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A systematic review of how missing data are handled and reported in multi-database pharmacoepidemiologic studies
Nicholas B Hunt1, Helga Gardarsdottir1,2,3, Marloes T Bazelier1
1Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands.
Pharmacoepidemiologic multi-database studies (MDBS) often have missing data. While over half of recent studies reported it, only two-thirds addressed it, risking bias and precision loss in drug safety evaluations.
Area of Science:
- Pharmacoepidemiology
- Health Informatics
- Biostatistics
Background:
- Multi-database studies (MDBS) are crucial for evaluating drug safety and effectiveness.
- Missing data in MDBS can lead to biased results and reduced precision.
- Standardized reporting and handling of missing data in MDBS are needed.
Purpose of the Study:
- To assess the reporting and handling of missing data in pharmacoepidemiologic MDBS.
- To identify common methods used to address missing data in these studies.
Main Methods:
- Systematic literature search of PubMed for pharmacoepidemiologic MDBS published 2018-2019.
- Inclusion criteria: studies using ≥2 distinct databases for the same drug outcome.
- Extracted data included MDBS strategies, missing data reporting (type, bias), and methods for addressing missing data.
Main Results:
- 62 studies were included, with most data from North America and Europe.
- 56% of studies reported missing data; 35% of those acknowledged potential bias.
- 19 studies reported methods to address missing data, with complete case analysis being most common (68%).
Conclusions:
- Just over half of recent pharmacoepidemiologic MDBS reported missing data.
- Two-thirds of studies reporting missing data also described how they addressed it.
- Increased vigilance in reporting and addressing missing data is essential to mitigate bias in MDBS.
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