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Klinimetrie bij het stellen van de functionele prognose na een CVA: hulp of last? Dr. G. Kwakkel.

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Presentation on theme: "Klinimetrie bij het stellen van de functionele prognose na een CVA: hulp of last? Dr. G. Kwakkel."— Presentation transcript:

1 Klinimetrie bij het stellen van de functionele prognose na een CVA: hulp of last?
Dr. G. Kwakkel

2 Identify patient’s problem
Define a meaningful question Determine the prognosis Select most appropriate therapy Evaluate efficacy

3 Doel van het (klinisch) meten
om te onderscheiden (diagnostiseren en/of klassificeren) om te voorspellen om (verandering) te evalueren Kirshner & Guyatt, J. Chron. Dis 1985; 38: 27

4 clinical decision making
outcome of ADL ? home at 6 months ? clinical decision making needs further help ? patients future

5 hypothetico-deductive reasoning?
pattern recognition hypothetico-deductive reasoning? problem solving ? intuition ? outcome of ADL ? home at 6 months? needs further help? patients future

6 (1) Prediction of what? Outcome of what? determinant

7 Interaction of Concepts
ICF 2001 Health Condition (disorder/disease) Body function&structure (Impairment) Activities (Limitation) Participation (Restriction) ? ? Environmental Factors Personal Factors

8 Which construct (at level of activity) do we exactly like to predict?
Neuro-psychology Clinical neurology Functional outcome (e.g., dexterity, walking ability, (I)ADL-independency determinant Neuro-physiology Neuroradiology Demographic factors

9 Functional Ambulation Categories
Barthel Index ARAT Arm-handvaardigheid Basic ADL ? Loopvaardigheid Functional Ambulation Categories

10 Construct validity of BI (N=89)
Correlation coefficient (rs) weeks

11 Construct validity of BI (N=89)
Correlation coefficient (rs) weeks

12 (2) Which determinants are valid?
Neuro-psychology Clinical neurology Functional outcome of basic ADLs determinant Neuro-physiology Neuroradiology Demographic factors

13 I . Key methodological criteria for prognostic research
internal validity reliable and valid measurements inception cohort appropriate end-points of observation control of patient drop-out statistical validity control for statistical significance adequate estimation of sample-size control for multicollinearity Kwakkel et al, Age & Ageing 1996;25:

14 r y.x1 r x1.x2 r y.x2 Factor x1 Outcome Y Factor x2
(explained variance) r x1.x2 r y.x2 Factor x2

15 Predictive value of volume of stroke according to MRI scan for outcome of ADL-independency at 6 months post stroke Schiemanck et al, Stroke. 2006;37:

16 Model 1 (AUC=0.83) = age and IBI
Receiver operating curves of model 1 (clinical) and model 2 (clinical imaging) (N=75) Model 1 (AUC=0.83) = age and IBI Model 2 (AUC =0.87) = Model 1 + volume MRI Schiemanck et al, Stroke. 2006;37: Schiemanck, S. K. et al. Stroke 2006;37: Copyright ©2006 American Heart Association

17 II. Key methodological criteria for prognostic research
external validity specification of inclusion and exclusion criteria description of additional treatment effects during period of observation cross-validation of the prediction model Kwakkel et al, Age & Ageing 1996;25:

18 78 Internal validity Statistical validity 13 (8) external validity

19 Valid predictors for ADL (and walking ability)
admission ADL (i.e., assessment specific) urinary (in)continence age* previous stroke (and other disabling co-morbidity) consciousness at onset severity of paresis sitting balance orientation in time and place level of social support inattention depression

20 Possible negative predictors for ADL
homonymous hemianopia conjugate deviation of the eyes fatigue dyspraxia dysphasia ??

21 Variables not related to outcome of ADL
gender ethnic origin side of stroke Kwakkel et al., Age & Ageing, 1996: 25:

22 Individual recovery patterns of Barthel Index (n=13)
BI-score weeks weeks

23 Mean recovery pattern of Barthel Index
prediction outcome

24 Regression model statistics for outcome of BI
Intercept Initial BI Sitting balance Soc. Support age * Model Nh Pooled Eigenvalue 4.291 0.363 0.226 0.110 0.023 0.106 0.120 CI 1.0 3.44 4.36 6.24 13.66 5.71 5.34 R-square 0.51 0.61 0.64 0.67 0.52 0.57

25 BI = 42.29 + (0.51 * IBI) + (20.93 * SB) + (10.35 * SS)
Final regression model for outcome of Barthel Index at 6 months post stroke BI = (0.51 * IBI) + (20.93 * SB) + (10.35 * SS) BI= (Initial) Barthel Index (ranging from 0-100) SB=initial sitting balance (yes/no on the TCT) SS= Social Support (yes/no: having a partner able to support)

26 Increment in explained variance for outcome of BI score (N=102)
model retesting

27 Effects of initial BI on outcome at 6 months post stroke (N=89)
Adjusted R2=0.50 (Initial BI)

28 Coefficient of Scalability: 0.72 (week 26) < CS <0.85 (week3)
Barthel Index bowel grooming bladder feeding transfer toilet use mobility bathing dressing stairs Rest. Neurology & Neuroscience 2004;22:

29 Logit item step difficulties (I) of the Rasch homogeneous 8-item Barthel scale (N=559).
Logit item step difficulties ({beta}I) of the Rasch homogeneous 8-item Barthel scale difficult 1.4 1.2 stairs 1.0 0.8 bathing 0.6 dress step 2 0.4 mobility step 2 0.2 toilet -0.2 dress step 1 -0.4 groom -0.6 -0.8 -1.0 transfer step 1 -1.2 van Hartingsveld, F. et al. Stroke 2006;37: -1.4 feeding easy Van Hartingsveld et al, Stroke. 2006;37: Copyright ©2006 American Heart Association

30 Take home message: Barthel Index gemeten in de eerste 2 weken na een CVA is een robuuste determinant voor het uiteindelijk te verwachten herstel op de BI na 6 maanden. Een klinimetrische testuitslag krijgt pas een prognostische (meer)waarde wanneer men deze relateert aan het moment waarop het CVA heeft plaatsgevonden. Functionele prognostiek is pas mogelijk wanneer men eveneens kennis heeft over de psychometrische eigenschappen van gebruikte meetinstrumenten.

31 Mijn dank voor uw aandacht!

32 Advantage of clinimetrics (2):
Clinical assessments increase the transparency in making client-related decisions within a team of professionals working together as a stroke team.

33 Increment in explained variance for outcome of BI, FAC and ARA score (N=102)

34 Steps to follow for getting relation coordination
consensus in clinimetrics: What do we measure systematically? How do we measure systematically? Who is measuring what? When do we measure the stroke patient?

35 Rehabilitation centre
Hospital Rehabilitation centre Home/ Nursing house % herstel

36 Rehabilitation centre
Hospital Rehabilitation centre Home/ Nursing house % herstel ?

37 Rehabilitation centre ‘learning from making functional prognosis’
Hospital Rehabilitation centre Home/ Nursing house ? % herstel ‘learning from making functional prognosis’

38 Clinimetrics (ICF 2001) activities participation pathology impairment
disability handicap MI-score FM-motor score Ashworth Scale Thumb-Finding Test Letter cancellation task, line-bisection task MMSE Scan. Stroke Scale Trunk Control Test Berg-Balance Scale Timed-Balance test Timed-Get-up & Go-Test FAC, 10-meter walking test ARA, Frenchay Arm Barthel Index FAI, EADL OCSP Stroke type Number of strokes Epilepsy HSP, GHS SHS SIP-68 NHP-part 1 Post-stroke Depression Carer Strain Index Satisfaction Questionnaires

39 Construct validiteit van de BI (N=89)
Pearson correlation coefficients with Barthel Index weeks

40 CONSENSUS Clinimetrics objectivity communication reliability validity
responsiveness hierarchy

41 Advantage of clinimetrics:
From perspective of a health care professional: Assessment contribute to set realistic and therapeutically attainable treatment goals (i.e., improves objectivity). From perspective of a (stroke) team: Clinical assessments increase the transparency in making client-related decisions within a team of professionals working together as a stroke team (i.e., improves communication).

42 Stroke Guidelines Multidisciplinary guidelines for stroke financed by the Dutch Heart Foundation

43 http://www.kngf.nl/ Praktijkrichtlijn Samenvattingskaart
Deskundigheidsbevorderingspakket Verantwoording en toelichting

44 Samenvattingskaart

45 Conclusion Not only differences in heterogeneity in stroke patients are responsible for lack of accuracy in predicting functional outcome, but also the methodological shortcomings in published prognostic research Kwakkel et al., Age & Ageing, 1996: 25:


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