5d20cc7a-09ad-4f19-93e0-f1a0b31e9bb5
5d20cc7a-09ad-4f19-93e0-f1a0b31e9bb5
5d20cc7a-09ad-4f19-93e0-f1a0b31e9bb5
EDGE
February 2013
Plus: Hospital OIG Hearing Loss 2013 Cardiology Sticky POS Double Dipping
BIGGER OPPORTUNITIES.
ICD-10-CM/PCS
(takes effect Oct.1, 2014)
2013
Draft
www.optumcoding.com www.optumcoding.com
2013
Draft
www.optumcoding.com
2013
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www.optumcoding.com
2013
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www.optumcoding.com
2013
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2013
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2013
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www.optumcoding.com
2013
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www.optumcoding.com
2013
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www.optumcoding.com
2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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2013
Draft
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2013
Draft
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
Draft
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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668%
INCREASE
ICD-9-CM
2013
Draft
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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2013
Draft
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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2013
Draft
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
A full suite of resources including the latest code set, mapping products, and expert training to help you make a smooth transition. www.optumcoding.com/ICD10
ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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2013
Draft
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
Draft
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
A full suite of resources including the latest code set, mapping products, and expert training to help you make a smooth transition. www.optumcoding.com/ICD10
ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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2013
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2013
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2013
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2013
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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2013
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2013
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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2013
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2013
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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2013
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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The Complete Ofcial Dr
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10
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ICD-10-CM
ICD-10-CM
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10
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ICD-10-CM
ICD-10-CM
ICD-10-CM
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
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ICD-10-CM
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ICD-10
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ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10-CM
The Complete Ofcial Draft Code Set
ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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ICD-10
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Contents
22
[Coding/Billing]
44
[Auditing/Compliance]
54
[Practice Management]
February 2013
[contents]
34
[Coding/Billing]
In Every Issue
7 Letter from the Chairman and CEO 9 Letter from Member Leadership 10 Kudos 12 AAPCCA 14 Letters to the Editor 14 Coding News
Special Features
29 AAPC Conference Guide 62 Minute with a Member
Features
16 Choose with Clarity Hearing Loss Equipment Codes
Marita Cable-Camilleis, CPC
Education
10 A&P Quiz 59 Newly Credentialed Members
Online Test Yourself Earn 1 CEU
Coming Up
Hospital Candidates Foot Amputations Compliance Professionals Fractures Therapy G Codes
On the Cover: Amy Lee Smith, MBA, CPC, CPC-H, CPMA, CIA, CRMA , infuses a dose of proper drug administration coding at the Infusion Center at Mary Immaculate Hospital (affiliated with Bon Secours Health System, Inc.) in Newport News, Va. Cover photo by Jennifer Terry Photography (www.jenniferterry.com).
www.aapc.com
February 2013
Be Green!
Why should you sign up to receive AAPC Cutting Edge in digital format? Here are some great reasons: You will save a few trees. You wont have to wait for issues to come in the mail. You can read AAPC Cutting Edge on your computer, tablet, or other mobile device -anywhere, anytime. You will always know where your issues are. Digital issues take up a lot less room in your home or office than paper issues. Go into your Profile on www.aapc.com and make the change!
February 2013
advertising index
Affymax, Inc. and Takeda Pharmaceuticals USA, Inc.........50 www.omontys.com AHA Central Office..........................................5 www.ahacentraloffice.com American Medical Association......................11 www.amabookstore.com CodingWebU.com. ............................................8 www.CodingWebU.com Contexo Media...............................................25 www.contexomedia.com HealthcareBusinessOffice, LLC.....................29 www.HealthcareBusinessOffice.com Ingenix is now OptumTM ..................................2
A leading health services business
Raemarie Jimenez, CPC, CPMA, CPC-I, CANPC, CRHC raemarie.jimenez@aapc.com Katherine Abel, CPC, CPMA, CPC-I, CMRS katherine.abel@aapc.com
Director of Publishing
Brad Ericson, MPC, CPC, COSC brad.ericson@aapc.com
Managing Editor
John Verhovshek, MA, CPC g.john.verhovshek@aapc.com
www.optumcoding.com Medicare Learning Network (MLN).............41 Official CMS Information for Medicare Fee-For-Service Providers http://www.cms.gov/MLNGenInfo NAMAS/DoctorsManagement................ 15, 64 www.NAMAS-auditing.com The Physicians Practice SOS Group............24
Taking the Business of Medicine to the Next Level
www.ppsosgroup.com The Coding Institute, LLC..............................57 www.SuperCoder.com ZHealth Publishing, LLC................................21 www.zhealthpublishing.com
Volume 24 Number 2
February 1, 2013
AAPC Cutting Edge (ISSN: 1941-5036) is published monthly by AAPC, 2480 South 3850 West, Suite B, Salt Lake City UT 84120-7208, for its paid members. Periodicals Postage Paid at Salt Lake City UT and at additional mailing office. POSTMASTER: Send address changes to: Cutting Edge c/o AAPC, 2480 South 3850 West, Suite B, Salt Lake City UT 84120-7208.
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February 2013
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t. Valentines Day, thanks to its Hallmark card association, is typically celebrated by exchanging cards, candy, and gifts. Being the researcher that I am (and that health care coders and billers are), I was curious to find out the story behind St. Valentine, and if he truly existed. I found out how this holiday became part of American culture.
AAPC members is apparent. Being a member saves me incalculable hours of work attempting to absorb the nuances of coding for psychiatry, working through nerve conduction study changes, and piecing together the elements of new evaluation and management (E/M) codes for transitional care management services. Calling on fellow AAPC members allows us to share ideas and our work load, and benefits our employers with a collaboration of many years of health care experience.
Cynthia Stewart, CPC, CPC-H, CPMA, CPC-I, CCS-P President, National Advisory Board
www.aapc.com February 2013 9
A&P QUIZ
By Rhonda Buckholtz, CPC, CPMA, CPC-I, CENTC, CGSC, COBGC, CPEDC
Test yourself to find out where your anatomy and physiology skills rank:
The physician documents that he removes a polyp found at 19 cm. What part of the colon is this considered? A. Anus B. Rectum C. Rectosigmoid D. Sigmoid The correct answer is on page 20.
Rhonda Buckholtz, CPC, CPMA, CPC-I, CENTC, CGSC, COBGC, CPEDC, is vice president of ICD-10 Training and Education at AAPC.
KUDOS
when she took the donation to the local Ronald McDonald House. She said, I had a little girl who looked so sick dressed up in a princess dress and tiara come up to me. She asked if I had drunk all that pop and beer by myself. We had a good laugh over that one. She gave me a hug and told me to thank the rest of those [coding] ladies for drinking so much! I went to my car and cried and laughed at the same time. The Minneapolis chapter invited attendees at Novembers AAPC state conference to pitch in and donate all of their pop tops. As a result, Dowling and her chapter collected quite a few pop tops at the event, and wound up with a 124-pound total for the year. Kudos to the charitable Dowling and her Minnesota AAPC colleagues!
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Chapter Life
Phoenix, Ariz.
In 2002, the Phoenix chapter lost one of their members, Germaine Steudler. The following year they honored her memory by supporting Community Alliance Against Family Abuse (CAAFA), an organization Steudler helped to start. The coders still collect household goods, clothing, and money to help support the shelter throughout the year. The Grand Canyon Coders have been recognized as one of CAAFAs supporters on the charitys website (www.caafaaz.org/Supporters.html).
Minneapolis, Minn.
In 2012, the Minneapolis local chapter participated in several charitable activities; two of these activities were organized by Louise Dowling, CPC . In the spring, Louise handed out dozens of little Ronald McDonald Cardboard Houses to members to collect pop tops. Members were encouraged to drop them off at chapter meetings for her to collect and deliver back to the charity. In all, 37.6 pounds of pop tops were collected after just two chapter meetings (read Kudos on page 10 for more information). The chapter also stepped up to donate 12 blankets and 65 towels for the Hennepin County Animal Shelter.
Cross, and the AAPC Chapter Association (AAPCCA) Hardship Scholarship Fund.
Tulsa, Okla.
Since 2005, the Tulsa, Okla. chapter (ProTulsa) has actively supported their local food bank, participating in the Backpack for Kids program, volunteering their time, collecting food items at meetings, and providing financial support. They have also collected teddy bears for local police departments and hospitals, who give them to children in abusive or other traumatic situations. In 2011, the chapter collected donations from members for the Society for the Prevention of Cruelty to Animals, the American Cancer Society, Alzheimers Association, American Red Cross, American Heart Association, and the Blood Bank of Tulsa. In 2012, ProTulsa continued their charitable work and also donated money to Project AAPC, the American Red
12 AAPC Cutting Edge
Gainesville, Ga.
The Gainesville, Ga. chapter supports the organization Challenged Child and Friends, which works to keep children with special needs in the mainstream by pairing them with other children in the community. At the chapters year-end party, members
photo by iStockphotohidesy
are encouraged to bring school supplies, learning toys, batteries, and any office supplies the organization needs.
Read the AAPC Local Chapter Handbook for more good advice and soon you will be on your way to becoming all you can be.
AAPCCA: Mentoring
By Judy A. Wilson, CPC, CPC-H, CPCO, CPC-P, CPPM, CPC-I, CANPC, CMRS
You can be a mentee, too. Everyone has an area that needs improvement, so heres an opportunity to get help from experts in the field. Becoming a mentee provides an opportunity to: Expand your knowledge in a certain field or specialty
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February 2013
13
Coding News
Ambulance Inflation Factored for 2013
The 2013 Ambulance Inflation Factor (AIF) has been released and went into effect Jan. 1. The Social Security Act (section 1834(l)(3) (B)) figures a yearly payment update based on the Urban Consumer Price Index (CPI-U) percentage increase for the 12-month period ending with June of the prior year. Prospective payment system and fee schedule update factors are adjusted by changes in economy-wide productivity, which are equal to the 10-year average of private, nonfarm business MultiFactor Productivity (MFP) annual changes. Medicare Part B coinsurance and deductible requirements apply to payments under the ambulance fee schedule. For 2013: MFP is 0.9 percent CPI-U is 1.7 percent AIF is 0.8 percent (The Affordable Care Act says the CPI-U is reduced by the MFP to get the AIF, even if it leads to a negative update.) See Centers for Medicare & Medicaid Services (CMS) transmittal 2620 for more information: www.cms.gov/Regulations-and-Guidance/ Guidance/Transmittals/Downloads/R2620CP.pdf. Here are few examples of changes made to CMS MSN message verbiage:
Receivables: $67,901 Credit Balance: - $4,521 (this is a negative number because it is money owed) Gross Charges: $587,857 (Total Receivables - Credits) / (Gross Charges / 365 Days) = Days in Accounts Receivable (A/R) or [$67,901 - (-$4,521)] / [$587,857 / 365 Days] = Days in A/R or $72,422 / $1,611 = 44.95 Days AAPC Cutting Edge
14
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Coding/Billing
V5095 Semi-implantable middle ear hearing prosthesis is for Vibrant Soundbridge (VSB), a semi-implantable electromagnetic hearing aid. Another middle ear implant, called Envoy Esteem, is fully implantable with no external components. This implant is also coded like the VSB semi-implant with CPT 69799 Unlisted procedure, middle ear. For an in-the-mouth (ITM) device called SoundBite, used for bone conductive loss, report L9900 Orthotic and prosthetic supply, accessory, and/or service component of another HCPCS L code. According to Consumer Reports (How To Buy a Hearing Aid, July 2009), you cannot truly compare hearing aids because no two people have the same kind of hearing loss (type, severity, and configuration). With so many hearing aidsclassified as monaural, binaural, and bilateralit is easier to keep track of them using a chart, like the one shown in Table A . If a patient is diagnosed as having unilateral hearing loss and one deaf ear, a choice of bilateral contra-lateral routing of signals (BICROS) may be appropriate. Contra-lateral routing of signals (CROS) is used when a patient has one ear with normal hearing and one deaf ear. One side of chart has the body-location variable and the other side lists hearing loss diagnosis variables mixed with manufacturers variables. Some hearing aids may be adjusted for high and/or low frequency hearing losses.
Not all assistive listening devices are specifically coded because of multi-functionality. Captioned telephones such as CapTel and CaptionCall may be included in the HCPCS Level II code V5274 Assistive listening device, not otherwise specified, or simply reported with V5268 Assistive listening device, telephone amplifier, any type. These
codes may also include hearing aid compatible smartphones. A modern digital hearing aid may have the ability to be controlled remotely by the patients cell phone. Some assisted listening devices have not yet been coded because they are geared more toward groups, rather than individuals. One example is the increasingly popular looping system that is more common in Great Britain and Scandinavia. In this setting, an electromagnetic wire is looped around a room (or a ticket booth) to the speaker microphone, so anyone nearby can turn on the telecoil (t-coil) switch of his or her custom-made hearing aid (or cochlear implant) to hear the speaker more clearly. Approximately 69 percent of all hearing aids have a t-coil, which can be turned on for hearingaid compatible phones with optional neck loops plugged in. T-coils (including related batteries, feedback-suppression capability, and directional microphones) are not currently specified in HCPCS Level II codes for hearing aids. Even a non-deaf person can hear better with a headphone and inductive loop receiver, which picks up signals from a loop system
Table A
CONDUCTIVE LOSS: MIXED LOSS:
while cutting off background noise. There are also personal loops just for television, which may be reported with V5270 Assistive listening device, television amplifier, any type.
Another system creates a public addresstype system with a wireless microphone, transmitting sound to receivers attached to loudspeakers and/or to those attached to hearing aids. For example, Inspiro is an FM transmitter for teachers to wear in the classroom, and the DynaMic is a cordless microphone designed to be used with it. To combine all three components (receiver(s), transmitter, and microphone), use V5281 Assistive listening device, personal FM/DM system, monaural, (1 receiver, transmitter, microphone), any type for one receiver or V5282 Assistive listening device, personal FM/DM system, binaural, (2 receivers, transmitter, microphone), any type for two receivers (one for each ear). Personal amplifiers (V5274), such as Pocketalkers, are useful when FM systems, infrared systems, and hearing loop (or induction loop) systems are not available.
Marita Cable-Camilleis, M.Ed., CPC, is treasurer of HLAAs Cape Cod chapter. She has severe hearing loss and has worn hearing aids since the age of three. She has done considerable research in the field of audiology.
BILATERAL CROS
DIGITAL PROGRAM
DIGITAL
BICROS
ANALOG
ANALOG
PROGRAM
DIGITAL
DISPOSABLE
SITE ON BODY
In the Mouth (ITM) Inner Ear: Cochlear Implant Middle Ear: Semi-implant (VSB) Completely In the Canal (CIC) In the Canal (ITC) L9900 L8690 L8691 L8614 L8619 V5095 V5242* V5248** V5243* V5249** In the Ear (ITE) V5050* V5130** Behind the Ear (BTE) V5060* V5140** Body Worn V5030* V5040* V5100*** V5120** In Eyeglasses Hearing Aids Not Classified Key: * = monaural ** = binaural V5070 V5080 V5150 V5298 *** = bilateral V5190 V5230 V5180 V5220 V5247* V5253** V5170 V5210 V5244* V5250** V5245* V5251** V5246* V5252** V5254* V5258** V5255* V5259** V5256* V5260** V5257* V5261** V5262* V5263** V5262* V5263** V5262* V5263** V5262* V5263**
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February 2013
17
Coding/Billing
he American Medical Association (AMA) was very busy last year, creating 74 new interventional radiology, endovascular, cardiac chamber, and coronary arterial interventional codes for 2013, while deleting 32 codes for many of the same types of procedures. Well focus on the chest drainage procedures and non-cardiac endovascular codes changes, which include retrieval of intravascular foreign body and thrombolysis.
Takeaways:
The AMA created 74 new interventional radiology, endovascular, cardiac chamber, and coronary arterial interventional codes and deleted 32 codes for many of the same types of procedures. These include intravascular FB removal and thrombolysis services. Differentiate separate from bundled thrombolysis services.
Note: Usually, a diagnostic angiogram is not necessary because broken catheters, lost coils, stents, and other intravascular foreign bodies are easily visible with fluoroscopy. Contrast injections are mostly used for guidance, as needed.
Coding/Billing: Endovascular
py, including follow-up catheter contrast injection, position change, or exchange, when performed; cessation of thrombolysis including removal of catheter and vessel closure by any method for the final day of therapy, when the infusion is concluded. If an infusion is three days or longer, 37213 will be repeated for each additional day that is not the initial or final day of treatment. Code 37213 cannot be reported the same day as 37211, 37212, or 37214. For a single day of therapy, only 37211 or 37212 may be reported for the thrombolysis. Do not report 37214 the same day as 37211 or 37212. Example 2: A 62-year-old patient has an ischemic right leg. Via left femoral arterial puncture, a contralateral sheath is placed into the right external iliac artery. Diagnostic angiography reveals acutely thrombosed right femoral-popliteal bypass graft with chronically occluded native superficial femoral artery (SFA) (75710 Angiography, extremity, unilateral, radiological supervision and interpretation). A thrombolysis catheter is advanced into the graft (36247 Selective catheter placement, arterial system; initial third order or more selective abdominal, pelvic, or lower extremity artery branch, within a vascular family) and catheterdirected thrombolytic infusion is initiated (37211). The patient is sent to ICU for monitoring. The patient is brought back later the same day. Followup imaging and catheter exchange for a longer infusion catheter is performed (no additional code because 37211 describes a single day of therapy). The patient is brought back on day two with imwww.aapc.com www.aapc.com February 2013 19
Coding/Billing: Endovascular
Thrombolysis infusion, follow-up angiography, and catheter exchanges performed on a single date of therapy (12 a.m. to 11:59 p.m.) are described by a single code.
aging performed, showing resolution of thrombus and an underlying 90 percent distal anastomotic stenosis. This is treated with a stent (37226 Revascularization, endovascular, open or percutaneous, femoral, popliteal artery(s), unilateral; with transluminal stent placement(s), includes angioplasty within the same vessel, when performed ). Excellent result is obtained. The sheath is removed (37214) for the final day of thrombolytic therapy. Note: If the entire procedure had been performed on a single day, you would not report 37214.
this catheter exchange is bundled with the new thrombolysis codes. Usually, after completion of the thrombolysis, an underlying cause (such as a stenosis) is identified. Treatment of that abnormality is additionally reported (e.g., angioplasty, atherectomy, stent placement). Mechanical arterial or venous thrombectomy may be reported in addition to prolonged thrombolysis infusion procedures. Codes 37184-37188 are used to describe these associated percutaneous thrombectomy procedures, when performed. Although the new codes for thrombolysis do simplify coding, it may be disappointing to the on-call physician who performs a follow-up angiogram and catheter exchange (both included with 37211, submitted earlier in the day) at 11:30 pm, and has nothing to code. Stay tuned: Next month, well review CPT 2013 changes to cervico-cerebral imaging.
David Zielske, MD, CPC-H, CIRCC, CCC, CCS, RCC, is an interventional radiologist and president of ZHealth Consulting and ZHealth Publishing in Brentwood, Tenn.
20
Coding/Billing
New Modifiers
Among the changes are seven new modifiers for Medicare reporting, which must be appended to HCPCS Level II codes G8978-G9176 (new for 2013) to describe a functional limitation (e.g., G8981G8983 Changing and maintaining body position functional limitation ). The modifiers describe the extent of the functional limitation.
CH CI CJ CK CL CM CN
0 percent impaired, limited or restricted At least 1 percent but less than 20 percent impaired, limited or restricted At least 20 percent but less than 40 percent impaired, limited or restricted At least 40 percent but less than 60 percent impaired, limited or restricted At least 60 percent but less than 80 percent impaired, limited or restricted At least 80 percent but less than 100 percent impaired, limited or restricted 100 percent impaired, limited or restricted
Coding/Billing: HCPCS II
Table 1
Trade Name
AMYVID Exparel Perjeta Voraxaze Eleyso Zaltrap EYLEA Nulojix Anascorp
drug-eluting stents, CMS designated new HCPCS Level II C codes to parallel the new CPT codes:
HCPCS = CPT
C9600 = 92920 C9601 = 92921 C9602 = 92924 C9603 = 92925 C9604 = 92937 C9605 = 92938 C9606 = 92941 C9607 = 92943 C9608 = 92944
Consult Table 3 on the next page for a list of other new HCPCS Level II codes, some of which were created to take the place of CPT codes for Medicare reporting. Another interesting code is Q9969 Tc-99m from non-highly enriched uranium source, full cost recovery add-on, per study dose, which is newly established to report Tc-99m from non-highly enriched uranium (HEU) sources. TC-99m is the most widely used radioisotope for diagnosing diseased organs. For 2013, CMS will make an additional payment of $10 to cover the marginal costs associated with non-HEU Tc-99m production. In some cases, newly-created CPT codes have taken the place of now-deleted HCPCS Level II codes. For example, Category III CPT code 0308T Insertion of ocular telescope prosthesis including removal of crystalline lens replaced C9732 for ocular telescope prosthesis with removal of crystalline lens, while many pathology procedures in the range S3711-S3860 have been deleted and replaced with new CPT codes describing molecular pathology and multianalyte assays with algorithmic analysis (e.g., 81200-81408, 81500-81512, 81599, and 86152-86153). Finally, V5267 has been revised to specify Hearing aid or assistive listening device/supplies/accessories, not otherwise specified, and 10 new codes have been added to describe personal FM/DM auditory devices, which are used with hearing aids to improve the signal-to-noise ratio, allowing the listener to hear better in the presence of background noise.
Mitosol Zortress
Erwinaze
Table 2
Product
MatriStem PSMX, RS, and PSM Memoderm, dermaspan, tranzgraft, or integuply Flex HD, Allopatch HD, or Matrix HD Epifix Grafix CORE Grafix PRIME hMatrix Mediskin Ez-Derm
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February 2013
23
Coding/Billing: HCPCS II
As always, there has been plenty of action when it comes to drug supply codes, as temporary codes transition to permanent status and new drugs are added.
HCPCS
C9733 G0452 G0453 G0454
CPT
N/A N/A 95941 N/A
Service
SPY and other non-ophthalmic fluorescent vascular angiography Molecular pathology procedure; physician interpretation and report Continuous intraoperative neurophysiology monitoring outside the operating room Physician documentation of face-to-face visit for durable medical equipment determination performed by nurse practitioner, physician assistant, or clinical nurse specialist Preparation with instillation of fecal microbiota by any method Phakic intraocular lens for correction of refractive error Treatment planning and care coordination management for cancer, initial Treatment planning and care coordination management for cancer, established patient with a change of regimen
S0354*
N/A
24
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21131
Coding/Billing
Lesser-used Modiers
Overlooking these modiers can result in improper reimbursement.
Takeaways:
HCPCS Level I modifiers are CPT modifiers. HCPCS Level II modifiers are developed by CMS. Both can be used with CPT codes. Both types of modifiers, when appended correctly, are excellent tools with which to tell the whole story of a procedure or service. Review the full set of modifiers in their entirety to ensure proper selection.
plied, there are a few exceptions. Among the most important are modifiers 63 Procedure performed on infants less than 4 kgs and 66 Surgical team.
Modifier 63
When a surgeon performs a procedure on an infant weighing less than 4 kg (4,000 g, or approximately 8.8 lbs), you may append modifier 63 to the CPT code to inform the payer of the increased complexity of the procedure due to the patients small size. At best, this could garner increased reimbursement. Be aware, however, that most CPT procedure codes performed on small infants include the notation, Do not report modifier 63 in conjunction with ... because the CPT code has already been valued to include this increased complexity. For example, see the parenthetical notation following 33502 Repair of anomalous coronary artery from pulmonary artery origin; by ligation and 33503 Repair of anomalous coronary artery from pulmonary artery origin; by graft, without cardiopulmonary bypass.
Although so-called CPT modifiers are generally familiar and often ap26 AAPC Cutting Edge
Modifier 66
Modifier 66 is applied when three or more
Coding/Billing: Modifiers
Level II includes quite a few modifiers beyond RT and LT that may be used within certain specialties to allow payment for multiple procedures that would otherwise appear to be duplicate billing.
surgeons complete parts of a procedure described by a single CPT code. Before solid organ transplantation codes were separated into codes for donor organ removal, backbench work, and recipient transplantation (e.g., the CPT section guidelines for Liver Transplantation), modifier 66 was appended to the transplant code to represent the separate surgical teams involved in each transplant stage. In the unusual situation, when there are three or more primary surgeons working on a procedure, ensure the medical necessity of multiple primary surgeons is documented. When submitting a claim with modifier 66, youll usually have to send the operative report, as well. Medicare and other payers that follow the National Correct Coding Initiative (NCCI), verify whether modifier 66 is allowed for the procedure by referring
to the Team Surgery column in the Medicare Physician Fee Schedule Relative Value File (downloadable from the CMS website: www.cms.gov/Medicare/Medicare-Fee-forService-Payment/PhysicianFeeSched/PFS-RelativeVal ue-Files.html).
extensor tendon, finger, primary or secondary; without free graft, each tendon), the coder would report 26418-F7, 26418-F8, and 26418-F9.
Fingers
FA Left hand, thumb F1 Left hand, second digit F2 Left hand, third digit F3 Left hand, forth digit F4 Left hand, fifth digit F5 Right hand, thumb F6 Right hand, second digit F7 Right hand, third digit F8 Right hand, forth digit F9 Right hand, fifth digit
Toes
TA Left foot, great toe T1 Left foot, second digit T2 Left foot, third digit T3 Left foot, forth digit T4 Left foot, fifth digit T5 Right foot, great toe T6 Right foot, second digit T7 Right foot, third digit T8 Right foot, forth digit T9 Right foot, fifth digit
Coronary Arteries
LC Left circumflex LD Left anterior descending RC Right coronary artery
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February 2013
27
Coding/Billing: Modifiers
The true value of a Level II modifier (in my humble opinion) lies with the modifiers that describe unusual payment situations.
number, and the charge is resubmitted with the correct provider number, you should append the appropriate CPT code with CC appended. GD Units of service exceeds medically unlikely edit value and represents reasonable and necessary services is used to override medically unlikely edits (MUEs), when appropriate. In 2007, Medicare implemented a set of MUEs that are applied to CPT codes to prevent reimbursement for more units of a service than are typically provided, but the edits may not apply in all circumstances. For example, a Medicare beneficiary may have required a total thyroidectomy to treat thyroid cancer, reported with 60252 Thyroidectomy, total or subtotal for malignancy; with limited neck dissection. Fifteen years later, the patient has a recurrence of thyroid cancer in a very small amount of retained thyroid tissue. The surgeon removes the remaining tissue, and should report the service with 60260 Thyroidectomy, removal of all remaining thyroid tissue following previous removal of a portion of the thyroid because the previous surgery was not technically a total thyroidectomy. But there is an MUE for total thyroidectomy because the total thyroid can be removed only once. In the case described, the second surgeon has a legitimate claim to override the MUE and to be paid for his service, and reports 60260-GD to describe the situation. You will likely have to submit an operative report and clearly document medical necessity, but the service should be reimbursed. GW Service not related to the hospice patients terminal condition is applied only for patients receiving hospice services. When a patient is in hospice care, physicians must report all services related to the hospice illness to the hospice provider. If the patient receives care for a non-related illness, append modifier GW to allow payment di28 AAPC Cutting Edge
rectly from the payer. For example, if a patient who is receiving hospice care at home for metastatic cancer is seen in a primary care office for an upper respiratory infection, the primary care office should report an evaluation and management (E/M) service with modifier GW.
Clinical Trials
Payers, particularly Medicare, often expect clinical research services to be identified on the claim with Q0 Investigational clinical service provided in a clinical research study that is in an approved clinical research study and Q1 Routine clinical service provided in a clinical research study that is in an approved clinical research study. These modifiers identify whether the services are part of routine care for the patients condition (care that would have been provided regardless of the research) or care that is not routine, and is part of the research.
ing the modifiers below, always verify with the billing office whether they are appropriate. CR Catastrophe/disaster related [may currently apply to superstorm Sandy services] CS Item or service related, in whole or in part, to an illness, injury, or condition that was caused by or exacerbated by the effects, direct or indirect, of the 2010 oil spill in the Gulf of Mexico, including but not limited to subsequent clean up activities ST Related to trauma or injury
Teaching Physicians
Coders in academic practices are very familiar with the GC, GE, and GR modifiers, and so should coders looking to make a career move to academic medicine. These modifiers describe services provided following Medicare or U.S. Department of Veterans Affairs (VA) rules for resident and attending physicians working together:
GC
This service has been performed in part by a resident under the direction of a teaching physician This service has been performed by a resident without the presence of a teaching physician under the primary care exception This service was performed in whole or in part by a resident in a department of veterans affairs medical center or clinic, supervised in accordance with VA policy
Surgical Misadventures
When it is appropriate to report (or internally track) a surgical misadventure, the coder should append the CPT code with one of the following:
PA PB PC
Surgical or other invasive procedure on wrong body part Surgical or other invasive procedure on wrong patient Wrong surgery or other invasive procedure on patient
GE
GR
Miscellaneous
The true value of a Level II modifier (in my humble opinion) lies with the modifiers describing unusual payment situations. The following are just a few examples: CA Procedure payable only in the inpatient setting when performed emergently on an outpatient who expires prior to admission. This modifier may be used when the hospital where the procedure was performed admits
Coding/Billing: Modifiers
a patient after a surgery is completed rather than before. FP Service provided as part of the annual family planning program is especially valuable when the patient only has Medicaid coverage for family planning. A coder may need to append GT Via interactive audio and video telecommunication systems for telehealth services. H9 Court-ordered notes services rendered due to a court order. HJ Employee assistance program is append-
ed for services provided as part of an employee assistance program. Large sections of Level II modifiers also apply to mental health services, durable medical equipment (DME), anesthesia, etc. Hopefully, this sampling of CPT and Level II modifiers will motivate you to review the two modifier sets in their entirety, ensuring proper reporting and appropriate reimbursement for your practice.
As with any code, policies for using modifiers may differ from payer to payer. Before applying any modifier, ensure the payer accepts the modifier and adhere to any published rules for its use.
Terri Brame, MBA, CHC, CPC, CGSC, CPCH, CPC-I , is the compliance education officer for the University of Arkansas for Medical Sciences. She is a past AAPC local chapter president, and has presented at two AAPC national conferences.
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Coding/Billing
Timely Tidbits:
For 2013, the American Medical Association (AMA) updated their CPT codebook to better explain the rules for timebased codes. The revised instructions can be found in the Introduction section of the CPT Professional Edition (page xii), under the subhead Time. The guidelines stipulate thatin the absence of specific instruction to the contrary (whether in a parenthetical reference, code-range-specific rules, or the code descriptor)there are five basic rules when reporting time-based services.
Takeaways:
The CPT 2013 codebook better defines time when length of time is not mentioned in the code. Five rules help define what codes should be reported when a length of time is not specified. Proper determination for length of time helps coding accuracy and eases revenue cycle management.
To be sure you are reporting all appropriate time, read all code descriptors and coding guidelines for the code category you are reporting.
troencephalographic (eg, 8 channel EEG) recording and interpretation, each 24 hours. For these codes, at least 12 hours of service must be documented to report the code. For services lasting fewer than 12 hours, you may need to append a modifier, such as modifier 52 Reduced services.
15 minutes, so you would report 99213. If, instead, the service lasted 22 minutes, the closest reference time is the 25 minutes of 99214, and you would report that code.
port the total units of time provided continuously. For instance, if intravenous hydration is given in the time described above, you would report 96360 Intravenous infusion, hydration; initial, 31 minutes to 1 hour once and +96361 Intravenous infusion, hydration; each additional hour (List separately in addition to code for primary procedure) twice.
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2. Therapeutic/Prophylactic/Diagnostic: See Table 1 for CPT codes to report for the administration of drugs and other substances (other than hydration). Do not report these codes for chemotherapy or other highly complex drugs/biological or when fluids are used to administer the drug(s); the fluid administration is incidental hydration and is not separately reportable. These codes are not reported by the physician in a facility setting. 3. Chemotherapy or other biologic agents/complex drugs: See Table 2 on the next page for appropriate CPT codes. Chemo includes other highly complex drugs or biologic agents such as: Non-radionuclide anti-neoplastic drugs Anti-neoplastic agents provided for treatment of non-cancer diagnoses Certain monoclonal antibody agents Other biologic response modifiers
Table 1: Diagnostic/Therapeutic/Prophylactic Infusion Codes CPT Code
96360
Use of these codes typically requires advanced practice training and competency; special considerations for preparation, dosage, or disposal; and usually entails significant patient risk and frequent monitoring far beyond that of therapeutic administrations. Physicians in the facility setting may not use chemotherapy codes. Report separate codes for each method of administration when chemotherapy is administered by different techniques. Medications administered independently as supportive management of chemotherapy are reported separately using 96360, 96361, 96365, or 96379, as appropriate. Along with three categories of drug administration, there are three methods by which drugs may be administered: 1. Injection: Do not use CPT 96372 Therapeutic, prophylactic, or diagnostic injection (specify substance or drug); subcutaneous or intramuscular for the administration of vaccines/toxoids. This code does not include injections for allergen immunotherapy. Although hospitals may report injection codes when the physi-
CPT Description
Intravenous infusion, hydration; initial, 31 minutes to 1 hour
Notes
Do not report if performed as concurrent infusion service; do not report hydration infusion of 30 minutes or less). Use for infusions of 31-90 minutes.
+96361
Intravenous infusion, hydration; each additional hour (List separately in addition to code for primary procedure) Intravenous infusion, for therapy, prophylaxis, or diagnosis (specify substance or drug); initial, up to 1 hour Intravenous infusion, for therapy, prophylaxis, or diagnosis (specify substance or drug); each additional hour (List separately in addition to code for primary procedure) Intravenous infusion, for therapy, prophylaxis, or diagnosis (specify substance or drug); additional sequential infusion of a new drug/substance, up to 1 hour (List separately in addition to code for primary procedure) Intravenous infusion, for therapy, prophylaxis, or diagnosis (specify substance or drug); concurrent infusion (List separately in addition to code for primary procedure)
Report for intervals of greater than 30 minutes beyond one-hour increments; also report for secondary or subsequent service after a different initial service through same IV access. Report for IV infusions of 16-90 minutes.
96365
+96366
Report for intervals of greater than 30 minutes beyond one-hour increments; also report for secondary or subsequent service after a different initial service through same IV access. Report in conjunction with 96365, 96374, 96409, or 96413 if provided as secondary service after a different initial service is administered through the same IV access. Report only once per sequential infusion of same infusate mix (multiple drugs mixed together in one bag is one infusate mix). Report only once per encounter. Report in conjunction with 96365, 96366, 96413, 96415, or 96416. Used for infusions running at the same time via the same IV accessmust be hung in separate bags.
+96367
+96368
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Cover: Coding/Billing
CPT Description
Chemotherapy administration, subcutaneous or intramuscular; non-hormonal anti-neoplastic Chemotherapy administration, subcutaneous or intramuscular; hormonal anti-neoplastic Chemotherapy administration; intravenous, push technique, single or initial substance/drug Chemotherapy administration; intravenous, push technique, each additional substance/drug (List separately in addition to code for primary procedure) Chemotherapy administration, intravenous infusion technique; up to 1 hour, single or initial substance/drug
Notes
96413
Report for infusions of 1690 minutes. Report 96361 to identify hydration as a secondary service through the same IV access. Report 96366, 96367, or 96375 to identify therapeutic infusion/injection as secondary service through same IV access.
+96415
Chemotherapy administration, intravenous infusion technique; each additional hour (List separately in addition to code for primary procedure) Chemotherapy administration, intravenous infusion technique; each additional sequential infusion (different substance/drug) up to 1 hour (List separately in addition to code for primary procedure)
Report in conjunction with 96413. Report for infusion intervals of greater than 30 minutes beyond one-hour increments. Report in conjunction with 96413. Report only once per sequential infusion. Report 96415 for additional hour(s) of sequential infusion.
+96417
cian is not present, physician offices may not. You may use injection codes to report non-antineoplastic hormonal therapy. 2. IV Push: CPT 96374 Therapeutic, prophylactic, or diagnostic injection (specify substance or drug); intravenous push, single or initial substance/drug is appropriate when intravenous (IV) push is the primary service. Add-on code +96375 Therapeutic, prophylactic, or diagnostic injection (specify substance or drug); each additional sequential intravenous push of a new substance/ drug (List separately in addition to code for primary procedure) may be reported with 96365, 96374, 96409, or 96413 to identify an IV push of a new drug when provided as a secondary service after a different initial service is administered through the same IV access. Add-on code +96376 Therapeutic, prophylactic, or diagnostic injection (specify substance or drug); each additional sequential intravenous push of the same substance/drug provided in a facility drug (List separately in addition to code for primary procedure) is used only when the same drug is administered twice in one encounter, but not within 30 minutes of each other. All of these IV push codes are reported for facilities only, and may be used for infusions lasting 15 minutes or less. 3. Infusion: Refer to Table 1 on the preceding page for infusion codes and their instructions. What makes your job so sticky is that these categories and methods can be combined in a number of different ways, all of which are coded differently.
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Cover: Coding/Billing
the actual chronological order of administration is not important for coding. The initial code is not necessarily the first service provided.
Table 3: Reporting infusion time Single infusion lasting: Can be coded (assuming documentation is complete):
IV push Initial hour Initial hour + 1 additional hour Initial hour + 2 additional hours Initial hour + 3 additional hours
15 minutes or less 16 - 90 minutes 91 - 150 minutes 151 - 210 minutes 211 - 270 minutes and so on
ing between 16 and 90 minutes. Only when an infusion lasts longer than 90 minutes can you code the additional hour code. Each additional hour means increments greater than 30 minutes over the initial hour. Do not include time spent keeping veins open (see Table 3 for examples).
The highest-ranking service provided is considered the initial service. For example, a patient comes into a hospital outpatient department for an antibiotic injection, but also receives a hydration infusion. The initial service is the antibiotic injection because the therapeutic injection ranks higher in the hierarchy than the hydration infusion.
Other Considerations
If a significant, separately identifiable evaluation and management (E/M) service is provided, report the appropriate E/M code with modifier 25 in addition to the infusion codes. A different diagnosis is not required; however, you cannot report 99211 Office or other outpatient visit for the evaluation and management of an established patient, that may not require the presence of a physician. Usually, the presenting problem(s) are minimal. Typically, 5 minutes are spent performing or supervising these services with infusion codes. If multiple infusions are administered, report only one initial service code, unless two separate IV sites are required. Per the Medicare Claims Processing Manual (chapter 4, section 230.2) as of 2007, only one initial service code can be reported per patient, per date of service, per separate IV access site. If there are multiple IV access sites, each site may be coded with an initial code and modifier(s), as appropriate, and must be supported by documentation in the record indicating it is medically reasonable and necessary for the drug or substance administrations to occur at separate intravenous access sites.
Amy Lee Smith, MBA, CPC, CPC-H, CPMA, CIA, CRMA , is a senior manager of internal audit with Bon Secours Health System, Inc., where she primarily performs coding and billing audits. She holds a bachelors and a masters degree in Business Administration with a concentration in finance from The College of William & Mary in Virginia. Ms. Smith is also a Certified Internal Auditor and certified in Risk Management Assurance.
Time Requirements
One of the biggest obstacles when coding drug administration is the common lack of documentation; start and stop times must be clearly and completely documented in the medical record by the clinician. The start time is normally well documented, but the stop time is quite often omitted. Check with your payer to see their requirements for these situations; some will accept a code for an IV push even if a stop time is not documented, while others will not. In general, an IV push code may be used for an infusion lasting 15 minutes or less (again, check with your payers for clarification). In drug administration terms, one hour means any infusion last-
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Coding/Billing
+33369 Cardiopulmonary bypass support for TAVR, central (eg, aorta, right atrium, pulmonary artery) cannulations
Here are some tips for applying these new codes correctly: The only currently approved device is the Sapien valve. Its indicated for patients with severe aortic stenosis who are not surgical candidates (determined by a cardiothoracic surgeon). The three add-on codes for cardiopulmonary bypass (C-P
38 AAPC Cutting Edge
bypass), when performed, are also based on approach. Only one C-P bypass code is submitted during TAVR. Open femoral (34812) and open brachial access (34834) are included in the TAVR codes. Temporary pacemaker placement for rapid pacing during TAVR, as well as catheter placements and balloon valvuloplasty, are included. Swan-Ganz placement and aortic/left ventricular (LV) measurements and imaging to guide and complete the TAVR are included. If a complete heart catheterization is performed, you may report it if no prior diagnostic study was performed or a suboptimal study is documented, or if there has been a clinical change in the patient since the prior study or during the procedure. Code for other percutaneous coronary/cardiac interventions that are performed and medically indicated. You may code for ventricular assist device or intra-aortic balloon pump (33990, 33991, 33967, 33970), if performed. TAVR requires two physicians to complete the procedure. Codes 33361-33365 and 0318T Implantation of catheterdelivered prosthetic aortic heart valve, open thoracic approach,
Coding/Billing: Cardiology
TAVR requires two physicians to complete the procedure. Codes 3336133365 and 0318T require modifier 62 for physician billing.
(eg, transapical, other than transaortic) require modifier 62 Two surgeons for physician billing. For example, each physician would report 33361-62 for a percutaneous TAVR. The C-P bypass codes do not have this requirement. Example: An elderly patient with severe aortic stenosis, who is not a surgical candidate, presents for a TAVR procedure. This is performed with C-P bypass via femoral cut-downs and rapid pacing with a temporary pacer. The TAVR is performed via percutaneous approach. Correct codes would be:
33361 Transcatheter aortic valve replacement (TAVR/TAVI) with
prosthetic valve; percutaneous femoral artery approach
puncture and removes oxygenated blood from the left LA back to the TandemHeart device (external on patient), and then returns it into a second catheter, placed usually via the femoral artery. You may report 34812 Open femoral artery exposure for delivery of endovascular prosthesis, by groin incision, unilateral when an open arterial exposure is performed to accommodate the larger catheters used in percutaneous VADs. Routine closure of artery is not reported separately. Removal and repositioning codes can only be used when at a different encounter. If on the same date of service but a different encounter, append modifier 59 Distinct procedural service to either 33992 Removal of percutaneous ventricular assist device at separate and distinct session from insertion or 33993 Repositioning of percutaneous ventricular assist device with imaging guidance at separate and distinct session from insertion.
Follow these tips for proper coding: VADs are for use in patients with impaired LV function. The new aforementioned codes are for percutaneous VADs. Impella device is via arterial access only, with a single catheter that forcefully removes blood from the LV via the distal portion of the catheter and discharges it into the proximal aorta. TandemHeart device has both venous and arterial access. The venous catheter is placed into the LA via a transseptal
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Coding/Billing: Cardiology
If VAD is placed prophylactically for an intervention and removed at its conclusion, do not report 33992. Repositioning of a percutaneous VAD without imaging guidance is not a reportable procedure. If an existing VAD is removed and replaced with a new VAD, code this as a new device placement. Do not report 33992 because the removal is bundled into the new device placement code.
Electrophysiology Ablations
Electrophysiology ablation codes 93651 and 93652 are deleted. New abbreviated versions of the codes are:
93653 Comprehensive electrophysiologic (EP) evaluation with ablation of supraventricular tachycardia (SVT)
93656 Comprehensive EP evaluation with ablation of atrial fibrillation via pulmonary vein isolation
Use these helpful tips for proper EP ablation coding: The five new ablation codes all include a diagnostic EP study at the time of ablation. Do not submit any combination of 93653, 93654, and 93656 together. If an additional mechanism is ablated, use add-on code +93655 or +93657. With ablation of SVT (93653), you may report mapping (+93609 Intraventricular and/or intra-atrial mapping of tachycardia site(s) with catheter manipulation to record from multiple sites to identify origin of tachycardia (List separately in addition to code for primary procedure) or +93613 Intracardiac electrophysiologic 3-dimensional mapping (List separately in addition to code for primary procedure)), transseptal procedure (+93462 Left heart catheterization by transseptal puncture through intact septum or by transapical puncture (List separately in addition to code for primary procedure)), and LV pacing/ recording (+93622 Comprehensive electrophysiologic evaluation
40 AAPC Cutting Edge
including insertion and repositioning of multiple electrode catheters with induction or attempted induction of arrhythmia; with left ventricular pacing and recording (List separately in addition to code for primary procedure)), when performed. Ablation of VT (93654) includes 3-D mapping (93613) and LV pacing/recording (93622), when performed. You can report transseptal procedure (93462), when performed. Pulmonary vein isolation for a-fib (93656) includes the transseptal procedure (93462) and LA pacing/recording (+93621 Comprehensive electrophysiologic evaluation including insertion and repositioning of multiple electrode catheters with induction or attempted induction of arrhythmia; with left atrial pacing and recording from coronary sinus or left atrium (List separately in addition to code for primary procedure)), when performed. You can report mapping (93609 or 93613) and LV pacing/recording, when performed. There is a gray zone regarding 93623; CPT states this code may be reported with 93656, but National Correct Coding Initiative (NCCI) Version 19.0 states not to report 93623 with any of the new ablation codes.
If thats goal #1, then start with the right tools. The Medicare Learning Network (MLN) develops informational resources just for Medicare Fee-For-Service providers. Billing errors can prevent physicians from receiving timely and proper reimbursement for common medical and surgical procedures. For example, the CMS Comprehensive Error Rate Testing (CERT) Program cites that a number of errors relate to non-compliance with Medicare coverage, coding, and billing rules. Evaluation and Management (E/M) Services: Complying with Documentation Requirements is an MLN educational tool. It describes common CERT Program errors and provides information on the documentation needed to support certain claims to Medicare. More learning starts now. Visit http://go.cms.gov/EM-Services.com
Coding/Billing: Cardiology
Defibrillation threshold testing (DFT testing) involves induction of arrhythmia and evaluation of sensing and pacing for arrhythmia termination, as well as reprogramming as necessary.
Add-on code +93655 may be reported with 93653, 93654, or 93656, when performed. Add-on code +93657 may be reported only with 93656, when performed. Some of the parentheticals may need updating. For example, a parenthetical note instructs you to use +93622 only with 93620, but the CPT introductory section states +93622 may be added to 93653. Likewise, only 93620 may be used with 93621, per a parenthetical note following 93621. Example: A patient presents with atrial fibrillation. A complete EP study is performed, followed by a transseptal puncture under intracardiac echocardiography (ICE) into the LA. A 3-D map is created, followed by ablations performed to achieve pulmonary vein isolation. After this was done, there was evidence of continued a-fib and a decision was made to perform additional right atrial ablations. The a-fib then ceased. The correct coding in this case is:
93656 93662 Intracardiac echocardiography during therapeutic/diagnostic intervention, including imaging supervision and interpretation (List separately in addition to code for primary procedure)
0325T Repositioning of electrode and/or generator 0326T EP evaluation (defibrillation threshold testing) 0327T Interrogation of device 0328T Programming of device with iterative adjustments
93613 +93657
Note: Do not code for the EP study (93620) or transseptal procedure (93462); they are included in 93656.
This is a newer type of defibrillator for treatment of arrhythmias that is totally implanted in the subcutaneous tissues, including the defibrillating lead. To apply the above codes, follow these tips: The generator and one lead are placed subcutaneously. This allows for easier insertion over traditional transvenous insertion of electrode, and results in fewer potential complications, such as venous stenosis and infected leads within the heart because the lead is in the subcutaneous tissues. This system does not allow pacing, as in a conventional defibrillator. To report removal of an existing subcutaneous lead and generator plus replacement with a new system, report 0322T, 0324T, and 0319T. At generator end of life, report replacement with 0323T when the depleted generator is removed and a new generator is inserted. Use the repositioning code 0325T when performed repositioning of an electrode and/or generator occurs at a different encounter than at the original insertion. Defibrillation threshold testing (DFT testing) involves induction of arrhythmia and evaluation of sensing and pacing for arrhythmia termination, as well as reprogramming as necessary, and is reported with 0326T. Report 0327T and 0328T at a different encounter than at the original placement for interrogation or programming of S-ICD (this is not DFT testing).
Coding/Billing: Cardiology
The removal of an existing IMD system and replacement with a new system is reported by the single code
Finally, youll find new Category III codes for left atrial hemodynamic monitor. Easier-to-follow abbreviated descriptions are:
0293T Insertion of LA hemodynamic monitor, complete with module and pressure sensor lead
0305T Programming of device with iterative adjustment 0306T Interrogation of device 0307T Removal of IMD system
This system monitors LA pressures to identify changes in patients with heart failure to allow potential earlier treatment. Tips to apply these codes correctly include: You may use the above codes alone, or when inserted into combination-type defibrillator devices. Transseptal code 93462 is bundled with these codes, as is ICE (93662). Use 0294T with 33230 Insertion of pacing cardioverterdefibrillator pulse generator only; with existing dual leads, 33231 Insertion of pacing cardioverter-defibrillator pulse generator only; with existing multiple lead, 33240 Insertion of pacing cardioverter-defibrillator pulse generator only; with existing single lead, 33262-33264 Removal of pacing cardioverter-defibrillator pulse generator with replacement of pacing cardioverter-defibrillator pulse generator , and 33249 Insertion or replacement of permanent pacing cardioverterdefibrillator system with transvenous lead(s), single or dual chamber.
David Dunn, MD, FACS, CIRCC, CPC-H, CCC, CCVTC, is vice president of ZHealth. He oversees physician coding and instructs ZHealth educational programs, and contributes to Dr. Zs Medical Coding Series. A graduate of Texas A&M University, he completed his M.D. at the University of Texas, his surgical residency at Scott & White Hospital, and his vascular surgery fellowship at Baylor College of Medicine. A diplomat of the American Board of Surgery, Dr. Dunn is also certified in vascular surgery. He is a fellow of the American College of Surgeons and a member of the Southern Association for Vascular Surgery. He is president-elect of the AAPC National Advisory Board.
IMD (AngelMed Guardian system) consists of an electrode placed into the right ventricle and a device. It monitors electrocardiogram signals for acute ST elevation changes and warns the patient via vibratory and auditory alerts. This allows the patient to potentially seek earlier treatment of impending ischemic events. Consider these tips when applying the above codes: The removal of an existing IMD system and replacement with a new system is reported by the single code, 0302T. Report codes 0305T and 0306T at a different encounter than at original placement for interrogation or programming of IMD.
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Auditing/Compliance
Double Dip Do
The second meaning of double dip is to use a single statement in the documentation of an E/M service more than once when determining the level of service provided. Contrary to what you may have heard, this type of double dipping can be appropriate, if done correctly. First, some background: Way back in December 1997, Barton C. McCann, MD, publicly remarked that when selecting an E/M service level, you cannot use one statement to count as two elements. McCann was not just any physician: He was executive medical officer of the Health Care Finance Administration (precursor to the Centers for Medicare & Medicaid Services), and his instructions mattered greatly to coders, payers, and health care regulators. McCanns intended meaning is that you cannot use a single documented item twice within the same component of the E/M service. For instance, if the physician documents pain since last Tuesday, you cannot count that statement in the history of present illness (HPI) as timing and duration. Its one or the other, but not both. Similarly, if the physician records no back pain, you cant count that statement in the review of systems (ROS) as relevant to both musculoskeletal and neurological body systems. In other words, you shouldnt use the same statement twice within the history or within the ROS. Thats your third legitimate dont. Taken in context, McCanns pronouncement about the inappropriateness of this type of double dipping was neither sensational nor controversial. Unfortunately, his words were immediately taken out of context and applied much more broadly to re-
photo by iStockphotoPannonia
flect a meaning he never intended. Specifically, McCanns statement was interpreted to mean that a single item could not apply to both the HPI and ROS. For example, suppose a patient presents with chest pain with dyspnea. Under the mistaken interpretation of McCanns statement, you would not be able to count the documentation as location and associated signs and symptoms in the history and as relevant to the respiratory system in the ROS.
Despite McCanns clarification, the you cant use the same documented item in both the history and ROS trope spread far and wide, and was repeated so often that it has been accepted as truth.
agement Services state that you cannot count a single item in both the history and ROS. Nothing in the American Medical Association (AMA) or national Medicare guidelines says so, either. And the man who is mistakenly credited with having said it was so has publicly stated that it isnt. Any payer or auditor who continues to insist on the validity of the double dip urban myth ought to know better, and should be challenged. The Truth Part 2: As long as an item is clearly documented, you may count it in both the history and ROS. Repetition of data is not required as long as it is appropriately referred to. Returning to our earlier example of the patient with documented chest pain with dyspnea, you may count dyspnea as both an associated sign/symptom for the HPI and for respiratory ROS (but you should not count chest pain for both cardiovascular and musculoskeletal systems in the ROS). But (and this is a big but), if a patient shows up with only one complaint, you shouldnt use that single complaint for both the history and ROS. Rather, you should look for documented evidence that the physician dug deeper to find more information to assist him or her in identifying what is wrong with the patient and how to treat it (in other words, you should be sure that the physician truly did provide an ROS). For example, if the patient presents with abdominal pain, and thats all the physician documents, you shouldnt report that single item in the history and ROS. But documentation of abdominal pain, no nausea means the physician asked additional questions beyond the presenting problem, which makes using the item in both the history and ROS acceptable. Similarly, documentation of cough alone isnt sufficient to count for both history and ROS; however, cough one week, no expectoration, moderate shortness of breath provides plenty of detail to support both the history and ROS elements. The bottom line: If the physician looks beyond the presenting problem, performing additional work to expand on the problem identified in the chief complaint and HPI, you may double dip and count a single element in both the history and ROS. Doing so is not only legitimate, it may mean the difference between, for example, a level III and a level IV E/M code assignment.
G.J. Verhovshek, MA, CPC, is managing editor at AAPC.
Despite McCanns clarification, the you cant use the same documented item in both the history and ROS trope spread far and wide, and was repeated so often that it has been accepted as truth. In fact, this (mis)understanding has become one of the greatest coding urban legends. And because payers and auditors do have freedom in how they apply documentation guidelines, some have, indeed, chosen to interpret the rules to mean a single item cannot be used in both the history and ROS. The Truth Part 1: There are no requirements for documented patient information to be stated or written in any specific format. Neither the 1995 or 1997 Documentation Guidelines for Evaluation and Man-
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Auditing/Compliance
Facility
Each October, the Office of Inspector General (OIG) reports on compliance issues it plans to monitor most closely in the new year. This information provides a road map your organization can use to develop a compliance audit plan for the year ahead. In reviewing the OIGs areas of concern for hospitals, you might catch potential noncompliance in your workplace, allowing you to take corrective action to reduce risk of Medicare and Medicaid fraud.
DRG Window
The Medicare program currently bundles all outpatient services delivered three days prior to an inpatient hospital admission. The Medicare program does not pay separately for these preadmission services when they are delivered in a setting owned or operated by the admitting hospital. This policy is commonly known as the DRG window, and prior OIG work identified improper payments in the DRG window. This study was developed to analyze claims data to determine how much CMS could save if it bundled outpatient services delivered up to 14 days prior to an inpatient hospital admission into the MS-DRG payment. To evaluate these DRG window payments,
photo by iStockphotocourtneyK
Hospitals should examine their provider-based clinics to determine if they are billing properly.
ine their provider-based clinics to determine if they are billing properly. If your facility has physician practices that do not meet the criteria for provider-based clinic billing, its critical these services are not billed as provider-based. diem rate if the patient was discharged to a swing bed in another hospital. This review will allow the OIG and CMS to examine swing bed policy to determine if a change in reimbursement policies should be made. with MCC has a relative weight of 1.8803. MS-DRG 870 Septicemia with mechanical ventilation, 96+ hours has a relative weight of 5.8399. This significant difference in relative weight will obviously result in a higher payment to the facility for mechanical ventilation services. Review any clinical documentation you have for mechanical ventilation in your facility: Are there areas for improving time recording? Are the minimum standards being met for the MS-DRG grouping 96hour rule?
for physician related-items read Get a Jump on 2013 Government Reviews on pages 48-49 of Januarys Cutting Edge.
Jillian Harrington, MHA, CPC, CPC-P, CPC-I, CCS-P, serves as a clinical technical editor for OptumInsight, and has nearly 20 years of experience in the health care industry. She is a former chief compliance officer and chief privacy official. She teaches CPT coding as an approved AAPC instructor, and is a former member of AAPCs ICD10 curriculum development team. She holds a bachelors degree in health care administration from State University of New York - Empire State College and a masters degree in health systems administration from the Rochester Institute of Technology.
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February 2013
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Auditing/Compliance
Coding Compass
e sure your place-of-service (POS) code matches the setting where the patient received the service (for faceto-face services), or the setting where the technical portion of the service was delivered (for non-face-to-face services, such as diagnostic test result interpretation). Although this may sound easy in theory, new Medicare guidance can make POS assignment tricky. In recent transmittal 2563, change request (CR) 7631, the Centers for Medicare &
48 AAPC Cutting Edge
Medicaid Services (CMS) clarified guidance for assigning POS codes on Medicare claims. That guidance has posed new questions that should be addressed regarding these claims. One of those questions came to light through Cynthia Stewart, CPC, CPC-H, CPMA, CPC-I, CCS-P, when she used the following coding scenario to point out discrepancies when reporting in compliance to the new POS reporting rules: An inpatient is transported to an outpa-
Attempting to avoid the denial by reporting an inpatient E/M service that was not performed, especially where that code results in the physician obtaining additional reimbursement, is not recommended.
spective of the setting where the patient actually receives the face-to-face encounter. In other words, reporting the inpatient hospital POS code 21 is a minimum requirement for purposes of triggering the facility payment under the PFS when services are provided to a registered inpatient. If the physician/practitioner is aware of the exact setting the beneficiary is a registered inpatient, the appropriate inpatient POS code may be reported consistent with the code list annotated in this section (instead of POS 21). For example, a physician/practitioner may use POS 31, for a patient in a SNF receiving inpatient skilled nursing care, POS 51, for a patient registered in a Psychiatric Inpatient Facility, and POS 61 for patients registered in a Comprehensive Inpatient Rehabilitation Facility. According to this provision, I see the issue where a physician performing an E/M service in an office setting for a patient who is currently a registered inpatient at a facility (and transported to the office location) would be required to report POS 21 for any physician service or procedure performed. The problem this instruction potentially creates is that while there is a facility payment rate for an outpatient E/M service, some carriers may not process a payment for an outpatient E/M service (e.g., 9920199215) when billed with POS 21 consistent with this rule. Where payment is denied, the provider is forced to appeal and validate that reporting is accurate under the above rule, consistent with the following revised instructions to the Medicare administrative carrier (MAC): 10.6 - Carrier Instructions for Place of Service (POS) Codes (Rev.2563, Issued: Oct.11, 2012, Effective: April 1, 2013)
For purposes of payment under the Medicare Physician Fee Schedule (MPFS), the POS code is generally used to reflect the actual setting where the beneficiary receives the face-to-face service. For example, if the physicians face-toface encounter with a patient occurs in the office, the correct POS code on the claim, in general, reflects the 2-digit POS code 11 for office. In these instances, the 2-digit POS code (Item 24B on the claim Form CMS-1500) will match the address and ZIP entered in the service location (Item 32 on the 1500 Form) the physical/geographical location of the physician. However, there are two exceptions to this general rule these are for a service rendered to a patient who is a registered inpatient or an outpatient of a hospital. In these cases, the correct POS code regardless of where the faceto-face service occurs is that of the appropriate inpatient POS code (at a minimum POS code 21) or that of the appropriate outpatient hospital POS code (at a minimum POS code 22) as discussed in section 10.5 of this chapter. So, if in the above example, the patient seen in the physicians office is actually an inpatient of the hospital, POS code 21, for inpatient hospital, is correct. In this example, the POS code reflects a different setting than the address and ZIP code of the practice location (the physicians office).* * Medicare Claims Processing Manual, Internet Only Manual (IOM), pub 100-4, chapter 26, section 10.6 (emphasis added). Although it is time consuming to appeal such denials, I have to assume that Medicare administrative contractors will eventually fix their payment systems to comply with this instruction, which is not yet updated in the processing manual on the CMS IOM website. The other option would be for the physician to go to the hospital to do the E/M and pro-
cedure work. Then, and only then, could the physician bill the inpatient codebecause only in that case is an inpatient E/M service provided. A word of caution: Nothing in the above instruction suggests or implies that it would be reasonable to interpret the change as instructing a provider to report an inpatient E/M code for an E/M service performed in an outpatient setting. It merely instructs the provider to use POS code 21 (or a more specific code, where the exact facility status is known) when the outpatient E/M service or other procedure is performed on a patient that is a current registered inpatient at a hospital. Note that the location of the service in block 32 would be the physicians office and ZIP code. I suspect carriers will reprogram their claims processing systems soon to deal with this payment problem, where it exists. Attempting to avoid the denial by reporting an inpatient E/M service that was not performed, especially where that code results in the physician obtaining additional reimbursement, is not recommended. Even if paid, the provider would have to disclose and refund the overpayment within 60 days, consistent with the reverse false claims provision of the False Claims Act and the draft implementing regulations.
Michael D. Miscoe, Esq., CPC, CASCC, CUC, CCPC, CPCO, CHCC, has a Bachelor of Science degree from the U.S. Military Academy, a Juris Doctorate degree from Concord Law School, is president of Practice Masters, Inc., and founding partner of Miscoe Health Law, LLC. He is a past member of AAPCs National Advisory Board and a current member of the Legal Advisory Board. He is admitted to the Bar in California and to practice law before the U.S. District Courts in the Southern District of California and the Western District of Pennsylvania. He has nearly 20 years of experience in health care coding and over 15 years as a coding and compliance expert testifying in civil and criminal cases. He is a national speaker and has been published in numerous national publications.
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February 2013
49
J0890
ESA administration
Consider the first once-monthly, non-EPO ESA offering less-frequent dose administration.
INDICATION AND LIMITATIONS OF USE
OMONTYS (peginesatide) Injection is indicated for the treatment of anemia due to chronic kidney disease (CKD) in adult patients on dialysis. OMONTYS is not indicated and is not recommended for use in patients with CKD not on dialysis, in patients receiving treatment for cancer and whose anemia is not due to CKD, or as a substitute for red blood cell (RBC) transfusions in patients who require immediate correction of anemia. OMONTYS has not been shown to improve symptoms, physical functioning, or health-related quality of life. increased risk for death and serious adverse cardiovascular reactions including myocardial infarction and stroke was observed. There is increased mortality and/or increased risk of tumor progression or recurrence in patients with cancer receiving ESAs. In controlled clinical trials of ESAs, ESAs increased the risk of death in patients undergoing coronary artery bypass graft surgery (CABG) and deep venous thrombosis (DVT) in patients undergoing orthopedic procedures. In 2 trials of OMONTYS (peginesatide) Injection, patients with CKD not on dialysis experienced increased specific cardiovascular events. Hypertension (see Contraindications): Appropriately control hypertension prior to initiation of and during treatment with OMONTYS. Reduce or withhold OMONTYS if blood pressure becomes difficult to control. Serious allergic reactions (see Contraindications): Serious allergic reactions have been reported with OMONTYS. Immediately and permanently discontinue OMONTYS and administer appropriate therapy if a serious allergic reaction occurs. Lack or loss of response to OMONTYS: Initiate a search for causative factors. If typical causes of lack or loss of hemoglobin response are excluded, evaluate for antibodies to peginesatide. Dialysis management: Patients receiving OMONTYS may require adjustments to dialysis prescriptions and/or increased anticoagulation with heparin to prevent clotting of the extracorporeal circuit during hemodialysis. Laboratory monitoring: Evaluate transferrin saturation and serum ferritin prior to and during OMONTYS treatment. Administer supplemental iron therapy when serum ferritin is less than 100 mcg/L or when serum transferrin saturation is less than 20%. Monitor hemoglobin every 2 weeks until stable and the need for RBC transfusions is minimized. Then, monitor monthly. Adverse reactions Most common adverse reactions in clinical studies in patients with CKD on dialysis treated with OMONTYS were dyspnea, diarrhea, nausea, cough, and arteriovenous fistula site complication.
03-12-00277-A.; 24102. 2012 Affymax, Inc. and Takeda Pharmaceuticals America, Inc. All rights reserved. Affymax, the Affymax logo, OMONTYS, and the OMONTYS logo are trademarks of Affymax, Inc. and/or its subsidiaries. Takeda and the Takeda logo are trademarks of Takeda Pharmaceutical Company Limited registered with the U.S. Patent and Trademark Office and used under license by Takeda Pharmaceuticals America, Inc.
Table 2 Adverse Cardiovascular Outcomes in Randomized Controlled Trials Comparing Higher and Lower Hemoglobin Targets in Patients With CKD
Population BRIEF SUMMARY OF FULL PRESCRIBING INFORMATION OMONTYS (peginesatide) Injection for intravenous or subcutaneous use WARNING: ESAs INCREASE THE RISK OF DEATH, MYOCARDIAL INFARCTION, STROKE, VENOUS THROMBOEMBOLISM, THROMBOSIS OF VASCULAR ACCESS AND TUMOR PROGRESSION OR RECURRENCE. Chronic Kidney Disease: In controlled trials, patients experienced greater risks for death, serious adverse cardiovascular reactions, and stroke when administered erythropoiesisstimulating agents (ESAs) to target a hemoglobin level of greater than 11 g/dL. No trial has identified a hemoglobin target level, ESA dose, or dosing strategy that does not increase these risks [see Warnings and Precautions]. Use the lowest OMONTYS dose sufficient to reduce the need for red blood cell (RBC) transfusions [see Warnings and Precautions]. INDICATIONS AND USAGE Anemia Due to Chronic Kidney Disease OMONTYS is indicated for the treatment of anemia due to chronic kidney disease (CKD) in adult patients on dialysis. Limitations of Use OMONTYS is not indicated and is not recommended for use: In patients with CKD not on dialysis because of safety concerns in this population [see Warnings and Precautions]. In patients receiving treatment for cancer and whose anemia is not due to CKD, because ESAs have shown harm in some settings and the benefit-risk factors for OMONTYS in this setting have not been evaluated [see Warnings and Precautions]. As a substitute for RBC transfusions in patients who require immediate correction of anemia. OMONTYS has not been shown to improve symptoms, physical functioning or health-related quality of life. CONTRAINDICATIONS OMONTYS is contraindicated in patients with: Uncontrolled hypertension [see Warnings and Precautions]. Serious allergic reactions to OMONTYS [see Warnings and Precautions]. WARNINGS AND PRECAUTIONS Increased Mortality, Myocardial Infarction, Stroke, and Thromboembolism In controlled clinical trials of other ESAs in patients with CKD comparing higher hemoglobin targets (13 - 14 g/dL) to lower targets (9 - 11.3 g/dL) (see Table 2), increased risk of death, myocardial infarction, stroke, congestive heart failure, thrombosis of hemodialysis vascular access, and other thromboembolic events was observed in the higher target groups. Using ESAs to target a hemoglobin level of greater than 11 g/dL increases the risk of serious adverse cardiovascular reactions and has not been shown to provide additional benefit. Use caution in patients with coexistent cardiovascular disease and stroke. Patients with CKD and an insufficient hemoglobin response to ESA therapy may be at even greater risk for cardiovascular reactions and mortality than other patients. A rate of hemoglobin rise of greater than 1 g/dL over 2 weeks may contribute to these risks. In controlled clinical trials of ESAs in patients with cancer, increased risk for death and serious adverse cardiovascular reactions was observed. These adverse reactions included myocardial infarction and stroke. In controlled clinical trials, ESAs increased the risk of death in patients undergoing coronary artery bypass graft surgery (CABG) and deep venous thrombosis (DVT) was observed in patients undergoing orthopedic procedures. The design and overall results of 3 large trials comparing higher and lower hemoglobin targets are shown in Table 2 (Normal Hematocrit Study (NHS), Correction of Hemoglobin Outcomes in Renal Insufficiency (CHOIR) and Trial to Reduce Cardiovascular Events with Aranesp Therapy (TREAT)).
Patients with CKD Patients with CKD on Patients with not on dialysis with hemodialysis with CKD not on dialysis coexisting CHF or hemoglobin < 11 g/dL with type II diabetes, not previously CAD, hematocrit hemoglobin administered 30 3% on 11 g/dL epoetin alfa epoetin alfa 14.0 vs. 10.0 12.6 (11.6, 13.3) vs. 10.3 (10.0, 10.7) All-cause mortality or non-fatal MI 13.5 vs. 11.3 13.0 (12.2, 13.4) vs. 11.4 (11.1, 11.6) All-cause mortality, MI, hospitalization for CHF, or stroke 1.34 (1.03 1.74) All-cause mortality 1.48 (0.97 2.27) 13.0 vs. 9.0 12.5 (12.0, 12.8) vs. 10.6 (9.9, 11.3) All-cause mortality, MI, myocardial ischemia, heart failure, and stroke 1.05 (0.94 1.17) Stroke 1.92 (1.38 2.68)
Hemoglobin Target; Higher vs. Lower (g/dL) Median (Q1, Q3) Achieved Hemoglobin level (g/dL) Primary Endpoint Hazard Ratio or Relative Risk (95% CI) Adverse Outcome for Higher Target Group Hazard Ratio or Relative Risk (95% CI)
Patients with Chronic Kidney Disease Not on Dialysis OMONTYS is not indicated and is not recommended for the treatment of anemia in patients with CKD who are not on dialysis. A higher percentage of patients (22%) who received OMONTYS experienced a composite cardiovascular safety endpoint event compared to 17% who received darbepoetin alfa in two randomized, active-controlled, open-label, multi-center trials of 983 patients with anemia due to CKD who were not on dialysis. The trials had a pre-specified, prospective analysis of a composite safety endpoint consisting of death, myocardial infarction, stroke, or serious adverse events of congestive heart failure, unstable angina or arrhythmia (hazard ratio 1.32, 95% CI: 0.97, 1.81). Increased Mortality and/or Increased Risk of Tumor Progression or Recurrence in Patients with Cancer receiving ESAs OMONTYS is not indicated and is not recommended for reduction of RBC transfusions in patients receiving treatment for cancer and whose anemia is not due to CKD because ESAs have shown harm in some settings and the benefit-risk factors for OMONTYS in this setting have not been evaluated. The safety and efficacy of OMONTYS have not been established for use in patients with anemia due to cancer chemotherapy. Results from clinical trials of ESAs in patients with anemia due to cancer therapy showed decreased locoregional control, progression-free survival and/or decreased overall survival. The findings were observed in clinical trials of other ESAs administered to patients with: breast cancer receiving chemotherapy, advanced head and neck cancer receiving radiation therapy, lymphoid malignancy, cervical cancer, non-small cell lung cancer, and with various malignancies who were not receiving chemotherapy or radiotherapy. Hypertension OMONTYS is contraindicated in patients with uncontrolled hypertension. Appropriately control hypertension prior to initiation of and during treatment with OMONTYS. Reduce or withhold OMONTYS if blood pressure becomes difficult to control. Advise patients of the importance of compliance with antihypertensive therapy and dietary restrictions. Serious Allergic Reactions Serious allergic reactions, including anaphylactic reactions, hypotension, bronchospasm, angioedema and generalized pruritus, may occur in patients treated with OMONTYS. Immediately and permanently discontinue OMONTYS and administer appropriate therapy if a serious allergic reaction occurs. Lack or Loss of Response to OMONTYS For lack or loss of hemoglobin response to OMONTYS, initiate a search for causative factors (e.g., iron deficiency, infection, inflammation, bleeding). If typical causes of lack or loss of hemoglobin response are excluded, evaluate the patient for the presence of antibodies to peginesatide. In the absence of antibodies to peginesatide, follow dosing recommendations for management of patients with an insufficient hemoglobin response to OMONTYS therapy. Contact Affymax, Inc. (1-855-466-6689) to perform assays for binding and neutralizing antibodies. Dialysis Management Patients may require adjustments in their dialysis prescriptions after initiation of OMONTYS. Patients receiving OMONTYS may require increased anticoagulation with heparin to prevent clotting of the extracorporeal circuit during hemodialysis.
Laboratory Monitoring Evaluate transferrin saturation and serum ferritin prior to and during OMONTYS treatment. Administer supplemental iron therapy when serum ferritin is less than 100 mcg/L or when serum transferrin saturation is less than 20%. The majority of patients with CKD will require supplemental iron during the course of ESA therapy. Following initiation of therapy and after each dose adjustment, monitor hemoglobin every 2 weeks until the hemoglobin is stable and sufficient to minimize the need for RBC transfusion. Thereafter, hemoglobin should be monitored at least monthly provided hemoglobin levels remain stable. ADVERSE REACTIONS The following serious adverse reactions are discussed in greater detail in other sections of the labeling: Increased Mortality, Myocardial Infarction, Stroke, and Thromboembolism [see Warnings and Precautions] Hypertension [see Warnings and Precautions] Serious allergic reactions [see Warnings and Precautions] Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of OMONTYS cannot be directly compared to rates in the clinical trials of other drugs and may not reflect the rates observed in practice. Patients with Chronic Kidney Disease Adverse reactions were determined based on pooled data from two active controlled studies of 1066 dialysis patients treated with OMONTYS and 542 treated with epoetin, including 938 exposed for at least 6 months and 825 exposed for greater than one year to OMONTYS. The population for OMONTYS was 20 to 93 years of age, 58.5% male, and the percentages of Caucasian, Black (including African Americans), and Asian patients were 57.9%, 37.4%, and 3.1%, respectively. The median weight adjusted dose of OMONTYS was 0.07 mg/kg and 113 U/week/kg of epoetin. Table 3 summarizes the most frequent adverse reactions ( 10%) in dialysis patients treated with OMONTYS. Table 3 Adverse Reactions Occurring in 10% of Dialysis Patients Treated with OMONTYS Dialysis Patients Treated with OMONTYS (N = 1066) 18.4% 17.4% 15.3% 18.4% 15.9% 16.1% 10.9% 15.4% 15.3% 10.9% 10.9% 10.7% 14.2% 13.2% 12.2% 11.4% 11.0% Dialysis Patients Treated with Epoetin (N = 542) 15.9% 19.6% 13.3% 19.4% 16.6% 16.6% 12.5% 15.9% 17.2% 12.7% 11.3% 9.8% 14.6% 11.4% 14.0% 11.8% 12.4%
Adverse Reactions Gastrointestinal Disorders Diarrhea Nausea Vomiting Dyspnea Cough Arteriovenous Fistula Site Complication Procedural Hypotension Nervous System Disorders Headache Muscle Spasms Pain in Extremity Back Pain Arthralgia Vascular Disorders Hypotension Hypertension Pyrexia Metabolism and Nutrition Disorders Hyperkalemia Infections and Infestations Upper Respiratory Tract Infection
Postmarketing Experience Because postmarketing reporting of adverse reactions is voluntary and from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Serious allergic reactions have been reported during postmarketing use of OMONTYS [see Warnings and Precautions]. Immunogenicity Of the 2357 patients tested during clinical trials, 29 (1.2%) had detectable levels of peginesatide-specific binding antibodies. There was a higher incidence of peginesatidespecific binding antibodies in patients dosed subcutaneously (1.9%) as compared to those dosed intravenously (0.7%). Peginesatide neutralizing antibodies were detected in vitro using a cell-based functional assay in 21 of these patients (0.9%). In approximately half of all antibody-positive patients, the presence of antibodies was associated with declining hemoglobin levels, the requirement for increased doses of OMONTYS to maintain hemoglobin levels, and/or transfusion for anemia of CKD. No cases of pure red cell aplasia (PRCA) developed in patients receiving OMONTYS during clinical trials. DRUG INTERACTIONS No formal drug/drug interaction studies have been performed. Peginesatide does not bind to serum albumin or lipoproteins as demonstrated in in vitro protein binding studies in rat, monkey and human sera. In vitro studies conducted with human hepatocytes or microsomes have shown no potential for peginesatide to induce or inhibit CYP450 enzymes. USE IN SPECIFIC POPULATIONS Pregnancy Pregnancy Category C There are no adequate and well-controlled studies in pregnant women. Peginesatide was teratogenic and caused embryofetal lethality when administered to pregnant animals at doses and/or exposures that resulted in polycythemia. OMONTYS should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Administration of peginesatide by intravenous injection to rats and rabbits during organogenesis was associated with embryofetal toxicity and malformations. Dosing was every third day in rats for a total of 5 doses and every fifth day in rabbits for a total of 3 doses (0.01 to 50 mg/kg/dose). In rats and rabbits, adverse embryofetal effects included reduced fetal weight, increased resorption, embryofetal lethality, cleft palate (rats only), sternum anomalies, unossification of sternebrae and metatarsals, and reduced ossification of some bones. Embryofetal toxicity was evident in rats at peginesatide doses of 1 mg/kg and the malformations (cleft palate and sternoschisis, and variations in blood vessels) were mostly evident at doses of 10 mg/kg. The dose of 1 mg/kg results in exposures (AUC) comparable to those in humans after intravenous administration at a dose of 0.35 mg/kg in patients on dialysis. In a separate embryofetal developmental study in rats, reduced fetal weight and reduced ossification were seen at a lower dose of 0.25 mg/kg. Reduced fetal weight and delayed ossification in rabbits were observed at 0.5 mg/kg/dose of peginesatide. In a separate embryofetal developmental study in rabbits, adverse findings were observed at lower doses and included increased incidence of fused sternebrae at 0.25 mg/kg. The effects in rabbits were observed at doses lower (5% - 50%) than the dose of 0.35 mg/kg in patients. Nursing Mothers It is not known whether peginesatide is excreted in human milk. Because many drugs are excreted into human milk, caution should be exercised when OMONTYS is administered to a nursing woman. Pediatric Use The safety and efficacy of OMONTYS in pediatric patients have not been established. Geriatric Use Of the total number of dialysis patients in Phase 3 clinical studies of OMONTYS, 32.5% were age 65 and over, while 13% were age 75 and over. No overall differences in safety or effectiveness were observed between these subjects and younger subjects. OVERDOSAGE OMONTYS overdosage can elevate hemoglobin levels above the desired level, which should be managed with discontinuation or reduction of OMONTYS dosage and/or with phlebotomy, as clinically indicated. Cases of severe hypertension have been observed following overdose with ESAs [see Warnings and Precautions]. Marketed by: Affymax, Inc. Palo Alto, CA 94304 Distributed and Marketed by: Takeda Pharmaceuticals America, Inc. Deerfield, IL 60015 OMONTYS is a trademark of Affymax, Inc. registered in the U.S. Patent and Trademark Office and used under license by Takeda Pharmaceuticals America, Inc. All other trademarks are the property of their respective owners. PEG096 R2_BS L-DSG-1112-1
Seizures have occurred in patients participating in OMONTYS clinical studies. During the first several months following initiation of OMONTYS, blood pressure and the presence of premonitory neurologic symptoms should be monitored closely. Advise patients to contact their healthcare practitioner for new-onset seizures, premonitory symptoms, or change in seizure frequency. Allergic and infusion-related reactions have been reported in patients treated with OMONTYS.
Practice Management
hinking from the health care administrators perspective, wouldnt it be nice if a patient scheduling model and throughput existed that could: Fill available schedule blocks; Decrease no-show rates; Reduce appointment handling and rescheduling workload; Enhance provider schedule flexibility; and Yield high patient satisfaction scores? Thinking from the patient perspective, wouldnt it be great if you: Got dependably an appointment when you actually needed it; Were seen reliably by your own provider; Were treated respectfully by your doctors office as being competent and capable of managing your own appointment choices; and Received regular follow-up reminders as necessary?
el (as developed and described in Murray and Tantaus September 2000 publication, Same-Day Appointments: Exploding the Access Paradigm). Like its Advanced Open Access predecessor, Modified Open Access pursues: Same-day care access as the norm for a practice A uniform schedule slot time length without special acuity limitations slots are intentionally designated to average the time a practice needs per patient and to eliminate the need for special appointment handling around acuity issues An emphasis on provider-specific continuity of care The goal of Modified Open Access and Murray and Tantaus model is to make the systems first priority be to take care of the patients who are established with a practice and who ultimately are the ones who take care of the practice. As we considered implementation logistics, our team addressed the concern of how to prevent open schedules from refilling with new or transient clientele who may ultimately block out established patients. To address this concern and preserve an open and accessible schedule for established patients, Modified Open Access differs from the Murray and Tantau model in placing limits on the interval beyond same-day for when appointments may be booked. It then utilizes several simple policy tools to ensure that established patients can always get in when they call for either acute or follow-up carethese are tools to maintain the promise of established patient care access.
Practice Management
In a nutshell, the model strives to optimize care provider access and utilization through the creation and maintenance of intentionally open schedule templates at the start of each day.
tients. The EPPA time is an internally set time on the clock each day. Before the EPPA time of the day, only established patients are allowed access to that days appointments. After the EPPA time passes, all patients, new and established, are given equal access to remaining appointments for that same day. In our busy practice setting, the EPPA time is usually set at 11a.m., but remains flexible and can be altered as needed, even on a daily basis. Before 11 a.m., only our established patients have access to the days twothirds open schedule, giving them priority status. After 11 a.m., both new and established patients are offered any remaining slots for that day. New patients who call for appointments before the days established EPPA time are politely informed that no appointments are available at that time, and are offered a callback if an appointment becomes available after the set EPPA time. After the EPPA time, new patients have equal access to any remaining slots for the day and the call-back list also can be used to fill in remaining open slots in the days schedule. The EPPA time may be adjusted to accommodate care demand trends observed by the practice. If the schedule is not filling, you can move the EPPA time to an earlier point in the day, effectively opening up the practice to more new patients. If established patient care demand risesfor instance, due to an influenza outbreakthen you can protect more established patient slots by moving the EPPA time to a later point in the day. Central to the models success is that established patients may, at any point, book an appointment up to a week in advance, but at no point are new patients offered appoint-
ments beyond today. This not only defends and sustains the models openness, it satisfies new patient needs. We found that new patients are happy to accept or be called back for same-day appointments when they are available. Our new patient volume actually increased compared to our prior traditional scheduling model experience. Tool No. 2: Receptionist Scripts To support this method of handling care demands, receptionist phone protocol scripts were developed to aid our receptionists (see Figure A and B). Although the model protocol can be integrated into the practice management scheduling software, scripts for our receptionists remain a valuable tool for implementation and training. They are also useful for understanding the models flow of patient call handling. The scripts encourage filling of first available slots, but our patient-centered emphasis remains on accommodating established patient appointment needs, up to the allowed full weeks advanced scheduling option. The scripts also introduce the next tool developed to support keeping the same-day access promise for established patients. Tool No. 3: Pressure-valve Slots Because patient care demand can be unpredictable in both volume and at what time, pressure-valve slots are a tool that allows for a second layer of capacity. Patients, who may not lock in appointments beyond one week in advance, need assurance that when they call, they have appointment access reliably. The pressure-valve slot tool is embedded in the model to ensure established patients can count on the availability of at least one same-day access option on any day. Heres how pressure-valve slots work: They are a scheduled interval of protected appointment slots built around the usual prac-
tice closing time that become available only if the days regular appointment slots have saturated. In our busy practice, pressurevalve slots span from one hour prior to our usual closing time to one hour after that time. These pressure-valve slots are available to established patients only, and always are open at the start of the day. If during any point of the day, no regular appointment slots remain open for an established patient calling for care, the pressure valveclosed till that pointthen opens, allowing the first available pressure-valve slot only to be offered to that established patient. The next available slot is only offered to a subsequent established patient requesting care. In our experience, pressure-valve slots rarely fill past usual closing time, but the capacity beyond the usual closing time allows responsiveness to care needs and demands of established patient clientele. In our primary care setting, pressure-valve care tends to be acute, urgent, and reflects the illnesses affecting the community; however, no limits are ever placed in the schedule on the nature of care requested. As the pressure-valve slots in a day progress across the interval, patients with lower acuity care needs tend to accept more readily the two-thirds open appointment options in the subsequent days. Pressure-valve slots help to keep at least one appointment available around closing time to established patients, which honors the promise of access. Tool No. 4: Follow-up Management Protocol If appointments are not locked in beyond one week for established patients, how are follow-up appointments handled beyond one week? To address this concern, a follow-up prompt and reminder system was developed using
February 2013 55
www.aapc.com
Practice Management
Figure A
Before ______ am
EPPA time
No
Figure B
After _______ am
EPPA time
Offer any remaining: same-day + Regular Appointment slots OR May I put your name on our call-back list or you may check with us again tomorrow after _____(EPPA time)
Offer 1st Available Pressure-Valve appointment Declined Offer PCP Appointment < 1 week
No
Please give us a call on or near the day you want to be seen and we will get you in.
56
Practice Management
our existing practice management software capabilities. The reminder systems foundation is based on the underlying principle: No matter what the scheduling model, it ultimately is the patients choice and decision whether to comply with the follow-up recommendations given by his or her provider. With this in mind, a three-tiered, follow-up reminder system was developed to encourage recommended return care interval compliance. The system starts with the providers recommended follow-up interval being delivered to the receptionist desk while the patient exits from an existing appointment. The first tier is a general interval follow-up card given to the exiting patient (e.g., follow up in early May). The existing patient reminder system then triggers daily batch mailing reminder cards at the providers recommend-
ed follow-up interval. After allowing a response interval, if no appointment is initiated by the patient, a final reminder is generated and sent. Although initiation of an appointment request falls into the patients hands, follow-up compliance is tracked and providers are kept aware of all patient-specific lapses.
rescheduling. With no locked-in appointments beyond one week, provider schedules had a significant increase in flexibility. Most importantly, patient satisfaction with provider continuity and access has been high. Implementation challenges and caveats, as well as spin-off benefits of the model, continue to be noted, and opportunities for software-driven enhancements and streamlining still remain.
David J. Moore, MD, MS, has served in primary care community health for nearly 20 years and is an assistant professor at the University of Kentuckys Center for Excellence in Rural Health. He has served in corporate medical director and site director roles in the Universitys partner relationship with the North Fork Valley Community Health Center in Hazard, Ky. He is a graduate of Harvard University School of Public Healths Masters in Health Care Management and a graduate of Wright State University School of Medicine and Family Medicine Residency in Dayton, Ohio.
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A H S G Dasthagir, CPC-A Abby Yip, CPC-A Adelina Kobeci, CPC-A Agnieszka Plonska, CPC-A Algin D N, CPC-A Alice A Calipes, CPC-A Alice E Johnson, CPC-A Alicia McCrudden, CPC-A Alwyn DN, CPC-A Amanda Breznau, CPC-A Amanda Hasser, CPC-A Amanda Soliday, CPC-A Ambar Solorzano, CPC-A Amrita Raveendran, CPC-A, CPC-H-A Amy Marie Meeks, CPC-A Amy Penman, CPC-A Amy Pridemore, CPC-A Andreena Marie Pulak, CPC-A Anil Singh, CPC-A Anissa Booth, CPC-A Anita Ehly, CPC-A Ann Bogari, CPC-A Ann Sweeney, CPC-A Annie Nguyen, CPC-A Antoinette Munsch, CPC-A Aranya (Joy) L Feagins, CPC-A Arlet Hopkins, CPC-A Arun Kumar Rajavel, CPC-A Ashal Mahoney, CPC-A Ashley Tucker, CPC-A Ashwini Rajan, CPC-A Barbara McQuade-Lantzy, CPC-A Barbara Rabatsky, CPC-A Barun Kumar, CPC-A Becky Banks, CPC-A
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Donna DiStefano, CPC-A Donna Ford, CPC-A Donna Place, CPC-A Donya Carol Tucker, CPC-A Edna Gonzalez, CPC-A Edwin Johnson, CPC-A Eileen Coutras, CPC-A Elena Delgado, CPC-A Elisabeth Parker, CPC-A Elizabeth Hewett, CPC-A Elyssa Ann Luebbering, CPC-A Emily E Walk, CPC-A Esmeraldo Batingana, CPC-A Evelyn D Knott, CPC-A Farine Ali, CPC-A Francelaine Saintelus, CPC-A Gail Nadeau, CPC-A Gail Yu, CPC-A Gary Edward Anderson, CPC-A Georgeta Moise, CPC-A Georgia Dodge, CPC-A Gina Conoan, CPC-A Gina Grady, CPC-A Gina L Fulcher, RDH, CPC-A Gopalakrishnan Thangavelu, CPC-A Gowri Manohari Natarajan, CPC-A Gwendolyn Lawhorn, CPC-A Harriet Cohen, CPC-A Heather Soss, CPC-A Heather Walsh, CPC-A Heidi Stutz, CPC-A Hilary Mulligan, CPC-A Holly Hindel, CPC-A Holly Christine Wideman, CPC-A Holly Henderson, CPC-A Holly Jarvis, CPC-A Horalia Acosta, CPC-A Huiyi Miao, CPC-A Indira Mahendrada, CPC-A Inge Barth, CPC-A Jackie Rogers, CPC-A Jackie Shoun Ringersma, CPC-A Jacquelyn Broten, CPC-A Jaiganesh Palani, CPC-A James Rausch, CPC-A James W Lim, CPC-A Jamie Krajewski, CPC-A Jamie Pylman, CPC-A Jamie Schwaller, CPC-A Janet L Holdeman, CPC-A Janet Yoder, CPC-A Jayanthi Vadivelu, CPC-A Jazsmine Jacobs, CPC-H-A Jean Havel, CPC-A Jean Morris, CPC-A Jeanette Robin Weiland, CPC-A Jeanne Uhing, CPC-A Jeannette Rosas, CPC-A Jenelle Keppley, CPC-A Jennifer Haselby, CPC-A Jennifer Swank, CPC-A Jennifer Austin, CPC-A Jennifer Courtney, CPC-A Jennifer Gabriela Dejamco, CPC-A Jennifer Lyn Moore, CPC-A Jennifer Mary Baumann, CPC-A Jennifer Meade, CPC-A Jennifer Porter, CPC-A Jennifer R Fair, CPC-A Jenny Estrada, CPC-A Jenny Sexton, CPC-A Jessica Fisher, CPC-A Jessica Hathaway, CPC-A Jessica Johnson, CPC-H-A Jessica Jose, CPC-A Jessica Schroeder, CPC-A Jill Doyle, CPC-A Jill R Ammons, CPC-A Jill Vierck, CPC-A Jill Visser, CPC-A
Jing Yun Wu, CPC-A Joan Elaine Erickson, CPC-A Joan Ferguson, CPC-A Joan Keller, CPC-A John Bennett, CPC-A John Bry, CPC-P-A Jordan C Burchell, CPC-A Jordan Heath, CPC-A Jordan Strombeck, CPC-A Josette Fuselier, CPC-A Joyce Favier, CPC-A Judy Block, CPC-A Judy J Taylor, CPC-A Judy Louise Ashey, CPC-A Julia Genther, CPC-A Julianne Johnson, CPC-A Julie A Miller, CPC-A Julie Kiekhoefer, CPC-A Kakasaheb Kachole, CPC-A Kandy Nies, CPC-A Kara Scott, CPC-H-A Karen Francis, CPC-A Karen J Musslewhite, CPC-A Karen Luckeroth, CPC-A Katherine Seebeck, CPC-A Kathleen Cott, CPC-A Kathleen Johnson, CPC-A Kathryne Leah Barnes, CPC-A Kathy Hudson, CPC-A Katrina Cartwright, CPC-A, CPC-P-A Katy Niemchick, CPC-A Kayla Lee Malone, CPC-A Keelie Dalonzo, CPC-A Kelli Pekios, CPC-A Kelly Hart, CPC-A Kelly McCormick, CPC-A Kelly Mckay, CPC-A Kelly Pethtel, CPC-A Kelsey Sorensen, CPC-A Kenny M. Lee, CPC-A Keri Marie Crowley, CPC-A Kim Bair, CPC-A, CPC-H-A Kim Cioe, CPC-A Kim Eskew, CPC-H-A Kim Greening, CPC-A Kim Nguyen, CPC-A Kimberly Biagioni, CPC-A Kimberly Lynne Miller, CPC-A Kiwanna Faulkner, CPC-A Kokiladevi Gopinath, CPC-A Komala Valli Selvaraj, CPC-A Komathi B, CPC-A Kristen Palmer, CPC-H-A Kristen Theisen, CPC-A Kristi Wilson, CPC-A Kristine Claire Lefebvre, CPC-A Kristine Johnson, CPC-A Krystal LaForrest, CPC-A Krystle Lister, CPC-A Kunal Chatterjee, CPC-A Lakenia Warren, CPC-A Lalima Mehrotra, CPC-A LaRena Fitz-Gerald, CPC-A Larry Poms, CPC-A LaTosha Bridgewater, CPC-A Laura Alber, CPC-A Lauren Gail Poe, CPC-A Laurie Richardson, CPC-A Laurie Hubbard, CPC-A Lavette D Neal, CPC-A Leah Trippanera, CPC-A Leigh Willard, CPC-A Leslie Boulette, CPC-H-A Lieu Doan, CPC-A Lina Ungureanu, CPC-A Linda Hatch, CPC-A Linda Heady, CPC-A Linda Tittle, CPC-A Lindsay Owens, CPC-A Linette Navarro, CPC-A
Lisa C Smith, CPC-A Lisa Campbell, CPC-A Lisa Davidson, CPC-A Lisa Fisher, CPC-A Lisa Hendricks, CPC-A Lisa Larson, CPC-A Lisa Robinson, CPC-A Lois Widener, CPC-A Lokesh Chaluvegowda, CPC-A Lora Bolton, CPC-A Lori Brown, CPC-A Lori Deniece Wise, CPC-A Lori Hewitt, CPC-A Lori Shinault, CPC-A Lucinda Jane Waber, CPC-A Lynette Valverde, CPC-A Lynn Archer, CPC-A Lynn Klim, CPC-A Lynn Kriedeman, CPC-A M McGehee, CPC-A Machelle Beckley, CPC-A Madhusmitha Gunjate, CPC-A Mahendran Selvam, CPC-A Mansoor Thangal, CPC-A Maranda Merjudio, CPC-A Marc A Cox, CPC-A Marcia Stewart, CPC-A Marcy Mote, CPC-A Maria Kathlyn Acosta, CPC-A Maria Lynn Schuster, CPC-A Marianne Amster, CPC-A Marianne Kusbit, CPC-A Marianne Moll, CPC-A Marilyn Bernache, CPC-A Marin Smith, CPC-A Marleen Hernandez, CPC-A Mary Anna Williford, CPC-A Mary Hollingsead, CPC-A Mary Jones, CPC-A Mary L Thomas, CPC-A Mary Lou Wojciechowski, CPC-A, CCC Mary Massey, CPC-A Mary T Hathorne, CPC-A Mary Wainio, CPC-A Maryann McMillan, CPC-A Marybeth Daley, CPC-A Massiel Javier, CPC-A Maura Carty, CPC-A Meenakshi Nain, CPC-A Megan Kime, CPC-A Megan Manning, CPC-A Meghan Allen, CPC-A Melanie D Briggs, CPC-A Melinda C Severt, CPC-A Melinda Trusty, CPC-A Melissa Bouchikas, CPC-A, CPC-H-A Melissa Lulling, CPC-A Melissa Mancini, CPC-A Melonie Gibson, CPC-A Michael Dosdos, CPC-A Michael Harmon, CPC-A Michelle Blackshear Harper, CPC-A Michelle Grist, CPC-A Mirian Gonzalez, CPC-A Monica Lynn Wenzell, CPC-A Morgan Jones, CPC-A Moses John Llamas, CPC-A Mrinalini Sekhar, CPC-A Nalagonda Priyanka, CPC-A Nancy Arias, CPC-A Nancy Quach, CPC-A Nandhini Jayakumar, CPC-A Naveen Selvaraj, CPC-A Nicole Walker, CPC-A Nicole Webb, CPC-A Ninette Santa Cruz, CPC-A Ondrea Maffeo, CPC-A Orsolya Simmons, CPC-H-A Paige McSain, CPC-A Pamela Beaver, CPC-A
Pamela Klaus, CPC-A Pamela S Long, CPC-A Pamela Tarpley, CPC-A Pamela Yap, CPC-A Patricia Alvis, CPC-A Patricia McAlister, CPC-A Patricia Murrin, CPC-A Pauline Ellen Thalmann, CPC-A Pavithra Ramalingam, CPC-A Phyllis Joanne Tabano Valencia, CPC-A Prabakar Murugan Sekar, CPC-A Prabha Chandrasekaran, CPC-A Prakash Shannugam Authoor, CPC-A Prathima Vaddepally, CPC-A Prem Vinoth Kumar, CPC-A Premila Kumarankandath, CPC-A Priya Gupta, CPC-A Purvi Shah, CPC-A Rachel D Ouellette, CPC-A Rachel Garena, CPC-A Rachell White, CPC-A Raghava Danwada, CPC-A Raghuraman Sundhararaju, CPC-A, CPC-H-A Rajasekar Rajendran, CPC-A Rajitha Goli, CPC-A Rajni Kanth, CPC-A Ramesh Sampath, CPC-A Ramona Merritt, CPC-A Ravikiran Nagabhushan, CPC-A Rebecca Cox, CPC-A Rebecca Pascucci, CPC-A Rebecca Ann Holderman, CPC-A Rebecca Barton, CPC-A Rebecca Cooper, CPC-A Rebecca Palmer, CPC-A Rebekah Voorhis, CPC-A Regina Oginski, CPC-A Reginald Brock, CPC-A Regine Delus, CPC-A Rena P Lening, CPC-A Renee Diaz, CPC-A Revathi E, CPC-A Rhonda Blankingship, CPC-A Rhonda Jane Hanna, CPC-A Robert Maars, CPC-A Robert Neklesa, CPC-A Robert Pezzillo, CPC-A Robert Simonds, CPC-A Roberta A Jackson, CPC-A Rona Perez, CPC-A Ronelle Bones, CPC-A Roopa Narayanan, CPC-A Ruth Case, CPC-A Ruth James, CPC-A Sabine Parmley, CPC-A Sally Valdez, CPC-A Samantha Messer, CPC-A Samantha Blattner, CPC-A Sandeep Kumar, CPC-A Sandhya Raghavan, CPC-A Sandy Steele, CPC-A Sarah Donaldson, CPC-A Sarah Hollier, CPC-A Sarah McCauley, CPC-A Sarah Moody, CPC-A Sarah Ward Coudon, CPC-A Sargunaraj Raja, CPC-A Sasipriya Madhav, CPC-A Satheesh Kumar, CPC-A Sattie Jugmohan, CPC-A Scott Kreutzer, CPC-A Shamanthkumar Mandava, CPC-A Shandi Ann McCutcheon, CPC-A Shanmugavadivel Virudhagiri, CPC-A Shannon Kropp, CPC-A Shannon Toenyan, CPC-A Shara Franklin, CPC-A Shareen Jalaludin, CPC-A Sharlene Sorenson, CPC-A Sharon Maureen Stovall, CPC-A
Shelly Figg, CPC-A Sher Kosage, CPC-A Sherry Sawyers, CPC-H-A Sherryann Sinanan-Ali, CPC-A Shiny Anand, CPC-A Shirlee Ann Kakaruk, CPC-A Shrimathi Raghupathy, CPC-A Shweta Taneja, CPC-A Simone Mathers, CPC-A Sintoria Johnson, CPC-A Sky Boggs, CPC-A Sonia Ithier Hopkins, CPC-A Sovena Homer, CPC-A Sreekanth Reddy, CPC-A Sri Bhanu Tejaswi Thummoju, CPC-A Srinath Dachepalli, CPC-A Srinivasan Vijayan, CPC-A Stacey Morache, CPC-A Staci Kuhnhenn, CPC-A Stacie Hyla Friedman, CPC-A Stacy Burney-Jones, CPC-A Stephanie Ann Honeycutt, CPC-A Stephanie Jo Weiner, CPC-A Stephanie McPherson, CPC-A Stephen S, CPC-A Steven Graessle, CPC-A Subha Ramachandran, CPC-A Sue Sansoucy, CPC-A Suganthi Raju, CPC-A Suja Chandrapaul, CPC-A Sulochanadevi Sundararajah, CPC-A Suman Patra, CPC-A Supriya Harishchandra Bhandakkar, CPC-A Suresh Babu, CPC-A Susan Gosselin, CPC-A Susan Redmond, CPC-H-A Suvega Selvaraj, CPC-A Suzanne Greene Lenske, CPC-A Suzanne M Matz, CPC-H-A Swathi Goud Kurra, CPC-A Tabatha JK Osteen, CPC-A Tabitha Foxx, CPC-A Tamara Jane Sutton, CPC-A Tania Cuevas, CPC-A Tasha Letrease Bryant, CPC-A Tellaboina Satyabhaskar, CPC-A Tena Hill Wynne, CPC-A Teresa A Hawken, CPC-A Teresa Lyon, CPC-A Terese Mastrofrancesco, CPC-A Terri Peebles, CPC-A Tiffani Dahl, CPC-A Tiffany Miklas, CPC-A Tiffany F Valery, CPC-A Tim Varghese, CPC-A Tina Schweitzer, CPC-A Tina Miller, CPC-A Tony Vakkachan, CPC-A Tora Arlene Knowles, CPC-A Tracey Denise Holzbog, CPC-A Tricia Carter, CPC-A Troiline Frezzell, CPC-A Unia Patterson, CPC-A Valerie Ortiz, CPC-A Valorie Ann Hoffmaster, CPC-A Venece R Martin, CPC-A Venkata Rakesh Chakravarthy, CPC-A, CPC-H-A Vicki Doherty, CPC-A Victoria Slavik, CPC-A Vijayadeepa Pandiyan, CPC-A Vipin Cheriyamoothore, CPC-A Vishnu Sharma, CPC-A Wendy Gonzalez, CPC-A Yutian Galloway, CPC-A Yvonne Rosenzweig, CPC-A Zak Federer, CPC-A Zelenne I Esteves, CPC-A
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Alicia Ajon Flynn, CPC, CGSC Amanda Banks Nelson, CPC-A, CRHC Amy Joanne Coffee, CPC, CPMA Amy Michelle Benton, CPC-A, CPCO, CPMA Angela M Wilson, CPC, CENTC Angela Scott, CPC, CPMA Annette Fay Rawlins, CPC, CCC Ashley D Miller, CPC, CHONC Barbara Struve, CPC, CEDC Beth Eve Schleeper, CPC, CPCO, CEMC Bobbi Jeanette Martin, CPC-H, CPMA Brenda Lea Parker, CPC, CPC-P, CPMA Brooke Thao, CPC, CEDC Candiss A Grannis, CPC-H, CIRCC Carolyn A Grifths, CPC, CHONC Cassandra Allison, CPMA Cathy E Roberge, CPC, CPPM Cathy S Jennings, CPC, CEDC, CHONC Charles B Harvey Jr, BSN, RN, CPC, CPMA Christine M Schaefer, CPC, CEMC, COBGC Clarence Milton Stewart, CPC, CSFAC Colette Mink, CPC, CPMA Connie Moering, CPC, CPEDC Courtney Polito, CPC, CPMA, COBGC Cristina M Nicoara, CPC, CPMA, CEMC Crystal Mayer, CPC, CPMA Cynthia A. James, CRHC Cynthia Anne Owens-Muller, CPC, CPMA Cynthia S Tucker, CPC, CPMA, COSC Darla Jeanell Morrison, CPC-A, CRHC David Carr, CPC-A, CPCO Deborah Kubida, CPC, COBGC Deidre Jandeska, CCC Dena Ferrante Wilcox, CPC, CCC, CEMC Denise Dula, CPC, COSC Diana M Morehead, CPC, CEMC Dianna Schrimsher, CPC, CHONC
Specialties
Donna Beaulieu, CPC, CPMA, CPC-I, CEDC Donna Kay Ring, CPC, CPMA, CEMC Edward Johnson, CPCO Eleinys Pupo, CPC, CPMA Elizabeth Ann Cook, CPC, CASCC Elizabeth Apicella, CPC, COSC Elizabeth Frias, CPC, CPMA Erin Terrones, CFPC Fiona B Lange, CPC, CPPM Gail Acton, CPC, CPMA, CEMC Gail Vogt-McGeehan, CIRCC Gigi Georgina Price, CHONC Gloria Brogan Ph.D ACS-AN, CPC, CPMA Heather Renee Smith, CPC, CPMA Helen Marie Gerdes, CPC, CCC Holly Brown, CPC, CPC-H, CEMC Jade Harden, CPC, CEDC James Thomas Carter, CPC, CPMA Jan Turley, CPC, CPMA Jennifer Westfall, CPC, CPMA, CGSC Jennifer Young, CPC, CPCO Jill D Conley, CPC, CEMC JoAnne M Wolf, RHIT, CPC, CEMC Johnita Smith, CRHC Jonathan Robert Sanford, CPC, CPC-H, CPPM Julie Brandt, CHONC Karen Guadalupi, CPRC Kathleen M Kampe, CPC, COSC Kathleen M Sherbrooke, CPC, CANPC Kathryn J Kasper, CPC, CPCD Kellie Dress, CPPM, CPRC Kerry Beth Atkins, CPC, CPMA, COBGC Kimberly Mathews, CPC, CPPM Krista Jackson, CPC, CPCO, CPC-P Kristina S Lauer, CPC, CHONC Laurie J Hartford, CPC, CCC, COBGC Leslie Dailey, CGSC Lori Ann Gelgut BBA, CPC, CPC-H, CCVTC Lori J Lawson, CPC, COBGC
Lydia Chitwood, CPC, CCVTC Malgorzata Tyszko, CRHC Margaret Coyle, CPC, CPC-H, CHONC Marilyn Glidden, CPC, CPMA, CGIC, CGSC Marilyn Kitchens Cecil, CPC, CPMA, CPCD, CPRC Marilyn L Koerner, CPC, CHONC Mary Bort, CPC, CANPC, COSC Mary Buike, CPC, CEMC Mary Gore, CPC, COBGC Mary Rikley, CPC, CPMA Maura Macri, CPPM Melanie Cooper, CPC, CEMC Melanie Lewis, CPC, CPMA, CPC-I, CEMC Michael Lee Taylor, CPC, CPMA Nancy Flowers, CPC, CPMA Nancy L Henry, CPC, CPPM Nancy Love Weith, CPC, CCVTC Naomi A Hinton, CPC, CPMA Nicole Marie Clatterbuck, CRHC Nikki Strang, CANPC Peter Weiser, CRHC Philip G Brown, CPC, CPMA, CASCC Rachel Elaine Briggs, CPC, CPMA, CEMC Robin Erinn Bay, CPC-A, CPMA Robin Szuchman, CPCD Rodolfo P Bangilan, CPC, CPC-H, CASCC Ruth Kerekes, CIRCC RuthAnn C Hansen, CPC, CPMA Sabrina R Leichtman, CPC, CENTC Sandra Gamboa, CPC, CPMA Sandra Ebersole, CHONC Sandy Colson, CPC, CPC-H, CPMA Sebrena Atencio, CPC, CEDC Shawn Dunn, CPC, CPMA Shawn Marie Muench, CPC, CANPC Sheena Lunsmann, CPC, COBGC Stacey Lynn Wilson, CPC, COSC Sunny Triana, CPC-A, CPMA Tanika Jennings, CPC, CHONC
Tanya Baker, CPC, CPMA Tara K. Johnson, CPC, CANPC, CGIC Tasha Todd, CPC, CANPC Teresa M Berry, CPC, CIRCC Terri Brown, CPC, CGSC Thelma Mae Bishoff, CPC, CPMA Tiffany Bobbitt, CPC-A, CPEDC Tiffany Nicole Taylor, CPC, CPMA Tina Louise Daley, CPC, CCC Tracy Alise Sarver, CPC, CEMC Tracy Lee Rada, CPC, CPMA, CEMC, COSC Trista L Johnson, CPC, COSC Vandna Chaudhary, CRHC Windy Baughman, CANPC
Aleida S Padron, CPC Allegra Wheeler, CPC Amanda Briggs, CPC Aniladiv Acuna, CPC-A Anisia L Torres, CPC Ann Forrister, CPC Ann Fullerton, CPC-A Anna Wade, CPC-A Avani Hart, CPC-A Brigette Burton, CPC Charlotte Perrone, CPC-A Chitra Lakshmanan, CPC Christine Schmotzer, CPC, CPC-H, CPMA, CEMC Dale Smith, CPC Darlean Yankovich, CPC Denise G Lopez, CPC Diana David, CPC-A Diana L Hutchings, CPC-A Dolores Zaldivar, CPC Eileen Camillone, CPC Eileen OCarroll McCully, CPC-A Emilio Sanchez, CPC-A
Evelyn Medina, CPC Freddy Mercado, CPC Gagan T Kadahalli, CPC-A Genoveva C Prieto, CPC Gisela Miller, CPC Heidi Beggan, CPC Heidy Villiers, CPC Joe Jose Moreno, CPC Johanna Marie Novoa, CPC Julia M Serrano, CPC-A Kerry L Fulks , CPC, CEDC Komal Meisuria, CPC Kristin Jacobs, CPC Maritza Isabel Vazquez Lopez, CPC Mary Deano, CPC-A Mirella Platon, CPC-A Monica Persaud, CPC-A Norma R Romero, CPC Odalys Rodriguez, CPC Rafaela Gallo, CPC Richard Campbell, CPC-A Ronna A Pate, CPC Rosalina Cespedes, CPC Shahina Jaffer, CPC Shari Brauch, CPC Sylvia Cram, CPC-A Thomas Allen Brown, CPC Tina L Pelton , CPC, CPC-H Tonia Haralson, CPC-A Vanmathi Sivaraman, CPC William Fiala, CPC Wilmieniza Yamson Sale, CPC-A Yeima Perez, CPC Yonaicris de las Maria Plasencia, CPC-A Yuanling B Nuez, CPC
r fo w 3 Ne 201
$299
COMPLIANCE
Approved
Ten Essential Tips for Efficient EMR Templates Key Steps to Develop a Quality Assurance Program Manage Contracts Like a Pro What are Government Audits Really Looking For? Teaching E/M Coding to Physicians: A Doctors Prospective Specialized Surgical Chart Auditing Getting to the Roots of Thriving Leadership and Management Ten Simple Indicators that Will Lead Your Practice to Financial Success Maximizing Systems Integration and Automation
Confident Compliance Planning What to Do When Your Compliance Plan Breaks OIGs Self Disclosure Protocol Conquering E/M Auditing Challenges Within EMRs Delivering Audit Results to Providers in an Effective Manner Developing a Successful Auditing Compliance Plan Key Steps in Hiring the Right Physician That Which is Measured Improves: Key Indicators and Data Analytics Create Simple and Effective Financial Dashboard
AUDITING
PRACTICE MANAGEMENT
CPPM
Approved
Tell us a little bit about your career how you got into coding, what youve done during your coding career, what youre doing now, etc.
I began working in the health care industry in 1999 as an insurance companys customer service representative, speaking to members and answering health benefit questions. After a year, I was transferred to the provider line and spoke with physician offices regarding submitted and denied claims. In 2004, I began working for a local urgent care center as a registrar, performing front desk duties and answering patients billing questions. While working at the urgent care office, I took surgical technician program classes at a local college and, upon finishing the course, began an internship at a local hospital. During the job search as a surgical tech, I realized I didnt enjoy the clinical side of health care; what I really enjoy is constantly learning and keeping up with guidelines and regulationsthe back office side of the industry. I even turned down a surgical tech position to
62 AAPC Cutting Edge
How do you spend your spare time? Tell us about your hobbies, family, etc.
I have been married for five years to Josh, with whom I love to spend time and travel. We enjoy going to the movies and being with family and friends. We also enjoy going to Disney World, which is only a short two hour and 30 minute drive for us. We bought annual passes two years ago and take advantage of it every chance we get. I am super excited the AAPC National Conference is at Disney World this year! I might bring my husband with me, so he can enjoy some Disney time while I attend the conference. We have a 7-year-old cocker spaniel who keeps us busy when were home.
ICD-10 Code Set Training Begins in Orlando Two Complete Tracks 26 Specialty Coding Sessions Six Auditing Sessions Four Billing Sessions Three Compliance Sessions Four Facility Sessions Six Practice Management Sessions CPPM Boot Camp available concurrent with this Event
NATIONAL CONFERENCE
Walt Disney World Resort - Florida
2013
AAPC
www.aapc.com/orlando2013
NAMAS CPMA Training will be offered as a pre-conference event at the AAPC National Conference April 11-12, 2013 Two day Live training event for CPMA examination prep 16 CPMA /CPC CEUs Convenience of same session testing on April 13, 2013