Personalised haemodynamic management targeting baseline cardiac index in high-risk patients undergoing major abdominal surgery: a randomised single-centre clinical trial.


Journal

British journal of anaesthesia
ISSN: 1471-6771
Titre abrégé: Br J Anaesth
Pays: England
ID NLM: 0372541

Informations de publication

Date de publication:
08 2020
Historique:
received: 17 12 2019
revised: 20 04 2020
accepted: 23 04 2020
entrez: 27 7 2020
pubmed: 28 7 2020
medline: 18 8 2020
Statut: ppublish

Résumé

Despite several clinical trials on haemodynamic therapy, the optimal intraoperative haemodynamic management for high-risk patients undergoing major abdominal surgery remains unclear. We tested the hypothesis that personalised haemodynamic management targeting each individual's baseline cardiac index at rest reduces postoperative morbidity. In this single-centre trial, 188 high-risk patients undergoing major abdominal surgery were randomised to either routine management or personalised haemodynamic management requiring clinicians to maintain personal baseline cardiac index (determined at rest preoperatively) using an algorithm that guided intraoperative i.v. fluid and/or dobutamine administration. The primary outcome was a composite of major complications (European Perioperative Clinical Outcome definitions) or death within 30 days of surgery. Secondary outcomes included postoperative morbidity (assessed by a postoperative morbidity survey), hospital length of stay, mortality within 90 days of surgery, and neurocognitive function assessed after postoperative Day 3. The primary outcome occurred in 29.8% (28/94) of patients in the personalised management group, compared with 55.3% (52/94) of patients in the routine management group (relative risk: 0.54, 95% confidence interval [CI]: 0.38 to 0.77; absolute risk reduction: -25.5%, 95% CI: -39.2% to -11.9%; P<0.001). One patient assigned to the personalised management group, compared with five assigned to the routine management group, died within 30 days after surgery (P=0.097). There were no clinically relevant differences between the two groups for secondary outcomes. In high-risk patients undergoing major abdominal surgery, personalised haemodynamic management reduces a composite outcome of major postoperative complications or death within 30 days after surgery compared with routine care. NCT02834377.

Sections du résumé

BACKGROUND
Despite several clinical trials on haemodynamic therapy, the optimal intraoperative haemodynamic management for high-risk patients undergoing major abdominal surgery remains unclear. We tested the hypothesis that personalised haemodynamic management targeting each individual's baseline cardiac index at rest reduces postoperative morbidity.
METHODS
In this single-centre trial, 188 high-risk patients undergoing major abdominal surgery were randomised to either routine management or personalised haemodynamic management requiring clinicians to maintain personal baseline cardiac index (determined at rest preoperatively) using an algorithm that guided intraoperative i.v. fluid and/or dobutamine administration. The primary outcome was a composite of major complications (European Perioperative Clinical Outcome definitions) or death within 30 days of surgery. Secondary outcomes included postoperative morbidity (assessed by a postoperative morbidity survey), hospital length of stay, mortality within 90 days of surgery, and neurocognitive function assessed after postoperative Day 3.
RESULTS
The primary outcome occurred in 29.8% (28/94) of patients in the personalised management group, compared with 55.3% (52/94) of patients in the routine management group (relative risk: 0.54, 95% confidence interval [CI]: 0.38 to 0.77; absolute risk reduction: -25.5%, 95% CI: -39.2% to -11.9%; P<0.001). One patient assigned to the personalised management group, compared with five assigned to the routine management group, died within 30 days after surgery (P=0.097). There were no clinically relevant differences between the two groups for secondary outcomes.
CONCLUSIONS
In high-risk patients undergoing major abdominal surgery, personalised haemodynamic management reduces a composite outcome of major postoperative complications or death within 30 days after surgery compared with routine care.
CLINICAL TRIAL REGISTRATION
NCT02834377.

Identifiants

pubmed: 32711724
pii: S0007-0912(20)30371-8
doi: 10.1016/j.bja.2020.04.094
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02834377']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

122-132

Informations de copyright

Copyright © 2020 British Journal of Anaesthesia. Published by Elsevier Ltd. All rights reserved.

Auteurs

Julia Y Nicklas (JY)

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine. Electronic address: j.nicklas@uke.de.

Oliver Diener (O)

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine.

Maximilian Leistenschneider (M)

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine.

Christina Sellhorn (C)

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine.

Gerhard Schön (G)

Department of Medical Biometry and Epidemiology.

Martin Winkler (M)

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine.

Guenter Daum (G)

Clinic and Polyclinic for Vascular Medicine, University Heart Center.

Edzard Schwedhelm (E)

Institute of Clinical Pharmacology and Toxicology.

Julian Schröder (J)

Department of Neurology.

Margit Fisch (M)

Department of Urology.

Barbara Schmalfeldt (B)

Department of Gynecology and Gynecologic Oncology.

Jakob R Izbicki (JR)

General-, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Michael Bauer (M)

Department of Anesthesiology and Intensive Care Medicine.

Sina M Coldewey (SM)

Department of Anesthesiology and Intensive Care Medicine; Septomics Research Center, Center for Sepsis Control and Care, Jena University Hospital, Jena, Germany.

Daniel A Reuter (DA)

Department of Anesthesiology, Rostock University Medical Center, University of Rostock, Rostock, Germany.

Bernd Saugel (B)

Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine; Outcomes Research Consortium, Cleveland, OH, USA.

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