Indicators for Osteomyelitis in Children With Sickle Cell Disease Admitted With Vaso-Occlusive Crises

Duaa A Tashkandi1, Ehab Hanafy2, Norah Alotaibi1

  • 1Pediatrics, King Salman Armed Forces Hospital, Tabuk, SAU.

Cureus
|September 6, 2024
PubMed

Insights

This study identified key indicators for diagnosing osteomyelitis in children with sickle cell disease (SCD). Early multidisciplinary evaluation is recommended for suspected cases, integrating clinical, lab, and MRI findings.

Area of Science:

  • Pediatric Hematology
  • Infectious Diseases
  • Musculoskeletal Infections

Background:

  • Sickle cell disease (SCD) predisposes patients to osteoarticular complications, including osteomyelitis.
  • Osteomyelitis commonly affects long bones and vertebrae in individuals with SCD.

Purpose of the Study:

  • To define diagnostic indicators for osteomyelitis in pediatric patients with SCD.
  • To improve early and accurate diagnosis of bone infections in this vulnerable population.

Main Methods:

  • A prospective, descriptive, and analytical study of pediatric patients with SCD.
  • Inclusion of retrospective data for eligible patients.
  • Evaluation of laboratory and radiological features for diagnosis of vaso-occlusive crisis (VOC) and osteomyelitis.

Main Results:

  • Leukocytosis (75%) and elevated CRP (50%) were common in osteomyelitis cases.
  • High ferritin levels (>5000 ng/mL) were observed in patients with osteomyelitis or concurrent VOC.
  • MRI revealed marrow edema and bone enhancement in three cases, with two complicated by osteomyelitis.

Conclusions:

  • An individualized, multidisciplinary approach is recommended for suspected osteomyelitis in SCD patients presenting with VOC.
  • Integrating clinical history, laboratory results, and MRI findings is crucial for diagnosis.
  • Collaboration between hematology, infectious disease, orthopedic surgery, and interventional radiology ensures comprehensive patient care.
Abstract

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