Knowledge-based, computerized, patient clinical decision support system for perioperative pain, nausea and constipation management: a clinical feasibility study

被引:0
作者
Noll, Eric [1 ]
Noll-Burgin, Melanie [2 ]
Bonnomet, Francois [3 ]
Reiter-Schatz, Aurelie [4 ]
Gourieux, Benedicte [4 ]
Bennett-Guerrero, Elliott [5 ]
Goetsch, Thibaut [6 ]
Meyer, Nicolas [6 ]
Pottecher, Julien [7 ]
机构
[1] Strasbourg Univ Hosp, Hautepierre Hosp, Dept Anesthesiol Intens Care & Perioperat Med, Strasbourg, France
[2] Grp Hosp St Vincent, Dept Pharm, Strasbourg, France
[3] Strasbourg Univ Hosp, Hautepierre Hosp, Dept Orthoped & Trauma Surg, Strasbourg, France
[4] Strasbourg Univ Hosp, Dept Pharm, Strasbourg, France
[5] Stony Brook Med, Dept Anesthesiol, Stony Brook, NY USA
[6] Strasbourg Univ Hosp, Dept Biostat, Strasbourg, France
[7] Strasbourg Univ Hosp, Hautepierre Hosp, Dept Anesthesiol & Intens Care, Strasbourg, France
关键词
Perioperative medicine; Postoperative pain; Postoperative nausea and vomiting; Clinical decision support system; Pain management; GUIDELINES;
D O I
10.1007/s10877-024-01148-z
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Opioid administration is particularly challenging in the perioperative period. Computerized-based Clinical Decision Support Systems (CDSS) are a promising innovation that might improve perioperative pain control. We report the development and feasibility validation of a knowledge-based CDSS aiming at optimizing the management of perioperative pain, postoperative nausea and vomiting (PONV), and laxative medications. This novel CDSS uses patient adaptive testing through a smartphone display, literature-based rules, and individual medical prescriptions to produce direct medical advice for the patient user. Our objective was to test the feasibility of the clinical use of our CDSS in the perioperative setting. This was a prospective single arm, single center, cohort study conducted in Strasbourg University Hospital. The primary outcome was the agreement between the recommendation provided by the experimental device and the recommendation provided by study personnel who interpreted the same care algorithm (control). Thirty-seven patients were included in the study of which 30 (81%) used the experimental device. Agreement between these two care recommendations (computer driven vs. clinician driven) was observed in 51 out 54 uses of the device (94.2% [95% CI 85.9-98.4%]). The agreement level had a probability of 86.6% to exceed the 90% clinically relevant agreement threshold. The knowledge-based, patient CDSS we developed was feasible at providing recommendations for the treatment of pain, PONV and constipation in a perioperative clinical setting.Trial registration number & date The study protocol was registered in ClinicalTrial.gov before enrollment began (NCT05707247 on January 26th, 2023).
引用
收藏
页码:907 / 913
页数:7
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