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基于证据的脑死亡潜在器官供者心脏停搏延迟检查表: DONORS 集群随机临床试验。

Evidence-Based Checklist to Delay Cardiac Arrest in Brain-Dead Potential Organ Donors: The DONORS Cluster Randomized Clinical Trial.

机构信息

Responsabilidade Social-Programa de Apoio ao Desenvolvimento Institucional do Sistema Único de Saúde (PROADI-SUS), Hospital Moinhos de Vento (HMV), Porto Alegre, Rio Grande do Sul, Brazil.

Central Estadual de Transplantes de Santa Catarina, Rua Esteves Júnior, Florianópolis, Santa Catarina, Brazil.

出版信息

JAMA Netw Open. 2023 Dec 1;6(12):e2346901. doi: 10.1001/jamanetworkopen.2023.46901.

Abstract

IMPORTANCE

The effectiveness of goal-directed care to reduce loss of brain-dead potential donors to cardiac arrest is unclear.

OBJECTIVE

To evaluate the effectiveness of an evidence-based, goal-directed checklist in the clinical management of brain-dead potential donors in the intensive care unit (ICU).

DESIGN, SETTING, AND PARTICIPANTS: The Donation Network to Optimize Organ Recovery Study (DONORS) was an open-label, parallel-group cluster randomized clinical trial in Brazil. Enrollment and follow-up were conducted from June 20, 2017, to November 30, 2019. Hospital ICUs that reported 10 or more brain deaths in the previous 2 years were included. Consecutive brain-dead potential donors in the ICU aged 14 to 90 years with a condition consistent with brain death after the first clinical examination were enrolled. Participants were randomized to either the intervention group or the control group. The intention-to-treat data analysis was conducted from June 15 to August 30, 2020.

INTERVENTIONS

Hospital staff in the intervention group were instructed to administer to brain-dead potential donors in the intervention group an evidence-based checklist with 13 clinical goals and 14 corresponding actions to guide care, every 6 hours, from study enrollment to organ retrieval. The control group provided or received usual care.

MAIN OUTCOMES AND MEASURES

The primary outcome was loss of brain-dead potential donors to cardiac arrest at the individual level. A prespecified sensitivity analysis assessed the effect of adherence to the checklist in the intervention group.

RESULTS

Among the 1771 brain-dead potential donors screened in 63 hospitals, 1535 were included. These patients included 673 males (59.2%) and had a median (IQR) age of 51 (36.3-62.0) years. The main cause of brain injury was stroke (877 [57.1%]), followed by trauma (485 [31.6%]). Of the 63 hospitals, 31 (49.2%) were assigned to the intervention group (743 [48.4%] brain-dead potential donors) and 32 (50.8%) to the control group (792 [51.6%] brain-dead potential donors). Seventy potential donors (9.4%) at intervention hospitals and 117 (14.8%) at control hospitals met the primary outcome (risk ratio [RR], 0.70; 95% CI, 0.46-1.08; P = .11). The primary outcome rate was lower in those with adherence higher than 79.0% than in the control group (5.3% vs 14.8%; RR, 0.41; 95% CI, 0.22-0.78; P = .006).

CONCLUSIONS AND RELEVANCE

This cluster randomized clinical trial was inconclusive in determining whether the overall use of an evidence-based, goal-directed checklist reduced brain-dead potential donor loss to cardiac arrest. The findings suggest that use of such a checklist has limited effectiveness without adherence to the actions recommended in this checklist.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT03179020.

摘要

重要性

目标导向护理对减少心脏骤停脑死亡潜在供体的损失的效果尚不清楚。

目的

评估在 ICU 中对脑死亡潜在供体进行临床管理的基于证据的目标导向检查表的有效性。

设计、地点和参与者:捐赠网络优化器官恢复研究(DONORS)是巴西的一项开放性、平行组集群随机临床试验。招募和随访于 2017 年 6 月 20 日至 2019 年 11 月 30 日进行。报告在前 2 年中有 10 例或更多脑死亡的医院 ICU 包括在内。连续的脑死亡潜在供体,年龄在 14 至 90 岁之间,在首次临床检查后符合脑死亡条件,在 ICU 中招募。参与者被随机分配到干预组或对照组。意向治疗数据分析于 2020 年 6 月 15 日至 8 月 30 日进行。

干预措施

干预组的医院工作人员被指示对干预组的脑死亡潜在供体每隔 6 小时使用一份包含 13 个临床目标和 14 个相应行动的基于证据的检查表,以指导护理,直至器官检索。对照组提供或接受常规护理。

主要结果和测量

主要结局是个体层面上心脏骤停导致脑死亡潜在供体的损失。一项预先指定的敏感性分析评估了干预组对检查表的遵守程度的影响。

结果

在 63 家医院筛查的 1771 名脑死亡潜在供体中,有 1535 名符合条件。这些患者包括 673 名男性(59.2%),中位(IQR)年龄为 51(36.3-62.0)岁。脑损伤的主要原因是中风(877 例[57.1%]),其次是创伤(485 例[31.6%])。在 63 家医院中,31 家(49.2%)被分配到干预组(743 例[48.4%]脑死亡潜在供体),32 家(50.8%)被分配到对照组(792 例[51.6%]脑死亡潜在供体)。70 名潜在供体(9.4%)在干预医院和 117 名潜在供体(14.8%)在对照组达到了主要结局(风险比[RR],0.70;95%CI,0.46-1.08;P = 0.11)。在遵守率高于 79.0%的患者中,主要结局发生率低于对照组(5.3%比 14.8%;RR,0.41;95%CI,0.22-0.78;P = 0.006)。

结论和相关性

这项集群随机临床试验在确定整体使用基于证据的、目标导向的检查表是否降低心脏骤停导致脑死亡潜在供体的损失方面没有定论。研究结果表明,在不遵守本检查表中推荐的操作的情况下,使用此类检查表的效果有限。

试验注册

ClinicalTrials.gov 标识符:NCT03179020。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8259/10722341/89114ca6f008/jamanetwopen-e2346901-g001.jpg

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