Nebulised Gentamicin/ genticin
Posted , 5 users are following.
Hello!
I have been diagnosed with suspected bronchiectasis and my consultant has suggested nebulised Genticin twice a day. I was just wondering if anybody else has had this treatment; how long you have had it for and whether it was successful?
Thanks!
1 like, 15 replies
Outhwaite
Posted
My friend has it,but as yet has had no antibiotics prescribed in her nebuliser. Have just read the following and it would sound like a good idea to try
http://www.newcastle-hospitals.org.uk/downloads/cardiothoracic/Patient_leaflet_Nebulised_inhaled_Gentamicin.pdf
Good luck, regards, Val.
supercough
Posted
fiona89941
Posted
lesley05714
Posted
Lung bleed last August and diagnosed with bronchiectasis with the specialist after a CT scan.
Off to the doctor again today, still coughing badly, very productive, using my flutter, getting very tired.
supercough lesley05714
Posted
fiona89941
Posted
I use an electronic nebuliser once a day it makes me cough the productive stuff up without much effort from me, a local supermarket sold them for 20.00 so I bought a spare to use as
at my partners house. It's a preventative to stop attracting infection so easily . I use it now my infection has cleared up.
What happened at the docs did you take sputum sample in?
Fiona
lesley05714
Posted
Yes I took a sample in and they have delivered it to the hospital lab' it will no doubt take a few days for the
results.
He also gave me 'Azithromycin' 250mg tablets to take, one every Monday and Thursday; probably to keep me going until I see the specialist again.
The doctor has sent a letter to my specialist to send for me, I don't understand the delay as I should have
had another CT scan in February.
Thank you for the info' on an electronic nebuliser, I'll look into that, it sounds very useful.
I do get tired with this 'flutter', I've given it a rest for a couple of days.
Sounds as if you are in control, the sputum test appears to be the answer.
Kind regards,
Lesley
lesley05714
Posted
I have a new set of tablets, recommended for the new bug that has been found...I appear to have a few lodgers! So new measures to deal with them... Ciprofloxacin 500mg twice every day for seven days.
This idea of a sputem test is excellent as these tablets recommended, are the first ones since Christmas that have really worked and I have only taken 3 days...4 more to go and feeling so much better.
My appointment has come through to see the specialist at the hospital, I am so pleased with my new doctor who really seems to care enough to chase the hospital and get the right tablets for me.
judi77460 lesley05714
Posted
I have been on Ciprofloxacin on and off for over twelve months now but unfortunately the pseudomonas infection is now resistant to that particular antibiotic and I am now on Gentamicin via a nebuliser after being in hospital for 2 weeks hooked up to an IV with Gentamicin and Timentin. Hope this doesn't happen to you.
Regards,
Judi
supercough
Posted
lesley05714
Posted
fiona89941
Posted
That's the drug that eventually stabilised my bugs, pseudomonas , my specialist said that they are usually present in bronchiestesis and flare up when an infection unsettles them.
I use my nebuliser everyday to prevent attracting a new infection.
From fiona
supercough fiona89941
Posted
judi77460 christopher15870
Posted
I was diagnosed with bronchiectasis in 1991 and really didn't treat it with the respect it deserved and have paid for that disrespect over the last 6 years, particularly the last 12 months. I have had continuous pseudomonas infections, which is the worst type of infection to have if you are diagnosed with bronchiectasis. Pseudomonas feeds on bronchiectasis. Until recently I have been treated with Ciprofloxacin, Bactrim DS and a course of Prednisolone all to no avail. I was hospitalised for 2 weeks and in that time I had IV antibiotics of Gentamicin and Timentin which whilst helping did not get rid of the infection. I have been sent home with the Gentamicin to be used in a nebuliser twice a day for at least the next 3-4 months as well as being on Erythromycin 400 mg twice a day for the rest of my life. I have also been using a product called HyperSal which is a 6% saline solution also to be used with a nebuliser. I have been using the Hypersal since May last year and it does help to bring up some of the "gunk" in my lungs. As I said treat brochiectasis with the respect it deserves. Make sure that you have regular sputum tests and chest x-rays. Don't be put off by your doctor saying that "your lungs are clear", this is what my doctor said but each time my results came back it showed the pseudomonas bug. Needless to say my GP and specialist now listen t me when I tell them "IT'S BACK AGAIN". The Gentamicin in the nebuliser appears to be working and finally clearing my lungs. I have found that using a portable nebuliser is better and more efficient than the larger nebuliser. Hope this information is of some use to you.
Regards,
Judi
sdawoolsey christopher15870
Posted
I strongly recommend walking 30 minutes each day, I hate walking but started this 6 mnonths ago & can see a remarkable difference.
I was diagnosed when I was 32, have had it since infancy &, while it is becoming increasingly scary as I get tired & sick, feel you need good treatment & support & understanding.
We need to create a BA (btronchiectasis anonymous) support group & get together regularly to have a laugh about this. There is not enough awareness about this disease & it strongly compared to cystic fibrosis.