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1.
J Ren Care ; 43(4): 209-218, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28371226

RESUMO

BACKGROUND: Patterns of healthcare encounters by patients in each stage of chronic kidney disease (CKD) have not been fully described. OBJECTIVE: This study describes patterns of healthcare resource use by patients with CKD. DESIGN: A retrospective descriptive design was used. PARTICIPANTS: Patients with Stages 1-5 CKD were identified in five existing de-identified healthcare insurance claims databases in the United States using codes from the International Classification of Diseases (ICD-9-CM). MEASUREMENTS: The databases contained more than 23,660,000 claims records from over 11 million subscribers who were continuously enrolled in a single 2014 health plan. All CKD patients' 2014 claims were extracted, yielding 1,987 unique people with 110,594 healthcare encounters. RESULTS: Healthcare resources are used to manage the causes of CKD and its multiple effects on health, and thus the number of healthcare encounters among people with more advanced disease was, as expected, relatively higher. There were more hospitalisations, emergency department visits and specialist encounters in this group. Surprisingly, however, even people in earlier stages of kidney disease experienced a median of 14-17 healthcare encounters during a single calendar year. CONCLUSIONS: Understanding patterns of healthcare encounters provides important information about the transition experiences of patients with CKD. Exploring ways to reduce the risks associated with transitions in care may prevent problems with home medication management, frequent emergency department visits and potentially avoidable hospitalisations.


Assuntos
Atenção à Saúde/métodos , Atenção à Saúde/estatística & dados numéricos , Recursos em Saúde/estatística & dados numéricos , Insuficiência Renal Crônica/psicologia , Insuficiência Renal Crônica/terapia , Arizona , California , Atenção à Saúde/normas , Feminino , Florida , Hospitalização/estatística & dados numéricos , Humanos , Revisão da Utilização de Seguros/estatística & dados numéricos , Masculino , Nevada , Insuficiência Renal Crônica/complicações , Estudos Retrospectivos
2.
J Aging Health ; 28(1): 165-79, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26112066

RESUMO

OBJECTIVE: The aim of the study is to assess the relationship between body mass index (BMI) class and Medicare claims among young-old (65-69), old (70-74), and old-old (75+) adults over a 10-year period. METHOD: We assessed costs by BMI class and age group among 9,300 respondents to the 1998 Health and Retirement Study (HRS) with linked 1998-2008 Medicare claims data. BMI was classified as normal (18.5-24.9), overweight (25-29.9), mild obesity (30-34.9), or severe obesity (35 or above). RESULTS: Annualized total Medicare claims adjusted for age, gender, ethnicity, education, and smoking history were 109% greater for severely obese young-old adults in comparison with normal weight young-old adults (US$9,751 vs. US$4,663). Total annualized claim differences between the normal weight and severely obese in the old and old-old groups were not statistically significant. DISCUSSION: Excess Medicare expenditures related to obesity may be concentrated among severely obese young-old adults. Preventing severe obesity among middle and older aged adults may have large cost implications for society.


Assuntos
Índice de Massa Corporal , Gastos em Saúde/estatística & dados numéricos , Medicare/economia , Fatores Etários , Idoso , Feminino , Humanos , Masculino , Obesidade/economia , Estados Unidos
3.
Am J Geriatr Psychiatry ; 22(5): 427-36, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-23933423

RESUMO

OBJECTIVES: The population of older patients with schizophrenia is increasing. This study describes health outcomes, utilization, and costs over 10 years in a sample of older patients with schizophrenia compared with older patients without schizophrenia. METHODS: An observational cohort study of 31,588 older adults (mean age: 70.44 years) receiving care from an urban public health system, including a community mental health center, during 1999-2008. Of these, 1,635 (5.2%) were diagnosed with schizophrenia and 757 (2.4%) had this diagnosis confirmed in the community mental health center. Patients' electronic medical records were merged with Medicare claims, Medicaid claims, the Minimum Dataset, and the Outcome and Assessment Information Set. Information on medication use was not available. MEASUREMENTS: Rates of comorbid conditions, healthcare utilization, costs, and mortality. RESULTS: Patients with schizophrenia had significantly higher rates of congestive heart failure (45.05% versus 38.84%), chronic obstructive pulmonary disease (52.71% versus 41.41%), and hypothyroidism (36.72% versus 26.73%) than the patients without schizophrenia (p <0.001). They had significantly lower rates of cancer (30.78% versus 43.18%) and significantly higher rates of dementia (64.46% versus 32.13%). The patients with schizophrenia had significantly higher mortality risk (hazard ratio: 1.25, 95% confidence interval: 1.07-1.47) than the patients without schizophrenia. They also had significantly higher rates of healthcare utilization. The mean costs for Medicare and Medicaid were significantly higher for the patients with schizophrenia than for the patients without schizophrenia. CONCLUSIONS: The management of older adult patients with schizophrenia is creating a serious burden for our healthcare system, requiring the development of integrated models of healthcare.


Assuntos
Continuidade da Assistência ao Paciente/economia , Continuidade da Assistência ao Paciente/estatística & dados numéricos , Custos de Cuidados de Saúde/estatística & dados numéricos , Serviços de Saúde para Idosos/economia , Serviços de Saúde para Idosos/estatística & dados numéricos , Serviços de Saúde Mental/economia , Serviços de Saúde Mental/estatística & dados numéricos , Esquizofrenia/economia , Idade de Início , Idoso , Estudos de Casos e Controles , Estudos de Coortes , Comorbidade , Feminino , Serviços de Saúde para Idosos/tendências , Nível de Saúde , Humanos , Masculino , Medicaid/economia , Prontuários Médicos , Medicare/economia , Esquizofrenia/epidemiologia , Esquizofrenia/mortalidade , Estados Unidos/epidemiologia
4.
J Eval Clin Pract ; 14(5): 854-60, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19018918

RESUMO

RATIONALE, AIMS AND OBJECTIVES: Evidence suggests that educational outreach ('academic detailing') improves evidence-based prescribing. We evaluated the impact of an academic detailing programme intended to increase new statin prescriptions. METHODS: In a 2 x 2 factorial design we evaluated the effect of an academic detailing programme with/without telephonic care management for patients. Eligible patients were continuously enrolled Medicaid members at high risk for cardiovascular disease utilization who were not receiving statin medication in the 18 months prior to the intervention. All primary care prescribers assigned to these patients were randomized by clinic to academic detailing. Two trained nurses provided the detailing to prescribers, including specific discussion about the use of statins in this high-risk patient population. Nurses left the prescribers with a summary of clinical practice guidelines, a one-page detailing sheet and a list of patients under the care of the prescriber who were candidates for statins. The primary outcome was the incidence of a new statin prescription claim during the 6-month intervention period and the subsequent 6 months. Logistic regression models were used to estimate main effects of the interventions and to adjust for potential confounding variables in the study. RESULTS: Forty-eight clinics were randomized, effectively randomizing a total of 284 patients and 128 prescribers. Among the 284 patients, 46 (16%) received a new statin claim during the evaluation period. Controlling for significant bivariate associations, the academic detailing intervention had no significant effect on new statin prescriptions compared with the control group (odds ratio = 0.8, 95% confidence interval: 0.4-1.6, P = 0.5). CONCLUSION: Among this Medicaid population at high risk for cardiovascular events, an academic detailing programme to increase statin prescriptions was not effective. To assist others to learn from our failed effort, we identify and discuss critical elements in the design and implementation of the programme that could account for these results.


Assuntos
Prescrições de Medicamentos/estatística & dados numéricos , Educação Médica Continuada/organização & administração , Medicina Baseada em Evidências/educação , Medicaid , Padrões de Prática Médica/organização & administração , Atenção Primária à Saúde/organização & administração , Doenças Cardiovasculares/prevenção & controle , Distribuição de Qui-Quadrado , Difusão de Inovações , Feminino , Fidelidade a Diretrizes , Humanos , Inibidores de Hidroximetilglutaril-CoA Redutases/uso terapêutico , Indiana , Modelos Logísticos , Masculino , Medicaid/organização & administração , Pessoa de Meia-Idade , Análise Multivariada , Guias de Prática Clínica como Assunto , Avaliação de Programas e Projetos de Saúde , Telefone , Estados Unidos
5.
Sex Transm Dis ; 35(4): 387-92, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18362860

RESUMO

BACKGROUND: To prevent congenital syphilis, the Centers for Disease Control and Prevention and professional organizations recommend universal prenatal syphilis screening. State-level or larger-scale evaluations of adherence to these guidelines have relied on administrative data. We measured prenatal syphilis screening rates in Indiana women with prenatal Medicaid coverage and also used electronic medical records to examine the completeness of syphilis screening claims in Medicaid administrative data. METHODS: In statewide Indiana Medicaid claims data, diagnosis and procedure codes were used to identify women who delivered an infant between October 1, 1998, and September 30, 2002. Claims for prenatal (that is, during the 40 weeks before and including the delivery date) syphilis screens, including the "obstetric panel" of tests, and for prenatal visits were extracted. A subset of the study population received prenatal care in a large public hospital and its affiliated clinics served by an electronic medical records system. For these women, claims data were compared with laboratory reports. RESULTS: Among 74,188 women with one delivery in Medicaid claims data, 60% had at least 1 prenatal syphilis screening claim, and 15% had 2 or more. Women with continuous Medicaid enrollment during pregnancy or with at least one prenatal visit claim had higher rates. Among the 3960 women for whom Medicaid claims and laboratory data were available, 49.8% had at least one prenatal syphilis screen in Medicaid claims, but 99.3% had at least one laboratory report of a syphilis screen. CONCLUSIONS: Measurements made using Medicaid administrative data appear to substantially underestimate true prenatal syphilis screening rates.


Assuntos
Hospitais Públicos/estatística & dados numéricos , Programas de Rastreamento/estatística & dados numéricos , Medicaid/estatística & dados numéricos , Sistemas Computadorizados de Registros Médicos/estatística & dados numéricos , Complicações Infecciosas na Gravidez/diagnóstico , Sífilis/diagnóstico , Feminino , Humanos , Indiana , Formulário de Reclamação de Seguro/estatística & dados numéricos , Registro Médico Coordenado , Gravidez , Cuidado Pré-Natal , Estados Unidos
6.
J Am Med Inform Assoc ; 10(4): 389-98, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12668695

RESUMO

The authors describe a research group that supports the needs of investigators seeking data from an electronic medical record system. Since its creation in 1972, the Regenstrief Medical Records System has captured and stored more than 350 million discrete coded observations on two million patients. This repository has become a central data source for prospective and retrospective research. It is accessed by six data analysts--working closely with the institutional review board--who provide investigators with timely and accurate data while protecting patient and provider privacy and confidentiality. From January 1, 1999, to July 31, 2002, data analysts tracked their activities involving 47,559 hours of work predominantly for physicians (54%). While data retrieval (36%) and analysis (25%) were primary activities, data analysts also actively collaborated with researchers. Primary objectives of data provided to investigators were to address disease-specific (35.4%) and drug-related (12.2%) questions, support guideline implementation (13.1%), and probe various aspects of clinical epidemiology (5.7%). Outcomes of these endeavors included 117 grants (including 300,000 US dollars per year salary support for data analysts) and 139 papers in peer-reviewed journals by investigators who rated the support provided by data analysts as extremely valuable.


Assuntos
Pesquisa Biomédica , Informática Médica/organização & administração , Sistemas Computadorizados de Registros Médicos , Estatística como Assunto/organização & administração , Coleta de Dados , Epidemiologia/organização & administração , Humanos , Pesquisadores
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