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CARDIAC IMAGING  
Year : 2012  |  Volume : 22  |  Issue : 3  |  Page : 170-177
Magnetic resonance imaging in the evaluation of congestive cardiac failure


Department of Radiology, Cardiothoracic Imaging Section, University Hospitals of Cleveland, Case Western Reserve University, Cleveland, Ohio, USA

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Date of Web Publication15-Feb-2013
 

   Abstract 

Congestive cardiac failure is the end-result of various cardiac disorders, and is a major contributor to morbidity, mortality, and financial burden throughout the world. Due to advances in the knowledge of the disease and scanner technology, magnetic resonance imaging (MRI) is playing an increasingly important role in the evaluation of cardiac failure, including in establishing diagnosis, problem solving, risk stratification, and monitoring of therapy. This review discusses and illustrates the role of MRI in the assessment of congestive cardiac failure.

Keywords: Cardiac failure; ischemia; magnetic resonance imaging

How to cite this article:
Rajiah P. Magnetic resonance imaging in the evaluation of congestive cardiac failure. Indian J Radiol Imaging 2012;22:170-7

How to cite this URL:
Rajiah P. Magnetic resonance imaging in the evaluation of congestive cardiac failure. Indian J Radiol Imaging [serial online] 2012 [cited 2019 Sep 17];22:170-7. Available from: http://www.ijri.org/text.asp?2012/22/3/170/107177

   Introduction Top


Congestive cardiac failure is the end result of various cardiac disorders [Table 1]. Due to an aging population and improved survival from coronary events, the prevalence of congestive cardiac failure has increased. It is a major cause of morbidity and mortality, and is an important cause of high healthcare cost. [1] Due to advances in knowledge about the disease and in scanner technology, magnetic resonance imaging (MRI) is playing an increasingly important role in the evaluation of various aspects of cardiac failure [Table 2]. A standardized protocol for the evaluation of cardiac failure is shown in [Table 3]. This review discusses and illustrates the role of MRI in the assessment of congestive cardiac failure.
Table 1: Causes of cardiac failure


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Table 2: Role of magnetic resonance imaging in the evaluation of congestive cardiac failure


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Table 3: Magnetic resonance imaging protocol suggested for evaluation of congestive cardiac failure


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   Establishing the Diagnosis Top


The diagnosis of cardiac failure is typically based on clinical symptoms and signs and investigations, including echocardiography. However, MRI is occasionally used for establishing the diagnosis when the diagnosis is indeterminate, usually due to discrepant ejection fractions as measured by different imaging techniques. MRI has high accuracy and reproducibility in the measurement of ventricular systolic function. [2] Diastolic function can also be evaluated using flow curves or time-volume curves, although this is not routinely performed in clinical practice.


   Establishing the Etiology Top


The principal utility of MRI in the evaluation of cardiac failure is its ability to characterize the underlying disease based on the pattern and location of scar/interstitial fibrosis using delayed enhancement imaging [Table 4]. [3] Establishing the etiology enables tailoring of treatment according to the cause. [3] Ischemic cardiomyopathy is the most common cause of cardiac failure (62%). [4] Subendocardial pattern of delayed enhancement is seen in early infarct and a transmural pattern is seen in established infarct, both conforming to a vascular territorial distribution. In acute myocardial infarction (MI), T2-weighted images show myocardial edema in the affected vascular territory [Figure 1]A. In severe acute MI, a dark area can be seen within the enhanced scar [Figure 1]B due to microvascular obstruction. Non-ischemic patterns of enhancement are mid-myocardial (linear, patchy, or at right ventricular insertion points), subepicardial, and global subendocardial/transmural. Non-ischemic dilated cardiomyopathy is a diagnosis of exclusion, made when the left ventricle is dilated, with poor systolic function, but with normal coronary arteries. In 10-28% of these patients, a mid-myocardial pattern of enhancement is seen in the basal and mid-septum [Figure 2]. [5] However, ischemic scar pattern is seen in 13% of clinically diagnosed non-ischemic cardiomyopathy. Myocarditis produces cardiac failure in severe cases. In addition to global or regional dysfunction, myocardial edema, and contrast enhancement (early and delayed) is seen in a mid-myocardial or subepicardial distribution. Typically, the enhancement decreases or disappears with time (in 88% of cases), but may persist occasionally. [6] Sarcoidosis involves the heart in 5-25% of patients and is associated with regional wall-motion abnormalities, myocardial edema, and thickening and mid-myocardial or subepicardial pattern of delayed enhancement [Figure 3]. [7] The disease activity may be monitored with T2-weighted imaging and, typically, the areas of delayed enhancement decrease following steroid therapy. [8] Hypertrophic cardiomyopathy is characterized by various patterns of myocardial hypertrophy, which is typically asymmetric septal. Although in the early stages there is hyperdynamic systolic function, in the late/burn-out phases there is diminished function with chamber dilation and wall thinning. Papillary muscle abnormalities may be seen. Eighty-eight percent of these patients have delayed enhancement, which is of a patchy mid-myocardial pattern, more common at Right ventricle (RV) insertion sites [Figure 4]. [9] Cardiac amyloidosis is characterized by thickened myocardium, atria, and interatrial septum, with diminished systolic function and bi-atrial enlargement. [10] Delayed enhancement is typically global subendocardial [Figure 5] progressing to transmural, but can also occasionally be patchy. A unique feature of cardiac amyloidosis is the alteration of T1 kinetics of gadolinium distribution, with nulling of the myocardium before the blood pool due to diffuse amyloid infiltration, resulting in higher gadolinium uptake and T1 shortening. T1 values can be mapped using Look-Locker or modified Look-Locker sequences (MOLLI). [11]
Figure 1 (A,B): Myocardial infarction. (A) Acute myocardial edema; the two-chamber T2-weighted black-blood image shows high signal in the apical anterior, apical inferior, and apical segments (arrows), consistent with myocardial edema in a patient with acute myocardial infarction. (B) Short-axis delayed-enhancement image shows a dark non-enhancing area (arrow) in the basal infero-lateral segment within a focal area of enhancing myocardial scar (arrowhead), consistent with microvascular obstruction within an acute myocardial infarction

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Figure 2: Non-ischemic dilated cardiomyopathy. Short-axis delayed-enhancement magnetic resonance imaging demonstrates a dilated left ventricle with linear mid-myocardial scarring in the basal septum (arrow); this is a characteristic pattern seen in non-ischemic dilated cardiomyopathy. The coronary arteries were normal in this patient

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Figure 3: Cardiac sarcoidosis. Four-chamber delayed-enhancement magnetic resonance imaging in a patient with known sarcoidosis and heart block shows diffuse myoepicardial enhancement (arrows) in a pattern consistent with cardiac sarcoidosis

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Figure 4: Hypertrophic cardiomyopathy. Short-axis delayed-enhancement image shows hypertrophied myocardium and patchy, sandy areas of delayed enhancement (arrows) in a pattern typical for hypertrophic cardiomyopathy

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Figure 5: Cardiac amyloidosis. Four-chamber delayed-enhancement magnetic resonance imaging shows diffuse subendocardial enhancement (arrows) extending to the mid-myocardium, involving the entire left ventricle, right ventricle, interatrial septum, atrial walls, and valves, consistent with cardiac amyloidosis

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Table 4: Various patterns of delayed enhancement


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Pericardial constriction is characterized by impaired filling of the cardiac chambers due to a thick (>4 mm) or non-compliant pericardium. [12] Other morphological features include conical or tubular deformity of ventricles, bi-atrial enlargement, pleural effusion, superior vena cava and inferior vena cava dilation, and pulmonary artery dilation. Diastolic septal bounce and abrupt cessation of diastolic filling may also be seen. Real-time imaging of the ventricular septum shows septal flattening or bowing towards the left ventricle during inspiration [Figure 6]. [13] MRI is a good modality for the evaluation of valvular heart disease, particularly in qualitative and quantitative estimation of valvular function [Figure 7]. [14] MRI is the ideal technique for the evaluation of various congenital heart diseases, being particularly useful in the evaluation of morphology and ventricular and valvular function following treatment. [15] Cardiac masses can present with new-onset heart failure. In addition to detecting cardiac masses, MRI can also characterize these masses and detect involvement of adjacent structures and obstruction of valve or compression of ventricles.
Figure 6: Constrictive pericarditis. Real-time image of the ventricular septum obtained after inspiration shows a flattened interventricular septum (arrow), consistent with constrictive pericarditis

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Figure 7: Valvular regurgitation. Four-chamber steady-state free-precession image shows severe tricuspid (straight arrow) and moderate mitral valvular (curved arrow) regurgitation

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Iron-overload cardiomyopathy is a major cause of cardiac failure in patients with hemolytic anemias and multiple blood transfusions. The T2* value of the myocardium can be detected using a single breath-hold, black-blood multi-echo sequence (Images obtained at various TEs), and this is directly related to myocardial iron level [Figure 8]. Using T2* imaging, iron chelation therapy can be initiated before the onset of symptoms and the myocardial T2* and ejection fraction can be improved. [16] This approach has resulted in markedly improved survival in thalassemia major patients in the United Kingdom. [17] Arrhythmogenic right ventricular dysplasia (ARVD) is characterized by progressive fibrofatty replacement of the right ventricular myocardium, with fat demonstrated using black-blood images and fibrous tissue using delayed enhancement. Global systolic dysfunction, regional wall-motion abnormalities and aneurysms indicate the diagnosis, which is usually based on the Task Force criteria. [18] Left ventricular non-compaction is characterized by a ratio of non-compacted to compacted myocardium of >2.3:1 and an abrupt transition from thick compacted myocardium to a thinned myocardium [Figure 9]. Delayed enhancement may be seen in the non-compacted myocardium. [19] Takotsubo cardiomyopathy (stress-induced cardiomyopathy) is characterized by acute onset of left ventricular dysfunction, with akinesis of the apical segments and hyperkinesis of the basal segments, myocardial edema, and no delayed enhancement. [20] The cardiac failure is usually reversible. Anderson-Fabry disease is a lysosomal disorder, presenting with concentric myocardial hypertrophy and increased ejection fraction in early stages and wall thinning and systolic dysfunction in later phases. Enhancement is seen in the mid-myocardial to epicardial layers, more commonly in the basal infero-lateral wall. [21]
Figure 8: Iron-overload cardiomyopathy. Short-axis black-blood T2*-weighted images acquired with progressively increasing echo time (TE) (mentioned in the top left of each image) shows progressive darkening of the myocardium with increasing TE; this is due to iron deposition

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Figure 9: Left ventricle non-compaction. Four-chamber steady-state free-precession image in a 27-year-old man shows prominent trabeculations (arrows) in the mid-and apical regions of the left ventricle and thinning of compacted myocardium, consistent with left ventricular non-compaction

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   Quantification Top


MRI has high accuracy and reproducibility in the measurement of ventricular function. [2] Global systolic function is evaluated using short-axis cine images whereas regional function can be evaluated visually or through myocardial tagging techniques. MRI is also highly accurate and reproducible in the measurement of scar. [22],[23] Scar can be measured either by qualitative, semi-quantitative, or quantitative means. Summed scar score and transmurality index are used in qualitative estimation of scar. [24] In the semi-quantitative technique, the signal intensity of remote normal myocardium is measured and scar is defined as tissue with signal intensity above a threshold of 2-6 standard deviations above the mean signal intensity of normal myocardium [Figure 10]. In manual planimetry, the areas of enhancement can be manually contoured and expressed as grams or percentage of cardiac mass.
Figure 10: Scar quantification. The endocardial and epicardial contours are segmented. The normal myocardium is selected (blue), and based on this value a threshold for abnormal myocardium is selected. This helps in quantitative estimation of scarred areas

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   Prognostic Information Top


MRI provides prognostic information in the various disorders that cause cardiac failure [Table 5]. Delayed enhancement implies adverse prognosis in most of these diseases, as scar is a substrate for ventricular arrhythmia and is associated with adverse cardiovascular events and sudden cardiac death. Scar size by MRI (irrespective of the cause) [Figure 10] also predicts survival and all-cause mortality, independent of left ventricular ejection fraction. [22],[23],[24]
Table 5: Adverse prognostic indicators in cardiac failure due to various causes


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Ischemic cardiomyopathy

In acute MI, micro-vascular obstruction implies poor prognosis due to association with adverse cardiovascular events, and adverse remodeling [25] Hemorrhage within the core of infarct also implies adverse prognosis due to association with larger infarct size, adverse remodeling and increase of LV end-systolic volume. [26] Myocardial salvage index (Area of high signal in T2-weighted images − Area of delayed hypernenhancement/Area of high signal in T2-weighted images) has a prognostic value comparable to infarct size and microvascular obstruction. [27] After the acute stage, infarct size is the most important predictor of functional recovery, with transmural scar associated with poor recovery following revascularization procedures [Figure 11]A. [28] Patients with silent MI have an increased (6- to 11-fold) risk for major cardiac events. [29] The presence of tiny amounts of scar, regardless of history of MI, is associated with higher risk of adverse events. [30] The infarct size is a better predictor of ventricular tachycardia (VT) than left ventricular ejection fraction or left ventricular volumes. [31] Higher infarct heterogeneity has a direct correlation with higher susceptibility to VT. Right ventricular function late after MI is also an important predictor of prognosis. [32] Peri-infarct ischemia is associated with higher incidence of cardiovascular events. [33]
Figure 11 (A,B): Prognostic markers. (A) Short-axis delayed-enhancement image shows transmural scar in the anterior wall and anteroseptum (arrows) in the left anterior descending (LAD) distribution. Due to the extensive scar in this vascular territory, a revascularization procedure such as coronary artery bypass surgery is unlikely to be successful. (B) Three-chamber delayed-enhancement image shows an extensive transmural scar in the basal and mid-lateral wall (arrow), which indicates low probability of success with cardiac resynchronization therapy

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Non-ischemic cardiomyopathy

As in ischemic disease, the presence of delayed enhancement generally implies adverse prognosis in non-ischemic disorders. Mid-myocardial scar in non-ischemic cardiomyopathy is associated with higher incidence of arrhythmias, adverse events, hospitalization, and mortality. [34] Parvovirus B19 myocarditis produces lateral wall enhancement and recovery within a few months, but herpesvirus six myocarditis produces septal enhancement and rapid progression to cardiac failure. [35] Severe hyperenhancement is associated with poor prognosis in sarcoidosis, [36] hypertrophic cardiomyopathy, [37] ARVD, [18] LV non-compaction, [38] Fabry's disease [39] and cardiac amyloidosis. [40] In cardiac amyloidosis, a 2 min post-contrast T1 difference between the subepicardium and the subendocardium of less than 23 ms decreased survival. [11] In iron-overload cardiomyopathy, myocardial T2* values of less than 20 ms indicate iron-overload and values less than 10 ms indicate severe iron-overload. Lower T2* values are generally associated with severe ventricular dysfunction, [41] Presence of non-compaction in the mid-ventricular level indicates the presence of relatively more severe disease and bad prognosis. [42]


   Prediction of Response to Therapy Top


MRI plays an important role in selecting patients who would benefit from surgical or interventional procedures. There is an inverse relationship between the amount of scar and the recovery of contractile function, following coronary revascularization procedures. [43] While myocardial segments with wall motion abnormalities and no/mild (<25%) scar have good likelihood of functional recovery following revascularization, segments with >75% hyperenhancement have been shown to have little or no potential for functional recovery following revascularization [Figure 11]A [43] In addition, cardiac resynchronization therapy (CRT) will not be effective if there is extensive scar in the lateral wall or septum that prevents electrical activation [Figure 11]B. [44] Three-dimensional whole-heart MR-venography can be used to assess the venous anatomy since variations in venous anatomy, including absence of common veins, may result in failure of the procedure and therefore warrant surgical epicardial lead placement.


   Monitoring of Therapy Top


Due to its high accuracy and reproducibility in the evaluation of systolic function, MRI is the ideal modality for serial follow-up to monitor response to various therapeutic interventions. MRI is also used for evaluating the efficacy of novel therapeutic strategies in reducing reperfusion injury and infarct size, increasing salvageable myocardium and altering prognostic indicators. The size of the scar in MI is a useful surrogate endpoint for new clinical trials on the efficacy of drugs in the treatment of MI. [32] A reduction of infarct size may alter ventricular remodeling and improve prognosis.


   Conclusion Top


MRI plays a pivotal role in various aspects of cardiac failure. It is useful in establishing the diagnosis and etiology. It enables risk stratification, provides prognostic information, and determines suitability for surgical/interventional procedures. The presence of scar or fibrosis implies adverse prognosis in several conditions that cause cardiac failure.

 
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Correspondence Address:
Prabhakar Rajiah
Radiology Department, University Hospitals Case Medical Center, 11100 Euclid Avenue, Cleveland OH 44106
USA
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-3026.107177

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