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1.
Am J Nephrol ; 46(2): 165-175, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28787713

RESUMEN

BACKGROUND: The persistent challenges of bridging healthcare disparities for African Americans (AAs) in need of kidney transplantation continue to be unresolved at the national level. This healthcare disparity is multifactorial: stemming from limited kidney donors suitable for AAs; inconsistent care coordination and suboptimal risk factor control; social determinants, low socioeconomic status, reduced access to care; and mistrust of clinicians and the healthcare system. SUMMARY: There are numerous opportunities to significantly lessen the disparities in kidney transplantation for AAs through the following measures: the adoption of new care and patient engagement models that include education, enhanced practice-level cultural sensitivity, and timely referral as well as increased research on the impact of the environment on genetic risk, and implementation of new transplantation-related policies. Key Messages: This systematic review describes pretransplant concerns related to access to kidney transplantation, posttransplant complications, and policy interventions to address the challenging issues associated with kidney transplantation in AAs.


Asunto(s)
Negro o Afroamericano/estadística & datos numéricos , Política de Salud , Disparidades en Atención de Salud/etnología , Fallo Renal Crónico/terapia , Trasplante de Riñón/estadística & datos numéricos , Negro o Afroamericano/genética , Pruebas Genéticas , Rechazo de Injerto/etnología , Rechazo de Injerto/genética , Accesibilidad a los Servicios de Salud , Disparidades en Atención de Salud/estadística & datos numéricos , Humanos , Fallo Renal Crónico/etnología , Fallo Renal Crónico/genética , Trasplante de Riñón/efectos adversos , Trasplante de Riñón/legislación & jurisprudencia , Trasplante de Riñón/métodos , Educación del Paciente como Asunto , Resultado del Tratamiento , Estados Unidos
2.
Am J Nephrol ; 46(2): 176-186, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28787720

RESUMEN

BACKGROUND: African Americans (AAs) suffer the widest gaps in chronic kidney disease (CKD) outcomes compared to Caucasian Americans (CAs) and this is because of the disparities that exist in both health and healthcare. In fact, the prevalence of CKD is 3.5 times higher in AAs compared to CAs. The disparities exist at all stages of CKD. Importantly, AAs are 10 times more likely to develop hypertension-related kidney failure and 3 times more likely to progress to kidney failure compared to CAs. SUMMARY: Several factors contribute to these disparities including genetic and social determinants, late referrals, poor care coordination, medication adherence, and low recruitment in clinical trials. Key Messages: The development and implementation of CKD-related evidence-based approaches, such as clinical and social determinant assessment tools for medical interventions, more widespread outreach programs, strategies to improve medication adherence, safe and effective pharmacological treatments to control or eliminate CKD, as well as the use of health information technology, and patient-engagement programs for improved CKD outcomes may help to positively impact these disparities among AAs.


Asunto(s)
Negro o Afroamericano/estadística & datos numéricos , Accesibilidad a los Servicios de Salud/tendencias , Disparidades en Atención de Salud/etnología , Diálisis Renal/tendencias , Insuficiencia Renal Crónica/terapia , Negro o Afroamericano/genética , Apolipoproteína L1/genética , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Disparidades en Atención de Salud/estadística & datos numéricos , Disparidades en Atención de Salud/tendencias , Humanos , Educación del Paciente como Asunto , Participación del Paciente/tendencias , Atención Dirigida al Paciente/estadística & datos numéricos , Atención Dirigida al Paciente/tendencias , Variantes Farmacogenómicas , Diálisis Renal/estadística & datos numéricos , Insuficiencia Renal Crónica/etnología , Insuficiencia Renal Crónica/genética , Factores Socioeconómicos , Estados Unidos
3.
Am J Nephrol ; 46(2): 156-164, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28787724

RESUMEN

BACKGROUND: Chronic kidney disease is a progressive disease, which terminates in end-stage renal diseases (ESRD) that requires either dialysis or kidney transplantation for the patient to survive. There is an alarming trend in the disparities of ESRD in African Americans (AAs). Currently, AAs represent more than 30% of incident ESRD cases, yet they constitute 15% of the overall US population. Despite the reductions in mortality, increases in access to patient-centered home dialysis and preemptive kidney transplantation for the overall US ESRD population over the last decade, disparities in the care of AAs with ESRD remain largely unaffected. SUMMARY: This review discusses patient-, community-, and practitioner-related factors that contribute to disparities in ESRD care for AAs. In particular, the review addresses issues related to end-of-life support, the importance of Apolipoprotein-1 gene variants, and the advent of pharmacogenomics toward achieving precision care. The need for accessible clinical intelligence for the ESRD population is discussed. Several interventions and a call to action to address the disparities are presented. Key Messages: Significant disparities in ESRD care exist for AAs. Strategies to enhance patient engagement, education, accountable partnerships, and clinical intelligence may reduce these disparities.


Asunto(s)
Negro o Afroamericano/estadística & datos numéricos , Disparidades en Atención de Salud/etnología , Fallo Renal Crónico/terapia , Trasplante de Riñón/tendencias , Diálisis Renal/tendencias , Negro o Afroamericano/genética , Apolipoproteína L1/genética , Progresión de la Enfermedad , Disparidades en Atención de Salud/estadística & datos numéricos , Disparidades en Atención de Salud/tendencias , Humanos , Fallo Renal Crónico/etnología , Fallo Renal Crónico/genética , Trasplante de Riñón/estadística & datos numéricos , Educación del Paciente como Asunto , Participación del Paciente , Variantes Farmacogenómicas , Estados Unidos
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