Obesity hypoventilation syndrome treated with non-invasive ventilation: Is a switch to CPAP therapy feasible?


Journal

Respirology (Carlton, Vic.)
ISSN: 1440-1843
Titre abrégé: Respirology
Pays: Australia
ID NLM: 9616368

Informations de publication

Date de publication:
04 2020
Historique:
received: 22 03 2019
revised: 20 08 2019
accepted: 03 09 2019
pubmed: 10 10 2019
medline: 23 6 2021
entrez: 10 10 2019
Statut: ppublish

Résumé

Obesity hypoventilation syndrome (OHS) can be treated with either continuous positive airway pressure (CPAP) or non-invasive ventilation (NIV) therapy; the device choice has important economic and operational implications. This multicentre interventional trial investigated the safety and short-term efficacy of switching stable OHS patients who were on successful NIV therapy for ≥3 months to CPAP therapy. Patients underwent an autotitrating CPAP night under polysomnography (PSG); if the ensuing parameters were acceptable, they were sent home on a fixed CPAP for a 4-6-week period. It was hypothesized that blood gas analysis, PSG parameters and lung function tests would remain unchanged. A total of 42 OHS patients were recruited, of whom 37 patients were switched to CPAP therapy. All patients had a history of severe obstructive sleep apnoea syndrome; chronic obstructive pulmonary disease (COPD) (Global Initiative for Obstructive Lung Disease (GOLD) I/II) was present in 52%. Regarding the primary outcome, 30 of 42 patients (71%, 95% CI: 55-84%) maintained daytime partial pressure of carbon dioxide (PaCO It is feasible to switch most stable OHS patients from NIV to CPAP therapy, a step that could significantly reduce health-related costs. The auto-adjusted CPAP device, used in combination with the analysis of the PSG and capnometry, is a valid titration method in OHS patients.

Sections du résumé

BACKGROUND AND OBJECTIVE
Obesity hypoventilation syndrome (OHS) can be treated with either continuous positive airway pressure (CPAP) or non-invasive ventilation (NIV) therapy; the device choice has important economic and operational implications.
METHODS
This multicentre interventional trial investigated the safety and short-term efficacy of switching stable OHS patients who were on successful NIV therapy for ≥3 months to CPAP therapy. Patients underwent an autotitrating CPAP night under polysomnography (PSG); if the ensuing parameters were acceptable, they were sent home on a fixed CPAP for a 4-6-week period. It was hypothesized that blood gas analysis, PSG parameters and lung function tests would remain unchanged.
RESULTS
A total of 42 OHS patients were recruited, of whom 37 patients were switched to CPAP therapy. All patients had a history of severe obstructive sleep apnoea syndrome; chronic obstructive pulmonary disease (COPD) (Global Initiative for Obstructive Lung Disease (GOLD) I/II) was present in 52%. Regarding the primary outcome, 30 of 42 patients (71%, 95% CI: 55-84%) maintained daytime partial pressure of carbon dioxide (PaCO
CONCLUSION
It is feasible to switch most stable OHS patients from NIV to CPAP therapy, a step that could significantly reduce health-related costs. The auto-adjusted CPAP device, used in combination with the analysis of the PSG and capnometry, is a valid titration method in OHS patients.

Identifiants

pubmed: 31597227
doi: 10.1111/resp.13704
doi:

Substances chimiques

Carbon Dioxide 142M471B3J

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

435-442

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© 2019 Asian Pacific Society of Respirology.

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Auteurs

Maria P Arellano-Maric (MP)

Department of Pneumology, Cologne Merheim Hospital, Kliniken der Stadt Köln, Germany.
Department of Pneumology, Pontificia Universidad Católica de Chile, Santiago, Chile.

Christine Hamm (C)

Department of Pneumology, Cologne Merheim Hospital, Kliniken der Stadt Köln, Germany.
Faculty of Health/School of Medicine, Witten/Herdecke University, Cologne, Germany.

Marieke L Duiverman (ML)

Department of Pulmonary Diseases/Home Mechanical Ventilation, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Groningen Research Institute of Asthma and COPD, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Sarah Schwarz (S)

Department of Pneumology, Cologne Merheim Hospital, Kliniken der Stadt Köln, Germany.
Faculty of Health/School of Medicine, Witten/Herdecke University, Cologne, Germany.

Jens Callegari (J)

Department of Pneumology, Cologne Merheim Hospital, Kliniken der Stadt Köln, Germany.
Faculty of Health/School of Medicine, Witten/Herdecke University, Cologne, Germany.

Jan H Storre (JH)

Department of Intensive Care, Sleep Medicine and Mechanical Ventilation, Asklepios, Fachkliniken Munich-Gauting, Gauting, Germany.
Department of Pneumology, University Medical Center Freiburg, Freiburg, Germany.

Claudia Schmoor (C)

Clinical Trials Center, University Medical Center, Freiburg, Germany.

Marc Spielmanns (M)

Faculty of Health/School of Medicine, Witten/Herdecke University, Cologne, Germany.
Department of Pneumology, St. Remigius Hospital, Opladen, Germany.

Wolfgang Galetke (W)

Department of Pneumology, Hospital der Augustinerinnen, Cologne, Germany.

Wolfram Windisch (W)

Department of Pneumology, Cologne Merheim Hospital, Kliniken der Stadt Köln, Germany.
Faculty of Health/School of Medicine, Witten/Herdecke University, Cologne, Germany.

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