PMID- 30474478 OWN - NLM STAT- MEDLINE DCOM- 20200217 LR - 20211204 IS - 1784-973X (Electronic) IS - 0001-5385 (Linking) VI - 74 IP - 5 DP - 2019 Oct TI - Effects of sacubitril/valsartan on functional status and exercise capacity in real-world patients. PG - 405-412 LID - 10.1080/00015385.2018.1521054 [doi] AB - Background: Sacubitril/valsartan significantly reduced heart failure(HF) hospitalisations and mortality in the PARADIGM-HF-trial. However real-world data on symptomatic and functional improvement are lacking. Methods: Between December 2016 and January 2018, we retrospectively collected baseline and follow-up data including New York Heart Association (NYHA)-functional class and Cardio-pulmonary exercise data(CPET) in all HF-patients receiving sacubitril/valsartan. Additionally, in patients with an implantable electric cardiovascular device (IECD) enrolled in remote telemonitoring, we quantified patient level activity before and after initiation. Results: A total of 201 patients (82% males) were identified. NYHA-functional class was reassessed after an average of 221 +/- 114 days. Overall, 3.3% of patients improved 2 NYHA classes, 28.7% improved 1 NYHA class, 64% remained stable and 4% deteriorated 1 NYHA class. Patients with symptomatic improvement exhibited a larger reduction in Left Ventricular End Systolic Volume(LVESV) and a larger increase in Left Ventricular Ejection Fraction(LVEF[p-value both <.05]). In total, 110 patients (55%) were equipped with an IECD capable of quantifying outpatient activity-level. On an average of 364 days before sacubitril/valsartan, an activity expressed as %-of-the-day was 13 +/- 2%, vs. 18 +/- 3% the 364 days following sacubitril/valsartan initiation. Signifying a 38% improvement in the out-patient activity level. CPET-data was obtained in paired-fashion in 45 patients (22%). VO(2max) at baseline (14.7 +/- 3.8 mL/kg/min) did not significantly change at follow-up (14.1 +/- 4.7 mL/min/kg; p = .237). Conclusion: Real-world patients exhibit significant symptomatic and functional improvement following the initiation of sacubitril/valsartan. However, larger prospective studies are necessary to assess the impact of sacubitril/valsartan on indices of maximal exercise performance measured during CPET. FAU - Lau, Chirik Wah AU - Lau CW AD - Department of Cardiology, Ziekenhuis Oost-Limburg , Genk , Belgium. FAU - Martens, Pieter AU - Martens P AD - Department of Cardiology, Ziekenhuis Oost-Limburg , Genk , Belgium. AD - Doctoral School for Medicine and Life Sciences, Hasselt University , Diepenbeek , Belgium. FAU - Lambeets, Seppe AU - Lambeets S AD - Department of Cardiology, Ziekenhuis Oost-Limburg , Genk , Belgium. FAU - Dupont, Matthias AU - Dupont M AD - Department of Cardiology, Ziekenhuis Oost-Limburg , Genk , Belgium. FAU - Mullens, Wilfried AU - Mullens W AD - Department of Cardiology, Ziekenhuis Oost-Limburg , Genk , Belgium. AD - Faculty of Medicine and Life Sciences, Biomedical Research Institute, Hasselt University , Diepenbeek , Belgium. LA - eng PT - Journal Article DEP - 20181125 PL - England TA - Acta Cardiol JT - Acta cardiologica JID - 0370570 RN - 0 (Aminobutyrates) RN - 0 (Angiotensin Receptor Antagonists) RN - 0 (Biphenyl Compounds) RN - 0 (Drug Combinations) RN - 0 (Tetrazoles) RN - 80M03YXJ7I (Valsartan) RN - WB8FT61183 (sacubitril and valsartan sodium hydrate drug combination) SB - IM CIN - Acta Cardiol. 2021 Feb;76(1):107. PMID: 31920152 MH - Aged MH - Aminobutyrates/*pharmacology MH - Angiotensin Receptor Antagonists/pharmacology MH - Biphenyl Compounds MH - Drug Combinations MH - Exercise Tolerance/*physiology MH - Female MH - Follow-Up Studies MH - Heart Failure/*drug therapy/physiopathology MH - Humans MH - Male MH - Motor Activity/*physiology MH - Retrospective Studies MH - Tetrazoles/*pharmacology MH - Time Factors MH - Treatment Outcome MH - Valsartan MH - Ventricular Function, Left/*physiology OTO - NOTNLM OT - NYHA functional class OT - Sacubitril/valsartan OT - cardiopulmonary exercise test OT - functionality OT - real world EDAT- 2018/11/27 06:00 MHDA- 2020/02/18 06:00 CRDT- 2018/11/27 06:00 PHST- 2018/11/27 06:00 [pubmed] PHST- 2020/02/18 06:00 [medline] PHST- 2018/11/27 06:00 [entrez] AID - 10.1080/00015385.2018.1521054 [doi] PST - ppublish SO - Acta Cardiol. 2019 Oct;74(5):405-412. doi: 10.1080/00015385.2018.1521054. Epub 2018 Nov 25.