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Integrative Therapies for People with Cystic Fibrosis

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Book cover Integrative Therapies in Lung Health and Sleep

Part of the book series: Respiratory Medicine ((RM,volume 4))

Abstract

Cystic fibrosis (CF) is the most common lethal autosomal inherited disorder affecting Caucasian populations. Due to improved treatments and multidisciplinary team care, the life expectancy of patients with CF has increased dramatically in the last 2 decades. Medical therapy for the majority of patients consists of regular sputum clearance, mucolytic therapy, antibiotics, pancreatic enzyme replacement, nutritional support, and anti-inflammatory agents such as azithromycin. Review by complementary and alternative medicine (CAM) therapists and the utilization of CAM medicines is common in people with CF and healthcare practitioners should encourage discussion with their patients about the use of such therapies. Data to date on the effectiveness of CAM therapy in CF are limited; therefore, adequately powered and carefully designed studies are required to enhance knowledge of the correct role of such therapies. Collaborations between academic centers established to evaluate CAM therapies with CF researchers would provide excellent opportunity to enhance the study of the role of CAM.

* Conflict of Interest Statement: Neither author has a financial or other interest in any of the products discussed in this chapter.

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Correspondence to Scott C. Bell MBBS, MD, FRACP .

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Butler, C.A., Bell, S.C. (2012). Integrative Therapies for People with Cystic Fibrosis. In: Chlan, L., Hertz, M. (eds) Integrative Therapies in Lung Health and Sleep. Respiratory Medicine, vol 4. Humana Press. https://doi.org/10.1007/978-1-61779-579-4_6

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