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Telegenetics.
Peterlin, Borut.
Afiliación
  • Peterlin B; Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Curr Opin Pediatr ; 32(6): 739-741, 2020 12.
Article en En | MEDLINE | ID: mdl-33027215
PURPOSE OF REVIEW: The aim of the article is to provide an update on recent evidence for utilization and challenges of implementation of telegenetics in the clinical practice. RECENT FINDINGS: Implementation of telegenetics in health systems is still limited, below 10%, somewhat higher for cancer genetic counseling. Nevertheless, telegenetic services have been shown useful in the COVID pandemic. Key factors for efficient implementation include a patient-centered approach, engaging the major stakeholders, and incorporating telegenetics into existing health policies. Main barriers remain: limitations to billing and reimbursement, licensure, proper equipment and technical issues, engagement of referring providers and patients, coordination of services with local health providers, and lack of decision-making power. Further rigorous studies are needed to investigate the outcomes of telegenetics and to motivate health policies for change. SUMMARY: Despite continuous evidence of the benefits of telegenetics, its use in health systems remains limited. Further, larger, prospective, randomized, long-term studies are needed to address the outcomes.Enabling factors contributing to the implementation of telegenetics are patient-centeredness, the involvement of major stakeholders, and aligning telegenetics with the existing national health policies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Telemedicina / Asesoramiento Genético Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: Curr Opin Pediatr Asunto de la revista: PEDIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Eslovenia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Telemedicina / Asesoramiento Genético Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: Curr Opin Pediatr Asunto de la revista: PEDIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Eslovenia