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Serum 25-Hydroxyvitamin D and Diet Mediates Vaso-Occlusive Related Hospitalizations in Sickle-Cell Disease Patients
Michael L McCaskill1, Olalekan Ogunsakin2, Tete Hottor3
1Department of Global Environmental Health Sciences, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA 70112, USA. mmccaski@tulane.edu.
Insights
Sickle cell disease (SCD) patients with low vitamin D levels experience more frequent hospital visits. Dietary intake of fish and milk is linked to reduced SCD crisis-related healthcare utilization.
Area of Science:
- Hematology
- Nutritional Science
- Public Health
Background:
- Sickle cell disease (SCD) is a genetic blood disorder characterized by mutated hemoglobin S.
- Patients with SCD often exhibit severe vitamin D deficiency.
- Vaso-occlusive crises are a common and debilitating manifestation of SCD.
Purpose of the Study:
- To investigate the association between vitamin D status and healthcare utilization for sickle cell disease crises.
- To explore dietary and behavioral factors influencing SCD crisis frequency and severity.
Main Methods:
- Analysis of de-identified patient records from the Sickle Cell Clinic of Southern Louisiana (2010-2014).
- A survey administered to 102 SCD patients assessing sun exposure, diet, and pain.
- Correlation of vitamin D levels (25(OH)D₃) with emergency room (ER) and hospital visit data.
Main Results:
- Patients with vitamin D levels below 14.1 ng/mL had significantly more crisis-related hospital visits (10 per year) compared to those with levels above 34 ng/mL.
- Infrequent consumption of fish and milk was associated with higher rates of hospital stays and ER visits.
- Daily intake of fish and milk correlated with fewer SCD-related ER visits.
Conclusions:
- Vitamin D deficiency is linked to increased healthcare utilization in sickle cell disease patients.
- Dietary patterns, specifically consumption of fish and milk, may play a role in mitigating SCD crisis frequency.
- Further research into vitamin D supplementation and dietary interventions for SCD management is warranted.
Abstract:
Sickle cell disease (SCD) is a genetic disorder resulting from the presence of mutated hemoglobin S (HbS). Homozygous carriers will present with early manifestations of painful vaso-occlusive crises. SCD patients have been reported to be severely deficient in vitamin D (<20 ng/mL). Four years (2010⁻2014) of individual de-identified Sickle Cell Clinic of Southern Louisiana (SCCSL-SCD) patient records were analyzed for vitamin D status and the level of crisis-related ER/hospital utilization. To determine the dietary, and behavioral mediators of SCD-crisis in our study population, a cohort of 102 SCCSL-SCD patients were administered a survey that evaluated sun exposure, dietary behaviors, and pain frequency and severity. Patients with circulating levels of 25(OH)D₃ less than 14.1 ng/mL reported having more crisis-related hospital visits per year (10) than patients with 25(OH)D₃ serum levels >34 ng/mL. The result of the dietary survey detailed a relationship between patients who reported to have "Almost Never" consumed fish or milk in their diets and more frequent hospital stays and ER visits than those who reported consuming these products on a daily basis. Those who consumed these foods in their diet several times a month also had fewer ER visits when compared to the "Almost Never" category.
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