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Empyema is a frequent complication in children hospitalised with pneumonia. Parenchymal changes have been demonstrated on chest radiographs and chest CT scans in empyema,1 and it is plausible that functional outcome may be affected. Studies that have used spirometry in children of school age to assess function following empyema have largely demonstrated normal lung function.2 The ventilation-perfusion (V/Q) scan has been used occasionally in follow-up,3 but evidence is lacking as to its value in this context.
We retrospectively reviewed V/Q scans of eight children originally recruited as part of a published study comparing video-assisted thoracoscopic drainage (VATS) with percutaneous chest drain insertion and urokinase for empyema.4 Our aim was to assess whether empyema causes functional abnormalities following clinical resolution.
All subjects in the original study consented to have a V/Q scan at follow-up. Ethical approval was obtained. Of the total 60 children recruited (median age 3.7 years, range 0.5–15.8), only 8 (median age 7 years, range 1.1–14.4) agreed to have a V/Q scan. Seven of these had VATS and one had percutaneous drain insertion with urokinase.
The median time from hospital discharge to V/Q scan and contemporaneous chest radiography was 6.5 months (range 4.5–13). All children had made a complete clinical recovery at assessment. All follow-up chest radiographs showed minor changes such as pleural shadowing. No major focal parenchymal defects were found on the V/Q scan in any of the children. Six of the V/Q scans showed normally distributed ventilation and perfusion. One scan, following a left empyema treated with VATS, showed global borderline reduction in the function of the left lung (fig 1B), which correlated well with the chest radiograph (fig 1A). Another V/Q scan showed a small focal abnormality in part of the right lower lobe on both ventilation and perfusion studies.
We found that V/Q scans in children with empyema at a median interval of 6.5 months following discharge did not demonstrate major focal defects.
The main limitation of our observation is the small number of children studied. All the children in our study were previously healthy and were reluctant to take part in a potentially unpleasant investigation (intravenous cannulation for injecting radioisotope) once the acute illness had resolved. The only paediatric study evaluating lung perfusion following empyema found that more than 50% of the children had diminished perfusion on the side of the empyema.3 However, the time to the perfusion scan spanned >10 years following empyema, with no details of patients’ ages, management, morbidity and interval infections.
The prognosis in children with empyema is excellent, with most making a complete clinical and radiological recovery.5 British Thoracic Society guidelines recommend that children should be followed up after discharge until complete clinical and near normal radiological resolution.5 However, there is a dearth of studies evaluating long-term functional outcome in children with empyema which needs to be addressed.
We conclude that medium-term lung function as assessed by V/Q scans in a small series of children with resolved empyema is normal or near normal. V/Q scans do not add additional information to functional assessment in a clinically well child following empyema.
Competing interests: None.
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