Literature DB >> 19410477

Late magnetic resonance surveillance of repaired coarctation of the aorta.

Rajesh Puranik1, Victor T Tsang, Smrithi Puranik, Rodney Jones, Seamus Cullen, Phillip Bonhoeffer, Marina L Hughes, Andrew M Taylor.   

Abstract

OBJECTIVE: Coarctation of the aorta has often been described as a simple form of congenital heart disease. However, rates of re-coarctation reported in the literature vary from 7% to 60%. Re-coarctation of the aorta may lead to worsening systemic hypertension, coronary artery disease and/or congestive cardiac failure. We aimed to describe the rates of re-coarctation in subjects who had undergone early coarctation repair (<2 years of age) and referred for clinically indicated or routine magnetic resonance (MR) surveillance.
METHODS: We retrospectively identified 50 consecutive subjects (20.2+/-6.9 years post-repair) imaged between 2004 and 2008. Patient characteristics, rates of re-coarctation and LV/aortic dimensions were examined.
RESULTS: Forty percent of subjects had bicuspid aortic valves (BAV). There were 40 cases of end-to-end repair and 10 cases of subclavian flap repair. Re-intervention with balloon angioplasty or repeat surgery had been performed in 32% of subjects. The MRI referrals were clinically indicated in 34% and routine in 66% of patients. Re-coarctation was considered moderate or severe in 34%, mild in 34% and no re-coarctation was identified in 32% of patients. There was no significant difference in the number of cases of re-coarctation identified in the clinically indicated versus routine referrals for MR imaging (p=0.20). There were no cases of aortic dissection or aneurysm formation identified amongst the subjects. The mean indexed left ventricular mass and ejection fraction was 72+/-16g/m(2) and 66+/-6%, respectively. Amongst those subjects with BAV there were larger aortic sinus (30+/-1mm vs 27+/-1mm, p=0.03) and ascending aortic (27+/-1mm vs 23+/-1mm, p=0.01) dimensions when compared to subjects with morphologically tricuspid aortic valves.
CONCLUSIONS: We demonstrate that many years after early repair of coarctation of the aorta, MR surveillance detects significant rates of re-coarctation. These findings were independent of whether or not there was a clinical indication for imaging. Those patients with BAV disease had larger ascending aortic dimensions and may require more frequent non-invasive surveillance.

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Mesh:

Year:  2009        PMID: 19410477      PMCID: PMC2706949          DOI: 10.1016/j.ejcts.2009.02.056

Source DB:  PubMed          Journal:  Eur J Cardiothorac Surg        ISSN: 1010-7940            Impact factor:   4.191


Introduction

Coarctation of the aorta has often been described as a simple form of congenital heart disease by cardiologists. However, rates of re-coarctation reported in the literature vary from 7% to 60% [1-4]. Re-coarctation of the aorta may lead to worsening systemic hypertension, coronary artery disease and/or congestive cardiac failure [5], making long-term follow-up of this condition more complex than initially thought. Repair of coarctation of the aorta in infancy has the reported benefits of increased long-term survival [6]. Despite this, late cardiovascular complications have been shown to develop even after apparently successful coarctation surgery [7-9]. Thus, recent attention has been given to the optimal long-term imaging strategy for this condition. Specifically, Therrien et al. have demonstrated that the combination of clinical examination plus magnetic resonance (MR) imaging is the most cost-effective non-invasive strategy to diagnose complications at the site of repair many years after coarctation surgery [5]. We therefore aimed to retrospectively examine findings from MR imaging for both clinically indicated and routine scans in individuals where early repair (<2 years of age) of coarctation was performed and who are now followed-up in our adult congenital heart disease service.

Materials and methods

Patient recruitment

Between 2004 and 2008 we retrospectively identified 50 consecutive subjects referred from our adult congenital heart disease service for MR follow-up of repaired coarctation of the aorta. In all subjects coarctation repair surgery was performed <2 years of age at our institution. Scans were regarded as either clinically indicated by the referring physician or as routine where no clinical indication was identified on physical examination or 2D-echocardiography. Patient characteristics including; age at repair, type of repair, re-intervention procedures required, associated cardiac conditions, body mass index, heart rate, and resting blood pressure were recorded. The local research ethics committee approved the study, and all subjects gave informed consent at the time of the MR scan.

Cardiac MR imaging

MR imaging was performed using 1.5T MR scanner (Avanto, Siemens Medical Systems, Erlangen, Germany).

Measurement of aortic dimensions

Dimensions of the aorta were determined from MR angiography. This was performed with a T1 weighted spoiled gradient echo sequence. Imaging parameters: TR = 3.3; TE = 1.0; flip angle = 25°; matrix = 256 × 256; which was triggered visually and was acquired in a 15 s breath-hold. Measurements were systematically made at the level of the sinus of Valsalva, proximal ascending aorta, transverse aortic arch, residual coarctation site, proximal descending aorta and distal descending thoracic aorta at the level of the diaphragm. Aortic re-coarctation was defined according to the percent residual coarctation diameter/descending thoracic aorta diameter at the level of the diaphragm where, no re-coarctation >80%, mild re-coarctation 61–80%, moderate re-coarctation 41–60% and severe re-coarctation <40%.

Aortic cine and flow imaging

Cine images of the entire thoracic aorta were acquired using retrospectively gated steady-state free precession (SSFP) MR imaging. Image parameters: TR = 2.4 ms; TE = 1.2 ms; flip angle = 78°; slice thickness = 6–8 mm; matrix = 144 × 192; field of view = 300–380 mm and temporal resolution = 25 phases; acquired during a single breath-hold. Specific attention was given to the region of the proximal descending aorta where previous aortic surgery was performed. Aortic flow data were acquired using a flow-sensitive gradient-echo sequence (TR, 27 ms; TE, 3.2 ms; flip angle, 30°; slice thickness, 5 mm; and matrix, 192 × 256) during free breathing. Imaging planes were located in the proximal ascending aorta [10]. Through-plane flow data (30 phases per cardiac cycle) were acquired by use of retrospective cardiac gating. Arterial blood flow was calculated from phase contrast images by use of a semiautomatic vessel edge-detection algorithm (Argus; Siemens Medical Systems, Erlangen, Germany) with operator correction. Aortic valve regurgitation fraction (RF %) was calculated as percent backward aortic flow/total aortic flow.

Assessment of ventricular volumes, function and mass using cine MR imaging

SSFP cine MR images of the heart were acquired in the vertical long-axis, four-chamber view and the short-axis view covering the entirety of both ventricles (9–12 slices). Image parameters used were as described above. Assessment of left ventricular volumes was performed by manual segmentation of short-axis cine images with endocardial outline at end-diastole and end-systole (Argus; Siemens Medical Systems, Erlangen, Germany). End-diastolic and end-systolic volumes were calculated by use of Simpson's rule, and from these volumes the ejection fraction was calculated. Left ventricular mass was determined in end-diastole via manual segmentation of the endo- and epi-cardium from short-axis images. This value was indexed to body surface area.

Statistical analysis

All data are presented as mean ± SD or median and range. Statistical comparison of parametric data was performed with a two-tailed unpaired Student's t-test. The relationship between dichotomous variables was tested with Fisher's exact test. A value of p < 0.05 was considered statistically significant. Statistical testing and data analysis were performed with GraphPad Prism Version 4.0 (San Diego, CA).

Results

Patient characteristics (Table 1)

The mean age of patients in the study and years from repair of coarctation was 22.0 ± 6.5 years and 20.2 ± 6.9 years, respectively. The median age at repair was 4.0 days (range 1–630 days) with 62% of repair surgery being performed by 1 month of age. End-to-end repair was used in 80% (40/50) of patients and subclavian flap surgery was used in the remainder. Thirty-two percent (16/50) of patients required a re-intervention procedure after the initial surgical repair (12 cases treated with percutaneous balloon procedures and four cases treated with surgery). Three patients required an additional procedure subsequent to their first re-intervention. Patients had normal resting haemodynamics and body mass index (Table 1).
Table 1

Patient characteristics.

n = 50
Mean age (years)22.0 ± 6.5
Median age at repair (days)4.0 (range 1.0–630)
Mean years since repair20.2 ± 6.9
Gender62% male, 38% female
Body mass index (kg/m2)24.5 ± 4.9
Heart rate (beats/min)74 ± 11
Blood pressure (mmHg)127/70 ± 15/9
Type of repair80% end-to-end 20% subclavian patch repair



Re-interventions post-initial surgery1st re-intervention performed in 36%
2nd re-intervention performed in 6%



Associated conditions at the time of surgeryBAV (n = 20), VSD (n = 8), sub-Ao stenosis (n = 5), AR (n = 3), MVD (n = 1)

Characteristics for all 50 patients are detailed with data presented as mean ± SD or median and range where stated. BAV: bicuspid aortic valve disease, VSD: ventricular septal defect, sub-Ao: sub aortic, AR: aortic regurgitation, MVD: mitral valve disease.

In regards to associated lesions, 40% (20/50) of patients had bicuspid aortic valves, 16% (8/50) of patients had a ventricular septal defect repaired at the time of coarctation surgery and 10% (5/50) of patients had sub-aortic stenosis resection performed. There were three patients with significant aortic valve regurgitation (regurgitation fraction >10%) and one patient with mitral valve disease. Scans were clinically indicated in 34% (17/50) of patients. Specifically, new-onset hypertension or hypertension refractory to therapy was the reason for referral in 14 cases. In a further three cases 2D echocardiography findings of increased peak velocity across the aortic arch led to the referral for MR imaging. The remaining 66% (33/50) of cases were regarded as routine scans, where there were no abnormal clinical/echo findings identified.

Cardiac MR imaging (Table 2, Figs. 1 and 2)

Re-coarctation of the aorta was identified in 68% (34/50) of patients. Specifically, mild re-coarctation was found in 34% (17/50) of patients and moderate or severe re-coarctation was found in 34% (17/50) of patients (Fig. 1). Eighty-two percent of patients in whom re-coarctation was identified had an end-to-end repair performed initially. There were no cases of aortic dissection or aneurysm formation identified amongst the cohort. There was no statistically significant difference in the number of cases of re-coarctation identified in either the clinically indicated or routine referrals for MR imaging (p = 0.20).
Fig. 1

Rates of re-coarctation. Pie graph showing the proportion of patients with no, mild or moderate/severe re-coarctation identified in follow-up MR imaging. Re-CoA: re-coarctation.

The dimensions of the entire thoracic aorta and functional data and dimensions for the left ventricle are summarised in Table 2. Twenty-eight percent (14/50) of patients had post-stenotic dilatation of the proximal descending aortic arch. The mean left ventricular ejection fraction and indexed mass were normal for the cohort, being 66 ± 6% and 72 ± 16 g/m2, respectively. When subjects in whom there was evidence of re-coarctation were compared with no re-coarctation, left ventricular ejection fraction and indexed mass were similar for both (67 ± 1% vs 66 ± 2%, p = 0.59 and 71 ± 3 g/m2 vs 74 ± 6 g/m2, p = 0.82, respectively).
Table 2

Aortic dimensions and left ventricular parameters.

n = 50Aortic dimensions (mm)
Sinus of Valsalva28 ± 5
Proximal ascending aorta25 ± 5
Transverse aortic arch16 ± 4
Region site of previous CoA surgery13 ± 4
Proximal descending aorta19 ± 4
Distal descending thoracic aorta (diaphragm level)17 ± 3

Aortic dimensions for the entire thoracic aorta and indexed parameters for left ventricular volumes, function and mass are detailed for the patients (n = 50). Data are presented as mean ± SD. CoA: coarctation, LV: left ventricle, EDV: end-diastolic volume, ESV: end-systolic volume, SV: stroke volume.

When patients with morphologically tricuspid aortic valves (n = 30) were compared with bicuspid aortic valves (n = 20), there was no difference in the number of cases reported to have re-coarctation (p = 0.14). However, patients with morphologically bicuspid aortic valves had larger aortic dimensions at the level of the sinus of Valsalva (30 ± 1 mm vs 27 ± 1 mm, p = 0.03) and proximal ascending aorta (27 ± 1 mm vs 23 ± 1 mm, p = 0.01) than patients with tricuspid aortic valves (Fig. 2). Aortic dimensions for the transverse arch and the descending thoracic aorta were similar between the groups.
Fig. 2

Aortic dimensions-tricuspid versus bicuspid aortic valves. Mean aortic dimensions for patients with morphologically tricuspid (n = 30) and bicuspid (n = 20) aortic valves are shown. Measurements were made at the level of the sinus of Valsalva and proximal ascending aorta. The results are expressed as mean ± SD, p < 0.05 was considered statistically significant.

Discussion

We demonstrate that many years after infantile repair of coarctation of the aorta, MR surveillance detects significant rates of re-coarctation. Specifically, we identified at least mild re-coarctation in over 2/3 of the cohort referred for follow-up scanning. These findings were independent of whether a clinical indication for imaging was identified. Additionally, those patients with bicuspid aortic valves had larger ascending aortic dimensions when compared to patients with morphologically tricuspid aortic valves. The rationale for early repair of coarctation of the aorta in infancy has been the reported benefits of increased long-term survival [6,11]. Despite this, late cardiovascular complications have been shown to develop even after apparently successful coarctation surgery [7-9]. Re-coarctation of the aorta may lead to worsening systemic hypertension, coronary artery disease and/or congestive cardiac failure [5]. Our data suggest significant rates of re-coarctation amongst patients in whom early operative repair of aortic coarctation was performed two decades prior. Therrien et al. have demonstrated that the combination of clinical examination plus MR imaging is the most cost-effective strategy to diagnose complications at the site of repair many years after coarctation surgery [5]. Although the sensitivity of echocardiography is reasonably high for detection of re-coarctation, this is tempered by lower image resolution (particularly in adults) and technical difficulties in obtaining a representative Doppler gradient in the presence of collateral vessel flow. The issue that remains unresolved and warrants further prospective investigation is the optimal timing of serial imaging in this group. We identified larger ascending aortic dimensions in patients with repaired coarctation of the aorta and morphologically bicuspid aortic valves which is consistent with previous descriptions [12]. It is recognised that bicuspid aortic valve disease is often associated with connective tissue disorders [13-17], which may lead to aortic dilatation even in the absence of haemodynamically significant aortic valve pathology. This leaves the patient at risk of aneurysm formation, aortic dissection and sudden death. Importantly amongst our cohort we were unable to identify aneurysm formation or dissection in either the region of coarctation repair or the ascending portion of the aorta. Although there is a paucity of data pertaining to the risk of aortic dissection in subjects with bicuspid aortic valve disease, it is generally believed that increasing risk is directly proportional to increasing aortic dimensions [18]. Hence current ACC/AHA guidelines recommend that patients with bicuspid aortic valves and dilated aortic root dimensions (>40 mm) should undergo routine yearly serial evaluation [18]. It can be argued that subjects with previously repaired coarctation and bicuspid aortic valve disease present a ‘high risk’ group amongst these subjects and in whom more frequent screening protocols may be warranted. The retrospective nature of this study and relatively small numbers presents a limitation to our findings. Serial prospective data detailing the rate of progression of re-coarctation and ascending aortic dimensions would have been ideal in order to more completely understand optimal timing for screening protocols. This is especially the case in those patients who have mild re-coarctation. The rate of progression and clinical significance of this group can only be accurately determined prospectively. The patients in our study were referred from our adult congenital heart disease service and although the majority of scans were deemed routine there may well still be a selection bias which explains the relatively high rate of re-coarctation identified. In conclusion, coarctation of the aorta has often been described as a simple form of congenital heart disease. Rates of re-coarctation in adult subjects who were repaired early in life suggest that this is in fact a complex condition, which requires intensive long-term surveillance in order to avert serious morbidity and/or mortality. In our study, there was a significant rate of re-coarctation identified in scans performed on a routine basis i.e. in which there was no obvious clinical indication. More frequent screening protocols may also be warranted in those patients who have bicuspid aortic valve disease in addition to previously repaired coarctation of the aorta.
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