PALLIATIVE CARE AND HOSPICE

When a healthcare provider recommends palliative care or hospice, patients and their families need guidance so they can make the most life-affirming decisions possible in their circumstances. The Task Force on Civil Rights in Health Care advises people to become informed and ask questions before electing a palliative care or hospice program.  

The goal of palliative care is to relieve symptoms—including pain and stress—at any stage in a serious illness. Palliative care can be provided in conjunction with curative or life-prolonging treatment. Hospice care is a subset of palliative care. It is focused on providing comfort care when a patient no longer has curative options or has chosen to forgo treatment because the burdens of treatment outweigh the benefits. 

When palliative care is provided by healthcare professionals who have genuine respect for the life of every person committed to their care, it can be a blessing for patients and their families. Palliative care should never be used to cause or hasten death.

Unfortunately, there is a growing trend to misapply palliative medications to make people die, particularly in the hospice care setting. 

Because people who are receiving hospice care have a limited life-expectancy, it is the “ideal” setting for stealth euthanasia – intentionally causing patients’ deaths while pretending to provide appropriate end-of-life care. Patients and families must be vigilant.

“Numerous reports from families of hospice and palliative care patients indicate that a one-size-fits-all pattern of administering a combination of opioids and anti-anxiety drugs has emerged. Whether or not patients have pain and/or agitation, they may begin to receive these drugs upon admission.” – “Drugs Commonly Used in Hospice and Palliative Care,” Making a Difference, A Guide for Defending the Medically Vulnerable,www.halovoice.org

A typical report that HALO receives from grieving family members is that their loved one, who had been alert and was not complaining of pain, was administered increasingly frequent and larger doses of pain medications and sedatives to the point where they were sleeping all the time and could not eat or drink. Some reported that patients were also denied usual medications to control blood pressure, diabetes, heart disease, infections, etc. Other groups receive similar reports. For instance, Murdered by Hospice, a Facebook group with over 700 members, exists to inform the public that hospice performs “euthanasia with or WITHOUT CONSENT” and states, “We are witnesses to medical murder of our loved ones.”

Is palliative care the antidote to assisted suicide?

There is merit in the argument that we should ensure patients do not choose assisted suicide because they are not receiving the best treatment available for management of pain and other symptoms of disease. However, Oregon’s experience suggests that palliative care is not the antidote to assisted suicide. An overwhelming majority of patients who have died by assisted suicide using Oregon’s so-called “death with dignity” law (in effect since 1997) have been enrolled in hospice care programs. The 2019 Oregon Death with Dignity Annual Report revealed that 90% of patients who killed themselves with a doctor-prescribed deadly dose of drugs were on hospice at the time of death.

The American Academy of Hospice and Palliative Medicine (AAHPM) “takes a position of studied neutrality on the subject of whether PAD [physician-assisted death] should be legally permitted or prohibited.” Neutrality gives the green light to assisted suicide as surely as support does.

Also, there is more than one way to assist a suicide. For instance, Voluntary Stopping Eating and Drinking (VSED) is facilitated by some hospices, particularly in states that do not permit assisted suicide by physician-prescribed drugs. VSED means that a patient, who is capable of eating and drinking, chooses to refuse food and fluids with the intention to cause death. This is suicide. When a hospice supports this decision by providing “comfort care” as the patient starves and dehydrates to death, the suicide is assisted – not prevented – by palliative care! 

Fraud and abuse are widespread in the palliative care and hospice industries.

The U.S. Department of Health and Human Services Office of Inspector General (HHS-OIG), released the results of its work which identified thousands of Medicare claims that indicate abuse and neglect of beneficiaries (i.e., patients receiving Medicare benefits). (See https://oig.hhs.gov/newsroom/media-materials/2019/hospice/ for more information.) 

For information about hospice fraud, simply Google “hospice fraud cases.” Prepare to be astounded at the extent and the dollar amount involved, and, even worse, the patient abuse.

Here is just one example. The FBI made arrests in February 2018 for healthcare fraud. Brad Harris, the owner of a Frisco-based (near Dallas, Texas) hospice company, his wife and 14 others were indicted in a $60 million Medicare fraud scheme that put financial interests over the needs of patients. Five of the defendants were doctors. Five were nurses. The FBI investigation, which began in 2014, initially focused on allegations that Novus Health Services sought federal reimbursements for patients recruited by Novus who did not qualify for hospice services and charged for services that were not medically necessary. Harris also had ordered nurses to increase drug dosages to speed patients’ deaths and maximize profits, according to an FBI affidavit. (Harris is an accountant, not a doctor.) Harris sent text messages to employees such as, “You need to make this patient go bye-bye.” 

Advice

If you are considering hospice for yourself or a loved one, do your homework. Know what questions to ask before choosing a hospice. The Healthcare Advocacy and Leadership Organization (HALO) provides a list of questions to ask a hospice before admission at https://www.halovoice.org/pdf/HALO_Questions-to-ask-a-Hospice.pdf. Providers who are doing things right and following the rules will be happy to let you know this and to compare themselves to other palliative care and hospice providers. Ask them for references – especially the contact information for families who have used/are using their services. Google the name of the hospice to check for fraud cases against it. Check out the records of the doctors and nurses providing care. 

To report neglect, abuse, or suspected fraud, call 1-800-MEDICARE.

Julie Grimstad is President of HALO (the Healthcare Advocacy and Leadership Organization)

2 thoughts on “PALLIATIVE CARE AND HOSPICE”

  1. I appreciate you explaining to us that hospice care is focused on providing comfort and assistance to patients who no longer have curative options and have decided to not proceed with treatment. It seems like my cousin does not have much left to live anymore due to her illness, so her parents are doing the best they can to support her while she’s still alive. I hope they find good end-of-life care services to assist them as well in looking after my cousin.

  2. Stella

    My dad had dementia. He was walking, talking, smiling, eating 2-3 times a day and drinking plenty on the day he went into hospice for a 5-day RESPITE visit to give my mom her first extended break as his caretaker in 2 1/2 years. HE WAS NOT ON ANY DRUGS FOR PAIN! We believe that he was comatose within 48 hours. My mother was expecting to pick him up on Friday at 1pm. She received a phone call at 4:15am on Friday to tell her that my dad was dying. Not a single time was my mother told, when she would call every day, that my dad was not given any of his daily meds, not eating or drinking and crying saying he wanted to go home. All of this we had to read in his medical records AFTER he was dead.They gave him AHR cream, xanax, atavan, morphine and FENTANYL!! He had NO PAIN. He had dementia!! My mother and my family are devastated and grieving with guilt. IT IS MURDER!

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