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- dornase alfa is a genetically engineered version of human DNAase
- the sputum of patients with cystic fibrosis (CF) contains large amounts
of DNA - the viscoelastic property of sputum in CF patients is due to the
inherent viscosity of DNA, and the mucus glycoproteins
- nebulised dornase alfa is a well tolerated and safe treatment option in
CF - dornase alfa reduces the viscosity of CF sputum by decreasing DNA strand
size
- there is evidence of medium-term improvement in lung function
NICE state that (1):
- a mucoactive agent should be offered to people with cystic fibrosis who
have clinical evidence of lung disease
- rhDNase (dornase alfa; recombinant human deoxyribonuclease) should be offered
as the first choice of mucoactive agent
- if clinical evaluation or lung function testing indicates an inadequate
response to rhDNase, consider both rhDNase and hypertonic sodium chloride
or hypertonic sodium chloride alone
- consider mannitol dry powder for inhalation for children and young people
who cannot use rhDNase and hypertonic sodium chloride because of ineligibility,
intolerance or inadequate response.
Reference:
Last reviewed 01/2018
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