BILL ANALYSIS Ó SB 19 Page 1 Date of Hearing: August 19, 2015 ASSEMBLY COMMITTEE ON APPROPRIATIONS Jimmy Gomez, Chair SB 19 (Wolk) - As Amended July 16, 2015 ----------------------------------------------------------------- |Policy |Health |Vote:|19 - 0 | |Committee: | | | | | | | | | | | | | | |-------------+-------------------------------+-----+-------------| | |Judiciary | |10 - 0 | | | | | | | | | | | |-------------+-------------------------------+-----+-------------| | | | | | | | | | | | | | | | ----------------------------------------------------------------- Urgency: No State Mandated Local Program: NoReimbursable: No SUMMARY: This bill requires the California Health and Human Services Agency (CHHSA) to establish and operate a statewide registry system to collect Physician Orders for Life-Sustaining Treatment (POLST) forms, and disseminate the information in the form to SB 19 Page 2 authorized users, including health care providers. FISCAL EFFECT: 1)Start-up costs of about $2.5 million over the first three years to develop the system (non-state funds). The California Health Care Foundation has commissioned a feasibility report to examine the concept of a POLST registry. According to a draft of the report, it will cost about $2.5 million to develop the information technology system for an online-accessible registry and set up the program. 2)Ongoing costs of about $1.3 million per year to staff, maintain, and market the system (General Fund or other unknown fund source). 3)Unknown potential cost savings due to avoided unwanted medical care (various fund sources). The primary purpose of a POLST and the POLST registry proposed in this bill is to document a patient's preferences for end-of-life treatment. This can either ensure that individuals receive all treatment possible to prolong life, or ensure that people do not receive medical care they do not wish to receive. According to experience in other states, most people who fill out a POLST form indicate their wishes for - and receive- much less intensive treatment. By creating a registry of POLST forms, the bill will improve access to POLST forms by emergency medical services and hospitals. In turn, this will lead to fewer emergency health care services for individuals who do not want those services. The size of this impact is unknown. COMMENTS: SB 19 Page 3 1)Purpose. This bill establishes an electronic POLST registry that allows individuals and health care providers to update and access information about an individual's end-of-life treatment options. 2)POLST. The POLST form is a voluntary form that documents patient preferences about medical interventions common in end-of-life treatment, including cardiopulmonary resuscitation (CPR), mechanical ventilation, intubation, and artificially administered nutrition. It is completed and signed by a patient or their authorized representative, and is also signed by a physician. A signed POLST form, or copy thereof, is a legally valid physician order that other health care providers, such as emergency medical services (EMS) personnel, can rely on to make treatment decisions. POLST is used widely in health care settings, but nursing homes and hospitals report problems with the flow of paper forms between settings. 3)POLST versus Advanced Health Care Directives (AHCD). POLST is designed for use by seriously ill or medically frail individuals who are close to the end of their lives. POLST also includes very specific instructions about certain medical interventions, is applicable to current treatment, and is a legally valid physician order. In contrast, AHCDs are more general legal documents that allow anyone 18 years or older to designate future treatment preferences and to appoint a health care representative. Unlike POLST, AHCDs do not carry the legal weight of a valid physician order. This means AHCDs can guide inpatient treatment by a physician who has reviewed the AHCD, but do not provide a legal basis for EMS personnel to follow a patient's treatment preferences. SB 19 Page 4 4)POLST Registry Supports Ongoing Policy Initiatives. This bill aligns with goals devised by Let's Get Healthy California, a public-private partnership coordinated by the CHHSA in 2012 to improve the health of Californians. LGHC, as well as a related 2014 California State Innovation Model (CalSIM) grant proposal to the federal government, identified improving end-of-life care, by reducing deaths in the hospital and increasing advanced care planning, as a key initiative. Although California was unsuccessful in the CalSIM grant application, some work is ongoing to implement the proposed initiative. This bill appears to be consistent with these efforts. 5)Readiness for a POLST Registry in California. A brief commissioned by the California Health Care Foundation (CHCF) assessing California's readiness for a POLST registry found support for the concept among health care providers involved in using and completing POLST forms. Stakeholders interviewed for the brief suggested piloting an electronic registry, developing a modern technology platform, expanding education about POLST, engaging state administrative leadership, and identifying funding sources to build and maintain the registry. It also notes both Oregon and New York have successful electronic POSLT registries. CHCF is currently exploring the idea of sponsoring a POLST pilot project and a decision on moving forward with funding a pilot project is pending. 6)Prior Legislation. a) SB 1357 (Wolk) of 2014 was substantially similar to this SB 19 Page 5 bill, and was held on the Suspense File of the Senate Appropriations Committee. b) AB 2452 (Pan) of 2014 required the Secretary of State to develop an online registry for advance health care directives, and was held in the Senate Judiciary Committee. 1)Staff Comments. a) Funding a POLST Registry. This bill specifies CHHSA shall implement the registry only after determining that sufficient nonstate funds have been received to allow for the development of the registry and any related startup costs. Interest from private foundations in establishing a POLST registry indicates it may be possible to fund the initial development cost with non-state sources. However, the bill does not specify an ongoing fund source, raising questions about an appropriate fund source for ongoing customer service staffing and maintenance of an IT system. Given the cost of providing aggressive and often unwanted end-of-life medical interventions, both in dollars and human terms, providing real-time access to POLST forms through an electronic registry appears to be a reasonable investment for the state. Some potential fund sources that could be considered for ongoing support include: GF. The benefits of a POLST registry would be widespread and statewide, and the GF would also likely incur savings in state-funded health programs from making all patient's end-of-life wishes more accessible, making the GF a reasonable long-term funding source in absence of a more specific funding source. Federal funds may be available through federal SB 19 Page 6 financial participation (FFP) for serving the Medi-Cal population or potentially through grants, though grant funding may prove unreliable as an ongoing fund source. Drawing down FFP to cover some of the cost would likely only be available through a federal waiver, and would generally require a nonfederal share to match any federal dollars. The Health Data and Planning Fund administered by the Office of Statewide Health Planning and Development is another non-GF source to consider. Fees charged to health care facilities support OSHPD's work in collecting and disseminating health care data, and bolstering California's health care workforce through improved training. Although the bill does not specify OSHPD as an administering agency, this fund would likely be a fiscally sound revenue source for a program of this size, and offers a reasonable nexus between the payers and the activities being funded. Hospitals and skilled nursing facilities that provide the majority of end-of-life care, which are the primary users of a POLST system, are also the primary payers into the fund. This fund received a GF loan repayment of $12 million in 2015-16. a) Pilot program? As mentioned above, the CHCF readiness assessment suggested an electronic POLST registry start with a pilot project, one that could be rapidly scalable after success was proven. Though a statewide POLST registry appears to be a reasonable long-term policy goal, the committee may wish to consider whether starting with a regional pilot may offer a better chance at success, and minimize potential fiscal risk associated with statewide implementation. SB 19 Page 7 Analysis Prepared by:Lisa Murawski / APPR. / (916) 319-2081