Physician Antipsychotic Overprescribing Letters and Cognitive, Behavioral, and Physical Health Outcomes Among People With Dementia

Author:

Harnisch Michelle1,Barnett Michael L.2,Coussens Stephen3,Thomas Kali S.4,Olfson Mark5,Berhane Kiros6,Sacarny Adam3

Affiliation:

1. PhD Economics Programme, Department of Economics, London School of Economics and Political Science, London, United Kingdom

2. Department of Health Policy and Management, Harvard T. H. Chan School of Public Health, Boston, Massachusetts

3. Department of Health Policy and Management, Mailman School of Public Health, Columbia University, New York, New York

4. Center for Equity in Aging, Johns Hopkins University School of Nursing, Baltimore, Maryland

5. Department of Psychiatry, Department of Epidemiology, Columbia University Irving Medical Center, New York, New York

6. Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, New York

Abstract

ImportanceAntipsychotics, such as quetiapine, are frequently prescribed to people with dementia to address behavioral symptoms but can also cause harm in this population.ObjectiveTo determine whether warning letters to high prescribers of quetiapine can successfully reduce its use among patients with dementia and to investigate the impacts on patients’ health outcomes.Design, Setting, and ParticipantsThis is a secondary analysis of a randomized clinical trial of overprescribing letters that began in April 2015 and included the highest-volume primary care physician (PCP) prescribers of quetiapine in original Medicare. Outcomes of patients with dementia were analyzed in repeated 90-day cross-sections through December 2018. Analyses were conducted from September 2021 to February 2024.InterventionsPCPs were randomized to a placebo letter or 3 overprescribing warning letters stating that their prescribing of quetiapine was high and under review by Medicare.Main Outcomes and MeasuresThe primary outcome of this analysis was patients’ total quetiapine use in days per 90-day period (the original trial primary outcome was total quetiapine prescribing by study PCPs). Prespecified secondary outcomes included measures of cognitive function and behavioral symptoms from nursing home assessments, indicators of depression from screening questionnaires in assessments and diagnoses in claims, metabolic diagnoses derived from assessments and claims, indicators of use of the hospital and other health care services, and death. Outcomes were analyzed separately for patients living in nursing homes and in the community.ResultsOf the 5055 study PCPs, 2528 were randomized to the placebo letter, and 2527 were randomized to the 3 warning letters. A total of 84 881 patients with dementia living in nursing homes and 261 288 community-dwelling patients with dementia were attributed to these PCPs. There were 92 874 baseline patients (mean [SD] age, 81.5 [10.5] years; 64 242 female [69.2%]). The intervention reduced quetiapine use among both nursing home patients (adjusted difference, –0.7 days; 95% CI, −1.3 to −0.1 days; P = .02) and community-dwelling patients (adjusted difference, −1.5 days; 95% CI, −1.8 to −1.1 days; P < .001). There were no detected adverse effects on cognitive function (cognitive function scale adjusted difference, 0.01; 95% CI, −0.01 to 0.03; P = .19), behavioral symptoms (agitated or reactive behavior adjusted difference, −0.2%; 95% CI −1.2% to 0.8% percentage points; P = .72), depression, metabolic diagnoses, or more severe outcomes, including hospitalization and death.Conclusions and RelevanceThis study found that overprescribing warning letters to PCPs safely reduced quetiapine prescribing to their patients with dementia. This intervention and others like it may be useful for future efforts to promote guideline-concordant care.Trial RegistrationClinicalTrials.gov Identifier: NCT05172687

Publisher

American Medical Association (AMA)

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