Scholte Johannes B J, van der Velde Johan I M, Linssen Catharina F M, van Dessel Helke A, Bergmans Dennis C J J, Savelkoul Paul H M, Roekaerts Paul M H J, van Mook Walther N K A
Department of Intensive Care Medicine, Luzerner Kantonspital, 6000, Luzern 16, Switzerland.
Department of Intensive Care Medicine, Maastricht University Medical Centre+, P.O. box 5800, 6202 AZ, Maastricht, The Netherlands.
BMC Pulm Med. 2015 Aug 12;15:86. doi: 10.1186/s12890-015-0087-y.
The significance of commensal oropharyngeal flora (COF) as a potential cause of ventilator-associated pneumonia (VAP) is scarcely investigated and consequently unknown. Therefore, the aim of this study was to explore whether COF may cause VAP.
Retrospective clinical, microbiological and radiographic analysis of all prospectively collected suspected VAP cases in which bronchoalveolar lavage fluid exclusively yielded ≥ 10(4) cfu/ml COF during a 9.5-year period. Characteristics of 899 recent intensive care unit (ICU) admissions were used as a reference population.
Out of the prospectively collected database containing 159 VAP cases, 23 patients were included. In these patients, VAP developed after a median of 8 days of mechanical ventilation. The patients faced a prolonged total ICU length of stay (35 days [P < .001]), hospital length of stay (45 days [P = .001]), and a trend to higher mortality (39 % vs. 26 %, [P = .158]; standardized mortality ratio 1.26 vs. 0.77, [P = .137]) compared to the reference population. After clinical, microbiological and radiographic analysis, COF was the most likely cause of respiratory deterioration in 15 patients (9.4 % of all VAP cases) and a possible cause in 2 patients.
Commensal oropharyngeal flora appears to be a potential cause of VAP in limited numbers of ICU patients as is probably associated with an increased length of stay in both ICU and hospital. As COF-VAP develops late in the course of ICU admission, it is possibly associated with the immunocompromised status of ICU patients.
口咽共生菌群(COF)作为呼吸机相关性肺炎(VAP)潜在病因的意义鲜有研究,因此尚不明确。所以,本研究旨在探讨COF是否会引发VAP。
对前瞻性收集的所有疑似VAP病例进行回顾性临床、微生物学和影像学分析,这些病例在9.5年期间支气管肺泡灌洗 fluid 仅产生≥10(4) cfu/ml 的COF。将近期899例重症监护病房(ICU)入院患者的特征作为对照人群。
在前瞻性收集的包含159例VAP病例的数据库中,纳入了23例患者。在这些患者中,VAP在机械通气中位数8天后发生。与对照人群相比,这些患者的ICU总住院时间延长(35天[P <.001]),住院时间延长(45天[P =.001]),且死亡率有升高趋势(39% 对 26%,[P =.158];标准化死亡率1.26对0.77,[P =.137])。经过临床、微生物学和影像学分析,COF是15例患者呼吸恶化的最可能原因(占所有VAP病例的9.4%),2例患者中为可能原因。
口咽共生菌群似乎是少数ICU患者VAP的潜在病因,可能与ICU和医院住院时间延长有关。由于COF-VAP在ICU入院后期发生,可能与ICU患者的免疫功能低下状态有关。