Efficacy of α-Blockers on Hemodynamic Control during Pheochromocytoma Resection: A Randomized Controlled Trial.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 06 11 2019
accepted: 27 01 2020
pubmed: 13 11 2019
medline: 4 2 2021
entrez: 13 11 2019
Statut: ppublish

Résumé

Pretreatment with α-adrenergic receptor blockers is recommended to prevent hemodynamic instability during resection of a pheochromocytoma or sympathetic paraganglioma (PPGL). To determine which type of α-adrenergic receptor blocker provides the best efficacy. Randomized controlled open-label trial (PRESCRIPT; ClinicalTrials.gov NCT01379898). Multicenter study including 9 centers in The Netherlands. 134 patients with nonmetastatic PPGL. Phenoxybenzamine or doxazosin starting 2 to 3 weeks before surgery using a blood pressure targeted titration schedule. Intraoperative hemodynamic management was standardized. Primary efficacy endpoint was the cumulative intraoperative time outside the blood pressure target range (ie, SBP >160 mmHg or MAP <60 mmHg) expressed as a percentage of total surgical procedure time. Secondary efficacy endpoint was the value on a hemodynamic instability score. Median cumulative time outside blood pressure targets was 11.1% (interquartile range [IQR]: 4.3-20.6] in the phenoxybenzamine group compared to 12.2% (5.3-20.2)] in the doxazosin group (P = .75, r = 0.03). The hemodynamic instability score was 38.0 (28.8-58.0) and 50.0 (35.3-63.8) in the phenoxybenzamine and doxazosin group, respectively (P = .02, r = 0.20). The 30-day cardiovascular complication rate was 8.8% and 6.9% in the phenoxybenzamine and doxazosin group, respectively (P = .68). There was no mortality after 30 days. The duration of blood pressure outside the target range during resection of a PPGL was not different after preoperative treatment with either phenoxybenzamine or doxazosin. Phenoxybenzamine was more effective in preventing intraoperative hemodynamic instability, but it could not be established whether this was associated with a better clinical outcome.

Identifiants

pubmed: 31714582
pii: 5622983
doi: 10.1210/clinem/dgz188
pmc: PMC7261201
pii:
doi:

Substances chimiques

Adrenergic alpha-Antagonists 0
Phenoxybenzamine 0TTZ664R7Z
Doxazosin NW1291F1W8

Banques de données

ClinicalTrials.gov
['NCT01379898']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Endocrine Society 2019.

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Auteurs

Edward Buitenwerf (E)

Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Thamara E Osinga (TE)

Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Henri J L M Timmers (HJLM)

Department of Internal Medicine, Section of Endocrinology, Radboud University Medical Center, Nijmegen, The Netherlands.

Jacques W M Lenders (JWM)

Department of Internal Medicine, Section of Vascular Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Medicine III, Technische Universität Dresden, Dresden, Germany.

Richard A Feelders (RA)

Department of Internal Medicine, Section of Endocrinology, Erasmus Medical Center, Rotterdam, The Netherlands.

Elisabeth M W Eekhoff (EMW)

Department of Internal Medicine, Endocrinology Section, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Harm R Haak (HR)

Department of Internal Medicine, Máxima Medical Center, Eindhoven, The Netherlands.
Department of Internal Medicine, Division of General Internal Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
Maastricht University, CAPHRI School for Public Health and Primary Care, Ageing and Long-Term Care, Maastricht, The Netherlands.

Eleonora P M Corssmit (EPM)

Department of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands.

Peter H L T Bisschop (PHLT)

Department of Endocrinology and Metabolism, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Gerlof D Valk (GD)

Department of Endocrine Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.

Ronald Groote Veldman (RG)

Department of Internal Medicine, Medical Spectrum Twente, Enschede, The Netherlands.

Robin P F Dullaart (RPF)

Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Thera P Links (TP)

Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Magiel F Voogd (MF)

Department of Anesthesiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Götz J K G Wietasch (GJKG)

Department of Anesthesiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Michiel N Kerstens (MN)

Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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Classifications MeSH