FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
Reply |
|
Thread Tools | Display Modes |
|
![]() |
#1 | ||
|
|||
Junior Member
|
I had trauma on my leg and subsequent pain and now doc wants to rule rsd out. How too little time passed for the bone scan to be of any use in making a diagnosis? In other words, have I had the rsd long enough for it to have affected the bones and thus no shown in a scan and thus not be an effective tool in making an rsd diagnosis?
|
||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-06-2009), Dew58 (07-06-2009) |
![]() |
#2 | |||
|
||||
Co-Administrator
Community Support Team
|
I don't know the answer to your question on the timing, but it might be good to have a starting /baseline scan anyway.
If something positive shows up then you'll know & have proof. Or if it is clear for now, then you'll have something to compare with if it is needed in the future.
__________________
Search the NeuroTalk forums - . |
|||
![]() |
![]() |
"Thanks for this!" says: |
![]() |
#3 | ||
|
|||
Junior Member
|
I don't know about bone scans, but the qiucker you can find out if you have this, the better chance you have of stopping it. My doctor usually uses a set of two nerve blocks to diagnose RSD, but if he finds that is the case, then he doesn't perform any more unlike some docs who will just keep doing them over and over. If you don't already have a pain management doctor, they know more about this disease than most orthos or family practice doctors. Might be a good idea to see one for diagnosis and hopefully quick treatment. Good luck!
|
||
![]() |
![]() |
"Thanks for this!" says: |
![]() |
#4 | |||
|
||||
Senior Member
|
Not sure what a good idea it is. I had a bone scan 6 months or so after getting CRPS and it was clear. So of course some people said, "no RSD." Disability carriers like that sort of stuff in particular.
Of course, two years later I had all of the requisite symptomatology that many alleged experts want to see up front before they make a diagnosis, but in the meantime they were sitting on their hands when I should have been getting appropriate care (heavy rounds of blocks, low dose ketamine infusions, etc.) when it could have made a difference: when I was still in the "acute stage" of CRPS. [I am advised that in Germany, the current "gold standard" is to pump local anesthetic right into the affected area for what may be a day or two. And guess what? It takes care of the problem.] If you have only had pain for the last five months, there are aggressive medical therapies out there that will do you no good if you don't jump on them now. Five months from now will, more likely than not, be too late. But I digress. As to the predictive accuracy of the 3-phase bone scan, check out the following abstract, from a respected peer reviewed journal: "Imaging in early posttraumatic complex regional pain syndrome: a comparison of diagnostic methods," Schürmann M, Zaspel J, Löhr P, Wizgall I, Tutic M, Manthey N, Steinborn M, Gradl G, Clin J Pain 2007 Jun;23(5):449-57.http://www.ncbi.nlm.nih.gov/pubmed/1...ubmed_RVDocSum Mike ps For an extended discussion of the value of early medical interventions, including links to articles that can be shared with your doctors, check out the "Are Nerve Blocks really worth it?" thread at http://neurotalk.psychcentral.com/thread90221.html Last edited by fmichael; 07-06-2009 at 02:22 PM. Reason: ps |
|||
![]() |
![]() |
"Thanks for this!" says: | AintSoBad (07-08-2009), ALASKA MIKE (07-06-2009) |
![]() |
#5 | |||
|
||||
Co-Administrator
Community Support Team
|
Good point Mike, I hadn't thought of that part of it.
Depending on your status related to medical ins, disability or work comp it may or may not be a good thing. I did a quick search also and here is more info - [bone scan to make a rsd diagnosis] http://www.google.com/search?q=bone+...ient=firefox-a {Some are older and some newer so check dates to get the latest info.}
__________________
Search the NeuroTalk forums - . |
|||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-06-2009) |
![]() |
#6 | ||
|
|||
Member
|
From a recent study printed in Medscape in 2008:
- A 3 phase bone scan may be helpful in revealing findings typical for the diagnosis of RSD. A false negative (misses RSD diagnosis in symptomatic people) is fairly common - It is considered sensitive and specific particularly if done < 20 wks of onset. But a study by Werner reported sensitivity at 44% - Sensitivity reported at 60% by Kozin, et al. And a 2007 article from Orthopedics Today: - The sensitivity of a 3 phase bone scan decreases with duration of the disease - It has poor sensitivity, approximately 50% So, not a great test for RSD, what is? It's a mixed bag. But do it sooner than later if you're going to do it at all and understand that this test will not be sensitive enough 50% of the time for RSD. In constrast, bone scanning is something like 97% sensitive when looking for bone tumors. |
||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-06-2009) |
![]() |
#7 | ||
|
|||
Member
|
I have had full body RSD for 9 years. I have had two bone scans during that time and my RSD is not affecting my bones so the scan was clear both times.
Take care, Sherrie |
||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-07-2009) |
![]() |
#8 | |||
|
||||
Member
|
i had bone scan about 6mths into rsd and it was positive for already bone loss in my shoulders right wrist, and legs and spine. so i would say its a 50/50 chance of it coming back postive or neg.. that actually test that i had 11yrs ago to dx it was phentolmine challenge and thermography !! also vascular testing .. hope that this helps.
carrie
__________________
hope this finds all in less pain . rsd DX 99 had since 98 full body and organ involement,fibro ,pelvic pain ,etc,,,,,, please check out our website to help bring awareness to RSD! . |
|||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-07-2009) |
![]() |
#9 | |||
|
||||
Member
|
i was diagnosed like a month after my initial injury. nothing showed up on my bone scans or mri's or ct's or xrays tho... other than my original injury- hairline fracture to my radial. was pretty much process of eliminating everything else
__________________
~*Andrea*~ |
|||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-07-2009) |
![]() |
#10 | |||
|
||||
Member
|
Had my 1st scan at 5 months after onset and it only showed my broken kneecap which I didn't know I had. The 2nd scan was done exactly a year later and it came back negative for anything at all. I was glad to know my break had healed!
Hugs, Karen
__________________
Laugh until you cry, don't cry until you laugh. Living, loving and laughing with RSD for 14 years and counting. |
|||
![]() |
![]() |
"Thanks for this!" says: | ALASKA MIKE (07-07-2009) |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
bad bone scan | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
bone density test vs bone scan | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Bone scan divergences? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
full body bone scan? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Bone scan results | Reflex Sympathetic Dystrophy (RSD and CRPS) |