A prospective study of carcinoid crisis with no perioperative octreotide.


Journal

Surgery
ISSN: 1532-7361
Titre abrégé: Surgery
Pays: United States
ID NLM: 0417347

Informations de publication

Date de publication:
01 2022
Historique:
received: 07 02 2021
revised: 09 03 2021
accepted: 19 03 2021
pubmed: 7 7 2021
medline: 19 2 2022
entrez: 6 7 2021
Statut: ppublish

Résumé

Carcinoid crises, defined as the sudden onset of hemodynamic instability in patients with neuroendocrine tumors undergoing operation, are associated with significantly increased risk of postoperative complications. Octreotide has been used prophylactically to reduce crisis rates as well as therapeutically to treat crises that still occur. However, studies using octreotide still report crisis rates of 3.4% to 35%, leading to the questioning of its efficacy. Patients with neuroendocrine tumors undergoing operation between 2017 to 2020 with no perioperative octreotide were prospectively studied. Clinicopathologic data were compared by χ One hundred and seventy-one patients underwent 195 operations. Crisis was documented in 49 operations (25%), with a mean duration of 3 minutes. Crisis was more likely to occur in patients with small bowel primary tumors (P = .012), older age (P = .015), and carcinoid syndrome (P < .001). Those with crises were more likely to have major postoperative complications (P = .003). Completely eliminating perioperative octreotide resulted in neither increased rate nor duration compared with previous studies using octreotide. We conclude perioperative octreotide use may be safely stopped, owing to inefficacy, though the need for an effective medication is clear given continued higher rates of complications.

Sections du résumé

BACKGROUND
Carcinoid crises, defined as the sudden onset of hemodynamic instability in patients with neuroendocrine tumors undergoing operation, are associated with significantly increased risk of postoperative complications. Octreotide has been used prophylactically to reduce crisis rates as well as therapeutically to treat crises that still occur. However, studies using octreotide still report crisis rates of 3.4% to 35%, leading to the questioning of its efficacy.
METHODS
Patients with neuroendocrine tumors undergoing operation between 2017 to 2020 with no perioperative octreotide were prospectively studied. Clinicopathologic data were compared by χ
RESULTS
One hundred and seventy-one patients underwent 195 operations. Crisis was documented in 49 operations (25%), with a mean duration of 3 minutes. Crisis was more likely to occur in patients with small bowel primary tumors (P = .012), older age (P = .015), and carcinoid syndrome (P < .001). Those with crises were more likely to have major postoperative complications (P = .003).
CONCLUSION
Completely eliminating perioperative octreotide resulted in neither increased rate nor duration compared with previous studies using octreotide. We conclude perioperative octreotide use may be safely stopped, owing to inefficacy, though the need for an effective medication is clear given continued higher rates of complications.

Identifiants

pubmed: 34226047
pii: S0039-6060(21)00452-9
doi: 10.1016/j.surg.2021.03.063
pii:
doi:

Substances chimiques

Antineoplastic Agents, Hormonal 0
Octreotide RWM8CCW8GP

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

88-93

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Sarah M Wonn (SM)

Department of Surgery, Oregon Health & Science University, Portland, OR.

Anna N Ratzlaff (AN)

Division of Surgical Oncology, Department of Surgery, Oregon Health & Science University, Portland, OR.

SuEllen J Pommier (SJ)

Division of Surgical Oncology, Department of Surgery, Oregon Health & Science University, Portland, OR.

Belinda H McCully (BH)

Division of Surgical Oncology, Department of Surgery, Oregon Health & Science University, Portland, OR.

Rodney F Pommier (RF)

Division of Surgical Oncology, Department of Surgery, Oregon Health & Science University, Portland, OR. Electronic address: pommierr@ohsu.edu.

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Classifications MeSH