RESUMEN
BACKGROUND: We aimed to characterize the association between differentiated thyroid cancer (DTC) patient insurance status and appropriateness of therapy (AOT) regarding extent of thyroidectomy and radioactive iodine (RAI) treatment. METHODS: The National Cancer Database was queried for DTC patients diagnosed between 2010 and 2016. Adjusted odds ratios (AOR) for AOT, as defined by the American Thyroid Association guidelines, and hazard ratios (HR) for overall survival (OS) were calculated. A difference-in-differences (DD) analysis examined the association of Medicaid expansion with outcomes for low-income patients aged <65. RESULTS: A total of 224,500 patients were included. Medicaid and uninsured patients were at increased risk of undergoing inappropriate therapy, including inappropriate lobectomy (Medicaid 1.36, 95% confidence interval [CI]: 1.21-1.54; uninsured 1.30, 95% CI: 1.05-1.60), and under-treatment with RAI (Medicaid 1.20, 95% CI: 1.14-1.26; uninsured 1.44, 95% CI: 1.33-1.55). Inappropriate lobectomy (HR 2.0, 95% CI: 1.7-2.3, P < .001) and under-treatment with RAI (HR 2.3, 95% CI: 2.2-2.5, P < .001) were independently associated with decreased survival, while appropriate surgical resection (HR 0.3, 95% CI: 0.3-0.3, P < .001) was associated with improved odds of survival; the model controlled for all relevant clinico-pathologic variables. No difference in AOT was observed in Medicaid expansion versus non-expansion states with respect to surgery or adjuvant RAI therapy. CONCLUSION: Medicaid and uninsured patients are at significantly increased odds of receiving inappropriate treatment for DTC; both groups are at a survival disadvantage compared with Medicare and those privately insured.
Asunto(s)
Cobertura del Seguro/estadística & datos numéricos , Radioisótopos de Yodo/administración & dosificación , Neoplasias de la Tiroides/terapia , Tiroidectomía/estadística & datos numéricos , Adulto , Anciano , Femenino , Humanos , Cobertura del Seguro/economía , Masculino , Medicaid/economía , Medicaid/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Medicare/economía , Medicare/estadística & datos numéricos , Persona de Mediana Edad , Radioterapia Adyuvante/economía , Radioterapia Adyuvante/estadística & datos numéricos , Neoplasias de la Tiroides/economía , Neoplasias de la Tiroides/mortalidad , Tiroidectomía/economía , Estados Unidos/epidemiologíaRESUMEN
BACKGROUND: The Affordable Care Act's (ACA) Medicaid expansion has increased insurance coverage and improved various cancer outcomes. Its impact in papillary thyroid cancer (PTC) remains unclear. METHODS: Non-elderly patients (40-64 years-old) with PTC living in low-income areas either in a 2014 expansion, or a non-expansion state were identified from the National Cancer Database between 2010 and 2016. Insurance coverage, stage at diagnosis, and RAI administration were analyzed using a difference-in-differences analysis. RESULTS: 10,644 patients were included. Compared with non-expansion states, the percentage of uninsured patients (adjusted-DD -2.6% [95%-CI -4.3to-0.8%],p = 0.004) and patients with private insurance decreased, and those with Medicaid coverage increased (adjusted-DD 9.7% [95%-CI 6.9-12.5%],p < 0.001) in expansion states after ACA implementation. The percentage of patients with pT1 did not differ between expansion and non-expansion states; neither did the use of RAI. CONCLUSIONS: Medicaid expansion has resulted in a smaller uninsured population in PTC patients, but without earlier disease presentation nor change in RAI treatment.
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Cobertura del Seguro/estadística & datos numéricos , Medicaid/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Patient Protection and Affordable Care Act/estadística & datos numéricos , Cáncer Papilar Tiroideo/patología , Neoplasias de la Tiroides/patología , Adulto , Bases de Datos Factuales/estadística & datos numéricos , Femenino , Humanos , Cobertura del Seguro/tendencias , Radioisótopos de Yodo/uso terapéutico , Masculino , Uso Excesivo de los Servicios de Salud , Persona de Mediana Edad , Áreas de Pobreza , Sector Privado/estadística & datos numéricos , Radioterapia Adyuvante , Cáncer Papilar Tiroideo/diagnóstico , Cáncer Papilar Tiroideo/radioterapia , Neoplasias de la Tiroides/diagnóstico , Neoplasias de la Tiroides/radioterapia , Estados UnidosRESUMEN
BACKGROUND: New guidelines for managing cervical precancer among women in the United States use risk directly to guide clinical actions for individuals who are being screened. These risk-based management guidelines have previously only been based on risks from a large integrated healthcare system. We present here data representative of women of low income without continuous insurance coverage to inform the 2019 guidelines and ensure applicability. OBJECTIVE: We examined the risks of high-grade precancer after human papillomavirus and cytology tests in underserved women and assessed the applicability of the 2019 guidelines to this population. STUDY DESIGN: We examined cervical cancer screening and follow-up data among 363,546 women enrolled in the Centers for Disease Control and Prevention's National Breast and Cervical Cancer Early Detection Program from 2009 to 2017. We estimated the immediate (prevalent) risks of cervical intraepithelial lesion grade 3 or cancer by using prevalence-incidence mixture models. Risks were estimated for each combination of human papillomavirus and cytology result and were stratified by screening history. We compared these risks with published estimates used in new risk-based management guidelines. RESULTS: Women who were up-to-date with their screening, defined as being screened with cytology within the past 5 years, had immediate risks of cervical intraepithelial neoplasia grade 3 or higher similar to that of women at Kaiser Permanente Northern California, whose data were used to develop the management guidelines. However, women in the Centers for Disease Control and Prevention's National Breast and Cervical Cancer Early Detection Program had greater immediate risks if they were never screened or not up-to-date with their screening. CONCLUSION: New cervical risk-based management guidelines are applicable for underinsured and uninsured women with a low income in the United States who are up-to-date with their screening. The increased risk observed here among women who received human papillomavirus-positive, high-grade cytology results, who were never screened, or who were not up-to-date with their cervical cancer screening, led to a recommendation in the management guidelines for immediate treatment among these women.
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Detección Precoz del Cáncer , Pacientes no Asegurados/estadística & datos numéricos , Lesiones Precancerosas/epidemiología , Neoplasias del Cuello Uterino/epidemiología , Adulto , Colposcopía/estadística & datos numéricos , Femenino , Humanos , Persona de Mediana Edad , Infecciones por Papillomavirus/epidemiología , Estados Unidos/epidemiología , Displasia del Cuello del Útero/epidemiologíaRESUMEN
BACKGROUND: Metastatic colorectal cancer (CRC) outcomes continue to improve, but they vary significantly by race and ethnicity. We hypothesize that these disparities arise from unequal access to care. MATERIALS AND METHODS: The Harris Health System (HHS) is an integrated health delivery network that provides medical care to the underserved, predominantly minority population of Harris County, Texas. As the largest HHS facility and an affiliate of Baylor College of Medicine's Dan L. Duncan Comprehensive Cancer Center, Ben Taub Hospital (BTH) delivers cancer care through multidisciplinary subspecialty that prioritize access to care, adherence to evidence-based clinical pathways, integration of supportive services, and mitigation of financial toxicity. We performed a retrospective analysis of minority patients diagnosed with and treated for metastatic CRC at BTH between January 2010 and December 2012. Kaplan-Meier survival curves were compared with survival curves from randomized control trials reported during that time period. RESULTS: We identified 103 patients; 40% were black, 49% were Hispanic, and 12% were Asian or Middle Eastern. Thirty-five percent reported a language other than English as their preferred language. Seventy-four percent of patients with documented coverage status were uninsured. Eighty-four percent of patients received standard chemotherapy with a clinician-reported response rate of 63%. Overall survival for BTH patients undergoing chemotherapy was superior to that of subjects enrolled in the CRYSTAL (Cetuximab Combined with Irinotecan in First-Line Therapy for Metastatic Colorectal Cancer) trial (median, 24.0 vs. 19.9 months; P = .014). CONCLUSION: HHS provides a health delivery infrastructure through which minority patients with socioeconomic challenges experience clinical outcomes comparable with highly selected patients enrolled in randomized control trials. Efforts to resolve CRC disparities should focus on improving access of at-risk populations to high-quality comprehensive cancer care.
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Neoplasias Colorrectales/mortalidad , Disparidades en Atención de Salud/estadística & datos numéricos , Grupos Minoritarios/estadística & datos numéricos , Proveedores de Redes de Seguridad/estadística & datos numéricos , Centros Médicos Académicos/economía , Centros Médicos Académicos/estadística & datos numéricos , Adulto , Negro o Afroamericano/estadística & datos numéricos , Anciano , Asiático/estadística & datos numéricos , Neoplasias Colorrectales/economía , Neoplasias Colorrectales/terapia , Femenino , Hispánicos o Latinos/estadística & datos numéricos , Humanos , Estimación de Kaplan-Meier , Masculino , Pacientes no Asegurados/estadística & datos numéricos , Persona de Mediana Edad , Aceptación de la Atención de Salud/estadística & datos numéricos , Ensayos Clínicos Controlados Aleatorios como Asunto/estadística & datos numéricos , Estudios Retrospectivos , Proveedores de Redes de Seguridad/economía , Factores Socioeconómicos , Población Blanca/estadística & datos numéricosRESUMEN
OBJECTIVE: To determine the prevalence of health insurance and associated factors among households in urban slum settings in Nairobi, Kenya. DESIGN: The data for this study are from a cross-sectional survey of adults aged 18 years or older from randomly selected households in Viwandani slums (Nairobi, Kenya). Respondents participated in the Lown scholars' study conducted between June and July 2018. SETTING: The Lown scholars' survey was nested in the Nairobi Urban Health and Demographic Surveillance System in Viwandani slums in Nairobi, Kenya. PARTICIPANTS: A total of 300 randomly sampled households participated in the survey. The study respondents comprised of either the household head, their spouses or credible adult household members. PRIMARY OUTCOME MEASURE: The primary outcome of this study was enrolment in a health insurance programme. The households were classified into two groups: those having at least one member covered by health insurance and those without any health insurance cover. RESULTS: The prevalence of health insurance in the sample was 43%. Being unemployed (adjusted OR (aOR) 0.17; p<0.05; 95% CI 0.06 to 0.47) and seeking care from a public health facility (aOR 0.50; p<0.05; 95% CI 0.28 to 0.89) was significantly associated with lower odds of having a health insurance cover. The odds of having a health insurance cover were significantly lower among respondents who perceived their health status as good (aOR 0.62; p<0.05; 95% CI 1.17 to 5.66) and those who were unsatisfied with the cost of seeking primary care (aOR 0.34; p<0.05; 95% CI 0.17 to 0.69). CONCLUSIONS: Health insurance coverage in Viwandani slums in Nairobi, Kenya, is low. As universal health coverage becomes the growing focus of Kenya's 'Big Four Agenda' for socioeconomic transformation, integrating enabling and need factors in the design of the national health insurance package may scale-up social health protection.
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Seguro de Salud/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Aceptación de la Atención de Salud/estadística & datos numéricos , Áreas de Pobreza , Salud Urbana/estadística & datos numéricos , Poblaciones Vulnerables/estadística & datos numéricos , Adolescente , Adulto , Anciano , Participación de la Comunidad/estadística & datos numéricos , Estudios Transversales , Composición Familiar , Femenino , Humanos , Kenia/epidemiología , Masculino , Persona de Mediana Edad , Programas Nacionales de Salud , PrevalenciaRESUMEN
BACKGROUND: Undocumented migrants in Israel, mostly originating from HIV endemic countries, are not covered by Israel's universal healthcare coverage. We initiated a Public-Private Partnership (PPP) to handle this public health and humanitarian challenge. The PPP venture included the Ministry of Health (MoH), pharmaceutical companies, pharmacies, and specialized HIV clinics, the Israeli HIV Medical Society (from the Israel Medical Association), and non-governmental organizations. This study describes the national policy process in conceptualizing and implementing access to HIV services for undocumented migrants through a PPP, and analyzes the preliminary results. METHODS: This case study describes the process of creating a temporary Public-Private Partnership to provide HIV care for undocumented migrants based on institutional records of the Department of Tuberculosis and AIDS (DTA) and memories and reflections from partners. This case was analyzed according to the OECD-DAC criteria for development assistance (relevance, effectiveness, efficiency, sustainability and impact). Demographic and serological data of patients referred between 2014 to 2018 were collected to monitor progress. and analyze preliminary medical and biological outcomes. Ethical approval was obtained from the Ministry of Health. RESULTS: Creating a policy to extend HIV care to undocumented migrants was a 15 year process that confronted several challenges within Israeli and international discourse, particularly concerning governmental response to the migration crisis. The use of a PPP model involving numerous stakeholders provided a solid, local feasibility demonstration that extending HIV care as a matter of policy would have positive implications for public health in Israel. During the first 2 years of the program (2014-2015), the MoH funded medical follow-up and the pharmaceutical companies provided antiretroviral treatment (ART) free of charge for only 100 patients at any given time, in addition to ART provided by the MoH for pregnant women. Since 2016, the MoH has fully covered this service and integrated it within the Israeli health system; this constitutes the major success of the PPP program. As of December 2018, the national program has monitored 350 patients and treated 316 (90.3%). The most prevalent disease present upon referral was Tuberculosis. CONCLUSIONS: To our knowledge, this study documents the first example of a successful PPP with government partnership in a high-income country to address undocumented migrants' lack of access to health services in general and HIV care in particular. In light of the intensification of North-South migration, this Israeli case study could be useful for other countries facing similar challenges. It also has lessons within Israel, as the country grapples with other health problems among uninsured communities.
Asunto(s)
Infecciones por VIH/terapia , Accesibilidad a los Servicios de Salud/organización & administración , Formulación de Políticas , Migrantes/estadística & datos numéricos , Conducta Cooperativa , Femenino , Infecciones por VIH/epidemiología , Accesibilidad a los Servicios de Salud/legislación & jurisprudencia , Humanos , Israel/epidemiología , Masculino , Pacientes no Asegurados/legislación & jurisprudencia , Pacientes no Asegurados/estadística & datos numéricos , Programas Nacionales de Salud/legislación & jurisprudencia , Migrantes/legislación & jurisprudenciaRESUMEN
Objectives: The objective of this study was to assess the diagnosis and management of anemic patients in free clinics around the Tampa Bay area.Methods: In this retrospective study we extracted data including demographics, chronic diseases, and laboratory values from medical charts of uninsured patients seen in 9 free clinics from January 2016 through December 2017 in the Tampa Bay area, FL, USA. Multiple logistic regression analysis was used to assess relationships between socioeconomic variables and a documented history of anemia.Results: From two years of documented data, 6971 patients were included, of which 367 (5%) had a documented diagnosis of anemia. Most were women (315, 86%), and the median age was 41 years (6-91). Among the 367 patients with anemia,191 (52%) patients had an unspecified type of anemia, 144 (39%) were diagnosed with IDA, 16 (4%) with anemia of chronic disease, and the remaining were other uncommon causes. Only 67% (97/144) of IDA patients had documented iron replacement. Colonoscopies were documented in only 32 (9%) of all patients with anemia, and in 23 (16%) IDA patients. Several chronic diseases were statistically associated and comorbid with a diagnosis of anemia.Conclusions: Uninsured patients with IDA are prescribed iron and undergo colonoscopies at sub-optimal rates. Increasing resources, awareness, and education of providers in these settings could lead to improved treatment practices and decrease the risk of morbidity and mortality.
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Anemia/epidemiología , Enfermedad Crónica/epidemiología , Disparidades en Atención de Salud/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Proveedores de Redes de Seguridad/estadística & datos numéricos , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Anemia Ferropénica/tratamiento farmacológico , Anemia Ferropénica/epidemiología , Niño , Colonoscopía/estadística & datos numéricos , Femenino , Florida/epidemiología , Conductas Relacionadas con la Salud , Disparidades en el Estado de Salud , Humanos , Hierro/uso terapéutico , Modelos Logísticos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores Socioeconómicos , Adulto JovenAsunto(s)
Pueblos Indígenas/estadística & datos numéricos , Calidad de la Atención de Salud/normas , Cicatrización de Heridas , Canadá , Servicios de Salud Comunitaria/métodos , Servicios de Salud Comunitaria/normas , Humanos , Pacientes no Asegurados/estadística & datos numéricos , Calidad de la Atención de Salud/estadística & datos numéricosRESUMEN
BACKGROUND: We sought to identify treatment disparities existing prior to publication of the 2015 American Thyroid Association Management Guidelines in order to identify patients with papillary thyroid cancer (PTC) at risk for receiving inadequate treatment. METHODS: Patients diagnosed with PTC from 2011 to 2013 were identified using Surveillance, Epidemiology and End Results database. High-risk disease was defined as T4, N1, or M1. Chi-square tests compared characteristics of patients with and without high-risk disease and characteristics of high-risk patients who did and did not receive radioactive iodine ablation (RAI). Likelihoods of having high-risk disease, of receiving RAI, and of cause-specific death were calculated using regression analyses. RESULTS: Sample included 32,229 individuals; 7894 (24.5%) had high-risk disease. Mean age was 50.0 years, 24,815 (77.0%) were female, and 21,318 (66.2%) were white. Odds of high-risk disease were greater among males (OR:2.04; 95% CI:1.92-2.16), Hispanics (OR:1.67; 95% CI:1.56-1.79) and Asians (OR:1.49; 95% CI:1.37-1.62), and uninsured (OR:1.24; 95% CI:1.07-1.43), and lower among patients ages 45-64 (OR:0.57; 95% CI:0.53-0.60), and ≥65 years (OR:0.54; 95% CI:0.50-0.59), and Blacks (OR:0.46; 95% CI:0.40-0.53). Most (69.3%) high-risk patients received RAI. Odds of receiving RAI were lower among patients age ≥65 years (OR:0.67; 95% CI:0.58-0.77), uninsured (OR:0.52; 95% CI:0.41-0.67), or with Medicaid (OR:0.58; 95% CI:0.50-0.69). RAI use reduced the risk of cause-specific mortality (HR:0.29; 95% CI:0.18-0.47). CONCLUSION: Knowledge of these treatment disparities will allow recognition of groups at risk for high-risk disease and receiving inadequate treatment.
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Disparidades en Atención de Salud/estadística & datos numéricos , Radioisótopos de Yodo/uso terapéutico , Disección del Cuello , Pautas de la Práctica en Medicina/estadística & datos numéricos , Cáncer Papilar Tiroideo/radioterapia , Neoplasias de la Tiroides/radioterapia , Tiroidectomía , Adulto , Negro o Afroamericano/estadística & datos numéricos , Factores de Edad , Anciano , Asiático/estadística & datos numéricos , Etnicidad/estadística & datos numéricos , Femenino , Disparidades en Atención de Salud/etnología , Hispánicos o Latinos/estadística & datos numéricos , Humanos , Modelos Logísticos , Masculino , Medicaid/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Persona de Mediana Edad , Estadificación de Neoplasias , Oportunidad Relativa , Modelos de Riesgos Proporcionales , Radioterapia Adyuvante/estadística & datos numéricos , Riesgo , Programa de VERF , Factores Sexuales , Cáncer Papilar Tiroideo/mortalidad , Cáncer Papilar Tiroideo/patología , Neoplasias de la Tiroides/mortalidad , Neoplasias de la Tiroides/patología , Estados Unidos , Población Blanca/estadística & datos numéricosRESUMEN
Taiwanese Labor, Government Employee, and Farmer Insurance programs provide 5 to 6 months of salary to enrollees who undergo hysterectomies or oophorectomies before their 45th birthday. These programs create incentives for more and earlier treatments, referred to as inducement and timing effects. Using National Health Insurance data between 1997 and 2011, we estimate these effects on surgery hazards by difference-in-difference and bunching-smoothing polynomial methods. For Government Employee and Labor Insurance, inducement is 11-12% of all hysterectomies, and timing 20% of inducement. For oophorectomies, both effects are insignificant. Enrollees' behaviors are consistent with rational choices. Each surgery qualifies an enrollee for the same benefit, but oophorectomy has more adverse health consequences than hysterectomy. Induced hysterectomies increase benefit payments and surgical costs, at about the cost of a mammogram and 5 pap smears per enrollee.
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Histerectomía/economía , Seguro por Discapacidad/economía , Adulto , Factores de Edad , Femenino , Humanos , Histerectomía/estadística & datos numéricos , Seguro/economía , Seguro por Discapacidad/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Persona de Mediana Edad , Modelos Econométricos , Programas Nacionales de Salud/economía , Programas Nacionales de Salud/estadística & datos numéricos , Ovariectomía/economía , Ovariectomía/estadística & datos numéricos , Medición de Riesgo , TaiwánRESUMEN
OBJECTIVE: Half of the TB patients in India seek care from private providers resulting in incomplete notification, varied quality of care and out-of-pocket expenditure. The objective of this study was to describe the characteristics of TB patients who remain outside the coverage of treatment in public health services. METHODS: Cross-sectional data from National Family Health Survey-4 (2015-16) were analysed using logistic regression analysis. TB treatment was the dependent variable. Sociodemographic factors and place where households generally seek treatment were independent variables. RESULTS: Prevalence of self-reported TB was 308.17/100 000 population (95% CI: 309.44-310.55/100 000 population) and 38.8% (95% CI: 36.5-41.1%) of TB patients were outside care of public health services - 3.3% did not seek treatment and 35.3% accessed treatment from private sector. Factors associated with not seeking treatment were age <10 years [OR = 3.43; 95% CI (1.52-7.77); P = 0.00]; no/preschool education [OR = 1.82; 95% CI (1.10-3.34); P = 0.02]; poorest wealth index [OR = 1.86; 95% CI (1.01-3.34); P = 0.04] and household's general rejection of the public sector when seeking health care [OR = 1.69; 95% CI (1.69-2.26); P = 0.00]. Factors associated with seeking treatment from private providers were female sex [OR = 1.29; 95% CI (1.11-1.50); P = 0.001], younger age of the patient [OR = 2.39; 95% CI (1.62-3.53); P = 0.00], higher education [OR = 1.82; 95% CI (1.11-2.98); P = 0.02] and household's general rejection of the public sector when seeking health care [OR = 4.56; 95% CI (3.95-5.27); P = 0.00]. Patients from households reporting 'poor quality of care' as the reason for not generally preferring public health services were more likely (OR = 1.48, 95% CI = 1.19-1.65; P = 00) to access private treatment. CONCLUSION: The study provides insights for efforts to involve the private health sector for accurate surveillance and patient groups requiring targeted interventions for linking them to the national programme.
Asunto(s)
Cobertura del Seguro/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Sector Público/estadística & datos numéricos , Tuberculosis/epidemiología , Tuberculosis/terapia , Adolescente , Adulto , Anciano , Niño , Estudios Transversales , Femenino , Humanos , India , Masculino , Persona de Mediana Edad , Programas Nacionales de Salud , Aceptación de la Atención de Salud/estadística & datos numéricos , Pobreza/estadística & datos numéricos , Prevalencia , Adulto JovenRESUMEN
This study was designed to assess the reasons for health insurance coverage in a population covered by the Family Health Strategy in Brazil. We describe overall health insurance coverage and according to types, and analyze its association with health-related and socio-demographic characteristics. Among the 31.3% of persons (95%CI: 23.8-39.9) who reported "health insurance" coverage, 57.0% (95%CI: 45.2-68.0) were covered only by discount cards, which do not offer any kind of coverage for medical care, but only discounts in pharmacies, clinics, and hospitals. Both for health insurance and discount cards, the most frequently cited reasons for such coverage were "to be on the safe side" and "to receive better care". Both types of coverage were associated statistically with age (+65 vs. 15-24 years: adjusted odds ratios, aOR = 2.98, 95%CI: 1.28-6.90; and aOR = 3.67; 95%CI: 2.22-6.07, respectively) and socioeconomic status (additional standard deviation: aOR = 2.25, 95%CI: 1.62-3.14; and aOR = 1.96, 95%CI: 1.34-2.97). In addition, health insurance coverage was associated with schooling (aOR = 7.59, 95%CI: 4.44-13.00) for complete University Education and aOR = 3.74 (95%CI: 1.61-8.68) for complete Secondary Education, compared to less than complete Primary Education. Meanwhile, neither health insurance nor discount card was associated with health status or number of diagnosed diseases. In conclusion, studies that aim to assess private health insurance should be planned to distinguish between discount cards and formal health insurance.
Resumo: Este estudo foi desenhado para avaliar a cobertura por plano de saúde e seus motivos em uma população coberta pela Estratégia Saúde da Família. Nesta análise, descrevemos a cobertura por plano de saúde, total e por tipos, e analisamos sua associação com características de saúde e sociodemográficas. Entre os 31,3% (IC95%: 23,8-39,9) de pessoas que relatavam cobertura por "plano de saúde", 57,0% (IC95%: 45,2-68,0) estavam cobertos por cartões de desconto, que não oferecem qualquer tipo de cobertura para assistência médica, apenas descontos em farmácias, clínicas e hospitais. Tanto no caso dos planos de saúde quanto no dos cartões de desconto, os motivos para cobertura mais frequentemente relatados foram "para a segurança" e "para ter melhor atendimento". Ambas as coberturas se associaram à idade (65+ versus 15-24 anos: odds ratio ajustada, ORa = 2,98; IC95%: 1,28-6,90; e ORa = 3,67; IC95%: 2,22-6,07, respectivamente) e ao nível econômico (desvio padrão adicional: ORa = 2,25; IC95%: 1,62-3,14; e ORa = 1,96; IC95%: 1,34-2,97). Além disso, a cobertura por plano de saúde se associou à escolaridade (ORa = 7,59; IC95%: 4,44-13,00) para Ensino Superior completo e ORa = 3,74 (IC95%: 1,61-8,68) para Ensino Médio completo, em comparação a menos do que o Ensino Fundamental completo. Por outro lado, nem a cobertura por plano de saúde nem a por cartão de desconto se mostraram associadas ao estado de saúde ou ao número de doenças diagnosticadas. Em conclusão, estudos que pretendam avaliar a cobertura por saúde suplementar deveriam ser planejados de forma a poderem distinguir entre cartões de desconto e planos de saúde formais.
Resumen: Este estudio se diseñó para evaluar la cobertura por seguro de salud y sus causas en una población cubierta por la Estrategia Salud de la Familia. En este análisis, describimos la cobertura por seguro de salud, total y por tipos, y analizamos su asociación con características de salud y sociodemográficas. Dentro del 31,3% (IC95%: 23,8-39,9) de personas que informaban contar con una cobertura por "seguro de salud" un 57,0% (IC95%: 45,2-68,0) estaban cubiertas por tarjetas de descuento, que no ofrecen cualquier tipo de cobertura para la asistencia médica, solamente descuentos en farmacias, clínicas y hospitales. Tanto en el caso de los seguros de salud, como en el de las tarjetas de descuento, los motivos de cobertura más frecuentemente relatados fueron "por seguridad" y "para tener una mejor atención". Ambas coberturas se asociaron a la edad (65+ versus 15-24 años: odds ratio ajustada, ORa = 2,98; IC95%: 1,28-6,90; y ORa = 3,67; IC95%: 2,22-6,07, respectivamente), y al nivel económico (desvío patrón adicional: ORa = 2,25; IC95%: 1,62-3,14; y ORa = 1,96; IC95%: 1,34-2,97). Además, la cobertura por seguro de salud se asoció a la escolaridad (ORa = 7,59; IC95%: 4,44-13,00) para la Enseñanza Superior completa y ORa = 3,74 (IC95%: 1,61-8,68) para el Nivel Medio completo, en comparación con los menores índices por la Enseñanza Fundamental completa. Por otro lado, ni la cobertura por seguro de salud, ni la por tarjeta de descuento, se mostraron asociadas al estado de salud o al número de enfermedades diagnosticadas. En conclusión, los estudios que pretendan evaluar la cobertura de seguro de salud privado se deberían planear de tal forma que puedan distinguir entre tarjetas de descuento y seguros de salud formales.
Asunto(s)
Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Seguro de Salud/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Adolescente , Adulto , Anciano , Brasil , Salud de la Familia , Femenino , Gastos en Salud/estadística & datos numéricos , Accesibilidad a los Servicios de Salud/economía , Humanos , Seguro de Salud/economía , Masculino , Persona de Mediana Edad , Programas Nacionales de Salud , Factores Socioeconómicos , Adulto JovenRESUMEN
Resumo: Este estudo foi desenhado para avaliar a cobertura por plano de saúde e seus motivos em uma população coberta pela Estratégia Saúde da Família. Nesta análise, descrevemos a cobertura por plano de saúde, total e por tipos, e analisamos sua associação com características de saúde e sociodemográficas. Entre os 31,3% (IC95%: 23,8-39,9) de pessoas que relatavam cobertura por "plano de saúde", 57,0% (IC95%: 45,2-68,0) estavam cobertos por cartões de desconto, que não oferecem qualquer tipo de cobertura para assistência médica, apenas descontos em farmácias, clínicas e hospitais. Tanto no caso dos planos de saúde quanto no dos cartões de desconto, os motivos para cobertura mais frequentemente relatados foram "para a segurança" e "para ter melhor atendimento". Ambas as coberturas se associaram à idade (65+ versus 15-24 anos: odds ratio ajustada, ORa = 2,98; IC95%: 1,28-6,90; e ORa = 3,67; IC95%: 2,22-6,07, respectivamente) e ao nível econômico (desvio padrão adicional: ORa = 2,25; IC95%: 1,62-3,14; e ORa = 1,96; IC95%: 1,34-2,97). Além disso, a cobertura por plano de saúde se associou à escolaridade (ORa = 7,59; IC95%: 4,44-13,00) para Ensino Superior completo e ORa = 3,74 (IC95%: 1,61-8,68) para Ensino Médio completo, em comparação a menos do que o Ensino Fundamental completo. Por outro lado, nem a cobertura por plano de saúde nem a por cartão de desconto se mostraram associadas ao estado de saúde ou ao número de doenças diagnosticadas. Em conclusão, estudos que pretendam avaliar a cobertura por saúde suplementar deveriam ser planejados de forma a poderem distinguir entre cartões de desconto e planos de saúde formais.
Abstract: This study was designed to assess the reasons for health insurance coverage in a population covered by the Family Health Strategy in Brazil. We describe overall health insurance coverage and according to types, and analyze its association with health-related and socio-demographic characteristics. Among the 31.3% of persons (95%CI: 23.8-39.9) who reported "health insurance" coverage, 57.0% (95%CI: 45.2-68.0) were covered only by discount cards, which do not offer any kind of coverage for medical care, but only discounts in pharmacies, clinics, and hospitals. Both for health insurance and discount cards, the most frequently cited reasons for such coverage were "to be on the safe side" and "to receive better care". Both types of coverage were associated statistically with age (+65 vs. 15-24 years: adjusted odds ratios, aOR = 2.98, 95%CI: 1.28-6.90; and aOR = 3.67; 95%CI: 2.22-6.07, respectively) and socioeconomic status (additional standard deviation: aOR = 2.25, 95%CI: 1.62-3.14; and aOR = 1.96, 95%CI: 1.34-2.97). In addition, health insurance coverage was associated with schooling (aOR = 7.59, 95%CI: 4.44-13.00) for complete University Education and aOR = 3.74 (95%CI: 1.61-8.68) for complete Secondary Education, compared to less than complete Primary Education. Meanwhile, neither health insurance nor discount card was associated with health status or number of diagnosed diseases. In conclusion, studies that aim to assess private health insurance should be planned to distinguish between discount cards and formal health insurance.
Resumen: Este estudio se diseñó para evaluar la cobertura por seguro de salud y sus causas en una población cubierta por la Estrategia Salud de la Familia. En este análisis, describimos la cobertura por seguro de salud, total y por tipos, y analizamos su asociación con características de salud y sociodemográficas. Dentro del 31,3% (IC95%: 23,8-39,9) de personas que informaban contar con una cobertura por "seguro de salud" un 57,0% (IC95%: 45,2-68,0) estaban cubiertas por tarjetas de descuento, que no ofrecen cualquier tipo de cobertura para la asistencia médica, solamente descuentos en farmacias, clínicas y hospitales. Tanto en el caso de los seguros de salud, como en el de las tarjetas de descuento, los motivos de cobertura más frecuentemente relatados fueron "por seguridad" y "para tener una mejor atención". Ambas coberturas se asociaron a la edad (65+ versus 15-24 años: odds ratio ajustada, ORa = 2,98; IC95%: 1,28-6,90; y ORa = 3,67; IC95%: 2,22-6,07, respectivamente), y al nivel económico (desvío patrón adicional: ORa = 2,25; IC95%: 1,62-3,14; y ORa = 1,96; IC95%: 1,34-2,97). Además, la cobertura por seguro de salud se asoció a la escolaridad (ORa = 7,59; IC95%: 4,44-13,00) para la Enseñanza Superior completa y ORa = 3,74 (IC95%: 1,61-8,68) para el Nivel Medio completo, en comparación con los menores índices por la Enseñanza Fundamental completa. Por otro lado, ni la cobertura por seguro de salud, ni la por tarjeta de descuento, se mostraron asociadas al estado de salud o al número de enfermedades diagnosticadas. En conclusión, los estudios que pretendan evaluar la cobertura de seguro de salud privado se deberían planear de tal forma que puedan distinguir entre tarjetas de descuento y seguros de salud formales.
Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Anciano , Adulto Joven , Pacientes no Asegurados/estadística & datos numéricos , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Seguro de Salud/estadística & datos numéricos , Factores Socioeconómicos , Brasil , Salud de la Familia , Gastos en Salud/estadística & datos numéricos , Accesibilidad a los Servicios de Salud/economía , Seguro de Salud/economía , Persona de Mediana Edad , Programas Nacionales de SaludRESUMEN
BACKGROUND: Root cause analysis is a technique used to assess systems factors related to "sentinel events"-serious adverse events within healthcare systems. This technique is commonly used to identify factors, which allowed these adverse events to occur, to target areas for improvement and to improve health care delivery systems. We sought to apply this technique to men presenting with metastatic prostate cancer (PCa). METHODS: We performed an in-depth case series analysis of 15 patients, who presented with metastatic disease at Johns Hopkins Sidney Kimmel Comprehensive Cancer Center using root cause analysis to refine a list of health system factors that lead to late stage presentation in the current era. RESULTS: Key factors in late diagnosis of PCa included lack of insurance, lack of routine PSA testing, comorbidities, reticence of patients to follow up actionable PSA, and aggressive disease. Three patients had aggressive disease that would not have been discovered at an early stage in the disease process, despite routine screening. However, analysis of the remaining 12 patients illuminated health system factors led to missing important diagnostic information, which might have led to diagnosis of PCa at a curable stage. CONCLUSIONS: The cases help highlight the need for systems based approaches to early diagnosis of PCa. A heterogeneous group of barriers to early diagnosis were identified in our series of patients including economic, health systems, and cultural factors. These findings underscore the need for individualized approaches to preventing delayed diagnosis of PCa. While limited by our single-institution scope, this approach provides a model for research and quality improvement initiatives to identify modifiable systems factors impeding appropriate diagnoses of PCa.
Asunto(s)
Detección Precoz del Cáncer , Metástasis de la Neoplasia , Neoplasias de la Próstata , Comorbilidad , Atención a la Salud/métodos , Atención a la Salud/normas , Detección Precoz del Cáncer/métodos , Detección Precoz del Cáncer/normas , Humanos , Masculino , Pacientes no Asegurados/estadística & datos numéricos , Persona de Mediana Edad , Modelos Organizacionales , Metástasis de la Neoplasia/diagnóstico , Metástasis de la Neoplasia/prevención & control , Antígeno Prostático Específico/análisis , Neoplasias de la Próstata/diagnóstico , Neoplasias de la Próstata/epidemiología , Neoplasias de la Próstata/patología , Mejoramiento de la Calidad , Medición de Riesgo/métodos , Factores de Riesgo , Vigilancia de Guardia , Estados Unidos/epidemiologíaRESUMEN
OBJECTIVE: Uninsured maternity patients comprise a small but complex group of patients and include marginalized Canadians, undocumented immigrants, visitors, and non-Canadians seeking health care and/or citizenship for their newborn. This is the first Canadian study to quantify these patients and to review health care providers' perspectives and practices of care. METHODS: Data for all deliveries in Calgary, Alberta over a 4-year period (2013-2016) were analyzed. All Calgary anaesthesiologists, family physicians, midwives, neonatologists, obstetricians, and pediatricians were surveyed about their care of these patients, ethical perspectives, and knowledge of liability protection when providing such care. RESULTS: This study found a trend of uninsured deliveries in Calgary (from 0.5% in 2013 to 0.8% in 2016; P < 0.0001) that is accounted for by non-Canadian patients. Midwives and physicians agree on provision of emergency care but not preventive care. Across medical specialties, fewer caregivers felt obliged to care for non-Canadian patients seeking citizenship for their newborn. Among physicians, 61% were aware of the Canadian Medical Protective Association's guidelines on liability coverage for non-Canadian patients, and only 28% consistently protected themselves legally. There is large variation regarding whether physicians bill for services when the patient is uninsured. CONCLUSION: In Calgary, the study observed an increase in numbers of uninsured maternity patients. Differing ethical perspectives on the care of these patients may lead to conflict within health care teams because of differences on ethical perspectives of care among team members. Health care providers require education to understand the implications and challenges of obstetrical care of non-Canadians.
Asunto(s)
Actitud del Personal de Salud , Parto Obstétrico/estadística & datos numéricos , Servicios de Salud Materna/tendencias , Pacientes no Asegurados/estadística & datos numéricos , Partería , Pautas de la Práctica en Medicina , Alberta/epidemiología , Femenino , Humanos , Embarazo , Encuestas y CuestionariosRESUMEN
Use of complementary and alternative medicine (CAM) among US children is 12% according to the 2012 National Health Interview Study. Certain pediatric populations have higher CAM use. We studied an uninsured population because limited access to care likely results in higher CAM use. We surveyed 250 uninsured patients in a free pediatric mobile clinic program. In the largely Hispanic population, rate of CAM use in the preceding 12 months was 45% among children and 59% among parents. Ninety-one percent of children who used CAM had parents who used CAM while only 32% of parents used CAM for themselves but did not use CAM for their children ( P < .001). Seven parents (3%) and 4 children (2%) had ever discussed their CAM use with a physician. Since CAM use is significant in this uninsured population and families do not generally discuss CAM with physicians, health care providers must ask about CAM use and provide guidance.
Asunto(s)
Terapias Complementarias/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Adulto , Instituciones de Atención Ambulatoria/estadística & datos numéricos , Niño , Terapias Complementarias/métodos , Femenino , Humanos , Masculino , Padres , TexasRESUMEN
Ghana has introduced a National Health Insurance Scheme (NHIS). Embedded in the NHIS is a policy to exempt poor and vulnerable groups from premiums and user fees. There has been some debate as to why the start-off age for exemption among the elderly is 70 years. Ghana has a shorter life expectancy than middle- and high-income countries and its current age of retirement is 60 years. This study explores the financial and social implications of continuing to charge premiums to people aged 60 to 69 years. Based on the analysis of data from a representative household survey, it is recommended that the exemption policy should be expanded to include all vulnerable elderly persons, regardless of age.
Asunto(s)
Política de Salud/economía , Accesibilidad a los Servicios de Salud/economía , Cobertura del Seguro/estadística & datos numéricos , Seguro de Salud/economía , Pacientes no Asegurados/estadística & datos numéricos , Anciano , Femenino , Ghana , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Humanos , Seguro de Salud/estadística & datos numéricos , Masculino , Programas Nacionales de Salud/normas , Pobreza/estadística & datos numéricos , Factores SocioeconómicosAsunto(s)
Servicios Médicos de Urgencia/normas , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Pacientes no Asegurados/estadística & datos numéricos , Seguridad del Paciente , Tiempo de Tratamiento/estadística & datos numéricos , California , Servicios de Salud Comunitaria , Prestación Integrada de Atención de Salud , Servicios Médicos de Urgencia/economía , Femenino , Humanos , MasculinoRESUMEN
INTRODUCTION: The collaborations between dental care providers and other health care providers are especially needed for underserved populations. There is a deficit of research focused on underserved populations who utilize a safety net facility such as a free clinic in the United States. The purpose of this study is to examine the association between health-related beliefs and oral health behaviors among uninsured adults utilizing a primary care free clinic providing oral health care. METHODS: Uninsured primary care patients utilizing a free clinic (N = 585) participated in a self-administered paper survey in May and June, 2016. RESULTS: More than 60% of free clinic patients reported a perceived need for dental treatment. Free clinic patients who brush their teeth more than once a day reported better perceived general health compared with those who do not brush their teeth more than once a day. Free clinic patients who had perceived a need for dental treatment reported worse perceived general health compared to those who did not report dental needs. CONCLUSIONS: The results of this study indicate a pressing need for the further development of dental care services at safety-net clinics. By including dental care in health promotion programs, it will have positive impacts not only on oral health but also on a healthy lifestyle and the general health of underserved populations utilizing a safety-net clinic. The implementation and evaluation of the integrated health programs, which include primary care and oral health care together, would be beneficial to reduce oral health disparities.
Asunto(s)
Actitud Frente a la Salud , Conductas Relacionadas con la Salud , Pacientes no Asegurados/psicología , Salud Bucal , Femenino , Necesidades y Demandas de Servicios de Salud , Estado de Salud , Humanos , Masculino , Pacientes no Asegurados/estadística & datos numéricos , Persona de Mediana Edad , Salud Bucal/estadística & datos numéricos , Atención Primaria de Salud/estadística & datos numéricos , Proveedores de Redes de Seguridad/estadística & datos numéricos , Encuestas y Cuestionarios , Cepillado Dental/estadística & datos numéricosRESUMEN
This paper examines first-generation Korean immigrants' barriers to healthcare in the US and their strategies for coping with these issues by analyzing survey data from 507 Korean immigrants and in-depth interviews with 120 Korean immigrants in the New York-New Jersey area. It reports that more than half of Korean immigrants have barriers to healthcare in the US, with the language barrier being the most frequent response, followed by having no health insurance. Korean immigrants are not passive, but rather active entities who display coping strategies for these barriers, such as seeing co-ethnic doctors in the US, seeking Hanbang (traditional Korean medicine) in the US, and taking medical tours to the home country. However, their coping strategies are far removed from formal US healthcare as their behaviors are still restricted to the informal healthcare within the ethnic community or home country. This study methodologically and theoretically contributes to the literature on immigrants' healthcare behaviors by using a mixed-method approach and developing a specific framework for one particular immigrant group.