Objective: To describe the spectrum of clinical features and management of community acquired pneumonia in the UK.
Design: Prospectively recorded clinical details for all children with possible pneumonia and chest x ray (CXR) changes in 13 hospitals in the North of England between 2001 and 2002.
Results: 89% of 711 children presenting to hospital with pneumonia were admitted; 96% received antibiotics, 70% intravenously. 20% had lobar CXR changes, 3% empyema and 4% required intensive care. Respiratory rate (RR), hypoxia and dyspnoea all correlated with each other and prompted appropriate interventions. Admission in children, not infants, was independently associated with RR, oxygen saturation, lobar CXR changes and pyrexia. Neither C-reactive protein, lobar CXR changes or pyrexia were associated with severity. Children over 1 year old with perihilar CXR changes more often had severe disease (p = 0.001). Initial intravenous antibiotics were associated with lobar CXR changes in infants and children and with dyspnoea, pyrexia and pleural effusion in children. The presence of pleural effusion increased duration of antibiotic treatment (p<0.001). Cefuroxime was the most often used intravenous antibiotic in 61%. Oral antibiotics included a penicillin in 258 (46%), a macrolide in 192 (34%) and a cephalosporin in 117 (21%). Infants stayed significantly longer (p<0.001) as did children with severe disease (p<0.01), effusions (p = 0.005) or lobar CXR changes (p⩽0.001).
Conclusions: There is a high rate of intravenous antibiotic administration in hospital admissions for pneumonia. Despite lobar CXR changes not being independently associated with severe disease, initial lobar CXR changes and clinical assessment in children independently influenced management decisions, including admission and route of antibiotics.
- BTS, British Thoracic Society
- CAP, community acquired pneumonia
- CRP, C-reactive protein
- CXR, chest x ray
- IF, immunofluorescence
- NG, nasogastric
- RR, respiratory rate
- community acquired pneumonia
- childhood pneumonia
- lobar pneumonia
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Published Online First 29 January 2007
Funding: This work was supported by a grant from Wyeth Vaccines UK. The sponsor played no role in the design, collection or analysis of data but did approve the design and agreed to the submission of the manuscript.
Competing interests: JEC has had research support and received sponsorship for meetings and lecture fees from Wyeth Vaccines UK. DS has had research support from Wyeth Vaccines UK.