Table 1.
Qualitative summary of studies included in the meta‐analysis assessing the impact of anticholinergic agent use on incident dementia
Study | Design | Study setting/participants | Patient characteristics | Drug exposure assessment | Dementia assessment | Follow‐up/study duration | Risk of bias | Reported association |
---|---|---|---|---|---|---|---|---|
Ancelin 2006 26 | Prospective cohort | General practitioner patients (France) | >60 years 77% women among users | Prevalent use at baseline and 1 year after | Neurologic examination based on DSM‐III‐R criteriaa | 7 years | Moderate | No |
N = 327 | ||||||||
Coupland 2019 8 | Nested case‐control | QResearch database (UK) | ≥55 years 63% women | 10 years: 1–11 years before index date | Clinical code for dementia recorded in practice records or Office of National Statistics death records, or prescription for donepezil, galantamine, memantine, or rivastigmine | N/A | Moderate | Yes |
N = 284,343 | ||||||||
Gray 2015 13 | Prospective cohort | Sampled patients (GroupHEALTH, USA) | ≥65 years 60% women | ≥10 years of GroupHEALTH care plan enrollment | Cognitive Abilities Screening Instrument used. If score was ≤85, patient had a diagnostic evaluation for dementiab | Mean (SD) follow‐up: 7.3 (4.8) years | Moderate | Yes/no depending on level of TSDD |
N = 3434 | ||||||||
Hong 2019 27 | Retrospective cohort | National Health Insurance Research Database (Taiwan) | ≥45 years 52% women | 1 year after index date | ICD‐9‐CM diagnosis code for dementia and record of mental function examination within the same visitc | Mean (SD) follow‐up: 5.9 (3.4) years among unexposed, 5.7 (3.4) years among exposed | Moderate | Yes |
N = 21,934 | ||||||||
Park 2017 28 | Nested case‐control | National Health Insurance Service (South Korea) | ≥65 years 72% women | 2 years before index date | ICD‐10‐CM diagnosis code for dementia | N/A | Moderate | Yes |
N = 11,124 | ||||||||
Richardson 2018 29 | Nested case‐control | Clinical Practice Research Datalink (UK) | 65–99 years 63% women | Median (IQR, range) = 7.1 (4.0–11.3, 1–16) years before index date | Read code for dementia or prescription for memantine, donepezil, rivastigmine, galantamine, or tacrine if diagnosis of dementia was recorded within 12 months | N/A | Moderate | Yes |
N = 324,703 |
Abbreviations: CM, clinical modification; DSM, Diagnostic and Statistical Manual of Mental Disorders; ICD, International Classification of Diseases; IQR, interquartile range; NINCDS–ADRDA, National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association.
When examination was not possible, medical records were examined in collaboration with the patient's general practitioner to determine presence/absence of dementia.
A study neurologist, geriatrician, or internist performed a physical/neurologic examination, as well as neuropsychological testing. Results of the assessment, laboratory testing, and clinical data from medical records were reviewed for diagnosis using DSM‐IV and NINCDS–ADRDA criteria. Patients diagnosed with incident dementia had at least one follow‐up examination to confirm the dementia diagnosis.
Mental function examinations to confirm dementia diagnosis included the Clinical Dementia Rating, Cognitive Abilities Screening Instrument, or Mini‐Mental State Examination.