Papadomichelakis Evangelos, Kontopidou Flora, Antoniadou Anastasia, Poulakou Garifalia, Koratzanis Evangelos, Kopterides Petros, Mavrou Irini, Armaganidis Apostolos, Giamarellou Helen
2nd Critical Care Department, Athens University Medical School, University General Hospital "ATTIKON", Rimini 1, Athens 12462, Greece.
Intensive Care Med. 2008 Dec;34(12):2169-75. doi: 10.1007/s00134-008-1247-9. Epub 2008 Aug 19.
To define the potential of resistant gram-negative colonization surveillance to predict etiology of subsequent infection and improve adequacy of empiric antimicrobial treatment.
Retrospective cohort study.
A mixed medical-surgical six-bed intensive care unit (ICU), from November 2003 to December 2006.
All patients having at least one episode of ventilator-associated pneumonia (VAP) or bloodstream infection (BSI) caused by a resistant gram-negative pathogen during the study period.
Colonization surveillance of the respiratory tract and gastrointestinal tract was systematically performed in all ICU patients. Tracheal aspirates were obtained twice weekly and rectal swabs once weekly. Both tracheal and rectal samples were cultured in antibiotic-enriched media (containing ceftazidime, ciprofloxacin, imipenem or piperacillin/tazobactam), to focus on resistant gram-negative pathogen isolation.
Colonization concordance between resistant, gram-negative pathogens of infectious episodes and previous, recent (<or=7 days) colonization of the respiratory and gastrointestinal tract was determined, based on species identity and antimicrobial susceptibility. Concordance was 82% in VAP and 86% in BSI cases and was further confirmed by molecular testing of 15 randomly selected cases by REP-PCR. Previous colonization had high sensitivity and specificity in VAP, but was less specific in BSI cases. Knowledge of previous colonization improved the rate of adequate empiric antimicrobial treatment (91 vs. 40% in VAP and 86 vs. 50% in BSI cases, P < 0.05).
Colonization surveillance for resistant gram-negative microorganisms is predictive of subsequent infection etiology and can improve empiric antimicrobial treatment adequacy in a critical care setting.
确定耐革兰阴性菌定植监测在预测后续感染病因及提高经验性抗菌治疗充分性方面的潜力。
回顾性队列研究。
2003年11月至2006年12月期间,一个拥有6张床位的内外科混合重症监护病房(ICU)。
在研究期间至少有1次由耐革兰阴性病原菌引起的呼吸机相关性肺炎(VAP)或血流感染(BSI)发作的所有患者。
对所有ICU患者系统地进行呼吸道和胃肠道的定植监测。每周两次采集气管吸出物,每周一次采集直肠拭子。气管和直肠样本均在富含抗生素的培养基(含头孢他啶、环丙沙星、亚胺培南或哌拉西林/他唑巴坦)中培养,以着重分离耐革兰阴性病原菌。
根据菌种鉴定和药敏情况,确定感染发作时的耐革兰阴性病原菌与呼吸道和胃肠道先前(近期,≤7天)定植之间的定植一致性。VAP病例中的一致性为82%,BSI病例中为86%,并通过对15例随机选择的病例进行REP-PCR分子检测进一步证实。先前的定植在VAP中具有高敏感性和特异性,但在BSI病例中特异性较低。了解先前的定植情况可提高经验性抗菌治疗的充分率(VAP中分别为91%和40%,BSI病例中分别为86%和50%,P<0.05)。
对耐革兰阴性微生物进行定植监测可预测后续感染病因,并可提高重症监护环境中经验性抗菌治疗的充分性。