Reform bills may extend Medicare coverage for kidney transplant drugs

Reform bills may extend Medicare coverage for kidney transplant drugs
September 14, 2009 — 10:51am ET | By Anne Zieger

Sinnce 1973, Medicare has covered treatment for any American citizen with end-stage renal disease, and 80 percent the bill for costly immunosuppressive medications. However, CMS will only pay the bill for 36 months if the patient wouldn’t otherwise qualify for Medicare, i.e. people under 65.

However, that limit has been under attack for a while. In March, for example, two Senators introduced a bill that would require Medicare to cover the costly drugs needed to fight kidney rejection for the life of the transplant. Now, the reform bill passed by the House includes a similar provision.

The measure could cost the government a great deal of money, as the immunosuppressive drugs can costs anywhere from $1,000 to $3,000. In fact, the Congressional Budget Office estimates that unlimited coverage would add $100 million per year to the $23 billion Medicare pays for its kidney program. That’s probably why previous attempts to lift the limit have never even made it to the voting stage. (On the other hand, is $100 million a year that big a deal against a $23 billion budget, given that lives are at stake?)

Given these costs, which under-65 patients know they’ll have to bear eventually, right now some kidney transplant candidates aren’t even putting themselves on the transplant lists, UPI reports.

Read more: http://www.fiercehealthcare.com/story/reform-bills-may-extend-medicare-coverage-kidney-transplant-drugs/2009-09-14#ixzz0RI1e0DR8

Medicare cover the treatment of end-stage renal disease (ESRD)

Government should take steps to promote wearable artificial kidney

Most inventions in the medical field are made abroad. We Indians are busy trying to be at par with developed nations in space science.. and rocket making. that is nice. But government should also be aware of the sufferings of patients and dedicated efforts to improve conditions of patients need to be taken
Government is spending money in non priority areas such as subsidising the Haj pilgrimage, one girl child etc. But patients in need of dialysis and urgent medical attention for life saving support systems are ignored. Perhaps this is because we are still ruled by the elite class who can affort treatment abroad and also get government healthcare benefits and they do not suffer due to medical problems. But it is not fair to turn a blind eye on the patients who need urgent life saving healthcare….
Now Americans have invented Wearable Artificial Kidney..read
http://www.nashuatelegraph.com/apps/pbcs.dll/article?AID=/20090913/HEALTH/309139991/-1/STYLE

At least our government should awake now to the needs of dying patients and try to promote such technologies in India by giving deserving subsidies… so that all of us can sing “saare jahan se achcha…”
not just those healthy wealthy elite classes

Cab driver gives his kidney

RIGHT TO LIFE OF KIDNEY PATIENTS SHOULD BE RESPECTED

Government is spending crores of rupees in non-priority sectors to appease certain communities with an eye on vote bank.. for example, it is giving subsidies to Haj and other pilgrimages, it is giving subsidies for single girl child etc. It is spending crores of rupees for inoculation in areas where the diseases are never heard of.. But it is turning blind eye to the sufferings of kidney patients who are spending all their earnings to support their life and are in dire need of emergent medical care. Government does not allow any one to die; euthanasia or mercy killing is not permitted. Patients have RIGHT TO LIFE; it is a constitutional right. Government should not spend any paise on pilgrimage etc. unless it meets the emergent life saving needs of kidney patients and patients who are supporting life through expensive medications.. Patients should form an ASSOCIATION to assert the Rights of Patients..

a Wearable Artificial Kidney for dialysis patients

ScienceDaily (Aug. 21, 2009) —
Researchers are developing a Wearable Artificial Kidney for dialysis patients, reports an upcoming paper in the Clinical Journal of the American Society of Nephrology (CJASN). “Our vision of a technological breakthrough has materialized in the form of a Wearable Artificial Kidney, which provides continuous dialysis 24 hours a day, seven days a week,” comments Victor Gura, MD (David Geffen School of Medicine at UCLA).

The device—essentially a miniaturized dialysis machine, worn as a belt—weighs about 10 pounds and is powered by two nine-volt batteries. Because patients don’t need to be hooked up to a full-size dialysis machine, they are free to walk, work, or sleep while undergoing continuous, gentle dialysis that more closely approximates normal kidney function.

Such a device could lead to a “paradigm change” in the treatment of dialysis patients. Despite enduring long hours on dialysis every week—with major limitations in activities, diet, and other areas of life—dialysis patients face high rates of hospitalization and death. The U.S. dialysis population currently exceeds 400,000, with costs of over $30 billion per year. “We believe that the Wearable Artificial Kidney will not only reduce the mortality and misery of dialysis patients, but will also result in significant reduction in the cost of providing viable health care,” says Gura.

The Wearable Artificial Kidney is successful in preliminary tests, including two studies in dialysis patients. The new study provides important information on the technical details that made these promising results possible.

“However, the long-term effect of this technology on the well-being of dialysis patients must be demonstrated in much-needed clinical trials,” adds Gura. “Although successful, this is but one additional step on a long road still ahead of us to bring about a much-needed change in the lives of this population.”

Other authors were Alexandra S. Macy, Masoud Beizai, and Carlos Ezon (Xcorporeal, Inc); and Thomas A. Golper, MD (Vanderbilt University Medical Center). Dr. Gura receives a salary from Xcorporeal, Inc.

Additionally, significant contributions to the development of this new device were made by Hans Dietrich Polaschegg, PhD, Andrew Davenport, MD, Claudio Ronco MD, Andre Kaplan, MD, and Eli Friedman, MD.

http://www.renalandurologynews.com/

Issues in Renal Disease: An Update

Issues in Renal Disease: An Update
Delicia Honen Yard
August 18 2009
Is CKD being defined too broadly and thus overdiagnosed?

Dr. Himmelfarb: The ASN per se doesn’t have a stand on this issue. But I would be very comfortable saying that the guidelines for classification and diagnosis of CKD promulgated by the National Kidney Foundation have had an overall benefit in developing a standardized approach to CKD. That said, controversy continues over whether the entire classification system for CKD should be based solely on the estimated glomerular filtration rate (eGFR) and whether, in essence, one size fits all for CKD. A number of efforts are under way to refine the CKD classification system, and many people feel that the classification scheme needs to be revised.

One major concern is whether the classification system, which doesn’t take into account age, tends to overdiagnose CKD in the elderly. Under the current system, about one third of people older than 70 will be classified as having CKD, yet it’s not clear that a high proportion of those individuals will progress to end-stage renal disease.

The CKD classification system is likely to be refined further in the future, but having the system, in my opinion, has been helpful in delineating the public health consequences of CKD.

Various drug combinations and dosages are continuously being tested in immunosuppressant regimens for renal transplant patients, but the best formula has yet to be determined. In what direction do you see this therapy moving?

Dr. Himmelfarb: There has been enormous progress in the development of immunosuppressive medications to prevent rejection of transplanted kidneys. And this has increased the choices of immunosuppressant combinations. While the short-term rates of rejection have declined, increasing attention is being paid to preventing long-term chronic allograft nephropathy or chronic rejection and minimizing the complications from immunosuppression. I think these trends are likely to continue.

Will we ever reach the point at which immunosuppressants will not be a lifetime prescription?

Dr. Himmelfarb: Within the transplant field, there are ongoing efforts to achieve what’s called tolerance, which would result in patients not having to take lifelong immunosuppressive medications. NIH has funded the Immune Tolerance Network, which sponsors studies on tolerance. So far achieving tolerance in humans has been difficult, and, at least for the time being, getting transplant recipients to continue on their immunosuppressive drugs is critically important.

What is the best approach to increasing the number of live kidney donors?

Dr. Himmelfarb: Like virtually every other organization, we would like to see increased availability of kidney transplants, and the best way to accomplish that is through educating the public about the relative safety of kidney donation. The ASN supports the Declaration of Istanbul, which promotes the idea that a kidney should not be a commodity that is bought and sold. This is somewhat of a controversial area—whether or not payments to live kidney donors would increase the number of kidney transplants that are performed.

Do you foresee the development of novel therapies that could replace traditional dialysis and transplants?

Dr. Himmelfarb: The ASN is certainly hopeful that new therapies will make our current therapies obsolete. One possibility would be the development of artificial implantable and/or wearable kidneys. Another would be organogenesis—essentially learning how to grow new kidneys.

Would you care to comment on the state of nephrology research?

Dr. Himmelfarb: Speaking as an individual, I think that many of the leading controversies in nephrology center on the lack of high-level evidence from randomized clinical trials to support practice recommendations.
Unfortunately, nephrology lags behind somewhat in performing the kind of randomized clinical trials that give us the highest level of evidence so that we can speak confidently about the best approaches to clinical practice. I don’t know why that is, but the nephrology community is attempting to address the problem. More clinical trials are currently being performed than in the past. But if we could achieve a higher level of evidence, then we could establish better consensus on how to optimize care for people with kidney disease. The ASN is, in general, a strong advocate for all kinds of kidney-disease research, including clinical, translational, and basic science studies.

Under new legislation, Medicare payments to dialysis centers will bundle medications with other dialysis services. What effect do you expect this to have on nephrology practices?

Dr. Himmelfarb: The major concern that ASN has with the legislation is to ensure that there are no unintended consequences whereby patients might be harmed because of possible underutilization of medications that are beneficial. In other words, if you’re being paid a fixed amount for the care of a patient, there could be a tendency to underutilize certain medications that may be beneficial. It’s really not on the part of the physicians: Nephrologists do not get reimbursed more or less money based on the prescription of medications for the dialysis patient. It’s the dialysis provider whose reimbursement will be affected by the prescription of medications. That’s one reason I don’t think this legislation will have a significant effect on nephrology practices; it will have a much greater effect on the dialysis provider.

Requesting extension of travell concession

Copy of Email to Chairman, Railway Board Etc.. requestion concession to patients travelling by train for routine checkups at hospitals post transplantation

From

Smitha V.P.
——————-
——-

To,
Chairman
Railway Board

Sir,

Kidney patients suffer a lot in all respects and the medical expenses are heavy. Even after transplant of kidney they have to go for routine checkup to the hospital every month. Since they are on immunosuppressive drugs to prevent rejection of transplanted kidney, they are still patients and their medical expenses are still heavy..

Therefore I request you to extend the railway concession granted to kidney patients travelling to hospital for dialysis and transplant to those who have undergone transplant and travelling to hospital for routine checkups..

Thank you

Yours faithfully

Smitha VP
Kozhikode, Kerala

Hail OBAMA…”No one in America should go broke because they get sick,” he said to loud applause.”

Obama is introducing health insurance reforms in america.. I hope that our masters, health minister, prime minister, chief ministers, health ministers of state and political parties too feel that same ..

Read this article in Reuters

No one in America should go broke because they get sick,” he said to loud applause.