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Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine

Hydroxyurea (HU) alone has the potential to prevent one out of every three deaths due to sickle cell disease (SCD) and almost all forms of disabilities caused by SCD. However, in Tanzania, only one out of every six registered SCD patients in the SPARCO-Tanzania Sickle Cell Cohort use HU. We conducte...

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Autores principales: Kilonzi, Manase, Mlyuka, Hamu, Jonathan, Agnes, Tutuba, Hilda, Chirande, Lulu, Rugajo, Paschal, Kida, Irene, Balandya, Emmanuel, Makani, Julie, Sirili, Nathanael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457563/
https://www.ncbi.nlm.nih.gov/pubmed/37638133
http://dx.doi.org/10.12688/f1000research.111300.1
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author Kilonzi, Manase
Mlyuka, Hamu
Jonathan, Agnes
Tutuba, Hilda
Chirande, Lulu
Rugajo, Paschal
Kida, Irene
Balandya, Emmanuel
Makani, Julie
Sirili, Nathanael
author_facet Kilonzi, Manase
Mlyuka, Hamu
Jonathan, Agnes
Tutuba, Hilda
Chirande, Lulu
Rugajo, Paschal
Kida, Irene
Balandya, Emmanuel
Makani, Julie
Sirili, Nathanael
author_sort Kilonzi, Manase
collection PubMed
description Hydroxyurea (HU) alone has the potential to prevent one out of every three deaths due to sickle cell disease (SCD) and almost all forms of disabilities caused by SCD. However, in Tanzania, only one out of every six registered SCD patients in the SPARCO-Tanzania Sickle Cell Cohort use HU. We conducted studies to understand factors influencing utilization of HU in Tanzania and discovered that among the reason for low utilization of HU include HU is classified as anticancer medication, only hematologists are supposed to prescribe HU, limited HU prescription to only National and Specialized hospitals, a special permit is required to access HU using National Health Insurance Fund (NHIF) scheme and limited importation and absence of local manufacturing of HU limit availability of this important drug in Tanzania. Therefore, with this brief, the government should allow prescription of HU to the district hospitals level, should allow all clinicians with a minimum of a Bachelor of Medicine to prescribe HU, and accessibility of HU through NHIF should be friendly.
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spelling pubmed-104575632023-08-27 Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine Kilonzi, Manase Mlyuka, Hamu Jonathan, Agnes Tutuba, Hilda Chirande, Lulu Rugajo, Paschal Kida, Irene Balandya, Emmanuel Makani, Julie Sirili, Nathanael F1000Res Policy Brief Hydroxyurea (HU) alone has the potential to prevent one out of every three deaths due to sickle cell disease (SCD) and almost all forms of disabilities caused by SCD. However, in Tanzania, only one out of every six registered SCD patients in the SPARCO-Tanzania Sickle Cell Cohort use HU. We conducted studies to understand factors influencing utilization of HU in Tanzania and discovered that among the reason for low utilization of HU include HU is classified as anticancer medication, only hematologists are supposed to prescribe HU, limited HU prescription to only National and Specialized hospitals, a special permit is required to access HU using National Health Insurance Fund (NHIF) scheme and limited importation and absence of local manufacturing of HU limit availability of this important drug in Tanzania. Therefore, with this brief, the government should allow prescription of HU to the district hospitals level, should allow all clinicians with a minimum of a Bachelor of Medicine to prescribe HU, and accessibility of HU through NHIF should be friendly. F1000 Research Limited 2022-05-20 /pmc/articles/PMC10457563/ /pubmed/37638133 http://dx.doi.org/10.12688/f1000research.111300.1 Text en Copyright: © 2022 Kilonzi M et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Policy Brief
Kilonzi, Manase
Mlyuka, Hamu
Jonathan, Agnes
Tutuba, Hilda
Chirande, Lulu
Rugajo, Paschal
Kida, Irene
Balandya, Emmanuel
Makani, Julie
Sirili, Nathanael
Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine
title Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine
title_full Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine
title_fullStr Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine
title_full_unstemmed Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine
title_short Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine
title_sort promoting access of hydroxyurea to sickle cell disease individuals: time to make it an essential medicine
topic Policy Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457563/
https://www.ncbi.nlm.nih.gov/pubmed/37638133
http://dx.doi.org/10.12688/f1000research.111300.1
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