کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5643880 1586472 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The SERVE-HF safety notice in clinical practice - experiences of a tertiary sleep center
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی عصب شناسی
پیش نمایش صفحه اول مقاله
The SERVE-HF safety notice in clinical practice - experiences of a tertiary sleep center
چکیده انگلیسی


- Treatment priority for heart failure patients with central sleep apnea is an optimal medical management of the heart failure.
- 10.3% of patients on ASV fulfilled the SERVE-HF inclusion criteria.
- Discontinuation of adaptive servoventilation was feasible in patients with chronic heart failure.
- Symptomatic patients requested and received treatment alternatives.

BackgroundIn May 2015, the results of the SERVE-HF trial - addressing adaptive servoventilation (ASV) in chronic congestive heart failure (CHF) patients with central sleep apnea (CSA) - prompted a field safety notice. It was recommended to identify CHF patients treated with ASV and to advise the discontinuation of the treatment. We aimed to analyze the identification process and effect of ASV discontinuation on affected patients.Methods126 patients treated with ASV on May 13th, 2015 at our institution were retrospectively analyzed. Treatment decisions, effect of ASV discontinuation and clinical course were followed for a year. Patients on ASV with CHF were compared to those without CHF.ResultsThe risk criteria of the safety notice were fulfilled by 10.3% of patients (13/126). Additional echocardiographies were performed in 38%. ASV was discontinued in 93% of patients without adverse events (emergency hospitalization in n = 1). CSA reappeared immediately. Day- or nighttime symptoms were reported by 61%. Symptomatic patients were started on alternative treatments. CHF and non-CHF patients differed in cardiac function and type of SDB. CHF patients had shorter overall treatment duration. Compliance to ASV was similar in both groups with a median usage of 412 min (269; 495)/night in the CHF group and 414.5 min (347; 480) in the non-CHF group.ConclusionIdentification of patients “at risk” is feasible but outcome of discontinuation of ASV cannot be evaluated based on these data. ASV withdrawal in patients with stable chronic CHF and CSA leads to an immediate return of sleep disordered breathing. Symptomatic patients may ask for alternative treatment options.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Sleep Medicine - Volume 37, September 2017, Pages 201-207
نویسندگان
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