Literature DB >> 29026400

Hydroxyurea therapy in adult Nigerian sickle cell disease: a monocentric survey on pattern of use, clinical effects and patient's compliance.

Ademola Samson Adewoyin1, Omokiniovo Sunday Oghuvwu2, Omolade Augustina Awodu1.   

Abstract

BACKGROUND: The clinical prospects of hydroxyurea therapy in the management of sickle cell disease (SCD) require evaluation in the Nigerian setting to develop indigenous guidelines. This survey examines the pattern of hydroxyurea therapy, its clinico-haematologic benefits and safety profile in Nigerian SCD subjects.
METHODS: A cross sectional pilot survey was carried out among 60 adult SCD subjects over 3 months. Data on clinical phenotypes, relevant haematological parameters and details of hydroxyurea therapy were obtained using a structured questionnaire through an interview process and case file review.
RESULTS: The median age was 30 years. Thirty-four (56.7%) of the subjects are aware of hydroxyurea therapy in SCD. Twenty-four (40%) SCD patients had previously used hydroxyurea. Only 4 subjects were fully compliant. Reasons for non-compliance included poor knowledge and lack of funds. In particular, hydroxyurea reduced leucocyte count and increased mean red cell volume (MCV) in compliant subjects.
CONCLUSION: Hydroxyurea use is low among Nigerian SCD subjects despite its proven efficacy/clinical prospects in the developed nations. Large scale multicenter studies and clinical trials are needed to form a basis for developing standard local treatment protocol for its use.

Entities:  

Keywords:  Hydroxyurea therapy; Nigerian sickle cell disease; clinical effects; patient's compliance; pattern of use

Mesh:

Substances:

Year:  2017        PMID: 29026400      PMCID: PMC5636256          DOI: 10.4314/ahs.v17i1.31

Source DB:  PubMed          Journal:  Afr Health Sci        ISSN: 1680-6905            Impact factor:   0.927


  29 in total

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Authors:  David C Rees
Journal:  Haematologica       Date:  2011-04       Impact factor: 9.941

Review 2.  Hydroxyurea for sickle cell disease.

Authors:  S Davies; A Olujohungbe
Journal:  Cochrane Database Syst Rev       Date:  2001

3.  Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease.

Authors:  H Hawker; H Neilson; R J Hayes; G R Serjeant
Journal:  Br J Haematol       Date:  1982-01       Impact factor: 6.998

Review 4.  What is the evidence that hydroxyurea improves health-related quality of life in patients with sickle cell disease?

Authors:  Deepika S Darbari; Julie A Panepinto
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2012

5.  Five years of experience with hydroxyurea in children and young adults with sickle cell disease.

Authors:  A Ferster; P Tahriri; C Vermylen; G Sturbois; F Corazza; P Fondu; C Devalck; M F Dresse; W Feremans; K Hunninck; M Toppet; P Philippet; C Van Geet; E Sariban
Journal:  Blood       Date:  2001-06-01       Impact factor: 22.113

6.  Sickle cell disease clinical phenotypes in children from South-Western, Nigeria.

Authors:  S A Adegoke; O O Adeodu; A D Adekile
Journal:  Niger J Clin Pract       Date:  2015 Jan-Feb       Impact factor: 0.968

Review 7.  Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.

Authors:  Sophie Lanzkron; John J Strouse; Renee Wilson; Mary Catherine Beach; Carlton Haywood; HaeSong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

Review 8.  Hydroxyurea for children with sickle cell disease.

Authors:  Matthew M Heeney; Russell E Ware
Journal:  Pediatr Clin North Am       Date:  2008-04       Impact factor: 3.278

9.  Pathophisiology of sickle cell disease and new drugs for the treatment.

Authors:  Lucia De Franceschi
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-12-20       Impact factor: 2.576

Review 10.  Hypertransfusion therapy in sickle cell disease in Nigeria.

Authors:  Ademola Samson Adewoyin; Jude Chike Obieche
Journal:  Adv Hematol       Date:  2014-08-07
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Journal:  J Trop Pediatr       Date:  2020-06-01       Impact factor: 1.165

4.  Implementation of the therapeutic use of hydroxyurea for sickle cell disease management in resource-constrained settings: a systematic review of adoption, cost and acceptability.

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Journal:  PLoS One       Date:  2021-02-17       Impact factor: 3.240

6.  Level of utilization and provider-related barriers to the use of hydroxyurea in the treatment of sickle cell disease patients in Jos, North-Central Nigeria.

Authors:  Akinyemi Od Ofakunrin; Edache S Okpe; Tolulope O Afolaranmi; Rasaq R Olaosebikan; Patience U Kanhu; Kehinde Adekola; Nantok Dami; Atiene S Sagay
Journal:  Afr Health Sci       Date:  2021-06       Impact factor: 0.927

7.  Hydroxyurea usage awareness among patients with sickle-cell disease in Saudi Arabia.

Authors:  Mortadah Alsalman; Hussain Alkhalifa; Ali Alkhalifa; Mustafa Alsubie; Nora AlMurayhil; Abdulaziz Althafar; Mohammed Albarqi; Abdulrahman Alnaim; Abdul Sattar Khan
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8.  Barriers to Therapeutic Use of Hydroxyurea for Sickle Cell Disease in Nigeria: A Cross-Sectional Survey.

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Journal:  Front Genet       Date:  2022-01-19       Impact factor: 4.599

9.  Outcome of Hydroxyurea Use in SCD and Evaluation of Patients' Perception and Experience in Nigeria.

Authors:  Reuben Ikechukwu Chianumba; Akinyemi O D Ofakunrin; Jack Morrice; Olaniyi Olanrewaju; Oluseyi Oniyangi; Aisha Kuliya-Gwarzo; Uche Nnebe-Agumadu; Hezekiah Alkali Isa; Obiageli Eunice Nnodu
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  9 in total

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