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California Compassionate Choices Act, AB 374, Passed by Assembly Judiciary Committee

By Frank D. Russo
Yesterday, on a strict party line vote,with all 7 Democrats supporting the measure and all 3 Republicans opposed, the Assembly Judiciary Committee passed AB 374, a bill described by its author as "the most important pro-choice bill in many years--The California Compassionate Choices Act."
The bill is based upon Oregon's successful Death with Dignity Act, approved in 1997. The Act allows to mentally capable, terminally ill adults, with six months or less to live to legally obtain and use prescriptions to end their suffering.
Passage came after a very emotional two hour hearing before a packed hearing room full of supporters and opponents of the bill. We are publishing today the testimony of one of the witnesses, Trudy Schaefer that had to be read by her daughter in support of AB 374.
While there was a lot of emotion, committee members also asked specific questions as they honed in on the provisions of the bill, how it would work, and how it compared with the Oregon law. The committee hearing can be viewed in the archives of the California Channel.
The author of the bill, Assemblymember Patty Berg delivered an elegant opening statement to the committee that set forth the critical issues for the proponents. She said:
This bill deals with a deeply personal choice available only to people who are dying of a terminal illness. it allows them to consider an option that a huge majority of Californians say they would like to have.But, much more than the specifics of the options, AB374 is about our fundamental right to privacy -- a civil right that is expressed as a freedom to choose.
It is about the freedom of the individual to make choices – and the freedom for your choices to be different from my choices.
The question before you today is not whether you approve of a terminally ill patient hastening his or her death. It is about whether you will uphold our right to privacy, and whether you believe in the right of the individual to choose.
… as soon as we allow the fears of one group or the religious beliefs of another to constrain this particular right, we will find that other rights ultimately are in the crosshairs.
What the opposition wants is not protection, but really to issue an ultimatum that imposes their personal and religious beliefs on all of California. And if we can learn anything from history it is that we are imperiled when freedom is constrained, not when it is advanced.
The dividing line on the bill between Democrats and Republicans broke appears to be based on deeply and sincerely held personal views, much like that of the abortion debate. Religious beliefs surfaced during the hearing, with one Catholic priest telling those who support the measure that they were going to Hell.
Berg's framing, and that of supporters is based on choice and individual autonomy. While there were questions about practicalities of the bill and how it would work in practice, with opponents claiming it would allow for insurance companies and those who stand to benefit, having undue influence, Berg pointed out the layers upon layers of protection written into the bill, and the Oregon experience.
Conservative Republican Assemblyman Anthony Adams saw it as a preservation of life issue and one that he had a duty to impose his belief on others. He stated, "You better darn well believe I want to impose my morality on these people."
Sacramento physician Dr. Richard Ikeda, who cares for elderly, low income patients as medical director of Health For All community clinics, told the committee that California patients deserve better choices and that AB 374 would benefit all California terminal patients, “All patients regardless of income or status deserve the best medical care that our state can offer. Ethical medical care respects my patient’s personal decision-making at the end of their life. I believe that my patients deserve access to, and information about, all options for medical care, including aid in dying. My patients are poor, not stupid."
Assemblymember Berg pointed to the committee the safeguards written into AB 374, saying:
The bill has multiple layers of safeguards to ensure that it applies only those whose lives are already at an end. it is based on Oregon's Death with Dignity Act, which has proven itself sound and trustworthy for nine years.The bill before you provides even more layers of protection and certainty than exist in the Oregon law. It has automatic triggers for a psychological or psychiatric evaluation; it ensures that patients get information on all available alternatives, in writing and of all the available alternatives in writing in their primary language; and it prevents family members or potential inheritors from playing any role at all.
Here are some of the protections written into AB 374:
1. The patient must be a terminally ill adult with six months or less to live.
2. The patient must be a resident of California.
3. The patient must make an informed decision. The patient’s attending physician must inform the patient of their medical diagnosis, prognosis, potential risks associated with taking the medication, the probable result of taking the medication, and provide in writing the feasible alternatives, including comfort care, hospice care, and pain control.
4. The patient cannot be coerced by next of kin or any third party. If any coercion is suspected, the patient will be prohibited from participating in the Act.
5. The patient must be evaluated by two physicians. A consulting physician must examine the patient and confirm the attending physician’s diagnosis and prognosis and that the patient is mentally capable, fully informed and acting voluntarily, free of coercion.
6. The patient must be mentally capable. Both physicians must verify that the patient is mentally capable of making and communicating health care decisions. If either physician suspects the patient's judgment may be impaired by medication or a psychiatric or psychological disorder, the patient must be referred to a licensed psychiatrist or psychologist for a psychological examination. If a patient is referred, then the process completely stops until the psychiatrist or psychologist has determined that the patient is mentally capable. If the patient is determined to not be mentally capable the patient will be denied the medication.
7. The patient must make two oral requests, and one written request for the prescription. The written request must be witnessed by two individuals who attest to the best of their knowledge and belief that the patient is competent, acting voluntarily, and not feeling any coercion to make the request.
8. There are two waiting periods. 15 days after the first oral request, at which time the written request can be made, and 48 hours after the second oral request and the writing of the prescription.
9. The patient can rescind their request at any time.
10. The patient must self-administer the prescription. No one else can administer the medication to the patient.
11. Physicians may refuse to participate with the Act. No doctor would ever be required to participate in the process in any way.
12. Anyone who violates the provisions of the Act will be prosecuted. The language of the Act provides that anyone who engages in illegal behavior is subject to punishment for a crime to the full extent of the law.
13. Both physicians must submit detailed reports to the Department of Health Services.
The Oregon Death with Dignity Act was a citizens' initiative passed twice by Oregon voters. The first time was in a general election in November 1994 when it passed by a margin of 51% to 49%. An injunction delayed implementation of the Act until it was lifted on October 27, 1997. In November 1997, a measure was placed on the general election ballot to repeal the Act. Voters chose to retain the Act by a margin of 60% to 40%.
Polls, including the California Field Poll have shown wide and consistent support in California for the approach of AB 374, including a Field Poll last year http://www.caforaidindying.org/pdf/FieldPoll06.pdf which reported that:
Over the twenty-seven years that The Field Poll has been tracking public sentiment on the issue of doctor-assisted suicide, a large majority of Californians have consistently endorsed the concept.
In a statewide survey completed last month, 70% of all adults and 69% of registered voters believe that incurably ill patients should have the right to ask for and get life-ending medication.
In the last session of the California legislature, AB 651, http://www.leginfo.ca.gov/pub/05-06/bill/asm/ab_0651-0700/ab_651_bill_20060615_amended_sen.pdf with similar provisions, failed in the California Senate Judiciary Committee by one vote. http://www.californiaprogressreport.com/2006/06/california_comp.html
The measure faces strong opposition by the Catholic Church as it did last year. Despite the opposition of the church, the Field poll mentioned above showed a majority of Catholics support the concepts of the bill.
The next step for AB 374 is the Assembly Appropriations Committee for what is supposed to be a fiscal and not a policy review. However, there is likely to be a similar division along party lines. The bill must pass the Appropriations Committee by June 1 and the Assembly Floor by June 8 to be able to get to the Senate in time to be considered for final passage this year.
Its chances are excellent given the coauthors and support from Democratic leadership in both houses. AB 374 lists as an author, in addition to Berg, the Speaker of the Assembly. Fabian Nunez, and the Majority Leader in the Senate, Gloria Romero. A wide coalition or organizations and individuals support compassionate care and will be lobbying for its passage.
Comments
Hard cases make bad law.
For every poignant patient wishing they could end it all with the assistance and sanction of the medical profession, as the Oregon experiment reveals, many more choose to die with dignity, struggling day after day, communicating with family and friends, willingly enduring the discomfort and disabilities of their disease. If PAS were legal in CA, the majority would still opt for this path. Though legal in Oregon, only 46 cases were reported in 2007 (292 since enacted in 1997). This corresponds to an estimated 1.47 physician-assisted suicides per 1,000 deaths. Not a landslide clamoring for this culture-altering change. http://tinyurl.com/2cbmrq
"Then what's the problem, why the panic, the resistance, since so few will choose this path?"
Because it will change, forever, our culture. Medicine, where physicians become complicit killers as well as compassionate healers - (read your history prior to Hippocrates). Families, where no one will know of the pressure, strident or silent, to opt out, saving heirs thousands of dollars. But we will never know . . . we will rarely peek inside their homes. Insurance companies, who are remarkably and shrewdly silent on this issue as they stand in the wings, eagerly anticipating reaping a bounty, since 22% of all US medical dollars are spent in the last year of life! http://tinyurl.com/2gqgau
Is it worth changing our entire culture irrevocably for 500 Californians or 5,000 Americans each year? Medicine will never be the same. Most cannot conceive of the devastation this will wreak on it. These figures do not tell the whole story, though, because as the Dutch experiment reveals, these numbers will soar beyond credulity.
Doctors will face the temptation to choose life or death. A country of 16.5 million, half the population of CA, after 15 years of looking the other way as doctors openly assisted in or actively euthanized their patients, the Remmelink Report provided by the Dutch Government, reports that in 1990, 400 patients were given the means to kill themselves, 2,300 patients asked their doctors to kill them, 1,040 doctors actively killed their patients without the patient's knowledge or consent, and 4,941 doctors administered lethal morphine injections without their patient's explicit consent. That's 8,681 euthanized patients, 69% of which were put to death solely at the physician's discretion. http://www.euthanasia.com/hollchart.html
Family members will face financial temptations. Hasn't the family deteriorated enough in the past 50 years? Dare we offer it one more nail? The legal temptation good people will wrestle with when confronted with the huge cost of medical care for mom or dad as "we" watch our inheritance spiral down the drain?
Don't insurance companies face enough temptations already? Annually they whittle away at our present coverage as healthcare costs increase exponentially. What coverage will they deny in the future as the seldom selected choice to take one's life fully integrates, becoming the duty to die?
If compassion is the true motivator behind this movement, rather than voting to give each other the right to kill ourselves, why not commit ourselves to the duty of compassion, comprehensive pain control and palliative care, all relatively inexpensive by comparison to high end life-sustaining medical intervention?
The relatively rare and hard cases touted as normative are poignant indeed. No one dares minimize these tragic situations. But are we willing to sacrifice another pillar tenuously supporting our culture? I hope not.
Michael McLaughlin
13601 SE 129th Avenue
Clackamas, OR 97015
503.522.1950
cmdawest@gmail.com
Posted by: Michael McLaughlin at March 28, 2007 01:04 PM
This was posted on ADAPT-CAL, an e-mail LISTSERVE on the subject of disability, as part of a continuing debate on physician-assisted suicide.
Marilyn Golden is a Policy Analyst for the Disability Rights Education and Defense Fund.
Given some of the issues about the legalization of assisted suicide that Marilyn Grunwald and others have mentioned, I would like to post some points and thoughts on that subject. I hope you will share them with everyone.
I want to thank Marilyn Grunwald for the kind words about me in her unpublished article. The thoughts below will explain why I think legalization (which is represented right now by AB 374 in the California Assembly) is a dangerous and mistaken step, especially given how our health care system functions today. Dangerous for people with disabilities - but dangerous for our society as a whole. And given the emphasis in what Marilyn Grunwald wrote, I will focus mostly on the society as a whole rather than specifically on PWD’s (People With Disabilities).
First, some general points. I can offer documentation on them if anyone wishes, but will not weigh this e-mail down with lengthy source documentation. By the way, these points have been collected by a number of people, including Paul Longmore and Catherine Campisi; they are not mine alone. After the general points, I will include the text of my recent Op Ed on this subject, which appeared in the San Jose Mercury News on March 1, 2007.
GENERAL POINTS ABOUT THE LEGALIZATION OF ASSISTED SUICIDE AND AB 374
1. A broad coalition opposes assisted suicide: Medical care providers: American Medical Association; California Medical Association; California Hospice and Palliative Care Association. Minority community advocates: League of United Latin American Citizens; La Raza Roundtable of Santa Clara County; Sacramento NAACP. Disability rights groups: California Foundation for Independent Living Centers; California Disability Alliance; Disability Rights Education and Defense Fund; and 16 other organizations representing people with disabilities. As well as organizations representing poor people and uninsured people.
2. These groups all fear the deadly mix of assisted suicide and our profit-driven health care system. The lethal prescription generally used for assisted suicide costs about $100, far cheaper than treatments for most prolonged illnesses. Pressures to cut costs by denying treatment already pose a significant danger. Legalizing assisted suicide would intensify that danger. To deny patients life-sustaining treatments while offering the “choice” of assisted suicide would subtly coerce them toward death.
3. How can California’s legislature consider assisted suicide while millions of low-income families have no access to health care? Is the legislature telling them, “We won’t provide health care, but we’ll make it easier for you to commit suicide when you’re uninsured and at your most vulnerable”? Legalization would place many people, particularly among the disadvantaged and marginalized, at significant risk.
4. AB 374 is modeled on Oregon’s flawed assisted suicide law. That law does not penalize doctors who fail to report assisting suicides. It gives the state no resources or authority to investigate violations or abuses. Moreover, the state destroys its paperwork after each annual report, making it impossible to verify those reports’ conclusions independently.
5. The just-released official Oregon report for 2006 supplies even less information than previous reports. For example, this year’s report no longer lists the number of lethal prescriptions written by individual doctors. In the past, doctors affiliated with the pro-assisted suicide advocacy group Compassion in Dying (since renamed Compassion & Choices) facilitated three out of four such deaths. The new report helps to hide that fact.
6. The Oregon law and the California bill contain “safeguards” that are merely paper protections, easily sidestepped. For example, they purport to limit assisted suicide to terminally ill people who have only six months to live. In fact, the number of days between an initial request for life-ending prescriptions and patients’ deaths has ranged as long as three years. This shows the inaccuracy and unreliability of six-month prognoses. It also indicates that people who are not terminal have been encouraged to take their lives. In the Netherlands, assisted suicide for people with terminal illness has spread to full-blown euthanasia (lethal injections by doctors) for people with chronic illness, people with mental health distress, and even depressed teenagers and infants with disabilities.
7. The Oregon law encourages “doctor shopping” for suicide. Proponents promised legalized physician-assisted suicide would occur in the context of long-standing doctor-patient relationships. Instead, many, and over time perhaps most, deaths have involved short-term relationships with pro-suicide doctors doing cursory examinations. In half the cases 1988-2004, the doctors knew the patients less than three months. The official reports identified the “Duration (weeks) of physician-patient relationship” as ranging from “0-1065.” In other words, some doctors prescribed lethal medications for patients they know for just a few days or not at all.
8. Oregon’s press has reported troubling examples of “doctor shopping,” medication failing, coercion, and deaths of people who did not meet eligibility criteria. Yet none of this has ever appeared in the official state reports. The Oregonian, the state’s major newspaper, complained in 2005 that the law’s reporting system “seems rigged to avoid finding” the answers. Its limitations keep hidden any abuses and irregularities.
9. Oregon’s law protects doctors from legal liability if they act in “good faith.” This is almost impossible to disprove. It legalizes negligence. Like Oregon’s law, the California bill does more to protect physicians from liability than to safeguard vulnerable individuals from harm.
10. Oregon’s data consistently shows that people seek assisted suicide because they fear “dependency,” “loss of autonomy,” and loss of “dignity.” These fears are conditioned by stigmatizing social mores and discriminatory practices that devalue sick people and people with disabilities. But rather than helping such persons to affirm their inherent human dignity, suicide advocates reinforce those prejudices. Dr. Nick Gideon’s, a proponent and practitioner of assisted suicide, declared, “You could palliate pain, but you could not palliate loss of independence.” [Los Angeles Times, March 11, 2007] Furthermore, if “dependency” and “indignity” justify assisted suicide, all people with significant disabilities and especially progressive disabilities will be at great risk.
11. Most people who died under Oregon’s assisted suicide law were suffering psychological distress, not intractable pain. End-of-life care specialists know that depression in most terminally ill patients is treatable, unless there is underlying psychopathology. Legalizing assisted suicide would trap depressed patients in their own requests for death, abandoning them to die in unacknowledged terror.
12. Although assisted suicide claims to support self-determination and choice, there is significant danger of coercion. Oregon’s reports indicate that some older people who feared becoming a financial or caretaking burden on their families chose death. Also, Elder abuse is rampant in the US. California’s Attorney General reports that two out of three perpetrators are family members. Such abuse can easily pressure elders to “choose” assisted suicide, as Oregon’s news media have reported. Despite extensive efforts by California’s legislature and law enforcement to deter elder abuse, assisted suicide could facilitate the ultimate abuse.
13. Assisted suicide endangers people with new disabilities or chronic diseases. People with new disabilities often feel despondent and even suicidal. But over time they typically find satisfaction in their lives. Working through this initial despair usually takes far longer than the brief two-week waiting period in Oregon’s law and the California bill. In that critical early stage, many disabled people could easily take this irrevocable fatal step.
14. In Oregon, assisted suicide is being practiced secretly, without accountability, and without real safeguards. Yet California’s AB 374 repeats the same serious flaws of the Oregon law.
– — – — – — – — – — – — – — – — – — – — – — – –
SAN JOSE MERCURY NEWS OP ED, March 1, 2007
Assisted Suicide Bill Puts Pressure on Patients to Die Sooner
Bad Medicine for California Marilyn Golden Policy Analyst, Disability Rights Education and Defense Fund (DREDF)
For the third time in as many years, a bill to legalize assisted suicide has been introduced in the California legislature. At first glance, it seems like a merciful policy. But a closer look uncovers many reasons legalization would be a dangerous mistake. For this reason, it is opposed by a broad coalition that includes many disability rights organizations, the American Medical Association and other medical groups, the American Cancer Society, the League of United Latin American Citizens (LULAC), the Coalition of Concerned Medical Professionals which does anti-poverty work in poor communities, and many other organizations. While religious groups are in the mix, the opposition to assisted suicide is a broad coalition of left, right, and center. Why such a spectrum of resistance to something that seems so humane?
Supporters of assisted suicide often talk superficially about choice and self-determination. It is crucial to look deeper. We need to think about how assisted suicide would actually function in our medical system and our society as they operate today. Once legalized, assisted suicide would have many unintended consequences. It would especially impact many people in vulnerable circumstances.
One major reason for the diverse opposition is the deadly mix between assisted suicide and profit-driven managed health care. The cost of the lethal prescription generally used for assisted suicide is about $100. That’s far cheaper than the cost of treatment for most prolonged illnesses. The incentive to save money by denying treatment already poses a significant danger. Again and again, HMO’s and managed care bureaucrats have overruled doctors’ treatment decisions, sometimes hastening patients’ deaths. This danger would be far greater if assisted suicide were legal. Denying patients access to life-sustaining treatments while offering them the “choice” of assisted suicide would subtly but coercively steer them toward death. While the proponents of legalization argue that it would guarantee choice, assisted suicide would actually result in deaths due to a lack of choice.
A 1998 study from Georgetown University’s Center for Clinical Bioethics underscores the link between profit-driven managed health care and assisted suicide. The research found that the greater the cost-cutting pressure, the greater the willingness to prescribe lethal drugs, if such prescriptions were legal. The study called for “a sobering degree of caution in legalizing [assisted suicide] in a medical care environment that is characterized by increasing pressure on physicians to control the cost of care.” Assisted suicide advocates tout the example of Oregon, which legalized the practice in 1997. But Oregon shines only if you don’t look too closely. Each year, Oregon publishes a statistical report that leaves out more than it reveals. In fact, several of these reports have admitted, “We cannot determine whether assisted suicide is being practiced outside the framework of the law.” The reports provide only general statistics, no details of individual cases. The statute gives the state neither the resources nor the authority to investigate violations. All of the information comes from doctors who prescribed the lethal drugs. Yet doctors who fail to report face no penalty. Autopsies are not required, so there’s no way to ascertain the person was actually terminally ill. The state has never reported on several prominent cases at variance with the law - these cases came to light only via the Oregon news media. Moreover, the State of Oregon destroys their paperwork after each annual report, so it’s impossible to independently verify their conclusions. The Oregonian, the state’s major newspaper, complained in 2005 that the law’s reporting system “seems rigged to avoid finding” the answers. Yet the California bill contains the same serious flaws as the Oregon statute on which it is modeled.
The bill’s absence of genuine oversight and its weak penalties will allow it to be stretched as has occurred in the Netherlands. Over the past 25 years, the Dutch approach to “death with dignity” for people with terminal illness has expanded into full-blown euthanasia (lethal injections administered by doctors) for people with chronic illness, people with mental health distress, and even depressed teenagers and infants with disabilities.
We should reject this bill as bad medicine for California.
Marilyn Golden Policy Analyst mgolden@dredf.org Disability Rights Education and Defense Fund
Posted by: Michael Lyon at April 5, 2007 12:11 PM
Your correpondents McLaughlin and Golden typify the dishonest approach of euthanasia opponents. The strident opposition to euthanasia is usually based on religious belief. But you don't hear that.
It's "dying people will be put under pressure by wicked family members or the health system" etc.
The simple fact of the matter is that some people face terrible deaths which even the best palliative care (if they can afford it} can not relieve. Some ask for their suffering to be terminated and their inevitable death to be advanced.
If they are rational and not under pressure (the bill provides appropriate measures to cover the situation),then who has the right to callously say "No, you must suffer and die like a dog because it is against my beliefs that your wish be granted"
70% of Californians have considered this and are in favour of the bill. In my country, Australia,the figure is 80% but medieval church driven politicians will not listen.
Be brave, Californians.
Posted by: Bryan J Milner at April 12, 2007 10:14 PM
I wholeheartedly support the Compassionate Choices Act, AB 374, as do many of my friends and family members.
As I get older, death is not what I fear the most. Rather it is the prospect of enduring months or years of either pain or physical dependency with no hope of recovery. I firmly believe that the decision to end my life when and if it no longer offers hope or pleasure is a fundamental right the flows inexorably from my constitutionally given right to life, liberty, and the pursuit of happiness.
It is not the right of any other person, group of persons, or their elected representatives to deny me that liberty which I hold most dear, the liberty to live and die with dignity. I, and only I, in consultation with my family and medical advisors, should be able to decide when and if death is the only avenue toward the final pursuit of my happiness.
I respect those whose religious beliefs do not allow them for choose death regardless of their circumstance. But the separation of Church and Sate should free me of others’ beliefs to follow my own conscience.
Every 18 minutes someone in the United States commits an unanticipated suicide, often by means too horrible for their surviving family members to contemplate. It is very possible that many seniors would to live longer and in peace, if they were assured that their final wishes for a dignified life and death would be carried out, in case they themselves were no longer physically able to end their lives. I know it would work for me.
Posted by: Sofia Freer at April 17, 2007 03:43 PM
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