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The silent and apparent neurological injury in transcatheter aortic valve implantation study (SANITY): concept, design and rationale
- Jonathon P Fanning1, 2, 3Email author,
- Allan J Wesley1, 4,
- David G Platts1, 2, 3, 9,
- Darren L Walters1, 3, 9,
- Eamonn M Eeles1, 7,
- Michael Seco5, 6,
- Oystein Tronstad2, 3, 8,
- Wendy Strugnell4,
- Adrian G Barnett10,
- Andrew J Clarke3, 8,
- Judith Bellapart1, 2,
- Michael P Vallely5, 6, 11, 12,
- Peter J Tesar3, 8 and
- John F Fraser1, 2, 3, 13
© Fanning et al.; licensee BioMed Central Ltd. 2014
Received: 27 January 2014
Accepted: 4 March 2014
Published: 5 April 2014
The incidence of clinically apparent stroke in transcatheter aortic valve implantation (TAVI) exceeds that of any other procedure performed by interventional cardiologists and, in the index admission, occurs more than twice as frequently with TAVI than with surgical aortic valve replacement (SAVR). However, this represents only a small component of the vast burden of neurological injury that occurs during TAVI, with recent evidence suggesting that many strokes are clinically silent or only subtly apparent. Additionally, insult may manifest as slight neurocognitive dysfunction rather than overt neurological deficits. Characterisation of the incidence and underlying aetiology of these neurological events may lead to identification of currently unrecognised neuroprotective strategies.
The Silent and Apparent Neurological Injury in TAVI (SANITY) Study is a prospective, multicentre, observational study comparing the incidence of neurological injury after TAVI versus SAVR. It introduces an intensive, standardised, formal neurologic and neurocognitive disease assessment for all aortic valve recipients, regardless of intervention (SAVR, TAVI), valve-type (bioprosthetic, Edwards SAPIEN-XT) or access route (sternotomy, transfemoral, transapical or transaortic). Comprehensive monitoring of neurological insult will also be recorded to more fully define and compare the neurological burden of the procedures and identify targets for harm minimisation strategies.
The SANITY study undertakes the most rigorous assessment of neurological injury reported in the literature to date. It attempts to accurately characterise the insult and sustained injury associated with both TAVI and SAVR in an attempt to advance understanding of this complication and associations thus allowing for improved patient selection and procedural modification.
Clinically apparent cerebrovascular events
Classification and definitions of neurological injury/impairment
A. Cerebrovascular events
Cerebral infarcts that are observed on magnetic resonance imaging (MRI) scans in the absence of any corresponding, clinically apparent cerebrovascular ischaemic event.
Acute episode of a focal or global neurological deficit with at least one of the following: change in the level of consciousness, hemiplegia, hemiparesis, numbness, or sensory loss affecting one side of the body, dysphasia or aphasia, hemianopia, amaurosis fugax, or other neurological signs or symptoms consistent with stroke.
Duration of a focal or global neurological deficit ≥ 24 hours; OR <24 hours if available neuroimaging documents a new hemorrhage or infarct; OR the neurological deficit results in death.
i. Ischemic: an acute episode of focal cerebral, spinal or retinal dysfunction caused by infarction of the central nervous system tissue.
ii. Haemorrhagic: an acute episode of focal or global cerebral or spinal dysfunction caused by intraparenchymal, intraventricular, or subarachnoid haemorrhage.
iii. Undetermined: insufficient information to allow categorization as ischemic or haemorrhagic.
i. Disabling stroke (Major): an mRS of 2 or more at 90 days and an increase in at least one mRS category from an individuals pre-stroke baseline.
ii. Non- disabling stroke (Minor): an mRS score of <2 at 90 days or one that does not result in an increase in at least one mRS category from an individual’s pre-stroke baseline.
Duration of a focal or global neurological deficit <24 hours, any available neuroimaging does not demonstrate a new haemorrhage or infarct.
• Exclusion of non-stroke causes for clinical presentation
o e.g. brain tumour, trauma, infection, hypoglycaemia, peripheral lesion, pharmacological influences etc.
• Determined by or in conjunction with the designated internal medicine specialist or neurologist.
• Diagnosis confirmed by at least one of the following:
• Neuroimaging procedure (CT scan or MRI brain) and/or
• Neurologist or neurosurgical specialist.
B. Neurocognitive impairment
Definition: Deterioration of intellectual function presenting as impaired memory or concentration presenting with temporal association to surgery.
Definition: An acute disturbance of consciousness and a change in cognition with tendency to fluctuate during the course of the day and occurring in patients without some other identifiable aetiology and following normal emergence from anaesthesia.
• In conjunction with CAM and MoCA assessment tools
Silent brain infarction
In neuroimaging studies, clinically apparent strokes account for only a minority of CVEs. Diffusion-weighted magnetic resonance imaging (DWI) studies have revealed the average incidence of new ischemic lesions as 75% post-TAVI, and as high as 93% [8, 9]. Comparatively, only 40–50% are evident on DWI studies following SAVR, and 22% following retrograde catheterisation of the aortic valve in AS [8, 10]. Understanding of these clinically silent CVEs is more limited than for clinically apparent strokes, with only a few published MRI-centred studies investigating their occurrence post-TAVI, amounting to fewer than 200 patients. The clinical relevance of this burden of infarct remains unknown, though has been suggested to correlate with increased risk of post-operative cognitive dysfunction (POCD) or post-operative delirium (POD) [11, 12]. Furthermore, DWI has recently been recommended as a useful surrogate endpoint for quantifying neurological injury due to the relative rarity of clinically apparent neurological injury .
Investigation into neurological injury post-TAVI has almost exclusively focused on CVEs, with little attention given to neurocognitive/neuropsychological disturbances. This reflects both the common occurrence and uncertain consequences of such events and the difficulties of their clinical detection. Two entities of particular interest are POD and POCD, which are outlined in Table 1. Though clinical experience suggests that these are common entities post-cardiovascular intervention, studies geared towards their detection following TAVI are sparse.
The underlying neurological insult resulting in injury is thought to be primarily an embolic phenomenon . Transcranial Doppler (TCD) studies have demonstrated microemboli at all stages of the TAVI procedure, with cumulative embolic loads exceeding 500 high-intensity signals (HITS, a validated surrogate of emboli) reported, especially during stages of aortic valve manipulation/TAVI deployment. A recent study employing embolic protection devices has demonstrated that a large number of such emboli are particulate in nature and include acute and chronic thrombus, atheromatous, calcific and valve/vascular tissue .
In addition to emboli, cerebral hypoperfusion is also likely a significant contributory factor, both in precipitating ischemia and magnifying the effects of microemboli . Indeed, a pilot study employing cerebral oximetry has confirmed statistically significant reductions in cerebral oxygen saturations most notably during periods of rapid ventricular pacing during valvuloplasty and valve deployment .
Generally, the data used to quantify and characterise the aetiology of the neurological insult is based on a limited number of small studies. Furthermore, no studies to date have correlated neurological insult detected by intraoperative monitoring and MRI evidence of neurological injury within the same cohort of patients.
Area of need
Clearly, current understanding of the nature and character of both the neurologic injury and the underlying insult associated with TAVI is incomplete. The paucity of data is the consequence of studies not specifically geared towards sensitive neurological insult/injury detection and the significant functional benefits of TAVI in patients who are ineligible or at high-risk for SAVR. However, the nature of neurological injury becomes of increasing interest as refinement of TAVI continues with the expectation that complications can and should be minimised. Indeed, the greatest barrier to TAVI extending into lower surgical risk and younger populations remain the risk of neurological injury.
The SANITY study (ACTRN12613000083796) aims to provide the most comprehensive characterisation to date of neurological insult and injury - both clinically apparent and silent – post-TAVI and SAVR. These encompass pre-existing patient factors, and both intra- and post-operative factors thought to influence neurological insult and injury during aortic valve interventions. It is hoped that improved understanding of these associations will permit detailed characterisation of neurological injury during TAVI compared to the gold-standard management of SAVR, and allow for the identification of predictors of such injury and previously unrecognised neuroprotective strategies.
Specifically, the objectives are:
Primary Objectives: Characterise neurological injury (MRI evidence of new ischaemic lesions) during the TAVI procedure compared with SAVR
- 1.Define the association between incidence of neurological insult (intraprocedural monitoring) and injury with:
Procedure (TAVI, SAVR)
TAVI access (transfemoral, transapical, transaortic)
- 2.Define the association between incidence of neurological insult, radiological evidence of injury and:
Clinically apparent neurological injury
New onset atrial fibrillation
Degree of vascular/aortic valve calcification
Rapid ventricular pacing and cerebral desaturation
Serological markers of neurological injury (S100B and GFAP)
Validate GFAP as a serological marker of neurological injury in cardiovascular intervention
SAVR than TAVI, due to the removal of the valvular source of embolisation, which in TAVI persists, pushed against the wall of the aorta and potentially acting as a nidus for calcific emboli and altered rheology, promoting thrombosis.
A transapical/transaortic than transfemoral approach. Transapical/transaortic routes minimise the risk of disrupting calcific plaques especially in the aortic arch, an inherent risk with femoral access.
This is a prospective, multicentre, non-randomised and observational study comparing the incidence of neurological injury associated with TAVI of the Edwards SAPIEN-XT (Edwards LifeSciences Irvine, CA, USA) under general anaesthetic versus bioprosthetic SAVR. Ethics approval has been obtained from the Human Research Ethics Committee of the Prince Charles Hospital, Brisbane, Australia (HREC/12/QPCH/291) and informed consent will be obtained from all participants prior to enrolment.
I. Informed consent for participation
I. Lacks capacity to consent for him or herself
II. Severe aortic stenosis
i. AVA <0.8 cm2
II. Pre-existing neurological impairment
ii. Mean aortic valve gradient >40 mmHg
i. Modified rankin score ≥ 3 (i.e. moderate disability; requiring some help, but able to walk without assistance)
iii. Peak jet velocity >4 m/s
III. Planned TAVI or SAVR
III. Contraindication to MRI (including incompatible metallic prosthesis/foreign body, inability to lie flat, claustrophobia requiring sedation)
i. STS score >8%
ii. Logistic EuroSCORE >20%
iii. Logistic EuroSCORE II >10%
IV. Non or poor English-speaking due to nature of and unknown validity in such populations cognitive testing
V. Previous aortic valve repair/replacement
VI. Coronary artery disease requiring revascularisation (including patients undergoing combined AVR and CABG)
Qualified medical or nursing personnel will administer a detailed, standardised questionnaire, either at the time of consent or, in cases of telephone consent, at first subsequent contact. This is aimed at identifying all pre-existing cerebrovascular and neurocognitive risk factors and assigning formal surgical-risk scores using the Society for Thoracic Surgeons Predicted Risk of Mortality (STS-PROM) scale and European System for Cardiac Operative Risk Evaluation (EuroSCORE) II. At each contact specific questioning and chart review will target transient ischemic events that might otherwise be missed using the neurological assessment protocol outlined below.
Neurological and cognitive assessment
There are no standards or recommendations guiding neurocognitive assessment in the TAVI population. Cognitive function will primarily be assessed with application of the Montreal Cognitive Assessment (MoCA). This tool is generally considered more sensitive for vascular cognitive impairment than the mini-mental state examination (MMSE) due to the inclusion of a thorough executive function assessment . Additionally, as appropriate, the Confusion Assessment Method (CAM) or the intensive care unit (ICU) equivalent – CAM-ICU, will be performed for the detection of delirium . These tests will be administered prior to the index procedure and at day 3, 6 weeks and 6 months post-index procedure.
Clinical neurological assessment
The National Institutes of Health Stroke Scale (NIHSS) is a widely validated tool, which facilitates the standardised objective quantification of impairment caused by stroke. Categorisation of stroke severity (no stroke, minor stroke, moderate stroke, moderate to severe stroke and severe stroke) is permitted, based on the overall score. Where stroke is identified (pre-existing or new), the modified Rankin Scale (mRS) will be applied to measure and monitor stroke-related disability. These assessments will be applied at the same time points as outlined for the cognitive assessment tools.
Numerous serological markers of neurological injury have been utilised previously in acute ischemic stroke (AIS), however few studies have evaluated their application specifically in patients undergoing cardiovascular interventions; thus, the ideal marker in this setting is unknown . Following careful consideration of strengths and weaknesses of each (Additional file 1: Table S1), GFAP and S100B were selected for use in the SANITY study. The time points for testing will be pre-procedure and daily for four days post-procedure.
Echocardiography (either transoesophageal or transthoracic) will be performed on all patients prior to and following the aortic valve procedure for the purposes of grading aortic stenosis and valve function. The TAVI Echocardiographic Calcification Score (TAVI-ECS) will be applied . Additionally, assessment for intra-cardiac thrombi and spontaneous echo contrast will be sought to aid assessment of pre-existing procoagulant state .
Carotid duplex ultrasound
It is feasible that carotid artery stenosis (CAS) may play a role, albeit currently undefined, in post-operative stroke . As such, carotid duplex ultrasound will be performed on all patients at baseline to identify CAS within the common, internal and external carotid arteries. Stenosis and plaque burden will be graded, taking into consideration all information from B-mode, pulsed-wave and colour-flow Doppler.
CT Chest/vascular calcification score
Arterial calcification correlates with atherosclerotic plaque burden . The Agaston Score Equivalent (ASE) is a widely used method of measuring the calcified plaque burden in coronary arteries using non contrast CT . Thus, a low dose, non-contrast acquisition will form part of the CT angiographic assessment of the aorta and the iliofemoral access arteries as routinely performed for TAVI suitability assessment and planning. These images will be loaded into Syngo.Via (Siemens Healthcare, Munich, Germany) and Calcium Score/ ASEs of the aorta will be quantitatively calculated for each of the aortic vessel segments, including the aortic root and valve leaflets. The correlation between the vascular and aortic valve plaque burden and neurological insult can thus be determined.
Magnetic resonance imaging (MRI)
Recognised as the most sensitive technique for the detection of acute ischemic cerebral infarcts, DWI detects the restriction of water diffusion in cerebral tissue caused by hypoxic oedema within minutes of ischemia onset. Increased signal intensity on DWI is reliably Detectable 4 hours post-insult and persists for up to 10 days . Lesions representing brain infarct can be quantified in number, size, and volume using this modality.
Susceptibility Weighted Imaging (SWI) is a relatively new MRI sequence which is highly sensitive to the local magnetic field inhomogeneity caused by paramagnetic substances including the haem group in haemoglobin. SWI is commonly used as an adjunct to DWI in the assessment of cerebral ischemia as it is extremely sensitive for detecting haemorrhagic transformation within regions of infarction; can demonstrate acute thromboemboli sufficient to occlude arteries and can detect micro-haemorrhage, suspected to originate from diapedesis of red blood cells across overtly permeable capillaries. Peak incidence of haemorrhagic transformation occurs between 48 hours and 5 days and can persist for years .
Patients will undergo a baseline MRI study <48 hours prior to intervention. This comprehensive study will include standard fast spin echo sequences, baseline DWI and SWI sequences and time of flight angiography of the circle of Willis to document pre-existing disease. At day 4 (±2) post-intervention, and following removal of temporary pacing wires where applicable, a limited study consisting of DWI, SWI, T2 Flair and T1-weighted imaging will be performed. This interval length allows for sufficient patient recovery post-procedure to safely undergo an MRI examination and allows for establishment of the MRI detectable changes and maximum evolution of the ischemic change . This limited acquisition is performed in 15 min for increased patient tolerance. A further limited examination after 6 months will include DWI and SWI, demonstrating DWI resolution, infarct complications and finally accounting for all SWI lesions.
Near infrared spectroscopic (NIRS)Cerebral Oximetry
Transcranial cerebral oximetry non-invasively monitors cerebral oxygen saturation (rSO2) in the frontal lobes of the brain and has been shown to correlate with cerebral venous oxygen saturation, which is traditionally considered the 'gold-standard’ for determining oxygen delivery/consumption . Accepted thresholds for cerebral ischemia are a rSO2 of <50% or a decline of >20% . This will be applied during the intra-operative period of the SANITY study with use of INVOS™ (Covidien, Boulder, CO) specifically to monitor the cerebral oxygen delivery compromise associated with the procedure, and in particular with rapid ventricular pacing [31, 32].
Invasive blood pressure
Hemodynamic instability leading to systemic hypotension may impair cerebral perfusion pressure beyond auto-regulatory capacity, resulting in hypoperfusion . While itself a cause of ischemia, low cerebral flow magnifies the effects of micro-emboli by impairing their clearance and permitting small emboli to lodge.
Intra-operative telemetry will be employed to measure the number and duration of rapid ventricular pacing episodes and to detect intra-operative rhythm abnormalities.
Quality of life
Quality of life (QoL) assessment during post-procedural follow-up is crucial to determining the clinical benefit of TAVI and fully appreciating the consequences of neurological and cognitive insult and injury. Recommendations of the VARC-2 necessitate both a health-specific measure and generalised measure of QoL . Following careful consideration of each (Additional file 2: Table S2), the heart failure specific Kansas City Cardiomyopathy Questionnaire (KCCQ) , and the generic European Quality of Life instrument-5D (EQ-5D)  were selected. These will be performed prior to and 6 months following index procedure.
Functional outcome measures and frailty
Functional capacity will be measured objectively by the six-minute walk test (6MWT), conducted according to American Thoracic Society guidelines . This simple, practical and inexpensive sub-maximal exercise test assesses functional capacity , is closely linked to activities of daily living and has been proposed as both a functional status indicator and an outcome measure . Similarly, gait speed is an important indicator of frailty , with slow gait a strong predictor of adverse outcomes, including disability, high healthcare utilisation and mortality .
Frailty describes a vulnerability to adverse events that is associated with, but separate from chronological age . Implicitly, all patients requiring TAVI as opposed to open aortic valve surgery must have frailty as a barrier to standard treatment. Frailty is therefore an important contributor to the choice of TAVI and a potential confounder regarding outcomes, including delirium . The SANITY study will utilise the Deficit accumulation score, which provides a robust measure of frailty and an appreciation of those who are unable to complete performance based tests - the frailest frail .
An estimated 100 patients will be recruited into this study, fifty in each of the two treatment arms (SAVR and TAVI) and at least 20 patients in each TAVI subgroup (transfemoral and transapical/transaortic). Fifty patients per group provides 90% power to detect differences in the incidence of new DWI lesions (primary endpoint) with two-sided statistical significance of 5%, assuming overall incidence estimates of 76% and 45% with TAVI and SAVR, respectively, as previously reported.
Multiple regression models will be used to adjust for potential confounders identified based upon clinical importance and statistical selection. The key output will be the estimated treatment difference and 95% confidence intervals for the primary group from the multiple regression models. Additionally, longitudinal analysis will be used to examine all outcomes with repeated data, again using multiple regression models. Treatment failure and withdrawal will be considered on an intention-to-treat basis, with the aim of providing a more realistic estimate of the difference between groups in clinical practice.
The SANITY Study offers the most comprehensive neurological/neurocognitive assessment of the TAVI and high-risk SAVR patient population to date. Additionally, well-established and recommended assessments are complemented by those that are novel and unique, thereby offering the potential of improved understanding of the interventions in question, correlation of risk factors and prognostic markers, and validation of assessment tools themselves. Such knowledge is vital to establishing both suitable assessment batteries and guidelines in this unique, high-risk group of patients, and to advancing strategies for neurological injury reduction.
Across all TAVI literature, the identification of risk-matched control groups has proven controversial. The validity of high-risk SAVR patients as a 'control group’ has previously been questioned, given that the level of health risk is a factor determining suitability for the procedure. Such difference also exists between access approaches, with transapical/transaortic typically considered a second line option where severe vascular disease excludes a transfemoral approach. Furthermore, these procedures differ vastly, most notably in the use of cardiopulmonary bypass, obscuring the exact cause of any difference identified between study groups. However, comparison between these two groups does offer clinical relevance as SAVR is the current 'gold-standard’ for eligible patients with AS and the challenge is in selecting the most appropriate procedure in patients who are considered suitable for both.
This study will be non-randomised and non-blinded. Though multiple regression analysis will be used to minimise confounding, this is not a substitute for blinding or randomisation, and unmeasured confounders may produce hidden bias.
Finally, a clinical follow-up duration of 6 months limits conclusions regarding delayed and late neurological injury. However, such a timeframe can be justified, given that DWI findings resolve within this period and reversible neurocognitive deficits generally resolve by 3 months . Consequently, the financial costs and patient burdens of prolonging follow-up cannot be ethically justified.
JPF supported by The Cardiac Society of Australia and New Zealand (CSANZ) Research Scholarship, The University of Queensland Research Scholarship and The Prince Charles Hospital Foundation (TPCHF) Research Grants. JFF supported by the Office of Health and Medical Research (OHMR) fellowship.
- Fanning JP, Platts DG, Walters DL, Fraser JF: Transcatheter aortic valve implantation (TAVI): Valve design and evolution. Int J Cardiol. 2013, 168 (3): 1822-1831. 10.1016/j.ijcard.2013.07.117.View ArticlePubMedGoogle Scholar
- Fanning JP, Walters DL, Platts DG, Eeles E, Bellapart J, Fraser JF: Characterization of Neurological Injury in Transcatheter Aortic Valve Implantation: How Clear Is the Picture?. Circulation. 2014, 129 (4): 504-515. 10.1161/CIRCULATIONAHA.113.004103.View ArticlePubMedGoogle Scholar
- Eggebrecht H, Schmermund A, Voigtlander T, Kahlert P, Erbel R, Mehta RH: Risk of stroke after transcatheter aortic valve implantation (TAVI): a meta-analysis of 10,037 published patients. Eurointervention. 2012, 8 (1): 129-138. 10.4244/EIJV8I1A20.View ArticlePubMedGoogle Scholar
- Vasques F, Messori A, Lucenteforte E, Biancari F: Immediate and late outcome of patients aged 80 years and older undergoing isolated aortic valve replacement: A systematic review and meta-analysis of 48 studies. Am Heart J. 2012, 163 (3): 477-485. 10.1016/j.ahj.2011.12.005.View ArticlePubMedGoogle Scholar
- O'Brien SM, Shahian DM, Filardo G, Ferraris VA, Haan CK, Rich JB, Normand SLT, DeLong ER, Shewan CM, Dokholyan RS, Peterson ED, Edwards FH, Anderson RP, Society of Thoracic Surgeons Quality Measurement Task Force: The Society of Thoracic Surgeons 2008 Cardiac Surgery Risk Models: Part 2, Isolated Valve Surgery. Ann Thorac Surg. 2009, 88 (1, Supplement): S23-S42. 10.1016/j.athoracsur.2009.05.056.View ArticlePubMedGoogle Scholar
- Tay ELW, Gurvitch R, Wijesinghe N, Nielispach F, Wood D, Cheung A, Ye J, Lichtenstein SV, Carere R, Thompson C, Webb JG: A high-risk period for cerebrovascular events exists after transcatheter aortic valve implantation. J Am Coll Cardiol Intv. 2011, 4 (12): 1290-1297. 10.1016/j.jcin.2011.08.012.View ArticleGoogle Scholar
- Miller DC, Blackstone EH, Mack MJ, Svensson LG, Kodali SK, Kapadia S, Rajeswaran J, Anderson WN, Moses JW, Tuzcu EM, Webb JG, Leon MB, Smith CR, PARTNER Trial Investigators and Patients; PARTNER Stroke Substudy Writing Group and Executive Committee: Transcatheter (TAVR) versus surgical (AVR) aortic valve replacement: occurrence, hazard, risk factors, and consequences of neurologic events in the PARTNER trial. J Thorac Cardiovasc Surg. 2012, 143 (4): 832-843. 10.1016/j.jtcvs.2012.01.055.View ArticlePubMedGoogle Scholar
- Astarci P, Glineur D, Kefer J, D'Hoore W, Renkin J, Vanoverschelde J-L, El Khoury G, Grandin C: Magnetic resonance imaging evaluation of cerebral embolization during percutaneous aortic valve implantation: comparison of transfemoral and trans-apical approaches using Edwards Sapiens valve. Eur J Cardiothorac Surg. 2011, 40 (2): 475-479.PubMedGoogle Scholar
- Kahlert PMD, Al-Rashid FMD, Dottger PMS, Mori KMS, Plicht BMD, Wendt DMD, Bergmann LMD, Desa , Kottenberg EMD, Schlamann MMD, Mummel P, Holle D, Thielmann M, Jakob HG, Konorza T, Heusch G, Erbel R, Eggebrecht H: Cerebral embolization during transcatheter aortic valve implantation: a transcranial doppler study. Circulation. 2012, 126 (10): 1245-1255. 10.1161/CIRCULATIONAHA.112.092544.View ArticlePubMedGoogle Scholar
- Omran H, Schmidt H, Hackenbroch M, Illien S, Bernhardt P, von der Recke G, Fimmers R, Flacke S, Layer GN, Pohl C: Silent and apparent cerebral embolism after retrograde catheterisation of the aortic valve in valvular stenosis: a prospective, randomised study. Lancet. 2003, 361 (9365): 1241-1246. 10.1016/S0140-6736(03)12978-9.View ArticlePubMedGoogle Scholar
- Rudolph JL, Schreiber KA, Culley DJ, McGlinchey RE, Crosby G, Levitsky S, Marcantonio ER: Measurement of post-operative cognitive dysfunction after cardiac surgery: a systematic review. Acta Anaesthesiol Scand. 2010, 54 (6): 663-677. 10.1111/j.1399-6576.2010.02236.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Saczynski JS, Marcantonio ER, Quach L, Fong TG, Gross A, Inouye SK, Jones RN: Cognitive Trajectories after Postoperative Delirium. N Engl J Med. 2012, 367 (1): 30-39. 10.1056/NEJMoa1112923.View ArticlePubMedPubMed CentralGoogle Scholar
- Meller S, Baumbach A, Voros S, Mullen M, Lansky A: Challenges in cardiac device innovation: is neuroimaging an appropriate endpoint? Consensus from the 2013 Yale-UCL Cardiac Device Innovation Summit. BMC Medicine. 2013, 11 (1): 257-10.1186/1741-7015-11-257.View ArticlePubMedPubMed CentralGoogle Scholar
- Van Mieghem NM, Schipper MEI, Ladich E, Faqiri E, van der Boon R, Randjgari A, Schultz C, Moelker A, Van Geuns R-J, Otsuka F, Serruys PW, Virmani R, De Jaegere PP: Histopathology of embolic debris captured during transcatheter aortic valve replacement. Circulation. 2013, 127 (22): 2194-2201. 10.1161/CIRCULATIONAHA.112.001091.View ArticlePubMedGoogle Scholar
- Caplan Lr HM: Impaired clearance of emboli (washout) is an important link between hypoperfusion, embolism, and ischemic stroke. Arch Neurol. 1998, 55 (11): 1475-1482. 10.1001/archneur.55.11.1475.View ArticlePubMedGoogle Scholar
- Bila RH, Augustine T, Hartley M, Humphries C, Roberts S, Moore R, Sogliani F: Cerebral oximetry monitoring during transcatheter aortic valve implantation (TAVI) [Conference Abstract]. Innovations: Technology and Techniques in Cardiothoracic and Vascular Surgery. 2012, 7 (2): 134-Google Scholar
- Kappetein AP, Head SJ, Genereux P, Piazza N, Van Mieghem NM, Blackstone EH, Brott TG, Cohen DJ, Cutlip DE, Van Es GA, Hahn RT, Kirtane AJ, Krucoff MW, Kodali S, Mack MJ, Mehran R, Rodés-Cabau J, Vranckx P, Webb JG, Windecker S, Serruys PW, Leon MB: Updated standardized endpoint definitions for transcatheter aortic valve implantation: the Valve Academic Research Consortium-2 consensus document. Eur Heart J. 2012, 33 (19): 2403-2418. 10.1093/eurheartj/ehs255.View ArticlePubMedGoogle Scholar
- Godefroy O, Fickl A, Roussel M, Auribault C, Bugnicourt JM, Lamy C, Canaple S, Petitnicolas G: Is the montreal cognitive assessment superior to the mini-mental state examination to detect poststroke cognitive impairment?: a study with neuropsychological evaluation. Stroke. 2011, 42 (6): 1712-1716. 10.1161/STROKEAHA.110.606277.View ArticlePubMedGoogle Scholar
- Inouye SK, Van Dyck CH, Alessi CA, Balkin S, Siegal AP, Horwitz RI: Clarifying confusion: the confusion assessment method. Ann Intern Med. 1990, 113 (12): 941-10.7326/0003-4819-113-12-941.View ArticlePubMedGoogle Scholar
- Seco M, Edelman JJB, Wilson MK, Bannon PG, Vallely MP: Serum biomarkers of neurologic injury in cardiac operations. Ann Thorac Surg. 2012, 94 (3): 1026-1033. 10.1016/j.athoracsur.2012.04.142.View ArticlePubMedGoogle Scholar
- Colli A, D’Amico R, Kempfert J, Borger MA, Mohr FW, Walther T: Transesophageal echocardiographic scoring for transcatheter aortic valve implantation: impact of aortic cusp calcification on postoperative aortic regurgitation. J Thorac Cardiovasc Surg. 2011, 142 (5): 1229-1235. 10.1016/j.jtcvs.2011.04.026.View ArticlePubMedGoogle Scholar
- Lenders GD, Paelinck BP, Wouters K, Claeys MJ, Rodrigus IE, Van Herck PL, Vrints CJ, Bosmans JM: Transesophageal echocardiography for cardiac thromboembolic risk assessment in patients with severe, symptomatic aortic valve stenosis referred for potential transcatheter aortic valve implantation. Am J Cardiol. 2013, 111 (10): 1470-1474. 10.1016/j.amjcard.2013.01.302.View ArticlePubMedGoogle Scholar
- American Heart Association: Heart disease and stroke statistics: 2005 update. 2004, Dallas, Texas: American Heart AssociationGoogle Scholar
- Aono Y, Ohkubo T, Kikuya M, Hara A, Kondo T, Obara T, Metoki H, Inoue R, Asayama K, Shintani Y, Hashimoto J, Totsune K, Hoshi H, Satoh H, Izumi S, Imai Y: Plasma fibrinogen, ambulatory blood pressure, and silent cerebrovascular lesions: the Ohasama study. Arterioscler Thromb Vasc Biol. 2007, 27: 963-968. 10.1161/01.ATV.0000258947.17570.38.View ArticlePubMedGoogle Scholar
- Allison MA, Criqui M, Wright CM: Patterns and risk factors for systemic calcified atherosclerosis. Ateriosclerosis Thrombosis and Vascular Biology. 2004, 24: 331-336. 10.1161/01.ATV.0000110786.02097.0c.View ArticleGoogle Scholar
- Agaston AS, Janowitz WR, Hildner FJ, Zusmer NR, Viamonte M, Detrano R: Quantification of coronary artery calcium using ultrafast computed tomography. J Am Coll Cardiol. 1990, 14 (4): 827-832.View ArticleGoogle Scholar
- Allen LM, Hasso AN, Handwerker J, Farid H: Sequence-specific MR Imaging Findings that are useful in Dating Ischemic Stroke. RadioGraphics. 2012, 32: 1285-1297. 10.1148/rg.325115760.View ArticlePubMedGoogle Scholar
- Schlaug G, Siewert B, Benfield A, Edelman RR, Warach S: Time course of the apparent diffusion coefficient (ADC) abnormality in human stroke. Neurology. 1997, 49 (1): 113-119. 10.1212/WNL.49.1.113.View ArticlePubMedGoogle Scholar
- Paarmann H, Heringlake M, Heinze H, Hanke T, Sier H, Karsten J, Schon J: Non-invasive cerebral oxygenation reflects mixed venous oxygen saturation during the varying haemodynamic conditions in patients undergoing transapical transcatheter aortic valve implantation. Interact Cardiovasc Thorac Surg. 2012, 14 (3): 268-272. 10.1093/icvts/ivr102.View ArticlePubMedGoogle Scholar
- Sa K, Pb S, Klein KUA: Transcranial doppler and near infrared spectroscopy in the perioperative period. Curr Opin Anaesthesiol. 2013, 26 (5): 543-548. 10.1097/01.aco.0000432517.70844.a6.View ArticleGoogle Scholar
- Bila RH, Augustine T, Hartley M, Humphries C, Roberts S, Moore R, Sogliani F: Cerebral oximetry monitoring during transcatheter aortic valve implantation (TAVI). Conference Abstract from: Innovations: Technology and Techniques in Cardiothoracic and Vascular Surgery 2012, Conference: 15th Annual Meeting of the International Society for Minimally Invasive Cardiothoracic Surgery, ISMICS 2012. 2012, Los Angeles, CA United States: Conference Publication: (var.pagings), 7(2):134Google Scholar
- Brodt J, Maratea E: Cerebral Oxygenation During Transcatheter Aortic Valve Implantation. Poster session presented at: Anesthesiology 2012. 2012, Washington, D.C., United States: American Society of Anesthesiologists Annual Meeting,Google Scholar
- Kapadia S: Three-Year Outcomes of Transcatheter Aortic Valve Replacement (TAVR) in "inoperable" Patients with severe Aortic Stenosis: The PARTNER Trial. 2012, Miami, FL, USA: Presentation at: Transcatheter Cardiovascular Therapies (TCT) 2012Google Scholar
- Chou CC, Lien LM, Chen WH, Wu MS, Lin SM, Chiu HC, Chiou HY, Bai CH: Adults with late stage 3 chronic kidney disease are at high risk for prevalent silent brain infarction: a population-based study. Stroke. 2011, 42 (8): 2120-2125. 10.1161/STROKEAHA.110.597930.View ArticlePubMedGoogle Scholar
- Green CP, Porter CB, Bresnahan DR, Spertus JA: Development and evaluation of the Kansas City Cardiomyopathy Questionnaire: a new health status measure for heart failure. J Am Coll Cardiol. 2000, 35 (5): 1245-1255. 10.1016/S0735-1097(00)00531-3.View ArticlePubMedGoogle Scholar
- Group TE: EuroQol - a new facility for the measurement of health-related quality of life. Health Policy. 1990, 16 (3): 199-208.View ArticleGoogle Scholar
- Eguchi K, Kario K, Hoshide S, Hoshide Y, Ishikawa J, Morinari M, Hashimoto T, Shimada K: Smoking is associated with silent cerebrovascular disease in a high-risk Japanese community-dwelling population. Hypertens Res. 2004, 27 (10): 747-754. 10.1291/hypres.27.747.View ArticlePubMedGoogle Scholar
- Eguchi K, Kario K, Shimada K: Greater impact of coexistence of hypertension and diabetes on silent cerebral infarcts. Stroke. 2003, 34 (10): 2471-2474. 10.1161/01.STR.0000089684.41902.CD.View ArticlePubMedGoogle Scholar
- Feiwell RJ, Besmertis L, Sarkar R, Saloner DA, Rapp JH: Detection of clinically silent infarcts after carotid endarterectomy by use of diffusion-weighted imaging. AJNR Am J Neuroradiol. 2001, 22 (4): 646-649.PubMedGoogle Scholar
- Fujishima M, Yao H, Terashi A, Tagawa K, Matsumoto M, Hara H, Akiguchi I, Suzuki K, Nishimaru K, Udaka F, Gyoten T, Takeuchi J, Hamada R, Yoshida Y, Ibayashi S: Deep white matter lesions on MRI, and not silent brain infarcts are related to headache and dizziness of non-specific cause in non-stroke Japanese subjects. Intern Med. 2000, 39 (9): 727-731. 10.2169/internalmedicine.39.727.View ArticlePubMedGoogle Scholar
- Gerriets T, Swarz N, Bachmann G, Kaps M, Kloevekorn WP, Sammer G, Tschernatsch M, Nottbohm R, Blaes F, Schönburg M: Evaluation of methods to predict early long-term neurobehavioral outcome after coronary artery bypass grafting. Am J Cardiol. 2010, 105 (8): 1095-1101. 10.1016/j.amjcard.2009.12.009.View ArticlePubMedGoogle Scholar
- McMillan GJ, Hubbard RE: Frailty in older inpatients: what physicians need to know. QJM. 2012, 105 (11): 1059-1065. 10.1093/qjmed/hcs125.View ArticlePubMedGoogle Scholar
- Eeles EMP, White SV, O'Mahony SM, Bayer AJ, Hubbard RE: The impact of frailty and delirium on mortality in older inpatients. Age Ageing. 2012, 41 (3): 412-416. 10.1093/ageing/afs021.View ArticlePubMedGoogle Scholar
- Rockwood K, Mitnitski A: Frailty in Relation to the Accumulation of Deficits. J Gerontol A: Biol Med Sci. 2007, 62 (7): 722-727. 10.1093/gerona/62.7.722.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2261/14/45/prepub
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