Abstract
AbstractPatients with sickle cell disease (SCD) suffer from impaired health-related quality of life (HRQoL). This study aimed to determine the level of HRQoL, sense of coherence (SOC), and self-efficacy (SE) in a sample of SCD patients, and to explore predictors of their physical and mental HRQoL. A cross-sectional descriptive study was conducted on 83 SCD patients of one university hospital. The data of the study was collected through Persian versions of the Short-Form Health Survey SF-36 (RAND 36-item), the Sense of Coherence Scale (SOC-13), and the Sickle Cell Self-Efficacy Scale (SCSES). The mean age of the patients was 26.34 ± 8.19 years old. Patients’ mean scores for the Physical Component Summary (PCS), Mental Component Summary (MCS), SOC, and SCSES were 40.57 ± 17.18 (range: 0–100), 50.44 ± 17.95 (range: 0–100), 52.40 ± 15.35 (range: 13–91), 26.40 ± 6.96 (range: 9–45), respectively. Regression models showed that the level of the patients’ SOC, was the main predictor of the MCS (β = 0.37, p < 0.001). However, the level of the patients’ SE was the main predictor of the PCS (β = 0.30, p = 0.004). Also, “blood transfusion history” in patients was a common predictor for both the PCS (β = − 0.28, p = 0.008) and the MCS (β = − 0.29, p = 0.003). These results can assist nurses and clinicians to plan clinical interventions for SCD patients by focusing on increasing the level of the SOC and SE and improving SCD patients’ HRQoL. Furthermore, measuring the level of the SOC and self-efficacy as screening tests are useful to find patients with a greater risk of impaired HRQoL.
Funder
Marie Cederschiöld University
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Reference59 articles.
1. Pandarakutty S, Murali K, Arulappan J, Al Sabei SD (2020) Health-related quality of life of children and adolescents with sickle cell disease in the Middle East and North Africa region: A systematic review. Sultan Qaboos Univ Med J 20:e280
2. Ashorobi D, Ramsey A, Yarrarapu SNS, Bhatt R (2022) Sickle cell trait. In: StatPearls. Treasure Island, StatPearls Publishing
3. Sedrak A, Kondamudi NP (2021) Sickle cell disease. StatPearls, StatPearls, Treasure Island, FL
4. Keikhaei B, Moradi-Choghakabodi P, Rahim F, Pedram M, Yousefi H, Zandian K, Samavat A (2018) A Neonatal screening for sickle cell disease in Southwest Iran. Iran J Pediatr Hematol Oncol 8:105–110
5. Badawy SM, Beg U, Liem RI, Chaudhury S, Thompson AA (2021) A systematic review of quality of life in sickle cell disease and thalassemia after stem cell transplant or gene therapy. Blood adv 5:570–83. https://doi.org/10.1182/bloodadvances.2020002948
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