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2.
Autism ; 21(8): 972-984, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-27663266

RESUMO

Our objective was to use a community-based participatory research approach to identify and compare barriers to healthcare experienced by autistic adults and adults with and without other disabilities. To do so, we developed a Long- and Short-Form instrument to assess barriers in clinical and research settings. Using the Barriers to Healthcare Checklist-Long Form, we surveyed 437 participants (209 autistic, 55 non-autistic with disabilities, and 173 non-autistic without disabilities). Autistic participants selected different and greater barriers to healthcare, particularly in areas related to emotional regulation, patient-provider communication, sensory sensitivity, and healthcare navigation. Top barriers were fear or anxiety (35% (n = 74)), not being able to process information fast enough to participate in real-time discussions about healthcare (32% (n = 67)), concern about cost (30% (n = 62)), facilities causing sensory issues 30% ((n = 62)), and difficulty communicating with providers (29% (n = 61)). The Long Form instrument exhibited good content and construct validity. The items combined to create the Short Form had predominantly high levels of correlation (range 0.2-0.8, p < 0.001) and showed responsiveness to change. We recommend healthcare providers, clinics, and others working in healthcare settings to be aware of these barriers, and urge more intervention research to explore means for removing them.


Assuntos
Transtorno Autístico/terapia , Pessoas com Deficiência/estatística & dados numéricos , Pesquisas sobre Atenção à Saúde/métodos , Pesquisas sobre Atenção à Saúde/estatística & dados numéricos , Acessibilidade aos Serviços de Saúde/estatística & dados numéricos , Adulto , Pesquisa Participativa Baseada na Comunidade/métodos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
3.
Ann Behav Med ; 49(1): 58-65, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25008432

RESUMO

BACKGROUND: Angina and depression are common in ischemic heart disease (IHD), but their association remains understudied. PURPOSE: This study was conducted in order to evaluate the association of 1 year change in depression with change in patient-reported outcomes of stable angina. METHODS: Five hundred sixty-nine stable angina patients completed the Seattle Angina Questionnaire and Patient Health Questionnaire (PHQ) at baseline and 1 year. Participants were divided into four groups: not depressed, new onset of depression at 1 year, remitted at 1 year, and persistently depressed. Associations between depression and angina symptoms were evaluated using regression models. RESULTS: Compared to those not depressed, newly depressed participants reported more angina (ß = -11.7, p < 0.001) and physical limitations (ß = -11.8, p < 0.001) and lower treatment satisfaction (ß = -15.03, p < 0.001) and quality of life (ß = -15.4, p < 0.001). Persistently depressed participants reported physical limitations (ß = -7.4, p < 0.05), lower treatment satisfaction (ß = -10.1, p < 0.001), and poorer quality of life (ß = -10.03, p < 0.001). CONCLUSIONS: Changes in depression scores and angina outcomes were significantly associated.


Assuntos
Angina Pectoris/diagnóstico , Depressão/diagnóstico , Isquemia Miocárdica/complicações , Qualidade de Vida , Idoso , Idoso de 80 Anos ou mais , Angina Pectoris/complicações , Efeitos Psicossociais da Doença , Depressão/complicações , Feminino , Nível de Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Inquéritos e Questionários , Avaliação de Sintomas , Veteranos
4.
Med Care ; 48(1): 38-44, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19952802

RESUMO

BACKGROUND: Chronic pain is costly to individuals and the healthcare system, and is often undertreated. Collaborative care models show promise for improving treatment of patients with chronic pain. The objectives of this article are to report the incremental benefit and incremental health services costs of a collaborative intervention for chronic pain from a veterans affairs (VA) healthcare perspective. METHODS: Data on VA treatment costs incurred by participants were obtained from the VA's Decision Support System for all utilization except certain intervention activities which were tracked in a separate database. Outcome data were from a cluster-randomized trial of a collaborative intervention for chronic pain among 401 primary care patients at a VA medical center. Intervention group participants received assessments and care management; stepped-care components were offered to patients requiring more specialized care. The main outcome measure was pain disability-free days (PDFDs), calculated from Roland-Morris Disability Questionnaire scores. RESULTS: Participants in the intervention group experienced an average of 16 additional PDFDs over the 12-month follow-up window as compared with usual care participants; this came at an adjusted incremental cost of $364 per PDFD for a typical participant. Important predictors of costs were baseline medical comorbidities, depression severity, and prior year's treatment costs. CONCLUSIONS: This collaborative intervention resulted in more pain disability-free days and was more expensive than usual care. Further research is necessary to identify if the intervention is more cost-effective for some patient subgroups and to learn whether pain improvements and higher costs persist after the intervention has ended.


Assuntos
Dor nas Costas/economia , Custos de Cuidados de Saúde/estatística & dados numéricos , Atenção Primária à Saúde/organização & administração , United States Department of Veterans Affairs/organização & administração , Fatores Etários , Idoso , Dor nas Costas/terapia , Doença Crônica , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Atenção Primária à Saúde/economia , Qualidade de Vida , Ensaios Clínicos Controlados Aleatórios como Assunto , Fatores Sexuais , Resultado do Tratamento , Estados Unidos , United States Department of Veterans Affairs/economia
5.
Health Serv Res ; 37(1): 121-43, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11949917

RESUMO

OBJECTIVE: To study the impact that physician, practice, and patient characteristics have on physician stress, satisfaction, mental, and physical health. DATA SOURCES: Based on a survey of over 5,000 physicians nationwide. Four waves of surveys resulted in 2,325 complete responses. Elimination of ineligibles yielded a 52 percent response rate; 1,411 responses from primary care physicians were used. STUDY DESIGN: A conceptual model was tested by structural equation modeling. Physician job satisfaction and stress mediated the relationship between physician, practice, and patient characteristics as independent variables and physician physical and mental health as dependent variables. PRINCIPLE FINDINGS: The conceptual model was generally supported. Practice and, to a lesser extent, physician characteristics influenced job satisfaction, whereas only practice characteristics influenced job stress. Patient characteristics exerted little influence. Job stress powerfully influenced job satisfaction and physical and mental health among physicians. CONCLUSIONS: These findings support the notion that workplace conditions are a major determinant of physician well-being. Poor practice conditions can result in poor outcomes, which can erode quality of care and prove costly to the physician and health care organization. Fortunately, these conditions are manageable. Organizational settings that are both "physician friendly" and "family friendly" seem to result in greater well-being. These findings are particularly important as physicians are more tightly integrated into the health care system that may be less clearly under their exclusive control.


Assuntos
Medicina de Família e Comunidade/organização & administração , Satisfação no Emprego , Saúde Mental , Saúde Ocupacional , Aptidão Física , Médicos de Família/psicologia , Adulto , Grupos Diagnósticos Relacionados , Medicina de Família e Comunidade/estatística & dados numéricos , Pesquisa sobre Serviços de Saúde , Inquéritos Epidemiológicos , Humanos , Pessoa de Meia-Idade , Modelos Psicológicos , Médicos de Família/classificação , Médicos de Família/estatística & dados numéricos , Estresse Psicológico/epidemiologia , Estados Unidos/epidemiologia , Local de Trabalho/psicologia
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