Literature DB >> 36126764

Cardiac Magnetic Resonance Imaging for the Diagnosis of Infective Endocarditis in the COVID-19 Era.

Sapan Bhuta1, Neha J Patel2, Jacob A Ciricillo2, Michael N Haddad2, Waleed Khokher2, Mohammed Mhanna3, Mitra Patel2, Cameron Burmeister1, Hazem Malas4, Joel A Kammeyer5.   

Abstract

INTRODUCTION: In the COVID-19 pandemic, to minimize aerosol-generating procedures, cardiac magnetic resonance imaging (CMR) was utilized at our institution as an alternative to transesophageal echocardiography (TEE) for diagnosing infective endocarditis (IE).
METHODS: This retrospective study evaluated the clinical utility of CMR for detecting IE among 14 patients growing typical microorganisms on blood cultures or meeting modified Duke criteria.
RESULTS: 7 cases were treated for IE. In 2 cases, CMR results were notable for possible leaflet vegetations and were clinically meaningful in guiding antibiotic therapy, obtaining further imaging, and/or pursuing surgical intervention. In 2 cases, vegetations were missed on CMR but detected on TEE. In 3 cases, CMR was nondiagnostic, but patients were treated empirically. There was no difference in antibiotic duration or outcomes over 1 year.
CONCLUSION: CMR demonstrated mixed results in diagnosing valvular vegetations and guiding clinical decision making. Further prospective controlled trials of CMR vs TEE are warranted.
Copyright © 2022. Published by Elsevier Inc.

Entities:  

Keywords:  COVID-19; Infective endocarditis; aerosol-generating procedure; cardiac magnetic resonance imaging; transesophageal echocardiography

Year:  2022        PMID: 36126764      PMCID: PMC9481470          DOI: 10.1016/j.cpcardiol.2022.101396

Source DB:  PubMed          Journal:  Curr Probl Cardiol        ISSN: 0146-2806            Impact factor:   16.464


Introduction

Infective endocarditis (IE) is a complex multifaceted disease involving any surface of the endocardium; particularly, native valves, chordae tendineae, congenital anomalies, prosthetic valves, and intracardiac devices. Additionally, depending on the clinical scenario and laterality of involvement, IE is associated with various intracardiac and extracardiac complications, including but not limited to valvular insufficiency, heart failure, paravalvular extension, atrioventricular conduction disturbance, myocarditis, pericarditis, septic pulmonary or systemic embolization, metastatic abscess, mycotic aneurysm, glomerulonephritis, and systemic immune reaction.1, 2, 3, 4 The diagnosis of IE is based upon a combination of clinical, microbiological, and echocardiographic findings as specified in the modified Duke criteria. , Given the significant morbidity and mortality of IE, prompt diagnosis and risk stratification is critical, as a delay in definitive management predisposes patients to further complications and portends worse outcomes. However, the diagnosis of IE remains challenging as patients present with a wide spectrum of clinical manifestations from asymptomatic, chronic illness with low-grade fever and nonspecific symptoms, systemic complications due to septic embolization, or acute rapidly progressive septic and cardiogenic shock. For patients undergoing diagnostic workup of suspected IE, imaging plays a critical role, and echocardiography is the first-line imaging modality. The goals of echocardiographic evaluation include assessing the anatomy of the valvular structures, identifying and characterizing the presence of vegetations, defining any resultant impairment in valvular function, assessing for paravalvular extension or abscesses, identifying involvement of prosthetic valves, examining indwelling catheters, assessing intracardiac devices such as a left ventricular assist device, and for patients with a cardiac implantable electronic device (CIED) such as a permanent pacemaker or implantable cardioverter-defibrillator (ICD), visualizing the leads if possible. While transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE) often serve complimentary roles, TEE as compared to TTE is a superior modality of imaging due to its enhanced spatial resolution resulting in higher sensitivity for identifying and characterizing valvular vegetations and paravalvular extension, particularly in the setting of prosthetic valves. , Three-dimensional (3D) TEE also allows for improved identification of valvular vegetation vs abscess, leaflet perforation, prosthetic paravalvular leak, prosthetic valve dehiscence, and vegetation size and localization. However, when there remains diagnostic uncertainty following TEE, particularly in the setting of prosthetic valves, paravalvular extension, and intracardiac devices, the modern diagnostic approach involves the utilization of multimodality imaging techniques such as leukocyte scintigraphy, 18F-fluorodeoxyglucose positron emission tomography / computed tomography (18FDG PET/CT), multidetector computed tomography (MDCT), and cardiac magnetic resonance imaging (CMR). , Recent advancements in radiotracers, multidetector scanners, iterative reconstruction algorithms, magnet field strength, and artificial intelligence models have allowed multimodality imaging to help improve diagnostic accuracy and inform management decisions. Particularly, CMR is a unique imaging modality that utilizes non-ionizing radiation to provide both anatomic and functional data in exquisite detail. Specifically, CMR allows for excellent visualization and quantitative assessment of valvular regurgitation/stenosis, ventricular volumes, ventricular systolic function, valvular vegetations, paravalvular extension, pericarditis, and myocarditis. , However, CMR is limited by the requirement of gadolinium contrast, preventing its use in advanced renal insufficiency (estimated glomerular filtration rate less than 30 mL/min) due to concern for the rare complication of nephrogenic systemic fibrosis, imaging artifacts secondary to mechanical prosthetic valves, incompatible CIEDs, ferromagnetic metallic implants, lengthy acquisition times, cost, and availability. Although CMR is now well accepted for identifying myopericardial complications and increasingly utilized for the quantitative assessment of valvular function, the exact role of CMR in the evidence-based diagnostic pathway of IE currently remains unclear due to a paucity of studies. , Additionally, while the gold standard for the diagnosis of IE, TEE is an aerosol-generating procedure (AGP) due to the traversal of a transesophageal probe through the aerodigestive tract, thus posing a potential SARS-CoV-2 transmission risk to healthcare personnel. , From the outset of the COVID-19 pandemic, CMR was utilized at our institution as an alternative to TEE in patients growing typical microorganisms on blood cultures or meeting modified Duke criteria for IE. We evaluate the clinical utility of CMR in diagnosing patients with IE.

Methods

Patient Population

This retrospective single center observational study consisted of 14 patients growing typical microorganisms (e.g., Staphylococci, Streptococci, and Enterococci) on blood cultures or meeting modified Duke criteria for IE who underwent CMR for the diagnostic evaluation of IE during the initial phase of the COVID-19 pandemic from March 14, 2020, to February 14, 2021, at ProMedica Toledo Hospital.

Imaging Protocol

Multiplanar multisequence gated CMR was performed with steady state free precession imaging and pre- and postcontrast delayed myocardial enhancement views obtained prior to and following the administration of intravenous gadolinium contrast. Additionally, contrast velocity flow imaging of the valves was performed to evaluate valvular function.

Data Retrieval

A total of 119 patients who underwent CMR between March 14, 2020, to February 14, 2021, were retrieved. Through manual chart review, 14 patients who demonstrated growth of typical microorganisms on blood cultures as noted above or met modified Duke criteria for IE were included in the analysis. Baseline demographic data, clinical course data, and imaging findings were retrieved manually from the electronic medical record and collated into a shared database for further analysis.

Statistical Analysis

Continuous variables have been expressed as the mean ± 1 standard deviation, and statistical significance was calculated using the Student's t-test. Categorical variables have been expressed as absolute numbers or percentages, and statistical significance was calculated using the Chi-squared test. A statistically significant difference between variables required a p-value ≤0.05. All statistical analysis was performed using Microsoft Excel 2010.

Approval

This retrospective observational study was approved as an expedited review by the Institutional Review Board (IRB) at the University of Toledo and ProMedica Toledo Hospital.

Results

Patient Characteristics

The study consisted of 14 patients with baseline demographic information as specified in Table 1 . The population was notable for 9 males (64%), ages ranging from 36 to 88 years old with an average age of 58 ± 15 years. Regarding risk factors: 1 patient (7%) had a history of IE; 2 patients (14%) had a history of intravenous drug use (IVDU); 3 patients (21%) had a history of heart failure (HF); 1 patient (7%) had a prosthetic valve; 0 patients (0%) had an intracardiac device, an indwelling catheter, or required dialysis.
Table 1

Baseline characteristics

Total14
Min age (years)36
Max age (years)88
Median age (years)55
Average age (years)58 ± 15
Male9 (64%)
History of infective endocarditis1 (7%)
History of intravenous drug use2 (14%)
History of heart failure3 (21%)
Prosthetic valve1 (7%)
Intracardiac device0 (0%)
Indwelling catheter0 (0%)
Dialysis dependent0 (0%)
COVID-19 positive via PCR1 (7%)
Modified Duke criteria met3 (21%)
Positive blood cultures14 (100%)
Methicillin-susceptible Staphylococcus aureus7 (50%)
Methicillin-resistant Staphylococcus aureus1 (7%)
Coagulase-negative Staphylococci (Staphylococcus lugdunensis)1 (7%)
Enterococcus faecalis4 (29%)
Enterococcus avium1 (7%)
Streptococcus constellatus (a subgroup of viridans streptococci)1 (7%)
Klebsiella oxytoca1 (7%)
Citrobacter youngae1 (7%)
Candida glabrata1 (7%)

All values are reported as n (%) unless otherwise specified Abbreviations: COVID-19 = coronavirus disease 2019, PCR = polymerase chain reaction

Baseline characteristics All values are reported as n (%) unless otherwise specified Abbreviations: COVID-19 = coronavirus disease 2019, PCR = polymerase chain reaction

Microbiological Data

All patients had positive blood cultures (MSSA 50%, MRSA 7%, Coagulase-negative staphylococci 7%, Enterococcus faecalis 29%, Enterococcus avium 7%, Viridans streptococci 7%, Klebsiella oxytoca 7%, Citrobacter youngae 7%, Candida glabrata 7%). Modified Duke criteria were confirmed in 3 cases (21%), possibly met in 9 cases (64%), and rejected in 2 cases (14%). 1 patient (7%) tested positive for COVID-19 via PCR. Further details regarding cultures, imaging findings, modified Duke criteria, final diagnosis, and management on a per case basis are outlined in Table 2 .
Table 2

Diagnostic findings, treatment regimens, and clinical outcomes

Patient #Blood culture speciation and sensitivitiesCMR resultsTTE resultsTEE resultsModified Duke criteriaDiagnosis & concominant indications for prolonged antibioticsTreatment regimenTreated specifically for IERepeat blood culture resultsIE readmissionDeath
1Enterococcus faecalis (ampicillin-susceptible)No evidence of IENo evidence of IENot performedPossibleEnterococcus faecalis bacteremia, pyelonephritis secondary to obstructing ureteral calculiUreteral stenting, amoxicillin / clavulanic acid x 4 weeks (patient refused ampicillin IV x 4 weeks)NoNegativeNoNo
2Methicillin-resistant Staphylococcus aureusNo evidence of IENo evidence of IENot performedRejectedMRSA bacteremia, left breast necrotizing fasciitis, and widely disseminated skin and soft tissue infection with multiple abscessesI&D, vancomycin IV x 2 weeks –> linezolid PO x 2 weeks (due to vancomycin reaction)NoNegativeNoNo
3Methicillin-susceptible Coagulase-negative Staphylococci (Staphylococcus lugdunensis)Patchy subepicardial and mid-myocardial enhancement - most suggestive of inflammatory or infectious process; mild thickening of the anterior and posterior mitral valve leafletsNo evidence of IESmall anterior mitral leaflet vegetation with moderate mitral regurgitationPossibleStaphylococcus lugdunensis bacteremia, native mitral valve endocarditis, and lumbar vertebral osteomyelitis / diskitis with associated phlegmonCefazolin IV x 6 weeks –> followed by chronic suppresive therapy with cephalexinYes-NoNo
4Methicillin-susceptible Staphylococcus aureusNo evidence of IENo evidence of IENot performedPossibleMSSA bacteremia, left 4th finger cellulitis and septic arthritis of the proximal interphalangeal joint, vertebral osteomyelitis / diskitis, psoas muscle abscessDaptomycin IV x 6 weeks (switched from cefazolin IV for logistics)No-NoNo
5Methicillin-susceptible Staphylococcus aureusNo evidence of IENo evidence of IENot performedDefiniteMSSA bacteremia and endocarditis with septic pulmonary emboliDaptomycin IV x 6 weeks (switched from cefazolin IV for logistics)Yes-NoNo
6Methicillin-susceptible Staphylococcus aureusMild nonspecific patchy delayed enhancement of the mid myocardium - represent a nonspecific fibrotic process possibly from inflammatory or infectious processesNo evidence of IENot performedPossibleMSSA bacteremia, vertebral osteomyelitis / diskitis, throacic paraspinal abscesses, lumbar epidural abscess, psoas muscless abscess, left ankle hardware infection in the setting of a remote left distal fibular metaphysis fracture s/p fixation, right shoulder subdeltoid bursa and shoulder region abscess, septic bursitis of left olecranonNafcillin IV x 6 weeks –> cefazolin IV x 2 weeksNoNegativeNoNo
7Methicillin-susceptible Staphylococcus aureusNo evidence of IENo evidence of IENot performedPossibleMSSA bacteremia and right 2nd toe osteomyelitisDebridement and amputation of right 2nd toe, cefazolin IV x 3 weeks –> cefalexin PO x 3 weeksNo-NoNo
8Streptococcus constellatus (a subgroup of viridans streptococci)Asymmetric focal thickening of the noncoronary aortic valve leaflet which could represent early calcifications and/or possible early vegetationNo evidence of IENot performedPossibleStrep constellatus bacteremia with presumed endocarditis complicated by mycotic aneurysm with intraparenchymal hemorrhage, septic pulmonary emboli, septic splenic emboli, and presence of ventricular septal defectCeftriaxone IV x 6 weeksYes-NoNo
9Methicillin-susceptible Staphylococcus aureusDelayed myocardial enhancement involving the basal septum the myocardium and basal lateral wall which is nonspecific and could relate to an inflammatory or infectious fibrotic processNo evidence of IENot performedRejectedMSSA bacteremia, vertebral osteomyelitis / diskitis, and epidural phlegmon vs abscessNafcillin IV x 6 weeksNo-NoNo
10Enterococcus faecalis (ampicillin-resistant), Enterococcus avium (ampicillin-susceptible), Klebsiella oxytoca (ampicillin-resistant, cefazolin-resistant), Citrobacter youngae (cephalosporin-resistant), Candida glabrata (micafungin-susceptible, fluconazole-intermediate)Possible mild delayed myocardial enhancement of the mid myocardium of the proximal septum and inferior lateral wall which is nonspecific and could represent inflammatory process or nonischemic fibrosisNo evidence of IENot performedPossibleCentral line related polymicrobial bacteremia/fungemia, diskitis, bilateral septic emboli, possible endocarditisImipenem IV x 6 weeks & micafungin IV x 6 weeksYesNegativeNoNo
11Methicillin-susceptible Staphylococcus aureusPossible delayed myocardial enhancement in a nonischemic distribution involving the proximal lateral and mid myocardium of the septum which could relate to inflammatory or infectious fibrotic processNo evidence of IENot performedPossibleMSSA bacteremia with septic arthritis of left hip, right shoulder / glenohumeral joint / acromioclavicular jointCefazolin IV x 6 weeksNo-NoNo
12Enterococcus faecalis (ampicillin-susceptible)No evidence of IE, but prosthetic aortic valve partly obscured by magnetic susceptibility artifactNo evidence of IENot performedPossibleRecurrent Enterococcus faecalis bacteremia, initially likely secondary to catheter associated urinary tract infection, later complicated by presumed prosthetic aortic valve endocarditis and confirmed epidural lumbar abscessVancomycin IV, ceftriaxone IV, and gentamicin IV x 6 weeksYesNegativeNoNo
13Methicillin-susceptible Staphylococcus aureusModerate aortic regurgitation with thickening versus nodule of the right coronary valve leaflet measuring 0.6 × 1.1 cm which could represent a nodule or vegetation, patchy delayed myocardial enhancement suggestive of a nonischemic inflammatory or infiltrative processDilated aortic root with moderate to severe aortic regurgitation; no valvular vegetations visualizedAortic valve demostrates severe eccentric regurgitation with aortic diastolic flow reversal, and the right coronary cusp appears partially torn with an echogenic structure consistent with vegetationDefiniteMSSA bacteremia and native aortic valve endocarditisSurgical aortic valve replacement, cefazolin IV x 6 weeksYes-NoNo
14Enterococcus faecalis (ampicillin-susceptible)No evidence of IESevere aortic regurgitation, small echogenicity on the left ventricular side of the aortic valve suspicious for vegetation, and moderate mitral regurgitationLarge, mobile vegetation on the aortic valve well over a cm in length, severe, wide-open aortic regurgitation with an eccentric jet, moderate to severe mitral regurgitation, mitral valve is diffusely thickened, and more focal thickening along P3 where a tiny vegetation is possibleDefiniteEnterococcus faecalis bacteremia with native aortic valve endocarditisSurgical aortic valve replacement and mitral valve repair, ceftriaxone IV & ampicillin IV x 6 weeksYes-NoNo

Abbreviations: CMR = cardiac magnetic resonance imaging, I&D = incision and drainage, IE = infective endocarditis, IV = intravenous, MRSA = methicillin-resistant Staphylococcus aureus, MSSA = methicillin-susceptible Staphylococcus aureus, PO = oral, s/p = status post, TEE = transesophageal echocardiography, TTE = transthoracic echocardiography

Diagnostic findings, treatment regimens, and clinical outcomes Abbreviations: CMR = cardiac magnetic resonance imaging, I&D = incision and drainage, IE = infective endocarditis, IV = intravenous, MRSA = methicillin-resistant Staphylococcus aureus, MSSA = methicillin-susceptible Staphylococcus aureus, PO = oral, s/p = status post, TEE = transesophageal echocardiography, TTE = transthoracic echocardiography

Clinical Performance of CMR

In total, 7 of 14 cases (50%) were treated for confirmed or presumed IE as outlined in Table 3 . In 2 of the 7 cases, CMR was notable for a possible leaflet vegetation and was clinically meaningful in guiding antibiotic therapy, obtaining further imaging, and in 1 case eventually pursuing surgical intervention. In another 2 of the 7 cases, leaflet vegetations were missed on CMR but detected on TEE. In the remaining 3 of the 7 cases, CMR results were unremarkable or obscured by artifact, but the patients were treated for IE based on either meeting definite modified Duke criteria in 1 case or empirically based on high clinical suspicion in 2 cases.
Table 3

CMR performance among patients treated for confirmed or presumed IE

Patient #CMR findingsTTE findingsTEE findingsModified Duke CriteriaDiagnosis of IEConcomitant indication for prolonged antibioticsCMR result clinically useful in guiding antibiotic therapyComments
3Equivocal (mild thickening of the anterior and posterior mitral valve leafletsNegativePositive (small anterior mitral valve leaflet vegetation, moderate mitral regurgitation)PossibleConfirmedYesNoCMR was not diagnostic. IE was diagnosed only by TEE. Additionally, treated with a prolonged antibiotic course for vertebral osteomyelitis / diskitis
5NegativeNegativeNot performedDefiniteConfirmedNoNoCMR was negative, but IE was diagnosed by modified Duke criteria (blood cultures, intravenous drug use, fever, and septic pulmonary emboli).
8Positive (asymmetric focal thickening of aortic valve leaflet - early calcification vs vegetation)NegativeNot performedPossiblePresumedNoYesCMR was the only advanced imaging study peformed and was abnormal, though not definitively diagnostic. There was already high clinical suspcion for IE given numerous embolic phenomena (mycotic aneurysm, septic pulmonary emboli, and septic splenic emboli) in the setting of a ventricular septal defect. Thus, treated empirically for IE.
10Negative (nonspecific delayed myocardial enhancement)NegativeNot performedPossiblePresumedYesNoDespite negative CMR, treated empirically for IE given bilateral septic pulmonary emboli in the setting of central line related polymicrobial bacteremia / fungemia. Additionally, treated with a prolonged antibiotic course for diskitis.
12Negative (prosthetic aortic valve partly obscured by magnetic susceptibility artifact)NegativeNot performedPossiblePresumedYesNoCMR demonstrated low diagnostic utility due to artifact from prosthetic valve. Regardless, treated empirically for prosthetic valve endocarditis given recurrent Enterococcus bacteremia. Additionally, treated with a prolonged antibiotic course for epidural lumbar abscess.
13Positive (moderate aortic regurgitation with lesion of right coronary aortic valve leaflet which could represent a nodule vs vegetation)Positive (moderate to severe aortic regurgitation, though no valvular vegetations visualized)Positive (severe aortic regurgitation, right coronary cusp partially torn with an echogenic structure consistent with vegetation)DefiniteConfirmedNoYesTTE demonstrated significant valvulopathy. While CMR was notable for a lesion, it was not definitively diagnostic. A TEE was completed for further characterization and clearly demonstrated both a valvular vegetation and the resultant valvular insufficiency. Subsequently underwent surgical aortic valve replacement.
14NegativePositive (severe aortic regurgitation, small echogenicity on the left ventricular side of the aortic valve suspicious for vegetation, and moderate mitral regurgitation)Positive (large, mobile vegetation on the aortic valve, severe, wide-open aortic regurgitation with an eccentric jet, moderate to severe mitral regurgitation, mitral valve diffusely thickened, and more focal thickening along P3 where a tiny vegetation is possible)DefiniteConfirmedNoNoIE clearly identified on TTE & TEE. IE missed on CMR, but the study was actually performed for purposes of a viability study to determine need for concomitant single vessel coronary artery bypass grafting during open heart surgery. Subsequently underwent surgical aortic valve replacement and mitral valve repair.

Abbreviations: CMR = cardiac magnetic resonance imaging, IE = infective endocarditis, TEE = transesophageal echocardiography, TTE = transthoracic echocardiography

CMR performance among patients treated for confirmed or presumed IE Abbreviations: CMR = cardiac magnetic resonance imaging, IE = infective endocarditis, TEE = transesophageal echocardiography, TTE = transthoracic echocardiography Furthermore, 6 of 14 cases (43%) were notable for delayed myocardial enhancement, most suggestive of an inflammatory or infectious fibrotic process, but these findings were deemed non-specific and did not guide medical decision making. In 3 of the 6 cases, patients were treated specifically for IE based on alternative findings. In the remaining 3 of the 6 cases, patients were not diagnosed with IE, but had concomitant indications for prolonged antibiotics.

Concomitant Indications for Prolonged Antibiotics

There was no significant difference in the duration of antibiotics for patients with CMR findings positive or equivocal versus negative for IE (6.0 vs 5.8 weeks, p=0.59). However, in 9 patients (64%) there were 13 separate indications for prolonged courses of antibiotics as outlined in Table 2. The indications included 7 cases (50%) of spinal involvement (e.g., vertebral osteomyelitis, diskitis, paraspinal or epidural phlegmon/abscess), 1 case (7%) of orthopedic hardware-related osteomyelitis, 1 case (7%) of septic arthritis, 2 cases (14%) of complicated skin and soft tissue infection, and 2 cases (14%) of psoas muscle abscesses.

Clinical Outcomes

Two cases (14%) underwent surgical valve replacement in addition to antibiotic therapy, of which only 1 of 2 cases had a vegetation visualized on CMR (Figure 1 ) as compared to 2 of 2 cases on TEE. Of the 5 cases (36%) that completed repeat blood cultures after antibiotic therapy, 100% remained negative. No readmissions for IE or deaths were reported among the entire study population over a follow up period of 1 year.
Figure 1

Vegetation of the right coronary valve leaflet measuring 0.6 × 1.1 cm associated with severe aortic insufficiency

Vegetation of the right coronary valve leaflet measuring 0.6 × 1.1 cm associated with severe aortic insufficiency

Discussion

Context

To the best of our knowledge, this is the third study ever conducted examining the real-world application of CMR as the primary imaging modality following TTE for the diagnosis of IE. Previously, Dursun et al. studied 16 patients with a preliminary diagnosis of IE and found 14 valvular vegetations in 11 patients on CMR; additionally, they noted delayed contrast enhancement attributable to extension of inflammation in numerous locations. They concluded that features of IE can be readily detected by CMR, via visualization of either valvular vegetations or delayed enhancement representing endothelial inflammation of the cardiovascular structures, and thus CMR could contribute to the diagnosis and management of IE. In contrast, Zatorska et al. studied 20 patients, and noted vegetation visualization was rather limited by the low spatial resolution of CMR, though they noted significant advantages in diagnosing perivalvular complications, assessing the degree of valvular insufficiency and resultant hemodynamic consequences, and evaluating the degree of myocardial inflammation.

Value of Findings

In our study, both the diagnostic accuracy and clinical utility of CMR for IE appear questionable. CMR detected valvular vegetations in 2 cases but also missed valvular vegetations in 2 cases; in comparison, when TEE was performed in 3 of these 4 cases, valvular vegetations were detected in all 3 cases. Additionally, in 1 case with a prosthetic aortic valve, magnetic susceptibility artifact reduced the diagnostic utility of the study. Moreover, 3 cases were treated empirically for IE regardless of CMR findings, based on clinical suspicion alone. Finally, 6 cases were notable for delayed myocardial enhancement, but these results were deemed non-specific and did not guide medical decision making. Taken together, these findings cast doubt on CMR as a viable diagnostic modality for IE at this time.

Pros and Cons of CMR

In theory, CMR confers many advantages in the diagnosis of IE. In addition to being a non-invasive modality utilizing non-ionizing radiation, there are multiple techniques available to gather a diverse array of clinical information. , Spin echo accurately defines cardiovascular anatomy, without the limitations of acoustic windows or attenuation artifacts due to body habitus associated with echocardiography and nuclear imaging respectively. Balanced steady state free precession cine quantifies ventricular cavity size and function, valvular function, and defines intracardiac masses. Phase contrast velocity mapping quantifies the severity of valvular regurgitation and stenosis. These quantitative measures are highly accurate, precise, and reproducible across studies as no geometric assumptions are required. Late gadolinium enhancement (LGE) patterns can help characterize myocarditis, and delayed hyperenhancement can help identify and characterize pericarditis. However, CMR is a rapidly evolving area of imaging. It requires deep local expertise and technical staff to appropriately protocolize and execute studies correctly. Electrocardiographic gating and breath holding or respiratory gating are required to achieve optimal temporal and spatial resolution. Magnetic susceptibility artifact from mechanical prosthetic valves and CIEDs can drastically affect diagnostic utility. Additionally, there are numerous considerations when contemplating a study including cardiac rhythm, renal function, CIED compatibility, ferromagnetic metallic implants, duration, cost, and availability of the modality.

Limitations

This study has several limitations. From a design perspective, the primary reason CMR was utilized was to prevent aerosol generation and thus protect healthcare workers. However, this risk must be balanced against the risk of transporting a critically ill or high-risk patient through the hospital to the MRI scanner, exposure risk to multiple personnel including nurses and technicians, contamination of the MRI room requiring full disinfection, and long acquisition times for MRI. , From a technical perspective, only 3 cases underwent TEE, thus limiting direct CMR versus TEE comparisons, particularly given TEE is the current gold standard. Additionally, the interpretation and management of delayed myocardial enhancement was unclear, thus confusing the clinical picture. Furthermore, regardless of the presence of IE, many patients had concurrent indications for prolonged antibiotic therapy, thus confounding the clinical picture. Finally, given such diverse clinical scenarios (e.g., type of organism, native vs prosthetic valve involvement, and underlying patient risk factors), small sample size, and low event rate of valvular vegetations, comparing long term outcomes is difficult.

Further Directions

The clinical scope of CMR continues to expand as capabilities increase and limitations are addressed. For spatial resolution, magnetic field strength is a critical factor with respect to image quality, signal-to-noise ratio, contrast-to-noise ratio, and acquisition time; newer magnet technologies allow significantly higher field strengths than the conventional 1.5 Tesla magnets, with many clinical laboratories utilizing 3 Tesla magnets, and research laboratories studying ultrahigh field strengths up to 9 Tesla with promising results and new challanges.20, 21, 22, 23 For temporal resolution, the recent development of four-dimensional (4D) flow CMR enables comprehensive assessment of blood flow via simultaneous velocity encoding that is resolved in all three dimensions of space and the dimension of time over multiple phases in the cardiac cycle. Recently this 4D flow CMR was utilized in conjunction with 3D TEE to characterize and intervene on a significant mitral paravalvular leak following a bioprosthetic mitral valve replacement for IE. For limitations related to electrocardiographic and respiratory gating as well as acquisition time, novel developments in post-processing promise to allow free-breathing, non-electrocardiographic techniques for obtaining sequences faster while preserving spatial and temporal quality.26, 27, 28 For limitations related to CIEDs, recent studies demonstrate that CMR in non-MRI-conditional systems, including those with hybrid configurations, is feasible and safe without clinically meaningful device parameter changes or adverse events. , Though, abandoned leads remain a challenge.31, 32, 33, 34 Recent advances in wideband LGE protocols, for both segmented and single-shot sequences, have demonstrated efficacy in accurately reducing device-related artifact, particularly with transvenous ICDs and cardiac resynchronization therapy devices.35, 36, 37

Conclusions

CMR may provide a viable alternative to TEE in settings where AGPs should be minimized, such as the COVID-19 pandemic. However, the role of CMR requires further clarification. In our study, CMR demonstrated mixed results in diagnosing valvular vegetations and guiding clinical decision making; additionally, a portion of patients were treated empirically for IE based on clinical suspicion alone, suggesting a lack of confidence in CMR as a valid diagnostic modality. Further prospective studies are needed to evaluate the performance of CMR relative to TEE for the diagnosis and management of IE. As CMR is a rapidly evolving technology, future developments may address current diagnostic limitations, particularly regarding temporal and spatial resolution.

Author Contributions

Sapan Bhuta: data collection/curation, formal analysis, writing - original draft, writing - review & editing. Neha J. Patel: data collection/curation, writing - review & editing. Jacob A. Ciricillo: data collection/curation. Michael N. Haddad: data collection/curation. Waleed Khokher: writing - review & editing. Mohammed Mhanna: writing - review & editing. Mitra Patel: writing - review & editing. Cameron Burmeister: writing - review & editing. Hazem Malas: writing - review & editing. Joel A. Kammeyer: Conceptualization, writing - review & editing, Supervision.

Disclosures

The authors have no relationships relevant to the contents of this paper to disclose.

Declaration of interests

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
  37 in total

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Authors:  Helge Skulstad; Bernard Cosyns; Bogdan A Popescu; Maurizio Galderisi; Giovanni Di Salvo; Erwan Donal; Steffen Petersen; Alessia Gimelli; Kristina H Haugaa; Denisa Muraru; Ana G Almeida; Jeanette Schulz-Menger; Marc R Dweck; Gianluca Pontone; Leyla Elif Sade; Bernhard Gerber; Pal Maurovich-Horvat; Tara Bharucha; Matteo Cameli; Julien Magne; Mark Westwood; Gerald Maurer; Thor Edvardsen
Journal:  Eur Heart J Cardiovasc Imaging       Date:  2020-06-01       Impact factor: 6.875

9.  Safety of magnetic resonance imaging in patients with cardiac implantable electronic devices with generator and lead(s) brand mismatch.

Authors:  Nareg Minaskeian; Sofia P Hajnal; Michael B Liu; Lindsay M Klooster; Katrina L Devick; Linda Schwartz; Clinton E Jokerst; Dan Sorajja; Luis Rp Scott
Journal:  J Appl Clin Med Phys       Date:  2022-01-23       Impact factor: 2.102

10.  Clinical intra-cardiac 4D flow CMR: acquisition, analysis, and clinical applications.

Authors:  Ahmet Demirkiran; Pim van Ooij; Jos J M Westenberg; Mark B M Hofman; Hans C van Assen; Linda J Schoonmade; Usman Asim; Carmen P S Blanken; Aart J Nederveen; Albert C van Rossum; Marco J W Götte
Journal:  Eur Heart J Cardiovasc Imaging       Date:  2022-01-24       Impact factor: 6.875

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