Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosis

被引:79
作者
Merlo, Christian A.
Boyle, Michael P.
Diener-West, Marle
Marshall, Bruce C.
Goss, Christopher H.
Lechtzin, Noah
机构
[1] Johns Hopkins Univ Hosp, Sch Med, Dept Med, Div Pulm & Crit Care Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ Hosp, Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
[3] Univ Washington, Med Ctr, Dept Med, Div Pulm & Crit Care Med, Seattle, WA 98195 USA
关键词
antibiotic resistance; cystic fibrosis; incidence; Pseudomonas aeruginosa; risk factors;
D O I
10.1378/chest.06-2888
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Infection with multiple antibiotic-resistant Pseudomonas aeruginosa (MARPA) in individuals with cystic fibrosis (CF) has caused much concern among caregivers, yet little is known about the risks associated with acquiring resistance. The main objective of the study was to estimate the incidence and identify risk factors for the acquisition of MARPA among individuals with CF. Methods: Five-year cohort study of individuals followed in the Cystic Fibrosis Foundation Registry from 1998 through 2002. Results: Demographics, anthropometrics, spirometry, respiratory culture results, comorbidities, antibiotic usage, and hospitalizations were collected. Of the 4,293 patients with P aeruginosa infection during the study period, MARPA developed in 341. The overall incidence of MARPA was 1.8%/yr. Independent risk factors for MARPA included CF-related diabetes mellitus (hazard ratio [HR], 1.64; 95% confidence interval [CI], 1.11 to 2.43), long-term inhaled tobramycin usage (HR, 2.08; 95% Cl, 1.56 to 2.77), and care at a CF center with a baseline MARPA prevalence in the top quartile (HR, 2.00; 95% CI, 1.31 to 3.04). Frequent courses of IV antibiotics and repeated hospitalizations were also found to independently increase the risk for MARPA. Conclusions: Infection with MARPA is common among patients with CF. Diabetes, long-term inhaled tobramycin usage, and frequent acute pulmonary exacerbations requiring hospitalization or IV antibiotics increase the risk for MARPA. Receiving CF care at a center with a high prevalence of resistant Pseudomonas also increases the risk for MARPA in patients with CF. Further study is needed to investigate the mechanisms of acquiring resistant strains and the clinical impact of MARPA on CF outcomes.
引用
收藏
页码:562 / 568
页数:7
相关论文
共 29 条
[1]   Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: a randomised, double-blind, controlled clinical trial [J].
Aaron, SD ;
Vandemheen, KL ;
Ferris, W ;
Fergusson, D ;
Tullis, E ;
Haase, D ;
Berthiaume, Y ;
Brown, N ;
Wilcox, P ;
Yazghatlian, V ;
Bye, P ;
Bell, S ;
Chan, F ;
Rose, B ;
Jeanneret, A ;
Stephenson, A ;
Noseworthy, M ;
Freitag, A ;
Paterson, N ;
Doucette, S ;
Harbour, C ;
Ruel, M ;
MacDonald, N .
LANCET, 2005, 366 (9484) :463-471
[2]  
[Anonymous], 2005, PAT REG 2004 ANN REP
[3]   The efficacy and safety of meropenem and tobramycin vs ceftazidime and tobramycin in the treatment of acute pulmonary exacerbations in patients with cystic fibrosis [J].
Blumer, JL ;
Saiman, L ;
Konstan, MW ;
Melnick, D .
CHEST, 2005, 128 (04) :2336-2346
[4]  
Brick J M, 1996, Stat Methods Med Res, V5, P215, DOI 10.1177/096228029600500302
[5]   Health and economic outcomes of antibiotic resistance in Pseudomonas aeruginosa [J].
Carmeli, Y ;
Troillet, N ;
Karchmer, AW ;
Samore, MH .
ARCHIVES OF INTERNAL MEDICINE, 1999, 159 (10) :1127-1132
[6]  
*CYST FIBR FDN, 1994, CONS C MICR INF DIS, P1
[7]  
Delamaire M, 1997, DIABETIC MED, V14, P29, DOI 10.1002/(SICI)1096-9136(199701)14:1<29::AID-DIA300>3.0.CO
[8]  
2-V
[9]   Phenotypic variability of Pseudomonas aeruginosa in sputa from patients with acute infective exacerbation of cystic fibrosis and its impact on the validity of antimicrobial susceptibility testing [J].
Foweraker, JE ;
Laughton, CR ;
Brown, DFJ ;
Bilton, D .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 55 (06) :921-927
[10]  
GRAMBSCH PM, 1994, BIOMETRIKA, V81, P515