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Most effective way to administer IVIG

Blood Cancers & Disorders | Last Active: Feb 15 8:13am | Replies (8)

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@lucy84

I do question how the IVIG treatments are being administered. When I go in for a 3 or 4 month check with my oncologist, my Ig #’s are always way below normal. Then, I take 4 infusions, two per week for two weeks. I have heard that other people take one treatment each month. The nurses always question me about the the way I am getting them and have commented that most people get one per month. I would like to hear from people who get the IVIG treatments, if they are getting blood work results back within normal range, and how they are being administered. Thanks.

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Replies to "I do question how the IVIG treatments are being administered. When I go in for a..."

Hello @lucy84

The regiment I was on after Car T was, once the levels fell below minimum, I would receive one treatment once a month for four consecutive months. (Regardless how the levels changed) My blood would be checked on a monthly basis and the treatment would start again once the levels dropped below the tolerance level. This went on for about 2 years after cancer treatment. My blood is still well below minimum levels however the treatments have been discontinued as I do not get infections. Treatments could start again if infections occur.

I had a reaction to the infusions and had to take take pre-meds before the infusions. Do you have a reaction?

Hi @lucy84

I have MCL stage 2A which was diagnosed last April. It's taken an indolent course so far and I have been on watch & wait with it. However, I also was diagnosed with CIDP and my neurologist started me on a four month trial of IVIG last October. I received the loading dose of five consecutive days followed by twice weekly infusions. I just had a new EMG which didn't show I responded to the treatment. My bloodwork was also affected by the IVIG. Everyone's treatment is different; some get IVIG 1x every 3 weeks, some 1x monthly, some 1x weekly and, some, like myself, receive it 2x/week. Hope that helps.