The Drug Regimen Prescribed for Sickle Cell Patients Attending a Clinic in Kumasi, Ghana, in a Period of One Year
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Author(s)
1Department
of Biochemistry and Biotechnology, College of Science, Kwame Nkrumah
University of Science and Technology, Kumasi, Ghana.
2Department of Child Health, College of Health Sciences, School of Medical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
3Department of Child Health, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
2Department of Child Health, College of Health Sciences, School of Medical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
3Department of Child Health, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
Objective: In order to manage the varied
pathophysiological features of sickle cell disease (SCD), an array of
drugs has to be used. The specific drugs used, however, depend on the
locality. This study was aimed at finding out the drug regimen
prescribed by clinicians to sickle cell disease patients who attended a
Sickle Cell Clinic in Kumasi, Ghana. Method: The setting for the study
is the Sickle Cell Clinic at the Komfo Anokye Teaching Hospital, Ghana,
and a questionnaire was used as the study instrument. Information on
drug prescription on each day of clinic visit was extracted from the
medical records of the patients. Results: The drugs prescribed were
“routine drugs” for SCD patients, analgesics, narcotics, anti-malarials,
antibiotics, haematinics and miscellaneous drugs. The top ten commonly
prescribed drugs were folic acid, diclofenac, ibuprofen, B-complex,
routine drugs, artesunate/amodiaquin, paracetamol, penicillin V,
amoxiclav and zincovit. Conclusion: Within the year, the drugs
prescribed included those that could prevent vitamin and zinc deficiency
due to continuing haemolysis, those that could mitigate the pain and
inflammation from vaso-occlusion and reperfusion injury, as well as
antibiotics to combat infections. Being a malarial-endemic region,
prophylaxis with daraprim and symptomatic malaria fever therapy were
common practices. This study has thus shown that the well-being of SCD
patients in our typical tropical terrain, depends on haematinic
vitamin/mineral supplements, anti-malarials,
analgesics-anti-inflammatory, antipyretics and antibiotics.
KEYWORDS
Cite this paper
Nsiah, K. , Osei-Akoto, A. and Ansong, D. (2014)
The Drug Regimen Prescribed for Sickle Cell Patients Attending a Clinic
in Kumasi, Ghana, in a Period of One Year. Open Journal of Blood Diseases, 4, 50-57. doi: 10.4236/ojbd.2014.44007.
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