When Ailments Pile Up, Asking Patients to Rethink Free Dialysis


[NYTimes]- Of all the terrible chronic diseases, only one —end-stage kidney disease — gets special treatment by the federal government. A law passed by Congress 39 years ago provides nearly free care to almost all patients whose kidneys have failed, regardless of their age or ability to pay.

But the law has had unintended consequences, kidney experts say. It was meant to keep young and middle-aged people alive and productive. Instead, many of the patients who take advantage of the law are old and have other medical problems, often suffering through dialysis as a replacement for their failed kidneys but not living long because the other chronic diseases kill them.

Kidney specialists are pushing doctors to be more forthright with elderly people who have other serious medical conditions, to tell the patients that even though they are entitled to dialysis, they may want to decline such treatment and enter a hospice instead. In the end, it is always the patient’s choice.

One idea, promoted by leading specialists, is to change the way doctors refer to the decision to forgo dialysis. Instead of saying that a patient is withdrawing from dialysis or agreeing not to start it, these specialists say the patient has chosen “medical management without dialysis.”

“That is the preferred term,” said Nancy Armistead, executive director of the Mid-Atlantic Renal Coalition, a Medicare contractor that collects data and patient grievances.

The phrase, she says, “acknowledges that death is imminent,” but it also sends an important message: “We are not just sending people home to die. We are offering palliative care.”

A committee of the Renal Physicians Association recently formulated guidelines to use in deciding when dialysis is appropriate. It provides questions that doctors should ask themselves before suggesting the treatment. One is the “surprise” question: Would I be surprised if this patient is dead within a year?

But, said the committee’s chairman, Dr. Alvin H. Moss, a nephrologist and ethicist at West Virginia University, the task ahead is like turning around an ocean liner.

“Clearly, when the program was initiated in the 1970s, the hope and expectation was that this program would return otherwise healthy people back into society so they could work and be productive,” said Dr. Manjula Kurella Tamura, a kidney specialist at Stanford. But, she added, “dialysis at the end of life is a different sort of treatment.”

Dialysis is difficult, especially for the old and sick. Most of the nation’s 400,000 dialysis patients spend several hours, three days a week, hooked up to a machine, and additional time traveling back and forth to the clinic.

They have to restrict salt and fluids, and the procedure is so exhausting that some patients rest for the remainder of the day. Although dialysis may alleviate symptoms like fluid accumulation in the legs or lungs, it can lead to dizziness, weakness, leg cramps, nausea and other problems. Complications like bloodstream infections or clogged blood vessels where the dialysis needles are placed are common, often requiring surgery or hospital stays. Ultimately, about one patient in five is unwilling to go on with it.

Yet it can be hard to say no.

An 84-year-old man being treated at a clinic in Elkins, W.Va., run by West Virginia University has been counseled against dialysis. He has high blood pressure and severe congestive heart failure, a condition as lethal as terminal cancer. His heart problems make it hard for him to breathe, and he is often in the hospital. In a telephone interview, the man said he saw friends suffer on dialysis and always thought he would refuse it. But he is getting ready to start anyway. The man, whose name is being withheld to protect his privacy, says he changed his mind after he “sat and thought about how good life is.”

“What choice do you really have?” he asked.

When Congress established the entitlement to pay for kidney patients in October 1972, dialysis and transplants were new procedures that were not covered by health insurance. There were horrifying stories — rich people got dialysis and lived while poor people died. In Seattle, a committee meted out dialysis by voting on who could get it. A man who was supporting a family, for example, took precedence over a single woman.

It also was expected at that time that fewer than 40 patients per million would need dialysis, and that most of those patients would be healthy — except for their failed kidneys — and under age 54.

Now more than 400 people per million start dialysis each year. More than a third of the patients are 65 or older, and they account for about 42 percent of the costs. People over 75 make up the fastest-growing group of dialysis patients. And most elderly dialysis patients have other serious diseases like diabetes, heart failure, stroke and even advanced dementia. One-third of them have four or more chronic conditions.

The federal program, said Dr. Peter S. Aronson, a professor of nephrology at Yale University’s School of Medicine “is so emblematic of good intentions misapplied.”

“The question,” Dr. Aronson said, “is how to dial it back.”

Recent studies have found that dialysis does not prolong life for many elderly people with other serious chronic illnesses. One study found that the procedure’s main effect is to increase the chances that such patients will die in the hospital rather than at home.

Meanwhile, costs are soaring — end-stage kidney disease will cost the nation an estimated $40 billion to $50 billion this year. And doctors are recommending dialysis sooner, even though recent studies have found that an early start confers no additional benefit.

Even so, Ms. Armistead said, when patents are ready to choose “medical management,” family members often struggle with the decision.

It also can be difficult to make some patients understand the gravity of their disease or their choices, said Barbara Weaner, a nurse practitioner at West Virginia University who works with dialysis patients.

“We live in a country where there is a lot of choice, where people tend to be afraid of dying and where palliative treatment is not always recognized as a good alternative,” Ms. Weaner said.

Her patients at the Elkins clinic illustrate her point. Those who are old and very sick often have a choice — they can have “medical management” without dialysis or they can have dialysis, which might fail to improve their lives. But for many, the first choice is not acceptable.

One patient, a 78-year-old woman whose name is being withheld, was not a good candidate for dialysis, her doctors said. She has complications from diabetes, high blood pressure, a heart valve problem and severe coronary artery disease. Her medical problems were so grave that dialysis was likely to lead to a series of medical interventions — hospital stays, drugs and doctor visits — but would not necessarily prolong her life. And her doctors told her that.

But she insisted on dialysis, saying, “Some life is better than no life.” In the seven months she has been on dialysis, she has been hospitalized four times, including twice for heart surgery.

“I go to dialysis because I want to live,” she said in a telephone interview. “I want dialysis.”


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My mother has been on dialysis since 2006. A couple of times the dialysis doctor that comes so often to the dialysis clinic has tried to persuade me to take my mother off of dialysis. When a family member has decided to keep their relative on dialysis the doctor needs to keep their mouth shut. Even with dialysis when God is ready for that patient to die he will take them and if there is a chance for the patient at all on dialysis leave the patient and the family along. I do not know if there are laws about doctors pressuring family about taking their relative off of dialysis there should be. If you know of any laws that protect family members about being pressured about taking their relative being taken off of dialysis I would like to know about it. I am sick and tired of this doctor telling me I need to take my mother off of dialysis. I do no need this kind of stress. He needs to keep his mouth shut about this and only answer the specific questions I do have and not keep telling me I need to take my mother off of dialysis. My father and brother are deceased, but I am sure if they were alive they would feel the same as I do.

Shirley, I am going through a similar situation. My mother has been a dialysis patient for 10 years now including a failed kidney transplant back in 1999. My mother’s health took a drastic turn in January of 2011. My mother has not ben able to make decisions for herself. Since that time not more than a day passes that our family is asked why we don’t just take my mother off of dialysis and let nature take its course. The even more annoying question has been askd what seems like thousands of times including every nurse I come across “You know your mother is very sick right.” I wonder how is it that seemingly intelligent people do not realize just how stupid that question is. Every new facility my mother goes to the doctor tries to bring in a palliative care team, chaplain, case manager, or hospice as if they are going to educate us. Why can’t this doctor just understand that we are aware my mother is “very sick” with lots of conflicting ailments and she will die probably in the very near future, but we as a family want choose to fight this battle until the very end. My father is the legal decsion maker for my mother but defers to myself and my brother. This doctor has even gone as far to try and convince my father to go against our wishes as her children. I grew up in “the hood” as some people call it and this sure feels like a good old fashioned shake down to me and I don’t like it. If anyone has any ideas how to get this doctor to back the off and leave my family in peace please let me know.