Statin associated adverse reactions in Latin America: a scoping review.

BMJ Open

Clinical Research Department, Fundación del Caribe para la Investigación Biomédica, Barranquilla, Atlantico, Colombia

Published: October 2021

AI Article Synopsis

  • The study aims to investigate the occurrence and types of adverse drug reactions (ADRs) in patients taking statins across published research from Latin American countries.
  • A literature review revealed 20 relevant studies (7 randomized controlled trials and 13 observational studies), showing statin-related ADR frequencies ranging from 0% to 35.1% in trials and 0% to 28.4% in observational studies, with muscle pain being the most reported issue.
  • The authors note variability in ADR reporting and suggest the need for standardized definitions and more thorough research to improve data consistency and understanding of statin-related side effects.

Article Abstract

Objectives: We aim to describe the frequency and type of adverse drug reactions (ADRs) in patients on statins in published studies from Latin American (LATAM) countries.

Design: Scoping review.

Methods: A literature search was conducted in three databases (PubMed, EMBASE and LILACS) in addition to a manual search in relevant journals from LATAM universities or medical societies. A snowballing technique was used to identify further references. Randomised controlled trials (RCTs) and observational studies between 2000 and 2020 were included. Studies were considered eligible if they included adults on statin therapy from LATAM and reported data on ADRs. Data on ADRs were abstracted and presented by study design.

Results: Out of 8076 articles, a total of 20 studies were included (7 RCTs and 13 observational studies). We identified three head-to-head statin RCTs, two statin-versus-policosanol RCTs and only two placebo-controlled trials. The statin-related ADRs frequency ranged from 0% to 35.1% in RCTs and 0% to 28.4% in observational studies. The most common ADRs were muscle-related events including myalgia and elevated creatine phosphokinase. Other reported ADRs were gastrointestinal symptoms, headache and altered fasting plasma glucose.

Conclusions: We identified differences in the frequency of ADRs in both observational studies and RCTs from LATAM countries. This could be due to the absence of standard definitions and reporting of ADRs as well as differences among the study's interventions, population characteristics or design. The variability of ADRs and the absence of definitions are similar to studies from other geographical locations. Further placebo-controlled trials and real-world data registries with universal definitions should follow.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488746PMC
http://dx.doi.org/10.1136/bmjopen-2021-050675DOI Listing

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