The Prevalence of Cholelithiasis in Nigerians with Sickle Cell Disease as Diagnosed by Ultrasound

Agholor, C. A. and Akhigbe, A. O. and Atalabi, O. M. (2014) The Prevalence of Cholelithiasis in Nigerians with Sickle Cell Disease as Diagnosed by Ultrasound. British Journal of Medicine and Medical Research, 4 (15). pp. 2866-2873. ISSN 22310614

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Abstract

Aim: To determine the prevalence of cholelithiasis in Nigerians with sickle cell disease in steady state, using ultrasonography.
Study Design: A prospective cross-sectional study.
Place and Duration of Study: Haematology Clinic, University of Benin Teaching Hospital, Benin City and Sickle Cell Centre, Benin City, Nigeria between July and December 2011.
Methodology: The study population was made up of non-pregnant sickle cell disease patients not in crisis and who have not had cholecystectomy. They were confirmed to have sickle cell disease through haemoglobin electrophoresis. All the patients were examined with a B-mode ultrasound machine with a curvilinear multifrequency transducer 2.5-7.5MHZ after an overnight or at least six hour fast. Calculi were diagnosed if highly echogenic structures, with acoustic shadowing were detected in the lumen of the gallbladder.
Results: There were 79 females and 71 males, aged between 10 months and 51 years. Of the 150 patients, 140 were homozygous for sickle cell disease (HbSS), while the remaining 10 were heterozygous for sickle cell disease (HbSC). The prevalence of cholelithiasis was 16.0%. It was related to age, sex and haemoglobin genotype. There was progressive increase in cholelithiasis with age which was more pronounced in the third and fourth decades. Cholelithiasis was also significantly more commonly seen in the HbSS group 23 (16.4%) out of 140 patients compared with the HbSC group 1 (10.0%) out of 10 patients. Cholelithiasis did not correlate with sex, although it was more commonly observed in females. The youngest patient with gall stones in this study was 2 years.
Conclusion: The prevalence of cholelithiasis in Nigerians with sickle cell disease was 16.0% and it was related to age and haemoglobin genotype.

Item Type: Article
Subjects: Pustaka Library > Medical Science
Depositing User: Unnamed user with email support@pustakalibrary.com
Date Deposited: 13 Jun 2023 05:03
Last Modified: 13 Jan 2024 04:49
URI: http://archive.bionaturalists.in/id/eprint/1155

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