Part 1.85End of Life Option Act
Section § 443
This section is the title of the End of Life Option Act. It specifies that people in California can refer to this section as such when discussing or using this law.
Section § 443.1
This section provides definitions for terms used in the context of California's aid-in-dying laws. It clarifies who qualifies as an 'adult,' 'qualified individual,' and defines an 'aid-in-dying drug' as one prescribed to these individuals to end their life due to a terminal disease. An 'attending physician' is the main doctor responsible for treating the terminal disease, while a 'consulting physician' provides a second opinion. To make an 'informed decision,' individuals must understand their diagnosis, risks and outcomes of the drug, and alternative treatments. 'Capacity to make medical decisions' means understanding and communicating about these choices. 'Medically confirmed' means a second physician verifies the incurability and prognosis of the disease.
The law spells out additional roles, such as 'mental health specialists' who ensure that individuals can decide without impairment. 'Self-administer' refers to the act of voluntarily taking the prescribed medication. A 'terminal disease' is one expected to lead to death within six months. The law distinguishes 'health care providers,' 'entities,' and 'public places' related to administering this process.
Section § 443.10
Before a doctor can prescribe a drug to help someone end their life under this law, they must first make sure the person knows what they're doing and chooses it on their own, called making an informed decision.
Section § 443.11
This law explains the process for requesting a prescription for a life-ending aid-in-dying drug in California. To make this request, the individual must be an adult of sound mind, confirmed by medical professionals to be terminally ill, and a resident of the state. They must confirm understanding of their medical condition, the risks of the drug, and available care alternatives, such as hospice. The request must be voluntary and can be withdrawn at any time.
The individual must acknowledge their family's awareness of the decision, or state that they have no family to inform. Two witnesses must sign the declaration, ensuring the individual is of sound mind and acting without coercion. Only one witness can be a relative or involved with the individual's health care facility.
If the request is verbalized in another language, the written request can be in English with a declaration from an interpreter. The interpreter must confirm the individual's understanding and intentions, and must not be a family member or have a financial interest in the person's estate. Interpreters must adhere to certain professional standards.
Section § 443.12
This law states that any agreement made after January 1, 2016, whether it's a contract, will, or other types, can't include terms that impact someone's choice to make, cancel, or take back a request for an aid-in-dying drug. This means you can't have conditions in contracts that depend on whether a person decides to ask for or withdraw an aid-in-dying drug.
In simple terms, if you sign a contract after this date, it can't legally affect your rights to choose an aid-in-dying drug.
Section § 443.13
This law ensures that a request for an aid-in-dying drug does not impact the sale, price, or terms of life, health, or annuity insurance policies. It clarifies that self-administering such a drug is not considered suicide, so insurance coverage remains unaffected. Furthermore, the law prohibits insurance carriers from discussing the availability of aid-in-dying drugs unless explicitly asked by the individual or their doctor. Communications from insurers must not mix treatment denials with aid-in-dying information.
Section § 443.14
This law provides protections and outlines responsibilities for those involved in the aid-in-dying process. If you're present when someone self-administers the aid-in-dying drug, you won't face civil or criminal liability just for being there. You can help prepare the drug, but can't help them take it. Healthcare providers and organizations can't punish someone for following or choosing not to follow this law. Participating in aid-in-dying is voluntary, and no one is forced to be involved if it conflicts with their conscience or ethics. If healthcare providers object, they must inform the individual and transfer medical records if the person switches care. Also, they must avoid misleading claims about their willingness to provide aid-in-dying prescriptions. The act emphasizes non-interference with anyone's professional standing or medical licenses for participation or refusal to participate in aid-in-dying practices.
Section § 443.15
This section allows a health care entity, like a hospital, to ban its staff and contractors from participating in medical aid-in-dying activities on its premises or during their work duties. However, the entity must inform these individuals about the policy when they start and remind them annually, typically by posting the policy online.
If someone breaks this rule, the entity can take non-monetary actions such as suspending employment or terminating contracts. However, this restriction doesn’t apply if the person is off-site or acting outside their work roles.
Participation includes roles like being an attending or consulting physician in aid-in-dying situations, but doesn’t include diagnosing or providing general end-of-life care information. The healthcare provider’s participation in such activities shouldn’t lead to claims of unprofessional conduct unless otherwise warranted.
Entities must publicly post their policy online and avoid misleading or coercive communication about their end-of-life care policies.
Section § 443.16
This section of the law states that healthcare providers cannot be punished for informing a patient that they have a terminal illness, giving information about the End of Life Option Act, or referring a patient to another doctor if asked.
Healthcare providers are also protected if they work with a terminal patient outside their official role in facilities that don't allow such activities, as long as they act independently. However, providers can face disciplinary action from their professional boards if they engage in unprofessional behavior or don't follow the rules set in this part thoroughly.
Section § 443.17
This law makes it a felony to tamper with someone's request for an aid-in-dying drug, such as altering, forging, or destroying their request without permission, especially if it leads to their death. It's also a felony to force someone to take the drug or to give it to them without consent. The term 'knowingly' is defined by the state penal code. Physicians and mental health specialists involved cannot be related to the patient or benefit from their estate. This doesn't limit civil lawsuits for negligence or intentional harm, nor does it affect other criminal penalties for related misconduct.
Section § 443.18
This section ensures that no one, including doctors, is allowed to intentionally end someone's life through methods like lethal injection or mercy killing. Anything done according to this part of the law won't be considered acts like suicide, assisted suicide, murder, or elder abuse.
Section § 443.19
This section mandates that the State Department of Public Health confidentially collects and reviews information related to aid-in-dying prescriptions. The collected data, which is protected to ensure patient and provider privacy, is not to be disclosed in legal proceedings.
Every year from July 1, 2017, the department must publish a report on their website with statistics and data about the use of aid-in-dying prescriptions. This includes details like the number of people receiving prescriptions, deaths from these prescriptions, and demographic details of those who died using aid-in-dying drugs.
Additionally, the department needs to make certain physician compliance forms available online, as outlined in another section of the law.
Section § 443.2
This section allows a terminally ill adult in California with the capacity to make medical decisions to request a prescription for a drug to help them end their life, known as aid-in-dying. To qualify, the person must be diagnosed with a terminal illness by their doctor, express their wish voluntarily, and be a California resident, proven by documents like a driver's license or tax return. They must document their request according to specific rules (see Section 443.3) and be able to take the drug themselves. Simply being old or disabled doesn't qualify someone for this. The individual must personally make the request without relying on others, such as a power of attorney or health care agents, to act on their behalf.
Section § 443.20
If a person has unused aid-in-dying drugs after the patient has passed away, they must personally take these drugs to a nearby facility that can safely dispose of them. If no such facility is available, the person must dispose of them following guidelines from the California State Board of Pharmacy or through an approved federal take-back program.
Section § 443.21
If a qualified person ends their life in a public area under this specific law, and it causes costs for any government body, that government can seek to recover these expenses from the deceased person's estate. The government can also claim reasonable attorney fees related to enforcing this claim.
Section § 443.215
This law will only be effective until January 1, 2031, and will be repealed after that date.
Section § 443.22
This section allows the Medical Board of California to update key forms used by physicians when complying with specific procedures. These forms include the attending physician checklist, compliance form, consulting physician compliance form, and attending physician follow-up form. Once updated, the State Department of Public Health must publish these forms online. Until any updates are made, these forms will remain as outlined in the 2015 legislation.
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NOTICE OF INCOMPLETE TEXT: The physician compliance and
follow-up forms appear in the published chaptered bill. See Sec. 1
of Chapter 1 (pp. 18–25), 2nd Ex. Session, Statutes of 2015.
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Section § 443.3
If someone wants to get a prescription for an aid-in-dying drug, they need to make two verbal requests at least 48 hours apart and submit a written request to their doctor. The doctor has to document these requests in the patient's medical record. Even if the request was made to a previous or non-participating doctor, it still counts.
The written request must follow a specific format laid out in another section. It has to be signed in front of two adult witnesses, and these witnesses must know the person, believe the person is signing voluntarily and is of sound mind, and they cannot have a role in the person's medical care as their doctor or mental health specialist.
One of the witnesses can be a family member or have a stake in the person's estate, or work at the facility where the person is being treated. However, none of these witnesses can be the patient's doctor or mental health professional.
Section § 443.4
This law allows a person to change their mind about using or requesting an aid-in-dying drug at any time, regardless of their mental state.
Before a prescription for such a drug is made, the attending doctor must personally offer the individual a chance to withdraw their request. If the person chooses a new doctor, the current doctor must share all important medical records related to their aid-in-dying request.
Section § 443.5
This section outlines the steps a doctor must take before prescribing an aid-in-dying drug. First, the doctor needs to ensure the patient can make medical decisions, doesn't suffer from impaired judgment due to a mental disorder, and is making the choice voluntarily.
The patient must have a terminal illness and be informed about their diagnosis, prognosis, and potential risks and outcomes of taking the drug. The doctor verifies these through a consulting physician and ensures the patient is not coerced. The doctor will also discuss the importance of having another person present when taking the drug, not doing it in public, and the option to notify family, among other counseling points.
The patient can withdraw their request anytime. If all conditions are met, the doctor can dispense the drug directly or via a pharmacist and complete necessary documentation.
Section § 443.6
Before someone can receive a drug to assist in dying, a second doctor (consulting physician) must do several things. They need to check the person's health and medical files and verify the first doctor's diagnosis and estimate of how long the person will live. The consulting doctor also has to ensure the person can make their own medical choices, is doing this of their own free will, and understands what it means. If there's any sign of a mental health issue, they must refer the person to a specialist. They also need to document all of this and send a form showing they've followed the rules to the first doctor.
Section § 443.7
This section outlines the duties of a mental health specialist when they receive a referral from a physician. The specialist must examine the patient's medical records and ensure the patient can make decisions and act voluntarily. They also need to confirm that the patient doesn't have impaired judgment from a mental disorder. Finally, they must document everything in the patient's records as required by the law.
Section § 443.8
This law details what must be recorded in a person's medical record when they request aid-in-dying drugs. It includes all oral and written requests, diagnoses, prognoses, and mental capacity assessments from attending and consulting physicians. Additionally, any mental health evaluations and the offer to withdraw the request must be documented. Finally, it requires a note confirming that all legal requirements have been met and the prescription details of the aid-in-dying drug.
Section § 443.9
If a doctor prescribes a medication for a patient to end their life, they must send specific documents to the State Department of Public Health within 30 days. These documents include the patient’s written request, and forms confirming the process was followed correctly by both the attending and consulting physicians.
Additionally, if the patient who was prescribed the medication passes away, whether from taking the medication or another cause, the doctor must also send a follow-up form to the State Department of Public Health within 30 days.