Table 4.
Management of other common complications of cystic fibrosis
Organ | Manifestation of cystic fibrosis | Treatment | Comments |
---|---|---|---|
Upper airway | Polyps18 | Topical steroids; antibiotics; surgery if medical management fails | Surgery may have medium term benefit, but recurrence common |
Sinusitis | Topical steroids; antibiotics; surgery if medical management fails | Most cases are asymptomatic (changes seen on x ray films or computed tomograms almost universal): no treatment required | |
Endocrine pancreas19 | Insulin deficiency; frank diabetes | Insulin; continue high fat diet; oral hypoglycaemic agents rarely useful | Deleterious impact on respiratory health and nutrition even before diabetes diagnosed |
Bones | Osteopenia; pathological fracture | Prevention: weight bearing exercise, high dairy intake, vitamin D and K therapy* (bisphosphonates if severe*) | |
Cystic fibrosis arthropathy | Anti-inflammatory agents | ||
Sweat gland | Electrolyte depletion leading to failure to thrive, acute collapse | Sodium and potassium chloride supplementation | |
Male reproductive tract | Bilateral absence of vas deferens | Sperm aspiration, and assisted fertilisation techniques | |
Female reproductive tract | Vaginal candidiasis; stress incontinence | Topical antifungal agents | Seek gynaecological advice |
*Treatments for which consensus is lacking.