Comparative Effectiveness and Safety of High-Intensity Statins (Atorvastatin vs Rosuvastatin) in Coronary Heart Disease Patients After Percutaneous Coronary Intervention (PCI) : A Literature Review

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Mira Susiladewi
Yose Ramda Ilhami
Yelly Oktavia Sari

Abstract

Background Coronary heart disease is one of the causes of morbidity and mortality worldwide, especially in Indonesia. Coronary heart disease is closely associated with dyslipidemia, particularly increased low-density lipoprotein (LDL), which plays an important role in the formation of atherosclerosis. High-intensity statin therapy is recommended for patients with coronary heart disease after percutaneous coronary intervention (PCI) to optimally reduce LDL and reduce the incidence of major adverse cardiovascular events (MACE) due to its pleiotropic effects. Objective To review the scientific evidence regarding the effectiveness, safety, and clinical outcomes of the use of high-intensity statins in patients with coronary heart disease after PCI based on the current literature. Methods The literature was obtained from the PubMed, Scopus, and Google Scholar databases published within the last ten years. The included studies consisted of randomized clinical trials, retrospective and prospective cohort studies, observational studies, systematic reviews and meta-analyses, and narrative reviews. The evaluated outcomes included LDL target achievement, major adverse cardiovascular events (MACE), and safety profiles including myopathy, hepatotoxicity, diabetes mellitus, and other adverse effects. Results Most studies showed that high-dose statins effectively reduced LDL levels and provided clinical benefits in patients with cardiovascular disease. A comparison of atorvastatin 40 mg and 80 mg showed similar effectiveness in reducing LDL, with a low incidence of adverse effects and still tolerable. In patients after PCI, atorvastatin 80 mg and rosuvastatin 40 mg had comparable effectiveness, although atorvastatin showed a better safety profile and cost efficiency. Several studies reported that the combination of moderate-dose statins with ezetimibe resulted in higher achievement of LDL targets compared with high-dose statin monotherapy. In addition, the combination was associated with lower risks of muscle-related adverse effects, increased liver enzymes, and diabetes mellitus. Nevertheless, most high-risk patients still do not achieve the recommended LDL target, so treatment intensification strategies are needed, including the addition of ezetimibe or PCSK9 inhibitors.

Article Details

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Review Article

How to Cite

Comparative Effectiveness and Safety of High-Intensity Statins (Atorvastatin vs Rosuvastatin) in Coronary Heart Disease Patients After Percutaneous Coronary Intervention (PCI) : A Literature Review. (2026). Journal of Pharmaceutical and Sciences, 9(3), 2815-2826. https://doi.org/10.36490/journal-jps.com.v9i3.1676

References

Agrawal D, Manchanda SC, Sawhney JPS, Kandpal B, Jain R, Mehta A, et al. To study the effect of high dose atorvastatin 40 mg versus 80 mg in patients with dyslipidemia. Indian Heart J. 2018;70 Suppl 3:S8-S12. https://doi.org/10.1016/j.ihj.2018.01.034

Allahyari A, Jernberg T, Hagström E, Leosdottir M, Lundman P, Ueda P. Application of the 2019 ESC/EAS dyslipidaemia guidelines to nationwide data of patients with a recent myocardial infarction: a simulation study. Eur Heart J. 2020;41(40):3900-3909. https://doi.org/10.1093/eurheartj/ehaa034

Ference BA, Ginsberg HN, Graham I, Ray KK, Packard CJ, Bruckert E, et al. Low-density lipoproteins cause atherosclerotic cardiovascular disease. 1. Evidence from genetic, epidemiologic, and clinical studies. A consensus statement from the European Atherosclerosis Society Consensus Panel. Eur Heart J. 2017;38(32):2459-2472. https://doi.org/10.1093/eurheartj/ehx144

Grundy SM, Stone NJ, Beam C, De Ferranti S, Hlatky MA, Lloyd-Jones D, et al. Correction to: 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol. Circulation. 2019;139(25):E1182-E1186. https://doi.org/10.1161/CIR.0000000000000625

Katzung BG. Basic and Clinical Pharmacology. 15th ed. New York: McGraw-Hill; 2021.

Kim J, Park KT, Jang MJ, Park TK, Lee JM, Yang JH, et al. High-intensity versus non-high-intensity statins in patients achieving low-density lipoprotein cholesterol goal after percutaneous coronary intervention. J Am Heart Assoc. 2018;7(21):e009517. https://doi.org/10.1161/JAHA.118.009517

Kim K, Bang WD, Han K, Kim B, Lee JM, Chung H. Comparison of the effects of high-intensity statin therapy with moderate-intensity statin and ezetimibe combination therapy on major adverse cardiovascular events in patients with acute myocardial infarction: a nationwide cohort study. J Lipid Atheroscler. 2021;10(3):291-303. https://doi.org/10.12997/jla.2021.10.3.291

Laranjo L, Lanas F, Sun MC, Chen DA, Hynes L, Imran TF, et al. World Heart Federation roadmap for secondary prevention of cardiovascular disease: 2023 update. Glob Heart. 2024;19(1):8. https://doi.org/10.5334/gh.1278

Lee B, Hong SJ, Rha SW, Heo JH, Hur SH, Choi HH, et al. Moderate-intensity statin plus ezetimibe vs high-intensity statin according to baseline LDL-C in the treatment of atherosclerotic cardiovascular disease: a post-hoc analysis of the RACING randomized trial. Atherosclerosis. 2023;386:117373. https://doi.org/10.1016/j.atherosclerosis.2023.117373

Mach F, Baigent C, Catapano AL, Koskinas KC, Casula M, Badimon L, et al. 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. Eur Heart J. 2020;41(1):111-188. https://doi.org/10.1093/eurheartj/ehz455

Oesterle A, Laufs U, Liao JK. Pleiotropic effects of statins on the cardiovascular system. Circ Res. 2017;120(1):229-243. https://doi.org/10.1161/CIRCRESAHA.116.308537

Rahhal A, Khir F, Aljundi AH, AlAhmad Y, Alzaeem H, Habra M, et al. Clinical outcomes of high-intensity doses of atorvastatin in patients with acute coronary syndrome: a retrospective cohort study using real-world data. Br J Clin Pharmacol. 2021;87(4):2043-2052. https://doi.org/10.1111/bcp.14613Digital Object Identifier (DOI)

Rossini E, Biscetti F, Rando MM, Nardella E, Cecchini AL, Nicolazzi MA, et al. Statins in high cardiovascular risk patients: do comorbidities and characteristics matter? Int J Mol Sci. 2022;23(16):9326. https://doi.org/10.3390/ijms23169326

Roy D, Mahapatra T, Manna K, Kar A, Rana MS, Roy A, et al. Comparing effectiveness of high-dose atorvastatin and rosuvastatin among patients undergone percutaneous coronary interventions: a non-concurrent cohort study in India. PLoS One. 2020;15(5):e0233230.

https://doi.org/10.1371/journal.pone.0233230

Shahjehan RD, Sharma S, Bhutta BS. Coronary artery disease. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 [cited 2026 Jun 15]. https://www.ncbi.nlm.nih.gov/books/NBK564304/

Sydhom P, Al-Quraishi B, El-Shawaf M, Osman MT, Naji N, Awwad N, et al. The clinical effectiveness and safety of low/moderate-intensity statins & ezetimibe combination therapy vs. high-intensity statin monotherapy: a systematic review and meta-analysis. BMC Cardiovasc Disord. 2024;24(1):660. https://doi.org/10.1186/s12872-024-04144-y

Thompson PD, Panza G, Zaleski A, Taylor B. Statin-associated side effects. J Am Coll Cardiol. 2016;67(20):2395-410. http://dx.doi.org/10.1016/j.jacc.2016.02.071

Zeliaś A, Bednarek A, Dykla D, Wysocka R, Szczygiel P, Dudek D. Lipid goal achievement one month after myocardial infarction: observational real-world study from the Polish population. Kardiol Pol. 2024;82(9):892-894.

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