By Cheryl Arenella, MD, MPH
According to a Harris Survey on End-of-Life Care conducted in 2002, the vast majority of Americans (86%) believe that people with terminal illness would most like to receive end-of-life care at home. Yet nearly 70% of deaths in America today occur in facilities, primarily in hospitals and long-term care facilities.
Given the overwhelming desire of Americans to die at home, what are the reasons for the gap between what Americans prefer and what is actually taking place? In this article, we will examine one of the factors responsible for the gap: our trepidation for caring for a severely ill person at home.
Caring for a seriously ill loved one at home can be intimidating and overwhelming. Most of us have no experience or training in caring for an ill person at home. Adding to our sense of overwhelming responsibility is the rapid advance of technology, which has made the array of home-based medical interventions bewildering.
There is little doubt that, when families commit to caring for a seriously ill loved one at home, they face many challenges. These families could benefit from additional support, especially the comprehensive, holistic support offered by hospice. Concerns often arise in three broad categories:
How can I make my home safe for my ill and frail sister?
Much as you would if a toddler were coming for a visit, do a safety inventory of your home, but tailored to the needs of your loved one:
The hospice nurse, home care nurse, or an occupational or physical therapist can assist you with this evaluation and help plan appropriate modifications. The nurse will instruct you in proper hand-washing technique.
My mother lives alone and insists on maintaining her independence. But I worry about her constantly!
While this situation may not be ideal from the viewpoint of the concerned family member, there are steps that can be taken to increase your loved one’s safety, while allowing autonomy as long as possible:
A hospice social worker or eldercare case manager can help to assess needs and create a safe environment for your loved one.
My father is confused. He turns on the stove, wanders, and does other unsafe things if he is not constantly monitored.
Caregivers of persons with Alzheimer’s disease and other dementias have learned to be creative in keeping a loved one safe by such techniques as:
PERSONAL CARE ISSUES
My husband is weak, and it is hard to help him out of bed, into and out of chairs, on and off the commode, and into and out of the tub.
My grown daughter can’t even get out of bed! How can I bathe her, change her, and change the bed with her in it?
Again, techniques have been developed to help you safely tend to your loved one’s care needs, even when he/she is bed bound. The hospice nurse or home health nurse can teach these to you.
How can I be sure my aunt is eating enough?
Many frail, chronically ill persons have diminished appetites. Serving normal sized meals can be a “turn off” for them. Instead:
A dietician can help you evaluate what the best meal plan is for your loved one. At times, nutritional supplements in the form of shakes or puddings may play a role.
MEDICAL CARE ISSUES
My husband is on so many medications, it is so hard to keep them all straight!
My father has developed a pressure sore on his lower back. I don’t know how to care for it!
The best care plan for management of pressure wounds is to prevent them:
In the event that a pressure ulcer develops:
My wife has what they called a “central intravenous catheter” in her upper chest. It has special bandages and requires special care. I’m worried that I’ll break it, or cause an infection.
Family members can be taught how to safely care for the site of an intravenous catheter. The hospice or home health nurse can instruct you in the proper techniques.
My son has a urinary catheter (a tube placed through the urethra into the bladder). How do I care for it?
The hospice or home health nurse can show you how to:
My grandfather is fed through a gastric feeding tube. How do I set it up?
The hospice nurse or home health nurse will show you:
There may come a time when your loved one no longer wants, or can no longer tolerate, the tube feedings. The hospice team, including the nurse, social worker and chaplain, can help prepare you for this time, and help you continue to keep your loved one comfortable even after the tube feedings are stopped.
My spouse has a colostomy bag. It’s kind of gross. I’m not sure I can handle it!
Many people find that, when it comes to caring for a loved one, tasks that at first seem objectionable become manageable. Just as we care for our infants with love, no matter what the task at hand, we can also care for our older loved ones with special care needs.
The hospice nurse or home health nurse can teach you how to:
My sister has a tracheostomy tube in her throat to breathe, and she needs to be suctioned through it frequently to keep the tube clear. I can’t do that, can I?
Family members can indeed be taught how to suction mucus and secretions from a tracheostomy tube. In fact, family members often become more “expert” in suctioning a loved one’s trach than the health care professionals, since the family member becomes, in essence, a “specialist” in the care of their loved one.
The nurse or respiratory therapist can teach you how to:
My mother’s last wish is to die at home, but she is on a ventilator. What can we do?
With careful planning, it is possible to take a loved one home from the hospital on a ventilator. The hospital will have to work closely with the hospice or home health agency as well as with the durable medical equipment company that provides the in-home ventilator.
Many, but not all, hospices will accept ventilator-dependent patients. Most hospices provide urgent care nurse visits on a 24-hour basis. The hospice interdisciplinary team is skilled in advance care planning, as well as in anticipating future care needs to keep your loved one comfortable.
My friend can no longer eat or drink. Won’t he suffer from thirst and hunger? How can I keep him comfortable?
When death is near, a person commonly loses the ability to swallow and can no longer eat or drink. Hunger does not generally occur in this situation. Observe the person for any signs of discomfort and notify your health care team if discomfort occurs. A dying person can be kept comfortable by:
The hospice interdisciplinary team has expertise in managing pain and other distressing symptoms. A recent national survey found that caregivers supported by hospice were more satisfied with the end-of-life care given their loved ones than those who were supported by home health agencies, nursing homes, or hospitals.
Increasingly, complicated, advanced medical care is capable of being delivered in the home setting. The responsibility for this care often falls on the shoulders of loved ones. However, programs such as hospice, home care, caregiver support networks, and educational resources are available to those who accept the challenge to allow loved ones to die at home, where most want to be. The experience, though never easy, is often rewarding for those who undertake it.
About the author: Dr. Cheryl Arenella does health care consulting for programs focused on improving end-of-life care. She has over 20 years of experience in the field of Hospice and Palliative Medicine. She is a former trustee of the American Board of Hospice and Palliative Medicine and served for many years as a Medical Director for a large Medicare certified hospice, where she provided medical oversight, direct patient care and administrative program support.