Wednesday, January 16, 2008

What is Bronchiectasis?

Cystic fibrosis is a chronic condition in which a mutation of the cystic fibrosis trans-membrane regulator (CFTR) protein causes the body to produce abnormally thick, sticky mucus. When this mucus becomes lodged in the respiratory passages, infection is likely to result. Blockage and subsequent infection can cause the airways to become weak and stretched out, scarred, and otherwise deformed. This condition is called bronchiectasis.

Nearly 50% of all reported instances of bronchiectasis are associated with the inflammation and infections associated with cystic fibrosis. Sometimes, the diagnosis of bronchiectasis is made prior to a formal diagnosis of cystic fibrosis. Bronchiectasis can also develop in patients who have allergic bronchopulmonary aspergilliosis (ABPA).

The severity of bronchiectasis is related to which of three types of the condition are present.

1) Fusiform (Cylindrical)

2) Varicose

3) (Saccular) Cystic

Cylindrical forms are often caused by acute bronchitis or other lung infection. In this form, the respiratory passages are only slightly widened, similar to how a garden hose would expand when filled with water. This type of bronchiectasis can be reversed, as there are no collapsed sections of the bronchial wall. Varicose bronchiectasis, is a more serious form, characterized by extended and collapsed portions of the bronchial wall. The most serious and irreversible form is cystic bronchiectasis, in which the bronchi are greatly ballooned.

Bronchiectasis is usually identified during a routine chest x-ray as part of a cystic fibrosis patient’s annual lab tests. Further imaging such as a CT scan as well as pulmonary function tests and a sputum cultures will help the doctor determine the underlying cause, extent and severity of lung damage.

Bronchodilators such as albuterol, are prescribed to help open the airways. Fluticason and ipatropium are useful in controlling inflammation. Percussive respiratory therapy and postural drainage designed to dislodge the mucus is also used. Patients with cystic fibrosis will often use a combination of respiratory therapy including nebulized antibiotics to help control infection, bronchodilators, mucolytics and a vibrating vest such as the InCourage or ThAIRapy vest. Each of these therapies is important not only to control infection, but to slow the rate of declining lung function. Bronchiectasis is less likely to develop if infections are treated early.

In 2005 the FDA approved an inhalation powder called Bronchitol. Phase II clinical studies demonstrated adequate safety and effectiveness in patients at risk for developing bronchiectasis. The medication works by stimulating mucus hydration, enabling the usually thick, sticky mucus to be cleared more easily. Nebulized hypertonic saline produces a similar effect.


Debra said...

Great article, Lauren. I have bronchiectisis, but am not sure which form. I know it's not cylindrical and I'm guessing it's cystic, but will have to ask my dr. Thanks for the info! Aspiemom

Anonymous said...

thanks for your post on bronchiectasisi we found out that my three and half year old has this, which one it is i'm not sure, its result of a CT scan, we will hear more next week from our team, but thanks to you i have some very "intelligent" questions for them. Thanks and wishing you good health.
Yvonne Dublin Ireland

Anonymous said...

Wonderful article, I have bronchiectisis and this article was very informative, thank you for posting.

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georg clerk said...

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Margla Clerk said...

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Zom Sanchez said...

God bless Dr. Monday for his marvelous work in my life, I was diagnosed ofBronchiectasis since 2013 and I was

taking my medications, I wasn't satisfied i needed to get the Bronchiectasis out of my system, I searched about

some possible cure for Bronchiectasis i saw a comment about Dr. Monday, how he cured HERPES,DIABETES,STROKE,ZIKA
and CANCER with his herbal medicine, I contacted him and he guided me. I asked for solutions, he

started the remedy for my health, he sent me the medicine through DHL COURIER SPEED POST. I took the

medicine as prescribed by him (DR. monday) and 3weeks later i was cured from Bronchiectasis.
Dr. Monday truly you are great.
Contact him through.


As a sign of gratitude for how my son was saved from cystic fibrosis , i decided to reach out to those still suffering from this.
My son suffered cystic fibrosis in the year 2013 and it was really tough and heartbreaking for me because he was my all and the symptoms were terrible, he always have shortness of breath , and he always complain of burning in the chest . we tried various therapies prescribed by our neurologist but none could cure him. I searched for a cure and i saw a testimony by someone who was cured and so many other with similar body problem, and he left the contact of the doctor who had the cure to cystic fibrosis. I never imagined cystic fibrosis has a natural cure not until i contacted him and he assured me my son will be fine. I got the herbal medication he recommended and my son used it and in one months time he was fully okay even up till this moment he is so full of life.cystic fibrosis has a cure and it is a herbal cure contact the doctor for more info on on how to get the medication. Thanks for reading my testimony.

Herbs Solutions By Nature said...

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Herbs Solutions By Nature said...

Thanks for sharing such wonderful knowledge! Natural Treatment for Bronchiectasis method to help in improving your breathing.