Participants were asked to refrain from smoking and drinking coffee or tea for 24 h before the study. The experimental session took place in the early afternoon, with the subjects supine in a quiet room at an environmental temperature between 20 and 23 °C. The recordings started after 20–30 min of rest. Participants were allowed to breathe spontaneously during the first 15 min of the recording and then were asked to breathe following a metronome. Two paced frequencies, fast and slow, were set and allocated in random order. Aim of the fast-paced breathing was to remove the spontaneous breath-by-breath variability during the breathing cycle while preserving the physiological average breathing rate: thus, the paced respiratory frequency was set at a constant rate between 15 and 12 bpm (according to the patient's preference), for 5 min. Aim of the slow-paced breathing was to evaluate the influence of a 10-s breathing cycle on cardiovascular variability: thus, the respiratory rate was paced at 6 bpm for 4 min. In both patients and controls the recorded signals included the continuous noninvasive finger blood pressure (Finapres, Ohmeda Inc., Englewood, Colorado, USA) and one-lead EKG, sampled at 200 Hz. The recorded signals also included the uncalibrated respiratory volume (RSP) by induction plethysmography (Respitrace, Ambulatory Monitoring, Ardsley, NY)15 (link) but due to a technical problem, this device was available for the experimental sessions of all the 10 controls and 17 HF patients. Oxygen saturation (SaO2) was measured at the end of each (free, fast-paced, and slow-paced) breathing condition in all participants.
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