Abstract |
We implemented a carbapenem-saving strategy in hemato-oncology patients from 2013, using an empirical combination of piperacillin-tazobactam and amikacin for high-risk hemato-oncology patients with febrile neutropenia, who remain hemodynamically unstable > 72 hours despite initial cefepime treatment. All-cause mortality was not different between the two periods (6.54 and 6.57 deaths per 1,000 person-day, P = 0.926). Group 2 carbapenem use significantly decreased after strategy implementation (78.43 vs. 67.43 monthly days of therapy, P = 0.018), while carbapenem-resistant gram-negative bacilli did not show meaningful changes during the study period. Our carbapenem-saving strategy could effectively suppress carbapenem use without an increase of overall mortality.
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Authors | Jae-Hoon Ko, Si-Ho Kim, Cheol-In Kang, Sun Young Cho, Nam Yong Lee, Doo Ryeon Chung, Kyong Ran Peck, Jae-Hoon Song |
Journal | Journal of Korean medical science
(J Korean Med Sci)
Vol. 34
Issue 2
Pg. e17
(Jan 14 2019)
ISSN: 1598-6357 [Electronic] Korea (South) |
PMID | 30636947
(Publication Type: Journal Article)
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Chemical References |
- Anti-Bacterial Agents
- Carbapenems
- Piperacillin, Tazobactam Drug Combination
- Amikacin
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Topics |
- Amikacin
(pharmacology, therapeutic use)
- Anti-Bacterial Agents
(therapeutic use)
- Carbapenems
(pharmacology, therapeutic use)
- Drug Resistance, Bacterial
- Enterobacteriaceae
(drug effects)
- Febrile Neutropenia
(drug therapy, microbiology, pathology)
- Humans
- Piperacillin, Tazobactam Drug Combination
(pharmacology, therapeutic use)
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