Back to Search Start Over

Polypharmacy and Medication Outcome Reporting Bias in Older Patients with COVID-19.

Authors :
Brown, Ronald B.
Source :
BioMed. Sep2023, Vol. 3 Issue 3, p320-328. 9p.
Publication Year :
2023

Abstract

Polypharmacy, the use of multiple and potentially inappropriate medications, is an increasing problem among older adults. The global polypharmacy prevalence is 34.6% in patients with COVID-19, and polypharmacy in COVID-19 increases with age. The present paper proposes that polypharmacy in older adults with COVID-19 and other comorbid conditions is linked to the medication outcome reporting bias of randomized controlled trials. Outcome reporting bias can occur when treatment efficacy is reported as relative risk reductions, which overestimates medication benefits and exaggerates disease/illness risk reductions compared to unreported absolute risk reductions. The comorbidities common in patients with COVID-19 include high blood pressure, cardiovascular disease, dementia or cerebrovascular disease, and diabetes. Accordingly, the present paper reassesses the relative and absolute risk reductions in clinical trials from a small convenience sample of antihypertension, statin, anticoagulant, and antihyperglycemic medications. Examples demonstrate a wide gap between reported relative risk reductions and unreported absolute risk reductions in medication clinical trials. This paper concludes that medication clinical trial outcome reporting bias is an important upstream factor that contributes to biased medication benefits and poor clinical decision making, leading to polypharmacy in older adults with COVID-19 and other comorbid conditions. Public health campaigns are urgently needed to educate the public about the link between polypharmacy and medication outcome reporting bias. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26738430
Volume :
3
Issue :
3
Database :
Academic Search Index
Journal :
BioMed
Publication Type :
Academic Journal
Accession number :
172394165
Full Text :
https://doi.org/10.3390/biomed3030027