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耐甲氧西林金黄色葡萄球菌(MRSA)医院获得性肺炎(NP)患者治疗临床成功的预测因素

Predictors of Clinical Success in the Treatment of Patients with Methicillin-Resistant Staphylococcus aureus (MRSA) Nosocomial Pneumonia (NP).

作者信息

Shorr Andrew F, Puzniak Laura A, Biswas Pinaki, Niederman Michael S

机构信息

Pulmonary Critical Care; Washington Hospital Center, Washington, DC, United States of America.

Infectious Diseases and Vaccines; Pfizer Inc, Collegeville, Pennsylvania, United States of America.

出版信息

PLoS One. 2015 Jul 21;10(7):e0131932. doi: 10.1371/journal.pone.0131932. eCollection 2015.

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) remains an important pathogen in nosocomial pneumonia and is associated with significant morbidity and mortality. Clinical outcomes for nosocomial pneumonia are dependent on patient age, co-morbidities, severity of illness and appropriate antibiotic therapy. The objective of this secondary analysis was to identify baseline clinical variables that are associated with clinical success at the end of the study observation period. Data from a randomized blinded trial (NCT00084266) comparing linezolid (600-mg twice daily) to vancomycin (15-mg/kg twice daily, dose-adjusted) for the treatment of culture-proven MRSA pneumonia were analyzed to evaluate baseline clinical and demographic factors that may predict clinical success at end of study (EOS) (7-30 days after end of treatment). A multivariate logistic regression was conducted to identify baseline factors that are associated with clinical success. Patients treated with linezolid (OR 1.55 95% CI: 1.013, 2.355), no vasopressor receipt (OR 2.30, 95% CI: 1.303, 4.069), unilateral involvement (OR 1.70, 95% CI: 1.078, 2.681) and normal renal function (eGFR 30-80 vs >80 OR 0.48, 95% CI: 0.303, 0.750) were more likely to have clinical success. From a clinical standpoint, identifying reliable predictors of outcome and who might benefit more from one therapy versus another can help inform treatment decisions.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)仍是医院获得性肺炎的重要病原体,与显著的发病率和死亡率相关。医院获得性肺炎的临床结局取决于患者年龄、合并症、疾病严重程度以及适当的抗生素治疗。这项二次分析的目的是确定在研究观察期结束时与临床成功相关的基线临床变量。分析了一项随机双盲试验(NCT00084266)的数据,该试验比较了利奈唑胺(每日两次,每次600毫克)和万古霉素(每日两次,每次15毫克/千克,剂量调整)治疗经培养证实的MRSA肺炎的效果,以评估可能预测研究结束时(EOS,治疗结束后7 - 30天)临床成功的基线临床和人口统计学因素。进行多因素逻辑回归以确定与临床成功相关的基线因素。接受利奈唑胺治疗的患者(比值比1.55,95%置信区间:1.013,2.355)、未接受血管升压药治疗的患者(比值比2.30,95%置信区间:1.303,4.069)、单侧受累患者(比值比1.70,95%置信区间:1.078,2.681)以及肾功能正常的患者(估算肾小球滤过率30 - 80与>80,比值比0.48,95%置信区间:0.303,0.750)更有可能获得临床成功。从临床角度来看,确定可靠的预后预测因素以及哪些患者可能从一种治疗方法中比另一种治疗方法中获益更多,有助于指导治疗决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52b/4510301/845cf174a942/pone.0131932.g001.jpg

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