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Author Topic: PTH high, calcitriol not working  (Read 6162 times)
Sydnee
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« on: October 27, 2012, 03:38:35 PM »

since  the last labs Ed's PTH went from about 300 to over 800.
He is on the highest dose of calcitriol Dr is not sure what to try next. We are at a wait and see. 

not sure what to think.
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After a hard fight to not start I started dialysis 9/13
started on PD
hoping for home hemo starting to build a fistula 1/14
cause PKD diagnosed age 14

Wife to Ed (who started dialysis 1/12 and got his kidney 10/13)
Mother to Gehlan 18, Alison 16, Jonathan 12, and Evalynn 7. All still at home.
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Cordelia
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« Reply #1 on: October 27, 2012, 03:48:06 PM »

What is the highest dose of calcitriol?

I'm on .5 daily. I take 2 of those little orange football shaped pills.
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
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Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
bleija
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« Reply #2 on: October 27, 2012, 05:11:49 PM »

is phosphorus under control, cant remember which the other.  is he on sensipar... that may be the next step. it is an expensive one.. i had medicare part d with extra help so i only paid 6.50 but im not sure if there is a generic
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jeannea
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« Reply #3 on: October 27, 2012, 05:33:19 PM »

No generic yet for Sensipar. I had to pay about $125 for it on my Part D plan.
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bleija
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« Reply #4 on: October 27, 2012, 07:11:55 PM »

didnt think so, havnt been off of it for that long lol ;)
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Lillupie
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« Reply #5 on: October 27, 2012, 07:32:29 PM »

I never did well on calcitriol. I understand that is what Medicare or the bundling want. But Hectoral (sp) works good, usually that has brought down my pth, then my center will put me on sensipar.

Lisa
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« Reply #6 on: October 27, 2012, 11:21:06 PM »

How is his phosphorus? If they are both high, and remain high consistently it might be an option to remove the parathyroid.
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1995 - Diagnosed with vesicoureteral reflux and had surgery to repair at age 11. Post surgery left side still had Stage I VUR, right side was okay. Both sides were underdeveloped.
2005 - Discovered renal function was declining, causing HBP. Regular monitoring began.

March 2008 - Started transplant evaluation for preemptive transplant due to declining function.

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Sydnee
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« Reply #7 on: October 28, 2012, 07:03:24 AM »

Phosphorus is normal. The only labs that are not normal are magnesium and calcium are a little low. And of course PTH is high.
Ed is on 2 pills twice a day .5 mg also.
 We are on blue cross blue shield with medicare as a second. Ed's work is changing drug coverage for next year.
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After a hard fight to not start I started dialysis 9/13
started on PD
hoping for home hemo starting to build a fistula 1/14
cause PKD diagnosed age 14

Wife to Ed (who started dialysis 1/12 and got his kidney 10/13)
Mother to Gehlan 18, Alison 16, Jonathan 12, and Evalynn 7. All still at home.
www.donate2benefit.webs.com
amanda100wilson
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« Reply #8 on: October 28, 2012, 07:51:49 AM »

gland removal is a last option usually reserved for tertiary hyperparathyroidism which this isn't  at the moment if this increase is recent.  tertiary is where the gland has enlarged to the point that it kicks out  PTH is an uncontrolled manner and medication does not control.  I am on huge doses of sensipar, but my PTH is still not controlled.  I am due to have my glands removed.  sensipar is probably the next step.
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bleija
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« Reply #9 on: October 28, 2012, 02:22:18 PM »

when i switched to hemo, my pth flew to almost 1600. they double m,y sensipar and it came back to normal, they even put me back down on my normal dose after i went back on pd. and now after my transplant i take a regular vit D supplement and nothing else for my parathyroid
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del
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« Reply #10 on: October 28, 2012, 05:09:47 PM »

Hubby takes 120mg of sensipar everyday to keep PTH controlled.  It is very expensive though.  Luckily I have good insurance.
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cdwbrooklyn
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« Reply #11 on: October 28, 2012, 05:34:00 PM »

I take both sensipar and calcitriol low dose and it helps.  If you look on the sensipar's website, you should be able to find a company that will fund it for you so you only pay $5 for it. 
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Dailysis patient for since 1999 and still kicking it strong.  I was called for a transplant but could not get it due to damage veins from extremely high blood pressure.  Have it under control now, on NxStage System but will receive dailysis for the rest of my life.  Does life sucks because of this.  ABOLUTELY NOT!  Life is what you make it good, bad, sick, or healthy.  Praise God I'm still functioning as a normal person just have to take extra steps.
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« Reply #12 on: October 28, 2012, 05:36:25 PM »

John was fighting High PTh too.  Over 1800, but they put him on cacitrol and sensipar and now it is 117 Pth last lab.  They have dropped his sensipar to 30 and his cacitrol to 3 times a week.

If you check with your SW where you go, ask about a card where all you have to pay is $5.00.  That is all we pay for Sensipar.

Like above post indicated, removing "body" parts should be the last resort.  Only if all else is exhausted, IMHO!

God Bless,
lmunchkin :kickstart;
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Simon Dog
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« Reply #13 on: January 10, 2013, 01:54:25 PM »

You can get the card on-line from www.sensipar.com.   It's only for insured patients to help with copays, and seems to be designed to reduce resistance to the expensive drug while still hammering 3rd parties.

Getting Sensipar from my insurance was quite an experience involving many phone calls by myself, my doc, and the pharmacy.   Nobody said "no", but there were so many approvals required that I feel like I need to bring it home in a briefcase handcuffed to my wrist.
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lmunchkin
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« Reply #14 on: January 10, 2013, 06:17:27 PM »

Getting Sensipar from my insurance was quite an experience involving many phone calls by myself, my doc, and the pharmacy.   Nobody said "no", but there were so many approvals required that I feel like I need to bring it home in a briefcase handcuffed to my wrist.

 :rofl; :rofl; :rofl; :rofl; :clap; :clap; :clap; :clap;
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
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KarenInWA
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« Reply #15 on: January 10, 2013, 07:05:55 PM »

I am over 13 months post-tx and I have been dealing with this, too. My reg neph ordered a PTH on me and it was 200. He put me on calcitriol 0.25mcg once a day and it went UP to 249 or 289, I can't remember which (too lazy to go find it right now). I didn't want to go on another expensive med yet, so I suggested I try taking 2000iu of Vitamin D once a day. I take the Vit D3 in the am, and the calcitriol in the pm. I had my PTH done today, about a month later, and it is down to 150! Now just hoping this trend continues...

KarenInWA
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1996 - Diagnosed with Proteinuria
2000 - Started seeing nephrologist on regular basis
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Dec 1, 2010 - Transplant Eval Appt - Listed on Feb 10, 2012
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« Reply #16 on: January 11, 2013, 07:57:37 AM »

Just curious as to why your Medicare is secondary to BCBS.... I work in a lab where I register all patients that come through and I was told that Medicare is always first. That way Medicare is billed and whatever is left minus copayment goes to secondary billing. Not sure if that would make a difference. ???

Maybe it's different with Pharmacy?
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Transplant Failed/Put on Hemodialysis - May 2005
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CebuShan
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« Reply #17 on: January 11, 2013, 08:23:17 AM »

If you already have insurance, Medicare becomes secondary for a certain amount of time. (I can't remember exactly how long it is.) Plus you have to wait so many months before Medicare will even kick in.
 I've been on D since 4/10 and just this month Medicare became primary for me.
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Simon Dog
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« Reply #18 on: January 11, 2013, 09:17:54 AM »

The Fresenius nurse I saw this AM told me that Sensipar is being added to the dialysis bundle as of 1/1/2014 and at that point I will get it through their pharmacy as part of the covered treatment plan  :2thumbsup;  I do wonder if the fact that a $$$ drug is bundled will cause the "system" to introduce barriers making it harder for docs to prescribe it.  In my case, it was straight from Vit D IU 50,000 2/weekly to Sensipar.   Perhaps cost issues will cause pressure to make sure Sensipar is used only as a drug of last resort.
« Last Edit: January 11, 2013, 09:20:04 AM by Simon Dog » Logged
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