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Published Online First: 1 February 2008. doi:10.1136/thx.2007.086785
Thorax 2008;63:447-452
Copyright © 2008 BMJ Publishing Group Ltd & British Thoracic Society.

RESPIRATORY INFECTION

Markers of treatment failure in hospitalised community acquired pneumonia

R Menéndez1,2, M Cavalcanti3, S Reyes1, J Mensa2,4, R Martinez1, M A Marcos1, X Filella5, M Niederman6, A Torres2,7

1 Servicio de Neumología, Hospital Universitario La Fe, Valencia, Spain
2 CIBER de Enfermedades Respiratorias (CIBERES)
3 PPG Pneumologia-UFRGS, Brasil
4 Servei de Malalties Infeccioses, Hospital Clínic, Barcelona, Spain
5 Servei de Bioquímica, Hospital Clínic, Barcelona, Spain
6 Winthrop University Hospital, Mineola, New York, USA
7 Servei de Pneumologia, Hospital Clínic, Barcelona, Spain

Dr R Menéndez, Servicio de Neumología, Hospital Universitario La Fe, Avda de Campanar 21, 46009 Valencia, Spain; rmenend{at}separ.es

Background: Lack of response to treatment in community acquired pneumonia (CAP) worsens outcome. We evaluated the systemic cytokine profile (tumour necrosis factor {alpha}, interleukin (IL)1, IL6, IL8 and IL10), C reactive protein (CRP) and procalcitonin (PCT) in patients with CAP who had treatment failure.

Methods: A prospective study was performed in hospitalised patients with CAP. Cytokines, PCT and CRP measurements were obtained on day 1 and after 72 h of treatment. Treatment failure was the endpoint evaluated, with separation of those with early (<=72 h) or late failure.

Results: 453 patients were included: 84 (18%) had treatment failure, of whom 38 (8%) were early failures. Median levels of IL6, PCT and CRP on days 1 and 3 and median levels of IL8 on day 1 were significantly higher in patients with any treatment failure. Logistic regression analysis demonstrated that values above the cut-off points for IL6 (>=169 pg/ml), IL8 (>=14 pg/ml) and CRP (>=21.9 mg/dl) on day 1 had independent predictive value for any treatment failure after adjustment for initial severity; relative risks (OR) found were 1.9, 2.2 and 2.6, respectively. Increased levels for CRP and PCT on day 1 were also independent predictors for early failure. Increased levels for IL6 and CRP were the best predictors of late failure.

Conclusions: Serum levels of CRP, IL6 and PCT on days 1 and 3 were independently associated with a higher risk of any treatment failure. Low levels of PCT and CRP on day 1 had a high negative predictive value for early failure.


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