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Seven versus 14 days of antimicrobial therapy for severe multidrug-resistant Gram-negative bacterial infections in intensive care unit patients (OPTIMISE) : a randomised, open-label, non-inferiority clinical trial
| dc.contributor.author | Arns, Beatriz | pt_BR |
| dc.contributor.author | Antonio, Ana Carolina Pecanha | pt_BR |
| dc.contributor.author | Antonio, Juliana Peçanha | pt_BR |
| dc.contributor.author | Zavascki, Alexandre Prehn | pt_BR |
| dc.contributor.author | OPTIMISE Study Group | pt_BR |
| dc.date.accessioned | 2025-03-01T06:45:24Z | pt_BR |
| dc.date.issued | 2024 | pt_BR |
| dc.identifier.issn | 1364-8535 | pt_BR |
| dc.identifier.uri | http://hdl.handle.net/10183/287974 | pt_BR |
| dc.description.abstract | Background Shorter courses of antimicrobial therapy have been shown to be non-inferior to longer durations for the management of several infections. However, data on critically ill patients with severe infections by multidrug-resistant Gram-negative bacteria (MDR-GNB) are scarce. In the duratiOn of theraPy in severe infecTIons by MultIdrug-reSistant gram-nEgative bacteria (OPTIMISE) trial, we assessed the non-inferiority of 7-day versus 14-day antimicrobial therapy for patients with intensive care unit (ICU)-acquired severe infections by MDR-GNB. Methods This was a randomised multicenter, open-label, parallel controlled, non-inferiority trial. Adult patients with severe infections by MDR-GNB initiated ≥ 48 h of ICU admission were eligible if they were hemodynamically stable and without fever > 48 h on the 7th day of appropriate antimicrobial therapy. Patients were 1:1 randomised to discontinue antimicrobial therapy on the 7th (± 1) day or to continue for a total of 14 (± 1) days. The primary outcome was clinical failure, defined as death or relapse of infection within 28 days of randomisation. An upper edge of the two-tailed 95% confidence interval (CI) of the delta between the clinical failure rate in the 7- and the 14-day lower than 10% in both intention-to-treat (ITT) and per protocol (PP) analyses was set as the non-inferiority criteria. Results A total of 106 patients composed the ITT population: 59 and 47 allocated to 7- and 14-day groups, respectively. The PP population included 75 patients: 47 and 28 in the 7- and 14-day groups, respectively. Clinical failure occurred in 42.4% and 44.7% of the ITT population in 7- and 14-day groups, respectively, (risk difference (RD) − 2.3, 95%CI − 21.3 to 16.7), and in 46.8% and 50.0% of the PP population in 7- and 14-day groups, respectively (RD − 3.2, 95%CI − 26.6 to 20.2). Most infections were of the respiratory tract (73/68.9%) and caused by carbapenem-resistant Enterobacterales (42/39.6%). The study was interrupted before reaching planned sample size due to low recruitment rate. Conclusion The OPTIMISE trial could not determine the non-inferiority of 7-day compared to 14-day therapy for severe infections caused by MDR-GNB due to early termination related to the low recruitment rate. Trial registration: NCT05210387 on January 13, 2022. | en |
| dc.format.mimetype | application/pdf | pt_BR |
| dc.language.iso | eng | pt_BR |
| dc.relation.ispartof | Critical care. London. Vol. 28 (Apr. 2023), 412, 12 p. | pt_BR |
| dc.rights | Open Access | en |
| dc.subject | Gram-negative bacteria | en |
| dc.subject | Klebsiella pneumoniae | pt_BR |
| dc.subject | Antimicrobial therapy | en |
| dc.subject | Acinetobacter baumannii | pt_BR |
| dc.subject | Pseudomonas aeruginosa | pt_BR |
| dc.subject | Antimicrobial resistance | en |
| dc.subject | Antiinfecciosos | pt_BR |
| dc.subject | Enterobacterales | en |
| dc.subject | Bacterias gram-negativas | pt_BR |
| dc.subject | Enterobacteriaceae | pt_BR |
| dc.subject | Resistência microbiana a medicamentos | pt_BR |
| dc.title | Seven versus 14 days of antimicrobial therapy for severe multidrug-resistant Gram-negative bacterial infections in intensive care unit patients (OPTIMISE) : a randomised, open-label, non-inferiority clinical trial | pt_BR |
| dc.type | Artigo de periódico | pt_BR |
| dc.identifier.nrb | 001242995 | pt_BR |
| dc.type.origin | Estrangeiro | pt_BR |
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