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Effect of resuscitative endovascular balloon occlusion of the aorta in nontraumatic out-of-hospital cardiac arrest: a multinational, multicenter, randomized, controlled trial

DC Field Value Language
dc.contributor.authorKim, Hee Eun-
dc.contributor.authorChu, Sheng-En-
dc.contributor.authorJo, You Hwan-
dc.contributor.authorChiang, Wen-Chu-
dc.contributor.authorJang, Dong-Hyun-
dc.contributor.authorChang, Chin-Hao-
dc.contributor.authorOh, So Hee-
dc.contributor.authorChen, Hsuan-An-
dc.contributor.authorPark, Seung Min-
dc.contributor.authorSun, Jen-Tang-
dc.contributor.authorLee, Dong Keon-
dc.date.accessioned2024-03-04T01:02:33Z-
dc.date.available2024-03-04T10:03:02Z-
dc.date.issued2024-02-13-
dc.identifier.citationTrials, Vol.25 no.118ko_KR
dc.identifier.issn1745-6215-
dc.identifier.urihttps://hdl.handle.net/10371/199030-
dc.description.abstractBackground
Out-of-hospital cardiac arrest (OHCA) is a significant public health issue worldwide and is associated with low survival rates and poor neurological outcomes. The generation of optimal coronary perfusion pressure (CPP) via high-quality chest compressions is a key factor in enhancing survival rates. However, it is often challenging to provide adequate CPP in real-world cardiopulmonary resuscitation (CPR) scenarios. Based on animal studies and human trials on improving CPP in patients with nontraumatic OHCA, resuscitative endovascular balloon occlusion of the aorta (REBOA) is a promising technique in these cases. This study aims to investigate the benefits of REBOA adjunct to CPR compared with conventional CPR for the clinical management of nontraumatic OHCA.

Methods
This is a parallel-group, randomized, controlled, multinational trial that will be conducted at two urban academic tertiary hospitals in Korea and Taiwan. Patients aged 20–80 years presenting with witnessed OHCA will be enrolled in this study. Eligible participants must fulfill the inclusion criteria, and written informed consent should be collected from their legal representatives. Patients will be randomly assigned to the intervention (REBOA-CPR) or control (conventional CPR) group. The intervention group will receive REBOA and standard advanced cardiovascular life support (ACLS). Meanwhile, the control group will receive ACLS based on the 2020 American Heart Association guidelines. The primary outcome is the return of spontaneous circulation (ROSC). The secondary outcomes include sustained ROSC, survival to admission, survival to discharge, neurological outcome, and hemodynamic changes.

Discussion
Our upcoming trial can provide essential evidence regarding the efficacy of REBOA, a mechanical method for enhancing CPP, in OHCA resuscitation. Our study aims to determine whether REBOA can improve treatment strategies for patients with nontraumatic OHCA based on clinical outcomes, thereby potentially providing valuable insights and guiding further advancements in this critical public health area.

Trial registration
ClinicalTrials.gov NCT06031623. Registered on September 9, 2023
ko_KR
dc.description.sponsorshipThis work is partly supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (no. NRF-2022R1F1A1074361), the Seoul National University Bundang Hospital Research Fund (no. 14-2019-021), and the Far Eastern Memorial Hospital (no. PI20230002).ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.titleEffect of resuscitative endovascular balloon occlusion of the aorta in nontraumatic out-of-hospital cardiac arrest: a multinational, multicenter, randomized, controlled trialko_KR
dc.typeArticleko_KR
dc.identifier.doi10.1186/s13063-024-07928-xko_KR
dc.citation.journaltitleTrialsko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2024-02-18T04:12:20Z-
dc.citation.number118ko_KR
dc.citation.volume25ko_KR
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