Efficacy of combination therapy with dexmedetomidine for benzodiazepines-induced disinhibition during endoscopic retrograde cholangiopancreatography.

benzodiazepine dexmedetomidine disinhibition endoscopic retrograde cholangiopancreatography endoscopic ultrasound

Journal

Therapeutic advances in gastroenterology
ISSN: 1756-283X
Titre abrégé: Therap Adv Gastroenterol
Pays: England
ID NLM: 101478893

Informations de publication

Date de publication:
2020
Historique:
received: 18 09 2019
accepted: 13 02 2020
entrez: 12 6 2020
pubmed: 12 6 2020
medline: 12 6 2020
Statut: epublish

Résumé

Benzodiazepines (BZDs) and analgesics are widely used for conscious sedation during endoscopic ultrasound (EUS) or endoscopic retrograde cholangiopancreatography (ERCP). However, endoscopic procedures are sometimes discontinued because of BZD-induced disinhibitory reactions such as excessive movement. We evaluated the usefulness of dexmedetomidine (DEX) for BZD-induced disinhibition in ERCP. Between February 2018 and August 2019, 22 patients who underwent EUS or ERCP were enrolled. All patients showed BZD-induced excessive movement at the first examination (BZD group) and received DEX at the second examination (DEX group). The initial DEX dose was 6 μg/kg/h for a 10-min loading, followed by 0.4 μg/kg/h during the procedure. BZDs and analgesics were administered before scope insertion. An additional sedative was administered to achieve a Ramsay sedation scale (RSS) of 4-5. Sedative effect, procedure completion rate, and changes in circulatory and respiratory dynamics were evaluated. Mean RSS scores were significantly higher ( The addition of DEX to BZD therapy yielded better sedative efficacy, lower excessive movement, a reduction in BZDs used, and a higher procedure complete rate. DEX may be used as an alternative method for BZD-induced inhibition during ERCP.

Sections du résumé

BACKGROUND BACKGROUND
Benzodiazepines (BZDs) and analgesics are widely used for conscious sedation during endoscopic ultrasound (EUS) or endoscopic retrograde cholangiopancreatography (ERCP). However, endoscopic procedures are sometimes discontinued because of BZD-induced disinhibitory reactions such as excessive movement. We evaluated the usefulness of dexmedetomidine (DEX) for BZD-induced disinhibition in ERCP.
METHODS METHODS
Between February 2018 and August 2019, 22 patients who underwent EUS or ERCP were enrolled. All patients showed BZD-induced excessive movement at the first examination (BZD group) and received DEX at the second examination (DEX group). The initial DEX dose was 6 μg/kg/h for a 10-min loading, followed by 0.4 μg/kg/h during the procedure. BZDs and analgesics were administered before scope insertion. An additional sedative was administered to achieve a Ramsay sedation scale (RSS) of 4-5. Sedative effect, procedure completion rate, and changes in circulatory and respiratory dynamics were evaluated.
RESULTS RESULTS
Mean RSS scores were significantly higher (
CONCLUSIONS CONCLUSIONS
The addition of DEX to BZD therapy yielded better sedative efficacy, lower excessive movement, a reduction in BZDs used, and a higher procedure complete rate. DEX may be used as an alternative method for BZD-induced inhibition during ERCP.

Identifiants

pubmed: 32523618
doi: 10.1177/1756284820911822
pii: 10.1177_1756284820911822
pmc: PMC7236568
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1756284820911822

Informations de copyright

© The Author(s), 2020.

Déclaration de conflit d'intérêts

Conflict of interest statement: The authors declare that there is no conflict of interest.

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Auteurs

Yuki Ikeda (Y)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Makoto Yoshida (M)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Kazuma Ishikawa (K)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Tomohiro Kubo (T)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Kazuyuki Murase (K)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Kohichi Takada (K)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Koji Miyanishi (K)

Department of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Masayoshi Kobune (M)

Department of Hematology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.

Junji Kato (J)

Department of Medical Oncology, Sapporo Medical University School of Medicine, South 1 West 16, Chuo-ku, Sapporo, Hokkaido 060-8543, Japan.

Classifications MeSH