How to monitor Pulmonary Fibrosis over time?
Vložit
- čas přidán 8. 02. 2024
- What to expect as follow-up for cases of interstitial lung disease (ILD) and pulmonary fibrosis? How will your doctor check whether the lung scarring is getting worse? What are the tests they may request? What questions will they ask? How often will you need to be seen? Do all cases of pulmonary fibrosis require long-term follow-up consultations?
These are some of the questions that I answer in this video.
I also explain why certain tests are done and when (lung function - spirometry and gas transfer, chest CT scans, blood tests, heart scans - echocardiogram, ECG and ECG monitoring etc.).
I also mention why you may be asked about your oxygen levels and whether you are doing any exercises for your lungs (i.e. formal pulmonary rehabilitation programs).
#pulmonaryfibrosis #ILD #interstitiallungdisease
Please leave comments below if you want me to cover other topics in ILD.
☕ Consider supporting my work by "buying a coffee" -- www.buymeacoffee.com/scstanel
📚 www.interstitiallungdisease.info
🐤 / scstanel
🎵 Podcast links:
SPOTIFY: open.spotify.com/show/4NHgvZw...
GOOGLE PODCASTS: podcasts.google.com/feed/aHR0...
The opinions presented on this channel are my own and do not constitute medical advice in specific cases. If you are watching/listening to this content as a patient, you must seek personalized advice from your own healthcare team (who can provide you with a consultation and appropriate treatment and advice. This information presented here may not apply in your case. If you are a health professional, please use your professional judgement when treating patients.
Thank you so much for this video. My Mom had idiopathic 🫁 fibrosis & passed away in 2010. My brother & I also, have familial idiopathic pulmonary fibrosis since last yr in May. 💓🙏✝️
I to have familial pf as well of my two brothers. One brother passed and the other had a dlt. 💗
I appreciate your videos. Your information is very helpful in coping with and managing pf. Thank you!
Great information! Thank you and very helpful.
Thank you Dr.
I follow you with your great explanation ♥️♥️
Can you make a video (or have you already) on the topic of getting diagnosed incidentally with pulmonary fibrosis when they were looking for something else? And what it means if you have a diagnosis of IPF but no symptoms yet?
Very helpful! Thank you so much!
Very helpful to me . Thank you.
Please make a video on nsip or op pattern shows on CT scan related with connective tissue disease
Hello doc just want to ask a friend of mine was done her treatment from ptb and been cured and the result was she had a residual fibrosis and she was worried that on her next medical it will be shown on her xray as she's applying for uk as a skilled worker, is it necessary to undergo sputum cultured test even the hospital where she was treated and the pulmologist give her a certificate of completion of treatment and totally cured. Thanks doc I'll wait for ur reply
My mom dignosed IPF last year and dr said she is responding very well fibrosis not progressing much she can run walk and eat very normally and i just want to say there is no need to worry more just do timely meditation ,medical advice, medical consultation, daily excercise plan ,daily suitable good fat diet and at last it not be cured but you definately slow down the progression and it has examples which lived beyond 5 years 10 years so no need to worry you can give person life more and more by taking care of above mentioned things
Hi Ravi, Can you please tell me which medications and treatment is your mom undergoing?
Hi Ravi,even my husband is suffering from IPF.ple tell us which medicine is your mom using?
Is there a connection between lichen sclerosis and hypersensitive pneumonitis ?
Pl video on fibritic NSIP
You mention, “ anti scarring” that’s new to me. What kind of medication is that? And a pulse ox is missing leading on how we feel
Thank you information. However, can we know the other types of lung fibrosis besides the severe idiopathic one ?
Can asthma lead to fibrosis in the lungs?.
My mother and two sisters all three died from familiar idiopathic pulmonary fibrosis at ages 63, 68 snd 72. My younger brother had a double lung transplant 6 years ago. I am the only child who did not inherit the gene. I am now 75 years old.
It is a shame that the horrendous disease is not considered important to treat aggressively in your country. Does your country have government funded health care?
It is ab unbelievably horrible disease from which to suffer and die.
Any advice or info on mechanic hands skin condition?
You should refer to a dermatologist for this condition.
People who are diagnosed with idiopathic pulmonary fibrosis here in the States all require oxygen beginning at an advanced stage in their disease. Eventually, they need oxygen for 24 hours a day.