Bone Disease among Children with Sickle Cell Disease: A Scoping Review of Incidence and Interventions

Mulyana, Aep Maulid and Rakhmawati, Windy and Pramukti, Iqbal and Lukman, Mamat and Wartakusumah, Riki and Mediani, Henny Suzana (2024) Bone Disease among Children with Sickle Cell Disease: A Scoping Review of Incidence and Interventions. Journal of Multidisciplinary Healthcare, 17. 3235 - 3246. ISSN 11782390

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Abstract

Background: Children with sickle cell disease (SCD) are more likely to have deficient serum levels of vitamin D for bone metabolism. However, appropriate interventions are essential to prevent its progression and alleviate symptoms. Purpose: The aim of this study is to determine interventions for managing bone disease in children with SCD. Methods: This study uses a scoping review. A literature review was conducted using PubMed, CINAHL, ScienceDirect, Scopus, and Google Scholar search engines. The study was eligible for inclusion if it included articles published from 2013 to 2023, full-text, and original study design. Study quality was assessed using the Joanna Briggs Institute (JBI) appraisal tool. Results: This review identified six studies and 114 children with SCD, including 57 boys (50) and 57 girls (50). The majority of SCD types experienced were HbSS (86.84), HbS-B<sup>0</sup> Thal (7.01), HbSC (5.27), and the HbSS Arab-Indian haplotype (0.88). Bone disease problems that often arise in children with SCD include Avascular Necrosis (AVN) (78.08), Osteonecrosis of the Femoral Head (ONFH) (18.42), and other bone problems (3.50). Meanwhile, four types of intervention findings were used in managing bone disease among children with SCD: 1). Surgical procedures 53 (41.09) included total hip arthroplasty (THA), Osteotomy, and Multiple epiphyseal drilling with Autologous Bone Marrow Implantation (AMBI); 2). Invasive procedures 67 (51.93) included intravenous bisphosphonates, hydroxyurea (HU), and core decompression (CD) with bone marrow aspirate concentrate injection: 3). Oral pharmacological or Vitamin D3 (cholecalciferol) 4 (3.10); 4). Non-pharmacology or physical therapy 5 (3.88). Conclusion: Our findings highlight that surgical, invasive, pharmacological, and physical therapy interventions positively impact increasing bone mineral density (BMD) and functional improvement of bone disease among children with SCD. The interventions provided excellent functional outcomes with minimal complications and no life-threatening side effects. © 2024 Elsevier B.V., All rights reserved.

Item Type: Article
Additional Information: Cited by: 3; All Open Access; Gold Open Access; Green Final Open Access; Green Open Access
Uncontrolled Keywords: alkaline phosphatase; bisphosphonic acid derivative; calcitriol; colecalciferol; hydroxyurea; parathyroid hormone; vitamin D; anemia; avascular necrosis; bacterial meningitis; beta thalassemia; blood transfusion; bone density; bone disease; bone marrow mesenchymal stem cell; bone metabolism; bone pain; cell differentiation; child; depression; follow up; haplotype; health care personnel; hip arthroplasty; human; hypocalcemia; incidence; intervention study; mortality rate; osteoblast; osteopenia; osteoporosis; osteotomy; physiotherapy; prevalence; quality control; quality of life; Review; scoping review; sickle cell anemia; thalassemia; vitamin D deficiency
Subjects: R Medicine > RJ Pediatrics
R Medicine > RT Nursing
Divisions: Faculty of Medicine, Public Health and Nursing > Nursing
Depositing User: Ngesti Gandini
Date Deposited: 10 Oct 2025 01:24
Last Modified: 10 Oct 2025 01:24
URI: https://ir.lib.ugm.ac.id/id/eprint/22725

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