solu medrol cpt code

) reviewed the CPT-4 codes for each study year (Table 1) to identify those that were believed to reflect the most common types of spinal injection procedures that radiologists perform, including lumbar discography (CPT-4 code 62290), cervical discography (CPT-4 code 62291), disk aspiration and/or injection (CPT-4 code 62287), epidural steroid injection (nonselective epidural injection or selective nerve root injection; CPT-4 code 62289 for lumbar injection or 62298 for cervical or thoracic injec

Debs, It sounds like you mights as well take the Medrol - try it his way and then if it doesn't work out, you can go back and as for the solu-medrol. I'm guessing it is very close- just the "solu" means it is a liquid form (soluble) - again that's just my guess. Sorry you have to tough it out and take the meds - we all are taking stuff we would rather not ingest but do so because we're adults and understand the alternative. :-) Let us know how it goes...

For those of you who have had to get the solu-medrol treatment IV for 5 days, how did this affect you and your body? It has been a couple weeks since I stopped the out-patient treatment for the IV. I am still awake a lot of the time when I should be sleeping. I got about 2 hours of sleep last night, and today, I lay down to rest and I can't still.

I was diagnosed with Lupus Nephritus IV , my doctor had me do a 3 day IV treatment of 1g solu Medrol , each, that was a week ago. I was already on prednisone 60 mg a day and right before the treatment Cellcept was added. I am feeling like I got hit by bus ! I read elsewhere that most of my current issues are withdrawal from the Solu Medrol . I was wondering if anyone else has had this treatment and how long it took to feel" normal" ?

i had on hand a solu-medrol had my boyfriend give me inj 1.5cc Im glute but he gave it too me about 1 inch to the left and now i have swelling at the site about the size of a quarter i am a nursing student and try to walk him through it and made sure he aspirated will i be ok???

Anyone have any ideas how to cope with the solu-medrol headaches? I slept about 3 1/2 hours, nurse is coming back in 2 1/2 for round 2 of the infusion, so have a couple of more days with the headaches.

CPT codes are the critical code numbers to tell your Insurance Co. when you call them for coverage information. They are the "procedure" codes that your Doctors office will bill to the insurance company. It is the first thing your Ins. company will ask for when you call them for coverage information. I am just trying to hunt down CPT codes myself and found that you have to ask for the "Billing dept.

I have a quick question for you all... My neurologist says he doesn't want to give me Solu-Medrol for this "flare" because he said it would affect the MRI results as well as the LP if we do it fairly soon. Is what he told me true or is he just making me suffer for no reason? I don't know any better and thought who best to ask than you guys. Thanks so much.

Famliy Dr started a Decadron taper saying that it looks like MS but symptoms worsened. Neuro started IV Solu-Medrol 500mg x5 days and today was the last dose. Still numb arm. Just curious if any of you have experienced anything like this or how long it may take to get some relief from Solu-Medrol. Any information is very much so appreciated. Kinda freaking out here!!! Thanks!

I will have my first solu-medrol treatment at the end of this week. I have read the opinion of one person who has had this treatment before and they said that you should not drive or work. It was not clear if they were referring to just hours after the treatment or the entire five day course. I really need to work, and in order to work, I really need to be able to drive. Please tell me your experience with solu-medrol, especially if you continued to work during the treatment course.

My question is whether this feeling is a side effect of Solu-medrol or an MS symptom that his not being relieved by the Solu-medrol? I would be grateful for any insight!

I had my first experience with Solu-Medrol infusion in early August. My relapse had just started and was worsening daily-right before I was due to start training for my new job! The immediate side-effects were quite obvious and well documented. I'm having less success finding out about long-term side-effects-in particular, rapid weight gain. I noticed the bloating quite early in my treatment, especially in my face and abdomen.

can some one tell me the code for billing static emg scanner?

I started my exacerbation in April of this year and immediately got on Solu-Medrol. I took the Solu-Medrol for 6 days at maximum dosage and tapered off with Prednisone. While my Optic Neuritis went away after only a couple of weeks or so, I soon had a Trigeminal Neuralgia attack. This only happened once, thank God, but a few days later, I began to experience difficulty walking. I still have difficulty walking, some days good, some days really bad, but the other symptoms have vanished.

I am on day 6 of pretty bad vertigo, I ended up calling my neuro in Seattle to discuss using the steroids and he had to call my Dr here in AZ to get him to order Solu Medrol. This has been a huge fiasco. The insurance girl here first tells me that this IV infusion is not covered by Tricare, so I get the CPT code and call to verify. They do accept that procedure and I don't need an auth or referral. By the time all these back and forth phone calls are done, its almost 5pm and they close.

I was told to call the hospital and see what the cost of use would be for the out patient surgery. My doctor gave me CPT code of 67108. I got my estamite from the hospital and it's a staggering $15,000 dollars for us just to use the room. I Googled CPT codes and one site was AMA. Both sites said $1500.00 for code 67108. Can anyone tell me what to expect the hospital to charge for this? Not for the surgery, just for the privilege of using the place.

I finished my IV Solu-Medrol on 9/19, and now only a little over 2 weeks later, my eye is hurting again. Could I already be relapsing? My vision is still o-kay, but the pain is definitely back.

It is usually referenced in codes, like the Current Procedural Terminology(CPT) code set is a medical code set maintained by the American Medical Association. Your primary care physician may be able to guide you appropriately, please discuss this with him. Hope this helped and do keep us posted.

He shouldnt be charging you for more than your session time, 60 min is not the lowest increment available. I saw a code for 45 min also. Call your doctors office and ask for billing and enquire about it. Or call your insurance company and ask them about it. Tell either how much time you spent with the actual DR, not time in the waiting room. CPT Code 92214 means: Offic/Outpt E&M Estab Mod-Hi established patient. CPT Code 90838 means: psychotherapy, 60 minutes Hope this helps!

A week later I had double vision which prompted my first round of Solu-Medrol. The drug did seem to help, and I saw a steady improvement until the beginning of April, where I estimate I was about 95% of normal. Only if I looked to the far left I saw double. Well, I began a new relapse mid April (other sensory symptoms) which I was given another round of Solu-Medrol in the beginning of May.

I am on day 4 without solu-medrol, but still have the increased appetite..Shouldn't this be going away soon? It's driving me nuts as I worked so hard to lose 48 pounds and sure don't want the solu to blow it. I'm not doing this again. The side effects were awful and the results have not been worth it at all.

my second brain MRI had that code, but not the first brain mri or spinal MRI (the CPT code listed the same for brain and spine; may be wrong). I researched the CPT code used for my spinal MRI, and they were standard MRIs without contrast. If the first brain MRI was ordered using the not-ms protocol CPT code, and the second one used the ms protocol CPT code. Wouldn't that mean that they were done differently and weren't adequate for noting changes?

i had a 3-day solu-medrol infusion last week after a c-spine MRI revealed possible myelitis. i have had all the yucky side effects from the steroids which are subsiding--thank heavens--but instead of feeling better, it seems as though my other symptoms are getting worse--buzzing, achey joints, etc. is this typical? is it the case where things will get worse before they get better?

I then have to sit for approximately 20 minutes and I can than walk normally again. Last week I went for an infusion of Solu-Medrol. I had one infusion for 3 days at 3 hrs. each. I feel pretty good afterwards and am not limping much at all anymore. My question is regarding side effects of Solu-Medrol. I realize that everyone is different but is there an average time frame for side effects? Today is the 3rd day AFTER the infusions were completed.

Solu medrol cpt code

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