Management of AKI
Management of AKI
Management of AKI
Version 1.0
This guideline recognises and respects the right for all patients, their families and carers, to
be treated with honesty, privacy and dignity at all times.
Purpose: To advise and inform all hospital staff, patients and the wider community of the
hospitals overarching policy for the management of patients with AKI
NHS England
Archive date ie date To be inserted by Information Governance Department when this document is
guideline no longer in superseded. This will be the same date as the implementation date of the new
force document.
Printed copies of this document may not be up to date. Please check the hospital intranet
for the latest version and destroy all previous versions.
Hospital documents may be disclosed as required by the Freedom of Information Act 2000.
As part of the hospitals networking arrangements and sharing best practice, the hospital
supports the practice of sharing documents with other organisations. However, where the
hospital holds copyright to a document, the document or part thereof so shared must not be
used by any third party for its own commercial gain unless the hospital has given its express
permission and is entitled to charge a fee.
Release of any strategy, policy, procedure, guideline or other such material must be agreed
with the Lead Director or Deputy/Associate Director (for hospital-wide issues) or Division
/Departmental management Team (for Divisional or Departmental specific issues). Any
requests to share this document must be directed in the first instance to Dr Ande, Dr Lewis,
Dr Kitchen, RN Manju Markose Critical Care Outreach team.
Page No
SECTION 1 - INTRODUCTION ..................................................................................... 4
1.1 Clinical Guideline statement and rationale .......................................................................... 4
1.2 Key Principles ...................................................................................................................... 4
1.3 Background Information ...................................................................................................... 4
1.4 Definitions ............................................................................................................................ 4
There have been concerns that suboptimal care may contribute to the development
of AKI. In 2009, the National Confidential Enquiry into Patient Outcome and Death
(NCEPOD) described systemic deficiencies in the care of patients who died from AKI,
with only 50% receiving 'good' care. Other deficiencies in care included failures in
prevention, recognition, treatment and timely access to specialist services.
1.4 Definitions
ABBREVIATION DEFINITION
ACEI Angiotensin-Converting Enzyme Inhibitors
AKI Acute Kidney Injury
ARB Angiotensin II Receptor Blockers
BP Blood Pressure
CCOT Critical Care Outreach Team
CKD Chronic Kidney Disease
CRP C Reactive Protein
eGFR estimated Glomerular Filtration Rate
MEWS Modified Early Warning Score
2.1 The responsible officers for this document are Dr Praveen Ande (Consultant
Nephrologist), Dr Robert Lewis (Consultant Anaesthetist), Dr Jessica Kitchen
(Consultant Acute Medicine, Nephrologist), and Manju Markose RN (Critical Care
Outreach Practitioner)
2.2 Patient Safety & Clinical Effectiveness Group will approve this document in
accordance with the Trust policy.
2.4 All Trust employees; bank, agency and locum staff; trainees; students and contracted
staff
To adhere to the guideline
To seek clarification from their line manager or the senior manager responsible
for the initiation and review of this guideline if unsure about any part of the
guideline or relevant document.
To be aware of the current version of this guideline and other documents and
how to access them
3. Assessment of AKI
3.3.1 Assess the risk of AKI in adult patients before surgery. Be aware that increased risk
is associated with:
Emergency surgery, especially when the patient has sepsis or hypovolaemia
Intra-peritoneal surgery
CKD (patients with an eGFR less than 60 ml/min/1.73 m2 are at particular risk)
[See Appendix 1]
Diabetes
Heart failure
Age 65 years or over
Liver disease
Use of drugs with nephrotoxic potential in the perioperative period
Use the risk factors identification form to inform the clinical management plan. (See
Appendix 2)
3.3.3 Include the risks of developing AKI in the routine discussion of risks and benefits of
surgery with the patient.
Any patient identified as having AKI as an inpatient will follow the AKI checklist and
AKI care bundle Appendix 2. Once AKI is detected according to their serum
creatinine rise, each patient should be assessed on a daily basis and the multi-
3.4.2a Be aware that in adult patients with CKD and no obvious acute illness, a rise in serum
creatinine may indicate AKI rather than a worsening of their chronic disease.
3.4.2b Ensure that AKI is considered when an adult patient presents with an illness with no
clear acute component and has any of the following:
CKD, especially stage 3B, 4 or 5, or urological disease
new onset or significant worsening of urological symptoms
symptoms suggesting complications of AKI
Symptoms or signs of a multi-system disease affecting the kidneys and other
organ systems (for example: signs or symptoms of AKI, plus a purpuric rash).
Any patient identified as having AKI as an in-patient will follow the AKI care bundle as
shown in Appendix 2. Once AKI is detected according to their serum creatinine rise,
each patient should be assessed on a daily basis according to the care bundle and
the multi-disciplinary team should ensure that all crucial components of the AKI Care
bundle are completed and any reasons for exemption clearly documented in the
nursing or medical notes.
3.5.1a Follow the recommendations in Monitoring Vital Signs (MEWS) and Intervention with
the Acutely Ill Adult Policy (see the 'M' page of the Policies and Guidelines A-Z in
hospital intranet).
3.5.1b When adults are at risk of AKI, check and record full set of vital signs using i-POD
touch (e-Observations) and urine output with a frequency appropriate for the patients
condition.
3.5.1c Monitor Urine Output at least 4hrly if not catheterised and hourly if catheter present -
ensuring all outputs clearly documented on fluid balance charts and running totals
calculated. Escalate appropriately for every patient if oliguria detected for more than
3 hours.
3.5.1d Ensure the recommendations on AKI care bundle are instituted in all circumstances
3.5.1e Increase the frequency of observations if abnormal physiologies are detected and
inform CCOT team and medical team where appropriate (MEWS > 4).
3.5.2a Offer intravenous volume expansion to patients having iodinated contrast agents if:
They are at increased risk of contrast-induced AKI because of risk factors, or if
they have an acute illness.
Offer IV fluids (eg Sodium Bicarbonate 1.26%) as per the guideline (Appendix 3).
3.5.2c Discuss care with the nephrology team before offering iodinated contrast agent to
patients with contraindications to intravenous fluids if:
they are at increased risk of contrast-induced AKI, or
they have an acute illness, or
they are on RRT.
3.5.3 Monitoring and preventing deterioration in patients with or at high risk of AKI
3.5.3a Seek advice from a Pharmacist about optimising medicines and drug dosing in adult
patients with or at risk of AKI.
3.5.3b Consider temporarily stopping ACE inhibitors and ARBs in patients with diarrhoea,
vomiting or sepsis until their clinical condition has improved and stabilised.
3.6.2 Monitor serum creatinine regularly in all patients with or at risk of AKI.
3.7.1a Identify the cause(s) of AKI and record the details in the patient's notes.
3.7.1b Perform urine dipstick testing for blood, protein, leucocytes, nitrites and Glucose in all
patients as soon as AKI is suspected or detected. Document the results and ensure
that appropriate action is taken when results are abnormal.
3.7.1c Do not routinely offer ultrasound of the urinary tract when the cause of the AKI has
been identified.
3.7.1d When pylonephrosis (infected and obstructed kidney[s]) is suspected in patients with
AKI, offer immediate ultrasound of the urinary tract (to be performed within 12 hours
of assessment).
3.7.1e When patients have no identified cause of their AKI or are at risk of urinary tract
obstruction, offer urgent ultrasound of the urinary tract (to be performed within 24
hours of assessment).
3.8.1b Consider loop diuretics for treating fluid overload or oedema while awaiting RRT or
renal function is recovering in a patient not receiving RRT.
3.8.2a Discuss any potential indications for RRT with a Nephrologist and/or critical care
specialist immediately to ensure that the therapy is started as soon as needed.
3.8.2b When a patient has significant comorbidities, discuss with them/relatives and within
the multidisciplinary team whether RRT would offer benefit.
3.8.2c Refer patients immediately for RRT if any of the following are not responding to
medical management:
Hyperkalaemia
Metabolic acidosis
Symptoms or complications of uraemia (for example, pericarditis or
encephalopathy)
Fluid overload
Pulmonary oedema
3.8.2d Base the decision to start RRT on the condition of the patient as a whole and not on
an isolated urea, creatinine or potassium value.
3.8.2e When there are indications for RRT, the Nephrologist and/or Critical Care Specialist
should discuss the treatment with the patient / relative or carer as soon as possible
and before starting treatment.
3.8.3a Refer patients with AKI to Nephrologist and/or Critical Care Specialist immediately if
they meet criteria for RRT therapy in recommendation.
3.8.3b Do not refer patients to a Nephrologist when there is a clear cause for AKI and the
condition is responding promptly to medical management, unless they have a renal
transplant.
3.8.3c Consider discussing management with Nephrologist when a patient with severe
illness might benefit from treatment, but there is uncertainty as to whether they are
nearing the end of their life.
3.8.3e Discuss the management of AKI with a Nephrologist as soon as possible and within
24 hours of detection when one or more of the following is present:
A possible diagnosis that may need specialist treatment (for example, vasculitis,
glomerulonephritis, tubule-interstitial nephritis or myeloma)
AKI with no clear cause
Inadequate response to treatment
Complications associated with AKI
Stage 3 AKI
a renal transplant
CKD stage 4 or 5
3.8.3f Monitor serum creatinine after an episode of AKI. Consider referral to a Nephrologist
when eGFR is 30 ml/min/1.73 m2 or less in patients who have recovered from an
AKI.
The management of the AKI guideline will be introduced to the Trust using the
following methods:
5.2 This guideline will be made available on the hospital intranet. All managers will be
asked to highlight this to all staff and attend teaching sessions as appropriate.
7.1 Once approved by the Patient Safety & Clinical Effectiveness Group, the responsible
officer will forward this guideline to the Information Governance Department for a
document index registration number to be assigned and for the guideline to be
recorded onto the central hospital master index and central document library of
current documentation.
7.2 In order that this guideline adheres to the hospitals Records Management Policy, the
responsible officer will arrange for staff to be advised when this guideline is
superseded and for arranging for this version to be removed from the hospitals
intranet. They will also advise the Information Governance Department who will
ensure that this guideline is removed from the current index and library, archived and
retained for 10 years from the archive date.
References
Academy of Medical Royal Colleges Acute Kidney Injury Competency Framework (2010)
[accessed online on 20/09/2014] www.aomrc.org.uk/9503-acute-kidneyinjury-a-competency-
framework.
Burgess, R. (2011), New Principles of best practice in clinical audit, 2ND edition, Radcliffe
Publishing Ltd
Davenport, A. (2010), Clinical guidelines for the protection of kidney function and prevention
of acute kidney injury in the intensive care unit: common sense rather than magic bullets?
Fallon, D. and Long, T. (2007), Ethics approval, ethical research and delusions of efficacy.
In Long, T. and Johnson, M (etal), Research Ethics in the real world: Issues and solutions for
Health and Social care, Churchill Livingston, London.
Kerr, M., Bedford, M., Matthews B, O. Donoghue,D. (2014). The economic impact of acute
kidney injury in England. Nephrology Dialysis Transplantation. April 21 2014.
National Institute of Health and Care Excellence (2013). Acute kidney injury: Prevention,
detection and management of acute kidney injury up to the point of renal replacement
therapy. Published in August 2013.
The National Enquiry in to Patient Outcomes and Death (2009), 'Adding insult in to injury'.
Neale, J. (2009), Research methods for health and social care, First Edition, Palgrave
Macmillan, United Kingdom.
Waikar, S.S., Liu, K.D., Chertow, G.M (2008) ,Diagnosis, epidemiology and outcomes of
acute kidney injury. Clinical Journal of American Society of Nephrology 3:844861.
Investigate for AKI, by measuring serum creatinine and comparing with baseline, in
patients with acute illness if any of the following are likely or present:
CKD (adults with an estimated glomerular filtration rate [eGFR] less than 60 ml/min/1.73
m2 are at particular risk)
Heart failure
Liver disease
Diabetes
History of AKI
Hypovolaemia
Sepsis
AKI Checklist
1. Seek cause
2. Assess fluid status
3. Review drug chart for nephrotoxic medicines
4. Consider Renal USS (within 24hrs if no obvious cause or obstruction likely)
5. Renal referral if Stage 3 AKI or not responding to treatment