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Published on: March 14, 2017
Gallstones in Ghanaian children with sickle cell disease
R Darko1, O P Rodrigues, J O Oliver-Commey
1Department of Surgery, Korle Bu Teaching Hospital, Accra, Ghana.
Insights
Gallstones are prevalent in Ghanaian children with sickle cell disease (SCD), appearing as early as age six. The study highlights a higher prevalence in males with SCD, underscoring the need for early detection and management.
Area of Science:
- Pediatric Gastroenterology
- Hematology
- Medical Imaging
Background:
- Sickle cell disease (SCD) is a genetic blood disorder associated with various complications.
- Gallstone formation is a known complication in SCD patients, but prevalence in African children is not well-defined.
- Ultrasonography is a reliable tool for diagnosing gallstones.
Purpose of the Study:
- To determine the prevalence and age of onset of gallstones in Ghanaian children with sickle cell disease (SCD) in steady state.
- To utilize ultrasonography as the primary diagnostic method.
- To investigate potential associations between gallstone prevalence and SCD genotype or splenic status.
Main Methods:
- A prospective, cross-sectional study was conducted at a Paediatric SCD clinic in Accra, Ghana.
- 315 children (aged 2-13 years) with confirmed SCD (HbSS, HbSC, or SbetaThal genotypes) were consecutively recruited.
- Ultrasonography was used to detect gallstones in the gallbladder or common bile duct.
Main Results:
- The overall prevalence of gallstones was 4% (13 out of 315 children).
- The youngest child with gallstones was 6 years old, with peak prevalence at 12 years.
- A significant male predominance was observed (12 males vs. 1 female), and patients with no detectable spleen did not have gallstones.
Conclusions:
- Gallstones are found at an early age in Ghanaian children with sickle cell disease.
- The high male-to-female ratio of gallstone prevalence in this SCD cohort warrants further investigation.
- Spleen status may play a role in gallstone formation in children with SCD.
Objective:
This prospective, cross-sectional study was done to define the prevalence and age of onset of gallstones in Ghanaina children with Sickle Cell Disease (SCD) in steady state, using ultrasonography.
Materials And Method:
The study was conducted at the Paediatric SCD clinic, Korle Bu Teaching Hospital, Accra, Ghana. Three hundred and fifteen (315) children comprising 162 males and 153 females aged 2 to 13 years with a confirmed diagnosis of SCD of haemoglobin SS, (HbSS), Haemoglobin SC, (HbSC) or Haemoglobin S-betathalassemia (SbetaThal) genotype whose parents/guardians gave informed conset, were recruited consecutively. The main outcome measure was the detection of gallstones in the gall bladder or common bile duct by ultrasonography.
Results:
Thirteen children, 12 males and 1 female had gallstone, giving an overall prevalence of 4%. The youngest was aged 6. Four children had sludge only. Peak age of prevalence was 12 years. All patients under 12 years with gallstone were males (92.3%). The very high male: female ratio in these sickle cell disease children is at variance with the normal male: female ratio of 1:4.6. Although twenty percent of all the patients were genotype SC, only one SC patient had gallstones, giving a prevalence rate of 0.3%, and a prevalence ratio of stone in SS: SC of 12:1. Twenty patients had no spleen detectable clinically or on ultrasoound examination and none of them had gallstones.
Conclusion:
Gallstones occur at an early age in children with sickle cell disease in Ghana.
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