Muga Test
Hello,
Sounds like the Muga test is common with Herceptin treatment? Anything to be worried about?
Comments
-
Hi Trinity - Yes, I got a MUGA before I began chemo and Herceptin, then once every 3 months while doing Herceptin only. Then, since I joined a clinical trial, I've had one every 3 months for the last year. Had what I SINCERELY hope is my last one yesterday.
As for the test itself - no problem. They draw blood and insert an IV tube - you wait for 30 minutes while they mix it with a radioactive isotope - they reinject it and withdraw the tube. Then you lie on your back for a series of 3 "pictures" approximately 10 minutes each. the only discomfort is during the last "shoot" when you have to put your hands over your head.
I've had no lowering of my ejection fraction during treatment.
Best wishes to you!
(Edited to add that I just saw your questions about a port - When I had mine, I always made sure to request that the imaging facility scheduled me with a tech who could access ports. That way I could avoid the "stick.")
-
I had a MUGA befoe I started herceptin. Not sure if I will have another at the 3 months mark. I was informed of symptoms to watch out for. If not symptoms my center does not test regularly.
Nothing to be scared about. I had no issues. It's not like the dye that some people are allergic to.
-
Suemed describes the procedure perfectly. It's really not that bad. I don't recall the arms thing, but I may have had them over my head the whole time? Anyway, I got a baseline and then two more. The third showed decreased EF (heart left ventricle ejection fraction). It was below 50, so I had to get an echocardiogram to confirm. When that showed low EF, I was taken off herceptin for 6 weeks and put on blood pressure meds. Did another echo and everything was fine, so I resumed herceptin. They now have me doing echos instead of mugas. I had no symptoms when my EF dropped.
-
As the others have said, you'll probably have a few Muga scans.
It was always one of the easiest for me. I'm sure you'll do fine.
Good luck!
-
Thank you everyone!
-
Trinity~ I sent you a privatte message
-
I don't know anything about Herceptin, but I do know about Muga tests, as I was on several cycles of A/C, so had to have them. Piece of cake - nothing to worry about:-)
-
Thanks everyone, in this case help before I asked. I am also scheduled for a MUGA next Wednesday Prior to starting EC and now know what to expect. It sounds like no problem and that I can actually drive myself.
Jean -
I have to disagree with all you ladies
I hated that stupid Muga scan! My heart always goes wacked when im nervous, i have no viens so getting the blood sucked, and i would be laying in that stupid machine with my hands up, my arms killing, for over an hour! In the end (i was in a trial) i asked for the echo. So much better just lay flat for five minutes and its over. However, im not sure which is better for you?? I was always a little worried when they told me not to go near prego women for a few hours after my muga. Kinda made me wonder what they inject back into you!
-
I know very little about Herceptin, but I did have MUGA prior to chemo (AC + T) and the only thing that really stands out in my mind about it is that I had my port implanted just three days before the test and I was apprehensive about it being accessed so soon. A chemo nurse was called down to access it and all went fine. I haven't had another one. I'm five months out from chemo.
-
I had chemo less than 24 hours after my port surgery. They would have even given me chemo the same day but there wasn't an opening. As long as they know how to access the port there should be a problem.
-
fightinhrd--wow! an hour? sorry you had such a bad experience! I think mine only took 20 minutes and I just had my left arm over my head for the first 10 minutes. I also use my port, so no arm stick.
My onc does them every 3 months while on Herceptin. From what I've read, this is pretty standard. My heart function did decrease so I was put on bp meds, and it went back up a bit. I have not had to miss any Herceptin infusions, but I now have to have a MUGA every 6 or 7 weeks.
-
My experience was similar to Suemed's except they only took 3 pictures the first time. The three pictures are looking at the heart from 3 different angles to get an accurate picture of how the volume of the chamber changes when the heart beats.
After the first time, they only took one picture and then did some preliminary calculations. I was told that as long as the one picture looks like the ejection fraction is staying above 50% that they would do one picture. If it is starting to get close to the borderline, they would do the full set so that they could make the more accurate calculation.
The techs at my lab couldn't do the port stick - only the chemo nurses were allowed to so I had an arm stick for it.
There is a short lived radioactive tag in the injection - that's how they can see how much blood is in the chamber. There isn't very much of it which is why they have to build up a picture over 10 minutes. There are two methods of getting your blood tagged.The other is to put first one chemical in (not the radioactive one but something that helps it attach), wait a while and then inject the radioactive stuff. The other is to draw blood, apply the two chemicals and inject it back in. The half-life of the radioactive element that they use is 6 hours so by 24 hours almost all of it has been excreted or decayed.
I would stay away from pregnant women and babies/young children for 24 hours just to be very careful.
-
Thanks everyone. I had it done today and it was fine. Hope the results are too. The last thing I need is another thing to worry about
-
They don't use my port for the MUGA injections - they mix your blood with radio active isotopes and then reinject it and my onc said they prefer not to have the radio active material injected through the port.
They have a lot of problems finding cooperative veins so I wish they could use it.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team