ﻣﺠﻠــﻪﻱ ﻋﻠﻤــﻲ ،ﭘﮋﻭﻫﺸــﻲ ﺩﺍﻧﺸــﮕﺎﻩ ﻋﻠــﻮﻡ ﭘﺰﺷـﮑﻲ ﺯﻧﺠــﺎﻥ
ﺩﻭﺭﻩﻱ ,٢٢ﺷﻤﺎﺭﻩﻱ ,٩١ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ ,١٣٩٣ﺻﻔﺤﺎﺕ ١٢١ﺗﺎ ١٣٠
ﺑﺮﺭﺳﻲ ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭ ﻣﻴﺎﻥ ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺟﺪﺍ ﺷﺪﻩ ﺍﺯ
ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺩﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫﺎﻱ ﺗﻬﺮﺍﻥ
۵
ﻟﻴﻠﻲ ﺷﮑﻮﻫﻲ ﺯﺍﺩﻩ ،۱ﺩﮐﺘﺮ ﺍﺷﺮﻑ ﻣﺤﺒﺘﻲ ﻣﺒﺎﺭﺯ ،۲ﺩﮐﺘﺮ ﻣﺤﻤﺪ ﺭﺿﺎ ﺯﺍﻟﻲ ،۳ﺩﮐﺘﺮ ﺭﺿﺎ ﺭﻧﺠﺒﺮ ،۴ﺩﮐﺘﺮ ﻣﺴﻌﻮﺩ ﺍﻝ ﺑﻮﻳﻪ
ﻧﻮﻳﺴﻨﺪﻩﻱ ﻣﺴﻮﻭﻝ :ﺗﻬﺮﺍﻥ ،ﺩﺍﻧﺸﮕﺎﻩ ﺗﺮﺑﻴﺖ ﻣﺪﺭﺱ ،ﺩﺍﻧﺸﮑﺪﻩﻱ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ
ﺩﺭﻳﺎﻓﺖ۹۲/۴/۹ :
mmmobarez@modares.ac.ir
ﭘﺬﻳﺮﺵ۹۲/۷/۱۵ :
ﭼﮑﻴﺪﻩ
ﺯﻣﻴﻨﻪ ﻭ ﻫﺪﻑ :ﺳﻮﻳﻪﻫﺎﻱ ﻣﻘﺎﻭﻡ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺍﻧﺘﻮﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ) (VREﺷﺎﻳﻊﺗﺮﻳﻦ ﻋﺎﻣﻞ ﺍﻳﺠﺎﺩ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺩﺭ ﺑﻴﻤﺎﺭﺍﻥ ﺑﺴﺘﺮﻱ ﻣﻲﺑﺎﺷﻨﺪ.
ﻫﺪﻑ ﺍﺯ ﺍﻳﻦ ﻣﻄﺎﻟﻌﻪ ﺑﺮﺭﺳﻲ ﻓﺮﺍﻭﺍﻧﻲ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮎ ﻓـﺴﻴﻮﻡ ﻭ ﻫﻤﭽﻨـﻴﻦ ﺗﻌﻴـﻴﻦ ﻣﻴـﺰﺍﻥ ﻣﻘﺎﻭﻣـﺖ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﻭ ﺩﻳﮕـﺮ
ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎﻱ ﻣﻮﺛﺮ ﺩﺭ ﺩﺭﻣﺎﻥ ﺍﻳﻦ ﻋﻔﻮﻧﺖﻫﺎ ﺩﺭ ﺑﻴﻤﺎﺭﺍﻥ ﺑﺴﺘﺮﻱ ﺩﺭ ﭼﻬﺎﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥ ﺁﻣﻮﺯﺷﻲ ﺩﺭ ﺷﻬﺮ ﺗﻬﺮﺍﻥ ﺑﻮﺩ.
ﺭﻭﺵ ﺑﺮﺭﺳﻲ :ﻧﻤﻮﻧﻪﮔﻴﺮﻱ ﺑﻪﻣﺪﺕ ۹ﻣﺎﻩ ﺍﺯ ﺷﻬﺮﻳﻮﺭ ﺳﺎﻝ ۱۳۹۰ﺗـﺎ ﺍﺭﺩﻳﺒﻬـﺸﺖ ۱۳۹۱ﺍﻧﺠـﺎﻡ ﭘـﺬﻳﺮﻓﺖ .ﻧﻤﻮﻧـﻪﻫـﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺍﺯ ﺑﻴﻤـﺎﺭﺍﻥ ﺑـﺴﺘﺮﻱ ﺩﺭ
ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫﺎﻱ ﻃﺎﻟﻘﺎﻧﻲ ،ﻟﻘﻤﺎﻥ ،ﻣﻔﻴﺪ ﻭ ﻟﺒﺎﻓﻲ ﻧﮋﺍﺩ ﺩﺭ ﺗﻬﺮﺍﻥ ﺟﻤﻊﺁﻭﺭﻱ ﮔﺮﺩﻳﺪ .ﺑﺮﺍﺳﺎﺱ ﺗﺴﺖﻫـﺎﻱ ﺑﻴﻮﺷـﻴﻤﻴﺎﻳﻲ ﻭ ﻣﻮﻟﮑـﻮﻟﻲ ﮔﻮﻧـﻪﻫـﺎﻱ ﺍﻧﺘﺮﻭﮐـﻮﮎ
ﺷﻨﺎﺳﺎﻳﻲ ﺷﺪﻧﺪ .ﺣﺴﺎﺳﻴﺖ ﺿﺪ ﻣﻴﮑﺮﻭﺑﻲ ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﻭ ﻣﻴﺰﺍﻥ ﺣﺪﺍﻗﻞ ﻏﻠﻈـﺖ ﻣﻬـﺎﺭﻱ ) (MICﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﺑـﻪ ﺭﻭﺵ ﺩﻳـﺴﮏ
ﺩﻳﻔﻴﻮﺯﻥ ﻭ ﺁﮔﺎﺭ ﺩﻳﻠﻮﺷﻦ ﺗﻌﻴﻴﻦ ﮔﺮﺩﻳﺪ .ﺣﻀﻮﺭ ﮊﻥﻫﺎﻱ vanAﻭ vanBﺩﺭ ﺳﻮﻳﻪﻫﺎﻱ VREﺗﻮﺳﻂ ﺗﺴﺖ PCRﻣﻮﺭﺩ ﺑﺮﺭﺳﻲ ﻗﺮﺍﺭ ﮔﺮﻓﺖ.
ﻳﺎﻓﺘﻪﻫﺎ :ﺩﺭ ﻣﺠﻤﻮﻉ ۸۶ﺍﻳﺰﻭﻟﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻲ ﺍﺯ ﻧﻤﻮﻧﻪﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺟﺪﺍ ﮔﺮﺩﻳﺪ ﮐﻪ ﺷﺎﻣﻞ ) ۵۲ﺩﺭﺻﺪ( ۴۵ﺍﻳﺰﻭﻟﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺑﻮﺩﻧﺪ ۴۲/۲ .ﺩﺭﺻﺪ
ﺍﺯ ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻣﻘﺎﻭﻡ ﺑﻮﺩﻩ ﻭ ﮊﻧﻮﺗﻴﭗ vanAﺭﺍ ﻧﺸﺎﻥ ﻣﻲﺩﺍﺩﻧﺪ .ﺗﻤﺎﻣﻲ ﺳﻮﻳﻪﻫﺎﻱ VREﻧﺴﺒﺖ ﺑﻪ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎﻱ
ﺁﻣﭙﻲﺳﻴﻠﻴﻦ ،ﺟﻨﺘﺎﻣﻴﺴﻴﻦ ،ﺳﻴﭙﺮﻭﻓﻠﻮﮐﺴﺎﺳﻴﻦ ﻭ ﺍﺭﻳﺘﺮﻭﻣﺎﻳﺴﻴﻦ ﻭ ۷۸ﺩﺭﺻﺪ ﺁﻥﻫﺎ ﺑﻪ ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘﻮﺋﻴﻦ ﻣﻘﺎﻭﻡ ﻭ ﻫﻤﮕﻲ ﻧﺴﺒﺖ ﺑﻪ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎﻱ ﻟﻴﻨﺰﻭﻻﻳﺪ
ﻭ ﮐﻮﻳﻨﻮﭘﺮﻳﺴﺘﻴﻦ -ﺩﺍﻟﻔﻮﭘﺮﻳﺴﺘﻴﻦ ﺣﺴﺎﺱ ﺑﻮﺩﻧﺪ .ﺩﺭ ﺳﻮﻳﻪﻫﺎﻱ ﻣﻘﺎﻭﻡ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ MIC50ﺑـﻴﺶ ﺍﺯ ۱۲۸ﻭ MIC90ﺑـﻴﺶ ﺍﺯ ۲۵۶ﻣﻴﻠـﻲﮔـﺮﻡ ﺩﺭ
ﻣﻴﻠﻲﻟﻴﺘﺮ ﺗﻌﻴﻴﻦ ﮔﺮﺩﻳﺪ.
ﻧﺘﻴﺠﻪ ﮔﻴﺮﻱ :ﺍﻓﺰﺍﻳﺶ ﺳﻮﻳﻪﻫﺎﻱ ﻣﻘﺎﻭﻡ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺍﻧﺘﺮﻭﮐﻮﮐﺲ ﻓﺴﻴﻮﻡ ﺑﺎ ﺍﻟﮕﻮﻫﺎﻱ ﻣﻘﺎﻭﻣﺘﻲ ﭘﺮ ﺧﻄﺮ ﺗﻬﺪﻳﺪﻱ ﺟﺪﻱ ﺩﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫﺎﻱ ﺍﻳﺮﺍﻥ ﺑﻮﺩﻩ،
ﻣﻮﺟﺐ ﻣﺤﺪﻭﺩﻳﺖ ﺩﺭ ﮔﺰﻳﻨﻪﻫﺎﻱ ﺩﺭﻣﺎﻧﻲ ﺑﺮﺍﻱ ﺑﻴﻤﺎﺭﺍﻥ ﻣﺒﺘﻼ ﺑﻪ ﻋﻔﻮﻧﺖﻫﺎﻱ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐﺲ ﻓﺴﻴﻮﻡ ﻣﻲ ﺷﻮﺩ.
ﻭﺍﮊﮔﺎﻥ ﮐﻠﻴﺪﻱ :ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ،ﻋﻔﻮﻧﺖ ﺍﺩﺭﺍﺭﻱ ،ﻣﻘﺎﻭﻣﺖ ،ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ
ﻣﻘﺪﻣﻪ
ﻋﻔﻮﻧـــﺖﻫـــﺎﻱ ﻣﺠـــﺎﺭﻱ ﺍﺩﺭﺍﺭﻱ ۳۰ﺗـــﺎ ۴۰ﺩﺭﺻـــﺪ ﺍﺯ
ﻣﺠﻤﻮﻉ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﮐﺘﺴﺎﺑﻲ ﺑﻴﻤﺎﺭﺳﺘﺎﻧﻲ ﺭﺍ ﺗـﺸﮑﻴﻞ ﻣـﻲﺩﻫﻨـﺪ
ﻭ ﺷﺎﻳﻊﺗﺮﻳﻦ ﻋﻔﻮﻧﺖ ﺍﻳﺠﺎﺩ ﺷﺪﻩ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ﻣﻲﺑﺎﺷﺪ.
ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ﻋﺎﻣـﻞ ﺷـﺎﻳﻊ ﺳﻴـﺴﺘﻴﺖ ،ﭘﺮﻭﺳـﺘﺎﺗﻴﺖ ﻭ ﺍﭘﻴـﺪﻣﻴﺖ
- ۱ﺩﺍﻧﺸﺠﻮﻱ ﺩﻛﺘﺮﺍﻱ ﺑﺎﻛﺘﺮﻱ ﺷﻨﺎﺳﻲ ،ﺩﺍﻧﺸﻜﺪﻩﻱ ﻋﻠﻮﻡ ﭘﺰﺷﻜﻲ ،ﺩﺍﻧﺸﮕﺎﻩ ﺗﺮﺑﻴﺖ ﻣﺪﺭﺱ ﺗﻬﺮﺍﻥ
- ۲ﺩﻛﺘﺮﺍﻱ ﺗﺨﺼﺼﻲ ﻣﻴﻜﺮﻭﺏ ﺷﻨﺎﺳﻲ ،ﺩﺍﻧﺸﻴﺎﺭ ﮔﺮﻭﻩ ﺑﺎﻛﺘﺮﻱ ﺷﻨﺎﺳﻲ ،ﺩﺍﻧﺸﻜﺪﻩﻱ ﻋﻠﻮﻡ ﭘﺰﺷﻜﻲ ،ﺩﺍﻧﺸﮕﺎﻩ ﺗﺮﺑﻴﺖ ﻣﺪﺭﺱ ﺗﻬﺮﺍﻥ
- ٣ﻓﻮﻕ ﺗﺨﺼﺺ ﮔﻮﺍﺭﺵ ﻭ ﻛﺒﺪ ،ﺍﺳﺘﺎﺩ ﻣﺮﮐﺰ ﺗﺤﻘﻴﻘﺎﺕ ﮔﻮﺍﺭﺵ ﻭﮐﺒﺪ ،ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﺷﻬﻴﺪ ﺑﻬﺸﺘﻲ ،ﺗﻬﺮﺍﻥ
- ٤ﺩﻛﺘﺮﺍﻱ ﺗﺨﺼﺼﻲ ﺑﺎﻛﺘﺮﻱ ﺷﻨﺎﺳﻲ ،ﺩﺍﻧﺸﻴﺎﺭ ﻣﺮﮐﺰ ﺗﺤﻘﻴﻘﺎﺕ ﺑﻴﻮﻟﻮﮊﻱ ﻣﻮﻟﮑﻮﻟﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﺑﻘﻴﻪ ﺍﻟﻪ ،ﺗﻬﺮﺍﻥ
- ٥ﺩﻛﺘﺮﺍﻱ ﺗﺨﺼﺼﻲ ﺑﺎﻛﺘﺮﻱ ﺷﻨﺎﺳﻲ ،ﻣﺮﻛﺰ ﺗﺤﻘﻴﻘﺎﺕ ﮔﻮﺍﺭﺵ ،ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﻜﻲ ﺷﻬﻴﺪ ﺑﻬﺸﺘﻲ
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ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ
ﺩﺭ ﺍﻓﺮﺍﺩ ﻣﺴﻦ ﻣﻲﺑﺎﺷﻨﺪ ﮐﻪ ﺩﺭ ﺍﻳﻦ ﺍﻓﺮﺍﺩ ،ﻋﻔﻮﻧﺖﻫـﺎﻱ ﺩﺳـﺘﮕﺎﻩ
)ﺩﻱ ﺁﻻﻧـﻴﻦ -ﺩﻱ ﺁﻻﻧـﻴﻦ( ﺩﺭ ﻣﺮﺣﻠـﻪﻱ ﺁﺧـﺮ ﭘـﻴﺶ ﺳــﺎﺯﻫﺎﻱ
ﺍﺩﺭﺍﺭﻱ ﻓﻮﻗﺎﻧﻲ ﻣﻲﺗﻮﺍﻧـﺪ ﻣﻨﺠـﺮ ﺑـﻪ ﺑـﺎﮐﺘﺮﻳﻤﻲ ﺷـﺪﻩ ،ﺩﺭ ﺯﻧـﺎﻥ
ﭘﻨﺘﺎﭘﭙﺘﻴﺪﻱ ﭘﭙﺘﻴﺪ ﻭ ﮔﻠﻴﻜﺎﻥ ﻛﻤـﭙﻠﻜﺲﻫـﺎﻳﻲ ﺗـﺸﻜﻴﻞ ﻣـﻲﺩﻫﻨـﺪ
ﺟــﻮﺍﻥ ﻋﺎﻣــﻞ ﺳﻴــﺴﺘﻴﺖ ﻣــﺰﻣﻦ ﻏﻴــﺮ ﺷــﺎﻳﻊ ﻣــﻲﺑﺎﺷــﺪ ).(۱
ﺑﺎﻋﺚ ﺍﺯ ﺑﻴﻦ ﺭﻓﺘﻦ ﺍﺳﺘﺤﻜﺎﻡ ﺳﺎﺧﺘﺎﺭﻱ ﺩﻳـﻮﺍﺭﻩﻱ ﺳـﻠﻮﻟﻲ ﻭ ﺩﺭ
ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ،ﮐﻮﮐﺴﻲﻫﺎﻱ ﮔﺮﻡ ﻣﺜﺒﺘﻲ ﻫﺴﺘﻨﺪ ﮐﻪ ﺑﺨﺸﻲ ﺍﺯ ﻓﻠﻮﺭ
ﻧﺘﻴﺠﻪ ﻣﺮﮒ ﺳﻠﻮﻝ ﻣﻲ ﺷﻮﺩ .ﺑﺮ ﺍﺳﺎﺱ ﺧـﺼﻮﺻﻴﺎﺕ ﻓﻨـﻮﺗﻴﭙﻲ ﻭ
ﺗﻨﻔﺴﻲ ﻓﻮﻗﺎﻧﻲ ،ﻣﺠﺎﺭﻱ ﺻﻔﺮﺍﻭﻱ ،ﺣﻔﺮﻩ ﻱ ﺩﻫﺎﻥ ،ﻣﺜﺎﻧﻪ ،ﻭﺍﮊﻥ ﻭ
) (vanA, vanB, vanD, vanE, vanG, vanL, vanM, vanNﻭ
ﺩﻳﮕﺮ ﻧﻘﺎﻁ ﻧﻴـﺰ ﮐﻠـﻮﻧﻴﺰﻩ ﺷـﻮﻧﺪ .ﻓﻠـﻮﺭ ﮐﻮﻣﻨـﺴﺎﻝ ﺧـﻮﺩ ﺑﻴﻤـﺎﺭ
ﻳـﮏ ﻧـﻮﻉ ﻣﻘﺎﻭﻣــﺖ ﺫﺍﺗـﻲ vanCﮔــﺰﺍﺭﺵ ﮔﺮﺩﻳـﺪﻩ ﺍﺳــﺖ.
ﻣﻬﻢﺗﺮﻳﻦ ﻣﻨﺒﻊ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻲ ﻣﺤﺴﻮﺏ ﻣـﻲﮔـﺮﺩﺩ )(۲
ﻣﻘﺎﻭﻣـﺖ ﻧـﻮﻉ vanAﻭ vanBﻏﺎﻟـﺐﺗـﺮﻳﻦ ﻧـﻮﻉ ﻣﻘﺎﻭﻣـﺖ
ﻣﻴﮑﺮﻭﺑﻲ ﺭﻭﺩﻩ ﻱ ﺍﻧﺴﺎﻥ ﻭ ﺣﻴﻮﺍﻧﺎﺕ ﺑﻮﺩﻩ ،ﻣﻲﺗﻮﺍﻧﻨﺪ ﺩﺭ ﺩﺳـﺘﮕﺎﻩ
ﮊﻧﻮﺗﻴﭙﻲ ﺗﺎ ﮐﻨﻮﻥ ﻫﻔﺖ ﻧﻮﻉ ﻣﻘﺎﻭﻣﺖ ﺍﮐﺘﺴﺎﺑﻲ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ
ﺩﻭ ﮔﻮﻧﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﻭ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﮑﺎﻟﻴﺲ ﺑـﻴﺶ ﺍﺯ
ﺩﺭ ﺍﻳﺠﺎﺩ ﻣﻘﺎﻭﻣﺖ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﻣـﻲﺑﺎﺷـﻨﺪ ،ﺩﺳـﺘﻪﻱ ﮊﻧـﻲ
ﺳﺎﻳﺮ ﮔﻮﻧﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮎ ﺩﺭ ﺍﻳﺠـﺎﺩ ﻋﻔﻮﻧـﺖﻫـﺎﻱ ﺍﻧﺘﺮﻭﮐـﻮﮐﻲ
vanAﻣﻘﺎﻭﻣــﺖ ﺳــﻄﺢ ﺑــﺎﻻ ﻭ ﻗﺎﺑــﻞ ﺍﻟﻘــﺎ ﺑــﻪ ﻭﻧﻜﻮﻣﺎﻳــﺴﻴﻦ
ﺩﺧﻴﻞ ﻣﻲﺑﺎﺷﻨﺪ ) .(۳ﻣﻬـﻢﺗـﺮﻳﻦ ﺩﻟﻴـﻞ ﺍﻫﻤﻴـﺖ ﺍﻧﺘﺮﻭﮐـﻮﮎﻫـﺎ
) (MIC ≥ 64 -1000 µg/mlﻭ ﺗﻴﻜـﻮﭘﻼﻧﻴﻦMIC ≥ 16-
ﻣﻘﺎﻭﻣﺖ ﺫﺍﺗﻲ ﺁﻥﻫـﺎ ﺑـﻪ ﺁﻧﺘـﻲﺑﻴﻮﺗﻴـﮏﻫـﺎﻱ ﻣﻌﻤـﻮﻝ ﻭ ﮐـﺴﺐ
) (512 µg/mlﺭﺍ ﺍﻳﺠــﺎﺩ ﻣــﻲﻛﻨــﺪ ﻛــﻪ ﻣﻌﻤــﻮﻻﹰ ﺍﺯ ﻃﺮﻳــﻖ
ﻣﻘﺎﻭﻣﺖ ﺩﺭ ﺑﺮﺍﺑﺮ ﺗﻘﺮﻳﺒﺎ ﺗﻤﺎﻣﻲ ﺁﻧﺘﻲﺑﻴﻮﺗﻴـﮏﻫـﺎﻱ ﺩﺭ ﺩﺳـﺘﺮﺱ
ﺗﺮﺍﻧﺴﭙﻮﺯﻭﻥ Tn1546ﻣﻨﺘﻘـﻞ ﻣـﻲﮔـﺮﺩﺩ .ﺩﺳـﺘﻪ ﮊﻧـﻲ vanB
ﺍﻧﺘﺮﻭﮐــﻮﮎﻫــﺎ ﺑـﻪﺧــﺼﻮﺹ ﺍﻧﺘﺮﻭﮐــﻮﮎﻫــﺎﻱ ﻣﻘــﺎﻭﻡ ﺩﺭ ﺑﺮﺍﺑــﺮ
) (MIC= 4 -16 µg/mlﻣﻲﺷﻮﺩ ﻭ ﺑﻪ ﺗﻴﻜـﻮﭘﻼﻧﻴﻦ ﺣـﺴﺎﺱ
ﻭﻧﮑﻮﻣﺎﻳــﺴﻴﻦ ) (VREﺑﻴﻤــﺎﺭﻱﺯﺍﻱ ﻋﻤــﺪﻩ ﺩﺳــﺘﮕﺎﻩ ﺍﺩﺭﺍﺭﻱ
ﺍﺳﺖ ﮐﻪ ﻣﻌﻤﻮﻻﹰ ﺑﺮ ﺭﻭﻱ ﻛﺮﻭﻣﻮﺯﻭﻡ ﻗـﺮﺍﺭ ﺩﺍﺭﻧـﺪ ﻭﻟـﻲ ﻣﻤﻜـﻦ
ﻣﻲﺑﺎﺷﻨﺪ .ﻃﺒﻖ ﻣﻄﺎﻟﻌﺎﺕ ﻭ ﻧﺘﺎﻳﺞ ﻣﻨﺘﺸﺮ ﺷـﺪﻩ ﺍﮐﺜـﺮ VREﻫـﺎ
ﺍﺳﺖ ﺑﺮ ﺭﻭﻱ ﭘﻼﺳﻤﻴﺪ ﻧﻴﺰ ﺣﻤـﻞ ﺷـﻮﺩ ) (۷- ۱۲ﺍﻭﻟـﻴﻦ ﻣـﻮﺭﺩ
ﻇﻬﻮﺭ ﺳـﻮﻳﻪﻫـﺎﻱ VREﮐﻨﺘـﺮﻝ ﻭ ﺩﺭﻣـﺎﻥ ﻋﻔﻮﻧـﺖ ﻧﺎﺷـﻲ ﺍﺯ
ﺑﻌﺪ ﺍﺯ ﺍﻳﺎﻻﺕ ﻣﺘﺤﺪﻩ ﻭ ﺗﺎ ﺑﻪ ﺍﻣﺮﻭﺯ ﻇﻬﻮﺭ VREﺩﺭ ﺑﺴﻴﺎﺭﻱ ﺍﺯ
ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺭﺍ ﺩﭼﺎﺭ ﻣﺸﮑﻞ ﮐﺮﺩﻩ ﺍﺳﺖ ،ﭼﺮﺍ ﮐـﻪ ﺍﻳـﻦ
ﮐﺸﻮﺭﻫﺎ ﺍﺯ ﺟﻤﻠﻪ ﺍﻳـﺮﺍﻥ ﮔـﺰﺍﺭﺵ ﺷـﺪﻩ ﺍﺳـﺖ .ﺑـﻪﻃـﻮﺭﻱﮐـﻪ
ﻧﻮﻉ ﺳﻮﻳﻪﻫـﺎ ﻋـﻼﻭﻩ ﺑـﺮ ﻣﻘﺎﻭﻣـﺖ ﺫﺍﺗـﻲ ﺩﺭ ﺑﺮﺍﺑـﺮ ﺑـﺴﻴﺎﺭﻱ ﺁﺯ
ﺍﻣﺮﻭﺯﻩ ﺑﻪ ﻋﻨﻮﺍﻥ ﻳﮏ ﭘﺎﺗﻮﮊﻥ ﻣﻬـﻢ ﺑﻴﻤﺎﺭﺳـﺘﺎﻧﻲ ﺩﺭ ﻧﻈـﺮ ﮔﺮﻓﺘـﻪ
ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎﻱ ﻣﻮﺟﻮﺩ ﻣﻲﺷﻮﻧﺪ )۵ﻭ .(۴ﻣﻨﺎﺳﺐﺗﺮﻳﻦ ﺩﺭﻣـﺎﻥ
ﻫﺰﻳﻨﻪﻫﺎﻱ ﺩﺭﻣﺎﻧﻲ ﻧﺎﺷﻲ ﺍﺯ ﺳﻮﻳﻪﻫﺎﻱ VREﺩﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫـﺎ،
ﺑــﺮﺍﻱ ﻋﻔﻮﻧــﺖﻫــﺎﻱ ﺍﻧﺘﺮﻭﮐــﻮﮐﻲ ﺗﺮﮐﻴ ـﺐ ﻳ ـﮏ ﺁﻧﺘ ـﻲﺑﻴﻮﺗﻴ ـﮏ
ﺍﻃﻼﻉ ﺍﺯ ﻧﻮﻉ ﭘﺎﺗﻮﮊﻥﻫﺎﻱ ﺩﺧﻴﻞ ﺩﺭ ﺍﻳﺠﺎﺩ ﻋﻔﻮﻧـﺖﻫـﺎﻱ ﺍﺩﺭﺍﺭﻱ
ﮔﻠﻴﮑﻮﭘﭙﺘﻴﺪ ﻣﺎﻧﻨﺪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻳـﺎ ﻳـﮏ ﺁﻧﺘـﻲﺑﻴﻮﺗﻴـﮏ ﺑﺘﺎﻻﮐﺘـﺎﻡ
ﻭ ﻫﻤﭽﻨﻴﻦ ﺍﻟﮕﻮﻫﺎﻱ ﻣﻘـﺎﻭﻣﺘﻲ ﺁﻥﻫـﺎ ﺩﺭ ﮐﻨﺘـﺮﻝ ﻭ ﺩﺭﻣـﺎﻥ ﺍﻳـﻦ
ﻣﺎﻧﻨــﺪ ﺟﻨﺘﺎﻣﻴــﺴﻴﻦ ﻣــﻲﺑﺎﺷــﺪ .ﮐــﻪ ﺍﮐﺜــﺮ ﺳــﻮﻳﻪﻫــﺎﻱ VRE
ﻣﻄﺎﻟﻌﻪ ﺑﺮﺭﺳﻲ ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﻭ ﻫﻤﭽﻨﻴﻨـﻴﻦ
ﺑــﻪ ﻏﻠﻈــﺖﻫــﺎﻱ ﺑــﺎﻻﻱ ﻭﻧﮑﻮﻣﺎﻳــﺴﻴﻦ ،ﺁﻣﻴﻨﻮﮔﻠﻴﮑﻮﺯﻳــﺪﻫﺎ ﻭ
ﻣﻘﺎﻳــﺴﻪ ﺍﻟﮕﻮﻫــﺎﻱ ﻣﻘﺎﻭﻣــﺖ ﺁﻧﺘــﻲﺑﻴــﻮﺗﻴﮑﻲ ﺩﺭ ﺳــﻮﻳﻪﻫــﺎﻱ
ﺑﺘﺎﻻﮐﺘﺎﻡﻫﺎ ﻣﻘﺎﻭﻣﺖ ﻧﺸﺎﻥ ﻣﻲﺩﻫﻨﺪ ) .(۶ﮔﻠﻴﻜﻮﭘﭙﺘﻴـﺪﻫﺎ ﺑـﺎ ﻣﻬـﺎﺭ
ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺟﺪﺍ ﺷﺪﻩ ﺍﺯ ﻋﻔﻮﻧﺖﻫـﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺑﻴﻤـﺎﺭﺍﻥ
ﺳﻨﺘﺰ ﺩﻳﻮﺍﺭﻩ ﺳﻠﻮﻟﻲ ﺑﺮ ﺑﺎﻛﺘﺮﻱﻫﺎﻱ ﮔﺮﻡ ﻣﺜﺒﺖ ﺗﺎﺛﻴﺮ ﻣﻲﮔﺬﺍﺭﻧـﺪ.
ﺑﺴﺘﺮﻱ ﺩﺭ ﺑﺨﺶﻫﺎﻱ ﻣﺨﺘﻠﻒ ﭼﻬﺎﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥ ﺁﻣﻮﺯﺷﻲﺩﺭ ﺷﻬﺮ
ﻣ ـﻲﺑﺎﺷــﺪ ) .(۴ﺩﺭ ﺑﺨــﺶﻫــﺎﻱ ﭘــﺮ ﺧﻄــﺮﻱ ﻫﻤﭽــﻮﻥ ICU
ﻣﺘﻌﻠﻖ ﺑﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﻣﻲﺑﺎﺷﻨﺪ ).(۱
ﺁﻧﺘــﻲﺑﻴﻮﺗﻴــﮏﻫــﺎ ﻗــﺎﺩﺭ ﺑــﻪ ﮐــﺴﺐ ﮊﻥﻫــﺎﻱ ﻣﻘﺎﻭﻣــﺖ ﺑــﻪ
ﻣﺎﻧﻨﺪ ﺁﻣﭙﻲﺳﻴﻠﻴﻦ ﺑﻪﻫﻤﺮﺍﻩ ﻳﮏ ﺁﻧﺘـﻲﺑﻴﻮﺗﻴـﮏ ﺁﻣﻴﻨﻮﮔﻠﻴﮑﻮﺯﻳـﺪﻱ
ﮔﻠﻴﻜﻮﭘﭙﺘﻴــﺪﻫﺎ ﺭﻭﻱ ﺳــﻄﺢ ﺧــﺎﺭﺟﻲ ﺳــﻠﻮﻝ ﺑــﺎ ﺍﻧﺘﻬﺎﻫــﺎﻱ
ﺑﺎﻋﺚ ﻳﻚ ﻣﻘﺎﻭﻣﺖ ﻗﺎﺑﻞ ﺍﻟﻘﺎ ﺳﻄﺢ ﭘﺎﻳﻴﻦ ﺗﺎ ﺑﺎﻻ ﺑﻪ ﻭﻧﻜﻮﻣﺎﻳﺴﻴﻦ
ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺍﺯ ﺍﺭﻭﭘﺎ ﮔﺰﺍﺭﺵ ﮔﺮﺩﻳـﺪ ﻭ ﻳـﮏ ﺳـﺎﻝ
ﻣ ـﻲﺷــﻮﻧﺪ )۱۴ﻭ .(۱۳ﺑــﺎ ﺗﻮﺟــﻪ ﺑــﻪ ﺍﻓــﺰﺍﻳﺶ ﻣــﺮﮒ ﻭﻣﻴ ـﺮ ﻭ
ﻋﻔﻮﻧﺖﻫﺎ ﺍﻫﻤﻴﺖ ﺑﺴﻴﺎﺭ ﺣﺎﻳﺰ ﺍﻫﻤﻴﺖ ﻣﻲﺑﺎﺷـﺪ .ﻫـﺪﻑ ﺍﺯ ﺍﻳـﻦ
ﺗﻬﺮﺍﻥ ﺑﻮﺩ.
ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ ،ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ ،ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ ،ﺩﻭﺭﻩﻱ ,٢٢ﺷﻤﺎﺭﻩﻱ ,٩١ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ ١٣٩٣
ﻟﻴﻠﻲ ﺷﻜﻮﻫﻲ ﺯﺍﺩﻩ ﻭ ﻫﻤﻜﺎﺭﺍﻥ
ﺭﻭﺵ ﺑﺮﺭﺳﻲ
ﻧﻤﻮﻧﻪﮔﻴﺮﻱ ﻭ ﺷﻨـﺎﺳـﺎﻳﻲ ﮔﻮﻧﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮎ :ﻧﻤــﻮﻧﻪﻫﺎﻱ
ﺍﺩﺭﺍﺭﻱ ﺍﺯ ﺑﻴﻤﺎﺭﺍﻥ ﺑﺴﺘﺮﻱ ﺩﺭ ﺑﺨـﺶﻫـﺎﻱ ﻣﺨﺘﻠـﻒ ﺍﺯ ﺟﻤﻠـﻪ
123
ﺩﺭﺟــــﻪﻱ ۴۵ ،ﺛﺎﻧﻴــــﻪ ۳۵ ،ﺳــــﻴﮑﻞ؛ ﺗﮑﺜﻴــــﺮ ﻧﻬــــﺎﻳﻲ:
۷۲ﺩﺭﺟﻪ ۵ﺩﻗﻴﻘﻪ ،ﻳﮏ ﺳﻴﮑﻞ ﺍﺳﺘﻔﺎﺩﻩ ﮔﺮﺩﻳﺪ ).(۱۵
ﺑﺮﺭﺳ ﻲ ﺣﺴﺎﺳﻴﺖ ﺁﻧﺘـ ﻲﻣﻴ ﮑﺮﻭﺑـ ﻲ ﻭ ﮊﻧﻮﺗﻴـﭗ ﻣﻘﺎﻭﻣـﺖ ﺑـﻪ
،ICUﻧﻔﺮﻭﻟﻮﮊﻱ ،ﭘﻴﻮﻧﺪ ﮐﻠﻴﻪ ،ﭘﻴﻮﻧﺪ ﮐﺒﺪ ،ﻫﻤﺎﺗﻮﻟﻮﮊﻱ ،ﮔﻮﺍﺭﺵ،
ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ :ﺣﺴﺎﺳﻴﺖ ﺁﻧﺘﻲﺑﻴـﻮﺗﻴﮑﻲ ﺩﺭ ﺑﺮﺍﺑـﺮ ﺩﻳـﺴﮏﻫـﺎﻱ
)ﻃﺎﻟﻘﺎﻧﻲ ،ﻣﻔﻴﺪ ،ﻟﻘﻤﺎﻥ ﻭ ﻟﺒﺎﻓﻲ ﻧﮋﺍﺩ( ﺩﺭ ﺷﻬﺮ ﺗﻬﺮﺍﻥ ﺩﺭ ﻓﺎﺻﻠﻪﻱ
ﺁﻣﭙﻲ ﺳﻴﻠﻴﻦ ) ۱۰ﻣﻴﮑﺮﻭﮔﺮﻡ( ،ﺟﻨﺘﺎﻣﻴـﺴﻴﻦ ) ۱۲۰ﻣﻴﮑﺮﻭﮔـﺮﻡ(،
ﺟﺮﺍﺣﻲ ،ﺍﺭﺗﻮﭘﺪﻱ ،ﻗﻠﺐ ﻭﺍﻧﮑﻮﻟﻮﮊﻱ ﭼﻬﺎﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥ ﺁﻣﻮﺯﺷـﻲ
ﺷﻬﺮﻳﻮﺭ ﺳﺎﻝ ۹۰ﺗﺎ ﺧـﺮﺩﺍﺩ ﺳـﺎﻝ ۹۱ﺟﻤـﻊ ﺁﻭﺭﻱ ﺷـﺪ .ﺍﻳـﻦ
ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ) ۳۰ﻣﻴﮑﺮﻭﮔـﺮﻡ( ،ﺗﻴﮑـﻮﭘﻼﻧﻴﻦ ) ۳۰ﻣﻴﮑﺮﻭﮔـﺮﻡ(،
ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘــــﻮﺋﻴﻦ ) ۳۰۰ﻣﻴﮑﺮﻭﮔــــﺮﻡ( ،ﺳﻴﭙﺮﻭﻓﻠﻮﮐــــﺴﺎﺳﻴﻦ
ﻧﻤﻮﻧﻪﻫﺎ ﺍﺯ ﺁﺯﻣﺎﻳﺸﮕﺎﻩﻫﺎﻱ ﻣﻴﮑﺮﻭﺏﺷﻨﺎﺳﻲ ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫﺎﻱ ﻣﻮﺭﺩ
) ۵ﻣﻴﮑﺮﻭﮔــﺮﻡ( ﺍﺭﻳﺘﺮﻭﻣﺎﻳـﺴﻴﻦ) ۱۵ﻣﻴﮑﺮﻭﮔــﺮﻡ( ،ﺗﺘﺮﺍﺳــﺎﻳﮑﻠﻴﻦ
ﺍﻧﺘﺮﻭﮐـﻮﮎ ﺗﺤـﺖ ﻋﻨـﻮﺍﻥ )Enterococcosel (BBL, USA
ﺩﺍﻟﻔﻮﭘﺮﻳـــﺴﺘﻴﻦ )ﺳﻴﻨﺮﺳـــﻴﺪ( ) ۱۵ﻣﻴﮑﺮﻭﮔـــﺮﻡ( ،ﻟﻴﻨﺰﻭﻻﻳـــﺪ
ﻣﻄﺎﻟﻌﻪ ﺟﻤﻊﺁﻭﺭﻱ ﺷﺪﻧﺪ .ﺳـﭙﺲ ﺑـﺮ ﺭﻭﻱ ﻣﺤـﻴﻂ ﺍﺧﺘـﺼﺎﺻﻲ
ﻛﺸﺖ ﺩﺍﺩﻩ ﺷﺪﻩ ،ﭘﺲ ﺍﺯ ۲۴ﺳﺎﻋﺖ ﺍﻧﻜﻮﺑﺎﺳﻴﻮﻥ ﺩﺭ ۳۵ﺩﺭﺟﻪﻱ
ﺳﺎﻧﺘﻲﮔﺮﺍﺩ ،ﺗﻐﻴﻴﺮ ﺭﻧﮓ ﻣﺤﻴﻂ ﺍﺯ ﺯﺭﺩ ﺑﻪ ﻗﻬﻮﻩﺍﻱ ﺗﻴـﺮﻩ ﺗـﺎ ﺳـﻴﺎﻩ
) ۳۰ﻣﻴﮑﺮﻭﮔﺮﻡ( ﮐﻠﺮﺍﻣﻔﻨﻴﮑﻞ ) ۳۰ﻣﻴﮑﺮﻭﮔﺮﻡ( ،ﮐﻮﻳﻨﻮﭘﺮﻳﺴﺘﻴﻦ -
) ۱۵ﻣﻴﮑﺮﻭﮔﺮﻡ( ﺑﻪ ﺭﻭﺵ ﺩﻳﺴﮏ ﺩﻳﻔﻴﻮﮊﻥ ﻭ ﻫﻤﭽﻨﻴﻦ ﺣـﺪﺍﻗﻞ
ﻏﻠﻈــﺖ ﻣﻬــﺎﺭﻱ ) (MICﻭﻧﮑﻮﻣﺎﻳــﺴﻴﻦ ﺑــﻪ ﺭﻭﺵ ﻣﻴﮑــﺮﻭ
ﻧﺸﺎﻥ ﺩﻫﻨﺪﻩﻱ ﻫﻴﺪﺭﻭﻟﻴﺰ ﺍﺳـﻜﻮﻟﻴﻦ ﺑـﻮﺩ .ﺍﻧﺘﺮﻭﻛـﻮﻙﻫـﺎ ﻭ ﻏﻴـﺮ
ﺁﮔﺎﺭ ﺩﺍﻳﻠﻮﺷﻦ ﻣﻄﺎﺑﻖ ﻣﻌﻴﺎﺭﻫـﺎﻱ CLSI ۲۰۱۱ﺗﻌﻴـﻴﻦ ﮔﺮﺩﻳـﺪ
ﺟﻬﺖ ﺗﺸﺨﻴﺺ ﺁﻥ ﺩﻭ ﺍﺯ ﻳﻜـﺪﻳﮕﺮ ﺍﺯ ﺭﺷـﺪ ﺩﺭ ﺑـﺮﺍﺙ ﺣـﺎﻭﻱ
ﺳــﻮﻳﻪﻫــﺎﻱ VREﺑــﺎ ﺍﺳــﺘﻔﺎﺩﻩ ﺍﺯ ﭘﺮﺍﻳﻤﺮﻫــﺎﻱ ﺍﺧﺘــﺼﺎﺻﻲ
ﺍﻧﺘﺮﻭﻛﻮﻙﻫﺎ ﻭ ﻫﺮ ﺩﻭ ﻗﺎﺩﺭ ﺑﻪ ﺗﺠﺰﻳﻪﻱ ﺍﺳﻜﻮﻟﻴﻦ ﻣﻲﺑﺎﺷـﻨﺪ ﻛـﻪ
%۶/۵ﻛﻠﺮﻳﺪ ﺳﺪﻳﻢ ﺑﺮﺭﺳﻲ ﮔﺮﺩﻳﺪ .ﺳﭙﺲ ﺑﻪ ﻣﻨﻈـﻮﺭ ﺗـﺸﺨﻴﺺ
ﮔﻮﻧﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮎ ﺑﺮ ﺍﺳﺎﺱ ﺗﺴﺖﻫﺎﻱ ﺑﻴﻮﺷﻴﻤﻴﺎﻳﻲ ﻫﻤﭽـﻮﻥ
ﺗﺨﻤﻴﺮ ﻗﻨﺪ ،ﺑﺮﺭﺳﻲ ﺣﺮﮐﺖ ﻭ ﺗﻮﻟﻴﺪ ﭘﻴﮕﻤﺎﻥ ﺑـﻪ ﻣﻨﻈـﻮﺭ ﺍﻓﺘـﺮﺍﻕ
ﺑﻬﺘﺮ ﺩﻭ ﮔﻮﻧﻪ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓـﺴﻴﻮﻡ ﻭ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓﮑـﺎﻟﻴﺲ
) .(۱۶ﺣـــﻀﻮﺭ ﮊﻥﻫـــﺎﻱ ﻣﻘﺎﻭﻣـــﺖ ﺑـــﻪ ﻭﻧﮑﻮﻣﺎﻳـــﺴﻴﻦ ﺩﺭ
), 5′-CTTTTTCCGGCTCGACTTCCT-3′
(vanA: 5ʹ- TACTGTTTGGGGGTTGCTC-3′
ﺑـــــــــﻪ ﻃـــــــــﻮﻝ ۷۳۴ﺟﻔـــــــــﺖ ﺑـــــــــﺎﺯ ﻭ
(vanB: GGGGGGGAGGATGGTGGGATAGAG
) ,GGAAGATACCGTGGCTCAAAC-3ﺑـﻪ ﻃـﻮﻝ
ﻛﻪ ﻧـﺴﺒﺖ ﺑـﻪ ﺩﻳﮕـﺮ ﮔﻮﻧـﻪﻫـﺎ ﺍﺯ ﻓﺮﺍﻭﺍﻧـﻲ ﺑـﺎﻻﺗﺮﻱ ﺩﺭ ﺍﻳﺠـﺎﺩ
۴۲۰ﺟﻔﺖ ﺑﺎﺯ ﺑﻪ ﺭﻭﺵ deblex PCRﻃﺒﻖ ﺷﺮﺍﻳﻄﻲ ﮐـﻪ ﺩﺭ
ﺍﺳﺎﺱ ﻭﺟﻮﺩ ﮊﻥﻫﺎﻱ ﺍﺧﺘﺼﺎﺻﻲ ﺍﻳﻦ ﺩﻭ ﮔﻮﻧـﻪ ﻳﻌﻨـﻲ ﮊﻥ ddl
ﺳـــﻮﻳﻪﻫـــﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐـــﻮﺱ ﻓـــﺴﻴﻮﻡ ATCC 51559ﻭ
ﻋﻔﻮﻧﺖﻫﺎ ﻭ ﺩﺭ ﻣﺤـﻴﻂ ﺑﺮﺧـﻮﺭﺩﺍﺭ ﻫـﺴﺘﻨﺪ ﺍﺯ ﺭﻭﺵ PCRﺑـﺮ
ﺍﺧﺘﺼﺎﺻﻲ ﺍﻧﺘﺮﻭﻛﻮﻛﻮﺱ ﻓـﺴﻴﻮﻡ ﻭ ﺍﺧﺘـﺼﺎﺻﻲ ﺍﻧﺘﺮﻭﻛﻮﻛـﻮﺱ
ﻓﻜﺎﻟﻴﺲ GAGGCAGACCAGATTGACG -3′, 5-
)TATGACAGCGACTCCGATTC-3′
E. faecium:
( ddl
ﺑـــــــــﻪ ﻃـــــــــﻮﻝ ۶۵۸ﺟﻔـــــــــﺖ ﺑـــــــــﺎﺯ ﻭ
) 5- ATCAAGTACAGTTAGTCT-3′,
E. faecalis:
(ddl
5- ACGATTCAAAGCTAACTG -3′ﺑﻪ ﻃﻮﻝ ۹۴۱ﺟﻔـﺖ
ﺑﺎﺯ ﺑﺎ ﺷﺮﺍﻳﻂ ﺩﻧﺎﺗﻮﺭﺍﺳﻴﻮﻥ ﺍﻭﻟﻴﻪ :ﺩﺭ ﺩﻣﺎﻱ ۹۴ﺩﺭﺟﻪ ،ﭘﻨﺞ ﺩﻗﻴﻘـﻪ
ﻭ ﻳﮏ ﺳﻴﮑﻞ؛ ﺩﻧﺎﺗﻮﺭﺍﺳﻴﻮﻥ :ﺩﺭ ﺩﻣﺎﻱ ۹۴ﺩﺭﺟﻪ ،ﻳﮏ ﺩﻗﻴﻘﻪ۳۵ ،
ﺳﻴﮑﻞ؛ ﺍﺗﺼﺎﻝ ۵۰ :ﺩﺭﺟﻬﻲ ﻳﮏ ﺩﻗﻴﻘﻪ ۳۵ ،ﺳـﻴﮑﻞ؛ ﺗﮑﺜﻴـﺮ۷۲ :
ﺁﺯﻣﺎﻳﺶ PCRﻗﺒﻠﻲ ﺫﮐﺮ ﺷﺪ ،ﻣﻮﺭﺩ ﺑﺮﺭﺳﻲ ﻗﺮﺍﺭ ﮔﺮﻓﺖ ).(۱۵
ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﮑﺎﻟﻴﺲ ATCC 512999ﺑﻪ ﻋﻨﻮﺍﻥ ﺳﻮﻳﻪﻫﺎﻱ
ﺍﺳﺘﺎﻧﺪﺍﺭﺩ ﺑـﻪﺗﺮﺗﻴـﺐ ﺟﻬـﺖ ﺗﻌﻴـﻴﻦ ﮊﻥﻫـﺎﻱ vanAﻭ vanB
ﻣﻮﺭﺩ ﺍﺳﺘﻔﺎﺩﻩ ﻗﺮﺍﺭ ﮔﺮﻓﺖ.
ﻳﺎﻓﺘﻪﻫﺎ
ﻓﺮﺍﻭﺍﻧـ ـ ﻲ ﮔﻮﻧـــﻪﻫـــﺎﻱ ﺍﻧﺘﺮﻭﮐـــﻮﮎ :ﺩﺭ ﻣﺠﻤـــﻮﻉ ۱۴۴
ﺍﻳﺰﻭﻟﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻲ ﺍﺯ ﻧﻤﻮﻧﻪﻫﺎﻱ ﺑﺎﻟﻴﻨﻲ ﺟﻤـﻊﺁﻭﺭﻱ ﮔﺮﺩﻳـﺪ ﮐـﻪ
) ۶۰(۸۶ﺩﺭﺻﺪ ﺳﻮﻳﻪ ﺍﺯ ﻧﻤﻮﻧـﻪﻫـﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺟـﺪﺍ ﺷـﺪﻧﺪ .ﮐـﻪ
۴۵ﺍﻧﺘﺮﻭﮐﻮﮐــﻮﺱ ﻓــﺴﻴﻮﻡ ) ۵۲ﺩﺭﺻــﺪ( ۳۹ ،ﺍﻧﺘﺮﻭﮐﻮﮐــﻮﺱ
ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ ،ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ ،ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ ،ﺩﻭﺭﻩﻱ ,٢٢ﺷﻤﺎﺭﻩﻱ ,٩١ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ ١٣٩٣
124
ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ
ﻓﮑﺎﻟﻴﺲ ) ۴۵/۳ﺩﺭﺻﺪ( ﻭ ۱) ۱/۶ﺩﺭﺻﺪ( ﺭﺍ ﺩﻳﮕﺮ ﮔﻮﻧـﻪﻫـﺎﻱ
ﺍﻧﺘﺮﻭﮐــﻮﮎ ﺗــﺸﮑﻴﻞ ﻣــﻲﺩﺍﺩﻧــﺪ ۱۸ .ﺍﻳﺰﻭﻟــﻪ ) ۴۰/۶ﺩﺭﺻــﺪ(
ﺍﺩﺭﺍﺭﻱ ﺍﻧﺘﺮﻭﮐﻮﮐــــﻮﺱ ﻓــــﺴﻴﻮﻡ ﺍﺯ ﺯﻧــــﺎﻥ ﻭ ۲۷ﺍﻳﺰﻭﻟــــﻪ
) ۵۹/۳ﺩﺭﺻﺪ( ﺍﺯ ﻣﺮﺩﺍﻥ ﺟﺪﺍ ﮔﺮﺩﻳﺪ .ﻓﺮﺍﻭﺍﻧـﻲ VREﺍﺯ ﻣﻴـﺎﻥ
۴۵ﺳــﻮﻳﻪ ﺍﻧﺘﺮﻭﮐﻮﮐــﻮﺱ ﻓــﺴﻴﻮﻡ ۱۹ﺳــﻮﻳﻪ ) ۴۲/۲ﺩﺭﺻــﺪ(
ﻧﺴﺒﺖ ﺑﻪ ﻭﺍﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻣﻘﺎﻭﻡ ﺑﻮﺩﻧﺪ ﺩﺭ ﺣـﺎﻟﻲ ﮐـﻪ ﻫـﻴﭻ ﮐـﺪﺍﻡ
ﺑﻪ ﺗﺮﺗﻴـﺐ ﺩﺍﺭﺍﻱ ﺑﻴـﺸﺘﺮﻳﻦ ﻣﻴـﺰﺍﻥ VREﺑﻮﺩﻧـﺪ )ﺟـﺪﻭﻝ .(۲
ﺟﺪﻭﻝ :١ﺍﻟﮕﻮﻫﺎﻱ ﻣﻘﺎﻭﻣﺖ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮑﻲ ﺩﺭ ﺳﻮﻳﻪﻫﺎﻱ ﻣﻘﺎﻭﻡ
ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ
ﺍﻟﮕﻮﻫﺎﻱ ﻣﻘﺎﻭﻣﺖ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮑﻲ
) (%ﺗﻌﺪﺍﺩ
ﺍﺯ ﺳـــﻮﻳﻪﻫـــﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐـــﻮﺱ ﻓﮑـــﺎﻟﻴﺲ ﻭ ﺍﻧﺘﺮﻭﮐﻮﮐـــﻮﺱ
)٣ (%١٥/٧
Am/Gm/Cip/Te/E/Chl/Ni
)١ (%٢/٥
Am/Gm/Cip/Te/E/Chl
ﺗﻤـﺎﻣﻲ VREﻫـﺎ ﺩﺍﺭﺍﻱ ﮊﻥ ﻣﻘﺎﻭﻣـﺖ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﻧـﻮﻉ
)٨ (%٤٢
ﮔﺎﻟﻴﻨــﺎﺭﻭﻡ ﺑــﻪ ﺍﻳــﻦ ﺁﻧﺘــﻲﺑﻴﻮﺗﻴــﮏ ﻣﻘــﺎﻭﻣﺘﻲ ﻧــﺸﺎﻥ ﻧﺪﺍﺩﻧــﺪ.
(vanA)Aﺑﻮﺩﻧﺪ )ﺷﮑﻞ .(۱ﺑﺨـﺶﻫـﺎﻱ ﭘﻴﻮﻧـﺪ ﮐﻠﻴـﻪ )۷۷/۷
ﺩﺭﺻــﺪ( ۶۶/۶) ICU ،ﺩﺭﺻــﺪ( ﻭ ﻧﻔﺮﻭﻟــﻮﮊﻱ ) ۵۵/۵ﺩﺭﺻــﺪ(
)٧ (%٣٦/٨
Am/Gm/Cip/Te/E/Ni
Am/Gm/Cip/Te/E
،Amﺁﻣﭙﻲ ﺳﻴﻠﻴﻦ , Gm:ﺟﻨﺘﺎﻣﻴﺴﻴﻦ , Cip:ﺳﻴﭙﺮﻭﻓﻠﻮﮐﺴﺎﺳﻴﻦ, Te:
ﺗﺘﺮﺍﺳﻴﮑﻠﻴﻦ , E:ﺍﺭﻳﺘﺮﻭﻣﺎﻳﺴﻴﻦ , Chl:ﮐﻠﺮﺍﻣﻔﻨﻴﮑﻞ , Ni:ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘﻮﺋﻴﻦ
ﺷﮑﻞ :۱ﺗﺼﻮﻳﺮ ﮊﻝ ﺁﮔﺎﺭﺯ ﺍﺯ ﻧﺘﺎﻳﺞ ﺗﮑﺜﻴﺮ ﮊﻥﻫﺎﻱ vanAﻭ vanBﺑﻪ ﺭﻭﺵ ،Duplex PCRﭼﺎﻫﮏ ﺷﻤﺎﺭﻩ ;۱ﻣﺎﺭﮐﺮ) 2 kbﻓﺮﻣﻨﺘﺎﺯ( ،ﭼﺎﻫﮏ
ﺷﻤﺎﺭﻩ ;۲ﻧﻤﻮﻧﻪ ﮐﻨﺘﺮﻝ ﻣﻨﻔﻲ ،ﭼﺎﻫﮏ ﺷﻤﺎﺭﻩ ;۳ﻧﻤﻮﻧﻪ ﮐﻨﺘﺮﻝ ﻣﺜﺒﺖ ﮊﻥ vanAﺳﻮﻳﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ) ( ATCC51559ﺑﻪ ﻃﻮﻝ 734 bpﻭ
ﮐﻨﺘﺮﻝ ﻣﺜﺒﺖ ﮊﻥ :vanBﺳﻮﻳﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﮑﺎﻟﻴﺲ ) (ATTCC 29212ﺑﻪ ﻃﻮﻝ ،420 bpﭼﺎﻫﮏ ﺷﻤﺎﺭﻩ ;۴ﻧﻤﻮﻧﻪ ﺗﺴﺖ ﻣﻨﻔﻲ،
ﭼﺎﻫﮏﻫﺎﻱ ﺷﻤﺎﺭﻩ ۸ ،۶،۷ ،۵ﻭ ۹ﻧﻤﻮﻧﻪﻫﺎﻱ ﺗﺴﺖ ﻣﺜﺒﺖ ﺩﺍﺭﺍﻱ ﮊﻥ .vanA
ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ ،ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ ،ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ ،ﺩﻭﺭﻩﻱ ,٢٢ﺷﻤﺎﺭﻩﻱ ,٩١ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ ١٣٩٣
ﻟﻴﻠﻲ ﺷﻜﻮﻫﻲ ﺯﺍﺩﻩ ﻭ ﻫﻤﻜﺎﺭﺍﻥ
ﻣﻘﺎﻭﻣﺖ ﺁﻧﺘ ﻲﺑﻴﻮﺗﻴ ﮑ ﻲ :ﺗﻤﺎﻣﻲ ﺳـﻮﻳﻪﻫـﺎﻱ VREﻧـﺴﺒﺖ ﺑـﻪ
ﺁﻧﺘــﻲﺑﻴﻮﺗﻴﮑﻬــﺎﻱ ﺗﻴﮑــﻮﭘﻼﻧﻴﻦ ،ﺁﻣﭙــﻲﺳــﻴﻠﻴﻦ ،ﺟﻨﺘﺎﻣﻴــﺴﻴﻦ،
125
ﻣــﺸﺎﻫﺪﻩ ﮔﺮﺩﻳـﺪ MIC50 ≥۱۲۸ﻣﻴﮑﺮﻭﮔــﺮﻡ ﺩﺭ ﻣﻴﻠـﻲﻟﻴﺘــﺮ ﻭ
MIC90 ≥ ۲۵۶ﻣﻴﮑــﺮﻭ ﮔــﺮﻡ ﺩﺭ ﻣﻴﻠـﻲ ﻟﻴﺘــﺮ ﺗﻌﻴــﻴﻦ ﮔﺮﺩﻳ ـﺪ.
ﺍﺭﻳﺘﺮﻭﻣﺎﻳــﺴﻴﻦ ،ﺳﻴﭙﺮﻭﻓﻠﻮﮐــﺴﺎﺳﻴﻦ ﻣﻘــﺎﻭﻡ ﺑﻮﺩﻧــﺪ .ﺑﻴــﺸﺘﺮﻳﻦ
ﺍﻟﮕﻮﻫﺎﻱ ﻣﻘﺎﻭﻣﺘﻲ ﻏﺎﻟﺐ ﺩﺭ ﺳـﻮﻳﻪﻫـﺎﻱ VREﺑـﻪﺗﺮﺗﻴـﺐ ﺑـﻪ
ﻣﻘﺎﻭﻣــﺖ ﭘــﺲ ﺍﺯ ﺁﻧﺘــﻲﺑﻴﻮﺗﻴــﮏﻫــﺎﻱ ﺫﮐــﺮ ﺷــﺪﻩ ﺩﺭ ﺑﺮﺍﺑــﺮ
ﺻــﻮﺭﺕ ﻣﻘﺎﻭﻣــﺖ ﻫﻤﺰﻣــﺎﻥ ﺑــﻪ ﺁﻣﭙــﻲﺳــﻴﻠﻴﻦ /ﺟﻨﺘﺎﻣﻴــﺴﻴﻦ/
ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘﻮﺋﻴﻦ ﺩﺭ ﻳﺎﺯﺩﻩ ) ۷۸ﺩﺭﺻﺪ( ﺳـﻮﻳﻪ ﻣـﺸﺎﻫﺪﻩ ﮔﺮﺩﻳـﺪ.
ﺳﺴﭙﺮﻭﻓﻠﻮﮐﺴﺎﺳﻴﻦ /ﺗﺘﺮﺍﺳﻴﮑﻠﻴﻦ /ﺍﺭﻳﺘﺮﻭﻣﺎﻳﺴﻴﻦ ﺩﺭ ۴۲ﺩﺭﺻـﺪ
ﭘﻨﺞ ﺳﻮﻳﻪ ) ۲۸/۵ﺩﺭﺻﺪ( ﺳﻮﻳﻪ ﻧﺴﺒﺖ ﺑﻪ ﮐﻠﺮﺍﻣﻔﻨﻴﮑﻞ ﻣﻘـﺎﻭﻡ ﻭ
ﻣــﻮﺍﺭﺩ ﻭ ﻣﻘﺎﻭﻣــﺖ ﻫﻤﺰﻣــﺎﻥ ﺑــﻪ ﺁﻣﭙــﻲﺳــﻴﻠﻴﻦ /ﺟﻨﺘﺎﻣﻴــﺴﻴﻦ/
ﺗﻤﺎﻣﻲ ﺁﻥﻫﺎ ﺑـﻪ ﮐﻮﻳﻨﻮﭘﺮﻳـﺴﺘﻴﻦ -ﺩﺍﻟﻔﻮﭘﺮﻳـﺴﺘﻴﻦ )ﺳﻴﻨﺮﺳـﻴﺪ( ﻭ
ﺳﺴﭙﺮﻭﻓﻠﻮﮐـــــﺴﺎﺳﻴﻦ /ﺗﺘﺮﺍﺳـــــﻴﮑﻠﻴﻦ /ﺍﺭﻳﺘﺮﻭﻣﺎﻳـــــﺴﻴﻦ/
ﻟﻴﻨﺰﻭﻻﻳــﺪ ﺣــﺴﺎﺱ ﺑﻮﺩﻧــﺪ .ﻣﻴــﺰﺍﻥ MICﻭﻧﮑﻮﻣﺎﻳــﺴﻴﻦ ﺍﺯ
ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘـــﻮﺋﻴﻦ ﺩﺭ ۳۹ﺩﺭﺻـــﺪ ﻣـــﻮﺍﺭﺩ ﻣـــﺸﺎﻫﺪﻩ ﮔﺮﺩﻳـ ـﺪ
۶۴ﺗــﺎ ۵۱۲ﻣﻴﮑﺮﻭﮔــﺮﻡ ﺩﺭ ﻣﻴﻠ ـﻲﻟﻴﺘــﺮ ﺩﺭ ﺳــﻮﻳﻪﻫــﺎﻱ VRE
)ﺟﺪﻭﻝ .(۱
ﺟﺪﻭﻝ :٢ﻣﻴﺰﺍﻥ )ﺩﺭﺻﺪ( ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭﻣﻴﺎﻥ ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺟﺪﺍ ﺷﺪﻩ ﺍﺯ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺑﻴﻤﺎﺭﺍﻥ
ﺑﺴﺘﺮﻱ ﺩﺭ ﺑﺨﺶﻫﺎﻱ ﻣﺨﺘﻠﻒ ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫﺎﻱ ﻣﻮﺭﺩ ﻣﻄﺎﻟﻌﻪ
ﺑﺨﺶﻫﺎﻱ ﺑﻴﻤﺎﺭﺳﺘﺎﻥ
E. faecium
VRE
ﺳﺎﻳﺮ ﺑﺨﺶﻫﺎ
ﻧﻔﺮﻭﻟﻮﮊﻱ
ﭘﻴﻮﻧﺪ ﮐﻠﻴﻪ
ﮔﻮﺍﺭﺵ
ICU
)٦ (%١٣/٣
)٩ (%٢٠
)٩ (%٢٠
)١٢ (%٢٦/٦
)٩ (%٢٠
٠
)٥ (%٥٥/٥
)٧ (%٧٧/٧
)٣ (%٢٥
)٦ (%٦٦/٦
ﺑﺤﺚ
ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺷﺎﻳﻊﺗﺮﻳﻦ ﻋﻔﻮﻧﺖ ﺑﻴﻤﺎﺭﺳـﺘﺎﻧﻲ ﺍﻳﺠـﺎﺩ
ﻳﮏ ﺑﻮﺩﻩ ﻭﻟﻲ ﺍﻣﺮﻭﺯﻩ ﺍﻳﻦ ﻧﺴﺒﺖ ﺩﺭ ﺣﺎﻝ ﮐـﺎﻫﺶ ﻣـﻲ ﺑﺎﺷـﺪ ﻭ
ﺷﺪﻩ ﺗﻮﺳﻂ ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ﻣﻲﺑﺎﺷـﻨﺪ .ﺩﺭ ﺑﻴـﺸﺘﺮ ﻣـﻮﺍﺭﺩ ﻧﻴـﺎﺯ ﺑـﻪ
ﺣﺎﻝ ﺍﻓﺰﺍﻳﺶ ﻣﻲﺑﺎﺷﺪ ) .(۱۷ﺩﺭ ﺑﺮﺧﻲ ﺍﺯ ﻧﺘﺎﻳﺞ ﮔﺰﺍﺭﺵ ﺷﺪﻩ ﺍﺯ
ﺷـﺮﻭﻉ ﺩﺭﻣـﺎﻥ ﺍﻳـﻦ ﻋﻔﻮﻧـﺖﻫـﺎ ﻗﺒــﻞ ﺍﺯ ﻧﺘـﺎﻳﺞ ﺁﺯﻣـﺎﻳﺶﻫــﺎﻱ
ﻣﻴﮑــﺮﻭﺏﺷﻨﺎﺳ ـﻲ ﻣـﻲﺑﺎﺷــﺪ ،ﻟــﺬﺍ ﺗﺠــﻮﻳﺰ ﺻــﺤﻴﺢ ﻭ ﻣﻨﻄﻘ ـﻲ
ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎ ﺩﺭ ﺍﻳﻦﮔﻮﻧﻪ ﻣﻮﺍﺭﺩ ﺑﺴﻴﺎﺭ ﺣﺎﻳﺰ ﺍﻫﻤﻴﺖ ﻣﻲﺑﺎﺷـﺪ.
ﺩﺭ ﺳﺎﻝﻫﺎﻱ ﺍﺧﻴﺮ ﻣﻄﺎﻟﻌﺎﺕ ﻓﺮﺍﻭﺍﻧـﻲ ﺩﺭ ﻣـﻮﺭﺩ ﺍﭘﻴـﺪﻣﻴﻮﻟﻮﮊﻱ ﻭ
ﻣﻘﺎﻭﻣﺖﻫﺎﻱ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮑﻲ ﺩﺭ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻲ ﺩﺭ ﺍﻳـﺮﺍﻥ
ﺻﻮﺭﺕ ﮔﺮﻓﺘﻪ ﺍﺳﺖ .ﺍﻣﺮﻭﺯﻩ ﺑﺎ ﺗﻮﺟﻪ ﺑﻪ ﺍﻓﺰﺍﻳﺶ ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎﻱ
ﻧﺴﺒﺖ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺑﻴﻤﺎﺭﺳﺘﺎﻧﻲ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺩﺭ
ﺍﻳ ـﺮﺍﻥ ﻧﻴ ـﺰ ﺷــﺎﻫﺪ ﮐــﺎﻫﺶ ﻧﻘــﺶ ﺍﻧﺘﺮﻭﮐﻮﮐــﻮﺱ ﻓﮑــﺎﻟﻴﺲ ﺩﺭ
ﻋﻔﻮﻧﺖﻫﺎﻱ ﺑﻴﻤﺎﺭﺳﺘﺎﻧﻲ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ﻫـﺴﺘﻴﻢ .ﺩﺭ ﻳـﮏ
ﻣﻄﺎﻟﻌﻪ ﮐﻪ ﺗﻮﺳﻂ ﺍﻣﺎﻧﻴﻨﻲ ﻭ ﻫﻤﮑﺎﺭﺍﻥ ﺩﺭ ﺍﻳـﺮﺍﻥ ﺩﺭ ﺳـﺎﻝ ۲۰۰۸
ﺍﻧﺠﺎﻡ ﮔﺮﻓﺖ ﻧﺴﺒﺖ ﻋﻔﻮﻧﺘﻬﺎﻱ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓﮑـﺎﻟﻴﺲ
ﺑﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ۱/۸ﺑﻪ ۱ﮔﺰﺍﺭﺵ ﺷﺪﻩ ﺍﺳـﺖ ) .(۱۸ﺩﺭ
ﻳ ـﮏ ﻣﻄﺎﻟﻌــﻪ ﺩﻳﮕــﺮ ﮐــﻪ ﺩﺭ ﺑﻴﻤﺎﺭﺳــﺘﺎﻥﻫــﺎﻱ ﺗﻬــﺮﺍﻥ ﺗﻮﺳــﻂ
ﭼﻨﺪ ﻣﻘﺎﻭﻣﺘﻲ ﺑﻪﻭﻳﮋﻩ ،ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐـﻮﮎ ﻓـﺴﻴﻮﻡ ﻣﻘـﺎﻭﻡ ﺑـﻪ
ﺳﻠﻄﺎﻥﺩﻻﻝ ﻭ ﻫﻤﮑﺎﺭﺍﻥ ﺩﺭ ﻫﻤﺎﻥ ﺳﺎﻝ ﺻـﻮﺭﺕ ﮔﺮﻓـﺖ ﺩﺭ ۳۰
ﺑﻴﺶ ﺍﺯ ﺳﺎﻳﺮ ﮔﻮﻧﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮎ ﻣﻲﺑﺎﺷـﺪ .ﻫـﺮ ﭼﻨـﺪ ﮐـﻪ ﺩﺭ
) .(۱۹ﻧﺘﺎﻳﺞ ﺣﺎﺻﻞ ﺍﺯ ﺍﻳﻦ ﺗﺤﻘﻴﻖ ﺣﺎﺿﺮ ﻧﻴﺰ ﭼﻨـﻴﻦ ﻣﻄﻠﺒـﻲ ﺭﺍ
ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻣﻴﺰﺍﻥ ﻋﻔﻮﻧﺖﻫﺎﻱ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓـﺴﻴﻮﻡ
ﮔﺬﺷﺘﻪ ﻧﺴﺒﺖ ﻋﻔﻮﻧﺖﻫﺎﻱ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﮑﺎﻟﻴﺲ ﺑﻴﺶ
ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺑﻮﺩﻩ ﺍﺳﺖ ﺑﻪﻃﻮﺭﻱ ﮐﻪ ﻧﺴﺒﺖ ﺁﻥ ﺩﻩ ﺑـﻪ
ﺻﺪ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ،ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺟﺪﺍ ﺷﺪﻩ ﺍﺳـﺖ
ﺗﺎﻳﻴـﺪ ﻣـﻲﮐﻨـﺪ ﻭ ﺳـﻬﻢ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓـﺴﻴﻮﻡ ﺣﺘـﻲ ﺑـﻴﺶ ﺍﺯ
ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﮑﺎﻟﻴﺲ ﺩﺭ ﺍﻳﺠﺎﺩ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﻣـﻲﺑﺎﺷـﺪ
ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ ،ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ ،ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ ،ﺩﻭﺭﻩﻱ ,٢٢ﺷﻤﺎﺭﻩﻱ ,٩١ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ ١٣٩٣
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ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ
ﺑﻪﻃﻮﺭﻱ ﮐﻪ ﻧـﺴﺒﺖ ﻋﻔﻮﻧـﺖ ﺍﺩﺭﺍﺭﻱ ﺣﺎﺻـﻞ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ
ﺩﺭ ﺑﻴﻤﺎﺭﺳــﺘﺎﻥﻫــﺎﻱ ﺗﻬــﺮﺍﻥ ﭘﺮﺩﺍﺧﺘــﻪﺍﻧــﺪ ﻧﻤﻮﻧــﻪﻫــﺎﻱ ﺍﺩﺭﺍﺭﻱ
ﻓﺴﻴﻮﻡ ﺑﻪ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﮑﺎﻟﻴﺲ ۱/۱۵ﺑـﻪ ۴۵) ۱ﺩﺭ ﺑﺮﺍﺑـﺮ (۳۹
۸۹ﺩﺭﺻﺪ ﺍﺯ ﻧﻤﻮﻧﻪﻫﺎ ﺭﺍ ﺗﺸﮑﻴﻞ ﻣﻲﺩﺍﺩﻧﺪ ﻭ ﺗﻨﻬﺎ ۴/۶ﺩﺭﺻـﺪ ﺍﺯ
ﻣﺸﺎﻫﺪﻩ ﮔﺮﺩﻳﺪ .ﻭ ﺩﺭ ﻭﺍﻗـﻊ ﺍﻭﻟـﻴﻦ ﮔﺰﺍﺭﺷـﻲ ﺍﺳـﺖ ﮐـﻪ ﺩﺭ ﺁﻥ
ﺍﻳﻦ ﺳﻮﻳﻪﻫﺎ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻣﻘﺎﻭﻡ ﺑﻮﺩﻧـﺪ .ﺗﻤـﺎﻣﻲ ﺳـﻮﻳﻪﻫـﺎﻱ
ﻧﺴﺒﺖ ﻋﻔﻮﻧـﺖﻫـﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓـﺴﻴﻮﻡ ﺑﻴـﺸﺘﺮ ﻣـﻲﺑﺎﺷـﺪ.
VREﺩﺍﺭﺍﻱ vanAﺑﻮﺩﻧـــﺪ ﻭ ﻣﻘﺎﻭﻣـــﺖ ﻫﻤﺰﻣـــﺎﻥ ﺑـــﻪ
ﻧــﺴﺒﺖ ﺑــﻪ ﺁﻧﺘــﻲﺑﻴﻮﺗﻴــﮏﻫــﺎﻱ ﻭﻧﮑﻮﻣﺎﻳــﺴﻴﻦ ،ﺁﻣﭙــﻲﺳــﻴﻠﻴﻦ،
ﺍﺭﻳﺘﺮﻭﻣﺎﻳﺴﻴﻦ ﺍﻟﮕـﻮﻱ ﻣﻘـﺎﻭﻣﺘﻲ ﻏﺎﻟـﺐ ﺑـﻮﺩﻩ ﻭ ﺩﺭ ۴۷ﺩﺭﺻـﺪ
ﺟﻨﺘﺎﻣﻴﺴﻴﻦ ،ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘـﻮﺋﻴﻦ ،ﺳﻴﭙﺮﻭﻓﻠﻮﮐـﺴﺎﺳﻴﻦ ،ﮐـﻪ ﻣﻌﻤـﻮﻻ
ﺳﻮﻳﻪﻫﺎﻱ VREﻣﺸﺎﻫﺪﻩ ﮔﺮﺩﻳـﺪ ) .(۳۱ﺩﺭ ﻣﻄﺎﻟﻌـﻪﻱ ﺣﺎﺿـﺮ
ﺗﻮﺳﻂ ﭘﺰﺷﮑﺎﻥ ﺟﻬﺖ ﺩﺭﻣﺎﻥ ﻋﻔﻮﻧﺖﻫـﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺍﻧﺘﺮﻭﮐـﻮﮐﻲ
ﻣﻨﻄﺒﻖ ﺑﺎ ﺍﻳﻦ ﺗﺤﻘﻴﻖ ﺍﺯ ﺍﻳﺮﺍﻥ vanA ،ﮊﻧﻮﺗﻴﭗ ﻏﺎﻟـﺐ ﺩﺭ ﻣﻴـﺎﻥ
ﻃﺒﻖ ﺗﺤﻘﻴﻖ ﮐـﻪ ﺗﻮﺳـﻂ ﺭﻫﺒـﺮ ﻫﻤﮑـﺎﺭﺍﻥ ﺍﻧﺠـﺎﻡ ﺩﺍﺩﻧـﺪ ﻧﻴﺘـﺮﻭ
ﻫﻤﺰﻣـــﺎﻥ ﺑـــﻪ ﻭﻧﮑﻮﻣﺎﻳـ ـﺴﻴﻦ ،ﺟﻨﺘﺎﻣﻴـ ـﺴﻴﻦ ،ﺁﻣﭙـ ـﻲﺳـ ـﻴﻠﻴﻦ،
ﻓﻮﺭﺍﻧﺘﻮﺋﻴﻦ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏ ﻧﺴﺒﺘﺎ ﻣﻮﺛﺮﻱ ﺑﺮﺍﻱ ﺩﺭﻣﺎﻥ ﻋﻔﻮﻧـﺖﻫـﺎﻱ
ﺳﻴﭙﺮﻭﻓﻠﻮﮐﺴﺎﺳﻴﻦ ﻭ ﺍﺭﻳﺘﺮﻭﻣﺎﻳﺴﻴﻦ ﺩﺭ ۴۲ﺩﺭﺻﺪ ﻣﻮﺍﺭﺩ ،ﺍﻟﮕﻮﻱ
ﺍﺩﺭﺍﺭﻱ ﻧﺎﺷ ـﻲ ﺍﺯ ﺳــﻮﻳﻪﻫــﺎﻱ VREﺑــﻮﺩﻩ ﺍﺳــﺖ ﻭ ﻣﻘﺎﻭﻣــﺖ
ﻣﻘﺎﻭﻣﺘﻲ ﻏﺎﻟﺐ ﺑﻮﺩﻩ ﻭ ﻣﻘﺎﻭﻣﺖ ﻫﻤﺰﻣﺎﻥ ﺑﻪ ﺁﻧﺘﻲﺑﻴﻮﻳﮏﻫﺎﻱ ﺫﮐﺮ
ﻫﻤﺰﻣﺎﻥ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻭ ﻧﻴﺘﺮﻭﻓﻮﺍﻧﺘـﻮﺋﻴﻦ ﺩﺭ ﺑﻴﻤـﺎﺭﺍﻥ ﺑـﺴﺘﺮﻱ
ﺷــﺪﻩ ﻭ ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘــﻮﺋﻴﻦ ﺩﺭ ۳۶ﺩﺭﺻــﺪ ﺳــﻮﻳﻪﻫــﺎﻱ VRE
ﻧﺘﺎﻳﺞ ﺣﺎﺻﻞ ﺍﺯ ﺍﻳﻦ ﻣﻄﺎﻟﻌﻪ ﺣﺎﮐﻲ ﺍﺯ ﻓﺮﺍﻭﺍﻧـﻲ ﺑـﺎﻻﻱ ﻣﻘﺎﻭﻣـﺖ
ﺗﺠﻮﻳﺰ ﻣﻲﮔﺮﺩﻧﺪ ).(۲۰
ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ،ﺟﻨﺘﺎﻣﻴﺴﻴﻦ ،ﺁﻣﭙـﻲ ﺳـﻴﻠﻴﻦ ،ﺳﻴﭙﺮﻭﻓﻠﻮﮐـﺴﺎﺳﻴﻦ ﻭ
ﺳــﻮﻳﻪﻫــﺎﻱ VREﺍﻧﺘﺮﻭﮐــﻮﮐﺲ ﻓــﺴﻴﻮﻡ ﻣــﻲﺑﺎﺷــﺪ .ﻣﻘﺎﻭﻣــﺖ
ﺑـﻴﺶ ﺍﺯ ﺑﻴﻤـﺎﺭﺍﻥ ﺳـﺮ ﭘـﺎﻳﻲ ﺑـﻮﺩﻩ ﺍﺳـﺖ ) ۴۲ .(۲۱ﺩﺭﺻــﺪ ﺍﺯ
ﻣﺸﺎﻫﺪﻩ ﺷﺪﻩ ﺍﺳﺖ.
ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﻧﺴﺒﺖ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﻣﻘـﺎﻭﻡ
ﺩﺭ ﺗﺤﻘﻴﻘﻲ ﮐـﻪ ﺗﻮﺳـﻂ ﮊﺍﻧـﻞ ﻭ ﻫﻤﮑـﺎﺭﺍﻥ ﺩﺭ ﺍﻳـﺎﻻﺕ ﻣﺘﺤـﺪﻩ
ﺑﻮﺩﻧﺪ ﮐﻪ ﺍﻳﻦ ﺭﻗﻢ ﺑﻴﺶ ﺍﺯ ﺍﺭﻗﺎﻡ ﮔﺰﺍﺭﺵ ﺷﺪﻩ ﺩﺭ ﺍﻳﺮﺍﻥ ﻭ ﺑﺮﺧﻲ
ﺻﻮﺭﺕ ﮔﺮﻓﺖ ﺁﻧﺘـﻲﺑﻴﻮﺗﻴـﮏﻫـﺎﻱ ﻟﻴﻨﺰﻭﻻﻳـﺪ ،ﻧﻴﺘﺮﻭﻓﻮﺍﻧﺘـﻮﺋﻴﻦ،
ﮐﺸﻮﺭﻫﺎﻱ ﺁﺳﻴﺎﻳﻲ ﻭ ﺍﺭﻭﭘﺎﻳﻲ ﻭﻟﻲ ﭘﺎﻳﻴﻦﺗـﺮ ﺍﺯ ﻧﺘـﺎﻳﺞ ﺁﻣﺮﻳﮑـﺎﻱ
ﮐﻠﺮﺍﻣﻔﻨﻴﮑــﻞ ،ﮐﻮﻳﻨﻮﭘﺮﻳــﺴﻴﺘﻴﻦ -ﺩﺍﻟﻔــﻮ ﭘﺮﻳــﺴﺘﻴﻦ ﻣــﻮﺛﺮﺗﺮﻳﻦ
ﻻﺗﻴﻦ ) ۴۸ﺩﺭﺻﺪ( ﻭ ﺁﻣﺮﻳﮑﺎﻱ ﺷﻤﺎﻟﻲ ) ۷۶ﺩﺭﺻﺪ( ﻣﻲﺑﺎﺷﺪ .ﺩﺭ
ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏ ﺩﺭ ﺩﺭﻣﺎﻥ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﻧﺎﺷﻲ ﺍﺯ ﺳـﻮﻳﻪﻫـﺎﻱ
ﻭﺍﻗﻊ ﻓﺮﺍﻭﺍﻧﻲ VREﺩﺭ ﺁﺳﻴﺎ ﮐﻤﺘﺮ ﺍﺯ ﺁﻣﺮﻳﮑﺎ ﻣﻲﺑﺎﺷﺪ ﻭ ﻳﮑﻲ ﺍﺯ
ﻣﻘﺎﻭﻡ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺑﺎ ۲/۴ ،۰/۶ ،۰/۳ﻭ
ﺩﻻﻳﻞ ﺁﻥ ﻇﻬﻮﺭ ﺩﻳﺮﺗﺮ ﺍﻳﻦ ﺳـﻮﻳﻪﻫـﺎ ﺩﺭ ﻗـﺎﺭﻩ ﺁﺳـﻴﺎ ﻣـﻲﺑﺎﺷـﺪ
۱۳/۶ﺩﺭﺻـــﺪ ﻣﻘﺎﻭﻣـــﺖ ﺑـــﻪ ﺗﺮﺗﻴـــﺐ ﻭ ﺁﻣﭙـــﻲﺳـــﻴﻠﻴﻦ ﻭ
) .(۲۲- ۲۸ﺩﺭ ﻣﻄﺎﻟﻌﻪﺍﻱ ﮐﻪ ﺩﺭ ﺍﻳﺎﻻﺕ ﻣﺘﺤـﺪﻩ ﺻـﻮﺭﺕ ﮔﺮﻓﺘـﻪ
ﺳﻴﭙﺮﻭﻓﻠﻮﮐﺴﺎﺳﻴﻦ ﺑﺎ ۹۶ﻭ ۱۰۰ﺩﺭﺻـﺪ ﻣﻘﺎﻭﻣـﺖ ﺍﺛـﺮ ﺑﺨـﺸﻲ
۸۰ﺩﺭﺻﺪ ﺳﻮﻳﻪﻫـﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓـﺴﻴﻮﻡ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ
ﺿﻌﻴﻔﻲ ﻋﻠﻴﻪ ﺍﻳﻦ ﺳﻮﻳﻪﻫﺎ ﺩﺍﺷﺘﻨﺪ ) .(۳۲ﮐﻪ ﺩﺭ ﺗﺤﻘﻴـﻖ ﺣﺎﺿـﺮ
ﻣﻘﺎﻭﻡ ﺑﻮﺩﻧﺪ ) ،(۲۹ﺗﻨﻬﺎ ﻣﻮﺭﺩﻱ ﮐﻪ ﺩﺭ ﺍﻳﺮﺍﻥ ﻧـﺴﺒﺖ VREﻫـﺎ
ﺗﺎﺛﻴﺮ ﻧﻴﺘﺮﻭﻓﻮﺭﺍﻧﺘﻮﺋﻴﻦ ﺑﺴﻴﺎﺭ ﭘﺎﻳﻴﻦ ﺑﺎ ﻣﻘﺎﻭﻣﺖ %۷۸ﻭ ﮐﻠﺮﺍﻣﻔﻨﻴﮑﻞ
ﺑﻴﺶ ﺍﺯ ﻧﺘﺎﻳﺞ ﺣﺎﺻﻞ ﺍﺯ ﺍﻳﻦ ﻣﻄﺎﻟﻌﻪ ﺑﻮﺩﻩ ،ﮔﺰﺍﺭﺷـﻲ ﺍﺳـﺖ ﮐـﻪ
ﺑﺎ %۲۸ﻣﺸﺎﻫﺪﻩ ﮔﺮﺩﻳﺪ .ﻟﻨﺰﻭﻻﻳﺪ ﻭ ﺳﻴﻨﺮﺳﻴﺪ ﺑﺎ ﻣﻘﺎﻭﻣـﺖ ﺻـﻔﺮ
ﺗﻮﺳﻂ ﻓﻴﺾ ﺁﺑﺎﺩﻱ ﻭ ﻫﻤﮑـﺎﺭﺍﻥ ﺩﺭ ﺳـﺎﻝ ۲۰۰۸ﺍﺯ ﺑﻴﻤﺎﺭﺳـﺘﺎﻥ
ﺩﺭ ﺻﺪ ﻣﻮﺛﺮﺗﺮﻳﻦ ﻭ ﺁﻣﭙﻲﺳﻴﻠﻴﻦ ،ﺟﻨﺘﺎﻣﻴﺴﻴﻦ ،ﺳﻴﭙﺮﻭﻓﻠﻮﮐﺴﺎﺳﻴﻦ
ﮔﺰﺍﺭﺵ ﮔﺮﺩﻳﺪﻩ ﺍﺳﺖ .ﺩﺭ ﺣـﺎﻟﻲﮐـﻪ ﺗﻌـﺪﺍﺩ ﻧﻤﻮﻧـﻪﻫـﺎﻱ ﻣـﻮﺭﺩ
ﻧﺎﻣﻨﺎﺳﺐﺗﺮﻳﻦ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏ ﺷﻨﺎﺧﺘﻪ ﺷﺪﻧﺪ .ﻳﮑﻲ ﺍﺯ ﺩﻻﻳـﻞ ﻋـﺪﻡ
ﺑﺮﺭﺳﻲ ﺩﺭ ﻣﻄﺎﻟﻌﻪﻱ ﻣﺎ ﺑﻴﺶ ﺍﺯ ﺍﻳﻦ ﺗﺤﻘﻴـﻖ ﻣـﺬﮐﻮﺭ ﻣـﻲﺑﺎﺷـﺪ
ﻣﻘﺎﻭﻣﺖ ﺑـﻪ ﻟﻴﻨﺰﻭﻻﻳـﺪ ﻭ ﺳﻴﻨﺮﺳـﻴﺪ ﻋـﺪﻡ ﺗﺠـﻮﻳﺰ ﻓـﺮﻭﺍﻥ ﺍﻳـﻦ
) .(۳۰ﺍﺧﻴﺮﺍ ﺩﺭ ﻳﮏ ﻣﻄﺎﻟﻌﻪ ﮐﻪ ﺗﻮﺳﻂ ﺻﺪﺍﻗﺖ ﻭ ﻫﻤﮑـﺎﺭﺍﻥ ﺩﺭ
ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏ ﺩﺭ ﺑﻴﻤﺎﺭﺳﺘﺎﻥﻫﺎﻱ ﺍﻳﺮﺍﻥ ﻭ ﻫﻤﭽﻨـﻴﻦ ﻋﺮﺿـﻪ ﺁﻥ ﺩﺭ
۲۰۱۲ﻣﻨﺘﺸﺮ ﺷﺪﻩ ،ﺑـﻪ ﺑﺮﺭﺳـﻲ ﻣﻘﺎﻭﻣـﺖ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻴﻦ ﺩﺭ
ﺳﺎﻝﻫﺎﻱ ﺍﺧﻴـﺮ ﻭ ﺑـﻪ ﻣﻘـﺪﺍﺭ ﭘـﺎﻳﻴﻦ ﺩﺭ ﺩﺍﺭﻭﺧﺎﻧـﻪﻫـﺎﻱ ﮐـﺸﻮﺭ
ﻟﺒﺎﻓﻲﻧﮋﺍﺩ ﺍﺭﺍﻳﻪ ﮐﺮﺩﻩﺍﻧﺪ ﮐﻪ ﺩﺭ ﺁﻥ ﻣﻴﺰﺍﻥ VREﻫـﺎ ۷۰ﺩﺭﺻـﺪ
ﺳﻮﻳﻪﻫﺎﻱ ﺍﻧﺘﺮﻭﮐﻮﮐﻮﺱ ﻓﺴﻴﻮﻡ ﺟﺪﺍ ﺷﺪﻩ ﺍﺯ ﻧﻤﻮﻧﻪﻫـﺎﻱ ﺑـﺎﻟﻴﻨﻲ
ﻭ ﺍﺭﻳﺘﺮﻭﻣﺎﻳﺴﻴﻦ ﺑﺎ ﻣﻘﺎﻭﻣﺖ ۱۰۰ﺩﺭﺻﺪ ﺩﺭ ﺳـﻮﻳﻪﻫـﺎﻱ VRE
ﻣﻲﺑﺎﺷﺪ ).(۳۳
ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ ،ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ ،ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ ،ﺩﻭﺭﻩﻱ ,٢٢ﺷﻤﺎﺭﻩﻱ ,٩١ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ ١٣٩٣
ﻟﻴﻠﻲ ﺷﻜﻮﻫﻲ ﺯﺍﺩﻩ ﻭ ﻫﻤﻜﺎﺭﺍﻥ
127
ﻣﻘﺎﻭﻣﺖ ﺑﺎﮐﺘﺮﻱﻫﺎﻱ ﺑﻴﻤﺎﺭﺳﺘﺎﻧﻲ ﺍﺯ ﺟﻤﻠﻪ ﺳﻮﻳﻪﻫﺎﻱ ﻣﻘـﺎﻭﻡ ﺑـﻪ
ﻃﺒــﻖ ﺍﻳــﻦ ﺗﺤﻘﻴــﻖ ﻭ ﺩﻳﮕــﺮ ﻣﻄﺎﻟﻌــﺎﺕ ﺑﻴﻤــﺎﺭﺍﻥ ﺑــﺴﺘﺮﻱ ﺩﺭ
.(۲۵) ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺍﻧﺘﺮﻭﮐﻮﮎ ﻣﻲﺷﻮﺩ
ﻧﻔﺮﻭﻟـﻮﮊﻱ ﺩﺭ ﻣﻌـﺰﺽ،ICU ،ﺑﺨﺶﻫﺎﻳﻲ ﭼﻮﻥ ﭘﻴﻮﻧـﺪ ﮐﻠﻴـﻪ
ﺍﻧﺘﺮﻭﮐﻮﮐـﻮﺱ ﻓـﺴﻴﻮﻡ ﺩﺭVRE ﺁﻟﻮﺩﮔﻲ ﺑﻴﺸﺘﺮﻱ ﺑﺎ ﺳﻮﻳﻪﻫﺎﻱ
ﻧﺘﻴﺠﻪﮔﻴﺮﻱ
ﺩﺭ ﻣﺠﻤـﻮﻉ ﺍﻓـﺰﺍﻳﺶ ﺳــﻮﻳﻪﻫـﺎﻱ ﻣﻘــﺎﻭﻡ ﺑـﻪ ﻭﻧﮑﻮﻣﺎﻳـﺴﻦ
ﺍﻧﺘﺮﻭﮐﻮﮐــﻮﺱ ﻓــﺴﻴﻮﻡ ﺑــﺎ ﻣﻘﺎﻭﻣــﺖ ﭼﻨﺪﮔﺎﻧــﻪ ﺩﺭ ﺑﺮﺍﺑــﺮ ﺳــﺎﻳﺮ
ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎﻱ ﻣﻮﺛﺮ ﺩﺭ ﺩﺭﻣﺎﻥ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ ﺟﺎﻱ ﺑﺴﻲ
ﮐﻪ ﺍﻳﻦ ﺍﻣﺮ ﻣﻲﺗﻮﺍﻧﺪ ﻧﺎﺷـﻲ ﺍﺯ ﺗﺠـﻮﻳﺰ.ﺗﺎﻣﻞ ﻭ ﻧﮕﺮﺍﻧﻲ ﻣﻲﺑﺎﺷﺪ
ﮐـﺴﺐ.ﺑﻲﺭﻭﻳﻪ ﺑﺮﺧﻲ ﺁﻧﺘـﻲﺑﻴﻮﺗﻴـﮏﻫـﺎ ﺩﺭ ﺑﻴﻤﺎﺭﺳـﺘﺎﻥ ﺑﺎﺷـﺪ
ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺗﻮﺳﻂ ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ﺗﺎﺛﻴﺮﺍﺕ ﺟﺪﻱ ﺑـﺮ
.ﺭﻭﻧﺪ ﺩﺭﻣﺎﻥ ﻭ ﮐﻨﺘﺮﻝ ﻋﻔﻮﻧﺖﻫﺎﻱ ﻧﺎﺷﻲ ﺍﺯ ﺍﻧﺘﺮﻭﮐﻮﮎﻫﺎ ﺩﺍﺭﺩ
ﺑﺴﺘﺮﻱ ﺑﻮﺩﻥ ﻃﻮﻻﻧﻲ ﻣﺪﺕ ﺩﺭ،ﻗﺮﺍﺭ ﺩﺍﺭﻧﺪ ﮐﻪ ﻣﻲﺗﻮﺍﻧﺪ ﻧﺎﺷﻲ ﺍﺯ
ﺿﻌﻒ ﺳﻴـﺴﺘﻢ ﺍﻳﻤﻨـﻲ ﺩﺭ ﺍﺛـﺮ ﻋﻮﺍﻣـﻞ ﺯﻣﻴﻨـﻪﺍﻱ ﻭ،ﺑﻴﻤﺎﺭﺳﺘﺎﻥ
ﻣﺼﺮﻑ ﺩﺍﺭﻭﻫﺎﻱ ﺳﺮﮐﻮﺏ ﮐﻨﻨﺪﻩ ﺳﻴﺴﺘﻢ ﺍﻳﻤﻨﻲ ﻭ ﮐﻬﻮﻟﺖ ﺳﻦ
ﻓﺸﺎﺭ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮑﻲ ﺩﺭ ﻣﺤﻴﻂﻫﺎﻱ ﺑﻴﻤﺎﺭﺳﺘﺎﻧﻲ ﺑـﻪ ﺩﻟﻴـﻞ ﺗﺠـﻮﻳﺰ
ﻓـﺮﺍﻭﺍﻥ ﻭ ﻏﻴـﺮ ﻣﻨﻄﻘـﻲ ﺑـﺴﻴﺎﺭﻱ ﺍﺯ ﺁﻧﺘـﻲﺑﻴﻮﺗﻴـﮏﻫـﺎ ﺑـﻪﻭﻳـﮋﻩ
ﺳﻔﺎﻟﻮﺳﭙﻮﺭﻳﻦﻫﺎ،ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﻭ ﺁﻧﺘﻲﺑﻴﻮﺗﻴﮏﻫﺎﻱ ﻭﺳﻴﻊ ﺍﻟﻄﻴﻒ
ﻭ ﻣﺘﺮﻭﻧﻴﺪﺍﺯﻭﻝ ﻣﻲﺑﺎﺷﺪ ﮐﻪ ﺑﺎﻋﺚ ﺑﻪ ﻫﻢ ﺧﻮﺭﺩﻥ ﻓﻠﻮﺭ ﻣﻴﮑﺮﻭﺑﻲ
ﺩﺳﺘﮕﺎﻩ ﮔﻮﺍﺭﺵ ﻭ ﻣﺠﺎﻝ ﺭﺷﺪ ﭘﺎﺗﻮﮊﻥﻫـﺎﻱ ﺭﻭﺩﻩﺍﻱ ﻭ ﺍﻓـﺰﺍﻳﺶ
References
vancomycin-sensitive
1- Fridken SK, Gynes RP. Antimicrobial resistant
strain: effect on interpretation of clonality. J Clin
in intensive care units. Clin Chest Med. 1999; 20:
Microbiol. 1999; 37: 3934-9.
303-16.
7- Boyd DA, Willey BM, Fawcett D, et al.
2- Murray BE. Vancomycin resistant enterococcal
Molecular
infections. New Engl J Med. 2000; 342: 710-21.
faecalis N06-0364 with low-level vancomycin
3- Gold HS. Vancomycin resistant enterococci:
resistance harboring a novel D-Ala-D-Ser gene
mechanisms and clinical observations. Clin Infect
cluster, vanL. Antimicrob Agents Chemother.
Dis. 2001; 33: 210-9.
2008; 52: 2667-72.
4- Zhanel G, Karlowsky JA, Hoban D. In vitro
8- McKessar SJ, Berry AM, Bell JM, et al.
activities
Genetic
of
six
fluoroquinolones
against
Enterococcus
characterization
characterization
of
faecium
of Enterococcus
vanG,
novel
Canadian isolates of vancomycin sensitive and
vancomycin resistance locus
vancomycin-resistant
faecalis. Antimicrob Agents Chemother. 2000; 44:
Enterococcus
species.
of
a
Enterococcus
Diagn Micr Infec Dis. 1998; 31: 343-7.
3224-8.
5- Lai K K. Treatment of vancomycin-resistant
9- Xu X, Lin D, Yan G, et al. vanM, a new
Enterococcus faecium infections. Arch Intern
glycopeptide resistance gene cluster found in
Med. 1996; 156: 2579-84.
Enterococcus
6- Suppola JP, Kolho E, Salmenlinna S, Tarkka E,
Chemother. 2010; 54: 4643-7.
Vuopio-Varkila J, Vaara M: vanA and vanB
10- Lebreton F, Depardieu F, Bourdon N, et al.
incorporate into an endemic ampicillin-resistant
D-Ala-D-Ser VanN-type transferable vancomycin
faecium.
Antimicrob
Agents
١٣٩٣ ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ,٩١ ﺷﻤﺎﺭﻩﻱ,٢٢ ﺩﻭﺭﻩﻱ، ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ، ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ،ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ
ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ
128
resistance in Enterococcus faecium. Antimicrobial
aminoglycosides and macroloids resistance among
Agents Chemother 2011; 55: 4606-12.
Enterococcus faecalis and Enterococcus faecium
11-
from hospital in Tehran. Pol J Microbiol. 2008;
Krcme´ry
V,
Sefton
A.
Vancomycin
resistance in gram-positive bacteria other than
57: 173-178.
Enterococcus spp. Int J Antimicrob Agents. 2000;
19- Soltan Dallal MM, Saifi M, Pourshafie MR,
14: 99-105.
Eshraghian MR. High-level gentamicin-resistant
12- Dutka-Malen S, Molinas C, Arthur M,
enterococcal isolates from urinary tract infection
Courvalin P. Sequence of the vanC gene of
in Iran. Infect Dis Clin Pract. 2008; 16: 41-45.
Enterococcus gallinarum BM4174 encoding a D-
20- Wagenlehner FME, Naber KJ. New drugs for
alanine: D-alanine ligase-related protein necessary
gram-positive uropathogens. Int J Antimicrob
for vancomycin resistance. Gene. 1992; 112: 53-8.
Agents. 2004; 24: 39-43.
13- Uttley AH, Collins CH, Naidoo J, George R.
21- Rahbar M, Hajia M, Farzanehkhah M.
Vancomycin resistant enterococci. Lancet. 1988;
Activity of nitrofurantoin against urinary tract
i: 57-8.
infection (UTI) isolates of vancomycin-resistant
14- Leclercq R, Derlot E, Duval J, et al. Plasmid-
Enterococci (VRE): Iran J Path. 2007; 2: 171-
mediated
174.
resistance
to
vancomycin
and
teicoplanin in Enterococcus faecium. N Engl J
22- Cattoir V, Leclercq R. Twenty-five years of
Med. 1988; 319: 157-61.
shared life with vancomycin-resistant enterococci:
15- Kariyama R, Mitsuhata R, Chow JW, Clewell
is it time to divorce? J Antimicrob Chemother.
DB, Kumon H. Simple and reliable multiplex
2012; 68: 731-42.
PCR
of
23- Werner G, Coque TM, Hammerum AM, et al.
Clin
Emergence and spread of vancomycin resistance
assay
for
vancomycin-resistant
surveillance,
isolates
enterococci.
J
Microbiol. 2000; 38: 3092-95.
16-
CLSI.
Performance
among enterococci in Europe. Euro Surveill.
Standards
for
2008; 13: pii: 19046.
Antimicrobial Susceptibility Testing; 21th ed.
24- Putnam SD, Sader HS, Moet GJ, Mendes Re,
Wayne, PA: Clinical and Laboratory Standards
Jones RN. Worldwide summary of telavancin
Institute. 2011; 31: 84-87.
spectrum and potency against gram-positive
17-
Mundy LM,
Sahm DF,
Gilmore M.
pathogens: 2007 to 2008 surveillance results.
Relationships between enterococcal virulence and
Diagn Microbiol Infect Dis. 2010; 67: 359-68.
antimicrobial resistance. Clin Microbiol Rev.
25- Salem- Bekhit MM, Mussa I, Muharram MM,
2000; 13: 513-22.
Alanayz
18- Emaneini M, Aligholi M, Aminshahi M.
antimicrobial resistance pattern of multidrug-
Characterization
resistant
of
glycopeptides,
FK,
Hefni
enterococci
HM.
isolated
Prevalence
from
and
clinical
١٣٩٣ ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ,٩١ ﺷﻤﺎﺭﻩﻱ,٢٢ ﺩﻭﺭﻩﻱ، ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ، ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ،ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ
ﻟﻴﻠﻲ ﺷﻜﻮﻫﻲ ﺯﺍﺩﻩ ﻭ ﻫﻤﻜﺎﺭﺍﻥ
129
specimens. Indian J Med Microbiol. 2012; 30:
30- Feizabadi MM, Sayadi S, Shokrzadeh L,
44-51.
Parvin M, Yadegarnia D. Increase in prevalence
R,
of vancomycin resistant isolates of Enterococcous
Ramasubramanian V, Abdul Ghafur K, Senthur
faecium at labbafinejad hospital. Iran J Clin Infect
Nambi
Diseases. 2008; 3: 73-77.
26-
Vidyalakshmi
P,
PR,
Gopalakrishnan
Thirunarayana
MA.
Clinical,
epidemiological, and microbiological profile of
31- Sedaghat M, Rahimi F, Pourshafie MR, Talebi
patients with vancomycin-resistant Enterococci
M. Studies of vancomycin resistance enteroccus
from a tertiary care hospital. J Glob Infect Dis.
faecium isolated from clinical samples from
2012; 4: 137-38.
Tehran,Iran. Current Research in Bacteriology.
27- Yilmaz NO, Agus N, Yurtsever SG, Ozer E,
2012; 5: 53-58.
Afacan G, Oner O. Prevalence and risk factors
32- Zhanel MM, Laing MN, Nichol KA, et al.
associated with vancomycin resistant enterococci
Antibiotic activity against urinary tract infection
colonization. R Ci med biol Salvador. 2009; 8:
(UTI)
283-291.
enterococci (VRE): results from the 2002 North
28- Talebi M, Rahimi F, Katouli M, Mollby R,
American
Pourshafie MR. Epidemiologic link between
Susceptibility Study (NAVRESS). J Antimicrob
wastewater
Chemother. 2003; 52: 382-388.
and
human
vancomycin-resistant
isolates
of
Vancomycin
vancomycin-resistant
Resistant
Enterococci
Enterococcus faecium isolates. Curr microbial.
33- Saifi M, Pourshafie MR, Sultan Dallal MM,
2008; 56: 447-68.
Katouli
29- Hidron AI, Edwards JR, Patel J, et al. NHSN
gentamicin-resistant E. faecium isolated from
annual update: antimicrobial-resistant pathogens
municipial
associated with healthcare-associated infections:
in Tehran, Iran. Lett Apple Microbiol. 2009; 49:
annual summary of data reported to the national
160-65.
M.
Clonal
wastewater
group
and
of
high
clinical
–level
samples
healthcare safety network at the centers for
disease control and prevention. 2006-2007. Infect
Control Hosp Epidemiol. 2008; 29: 996-1011.
١٣٩٣ ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ,٩١ ﺷﻤﺎﺭﻩﻱ,٢٢ ﺩﻭﺭﻩﻱ، ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ، ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ،ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ
ﻓﺮﺍﻭﺍﻧﻲ ﻣﻘﺎﻭﻣﺖ ﺑﻪ ﻭﻧﮑﻮﻣﺎﻳﺴﻴﻦ ﺩﺭ ﻋﻔﻮﻧﺖﻫﺎﻱ ﺍﺩﺭﺍﺭﻱ
130
Frequency of Vancomycin -Resistant Enterococcus Faecium Strains Isolated from Urinary
Tract Infections (UTI) in 4 Hospitals of Tehran
Shokoohizadeh L1, Mohabati Mobarez A1, Zali MR2, Ranjbar R3, Alebouyeh M2
1
2
Dept. of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
Research Center of Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran
3
Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Correspond Author: Dept. of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
E-mail: mmmobarez@modares.ac.ir
Received: 30 Jun 2013
Accepted: 7 Oct 2013
Background and Objective: Vancomycin-resistant enterococci (VRE) are the major causative agents of
urinary tract infections (UTIs) in hospitalized patients. The aim of this study was to determine the prevalence
of urinary tract infections caused by enterococcus faecium and the level of resistance to vancomycine and
other antibiotics which are effective in enterococcal infection therapy of hospitalized patients in four
university teaching hospitals of Tehran.
Materials and Methods: This study was carried out between September 2011 and May 2012. Urine samples
were collected from hospitalized patients in Taleghani, Loghman, Mofid and Labaffi nejad Hospitals in
Tehran. Enterococcus species were detected by biochemical and molecular tests. Antimicrobial susceptibility
and minimum inhibitory concentration (MIC) of vancomycine were determined by disk diffusion and agar
dilution methods. The presence of vanA and vanB genes were investigated in VRE strains by PCR.
Results: 86 enterococci were isolated from urine samples of which 45(52%) were E.faecium. 42.2% of E.
faecium isolates were resistant to vancomycin (VRE) and showed vanA genotype. All VRE isolates were
resistant to ampicillin, gentamicin, ciprofloxacin and erythromycin, and 78% were resistant to nitrofurantoin.
Furthermore, all VRE isolates were sensitive to linezolide and quiopristin-dalfopristin. MIC50 ≥ 128 and
MIC90 ≥ 256 were detected in the VRE strains.
Conclusion: The increase in the prevalence of vancomycin resistant E. faecium with high risk resistance
profiles is a serious threat for some Iranian hospitals and limits the therapeutical options for patients infected
with E. faecium.
Keywords: Enterococcus faecium, Urinary tract infections, Vancomycin, resistance
١٣٩٣ ﺧﺮﺩﺍﺩ ﻭ ﺗﻴﺮ,٩١ ﺷﻤﺎﺭﻩﻱ,٢٢ ﺩﻭﺭﻩﻱ، ﺩﺭﻣﺎﻧﻲ ﺯﻧﺠـﺎﻥ، ﭘﮋﻭﻫﺸﻲ ﺩﺍﻧﺸﮕﺎﻩ ﻋﻠﻮﻡ ﭘﺰﺷﮑﻲ ﻭ ﺧﺪﻣﺎﺕ ﺑﻬﺪﺍﺷﺘﻲ،ﻣﺠﻠﻪﻱ ﻋﻠﻤﻲ