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Aortic Valve - Science topic

The valve between the left ventricle and the ascending aorta which prevents backflow into the left ventricle.
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Hi all! I am hoping that this is a simple ID for someone who knows what they're doing.
I am looking at transverse sections of the base of the heart. In several there are small groups of large, round cells. They appear to be highly organized and always appear near the left atria, which makes me believe they are part of an established organ. I was leaning towards parathyroid, but the reference images don't quite convince me. Then I found a piece that appears to be within the mitral (?) valve of one sample, so I'm at a loss again.
I have attached images from two different samples: one where there are 3 distinct pieces all within fat and one with the valvular location. Initially I thought that was an embolus of some sort in the valve, but I'm thinking now it may just be atria that got smushed down during embedding.
I promise I"m taking all of my images to a histologist for final say, but I would like to have some idea of what's going on before then. Any input would be very much appreciated!
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These are the ganglionated plexuses of the heart which lie within the epicardial fat predominantly in the atria. You can also see the beginning of a nerve in "high zoom top.png". The individual cells are called ganglion cells. You can confirm using immunohistochemistry such as PGP9.5 or NSE.
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You have invented a new type of artificial aortic valve, the performance of which you are now assessing in the first human heart. You have catheterized the aorta and placed a pressure transducer there. The ECG and aortic pressure are recorded simultaneously from your subject and are shown below (Note: The large voltage spike of the ECG corresponds to the beginning of ventricular contraction, while the more diffuse subsequent peak corresponds to repolarization and relaxation of the ventricular muscle)
a) You are concerned about the results of your tests. What is it about the pressure data that concerns you? (b) What do you think the general problem with your valve is, and how might you improve it?
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is there a image of tracing
I'm unable to see
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The valve will deform under burst pressure in IC-engine.
Generally speaking, when designing valve structure, what is the allowable bending stress for valve of silcrome 1 material?
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That's a good question
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I am looking for a protocol (cheap and effective way) that I could use to isolate multiple types of cells and be able to sort them out. For instance, I want to isolate multiple sub populations of interstitial cells in the aortic valve.
Any help/recommendation would be greatly appreciated. Thanks.
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Just seeing this thread now, but I am going to answer this here in case it is helpful to anyone who might stumble upon this .... You could look up this website: www.rnassist.com. This product called vivoPHIX enables tissue fixation and then dissociation for tissues, prior to downstream applications !
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The cuff-based blood pressure (BP) measurement can be affected by patient posture, compliance, etc. I wonder if the the left ventricle blood pressure that causes opening of aortic valve (which is also before the blood ejection) is the true blood pressure. Just a thought. Is there any animal/modeling study about measuring BP from different locations in cardiovascular system? Thanks
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Thierry C Gillebert Thank you very much for your answer. It was really helpful.
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Bicuspid aortic valve are asymptomatic mostly , but i would like to collecting data about the initial symptoms and sign in adult persons?
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As far as we know there is no difference in symptom progression due to bicuspid aortic valve disease in diabetic patients. This could be related to a poor representation of this patients in clinical trials. Usually symptoms depends on the degree of valve dysfunction. You should expect dyspnea, chest pain o syncope when valve disease is advanced. Perhaps chest pain could presente earlier in diabetic patients who are more prompt to develop coronary disease and relative ischemia in bicuspid valve advanced stenosis or regurgitation.
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A - Tricuspid Regurtitation
B - Mitral Regurgitation
C- Aortic Regurgitation
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Aortic stenosis followed by mitral regurgitation. However, we observe sometimes in patients with chronic IE a combined aortic vitium (Stenosis & regurgitation)
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what is the best aortic valve procedure and valve size for a 52 years old female  87kg 163cm with calcific bicuspid severe aortic stenosis , peak gradient 55mmhg. aortic annular diameter of 2 cm ,mod MR mod TR  EF 45 % atrial fib  and hyperthyroidism?
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Thank you all for this interesting discussion
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I have a 3-D geometry model of a aortic valve and the while importing it into the Mesh module generates the following message:
"Too many NURBS surface . Will take longer than usual to mesh it ".
Is there any strategy I can apply to reduce the Non-uniform rational Basis spline (NURBS) surfaces so as to make my meshing easier.
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Which program are you using in the first place to create the NURBS geometry? You may have the option to create a less detailed geometry at that point. Otherwise I would suggest using a 3D modelling software such as SolidWorks or similar to simplify your geometry before importing to Ansys. 
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Hello. I've posted a question before, however, it may have been a bit wordy, so i'll try to be more brief here. 
We are working with 2.5mm mouse thoracic aortic rings in a 25mL Radnoti tissue bath @ 37 degrees Celsius . Right now the buffer is Krebs ringer. We are oxygenating with 100% O2 (I've read that may be incorrect?). Passive tension is at 1.5 grams (but we've tried lower). As of yet we have not had a measurable response (we've tried insanely high concentrations of KCL, and L- phenylephrine in a desperate attempt to get any type of signal). 
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Thank you for your response! I will investigate this further.
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A 53 years old female with root aortic aneurysm, mitral and aortic valve regurgitation, and multiple bullae of lung. She had history of spontaneous pneumothorax 2 years ago. There was no history of smoking. ANA test and anti ds-dna test were negative. We haven't explore for  skeletal and ophthalmic disorders yet, but the patient didn't have any complaint about these organs. What is the possible etiology of these disorders? Are they related to connective tissue disease?
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We could try to arrange DNA testing in our lab? We have been sequencing the FBN1 gene for several years now and this could potentially be performed without cost if your patient cannot afford this.
Let me know if this would be usefull.
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Does anybody have experience in management of young patients with calcific aortic valve disease. Are there any data on prognosis of these young adults available? 
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There is a very recent case report with free text available: 
Ann Card Anaesth. 2016 Jan-Mar;19(1):166-8. doi: 10.4103/0971-9784.173041.
Perceval S aortic valve implantation in an achondroplastic Dwarf.
Baikoussis NG1, Argiriou M, Argiriou O, Dedeilias P.
Author information
 
Abstract
Despite cardiovascular disease in patients with dwarfism is not rare; there is a lack of reports referring to cardiac interventions in such patients. Dwarfism may be due to achondroplasia or hormonal growth disorders. We present a 58-year-old woman with episodes of dyspnea for several months. She underwent on transthoracic echocardiography, and she diagnosed with severe aortic valve stenosis. She referred to our department for surgical treatment of this finding. In accordance of her anthropometric characteristics and her very small aortic annulus, we had the dilemma of prosthesis selection. We decided to implant a stentless valve to optimize her effective orifice area. Our aim is to present the successful Perceval S valve implantation and the descriptions of the problems coming across in operating on these special patients. To our knowledge, this is the first case patient in which a Perceval S valve is implanted according to the international bibliography.
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I have adult mouse hearts embedded in paraffin and I was hoping to obtain cross sections of the valves (especially the Aortic valves) as that is the my structure of interest. Is there any way to achieve a cross section of the valves such that I can see all the valve leaflets by orientating the heart in some particular way? Any technique for this? Thanks in advance and any input is much appreciated.
More specifically, I am having issues achieving all 3 leaflets in one cross section (sometimes I get 2 leaflets and keep cutting a little bit and get the third one).
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It is easier to obtain a good orientation in paraffin sections.
You can start cutting with the microtome or cryostat from the aorta and observe the sections to detect when the first commissure appears. Then, you slightly re-orient the block and cut several more sections until you obtain the distal part of the three commissures in the same section.
Alternatively, before or after fixation you can carefully cut the aorta transversally at the most distal level of the commissures, in order to obtain a complete transversal plain. Then you just cut exactly with that orientation in the microtome or criostat.
Hope this helps
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External reinforced aortic root replacement (reinforced Ross operation) have been shown to limit or abolish root dilatation (depending on the techniques used). In the pediatric or young children and adolescence do you use it? If yes, which is the cutoff to decide to use reinforced Ross operation: patient age or size, native aortic root size (dilated) or pulmonary autograft size? Coronary position?
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  1. The pulmonary autograft is the ideal substitute for aortic valve disease in children and young adult. Accumulating evidence suggest that the advantages of the pulmonary autograft are represented by acceptance to the same self-biological, an absent immune and inflammatory responses, the ability of the growing pulmonary autograft to match the somatic growth and the avoidance of life-long anticoagulation. In adult population, the use of pulmonary autograft is indicated for surgical treatment of bicuspid aortic valve that is the most common congenital heart defect affecting 1,3% of the population worldwide. The disadvantage of the pulmonary autograft implanted in aortic position is the dilatation process when it is subjected to systemic-pressure load.
  2. However, observations elegantly discussed by Horer et al. concerning the differential potential of dilation at the various segments of the aorta, i.e. annulus, Valsalva sinuses (0,5 mm/year) and sinutubular junction (increase of 0,7-0,9 mm/year), outlined the need to tailor mechanical features of PA reinforcements in their different parts. This induced to reconsider their design with the aim to better adapt to the normal physiology of the aortic root improving the resistance of the zones, which are meant to majorly suffer from dilatative degeneration. In the context of Ross procedure the potential of dilation of Valsalva sinuses is a pivotal problem as it might affect the status of the reimplanted coronaries. Additionally, mechanical stress associated to progressive overstrain of the graft under systemic pressure might affect PA integrity and the endothelialization process16; therefore in this context prevention of graft stretching is crucial.
  3. Previous experience with a prosthetic Dacron graft with an artificial aortic root configuration (Valsalva graft) as external reinforcement of the PA has been reported by Carrel et al. This approach was attempted with the aim to to prevent neoaortic root dilatation and prevent the dynamic function of Valsalva sinuses. Surely, this techique would carry the advantage graft to allow the most physiologic pressure and flow patterns within the autograft in respect to a straight Dacron graft. Indeed the autograft encased in a straight Dacron prosthetic graft would be dramatically impaired in its pulsatility and compliance. Moreover, we previously demonstrated as Dacron graft and other synthetic polyesters severely impair aortic compliance when used as vascular replacement16 and elicit a strong inflammatory reaction with significant damage to vessel wall when used a PA reinforcement1. From these standpoints we focused in improving the biomechanical behaviour of the reinforced PA using a composite biodegradable and auxetic material. 
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The focused thing in this case is atrial fibrillation, so one should follow the CHA2DS2 VASc  score in deciding the anticougulant therapy. Considering  findings from the ADVANCE study, one is to aware of the increased risk of thromboembolism in TAVR patient. Weighing the risk for bleeding ( BLED score ), I may opt for anti-cougulants if the bleeding risk is low.
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50 years post mechanical AVR, off pump well for 1 hour, no support, normal ECG, normalTEE. Sudden  drop of BP from 100 TO 50 over 1 minute with bradyc, distension, no response at all  to vasopressors or inotropes boluses. CPB resumed for 30 min, off pump well. post op OK. Discharged 7 d postop.
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The sudden bradycardia and cardiac distention does not fit with hypovolaemia. Although it is a bit late, gas emobism from an inadequtely vented LV, down the right coronary artery would precipitate ischaemia of the sinoartrial node so bradycardia as well as RV dysfuntion and distention.
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Please let me know if there is any standard reference for
1. Max and Min load acting on a heart valve (artificial/real).
Are the max and Min values acting on the valve disc 120 and 80 mm Hg?
2. Types and orientation of loads/pressure acting on a valve during opening and closing operation (eg: aortic valve)
In addition to the disc and wall supports, will there be any additional forces.....
3. Bio-mechanics of heart valve (free body diagram, external loads, internal reactions etc)
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Hi Subhash,
1. that depends on the valve you're looking at.
120mmHg is the aortic pressure during end-systole. The aortic valve is open, thus there is no load on it (if wall shear stress or other are neglected). The main load on this valve is reached shortly after valve closure. Here is a picture were you can see some pressure gradients during the heart cycle: http://howmed.net/physiology/cardiac-cycle/  The max load on the aortic valve occurs after valve closure (pAorta - pLeftVentricle: ~100 mmHg).
Another question is if you are looking at healthy or diseased hearts.
2+3. You can find several publications on this topic I guess. Maybe start with the book 'Biomechanics - Mechanical Properties of Living Tissues' or '
Biomechanics: Motion, Flow, Stress, and Growth', both by Yuan-Cheng Fung
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I want to measure aorta diameter but the shape is not find round.
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maybe this reference also can help you:
Importance of Measurement of the Diameter of the Aorta during Peroperative Blood Flow Monitoring; 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society; p.2402 - 2403; DOI: 10.1109/IEMBS.1992.5761425.
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Transcatether prothesis
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Dear Roberto how, are you?
I think that TF should be consider theoretically less invasive compare to TA, DAo or subclavian but in my opinion proximal access site allow a more precise valve positioning.
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Aortic to right atrial fistula after the operation of the aortic valve replacement.
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Was this an isolated AVR or a root? Was it done for endocarditis?
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One of the concepts recently quoted in a meeting was that one should look at using relatively cheaper heart valves on the shelf, rather than go for a more expensive valve, even though it may be the "Ferrari" of valves. What are your thoughts on this?
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That's a tough one, 'cause price of valves varies, according to several factors: a) total amount of valves sold to your institution/ group, b) country (even local area or region) where you practice, c) time-frame of payment (hospital to company), d) whether the company/ agent sells other fungibles or expendables to your hospital/ group (can afford to sell cheaper valves if fringe benefits on other entries, i.e. pacemakers).
The center I work in buys mechanicals (SJM, Carbomedix) for somewhere in between 2500 and 2800 Euro, slightly less for BPV's (periardial or porcine). Then again, this is a public institution, with all nuances you might think of. These are well-functioning valves, beyond all doubt, as are ATS, On-X and most BPV's.
Choose your pick of both types, at least two providers on each, and be confident and comfortable with them.