Outcome measures in pediatric polypharmacy research: a scoping review
Negar Golchin1, Hannah Johnson2, Paul M Bakaki2
1School of Pharmacy, University of Washington, Seattle, Washington, USA.
Insights
This scoping review analyzed pediatric polypharmacy research, finding most studies focus on prevalence, prognosis, and adverse drug reactions. Researchers highlight the harms of polypharmacy, urging careful consideration of benefits versus risks.
Area of Science:
- Pharmacology
- Pediatric Medicine
- Health Outcomes Research
Background:
- Pediatric polypharmacy research has employed various interpretation methods.
- This study represents the first scoping review to explore outcome measures in pediatric polypharmacy research.
Purpose of the Study:
- To systematically describe the outcome measures assessed within the existing body of pediatric polypharmacy research.
Main Methods:
- A comprehensive search of multiple electronic databases was conducted in July 2017.
- Data extraction focused on study characteristics and outcome measures, with synthesis of reported harms and benefits.
- Included studies were analyzed for prevalence, prognosis, and adverse drug reaction outcomes.
Main Results:
- Out of 363 analyzed studies, polypharmacy prevalence was the most frequent outcome (31.4%), followed by prognosis (25.6%) and adverse drug reactions (16.5%).
- A significant majority of studies (73.0%) reported harms, including adverse drug reactions, side effects, and drug-drug interactions.
- Benefits were reported in 22.9% of studies, often related to efficacy, complex disease treatment, or treatment augmentation.
Conclusions:
- The majority of pediatric polypharmacy studies concentrate on prevalence, prognosis, and adverse drug reaction outcomes.
- Findings underscore the significant harms associated with pediatric polypharmacy.
- Clinicians must meticulously balance the potential benefits against the harms when prescribing multiple medications for pediatric patients.
Introduction:
Various methods have been used to interpret the reports of pediatric polypharmacy across the literature. This is the first scoping review that explores outcome measures in pediatric polypharmacy research.
Objectives:
The aim of our study was to describe outcome measures assessed in pediatric polypharmacy research.
Methods:
A search of electronic databases was conducted in July 2017, including Ovid Medline, PubMed, Elsevier Embase, Wiley Cochrane Central Register of Controlled Trials (CENTRAL), EBSCO CINAHL, Ovid PsyclNFO, Web of Science Core Collection, ProQuest Dissertations and Thesis A&I. Data were extracted about study characteristics and outcome measures, and also synthesized by harms or benefits mentioned.
Results:
The search strategy initially identified 8169 titles and screened 4398 using the inclusion criteria after de-duplicating. After the primary screening, a total of 363 studies were extracted for the data analysis. Polypharmacy (prevalence) was identified as an outcome in 31.4% of the studies, prognosis-related outcomes in 25.6%, and adverse drug reactions in 16.5%. A total of 265 articles (73.0%) mentioned harms, including adverse drug reactions (26.4%), side effects (24.2%), and drug-drug interactions (20.9%). A total of 83 studies (22.9%) mentioned any benefit, 48.2% of which identified combination for efficacy, 24.1% combination for treatment of complex diseases, and 19.3% combination for treatment augmentation. Thirty-eight studies reported adverse drug reaction as an outcome, where polypharmacy was a predictor, with various designs.
Conclusions:
Most studies of pediatric polypharmacy evaluate prevalence, prognosis, or adverse drug reaction-related out-comes, and underscore harms related to polypharmacy. Clinicians should carefully weigh benefits and harms when introducing medications to treatment regimens.
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