2022
DOI: 10.1177/2333794x221141356
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Acute Complications of Sickle Cell Disease in Children Under 5 Years at a Level II Hospital

Abstract: The aim of this study was to characterize the acute complications that required hospitalization in children under 5 years with Sickle Cell Disease. The population included 70 patients, 64% of African ascendency and 95.7% homozygotic for the HbS. We analyzed data from 337 hospitalizations. The first hospitalization occurred before 12 months in 38.6% and the average hospital admission per child was 3.92. The mean duration per hospitalization was 5.36 days. The most common diagnosis was vaso-occlusive crisis (36.… Show more

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(2 citation statements)
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“…Although most abnormal hemoglobins have limited clinical significance, a small number of homozygotes or if combined with thalassemia will present with significant anemia, such as Hb S/S and Hb E/β 0 . 6 , 7 …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although most abnormal hemoglobins have limited clinical significance, a small number of homozygotes or if combined with thalassemia will present with significant anemia, such as Hb S/S and Hb E/β 0 . 6 , 7 …”
Section: Introductionmentioning
confidence: 99%
“…Although most abnormal hemoglobins have limited clinical significance, a small number of homozygotes or if combined with thalassemia will present with significant anemia, such as Hb S/S and Hb E/β 0 . 6,7 The study of hemoglobinopathy in China was initiated in the 1960s, and in the 1980s, Chinese scientists conducted a general survey of hemoglobinopathy in nearly one million people covering 28 provinces nationwide. That survey showed that the average carrier rate of abnormal hemoglobin in Chinese population was 0.33%, and the distribution showed a significant difference between the south (0.37%) and the north (0.29%).…”
Section: Introductionmentioning
confidence: 99%