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Acute multifocal haematogenous osteomyelitis in children
T Sreenivas1, A R Nataraj, Jagdish Menon
1Department of Orthopedics, Jawaharlal Institute of Post Graduate Medical Education and Research (JIPMER), Dhanvantri Nagar, Pondicherry, 605006 India.
Insights
Acute multifocal osteomyelitis in children requires prompt diagnosis and treatment to prevent sepsis. Staphylococcus aureus, including methicillin-resistant strains (MRSA), is a common cause, highlighting the need for early intervention.
Area of Science:
- Pediatric Infectious Diseases
- Orthopedic Surgery
- Microbiology
Background:
- Haematogenous multifocal osteomyelitis in children is a severe condition with a high risk of rapid sepsis development.
- Early and effective treatment is crucial for favorable outcomes.
Purpose of the Study:
- To analyze the clinical presentation, causative organisms, laboratory findings, and risk factors of acute multifocal haematogenous osteomyelitis in children.
- To assess treatment outcomes and identify potential trends in microbial resistance.
Main Methods:
- Retrospective analysis of 26 pediatric patients diagnosed with acute multifocal osteomyelitis over five years.
- Inclusion criteria: patients over 1 year old with involvement of two or more bones, presenting within one week of symptom onset.
- Evaluation included clinical examination, blood tests, and local ultrasound.
Main Results:
- The average age of presentation was 4.9 years, with a female predominance (1.4:1 ratio).
- Lower limbs were most commonly affected (92%), particularly the tibia (73.1%).
- Staphylococcus aureus was the predominant pathogen, with 50% of isolates being methicillin-resistant S. aureus (MRSA). Blood cultures were positive in 38.5% of cases.
Conclusions:
- Early diagnosis and timely, adequate treatment are essential for managing acute multifocal haematogenous osteomyelitis in children.
- The high prevalence of MRSA indicates a shift in causative agents for multifocal bone infections in this population.
Purpose:
Haematogenous multifocal osteomyelitis in children represents a dangerous form of osteomyelitis in which sepsis can develop quickly if it is not treated early. A retrospective analysis of 26 children with acute multifocal haematogenous osteomyelitis over a period of 5 years was undertaken in order to assess the clinical presentation, infective organism, laboratory investigations and risk factors involved.
Methods:
Children more than 1 year of age with two or more bones involvement presenting within one week from the onset of symptoms were included in this study. All of the children were evaluated by clinical examination, blood tests and local ultrasound.
Results:
The average age at presentation was 4.9 years and girls were affected more than boys, with a female to male ratio of 1.4. Lower limbs were affected in 92% of cases, and, specifically, the tibia in 73.1% of the patients. Blood culture was positive in 38.5% of our cases. The predominant microorganism isolated from surgical samples was Staphylococcus aureus, among which methicillin-resistant S. aureus (MRSA) was found in 50% of the patients. Surgical drainage of the pus was done in 24 cases, followed by appropriate antibiotics, and two cases were treated by conservative means. All of the children were successfully treated except for four, who developed chronic osteomyelitis and sequelae.
Conclusion:
We conclude that acute multifocal haematogenous osteomyelitis in children needs early diagnosis by a high index of clinical suspicion and adequate treatment with timely intervention. The predominance of MRSA in our study shows the changing trend in its association with multiple bone involvement.
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