Martin, Alexander James; van der Velden, Fabian Johannes Stanislaus; von Both, Ulrich; Tsolia, Maria N; Zenz, Werner; Sagmeister, Manfred; Vermont, Clementien; de Vries, Gabriella; Kolberg, Laura; Lim, Emma; Pokorn, Marko; Zavadska, Dace; Martinón-Torres, Federico; Rivero-Calle, Irene; Hagedoorn, Nienke N; Usuf, Effua; Schlapbach, Luregn; Kuijpers, Taco W; Pollard, Andrew J; Yeung, Shunmay; ... (2023). External validation of a multivariable prediction model for identification of pneumonia and other serious bacterial infections in febrile immunocompromised children. Archives of disease in childhood, 109(1), pp. 58-66. BMJ Publishing Group 10.1136/archdischild-2023-325869
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OBJECTIVE
To externally validate and update the Feverkids tool clinical prediction model for differentiating bacterial pneumonia and other serious bacterial infections (SBIs) from non-SBI causes of fever in immunocompromised children.
DESIGN
International, multicentre, prospective observational study embedded in PErsonalised Risk assessment in Febrile illness to Optimise Real-life Management across the European Union (PERFORM).
SETTING
Fifteen teaching hospitals in nine European countries.
PARTICIPANTS
Febrile immunocompromised children aged 0-18 years.
METHODS
The Feverkids clinical prediction model predicted the probability of bacterial pneumonia, other SBI or no SBI. Model discrimination, calibration and diagnostic performance at different risk thresholds were assessed. The model was then re-fitted and updated.
RESULTS
Of 558 episodes, 21 had bacterial pneumonia, 104 other SBI and 433 no SBI. Discrimination was 0.83 (95% CI 0.71 to 0.90) for bacterial pneumonia, with moderate calibration and 0.67 (0.61 to 0.72) for other SBIs, with poor calibration. After model re-fitting, discrimination improved to 0.88 (0.79 to 0.96) and 0.71 (0.65 to 0.76) and calibration improved. Predicted risk <1% ruled out bacterial pneumonia with sensitivity 0.95 (0.86 to 1.00) and negative likelihood ratio (LR) 0.09 (0.00 to 0.32). Predicted risk >10% ruled in bacterial pneumonia with specificity 0.91 (0.88 to 0.94) and positive LR 6.51 (3.71 to 10.3). Predicted risk <10% ruled out other SBIs with sensitivity 0.92 (0.87 to 0.97) and negative LR 0.32 (0.13 to 0.57). Predicted risk >30% ruled in other SBIs with specificity 0.89 (0.86 to 0.92) and positive LR 2.86 (1.91 to 4.25).
CONCLUSION
Discrimination and calibration were good for bacterial pneumonia but poorer for other SBIs. The rule-out thresholds have the potential to reduce unnecessary investigations and antibiotics in this high-risk group.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine 04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine > Paediatric Infectiology |
UniBE Contributor: |
Agyeman, Philipp Kwame Abayie |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
0003-9888 |
Publisher: |
BMJ Publishing Group |
Language: |
English |
Submitter: |
Pubmed Import |
Date Deposited: |
30 Aug 2023 11:30 |
Last Modified: |
16 Dec 2023 00:13 |
Publisher DOI: |
10.1136/archdischild-2023-325869 |
PubMed ID: |
37640431 |
Uncontrolled Keywords: |
Allergy and Immunology Infectious Disease Medicine Paediatric Emergency Medicine Paediatrics |
BORIS DOI: |
10.48350/185870 |
URI: |
https://boris.unibe.ch/id/eprint/185870 |