Positive airway pressure telehealth models and long-term therapy termination: a healthcare database analysis.


Journal

ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 28 06 2023
accepted: 21 11 2023
medline: 27 2 2024
pubmed: 27 2 2024
entrez: 27 2 2024
Statut: epublish

Résumé

Telemonitoring-guided interventions can improve short-term positive airway pressure (PAP) therapy adherence, but long-term effects are unknown. This study investigated long-term PAP therapy termination in patients with sleep apnoea managed with standard care, telemonitoring-guided proactive care or telemonitoring-guided proactive care + patient engagement tool. German healthcare provider data were analysed retrospectively. Individuals aged 18-100 years who started PAP from 2014 to 2019 and had device type/interface data were included. Time-to-termination periods were analysed using Kaplan-Meier plots and Cox proportional hazards regression, adjusted for age, sex, insurance type, and device and mask type. The per-protocol population (valid telemonitoring data) included 104 612 individuals (71% male; 95% aged >40 years). Mean follow-up was 3.3±2.0 years. The overall therapy termination rate was significantly lower in the telemonitoring-guided proactive care group Use of telemonitoring-guided proactive care and a patient engagement tool was associated with lower rates of PAP therapy termination.

Sections du résumé

Background UNASSIGNED
Telemonitoring-guided interventions can improve short-term positive airway pressure (PAP) therapy adherence, but long-term effects are unknown. This study investigated long-term PAP therapy termination in patients with sleep apnoea managed with standard care, telemonitoring-guided proactive care or telemonitoring-guided proactive care + patient engagement tool.
Methods UNASSIGNED
German healthcare provider data were analysed retrospectively. Individuals aged 18-100 years who started PAP from 2014 to 2019 and had device type/interface data were included. Time-to-termination periods were analysed using Kaplan-Meier plots and Cox proportional hazards regression, adjusted for age, sex, insurance type, and device and mask type.
Results UNASSIGNED
The per-protocol population (valid telemonitoring data) included 104 612 individuals (71% male; 95% aged >40 years). Mean follow-up was 3.3±2.0 years. The overall therapy termination rate was significantly lower in the telemonitoring-guided proactive care group
Conclusions UNASSIGNED
Use of telemonitoring-guided proactive care and a patient engagement tool was associated with lower rates of PAP therapy termination.

Identifiants

pubmed: 38410706
doi: 10.1183/23120541.00424-2023
pii: 00424-2023
pmc: PMC10895437
pii:
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

Copyright ©The authors 2024.

Déclaration de conflit d'intérêts

Conflict of interest: H. Woerhle has received lecture/consulting fees from AstraZeneca, Allergopharma, Bioprojet, Boehringer Ingelheim, Chiesi, GSK, Novartis, Inspire, Jazz and ResMed, and research support from ResMed and Novartis. Conflict of interest: C. Schoebel has received grants from AstraZeneca, ResMed and Bayer, consulting fees from ResMed, Idorsia, Bristol-Myers Squibb and Astra Zeneca, and honoraria/lecture fees from Berlin Chemie, Takeda and Mementor; he also has unpaid roles as treasurer of the German Sleep Society, head of the Telemedicine Working Group of the German Society for Internal Medicine, and treasurer of the Sleep Apnea Working Group of the German Cardiac Society. Conflict of interest: J.H. Ficker has received grants and personal/lecture fees from ResMed and Inspire. Conflict of interest: A. Graml and J. Schnepf are employees of ResMed. Conflict of interest: I. Fietze reports support and grants from ResMed and Löwenstein Medical, personal fees from ResMed and Bioprojet, and has an unpaid role as director of the German Sleep Foundation. Conflict of interest: P. Young reports personal fees from Sanofi Genzyme, Biomarin, UCB Pharma, Medice, ResMed, Löwenstein Medical and Vanda, and grants from Lowensteinstiftung and the German Ministry of Education and Science (BMBF). Conflict of interest: M. Arzt has received grant support from ResMed, the ResMed Foundation, Philips Respironics and the Else-Kroehner Fresenisus Foundation, and lecture and/or consulting fees from ResMed, WITA Italia and Philips Respironics.

Auteurs

Holger Woehrle (H)

Sleep and Ventilation Center Blaubeuren, Lung Center Ulm, Ulm, Germany.

Christoph Schoebel (C)

Department of Sleep Medicine, University Duisburg-Essen, Essen, Germany.

Joachim H Ficker (JH)

Department of Respiratory Medicine, Allergology and Sleep Medicine, General Hospital Nuernberg and Paracelsus Medical University, Nuernberg, Germany.

Andrea Graml (A)

ResMed Science Center, ResMed Germany, Martinsried, Germany.

Jürgen Schnepf (J)

ResMed Science Center, ResMed Germany, Martinsried, Germany.

Ingo Fietze (I)

Centre for Sleep Medicine, CCM-CC11, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Peter Young (P)

Department for Neurology, Medical Park, Bad Feilnbach, Germany.

Michael Arzt (M)

Department of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.

Classifications MeSH