Feasibility of a transmucosal sublingual fentanyl tablet as a procedural pain treatment in colonoscopy patients: a prospective placebo-controlled randomized study.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
01 12 2020
Historique:
received: 12 06 2020
accepted: 17 11 2020
entrez: 2 12 2020
pubmed: 3 12 2020
medline: 2 4 2021
Statut: epublish

Résumé

Since patients often experience pain and unpleasantness during a colonoscopy, the present study aimed to evaluate the efficacy and safety of sublingually administered fentanyl tablets for pain treatment. Furthermore, since the use of intravenous drugs significantly increases colonoscopy costs, sublingual tablets could be a cost-effective alternative to intravenous sedation. We conducted a prospective placebo-controlled randomized study of 158 patients to evaluate the analgesic effect of a 100 µg dose of sublingual fentanyl administered before a colonoscopy. Pain, sedation, nausea, and satisfaction were assessed during the colonoscopy by the patients as well as the endoscopists and nurses. Respiratory rate and peripheral arteriolar oxygen saturation were monitored throughout the procedure. There were no differences between the fentanyl and placebo groups in any of the measured variables. The median pain intensity values, as measured using a numerical rating scale, were 4.5 in the fentanyl group and 5 in the placebo group. The sedation and oxygen saturation levels and the respiratory rate did not differ between the groups. The majority of the colonoscopies were completed.Our results indicate that a 100 µg dose of sublingual fentanyl is not beneficial compared to the placebo in the treatment of procedural pain during a colonoscopy.

Identifiants

pubmed: 33262414
doi: 10.1038/s41598-020-78002-0
pii: 10.1038/s41598-020-78002-0
pmc: PMC7708418
doi:

Substances chimiques

Analgesics, Opioid 0
Placebos 0
Fentanyl UF599785JZ

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

20897

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Auteurs

Mari Fihlman (M)

Department of Anaesthesiology and Intensive Care, University of Turku, Kiinamyllynkatu 4-8, P.O. Box 52, 20520, Turku, Finland. mari.fihlman@tyks.fi.
Division of Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital, Turku, Finland. mari.fihlman@tyks.fi.

E Karru (E)

Department of Anaesthesiology and Intensive Care, University of Turku, Kiinamyllynkatu 4-8, P.O. Box 52, 20520, Turku, Finland.

P Varpe (P)

Department of Digestive Surgery, Turku University Hospital, Turku, Finland.

H Huhtinen (H)

Department of Digestive Surgery, Turku University Hospital, Turku, Finland.

N Hagelberg (N)

Pain Clinic, Turku University Hospital, Turku, Finland.

T I Saari (TI)

Department of Anaesthesiology and Intensive Care, University of Turku, Kiinamyllynkatu 4-8, P.O. Box 52, 20520, Turku, Finland.
Division of Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital, Turku, Finland.

K T Olkkola (KT)

Department of Anaesthesiology, Intensive Care, and Pain Medicine, University of Helsinki and HUS Helsinki University Hospital, Helsinki, Finland.

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Classifications MeSH