Improving quality of life for people with dementia: the ADI-Stroud symposia

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Improving quality of life for people with dementia: the ADI-Stroud symposia Sube Banerjee - I stitute of Ps hiat, Ki g s College Lo do Barry Gurland - Stroud Center, Columbia University Nori Graham - Alzhei e s Disease I te atio al

Understanding quality of life

Quality of life Intuitively understood Part of common discourse personal political Broad, unifying and holistic concept Continuous and fundamental human process

Health related quality of life...an i dividual s pe eptio of their position in life...in relation to their goals, expectations, standards and concerns WHOQOL...the impact of a perceived health state on [living] a subjectively fulfilling life Bullinger et al 1993

Quality of life -- particularly important in dementia Dementias are more complex than simple disorders coronary heart disease diabetes surgical care Non-linear and unpredictable process Multiple pathologies Link between symptoms and qol is not clear, simple or predictable Interventions are usually complex need to avoid OSPD syndrome

Quality of life in dementia What really matters to people with dementia and their carers What really matters to clinicians The true goal of intervention What should really matter to policy makers and researchers More than just a combination of health assessments cognition and behaviour are not very good proxies for quality of life

How to measure it Different levels require different approaches individual level population level Measurement derived from the experiences and values of people with dementia rather than the p e o eptio s of e pe ts Patient Reported Outcome Measure (PROM)

Measurement of quality of life Individual level DEMQOL

Measurement at the individual level Much excellent work in instrument development eg PDS Dejong et al (1989) DQOL Brod et al (1999) QOL AD Logsdon et al (1999) ADRQL Black et al (2000) QOLAS Selai et al (2001) Evolving field with progressive refinement of methodology

Development of the system Initial field test 111 pairs Conceptual framework bottom up + top down Psychometrics Item reduction Final field test 105 pairs DEMQOL DEMQOL-Proxy

Smith et al (2005). Health Tech Ass http://www.ncchta.org/fullmono/mon910.pdf

The system Two interviewer administered self-report instruments different items work in the two groups measuring the same thing DEMQOL 28 item self report for people with dementia 5 to 30 minutes Score 28 to 112 DEMQOL-Proxy 31 item carer report on qol of person with dementia 5 to 10 minutes Score 31 to 124 Administration manuals for each

Study ID DEMQOL Instructions: Read each of the following questions (in bold) verbatim and show the respondent the response card. I would like to ask you about your life. There are no right or wrong answers. Just give the answer that best describes how you have felt in the last week. Don t worry if some questions appear not to apply to you. We have to ask the same questions of everybody. Before we start we ll do a practise question; that s one that doesn t count. (Show the response card and ask respondent to say or point to the answer.). In the last week, how much have you enjoyed watching television? a lot quite a bit a little not at all Follow up with a prompt question: Why is that? or Tell me a bit more about that.

First I m going to ask about your feelings. In the last week, have you felt. 1. cheerful? ** a lot quite a bit a little not at all 2. worried or anxious? a lot quite a bit a little not at all 3. that you are enjoying life? ** a lot quite a bit a little not at all 4. frustrated? a lot quite a bit a little not at all 5. confident? ** a lot quite a bit a little not at all 6. full of energy? ** a lot quite a bit a little not at all 7. sad? a lot quite a bit a little not at all 8. lonely? a lot quite a bit a little not at all 9. distressed? a lot quite a bit a little not at all 10. lively? ** a lot quite a bit a little not at all 11. irritable? a lot quite a bit a little not at all 12. fed-up? a lot quite a bit a little not at all 13. that there are things that you wanted to do but couldn t? a lot quite a bit a little not at all NU DK OP Next, I m going to ask you about your memory. In the last week, how worried have you been about. 14. forgetting things that happened recently? a lot quite a bit a little not at all 15. forgetting who people are? a lot quite a bit a little not at all 16. forgetting what day it is? a lot quite a bit a little not at all

DEMQOL missing data 70 60 pwd proxy 50 40 30 20 10 0 mild/mod severe

DEMQOL system results High acceptability High feasibility High internal consistency Good test retest reliability Good evidence of validity content convergent (SF12 MCS) discriminant (no effect age and gender) More work needed on responsiveness Smith et al (2007). Psych Med

DEMQOL-Proxy: Linear regression of clinical variables with DEMQOL-Proxy Beta coefficient p-value NPI total 0.52 <0.001 Patient age 0.32 0.016 MMSE -0.16 0.281 Carer GHQ 0.07 0.623 ADL (BI) 0.02 0.924 Banerjee et al (2006) JNNP

Quality of life measuring quality of care - Croydon Memory Service Model Evaluation

What is good quality care? - data on first 780 cases 95% acceptance rate 94% appropriate referrals 18% minority ethnic groups 19% under 65 years of age Banerjee et al (2007). IJGP.

Outcome: improvement in self-rated quality of life - DEMQOL Part of routine assessment Preliminary data 109 cases 6 month follow-up p=0.029 92 91 90 89 88 87 baseline 6m Banerjee et al (2007) IJGP

Outcome: improvement in proxy-rated quality of life DEMQOL-Proxy Part of routine assessment Preliminary data 141 cases 6 month follow-up p=0.041 100 98 96 94 92 baseline 6m

Change in DEMQOL for those below mean (<90) 88 88 86 86 84 84 82 80 78 76 82 80 78 76 74 74 baseline 6m 72 baseline 12m 6 month DEMQOL change 8.3pt, paired t=4.99, p<0.001, Cohe s d = 0.79 12 month DEMQOL change 7.8pt, paired t=3.88, p<0.001, Cohe s d = 0.60

Distribution of DEMQOL scores by CDR score 110.00 100.00 MAINTAIN A GOOD QUALITY OF LIFE FOR THOSE WITH GOOD LIFE QUALITY DEMQOL score 90.00 80.00 70.00 DRIVE UP THE QUALITY OF LIFE FOR THOSE WITH POOR QUALITY OF LIFE 60.00 0.50 1.00 1.50 2.00 2.50 3.00 cdr score

Changes over time in real world clinical practice, DEMQOL scores from the Croydon Memory Service routine practice data from patients remaining in service baseline, 6 months and 12 months indication of the possibility of change one element of responsiveness

GENERATION OF PREFERENCE-BASED INDICES FROM DEMQOL AND DEMQOL-PROXY FOR USE IN ECONOMIC EVALUATION

Introduction Economic evaluation using cost utility analysis can inform resource allocation between emerging interventions Cost per Quality Adjusted Life Year (QALY) can be used The Q o utilit e ui es a health state value s o ed usi g p efe e e information Typically generic preference based measures (PBMs) of health (eg EQ- 5D/SF-6D) are used Generally these animals do not work well in dementia 17/07/2013 The University of Sheffield

Five linked stages Adapt DEMQOL and DEMQOL-Proxy using psychometric and Rasch analysis to develop a health state classification system with one item per dimension Classification system amenable to preference valuation and the subsequent generation of QALYs using dementia specific preference based measures 1. derivation of the health state classification 2. main population valuation survey 3. patient/carer valuation survey 4. modelling, and 5. application to trial data 1. Derivation of the health state classification Step I Establish dimensions using EFA Step II Eliminate items per dimension using Rasch analysis Step III Select items per dimension using Rasch analysis and clinical input Step IV Exploration of item level reducing per dimension Step V Validation repeat steps I to IV on other datasets

Lots of scie tific stuff Disordered response levels Differential item functioning Fit to Rasch models

Results Mean observed TTO values range from 0.18 to 0.95 for DEMQOL-5D and from 0.33 to 0.96 for DEMQOL-P- 4D. The best performing models for each measure were main effects models estimated using individual level data. Overall the regression models have: good predictive ability (for example MAE 0.043-0.067) consistent coefficients, and comparable in their performance to other measures including: generic EQ-5D (MAE 0.039) SF-6D (MAE 0.073-0.079) asthma-specific AQL-5D (0.046-0.057 and cancer-specific EORTC-8D (0.046 to 0.054)

Conclusions A system ready to use. It is feasible to estimate preference-based single index measures from the DEMQOL and DEMQOL- Proxy for use in economic evaluation. These measures will enable economic evaluation using (good) QALYs to be undertaken on people with dementia across the full severity range of dementia.

What i dividual easures ca t do Constrained by measurability The tyranny of the four point scale Love, touch, choice, liberty, personhood, dignity, respect Many of the big questions out of range Strategy Policy Choice (eg of care home)

Use of a population level quality of life framework in dementia Framework with which to judge policies and practice internationally, nationally, locally Design services, systems and policies that truly meet the needs of people with dementia and their carers designed to maintain and enhance life quality Operationalise broad political and policy statements help to turn rhetoric into reality

A population framework for understanding quality of life in dementia and evaluating public policy and service Stroud symposia ADI-QOL

Rationale for the series To develop a cross-national understanding of what determines good and bad quality of life in dementia improve or impair quality of life in dementia To generate a cross-national framework with which to judge services and policy for people with dementia

The ADI/Stroud workshops Washington the nature of quality of life in dementia Christchurch 100 participants 150 participants what makes quality of life in dementia better and worse Barcelona 50 participants practical actions to promote or inhibit quality of life Dominican Republic 100 participants relationship between carer and the person with dementia Kyoto 170 participants the role of choice in quality of life in dementia Istanbul spirituality and quality of life Berlin effect and timing of diagnosis Singapore review and future use 40 participants 50 participants 50 participants

Contributors 120 100 60 80 40 60 40 20 20 0 carers profs resch pwd 0 n am s am asia europe africa

Methodology for generating the ADI-QOL model the small print! NVivo 2 qualitative data handling computer package used to aid storage, coding, and retrieval of the data. Transcripts analysed using qualitative thematic analysis. They were coded in detail for concepts using open coding. Codes derived directly from data, not from pre-determined theory. Two people (RW, SB) read the transcripts thoroughly, worked to develop a coding framework. Any discrepancies discussed until consensus reached. All of the transcripts were coded at a detailed conceptual level, with new codes emerging. Once all coded, transcripts read again from the beginning to ensure that instances of concepts defined by later codes were captured. Detailed codes were re-examined and codes were grouped into themes, forming conceptual domains drawn from the text itself to ensure the themes were fully grounded in the data.

Elements of quality of life in dementia: frequency of endorsement respect education spirituality love communication time choice 0 50 100 150

Background themes Subjective individually-defined Important cultural ele e ts, ut Possible to find supracultural transcendent themes not the same as disease progression inter-dependence of quality of life for carer and person with dementia Five domains Personhood Communication Environment Health Quality of Care

Making it better -- personhood Choice/decision making (43) love (33) cultural appropriateness (19) respect (18) knowing personal history (13) spirituality (11) treat as individual (10) Involvement creativity belonging genuineness feeling useful tolerance independence dignity work with retained skills treat like an adult freedom/autonomy trust acceptance

Making it worse -- personhood Infantalisation (17) treating as a disease (10) being stopped doing things (9) forced to do things (9) denying choice (7) rejection/exclusion (6) abuse role stripping over-organisation over protection denial of individuality disrespect made to feel not worthwhile indifference loss of autonomy disgust dishonesty laughing at people with dementia

Making quality of life better in dementia Communication touch Environment security Personhood choice Quality of life Health physical care Quality of care carer support

Making quality of life worse in dementia Communication Lack of time Environment restriction Personhood infantilisation Quality of life Health medication Quality of care denial

Sub-domains Communication Health Physical Health Mental, Emotional Health Cognitive Health Quality of Life in Dementia Quality of Care Environment Social Environment Physical Environment Personhood Empowerment Spirituality Respect Identity

ADI-QOL model of quality of life in dementia Funding for Services Quality of Care Health Quality of Life Public Attitudes & Understanding Com m unication Environm ent Inner ring (individual) Quality of care Health Communication Environment Personhood Personhood Government & Social Policy Outer ring (societal) Service funding Public attitudes Policy

How we might use the framework? Systematic framework to judge service eg care home policy eg NSF Assess by domain then domain content Who can use it? service themselves inspectors customers What do you do? Use any information you have enquiry observation consensus Useful information where there is none Tells you where to look and what to look for Value in repetition

Quality of care in dementia: challenges and solutions informed by and judged by the ADI-QOL framework

National Dementia Strategy - England Published 2 Feb 2009 Five year plan 17 interlinked objectives 150 million extra funding Four key themes Improving awareness Early and better diagnosis Improved quality of care Delivering the Strategy

National Dementia Strategy - England Published 2 Feb 2009 Five year plan 17 interlinked objectives Public Attitudes & Understanding 150 million extra funding Funding for Services Health Communication Four key themes Quality of Care Quality of Life Environment Improving awareness Early and better diagnosis Personhood Improved quality of care Delivering the Strategy Government & Social Policy

Objectives of the National Dementia Strategy - England

Objectives of the National Dementia Strategy - England Public Attitudes & Understanding Funding for Services Health Communication Quality of Care Quality of Life Environment Personhood Government & Social Policy

Living well with dementia in care homes Reduced use of antipsychotic medication

Ministerial review of use of antipsychotics in dementia Published November 2009 Comprehensive review Negative effects Positive effects Analysis of reasons for current clinical behaviour Practical clinical plan to deal with problems found

New data and extrapolation NHS Information Centre for Health and Social Care completed analyses using the IMS Disease Analyzer Practices from England, Wales, Scotland and Northern Ireland a representative UK sample by age and sex. 1,098,627 patients 12-month period from 1 April 2007 to 31 March 2008. 192,190 people (17.5%) over the age of 65 10,255 (5.3%) received a prescription for an antipsychotic. Estimates for the report 25% people with dementia receiving an antipsychotic 180,000 people with dementia receiving an antipsychotic Includes people with dementia at home as well as people in care homes

Summary of risks and benefits at a population level of the use of antipsychotics for BPSD in people with dementia data suggest that treating 1,000 people with BPSD with an atypical antipsychotic drug for around 12 weeks would result in an additional 91 200 patients with behaviour disturbance showing clinically significant improvement an additional 10 deaths; an additional 18 CVAEs,» around half of which may be severe; no additional falls or fractures; and an additional 58 94 patients with gait disturbance. For UK 1,800 deaths per year 1,620 severe CVAEs per year

Analysis of why Symptom of underlying system failure in health and social care for people with dementia 1960s response to a 21 st century challenge Why lack of response to clear warnings It is complicated System does not allow change» Knowledge» Attitudes» Provision Simple stuff eg specialists shouting at GPS does not work Need to treat the cause as well as the symptoms

Action Provision of specialist input Use quality improvement mechanisms Improve skills in primary and social care

Action Public Attitudes & Understanding Provision of specialist input Use quality improvement mechanisms Funding for Services Quality of Care Health Quality of Life Communication Environment Personhood Improve skills in primary and social care Government & Social Policy

Final thoughts Concepts of quality of life are important and useful everything we do for people with dementia and their carers is about enhancing or maintaining good quality of life Intervention at multiple levels likely to lead to the greatest quality improvement international, national, local, individual Different levels need different interventions and measures We now have the materials and methods to plan, assess and improve qol in dementia

Thank you!