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1.
J Clin Rheumatol ; 28(4): 183-189, 2022 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-35616508

RESUMEN

BACKGROUND: The patient-doctor relationship (PDR) is a complex phenomenon with strong cultural determinants, which impacts health-related outcomes and, accordingly, does have ethical implications. The study objective was to describe the PDR from medical encounters between 600 Mexican outpatients with rheumatic diseases and their attending rheumatologists, and to identify factors associated with a good PDR. METHODS: A cross-sectional study was performed. Patients completed the PDRQ-9 (Patient-Doctor Relationship Questionnaire, 9 items), the HAQ-DI (Health Assessment Questionnaire Disability Index), the Short-Form 36 items (SF-36), a pain-visual analog scale, and the Ideal Patient Autonomy Scale. Relevant sociodemographic, disease-related, and treatment-related variables were obtained. Patients assigned a PDRQ-9 score to each patient-doctor encounter. Regression analysis was used to identify factors associated with a good PDR, which was defined based on a cutoff point established using the borderline performance method. RESULTS: Patients were primarily middle-aged female subjects (86%), with substantial disease duration (median, 11.1 years), without disability (HAQ-DI within reference range, 55.3%), and with deteriorated quality of life (SF-36 out of reference range, 73.7%-78.6%). Among them, 36.5% had systemic lupus erythematosus and 31.8% had rheumatoid arthritis. There were 422 patients (70.3%) with a good PDR and 523 medical encounters (87.2%) involved certified rheumatologists.Patient paternalistic ideal of autonomy (odds ratio [OR], 3.029; 95% confidence interval [CI], 1.793-5.113), SF-36 score (OR, 1.014; 95% CI, 1.003-1.025), female sex (OR, 0.460; 95% CI, 0.233-0.010), and being certified rheumatologist (OR, 1.526; 95% CI, 1.059-2.200) were associated with a good PDR. CONCLUSIONS: Patient-related factors and the degree of experience of the attending physician impact the quality of the PDR, in Mexican outpatients with rheumatic diseases.


Asunto(s)
Calidad de Vida , Enfermedades Reumáticas , Estudios Transversales , Evaluación de la Discapacidad , Femenino , Humanos , Persona de Mediana Edad , Relaciones Médico-Paciente , Enfermedades Reumáticas/terapia , Encuestas y Cuestionarios
2.
PLoS One ; 15(10): e0240897, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33119715

RESUMEN

INTRODUCTION: In patient-doctor interaction both parties play a role. Primary objective was to determine if the concordance among rheumatologists and their patients of their ideal of autonomy was associated with a better patient-doctor relationship. Secondary objective was to describe factors associated to a patient paternalistic ideal of autonomy (PPIA). MATERIALS AND METHODS: This cross-sectional study had 3 steps. Step-1 consisted in translation/cultural local adaption of Ideal Patient Autonomy Scale (IPAS), a 14-items Dutch questionnaire. Step-2 consisted of IPAS validity and reliability in 201 outpatients. Step-3 consisted of the application of IPAS and the patient-doctor relationship questionnaire (PDRQ) to 601 outpatients with a medical encounter, and of IPAS to the 21 attending rheumatologists. Each patient-physician encounter was classified into with/without concordance in the ideal of autonomy and PRDQ scores were compared (Man Whitney U test). Regression analysis was used for associations. RESULTS: Step-1 followed ISPOR task force recommendations. Patients from Step-2 and Step-3 were representative outpatients with rheumatic diseases. IPAS structure underwent a modification; the 14 items were redistributed into four subscales, further combined into PPIA vs. patient-centered autonomy ideal. IPAS was valid and reliable. There were 497 patients with a preferred ideal of autonomy, primarily (84.9%) PPIA. There were 363 patient-doctor encounters with concordance in the autonomy ideal and their PDRQ-9 scores were higher. Religious beliefs and higher PDRQ-9 item 8 score ("I feel pleased with my doctor´s treatment") were associated to a PPIA. CONCLUSIONS: Concordance of autonomy ideal among patients and their rheumatologists positively impacts on the patient-doctor relationship.


Asunto(s)
Pacientes/psicología , Relaciones Médico-Paciente , Médicos/psicología , Enfermedades Reumáticas/epidemiología , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Atención Primaria de Salud , Psicometría , Enfermedades Reumáticas/psicología , Reumatólogos/psicología , Encuestas y Cuestionarios
4.
Am J Kidney Dis ; 67(3): 499-506, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26709109

RESUMEN

The costs of health care place developing countries under enormous economic pressure. Latin America is a region characterized by wide ethnic and per capita gross domestic product variations among different countries. Chronic kidney failure prevalence and incidence, as well as provision of renal replacement therapy (RRT), have increased in all Latin American countries over the last 20 years. From an ethical point of view, life-sustaining therapies such as RRT should be available to all patients with chronic kidney disease who might benefit. However, even among Latin American countries with similar per capita incomes and health care expenditures, only some have been able to achieve universal access to RRT. This indicates that it is not just a problem of wealth or distribution of scarce health care resources, but one of social justice. Strategies to increase the availability of RRT and renal palliative-supportive care, as well as implementation of interventions to prevent chronic kidney disease development and progression, are needed in Latin America and other developing countries.


Asunto(s)
Costos y Análisis de Costo/estadística & datos numéricos , Asignación de Recursos para la Atención de Salud , Disparidades en Atención de Salud , Fallo Renal Crónico , Terapia de Reemplazo Renal , Países en Desarrollo , Asignación de Recursos para la Atención de Salud/organización & administración , Asignación de Recursos para la Atención de Salud/estadística & datos numéricos , Disparidades en Atención de Salud/ética , Disparidades en Atención de Salud/estadística & datos numéricos , Humanos , Incidencia , Fallo Renal Crónico/economía , Fallo Renal Crónico/epidemiología , Fallo Renal Crónico/terapia , América Latina/epidemiología , Prevalencia , Terapia de Reemplazo Renal/ética , Terapia de Reemplazo Renal/métodos , Terapia de Reemplazo Renal/estadística & datos numéricos
5.
Hastings Cent Rep ; 19(4): S27-9, 1989.
Artículo en Inglés | MEDLINE | ID: mdl-11650229

RESUMEN

KIE: Agazzi's bibliographic essay of recent titles in Italian on biomedical issues also discusses the Catholic versus the secular approaches to bioethics in Italy. Among the publications mentioned are several of a philosophical or theological nature: M. Mori's volume on artificial insemination, and second editions of well-established textbooks on biomedical ethics by S. Leone, E. Sgreccia, S. Spinsanti, and D. Tettamanzi. Legal issues in reproductive technologies are addressed in the Santosuosso Commission's report on regulating artificial procreation, and in a book discussing the report. Secular writings on ethical issues have appeared in issues cited here of the journals Prospettive Settanta and Biblioteca della Libertà. Also mentioned in Agazzi's essay are a critique of the Vatican Congregation for the Doctrine of the Faith's Instruction on Respect for Human Life, and a booklet of articles related to the 20th anniversary of the encyclical Humanae Vitae.^ieng


Asunto(s)
Bioética , Discusiones Bioéticas , Catolicismo , Humanos , Italia , Jurisprudencia , Filosofía , Religión , Técnicas Reproductivas Asistidas , Teología
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