Clinical Trials Directory

Trials / Completed

CompletedNCT06131892

Defibrillation in Accidental Hypothermia

Defibrillation in Accidental Hypothermia: a Retrospective Study of the International Hypothermia Registry

Status
Completed
Phase
Study type
Observational
Enrollment
63 (actual)
Sponsor
University Hospital, Geneva · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Hypothermia (core temperature ≤35°C) is a frequent and life-threatening complication after mountain accidents, near-drowning, and intoxications, and can provoke arrhythmia, reduced cardiac contractility, and cardiac arrest. The hypothermic heart may be insensitive to defibrillation with a core temperature \<30°C. Also, below \<30°C after successful defibrillation, a perfusing rhythm often degenerates to ventricular fibrillation (VF) again. Repeated defibrillation can induce myocardial injury. Thus, the guidelines of the European Resuscitation Council (ERC) suggest delaying further defibrillation attempts until the core temperature is \>30°C if VF persists after 3 shocks. Epinephrine should be withheld if core temperature is \<30°C. Advanced Life Support (ALS) guidelines of the American Heart Association (AHA) state that it may be reasonable to perform further defibrillation attempts according to the standard algorithm and to consider administration of a vasopressor during cardiac arrest (Table 1). This discrepancy between ERC and AHA guidelines can be explained by the different interpretations of mainly animal data, which show that vasopressors increase the chances of successful defibrillation \<30°C, defined as return of spontaneous circulation (ROSC) for at least 30 seconds. The guidelines of the Wilderness and Environmental Medicine Society (WMS) state that a single shock at a maximum power can be given for patients with a temperature \<30°C. The aim of this study is to evaluate clinical course of hypothermic patients(\<30°C) undergoing defibrillation. The primary aim is to evaluate the success ratio of defibrillation, defined as ROSC for at least 30 seconds. Secondary aims are the recurrence rate of ventricular fibrillation, the number of defibrillation attempts per patient, the presence of cardiac dysfunction after defibrillation and the cerebral performance category (CPC) score at the end of hospitalization.

Conditions

Interventions

TypeNameDescription
OTHERDefibrillationDefibrillation

Timeline

Start date
2023-04-01
Primary completion
2023-09-30
Completion
2023-09-30
First posted
2023-11-14
Last updated
2023-11-18

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT06131892. Inclusion in this directory is not an endorsement.