Ertapenem usage in cancer patients with and without neutropenia: a report on 97 cases from a comprehensive cancer center
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Abstract
Purpose
Ertapenem is being increasingly utilized in cancer patients, but published data regarding its usage are limited. Our objective was to describe the various indications for ertapenem therapy and its safety and efficacy in cancer patients.
Methods
We conducted a retrospective cohort study of cancer patients who received monotherapy with ertapenem for at least 72 h, between January 2007 and February 2013.
Results
Among 97 unique patients who received ertapenem monotherapy, the most common indications were: (1) To facilitate discharge from the hospital of stable patients still requiring antimicrobial therapy (46 %). (2) Primary therapy of various documented infections (bacteremia, pneumonia, urinary tract infection, skin and skin structure infection) with ertapenem (28 %). (3) De-escalation from a different broad-spectrum agent or regimen to ertapenem within the hospital setting in patients not ready for discharge (25 %). The median age of the 97 patients studied was 59 years (range 9–87 years) with 52 % being men. Most patients had underlying hematologic malignancies (54 %), and 7 % were recipients of hematopoietic stem cell transplantation. Twenty-nine patients (30 %) were neutropenic, 26 % were diabetic, and 6 % had chronic lung disease. Primary ertapenem monotherapy was successful in all patients, de-escalation in 95.8 % of patients, and the strategy of discharge on outpatient therapy with ertapenem in 95.6 % of patients. Patients failing de-escalation or early discharge responded to alternative regimens. We documented no significant ertapenem associated toxicity or adverse events.
Conclusions
Ertapenem appears to be safe and effective for several indications in cancer patients.
Keywords
Ertapenem De-escalation Neutropenia Cancer patientsNotes
Acknowledgments
This study was presented in part at The 49th Annual Meeting of Infectious Diseases Society of America (IDSA), Boston, MA, October 20–23, 2011. This work was supported in part by a research grant from Merck Inc., which did not have any role in the study design, collection, analysis or interpretation of data; nor did they have any influence on the writing of the report, or the decision to submit the article for publication.
Conflict of interest
All authors wish to declare that they have no conflicts of interest.
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