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J Am Coll Cardiol, 2005; 45:1435-1440, doi:10.1016/j.jacc.2005.01.037 © 2005 by the American College of Cardiology Foundation |
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* Division of Utah Artificial Heart Program, Salt Lake City, Utah
Department of Cardiology, LDS Hospital, Salt Lake City, Utah
University of Utah School of Medicine, Salt Lake City, Utah.
Manuscript received September 19, 2004; revised manuscript received January 1, 2005, accepted January 11, 2005.
* Reprint requests and correspondence: Dr. Steven C. Horton, 324 10th Avenue, Suite 206, Salt Lake City, Utah 84103. (Email: schorton{at}msn.com).
| Abstract |
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BACKGROUND: Mechanical circulatory support, primarily with a LVAD, is increasingly used for treatment of advanced heart failure as a bridge to transplant and for long-term treatment of heart failure. The LVAD dysfunction is a recognized complication. To date, no studies have defined the role of transthoracic echocardiography in evaluating long-term mechanical complications of chronic LVAD support.
METHODS: Transthoracic echocardiography was used in a protocol designed to detect the common types of mechanical malfunction. Patients were followed up with serial echocardiograms, and clinical validations were made with findings from a catheter-based protocol and inspection at the time of cardiac transplant or corrective surgery.
RESULTS: Thirty-two patients with 44 LVADs were followed up during a four-year period using this protocol that correctly identified 11 patients with inflow valve regurgitation, 2 with intermittent inflow conduit obstruction, 1 with severe kinking of the outflow graft, and 9 with new insufficiency of the native aortic valve.
CONCLUSIONS: As LVAD use for end-stage heart failure becomes widespread, and durations of support are extended, dysfunction will be increasingly prevalent. Transthoracic echocardiography provides a practical method to accurately identify the causes of mechanical dysfunction with patients on chronic LVAD support.
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The LVAD malfunction is an important cause of morbidity and mortality. Device failure was the second most common cause of death in the REMATCH trial; at 24 months post-implant, 35% of patients suffered device failure (3). As cardiologists provide care for more LVAD patients, it is important that they be able to troubleshoot a malfunctioning device.
Diagnosis of LVAD component malfunction remains a challenge. Diagnostic studies have not been standardized. A systematic catheter-based approach for the diagnosis of LVAD system malfunction has been reported but not one principally utilizing echocardiography (4).
Transesophageal echocardiography (TEE) is ideal for defining LVAD dysfunction in both the pre-operative and intra-operative setting (57). However, no studies have used echocardiography, especially the less invasive transthoracic echocardiography (TTE), to evaluate the long-term mechanical complications of discharged patients with chronic LVAD support.
Therefore, we prospectively followed up with patients discharged from the hospital with the HeartMate LVAD (Thoratec Corp., Pleasanton, California) and performed serial examinations with TTE to see if this noninvasive test could identify the common types of LVAD dysfunction.
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Twelve (38%) of the patients followed up with echocardiography underwent 17 angiographic evaluations for suspected LVAD dysfunction. Echocardiograms were performed within a 30-day window of the angiographic studies. All patients had their findings correlated at the time of corrective surgery. Eighteen patients with stable functioning LVADs underwent cardiac transplantation, and LVAD components were examined at that time.
Statistical analysis. Data for discrete variables are presented as percentages with sample sizes, and data for continuous variables are presented as mean with standard deviations or mean with range in the case of time periods. For tests of significance, the chi-square test was used for discrete variables and the t test was used for continuously distributed variables.
| Results |
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IVR. Eleven of the 42 LVADs (26%) had findings of IVR, with 3 of the LVADs developing new IVR during the study period. By the end of the study period, 9 of the 11 LVADs had progressed to having severe IVR. Doppler-echocardiography identified all eight patients with IVR by angiography and confirmed by surgery to have severely deformed inflow valves. Eighteen patients (56%) found to be IVR-free on echocardiography had successful cardiac transplantation. The inflow valves were inspected at explant. Seventeen patients had normal inflow valves, and one had only a minor gap between two inflow valve leaflets. Thus, absence of IVR was correctly identified in 100% of cases.
Pulsed Doppler at the inflow cannula found significant variability of the IVR flow relative to the native cardiac cycle. The IVR waveforms were denser with higher velocities when they occurred during native left ventricular (LV) diastole (Fig. 4).
Table 2 depicts the differences found in patients with IVR compared with patients without IVR. Normal function is associated with an outflow graft peak velocity of about 2.1 m/s and a calculated stroke volume of approximately 76 cc. Outflow graft velocities, VTI, and stroke volume were all significantly reduced in patients with IVR. Consistent with a decompressed heart, LV diastolic dimensions were generally normal in patients without IVR, and significantly dilated in patients with IVR.
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Outflow valve regurgitation. No cases of outflow valve regurgitation were found in the 71 TTEs. Absence of outflow regurgitation was confirmed in the 15 angiographic studies, and no deformities of the outflow valve were seen at surgery.
Inflow conduit obstruction. Two patients (6%) had significant obstruction to flow at the inflow conduit. In both cases, the usual laminar LVAD diastolic inflow into the apical cannula became intermittently interrupted (Fig. 6). In both cases, the intermittent obstruction was not clinically compromising.
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Native aortic valve disease. Of the 28 patients without aortic insufficiency before LVAD placement, 9 patients (32%) had mild, insignificant, aortic insufficiency during follow-up.
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Normally functioning LVAD. This study shows that the inflow cannula and its orientation within the LV as well as the outflow graft can be imaged. A stable functioning LVAD is generally associated with a normal-sized LV. Flow into the apical cannula during LVAD filling is unidirectional and laminar. Normal peak velocities and their associated stroke volumes within the outflow graft were defined. Infrequent opening of the aortic valve is seen in the stable LVAD, consistent with nonejecting decompressed LV.
IVR. Inflow valve regurgitation can be caused by a torn cusp or commissural dehiscence of the prosthetic (porcine) valve. This valve is under high mechanical stress as it opposes high pump chamber pressures. The rigid pumping chamber is unlike biological systems, which are compliant. Hypertension and outflow graft twisting increase afterload to the LVAD and may lead to inflow valve regurgitation (8).
Inflow valve regurgitation is the most common cause of LVAD dysfunction and was associated with a nondecompressed, dilated LV, and frequent opening of the aortic valve. Color flow Doppler directly visualizes IVR as a turbulent flow originating at the inflow cannula during the LVAD ejection period. Outflow graft flows are reduced significantly in LVADs with IVR.
Pulsed Doppler of the inflow cannula shows significant variability of the IVR flow in relation to the native cardiac cycle Ejection of the LVAD into the low pressures of LV diastole allows for a larger volume of IVR. When the LVAD ejects during LV systole, the LV pressures are higher, and a smaller regurgitant volume of IVR is ejected.
Native aortic valve distortion. The native aortic valve may become fused and cause aortic stenosis or insufficiency (9). Connelly et al. (10) examined hearts of patients with LVADs and found commissural fusion was more common in patients with VE HeartMates than pneumatic HeartMates (p < .0002). Hence, with effective LV decompression, aortic valve opening is minimized leading to commissural fusion.
This observational study is limited by its moderate number of patients but reflects the literature regarding the types of LVAD malfunctions that have been reported. Our practice has been to perform catheterization before corrective surgery to confirm LVAD dysfunction identified with TTE. In cases of inadequate visualization with TTE, we recommend TEE. All patients undergo TEE at the time of corrective surgery.
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