BILL ANALYSIS                                                                                                                                                                                                    Ó



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          Date of Hearing:   June 14, 2016


                            ASSEMBLY COMMITTEE ON HEALTH


                                   Jim Wood, Chair


          SCR  
          117 (Pan) - As Introduced March 7, 2016


          SENATE VOTE:  38-0


          SUBJECT:  Palliative care.


          SUMMARY:  Encourages the state to study the status and  
          importance of coordinated palliative care and to develop  
          solutions, tools, and best practices for providing better  
          patient-centered care and information to individuals with  
          chronic diseases.  Specifically, this resolution: 


          1)Resolves that the Legislature encourage the state to do both  
            of the following:


             a)   Study the status and importance of coordinated  
               palliative care as a patient quality of life issue, as a  
               way to improve the quality and delivery of healthcare  
               services, and as a way to more effectively spend limited  
               healthcare dollars; and,



             b)   Develop solutions, tools, and best practices for  








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               providing better patient-centered care and information to  
               individuals with chronic diseases in California.


          2)Makes various findings and declarations regarding palliative  
            care, including the following:


             a)   Palliative care means patient- and family-centered  
               medical care that optimizes quality of life by  
               anticipating, preventing, and treating suffering caused by  
               serious illness; 


             b)   Patients with complex, chronic health issues should be  
               offered palliative care as it is appropriate at any age and  
               can be provided along with curative treatment; 


             c)   Palliative care can provide substantial cost reductions  
               while improving a patient's quality of life; 


             d)   A population trained about the benefits of palliative  
               care boosts our medical and social care workforce; 


             e)   The California Health and Human Services Agency's Let's  
               Get Healthy California Task Force identified palliative  
               care as one of its top priorities and indicators for all  
               Californians to enjoy optimal health in its 2012 report;  
               and,


             f)   The formation of a state palliative care and quality of  
               life interdisciplinary advisory council and a palliative  
               care information and education program within the  
               Department of Public Health (DPH) would maximize the  
               effectiveness of palliative care initiatives in the state  








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               by ensuring that comprehensive and accurate information,  
               education about palliative care is available to the public,  
               healthcare providers, and healthcare facilities. 


          





          EXISTING LAW: 



          1)Establishes DPH to protect and improve the health of  
            communities through education, promotion of healthy  
            lifestyles, and research. 


          2)Establishes the Medi-Cal program, administered by the  
            Department of Health Care Services (DHCS).  Requires DHCS, in  
            consultation with interested stakeholders, to establish  
            standards and provide technical assistance for Medi-Cal  
            managed care plans to ensure delivery of palliative care  
            services.  Establishes a pediatric palliative care pilot  
            project for Medi-Cal beneficiaries under age 21.


          3)Defines "palliative care" as a medical treatment,  
            interdisciplinary care, or consultation provided to a patient  
            or family members, or both, that has as its primary purpose  
            the prevention of, or relief from, suffering and the  
            enhancement of the quality of life, rather than treatment  
            aimed at investigation and intervention for the purpose of  
            cure or prolongation of life, as described.  In some cases,  
            disease-targeted treatment may be used in palliative care.










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          4)Defines "hospice care" as a specialized form of  
            interdisciplinary health care that is designed to provide  
            palliative care, alleviate the physical, emotional, social,  
            and spiritual discomforts of an individual who is experiencing  
            the last phases of life due to the existence of a terminal  
            disease, and provide supportive care to the primary caregiver  
            and the family of the hospice patient, and that meets  
            specified criteria.


          FISCAL EFFECT:  According to the Senate Appropriations  
          Committee, pursuant to Senate Rule 28.8, negligible state costs.


          COMMENTS:  


          1)PURPOSE OF THIS BILL.  According to the author, palliative  
            care provides us an opportunity to defragment our health care  
            system and improve both the lives of those who suffer from  
            serious illness, such as cancer, and the lives of those who  
            care for them.  It is important that we study the status and  
            importance of coordinated palliative care to develop solutions  
            and best practices for providing better patient-centered care  
            and information to individuals with chronic disease.

          2)BACKGROUND. 



             a)   Medi-Cal and palliative care.  SB 1004 (Hernandez),  
               Chapter 574, Statutes of 2014, requires DHCS to establish  
               standards and provide technical assistance for Medi-Cal  
               managed care plans to ensure delivery of palliative care  
               services.  DHCS issued a draft policy paper for SB 1004 in  
               October 2015 to establish minimum standard palliative care  
               services and eligible conditions for Medi-Cal  
               beneficiaries.  DHCS received a significant number of  
               comments from stakeholders and is currently revising the  








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               policy paper to reflect stakeholder feedback and additional  
               data analysis.

             b)   Institute of Medicine (IOM) Report.  "Dying in America,"  
               a 2014 IOM report, noted that improving the quality and  
               availability of medical and social services for patients  
               and their families could not only enhance quality of life  
               through the end of life, but may also contribute to a more  
               sustainable care system.  Among the report's findings and  
               recommendations were the following:



               i)     Some evidence suggests that, on average, palliative  
                 care and hospice patients may live longer than similarly  
                 ill patients who do not receive such care;

               ii)    Although professional guidelines and expert advice  
                 increasingly encourage oncologists, cardiologists, and  
                 other disease-oriented specialists to counsel patients  
                 about palliative care, widespread adoption of timely  
                 referral to palliative care appears slow;



               iii)   Most people nearing the end of life are not  
                 physically, mentally, or cognitively able to make their  
                 own decisions about care.  The majority of these patients  
                 will receive acute hospital care from physicians who do  
                 not know them.  Therefore, advance care planning is  
                 essential to ensure that patients receive care reflecting  
                 their values, goals, and preferences;



               iv)    There is insufficient attention to palliative care  
                 in medical and nursing school curricula;










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               v)     Palliative care should encompass access to an  
                 interdisciplinary palliative care team; and,



               vi)    State regulatory agencies should include education  
                 and training in palliative care in licensure requirements  
                 for physicians, nurses, chaplains, social workers, and  
                 others who provide health care to those nearing the end  
                 of life.



             c)   California Specific Report.  In December 2015 the  
               California HealthCare Foundation and the Coalition for  
               Compassionate Care of California published a report titled  
               "Dying in California:  A Status Report on  
               End-of-Life-Care."  The report found that growing demand  
               far outpaces the capacity of services.  Palliative care  
               specialists are in short supply, and certification programs  
               are limited.  Reliable funding streams do not yet exist.   
               While knowledge is growing about best practices and quality  
               standards, they have not yet been broadly implemented.   
               Specialty palliative care is currently unavailable in many  
               geographic areas and in many care settings.  So far,  
               consumer demand for better care at the end of life has not  
               created the type of powerful change seen for widespread  
               adoption of palliative care services.  

             d)   California State University (CSU) Institute for  
               Palliative Care (Institute).  The CSU Institute was founded  
               in 2012 as America's first statewide educational and  
               workforce development initiative focused on offering health  
               care professionals training in high-quality palliative  
               care.  More health care professionals receive training from  
               the CSU system than any other program in California.   
               According to CSU, the Institute is integral to  
               incorporating palliative care curriculum into the training  








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               of future nurses, social workers, public health, and other  
               allied professions (such as home health aides).  Located on  
               the CSU San Marcos campus, the Institute also offers  
               professional development and continuing education courses  
               to enhance the skills of current health care professionals.  




          3)SUPPORT.  The American Cancer Society Cancer Action Network,  
            the sponsor for this resolution argues that, while California  
            has made important strides in palliative care, there is still  
            more to do in ensuring access and affordability.  The  
            California Catholic Conference writes that a comprehensive  
            approach is needed and should include, for example, expanding  
            instruction in palliative care at medical schools and other  
            institutions providing health care instruction, and ensuring  
            increased access to palliative care for patients, and  
            providing safe and appropriate levels of staffing and salary  
            scales in care facilities serving elderly persons and persons  
            with life-threatening chronic illnesses.  The Alliance of  
            Catholic Health Care writes Catholic hospitals are leaders in  
            the provision of palliative care.  Over 95% of our Catholic  
            and affiliated community hospitals operate palliative care  
            programs, compared to a little more than 50% of California  
            hospitals as a whole.  Palliative care improves the quality of  
            life for patients and their families facing chronic and  
            life-threatening illness by preventing and relieving  
            suffering.
          
          4)PREVIOUS LEGISLATION.  AB 1745 (Chan), Chapter 330, Statutes  
            of 2006, requires the Department of Health Services (now DHCS)  
            to develop a Medi-Cal pediatric palliative care pilot project.  
             


          
          5)RELATED LEGISLATION.









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             a)   SB 1002 (Monning) would have required DPH to establish  
               and maintain a toll-free telephone number for the purpose  
               of receiving and responding to inquiries regarding the End  
               of Life Option Act.  SB 1002 was held in the Senate  
               Appropriations Committee on the Suspense File.

             b)   ABX2 15 (Eggman), Chapter 1, Statutes of 2015, Second  
               Extraordinary Session, establishes the End of Life Option  
               Act, which permits a competent, qualified individual who is  
               an adult with a terminal disease to receive a prescription  
               for an aid-in-dying drug if certain conditions are met.   
               ABX2 15 became effective on June 9, 2016.  



          REGISTERED SUPPORT / OPPOSITION:




          Support


          American Cancer Society Cancer Action Network (sponsor)


          Alliance of Catholic Health Care


          California Catholic Conference


          California Medical Association


          California State Retirees









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          Alliance of Catholic Health Care


          Providence Health & Services




          Opposition


          None on file.




          Analysis Prepared by:John Gilman / HEALTH / (916)  
          319-2097