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Evaluation of the Impact of a Tourniquet Training Program: A Cross-Sectional Study

Author

Listed:
  • Valentín González-Alonso

    (Departamento Simulación, Escuela Militar de Sanidad (EMISAN), Ministerio de Defensa, 28047 Madrid, Spain)

  • María del Carmen Usero-Pérez

    (Departamento de Enfermería, Escuela Militar de Sanidad (EMISAN), 28047 Madrid, Spain)

  • Raquel Seguido Chacón

    (Servicio de Sanidad de la Guardia Real, Ministerio de Defensa, 28048 Madrid, Spain)

  • Alicia Gómez de la Fuente

    (Servicio de Sanidad de la Guardia Real, Ministerio de Defensa, 28048 Madrid, Spain)

  • Jonathan Cortés-Martín

    (Departamento de Enfermería, Facultad de Ciencias de la Salud, Universidad de Granada, 18071 Granada, Spain)

  • Raquel Rodríguez-Blanque

    (Departamento de Enfermería, Facultad de Ciencias de la Salud, Universidad de Granada, 18071 Granada, Spain
    Hospital Clinico Universitario San Cecilio, 18016 Granada, Spain)

  • Juan Carlos Sánchez-García

    (Departamento de Enfermería, Facultad de Ciencias de la Salud, Universidad de Granada, 18071 Granada, Spain)

Abstract

Among the main preventable causes of death in the area of operations is external exsanguinating hemorrhage in the extremities, hence the importance of the tourniquet as a therapeutic tool in this type of injury and, therefore, of the training of personnel participating in international missions. The main objective of this study is to determine the impact of training in the application of this device. This is a quasi-experimental, prospective, cross-sectional study, carried out with 97 healthy volunteers, military personnel who perform their work in the Royal Guard barracks of El Pardo. The study was conducted between June 2019 and July 2021. The correct determination of the device placement site and the times of correct device placement were evaluated by determining whether there was blood flow using Doppler ultrasound measurements. Statistically significant results were obtained for application time (76.68 s to 58.06 s; p < 0.001), correct device placement ( p < 0.001), and achievement of complete ischemia in the upper extremity (23.7% pretest vs. 24.7% post-test; p < 0.001). In the lower extremity, after training, longer application duration (43.33 s to 47.30 s) and lower ischemia achievement (59.8% pretest vs. 37.8% post-test) were obtained. Standardized and regulated training improves device application. More intensive training is necessary to obtain better results.

Suggested Citation

  • Valentín González-Alonso & María del Carmen Usero-Pérez & Raquel Seguido Chacón & Alicia Gómez de la Fuente & Jonathan Cortés-Martín & Raquel Rodríguez-Blanque & Juan Carlos Sánchez-García, 2023. "Evaluation of the Impact of a Tourniquet Training Program: A Cross-Sectional Study," IJERPH, MDPI, vol. 20(3), pages 1-10, February.
  • Handle: RePEc:gam:jijerp:v:20:y:2023:i:3:p:2742-:d:1057080
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