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Use of the clinical pulmonary infection score to guide therapy for ventilator-associated pneumonia risks antibiotic overexposure in patients with trauma

机译:使用临床肺部感染评分指导呼吸机相关性肺炎的治疗可能会给创伤患者带来抗生素过度暴露的风险

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BACKGROUND: The clinical pulmonary infection score (CPIS) has been advocated to guide both the diagnosis and duration of therapy in ventilator-associated pneumonia (VAP). However, the clinical, physiologic, and radiologic components of the CPIS may be difficult to differentiate from the systemic effects of injury and inflammation, unnecessarily prolonging VAP therapy. This study evaluates the use of CPIS in determining the appropriate duration of antimicrobial therapy for VAP in patients with critical illness and trauma. METHODS: Patients with VAP (?10 CFU/mL in bronchoalveolar lavage [BAL] effluent) over 6 years were evaluated. Duration of antimicrobial therapy was determined by microbiologic resolution (≤10 CFU/mL) on repeated BAL. Recurrence was defined as >10 CFU/mL on BAL performed within 2 weeks of appropriate therapy. A CPIS of less than 6 was used as a threshold for VAP resolution. RESULTS: Of the patients with VAP, 1,028 were identified: 523 had community-acquired pathogens (mean CPIS, 6.9), and 505 had hospital-acquired (HA) pathogens (mean CPIS, 6.3). Using a CPIS of less than 6 yielded a sensitivity and specificity of 69% and 51% for community-acquired pathogens and 72% and 53% for HA pathogens, respectively. Antimicrobial therapy would have continued inappropriately in 59% of patients. Overall recurrence was 1%, occurring only with HA pathogens (mean CPIS, 5.9). CONCLUSION: CPIS should not be used to determine VAP resolution in patients with critical injury and trauma. It cannot reliably differentiate VAP from the systemic inflammatory response syndrome in the face of confounding clinical factors. Using CPIS to determine appropriate duration of antimicrobial therapy for patients with trauma is costly and could be harmful by unnecessarily prolonging exposure to antibiotics. LEVEL OF EVIDENCE: Therapeutic study, level III.
机译:背景:已提出临床肺部感染评分(CPIS),以指导呼吸机相关性肺炎(VAP)的诊断和治疗持续时间。但是,CPIS的临床,生理和放射学成分可能难以与损伤和炎症的全身作用区分开,从而不必要地延长了VAP治疗的时间。这项研究评估了CPIS在确定危重疾病和外伤患者VAP抗菌治疗适当时机方面的应用。方法:对6年内VAP(支气管肺泡灌洗液[BAL]中≥10CFU / mL)的患者进行评估。抗菌治疗的持续时间由重复BAL的微生物学分辨率(≤10 CFU / mL)确定。复发定义为在适当治疗后2周内BAL≥10 CFU / mL。小于6的CPIS用作VAP分辨率的阈值。结果:在VAP患者中,鉴定出1,028名:523名社区获得性病原体(平均CPIS,6.9),505名医院获得性(HA)病原体(平均CPIS,6.3)。使用小于6的CPIS对社区获得的病原体和HA病原体分别产生69%和51%的敏感性和特异性,对于HA病原体分别为72%和53%。 59%的患者将继续不适当地进行抗菌治疗。总体复发率为1%,仅发生于HA病原体(平均CPIS,5.9)。结论:CPIS不应用于确定重伤和创伤患者的VAP分辨率。面对混杂的临床因素,它不能可靠地将VAP与全身性炎症反应综合征区分开。使用CPIS为创伤患者确定合适的抗微生物治疗时间是昂贵的,并且由于不必要地延长接触抗生素的时间而可能有害。证据级别:治疗研究,三级。

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