Bone Scan Next Week-Injection
I'm having a bone scan next Wednesday and they tell me I will be injected w/ contrast. My question is--is this a running IV injection, is it just a needle/syringe injection into a vein? I have already told them it can't be my arms(bilateral LE) and I need lidocane for a foot stick. I was told they will not use lidocane as it causes the veins to constrict but that they work with cancer pts. all of the time and not to worry, they'll find a place to inject me!! Well, that put me off just alittle and I am concerned!!! Anyone ever have this done?? Where did they inject you and how much fluid was injected? Is this a radioactive solution? Any info you can share would be appreciated!
Thanks! katiejane
Comments
-
KatieJane, I had a bone scan prior to surgery, they injected the isotope solution into my arm, and it was a relatively big syringe, and it made my vein a little sore. Then, I got kind of achey. Then, it settled down, and I had the scan--and the kind technician told me it was okay as she helped me off the table.
So, it's an injection, and they made need a "decent" vein.
Working with cancer patients doesn't equate to working with people with bilateral LE.
Let us know how it goes.
Kira
-
Thanks Kira, My thoughts exactly. The gal I was speaking with had NO IDEA what I was talking about! I guess if I get in there and they can't use my foot then I'm S.O.L. My L side isn't my worst side and the LE is mostly in the armpit around to my back. I do allow occassional blood draws on that L hand but just not sure about an injection. It's probably between 30-60 mls of fluid. What do you think? I'm worried half sick about this! Thanks, katiejane
-
When I had my bone scan 3 weeks ago, an IV was inserted in the top of my hand and the isotope soluttion was inserted with a syringe. They used the smallest needle possible. It is radioactive and will be out of your body in about 24 - 36 hours. I was told to drink lots of water to help flush my system out.
-
KatieJean, with bilateral LE, I'd be very reluctant, to the point of refusal, to let someone inject a possibly vein irritating isotope into either of my arms.
Could you get the supervisor or head nuclear medicine radiologist to back you up?
New page on stepupspeakout:---
http://www.stepup-speakout.org/essential%20informat%20for%20healthcare%20providers.htm
For patients with bilateral lymphedema or bilateral risk, learn how to take leg blood pressures, foot blood draws and foot or neck IV's if necessary. http://www.medscape.com/viewarticle/471829
Concerns have been raised over the safety of intravenous lines in the lower extremity: they have been associated with a higher risk of infection, should be avoided when artificial joints are in the limb and this author could find no study that documented increased risk of deep vein thrombosis. The higher risk of infection needs to be weighed against the risk of exacerbation or triggering of lymphedema with the use of an IV in a limb with compromised lymphatic function.
You're going to be worried enough about the test, you don't need to worry about your LE also. IMO.
Kira
-
KatieJane, I just had a needle injection....no biggie then the bone scan. The anticipation was worse than the test!
-
Ok ladies......I spoke with nuclear medicine today(where bone scans are done) & exchanged info with one of the gentlemen who actually does the injection/scan. He was very kind and addressed my concerns with the injection. He acknowledged that my LE was a big concern and said he/they will not inject into either of my arms or hands. I do have a decent vein on my ankle and he was pleased to hear that! He also said they have had to do the injection in the neck as well but preferred to save that one for in patients. He was very reassuring and thanked me for giving them a "heads up". It was so nice to speak to someone who has some knowledge of LE!
Thank you all for your input and support! Also, the amount of fluid injected for the scan is 1 ccor ml!! Katiejane
-
Wonderful news, Katiejane! I love to hear about those folks who do take LE seriously and accommodate your needs! Thanks for letting us know!
Dawn
-
Oh, Katiejane, what a gift! Bless him!
You must feel so much better. So glad you persisted in the face of such an intimidating situation. Brava!
We're all with you on this, and we'll be keeping you in our thoughts for next Wednesday. Looking forward to good news!
Binney -
Thanks to all of you for your support and kind words! I will post results as soon as I have them! You know, words cannot even begin to voice what is in my heart for all of you..
Thank you, thank you, thank you!!!!!!! Many Hugs!!! katiejane
-
Well, I had the bone scan today and the scan itself is a piece of cake!! And the guy who did my injection used a vein in my ankle!
There were absolutely no problems! I was even able to watch the screen as the results(films) materialized. Very interesting!! I did have to do two follow up x-rays-one on my neck where I've had arthritis for years and one on each tibia/fibula. I have seen results of cancer + bone scans and this didn't appear to look anything like those but I am anxiously awaiting the "official" word from the radiologist. Keepin' my fingers crossed!
katiejane
-
KatieJane, so glad it went well, and my fingers are crossed for some arthritis, and a good official report. I'm so glad they used your ankle, and now it's just a short wait (I hope) before it's fully behind you.
Hugs
Kira
-
Thanks Kira! Still waiting!
-
Glad to hear they did the job well, Katie Jane!
Dawn
-
Waiting with you KJ -- looking forward to that all-clear whistle!
Binney
-
Hi all ! Here it is, 8:45 pm and I just received a phone call from my Internal Med. Doc with the all clear on the bone scan!!!! YAY! I guess the radiologist discovered bone splints (bilateral) in the tibia/fib area. Certainly not what I expected but certainly a very welcome diagnosis!!!!!! And guess what caused these shin splints???? New custom orthotics(sp?) that I have been wearing on my 12 hours shifts! All I could do was laugh!!!! I've never heard of such a thing! Anyway, thanks for all of your support! Katiejane
-
Yeah!!!
12 hours shifts--that's a long time to be on your feet!
So glad it's over and and it's all good!
Kira
-
Katiejane, I LOVE good news!
Hooray! Do something chocolate!
Binney -
Thanks ladies for all of the support! Binney, something chocolate is right up my alley!!!!!!!!!!!!
Katiejane
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