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Updated: Jul 25, 2026

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Preoperative transfusion versus no transfusion policy in sickle cell disease patients: a randomized trial
Mohamed Elshinawy1,2, Nada Al Marhoobi3, Rashid Al Abri4
1Department of Child Health, Pediatric Hematology/Oncology Unit, Sultan Qaboos University Hospital, Muscat, Oman.
Insights
Pediatric patients with sickle cell disease (SCD) undergoing adenotonsillectomy do not require pre-operative transfusions if hemoglobin is above 7.5 g/dL. This approach is safe and does not increase complication risks.
Area of Science:
- Pediatric Hematology
- Surgical Complications
- Transfusion Medicine
Background:
- Children with sickle cell disease (SCD) often receive pre-operative transfusions before adenotonsillectomy to prevent complications.
- The necessity and impact of these transfusions on surgical outcomes are not fully understood.
Purpose of the Study:
- To compare the efficacy of preoperative simple transfusion versus no transfusion in pediatric SCD patients undergoing adenotonsillectomy.
- To evaluate the incidence of surgical and SCD-related complications in both groups.
Main Methods:
- Prospective randomized controlled trial involving pediatric patients with SCD.
- Patients were randomized into two groups: preoperative simple transfusion and no transfusion.
- Data collected on postoperative complications and hospital stay duration.
Main Results:
- Overall postoperative SCD-related complications occurred in 4.3% of patients.
- No significant difference in surgical or SCD-related complications between transfusion and no-transfusion groups (p=0.6 and p=0.8).
- Homozygous sickle cell anemia patients had a 4.9% complication rate.
Conclusions:
- Preoperative PRBCs transfusion is not necessary for SCD patients with hemoglobin >7.5 g/dL before adenotonsillectomy.
- This transfusion strategy does not elevate the risk of postoperative surgical or SCD-related complications.
Background:
Many children with sickle cell disease (SCD) indicated for adenotonsillectomy receive pre-operative transfusion therapy, either simple or exchange transfusion, in order to reduce surgical and sickle cell disease-related complications.
Subjects And Methods:
This is a prospective randomized controlled clinical trial aiming to compare between preoperative simple transfusion and no transfusion in pediatric patients with sickle SCD admitted in Sultan Qaboos University Hospital, Muscat, Oman for adenotonsillectomy during the period from January 2014 through June 2018. They were randomly assigned into two arms (simple transfusion and no transfusion).
Results:
Postoperative SCD-related complications have been encountered in 6 out of 138 patients (4.3%). There was no statistically significant difference between the two studied groups as regards the development of surgical or SCD-related complications (p = 0.6 and 0.8 respectively). The length of postoperative hospital stay was comparable in the two groups. (p = 0.607). SCD-related complications occurred exclusively in cases with homozygous sickle anemia (4 out of 81 = 4.9%).
Conclusion:
Sickle cell disease patients with a hemoglobin level above 7.5 g/dL do not need PRBCs transfusion prior to adenotonsillectomy. This approach did not increase the risk of postoperative surgical or SCD-related complications.
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