Drug Interactions in the Treatment of Chronic Heart Failure: Analysis of Clinical Guidelines

Cover Page


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Background. According to Russian epidemiological studies, the prevalence of chronic heart failure (CHF) in the general population is high and amounts to 7–10%. Therapy of any disease, and especially chronic disease, is associated with the prescription of drugs. With the development of evidence-based medicine and implementation of its achievements in real clinical practice all over the world there is an increase in the number of prescribed drugs. This explains the high relevance of the problem of drug-drug interactions. Aims — analysis of interactions of drugs recommended for prescription to patients suffering from CHF. Methods. Based on the Clinical Guidelines (CG), all possible interdrug interactions of recommended medicinal products were analysed. Information on potential drug-drug interactions was obtained from the specialised website Drugs.com. Know more. Be sure (https://www.drugs.com/interactions/list/). Results. ACE inhibitors / ARA II / valsartan+sacubitril, beta-adrenoblockers and aldosterone antagonists are recommended as part of combination therapy for treatment according to CG for all patients with symptomatic heart failure (class II–IV) and reduced LV ejection fraction < 40%. Amiodarone, verapamil and diltiazem are among the drugs not recommended for use in patients with the diagnosis of CHF. Also, according to clinical guidelines, HMG-CoA reductase inhibitors (atorvastatin, lovastatin, pitavastatin, rosuvastatin, simvastatin, fluvastatin), direct renin inhibitors (heparin), COX-2 inhibitors (parecoxib, polmacoxib, celecoxib, etoricoxib) are among the unrecommended drugs in chronic heart failure.For ACE inhibitors, no adverse effects from interaction with beta-blockers have been identified. This combination is widely used and recommended by the CG. According to the “Major” type for ACE inhibitors with drugs indicated for use in CHF according to CG, 4 potential interactions were identified: with valsartan-sacubitril; angiotensin II receptor antagonists; with aldosterone antagonist (spironolactone); with loop and thiazide diuretics. Therefore, the appointment of angiotensin II receptor antagonists is carried out in case of ineffectiveness of initial therapy with ACE inhibitors, when changing the treatment tactics. These drugs are not used in combination with each other due to the risk of hyperkalemia. The prescription and use of diuretics while taking ACE inhibitors should be controlled by a physician also due to the risk of hyperglycaemia. In Moderate type, potential interactions with dapagliflozin, eplerenone, cardiac glycosides and heparin have been identified for ACE inhibitors. For beta-blockers, no potential Major-type interactions were identified with drugs from CG. Combinations with dapagliflozin, loop and thiazide diuretics, cardiac glycosides, spironolactone and ivabradine require special attention. It is recommended to avoid the combination of beta-blockers with valsartan. Of the recommended angiotensin II receptor antagonists, no risk of potential interactions with beta-blockers has been identified for candesartan and losartan.

Full Text

Restricted Access

About the authors

Olga V. Zhukova

Plekhanov Russian University of Economics

Author for correspondence.
Email: ov-zhukova@mail.ru
ORCID iD: 0000-0002-6454-1346

PhD in Pharmacology, Assistant Professor

Russian Federation, Moscow

Nikolay L. Shimanovsky

Plekhanov Russian University of Economics

Email: shimann@yandex.ru
ORCID iD: 0000-0001-8887-4420

MD, PhD, Professor, Corresponding Member of the RAS

Russian Federation, Moscow

Valery V. Beregovykh

Russian Academy of Sciences

Email: beregovykh@ramn.ru
ORCID iD: 0000-0002-0210-4570

PhD in Technical Sciences, Professor, Academician of the RAS

Russian Federation, Moscow

References

  1. Roger VL. Epidemiology of Heart Failure: A Contemporary Perspective. Circ Res. 2021;128(10):1421–1434. doi: https://doi.org/10.1161/CIRCRESAHA.121.318172
  2. Braunwald E. Shattuck lecture — cardiovascular medicine at the turn of the millennium: triumphs, concerns, and opportunities. N Engl J Med. 1997;337(19):1360–1369. doi: https://doi.org/10.1056/NEJM199711063371906
  3. Резник Е.В., Никитин И.Г. Алгоритм лечения больных с хронической сердечной недостаточностью с низкой фракцией выброса левого желудочка // Архивъ внутренней медицины. — 2018. — Т. 8. — № 2. — С. 85–99. [Reznik EV, Nikitin IG. Algorithm for the treatment of patients with chronic heart failure with reduced left ventricular ejection fraction. The Russian Archives of Internal Medicine. 2018;8(2):85–99. (In Russ.)] doi: https://doi.org/10.20514/2226-6704-2018-8-2-85-99
  4. Savarese G, Becher PM, Lund LH, et al. Global burden of heart failure: a comprehensive and updated review of epidemiology. Cardiovasc Res. 2022;118(17):3272–3287. doi: https://doi.org/10.1093/cvr/cvac013
  5. Azad N, Lemay G. Management of chronic heart failure in the older population. J Geriatr Cardiol. 2014;11(4):329–337. doi: https://doi.org/10.11909/j.issn.1671-5411.2014.04.008
  6. Koudstaal S, Pujades-Rodriguez M, Denaxas S, et al. Prognostic burden of heart failure recorded in primary care, acute hospital admissions, or both: a population-based linked electronic health record cohort study in 2.1 million people. Eur J Heart Fail. 2017;19(9):1119–1127. doi: https://doi.org/10.1002/ejhf.709
  7. Benjamin EJ, Blaha MJ, Chiuve SE, et al. Heart disease and stroke statistics-2017 update: A report from the American Heart Association. Circulation. 2017;135(10):e146–e603. doi: https://doi.org/10.1161/CIR.0000000000000485
  8. Romagnoli KM, Nelson SD, Hines L. Information needs for making clinical recommendations about potential drug-drug interactions: a synthesis of literature review and interviews. BMC Med Inform Decis Mak. 2017;17(1):21. doi: https://doi.org/10.1186/s12911-017-0419-3
  9. Сычев Д.А., Отделeнов В.А., Краснова Н.М., и др. Полипрагмазия: взгляд клинического фармаколога // Терапевтический архив. — 2016. — Т. 88. — № 12. — С. 94–102. [Sychev DA, Otdelenov VA, Krasnova NM, et al. Polypragmasy: A clinical pharmacologist’s view. 2016;88(12):94–102. (In Russ.)] doi: https://doi.org/10.17116/terarkh2016881294-102
  10. Марцевич С.Ю., Лукина Ю.В., Драпкина О.М. Основные принципы комбинированной медикаментозной терапии — фокус на межлекарственное взаимодействие // Кардиоваскулярная терапия и профилактика. — 2021. — Т. 20. — № 7. — С. 3031. [Martsevich SYu, Lukina YuV, Drapkina OM. Basic principles of combination therapy: focus on drug-drug interaction. Cardiovascular Therapy and Prevention. 2021;20(7):3031. (In Russ.)] doi: https://doi.org/10.15829/1728-8800-2021-3031
  11. Nobili A, Marengoni A, Tettamanti M, et al. Association between clusters of diseases and polypharmacy in hospitalized elderly patients: results from the REPOSI study. Eur J Intern Med. 2011;22(6):597–602. doi: https://doi.org/10.1016/j.ejim.2011.08.029
  12. Хроническая сердечная недостаточность: клинические рекомендации, 2020. [Chronic heart failure: clinical recommendations. (In Russ.)] Available from: https://cr.minzdrav.gov.ru/recomend/156_1
  13. Velazquez EJ, Morrow DA, DeVore AD, et al. Angiotensin–Neprilysin Inhibition in Acute Decompensated Heart Failure. N Engl J Med. 2019;380(6):539–548. doi: https://doi.org/10.1056/NEJMoa1812851
  14. Maggioni AР, Anand I, Gottlieb SO, et al. Effects of Valsartan on Morbidity and Mortality in Patients with Heart Failure Not Receiving Angiotensin — Converting Enzyme inhibitors. J Am Coll Cardiol. 2002;40(8):1414–1421. doi: https://doi.org/10.1016/s0735-1097(02)02304-5
  15. Dimopoulos K, Saukhe TV, Coats A, et al. Meta-analyses of mortality and morbidity effects of an angiotensin receptor blocker in patients with chronic heart failure already receiving an ACE inhibitor (alone or with a beta-blocker). Int J Cardiol. 2004;93(2–3):105–111. doi: https://doi.org/10.1016/j.ijcard.2003.10.001
  16. Torp-Pedersen C, Metra M, Spark P, et al. The safety of amiodarone inpatients with heart failure. J Card Fail. 2007;13(5):340–345. doi: https://doi.org/10.1016/j.cardfail.2007.02.009
  17. Carpenter M, Berry H, Pelletier AL. Clinically Relevant Drug-Drug Interactions in Primary Care. Am Fam Physician. 2019;99(9):558–564.
  18. Изможерова Н.В., Попов А.А., Курындина А.А., др. Полиморбидность и полипрагмазия у пациентов высокого и очень высокого сердечно-сосудистого риска // Рациональная фармакотерапия в кардиологии. — 2022. — Т. 18. — № 1. — С. 20–26. [Izmozherova NV, Popov AA, Kuryndina AA, et al. Polymorbidity and Polypragmasia in High and Very High Cardiovascular Risk Patients. Rational Pharmacotherapy in Cardiology. 2022;18(1):20–26. (In Russ.)] doi: https://doi.org/10.20996/1819-6446-2022-02-09
  19. Karatzia L, Aung N, Aksentijevic D. Artificial intelligence in cardiology: Hope for the future and power for the present. Front Cardiovasc Med. 2022;9:945726. doi: https://doi.org/10.3389/fcvm.2022.945726

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2023 "Paediatrician" Publishers LLC



This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies