Tracking Colistin-Treated Patients to Monitor the Incidence and Outcome of Carbapenem-Resistant Gram-Negative Infections

被引:19
作者
Kadri, Sameer S. [1 ,3 ]
Hohmann, Samuel F. [7 ,8 ]
Orav, E. John [5 ]
Bonne, Stephanie L. [9 ]
Moffa, Matthew A. [10 ]
Timpone, Joseph G. [10 ]
Strich, Jeffrey R. [11 ]
Palmore, Tara [2 ]
Christopher, Kenneth B. [6 ]
Varughese, Christy [4 ]
Hooper, David C. [3 ]
Danner, Robert L. [1 ]
机构
[1] NIH, Dept Crit Care Med, Ctr Clin, Bethesda, MD 20892 USA
[2] NIH, Hosp Epidemiol Serv, Ctr Clin, Bethesda, MD 20892 USA
[3] Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Dept Pharm, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[6] Brigham & Womens Hosp, Div Renal, Boston, MA 02115 USA
[7] Rush Univ, Univ HealthSyst Consortium, Chicago, IL 60612 USA
[8] Rush Univ, Dept Hlth Syst Management, Chicago, IL 60612 USA
[9] Barnes Jewish Hosp, Dept Gen Surg, St Louis, MO 63110 USA
[10] Georgetown Univ Hosp, Div Infect Dis & Travel Med, Washington, DC 20007 USA
[11] Georgetown Univ Hosp, Dept Med, Washington, DC 20007 USA
基金
美国国家卫生研究院;
关键词
colistin; carbapenem resistance; gram-negative infection; extensively drug resistant; surveillance; PSEUDOMONAS-AERUGINOSA COLONIZATION; CRITICALLY-ILL PATIENTS; CYSTIC-FIBROSIS; EPIDEMIOLOGY; MORTALITY; ENTEROBACTERIACEAE; COMBINATION; PREDICTORS; EFFICACY; THERAPY;
D O I
10.1093/cid/ciu741
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Background. Existing surveillance mechanisms may underestimate the incidence of carbapenem-resistant gram-negative infections (CRGNIs). Although carbapenem resistance increases the risk of death, the trend in mortality over time is unknown. Methods. A retrospective cohort study was conducted at 40 academic medical centers using a discharge database to identify adult hospital admissions without cystic fibrosis in 2006-2012 and received intravenous colistin for >3 consecutive days or died during therapy (termed colistin cases). The primary outcomes were the number of colistin cases per 100 000 admissions per year and change in the hospital mortality rate over time compared with the rate of discharges to home. Secondary outcomes included median overall and intensive care unit lengths of stay. Results. From 2006 to 2012, a total of 5011 unique patients were identified as colistin cases. The number per 100 000 admissions per year increased from 35.56 to 92.98 during the 7-year study (P < .001). The odds of in-hospital death among colistin cases (compared with discharge to home) decreased by a mean of 5.2%/y (P = .04), whereas discharge to an institution (P = .24) or hospice (P = .89) remained steady over time. The median overall and intensive care unit lengths of stay decreased by 7.5 and 6 days, respectively (P < .001). In a 4-hospital chart review, 81.6% of colistin cases were found to have culture-positive CRGNIs. Conversely, 53% of extensively drug-resistant bloodstream CRGNIs at 2 of these hospitals met colistin case criteria. Conclusions. Colistin cases represent a severely ill population with a high probability of having culture-confirmed CRGNIs. Colistin tracking is a novel strategy for monitoring the incidence and mortality of CRGNIs, particularly those caused by extensively drug-resistant bacteria. Although the incidence of colistin cases nearly tripled within 7 years, more of these patients are surviving hospitalization and going home.
引用
收藏
页码:79 / 87
页数:9
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