Prevalence of Red Blood Cell Alloimmunization among Children with Sickle Cell Disease in Southern Region of Saudi Arabia: A Single-Center Experience

Authors

  • Badriah Gharamah Al Asmari Department of Pediatric, Armed Forces Hospital Southern Region, Khamis Mushait, KSA.
  • Mohammed Alpakra Department of Pediatric, Armed Forces Hospital Southern Region, Khamis Mushait, KSA.
  • Ali Mujtaba Tahir Department of Pediatric, Armed Forces Hospital Southern Region, Khamis Mushait, KSA.
  • Ali Abdullah Hawan Department of Pathology, Armed Forces Hospital Southern Region, Khamis Mushait, KSA.
  • Nagwan Nabil Mohamed Hossameldin Department of Transfusion Medicine, Blood Bank, Armed Forces Hospital Southern Region, Khamis Mushait, KSA.
  • Mahnoor Saeed Azra Naheed Medical College, Lahore, Pakistan.
  • Abdulaziz Mohammed Alsharaef Department of Pathology, Armed Forces Hospital Southern Region, Khamis Mushait, KSA.
  • Jamilah Hadi Eissa Al Ali Batterjee Medical College, Aseer, KSA.

Keywords:

Sickle Cell Disease, Alloimmunization, Blood Transfusion, Hemoglobin, Pediatric Hematology

Abstract

Abstract: Background: Sickle cell disease (SCD), carrying a varied worldwide prevalence, is a commonly encountered entity in Kingdom of Saudi Arabia and Mediterranean. It is characterized by a range of complications. Blood transfusion is essentially required for both episodic and chronic indications. These blood transfusions inherently imply various risks including alloimmunization.

Objective: To ascertain the incidence of red blood cell alloimmunization in children having sickle cell disease (SCD).

Materials and Methods: Retrospective cross-sectional study was conducted at the Department of Pediatric Medicine, Armed Forces Hospital Southern Region, Khamis Mushait, Saudi Arabia, after obtaining permission from Research Ethics Committee (REC certificate number AFHS-RMREC/2024/Pediatrics/745). The data was collected for last three years 1st July 2021 to 30th June 2024, regarding pediatric patients having sickle cell disease while aged one to fourteen years.

Result: 188 patients of sickle cell disease - all with Saudi ethnicity - were selected with 81 (43%) patients being female and 107 (57%) male. The mean age was 6 years 2 months. Each patient had an average of 2.3 admissions during the course of the disease. Out of these 188 patients, 14 (7.4%) patients were found to have alloimmunization. Mean age at which they developed alloimmunization was 6 years 8 months. 12 patients were on hydroxyurea and 7 patients (50%) underwent splenectomy. On average these cases received 13 transfusions. In contrast, only three (21.4%) patients had undergone exchange transfusion. The most commonly identified single alloantibody was anti-E as seen in 3 patients (21.4%), followed by anti-M in two cases (14.3%). In 4 cases (28.6%), there was an indeterminate antibody (with no specific pattern). Two (14.3%) children were having combination of alloantibodies.

Conclusion: Among the children from southern region of Kingdom of Saudi Arabia, the incidence of alloimmunization in SCD was 7.4%.

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Published

27.03.2025

How to Cite

1.
Al Asmari BG, Alpakra M, Tahir AM, Hawan AA, Hossameldin NNM, Saeed M, et al. Prevalence of Red Blood Cell Alloimmunization among Children with Sickle Cell Disease in Southern Region of Saudi Arabia: A Single-Center Experience. Nat J Health Sci [Internet]. 2025 Mar. 27 [cited 2025 Jun. 22];10(1):3-7. Available from: https://ojs.njhsciences.com/index.php/njhs/article/view/710

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Research Article

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