BILL ANALYSIS                                                                                                                                                                                                    



                                                                  ACR 74
                                                                  Page  1


          ASSEMBLY THIRD READING
          ACR 74 (Portantino and Hill)
          As Amended February 24, 2010
          Majority vote 

           HEALTH              18-0                                        
           
           -------------------------------- 
          |Ayes:|Monning, Adams, Ammiano,  |
          |     |Carter, Conway, De La     |
          |     |Torre, De Leon, Emmerson, |
          |     |Eng, Gaines, Hayashi,     |
          |     |Hernandez, Jones, Bonnie  |
          |     |Lowenthal, Nava, V.       |
          |     |Manuel Perez, Salas,      |
          |     |Audra Strickland          |
          |     |                          |
           -------------------------------- 
           SUMMARY  :  States that the Legislature desires to find ways to  
          help California gain a viable public umbilical cord blood  
          banking system to ensure that all races and ethnicities have an  
          equal probability of finding a match when medically necessary.   
          Specifically,  this resolution  :  

          1)Makes a number of legislative findings and declarations  
            related to the public and private umbilical cord blood  
            collection industry as a treatment for blood cancers and other  
            diseases, the lack of public knowledge about the differences  
            of the public and private umbilical cord blood banking  
            systems, the lack of genetic diversity of public umbilical  
            cord blood inventories, the importance of using umbilical cord  
            blood that is not suitable for transplantation for research  
            institutions to explore the potential of umbilical cord blood  
            stem cells to treat medical conditions, and the importance of  
            building a viable public banking system.

          2)States the Legislature's desire to find ways to help  
            California gain a viable public umbilical cord blood banking  
            system to ensure that all races and ethnicities have an equal  
            probability of finding a match when medically necessary.

          3)States the Legislature's support for research being done with  
            collected units that are not suitable for transplantation.









                                                                  ACR 74
                                                                  Page  2


           EXISTING LAW  :

          1)Requires the California Department of Public Health (DPH) to  
            establish, by January 1, 2010, and until January 1, 2015, the  
            Umbilical Cord Blood Collection Program (UCBCP) for the  
            purpose of collecting and storing umbilical cord blood and  
            increasing the amount of umbilical cord blood that is donated  
            in the state and added to the National Cord Blood Inventory.

          2)Authorizes the UCBCP, to the extent private or public funds  
            are identified and secured for these purposes, to contract  
            with blood banks that are licensed or accredited to provide  
            umbilical cord blood banking storage services, for the purpose  
            of collecting and storing umbilical cord blood for public  
            transplantation services.  Permits DPH to implement any  
            additional standards for blood banks to collect and store  
            umbilical cord blood through the adoption of regulations.

          3)Requires DPH, contingent upon private funding, to conduct the  
            Umbilical Blood Community Awareness Campaign to provide  
            awareness and information regarding umbilical cord blood  
            banking options using print media, radio, the Internet,  
            outdoor advertising and other media, to establish an Internet  
            Web site, and to undertake public education activities related  
            to umbilical cord blood donation to targeted populations, as  
            appropriate.

           FISCAL EFFECT  :   None

           COMMENTS  :   According to the author, most cord blood is  
          collected for private usage and although this service is a great  
          benefit to individuals, it does not ensure the general public  
          has access to this potential treatment for a variety of medical  
          conditions.  The author believes that this resolution will help  
          increase awareness for the need to create a public cord blood  
          banking system that will bring the benefits of this resource to  
          a broad and more diverse group of Californians.

          According to information from the National Marrow Donor Program  
          (NMDP), cord blood, which is the blood collected from the  
          umbilical cord and placenta after a baby is born, is rich in  
          blood-forming cells that can be used in transplants for patients  
          with leukemia, lymphoma, and many other life-threatening  
          diseases.  Cord blood is one of three sources of cells used in  








                                                                  ACR 74
                                                                  Page  3


          transplants; the other two are bone marrow and peripheral blood  
          stem cells.  The NMDP estimates that, on any given day, more  
          than 6,000 patients around the world are searching the NMDP's  
          registry for a matching bone marrow or cord blood donor.  Since  
          cord blood is stored and ready to use and it does not require a  
          perfect donor match, the NMDP states that it is especially  
          useful for patients who need a transplant quickly, patients who  
          have difficulty finding a matched bone marrow donor, and  
          patients from racially diverse communities who often have  
          uncommon tissue types.  Patients are more likely to match  
          someone who shares their racial and ethnic heritage.  The NMDP  
          reports that, in 2008, 36% of the 90,000 cord blood units in its  
          registry went to patients from racially or ethnically diverse  
          communities and the need for cord blood donations from these  
          populations remains high.

          Public and private banks provide for the collection and storage  
          of cord blood.  Public banks promote related and unrelated  
          donation, similar to the current collection of whole blood units  
          in the U.S., for transplantation or research purposes.  Private  
          banks store cord blood from an individual for subsequent use by  
          the same individual or his or her family members should the need  
          arise.  Private banks typically charge between $1,000 and $2,000  
          in collection fees and between $50 and $125 annually for  
          storage.  Public banks do not charge for cord blood that is  
          donated for public use.  The American Association of Blood Banks  
          (AABB) and the Foundation for the Accreditation of Cellular  
          Therapy (FACT) provide voluntary accreditation of cord blood  
          banks using standards governing all aspects of operation,  
          including collection, processing, and transplantation.   
          According to their respective Web sites, 25 facilities  
          nationwide are currently accredited by the AABB and eight  
          currently have FACT accreditation.

           
          Analysis Prepared by  :    Martin Radosevich / HEALTH / (916)  
          319-2097 


                                                                FN: 0003802