4.5 Article

Efficacy and safety of de-escalation therapy to ertapenem for treatment of infections caused by extended-spectrum-β-lactamase-producing Enterobacteriaceae: an open-label randomized controlled trial

期刊

BMC INFECTIOUS DISEASES
卷 17, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12879-017-2284-1

关键词

ESBL; Enterobacteriaceae; Carbapenem; De-escalation; Ertapenem

资金

  1. Merck Investigator Studies Program (MSP)
  2. Merck, Sharp Dohme Corp.
  3. Health Systems Research Institute (Thailand)
  4. Chalermphrakiat Grant, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand

向作者/读者索取更多资源

Background: Carbapenem antibiotics are considered the treatment of choice for serious extended-spectrum betalactamase (ESBL)-producing Gram-negative bacteria (GNB) infections. The study objectives were to evaluate efficacy and safety of de-escalation therapy to ertapenem for treatment of infections caused by extended-spectrum-beta-lactamase- producing Enterobacteriaceae. Methods: We conducted a randomized controlled trial of adult patients with documented ESBL-producing Enterobacteriaceae infections who had received any group 2 carbapenem for less than 96 h. In the intervention group, the previously-prescribed group 2 carbapenem was de-escalated to ertapenem. In the control group, the group 2 carbapenem was continued. Results: During June 2011-December 2014, 32 patients were randomized to the de-escalation group and 34 to the control group. Most common sites of infection were urinary tract infection (42%). Characteristics of both groups were comparable. By using a 15% predefined margin, ertapenem was non-inferior to control group regarding the clinical cure rate (%Delta = 14.0 [ 95% confidence interval: -2.4 to 31.1]), the microbiological eradication rate (%Delta = 4.1 [-5.0 to 13.4]), and the superimposed infection rate (%Delta = -16.5 [-38.4 to 5.3]). Patients in the de-escalation group had a significantly lower 28-day mortality rate (9.4% vs. 29.4%; P =.05), a significantly shorter median length of stay (16.5 days [ 4.0-73.25] vs. 20.0 days [ 1.0-112.25]; P =.04), and a significantly lower defined daily dose of carbapenem use (12.9 +/- 8.9 vs. 18.4 +/- 12.6; P =.05). Conclusions: Ertapenem could be safely used as de-escalation therapy for ESBL-producing Enterobacteriaceae infections, once the susceptibility profiles are known. Future studies are needed to investigate ertapenem efficacy against ESBL-producing Enterobacteriaceae pneumonia to determine its applicability in life-threatening conditions.

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