Title: Dysfunctional but viable myocardium Ischemic heart disease assessed by MRI and SPECT
1Dysfunctional 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
3Aim
- To further elucidate the pathophysiology of
dysfunctional but viable myocardium in patients
with ischemic heart disease.
4Outline 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
5Study 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
6Background
- 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.
7Aims
- 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.
8Methods
- 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)
9Methods
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11Results
12Results
Kendalls W 1.0 (plt0.001) 0.85 (plt0.001)
13Conclusions
- 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.
14Study 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
15Background
- Regional LV function in patients with IHD may be
influenced by many factors.
16Aims
- 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.
17Methods
- 20 patients
- 6 months after revascularization
- Cine CMR
- Delayed enhancement CMR
- 20 matched controls
- Cine CMR
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22Multivariate analysis of parameters contributing
to wall thickening
- t p
- Infarct transmurality -4.5 lt0.001
- Number dysf. adjacent seg. -22.9 lt0.001
23Conclusion
- 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.
24Study 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
25Background
- An understanding of the relationship between LVEF
and infarct size is important when assessing the
potential benefit of revascularization in
patients with IHD.
26Aims
- To explore the relationship between LVEF and IS.
- To determine a maximum predicted LVEF for a given
IS.
27Methods
- 297 patients clinically referred for viability
assessment by CMR - LVEF
- Infarct size ( LVM)
28Methods
A
LVEF ()
B
?
C
Infarct size (LVM)
29Patient characteristics (IHD)
30Distribution of infarctions
31Distribution of number of coronary artery vessel
territories
32Results
33Cine
Contrast
2ch
4ch
LVEF29
IS36
34Cine
Contrast
2ch
4ch
LVEF25
IS6
35Conclusions
- 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.
36Study 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
37Background
- The time course of recovery of LV function and
perfusion after revascularization is not fully
understood.
38Aims
- To study the effect of presence of infarction on
the time course of recovery of perfusion and
function after elective revascularization.
39Methods
- 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.
40Patient characteristics
- 14 men, 1 woman
- mean age 68 years (range 52-84)
- 3VD n6
- 2VD n6
- 1VD n3
- LVEF 49 ? 10
41Distribution of infarct transmuralities
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43Conclusions
- 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.
44Summary
- 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
45Conclusion
- 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.
46www.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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48The ischemic cascade
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52Mahrholdt et al 2005 Eur Heart J
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