Angiotensin-Converting Enzyme Inhibitor Washout Period Prior to Angiotensin Receptor/Neprilysin Inhibitor Initiation

Kaanan Shah1, Stella Mabhugu1, Jessica Obioma1,2

  • 1College of Pharmacy, The University of North Texas Health Science Center, Fort Worth, TX, USA.

PubMed

Insights

Most patients (67%) switching from ACE inhibitors to ARNIs did not receive the recommended 36-hour washout, but this did not increase adverse events or heart failure readmissions.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Pharmacy

Background:

  • The 2022 AHA-ACC HFSA Guideline recommends Angiotensin Receptor/Neprilysin Inhibitors (ARNIs) for heart failure with reduced ejection fraction (HFrEF).
  • A 36-hour washout period is advised when switching from Angiotensin-Converting Enzyme Inhibitors (ACEi) to ARNIs to mitigate adverse effects like angioedema.
  • This study examines adherence to this washout protocol in a real-world clinical setting.

Purpose of the Study:

  • To determine the rate of adherence to the 36-hour washout period when transitioning patients from ACEi to ARNI.
  • To evaluate secondary outcomes including 90-day heart failure exacerbation readmissions and adverse events (angioedema, hypotension, AKI, hyperkalemia).

Main Methods:

  • Retrospective cohort study of HFrEF patients transitioned from ACEi to ARNI between March 2016 and December 2022.
  • Exclusion criteria included lack of ACEi or ARNI use during admission or ejection fraction >40%.
  • Pearson chi-square analysis was used for categorical data.

Main Results:

  • Of 33 patients, only 67% received the full 36-hour washout period.
  • No significant differences were observed in hospital readmission rates or adverse events between groups.
  • No patients experienced hyperkalemia or angioedema.

Conclusions:

  • This study highlights potential deviations from recommended washout protocols when switching from ACEi to ARNI in HFrEF patients.
  • The observed adherence rate suggests a need for further investigation into prescribing practices.
  • Larger, multicenter studies are warranted to validate these findings and explore the pharmacist's role in protocol adherence.
Abstract

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