Frontiers in Medicine (Apr 2020)

Adaptive Servo-Ventilation: A Comprehensive Descriptive Study in the Geneva Lake Area

  • Chloé Cantero,
  • Dan Adler,
  • Dan Adler,
  • Patrick Pasquina,
  • Christophe Uldry,
  • Bernard Egger,
  • Maura Prella,
  • Alain Bigin Younossian,
  • Antoine Poncet,
  • Antoine Poncet,
  • Paola Soccal-Gasche,
  • Paola Soccal-Gasche,
  • Jean-Louis Pepin,
  • Jean-Louis Pepin,
  • Jean-Paul Janssens,
  • Jean-Paul Janssens

DOI
https://doi.org/10.3389/fmed.2020.00105
Journal volume & issue
Vol. 7

Abstract

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Background: Use of adaptive servo-ventilation (ASV) has been questioned in patients with central sleep apnea (CSA) and chronic heart failure (CHF). This study aims to detail the present use of ASV in clinical practice.Methods: Descriptive, cross-sectional, multicentric study of patients undergoing long term (≥3 months) ASV in the Cantons of Geneva or Vaud (1,288,378 inhabitants) followed by public or private hospitals, private practitioners and/or home care providers.Results: Patients included (458) were mostly male (392; 85.6%), overweight [BMI (median, IQR): 29 kg/m2 (26; 33)], comorbid, with a median age of 71 years (59–77); 84% had been treated by CPAP before starting ASV. Indications for ASV were: emergent sleep apnea (ESA; 337; 73.6%), central sleep apnea (CSA; 108; 23.6%), obstructive sleep apnea (7; 1.5%), and overlap syndrome (6; 1.3%). Origin of CSA was cardiac (n = 30), neurological (n = 26), idiopathic (n = 28), or drug-related (n = 22). Among CSA cases, 60 (56%) patients had an echocardiography within the preceding 12 months; median left ventricular ejection fraction (LVEF) was 62.5% (54–65); 11 (18%) had a LVEF ≤45%. Average daily use of ASV was [mean (SD)] 368 (140) min; 13% used their device <3:30 h. Based on ventilator software, apnea-hypopnea index was normalized in 94% of subjects with data available (94% of 428).Conclusions: Use of ASV has evolved from its original indication (CSA in CHF) to a heterogeneous predominantly male, aged, comorbid, and overweight population with mainly ESA or CSA. CSA in CHF represented only 6.5% of this population. Compliance and correction of respiratory events were satisfactory.Clinical Trial Registration:www.ClinicalTrials.gov, identifier: NCT04054570.

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