Empiric treatment in hospitalized community-acquired pneumonia.: Impact on mortality, length of stay and re-admission

被引:33
作者
Calzada, S. Reyes [1 ]
Tomas, R. Martinez
Romero, M. J. Cremades
Moragon, E. Martinez
Cataluna, J. J. Soler
Villanueva, R. Menendez
机构
[1] Hosp Univ La Fe, Serv Pneumol, Valencia, Spain
[2] Hosp Sagunto, Valencia, Spain
关键词
community-acquired pneumonia; treatment; mortality; length of stay;
D O I
10.1016/j.rmed.2007.04.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate adherence to guidelines when choosing an empirical treatment and its impact upon the prognosis of community-acquired pneumonia (CAP). Methods: A prospective multicentre study was conducted in 425 CAP patients hospitalized on ward. Initial empirical treatment was classified as adhering or not to Spanish guidelines. Adherent treatment was defined as an initial antimicrobial regimen consisting of beta-lactams plus macrolides, beta-lactam monotherapy and quinolones. Non-adherent treatments included macrolide monotherapy and other regimens. Initial severity was graded according to pneumonia severity index (PSI). The end point variables were mortality, length of stay (LOS) and re-admission at 30 days. Results: Overall 30-day mortality was 8.2%, the mean LOS was 8 +/- 5 days, and the global re-admission rate was 7.6%. Adherence to guidelines was 76.5%, and in most cases the empirical treatment consisted of beta-lactam and macrolide in combination (57.4%). Logistic regression analysis showed that other regimens were associated with higher mortality OR = 3 (1.2-7.3), after adjusting for PSI and admitting hospital. Beta-lactam monotherapy was an independent risk factor for re-admission. LOS was independently associated with admitting hospital and not with antibiotics. Conclusions: A high adherence to CAP treatment guidelines was found, though with considerable variability in the empirical antibiotic treatment among hospitals. Non-adherent other regimens were associated with greater mortality. Beta-lactam monotherapy was associated with an increased re-admission rate. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1909 / 1915
页数:7
相关论文
共 37 条
[1]  
ALMIRALL J, 1993, EUR RESPIR J, V6, P14
[2]  
AMBROSINO N, 2003, EUR LUNG WHITE BOOK, P55
[3]   Impact of initial antibiotic choice on clinical outcomes in community-acquired pneumonia - Analysis of a hospital claims-made database [J].
Brown, RB ;
Iannini, P ;
Gross, P ;
Kunkel, M .
CHEST, 2003, 123 (05) :1503-1511
[4]   Why don't physicians follow clinical practice guidelines? A framewouk for improvement [J].
Cabana, MD ;
Rand, CS ;
Powe, NR ;
Wu, AW ;
Wilson, MH ;
Abboud, PAC ;
Rubin, HR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (15) :1458-1465
[5]   Decreased mortality after implementation of a treatment guideline for community-acquired pneumonia [J].
Dean, NC ;
Silver, MP ;
Bateman, KA ;
James, B ;
Hadlock, CJ ;
Hale, D .
AMERICAN JOURNAL OF MEDICINE, 2001, 110 (06) :451-457
[6]  
Dorca J, 1997, Arch Bronconeumol, V33, P240
[7]   Antimicrobial selection for hospitalized patients with presumed community-acquired pneumonia: A survey of nonteaching US community hospitals [J].
Dudas, V ;
Hopefl, A ;
Jacobs, R ;
Guglielmo, BJ .
ANNALS OF PHARMACOTHERAPY, 2000, 34 (04) :446-452
[8]   Development and validation of a clinical prediction rule for severe community-acquired pneumonia [J].
Espana, Pedro P. ;
Capelastegui, Alberto ;
Gorordo, Inmaculada ;
Esteban, Cristobal ;
Oribe, Mike ;
Ortega, Miguel ;
Bilbao, Amaia ;
Quintana, Jose M. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (11) :1249-1256
[9]   A prediction rule to identify low-risk patients with community-acquired pneumonia [J].
Fine, MJ ;
Auble, TE ;
Yealy, DM ;
Hanusa, BH ;
Weissfeld, LA ;
Singer, DE ;
Coley, CM ;
Marrie, TJ ;
Kapoor, WN .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (04) :243-250
[10]   Impact of atypical coverage for patients with community-acquired pneumonia managed on the medical ward: Results from the United States community-acquired pneumonia project [J].
Frei, CR ;
Koeller, JM ;
Burgess, DS ;
Talbert, RL ;
Johnsrud, MT .
PHARMACOTHERAPY, 2003, 23 (09) :1167-1174