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Christopher M. Kramer MD George A. Beller MD/Lantheus Medical Imaging Distinguished Professor of Cardiovascular Medicine Chief, Cardiovascular Division University of Virginia Health Advances in CMR: Will It Ever Become the Go To Test?

Advances in CMR: Will It Ever Become the Go To Test?

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Page 1: Advances in CMR: Will It Ever Become the Go To Test?

Christopher M. Kramer MD

George A. Beller MD/Lantheus Medical Imaging

Distinguished Professor of Cardiovascular Medicine

Chief, Cardiovascular Division

University of Virginia Health

Advances in CMR:

Will It Ever Become the Go To Test?

Page 2: Advances in CMR: Will It Ever Become the Go To Test?

Disclosures

Research grant

Regeneron

Biotelemetry

Myokardia

Consultant

Cytokinetics

Page 3: Advances in CMR: Will It Ever Become the Go To Test?

Go To Test?

Ischemic Heart Disease – hopefully

Cardiomyopathies/HF - definitely

Page 4: Advances in CMR: Will It Ever Become the Go To Test?

CMR in Ischemic Heart Disease

Structure and function

Viability

Stress perfusion

Contraindications

GFR<30 – gadolinium

Cardiac devices – no longer

Limitations

Scanner access

Physician training

Page 5: Advances in CMR: Will It Ever Become the Go To Test?

LV structure and function

Steady state free precession imaging

Page 6: Advances in CMR: Will It Ever Become the Go To Test?

Axial Short-axis

Clark CJ et al JACC CVImaging 2012;5:28-37

RV structure and function

Page 7: Advances in CMR: Will It Ever Become the Go To Test?

Infarct detection/transmurality

Technique - inversion recovery, nulling of normal

myocardial signal

Infuse 0.15-0.2 mM/kg of Gd-DTPA

Image 10-20 minutes later –

Gd becomes trapped

in necrotic scar,

delayed washout

Simonetti et al Radiology 2001;218:215

Page 8: Advances in CMR: Will It Ever Become the Go To Test?

Transmural extent of hyperenhancement

(%)= area A x 100 / (area A + area B)

Kim, et al. N Engl J Med 2000;343: 1445-53

Transmural extent of LGE

Page 9: Advances in CMR: Will It Ever Become the Go To Test?

Improved sensitivity vs. SPECT

Wagner A, et al. Lancet 2003;9355:374

6 pts. (13%) with

subendocardial

infarction had no

evidence of infarction

by SPECT

85/181 segments with

subendocardial

infarction had negative

SPECT

Page 10: Advances in CMR: Will It Ever Become the Go To Test?

Detecting unrecognized infarcts

ICELAND MI study

936 pts., 67-93 yrs.

91 recognized MI

157 unrecognized MI

6.4 yrs. f/u

Adjusted HR 1.45

Absolute risk↑ 8%

Schelbert E et al, JAMA, 2012;308:890-896

Page 11: Advances in CMR: Will It Ever Become the Go To Test?

Viability - LGE

50 pts. imaged before revascularization

804/2093 segments dysfunctional at baseline

694/2093 had areas of hyperenhancement

Kim R et al. N Engl J Med. 2000;343:1445

Page 12: Advances in CMR: Will It Ever Become the Go To Test?

Viability - LGE

Kim R et al. N Engl J Med. 2000;343:1445

Page 13: Advances in CMR: Will It Ever Become the Go To Test?

Meta-analysis

J Romero et al, JACC CV

Imaging 2012;5:509-12

Page 14: Advances in CMR: Will It Ever Become the Go To Test?

Stress perfusion CMR

First pass contrast-

enhanced CMR

Stress

Rest

Page 15: Advances in CMR: Will It Ever Become the Go To Test?

Myocardial perfusion

Klem I et al, J Am Coll Cardiol 2006;47:1630

Sensitivity 89%

Specificity 87%

Accuracy 88%

Page 16: Advances in CMR: Will It Ever Become the Go To Test?

Standard clinical exam in IHD

0

Scout

imaging

10min

Adenosine

stress

perfusion

20

Cine

Function

15

Rest

perfusion

25

Late

gadolinium

enhancement

Page 17: Advances in CMR: Will It Ever Become the Go To Test?

• CE-MARC study

• 752 pts, 1 center (Leeds)

• 39% with CAD

• >50% stenosis on QCA

• LGE and MR coronary

angiography also used

Greenwood J et al. Lancet 2012;379:393-5

Comparative effectiveness - CE MARC

Page 18: Advances in CMR: Will It Ever Become the Go To Test?

MR INFORMFFR-

INFORMED

(n=464)

MR-

INFORMED

(n=454)

Age 62 ± 9 62 ± 10

Gender (Male) 329 (73%) 335 (72%)

Ejection Fraction 59 ± 8 61 ± 7

Ethnicity (Caucasian) 419 (91%) 409 (90%)

CCS class II

III

415 (90%)

48 (10%)

407 (90%)

45 (10%)

Diabetes 138 (30%) 112 (25%)

Previous MI 33 (7%) 39 (9%)

Known CAD 52 (11%) 72 (16%)

Current Smoking 76 (16%) 82 (18%)

E Nagel et al. NEJM 2019;380:2418-28

Page 19: Advances in CMR: Will It Ever Become the Go To Test?

MR INFORM - Revascularization rate

3.5

44.252.3

FFR-INFORMED

no angio

revasc

no revasc

1.5

36.0

62.4

MR-INFORMED

no MR

revasc

no revasc

Revascularization rate

p = 0.0053

E Nagel et al. NEJM 2019;380:2418-28

Page 20: Advances in CMR: Will It Ever Become the Go To Test?

MR INFORM - Outcomes

E Nagel et al. NEJM 2019;380:2418-28

Page 21: Advances in CMR: Will It Ever Become the Go To Test?

Prognostic utility of stress CMR

19 studies, 11,636 pts., 32% ischemia, 29% LGE

Lipinski M et al. JACC 2013;62:826-38

Page 22: Advances in CMR: Will It Ever Become the Go To Test?

Prognostic utility of stress CMR

Page 23: Advances in CMR: Will It Ever Become the Go To Test?

So why isn’t it used as much as it should be?

Politics and economics, not the science

Scanner access

Lack of trained readers

Reimbursement

Cardiology/Radiology divide

Competing interests

Page 24: Advances in CMR: Will It Ever Become the Go To Test?

Cardiomyopathies/HF

Page 25: Advances in CMR: Will It Ever Become the Go To Test?

Replacement vs. interstitial fibrosis

Salerno M, Kramer CM. JACC CV Imaging, 2013;6:806-22

Page 26: Advances in CMR: Will It Ever Become the Go To Test?

T1 mapping – myocardial fibrosis

Schelbert EB et al J Am Coll Cardiol

2014;63:2188

Page 27: Advances in CMR: Will It Ever Become the Go To Test?

SSFP Cine imaging

Page 28: Advances in CMR: Will It Ever Become the Go To Test?

Parametric mapping – T1/T2

T1 map

Normal T1

= 1150ms

T2 map

Normal T2

<60 ms

Page 29: Advances in CMR: Will It Ever Become the Go To Test?

Myocarditis

Mahrholdt et al Circulation 2004;109:1250

32 pts. with myocarditis

Enhancement in 28/32-88%

Lateral free wall most common

Biopsy in area of contrast enhancement in 21 – 19 with active myocarditis

Page 30: Advances in CMR: Will It Ever Become the Go To Test?

Lake Louise II

Ferreira V et al J Am Coll Cardiol, 2018;72:3158-76

Page 31: Advances in CMR: Will It Ever Become the Go To Test?

Dilated cardiomyopathy

Page 32: Advances in CMR: Will It Ever Become the Go To Test?

Midwall LGE and prognosis

Gulati A. JAMA, 2013;309:896-908

472 patients

Page 33: Advances in CMR: Will It Ever Become the Go To Test?

Hypertrophic Cardiomyopathy

LV mass, volumes, 3D

hypertrophy

LV outflow tract gradient,

mitral regurgitation

Late gadolinium

enhancement (50-60%)

LV fibrosis/scar

- Global/regional

Page 34: Advances in CMR: Will It Ever Become the Go To Test?

HCMR study

Improved prediction of outcome in HCM with:

• Standard clinical predictors

• CMR – LGE and T1 mapping

• Biomarkers

• Genetics

• www.hcmregistry.org

2755 patients, 44 sites - N.A., Europe

Kramer CM et al, Am Heart J 2015;170:223-30

Page 35: Advances in CMR: Will It Ever Become the Go To Test?

Baseline characteristics

Neubauer S, ……, Kramer CM. J Am Coll Cardiol, 2019; in press

Page 36: Advances in CMR: Will It Ever Become the Go To Test?
Page 37: Advances in CMR: Will It Ever Become the Go To Test?

Sarcoidosis – meta-analysis

11 studies, 805 patients, f/u 3.0±1.7 yrs.

Combined outcome - all cause mortality, arrhythmogenic events

Coleman GC et al JACC CV Imaging, 2017;10:411-20

Page 38: Advances in CMR: Will It Ever Become the Go To Test?
Page 39: Advances in CMR: Will It Ever Become the Go To Test?
Page 40: Advances in CMR: Will It Ever Become the Go To Test?

Amyloidosis, LGE, and prognosis

Fontana M et al, Circulation, 2015;132:1570-9

Page 41: Advances in CMR: Will It Ever Become the Go To Test?

Amyloidosis - native T1, ECV

Karamitsos TD et al, JACC CV Imaging 2013;6:488-97

Martinez-Naharro et al, JACC CV Imaging 2018 pii:S1936-878X

Page 42: Advances in CMR: Will It Ever Become the Go To Test?

Summary

Go To Test?

Ischemic heart disease – hopefully

Cardiomyopathies/HF-definitely