Literature DB >> 7643945

Effect of rhDNase on lung function and quality of life in adult cystic fibrosis patients.

H G Heijerman1, R N van Rossem, W Bakker.   

Abstract

Accumulation of viscous sputum enhances lung damage in patients with cystic fibrosis. High contents of DNA, released by leucocytes, are the major cause of the high viscosity of this sputum. Recombinant human DNase I (rhDNase) decreases viscoelastic properties of sputum in cystic fibrosis and improves lung function. We have investigated the effect of rhDNase over a period of 6 weeks, 2.5 mg once daily, on lung function and quality of life in 12 adult patients with cystic fibrosis. Significant improvements in FEV1, IVC and daily peak flow values were measured. Airway resistance and FVC did not improve significantly. The cause of the improvements found is probably due to recruitment of previously, due to mucus plugging, unventilated lung areas. In addition, the awareness of symptoms related to sputum retention improved, although subjective parameters on general well-being and physical condition remained unchanged.

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Year:  1995        PMID: 7643945     DOI: 10.1016/0300-2977(95)00022-f

Source DB:  PubMed          Journal:  Neth J Med        ISSN: 0300-2977            Impact factor:   1.422


  9 in total

1.  Recombinant human DNase (rhDNase) in cystic fibrosis: is it cost effective?

Authors:  S P Conway
Journal:  Arch Dis Child       Date:  1997-07       Impact factor: 3.791

Review 2.  Dornase alfa. A review of pharmacoeconomic and quality-of-life aspects of its use in cystic fibrosis.

Authors:  K L Goa; H Lamb
Journal:  Pharmacoeconomics       Date:  1997-09       Impact factor: 4.981

Review 3.  Quality of life in cystic fibrosis.

Authors:  J Abbott; K Webb; M Dodd
Journal:  J R Soc Med       Date:  1997       Impact factor: 18.000

Review 4.  Timing of dornase alfa inhalation for cystic fibrosis.

Authors:  Ruth Dentice; Mark Elkins
Journal:  Cochrane Database Syst Rev       Date:  2016-07-26

Review 5.  Quality of life in children and adolescents with cystic fibrosis: implications for optimizing treatments and clinical trial design.

Authors:  Janice Abbott; Louise Gee
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

6.  Dornase alfa for cystic fibrosis.

Authors:  Connie Yang; Mark Montgomery
Journal:  Cochrane Database Syst Rev       Date:  2021-03-18

7.  Timing of dornase alfa inhalation for cystic fibrosis.

Authors:  Ruth Dentice; Mark Elkins
Journal:  Cochrane Database Syst Rev       Date:  2021-03-09

8.  Timing of dornase alfa inhalation for cystic fibrosis.

Authors:  Ruth Dentice; Mark Elkins
Journal:  Cochrane Database Syst Rev       Date:  2018-11-12

Review 9.  Dornase alfa for cystic fibrosis.

Authors:  Connie Yang; Mark Montgomery
Journal:  Cochrane Database Syst Rev       Date:  2018-09-06
  9 in total

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