Guideline-concordant therapy and outcomes in healthcare-associated pneumonia

被引:91
作者
Attridge, R. T. [1 ,2 ,6 ]
Frei, C. R. [1 ,6 ]
Restrepo, M. I. [3 ,4 ,5 ]
Lawson, K. A. [6 ]
Ryan, L. [1 ,6 ]
Pugh, M. J. V. [3 ,5 ]
Anzueto, A. [3 ,5 ]
Mortensen, E. M. [3 ,4 ,5 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Pharmacotherapy Educ & Res Ctr, Sch Med, San Antonio, TX 78229 USA
[2] Univ Incarnate Word, Feik Sch Pharm, San Antonio, TX USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA
[4] S Texas Vet Hlth Care Syst, VERDICT Res Program, San Antonio, TX USA
[5] S Texas Vet Hlth Care Syst, Audie L Murphy Div, San Antonio, TX USA
[6] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
Drug resistance; guidelines for management of pneumonia; health outcomes; pneumonia; COMMUNITY-ACQUIRED PNEUMONIA; HOSPITALIZED-PATIENTS; RESISTANT BACTERIA; EPIDEMIOLOGY; MORTALITY; PREDICTION; CULTURE;
D O I
10.1183/09031936.00141110
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Healthcare-associated pneumonia (HCAP) guidelines were first proposed in 2005 but have not yet been validated. The objective of this study was to compare 30-day mortality in HCAP patients treated with either guideline-concordant (GC)-HCAP therapy or GC community-acquired pneumonia (CAP) therapy. We performed a population-based cohort study of >150 hospitals in the US Veterans Health Administration. Patients were included if they had one or more HCAP risk factors and received antibiotic therapy within 48 h of admission. Critically ill patients were excluded. Independent risk factors for 30-day mortality were determined in a generalised linear mixed-effect model, with admitting hospital as a random effect. Propensity scores for the probability of receiving GC-HCAP therapy were calculated and incorporated into a second logistic regression model. A total of 15,071 patients met study criteria and received GC-HCAP therapy (8.0%), GC-CAP therapy (75.7%) or non-GC therapy (16.3%). The strongest predictors of 30-day mortality were recent hospital admission (OR 2.49, 95% CI 2.12-2.94) and GC-HCAP therapy (OR 2.18, 95% CI 1.86-2.55). GC-HCAP therapy remained an independent risk factor for 30-day mortality (OR 2.12, 95% CI 1.82-2.48) in the propensity score analysis. In nonsevere HCAP patients, GC-HCAP therapy is not associated with improved survival compared with GC-CAP therapy.
引用
收藏
页码:878 / 887
页数:10
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