In keeping with my commitment to spread the word on the value of mechanical circulatory support devices, The University of Virginia Medical Center in the linked article below offers a snapshot of where matters stand. Left ventricular assist devices are becoming more abundant for congestive heart failure patients. Simply put, LVADs work.
I've had my Thoratec HeartMate II LVAD for three years and a few days. The company's website carries a note that some 13,000 HM II's have been implanted worldwide.
Last year at this time the figure was 10,000. Progress comes in increments, but 3,000 new pumps worldwide in a year is pretty significant. Other manufacturers, of course, are not represented in the 13,000 figure. The more pumps and pump owners the merrier, from my perspective.
Here is the link to the UVA cardiologist's post http://www.dailyprogress.com/lifestyles/vital-signs-learn-the-facts-about-heart-failure-and-the/article_2001cbf6-98a4-11e2-8164-0019bb30f31a.html
I have continued on my LVAD journey these last few days as an inpatient at the University of Minnesota Medical Center. I had some symptoms of a blood clot in my pump and a kidney infection to boot. The infection was resolved with antibiotics. The clot is another matter.
Since the pump is not susceptible to internal inspection while installed, the docs use a series of tests to confirm their clot theory. Meanwhile, the patient gets a continuing dose of heparin by IV, which is a strong anti-coagulant. Heparin keeps the blood flowing, avoiding a stroke.
One option for a clot in the pump is to have another LVAD implanted. Another option is a new heart. Fortunately for me, another LVAD was ruled out "at this time." A new heart is the eventual goal, but none is on the horizon.
I've been on the UMMC heart transplant waiting list since Hallowe'en, 2011. In that time, I've had two 'dry runs'. The good news for me is that my HM II has allowed me to have a life awaiting a new heart. For that I am grateful every day.
My HeartMate II LVAD was a life saver. Established, April 2, 2010. The occasional entries for this blog were battery powered for 38 months. I owe continued life to the wonderful people at Thoratec, my cardiologists, Mayo Clinic surgeons, the University of Minnesota Fairview LVAD and transplant teams, and most importantly my caregiving family. On June 8, 2013, I was blessed with a heart transplant and now am no longer bionic. The journey of life continues.
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Here is my story of congestive heart failure and a return to life with a left ventricular assist device, my HeartMate II, an LVAD, ...
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I've been driving for several decades and have a decent driving record. To be practical, having an LVAD is no impediment for me t...
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This is another in a series of recollections of my time as a trial lawyer. It is made possible by my HeartMate II, left ventricular as...
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For the last five weeks, I have been fighting a driveline site infection. From reviews of the infected area by the LVAD support team at the...
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One of the attractions of the Christmas season in Chicago, was to see the animated figures in the windows at Marshall Field's. All of th...
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Since September, 2010, I have been attending monthly gatherings in Fargo of those who have LVADs and some who have had heart transplants...
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Yippee Ki Yay, driveline infection. I write with apologies to Johnny Mercer, fabled songwriter, and John McClane, fabled Bruce Willis good...
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This was the week that was. In the spirit of a Japanese proverb: Fall seven times, stand up eight. LVADs have their share ...
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I got the chance to be a "show and tell" exhibit for 60 plus EMTs at F-M Ambulance, the ambulance service in the Fargo-Moo...
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This reminiscence is made possible by my 27 month old HeartMate II LVAD, without which I would not be alive. At the time of th...
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