Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Dec 12;64(6):2401371.
doi: 10.1183/13993003.01371-2024. Print 2024 Dec.

The modified Baveno classification for obstructive sleep apnoea: development and evaluation based on the ESADA database

Affiliations

The modified Baveno classification for obstructive sleep apnoea: development and evaluation based on the ESADA database

Sandhya Matthes et al. Eur Respir J. .

Abstract

Background: The "Baveno classification" replaced the apnoea-hypopnoea index (AHI) with symptoms and comorbidities for treatment indication in obstructive sleep apnoea (OSA). This study evaluates a modified Baveno classification which adds a validated cardiovascular disease (CVD) risk score and acknowledges severe breathing disturbances.

Method: OSA patients from the European Sleep Apnoea Database (ESADA) were retrospectively allocated into CVD risk groups 1-3 based on the SCORE2 risk prediction model and European Society of Cardiology guidelines. AHI ≥30 events·h-1 conferred strong treatment indication. When AHI was <30 events·h-1, symptoms and CVD risk dictated allocation to the weak, intermediate or strong treatment indication group. Changes in Epworth Sleepiness Scale (ESS) score and office systolic blood pressure (SBP) at follow-up (12-24 months) under positive airway pressure (PAP) were assessed.

Results: 8625 patients were analysed (29% female; median (interquartile range) age 56 (49-64) years and body mass index 31.9 (28.4-36.3) kg·m-2). Treatment indication was weak in 501 (6%), intermediate in 2085 (24%) and strong in 6039 (70%). There was a continuous increase in age, SBP, C-reactive protein and glycosylated haemoglobin from weak to strong (p<0.001). PAP prescription increased from 52% to 64% to 93% (weak to strong; p<0.001). The change in ESS score was -2, -4 and -5, respectively (p<0.001). Reductions of ≥3 mmHg median SBP occurred when AHI was ≥30 events·h-1 and in symptomatic patients with CVD risk levels >1 when AHI was <30 events·h-1.

Conclusion: This analysis provides supporting evidence for the key role of CVD risk assessment and severe breathing disturbances in the identification of OSA patients most likely to benefit from treatment.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest: S. Matthes reports travel grants from Chiesi and Boehringer. L. Grote has performed educational activities for AstraZeneca, Lundbeck, ResMed, Philipps and Itamar, has interests in two patents licensed to Desitin GMBH, and provides medical advice to Onera BV. J. Hedner has provided scientific advice to SomnoMed and is a part owner of two patents, outside the submitted work. J-L. Pépin is funded by the French National Research Agency in the framework of the “Investissements d'avenir” programme (ANR-15-IDEX-02) and “e-health and integrated care and trajectories medicine and MIAI artificial intelligence” (ANR-19-P3IA-0003) Chairs of excellence from the Grenoble Alpes University; and reports income related to medical education from ResMed, Bioprojet, Jazz and Zoll. W.T. McNicholas reports participation in the Horizon 2020 research and innovation programme under grant agreement number 965417: Sleep Revolution, and is a board member at ESRS. J. Verbraecken reports grants and fees from SomnoMed, AirLiquide, Atos Medical, Vivisol, Mediq Tefa, Medidis, Micromed OSG, Bioprojet, Desitin, Epilog, Idorsia, Inspire Medical Systems, Löwenstein Medical, Ectosense, Philips, ProSomnus, ResMed, Sefam, SD Worx, SOS Oxygène, Tilman, Total Care, Vlaamse Gemeenschap, Vlerick and Zoll Itamar, outside the submitted work, and consultancy for Bioprojet and Epilog. G. Parati reports honoraria for lectures from Omron, SOMNOmedics, Merck and ReCor. W.J. Randerath reports grants and personal fees from Philips Respironics, Loewenstein Medical, ResMed, Bayer Vital, Bioprojet and Vanda Pharma, outside the submitted work. The remaining authors have no potential conflicts of interest to disclose.

LinkOut - more resources