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Controlled Clinical Trial
. 2011 Feb;100(2):107-15.
doi: 10.1007/s00392-010-0216-9. Epub 2010 Sep 12.

Adaptive servoventilation improves cardiac function and respiratory stability

Affiliations
Controlled Clinical Trial

Adaptive servoventilation improves cardiac function and respiratory stability

Olaf Oldenburg et al. Clin Res Cardiol. 2011 Feb.

Abstract

Cheyne-Stokes respiration (CSR) in patients with chronic heart failure (CHF) is of major prognostic impact and expresses respiratory instability. Other parameters are daytime pCO₂, VE/VCO₂-slope during exercise, exertional oscillatory ventilation (EOV), and increased sensitivity of central CO₂ receptors. Adaptive servoventilation (ASV) was introduced to specifically treat CSR in CHF. Aim of this study was to investigate ASV effects on CSR, cardiac function, and respiratory stability. A total of 105 patients with CHF (NYHA ≥ II, left ventricular ejection fraction (EF) ≤ 40%) and CSR (apnoea-hypopnoea index ≥ 15/h) met inclusion criteria. According to adherence to ASV treatment (follow-up of 6.7 ± 3.2 months) this group was divided into controls (rejection of ASV treatment or usage <50% of nights possible and/or <4 h/night; n = 59) and ASV (n = 56) adhered patients. In the ASV group, ventilator therapy was able to effectively treat CSR. In contrast to controls, NYHA class, EF, oxygen uptake, 6-min walking distance, and NT-proBNP improved significantly. Moreover, exclusively in these patients pCO₂, VE/VCO₂-slope during exercise, EOV, and central CO₂ receptor sensitivity improved. In CHF patients with CSR, ASV might be able to improve parameters of SDB, cardiac function, and respiratory stability.

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Figures

Fig. 1
Fig. 1
Flow-chart of study population
Fig. 2
Fig. 2
Changes in left ventricular ejection fraction (EF) from baseline to follow-up in ASV-treated patients and controls. Top absolute differences (follow-up EF–baseline EF); bottom relative changes compared to baseline EF
Fig. 3
Fig. 3
Changes in parameters of respiratory stability. Top daytime capillary pCO2; middle changes in central CO2-receptor sensitivity as measured by hyperoxic–hypercapnic ventilatory response (HCVR); bottom changes in VE/VCO2-slope during cardiopulmonary exercise testing

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