Reduced congestion and improved response to a fluid/sodium challenge in chronic heart failure patients after initiation of sacubitril/valsartan: The NATRIUM‐HF study

Author:

Mebazaa Alexandre12,Davison Beth A.13,Biegus Jan4,Edwards Christopher3,Murtagh Gillian5,Varounis Christos5,Hayrapetyan Hamlet6,Sisakian Hamayak7,Ter‐Grigoryan Victor R.8,Takagi Koji3ORCID,Novosadova Maria3,Ponikowski Piotr4,Cotter Gad13

Affiliation:

1. U 942 Inserm MASCOT Paris France

2. Department of Anesthesiology and Critical Care Medicine AP‐HP, Saint Louis Lariboisière University Hospitals, Université de Paris Paris France

3. Momentum Research, Inc. Durham NC USA

4. Institute of Heart Diseases, Wroclaw Medical University Wroclaw Poland

5. Abbott Laboratories Abbott Park Chicago IL USA

6. Cardiology Center of Erebouni MC, Yerevan State Medical University Yerevan Armenia

7. Yerevan State Medical University, University Hospital Yerevan Armenia

8. Nairi Medical Center Yerevan Armenia

Abstract

AbstractAimsThe effects of initiating sacubitril/valsartan in patients with stable heart failure with reduced ejection fraction (HFrEF) on response to fluid and sodium expansion are unknown.Methods and resultsWe have explored changes in natriuresis, diuresis, and congestion in response to the administration of intravenous fluid/sodium load in patients with HFrEF before as compared to after the initiation of sacubitril/valsartan. At baseline (before sacubitril/valsartan initiation) and 2 and 3 months after the initiation, patients underwent an evaluation that consisted of three phases of 3 h: the rest phase (0–3 h), the load phase (3–6 h) in which 1 L of intravenous Ringer solution was administered, and the diuretic phase (6–9 h) at the beginning of which furosemide was administered. Overall, 216 patients completed the study. In comparison to baseline values, at 2 and 3 months after sacubitril/valsartan initiation, patients' diuresis and natriuresis in response to Ringer administration significantly increased (mean difference: 38.8 [17.38] ml, p = 0.0040, and 9.6 [2.02] mmol, p < 0.0001, respectively). Symptoms and signs of congestion after the fluid/sodium challenge were significantly decreased at months 2 and 3 compared to baseline. Compared to baseline, there was also an increment of natriuresis after furosemide administration on sacubitril/valsartan (9.8 [5.13] mmol, p = 0.0167). There was a significant decrease in body weight in subsequent visits when compared to baseline values (−0.50 [−12.7, 7.4] kg at 2 months, and −0.75 [−15.9, 7.5] kg at 3 months; both p < 0.0001).ConclusionsThe initiation of sacubitril/valsartan in HFrEF patients was associated with improvements in natriuresis, diuresis, and weight loss and better clinical adaptation to potentially decongestive stressors.

Funder

Abbott Laboratories

Publisher

Wiley

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