Document Type

Article

Publication Date

2-23-2021

Comments

This is an Accepted Manuscript of an article published by Taylor & Francis in Hemoglobin on Februrary 23, 2021, available online: https://doi.org/10.1080/03630269.2021.1889582.

Abstract

Transition of adolescents with sickle cell disease to adult programs is associated with increased morbidity and mortality. The reasons for this poor outcome are not well known. This report describes the various factors that affect the outcome of the transition process. These include four inter-personal factors: country of residence, region within the country of residence, the health care system and intra-personal factors. Each factor is described in some detail. Understanding these factors and the establishment of guidelines or recommendations could improve the outcome of this critical transition in the life of patients with sickle cell disease.

Language

English

Available for download on Wednesday, February 23, 2022

Included in

Hematology Commons

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