Just Diagnosed with GERD, Bronchiectasis and MAC

Posted by nora49 @nora49, Aug 28, 2022

Hello. I was just diagnosed with GERD, broncheastis, and MAC. I have just begun antibiotic treatment: 3 antibiotics, 3 days a week. This is all new to me. I've never had a serious medical issue before this, and I am glad I found this group.

Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.

@masydnor

I was diagnosed 3 years ago with MAC and bronchiectasis . It was a finding on a CT scan for my heart. I have been getting CT scans every year. This year there was change to my CT scan. He wants to repeat the scan in Jan. And start medication at that time. I still have no symptoms at this time.

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A CT scan alone is not sufficient information with which to begin treatment - the culture will show the type of MAC (there are several) and what antibiotics it is sensitive to.

Have they done a sputum culture yet? Recommended using airway clearance with saline to try to stop/slow the infection? Are you seeing a pulmonologist or ID doc experienced in treating MAC? MAC is still quite uncommon, so many do not have experience treating it.

Sorry for so many questions, but you might want to do a little studying before you commit to treatment with antibiotics.
Here is a link to a recent educational conference at the Medical University of South Carolina where "To treat or Not?" is discussed in the first session
Defining NTM lung disease, Patrick Flume, M.D.
https://vimeo.com/748857824/f945551d7a

Mycobacteria & the Environment, Susan Dorman, M.D.
https://vimeo.com/748857970/cb56fff367

Non-Pharmacologic Therapies, Wayne Barfield, RT & Christina Mingora, M.D.
https://vimeo.com/748903816/ebd06f05f0

Antibiotic Treatment of NTM Lung Disease, Patrick Flume, M.D.
https://vimeo.com/748850475/29d1720a6a

Drug Toxicity and Monitoring, Wendy Bullington, PharmD
https://vimeo.com/748850940/308f6f46dc

Emotional Wellness and Quality of Life While Living with NTM, Lillian Christon, PhD
https://vimeo.com/748852151/d898a90471

What is in the Drug Pipeline? Susan Dorman, M.D.
https://vimeo.com/748857496/79c4311b74

Patient Advocacy, Sue Gray, RN
https://vimeo.com/748857141/64336c3d84

Panel Q&A
https://vimeo.com/748853414/a9965f853d

Patient Perspectives, Faculty Panel
https://vimeo.com/748858168/b5fc5364c5

I hope this information will help you.
Sue

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I will be getting the bronchoscope in January as well to determine type. I do see a pulmonologist that specializes in MAC. Up to this point he has not recommended any treatment, but now that there are changes to the scan he will be moving forward with treatment. No airway treatment has been discussed yet as I have to symptoms not a cough or anything.

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@masydnor

I was diagnosed 3 years ago with MAC and bronchiectasis . It was a finding on a CT scan for my heart. I have been getting CT scans every year. This year there was change to my CT scan. He wants to repeat the scan in Jan. And start medication at that time. I still have no symptoms at this time.

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Just to be clear, the airway clearance process (via PEP device and nebulized saline) is to mitigate the progression of your bronchiectasis. It's not to treat your MAC infection (although a small percentage of people have been known to clear their infection via airway clearance).
This process also mitigates the risk of 'exacerbations' such as pneumonia that could land you in hospital. Airway clearance for bronchiectasis patients is recommended regardless of being asymptomatic.

Unfortunately, a large number of pulmos in the US are not aware of the importance of airway clearance and, consequently, fail to educate their patients accordingly. Insmead currently have a bronchiectasis drug under trial and plan to do a nationwide educational roadshow to socialize this concept with physicians.

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@masydnor

I will be getting the bronchoscope in January as well to determine type. I do see a pulmonologist that specializes in MAC. Up to this point he has not recommended any treatment, but now that there are changes to the scan he will be moving forward with treatment. No airway treatment has been discussed yet as I have to symptoms not a cough or anything.

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Is there a reason they're getting a sample via bronchoscopy vs sputum induction? If they don't know about sputum induction, I recommend you go to a specialist who does. Bronchoscopy is expensive, time consuming, and not without risk (both from the procedure and from the anesthesia). For the purpose of obtaining a sample to determine AFB status, a sputum induction is considered standard per NTM diagnostic guidelines. Once they have the sample, they should be able to tell you the following if you're AFB positive:

1. Species
2. Colony count
3. Drug susceptibility

If you do go on treatment, standard protocol recommends getting monthly sputum samples.

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