Epidemiology and clinical outcomes associated with extensively drug-resistant (XDR)
Journal
Infection control and hospital epidemiology
ISSN: 1559-6834
Titre abrégé: Infect Control Hosp Epidemiol
Pays: United States
ID NLM: 8804099
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
pubmed:
1
10
2020
medline:
1
9
2021
entrez:
30
9
2020
Statut:
ppublish
Résumé
Although infections caused by Acinetobacter baumannii are often healthcare-acquired, difficult to treat, and associated with high mortality, epidemiologic data for this organism are limited. We describe the epidemiology, clinical characteristics, and outcomes for patients with extensively drug-resistant Acinetobacter baumannii (XDRAB). Retrospective cohort study. Department of Veterans' Affairs Medical Centers (VAMCs). Patients with XDRAB cultures (defined as nonsusceptible to at least 1 agent in all but 2 or fewer classes) at VAMCs between 2012 and 2018. Microbiology and clinical data was extracted from national VA datasets. We used descriptive statistics to summarize patient characteristics and outcomes and bivariate analyses to compare outcomes by culture source. Among 11,546 patients with 15,364 A. baumannii cultures, 408 (3.5%) patients had 667 (4.3%) XDRAB cultures. Patients with XDRAB were older (mean age, 68 years; SD, 12.2) with median Charlson index 3 (interquartile range, 1-5). Respiratory specimens (n = 244, 36.6%) and urine samples (n = 187, 28%) were the most frequent sources; the greatest proportion of patients were from the South (n = 162, 39.7%). Most patients had had antibiotic exposures (n = 362, 88.7%) and hospital or long-term care admissions (n = 331, 81%) in the prior 90 days. Polymyxins, tigecycline, and minocycline demonstrated the highest susceptibility. Also, 30-day mortality (n = 96, 23.5%) and 1-year mortality (n = 199, 48.8%) were high, with significantly higher mortality in patients with blood cultures. The proportion of Acinetobacter baumannii in the VA that was XDR was low, but treatment options are extremely limited and clinical outcomes were poor. Prevention of healthcare-associated XDRAB infection should remain a priority, and novel antibiotics for XDRAB treatment are urgently needed.
Identifiants
pubmed: 32993829
pii: S0899823X2000450X
doi: 10.1017/ice.2020.450
pmc: PMC8428801
mid: NIHMS1737842
doi:
Substances chimiques
Anti-Bacterial Agents
0
Pharmaceutical Preparations
0
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
305-310Subventions
Organisme : HSRD VA
ID : I01 HX002169
Pays : United States
Organisme : HSRD VA
ID : IK6 HX003156
Pays : United States
Références
N Engl J Med. 2020 Apr 2;382(14):1309-1319
pubmed: 32242356
J Glob Antimicrob Resist. 2018 Sep;14:51-57
pubmed: 29471109
Drugs. 2018 Jan;78(1):65-98
pubmed: 29230684
J Infect. 2015 Feb;70(2):144-52
pubmed: 25246361
Emerg Infect Dis. 2018 Apr;24(4):727-734
pubmed: 29553339
Clin Infect Dis. 2016 Sep 1;63(5):642-650
pubmed: 27358355
Crit Care. 2007;11(3):134
pubmed: 17543135
Infect Control Hosp Epidemiol. 2016 Oct;37(10):1212-8
pubmed: 27406609
Medicine (Baltimore). 2018 Sep;97(39):e12278
pubmed: 30278498
Am J Infect Control. 2017 Nov 1;45(11):1183-1189
pubmed: 28757086
Infect Control Hosp Epidemiol. 2020 Jan;41(1):1-18
pubmed: 31767041
Infect Control Hosp Epidemiol. 2016 Nov;37(11):1288-1301
pubmed: 27573805
JAMA. 2015 Oct 13;314(14):1479-87
pubmed: 26436831
Clin Microbiol Infect. 2012 Mar;18(3):268-81
pubmed: 21793988
Lancet Infect Dis. 2020 Oct;20(10):1108-1109
pubmed: 32505229
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
Antimicrob Agents Chemother. 2017 Mar 24;61(4):
pubmed: 28069649
Clin Microbiol Rev. 2017 Jan;30(1):1-22
pubmed: 27795305