Title of article
Efficacy of Human Recombinant DNase in Pediatric Patients with Cystic Fibrosis
Author/Authors
Furuya، نويسنده , , Mar??a Elena Y and Lezana-Fern?ndez، نويسنده , , José Luis and Vargas، نويسنده , , Mario H and Hern?ndez-Sierra، نويسنده , , Juan Francisco and Ram??rez-Figueroa، نويسنده , , Jorge Luis، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
5
From page
30
To page
34
Abstract
Background
espiratory complications in cystic fibrosis (CF) arise from abnormally viscid mucus, and rhDNase has shown to be effective in enhancing mucous clearance. We explored the responses to rhDNase in a Mexican population of CF patients.
s
ts with CF received aerosolized rhDNase (2.5 mg daily) during 3 months, followed by daily aerosolized placebo during 3 months.
s
l of 21 CF patients entered the study (11.1 ± 0.5 years of age, mean ± SEM, 10 girls): 15 patients (71%) had basal forced vital capacity (FVC) higher than the 70% predicted value, and the remainder of the patients had an FVC of between 30 and 70%. As a group, rhDNase progressively increased the forced expiratory flow at 1 sec (FEV1) as well as the FVC, reaching statistical significance (p <0.005) at the end of the third month of treatment. Sputum production and difficulty to expectorate or to breathe also improved during the rhDNase treatment period (p <0.05 to p <0.001). All these changes progressively decreased to basal values after 3 months with aerosolized placebo. Adverse reactions were almost null, with a sole patient reporting dysphonia.
sions
lized rhDNase was effective in progressively improving respiratory function and symptoms in most CF patients.
Keywords
Dornase alpha , respiratory function tests , cystic fibrosis , Mucoviscidosis , rhDNase
Journal title
Archives of Medical Research
Serial Year
2001
Journal title
Archives of Medical Research
Record number
1793987
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