Subject: Pricing Health Care: A Better Way to Die Date: Published: 5/19/93 (94 lines) Source: Wall Street Journal. Copyright Dow Jones & Co. Inc. Pricing Health Care: A Better Way to Die ---- By Carol Raphael News reports on the activities of Jack Kevorkian have drawn attention to the needs of the terminally ill and the wrenching decisions faced by them, their families and their physicians. In my experience, most patients are less terrified of the act of dying than of dying an agonizing, impersonal and undignified death. Unfortunately, lost in the swirl of controversy is the recognition that there already exists an alternative approach to the excruciating pain and devastating alienation that too often is the unnecessary lot of the dying patient. That alternative is organized hospice care, a proven, effective and compassionate service to help the terminally ill patient through the dying process with dignity and in comfort. Hospice care also helps the family through its loss and bereavement. In contrast, hospitalization is costly, often inappropriate and frequently unwanted by the patient, while Dr. Kevorkian's desperate remedy for pain represents a medical and moral breakdown in our health care system. Hospice offers terminally ill individuals the option of spending their final weeks and months in the comfort and privacy of their own homes; in 90% of the cases we see at the Visiting Nurse Service of New York, the patient takes an active role in the decision to seek hospice care. The hospice team -- nurse, physician, pastoral care counselor, social worker, home health aide and volunteer -- works collaboratively with the patient, the patient's family and the patient's physician to ensure maximum pain management, symptom control and comfort. While more than 75% of our hospice patients have advanced cancers, the services are appropriate for all dying patients, including those with Alzheimer's, cardiac disease, AIDS and severe degenerative neuro-muscular disorders, such as Lou Gehrig's Disease. Children, too, can be well served by hospice care. The process of dying is never an easy one, but the final days can be comforting for all involved; 98% of the patients in our hospice program die at home. And the need for service does not end with death; bereavement counseling is available to family members for a year after the death of a loved one. Visiting Nurse Service of New York serves 30% of New York City's annual hospice population of approximately 2,000, yet we know that the number of people in hospice care is only a fraction of the number of terminally ill who could benefit from it. Many families are still uninformed about hospice care or believe that hospice service is some form of institutional care. Part of the reason is that hospice care is new -- it started in Europe in the 1960s, where it is often institution-based, and was first introduced in the U. S. in the 1970s, where it is largely home-based. Indeed, Medicare regulations require that certified hospice programs provide at least 80% of care in the patient's home. Initially a cost-saving regulation, it has proved to be a wise decision. Many physicians still do not fully understand the value of hospice care for their patients. They may think they have to give up care of the patient. They don't. In fact, all orders for service in hospice care must be signed by the patient's physician, who can be an integral part of the hospice team. In addition, trained hospice medical directors can work with those physicians who may have little or no training in aggressive pain management, feel unprepared to care for a patient seeking only palliative care, or are uncomfortable talking about death and dying. We tell physicians that they should view a referral to hospice care as they would a referral to any other specialist. And physicians who do refer patients to hospice care are likely to do it again. One of the surprising statistics about the American health care system is that our overwhelming reliance on caring for the dying in the hospital means, for example, that we spend 28% of all Medicare dollars for care in the last year of patients' lives and half of that for care in the last two months. Here, too, hospice is a rational alternative. The most recent study of hospice costs shows that when terminally ill patients are cared for at home, they spend six fewer days in the hospital and incur nearly 20% less in costs over a six-month period. When a day of hospice care directly replaces a day in the hospital, the savings can be more than $500 per patient per day. When a cure is no longer a reasonable expectation, the physician has an obligation to minister to his or her patient, to relieve pain, and to comfort and sustain the patient's family. Modern hospice care can help the physician meet that basic obligation. --- Ms. Raphael is chief executive officer of Visiting Nurse Service of New York, the largest nonprofit provider of home health care in the U. S. [This article is made available here by Dow Jones Co. for the personal and non-commercial use of callers to this bbs, in the hope that it will be of some help to those who are suffering from the disease and others who are seeking to help them.]