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Original research article
Adaptive servoventilation versus oxygen therapy for sleep disordered breathing in patients with heart failure: a randomised trial
  1. Kimihiko Murase1,
  2. Koh Ono2,
  3. Tomoya Yoneda3,
  4. Moritake Iguchi4,
  5. Takafumi Yokomatsu5,
  6. Tetsu Mizoguchi5,
  7. Toshiaki Izumi6,
  8. Masaharu Akao4,
  9. Shinji Miki5,
  10. Ryuji Nohara6,
  11. Kenji Ueshima7,
  12. Michiaki Mishima1,
  13. Takeshi Kimura3,
  14. David P White8 and
  15. Kazuo Chin9
  1. 1Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan
  2. 2Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan
  3. 3Clinical Laboratory Medicine, Kyoto University Hospital, Kyoto, Japan
  4. 4Department of Cardiovascular Medicine, Kyoto Medical Centre, Kyoto, Japan
  5. 5Department of Cardiovascular Medicine, Kyoto Mitsubishi Hospital, Kyoto, Japan
  6. 6Department of Cardiovascular Medicine, Kitano Hospital, Osaka, Japan
  7. 7Department of EBM Research, Institute for Advancement of Clinical and Translational Research, Kyoto University Hospital, Kyoto, Japan
  8. 8Division of Sleep Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA
  9. 9Department of Respiratory Care and Sleep Control Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan
  1. Correspondence to Dr Kazuo Chin; chink{at}kuhp.kyoto-u.ac.jp

Abstract

Background Both adaptive servoventilation (ASV) and nocturnal oxygen therapy improve sleep disordered breathing (SDB), but their effects on cardiac parameters have not been compared systematically.

Methods and results 43 patients with chronic heart failure (CHF; left ventricular ejection fraction (LVEF) ≤50%) with SDB were randomly assigned to undergo ASV (n=19, apnoea hypopnoea index (AHI)=34.2±12.1/h) or oxygen therapy (n=24, 36.9±9.9/h) for 3 months. More than 70% of SDB events in both groups were central apnoeas or hypopnoeas. Although nightly adherence was less for the ASV group than for the oxygen group (4.4±2.0 vs 6.2±1.8 h/day, p<0.01), the improvement in AHI was larger in the ASV group than in the oxygen group (−27.0±11.5 vs −16.5±10.2/h, p<0.01). The N-terminal pro-brain natriuretic peptide (NT-proBNP) level in the ASV group improved significantly after titration (1535±2224 to 1251±2003 pg/mL, p=0.01), but increased slightly at follow-up and this improvement was not sustained (1311±1592 pg/mL, p=0.08). Meanwhile, the level of plasma NT-proBNP in the oxygen group did not show a significant change throughout the study (baseline 1071±1887, titration 980±1913, follow-up 1101±1888 pg/mL, p=0.19). The significant difference in the changes in the NT-proBNP level throughout the study between the 2 groups was not found (p=0.30). Neither group showed significant changes in echocardiographic parameters.

Conclusions Although ASV produced better resolution of SDB in patients with CHF as compared with oxygen therapy, neither treatment produced a significant improvement in cardiac function in the short term. Although we could not draw a definite conclusion because of the small number of participants, our data do not seem to support the routine use of ASV or oxygen therapy to improve cardiac function in patients with CHF with SDB.

Trial registration number NCT01187823 (http://www.clinicaltrials.gov).

  • Sleep Disordered Breathing
  • Chronic Heart Failure
  • Adaptive Servo Ventilation
  • Nocturnal Oxygen Therapy

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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