End Of Life Option Act Essay Time

This 2015 bill is the 8th attempt by doctor-prescribed suicide activists in California to transform a prescription for a lethal dose of drugs into a “medical treatment.”  It is patterned after Oregon’s “Death with Dignity Act.” 

Under the amended[1] “End of Life Option Act” (SB 128):

Government bureaucrats and profit-driven health insurance programs could cut costs by denying payment for treatment that patients need and want, while approving payment for less costly assisted suicide deaths.  

This has already been documented in Oregon – the state with the law upon which the California proposal is based.  The Oregon Health Plan (OHP) has notified some patients that medications prescribed to extend their lives or improve their comfort level would not be covered, but that the OHP would pay for a lethal drug prescription.[2]

Referring to payment for assisted suicide, the Oregon Department of Human Services explains, “Individual insurers determine whether the procedure is covered under their policies, just as they do any other medical procedure.”[3]

The bill, as amended, would not permit insurance companies to include denial of treatment and information about the availability of payment for assisted suicide in the same communication.[4]  However, the insurance provider could let the patient know that the cost for the lethal drug overdose is included in coverage if the patient, the attending physician or the patient’s designee asks what interventions would be covered.

California’s Capital Public Radio recently reported that health care – particularly for poor patients – has become increasingly difficult to provide.[5]

If the California bill is approved, will health insurance programs and government health programs do the right thing – or the cheap thing?

Family members, health care providers and others could advise, suggest, or encourage vulnerable individuals to request doctor-prescribed suicide.  

The bill would penalize anyone for “knowingly coercing or exerting undue influence”[6] on an individual to request the lethal prescription.  Additionally, it requires that the physician discuss the patient’s request “outside of the presence of any other persons” to determine whether the patient “is feeling coerced or unduly influenced by another person.”[7] However, “coercion” and “undue influence” have a very narrow legal meaning and do not include suggesting, advising, or encouraging a patient to request doctor-prescribed suicide.[8]

Since victims of domestic abuse, including elder abuse, are extremely vulnerable to persuasion from their abusers, it takes little imagination to understand how the bill could put abused individuals at risk of being persuaded to request doctor-prescribed suicide.  Victims of such abuse are unlikely to share their fears with outsiders or to reveal that they are being pressured by family members to request assisted suicide.[9]

“Doctor shopping” could take place until a health care professional can be found to declare that the patient is qualified for the lethal prescription.

If an attending physician believes a patient does not have the ability to make an informed decision or that the patient is being pressured to request the prescription for assisted suicide, nothing in the bill prohibits a health provider, family member or another person from arranging for the patient to be evaluated by other health care professionals until one is found who would declare the patient capable of choosing assisted suicide.

This has taken place in Oregon where it has been noted that “a psychological disorder — senility, for example — does not necessarily disqualify a person.”[10]

A woman died of assisted suicide under Oregon’s “Death with Dignity Act,” even though she was suffering from early dementia. Her own physician had declined to provide a lethal prescription for her. When counseling to determine her capacity was sought, a psychiatrist determined that she was not eligible for assisted suicide since she was not explicitly pushing for it and her daughter seemed to be coaching her to do so. She was then taken to a psychologist who determined that she was competent but possibly under the influence of her daughter who was “somewhat coercive.”

Finally, she was assessed by a managed care ethicist who determined that she qualified for assisted suicide, and the lethal dose was prescribed.[11]

An individual could request doctor-prescribed suicide based on fear of being a burden to others.   

Under the bill, the written request is to indicate whether the individual informed or decided not to inform his or her family of the request for assisted suicide.[12]  But such family notification by the person is not required.  If an individual fears becoming a burden and if loved ones are unaware of that concern, they are unable to reassure the person of their care and love.

In the last official Oregon report, fear of becoming a burden on others was given as a reason for requesting lethal drugs by more than 57 % of those who died using that state’s assisted-suicide law.[13]

The oral requests could be made by phone and the written request could be sent by mail or electronic means.   

Just as with Oregon’s assisted-suicide law, the bill requires that a person make two oral requests and a written request to the attending physician before receiving the prescription for doctor-prescribed suicide.[14]

Nothing in the proposal requires that any of those requests be made in the presence of the physician. The patient could, in fact, phone in the oral requests and mail the written request.

Someone who would benefit financially from the person’s death could serve as a witness to the patient’s written request.   

The bill requires that there be two witnesses to the individual’s written request for doctor-prescribed suicide.  The witnesses must attest that the patient is “competent,” “acting voluntarily” and “not being coerced to sign the request.”[15]  Only one of those witnesses shall not be a relative or someone entitled to any portion of the person’s estate upon death.[16]

This provides little protection since it permits one witness to be a relative or someone who is entitled to the patient’s estate.  The second witness could be a “best friend” of the first witness, and no one would know.

There are no protections for the person once the assisted-suicide prescription is filled. 

Like the Oregon law, the bill only addresses activities taking place up until the doctor writes the lethal prescription.  There are no provisions to insure that the patient is competent at the time the overdose is taken or that he or she knowingly and willingly takes the drugs.

Due to this lack of protection at the time of their deaths, the bill would put patients at enormous risk.  For example, someone who would benefit from the individual’s death could trick or even force the person into taking the fatal drugs, and no one would know.

Why are there no safeguards at the most important part of the process – at the time the patient takes the drugs that will cause death?

The death certificate would not reflect the actual cause of death.

The bill requires that the cause of death listed on a death certificate shall be “the underlying terminal disease,”[17] rather than the lethal drug overdose.

There is an illusion of choice.  Yet the bill, if passed, would constrict patient choice.

“Choice” is an appealing word, but inequity in health care is a harsh reality.

Under the bill, before writing a prescription for death, a doctor must discuss “the feasible alternatives or additional treatment opportunities, including but not limited to, comfort care, hospice care, palliative care, and pain control.”[18]  However, discussing all options does not mean that the patient will have the ability to access those options.

Patients may find that their insurance will not cover the “feasible alternatives” their doctors informed them about but, instead, will pay for doctor-prescribed suicide.

If doctor-prescribed suicide becomes just another “end of life option,” and a cheap option at that, the standard of care and provision of health care changes.  There will be less and less focus on extending life and eliminating pain, and more and more focus on the “efficient and inexpensive treatment option” of death.

If doctor-prescribed suicide is legalized in California, it could become the only “medical treatment” to which many people have equal access.  The last to receive health care could be the first to receive doctor-prescribed suicide.

Physicians would be able to write assisted-suicide prescriptions for mentally ill or depressed patients.

Before receiving a prescription for death, patients do not need to have a psychological or psychiatric evaluation.  A counseling referral is made “if appropriate.”[19] If a counseling referral is made, it may consist of only one consultation and is only for the purpose of determining whether the psychiatric or psychological disorder or depression is “causing impaired judgment.”[20]

Even if the counselor determines that the patient has a mental disorder or disease, the prescription for suicide could still be written as long as the counselor thinks that the patient’s judgment is not impaired and, therefore, he or she can make an informed decision.

This provision is the same as that contained in Oregon’s law where, in 2014, only 3 of the 155 patients who received lethal prescriptions were referred for a psychological evaluation.[21]  A study about Oregon’s law found that it “may not adequately protect all mentally ill patients.”[22]

Individuals who could live for many years would be eligible for assisted suicide.

Under the bill, doctors would be permitted to prescribe assisted suicide to patients who have a “terminal disease” which is defined as “an incurable and irreversible disease that has been medically confirmed and will, within reasonable medical judgment, result in death within six months.”[23]

However, that definition does not require that the individual is expected to die within six months, even with medical treatment, nor does it require that the condition be uncontrollable. Therefore, it is possible that a person could be considered “terminal” for the purpose of qualifying for assisted suicide even though, with medical treatment, he or she could live much longer.[24]

For example, diabetes can be both incurable and irreversible but it is controllable.  An insulin-dependent diabetic who stops taking insulin will, within reasonable medical judgment, die within six months.  Thus, under the bill, diabetics could be eligible for doctor-prescribed suicide even though they could live virtually normal lives with insulin.

There is documentation that this has occurred under Oregon’s assisted-suicide law.  In the latest official report from Oregon, diabetes is noted as the underlying terminal condition that made the patient eligible for a lethal prescription.[25]

Drugs for suicide could be mailed to a patient.

Nothing in the bill requires the patient to obtain the drugs in person.  The bill permits the lethal drugs to be delivered by “personal delivery, United Parcel Service, United States Postal Service, Federal Express, or by messenger service.”[26]  The amended version of the bill requires that a signature is required at delivery.[27]

However, even with a required signature, services such as Federal Express, UPS and the USPS only require the signature of the person accepting the delivery, not the person to whom the package is addressed.  There are no protections to prevent unintended individuals from signing for the package of drugs.

In addition, the bill permits the assisted-suicide drugs to be dispensed to “a person expressly designated by the patient.”[28]  That designated person could be an abusive spouse or heir who persuaded the patient to request the prescription and who was one of the two witnesses to the patient’s written request for doctor-prescribed suicide.

A representative of an assisted-suicide advocacy organization could witness a vulnerable patient’s written request. 

In Oregon, members of the assisted-suicide advocacy group that spearheaded the state’s law have acknowledged that they play a key role in the vast majority of deaths under the state’s assisted-suicide law.[29]  The same advocacy organization is a major promoter of SB 128.

There is no way to know if reporting by physicians and pharmacists is accurate and there are no provisions for investigating or enforcing of the law’s requirements.

The State Public Health Officer may review records of prescribing physiciansandis to make a annual statistical report related to activities of physicians and pharmacists under the end of life options act.[30]  All data contained in the annual reports would be provided by the prescribing physicians and the pharmacists who dispensed the lethal drugs. However, the bill contains nothing that gives enforcement or investigative authority to the State Public Health Officer so there is no way to ensure the accuracy of information in the annual report.

This is similar to the Oregon law, where the first official summary of the law’s utilization stated that information in the report may not have been accurate or complete.  “[F]or that matter, the entire account could have been a cock-and-bull story.  We assume, however, that physicians were their careful and accurate selves.”[31]

A medical epidemiologist with the Oregon Health Division and co-author of the state’s first official report said neither the law approved by voters nor the legislature had given any enforcement powers to the Health Division. She noted that the division had to rely on the word of doctors who are not required to be at the patient’s bedside when the lethal drugs are taken.  For that reason, the doctors who provide information for the annual reports may not have knowledge about any complications.[32]

A health care facility could not prevent deaths from doctor-prescribed suicide on its premises.

The bill states that a health care provider may prohibit its employees, independent contractors, and others from “participating in activities under this part” while on the premises.[33]  However, it defines “participating in activities under this part” to include only the duties of the attending physician, the consulting physician or the activity of delivering or dispensing the lethal overdose.[34]

This does not permit the facility to prohibit employees or others from promoting doctor-prescribed suicide, witnessing the written request, or transporting a resident of a nursing home or senior living facility to an off premises physician to obtain the prescription and to an off premises pharmacy to get the lethal drugs which will be brought back to and used on the premises.

Health care providers and facilities could be compelled to violate their principles and policies.

The bill states that a person or entity “is not required to take any action in support of a patient’s decision under this part, except as required by Sections 442 through 442.7 inclusive.”[35]  Those sections require that a health care provider who gives a patient a terminal diagnosis must also give comprehensive information and counseling regarding legal end-of-life options.[36]The California Department of Public Health has made it clear that, if a health care provider does not wish to comply, that provider must refer to someone who will.[37]

If SB 128 passes, doctor-prescribed suicide will be a “legal end-of-life option.”

The overall suicide rate in California could dramatically increase.

Already more people in California die annually from suicide than from motor vehicle accidents,[38] and suicides vastly outnumber homicides[39] in the state.

Starting two years after its doctor-prescribed suicide law went into effect, Oregon’s suicide rate skyrocketed, making it 41% higher than the nation’s average.[40]

If California adopts SB128, will the overall suicide rate in California also increase?

Note:  Supporters of SB 128 point to Oregon to claim that there are no problems with the law and that safeguards are meticulously followed and monitored.  Yet, in closed-door sessions, they acknowledge that this is not true.  For documented information about this contradiction, see “The Oregon Experience.”[41]

[1]  SB 128 was amended in the Senate on April 14, 2015.

[2]  KATU Television, “Letter noting assisted suicide raises questions” (interview about one such case and the response of the Oregon Health Plan). Available at:  http://www.katu.com/news/26119539.html  (last accessed 1/29/15).

[3]  Oregon Dept. of Human Services, “FAQs about the Death with Dignity Act.”  Available at: http://public.health.oregon.gov/ProviderPartnerResources/EvaluationResearch/DeathwithDignityAct/Pages/faqs. aspx (last accessed 12/30/14).

[5]  “Pauline Bartolone, “Doctors Medical Center Closure Shows Struggle of Hospitals that Serve the Poor,” April, 20, 2015.  Available at: http://www.capradio.org/articles/2015/04/20/doctors-medical-center-closure-shows-struggle-of-hospitals-that-serve-the-poor (last accessed 4/29/15).

[7]  Section 443.5 (a) (5).

[8]  For example: “coercion” generally means imposing one’s will on another by means of force or threats and “undue influence” includes such activities as controlling the necessities of life such as medication, access to information, interaction with others or access to sleep.

[9]  For example, statistics indicate, “Only four percent of reported elder abuse cases come from the elder person; 96 percent of the reports come from somewhere else.” Gazette.net (Maryland), “A safe place for abused seniors,” February 9, 2015. Available at http://www.gazette.net/article/20150209/NEWS/150209456/1007&source=RSS &template=gazette (last accessed 4/29/15).

[10]  “Physician-assisted suicide: A family struggles with the question of whether mom is capable of choosing to die,” Oregonian, February 4, 2015. Available at: http://www.oregonlive.com/health/index.ssf/2015/02/physician-assisted_suicide_a_f.html (last accessed 4/20/15).

[13]  Official report for 2014 deaths under Oregon’s Death with Dignity Act, pg. 5.  Available at:     http://public.health.oregon.gov/ProviderPartnerResources/EvaluationResearch/DeathwithDignityAct/Documents/ year17.pdf  (last accessed 4/6/15).

[15]  Section 443.3 (b) (3).

[16]  Section 443.3 (c) (1).

[18]  Section 443.5 (a) (2) (E).

[19]  Section 443.5 (a) (4).

[21]  Official report for 2014 deaths under Oregon’s Death with Dignity Act, p. 5.  Available at: http://public.health.oregon.gov/ProviderPartnerResources/EvaluationResearch/DeathwithDignityAct/Documents/

year17.pdf (last accessed 4/6/15).

[22]  Linda Ganzini, Elizabeth R. Goy, Steven K. Dobscha, “Prevalence of depression and anxiety in patients requesting physicians’ aid in dying: cross sectional survey,” British Medical Journal, Oct. 25, 2008, pp. 973-978.

[24]  According to data regarding predicted life expectancy, a prognosis of six months is typically given as a median for patients with a similar diagnosis and can be completely inaccurate when applied to a particular patient. “[I]f a patient is told she has a year median survival, it means that half of similar patients will be alive at the end of a year and half will have died.  It’s possible that the person’s cancer will advance quickly and she will live less than the median.  Or, if she is in good health and has access to the latest in treatments, she might outlive the median, sometimes by many years.”  Amanda Aronczyk, “Cancer Patients and Doctors Struggle to Predict Survival,” NPR, February 10, 2015. Available at: http://www.npr.org/blogs/health/2015/02/10/384011538/cancer-patients-and-doctors-struggle-to-predict-survival (last accessed 4/30/15).

[25]  Official report for 2014 deaths under Oregon’s Death with Dignity Act, p. 6, fn. 6.  Available at: http://public.health.oregon.gov/ProviderPartnerResources/EvaluationResearch/DeathwithDignityAct/Documents/ year17.pdf (last accessed 4/6/15).

[29]  Officers of Compassion in Dying/Compassion & Choices of Oregon were the chief proponents of Oregon’s assisted-suicide law.  They have proclaimed themselves stewards of the law. According to one spokesperson for the organization, in 2009, it was involved in 97% of deaths under the law.  For documentation see: “The Proportion of Oregon Assisted Suicides by Compassion & Choices Organization.”  Available at: http://www.patientsrightscouncil.org/site/oregon-assisted-suicide-deaths (last accessed 4/29/15).

[31]  Center for Disease Prevention & Epidemiology – Oregon Health Division, “A Year of Dignified Death,” March 16, 1999, Vol. 47, No. 6,  p. 2.  Available at: http://public.health.oregon.gov/DiseasesConditions/CommunicableDisease/CDSummaryNewsletter/Documents/1999/ohd4806.pdf (last accessed 4/29/15).

[32]  Joe Rojas-Burke, “Suicide critics say lack of problem in Oregon is odd,” Oregonian, February 24, 2000.

[33]  Section 443.12 (e) (1). (Emphasis added.)

[34]  Section 443.12 (e) (6) (B).

[35]  Section 443.12 (d) (1).

[36]  Cal. Health & Safety Code Sec. 442.5–442.7.

[37]  Letter from California Department of Public Health to All Health Care Facilities, November 12, 2014.  Available at:  http://coalitionccc.org/wp-content/uploads/2014/12/ab2139_end_of_life_CDOH-mandate.pdf?utm_source=Coalition+for+Compassionate+Care+of+California&utm_campaign=26f942e282-January_2015_public_policy1_16_2015&utm_medium=email&utm_term=0_fe8bdd104b-26f942e282-165203937

(last accessed 4/30/15).

[38]  In 2010, there were 3,913 suicide deaths and 2,922 deaths from motor vehicle accidents in California.
National Vital Statistics Reports Volume 61, Number 4, “Deaths: Final Data for 2010”, May 8, 2013, p. 88.  Available at: http://www.cdc.gov/nchs/data/nvsr/nvsr61/nvsr61_04.pdf (last accessed 01/29/2015).

[39]  In 2010, there were 3,913 suicide deaths and 1,954 homicide deaths in California.
National Vital Statistics Reports Volume 61, Number 4, “Deaths: Final Data for 2010”, May 8, 2013, pp. 88, 89.  Available at: http://www.cdc.gov/nchs/data/nvsr/nvsr61/nvsr61_04.pdf (last accessed 01/29/2015).

[40]  Oregon’s suicide rate increased by 49.3 percent, making it 41 percent higher than the national rate.  Available at: http://www.oregonlive.com/health/index.ssf/2013/05/report_oregons_suicide_rate_hi.html (last accessed 01/31/15).

[41]  “The Oregon Experience.”  Available at: http://www.patientsrightscouncil.org/site/the-oregon-experience (last accessed 1/30/15).


The End of Life Option Act went into effect on June 9, 2016. It allows for California residents, age 18 and older, to request life-ending medication from their doctor if they are suffering from a terminal illness and want to set their own timetable for their death.
Between June 9 and December 31, 2016, 258 people initiated the process, according to the report. One hundred ninety-one people were prescribed the lethal medication, of which 111 patients "were reported by their physician to have died following ingestion of aid-in-dying drugs prescribed under EOLA." Twenty-one people died as a result of their underlying terminal illness, and the outcome of the other 59 people who were prescribed drugs "is currently undetermined, as there has been no outcome reported for these individuals within the time period covered by this report."
The majority of the 111 people who utilized the law were cancer patients, according to the report. The median age at time of death was 73. Most patients were white (89.5%), enrolled in hospice/palliative care (83.8%), and were covered by some type of health insurance (96.4%). Sixty women and 51 men died as a result of ingesting aid-in-dying drugs.
"The state's data show that even during the early months of the law's implementation, the law was working well and terminally ill Californians were able to take comfort in knowing that they had this option to peacefully end intolerable suffering," Compassion & Choices California State Director Matt Whitaker said in a statement. "We continue to work to ensure that every terminally ill Californian has equal access to all end-of-life care options, including hospice, pain control, palliative care and medical aid in dying." The nonprofit organization helped to get the law passed in California, and advocates for similar legislation nationwide.
In California, a mentally capable adult is eligible to partake in the End of Life Option Act if he or she is determined to have a terminal illness -- meaning they have six months or less to live. The patient must make two verbal requests of their doctor, at least 15 days apart, as well as one written request. The patient must affirm his or her request 48 hours before ingesting the medication, which they must be able to self-administer, without the help of a physician, family member or friend.
Physician-assisted aid-in-dying is different from euthanasia (commonly referred to as physician-assisted suicide), which is illegal in all 50 states. Aid-in-dying advocates such as former California state Sen. Lois Wolk and state Sen. Bill Monning -- who co-authored the End of Life Option Act -- dislike the term "suicide," because it implies an impulsive and irrational act.
"Is this suicide?" CNN Chief Medical Correspondent Dr. Sanjay Gupta pointedly asked the pair in an interview last year.
"No, not at all," said Wolk.
"The person is dying. The people we've met with -- they want to live," said Monning. "They're not choosing death. That decision has been made unfortunately because of an uncontrolled disease, a terminal cancer. ... What this does is allows them to gain autonomy, self-determination in what will be the path of that certain death."
Both Wolk and Monning said it was important that any attempt to influence a person to hasten his or her own death under their bill would be cause for felony prosecution.
"The health plans cannot influence a patient in their choices," said Monning. "They're not mandated to cover the costs. Some may, some may not ... but no plan can say, 'You can't pursue (an expensive or long-term) treatment option; we want you to use this end of life option.' That's cause for a felony."
Under California's law, the cause of death that is listed on an official death certificate is the underlying terminal illness, such as cancer -- not "suicide" or use of the End of Life Option Act. That has important implications not only for patient confidentiality, but also for sensitive family matters such as a will or life insurance.

The legacy of Brittany Maynard

In 2014, 29-year-old Brittany Maynard brought the right-to-die movement back into the country's consciousness. On New Year's Day, she found out that she had brain cancer. After multiple procedures to remove part of the tumor, Maynard learned that it had come back and was more aggressive. Doctors said she had fewer than six months to live.
"I do not want to die. But I am dying," she wrote in an emotional essay for CNN in October 2014. "And I want to die on my own terms."
Because California had not yet legalized medical aid in dying, Maynard and her husband, Dan Diaz, moved to Oregon to utilize that state's Death With Dignity law.
Oregon was the first state to enact such a law, in 1997. In the 18 years after, 1,545 prescriptions have been written for a lethal dose of medication, of which 991 patients used that prescription to hasten their death, according to a study released in April. Most of those patients, like Maynard, had cancer.
Maynard made a series of videos with Compassion & Choices, the medical aid-in-dying advocacy group.
"I can't even tell you the amount of relief it provides me to know that I don't have to die the way that it's been described to me that my brain tumor would take me on its own," Maynard said in the first video.
Maynard and Diaz had been married just over a year when she was diagnosed with cancer. Uprooting their lives in California to move to Oregon was challenging for their entire family.
"That was one of the worst things, having to leave our home at that time," Diaz told CNN's Dr. Sanjay Gupta in an interview last year. "We move to Oregon; Brittany applies for this (lethal) medication; she puts it in the cupboard, and that's it.
"We continue doing everything we can to extend her life," Diaz said. "The fact that we had that medication, it didn't change anything with regards to her battling cancer or her fighting. When you have cancer, you fight. That's what you do."
On the morning of November 1, 2014, Maynard had a small seizure.
"It passed," Diaz said, "so we slept a little bit later that day. ... We had breakfast. Brittany wanted to go for a walk, so we did. We took the dogs -- because, again -- being outdoors, that's what fed Brittany's soul.
"When we got back to the house ... she just told me, she says, 'Dan, it's time. It's my time,' " he recalled. "The suffering that she had endured leading up to that day, the seizure that morning, was a reminder of what she was risking -- that if a seizure or a stroke occurs as her symptoms get worse, if she loses the ability to self-administer, if she suffers a stroke and she loses the ability to stand, walk or swallow, all of a sudden she's now trapped in her own body, and she's trapped dying the very way she was trying to avoid.
"It was around 4 o'clock in the afternoon," Diaz remembered. "She wrote a final passage in her Facebook, kind of a letter to all her friends and loved ones, and within five minutes of taking that medication, Brittany fell asleep, just like I've seen her do a thousand times before. In 30 minutes, the medication slows brain function, including the parts that control breathing, so her respirations drop to a point where she passed away. That was the gentle passing that Brittany had, and that's not the gentle passing that she would have had if the brain tumor would have continued to run its course."


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