Shortness of breath may require prompt action
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What I have recently learned may be useful to some PMR victims who experience shortness of breath on exertion.
I am an almost 82 yr male who has maintained a high fitness level until PMR - diagnosed last August but almost certainly affected as early as the previous August. A typical beginning medrol dosage of 16mg/day brought immediate miraculous relief. My aerobic capability returned completely.
As I began to reduce dosage, I noticed in retrospect a reduction in aerobic "fitness" as some stiffness of my back also increased. Because the stiffness increased but was still tolerable I paid inadequate attention to the aerobic change. As I reduced dosage further (last low dosage was 3.5mg/day) there was drastic shortness of breath with little exertion. It was not acceptable.
I did considerable online research and found a small number of medical papers noting an association of interstitial lung disorder with PMR. I increased my medrol to 12mg/day and noticed a change in aerobic capability almost as dramatic as the initial (miraculous) relief of PMR on first starting medrol.
Had I not increased medrol I am firmly convinced that my lungs would have suffered irreversible damage.
I believe that anyone suffering from PMR should pay close attention to aerobic capability as they try to wean from medrol. While lower doses of medrol may lower the risks associated corticosteroids they may endanger the lungs. For those noticing aerobic insufficiency I suggest serious consultation with their physicians. But it may be necessary to make your own decisions. In my case two rheumatologists told me there was no relation of shortness of breath to PMR or medrol.
PS, I walked today at a rate of 12min40sec to the mile with no distress whatsoever. And I have been down to 10.5mg/day for 10 days.
0 likes, 21 replies
Anniecurd philoso4
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dan38655 philoso4
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It never occurred to me that this could be a permanent condition or damage the lungs, and as I have found myself under-medicated to a lesser degree at times, my aerobic capacity always seemed to return.
FlipDover_Aust philoso4
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Oregonjohn-UK FlipDover_Aust
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philoso4 Oregonjohn-UK
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Oregonjohn-UK philoso4
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The other post is an association with PMR with UIP, 'exacerbated pulmonary fibrosis', it doesn’t mean that everyone will succumb to it. Same as most don’t contract osteoporosis but steroids can bring it on. Remerber we are all different and react to meds in different ways.
Oregonjohn-UK philoso4
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dan38655 Oregonjohn-UK
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FlipDover_Aust Oregonjohn-UK
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EileenH Oregonjohn-UK
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However, this is from webmd/interstitial lung disease if you want to have a full read:
"Interstitial lung disease is a general category that includes many different lung conditions. All interstitial lung diseases affect the interstitium, a part of the lungs' anatomic structure.
The interstitium is a lace-like network of tissue that extends throughout both lungs. The interstitium provides support to the lungs' microscopic air sacs (alveoli). Tinyblood vessels travel through the interstitium, allowing gas exchange between bloodand the air in the lungs. Normally, the interstitium is so thin it can't be seen on chest X-rays or CT scans.
Types of Interstitial Lung Disease
All forms of interstitial lung disease cause thickening of the interstitium. The thickening can be due to inflammation, scarring, or extra fluid (edema). Some forms of interstitial lung disease are short-lived; others are chronic and irreversible.
Some of the types of interstitial lung disease include:
Interstitial pneumonia: Bacteria, viruses, or fungi may infect the interstitium of the lung. A bacterium called Mycoplasma pneumonia is the most common cause.
Idiopathic pulmonary fibrosis : A chronic, progressive form of fibrosis (scarring) of the interstitium. Its cause is unknown.
Nonspecific interstitial pneumonitis: Interstitial lung disease that's often present with autoimmune conditions (such as rheumatoid arthritis or scleroderma). ...
... Who is at risk from interstitial lung disease? Anyone can develop interstitial lung disease. Men and women of any age can be affected. Interstitial lung disease is more common in people with autoimmune disease, including lupus, rheumatoid arthritis, and scleroderma."
So it is an aspect of several autoimmune disorders not just PMR and probably reflects the way the label you get for your symptoms depends on the ones that are predominant and match a historical paper describing them.
And the management? Corticosteroids. Azathioprine and methotrexate are also thought to be worth trying. Plus a lot of other far heavier-duty immunosuppressants if they don't work.
EileenH philoso4
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philoso4 EileenH
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EileenH philoso4
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philoso4 EileenH
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philoso4 EileenH
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http://my.clevelandclinic.org/health/diseases_conditions/hic_Pneumonia/hic-nonspecific-interstitial-pneumonia
"Nonspecific interstitial pneumonitis: Interstitial lung disease that's often present with autoimmune conditions (such as rheumatoid arthritis or scleroderma).
What are the symptoms of nonspecific interstitial pneumonia?
A person may have these symptoms:
a dry cough
shortness of breath, which may occur after effort or become worse over time
difficult or labored breathing
fatigue
No one is really sure what causes NSIP. Many researchers believe that it is an autoimmune disease, because of the similarities between NSIP and certain connective tissue diseases, such as systemic sclerosis.
Most patients with the cellular type of NSIP respond well to treatment with oral corticosteroids, such as prednisone."