Han 2008.
Study characteristics | ||
Methods | Design: retrospective cohort Setting: community Country: USA Duration of follow‐up: 1 year Covariates controlled for: age, education, race, living arrangement, before enrolment. history of alcohol use and smoking, and depressive symptoms, ADL function, Charlson Comorbidity Index |
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Participants | Participants numbers: 544 Population type: older adults Sex: 100% men Age (mean): 74 years |
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Prognostic factors | Anticholinergic burden measurement method: clinician‐rated | |
Outcomes | Outcomes assessed: cognitive decline Outcome ascertainment cognitive decline: HVRT, IADL Diagnostic criteria cognitive decline: scores on cognitive testing |
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Source of funding | Claude D. Pepper Older Americans Independence Center at Yale University School of Medicine | |
Notes | ||
Item | Authors' judgement | Support for judgement |
Study participation | No | Men only with hypertension. |
Study attrition | Unclear | Attrition was high but just below the 20% high risk mark. Conducted analysis to investigate potential impact of missing values on final model and did not alter conclusions but did not explain what these missing data analyses entailed. |
Prognostic factor measurement | Unclear | No measurement of dosage or frequency of use. No measurement of non‐VA sources of drugs. Conducted repeated measurements over the follow‐up period for the 12 months preceding each assessment at 1 and 2 years. |
Outcome measurement | Unclear | No mention of blinding. Unclear if anticholinergic burden was applied before or after cognitive assessment score was determined. |
Study confounding | Yes | Only men in sample so no sex. Controlled for comorbidities via Charlson Comorbidity Index along with depression. |
Reverse causation | No | Anticholinergic burden exposure time frame defined as the 12 months preceding each follow‐up at 1 year and 2 years. (so seems to have covered medication use right up to the point of each follow‐up assessment). |
Statistical analysis and reporting | Unclear | No assessment of assumptions. Referred to a protocol but was not a protocol specifically for this study so no mention of an analysis plan. |