The clinical spectrum of Staphylococcus aureus infections in children admitted to Chris Hani Baragwanath Academic Hospital, South Africa: A retrospective, descriptive study
P Raphulu (née Manenzhe), J Wadula, DP Moore, KL Petersen
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引用次数: 0
Abstract
Background. Staphylococcus aureus infection is associated with considerable morbidity and mortality. There are relatively few studiesdescribing invasive S. aureus infections in children, particularly in low- and middle-income countries.Objectives. To describe the clinical spectrum and outcomes associated with S. aureus infection in children <14 years of age hospitalised atChris Hani Baragwanath Academic Hospital (CHBAH), South Africa, and to identify risk factors of invasive disease.Methods. A retrospective, descriptive study was conducted at CHBAH to define the spectrum of clinical presentation, risk factors,duration of treatment and outcomes of paediatric S. aureus infections for the period January through December 2013. Data were soughtfor all children <14 years of age.Results. Four hundred and twenty-two episodes of S. aureus infection were identified. Three hundred and forty-two (81%) infectionswere caused by methicillin-susceptible S. aureus (MSSA) and 80 (19%) by methicillin-resistant S. aureus (MRSA). Clinical data wereobtained for 286 (67.8%) cases, on which all further analyses were based. Clinical presentations for MSSA bacteraemia included skin andsoft tissue infection (45%), pneumonia (10%), meningitis (6%), bone/joint infections (5%) and urinary tract infections (3%). Five (8.3%)cases of MRSA were community-acquired. Admission to intensive care unit (ICU) was the only risk factor associated with MRSA infection(adjusted odds ratio (aOR) 125.55; 95% confidence interval (CI) 11.67 - 1 350.68). Hospital-acquired S. aureus infection was the only factorassociated with mortality on multivariate analysis (aOR 8.70; 95% CI 1.55 - 48.77).Conclusion. S. aureus is frequently isolated in paediatric bacterial infections. Closer attention to infection control would impact on MRSAand S. aureus mortality rates in our setting.