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National Guideline Alliance (UK). Cystic Fibrosis: Diagnosis and management. London: National Institute for Health and Care Excellence (NICE); 2017 Oct 25. (NICE Guideline, No. 78.)
D.1. Diagnosis of cystic fibrosis
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D.2. Information and support
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D.3. Service configuration
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D.4. Multidisciplinary teams
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D.5. Transition from paediatric to adult services
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D.6. Complications of cystic fibrosis
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D.7. Monitoring for pulmonary disease onset in people with CF without clinical signs or symptoms of lung disease
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D.8. Monitoring for evolving pulmonary disease in people with CF with established lung disease
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D.9. Monitoring for pulmonary disease
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D.10. Airway clearance techniques
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D.11. Mucoactive agents
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D.12. Pulmonary Infection prophylaxis
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D.13. Pulmonary Infection - Antimicrobials for the treatment of acute pulmonary infection or those with an exacerbation
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D.14. Pulmonary Infection - Antimicrobial agents for chronic pulmonary infection
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D.15. Immunomodulatory agents
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D.16. Nutritional interventions
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D.17. Exocrine pancreatic insufficiency
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D.18. Treatment and secondary prevention for distal intestinal obstruction syndrome
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D.19. Monitoring for liver disease
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D.20. Ursodeoxycholic acid for cystic fibrosis-related liver disease
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D.21. Monitoring for CFRD
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D.22. Monitoring for low BMD
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D.23. Exercise
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D.24. Psychological assessment
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D.25. Cross infection control
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- Diagnosis of cystic fibrosis
- Information and support
- Service configuration
- Multidisciplinary teams
- Transition from paediatric to adult services
- Complications of cystic fibrosis
- Monitoring for pulmonary disease onset in people with CF without clinical signs or symptoms of lung disease
- Monitoring for evolving pulmonary disease in people with CF with established lung disease
- Monitoring for pulmonary disease
- Airway clearance techniques
- Mucoactive agents
- Pulmonary Infection prophylaxis
- Pulmonary Infection - Antimicrobials for the treatment of acute pulmonary infection or those with an exacerbation
- Pulmonary Infection - Antimicrobial agents for chronic pulmonary infection
- Immunomodulatory agents
- Nutritional interventions
- Exocrine pancreatic insufficiency
- Treatment and secondary prevention for distal intestinal obstruction syndrome
- Monitoring for liver disease
- Ursodeoxycholic acid for cystic fibrosis-related liver disease
- Monitoring for CFRD
- Monitoring for low BMD
- Exercise
- Psychological assessment
- Cross infection control
- Review protocols - Cystic FibrosisReview protocols - Cystic Fibrosis
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