IMPLEMENTING STANDARDS FOR QUALITY PALLIATIVE CARE. Monica Malec, MD University of Chicago

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Transcription:

IMPLEMENTING STANDARDS FOR QUALITY PALLIATIVE CARE Monica Malec, MD University of Chicago

Nothing to disclose

OBJECTIVES Utilize the eight domains of palliative care as the structure for palliative care consultation Identify quality indicators appropriate for each of the eight domains of palliative care Implement quality improvement processes to identify opportunities for improvement in palliative care structure, process, and outcomes

WHY IMPLEMENT STANDARDS? Set goals for care delivery Continuous quality improvement Establish uniformity to allow for benchmarking and comparison Build sustainable systems and practices

NATIONAL CONSENSUS PROJECT FOR QUALITY PALLIATIVE CARE To build a national consensus around the definition, philosophy and principles of palliative care To promote consistent and high quality care Clinical practice guidelines for quality palliative care released 2004, revised 2009 Established the eight domains of palliative care

EIGHT DOMAINS OF PALLIATIVE CARE 1.Structure and process of care 2.Physical aspects of care 3.Psychosocial and psychiatric aspects of care 4.Social aspects of care 5.Spiritual, religious, existential aspects of care 6.Cultural aspects of care 7.Care of the imminently dying patient 8.Ethical and legal aspects of care

EIGHT DOMAINS OF PALLIATIVE CARE: HOW THEY HELP Delineate the core essential elements of palliative care Differentiate palliative care from other types of care Support the structure of palliative care

Palliative care is both a philosophy of care and a highly structured system for delivering care NCP 2004

CLINICAL PRACTICE GUIDELINES FOR QUALITY PALLIATIVE CARE Patient population Patient and family centered care Timing of palliative care Comprehensive care Interdisciplinary team Attention to relief of suffering Communication skills Skill in the care of the dying and bereaved Continuity across care settings Equitable access Quality assessment and performance improvement

NATIONAL QUALITY FORUM Identified palliative care and hospice as national priority areas for healthcare quality improvement A Framework for Palliative and Hospice Care Quality Measurement and Reporting Adopted the NCP Clinical Practice Guidelines for Quality Palliative Care 38 preferred practices within the eight domains of palliative care

WHAT IS QUALITY? Increases the likelihood of desired health outcomes Consistent with current professional standards of care

WHAT IS QUALITY? Institute of medicine Six aims of quality healthcare delivery Safe- First do no harm Beneficial- influences important outcomes or processes linked to desirable outcomes Patient centered- based on the goals and preferences of the patient Efficient-designed to meet the actual patient needs Timely- right patient, right time Equitable- available to all who could benefit

HOW IS QUALITY MEASURED? DONABEDIAN MODEL Where we work Structure Process What we do What happens Outcome

Structure and process measures are most useful if changes in them demonstrably improve outcomes Outcomes measures are most useful if they can be linked to to specific structure or process measures that, if changed, improve the outcome

QUALITY INDICATORS Valid supported by evidence or expert consensus Reliable reproducible from center to center Feasible easily measurable Actionable under the control of providers

Quality indicators are intended to evaluate whether care meets a minimal standard of quality Practice guidelines define best practices, highest quality care Preferred practices are best practices linked to specific desired outcomes

PREFERRED PRACTICES Specificity Benefit Evidence of effectiveness Generalizability Readiness Measurability

Preferred practices are intended to provide the foundation for comprehensive program evaluation BUT No standard set of outcomes for palliative care exists SO Should be used as tools for promoting improved quality

CANCER QUALITY ASSIST PROJECT RAND, Karl Lorenz Addressing Symptoms, Side effects and Indicators of Supportive Treatment Developed process quality indicators for supportive cancer care 92 of 133 indicators deemed valid and feasible 41 validated

ACOVE PROJECT RAND, Neil Wenger, MD and ACOVE invesigators Assessing Care Of Vulnerable Elders Developed process quality indicators for the vulnerable elderly 392 indicators judged valid over 26 conditions Based on clinical evidence and expert opinion validated

NATIONAL QUALITY FORUM In February 2012, NQF endorsed 14 quality measures for palliative and end of life care

NQF ENDORSED MEASURES Pain screening Pain Assessment Patients treated with opioids given a bowel regimen Patients with advanced cancer assessed for pain at outpatient visits Dyspnea screening Dyspnea treatment

NQF ENDORSED MEASURES Patients admitted to ICU who have care preferences documented Treatment preferences Percentage of hospice patients with documentation of spiritual/religious concerns or desire not to discuss Comfortable dying Hospitalized patients who die an expected death with an ICD that has been deactivated

NQF ENDORSED MEASURES Family Evaluation of Hospice Care CARE-Consumer Assessments and Reports of End of Life Bereaved Family Survey

MEASURING WHAT MATTERS Partnership between AAHPM and HPNA Consensus project to identify a set of recommended performance measures for use in all hospice and palliative care programs Goal is for programs to adopt these measures to lay the groundwork for benchmarking and meaningful comparison

MEASURING WHAT MATTERS 75 initial published measures mapped to the domains of care Technical advisory panel rated the indicators on scientific soundness and referred 34 measures to clinical user panel Clinical user panel rated the measures on 3 areas of performance How meaningful is it to patients and families How actionable is it for providers and organizations How large is the potential impact

MEASURING WHAT MATTERS Clinical User Panel achieved consensus on top 12 measures Draft list sent to membership of AAHPM, HPNA, other organizations and patient advocacy groups for feedback Top 10 measures across 6 domains selected No measures selected for social or cultural aspects of care or care of the imminently dying

STRUCTURE AND PROCESS OF CARE Comprehensive Assessment Hospice % patients enrolled for greater than 7 days for whom comprehensive assessment was completed within 5 days Palliative care % seriously ill patients receiving palliative care in an acute hospital setting for longer than 1 day for whom comprehensive assessment was completed

PHYSICAL ASPECTS OF CARE Pain Treatment(Any) % of patients receiving medication vs non-medication treatment of pain within 24 hours of positive screen for moderate to severe pain

PHYSICAL ASPECTS OF CARE Screening for physical symptoms % of patients screened for physical symptoms(pain, dyspnea, nausea, constipation) during the initial(admission) visit

PHYSICAL ASPECTS OF CARE Dyspnea screening and management % of patients with advanced or serious life threatening illness that are screened for dyspnea % of patients with moderate to severe dyspnea with a documented management plan

PSYCHOLOGICAL AND PSYCHIATRIC ASPECTS OF CARE Discussion of emotional or psychological needs % of seriously ill patients with chart documentation of a discussion regarding emotional or psychological needs

SPIRITUAL, RELIGIOUS, AND EXISTENTIAL ASPECTS OF CARE Discussion of spiritual/religious concerns % of patients with documentation of discussion of spiritual/religious concerns or documentation that the patient or caregiver do not want to discuss these issues

ETHICAL AND LEGAL ASPECTS OF CARE Documentation of Surrogate % of seriously ill patients with the name and contact information for the patients surrogate decision-maker in the chart or documentation that there is no surrogate

ETHICAL AND LEGAL ASPECTS OF CARE Treatment preferences % of patients with chart documentation of preferences for lifesustaining treatments, documentation should reflect patient selfreport

ETHICAL AND LEGAL ASPECTS OF CARE Treatment preferences followed If a vulnerable elder has documented treatment preferences to withhold or withdraw life-sustaining treatment, then these treatment preferences should be followed

GLOBAL MEASURE The Family Evaluation of Palliative Care(FEPC) The FEPC is a post-death survey that captures family members perception about the quality of palliative care their lived ones received

So now what do I do?

THE DEMING CYCLE Series of steps to learn how to continually improve a process Introduced to Deming by his mentor Shewhart Developed for process/product improvement on the manufacturing floor Effective in healthcare improvement Intended to be rapid cycles

THE DEMING CYCLE

PLAN Determine quality priorities- what do you want to improve Create a driver diagram Helps breakdown the project into logical steps It outlines your theory about how your system works

DRIVER DIAGRAM

DRIVER DIAGRAM www.ihi.org Accessed 3/11/2015

DO Put the plan into action

STUDY Collect (just) enough data Keep it small at first just a few patients Monitor success and areas for improvement

ACT Apply what you learned Refine intervention and repeat until perfected Implement when ready Add another project!

RESOURCES National Quality Forum www.qualityforum.org Peace Hospice and Palliative care Quality Measures www.med.unc.edu/pcare/resources Institute for Healthcare Improvement www.ihi.org Measuring What Matters www.aahpm.org

Not everything that counts can be counted, not everything that can be counted counts Albert Einstein