FIELD: medicine.
SUBSTANCE: cathelicidin LL 37 is measured in a single portion of pharyngeal aspirate on the 1st-2nd day of life. If cathelicidin LL 37 is equal to 10.2 ng/ml or more, the favourable clinical outcome of congenital pneumonia in small premature infants is predicted, while the measured value of less than 10.2 ng/ml shows the lethal outcome.
EFFECT: method enables high-accuracy prediction of the clinical outcomes of congenital pneumonia in small premature infants, the timely correction and enhancement of the prescribed therapy and thereby the improvement of the clinical outcome that leads to reducing the cost of treatment and prevents the further health conditions of the infant.
1 tbl, 3 ex
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Authors
Dates
2015-02-27—Published
2013-10-18—Filed