Clinical Outcome of Cefiderocol for Infections with Carbapenem-Resistant Organisms
Cefiderocol is a novel cephalosporin recently approved by the FDA to aid clinicians in the fight against multidrug-resistant (including carbapenem-resistant) gram-negative organisms. The primary objective of this study is to evaluate the 14- and 28-day mortality associated with cefiderocol. We perfo...
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2023-05-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_706df2d6ad8d44afab86d42d13b078b2 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Monirul I. Sajib |e author |
700 | 1 | 0 | |a Melinda Monteforte |e author |
700 | 1 | 0 | |a Roderick Go |e author |
245 | 0 | 0 | |a Clinical Outcome of Cefiderocol for Infections with Carbapenem-Resistant Organisms |
260 | |b MDPI AG, |c 2023-05-01T00:00:00Z. | ||
500 | |a 10.3390/antibiotics12050936 | ||
500 | |a 2079-6382 | ||
520 | |a Cefiderocol is a novel cephalosporin recently approved by the FDA to aid clinicians in the fight against multidrug-resistant (including carbapenem-resistant) gram-negative organisms. The primary objective of this study is to evaluate the 14- and 28-day mortality associated with cefiderocol. We performed a retrospective chart review of all adult patients admitted at Stony Brook University Hospital between October 2020 and December 2021 and received cefiderocol for at least 3 days. Patients were excluded if they received more than one course of cefiderocol therapy or remained hospitalized at the time of this study. A total of 22 patients met the inclusion criteria. The all-cause mortality on day 28 for all patients was 13.6%, whereas this rate for patients with BSI was 0%, with cUTI was 0% and with LRTI was 16.7%. The all-cause mortality on day 28 for patients who received the dual antibiotics (in conjunction with cefiderocol) was 0%, compared to 25% for patients who only received cefiderocol (<i>p</i> = 0.25). We noted treatment failure in two patients (9.1%). Our findings suggest that cefiderocol could possibly be associated with lower all-cause mortality than previously thought. In our study, we did not find any significant difference between cefiderocol's use in combination with another antibacterial agent and its use as a monotherapy. | ||
546 | |a EN | ||
690 | |a cefiderocol | ||
690 | |a gram-negative infection | ||
690 | |a multidrug-resistant infection | ||
690 | |a Therapeutics. Pharmacology | ||
690 | |a RM1-950 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Antibiotics, Vol 12, Iss 5, p 936 (2023) | |
787 | 0 | |n https://www.mdpi.com/2079-6382/12/5/936 | |
787 | 0 | |n https://doaj.org/toc/2079-6382 | |
856 | 4 | 1 | |u https://doaj.org/article/706df2d6ad8d44afab86d42d13b078b2 |z Connect to this object online. |