Informations générales (source: ClinicalTrials.gov)

NCT04123977 Statut inconnu
Evaluation of Patient Analgesia After Bloc Serratus for the Management of Thoracic Trauma (TraumaThorax)
Observational
  • Plaies et blessures
University Hospital, Strasbourg, France (Voir sur ClinicalTrials)
octobre 2019
octobre 2020
29 juin 2024
Thorax traumas are very common in severe traumatology, including road accidents, representing the second most frequent site (after head injury, according to the FIRST study). These thoracic lesions are the cause of many complications (pneumothorax, hemothorax, lung infections, atelectasis). The national recommendations recommend the use of multi-modal analgesia with the use of regional loco anaesthesia for pain management and prevention of respiratory complications, including infectious complications. The loco-regional anaesthesia of choice is thoracic epidural or paravertebral block, but these techniques are not without risks, and are contraindicated in many situations (severe head trauma, patient under curative anticoagulation, pelvic trauma...). The anterior Serratus block appears to be a quality localoregional anaesthesia in thoracic surgery, and a few cases in the literature have shown an interest in severe traumatology. The investigators perform this anterior Serratus block almost systematically in patients with thoracic trauma in the Hautepierre surgical intensive care unit.

Etablissements

Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Service de Réanimation chirurgicale_ Hôpital de Hautepierre - 67091 - Strasbourg - France Julien POTTECHER, MD, PhD En recrutement Contact (sur clinicalTrials)

Critères

Tous
Inclusion criteria:

- Adult patient (≥18 years old)

- Gender (Male and Female)

- Patient hospitalised in surgical intensive care or continuous trauma care with
thorax trauma who received anterior Serratus block analgesia from January 1, 2018 to
February 28, 2019

- Patient who has given his consent to the reuse of his data for the purposes of this
research

Criteria for non-inclusion:

- Patient who has expressed opposition to participating in the study

- Impossibility of giving the subject informed information (difficulties in
understanding the subject,...)

- Subject under the protection of justice

- Subject under guardianship or curatorship