Related Experiment Video
Updated: Nov 18, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Risk Factors and Complications Among Pediatric Patients With Sickle Cell Anemia: A Single Tertiary Center
Fatma Alzahrani1, Anas M Fallatah2, Fatimah M Al-Haddad3
1Pediatrics, King Abdulaziz University Hospital, Jeddah, SAU.
Insights
Pediatric sickle cell anemia patients with high white blood cell counts, elevated systolic blood pressure, and hypoxia face increased risks of complications. Early identification and management of these factors are crucial for improving patient outcomes and quality of life.
Area of Science:
- Pediatrics
- Hematology
- Genetics
Background:
- Sickle cell anemia (SCA) is a prevalent genetic disorder in Saudi Arabia, causing red blood cell malformation and leading to severe systemic complications.
- These complications, including vaso-occlusive crisis (VOC) and stroke, are the primary drivers of mortality in SCA patients.
- Understanding risk factors for SCA complications is vital for reducing mortality and enhancing patient quality of life.
Purpose of the Study:
- To identify risk factors associated with SCA complications in pediatric patients.
- To investigate the relationship between clinical parameters and the occurrence of complications in children with SCA.
Main Methods:
- A retrospective study was conducted from January 2012 to June 2019 at King Abdulaziz University Hospital, Jeddah, KSA.
- Data were collected from electronic medical records of 102 pediatric SCA patients, excluding those with thalassemia or other chronic diseases.
- Statistical analysis was performed to determine significant risk factors for SCA complications.
Main Results:
- Urinary tract infection (UTI) and vaso-occlusive crisis (VOC) were the most frequent complications, followed by acute chest syndrome (ACS) and stroke.
- While HbSS genotype was common, no significant association was found between genotype and complication development.
- High white blood cell (WBC) counts, elevated systolic blood pressure (SBP), and hypoxia were significantly linked to an increased incidence of complications (p<0.05).
Conclusions:
- Pediatric patients with SCA exhibiting high WBC counts, elevated SBP, and hypoxia are at a higher risk of developing complications.
- Healthcare providers should implement measures to mitigate these risks, including patient/family education on risk factors, immunizations, and precautionary strategies.
- Proactive management of identified risk factors can significantly improve the quality of life for children with sickle cell anemia.
Abstract:
Background and objective Sickle cell anemia (SCA) is one of the common genetic diseases in the Kingdom of Saudi Arabia (KSA). This disease results from a genetic mutation that causes malformation of the red blood cells (RBCs), leading to various systemic complications, including vaso-occlusive crisis (VOC), acute chest syndrome (ACS), osteomyelitis, avascular necrosis (AVN), and stroke, to name a few. The leading cause of mortality in SCA is these systemic complications rather than the disease itself. Understanding the risk factors of these complications can help reduce mortality in these patients and improve their quality of life. In this study, we aimed to determine the risk factors of SCA complications among pediatric patients with SCA at King Abdulaziz University Hospital (KAUH) in Jeddah, KSA. Methods This retrospective study was carried out from January 2012 till June end 2019. It was conducted among pediatric patients with SCA. Patients were screened for eligibility, and we excluded those with thalassemia and those who had a medical history of chronic diseases. Data were collected from patients' electronic medical records. Results The study included 102 pediatric patients with SCA; their mean age was 7.88 ±4.22 years; almost half of them were females (56%) and 44% were males. The dominant body mass index (BMI) classification among them was normal (49%). Urinary tract infection (UTI) was the most common complication with 38 cases followed by VOC with 32 cases. Other complications observed were ACS (25.5%) followed by stroke (15.7%). HbSS was the most prominent genotype among these patients, and it was associated with a higher rate of complications. However, there was no significant relationship between genotype and patients developing complications. Finally, patients with high white blood cell (WBC) counts, elevated systolic blood pressure (SBP), and hypoxia developed more complications, and there was a significant relationship between these conditions and the development of complications (p<0.05). Conclusion Based on our findings, patients with high WBC count, elevated SBP, and hypoxia are at greater risk of developing complications. Accordingly, healthcare providers should consider putting in place all measures required to provide a good quality of life for these patients, including raising awareness about the risk factors that lead to these complications, appropriate immunizations, and precautionary measures to promote these patients' welfare.
More Related Videos
05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
08:23Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
Related Concept Videos
Hemodialysis II: Procedure and Complications
Factors Affecting the Risk of Infection
The integrity and count of the white blood cells help the body resist pathogens and fight infection. When impaired, it reduces the body's resistance to pathogens. The acidic pH levels of the gastrointestinal, genitourinary tracts, and skin...
Multiple Allele Traits
Pharmacokinetics in Pediatric Patients: Drug Excretion
Peritoneal Dialysis II: Peritoneal Dialysis Systems and Complications
Pharmacokinetics in Pediatric Patients: Drug Distribution