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1.
BMJ Open Qual ; 12(4)2023 12 22.
Artículo en Inglés | MEDLINE | ID: mdl-38135304

RESUMEN

OBJECTIVES: Low-value esophagogastroduodenoscopies (EGDs) for uncomplicated gastro-oesophageal reflux disease (GERD) can harm patients and raise patient and payer costs. We developed an electronic health record (EHR) 'eMeasure' to detect low-value EGDs. DESIGN: Retrospective cohort of 518 adult patients diagnosed with GERD who underwent initial EGD between 1 January 2019 and 31 December 2019. SETTING: Outpatient primary care and gastroenterology clinics at a large, urban, academic health centre. PARTICIPANTS: Adult primary care patients at the University of California Los Angeles who underwent initial EGD for GERD in 2019. MAIN OUTCOME MEASURES: EGD appropriateness criteria were based on the American College of Gastroenterology 2012 guidelines. An initial EGD was considered low-value if it lacked a documented guideline-based indication, including alarm symptoms (eg, iron-deficiency anaemia); failure of an 8-week proton pump inhibitor trial or elevated Barrett's oesophagus risk. We performed manual chart review on a random sample of 204 patients as a gold standard of the eMeasure's validity. We estimated EGD costs using Medicare physician and facility fee rates. RESULTS: Among 518 initial EGDs performed (mean age 53 years; 54% female), the eMeasure identified 81 (16%) as low-value. The eMeasure's sensitivity was 42% (95% CI 22 to 61) and specificity was 93% (95% CI 89 to 96). Stratifying across clinics, 62 (74.6%) low-value EGDs originated from 2 (12.5%) out of 16 clinics. Total cost for 81 low-value EGDs was approximately US$75 573, including US$14 985 in patients' out-of-pocket costs. CONCLUSIONS: We developed a highly specific eMeasure that showed that low-value EGDs occurred frequently in our healthcare system and were concentrated in a minority of clinics. These results can inform future QI efforts at our institution, such as best practice alerts for the ordering physician. Moreover, this open-source eMeasure has a much broader potential impact, as it can be integrated into any EHR and improve medical decision-making at the point of care.


Asunto(s)
Registros Electrónicos de Salud , Reflujo Gastroesofágico , Adulto , Humanos , Femenino , Anciano , Estados Unidos , Persona de Mediana Edad , Masculino , Estudios Retrospectivos , Medicare , Reflujo Gastroesofágico/diagnóstico , Reflujo Gastroesofágico/complicaciones , Endoscopía del Sistema Digestivo/métodos
2.
JAMA Intern Med ; 183(8): 885-889, 2023 08 01.
Artículo en Inglés | MEDLINE | ID: mdl-37167598

RESUMEN

This cross-sectional cost analysis uses data from the 2018 Health and Retirement Study to estimate the potential future Medicare spending and beneficiary costs for lecanemab.


Asunto(s)
Gastos en Salud , Medicare , Humanos , Anciano , Estados Unidos , Costos y Análisis de Costo
3.
PLoS One ; 17(12): e0277409, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36538552

RESUMEN

Among patients with Alzheimer's disease and its related dementias (ADRD) with behavioral disturbances, antipsychotic prescriptions have limited efficacy and increase the risk of death. Yet, physicians continue to routinely prescribe low-value antipsychotic medications for behavioral disturbances among patients with ADRD. We designed a pragmatic randomized-controlled trial to measure the impact of a behavioral economic electronic health record (EHR) clinical decision support (CDS) intervention to reduce physician prescriptions of new antipsychotic medications among patients with ADRD. Utilizing a pragmatic parallel arm randomized-controlled trial design, the study will randomize eligible physicians from a large academic health system to either receive a EHR CDS intervention or not (control) when they prescribe a new antipsychotic medication during visits with patients with ADRD. The intervention will include three components: 1) alerts prescribers that antipsychotic prescriptions increase mortality risk (motivating physicians' intrinsic desire for non-malfeasance); 2) offers non-pharmacological behavioral resources for caregivers; 3) auto-defaults the prescription to contain the lowest dose and number of pill-days (n = 30) without refills if the prescriber does not cancel the order (appealing to default bias). Over 1 year, we will compare the cumulative total of new antipsychotic pill-days prescribed (primary outcome) by physicians in the intervention group versus in the control group. The study protocol meets international SPIRIT guidelines. Behavioral economics, or the study of human behavior as a function of more than rational incentives, considering a whole host of cognitive and social psychological preferences, tendencies, and biases, is increasingly recognized as an important conceptual framework to improve physician behavior. This pragmatic trial is among the first to combine two distinct behavioral economic principles, a desire for non-malfeasance and default bias, to improve physician prescribing patterns for patients with ADRD. We anticipate this trial will substantially advance understanding of how behavioral-economic informed EHR CDS tools can potentially reduce harmful, low-value care among patients with ADRD.


Asunto(s)
Enfermedad de Alzheimer , Antipsicóticos , Sistemas de Apoyo a Decisiones Clínicas , Humanos , Anciano , Antipsicóticos/uso terapéutico , Enfermedad de Alzheimer/tratamiento farmacológico , Registros Electrónicos de Salud , Prescripciones , Ensayos Clínicos Controlados Aleatorios como Asunto
4.
JAMA Health Forum ; 3(1): e214495, 2022 01.
Artículo en Inglés | MEDLINE | ID: mdl-35977233

RESUMEN

This cross-sectional study examines upper bound and lower bound annualized Medicare costs for administering aducanumab to beneficiaries with the approved indications of mild cognitive impairment or mild dementia.


Asunto(s)
Disfunción Cognitiva , Demencia , Anciano , Anticuerpos Monoclonales Humanizados , Disfunción Cognitiva/tratamiento farmacológico , Estudios Transversales , Humanos , Medicare , Estados Unidos
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