Cefiderocol treatment for carbapenem-resistant
Journal
JAC-antimicrobial resistance
ISSN: 2632-1823
Titre abrégé: JAC Antimicrob Resist
Pays: England
ID NLM: 101765283
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
received:
09
08
2021
accepted:
25
10
2021
entrez:
22
11
2021
pubmed:
23
11
2021
medline:
23
11
2021
Statut:
epublish
Résumé
To analyse the impact of cefiderocol use on outcome in patients admitted to the ICU for severe COVID-19 and further diagnosed with carbapenem-resistant Retrospective multicentre observational study was performed at four Italian hospitals, from January 2020 to April 2021. Adult patients admitted to ICU for severe COVID-19 and further diagnosed with CR-Ab infections were enrolled. Patients treated with cefiderocol, as compassionate use, for at least 72 h were compared with those receiving alternative regimens. Primary endpoint was all-cause 28 day mortality. The impact of cefiderocol on mortality was evaluated by multivariable Cox regression model. In total, 107 patients were enrolled (76% male, median age 65 years). The median time from ICU admission to CR-Ab infection diagnosis was 14 (IQR 8-20) days, and the main types of CR-Ab infections were bloodstream infection (58%) and lower respiratory tract infection (41%). Cefiderocol was administered to 42 patients within a median of 2 (IQR 1-4) days after CR-Ab infection diagnosis and as monotherapy in all cases. The remaining patients received colistin, mostly (82%) administered as combination therapy. All-cause 28 day mortality rate was 57%, without differences between groups (cefiderocol 55% versus colistin 58% Our study confirms the potential role of cefiderocol in the treatment of CR-Ab infection, but larger clinical studies are needed.
Identifiants
pubmed: 34806011
doi: 10.1093/jacamr/dlab174
pii: dlab174
pmc: PMC8599913
doi:
Types de publication
Journal Article
Langues
eng
Pagination
dlab174Informations de copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy.
Références
JAMA. 2016 Feb 23;315(8):801-10
pubmed: 26903338
Lancet Infect Dis. 2021 Feb;21(2):153-155
pubmed: 33058794
Clin Infect Dis. 2021 Nov 2;73(9):1664-1676
pubmed: 33618353
MMWR Morb Mortal Wkly Rep. 2020 Dec 04;69(48):1827-1831
pubmed: 33270611
Clin Microbiol Infect. 2019 Aug;25(8):951-957
pubmed: 30914347
Expert Rev Clin Pharmacol. 2021 Jul;14(7):777-791
pubmed: 33849355
J Glob Antimicrob Resist. 2020 Dec;23:292-296
pubmed: 33065329
Infect Control Hosp Epidemiol. 2021 Apr 16;:1-6
pubmed: 33858547
Int J Mol Sci. 2021 Mar 17;22(6):
pubmed: 33802761
Ann Intern Med. 2002 Nov 19;137(10):791-7
pubmed: 12435215
Antimicrob Agents Chemother. 2018 Jan 25;62(2):
pubmed: 29158270
Clin Infect Dis. 2021 Jun 1;72(11):2021-2024
pubmed: 32941593
Lancet Infect Dis. 2021 Feb;21(2):226-240
pubmed: 33058795
Open Forum Infect Dis. 2020 May 21;7(6):ofaa185
pubmed: 32548207
JAMA. 2020 Oct 6;324(13):1330-1341
pubmed: 32876694
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
Am J Infect Control. 2008 Jun;36(5):309-32
pubmed: 18538699
J Antimicrob Chemother. 2019 Nov 1;74(11):3399-3401
pubmed: 31369095
Lancet Infect Dis. 2018 Mar;18(3):318-327
pubmed: 29276051
Lancet Infect Dis. 2019 Jan;19(1):56-66
pubmed: 30409683