Molecular and clinical epidemiology of carbapenem-resistant Enterobacterales in the USA (CRACKLE-2): a prospective cohort study

医学 内科学 前瞻性队列研究 流行病学 队列研究 分子流行病学 环境卫生 队列 生物 基因型 遗传学 基因
作者
David van Duin,César A. Arias,Lauren Komarow,Liang Chen,Blake Hanson,Gregory Weston,Eric Cober,Omai B. Garner,Jesse T. Jacob,Michael J. Satlin,Bettina C. Fries,Julia Garcia‐Diaz,Yohei Doi,Sorabh Dhar,Keith S. Kaye,Michelle Earley,Andrea M. Hujer,Kristine M. Hujer,Tatiana Domitrovic,William C. Shropshire
出处
期刊:Lancet Infectious Diseases [Elsevier BV]
卷期号:20 (6): 731-741 被引量:328
标识
DOI:10.1016/s1473-3099(19)30755-8
摘要

Summary

Background

Carbapenem-resistant Enterobacterales (CRE) are a global threat. We aimed to describe the clinical and molecular characteristics of Centers for Disease Control and Prevention (CDC)-defined CRE in the USA.

Methods

CRACKLE-2 is a prospective, multicentre, cohort study. Patients hospitalised in 49 US hospitals, with clinical cultures positive for CDC-defined CRE between April 30, 2016, and Aug 31, 2017, were included. There was no age exclusion. The primary outcome was desirability of outcome ranking (DOOR) at 30 days after index culture. Clinical data and bacteria were collected, and whole genome sequencing was done. This trial is registered with ClinicalTrials.gov, number NCT03646227.

Findings

1040 patients with unique isolates were included, 449 (43%) with infection and 591 (57%) with colonisation. The CDC-defined CRE admission rate was 57 per 100 000 admissions (95% CI 45–71). Three subsets of CDC-defined CRE were identified: carbapenemase-producing Enterobacterales (618 [59%] of 1040), non-carbapenemase-producing Enterobacterales (194 [19%]), and unconfirmed CRE (228 [22%]; initially reported as CRE, but susceptible to carbapenems in two central laboratories). Klebsiella pneumoniae carbapenemase-producing clonal group 258 K pneumoniae was the most common carbapenemase-producing Enterobacterales. In 449 patients with CDC-defined CRE infections, DOOR outcomes were not significantly different in patients with carbapenemase-producing Enterobacterales, non-carbapenemase-producing Enterobacterales, and unconfirmed CRE. At 30 days 107 (24%, 95% CI 20–28) of these patients had died.

Interpretation

Among patients with CDC-defined CRE, similar outcomes were observed among three subgroups, including the novel unconfirmed CRE group. CDC-defined CRE represent diverse bacteria, whose spread might not respond to interventions directed to carbapenemase-producing Enterobacterales.

Funding

National Institutes of Health.
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