Badr, M., Mohammed, M., Abdel Fattah, N., Ahmed, M. (2022). Assess The Quality of Life and Epidemiological Aspect of Pediatric with Sickle Cell Disease at Zagazig University Hospital. The Egyptian Journal of Hospital Medicine, 87(1), 1131-1136. doi: 10.21608/ejhm.2022.223141
Mohamed Ahmad Badr; Mervat Atfy Mohammed; Nelly Raaft Abdel Fattah; Marwa Gouda Abd El Hamied Ahmed. "Assess The Quality of Life and Epidemiological Aspect of Pediatric with Sickle Cell Disease at Zagazig University Hospital". The Egyptian Journal of Hospital Medicine, 87, 1, 2022, 1131-1136. doi: 10.21608/ejhm.2022.223141
Badr, M., Mohammed, M., Abdel Fattah, N., Ahmed, M. (2022). 'Assess The Quality of Life and Epidemiological Aspect of Pediatric with Sickle Cell Disease at Zagazig University Hospital', The Egyptian Journal of Hospital Medicine, 87(1), pp. 1131-1136. doi: 10.21608/ejhm.2022.223141
Badr, M., Mohammed, M., Abdel Fattah, N., Ahmed, M. Assess The Quality of Life and Epidemiological Aspect of Pediatric with Sickle Cell Disease at Zagazig University Hospital. The Egyptian Journal of Hospital Medicine, 2022; 87(1): 1131-1136. doi: 10.21608/ejhm.2022.223141
Assess The Quality of Life and Epidemiological Aspect of Pediatric with Sickle Cell Disease at Zagazig University Hospital
Background: Sickle cell disease is considered one of the most common inherited diseases in the world. Quality of life is a broad multidimensional concept that usually includes subjective evaluations of both positive and negative aspects of life. Objective: To assess the quality of life and epidemiological aspect of pediatrics with sickle cell disease at Zagazig University Hospital. Patients and Methods: A cross-sectional study was conducted in the Outpatient Clinic and Pediatric Hematological Department in Zagazig University Hospital including30 children with sickle cell anemia. We used two tools, the first was: Structure interview questionnaire sheets, and the second: was the Pediatric Quality of Life Inventory that was used to assess children's quality of life. Results: The mean age of SCD patients is 10.65±3.41years.Our study showed that males (66.7%). In our study, we used the WHOQOL-BREF criteria for measuring QOL in SCD and found that children with SCD scored positive 76.7% in physical activity, 50% in emotional aspect, 63.3% in the social aspect, 46.4% in school aspect, and the total QOL assessment is 63.3%. Concerning the school achievements of children with SCD, the results of this study revealed that 53.3% of students didn't pay attention in class and 66.7% of the children forget things. There were statistically significant differences in all school health subitems. Conclusion: It was concluded that sickle cell disease is a chronic disease that had a negative impact on QOL that includes physical, emotional, social, and school functioning. Our results reflected that all aspects of QOL were affected especially school functioning.