versão On-line ISSN 1027-202X
S. Afr. J. radiol. (Online) vol.19 no.1 Cape Town 2015
Antoinette ReindersI; Coert S. de VriesI; G. JoubertII
IDepartment of Clinical Imaging Sciences, University of the Free State, South Africa
IIDepartment of Biostatistics, University of the Free State, South Africa
BACKGROUND: Transcatheter aortic valve implantation (TAVI) provides an acceptable alternative for aortic valve replacement in the elderly, but needs accurate pre-procedural imaging to optimise intervention.
OBJECTIVES: To evaluate an alternative manual aortic valve calcification scoring system with computed tomography, for patients undergoing TAVI. We hypothesise a correlation between the Free State aortic valve calcium computed tomography score (FACTS) scoring system, valve plaque density and procedure-related complications.
METHODS: Twenty patients suitable for TAVI were selected according to standard international guidelines and received multimodality imaging prior to intervention. Images were reviewed by two reviewers who were blinded to each other's scores. Where large inter-individual score variations existed, retraining was done and scores repeated, using a double-blinded method. Matched scores were included in the final analysis. Rosenhek calcification scores were used as a standard of reference.
RESULTS: The study comprised 9 (45%) men and 11 (55%) women, with a median age of 83.5 years. Median EuroSCORE was 15.5. FACTS scores ≥6 were associated with the presence of a paravalvular leak (p = 0.01). Procedure-related complications (left bundle branch block, repositioning of the valve and anaemia) were seen in patients with plaques measuring ≥1000 HU (p = 0.07
CONCLUSION: The FACTS score and averaged valve plaque HU showed potential for predicting a paravalvular leak and procedure-related complications, and could be valuable in the future for optimising patient selection for TAVI.
Aortic stenosis is a global major debilitating health concern that is associated with high mortality and morbidity in the elderly population. Until recently, the only treatment for such patients was surgical aortic valve replacement, showing reasonable peri-operative results, but excluding a large number of symptomatic patients owing to unacceptably high peri-operative risk as indicated by a European Society of Cardiology score >20% (EuroSCORE) or Society of Thoracic Surgeons (STS) score >10.1
In the above pre-interventional scoring systems, patients are allocated specific numerical values according to comorbid conditions such as hypertension, hypercholesterolaemia and chronic obstructive pulmonary disease. Since the early 1990s, alternative routes for aortic valve replacement have been sought. 1,2,3 Transcatheter aortic valve replacement (TAVI) has emerged as a suitable and clinically better-tolerated alternative to surgical aortic valve replacement in selected patients.1 Results from the PARTNER trial (cohort B) showed an absolute reduction in one-year mortality of 20% with marked and durable improvement in functional status and reduced hospitalisation in patients who had undergone TAVI, compared with those who had been treated medically.1
Because TAVI is carried out in selected high-risk patients, pre-interventional assessment of the cardiac and aorta iliac anatomy is of the utmost importance.4 Trials have shown multi-detector computed tomography (MDCT) emerging as a valid alternative, and is in some institutions preferred to catheter angiography in assessing the aorta and ilio-femoral circulation prior to valve deployment. This trend is of particular importance in planning a percutaneous entry site as well as artificial valve sizing. MDCT is often also used as an adjunct to trans-oesophageal echocardiography in assessing the aortic annulus and valve cusps.4,5 This fast-growing approach has intertwined the interventional cardiologist's and radiologist's expertise, as well as heralded the start of a dedicated 'heart team' for adequate assessment of the suitability of a patient prior to TAVI.
Several MDCT acquisition protocols, including dual energy virtual non-contrast (DEVNC),6 have been suggested and reviewed in quantifying the aortic valve and annulus prior to percutaneous intervention with TAVI. Some authors advocate the Agatston7,8 calcium scoring method, whilst others rely on a 'gestalt' or manual scoring system based on the Rosenhek diagrammatic calcium score9 in an attempt to predict post-procedural outcomes in these high-risk patients. Heinsig8 alluded to the fact that patients with a high Agatston aortic valve calcification burden were more prone to paravalvular leaks (PVL) as well as a subsequent increase in hospital morbidity and one-year mortality post TAVI. He demonstrated this within a study population of 120 patients.7, 8 Although the Agatston aortic valve calcium score (AVCS) and its ability to predict the probability of a post-procedural paravalvular leak have been extensively written about in larger study groups,7,8,9 it has fallen out of favour at some institutions owing to its labour-intensive and time-consuming reconstructions. Manual scoring systems, on the other hand, have failed to accurately predict complications in patients undergoing TAVI as they do not take into consideration the density of the calcified plaque.
The aim of the present study was to describe our local experience with MDCT in evaluating patients with clinically significant aortic stenosis, in preparation for TAVI, specifically proposing an alternative manual system for grading the calcification of the aortic valves annulus as well as the cusps, denoting calcification burden and density with single-source MDCT. We aimed to hypothesise a link between the Free State aortic valve calcium CT score (FACTS) and valve plaque averaged Hounsfield units (AHU), with patient/procedure-related complications. We regarded complications such as paravalvular leak, stroke, death and myocardial infarction as major complications, and complications such as anaemia, left bundle branch block, and repositioning of the valve post/during the procedure as minor complications.
Research method and design
Materials and setting
A total of 20 patients from July 2011 - January 2013 were included. Consent was obtained from the hospital superintendent, prospective patients and the Faculty of Health Sciences Ethics Committee, University of the Free State, prior to the study (ECUFS no. 148/2012). Patients were evaluated by the Department of Cardiology, University of the Free State, and found eligible for TAVI. All fulfilled the criteria for clinically significant aortic stenosis, as determined by standardised inclusion criteria.10 No additional cardiac rhythm stabilising drugs were added to the patients' usual drug regime. Renal function was confirmed to be fit for intravenous contrast administration (Omnipaque 350, GE Healthcare Ireland, Cork, Ireland) prior to imaging. Exclusion criteria for imaging were severely impaired renal function <40 ml/min/1.73 m2 or previous severe adverse reaction to iodinated contrast material, such as anaphalactoid reaction, severe bronchospasm and cardiorespiratory collapse.11 Patients were evaluated by cardiac echocardiography (trans-oesophageal echocardiography (TEE) and trans-thoracic echo (TTE)) prior to and after TAVI at the cardiology interventional suite by dedicated echocardiographers using the Sellers technique as a guideline; see Table 1.
This was a pro- and retrospective, double-blinded, cohort analytical study.
Examinations were done on a single source, dual energy, high definition 64-detector CT scanner (HD750 Discovery, General Electric, Milwaukee). Patients were scanned using one of two standardised CT protocols, dependent on body weight (≥70 kg, 120 kV, 160 ml 350 Omnipaque; and ≤70 kg 100 kV 160 ml 350 Omnipaque), with ECG-prospectively gated, single-source energy scan of the chest, including gated cardiac CT and ungated single-source CTA of the abdomen and pelvis. Scan parameters were set with acquisition thickness of 0.625 mm, small field of view of 25 cm, a pitch of 0.16:1 and gantry rotation speed of 0.25 sec. - 0.35 sec., with kV and mAs dependent on body habitus. Scans were done in a craniocaudal direction on 75% of the RR interval. Automated bolus injection was implemented with the region of interest placed over the ascending aorta with scanning of the chest commencing at an attenuation value of 120 HU. Contrast was administered via an automated pump at 5 ml/sec., with a 40 ml saline bolus 'chaser' given after contrast injection.
Images were reviewed weekly by a qualified radiologist and a training fellow at the University of the Free State, Universitas Hospital Complex. Post processing of images took place on an Advantage Workstation 4.5 (General Electric) and analyses were performed using standard software (Reformat, General Electric). Data were loaded into a standard multiplanar reformat package, with image reconstructions in the coronal, sagittal and axial orientation and analysed using a multiplanar oblique tool. The coronal image was used to visualise the left ventricular outflow tract, with placement of the oblique tool in the middle of the ascending aorta, producing a sagittal oblique view. Placement of the oblique tool was in the centre axis of the ascending aorta, producing true axial images in the aortic leaflets and annulus planes, on which the calcification scoring was done. The aortic annulus and valve leaflets calcification burden was scored using a bone window level (WW2000 WL350).
Two views were used with the FACTS scoring of the aortic valve. The first view visualised the entire aortic annulus on the modified true axial views as done by using the multiplanar oblique tool. Outer ring scoring was done on this initial view. The second view visualised the distal ends of the leaflets as they converged; inner ring scoring was done on this view. The aortic annulus was divided into quarters on the first view and scored. One point was given for every calcification/plaque seen on the individual regions as described. The total score added to 16, where each valve had 4 possible sections as well as the annulus, which was also divided into 4 sections (Figure 1).
FACTS, Rosenhek and HU Score
FACTS scores were done individually and each observer blinded to the other's score. These scores were correlated to the Rosenhek diagrammatic calcium valve scoring system (Figure 2). The diagrammatic Rosenhek scoring system is shown in Figure 3.
Patients for whom the observers' FACTS scores showed a difference >15%/2 points were rescored, after retraining, by the same two observers and included in the final data set for statistical analysis. An agreement score was seen as a difference of up to 10%-15%/2 points between observers. Complications were associated with scores where the two observers were in agreement after the final scoring. Eighteen patients' FACTS scores and 16 patients' Rosenhek scores matched in the final analysis.
HUs were done separately to the FACTS scores and calculated on each aortic valve cusp. The largest calcified plaque density was taken on each valve cusp and summed. This figure was divided by a factor of 3 for an average score and grouped to either ≥1000 HU or <1000 HU as agreed upon between the observers, taking an HU ≥1000 as denoting calcified bone on routine CT. Correlations between the two observers' AHU scores were measured and 18 scores matched according to category.
All data (original and rescored) were captured and typed into a Microsoft Excel spreadsheet for statistical analysis. Age, race, sex, comorbid factors, grades of dyspnoea, left ventricular outflow fraction (prior and after the procedure) and presence of aortic regurgitation, complications and the presence of a pacemaker prior to and after procedures were included. Complications considered as major were stroke, myocardial infarction, death, paravalvular leak and 'other'. 'Other' included minor complications such as repositioning of the valve, anaemia post procedure and left bundle branch block. Patients' were followed up at 30, 90 and 180 days. No patients died during the follow-up period.
A total of 20 patients (9 men [45%] and 11 women [55%]), who happened to all be white, were enrolled in the study. Only 18 patients' FACTS scores were used in the final analysis. Patient demographics are shown in Table 2.
New York Heart association (NYHA) criteria were recorded prior to and following the procedure, with 35% of patients being NYHA 2, 50% NYHA 3, and 15% NYHA 4 prior to the procedure and showed marginal improvement post TAVI (NYHA 1 (10%), NYHA 2 (70%), and NYHA 3 (20%), but this was not statistically significant (p = 0.41). The median age of the patients was 83.5 years (range 68-95 years), with a EuroSCORE median of 15.5 (range: 5-22).
Sixteen (80%) of the 20 patients had a grade 1 aortic incompetence prior to TAVI, and 17 (85%) had paravalvular leak (PVL) post TAVI, of whom 10 patients had grade 1 PVL, 5 patients had grade 2 PVL, and 1 patient had grade 3 PVL. FACTS scores ≥6 were significantly associated with the presence of a paravalvular leak (p = 0.01) post TAVI. Grade 1 PVL = mild PVL, Grade 2 PVL = moderate PVL, and Grade 3 PVL = severe PVL. The FACTS scores were similar to the Rosenhek score in this regard, and both major and 'other' complications were seen to arise at a Rosenhek score >2, but were not statistically significant (p = 1.00; 'other' complications p = 0.09). No patient suffered from a myocardial infarction or death during or immediately after the procedure (see Figure 2). Nine patients fell into the 'other' complication category. The totals of complications were similar in both Rosenhek score groups, with both groups having close to the same number of complications in the 'other' category.
The median left ventricular ejection fraction (LVEF) was 56.5% (range 27%-77%) and marginally increased to 61.5% (range 29%-75%) at follow-up. Comorbid conditions (see Figure 4) prior to TAVI were recorded and were as follows: hypertension − 80%, diabetes − 15%, renal impairment − 10%), ischaemic heart disease − 35%), hypercholesterolaemia − 24%, chronic lung disease − 65%, peripheral vascular disease − 65%, and congestive cardiac failure − 5%.
Four patients received pacemakers; 1 was inserted prior to TAVI and 3 post TAVI. Left bundle branch block is a known complication of the TAVI procedure. All of our patients had degenerative aortic stenosis. An AHU ≥1000 was associated with 'other complications' amongst which left bundle branch block, anaemia post procedure and repositioning of the valve were seen; this was close to being statistically significant (p = 0.07). A graph of AHU v. complications is shown in Figure 5. AHUs ranged from 795 to 1336.
Only one female patient had a transient ischaemic event, which resolved in 24 hours. She had high FACTS and AHU scores (FACTS = 9 and AHU ≥1000). Male patients also had a higher incidence and grade of PVL than female patients, which we associated with a plaque density ≥1000 HU. One patient had a grade 3 PVL that was the result of initial incorrect positioning of the artificial valve, with a grade 1 PVL after repositioning of the Medtronic valve.
Plaques ≥1000 HU were associated with comorbidities; diabetes was found to be the main comorbid factor in plaque density differences, as seen in Figure 6.
No adverse events were recorded either during or after image acquisition. All TAVI procedures were performed after multidisciplinary discussion, using a transfemoral approach by a dedicated cardiac team, using the self-expandable Medtronic CoreValve.
Results were summarised by frequencies and percentages (categorical variables) and means or percentiles (numerical variables, depending on the distribution of the data). Groups were compared using chi-squared, Fisher's exact test or McNemar's test for categorical variables, the Kruskal-Wallis test, or Mann-Whitney test for numerical variables.
Benefits and hazards: If an association between plaque burden and density could be drawn to FACTS score ≥6 and HU ≥1000, pre-procedural evaluation could be streamlined and post-procedural complications be anticipated and timeously treated.
Recruitment procedures: Patients undergoing pre-interventional imaging were asked to take part in the study. Prospective and retrospective data capturing was done. No monetary compensation was offered to patients for taking part in the study. There was no discrimination against patients who declined participation.
Informed consent: Each patient received an information document, explaining the goal of the study and the imaging procedure involved. Patients were asked to sign this document prior to imaging, if they agreed to participate in the study.
Data protection: Patients' data were captured onto a standardised Excel sheet and numbers allocated to each patient. Only the first observer/researcher had access to patients' names. Confidentiality was maintained in all circumstances.
All TAVI procedures were performed by a dedicated cardiology team with the same two operators, with the standard use of a transfemoral approach. All patients' aortic valves were reviewed, and calcified valve plaques scored by the same two radiology reviewers on the same GE workstation, using a standard double-blinded method.
TAVI is an established percutaneous method for the treatment of critical aortic stenosis1,2,3,4,5,6,7,8,9,10,11,12 in high-risk patients and is relatively new in the South African context.12 The Agatston calcification scoring system5,7,8,10 for aortic valve calcification has been proposed in the past as well as manual valve plaque calcification scoring systems9 with and without the use of computer software, linking complications such as paravalvular leak and long-term patient survival to these scores13,14,15 and proposing better patient selection prior to intervention.
We aimed to introduce an alternative manual scoring system that was easy to implement, took plaque density into account, was not time consuming, and at the same time could predict clinically significant adverse patient outcomes. In our small study sample, we found that a FACTS score ≥6 was significantly associated with the presence of a paravalvular leak. Literature has shown that paravalvular leak post TAVI is an independent risk factor for longer hospital stay as well as an increased mortality risk factor at one-year follow-up.7 Procedure-related complication was close to statistically significantly associated with average valve plaque densities ≥1000 HU. Unfortunately, we were not able to differentiate between grades of paravalvular leak in our study, which could be attributed to our attempt to introduce a new manual scoring system and/or that our study population was small. Nevertheless, all the artificial valves were inserted by the same dedicated cardiology team, so the fact that an association between AHU score and complications such as anaemia, left bundle branch block and repositioning of the artificial valve could be shown is, we feel, some achievement.
We used the Rosenhek score as a reference standard, although in hindsight the two scoring systems are inherently different in that the FACTS and AHU scores offer quantification as well as qualification of the calcified plaques versus the first-mentioned score that only relies on a 'gestalt' or quantification of the calcification burden of the aortic valves, excluding the aortic annulus. Our score included the aortic annulus which, we postulate, could play a role in the pathology of paravalvular leaks post TAVI in our population. A possible reason for this could be the limited pliability of the aortic annulus with bulky calcified plaque. The Rosenhek score could also not differentiate between specific complications (e.g. stroke v. PVL) in our small study population but was, however, associated with no complications if the score was <2, when compared with the FACTS score; and, interestingly, the Rosenhek scores were seen to match in 80% of cases between the two observers, in the final statistical analysis. The LVEF and NYHA only marginally improved after TAVI procedure and were found to be statistically unrelated to either the FACTS or AHU scores. Pacemaker insertion could also be linked to high AHU scores, although this was not statistically significant and is a known complication of the Medtronic CoreValve.13
In our study population, complications were minimal, which could be due to the small study size or because the TAVIs were done meticulously by a qualified cardiac team. Moderate inter-individual variations were seen with the FACTS scores initially but, after retraining, the differences were markedly less. One explanation for the variation could be the relative inexperience of both observers with a new scoring system or because of the lack of experience in calcification scoring. Only two observers scored in this article. Maybe a larger number of observers could have improved the results. The FACTS and AHU scores were looked at individually and could have been incorporated into a single scoring system.
We recommend the incorporation of the AHU with the FACTS score in future for a uniform score, giving a specific numeral value to a specific HU density as well as a larger sample size. Individual scoring of the annulus versus the cusp calcification could also be considered for future studies.
The FACTS and AHU scores are easy to implement, not labour intensive or time consuming, and show promise in providing important added information for patients undergoing pre-interventional assessment for the TAVI procedure, especially in determining the risk of paravalvular leak, left bundle branch block, repositioning of the artificial aortic valve and anaemia. A larger study sample is necessary to confirm these preliminary findings.
The authors thank Dr W. Harmse, diagnostic radiologist and current fellow in Interventional Radiology, Alberta Health Services, Foothills Medical Centre; Professor S. Brown, Department of Paediatric Cardiology, University of the Free State; Professor H. Theron, Head of Department Cardiology, Universitas Academic Hospital, University of the Free State; and Mrs C. Swanepoel, Chief Radiographer Computed Tomography, Department of Clinical Imaging Sciences, University of the Free State, for their invaluable contribution to the completion and publication of the study.
The authors declare that they have no financial or personal relationships which may have inappropriately influenced them in writing this article.
A.R. (University of the Free State) protocol and study design, first blinded observer, writing and planning of the article draft and final version, main corresponding author. C.S.d.V. (University of the Free State) second blinded observer, study coordinator, protocol and final article draft reviewer. Professor G.J. (University of the Free State) is thanked for reviewing the statistics and protocols and for her invaluable input in the final draft of this article.
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1 Logeman Street
Universitas 9301, Bloemfontein, South Africa
Received: 03 Dec. 2014
Accepted: 12 Feb. 2015
Published: 04 June 2015