Treatment of Cystic Fibrosis

There is no cure for cystic fibrosis (also known as mucoviscidosis). But here at the USZ, the symptoms of the disease can be successfully treated and medication prescribed to improve the course of the disease.

Nutrition for Cystic Fibrosis

You can also do something for your own health (or the health of your loved one). Above all, by paying attention to proper nutrition: Researchers recommend eating predominantly high-calorie, vitamin-rich foods and taking additional fat-soluble vitamins. And in contrast to the dietary tips for many other diseases, the following applies to cystic fibrosis: don’t skimp on salt when cooking and seasoning.

Training and Support

It is best to take part in training courses that are offered to you if you have CF. Here you will learn how to deal with cystic fibrosis at different stages of life (both as an affected person and as a relative). CF training courses not only cover medical aspects, but usually also social, psychological, legal and financial issues.

To this end, you will also be supported by an interdisciplinary team of medical specialists, social workers, and a certified nurse (CF-Nurse). Since the disease generally manifests itself during childhood, these training sessions are offered by the children’s hospital.

Medications and Therapies

If you are in contact with doctors and therapists who specialize in cystic fibrosis, they will recommend some of the following treatments and medications:

  • Mucolytic drugs (mucolytics ) are intended to liquefy the mucus in the lungs.
  • Bronchodilators are active substances that dilate the bronchial tubes. They are often inhaled, for example with a spray (metered dose inhaler).
  • Inhalations with a high-percentage saline solution also have an expectorant effect.
  • The purpose of antibiotics is to fight bacteria and the respiratory tract infections they cause.
  • Autogenic drainage is a physiotherapeutic exercise with a special breathing technique. It makes it easier to cough up phlegm.
  • Ivacaftor, lumacaftor and tezacaftor are active substances that can improve lung function and the function of other organs in some CF patients (depending on the form of the genetic mutation). In addition, the frequency of infections is often reduced.
  • Pancreatic enzymes (usually in the form of capsules containing the digestive enzyme pancreatin) support the work of the pancreas. This can improve digestion and often prevent weight loss.

Management Team

Macé Schuurmans, PD Dr. med.

Senior Physician, Department of Pulmonology

Tel. +41 44 255 39 26
Specialties: Transplant pneumology , Cystic fibrosis , Stop smoking

Carolin Steinack, PD Dr. med.

Senior Physician, Department of Pulmonology

Tel. +41 44 255 38 28
Specialties: Head of Interventional Lung Center

Christian Clarenbach, Prof. Dr. med.

Senior Physician, Department of Pulmonology

Tel. +41 44 255 38 28
Specialties: Head of Interstitial and Rare Lung Diseases

For Patients

As a patient, you cannot schedule a consultation directly. Please ask your family doctor or specialist to refer you. If you have any questions, please use our contact form.

Contact Form

For Referring Physicians

Refer your patient online, by email, or by mail.

 

University Hospital of Zurich
Department of Pulmonology
Attn: (insert name of doctor here)
100 Rämistrasse
8091 Zurich

Tel. +41 44 255 33 93
Mail cf@usz.ch
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