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Gastropulmonary Route of Infection and the Prevalence of Microaspiration in the Elderly Patients with Ventilator-Associated Pneumonia Verified by Molecular Microbiology-GM-PFGE

机译:分子微生物学-GM-PFGE验证老年呼吸机相关性肺炎患者的胃肺感染途径和微抽吸发生率

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Gastropulmonary route of infection was considered to be an important mechanism of ventilator-associated pneumonia (VAP). However there is little evidence to support this assumption. Moreover, the prevalence of microaspiration in elderly ventilated patients was not well understood. To confirm gastropulmonary infection route and investigate the prevalence of microaspiration in elderly ventilated patients using genome macrorestriction-pulsed field gel electrophoresis (GM-PFGE). Patients over 60 years old, expected to receive mechanical ventilation longer than 48 h, were prospectively enrolled from October 2009 to January 2012. Clinical data were collected and recorded until they died, developed pneumonia, or were extubated. Samples from gastric fluid, subglottic secretion and lower respiratory tract (LRT) were collected during the follow-up for microbiological examination. To evaluate the homogeneity, GM-PFGE was performed on strains responsible for VAP that had the same biochemical phenotype as those isolated from gastric juice and subglottic secretions sequentially. Among 44 VAP patients, 76 strains were isolated from LRT and considered responsible for VAP. Twenty-two isolates had the same biochemical phenotype with the corresponding gastric isolates. The homology was further confirmed using GM-PFGE in 12 episodes of VAP. Nearly 30 % of VAPs were caused by microaspiration based on the analysis of bacterial phenotype or GM-PFGE. In addition, 58.3 % patients with gastric colonization developed VAP, especially late-onset VAP (LOP). Gastropulmonary infection route exists in VAP especially LOP in elderly ventilated patients. It is one of the important mechanisms in the development of VAP.
机译:胃肠道感染途径被认为是呼吸机相关性肺炎(VAP)的重要机制。但是,没有证据支持这一假设。此外,对老年通气患者微吸的发生率还没有很好的了解。使用基因组大限制性脉冲场凝胶电泳(GM-PFGE)来确定老年通气患者的胃肺感染途径并研究其微抽吸的发生率。预期于2009年10月至2012年1月入选60岁以上,预期接受机械通气时间超过48小时的患者。收集并记录临床数据,直到他们死亡,发展为肺炎或拔管。在随访期间收集了胃液,声门下分泌物和下呼吸道(LRT)的样本进行微生物学检查。为了评估同质性,对负责VAP的菌株进行了GM-PFGE,这些菌株的生化表型与从胃液和声门下分泌物中分离出的那些相同。在44例VAP患者中,从LRT分离出76株,并认为是导致VAP的原因。 22个分离株与相应的胃分离株具有相同的生化表型。使用GM-PFGE在12次VAP中进一步证实了同源性。根据细菌表型或GM-PFGE的分析,近30%的VAP是由微吸引起的。此外,有58.3%的胃部定植患者发生了VAP,尤其是迟发性VAP(LOP)。 VAP尤其是老年通气患者的LOP中存在胃肺感染途径。它是VAP发展中的重要机制之一。

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