Children, Vol. 12, Pages 959: Investigating Different Clinical Manifestations of Staphylococcus aureus Infections in Childhood—Can D-Dimer and Fibrinogen Predict Deep Tissue Invasion?


Children, Vol. 12, Pages 959: Investigating Different Clinical Manifestations of Staphylococcus aureus Infections in Childhood—Can D-Dimer and Fibrinogen Predict Deep Tissue Invasion?

Children doi: 10.3390/children12080959

Authors:
Pınar Önal
Gözde Apaydın Sever
Beste Akdeniz Eren
Gülşen Kes
Ayşe Ayzıt Kılınç Sakallı
Fatih Aygün
Gökhan Aygün
Haluk Çokuğraş
Fatma Deniz Aygün

Background: Staphylococcus aureus is a significant pathogen causing both local and systemic infections in children, with deep tissue involvement leading to severe complications. This study aimed to assess clinical manifestations and identify risk factors for deep tissue involvement in pediatric S. aureus infections. Methods: All children between 1 month and 18 years who had S. aureus growth in blood, pus, or joint fluid culture were included. Results: A total of 61 patients (median age 55 months) were included, with 22.9% having deep tissue infections. Osteoarticular infections, pyomyositis, and pulmonary involvement were common. Deep-seated infections were significantly associated with community-acquired infections and positive hemocultures after 72 hours (p < 0.01). Laboratory results showed significantly higher levels of C-reactive protein, sedimentation rate, D-dimer, and fibrinogen in the group with deep-seated infections (p = 0.02, p = 0.018, p = 0.01, and p = 0.015, respectively). The decision tree model showed that the first indicator of deep-seated infection was a D-dimer level above 1.15 mg/L, followed by a fibrinogen level above 334 mg/dL. Conclusions: Deep-seated S. aureus infections are more frequently associated with community-acquired cases, persistent hemoculture positivity, and methicillin-susceptible Staphylococcus aureus (MSSA) strains. Additionally, elevated D-dimer and fibrinogen levels may serve as valuable markers for identifying deep-seated infections in pediatric patients.



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