Really now.. I need to know what RNA is. How are you feeling? Did you make it to work? Keep ur chin up. lol That way the pups won't lick you in the mouth.
Hubby is right. It ain't over yet. Promise me you'll rest.. xxxxx. (no kisses, the pups will give you some) Karen :)
I'm going to a Gastroenterologist. MD. (What's a PI?) I'm starting to wonder about this guy. I have called 3 times in the past week and I don't get called back. This just ain't right. I don't need a nonresponsive doc to add into this mix - no way!!!
HCV RNA quantitative test to determine the amont of virus in your blood. It gives you a number for your Viral load.
at least that's how I understand it....and I don't know what PI is!!! Liz
When he asked if you were taking the PI's he is asking are you on triple therapy
According to your previous post you started triple therapy with Incivek on July 15th and it is a response guided therapy. Your vl was over 1000 IU/mL and according to the futility rules provided by Vertex you should stop all treatment now. The pegylated interferon and ribavirin are not able to destroy the protease inhibitor (Incivek) resistant variants. I'm sorry to say but SVR, even with a treatment duration of 48 weeks is highly unlikely.
HCV-RNA - hepatitis C virus-ribonucleic acid
Correction: All three drugs should be stopped with viral load of 1000 IU/mL or above at weeks 4 or 12.
Sorry about your news, as lynda says tx should be stopped.
Stopping Rules
According to the telaprevir label, all 3 drugs should be discontinued if HCV RNA is ≥ 1000 IU/mL at treatment Weeks 4 or 12. This rule exists because it was shown in clinical trials that if HCV RNA levels did not drop < 1000 IU/mL at Week 4, the likelihood of achieving SVR was exceedingly low. Continuing telaprevir alone without adequate virologic suppression increases the likelihood for emergence of resistance variants. The label also specifies that if HCV RNA is detectable at Week 24, pegIFN/RBV should be discontinued.
The above is from clinical care options site.
http://www.clinicaloptions.com/Hepatitis/Annual%20Updates/2011%20Annual%20Update/Modules/DAA%20Naive/Pages/Page%206.aspx
doc said since my viral number was low the first time that he wanted to go a little more, that it was a gray area.
yes, i'm doing the triple therapy - sorry i didn't put that together with the letters PI - a little of this technical stuff goes a long way with me and it gets confusing. all i want to do is get well.
I certainly feel pretty FUTILE now for sure - futility rules or not - thanks hrsepwrguy and lynda607.
sorry if i seem slow.
Futile Shmutile. I feel such a bond w/ you cuz we started on the same day. So I'm feelin mad right now. Let's wait n see... Go for the 2nd opinion if you have that option w/ ur insurance. For some reason they have you a week ahead of me on blood work. What was ur first set? when was it done? forgetful.... Must be the PI...
Magnum PI? (LOL - showing age!)
We started on the 15th with first shot.
Did one July 29, and one Aug 12....that's what I got back today.
I think. My calender is on my desk at school. (of course)
No apology needed. I guess the results are the reason the doctor wants the repeat? Even tho the doctor doesn't usually do the lab tests, it is worrisome when the doc isn't top notch and unresponsive. Not returning calls you do not deserve. Please keep us informed.
I'd be huggin my puppies too. (Don't tell Karen) but I kiss mine too. You and the hubby and the puppies stick together and you'll find a way to beat this thing. I've seen some posts on here lately about some new trials. They always get me confused when they refer to the drugs by the study names so I don't know what the drugs are, just don't give up. This sounds like a good time to find a good hep c doctor that participates in trials and get in so they know you are out looking for some of the new stuff. Your participation may cure you and help others for whom the triple therapy doesn't work. I wish you all the best. Someone once said you can't win if you don't play the game. You're playing and you will win, if not this time, next time.
G
G
Although it may seem bleak right now hang in there as best as you can.
There will be time to access what has happened and learn from this experience.
That your Gastro has not responded in a timely manner to your inquires is a poor reflection of their commitment to patient care.
That the doctor didn't follow the proper protocol for treatment is inexcusable and unprofessional.
If you doc won't help you...I would talk to another Gastro maybe in your doc's office or somewhere else and get their approval to stop treatment. Does Vertex have a help line for patients? Maybe they can advice. You DO NOT want to develop resistance by continuing treatment with no chance of SVR. That would be something that you couldn't correct as easily as finding a new doc etc. I believe resistance lasts for a number of years as far as is currently known. Everything else you can change to help you to continue to fight your hep.
Tip to get a response from your doctor's office:
One trick I have done in the past - is to go to the doctor's office (I usually will dress up in a tie and suit so they see me as a serious business person) and wait there until someone will see you. Yes, you need to be a pain in the a$$ but this is YOUR LIFE that we are talking about here. What better time spent. Be willing to sit there for hours if you need to. Try to stay claim and know exactly what you want before going there. You don't want to get all emotional and crazy that will work against you. Make your needs known and calmly stick to your guns. Don't let anyone brush you off. You pay for their services and you are under the care of the doctor. They need to treat you with respect and dignity. Eventually they will have someone see you as you will make them uncomfortable and they will be forced to deal with you. (On the phone you are just a voice and they can hang up to get rid of you). Explain your dilemma, calmly and a clearly as you can and that you need an answer today. Not later or tomorrow. Let then know you are willing to wait all day if need be. They will get the message.
Good luck. Let us know what happens.
Hector
Oh my cctex, I do not see your doctor's logic. I don't think there is much grey area to it, given the data provided in all the trials. Regardless of the 293 viral load at two weeks, your 4 week viral load increased and was well over the the 4 week 1000 IU/mL established protocol. That is something you do not want to see, especially when the patient is treating with a protease inhibitor.
Good Luck. I hope things work out.
Thank you! Made me feel better to hear kind words.
Thank you for commenting in such a positive way! This response helped me a lot! I think I will do just as you suggest. I don't think I am being taken seriously and it's just not right. I used to have the BEST doctor in our area, he retired just this year. This has been a very strange experience for me. I'm used to a completely different "bedside manner."
Thanks again, and have a great weekend!
Good for you. Demand the respect you deserve as a patient and as a human being. Don't let anyone treat you differently.
Have a great weekend!
Cheers!
Hector
Sorry about these results....an increase in viral load is something you don"t want to see during treatment and given the fact this is well above the discontinuation protocol for in civek I would agree with the others to stop.
It would seem odd the doctor is saying this is a grey area when all there is to base therapy on at this point is what has been tried in trials and there was no grey area in those about possible resistance developing .. unfortunately in some resistance variants were seen early on
Hector has given you great advice ..to get in touch with a help line at Vertex and discuss with a knowledgeable doctor or virologist there(if possible) to discuss the advice your own doctor has given you to continue past the discontinuation period.
Best to you
Will
Well girl, almost ALL of the forum experts have weighed in. :D There are always options. Hector, you crack me up. I do the same thing. I dress to the 9's for every lab n Dr. appt. Drop emotion at the door and go straight for logic. Give you a chance to show those legs in a nice skirt. haha!
Remember, in Oklahoma, lipstick and mascara are considered war paint. You Texas girls can do that. Tease that hair a little? :) Dream sweet. Karen xxx
But Karen, I'm a Beach Texan & not a Big Hair Texan!! WAIT! I know, I'll put my librarian duds on & give him THE LOOK like I give the kids that are misbehaving in the library if he doesn't listen to me. I'm thinkin' I'm gonna fire him. I'm calling Vertex 1st thing in the morning. Thanks again every one.
Karen,
I keep my legs well hidden. Trust me, no one wants to see these legs. No jacket and tie and shorts fashion faux pas for me! I also don't wear socks with flip flops you'll be happy to know. ha ha!
Since I am on disability it is a chance for me to wear my best clothes.
Funny story...I got listed for a liver transplant at a transplant center back east and always used to dress up for my appointments. I used to go and hang out in the cafeteria a lot while I waited for appointments or tests. I can't tell you how many times the cashiers thought I was a doctor or worked there (employees get a discount on the food). All because of how I dressed. I am 59 years old and an a WASP like most people at this very New England transplant center so...Although I couldn't flash my legs or bat an eye I still was able to use the "apparent" authority of being a 59 year old professional to my advantage without saying a word.
Bottom line: If it works for you use it.
And I didn't even have my voodoo dolls then! Look out I got my mojo working now and I am ready to conjure up some spells. ~~~~~~~~~~~
Hector
;-)
Hi, just wanted to say this is not something the "forum experts" came up with. This is the guidelines that the real experts have decided. Clinical care options is one of the top sites with many of the worlds leading hepatologist base their finding. Doctors, researchers, and real time trials have decided this. There are other sites where doctors have the same opinion regarding when to stop treatment.
The good people here care alot and sure don't want to see anyone jeopardize their health or their future chances at treatment. As always one should consult with a Doctor before deciding anything.... Wishing you the best in your treatment.