Practical impact of a decision support for goal-directed fluid therapy on protocol adherence: a clinical implementation study in patients undergoing major abdominal surgery.
Abdomen
/ surgery
Aged
Algorithms
Anesthesiology
/ methods
Decision Support Systems, Clinical
Female
Fluid Therapy
/ methods
Goals
Guideline Adherence
Humans
Intraoperative Care
/ methods
Male
Middle Aged
Monitoring, Intraoperative
/ methods
Monitoring, Physiologic
/ methods
Postoperative Complications
Prospective Studies
Surgical Procedures, Operative
/ methods
Cardiac output monitoring
Decision-assisted resuscitation
Goal-directed therapy
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
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
15-24Commentaires et corrections
Type : CommentIn
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