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Frequency of Screening and Spontaneous Breathing Trial Techniques

医学 自主呼吸试验 随机对照试验 机械通风 呼吸 通风(建筑) 病危 重症监护 心理干预 临床试验 麻醉 重症监护室 重症监护医学 外科 内科学 护理部 机械工程 工程类
作者
Karen E. A. Burns,Jessica C. Wong,Leena Rizvi,Myriam Lafrenière‐Roula,Kevin E. Thorpe,John W. Devlin,Deborah J. Cook,Andrew Seely,Peter Dodek,Maged Tanios,Thomas Piraino,Audrey Gouskos,Kenneth C. Kiedrowski,Phyllis Kay,Susan L. Mitchell,George W. Merner,Michaël Mayette,Frédérick D’Aragon,François Lamontagne,Bram Rochwerg
出处
期刊:JAMA [American Medical Association]
卷期号:332 (21): 1808-1808 被引量:4
标识
DOI:10.1001/jama.2024.20631
摘要

Importance The optimal screening frequency and spontaneous breathing trial (SBT) technique to liberate adults from ventilators are unknown. Objective To compare the effects of screening frequency (once-daily screening vs more frequent screening) and SBT technique (pressure-supported SBT with a pressure support level that was >0-≤8 cm H 2 O and a positive end-expiratory pressure [PEEP] level that was >0-≤5 cm H 2 O vs T-piece SBT) on the time to successful extubation. Design, Setting, and Participants Randomized clinical trial with a 2 × 2 factorial design including critically ill adults who were receiving invasive mechanical ventilation for at least 24 hours, who were capable of initiating spontaneous breaths or triggering ventilators, and who were receiving a fractional concentration of inspired oxygen that was 70% or less and a PEEP level of 12 cm H 2 O or less. Recruitment was between January 2018 and February 2022 at 23 intensive care units in North America; last follow-up occurred October 18, 2022. Interventions Participants were enrolled early to enable protocolized screening (more frequent vs once daily) to identify the earliest that patients met criteria to undergo pressure-supported or T-piece SBT lasting 30 to 120 minutes. Main Outcome and Measures Time to successful extubation (time when unsupported, spontaneous breathing began and was sustained for ≥48 hours after extubation). Results Of 797 patients (198 in the once-daily screening and pressure-supported SBT group, 204 in once-daily screening and T-piece SBT, 195 in more frequent screening and pressure-supported SBT, and 200 in more frequent screening and T-piece SBT), the mean age was 62.4 (SD, 18.4) years and 472 (59.2%) were men. There were no statistically significant differences by screening frequency (hazard ratio [HR], 0.88 [95% CI, 0.76-1.03]; P = .12) or by SBT technique (HR, 1.06 [95% CI, 0.91-1.23]; P = .45). The median time to successful extubation was 2.0 days (95% CI, 1.7-2.7) for once-daily screening and pressure-supported SBT, 3.1 days (95% CI, 2.7-4.8) for once-daily screening and T-piece SBT, 3.9 days (95% CI, 2.9-4.7) for more frequent screening and pressure-supported SBT, and 2.9 days (95% CI, 2.0-3.1) for more frequent screening and T-piece SBT. An unexpected interaction between screening frequency and SBT technique required pairwise contrasts that revealed more frequent screening (vs once-daily screening) and pressure-supported SBT increased the time to successful extubation (HR, 0.70 [95% CI, 0.50-0.96]; P = .02). Once-daily screening and pressure-supported SBT (vs T-piece SBT) did not reduce the time to successful extubation (HR, 1.30 [95% CI, 0.98-1.70]; P = .08). Conclusions and Relevance Among critically ill adults who received invasive mechanical ventilation for more than 24 hours, screening frequency (once-daily vs more frequent screening) and SBT technique (pressure-supported vs T-piece SBT) did not change the time to successful extubation. However, an unexpected and statistically significant interaction was identified; protocolized more frequent screening combined with pressure-supported SBTs increased the time to first successful extubation. Trial Registration ClinicalTrials.gov Identifiers: NCT02399267 and NCT02969226
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