Acute pulmonary pressure change after transition to sacubitril/valsartan in patients with heart failure reduced ejection fraction

被引:25
作者
Tran, Jeffrey S. [1 ]
Havakuk, Ofer [1 ,2 ]
Mcleod, Jennifer [3 ]
Hwang, Jennifer [1 ]
Kwong, Hoi Yan [1 ]
Shavelle, David [1 ]
Zile, Michael R. [4 ]
Elkayam, Uri [1 ]
Fong, Michael W. [1 ]
Grazette, Luanda P. [5 ]
机构
[1] Univ Southern Calif USC, Keck Sch Med, Dept Internal Med, Los Angeles, CA USA
[2] Tel Aviv Univ, Dept Cardiol, Tel Aviv Med Ctr, Tel Aviv, Israel
[3] Albert Einstein Coll Med, Montefiore Einstein Ctr Heart & Vasc Care, Dept Med, New York, NY USA
[4] Med Univ South Carolina, RHJ Dept Vet Affairs Med Ctr, Div Cardiol, Charleston, SC 29425 USA
[5] Univ Miami, Miller Sch Med, Cardiovasc Div, Miami, FL 33136 USA
关键词
Heart failure; Pulmonary hypertension; Remote monitoring; Heart failure reduced ejection fraction; Implantable monitors; Neprilysin;
D O I
10.1002/ehf2.13225
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Sacubitril/valsartan combines renin-angiotensin-aldosterone system inhibition with amplification of natriuretic peptides. In addition to well-described effects, natriuretic peptides exert direct effects on pulmonary vasculature. The effect of sacubitril/valsartan on pulmonary artery pressure (PAP) has not been fully defined. Methods and results This was a retrospective case-series of PAP changes following transition from angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) to sacubitril/valsartan in patients with heart failure reduced ejection fraction and a previously implanted CardioMEMS (TM) sensor. Pre-sacubitril/valsartan and post-sacubitril/valsartan PAPs were compared for each patient by examining averaged consecutive daily pressure readings from 1 to 5 days before and after sacubitril/valsartan exposure. PAP changes were also compared between patients based on elevated trans-pulmonary gradients (trans-pulmonary gradient >= 12 mmHg) at time of CardioMEMS (TM) sensor implantation. The cohort included 18 patients, 72% male, mean age 60.1 +/- 13.6 years. There was a significant decrease in PAPs associated with transition from ACEI/ARB to sacubitril/valsartan. The median (interquartile range) pre-treatment and post-treatment change in mean, systolic and diastolic PAPs were -3.6 (-9.8, -0.7) mmHg (P < 0.001), -6.5 (-15.0, -2.0) mmHg (P = 0.001), and -2.5 (-5.7, -0.7) (P = 0.001), respectively. The decrease in PAPs was independent of trans-pulmonary gradient (F(1,16) = 0.49, P = 0.49). Conclusions In this retrospective case series, transition from ACEI/ARB to sacubitril/valsartan was associated with an early and significant decrease in PAPs.
引用
收藏
页码:1706 / 1710
页数:5
相关论文
共 15 条
[1]  
Almufleh A, 2017, AM J CARDIOVASC DIS, V7, P108
[2]   Effects of combined angiotensin II receptor antagonism and neprilysin inhibition in experimental pulmonary hypertension and right ventricular failure [J].
Andersen, Stine ;
Axelsen, Julie Birkmose ;
Ringgaard, Steffen ;
Nyengaard, Jens Randel ;
Hyldebrandt, Janus Adler ;
Bogaard, Harm Jan ;
de Man, Frances S. ;
Nielsen-Kudsk, Jens Erik ;
Andersen, Asger .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2019, 293 :203-210
[3]   Effects of natriuretic peptides on vascular smooth-muscle cells derived from different vascular beds [J].
Arjona, AA ;
Hsu, CA ;
Wrenn, DS ;
Hill, NS .
GENERAL PHARMACOLOGY, 1997, 28 (03) :387-392
[4]   Pulmonary hypertension related to left heart disease: Insight from a wireless implantable hemodynamic monitor [J].
Benza, Raymond L. ;
Raina, Amresh ;
Abraham, William T. ;
Adamson, Philip B. ;
Lindenfeld, JoAnn ;
Miller, Alan B. ;
Bourge, Robert C. ;
Bauman, Jordan ;
Yadav, Jay .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2015, 34 (03) :329-337
[5]   Neprilysin inhibition for pulmonary arterial hypertension: a randomized, double-blind, placebo-controlled, proof-of-concept trial [J].
Hobbs, Adrian J. ;
Moyes, Amie J. ;
Baliga, Reshma S. ;
Ghedia, Dipa ;
Ochiel, Rachel ;
Sylvestre, Yvonne ;
Dore, Caroline J. ;
Chowdhury, Kashfia ;
Maclagan, Kate ;
Quartly, Harriet L. ;
Sofat, Reecha ;
Smit, Angelique ;
Schreiber, Benjamin E. ;
Coghlan, Gerry J. ;
MacAllister, Raymond J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2019, 176 (09) :1251-1267
[6]   LCZ696, Angiotensin II Receptor-Neprilysin Inhibitor, Ameliorates High-Salt-Induced Hypertension and Cardiovascular Injury More Than Valsartan Alone [J].
Kusaka, Hiroaki ;
Sueta, Daisuke ;
Koibuchi, Nobutaka ;
Hasegawa, Yu ;
Nakagawa, Takashi ;
Lin, BoWen ;
Ogawa, Hisao ;
Kim-Mitsuyama, Shokei .
AMERICAN JOURNAL OF HYPERTENSION, 2015, 28 (12) :1409-1417
[7]   Neprilysin inhibitors as a new approach in the treatment of right heart failure in the course of chronic obstructive pulmonary disease. Response to the letter of Siniorakis et al [J].
Liczek, Maciej ;
Panek, Iga ;
Damianski, Piotr ;
Jeczen, Olga ;
Jazwiec, Jedrzej ;
Kuna, Piotr ;
Panek, Michal .
ADVANCES IN RESPIRATORY MEDICINE, 2018, 86 (05) :257-259
[8]   Angiotensin-Neprilysin Inhibition versus Enalapril in Heart Failure [J].
McMurray, John J. V. ;
Packer, Milton ;
Desai, Akshay S. ;
Gong, Jianjian ;
Lefkowitz, Martin P. ;
Rizkala, Adel R. ;
Rouleau, Jean L. ;
Shi, Victor C. ;
Solomon, Scott D. ;
Swedberg, Karl ;
Zile, Michael R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (11) :993-1004
[9]  
Menendez Juan Tamargo, 2016, Card Fail Rev, V2, P40, DOI 10.15420/cfr.2016:1:1
[10]   Transplant candidates with severe left ventricular dysfunction managed with medical treatment: Characteristics and survival [J].
Rickenbacher, PR ;
Trindade, PT ;
Haywood, GA ;
Vagelos, RH ;
Schroeder, JS ;
Willson, K ;
Prikazsky, L ;
Fowler, MB .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 27 (05) :1192-1197