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Dysfunctional but viable myocardium Ischemic heart disease assessed by MRI and SPECT

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Title: Dysfunctional but viable myocardium Ischemic heart disease assessed by MRI and SPECT


1
Dysfunctional but viable myocardiumIschemic
heart disease assessed by MRI and SPECT
  • Martin Ugander, MD
  • Department of Clinical Sciences, Lund
  • Department of Clinical Physiology
  • Lund University

2
  • Supervisor Håkan Arheden, MD, PhD
  • Clinical Physiology, Lund
  • Co-supervisor Peter Cain, MBBS, PhD
  • Wesley Heart Clinic, Brisbane, AU
  • Funding
  • Swedish Research Council
  • Swedish Heart Lung Foundation
  • Faculty of Medicine at Lund University
  • Region of Scania

3
Aim
  • To further elucidate the pathophysiology of
    dysfunctional but viable myocardium in patients
    with ischemic heart disease.

4
Outline of Studies
  • Study I - Method for quantitative MRI SPECT
  • Study II - Wall thickening vs. Infarct
    transmurality
  • Study III - LVEF vs. Infarct size
  • Study IV - Time course of perfusion function
  • after revascularization

5
Study I
  • Quantitative polar representation of left
    ventricular myocardial perfusion, function and
    viability using SPECT and cardiac magnetic
    resonance initial results
  • Cain PA, Ugander M, Palmer J, Carlsson M, Heiberg
    E, Arheden H.
  • Clin Physiol Funct Imag 2005 (25) 215-222

6
Background
  • Clinical management of CAD involves complex
    assessment of the extent and severity of changes
    in function, perfusion and viability.
  • No adequate research tools for quantitative
    assessment exist.

7
Aims
  • To explore the feasibility of integrative
    quantitative representation of LV perfusion,
    function and viability in polar plots.
  • To determine agreement between visual scoring and
    quantitative measures.

8
Methods
  • 10 patients scheduled for CABG
  • rest/stress SPECT
  • Cine and delayed enhancment CMR
  • Quantification with in-house software
  • Comparison with visual scoring using Kendalls
    coefficient of concordance (W)

9
Methods
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Results
12
Results
Kendalls W 1.0 (plt0.001) 0.85 (plt0.001)
13
Conclusions
  • Side-by-side quantitative polar representation of
    LV perfusion, function and viability is feasible
    and may aid in the complex assessment of these
    parameters.
  • The agreement between quantitative measurement
    and visual scoring was very good.

14
Study II
  • Infarct transmurality and adjacent segmental
    function as determinants of wall thickening in
    revascularized chronic ischemic heart disease
  • Ugander M, Cain PA, Perron A, Hedström E, Arheden
    H.
  • Clin Physiol Funct Imag 2005 (25) 209-214

15
Background
  • Regional LV function in patients with IHD may be
    influenced by many factors.

16
Aims
  • To explore how regional wall thickening in
    patients with chronic IHD is affected by both
    infarct transmurality and the function of
    adjacent segments.
  • To compare with results from healthy subjects.

17
Methods
  • 20 patients
  • 6 months after revascularization
  • Cine CMR
  • Delayed enhancement CMR
  • 20 matched controls
  • Cine CMR

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Multivariate analysis of parameters contributing
to wall thickening
  • t p
  • Infarct transmurality -4.5 lt0.001
  • Number dysf. adjacent seg. -22.9 lt0.001

23
Conclusion
  • The number of dysfunctional adjacent segments is
    a greater determinant than infarct transmurality
    on regional wall thickening.
  • Infarction is difficult to assess by resting
    function alone.
  • DE CMR is an important tool in this setting.

24
Study III
  • A maximum predicted left ventricular ejection
    fraction in relation to infarct size in patients
    with ischemic heart disease
  • Ugander M, Ekmehag B, Arheden H.
  • Submitted

25
Background
  • An understanding of the relationship between LVEF
    and infarct size is important when assessing the
    potential benefit of revascularization in
    patients with IHD.

26
Aims
  • To explore the relationship between LVEF and IS.
  • To determine a maximum predicted LVEF for a given
    IS.

27
Methods
  • 297 patients clinically referred for viability
    assessment by CMR
  • LVEF
  • Infarct size ( LVM)

28
Methods
A
LVEF ()
B
?
C
Infarct size (LVM)
29
Patient characteristics (IHD)
30
Distribution of infarctions
31
Distribution of number of coronary artery vessel
territories
32
Results
33
Cine
Contrast
2ch
4ch
LVEF29
IS36
34
Cine
Contrast
2ch
4ch
LVEF25
IS6
35
Conclusions
  • LVEF cannot be used to estimate IS.
  • IS cannot be used to estimate LVEF.
  • LVEF can be used to estimate a maximum predicted
    IS.
  • IS can be used to estimate a maximum predicted
    LVEF.

36
Study IV
  • Influence of the presence of chronic
    non-transmural myocardial infarction on the time
    course of perfusion and functional recovery after
    revascularization.
  • Ugander M, Cain PA, Johnsson P, Palmer J, Arheden
    H.
  • Manuscript

37
Background
  • The time course of recovery of LV function and
    perfusion after revascularization is not fully
    understood.

38
Aims
  • To study the effect of presence of infarction on
    the time course of recovery of perfusion and
    function after elective revascularization.

39
Methods
  • 15 patients (inclusion ongoing)
  • first time elective CABG (n13) or PCI (n2)
  • Imaging
  • rest/stress SPECT
  • cine and delayed enhancement CMR
  • Before revasc., 1 6 months after revasc.

40
Patient characteristics
  • 14 men, 1 woman
  • mean age 68 years (range 52-84)
  • 3VD n6
  • 2VD n6
  • 1VD n3
  • LVEF 49 ? 10

41
Distribution of infarct transmuralities
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Conclusions
  • Dysfunctional segments without infarction
    improved both perfusion and function at 1 month.
  • Segments with infarction showed improved
    perfusion at 1 month and improved function at 6
    months.
  • This may reflect more severe ischemic burden in
    segments with infarction.

44
Summary
  • Study I - Method for quantitative MRI SPECT
  • Study II - Wall thickening vs Infarct
    transmurality
  • Study III - LVEF vs Infarct size
  • Study IV - Time course of perfusion function
  • after CABG

45
Conclusion
  • It is important to perform quantitative
    assessment of function,perfusion and viability in
    combination when studying the pathophysiology of
    dysfunctional but viable myocardium in IHD.

46
www.med.lu.se/cmr
Henrik Engblom, MD, PhD-student
Bo Hedén, MD PhD
Einar Heiberg ,PhD
Håkan Arheden, MD PhD
Ann-Helen Arvidsson, tech
Henrik Mosén, MD, PhD
Christel Carlander, tech
Karin Markenroth, PhD
Marcus Carlsson, MD, PhD-student
Erik Bergvall, MSc, PhD-student
Martin Ugander, MD, PhD-student
Erik Hedström, PhD
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The ischemic cascade
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Mahrholdt et al 2005 Eur Heart J
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