말기암환자 죽음 통보 긍정적
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미국 대나-파버 암연구소의 알렉시 라이트 박사는 모든 항암치료가 실패, 더 이상 치료방법이 없어 살 수 있는 시간이 1년이 안 되는 말기암환자 603명을 추적조사한 결과 놀랍게도 이 사실을 의사로부터 정식으로 통보받은 환자가 우울증이 나타난 경우는 7%로 이런 사실을 통보받지 않은 환자와 차이가 없었고 불안과 걱정도 비슷한 것으로 나타났다고 밝혔다.
오히려 죽음통보를 받은 환자는 그렇지 않은 환자에 비해 죽기 전 마지막 며칠을 병원에서 생명유지장치에 매달려 보낸 경우가 훨씬 적었다.
전체 환자 중에서 지금까지 사망한 323명의 경우 미리 죽음통보를 받은 환자는 그렇지 않은 환자에 비해 죽기 전 마지막 한 주를 병원 중환자실에서 보낼 가능성이 3분의 1, 인공호흡장치에 매어있을 가능성이 4분의 1, 심폐소생술을 받을 가능성이 6분의 1인 것으로 나타났다.
돈만 들어가고 효과도 없는 치료를 피하려고 한 것이다.
이런 환자의 가족들은 환자의 사망 후에도 훨씬 마음의 평온을 느낄 수 있었던 것으로 밝혀졌다.
조지타운 대학 종합암센터의 존 마셜 박사는 죽음을 통보받은 환자에게는 “슬픈 소식이겠지만 그로 인한 긴장은 곧 사라지게 된다”고 말한다.
한편 말기암환자에 대한 죽음통보가 이러한 긍정적인 측면이 있음을 확신하게 된 캘리포니아 주 의회는 이와 함께 환자는 자신이 처한 상황을 알 권리가 있다는 취지에서 죽어가는 말기암환자가 어떤 선택을 해야할지를 물어올 때 의사는 정확하고 완전한 답변을 해 주도록 규정한 법안을 통과시켰다.
주 하원을 통과한 이 법안은 이제 상원으로 가게 되는데 일부 의사들은 이 규정이 의사의 의료행위를 간섭하는 것이라면서 반대하고 있다.
By MARILYNN MARCHIONE, AP Medical Writer Sun Jun 15, 2:08 PM ET
CHICAGO - One look at Eileen Mulligan lying soberly on the exam table and Dr. John Marshall knew the time for the Big Talk had arrived. He began gently. The chemotherapy is not helping. The cancer is advanced. There are no good options left to try. It would be good to look into hospice care.
"At first I was really shocked. But after, I thought it was a really good way of handling a situation like that," said Mulligan, who now is making a "bucket list" — things to do before she dies. Top priority: getting her busy sons to come for a weekend at her Washington, D.C., home.
Many people do not get such straight talk from doctors, who often think they are doing patients a favor by keeping hope alive.
New research shows they are wrong.
Only one-third of terminally ill cancer patients in a new, federally funded study said their doctors had discussed end-of-life care. Surprisingly, patients who had these talks were no more likely to become depressed than those who did not, the study found. They were less likely to spend their final days in hospitals, tethered to machines. They avoided costly, futile care. And their loved ones were more at peace after they died.
Convinced of such benefits and that patients have a right to know, the California Assembly just passed a bill to require that health care providers give complete answers to dying patients who ask about their options. The bill now goes to the state Senate.
Some doctors' groups are fighting the bill, saying it interferes with medical practice. But at an American Society of Clinical Oncology conference in Chicago earlier this month, where the federally funded study was presented, the society's president said she was upset at its finding that most doctors were not having honest talks.
"That is distressing if it's true. It says we have a lot of homework to do," said Dr. Nancy Davidson, a cancer specialist at Johns Hopkins University in Baltimore.
Doctors mistakenly fear that frank conversations will harm patients, said Barbara Coombs Lee, president of the advocacy group Compassionate Choices.
"Boiled down, it's 'Talking about dying will kill you,'" she said. In reality, "people crave these conversations, because without a full and candid discussion of what they're up against and what their options are, they feel abandoned and forlorn, as though they have to face this alone. No one is willing to talk about it."
The new study is the first to look at what happens to patients if they are or are not asked what kind of care they'd like to receive if they were dying, said lead researcher Dr. Alexi Wright of the Dana-Farber Cancer Institute in Boston.
It involved 603 people in Massachusetts, New Hampshire, Connecticut and Texas. All had failed chemotherapy for advanced cancer and had life expectancies of less than a year. They were interviewed at the start of the study and are being followed until their deaths. Records were used to document their care.
Of the 323 who have died so far, those who had end-of-life talks were three times less likely to spend their final week in intensive care, four times less likely to be on breathing machines, and six times less likely to be resuscitated.
About 7 percent of all patients in the study developed depression. Feeling nervous or worried was no more common among those who had end-of-life talks than those who did not.
That rings true, said Marshall, who is Mulligan's doctor at Georgetown University's Lombardi Comprehensive Cancer Center. Patients often are relieved, and can plan for a "good death" and make decisions, such as do-not-resuscitate orders.
"It's sad, and it's not good news, but you can see the tension begin to fall" as soon as the patient and the family come to grips with a situation they may have suspected but were afraid to bring up, he said.
From an ethics point of view, "it's easy — patients ought to know," said Dr. Anthony Lee Back of the Fred Hutchinson Cancer Center in Seattle. "Talking about prognosis is where the rubber meets the road. It's a make-or-break moment — you earn that trust or you blow it," he told doctors at a training session at the cancer conference on how to break bad news.
People react differently, though, said Dr. James Vredenburgh, a brain tumor specialist at Duke University.
"There are patients who want to talk about death and dying when I first meet them, before I ever treat them. There's other people who never will talk about it," he said.
"Most patients know in their heart" that the situation is grim, "but people have an amazing capacity to deny or just keep fighting. For a majority of patients it's a relief to know and to just be able to talk about it," he said.
Sometimes it's doctors who have trouble accepting that the end is near, or think they've failed the patient unless they keep trying to beat the disease, said Dr. Otis Brawley, chief medical officer at the American Cancer Society.
"I had seven patients die in one week once," Brawley said. "I actually had some personal regrets in some patients where I did not stop treatment and in retrospect, I think I should have."
James Rogers, 67 of Durham, N.C., wants no such regrets. Diagnosed with advanced lung cancer last October, he had only one question for the doctor who recommended treatment.
"I said 'Can you get rid of it?' She said 'no,'" and he decided to simply enjoy his final days with the help of the hospice staff at Duke.
"I like being told what my health condition is. I don't like beating around the bush," he said. "We all have to die. I've had a very good life. Death is not something that was fearful to me."
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On the Net:
Institutes of Health, hospice information: http://tinyurl.com/3ngrvg
Cancer Society, hospice care: http://tinyurl.com/4gvf2g


