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Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: poor adherence and the need to address it.

12:48 EDT 23rd May 2013 | BioPortfolio

Summary of "Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: poor adherence and the need to address it."

No Summary Available

Affiliation

Regional Paediatric CF Unit, Leeds Teaching Hospitals NHS Trust, Leeds, UK.

Journal Details

This article was published in the following journal.

Name: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Pages:

Links

Medical and Biotech [MESH] Definitions

Inhalation Spacers

A variety of devices used in conjunction with METERED DOSE INHALERS. Their purpose is to hold the released medication for inhalation and make it easy for the patients to inhale the metered dose of medication into their lungs.

Anthracosis

A diffuse parenchymal lung disease caused by accumulation of inhaled CARBON or coal dust. The disease can progress from asymptomatic anthracosis to massive lung fibrosis. This lung lesion usually occurs in coal miners, but can be seen in urban dwellers and tobacco smokers.

Medication Therapy Management

Assistance in managing and monitoring drug therapy for patients receiving treatment for cancer or chronic conditions such as asthma and diabetes, consulting with patients and their families on the proper use of medication; conducting wellness and disease prevention programs to improve public health; overseeing medication use in a variety of settings.

Pneumoconiosis

A diffuse parenchymal lung disease caused by inhalation of dust and by tissue reaction to their presence. These inorganic, organic, particulate, or vaporized matters usually are inhaled by workers in their occupational environment, leading to the various forms (ASBESTOSIS; BYSSINOSIS; and others). Similar air pollution can also have deleterious effects on the general population.

Asbestosis

A form of pneumoconiosis caused by inhalation of asbestos fibers which elicit potent inflammatory responses in the parenchyma of the lung. The disease is characterized by interstitial fibrosis of the lung, varying from scattered sites to extensive scarring of the alveolar interstitium.

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