How Similar Are Drug Data and Disease Self-report? Estimating the Prevalence of Chronic Diseases in Less Developed Settings
Seyed Reza Abdipour Mehrian, Zahra Ghahramani, Mohammad Reza Akbari, Elham Hashemi, Ehsan Shojaeefard, Reza Malekzadeh, Bita Mesgarpour, Abdullah Gandomkar, Mohammad Reza Panjehshahin, Jafar Hasanzadeh, Fatemeh Malekzadeh, Hossein Molavi Vardanjani

TL;DR
This study compares drug data and self-reports to estimate chronic disease prevalence in a less-developed region of Iran, finding significant discrepancies.
Contribution
The study introduces a comparative analysis of drug data and self-reports for disease prevalence estimation in resource-limited settings.
Findings
Drug data and self-reports showed high similarity for diabetes (54%) and hypertension (53%).
Low similarity was observed for IBS (2%), stroke (5%), and depression (9%).
Combining drug data with self-reports is recommended for better disease prevalence estimates in less-developed regions.
Abstract
Drug data has been used to estimate the prevalence of chronic diseases. Disease registries and annual surveys are lacking, especially in less-developed regions. At the same time, insurance drug data and self-reports of medications are easily accessible and inexpensive. We aim to investigate the similarity of prevalence estimation between self-report data of some chronic diseases and drug data in a less developed setting in southwestern Iran. Baseline data from the Pars Cohort Study (PCS) was re-analyzed. The use of disease-related drugs were compared against self-report of each disease (hypertension [HTN], diabetes mellitus [DM], heart disease, stroke, chronic obstructive pulmonary disease [COPD], sleep disorder, anxiety, depression, gastroesophageal reflux disease [GERD], irritable bowel syndrome [IBS], and functional constipation [FC]). We used sensitivity, specificity, positive…
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Taxonomy
TopicsHealth Systems, Economic Evaluations, Quality of Life · Advanced Causal Inference Techniques · Pharmaceutical Economics and Policy
