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Hospital Ruber Juan Bravo · C/ Juan Bravo 39, planta 9 · 28006 Madrid
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Cystic fibrosis

Cystic fibrosis in adults

Cystic fibrosis is no longer a paediatric condition. There are more adults living with it every year, and their digestive and liver care needs a specialist who knows the disease.

The digestive side of a respiratory disease

Cystic fibrosis is associated above all with the lungs, but it affects almost the whole digestive tract. With improved respiratory outlook and the arrival of CFTR modulators, digestive and liver problems have moved to the foreground in adult life.

What we monitor

  • Exocrine pancreatic insufficiency. Adjusting the enzyme dose, which is almost always inadequate, and monitoring fat absorption
  • Liver involvement. From isolated enzyme elevation to focal biliary cirrhosis. Follow-up with ultrasound and elastography
  • Nutritional status. Weight, body composition, fat-soluble vitamins and bone density
  • Distal intestinal obstruction syndrome. Recognising and treating it without ending up in theatre
  • Gastro-oesophageal reflux, very common and with direct respiratory impact
  • Cystic fibrosis-related diabetes
  • Gallstones and their complications

Transition from paediatric care

This is one of the highest-risk moments in the whole condition. The patient moves from a team that has known them since childhood to an adult service that is often not set up for it, and some are lost along the way.

A stable digestive clinic, with the same person year after year, is one of the most valuable things at this stage.

Liver disease in adults has a better outlook than assumed

I contributed to a study published in the Revista Española de Enfermedades Digestivas analysing the course of liver involvement in adults with cystic fibrosis at a tertiary referral centre, which found a more benign course than expected. Also to an ultrasound study on the prevalence of biliary manifestations, presented at UEG Week.

My work in this area

I have been principal investigator at La Princesa University Hospital in several international clinical trials on exocrine pancreatic insufficiency in cystic fibrosis, including the SOLUTION, PANC 2002 and MS1819 studies, aimed at optimising enzyme replacement therapy.

Few gastroenterologists have specific experience of this condition in adults, which is why I work in close coordination with the respiratory units that follow these patients.

Frequently asked questions
Do I need a gastroenterologist if my respiratory team already follows me?
In most cases yes, working alongside them. Respiratory and digestive follow-up answer to different logics, and matters such as enzyme dosing, liver status or bone density need specific assessment.
I'm on CFTR modulators. Does that change anything digestive?
Yes, considerably. They change nutritional status, weight and sometimes pancreatic function and the liver profile. That is a reason to review digestive follow-up, not to skip it.
Do you see patients travelling from elsewhere?
Yes. It is an uncommon condition and many patients travel. Where possible I arrange the consultation and tests together to keep the number of trips down, and follow up by video between reviews.

Shall we look at your case?

Private practice in the Salamanca district of Madrid, with no waiting times. In person or by video. Invoice valid for reimbursement policies.