| Literature DB >> 27275341 |
Asmaa Ghmaird1, Mohammad Mohammad Alnoaiji2, Sawsan Al-Blewi3, Shaimaa Zaki4, Ahmad El-Lewi5, Nehal Ahmad5.
Abstract
BACKGROUND: Sickle cell disease is a common genetic disease in Saudi Arabia; it is an autosomal recessive disorder characterized by production of abnormal hemoglobin S and is associated with high morbidity and mortality. Acute splenic sequestration is a life-threatening complication for this disease. Prophylactic splenectomy is the only effective strategy for preventing future life-threatening episodes. AIM: The aim of this study was to study hospital records for all children aged 2 to 12 year old with Sickle cell disease who underwent splenectomy in Tabuk in Saudi Arabia.Entities:
Keywords: acute chest syndrome; blood transfusion; pediatrics; sickle cell disease; spleen sequestration; splenectomy
Year: 2016 PMID: 27275341 PMCID: PMC4884228 DOI: 10.3889/oamjms.2016.034
Source DB: PubMed Journal: Open Access Maced J Med Sci ISSN: 1857-9655
The patient’s demographics
| Age (mean ± standard deviation) | 10 ± 4 |
| Gender | |
| Male | 13 (54.2) |
| Female | 11 (45.8) |
Figure 1Blood transfusion pre and ostoperative.
Figure 2Painful crisis pre and postoperative.
The technique details of operation
| Variable | Frequency | Percent | |
|---|---|---|---|
| Type of procedure | Complete | 24 | 100.0 |
| Technique of procedure | Laparoscopic | 8 | 33.3 |
| Open | 13 | 54.2 | |
| Laparoscopic turn to open | 3 | 12.5 | |
| Concurrent procedures | None | 17 | 70.8 |
| Cholycystectomy | 7 | 29.2 | |
Hb electrophoresis
| Variable | Median | Inter quartile range | |
|---|---|---|---|
| Percentile 25 | Percentile 75 | ||
| Hb electrophoresis A1 | .00 | .00 | 2.60 |
| Hb electrophoresis A2 | 3 | 2 | 3 |
| HB electrophoresis S | 70.70 | 61.00 | 79.40 |
| Hb electrophoresis F | 20.30 | 16.10 | 29.00 |