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Hello Protagor,
Genotype 1 is easier to cure than Genotype 3.
Cirrhosis makes patients harder to cure and both patients have cirrhosis.
Women are (slightly) easier to cure than men
While it is entirely possible both patients will be cured with 12 weeks Sof+Dac+Riba
1) The response of the man with GT1 is slow – a viral load of 148 @ 4 weeks is unusually high. I would estimate his current chances of cure at 85-90% rather than the ~95% we expect
2) The response of the woman with GT3 is much better (at 4 weeks test) but expected cure rate for GT3 with cirrhosis is 90% with 12 weeks treatment.
The effect of extra treatment is small. In rough terms adding 4 weeks (so 16 weeks total) might add 4% to cure rate, adding another 4 weeks (so 20 weeks total) might add an extra 2% and adding another 4 weeks (so 24 weeks total) might add 1%
What you should see is that going from 12 weeks to 16 does add quite a bit to cure rate, but each extra lot of treatment adds less benefit.
For both patients I would suggest going out to 16 weeks total or longer if this can be afforded. For GT3 patient I would like more than 16 weeks if this is possible.
Daclatasvir does have some drug and food interactions that can either raise or lower the levels in the blood. Are any other medications being taken? What does diet of both people look like – is it the same food every day or is there good variety? (if good day to day variety any problem food does not tend to appear for many days in a row).
YMMV
Hello Oregondaisy,
Yes, you are cured.
Best wishes
James
YMMV
Hi Sven,
Ah the 70’s – you’d never get away with an 8 minute song these days, not even > 4 minutes – unless of course it was:
https://www.youtube.com/watch?v=fJ9rUzIMcZQ
YMMV
Hi Chris1234,
Mavyret is a very clean drug combination that tends to cause very few side effects. The most important thing is simply to take the 3 pills at roughly the same time of day, every day, and not forget to take them.
The effect of treatment tends to depend on how symptomatic you are.
During the first week, the vast majority of the virus is killed off and some patients notice a mild flu like illness.
By week 2, if you’ve been (say) getting some brain fog you may well find that starting to clear.
By week 4 it’s not unusual for patients to say “I have not felt this good for 20 years”
YMMV
Hi KarenB,
The waiting for the results can be hard. Trust the statistics – the odds are very much in your favour.
Best wishes
YMMV
15 September 2019 at 3:37 pm in reply to: Cirrhosis and Resistant Hep C – New Symptoms are they serious? #29444Hi G,
There is a 96% chance this treatment will cure you. Cured you are unlikely to die of liver disease, your liver function will improve, but you will still require monitoring for HCC.
In the event you’re in the 4% (again) then yes, your disease will progress and it will quite possibly kill you.
Transplanting the livers of patients with end-stage Hep C is common – it’s the commonest cause of liver transplantation. Patients with active Hep C are transplanted and then cured post-transplant – we find that Hep C is much easier than cure post transplant than with cirrhosis. Because the DAAs have been doing such a good job getting rid of Hep C it’s much easier to find a liver transplant these days as the demand (from Hep C) has virtually disappeared.
YMMV
Hello KarenB,
Your enzymes look great. You can have a sneak peek at them before SVR12 if you are worrying. If they stay down you are good.
YMMV
15 September 2019 at 3:40 am in reply to: My doctor is insisting on another Ultasound. Treatment 8/16 #29442Hello beahavan,
Although there is a form of HCC that does not produce AFP the pre test probability of you having an HCC are the less than the general population (without HCV) because of all the monitoring we have done excluding it.
YMMV
12 September 2019 at 1:05 pm in reply to: My doctor is insisting on another Ultasound. Treatment 8/16 #29435Hello beahaven – from your F0-F1 starting point your HCC risk is pretty much the same as the general population (ie very small).
Normal, F0 and F1 are all close together. F3 and F4 are close together. F2 is a middle ground. You are at the lowest possible end for fibrosis and the lowest possible risk for HCC. While there is a push to extend surveillance to F3 patients there is not a push to extend it to F2 or F1 or F0.
Your doctor would seem to be being over cautious. Monitoring your AFP is almost certainly sufficient (if you are of a paranoid disposition), particularly if funds are tight.
If you were my patient I would not be monitoring you for HCC (with either AFP or U/S) and would have declared you cured.
The occasional patient with F0, F1 and F2 will get an HCC. So to will the occasional patient who does not have Hep C (or Hep or any other liver issue.
YMMV
Hello vikamb,
Your mother’s results are as expected.
Her liver enzymes (AST/ALT) are improved
The change in platelets from 74 to 71 is not significant as is the change in bilirubin from 1.9 -> 2.2
The anaemia is from the ribavirin – we can see the haemogobin fall to around 9.5 quite quickly but this has been stable so is unlikely to fall any further.
Good food is good medicine but the seasons do as they please and we can’t eat what has not grown.
Things are definitely heading in the right direction.
YMMV
No, it only applies to daclatasvir
YMMV
Hello Apogal,
Fingers crossed it becomes less and less.
YMMV
8 September 2019 at 6:43 pm in reply to: Cirrhosis and Resistant Hep C – New Symptoms are they serious? #29422Hi G,
Drop me a line by email and we’ll get going.
Best Regards
James
YMMV
Hello Apogal,
Itch is very common with Hep C and while there is no 100% guarantee most patients troubled by itch before treatment find it goes away on/after treatment.
Please keep us updated about what you notice.
YMMV
7 September 2019 at 2:47 pm in reply to: Cirrhosis and Resistant Hep C – New Symptoms are they serious? #29419Hi barry666,
I’m pretty sure I copied you into an email to Prof Gane so you have my email address.
If you can get your specialist or GP to a) Prescribe you 16 weeks Maviret and b) Fill in a Medsafe form for 16 weeks Sofosbuvir we can (potentially) get just cracking now for you.
YMMV
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