This site/blog explains everything about Raynaud's Phenomenon in normal human language,
no sophisticated and scientific words, but everything discussed here have a scientific base.

This blog is created, in the hope that it will help the people affected by this disease.
Kindly use "Index" for a better experience. (Given on right hand side.)

Saturday, January 07, 2012

Raynaud's And Scleroderma

Although over 90% of patients with Scleroderma have Raynaud's, the chances of someone with Raynaud's developing Scleroderma are small - it is less than 2% women and 6% in men. But the chances of someone with Scleroderma developing Raynaud's are pretty high.

A little about Scleroderma:

The word Scleroderma means hardening of the skin, although the condition is not limited to the skin.  It is a disease of the connective tissue, which is the tissue that holds our bodies together.

Therefore, not only the skin can be affected, but also internal organs.  The majority of sufferers have the mild form where there is limited skin involvement, usually of the hands and feet, becoming stiff and shiny.  The gullet may also be affected making eating and swallowing difficult.

Some patients also form tiny deposits of calcium under the skin (calcinosis) which can cause ulcers.  In the more severe form, called diffuse Scleroderma, wide areas of skin and internal organs such as the lungs, bowel heart and kidneys are affected.  Localised Scleroderma can be divided into two types: 

    Morphea Scleroderma
    Linear Scleroderma

How are these conditions diagnosed?

The history of the disease is most important.  Blood tests may help, as can examining the small blood vessels at the base of the nail, which is called nail fold capillaroscopy.

The diagnosis of the Scleroderma is based on the finding of the clinical features of the illnesses. In addition, nearly all patients with Scleroderma have blood tests that suggest autoimmunity, because antinuclear antibodies (ANAs) are usually detectable. A particular antibody, the anticentromere antibody, is found almost exclusively in the limited, or CREST, form of scleroderma. Anti-Scl 70 antibody (antitopoisomerase-I antibody) is most often seen in patients with the diffuse form of scleroderma.

Other tests are used to evaluate the presence or extent of any internal disease. These may include upper and lower gastrointestinal tests to evaluate the bowels, chest X-rays, lung-function testing (pulmonary function test), and CAT scanning to examine the lungs, EKG and echocardiograms, and sometimes heart catheterization to evaluate the pressure in the arteries of the heart and lungs.

Is it hereditary?
There is no evidence at present that either Raynaud's or Scleroderma are directly inherited.  There is however a genetic predisposition, so that the chances of being affected are greater if a relative has the problem.

The Treatment:

Just like the Rraynaud's, there is no cure for Scleroderma at present but there are many effective treatments available to alleviate specific symptoms. As each case is different you should discuss these issues with your doctor.

Your General Physician  or specialist may prescribe a vasodilator, which is a drug that relaxes the blood vessels. Occasionally, your specialist may feel an operation called a sympathectomy may be of benefit. This involves either cutting or destroying the nerves that cause the arteries to constrict.  This operation is more successful for Raynaud's of the feet, however it is not recommended for the majority of cases as it does not usually produce longer term benefits.

People who develop Raynaud's as teenagers often have a form that is benign and will disappear with age.  Unfortunately this is not true in all cases, and sometimes Raynaud's does persist.

Treatment of scleroderma is directed toward the individual feature(s) affecting different areas of the body.

Aggressive treatments of elevations in blood pressure have been extremely important in preventing kidney failure. Blood-pressure medications, particularly the angiotensin converting enzyme (ACE) inhibitor class of drugs, such as captopril (Capoten), are frequently used.

Recent data indicate that colchicine can be helpful in decreasing the inflammation and tenderness that periodically accompanies the calcinosis nodules in the skin. Skin itching can be relieved with lotions (emollients) such as Eucerin and Lubriderm.

Mild Raynaud's phenomenon may require only hand warming and protection. Low-dose aspirin is often added to prevent tiny blood clots in the fingers, especially in patients with a history of fingertip ulcerations. Moderate Raynaud's phenomenon can be helped by medications that open up the arteries, such as nifedipine (Procardia, Adalat) and nicardipine (Cardene), or with topical nitroglycerin applied to the most affected digit (most effective on the sides of the digit where the arteries are). Gently applied finger splinting can protect tender tissues. (It is important to not constrict the tiny arteries on the sides of the fingers when protecting them with splints, braces, or band-aid materials.) A class of medications that is typically used for depression, called serotonin reuptake inhibitors, such as fluoxetine (Prozac), can sometimes improve the circulation of the affected digit. Severe Raynaud's phenomenon can require surgical procedures, such as those to interrupt the nerves of the finger that stimulate constriction of the blood vessels (digital sympathectomy). Ulcerations of the fingers can require topical or oral antibiotics.

Esophagus irritation and heartburn can be relieved with omeprazole (Prilosec), esomeprazole (Nexium), or lansoprazole (Prevacid). Antacids can also be helpful. Elevating the head of the bed can reduce the back-flow of acid into the esophagus that causes inflammation and heartburn. Avoiding caffeine and cigarette smoking also helps.

Constipation, cramping, and diarrhea is sometimes caused by bacteria that can be treated with tetracycline or erythromycin. Studies have shown that erythromycin could also be used. Increased fluid intake and fiber intake are good general measures.

Irritated, itchy dry skin can be helped by emollients such as Lubriderm, Eucerin, Bag Balm histamine 2 blockers, or trazodone (Desyrel).

Telangiectasias, such as those on the face, can be treated with local laser therapy. Sun exposure should be minimized as it can worsen telangiectasias.

Approximately 10% of patients with the CREST variant develop elevated pressures in the blood vessels to the lungs (pulmonary hypertension). Abnormally elevated blood pressure of the arteries supplying the lungs is often treated with calcium antagonist medications, such as nifedipine (Procardia), and blood-thinning drugs (anticoagulation). More severe pulmonary hypertension can be helped by continuous intravenous infusion or inhalation of prostacyclin (Iloprost). Taken by mouth, bosentan (Tracleer), is now also available to treat pulmonary hypertension. In addition, sildenafil (Viagra) and tadalafil (Cialis) have been FDA approved to treat pulmonary hypertension.

Additionally, medications are used to suppress the overly active immune system that seems to be spontaneously causing the disease in organs. Medications used for this purpose include penicillamine, azathioprine (Imuran, Azasan), and methotrexate (Rheumatrex, Trexall). Recent research has found that low-dose penicillamine (Depen, Cuprimine) (125 mg every other day) is as effective as previously used high doses of penicillamine, with less toxicity. Serious inflammation of the lungs (alveolitis) can require immune suppression with cyclophosphamide (Cytoxan) along with prednisone (Deltasone, Liquid Pred). The optimal treatment of scleroderma lung disease is an area of active research. Stem-cell transplantation is being explored as a possible option.

No medication has been found to be universally effective for all patients with scleroderma. In an individual patient, the illness may be mild and not require treatments. In some, the disease is ravaging and relentless.

One can find more info about medications for Scleroderma on following website:
http://www.hopkinsscleroderma.org/patients/scleroderma-treatment-options/

Precautions:

There are several things you can do which may help.  The most important is to stop smoking, take regular exercise and keep warm.
Most of the precautions are same as with Raynaud's.
Here are the Do's For the Patient's of Raynaud's Phenomenon.
And these are the Don'ts For the Patients of Raynaud's Phenomenon.



Smoking
If you are a smoker you must make a sincere and determined effort to give up completely. Tobacco is harmful as it causes the blood vessels to constrict, decreasing the blood flow to the fingertips.  Your GP should be able to discuss strategies for you to give up smoking or arrange for you to see a smoking cessation counsellor.  Nicotine replacement may also help and you should discuss this with your doctor or pharmacist.
One can find more detailed information of smoking on human body here: Raynaud's Phenomenon and Smoking

Eating for warmth
Eating and drinking can help you keep warm.  Try to eat lots of small meals to maintain your energy; high protein foods, milk, meat, fish, and fresh vegetables are best.  Hot meals and plenty of hot drinks are essential.
(I am currently working on a post completely about diet for Raynaud's, I will publish it as soon as possible.)

Exercise
Gentle exercise will help your circulation. Try to avoid sitting for long periods. Get up and walk around the room, moving arms and legs to maintain the circulation.  Do not however let your fingers or toes get cold. In cold weather take exercise indoors.

Clothing
Tight clothing should be avoided as this may restrict blood flow.  Hands and feet should always be adequately covered.  A scarf should be used to keep the face warm in cold weather.
One should wear a hat, because most of the body heat gets released from the head.
So, keep the head and trunk warm, because the core temperature of the body is the thing which really matters.
Feet are especially prone to cooling, therefore a good thick pair of socks is essential. Wet shoes and clothes should be changed as soon as possible.

One can find more information about clothing, skin protection, and the effect of alcohol regarding Raynaud's in the index.


Warm Regards,
Kiran Nayak :-)

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Saturday, November 19, 2011

What is more severe Raynaud's Primary or Secondary?

        As explained in my previous post, Raynaud's Primary or Secondary?,
The names Primary and Secondary have nothing to do with the severity of the Raynaud's Phenomenon.
As a matter of fact, there are very few patients of Secondary in comparison with Primary.

        One might say, "That's not correct, I have heard a lot about Secondary being more complex and difficult to treat, and it is more dangerous." Well, that is true. But it has got nothing to do with the severity.
        It is not very rare that Primary form is more sever than the Secondary. Then what has to do with the severity?
        Well the answer lies in my previous post. Don't worry, you don't have to visit the post. (But if you want more information about the difference between Primary and Secondary form then I can't help it, you must visit that post :p )
        In simple and non-techy language, the name Secondary Raynaud's is given to Raynaud's Phenomenon when, the Phenomenon is a result of some other disease which the patient already has.

Now, my most favourite part, the assumptions!

Suppose, Mark Z. is perfectly fit and fine on medical terms, but all of a sudden he generated Primary Raynaud's on February 1st 2011.
Assumption second: Bill G. has been suffering from Lupus since 98. But his Lupus gave him the gift of Raynaud's exactly on February 1st 2011.
Assumption third: Mark and Bill and neighbours, so all the environmental conditions are same for them.
So, technically Mark has Primary and Bill has Secondary Raynaud's.
Now we will assume that as of February 1st, Mark and Bill has the same severity of Raynaud's.
But Mark did not take care of his Raynaud's, he smoked a lot of cigarettes, drank a lot drinks containing caffeine, consumed medicines containing beta-blockers.
And on the other hand, Bill behaved like a good boy, and did no bad things.
So, on March 1st 2012, the severity of Mark's Raynaud's became more than of Bill's.
Here you saw, how severity has nothing to with the form of Raynaud's.

        Now, one might ask, "Then why is it said that Secondary is more complex than Primary? And furthermore, why is it more difficult to treat than Primary?
Well, for the answer, we will consult Bill!
Here is Bill's answer: "As you know, I am suffering from Lupus since a long time now, my body is a little fragile. When my doctors found out that I am also suffering from Raynaud's, they had to be very careful about my medicines. Because they did not want to give me some medicines that would increase my problems with Raynaud's."
So, you can guess why is it said to be complex/difficult to treat.
        And while it is the primary form, the doctors or the patients don't have to worry about anything except Raynaud's.
        If we take a look at Mark, we can see that Mark has to take the precautions only for Raynaud's. But as his severity has increased, his doctors think that it is time to threaten Mark and prescribe some medicines for him. (This kind of threatening includes "quit smoking, or your body will..." A word to the wise!) Here, doctor doesn't have to be as careful as he has to be with Bill's case. Both, Bill, and Mark are treated by the same doctor, named Timothy G.

Conclusions:
  • Severity has nothing to do with form of Raynaud's.
  • The only difference is, Secondary Raynaud's is difficult/complex to treat, than the Primary Raynaud's.
  • In case of Secondary form, person has Raynaud's and something more. And this persons needs to take care of all of them.
  • With Secondary, as there are more than one diseases in the body, it is a real troublemaker.
  • You should read the difference between primary and secondary form, and precautions on this blog. :D


Warm Regards,
Kiran Nayak :-)

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Thursday, November 17, 2011

Raynaud's Discussion Groups / Support Groups / Facebook Groups

There are several user groups on internet, on forums and websites.
I have visited almost all of them.
But in the end I prefer two facebook groups.
The first one (as of January 25th 2011) has 235 members.
It is very active and helpful group.
This group is public and anyone can join it.
Here is the link to this group:
http://www.facebook.com/groups/raynauds/

The another active group.
The members of second group, (including me) are members of the first group as well.
However, this second group is a secret group. That is, it is literally invisible who is not a member of that group.
Only members can see it, and only members can invite their facebook friends.
But me and other members keep both of these groups updated on same levels. That is if we find something new, we discuss about it on both the groups.
If someone posts something only on one group, then we post the same to the other group.
The second group was created for the persons who want to keep their Raynaud's as a secret.


Warm Regards,
Kiran :)

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