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Continuous monitoring of patients in and after the acute admission ward to improve clinical pathways: study protocol for a randomized controlled trial (Optimal-AAW).
Garssen, Sjoerd H; Kant, Niels; Vernooij, Carlijn A; Mauritz, Gert-Jan; Koning, Mark V; Bosch, Frank H; Doggen, Carine J M.
Affiliation
  • Garssen SH; Clinical Research Center, Rijnstate Hospital, Arnhem, The Netherlands.
  • Kant N; Department of Patient Care and Monitoring, Philips Research, Eindhoven, The Netherlands.
  • Vernooij CA; Department of Health Technology and Services Research, Technical Medical Center, University of Twente, Enschede, The Netherlands.
  • Mauritz GJ; Clinical Research Center, Rijnstate Hospital, Arnhem, The Netherlands.
  • Koning MV; Department of Health Technology and Services Research, Technical Medical Center, University of Twente, Enschede, The Netherlands.
  • Bosch FH; Department of Anesthesiology, Rijnstate Hospital, Arnhem, The Netherlands.
  • Doggen CJM; Department of Patient Care and Monitoring, Philips Research, Eindhoven, The Netherlands.
Trials ; 24(1): 405, 2023 Jun 15.
Article in En | MEDLINE | ID: mdl-37316919
BACKGROUND: Because of high demand on hospital beds, hospitals seek to reduce patients' length of stay (LOS) while preserving the quality of care. In addition to usual intermittent vital sign monitoring, continuous monitoring might help to assess the patient's risk of deterioration, in order to improve the discharge process and reduce LOS. The primary aim of this monocenter randomized controlled trial is to assess the effect of continuous monitoring in an acute admission ward (AAW) on the percentage of patients who are discharged safely. METHODS: A total of 800 patients admitted to the AAW, for whom it is equivocal whether they can be discharged directly after their AAW stay, will be randomized to either receive usual care without (control group) or with additional continuous monitoring of heart rate, respiratory rate, posture, and activity, using a wearable sensor (sensor group). Continuous monitoring data are provided to healthcare professionals and used in the discharge decision. The wearable sensor keeps collecting data for 14 days. After 14 days, all patients fill in a questionnaire to assess healthcare use after discharge and, if applicable, their experience with the wearable sensor. The primary outcome is the difference in the percentage of patients who are safely discharged home directly from the AAW between the control and sensor group. Secondary outcomes include hospital LOS, AAW LOS, intensive care unit (ICU) admissions, Rapid Response Team calls, and unplanned readmissions within 30 days. Furthermore, facilitators and barriers for implementing continuous monitoring in the AAW and at home will be investigated. DISCUSSION: Clinical effects of continuous monitoring have already been investigated in specific patient populations for multiple purposes, e.g., in reducing the number of ICU admissions. However, to our knowledge, this is the first Randomized Controlled Trial to investigate effects of continuous monitoring in a broad patient population in the AAW. TRIAL REGISTRATION: https://clinicaltrials.gov/ct2/show/NCT05181111 . Registered on 6 January 2022. Start of recruitment: 7 December 2021.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Critical Pathways / Hospitalization Type of study: Clinical_trials / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Trials Journal subject: MEDICINA / TERAPEUTICA Year: 2023 Type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Critical Pathways / Hospitalization Type of study: Clinical_trials / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Trials Journal subject: MEDICINA / TERAPEUTICA Year: 2023 Type: Article Affiliation country: Netherlands