Community Acquired Pneumonia Clinical Trial
Official title:
Diagnostic and Prognostic Values of Pleural Fluid Procalcitonin in Parapneumonic Pleural Effusion
Key words : serum, pleural effusion, procalcitonin, pneumonia Pneumonia is the common cause
of pleural effusion (ranged 2nd) and bacterial infection is the main etiology of pneumonia.
Procalcitonin, the prohormone of calcitonin, is a 116 amino-acid protein produced by C-cell
of the thyroid gland. During severe infection, procalcitonin is probably produced by
extra-thyroid tissues and the concentration increased rapidly in bacterial infection but
remains low in viral infections. However, the exact origin and pathophysiological role of
procalcitonin during sepsis is not clear and it is not a marker of infection as such, since
localized infections or infections with no systemic manifestation cause a little if any
increase in procalcitonin levels. This study will focus on assessing the value of
procalcitonin in pleural effusion for diagnosis, severity and prognosis among
community-acquired pneumonia with pleural effusion, such as in serum. 100 patients with
clinical pneumonia infection score over six points diagnosed of community-acquired pneumonia
and proved to have pleural effusion by chest sonography on admission will be studied
prospectively. Serum and effusion procalcitonin levels will be measured initially and 3 days
later after medical therapy. Bacterial pneumonia will be identified if bacteria was cultured
from any one of the three kinds of specimen, including blood, pleural effusion or
bronchoalveolar lavage. Then we will divide one hundred of patients into bacterial or
non-bacterial groups. Finally, we will analyze demographic and procalcitonin data of serum
and pleural effusion between these two groups and compare the difference between the severe
or mild and response or non-response bacterial community-acquired pneumonia statistically.
The aim of the study will be to verify whether procalcitonin levels measured in the serum
and pleural effusion could serve as a predictor for bacterial community-acquired pneumonia
with pleural effusion and the different levels will also be indicative of severity and
prognosis. We hope that the predictor from pleural effusion will be more sensitive or
specific than that from serum and could be detectable in localized bacterial infection.
In this study, the first goal will be to determine the sensitivity, specificity, and predictive value of serum and pleural effusion PCT level in CAP with pleural effusion. The second goal will be to decide an appropriate value in serum or pleural effusion to assess as an index of severity and prognosis in bacterial CAP with pleural effusion. ;
Observational Model: Cohort, Time Perspective: Prospective
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