Factors associated with failure of intraosseous access in prehospital trauma treatment by military medical personnel.

ACCIDENT & EMERGENCY MEDICINE EDUCATION & TRAINING (see Medical Education & Training) INTENSIVE & CRITICAL CARE Trauma management

Journal

BMJ military health
ISSN: 2633-3775
Titre abrégé: BMJ Mil Health
Pays: England
ID NLM: 101761581

Informations de publication

Date de publication:
08 Oct 2024
Historique:
received: 16 05 2024
accepted: 20 09 2024
medline: 10 10 2024
pubmed: 10 10 2024
entrez: 9 10 2024
Statut: aheadofprint

Résumé

Intraosseous devices have become an alternative to peripheral intravenous (PIV) access. Despite the established success of intraosseous devices in laboratory and simulator studies, there is a lack of data regarding their real-world utilisation in prehospital settings. Therefore, this study aims to evaluate the success rates of intraosseous access in a prehospital military context and identify factors associated with failure. Using the Israel Defense Forces (IDF) Trauma Registry, we retrospectively collected data from 2010 to 2023. The primary outcome was the first pass success rate of intraosseous access, and logistic regression models were applied to identify variables associated with first pass failure. The study included 172 trauma patients who underwent attempted intraosseous access with 46.5% cases which were classified as military events. The median age was 22 years, and 17.3% were paediatric patients. First pass success was achieved in 67.4% of cases, with a cumulative success rate of 80.8% after multiple attempts. Moreover, significant differences were noted when examining the success rate of the three intraosseous devices used by the IDF teams, with the highest success rate being documented for the NIO Adult versus the EZ-IO or the BIG (81.4%; 76.7%; 62.4%). However, logistic regression analysis revealed that the number of PIV access attempts was the only variable significantly associated with decreased odds of achieving first pass intraosseous access. These findings suggest that intraosseous devices are a viable alternative for establishing vascular access in prehospital military settings. However, success rates were slightly lower than previous reports, potentially due to the severity of injuries in the study cohort. Our analyses revealed a higher number of PIV access attempts correlated with reduced first pass intraosseous success, possibly stemming from caregiver proficiency in obtaining vascular access. Further research is needed to explore additional factors affecting intraosseous access success rates.

Identifiants

pubmed: 39384217
pii: military-2024-002783
doi: 10.1136/military-2024-002783
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Mor Rittblat (M)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel rittblat@gmail.com.
Department of Preventive Medicine and Epidemiology, School of Public Health, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Military Medicine and 'Tzameret', Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Plastic and Reconstructive Surgery, Hadassah Hebrew University Medical Centre, Jerusalem, Israel.

D Kotovich (D)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Department of Plastic and Reconstructive Surgery, Hadassah Hebrew University Medical Centre, Jerusalem, Israel.

N Tsur (N)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Department of Plastic and Reconstructive Surgery, Hadassah Hebrew University Medical Centre, Jerusalem, Israel.

Z Beer (Z)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Department of Military Medicine and 'Tzameret', Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

I Radomislensky (I)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
The Israel National Center for Trauma & Emergency Medicine Research, Gertner Institute of Epidemiology and Health Policy Research, Tel Hashomer, Ramat Gan, Israel.

S Gendler (S)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.

O Almog (O)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Department of Military Medicine and 'Tzameret', Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

A M Tsur (AM)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Department of Otolaryngology-Head and Neck Surgery, Rabin Medical Center, Tel Aviv University, Petach Tiqva, Israel.

G Avital (G)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Division of Anesthesia, Intensive Care & Pain Management, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

T Talmy (T)

Israeli Defense Forces Medical Corps, Tel Hashomer, Ramat Gan, Israel.
Department of Military Medicine and 'Tzameret', Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
Division of Anesthesia, Intensive Care & Pain Management, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Classifications MeSH