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1.
J Infect ; 83(3): 321-331, 2021 09.
Article in English | MEDLINE | ID: mdl-34265316

ABSTRACT

OBJECTIVES: The Pre-school Osteoarticular Infection (POI) study aimed to describe the burden of disease, epidemiology, microbiology and treatment of acute osteoarticular infections (OAI) and the role of Kingella kingae in these infections. METHODS: Information about children 3-60 months of age who were hospitalized with an OAI to 11 different hospitals across Australia and New Zealand between January 2012 and December 2016 was collected retrospectively. RESULTS: A total of 907 cases (73%) were included. Blood cultures grew a likely pathogen in only 18% (140/781). The peak age of presentation was 12 to 24 months (466/907, 51%) and Kingella kingae was the most frequently detected microorganism in this age group (60/466, 13%). In the majority of cases, no microorganism was detected (517/907, 57%). Addition of PCR to culture increased detection rates of K. kingae. However, PCR was performed infrequently (63/907, 7%). CONCLUSIONS: This large multi-national study highlights the need for more widespread use of molecular diagnostic techniques for accurate microbiological diagnosis of OAI in pre-school aged children. The data from this study supports the hypothesis that a substantial proportion of pre-school aged children with OAI and no organism identified may in fact have undiagnosed K. kingae infection. Improved detection of Kingella cases is likely to reduce the average length of antimicrobial treatment.


Subject(s)
Arthritis, Infectious , Kingella kingae , Neisseriaceae Infections , Arthritis, Infectious/diagnosis , Arthritis, Infectious/epidemiology , Child , Child, Preschool , Humans , Infant , Kingella kingae/genetics , Neisseriaceae Infections/diagnosis , Neisseriaceae Infections/epidemiology , Polymerase Chain Reaction , Retrospective Studies
2.
Pediatr Pulmonol ; 53(10): 1387-1390, 2018 10.
Article in English | MEDLINE | ID: mdl-29984485

ABSTRACT

BACKGROUND: In cystic fibrosis (CF), irreversible lung disease arises in early life, and is often asymptomatic and unrecognised. Chest computed tomography (CT) scans have been used to detect asymptomatic lung disease in research; however, the clinical utility of chest CT is unknown. This study aimed to determine the effect of surveillance CT in early life on the clinical management of patients with CF. WORKING HYPOTHESIS: Surveillance CT in early life changes the management of patients with CF. METHODS: A medical record review of patients in the AREST-CF cohort who had chest CT at 1 and 3 years of age was performed. Information extracted included CT scan findings and the effect of CT results on clinical management. RESULTS: The chest CT scans and records of 50 subjects with CF were reviewed. The majority of CT scans (n = 75; 75%) were abnormal. N = 31 (31%) of scans overall led to a direct change in management. The number of CT scans needed to be performed to lead to a treatment change was 3.2. The majority (n = 18, 58%) of changes in management were prompted by the finding of bronchiectasis. CONCLUSION: To the authors knowledge, this is the first study to highlight that early life surveillance CT frequently results in changes in clinical management, and hence may have a role beyond research and in routine care. If this can be shown to contribute to improved outcomes (such as reduced rates of bronchiectasis), then, as radiation doses diminish, chest CT could have an important clinical role.


Subject(s)
Cystic Fibrosis/diagnostic imaging , Cystic Fibrosis/therapy , Lung/diagnostic imaging , Tomography, X-Ray Computed , Bronchiectasis/diagnostic imaging , Bronchiectasis/etiology , Bronchiectasis/therapy , Child , Child, Preschool , Cystic Fibrosis/complications , Female , Humans , Male , Retrospective Studies , Tomography, X-Ray Computed/methods
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