Aspergillus after Bronchiectasis/MAC
History of brocniectasis/MAC diagnosis at NJH in December 2018. Had right lower portion of right lung removed June 2018 due to unidentified mass (mycobacteria). NJH stay of 10 days, went home with treatment plan of 2xdaily airway clearance. Slowly regained health and been doing fairly well until recently. November 2023 got sputum result of Aspergillus flavus. Johns Hopkins doctor ignored despite my repeated attempts for info. Finally responded, 2 mo. later that never treat till 2nd positive sputum….but did not order 2nd sputum. Sputum ordered by primary physician and result was Aspergillus Fumigatus. Found another pulmonary doc with MAC experience. He ordered 3rd sputum which recently came back Aspergillus Niger. No contact from physician and no treatment offered or discussed at all with me. I do have appointment next month. I am having symptoms similiar to when MAC first began. I am nearing 70 so not sure I even want treatment but would like information. What should I expect from physicians? On,y one who seems concerned is my primary care physician.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
I am very much like you, using saline/albuterol and vest causes hemoptysis even frequent use of Aerobika alone. I do postural drainage mostly.
I am 79years old. I was diagnosed Bronchiectasis 7 years ago and MAI at end of 2022. The reason brought me to seek a pulmonologist help was I found my sputum had tiny blood spots. Augusta University hospital pulmonologist Dr Gonzales had been my doctor since. After a series of examinations I was diagnosed with MAI. By then there was a clinic group I could join al because my hemolysis I was so concerned I refused the chance of clinical trial instead I agreed starting big 3 treatments. 6 months later added Aricyce treatment due to continued MAI culture positive. I tolerated the treatment well and got 12 times continually negative culture reports. But I still feel tired and bloody spotting often happens in my sputum. Ct scan shows my right lung inflammation was worsen .my Dr ordered bronchoscope which finds Asbergillus infection. I received Voriconazole treatment since then, At first few days of treatment I felt very sick (I think the fungus infection was flared up) but gradually I felt better and blood spotting all stopped Up to now 35 days . My anti fungus treatment totally would be 6-8 weeks depending my condition and side effects I have. This my experience of MAI and Asbergillus infection. Only after Asbergillus infection started under control my sputum turned white and no blood. I feel much better now.
So, Asbergillus infection. did not show in your routine sputum culture?
Thanks for sharing your experience and hope you continue to feel better.
No, the sputum culture didn’t show Asbergillus . I think my doctor needed giving specific order to lab to look for asbergillus . But by then my overall health was looking ok. During MAI treatment, my sputum converted but I feel more tired and continue having blood spots in my sputum plus CT scan found my right lung infection getting worse. My doctor discussed with me and decided to have bronchoscope done. This time I think my Dr thought the possibility of cancer and Asbergillus infection. Thank God The report only found Aspergillus not cancer.
Aspergillus needs special dye (which is different from the dye to stain the acid-fast bacilli ) in order to see under microscope .
Liangni1, I am very similar, but have been on voriconazole for 18 months now.
Would you please tell me why you are still on Voriconazole? Because not affective? Are there any side effect from this medication?
Unfortunately, I have a permanent fair sized cavity. A fungal ball has developed in it and will caused lung bleeding. Voriconazole has been keeping the ball at bay so I can avoid a lobectomy. Side effects not too bad, sun sensitive skin, thin outer skin layer and tingly toes. Dr wanted me to switch to Cresemba but with Medicare part d my copay is over $1000 per month.
I have a school mate who is same age as me. He had lobectomy 3 years ago. I don’t know the reason of surgery but he recovered very well. Maybe lobectomy can help you too. I think you should consult your doctor. After 18 month Voriconazole treatment the fungus has been confined to the ball,this may be the best time to do it.
I've seen 8 Doctors and surgeons. Already had a failed resection (no fun, all the pain with no gain). My lung has adhered to chest wall causing an elevated risk for a lobectomy.
As long as voriconazole (or Cresemba if needed) maintains my fairly decent quality of life, I'll keep the status quo.