I am so sorry to hear you had pneumonia I had double pneumonia about 5 years ago and ended up in resuscitation then on ICU and not nice at all
Usually they give you a xray 6 weeks later to see if it has cleared and as you have fluid I wonder are you on some kind of water tablet to help ?
I really do not know much about this but wanted to reply as I know what having pneumonia is like as well as having heart issues
Are they going to get another xray doe at some stage ?
I would keep to the fluid intake start writing a list of questions you have and maybe see if you can talk to your Doctor or ask when you next have a follow up appointment which hopefully you have
I hope someone will come along that will be able to help answer your question and keep us updated how you get on x
I was advised to keep my fuid intake to no more than 2L per day. Now I've been out on Forxiga ibe been to to drink plenty of fluid. I wish they'd make their minds up.
I also have heart failure and my lungs and lower body were full of fluid a year ago when I was first diagnosed and advised to only have 1.5 litres of fluid a day. At the time I was put on Furosemide drip to quickly release the fluid, then this was changed to the tablet form and now Dapagliflozin and Spironolactone going forward to keep the fluid at bay. Now that the hesrt failure gas improved significantly, I have been advised there is no limit to the amount of fluid I can have.
Unfortunately the fluid can return which is why we have to take meds to try to keep it at bay. I only need to take Furosemide now if I feel like I have some fluid back. With you being on Furosemide and Dapagliflozin, this should help to get rid of the extra fluid.I was on 1.5 litres for about 9 months once the fluid had disappeared and my HF had improved. It was very severe to start with...EF was just 10%, but is now 45-50% and I have no symptoms thus far. I was in a really bad way to start with, but am now back Weight training and enjoying my life again. I also have an ICD.
I went through a grieving process to begin with trying to get to grips with hoe my life has changed, but now I have the attitude that I'm one of the lucky ones that is still here, so I'm making the most of this 2nd chance and concentrating on the things I can do rather than the things I can't do
You can still live a normal life with heart failure depending on how your body responds to the meds. It can be improved.
How are you coming along with your HF? Have you got your head around it all?
I have had lung fluid and fluid around heart at various times.Spironolactone and flurosimide worked well for some time but I had a problem with high potassium so Spiron. was dropped and Amlodopine...a very small dose went in its place with the furosimide.... and tha seemed to do the trick . But yours sounds more serious so you may have to pay careful heed to your docs. But gathering a few ideas from this site may help you to discuss your case better with your docs.
You seem to describe a similar situation to me... In September I became very ill with a bad case of pneumonia and ended up in hospital. I also had recently discovered AF, so while being in the hospital I developed pleural effusion, a complication caused by pneumonia. At first, the consultants thought of water pills but then decided on draining the liquid (about one litre). The procedure was quick and painless. The relief was immediate, the pressure on the chest was gone. Subsequent X-rays showed the lungs clear of liquid. The consultants were the heroes of the time spent in the hospital.
Pneumonia plays havoc on the system and it takes time to recover. I wish you all the best.
Hi I have heart failure EF 23% last year. Before that it was 10% then 15% and I was told to only have 1.5 litres a day. That includes gravies or any liquid. I find it difficult to work out. I was on furosemide until it stopped working and my fluid began to build up. They changed me to Bumetanide and I’m no longer struggling with the fluid retention.
as an ex nurse i am concerned at such a low restriction and that this is not time limited
as far as i am aware any fluid restriction should be temporary and you cardiologist should have been clear about a time limit - also 1 litre a day is very low - the norm is 30ml per kilo (1l =1000ml) fluid intake, this includes drinks and the fluid in foods - please contact you cardiologist and/or GP to question this, particularly if it is not helping you to feel better
Thanks so much for your reply, I did get in touch with the cardiology nurses today. They are going to see me next week. It was the consultant who looked at the chest x-ray who advised the fluid intake.Thanks for your concern 👍
Hi Cosychair. Sorry to hear about your symptoms and I am replying because I have developed similar symptoms since mid December which feel like a return of fluid on the lungs. I have had heart failure for 10 years which was well under control until late last year. I had a chest Xray 2 weeks ago but not seen results yet. I have been back on Furosemide for 2 weeks and hoping that this will help and see the GP again next week. I am interested to share outcomes and will post anything relevant if and when there are any changes to my symptoms.
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