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Palonosetron as prophylaxis for post-discharge nausea and vomiting: a prospective, randomised, double-blind, placebo-controlled trial in ambulatory surgery
Umeå universitet, Medicinska fakulteten, Institutionen för kirurgisk och perioperativ vetenskap, Anestesiologi och intensivvård.ORCID-id: 0000-0002-0359-9085
Umeå universitet, Medicinska fakulteten, Institutionen för kirurgisk och perioperativ vetenskap, Anestesiologi och intensivvård.ORCID-id: 0000-0002-8802-2321
Umeå universitet, Medicinska fakulteten, Institutionen för kirurgisk och perioperativ vetenskap, Anestesiologi och intensivvård.ORCID-id: 0000-0003-2935-7161
Umeå universitet, Medicinska fakulteten, Institutionen för kirurgisk och perioperativ vetenskap, Anestesiologi och intensivvård.ORCID-id: 0000-0002-2924-8021
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2023 (engelsk)Inngår i: British Journal of Anaesthesia, ISSN 0007-0912, E-ISSN 1471-6771, Vol. 131, nr 2, s. 276-283Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

BACKGROUND: Approximately 25% of ambulatory surgery patients experience post-discharge nausea and vomiting (PDNV). We aimed to investigate whether palonosetron, a long-acting anti-emetic, decreases the incidence of PDNV in high-risk patients.

METHODS: In this prospective, randomised, double-blind, placebo-controlled trial, 170 male and female patients undergoing ambulatory surgery under general anaesthesia, with a high predicted risk for PDNV, were randomised to receive either palonosetron 75 μg i.v. (n=84) or normal saline (n=86) before discharge. During the first 3 postoperative days (PODs), we measured outcomes using a patient questionanaire. The primary outcome was the incidence of a complete response (no nausea, vomiting, or use of rescue medication) until POD 2. Secondary outcomes included the incidence of PDNV each day until POD 3.

RESULTS: The incidence of a complete response until POD 2 was 48% (n=32) in the palonosetron group and 36% (n=25) in the placebo group (odds ratio 1.69 [95% confidence interval: 0.85-3.37]; P=0.131). No significant difference in the incidence of PDNV was observed between the two groups on the day of surgery (47% vs 56%; P=0.31). Significant differences in the incidence of PDNV were found on POD 1 (18% vs 34%; P=0.033) and POD 2 (9% vs 27%; P=0.007). No differences were observed on POD 3 (15% vs 13%; P=0.700).

CONCLUSIONS: Compared with placebo, palonosetron did not reduce the overall incidence of PDNV up to POD 2. The lower incidence of PDNV on POD 1 and POD 2 in the palonosetron group requires further investigation.

sted, utgiver, år, opplag, sider
Elsevier, 2023. Vol. 131, nr 2, s. 276-283
Emneord [en]
5HT-3 antagonist, PDNV, PONV, ambulatory surgery, day-care surgery, palonosetron, post-discharge nausea and vomiting, prophylaxis
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-209021DOI: 10.1016/j.bja.2023.04.034ISI: 001147658200001PubMedID: 37246062Scopus ID: 2-s2.0-85160219043OAI: oai:DiVA.org:umu-209021DiVA, id: diva2:1762186
Forskningsfinansiär
Region VästernorrlandVisare NorrTilgjengelig fra: 2023-06-02 Laget: 2023-06-02 Sist oppdatert: 2024-08-23bibliografisk kontrollert

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Moraitis, AntonioMyrberg, TomiHultin, MagnusNyström, HelenaWalldén, Jakob

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