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Using Meta-Ethnography to Determine the Attributes for a Discrete Choice Experiment Authors: Hareth Al-Janabi 1 , Joanna Coast 2 , Terry Flynn 1 Discussant: Stéphanie Payet 3 28, rue d’Assas 75006 Paris France Tel . 01 44 39 16 90 Fax 01 44 39 16 92 E-mail : [email protected] - Web : www.rees-france.com CES-HESG Workshop 2 nd British-French meeting on health economics London, 4-6 January 2006 1: MRC Helth Service Research Collaboration, University of Bristol, 2: Health Economics Facility, Health Services Management Center, University of Birmingham, 3: REES France, Paris

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Page 1: Using Meta-Ethnography to Determine the Attributes for · PDF fileUsing Meta-Ethnography to Determine the Attributes for a Discrete Choice Experiment Authors: Hareth Al-Janabi1, Joanna

Using Meta-Ethnography to

Determine the Attributes for a

Discrete Choice Experiment

Authors: Hareth Al-Janabi1, Joanna Coast2, Terry Flynn1

Discussant: Stéphanie Payet3

28, rue d’Assas

75006 Paris – France

Tel . 01 44 39 16 90 – Fax 01 44 39 16 92

E-mail : [email protected] - Web : www.rees-france.com

CES-HESG Workshop

2nd British-French meeting on health economics

London, 4-6 January 2006

1: MRC Helth Service Research Collaboration, University of Bristol,

2: Health Economics Facility, Health Services Management Center, University of Birmingham,

3: REES France, Paris

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Summary of the paper

Application to the case of informal

care for older people

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General Approach (Noblit & Hare)

1. Getting started

2. Deciding what is relevant to the initial

interest

3. Reading the studies

4. Determining how the studies are related

5. Translating the studies into one another

6. Synthesising the studies

7. Expressing the synthesis

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1. Getting Started

Defining the aim of the meta-ethnography

and what will be the focus of the synthesis

Ex : Synthesise research that will uncover

the areas over which carers for older people

display strong preferences

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2. Deciding What is Relevant to the Initial Interest

Need for a trade-off between

Obtaining a high number of studies

Make the synthesis simple

Defining the inclusion and exclusion criteria

Planning and conducting the search

Sifting the papers to select the final set

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Initially Included Studies

Study Carer

gender

Relation Ethnic group Recipient

Aberg Both Anyone NS Very old

Adamson Both Relative Black/S. Asian Dementia

Baker Both Anyone Minorities HIV women

Cheung Both Spouse NS Multiple

scelosis

De Graaf Both Relative Turkish/Morrocans Terminal

illness

Harris Male Spouse NS Alzheimers

Lewis Female Daughter NS NS

McGarry Both Relative (>75) NS NS

Neufeld Female Relative NS NS

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3. Reading the Studies

Article 1 Article 2 Article 3 …

Title

Year

Carers

Recipients

Analysis methods

Research methods

Location

Concepts

Quotes

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4. Determining How the Studies are Related

Creating concepts from the comparison of

the studies

No ‘best’ method alphabetical pairing

Ex : « Control » emerged as a concept

Cheung : events overwhelm carers no control

Harris : satisfaction of carers who developed a

routine control

Return to the texts : no concept forgotten

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5. Translating the Studies into One Another

Categorising the findings

Concept 1 Concept 2 Concept 3

quote (1,1)

quote (2,6)

quote (4,3)

quote (2,1)

quote (1,2)

quote (3,1)

quote (2,1)

quote (4,1)

Link

Study-specific concept

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5. Translating the Studies into One Another

The same concept can have different

translations according to the study

Ex : « Commitment »

Adamson : Carers draw on religion and culture

and feel duty-bound to care for sick relative

Lewis : Carers commited to ensuring their

elderly receives quality care

Making the relevance of concepts in each study explicit

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6. Synthesising the Studies

Separating out concepts between those which

describe the caring experience

influence the quality of the caring experience

Is the quality of the caring experience derived from the concept per se ?

Or does the concept influence a higher over-arching concept which directly influences the quality of the caring experience ?

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7. Expressing the Synthesis

5 attributes

Relationship between carer and recipient

Formal support in caring

Informal support in caring

Strain

Role in society

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Authors’ Discussion

No consensus on

Synthesise different qualitative approaches

Synthesise qualitative and quantitative evidence

How many studies to include in the meta-ethnography

vs ethnography and interviews : need qualitative research and less rich

vs literature review and expert opinion : need familiarity with qualitative methods

Limitations of the method

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Authors’ Discussion

An interpretation beyond that obtained from a literature review

High transparency

Time needed smaller than that of interviews

Potential for excluding important attributes lower than that of

ethnography

interviews/focus group

researcher opinion

Advantages over alternative methods

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Discussion

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General Comments

Confusion between themes and concepts

« A grid was created (…) listing the study characteristics and the themes and quotes »

« Quotes and themes (…) were categorised using the concepts »

Two issues

The choice of the development method

The justification for the genesis of attributes from this method

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The « Plus » of Meta-Ethnography

More than the « sum of the parts »

Translation stage

Allow to gain familiarity with the general

understanding of the phenomenon

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What Could be Improved ?

Find an other threshold for the final set to

be analysed ?

How to choose papers among those

sharing the same characteristics ?

Validation by an expert : relate the methods

instead of confronting them

Harmonisation needed for the notations

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Further Domains of Application

Development of levels of attributes

Dimensions for quality of life scales

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Further Information

Publications: Britten and al. Using meta ethnography to synthesise

qualitative research: a worked example. J Health Serv Res Policy. 2002 Oct;7(4):209-215

Pound and al. Resisting medicines: a synthesis of qualitative studies of medicine taking. Social science & medicine. 2005 Jan;61:133-155

Walter and al. Lay understanding of familial risk of common chronic diseases: a systematic review and synthesis of qualitative research. Ann Fam Med. 2004 Nov;2(6):583-594

Mays and al. Systematically reviewing qualitative and quantitative evidence to inform management and policy making in the health field. J Health Serv Res Policy. 2005 Jul;10(1):6-20