Non-CF bronchiectasis - experience wi... - Bronchiectasis Su...

Bronchiectasis Support

951 members435 posts

Non-CF bronchiectasis - experience with surgery?

yesandno profile image
5 Replies

Hi, I am 30 and was diagnosed with non-CF bronchiectasis about a year ago. It is limited to two lung segments. I have chronic Pseudomonas infection with productive cough but no other symptoms. I have now started inhalation with 6% NaCl which really helps with chest clearance and am also trying a Pseudomonas eradication therapy, but I am not very optimistic about that. Since my condition is limited to two lung segments I am thinking about getting surgery to remove the lung segments that are affected. I was curious if anyone had experience with surgery and could tell me about their experience. Thank you!

Written by
yesandno profile image
yesandno
To view profiles and participate in discussions please or .
Read more about...
5 Replies
Mooka profile image
Mooka

What is your therapy for getting rid of the pseudomonas? To consider surgery at this stage seems drastic. I think it’s more usual to control the numbers with pseudomonas rather than eradicate it as it has a habit of finding a corner to hide in.

yesandno profile image
yesandno in reply toMooka

I am getting Cipro and Tobramycin inhalations as eradication therapy. Surgery has the potential of getting rid of the bronchiectasis once and for all, conservative therapy can only slow down the disease. There are minimally invasive procedures and the lung segments that would get removed are not functional. I think the earlier, the better. I would really be interested to hear from people who had surgery for focal bronchiectasis.

Mooka profile image
Mooka in reply toyesandno

In that case you would be better posing on the BLF site. I believe there are people on there with Bronchiectasis who have had surgery and some that have refused it. I take it you aren’t based in the uk?

yesandno profile image
yesandno in reply toMooka

thank you for your advice! and no, I am not based in the UK.

Mooka profile image
Mooka in reply toyesandno

It’s another community on HealthUnlocked. healthunlocked.com/communities

Search on this page. It’s the British lung foundation. I hope you get some good advice on here.

Not what you're looking for?

You may also like...

Bronchiectasis flare with sputum growth of pseudomonas

Flare up , sputum cults grew pseudomonas. Am being tx. With Cipro and prednisone. Any new...
lvn0619 profile image

Feeling good with Bronchiectasis

Hi I first went to my GP with acid reflux 5years ago and from there I was diagnosed via CT scans...
MelAidJack profile image

Non-typical bronchiectasis symptoms

Hello. I've joined this group in the hope that some of you might be able to shine some light on my...
Pompey24 profile image

Bronchitis or bronchiectasis?

Hello All. I rang up to see about the results of my CT scan, and was told that it was mild...

Anyone with Bronchiectasis who has had Covid 19? How great is the risk for people with mild Bronchiectasis?

Have you had or heard of anyone with Bronchiectasis who has had Covid-19? How did they get on? I’ve...
BelindaRuns profile image

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.