(Stroke. 2006;37:2035.)
© 2006 American Heart Association, Inc.
Original Contributions |
From the Departments of Neuroradiology (Michèle Hamon, P.C.), Cardiology (S.G., R.S., T.L., G.G., Martial Hamon), and Statistics (R.M.), University Hospital of Caen, Normandy, France; and the Department of Neuroradiology (C.O.), Sainte-Anne Hospital, Paris Descartes University, Paris, France.
Correspondence to Martial Hamon, Service de Cardiologie, Centre Hospitalier Universitaire de Caen, Avenue Côte de Nacre, 14033 Caen, Normandie, France. E-mail hamon-m{at}chu-caen.fr
| Abstract |
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Methods This prospective study involved 46 patients with severe aortic valve stenosis. To assess the occurrence of cerebral infarction, all patients underwent cerebral DW MRI and neurological assessment within 24 hours before and 48 hours after cardiac catheterization and retrograde catheterization of the aortic valve. A subgroup was monitored by transcranial power M-mode Doppler during cardiac catheterization to observe cerebral blood flow and track emboli.
Results One patient had a focal diffusion abnormality on DW MRI before cardiac catheterization. After catheterization, we detected only 1 additional acute cerebral diffusion abnormality in a single case (2.2%), although cerebral microemboli were detected in all transcranial Doppler-monitored patients during cardiac catheterization, as expected. All patients remained asymptomatic. Based on these results a mid-point incidence of 5.9% (95% CI, 0.01 to 12.5) for abnormalities on DW MRI in asymptomatic cardiac catheterization patients in our center can be assigned.
Conclusions Unsuspected cerebral infarctions can be detected by DW MRI after cardiac catheterization, but this phenomenon remains unfrequent in our series. Further studies are needed to identify factors explaining the discrepancy between these results and those of previous studies.
Key Words: cardiac catheterization cerebral embolism diffusion magnetic resonance imaging magnetic resonance imaging ultrasonography, Doppler, transcranial
| Introduction |
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Indeed the high sensitivity of DW MRI suggests that this technique could allow an improved estimate of cerebral ischemic events associated with cardiovascular-catheter procedures.9 We therefore performed DW MRI before and after cardiac catheterization to prospectively assess both clinically silent and apparent cerebral embolisms.
| Patients and Methods |
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Cardiac Catheterization
All patients were examined clinically and assessed for any history of previous cerebral embolism. Transthoracic echocardiography, 12-lead surface ECG, and coronary angiography were performed for all patients. Cardiac catheterizations were undertaken by expert interventional cardiologists using a standard Seldinger technique using 5 French (F) catheters. Sheaths were removed immediately after the procedure in all patients. We gave 5000 IU of unfractionated heparin intravenously to all patients at the beginning of the procedure. Retrograde catheterization of aortic valve was attempted in a right oblique projection using a long exchange guide wire (0.035 inch, 260 cm length to ensure exchange of the pigtail catheter) using a left amplatz 1 catheter or a right Judkins catheter. During attempts to cross the aortic valve, the wire was regularly withdrawn and cleaned and the catheter flushed every 2 minutes according to Grossmans recommendations.10 When the pigtail catheter was placed in the left ventricle, the wire was withdrawn and the catheter vigorously aspirated and pressure measurements performed. After left ventriculography, the catheter was rapidly withdrawn from the left ventricle into the ascending aorta with simultaneous pressure measurements. Maximum and mean pressure gradients were established. We recorded the duration of the whole procedure and fluoroscopic time in all patients.
MRI
MRI was done within 24 hours before and 48 hours after cardiac catheterization. We performed MRI examinations with 1.5 Tesla system (GE Health Care). The imaging protocol included a DW single-shot spin echo echoplanar sequence acquired in the AC-PC (anterior commissure-posterior commissure) plane with 24 contiguous sections (diffusion gradient b values of 0 and 1000 s/mm2, repetition time [TR] 6000 ms, echo time [TE] 120 ms, slice thickness 6 mm with no gap, matrix of 128x128 pixels, and field of view of 240 mm); fluid-attenuated inversion recovery (FLAIR; TR/TE 10 000/160 ms, inversion time 2200 ms); and T2-weighted turbo spin echo sequences (TR/TE 3500/94 ms). For DW MRI, the diffusion gradients were successively and separately applied in 3 orthogonal directions for a total acquisition time of 24 seconds. Trace images were then generated and apparent diffusion coefficient maps calculated with a dedicated software tool (Functool; General Electric). The image analysis was performed independently by 2 experienced neuroradiologists (Michèle Hamon, C.O.) who were blinded to the clinical data and were unaware of the technical aspects of the angiographic cardiac procedure. For analysis of DW MRI, the neuroradiologists were asked to determine the presence, size, number, and vascular distribution of any focal diffusion abnormalities (bright lesions) in a pattern consistent with embolic lesions.
TCD
TCD studies for this work were performed with the TCD power M-mode Doppler 100 (PMD100, Spencer Technologies) which calculates a power M-mode Doppler image concurrently with a 2-MHz single-gate spectrogram as previously described.11
Microembolic signals present a unique signature or "track" in the power M-mode Doppler image (slope consistent with the speed of blood flow across the vessel segments in view) which defines them as representing emboli and facilitating exclusion of potential artifacts. In partcular, artifacts tend to show significant power signature at all gates simultaneously, whereas true embolic signals have a progression across depth as time changes.12 The number of microembolic signals for all TCD recordings was assessed by an independent investigator unaware of the DW-MRI results.
Statistical Analysis
Baseline characteristics of the study population are presented as counts and percents for categorial variables and as mean±SD for continuous variables.
statistic was calculated to determine interobserver agreement. The number of lesions in our population of patients recruited was estimated by the adjusted Wald interval at 95% in accordance with the method recommended by Agresti and Coull.13 With small sample sizes, as recommended we have used the mid-point of the adjusted Wald interval instead of the observed proportion.14 The statistical analyses were performed using SPSS 10.0.7 program.
| Results |
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Successful transcranial Doppler recordings were made in the final 12 consecutive patients in the series (26%). In all patients with TCD recordings, we identified systematic cerebral microembolism with a mean of 72±37 high-intensity transient signals per procedure.
A total of 92 DW MRI were evaluated blindly. All patients underwent cerebral DW MRI (5±2 hours) before and (13±10 hours) after cardiac catheterization. Before cardiac catheterization, 1 patient had a hyperintense focal lesion on DW MRI. After the procedure only 1 new acute focal bright cerebral diffusion abnormality was found in a single case. This case was an 82-year old woman with normal left ventricular ejection fraction without carotid stenosis or atrial fibrillation but with prior history of hypertension, hypercholesterolemia and diabetes. The duration of the catheterization procedure was 22 minutes with a fluoroscopic time of 7 minutes.
No diffuse alterations in DW MRI or pattern of watershed ischemia were found in any patient. Subsequent comparison of pre- and postcardiac catheterization studies by the 2 readers indicated 98% agreement with a
value of 0.93 (given the small and focal lesion documented in only 1 case mutual assessment was required for full agreement). Statistical analysis yielded an upper boundary of 12.5% for the incidence of abnormalities on DW MRI in asymptomatic patients who had undergone cardiac catheterization with retrograde catheterization of severe aortic valve stenosis in our center; this value can be assigned with 95% confidence with a mid-point of 5.9% and is significantly different compared with previous studies (P<0.02; Table 2) especially in patients explored for aortic valve stenosis (P<0.002).
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| Discussion |
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Based on a previous study of Omran et al3 in patients with aortic stenosis who had undergone retrograde catheterization of the aortic valve, a 22% rate of silent cerebral infarction was expected in our series of patients. However, in our prospective evaluation including 46 patients and using serial cerebral DW MRI, we identified only 1 asymptomatic patient (2.2%) with such an event in association with retrograde catheterization of the aortic valve.
Other groups have recently documented that silent acute brain injury can also be associated with percutaneous cardiac interventions (PCI), with possible cognitive impairment for patients in whom new lesions are identified on DW MRI.4,5 It seems that only the length of the procedure or the procedural fluoroscopy time can be independently associated with the risk of cerebral infarction in these studies. These 2 parameters are related to the overall influence of the catheter manipulation, including additional periods of time required while the catheter acts as a embolic source; this factor may lead to thrombus formation or affect the vessel wall during manipulation or placement in patients vascular system. In addition, as previously assumed, plaque debris broken off from the aorta or the aortic arch, blood clots from the tip of the catheter, or air embolism risk must also be considered in assessing microembolism during heart catheterization. It appears likely that all these well-recognized risks of cerebral embolism for patients who undergo heart catheterization can be related to the duration of the procedure. It is notable that in our study the mean fluoroscopy time needed to cross the aortic valve was shorter than in the study of Omran et al.
All our catheterization procedures were performed at a high-volume center (>3000 diagnostic and 1300 interventional procedures per year) with standard techniques that appear similar to those recently reported and that are associated with a high rate of acute brain injury, as documented by DW MRI.3,4,5 All reported studies (see Table 2) used heparin during the procedure with standard commercially available materials for catheters and contrast media. The only characteristic that could have influenced the results in addition to the length of the procedure is the size of catheters used; in previous studies, catheters were 6 F and sometimes 7 F for PCI. Smaller catheters, such as the 5 F used in all our cases, could have minimized the risk of arterial injury and the source of embolism during retrograde passage of the aortic valve.
Because all cardiac catheterizations are associated with microembolism as detected by TCD (confirmed in our substudy analysis), it has been suggested that most of these microembolisms are likely benign microbubbles.6,7 However, some recent studies have raised the possibility that some microparticles embolized during heart catheterization could be responsible for acute brain injuries.3,4,5 In fact, the most likely sources of embolic material are catheters and guidewires that dislodge atheromatous material from the aortic arch. Visible aortic debris may be seen on withdrawal of catheters during PCI cases. Patients with a large atherosclerotic burden in the aorta (such as those with advanced coronary artery disease), as documented by transesophageal echocardiography, have an increased risk of cardiac catheterization-induced stroke.16,17,18 The more extensive coronary artery disease and longer fluoroscopy times identified in previous studies as risk factors for stroke can be considered as surrogate markers of prolonged, complex catheter manipulations in a severely atherosclerotic aorta. It has been shown that patients with cardiac catheterization-induced stroke often have multiple acute lesions (often tiny, cortical, and in different vascular territories) on DW MRI distinct from the occasional symptomatic lesion and consistent with a shower of embolic material. Given the rate of these unsuspected lesions and the potential consequences related to cognitive impairment, other studies are warranted to determine the risk factors associated with these deleterious effects of heart catheterization.
Among potential limitations of the present study one could argue that differences might exist in the interpretation of cerebral DW MRI. Such differences in MR image interpretation between centers seem unlikely because DW MRI has been routinely used for diagnosis of infarcted brain tissue for several years now and all images were evaluated by experienced neuroradiologists. Another issue is related to the delay between the cardiac catheterization and the postprocedural DW MRI. Indeed the optimal time to detect potential ischemic lesions using DW MRI is unknown. However, it has been documented that 24- to 48-hour DW MRI did not increase diagnostic accuracy in any case in which the 2- to 4-hour study was negative suggesting that early assessment could be performed in asymptomatic patients.19 Finally, given the number of high-intensity transient signals observed during each catheterization procedure we cannot exclude diffuse and subtle brain injury undetectable by DW MRI in some cases. The ability of neuropsychological tests to address this specific issue warrants further study.
In conclusion, in this prospective study we confirm that cerebral microembolism as detected by TCD occurs for all patients during cardiac catheterization without correlation with the risk of brain injury. Even after retrograde catheterization of valvular aortic stenosis, new cerebral lesions on DW MRI is unfrequent in our center. Further studies are warranted to identify factorsincluding catheterization methods, pharmacological environment, and selection of materials20,21 that could explain this discrepancy with previous studies. Finally, performing pre- and postprocedure DW MRI could be used to monitor the procedure-related frequency of ischemic lesions and to assess the benefit of changes in practice to improve the safety of cardiac angiography and catheterization.
Received January 28, 2006; revision received March 21, 2006; accepted May 3, 2006.
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