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Remote monitoring of COVID-19 positive high-risk patients in domestic isolation: A feasibility study
Author(s) -
David Wurzer,
Paul Spielhagen,
Adonia Siegmann,
Ayca Gercekcioglu,
Judith Gorgass,
Simone Henze,
Yuron Kolar,
Felix Koneberg,
Sari Kukkonen,
Hannah McGowan,
Stefanie Schmid-Eisinger,
Alexander Steger,
Michael Dommasch,
Hans-Ulrich Haase,
Alexander Müller,
Eimo Martens,
Bernhard Haller,
Katharina M. Huster,
Georg Schmidt
Publication year - 2021
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0257095
Subject(s) - medicine , diabetes mellitus , covid-19 , emergency medicine , pediatrics , disease , infectious disease (medical specialty) , endocrinology
Background If a COVID-19 patient develops a so-called severe course, he or she must be taken to hospital as soon as possible. This proves difficult in domestic isolation, as patients are not continuously monitored. The aim of our study was to establish a telemonitoring system in this setting. Methods Oxygen saturation, respiratory rate, heart rate and temperature were measured every 15 minutes using an in-ear device. The data was transmitted to the Telecovid Centre via mobile network or internet and monitored 24/7 by a trained team. The data were supplemented by daily telephone calls. The patients´ individual risk was assessed using a modified National Early Warning Score. In case of a deterioration, a physician initiated the appropriate measures. Covid-19 Patients were included if they were older than 60 years or fulfilled at least one of the following conditions: pre-existing disease (cardiovascular, pulmonary, immunologic), obesity (BMI >35), diabetes mellitus, hypertension, active malignancy, or pregnancy. Findings 153 patients (median age 59 years, 77 female) were included. Patients were monitored for 9 days (median, IQR 6–13 days) with a daily monitoring time of 13.3 hours (median, IQR 9.4–17.0 hours). 20 patients were referred to the clinic by the Telecovid team. 3 of these required intensive care without invasive ventilation, 4 with invasive ventilation, 1 of the latter died. All patients agreed that the device was easy to use. About 90% of hospitalised patients indicated that they would have delayed hospitalisation further if they had not been part of the study. Interpretation Our study demonstrates the successful implementation of a remote monitoring system in a pandemic situation. All clinically necessary information was obtained and adequate measures were derived from it without delay.

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