Prehospital Partial Resuscitative Endovascular Balloon Occlusion of the Aorta for Exsanguinating Subdiaphragmatic Hemorrhage

Author:

Lendrum Robbie A.123,Perkins Zane123,Marsden Max134,Cochran Claire3,Davenport Ross13,Chege Frank2,Fitzpatrick-Swallow Virginia5,Greenhalgh Rob12,Wohlgemut Jared M.3,Henry Christine L.2,Singer Ben123,Grier Gareth1,Davies Gareth6,Bunker Nick1,Nevin Daniel123,Christian Mike127,Campbell Marion K.8,Tai Nigel134,Johnson Austin9,Jansen Jan O.10,Sadek Samy12,Brohi Karim13

Affiliation:

1. Bart’s Health National Health Service Trust, London, United Kingdom

2. London’s Air Ambulance, London, United Kingdom

3. Centre for Trauma Sciences, Queen Mary University of London, London, United Kingdom

4. Academic Department of Military Surgery and Trauma, Research and Clinical Innovation, Defense Medical Services, Birmingham, United Kingdom

5. Home Office Registered Forensic Pathologist, Wantage, United Kingdom

6. Manx Care, Nobles Hospital, Douglas, Isle of Man

7. Department of Critical Care Medicine, University British Columbia, Vancouver, British Columbia, Canada

8. Health Services Research Unit, University of Aberdeen, Aberdeen, Scotland

9. University of Utah Health, Salt Lake City

10. Department of Surgery, University of Alabama at Birmingham

Abstract

ImportanceHemorrhage is the most common cause of preventable death after injury. Most deaths occur early, in the prehospital phase of care.ObjectiveTo establish whether prehospital zone 1 (supraceliac) partial resuscitative endovascular balloon occlusion of the aorta (Z1 P-REBOA) can be achieved in the resuscitation of adult trauma patients at risk of cardiac arrest and death due to exsanguination.Design, Setting, and ParticipantsThis was a prospective observational cohort study (Idea, Development, Exploration, Assessment and Long-term follow-up [IDEAL] 2A design) with recruitment from June 2020 to March 2022 and follow-up until discharge from hospital, death, or 90 days evaluating a physician-led and physician-delivered, urban prehospital trauma service in the Greater London area. Trauma patients aged 16 years and older with suspected exsanguinating subdiaphragmatic hemorrhage, recent or imminent hypovolemic traumatic cardiac arrest (TCA) were included. Those with unsurvivable injuries or who were pregnant were excluded. Of 2960 individuals attended by the service during the study period, 16 were included in the study.ExposuresZI REBOA or P-REBOA.Main Outcomes and MeasuresThe main outcome was the proportion of patients in whom Z1 REBOA and Z1 P-REBOA were achieved. Clinical end points included systolic blood pressure (SBP) response to Z1 REBOA, mortality rate (1 hour, 3 hours, 24 hours, or 30 days postinjury), and survival to hospital discharge.ResultsFemoral arterial access for Z1 REBOA was attempted in 16 patients (median [range] age, 30 [17-76] years; 14 [81%] male; median [IQR] Injury Severity Score, 50 [39-57]). In 2 patients with successful arterial access, REBOA was not attempted due to improvement in clinical condition. In the other 14 patients (8 [57%] of whom were in traumatic cardiac arrest [TCA]), 11 successfully underwent cannulation and had aortic balloons inflated in Z1. The 3 individuals in whom cannulation was unsuccessful were in TCA (failure rate = 3/14 [21%]). Median (IQR) pre-REBOA SBP in the 11 individuals for whom cannulation was successful (5 [46%] in TCA) was 47 (33-52) mm Hg. Z1 REBOA plus P-REBOA was associated with a significant improvement in BP (median [IQR] SBP at emergency department arrival, 101 [77-107] mm Hg; 0 of 10 patients were in TCA at arrival). The median group-level improvement in SBP from the pre-REBOA value was 52 (95% CI, 42-77) mm Hg (P < .004). P-REBOA was feasible in 8 individuals (8/11 [73%]) and occurred spontaneously in 4 of these. The 1- and 3-hour postinjury mortality rate was 9% (1/11), 24-hour mortality was 27% (3/11), and 30-day mortality was 82% (9/11). Survival to hospital discharge was 18% (2/11). Both survivors underwent early Z1 P-REBOA.Conclusions and RelevanceIn this study, prehospital Z1 P-REBOA is feasible and may enable early survival, but with a significant incidence of late death.Trial RegistrationClinicalTrials.gov Identifier: NCT04145271

Publisher

American Medical Association (AMA)

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