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- Yes I experienced failure of the port due to device malfunction.
- Yes I experenced difficulty with access and blood return.
- No I experienced no problems.

Poll Results
-
Yes I experienced failure of the port due to device malfunction.43% (25)
-
Yes I experenced difficulty with access and blood return.41% (24)
-
No I experienced no problems.16% (9)
I am sorry to hear of your terrible experience. Unfortunately, there are no doctors on this board.
I would suggest consulting with a lawyer if you decide you want to pursue it legally. Before deciding how your doctors will react, you may want to speak with him/her/them and see how they would feel if you went after the company you feel created the situation. I hope you can have open and honest conversations with him/her/them.
Finally, I would also strongly urge you to seek some counseling. That was a very traumatic experience for you as you describe it, and a good therapist or counselor can help you work through it. The hospital you were in may have a patient advocate who could recommend someone.
In support,
Byroney
My wife has several chronic health conditions and for three years has relied on a Hickman-type central venous catheter for nutritition, hydration, and medication. So - we're familiar with the benefits and drawbacks. One drawback is the risk of line sepsis; in early August her Hickman double-lumen line became infected and had to be replaced. This time a BARD PowerLine Port was installed. Last Saturday one of the external lumens failed - we're not certain of the precise failure mechanism but the end cap appeared to separate from the line - it never actually broke off but there was steady dripping where the end cap and line join. We clamped the line and called the Vascular Surgeon. We saw him in his office on 15 Sept., and scheduled surgery today (17 Sept) to remove the PowerLine Port and implant a Hickman. Last night (the night before surgery) the second lumen failed - its mode of failure appeared to be the same as the first. It's now 6 PM Friday, 17 Sept.; my wife had her new double-lumen Hickman installed today; and today's procedure went well. The remaining concern now is infection - when each of those ports failed fluid leaked out, meaning of course that external contaminants could have gotten in.
BTW, the poll allows you to select only one response. My wife's Power Port definitely malfunctioned, and that's the response I selected; but from the time it was first installed blood return was problematic - four out of five weekly blood draws were possible only after TPA was administered.
We're sorry to hear about your experience. Like you we're in a quandary - we'd sing praises of our Doctors to anyone who asks, but what can you say about a piece of hardware with these problems? I'm an Engineer with a full career of experience in Test & Evaluation. What kinds of tests and analyses was BARD required to perform, before they were allowed to put this equipment on the market?
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90222
I have now contacted an attorney with my MDs blessing regarding this matter. I am actually having PTSD regarding this incident. I am still suffering quite badly from anxiety and recurring nightmares. I, like your wife, am suffering from multiple medical issues at present, and have had TONS of procedures done including colostomy and stents placed in my renal arteries. I have never experienced any kind of after affects from those procedures. This thing with the port was a different animal all together. My attorney said he needs to establish the scope of the problem with these devices before he will take on my case. He currently has an RN reviewing all info and she indicated that if the device was made shoddily in a below par location then there would be a case, however if the problem is actually the design flaw of the device which is causing it to malfunction, the law says they cannot pursue compensation in that instance, so I'm waiting to hear back from them about all that. I hope your wife will do well with her new device and that she will be safe from returning infection. My Bard drained, as well, when it was in place. Best of luck to you both.
Raesofhope
I was diagnosed with a huge DVT in my left leg on April 12, 1997. I was admitted, put on a heparin drip (IV) and then gradually switched to oral Coumadin. I was released from the hospital on April 19, 1997. The next morning, Sunday, April 20, 1997, I awoke at 2:00 am with terrible trouble breathing, chest pain and vomiting blood. I was rushed back to the hospital and diagnosed with a Pulmonary Embolism (PE) in my left lung. Part of the large clot in my leg had broken off, traveled up the vena cava vein through my heart and lodged in my lung. They surgically inserted a Greenfield Filter into my vena cava through a tiny incision on the left side of my groin area and kept me in the ICU for 3 days to ensure my blood was properly anti-coagulated. I have been on an oral anti-coagulant since then and will be for the rest of my life.
While your DVT is in your arm, a PE would probably take a similar path. I think I have described fairly well the symptoms to watch for.
I pray your body naturally absorbs the DVT in your arm and you have no further complications.
you might want to take a look at another thread on BARD ports -- http://forums.webmd.com/3/chronic-disease-and-disability-exchange/forum/817/1?@guest .
-- susie margaret
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