Feasibility of remote digital monitoring using wireless Bluetooth monitors, the Smart Angel™ app and an original web platform for patients following outpatient surgery: a prospective observational pilot study.


Journal

BMC anesthesiology
ISSN: 1471-2253
Titre abrégé: BMC Anesthesiol
Pays: England
ID NLM: 100968535

Informations de publication

Date de publication:
08 10 2020
Historique:
received: 11 06 2020
accepted: 29 09 2020
entrez: 9 10 2020
pubmed: 10 10 2020
medline: 14 9 2021
Statut: epublish

Résumé

Remote monitoring of mean arterial blood pressure (MAP), heart rate (HR) or oxygen saturation (SpO Adults scheduled for elective outpatient surgery were prospectively enrolled. In the first 5 postoperative days, patients completed a self-report questionnaire (pain, comfort, nausea, vomiting) and recorded SpO From May 2018 to September 2018, data were available for 29 out of 30 patients enrolled (1 patient was not discharged from hospital after surgery). The remote monitoring technology recorded 2038 data items (62%) compared with 2656 (82%) items recorded on the paper form (p = 0.001). The most common errors with the remote technology were software malfunctioning when starting the MAP monitor and malfunctioning between the tablet and the Bluetooth monitor. No serious adverse events were noted. The SUS score for the system was 85 (68-93) for 26 patients. This work evaluates the ability of a pilot system for monitoring remote physiological data using digital technology after ambulatory surgery and highlights the digital limitations of this technology. Technological improvements are required to reduce malfunctioning (4G access, transmission between apps). ClinicalTrials.gov ( NCT03464721 ) (March 8, 2018).

Sections du résumé

BACKGROUND
Remote monitoring of mean arterial blood pressure (MAP), heart rate (HR) or oxygen saturation (SpO
METHODS
Adults scheduled for elective outpatient surgery were prospectively enrolled. In the first 5 postoperative days, patients completed a self-report questionnaire (pain, comfort, nausea, vomiting) and recorded SpO
RESULTS
From May 2018 to September 2018, data were available for 29 out of 30 patients enrolled (1 patient was not discharged from hospital after surgery). The remote monitoring technology recorded 2038 data items (62%) compared with 2656 (82%) items recorded on the paper form (p = 0.001). The most common errors with the remote technology were software malfunctioning when starting the MAP monitor and malfunctioning between the tablet and the Bluetooth monitor. No serious adverse events were noted. The SUS score for the system was 85 (68-93) for 26 patients.
CONCLUSION
This work evaluates the ability of a pilot system for monitoring remote physiological data using digital technology after ambulatory surgery and highlights the digital limitations of this technology. Technological improvements are required to reduce malfunctioning (4G access, transmission between apps).
TRIAL REGISTRATION
ClinicalTrials.gov ( NCT03464721 ) (March 8, 2018).

Identifiants

pubmed: 33032541
doi: 10.1186/s12871-020-01178-5
pii: 10.1186/s12871-020-01178-5
pmc: PMC7545846
doi:

Banques de données

ClinicalTrials.gov
['NCT03464721']

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

259

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Auteurs

Thierry Chevallier (T)

Department of Biostatistics, Epidemiology, Public Health and and Methodological innovation (BESPIM), Nîmes University Hospital, University Montpellier 1, Montpellier, France.

Gautier Buzancais (G)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Bob-Valéry Occean (BV)

Department of Biostatistics, Epidemiology, Public Health and and Methodological innovation (BESPIM), Nîmes University Hospital, University Montpellier 1, Montpellier, France.

Pierre Rataboul (P)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Christophe Boisson (C)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Natacha Simon (N)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Ariane Lannelongue (A)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Noémie Chaniaud (N)

UR 7273 CRP-CPO, Université Picardie Jules Verne, Chemin du Thil, 80000, Amiens, France.

Yann Gricourt (Y)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Jean-Yves Lefrant (JY)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France.

Philippe Cuvillon (P)

Staff anesthesiologists, Department of Anesthesiology and Pain Management, Centre Hospitalo-Universitaire (CHU) Carémeau, Place du Professeur Debré, Nîmes, and Montpellier University 1, Montpellier, France. philippe.cuvillon@chu-nimes.fr.

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