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                    "lastName": "Lombardi"
                },
                {
                    "creatorType": "author",
                    "firstName": "Krishi",
                    "lastName": "Akenapalli"
                },
                {
                    "creatorType": "author",
                    "firstName": "Richard D.",
                    "lastName": "Boyce"
                }
            ],
            "abstractNote": "IMPORTANCE: The incidence of potentially inappropriate medication (PIM) prescribing among older adults is not as well studied as its prevalence. Estimates of factors associated with PIM incidence, such as patient age, sex, race-ethnicity, medication subsidy support, and comorbidity, are also limited.\nOBJECTIVE: To estimate the incidence of PIM prescribing in older adult outpatients, as well as the incidence and predictors for each PIM class, in a large outpatient electronic health records (EHR) cohort.\nDESIGN: Retrospective study of PIM prescribing among outpatients with encounters leading to prescription orders, 2015-2018, excluding prevalent cases.\nSETTING: Outpatients receiving care from a multi-site health system in western Pennsylvania.\nPARTICIPANTS: 342,405 patients, contributing 893,754 person-years of follow-up.\nMAIN OUTCOMES AND MEASURES: The incidence of PIM prescribing based on automated coding of 2019 Beers criteria. A multivariable Poisson regression model was estimated to assess the impact of age, sex, race-ethnicity, comorbidity, and medication subsidy (PACE/PACENET) on PIM risk. For each PIM class, the association between predictors and time to PIM prescribing was evaluated using proportional hazard models.\nRESULTS: The incidence rate (IR) for 1 or more PIM was 193.5 per 1000 person-years, led by short- and intermediate-acting benzodiazepines (37.6), first-generation antihistamines (32.8), and skeletal muscle relaxants (22.0). The incidence of PIM prescribing was 15% higher among white patients and 35% lower among males. High comorbidity (Charlson score ≥ 3) was associated with a 59% higher risk. Participation in the PACE/PACENET program, a medication subsidy program, was associated with an 83% increase in incidence. Each additional year of age was associated with a 1.2% reduction in incidence.\nCONCLUSIONS AND RELEVANCE: This study establishes benchmarks for the incidence of PIM prescribing in outpatients and identifies important disparities in PIM risk, which vary by PIM class.",
            "publicationTitle": "Journal of the American Geriatrics Society",
            "publisher": "",
            "place": "",
            "date": "2025-03",
            "volume": "73",
            "issue": "3",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "728-736",
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                    "tag": "Aged",
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                    "type": 1
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                    "tag": "Electronic Health Records",
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                    "type": 1
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                    "tag": "Pennsylvania",
                    "type": 1
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                    "tag": "Potentially Inappropriate Medication List",
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                    "tag": "Retrospective Studies",
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                    "tag": "incidence",
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            "title": "Prodromal features and risk of neurodegenerative disorders diagnosis in outpatients with REM sleep behavior disorder",
            "creators": [
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                    "creatorType": "author",
                    "firstName": "Lana M.",
                    "lastName": "Chahine"
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                {
                    "creatorType": "author",
                    "firstName": "Anne",
                    "lastName": "Newman"
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                {
                    "creatorType": "author",
                    "firstName": "Richard D.",
                    "lastName": "Boyce"
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                    "creatorType": "author",
                    "firstName": "Maria M.",
                    "lastName": "Brooks"
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            "abstractNote": "STUDY OBJECTIVES: Individuals with isolated REM sleep behavior disorder (iRBD) are at high risk of neurodegenerative parkinsonian disorders or dementia (NPD). Determining which characteristics predict greatest risk could improve clinical care. Our objectives were to utilize electronic health record (EHR) data to apply prodromal PD research diagnostic criteria to iRBD outpatients and determine their utility for identifying iRBD cases at high vs low risk for NPD diagnosis.\nMETHODS: This was a retrospective cohort study at a tertiary care center in Western Pennsylvania. Diagnosis of iRBD was confirmed with expert manual chart review. Prodromal risk markers and signs/symptoms were determined with diagnostic codes. Multivariable Cox proportional hazards models examined a range of covariates as predictors of time to NPD diagnosis.\nRESULTS: Of 448 iRBD cases, 82 (18.30%) were diagnosed with NPD. Forty-nine (10.93%) had >80% prodromal PD probability. There was no difference in time to NPD among those who met vs did not meet >80% probability (log rank p=0.49). In a Cox model that included all assessed criteria features, risk of diagnosis was associated with male sex (HR=2.06, 95%CI 1.04-1.10), older baseline age (HR=1.07; 95%CI 1.05-1.10), and cognitive dysfunction diagnostic code (HR= 2.83, 95%CI 1.79-4.46). Time to NPD diagnosis among predicted high- vs low- risk cases was significantly different (Log-rank test p=0.012).\nCONCLUSIONS: In outpatients with iRBD, a model combining individual PD risk factors and prodromal features accurately identifies individuals at high risk for NPD diagnosis. Results demonstrate the potential of EHR data to translate research on prodromal PD to the clinic.",
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            "abstractNote": "BACKGROUND AND OBJECTIVES: Isolated REM sleep behavior disorder (iRBD) carries increased risk of neurodegenerative parkinsonian disorder or dementia (NPD) but is difficult to accurately screen for in the community. Health care data offer the opportunity to identify large numbers of iRBD cases among outpatients. We aimed to determine the positive predictive value (PPV) of an RBD International Classification of Disorders (ICD) code for actual iRBD based on manual review of the electronic health record (EHR), examine risk of NPD diagnosis, and explore whether a statistical model developed using selected EHR data can identify individuals with the RBD ICD code who have high probability for actual iRBD.\nMETHODS: In this retrospective cohort study, a search of the EHR at a single health care system was conducted to identify outpatients who received the ICD9 or ICD10 RBD code in 2011-2021. The EHR for each case was manually reviewed. Secondary RBD cases were excluded. Remaining cases were classified as no iRBD or actual iRBD (possible, probable, or definite). Incident cases of NPD were identified. PPV of presence of the RBD ICD code for actual iRBD was calculated. Cumulative incidence of NPD with death as a competing event was compared in those with vs without iRBD. Least absolute shrinkage and selection operator (LASSO) regression was used to build a prediction model for iRBD, and the model was validated in an independent data set.\nRESULTS: Among 1,130 cases with the RBD ICD code, 499 had secondary causes of RBD. For the remaining 628 cases, EHR review indicated no iRBD in 168 (26.8%). PPV of the RBD ICD code was 73.25%. Over a median follow-up of 4.7 years, compared with the no iRBD group, the iRBD group had a higher risk of NPD (subdistribution hazard ratio = 10.4 [95% CI 2.5-43.1]). The LASSO prediction model for iRBD had an area under the receiver operating characteristic curve of 0.844 (95% CI 0.806-0.880).\nDISCUSSION: PPV of an RBD ICD code is moderate. In the real-world setting, patients with iRBD had a high risk of incident diagnosis of NPD over 4.7 years. Results indicate feasibility of using statistical models developed using EHR data to accurately predict iRBD.",
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