2017
DOI: 10.1002/ejhf.790
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Design of the effect of adaptive servo‐ventilation on survival and cardiovascular hospital admissions in patients with heart failure and sleep apnoea: the ADVENT‐HF trial

Abstract: The ADVENT-HF trial will help to determine whether treating SDB by ASV in patients with HFrEF improves morbidity and mortality.

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Cited by 106 publications
(74 citation statements)
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References 52 publications
(63 reference statements)
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“…7 Entry criteria included: (1) men or women 18 years of age of older; (2) American Heart Association stages B, C, and D HF due to ischemic, idiopathic, or hypertensive causes for at least 3 months; (3) reduced LVEF (≤ 45%), as determined by twodimensional echocardiography; (4) on optimal medical therapy conforming to contemporary national or American Heart Association guidelines, as determined by the patient's cardiologist; (5) presence of CSR-CSA during the baseline sleep study, defined as apnea-hypopnea index (AHI) ≥ 15 with ≥ 50% of events central in nature and a crescendo-decrescendo pattern of hyperpnea. The exclusion criteria were: (1) HF due to primary valvular heart disease, (2) presence of a left ventricular assistive device, (3) transplanted heart or expected to receive a transplanted heart within the next 6 months, (4) pregnancy, (5) current use of adaptive servoventilation, or continuous or bilevel positive airway pressure.…”
Section: Subjectsmentioning
confidence: 99%
“…7 Entry criteria included: (1) men or women 18 years of age of older; (2) American Heart Association stages B, C, and D HF due to ischemic, idiopathic, or hypertensive causes for at least 3 months; (3) reduced LVEF (≤ 45%), as determined by twodimensional echocardiography; (4) on optimal medical therapy conforming to contemporary national or American Heart Association guidelines, as determined by the patient's cardiologist; (5) presence of CSR-CSA during the baseline sleep study, defined as apnea-hypopnea index (AHI) ≥ 15 with ≥ 50% of events central in nature and a crescendo-decrescendo pattern of hyperpnea. The exclusion criteria were: (1) HF due to primary valvular heart disease, (2) presence of a left ventricular assistive device, (3) transplanted heart or expected to receive a transplanted heart within the next 6 months, (4) pregnancy, (5) current use of adaptive servoventilation, or continuous or bilevel positive airway pressure.…”
Section: Subjectsmentioning
confidence: 99%
“…ADVENT-HF (a multicenter, randomized study to assess the effects of ASV on survival and frequency of cardiovascular hospital admissions in patients with HF and sleep apnea) is a randomized, parallel-group, open-label trial engaging centers with precertified sleep and echocardiography laboratories located in Canada, the USA, Brazil, Spain, Germany, Italy, England, France and Japan, designed to assess the effect of treating SDB with a peak-airflow triggered ASV (pf-ASV) algorithm on morbidity and mortality of patients with HFrEF. 83 The results of observational and short-term small-sized randomized trials with surrogate endpoints published by 2009, when ADVENT-HF was conceived, signaled the potential for reduced cardiovascular events and improved survival if HFrEF patients were provided effective treatment of both sleep-related breathing disorders. It was generally acknowledged, however, that clinically-indicated treatment should not be denied those patients describing excessive daytime sleepiness.…”
Section: Advent-hf: a Pivotal Hf Trialmentioning
confidence: 99%
“…57 Ultimately, further trials will be required to mediate these discrepant results, and studies with newer generation ASV devices in HFrEF and SDB are ongoing. 58 …”
Section: Central Sleep Apneamentioning
confidence: 99%