Doxapram as an additive to propofol sedation for endoscopic retrograde cholangiopancreatography: a placebo-controlled, randomized, double-blinded study.


Journal

Surgical endoscopy
ISSN: 1432-2218
Titre abrégé: Surg Endosc
Pays: Germany
ID NLM: 8806653

Informations de publication

Date de publication:
12 2020
Historique:
received: 09 07 2019
accepted: 24 12 2019
pubmed: 30 1 2020
medline: 29 5 2021
entrez: 30 1 2020
Statut: ppublish

Résumé

Endoscopic retrograde cholangiopancreatography (ERCP) requires moderate to deep sedation, usually with propofol. Adverse effects of propofol sedation are relatively common, such as respiratory and cardiovascular depression. This study was conducted to determine if doxapram, a respiratory stimulant, could be used to reduce the incidence of respiratory depression. This is a single-center, prospective randomized double-blind study performed in the endoscopy unit of Helsinki University Central Hospital. 56 patients were randomized in a 1:1 ratio to either receive doxapram as an initial 1 mg/kg bolus and an infusion of 1 mg/kg/h (group DOX) or placebo (group P) during propofol sedation for ERCP. Main outcome measures were apneic episodes and hypoxemia (SpO There were no statistically significant differences in apneic episodes (p = 0.18) or hypoxemia (p = 0.53) between the groups. There was a statistically significant rise in etCO Doxapram was not effective in reducing respiratory depression caused by deep propofol sedation during ERCP. Further studies are warranted using different sedation protocols and dosing regimens. Clinical trial registration ClinicalTrials.gov ID NCT02171910.

Sections du résumé

BACKGROUND
Endoscopic retrograde cholangiopancreatography (ERCP) requires moderate to deep sedation, usually with propofol. Adverse effects of propofol sedation are relatively common, such as respiratory and cardiovascular depression. This study was conducted to determine if doxapram, a respiratory stimulant, could be used to reduce the incidence of respiratory depression.
METHODS
This is a single-center, prospective randomized double-blind study performed in the endoscopy unit of Helsinki University Central Hospital. 56 patients were randomized in a 1:1 ratio to either receive doxapram as an initial 1 mg/kg bolus and an infusion of 1 mg/kg/h (group DOX) or placebo (group P) during propofol sedation for ERCP. Main outcome measures were apneic episodes and hypoxemia (SpO
RESULTS
There were no statistically significant differences in apneic episodes (p = 0.18) or hypoxemia (p = 0.53) between the groups. There was a statistically significant rise in etCO
CONCLUSIONS
Doxapram was not effective in reducing respiratory depression caused by deep propofol sedation during ERCP. Further studies are warranted using different sedation protocols and dosing regimens. Clinical trial registration ClinicalTrials.gov ID NCT02171910.

Identifiants

pubmed: 31993819
doi: 10.1007/s00464-019-07344-2
pii: 10.1007/s00464-019-07344-2
pmc: PMC7644472
doi:

Substances chimiques

Hypnotics and Sedatives 0
Doxapram 94F3830Q73
Propofol YI7VU623SF

Banques de données

ClinicalTrials.gov
['NCT02171910']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5477-5483

Références

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Auteurs

Jarno Jokelainen (J)

Department of Anesthesia and Intensive Care Medicine, South Karelia Central Hospital, Valto Käkelän katu 1, 53130, Lappeenranta, Finland. jarno.jokelainen@gmail.com.
University of Helsinki, Helsinki, Finland. jarno.jokelainen@gmail.com.

Anna Belozerskikh (A)

Department of Anesthesia and Intensive Care Medicine, Helsinki University Central Hospital, Helsinki, Finland.

Harri Mustonen (H)

University of Helsinki, Helsinki, Finland.
Department of Gastroenterological and General Surgery, Helsinki University Hospital, Helsinki, Finland.

Marianne Udd (M)

University of Helsinki, Helsinki, Finland.
Department of Gastroenterological and General Surgery, Helsinki University Hospital, Helsinki, Finland.

Leena Kylänpää (L)

University of Helsinki, Helsinki, Finland.
Department of Gastroenterological and General Surgery, Helsinki University Hospital, Helsinki, Finland.

Outi Lindström (O)

University of Helsinki, Helsinki, Finland.
Department of Gastroenterological and General Surgery, Helsinki University Hospital, Helsinki, Finland.

Maxim Mazanikov (M)

Department of Anesthesia and Intensive Care Medicine, Helsinki University Central Hospital, Helsinki, Finland.

R Pöyhiä (R)

University of Helsinki, Helsinki, Finland.
Kauniala Hospital, Kauniainen, Finland.

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