Treatment of cystic fibrosis as an add-on therapy to
standard care
▶BY INHALATION OF POWDER
▶Adult: Maintenance 400 mg twice daily, an initiation
dose assessment must be carried out under medical
supervision, for details of the initiation dose regimen,
consult product literature
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Bronchial hyperresponsiveness to
inhaled mannitol. impaired lung function (forced
expiratory volume in 1 second < 30% of predicted). non-
CF bronchiectasis
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Asthma. haemoptysis
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Patients must be assessed for
bronchial hyperresponsiveness to inhaled mannitol before
starting the therapeutic dose regimen; an initiation dose
assessment must be carried out under medical
supervision—for details of the initiation dose regimen,
consult product literature.
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NICE decisions
▶Mannitol dry powder for inhalation for treating cystic fibrosis
(November 2012) NICE TA266
Mannitol (Bronchitol ®) dry powder for inhalation is
recommended as an option for treating cystic fibrosis in
adults:
. who cannot use dornase alfa (rhDNase) because of
ineligibility, intolerance or inadequate response to
rhDNase, and
. whose lung function is rapidly declining (forced
expiratory volume in 1 second decline greater than
2% annually), and
. for whom other osmotic agents are not considered
appropriate.
Patients whose treatment was started within the NHS
before this guidance was published should have the option
to continue treatment, until they and their NHS clinician
consider it appropriate to stop.
www.nice.org.uk/guidance/ta266
Scottish Medicines Consortium (SMC) decisions
SMC No. 837/13
The Scottish Medicines Consortium has advised (December
2013) that mannitol (Bronchitol ®) is accepted for restricted
use within NHS Scotland for the treatment of cystic
fibrosis in adults as an add-on therapy to best standard of
care. Mannitol is restricted to patients who are not
currently using dornase alfa due to lack of response,
intolerance, or ineligibility and have rapidly declining lung
function and in whom other osmotic agents are considered
unsuitable.
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