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Honoring Patients ’ Wishes for Advanced Illness Care: The Evolution of State POLST Programs

Honoring Patients ’ Wishes for Advanced Illness Care: The Evolution of State POLST Programs. Charlie Sabatino - ABA Commission on Law & Aging Naomi Karp - Consumer Financial Protection Bureau (formerly AARP Public Policy Institute) February 16, 2012. Components.

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Honoring Patients ’ Wishes for Advanced Illness Care: The Evolution of State POLST Programs

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  1. Honoring Patients’ Wishes for Advanced Illness Care: The Evolution of State POLST Programs Charlie Sabatino - ABA Commission on Law & Aging Naomi Karp - Consumer Financial Protection Bureau (formerly AARP Public Policy Institute) February 16, 2012

  2. Components • Exploratory survey in 2010 of key informants in 12 states that ostensibly recognize POLST statewide. • Maryland included as an outlier state • 52 telephone interviews: all open-ended questions. Ranged from 3 to 7 per state • Analysis of themes and experience in establishing & implementing POLST • Legislative/regulatory review.

  3. Legislative/Regulatory Comparison • Research analyzed and compared all statutes/regulations • Report includes statutory chart with 17 elements

  4. Survey Preliminary Findings • The Survey content can be organized by: • Strengths or facilitating elements that supported efforts. • Barriers and Issues in establishing and implementing. • Training and Educational Matters. • Monitoring & Evaluation Matters. • Comments on ensuring quality of POLST conversations. • Establishing vs. implementing stages were not distinct. • Caveat: Because issues and factors that respondents identified were in response to open-ended questions, any frequencies we provide should be taken with a grain of salt.

  5. Strengths or Facilitating Elements Most commonly identified: • Core group of physician champions • Deliberately incremental strategy • Well-established statewide organization that effectively brings together statewide coalition • Availability of financial support in cash or in kind. Unique chemistry? Of 24 “strengths” identified, 19 were mentioned in only 1 or 2 states.

  6. Barriers and Salient Issues Most commonly identified: • Nature of consent required (signature - mandatory or optional) • Form content issues • Confusion between ADs and POLST • Registries and EHR (looking forward) Next most: • Surrogate ID and authority • Changing institutional policies & procedures • Perception: POLST too cumbersome/time-consuming • Cross cultural issues

  7. Training & Education Themes The most important implementation issue. Biggest barrier: Lack of or minimal funding. Success requires: • Ability to organize regular ongoing trainings, • Extensive web-based clearinghouse of resources, curricula, guides, media, etc • Ability to reach physicians

  8. Monitoring & Evaluation Themes • Majority (8) lack any formal monitoring/evaluation • What works: expert work group/committee (periodically solicits & reviews feedback from stakeholders). • One challenge: getting DOH to focus on POLST in compliance monitoring • Ideal: rigorous published evaluation over time

  9. Quality of the Conversation • Virtually all saw this as a training function • Range of resources cited: 8-step guide, video vignettes, EPEC, facilitator training, tool in development for patient/family feedback.

  10. Respondents’ Recommendations • Find the Champions. • Be inclusive. • Build coalitions on local level, too. • Start with pilots. • Framing the issue: patient’s rights. • Follow the lead of existing POLST states. • Know your state. • Devise a legislative strategy if going that route. • Allow space to design and revise form. • Create infrastructure for the long haul. • Funding can be key.

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