Practical impact of a decision support for goal-directed fluid therapy on protocol adherence: a clinical implementation study in patients undergoing major abdominal surgery.


Journal

Journal of clinical monitoring and computing
ISSN: 1573-2614
Titre abrégé: J Clin Monit Comput
Pays: Netherlands
ID NLM: 9806357

Informations de publication

Date de publication:
02 2019
Historique:
received: 28 01 2018
accepted: 15 05 2018
pubmed: 21 5 2018
medline: 6 8 2019
entrez: 21 5 2018
Statut: ppublish

Résumé

The purpose of this study was to assess the effects of using a real time clinical decision-support system, "Assisted Fluid Management" (AFM), to guide goal-directed fluid therapy (GDFT) during major abdominal surgery. We compared a group of patients managed using the AFM system with a historical cohort of patients (control group) who had been managed using a manual GDFT strategy. Adherence to the protocol was defined as the relative intraoperative time spent with a stroke volume variation (SVV) < 13%. We hypothesised that patients in the AFM group would have more time during surgery with a SVV < 13% compared to the control group. All patients had a radial arterial line connected to a pulse contour analysis monitor and received a 2 ml/kg/h maintenance crystalloid infusion. Additional 250 ml crystalloid boluses were administered whenever measured SVV ≥ 13% in the control group, and when the software suggested a fluid bolus in the AFM group. We compared 46 AFM-guided patients to 38 controls. Patients in the AFM group spent significantly more time during surgery with a SVV < 13% compared to the control group (median 92% [82, 96] vs. 76% [54, 86]; P < 0.0005), and received less fluid overall (1775 ml [1225, 2425] vs. 2350 ml [1825, 3250]; P = 0.010). The incidence of postoperative complications was comparable in the two groups. Implementation of a decision support system for GDFT guidance resulted in a significantly longer period during surgery with a SVV < 13% with a reduced total amount of fluid administered. Trial registration: Clinical Trials.gov (NCT03141411).

Identifiants

pubmed: 29779129
doi: 10.1007/s10877-018-0156-x
pii: 10.1007/s10877-018-0156-x
doi:

Banques de données

ClinicalTrials.gov
['NCT03141411']

Types de publication

Journal Article Observational Study

Langues

eng

Pagination

15-24

Commentaires et corrections

Type : CommentIn

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Auteurs

Alexandre Joosten (A)

Department of Anesthesiology, CUB Erasme, Hopital ERASME, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium. Alexandre.Joosten@erasme.ulb.ac.be.

Reda Hafiane (R)

Department of Anesthesiology, CUB Erasme, Hopital ERASME, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Marco Pustetto (M)

Department of Anesthesiology, CUB Erasme, Hopital ERASME, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Luc Van Obbergh (L)

Department of Anesthesiology, CUB Erasme, Hopital ERASME, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Thierry Quackels (T)

Department of Urology, CUB Erasme, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Alexis Buggenhout (A)

Department of Colorectal Surgery, CUB Erasme, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Jean-Louis Vincent (JL)

Department of Intensive Care, CUB Erasme, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Brigitte Ickx (B)

Department of Anesthesiology, CUB Erasme, Hopital ERASME, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.

Joseph Rinehart (J)

Department of Anesthesiology & Perioperative Care, University of California Irvine, 101 the City Drive South, Orange, CA, USA.

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Classifications MeSH