Anyone experience Blood Clot near port ??

KathyA · 10-05-2006, 03:49 PM

I just came back from treatment. I have a swollen arm and hand the doc thinks it is a blood clot near the port. He put me on coumadin and I will see him again on monday. Today is Thursday. He suggested an ultra sound but said he really didn't care if I had one or not since where he belives the clot is does not usually show well in the ultrasound and he would put me on coumadin anyway. Does anyone have any experience with ports and blood clots? I'd love to hear.

I'm beat. This is my 3rd port in 1 year 4 months. This is my fourth different treatment in the same amount of time. Taxotere + carboplatin, navelbine, gemzar and now navelbine again all along with herceptin. Tumors to lung, liver and bone the cicle seems to be stable, increase, stable increase.

Thanks for listening.
kathy

EllaD · 10-05-2006, 08:13 PM

KathyA,

I had a swollen arm on the port side right after my first chemo. It was very painful though. I had a doppler ultrasound since they thought it was a clot. Turned out to be phlebitis. I began chemo only 10 days after my third surgery for the bc. Apparently my veins were infected from one of the iv's in the hospital, my white count dropped so that I couldn't fight any infection.

I hope things go better for you.

EllaD

lisahammo · 10-05-2006, 08:35 PM

Hi Kathy

I am on to my second port, and all seems to be going well with it now. My first port only lasted about 6 weeks before I too, developed a blood clot. My arm turned blue, and swelled up. Nothing showed on ultrasound, doppler or anything, but they took the port pretty quickly. There was never any sign of the clot, but it was obviously there somewhere. I was put on Clexane injections twice daily for a month, and they had to struggle to find a vein for treatment.

They swapped sides with a different type of port about 12 months later, and as I said, no problems since.

Good luck. It just feels like the last damn straw. It is so frustrating, and enough to tip you over the edge. Just keep telling yourself, you have no choice, you have to keep going.

Love Lisa

Ruth T · 10-06-2006, 06:35 AM

Hi Kathy,
I had a clot from my port. My armpit was red swollen and very sore so the surgeon had me go for a doppler ultrasound and they found it. Put me on Lovanex shots (in the stomach) for 5 days and coumadin daily.They say it will resolve itself but no telling how long. One dr said maybe six weeks. The surgeon won't remove the port until it's resolved because of the chance of some clot moving during removal. They were able to use the port for my last chemo treatment though. I guess alot more have better luck with their ports- it's been very discouraging. I also have to see the dr regulary for the INR/ PT levels of the blood.This isn't a very encouraging post, but I wanted to share that you are not alone! Hang in there!
Ruth T.

KathyA · 10-06-2006, 08:17 AM

Thanks so much for replying. Ruth the note wasn't discouraging for me. I'm happy to believe now that I won't have to have this port out and that the drugs will help. I will ask for the ultrasound since all you gals were able to see one or no clot and that you were able to act accordingly. It's a new day and I feel better already.

Wishing you all blessings and better health.

Kathy

John21 · 10-06-2006, 10:23 AM

Don't you take coumadin everyday to keep your port working. My wife has for ever.

John

KathyA · 10-06-2006, 01:09 PM

John
My Onc says he used to give coumadin regularly to all his patience except now he says that there is research out now that showed that people got the blood clots just as much with coumadin as without it. Now he says he just gives it if there is evidence of a clot.

Best to you and your wife. thank you for responding.
Kathy

Razz · 05-04-2007, 09:01 AM

I had an infusaport inserted in my left side in February which had been accessed three times without any adverse effects for early onset estrogen positive, Her/2 neu positive breast cancer. Then after being accessed for the fourth time my arm became achy (like I had slept on it for too long), swollen and different in colour (red and blotchy) to my right arm. Investigations into these symptoms revealed a clot in my interior jugular and subsequent treatment with self administered Clexane injections. Mistakenly I thought my biggest worry from this would be the clot moving to my lung. (Well maybe it is!!) However discussions with my oncologist revealed another worry…I was about to commence Tamoxifen which doesn’t react well with Clexane. Three options were offered to me to deal with this (I won’t bore you with all of these details). After listening and trying to digest all three, I asked my oncologist what she felt would be my best course of action, this was ovary removal! I was wondering if anyone has had this faced this dilemma and all of the associated side effects, not the least being rapid onset menopause at 45.

Jen · 05-04-2007, 05:05 PM

John21

My daughter had a subcutaneous vascular access device (Mediport) for intermittent antibiotic infusions and wasn't on any anticoaggulant except for flushing the port once a month w/ 5ml of 100iu/ml heparin and 2ml of 100iu/ml heparin if it was accessed and not being used. She never developed any blood clots but the port did quit working after about 6 years due to the formation of a fibrin sheath on the tip of the catheter. Hope that info helps.

StephN · 05-04-2007, 06:49 PM

Add me to the clot problem list! Also to do with my central venous line - second one which was placed last Aug.

I got home a bit ago from a 24-hour hospital stay while a whole raft of different docs and residents went over me to decide what to do. I am also started on the Lovenox shots - only TWICE a day to start with. These are pricey little devils at approx $44 each.

I am posting a separate thread, but appreciate that these messages were here to greet me since I have been away from my computer for a couple of days.

JeanBeanie · 04-11-2013, 08:25 AM

Count me in.. I just got the news this past Tuesday clot in the neck near my port. Get 2 shots a day in the stomach.
Not sure how long the shots will be I have an aultrasound on the 22nd of April. This does stink just another issue on our list. I had the port in for two years and they do not want to remove or change position if they don't have too.