Abstract

Objectives: Despite the numerous advances in management strategies, treating osteomyelitis in individuals with sickle cell disease (SCD) remains a significant challenge, leading to severe long-term consequences. This study aimed to assess the key factors potentially linked to a complex progression of osteomyelitis in patients diagnosed with SCD. Methods: A cohort of 34 patients was identified and their progress was monitored over a span of 12 months during a 10-year period (2010–2020). The variables under investigation encompassed demographic and clinical traits, laboratory analyses and imaging data, as well as the treatment strategies employed. Results: The risk prediction model pinpointed 5 factors (severity of SCD, involvement of lower limbs, presence of bacteraemia, magnetic resonance image [MRI] findings and utilisation of surgical debridement) that exhibited an area under the curve (AUC) exceeding 0.7. Causative organisms were identified in 9 out of the total 34 patients (26.47%). A total of 17 patients displayed a severe course of SCD (AUC = 7.88), with MRI being highlighted as a valuable contributing factor (AUC = 7.88). Furthermore, 13 patients (38.2%) underwent surgical debridement, a procedure that yielded a statistically significant P value of 0.012 and an AUC of 0.714. Conclusion: Osteomyelitis within the context of severe SCD, particularly when accompanied by lower extremity infection, bacteraemia, positive MRI findings and the need for surgical debridement, emerges as a cluster of risk factors predisposing individuals to osteomyelitis relapse and a more complex disease course. Keywords: Anemia, sickle cell; Bacteremia; Debridement; Disease Severity; Osteomyelitis.

Publication details

DOI
10.18295/squmj.12.2023.083
Journal
Sultan Qaboos University Medical Journal, 24(1), 58-62
Publisher
Sultan Qaboos University
Open access
Gold open access
License
CC BY-ND 4.0

Cite this article

APA 7

Al Hashmi, A. Z., Al Fazari, E., Al Ward, M., Al Masruri, R., Al Balushi, S., Al Mutani, M., Al Ghaithi, A., & Al Baluki, W. (2025). Predictors of Developing a Complex Course of Osteomyelitis in Patients with Sickle Cell Anaemia. Sultan Qaboos University Medical Journal, 24(1), 58-62. https://doi.org/10.18295/squmj.12.2023.083

MLA 9

Al Hashmi, Al Zahra, et al. "Predictors of Developing a Complex Course of Osteomyelitis in Patients with Sickle Cell Anaemia." Sultan Qaboos University Medical Journal, vol. 24, no. 1, 2025, pp. 58-62. https://doi.org/10.18295/squmj.12.2023.083.

Chicago (author–date)

Al Hashmi, Al Zahra, Ethar Al Fazari, Mustafa Al Ward, Reema Al Masruri, Shahad Al Balushi, Mohammed Al Mutani, Ahmed Al Ghaithi, and Wafa Al Baluki. 2025. "Predictors of Developing a Complex Course of Osteomyelitis in Patients with Sickle Cell Anaemia." Sultan Qaboos University Medical Journal 24 (1): 58-62. https://doi.org/10.18295/squmj.12.2023.083.

Harvard

Al Hashmi, A. Z., Al Fazari, E., Al Ward, M., Al Masruri, R., Al Balushi, S., Al Mutani, M., Al Ghaithi, A. and Al Baluki, W. (2025) 'Predictors of Developing a Complex Course of Osteomyelitis in Patients with Sickle Cell Anaemia', Sultan Qaboos University Medical Journal, 24(1), pp. 58-62. doi:10.18295/squmj.12.2023.083.

Vancouver

Al Hashmi AZ, Al Fazari E, Al Ward M, Al Masruri R, Al Balushi S, Al Mutani M, et al. Predictors of Developing a Complex Course of Osteomyelitis in Patients with Sickle Cell Anaemia. Sultan Qaboos University Medical Journal. 2025;24(1):58-62. doi:10.18295/squmj.12.2023.083

IEEE

A. Z. Al Hashmi, E. Al Fazari, M. Al Ward, R. Al Masruri, S. Al Balushi, M. Al Mutani, A. Al Ghaithi, and W. Al Baluki, "Predictors of Developing a Complex Course of Osteomyelitis in Patients with Sickle Cell Anaemia," Sultan Qaboos University Medical Journal, vol. 24, no. 1, pp. 58-62, 2025, doi: 10.18295/squmj.12.2023.083.