Priyanka Chopra, NFL, and Organ Donation: How’s That for a Mash?

Priyanka Chopra, organ donation, Dr. Chris Barry, bLifeNY, #WLY, transplantationYes, Priyanka Chopra really is coming to Rochester, NY this October 5th to deliver a keynote address on organ donation awareness at our Transplant Gala. And yes, she will debut her single “In My City” September 13th on the NFL Network’s Thursday Night Kickoff (before and after each show for 13 weeks!). Singing along will be will.i.am, production by RedOne and Brian Kennedy, and management by Troy Carter of Lady Gaga fame.

So you’re probably thinking “WHAA…?” Why would this woman who is already a Bollywood superstar and now poised to splash in to yet another multibillion dollar industry care about organ donation?

Well, I submit to you that she is compassionate, intelligent, and grounded. She was certainly very real when I met her–no airs about her, just a calmly focused intensity and kindness. She is sincerely passionate about organ donation awareness and has already publicly pledged to become a donor. It’s a difficult subject to get people to seriously think about and her massive international influence will help save or improve hundreds of thousands of lives. Once again, I salute you Priyanka Chopra for your courage and foresight. Can’t wait to see you again on October 5th!
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Priyanka Chopra, organ donation, Dr. Chris Barry, bLifeNY, #WLY, transplantation

Priyanka Chopra, organ donation, Dr. Chris Barry, bLifeNY, #WLY, transplantation

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Organ Donation Persuasive Speech: Dr. Chris Barry TEDx

Here is an organ donation persuasive speech that I gave at TEDxFlourCity in Rochester, NY in June 2012. I hope you enjoy it and consider sharing with your family, friends, and loved ones.


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organ donation persuasive speech Dr Barry TEDxorgan donation persuasive speech

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Priyanka Chopra is coming to Rochester, NY for the Transplant Gala!

 

 

The University of Rochester Medical Center’s Center for Transplantation will be celebrating the 20th anniversary of the liver transplant program on Friday October 5th, 2012. There will be a VIP Reception from 6-7 pm and the main event will start at 6:30 pm at the Riverside Convention Center in downtown Rochester, New York.

Our keynote speaker and special guest will be Bollywood superstar Priyanka Chopra. Please note that Ms. Chopra will not be performing for this event. She will deliver an address promoting organ donation awareness.

General tickets will be $175 per person ($75 tax deductible). Higher sponsorship opportunities are available as described above.

Become a Table Captain to ensure your group of 10 sits together at the gala. The role of a table captain is to fill all the seats at your reserved table. To recognize your role as table captain, your name will be listed in the evening’s event program. Money for your table is due on Friday, September 21st. by 4:30pm.

Questions? Contact Charice Hoyt-Davis via eamil c.hoyt-davis@rochester.edu or 585-461-2553.

Send check payable to University of Rochester to:

Charice Hoyt-Davis

U of R Alumni & Advancement Center

300 East River Road

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Rochester, NY 14627-8996

To pay by credit card, contact:

Charice Hoyt-Davis at 585-461-2553

This year we celebrate the 20th anniversary of the liver transplant program at the University of Rochester, led by Division Chief Dr. Mark Orloff and originally founded by Dr. Seymour Schwartz. We are the only liver transplant program in upstate New York and since beginning 20 years ago, we have had the privilege to perform over 1500 liver transplants with remarkable success rates. The amazing success of transplant has ironically led to our greatest challenge: that is, far more people are awaiting transplants than there are donor organs available. We decided to highlight this challenge as the major theme of our 20th Anniversary Gala on October 5th, 2012.

A remarkable, almost magical set of circumstances evolved during our planning of the gala. We thought it would be fun to throw a Bollywood themed party, in part to celebrate the significant contributions of our Indian colleagues at the U of R to excellence in medicine and research, but also Indians know how to have fun and a Bollywood party would simply be a blast. As a division, we would not be able to achieve such clinical and intellectual excellence without the contributions of our colleagues such as our transplant surgeon Dr. Randeep Kashyap, our transplant hepatologists Dr. Ben Maliakkal and Dr. Gopal Ramaraju, the chief of gastroenterology Dr. Vivek Kaul, our anesthesiologist Dr. Ashwani Chhibber and imaging scientist Dr. Vikram Dogra.

As we continued planning, we realized that one of our patients, Dr. Ashok Chopra who came all the way from India specifically to URMC to receive his care, had quite a famous daughter. Wouldn’t it be wonderful and powerful to have Priyanka Chopra deliver a keynote address promoting organ donation? Her fame and her social conscience to help make the world a better place in so many ways could send an important message to people around the world that organ donation is a miraculous endeavor and that we shouldn’t be so uncomfortable to at least think about it. Organ donation, after all, touches the lives and saves the lives of hundreds of thousands of people.

So we asked her and she graciously and immediately said yes, she would love to have an opportunity to speak about such an important cause. It’s a difficult cause, because so many of us feel uncomfortable facing such things. And her willingness to speak up demonstrates true courage and forward thinking on her part. We hope to continue this work in India with the help of the transplant surgeons we have trained here and who have returned home. Our former fellows are positioned to become leaders in the emerging field of deceased organ donation in India. It won’t be easy, we’re talking about cultural change. But with the support of the Chopra family and our connections to transplant in India, we hope to save many more lives in India through this initiative.

So join us on October 5th for what should prove to be the biggest party of the year in Rochester. Funds raised will go to URMC Transplant’s 4 Pillars of Care: patient Care, social Activism (organ donation awareness), Research, and Education.

Follow bLifeNY on Twitter (@bLifeNY).

Friend us on FaceBook: bLifeNY

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Facebook and Organ Donation–Yay!

We are truly psyched here at bLifeNY.org that the good people at Facebook are encouraging its 900 million members to consider becoming organ donors. An article in today’s New York Times and an interview on ABC News with Mark Zuckerberg explain FB’s foray into social entrepreneurship by promoting organ donation awareness. This is a perfect vehicle for all of us to begin the conversation about organ donation and transplantation, learn more about what is exactly involved, and to start having thoughtful conversations with our friends and loved ones about the subject. Hopefully, many people will be moved to register their intentions to become an organ donor and thousands of lives can be saved or improved.

Remember the facts:

1. You can’t be too sick or too old to register to become an organ donor (the transplant professionals determine organ suitability when it’s time).

2. All religious traditions throughout the world support an individual’s decision to become a donor.

3. Health care professionals provide the same level of care to everyone, regardless of their organ donation status.

Some online pharmacies allow you to order your prescription pharmaceuticals online, and have your order filled but not shipped until the prescription arrives. cheap cialis india The product gets delivered all over the world now sildenafil professional can experience the magical effects of the powerful Amazon fruit. This very well could be the cause of cialis properien stress. Makhlouf and Deek have considered surgery when splinting cannot correct acute deformities; however, we will sildenafil tab review the present literature for acute open and chronic deformities. 4. Organ donation is a gift. There are no costs associated with registering to become or being an organ donor.

5. The organ donation allocation process is inherently fair.

6. You need to enroll in your state organ donation registry and talk with your family and friends about your decision in order to ensure that your wishes are fulfilled.

Think about it. Learn more. Talk to your friends and family. And if you really want to help make the world a better place, consider registering to become an organ donor (Donate Life America or go to the New York Donate Life Registry if you live in NY).

Friend us on our FB page and post your thoughts and intentions on your own page!

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April is Donate Life Month

This month we are celebrating organ donors, donor families, transplant recipients, and the success of transplant medicine with Donate Life Month. Finger Lakes Donor Recovery Network has produced two great new videos:

The URMC Center for Transplantation River Run takes place this Sunday April 22 to raise awareness on organ donation and to raise money for the transplant patient needs fund. The event starts with a proclamation from the Monroe County Legislature, delivered by Josh Barouth,  to celebrate donors, their families, and recipients.

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bLifeNY.org continues to flourish on many fronts. Two student organizations are being established: bLifeUR at the University of Rochester and bLifeRIT at Rochester Institute of Technology. On May 5th, bLife will have a booth at the Imagine RIT festival. We will be encouraging people to recycle themselves!

Also, Matt Randall, our Brighton High School student bLifeNY member, recently wrote a nice article in the BHS newspaper. Thanks Matt!

Finally, listen up for Rob Kochik (Executive Director of Finger Lakes Donor Recovery Network) and I on WXXI’s  radio show Healthy Friday on April 20 at noon. We will talk about, can you guess?, organ donation awareness.

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Organ Donation: What Does it Take to Engender a Cultural Shift?

bLifeNY wants a cultural shift around organ donation awarenessWe created bLifeNY.org to engage and educate the public about the importance of organ donation with a particular focus on New York State, which ranks 48th in the nation in terms of organ donor registration. As a transplant surgeon, I am saddened on a daily basis by the discrepancy between the number of people on the waitlist for transplantation and the number of available donor organs. Nationally, nineteen people die every day awaiting this precious gift and this problem is particularly acute in New York. Many noble efforts exist to impress upon the public the necessity and goodness of organ donation (for example, Donate Life America and organdonor.gov), but there remains a pervasive cloud of misinformation and undereducation that impedes these efforts.

What exactly is the problem and how do we go about tackling it?

Transplant clearly works and it works well. Apparently, this is not widely appreciated, even among many health care professionals. Transplantation is one of the most successful endeavors of modern medicine. With the advent of highly effective antirejection medicines, improved surgical and anesthetic techniques, and medicines to prevent or treat infections common to patients with suppressed immune systems, transplant has become the treatment of choice for end stage organ failure. Patients do very well overall, with greater than 70% long term success rates. It’s important to realize that transplant is not only a life saving and life prolonging treatment, but it is also life transforming. People get their lives back, they don’t just maintain.

Organ donation saves lives. A single deceased organ donor can save eight, or even nine, lives (heart, two lungs, two kidneys, one liver or a liver split into two pieces, pancreas, and intestines) and dramatically improve the lives of up to 50 people through tissue donation (corneas, skin, bone, etc.). Also, a healthy person can donate one kidney or a portion of liver to a friend or loved one. Becoming an organ donor is an extraordinary event. It is a miracle in the purest spiritual sense.

Studies show that most people support the notion of organ donation. So why are so few people actually registered to become donors?

Well, organ donation is icky. It requires consideration of death, loss, tragedy, and alteration of self. These are profoundly disturbing issues and emotions. People don’t like to think about these things. The challenge of organ donation awareness is to shift the perspective and provide appropriate environments for thoughtful consideration.

Education is the key. People need to know things such as transplantation is incredibly successful, that you’re not necessarily to old, too sick, or too gay to be an organ donor, and that the process is respectful, compassionate, and inherently fair. The public deserves to be educated and health care providers (especially early on in their training) need to be educated.

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Environmental decision making is also critical. The two most common venues for consideration of organ donation are the DMV and the ICU. Neither of these environments is conducive to contemplation of end of life decisions. They are, of course, important venues and efforts are ongoing to improve intervention efficacy, but other venues may be even more effective. For example, we believe that organ donation should always be discussed in the context of estate planning. When an individual first meets with an attorney or other estate planning professional, organ donation education and the opportunity to register one’s intention to donate should be coupled to discussions of living wills, health care proxies, and advanced directives. This is a highly appropriate environment for thoughtful consideration of organ donation, especially if accompanied by effective education.

Other appropriate environments include the primary care physician’s office during a well visit and institutional or corporate HR departments during benefits and retirement sessions

In Malcolm Gladwell’s book “The Tipping Point”, he identified three types of people necessary to create an environment conducive to bringing a social phenomenon to a “tipping point” or going viral. These are Connectors, Mavens, and Salesmen. Connectors are those people who know a lot of people and who are facile in cultivating large clouds of “loose acquaintances”. Social media experts (for example, most all young people these days) must be enlisted in the effort to increase organ donation awareness. The mavens are “collectors of information” and information experts. Transplant professionals such as surgeons, physicians, nurses, organ procurement professionals can all be engaged to fulfill this maven role. Salesmen are those who possess the power of persuasion. This is a rare talent that is not necessarily cultivated in the field of medicine and perhaps is not entirely teachable. For the message of organ donation’s importance to enter the popular consciousness, the right mix of connectors, mavens, and salesmen must be assembled.

But this won’t be enough. We also need stickiness and tenacity. Organ donation is icky, but “recycle yourself” is sticky. When people hear “recycle yourself”, they smile. They get it right away. It shifts your perspective away from the less palatable aspects of organ donation and allows you to consider donation in a more comfortable, positive light. Viral phenomena require sticky concepts. Sticky thoughts and slogans need to be identified and run with relentlessly. If something is truly sticky, it may not require too much repetition. But if it works, we must work it. All too often, researchers identify an educational intervention that is effective in motivating people to become organ donors, but after its publication and perhaps some good press, the intervention is not routinely replicated and practiced by others. Again, if it works, we must all continue to work it.

So, here’s what we must do to engender a cultural shift regarding organ donation awareness and action. We need to identify and cultivate the Connectors, Mavens, and Salesmen. We need to say something sticky. We need to encourage thoughtful and informed conversations. We need to be relentless. And we need to demand action. It’s not enough to educate and cultivate favor. Registering one’s intention to become an organ donor is the real prize.

(This blog post ultimately morphed into my TEDx talk on organ donation. Check it out!)

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Paired Donor Exchange and Non Directed Donation for Kidney Transplantation

Paired donor exchange involves two kidney recipients exchanging their intended donors with one another. If a donor has an incompatible blood type or has antigens to the recipient, they can instead donate to another unknown, but compatible, recipient in exchange for that recipient’s donor. In this way both donors can provide healthy kidneys to both recipients when transplant would have previously not been possible. A non directed kidney donation “chain” begins with an altruistic donor donating a kidney to an incompatible pair, and the donor from that pair passes his or her kidney on to another recipient or incompatible pair. I will briefly describe the basis of “matching” in kidney transplantation, and then describe paired donor exchange and non directed donation in more detail.

A successful kidney transplant requires first and foremost an appropriate “match” between the donor and recipient. In the matching process, we consider ABO blood type compatibility, Human Leukocyte Antigen (HLA) tissue types of the donor and recipient, and whether or not the recipient has antibodies against the donor (usually in the form of anti-HLA antibodies). We identify six HLAs that are most predictive of rejection to determine the degree of tissue typing match between donor and recipient. A “perfect match” is when all six HLAs are the same. This happens with identical twins, in siblings 25% of the time, and very rarely between two unrelated individuals. Perfect match kidneys last longer and the recipients require less term immunosuppression.

Currently, our standard immunosuppressive drugs are so good that it is unusual for a recipient to lose one’s kidney due to rejection in the first several years from transplant. The drugs are quite effective in preventing a severe rejection and even if some rejection occurs, there are even stronger medicines available to completely reverse the process. So nowadays, a good match simply means a compatible blood type and the absence of antibodies in the recipient’s blood directed against the donor’s tissues (or “antigens”). This is especially true with living kidney donation, where recipients do not even have to be related to their donors (e.g., husband to wife, friend to friend) to enjoy excellent outcomes.

We can, however, develop antibodies to HLAs. This is called “sensitization” and can occur as a result of multiple pregnancies, multiple blood transfusions, or previous transplantation. The presence of specific antibodies in a recipient to a particular donor’s HLAs is detected by a crossmatch assay. If the crossmatch assay is positive, the likelihood of immediate rejection is high. People who are highly sensitized have antibodies to many different HLAs and are therefore difficult to transplant.

So what happens when a sensitized patient wants to receive a living donor kidney transplant from a friend or loved one, but they are either the wrong blood type or crossmatch positive? Here at the University of Rochester, we have protocols to reduce the amount of ABO antibodies or HLA antibodies. These programs are state of the art and involve highly sophisticated treatments and medications. Very often they are successful in allowing transplants between ABO incompatible pairs or crossmatch positive pairs. They are not successful 100% of the time in reducing the antibodies, however, and sometimes we can not proceed with the transplant.

There are alternative approaches that are complementary to pharmacologic desensitization. Paired donor exchange and non directed donation involve the sharing of organs between pools of donors and recipients to achieve combinations that obviate existing ABO mismatch and HLA sensitization barriers.

The simplest scenario of a paired donor exchange (see Figure “Two Pair Exchange”) is one where a donor pair is ABO incompatible (say Jane, who is blood type A, wants to donate to Joe, who is blood type B) but complementary with another ABO incompatible pair (Frank, blood type B, wants to donate to Gertrude, blood type A). Well, why not have Jane donate to Gertrude (A to A) and Frank to Joe (B to B)? Even if Jane and Joe don’t know Frank and Gertrude, this scenario is ethical because all are benefiting. It is also medically simpler because no fancy immune system manipulations are necessary other than standard immunosuppression.

Paired donor exchange can be expanded to three pairs, allowing the exchange of crossmatch positive pairs with crossmatch negative pairs (see Figure “Three Pair Exchange”).
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Another similar approach is to perform non directed “chain” donations (see Figure “Chains”). Chains, by necessity, always start with an altruistic, or “Good Samaritan”, donor who wishes to donate his kidney out of the goodness of his or her heart to a complete stranger. (People like this do exist in this world.) Through a sophisticated computer algorithm, a virtual crossmatch chain is set up to maximize the amount of potential crossmatch negative transplants among a large pool of recipients.

As you can imagine, this endeavor can quickly become logistically complicated. In a simple paired donor exchange performed at a single hospital, four separate surgical teams and four operating rooms need to be available simultaneously. Such a scenario is possible only in the most dedicated and larger transplant centers such as the University of Rochester. In order for non directed donation chains to be of maximum benefit, the pool of participating donors and recipients must be large, and multiple transplant centers must be involved. Usually, simultaneous surgeries are performed at different hospitals and, sometimes, transcontinental exchanges are necessary.

Safeguards to ensure fair exchanges are critical. These include performing the donor surgeries at the same time to prevent a donor from backing out and leaving a recipient without an organ. This is also the case with the transplant operations. Furthermore, the donor/recipient pairs remain anonymous prior to transplant to prevent any coercion on the donors.

Ethical considerations are paramount. For the healthy donor undergoing the risks of surgery to help someone else, we must do everything possible to ensure that the outcome has a high likelihood of success. Recipients benefitting from this strategy should be those most in need, for example, highly sensitized patients. Finally, society as a whole must benefit. Non directed donations and paired exchanges do not disadvantage patients on the deceased donor waiting list because donor kidneys do not come from the pool utilized by those on the list, and chain donations are usually terminated by a donation to the highest person on the deceased donor waiting list.

In this country, the fastest growing source of kidneys is from live donors. Several hundred kidneys have been transplanted over the past several years using paired donor exchange and non directed donation strategies. Combining these strategies with pharmacologic desensitization protocols allows even more people to be transplanted because they increase the chances of finding a donor with a low level crossmatch more amenable to successful desensitization. Every time someone is transplanted using a live donor, one less person is added to the deceased donor waiting list.

Here at the University of Rochester, we are beginning to participate in a kidney donor exchange network encompassing more than 80 other transplant centers. We also have well established state of the art protocols to pharmacologically desensitize highly sensitized patients. Combining these modalities allows more people to be transplanted and maximizes the probability of achieving the best possible outcomes.

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Liver Transplant for Hepatocellular Carcinoma (HCC)

HCC, or HepatoCellular Carcinoma, is a type of cancer that begins in the liver. People with terminal scarring of their livers (cirrhosis), regardless of the original cause, are at higher risk of developing HCC. People infected with Hepatitis B or Hepatitis C viruses have an even higher risk. Although the presence of active cancer usually precludes the possibility of undergoing a transplant (because the immune suppressing drugs given afterwards can cause a cancer to grow uncontrollably), HCC can potentially be cured with liver transplant, and this is commonly practiced.

There are defined criteria that must be met in order to be considered a good candidate for liver transplant for HCC. These are referred to as the “Milan Criteria” and basically it comes down to if the tumor or tumors are not too large or numerous and they haven’t spread outside of the liver or into the blood vessels of the liver, then transplant is the best option for achieving a complete cure. Specifically, if there is one tumor, it can’t be greater than 5 centimeters (2 inches), and if there are multiple tumors, they can number no more than 3 and each has to be between 2 and 3 centimeters (1 ¼ inch).

When people are placed on the waiting list for liver transplant, where you are on the list depends on how sick your liver is. We estimate the function of your liver by calculating your MELD score (Model for End Stage Liver Disease). This score is obtained by a simple blood test in which the bilirubin (the yellow pigment that causes jaundice), the creatinine (a measure of your kidney function), and INR (a measure of how thin your blood is) values are used in a mathematical formula that generates a number between 6 (perfectly normal) and 40 (critically ill). The higher your MELD score, the sicker your liver, and the higher you are on the list.

This allocation system puts people with HCC at a disadvantage because the liver function is often nearly normal when an early HCC is first diagnosed. If a patient had to wait until their MELD score progressed to within the range of receiving organ offers (here in New York State, MELD scores need to be close to 30 or above to receive an offer), the HCC may grow or spread while waiting. The United Network of Organ Sharing (UNOS, the national oversight agency for transplantation in the U.S.) allows “exception” MELD points to patients with HCC who are within the Milan Criteria. Upon being placed on the waiting list, the MELD score automatically starts at 22 and every 3 months, if still within criteria, an additional 2 points are added. Most HCC patients undergoing transplant have “exception” MELD scores of around 30, but their true (or “biologic”) MELD scores are much lower. That means that most HCC patients are not terribly sick or may even feel completely healthy at the time of their transplant.

HCC is almost always diagnosed with a CAT scan or MRI. These imaging studies demonstrate tell-tale characteristics that usually make biopsy of the tumor unnecessary. If there is any doubt, then biopsy will be performed, but this is rare. We often proceed to treatment based solely on imaging studies and other clinical information alone. A blood test called “AFP” (Alpha FetoProtein) is always checked, as it can be elevated in up to 60% of patients with HCC, but it can be normal despite the presence of tumor. Also, the AFP level doesn’t necessarily correlate with how extensive the tumor is, but steadily increasing levels or extremely high levels do raise concern for a more advanced or aggressive tumor.
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Once the diagnosis of HCC is made and the patient is deemed to be a good candidate for transplant, the patient is immediately put on the list with exception points and offered treatment to slow down or halt the growth of the tumor while waiting for the MELD points to accrue (this can take between 9 and 15 months in New York State). If the patient is not a good candidate for transplant because of medical, surgical, or social reasons, HCC treatment will still be offered. If the HCC is discovered too late and the tumor has already spread outside of the liver or into the liver blood vessels, then palliative care or comfort care approaches are considered. Finally, if the HCC is slightly outside of the Milan criteria (for example, 4 tumors instead of 3, or a single tumor measuring 5.5 centimeters), then the possibility exists to try to “downsize” the tumor to get the patient within Milan Criteria so that they can be transplanted.

Two basic approaches to HCC tumor control exist: catheter based “embolization” therapies and directed needle “ablation” therapies. For embolizations, a catheter is placed in the groin and directed into the liver where chemotherapy (“TACE” or TransArterial ChemoEmbolization) or radiation coated glass beads are injected directly into the tumor. Large portions of the liver can be treated at one time with these methods. Tumor ablations are usually performed by placing needles through the skin directly into the tumor to deliver energy (most often radiofrequency waves) that kills the tumor. This is known as “RFA” or RadioFrequency Ablation. These procedures are most always performed by the Interventional Radiologists using conscious sedation and do not require admission to the hospital afterwards. These two approaches are very effective in keeping the HCC in check prior to transplant, but they are not considered curative therapies.

Liver cancer can also be surgically removed. Although the results can be quite good, the recurrence rates can be as high as 50% or greater within 5 years of surgery. With liver transplantation for HCC, survival rates are greater than 80% at 5 years and the recurrence rate is 12% or less at 5 years. These excellent results are achieved because not only is the tumor taken out at the time of transplant, but also the diseased liver that is predisposed to forming tumors. Sometimes surgical removal (or “resection”) is considered if the patient is not a good transplant candidate or, rarely, in order to improve one’s chances for ultimately getting a liver transplant. But the most common course of action, if possible, is to list for transplant, apply for exception points if within the Milan Criteria, and to begin tumor embolization and/or ablation treatment as soon as possible to stay within criteria or to attempt “downsizing” if slightly outside of criteria.

As you can see, treatment decision pathways for HCC are complicated and can vary greatly depending on the individual’s clinical situation. Nonetheless, excellent results can be achieved if the HCC is caught early. Our multidisciplinary approach to HCC and transplant here at the University of Rochester Medical Center involves surgeons, hepatologists, oncologists, interventional radiologists, imaging scientists, pathologists, and nurse coordinators, all of the highest order, working together to deliver state of the art and highly personalized care.

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Two Organ Donation Videos

Here is a beautiful video on organ donation awareness from South Africa. Concise, poignant, and powerful. Be an organ donor. Don’t take someone else with you.

http://vimeo.com/31359689

Here is a longer video produced by Malcolm Spaull at Rochester Institute of Technology’s School of Film and Animation for the 25th Anniversary Celebration of the Finger Lakes Donor Recovery Network. Three very moving stories from organ donor families. One can find meaning and purpose even at the moment of great loss.

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If you want to register to become an organ donor in New York State, click here. Or, if you don’t live in NY, visit Donate Life America.

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Guest Blog: A Kidney Donor’s Perspective

The following was written by one of my patients who graciously agreed to donate one of her kidneys to her brother in law for transplant. Her perspective emphasizes the many gifts given to many people through living donor kidney transplantation.

Two years ago, this month, I donated my left kidney to my brother-in-law….I’ll call him “Bob”.  Today, both Bob and I are both doing great.  Bob has his health back and is again on his bicycle, sailing his boat, working on his farm, and enjoying life.  Over the summer, he walked his beautiful daughter down the aisle, and next week he will be at his son’s wedding.  Bob has his life back.  My sister has her husband back.  Bob’s children have their father back.

 

As for me, with the exception of a relatively short recuperation period, my physical health has not changed.  I continue to run, ski, cycle, play tennis and do many other outdoor activities that inspire me.  The only physical reminder I have is my scar and the little itch it sometimes brings.  My spiritual life, however, has changed.  I now live knowing that I truly helped to save someone else’s life.  Not only that, I helped give Bob back a life he once knew… renewed energy, renewed spirit, and free of machines.  If ever I question my own life and choices, I need only remind myself of the powerful gift I have given.  If ever I question my ability to do something, I remind myself of this emotionally difficult undertaking.         I too, am a stronger, more balanced, and happier person.

 
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The decision whether or not to donate a kidney can certainly be a difficult one.  For me, however, once I understood the severity of Bob’s illness, there was no question in my mind that I would get match tested.  Somehow, even before knowing I was a blood match, I knew that I would be giving Bob one of my kidneys.  There was no looking back or turning around for me…I trusted the research, I trusted the doctors, and I trusted my family who completely supported me.

 

The only true moment of fear for me was waking up the morning of the surgery.  I was terrified.  But, with my husband by my side, I got out of bed and went forward.  A decision I will never regret.  A decision that I hope has helped my three young children, my many friends, and those unknown to me, to understand the power and necessity of giving.”

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