Risk factors for recurrent severe anemia among previously transfused children in Uganda: an age-matched case-control study

被引:8
|
作者
Dhabangi, Aggrey [1 ]
Idro, Richard [2 ]
John, Chandy C. [3 ]
Dzik, Walter H. [4 ]
Opoka, Robert [2 ]
Ssenyonga, Ronald [5 ]
van Hensbroek, Michael Boele [6 ]
机构
[1] Makerere Univ, Coll Hlth Sci, Child Hlth & Dev Ctr, Mulago Upper Hill Rd,POB 6717, Kampala, Uganda
[2] Makerere Univ, Dept Pediat & Child Hlth, Coll Hlth Sci, Kampala, Uganda
[3] Indiana Univ Sch Med, Ryan White Ctr Pediat Infect Dis & Global Hlth, Indianapolis, IN 46202 USA
[4] Harvard Univ, Massachusetts Gen Hosp, Dept Pathol Transfus, Boston, MA 02115 USA
[5] Makerere Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Clin Trials Unit,Coll Hlth Sci, Kampala, Uganda
[6] Univ Amsterdam, Dept Global Child Hlth, Emma Childrens Hosp, Acad Med Ctr, Amsterdam, Netherlands
关键词
Recurrent severe anemia; Children; Transfusion; Malaria; Hemoglobinuria; Sickle cell anemia; BURDEN;
D O I
10.1186/s12887-019-1398-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundIn resource-poor settings, transfused children often experience recurrence of severe anemia (SA) following discharge from hospital. This study determined the factors associated with recurrent severe anemia (RSA) among previously transfused Ugandan children aged less than 5years.MethodsA case-control study was conducted in five hospitals in Uganda from March 2017 to September 2018. We prospectively enrolled 196 hospitalised children who had been transfused for severe anemia 2weeks to 6months prior to enrollment. Of these, 101 children (cases) were re-admitted with a hemoglobin [Hb] level of 6g/dL and required transfusion; and 95 children (age-matched controls) were admitted for other clinical illness with a Hb >6g/dL. Children known to have sickle cell anemia, cancer, or bleeding disorders were excluded. Clinical and laboratory evaluation were done. Conditional logistic regression adjusted for age, was used to determine factors associated with RSA.ResultsThe median time (IQR) between the earlier transfusion and enrollment was 3.5 (1.9-5.7) months for cases, and was 5.0 (2.9-6.0) months for controls (p-value=0.015). Risk factors (adjusted odds ratio, 95% confidence interval, and significance) for development of RSA were: hemoglobinuria (36.33, 2.19-600.66, p=0.012); sickle cell anemia - newly diagnosed (20.26, 2.33-176.37, p=0.006); history of earlier previous transfusions (6.95, 1.36-35.61, p=0.020) and malaria infection (6.47, 1.17-35.70, p=0.032).ConclusionMalaria chemoprevention, follow up visit for Hb check after discharge from hospital and sickle cell screening among previously transfused children represent practical strategies to prevent and identify children at risk for recurrent severe anemia. The cause of hemoglobinuria in children merits further investigations.
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页数:7
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