Prospective Evaluation of a Modified Apnea Test in Brain Death Candidates that Does Not Require Disconnection from the Ventilator.

Apnea test Apneic oxygenation Brainstem areflexia Irreversible loss of brain function Ventilator-based

Journal

Neurocritical care
ISSN: 1556-0961
Titre abrégé: Neurocrit Care
Pays: United States
ID NLM: 101156086

Informations de publication

Date de publication:
01 Jul 2024
Historique:
received: 05 10 2023
accepted: 05 06 2024
medline: 2 7 2024
pubmed: 2 7 2024
entrez: 1 7 2024
Statut: aheadofprint

Résumé

The apnea test (AT) is an important component in the determination of brain death/death by neurologic criteria (BD/DNC) and often entails disconnecting the patient from the ventilator followed by tracheal oxygen insufflation to ensure adequate oxygenation. To rate the test as positive, most international guidelines state that a lack of spontaneous breathing must be demonstrated when the arterial partial pressure of carbon dioxide (PaCO The mAT was performed in all 140 BD/DNC candidates registered between January 2019 and December 2022: after 10 min of preoxygenation, (1) positive end-expiratory pressure was increased by 2 mbar (1.5 mm Hg), (2) ventilation mode was switched to continuous positive airway pressure, and (3) apnea back-up mode was turned off (flow trigger 10 L/min). The mAT was considered positive when spontaneous breathing did not occur upon PaCO The mAT was possible in 139/140 patients and had a median duration of 15 min (interquartile range 13-19 min). Severe complications were not evident. In 51 patients, the post-mAT arterial partial pressure of oxygen (PaO The mAT is a safe and protective means of identifying patients who no longer have an intact central respiratory drive, which is a critical factor in the diagnosis of BD/DNC. Clinical trial registration DRKS, DRKS00017803, retrospectively registered 23.11.2020, https://drks.de/search/de/trial/DRKS00017803.

Sections du résumé

BACKGROUND BACKGROUND
The apnea test (AT) is an important component in the determination of brain death/death by neurologic criteria (BD/DNC) and often entails disconnecting the patient from the ventilator followed by tracheal oxygen insufflation to ensure adequate oxygenation. To rate the test as positive, most international guidelines state that a lack of spontaneous breathing must be demonstrated when the arterial partial pressure of carbon dioxide (PaCO
METHODS METHODS
The mAT was performed in all 140 BD/DNC candidates registered between January 2019 and December 2022: after 10 min of preoxygenation, (1) positive end-expiratory pressure was increased by 2 mbar (1.5 mm Hg), (2) ventilation mode was switched to continuous positive airway pressure, and (3) apnea back-up mode was turned off (flow trigger 10 L/min). The mAT was considered positive when spontaneous breathing did not occur upon PaCO
RESULTS RESULTS
The mAT was possible in 139/140 patients and had a median duration of 15 min (interquartile range 13-19 min). Severe complications were not evident. In 51 patients, the post-mAT arterial partial pressure of oxygen (PaO
CONCLUSIONS CONCLUSIONS
The mAT is a safe and protective means of identifying patients who no longer have an intact central respiratory drive, which is a critical factor in the diagnosis of BD/DNC. Clinical trial registration DRKS, DRKS00017803, retrospectively registered 23.11.2020, https://drks.de/search/de/trial/DRKS00017803.

Identifiants

pubmed: 38951444
doi: 10.1007/s12028-024-02035-w
pii: 10.1007/s12028-024-02035-w
doi:

Banques de données

DRKS
['DRKS00017803']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

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Auteurs

Johann Lambeck (J)

Department of Neurology and Clinical Neurophysiology (Klinik für Neurologie und Neurophysiologie), Freiburg University Medical Center (Universitätsklinikum Freiburg), Breisacherstr. 64, 79106, Freiburg, Germany. johann.lambeck@uniklinik-freiburg.de.

Jürgen Bardutzky (J)

Department of Neurology and Clinical Neurophysiology (Klinik für Neurologie und Neurophysiologie), Freiburg University Medical Center (Universitätsklinikum Freiburg), Breisacherstr. 64, 79106, Freiburg, Germany.

Christoph Strecker (C)

Department of Neurology and Clinical Neurophysiology (Klinik für Neurologie und Neurophysiologie), Freiburg University Medical Center (Universitätsklinikum Freiburg), Breisacherstr. 64, 79106, Freiburg, Germany.

Wolf-Dirk Niesen (WD)

Department of Neurology and Clinical Neurophysiology (Klinik für Neurologie und Neurophysiologie), Freiburg University Medical Center (Universitätsklinikum Freiburg), Breisacherstr. 64, 79106, Freiburg, Germany.

Classifications MeSH