Jump to content
Main menu
Main menu
move to sidebar
hide
Navigation
Main page
Recent changes
Random page
Help about MediaWiki
Special pages
Niidae Wiki
Search
Search
Appearance
Create account
Log in
Personal tools
Create account
Log in
Pages for logged out editors
learn more
Contributions
Talk
Editing
Cystic fibrosis
(section)
Page
Discussion
English
Read
Edit
View history
Tools
Tools
move to sidebar
hide
Actions
Read
Edit
View history
General
What links here
Related changes
Page information
Appearance
move to sidebar
hide
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
=== Gastrointestinal === Problems with the gastrointestinal system including constipation and obstruction of the gastrointestinal tract including distal intestinal obstruction syndrome are frequent complications for people with cystic fibrosis.<ref name="pmid34936085" /> Treatment of gastrointestinal problems is required in order to prevent a complete obstruction, reduce other CF symptoms, and improve the quality of life.<ref name="pmid34936085" /> While stool softeners, laxatives, and prokinetics (GI-focused treatments) are often suggested, there is no clear consensus from experts as to which approach is the best and comes with the least risks.<ref name="pmid34936085" /> Mucolytics or systemic treatments aimed at dysfunctional CFTR are also sometimes suggested to improve symptoms.<ref name=":0" /> The evidence supporting these recommendations is very weak and more research is needed to understand how to prevent and treat GI problems in people with CF.<ref name=":0">{{Cite journal |last1=Carroll |first1=Will |last2=Green |first2=Jessica |last3=Gilchrist |first3=Francis J. |date=22 December 2021 |title=Interventions for preventing distal intestinal obstruction syndrome (DIOS) in cystic fibrosis |journal=The Cochrane Database of Systematic Reviews |volume=2021 |issue=12 |pages=CD012619 |doi=10.1002/14651858.CD012619.pub3 |issn=1469-493X |pmc=8693853 |pmid=34936085}}</ref> In addition, there is a risk of gastrointestinal malignancy, especially in the transplanted patient, and screening procedures may be considered at an earlier age.<ref>{{Cite journal |last1=Vyas |first1=Aditya Pradeep |last2=Ananthaneni |first2=Anil |last3=Abdehou |first3=Sam |last4=Pandit |first4=Sudha |date=2023-08-29 |title=Esophageal squamous cell carcinoma at the site of tracheo-esophageal fistula repair in a patient with cystic fibrosis |journal=BMJ Case Reports |volume=16 |issue=8 |pages=e253542 |doi=10.1136/bcr-2022-253542 |issn=1757-790X |pmc=10465901 |pmid=37643818|pmc-embargo-date=August 29, 2025 }}</ref>
Summary:
Please note that all contributions to Niidae Wiki may be edited, altered, or removed by other contributors. If you do not want your writing to be edited mercilessly, then do not submit it here.
You are also promising us that you wrote this yourself, or copied it from a public domain or similar free resource (see
Encyclopedia:Copyrights
for details).
Do not submit copyrighted work without permission!
Cancel
Editing help
(opens in new window)
Search
Search
Editing
Cystic fibrosis
(section)
Add topic