Benefits of early administration of Sacubitril/Valsartan in patients with ST-elevation myocardial infarction after primary percutaneous coronary intervention

Coron Artery Dis. 2021 Aug 1;32(5):427-431. doi: 10.1097/MCA.0000000000000955.

Abstract

Objective: To evaluate the effects of early administration of Sacubitril/Valsartan (Sac/Val) in patients with ST-elevation myocardial infarction after primary percutaneous coronary intervention (pPCI).

Methods: This prospective, controlled, single-center study randomized 186 ST-segment elevation myocardial infarction patients to one of the following two groups: Sac/Val group: early administration of Sac/Val within 24 hours after pPCI; control group: conventional angiotensin-converting enzyme inhibitors (ACEI) application. The creatine Kinase (CK) peak after the surgery, the incidence of acute heart failure during hospitalization, level of NT-proBNP and left ventricular ejection fraction (LVEF) measured by ultrasound before discharge and soluble suppression of tumorigenicity2 (sST2), LVEF, infarct size determined by single photon emission computed tomography (SPECT), readmission rate within 6 months were recorded and compared between two groups.

Results: Compared to the control group, Sac/Val could decrease the CK peak and the incidence of acute heart failure after pPCI; the level of NT-proBNP was lower and LVEF was higher before discharge in the Sac/Val group. After 6 months, the patients who had taken Sac/Val had a higher LVEF, a smaller infarct size determined by SPECT, lower sST2 and readmission rate.

Conclusion: Patients with ST-elevation myocardial infarction after primary percutaneous coronary intervention could benefit from early administration of Sacubitril/Valsartan, the effect was superior to conventional ACEI.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aminobutyrates* / administration & dosage
  • Aminobutyrates* / adverse effects
  • Angiotensin Receptor Antagonists / administration & dosage
  • Angiotensin Receptor Antagonists / adverse effects
  • Angiotensin-Converting Enzyme Inhibitors / administration & dosage
  • Angiotensin-Converting Enzyme Inhibitors / adverse effects
  • Anterior Wall Myocardial Infarction* / complications
  • Anterior Wall Myocardial Infarction* / epidemiology
  • Anterior Wall Myocardial Infarction* / surgery
  • Biphenyl Compounds* / administration & dosage
  • Biphenyl Compounds* / adverse effects
  • Drug Combinations
  • Drug Monitoring / methods
  • Early Medical Intervention / methods
  • Echocardiography / methods
  • Echocardiography / statistics & numerical data
  • Female
  • Heart Failure* / etiology
  • Heart Failure* / physiopathology
  • Heart Failure* / prevention & control
  • Humans
  • Male
  • Middle Aged
  • Natriuretic Peptide, Brain / blood
  • Peptide Fragments / blood
  • Percutaneous Coronary Intervention* / adverse effects
  • Percutaneous Coronary Intervention* / methods
  • Postoperative Complications* / blood
  • Postoperative Complications* / physiopathology
  • Postoperative Complications* / prevention & control
  • Stroke Volume
  • Treatment Outcome
  • Valsartan* / administration & dosage
  • Valsartan* / adverse effects

Substances

  • Aminobutyrates
  • Angiotensin Receptor Antagonists
  • Angiotensin-Converting Enzyme Inhibitors
  • Biphenyl Compounds
  • Drug Combinations
  • Peptide Fragments
  • pro-brain natriuretic peptide (1-76)
  • Natriuretic Peptide, Brain
  • Valsartan
  • sacubitril and valsartan sodium hydrate drug combination