Adewoyin Ademola Samson, Oghuvwu Omokiniovo Sunday, Awodu Omolade Augustina
Department of Haematology and Blood Transfusion, University of Benin Teaching Hospital, PMB 1111, Benin City, Nigeria.
Department of Internal Medicine, Clinical Pharmacology and Therapeutics Unit, University of Benin Teaching Hospital, PMB 1111, Benin City, Nigeria.
Afr Health Sci. 2017 Mar;17(1):255-261. doi: 10.4314/ahs.v17i1.31.
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.
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.
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.
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.
在尼日利亚的环境中,需要对羟基脲疗法治疗镰状细胞病(SCD)的临床前景进行评估,以制定本土指南。本调查研究了尼日利亚SCD患者中羟基脲疗法的模式、其临床血液学益处和安全性。
在3个月内对60名成年SCD患者进行了横断面试点调查。通过访谈过程和病例档案审查,使用结构化问卷获取了关于临床表型、相关血液学参数和羟基脲疗法细节的数据。
中位年龄为30岁。34名(56.7%)受试者知晓SCD中的羟基脲疗法。24名(4%)SCD患者曾使用过羟基脲。只有4名受试者完全依从。不依从的原因包括知识匮乏和资金短缺。特别是,羟基脲使依从性受试者的白细胞计数降低,平均红细胞体积(MCV)增加。
尽管羟基脲在发达国家已被证明有效/具有临床前景,但在尼日利亚SCD患者中的使用较少。需要进行大规模多中心研究和临床试验,为制定其使用的标准本地治疗方案奠定基础。