Dr. Kazi AbulFazal Ferdous provides an overview of echocardiographic evaluation of aortic stenosis. 2D echocardiography is used to evaluate aortic valve anatomy and differentiate valve subtypes. Doppler echocardiography determines the aortic valve area using the continuity equation and measures transaortic jet velocity. Together, valve area and jet velocity classify aortic stenosis severity and distinguish pseudo-severe from true severe stenosis by observing changes with increased flow. Progression is monitored through serial echocardiograms, with more frequent evaluation for severe stenosis.
there is detailed analysis of mitral valve segments by 2d transesophageal echo cardiography. There is a review on this and simplified approach how one can identify the pathological segment with great accuracy using two dimensional tee.
Echo assesment of Aortic Stenosis and Regurgitationdrpraveen1986
A simple ppt presentation on echo assesment of AS and AR. Don forget to leave a comment if u find this ppt useful. - Dr. Praveen Babu, Vijaya HOspital, Chennai
most important aspect for successful placement of LV lead is understanding of coronary os. anatomy and proper imaging and identification of selected vein.also important to know various method for CS cannulation.
there is detailed analysis of mitral valve segments by 2d transesophageal echo cardiography. There is a review on this and simplified approach how one can identify the pathological segment with great accuracy using two dimensional tee.
Echo assesment of Aortic Stenosis and Regurgitationdrpraveen1986
A simple ppt presentation on echo assesment of AS and AR. Don forget to leave a comment if u find this ppt useful. - Dr. Praveen Babu, Vijaya HOspital, Chennai
most important aspect for successful placement of LV lead is understanding of coronary os. anatomy and proper imaging and identification of selected vein.also important to know various method for CS cannulation.
preop TEE assessment of atrial septal defect is very important for making decision for device closure, properly assessed adequate rims of ASD will reduce risk of device embolization to almost nil.
Brain arteriovenous malformations (bAVM) are abnormal connections of arteries and veins in the brain, forming a tangled web of vessels instead of a normal capillary network treated with multimodalities including, SRS, embolisation and Microneurosurgery.
This slides updates the management of AVM highlighting the importance of SM grading, Pollock radiation grading etc.
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
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Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Best Ayurvedic medicine for Gas and IndigestionSwastikAyurveda
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
17. AORTIC STENOSIS
Most common :-
Bicuspid aortic valve with calcification
Senile or Degenerative calcific AS
Rheumatic AS
Less common:-
Congenital
Type 2 Hyperlipoproteinemia
EAE/ASE recommendations for Echocardiographic assessmentof valve
stenosis, European Journal of Echocardiography 2009
19. Aortic sclerosis
About 25% of all adults over age 65 yrs have aortic valve sclerosis.
Thickened calcified cusps with preserved mobility.
No significant obstruction to LV outflow.
Typically associated with peak doppler velocity of < 2.5 m/sec.
In Cardiovascular Health Study ,for group of patients 65
yrs,the aortic valve was normal in 70% of cases,sclerotic in 29% and
stenotic in 2%.
JACC.1997;29(3):630-4.
In Euro Heart Survey of 4910 pts in 25 countries,AS was the most
frequent lesion,accounting for 43% of patients with VHD.
Eur Heart J.2003;24(13):1231-43.
20.
21. Calcific Aortic Stenosis
10-15% of aortic sclerosis patients progress to severe AS.
Nodular calcific masses on aortic side of cusps.
No commissural fusion.
Free edges of cusps are not involve
Stellate- shaped systolic orifice.
d.
Cosmi et al,Arch Int Med 2002;162(20):2345-7.
22. Calcific Aortic Stenosis
Plax (Parasternal long axis) view
showing echogenic and immobile
aortic valve.
Marked increase in echogenicity.
Reduced systolic opening.
23. Calcific Aortic Stenosis
Parasternal short-axis view
showing calcified aortic valve
leaflets. Immobility of the cusps
results in only a slit like aortic
valve orifice in systole.
Used for valve area
(planimetry).
24. Imp points.
Directly planimetered aortic valve areas should be interpreted with
caution because of the complex anatomy of the orifice and calcific
shadowing and reverberation, even with 3D imaging.
Direct measurement of valve area on imaging reflects anatomic valve
area, whereas the doppler data provide functional area.
27. Bicuspid Aortic Valve (BAV)
Accounts for 2/3rd of cases of severe AS in adults < 70 yrs.
1/3rd of cases in adults > 70 yrs of age.
Severe AS of a BAV is difficult to be differentiated from that of
tricuspid one.
Usual view for differentiation is PARASTERNAL SHORTAXIS
VIEW at the level of great vessels in systole.
PARASTERNAL Long axis view shows systolic bowing of the
leaflets into aorta – “Dome like”.
M MODE – Eccentric closure line (to be taken at the tips of bowed
leaflets).
28. Two cusps are seen in systole with only two commissures framing an
elliptical systolic orifice (the fish mouth appearance).
Diastolic images may mimic a tricuspid valve when a raphe is
present.
Bicuspid Aortic valve
30. Bicuspid Aortic valve
In children, valve may be stenotic
without extensive calcification.
In adults, stenosis typically is
due to calcific changes, which
often obscures the number of
cusps, making determination of
bicuspid vs. tricuspid valve
32. Types of BAV
FUSION OF CUSPS FREQUENCY LEAFLET
CLOSURE LINE
REMARKS
RIGHTAND LEFT 70 -80% Anterolateral–
posteromedial closure
line
Larger anterior
leaflet.
RIGHTAND
NONCORONARY
20-30% Anterior–posterior
closure line
Larger
rightward leaflet
LEFTAND
NONCORONARY
1-2% Medial – lateral closure
line
Many bicuspid aortic valves have a raphe in the larger leaflet.
Clear identification of number of leaflets is possible only in systole.
Schaefer et al ,Am J Cardiol 99(5);686-90.2007
37. Subvalvular aortic stenosis
(1) Thin discrete membrane consisting of endocardial fold and fibrous
tissue.
(2) A fibromuscular ridge
(3) Diffuse tunnel-like narrowing of the LVOT
(4) Accessory or anomalous mitral valve tissue.
Young adults Valvenot stenotic
But high gradients think of subvalvularAS.
TEE – confirmation.
38. Supravalvular Aortic stenosis
Type I - Thick, fibrous ring above the aortic valve with less
mobility and has the easily identifiable 'hourglass' appearance
of the aorta.
39. Type II - Thin, discrete fibrous membrane located above the aortic
valve
The membrane usually mobile and may demonstrate doming during
systole.
Type III - Diffuse narrowing
Supravalvular Aortic stenosis
40. Rheumatic Aortic Stenosis
Characterized by
Commissural fusion
Triangular systolic orifice
Thickening & calcification
Accompanied by rheumatic mitral valve changes.
30% of patients with MS,aortic valve is also affected in
RHD.
41. Rheumatic aortic stenosis
Parasternal short axis view showing commissural
fusion, leaflet thickening and calcification, small
triangular systolic orifice
42. Differentiation of
Rheumatic vs Calcified AS
RHEUMATIC AS CALCIFIC AS
COMMISSURES FUSED FREE
LEAFLETS TIPS TO BASE BASE TO TIPS
ORIFICE TRIANGULAR STELLATE SHAPED
AGE OF PATIENT NO PARTICULAR USUALLY ELDERLY
MITRAL VALVE 30% OF MS CASES MAC +
OTHERS TIPS THICKENED,
CALCIFIED (INEXTREME)
TIPS ARE FREE (CALCIFIC
NODULES CAN BE
PRESENT not at TIPS)
46. Maximal aortic cusp separation (MACS)
Vertical distance between right CC and non CC during systole
M Mode- Aortic Stenosis
Aortic valve area MACS Measurement Predictive value
NormalAVA >2Cm2 Normal MACS >15mm 100%
AVA>1.0 > 12mm 96%
AVA< 0.75 < 8mm 97%
Gray area 8-12 mm …..
DeMaria A N et al. Circulation.Suppl II. 58:232,1978
48. Limitations
Single dimension
Asymmetrical AV involvement
Calcification / thickness
↓ LV systolic function
↓ CO status
M Mode- Aortic Stenosis
54. Qualitative information of stenosis
by 2D echo
Thickened calcified cusps that display preserved mobility define
aortic sclerosis (peak doppler velocity of 2.5 m/sec).
Heavily calcified cusps with little or no mobility suggest severe aortic
stenosis.
If one cusp is seen to move normally, critical aortic stenosis has
been excluded.
Can lead to overestimation of severity.
To be combined with doppler assessment.
55. A. Evaluate the anatomy of the AV
EAE/ASE recommendations for Echocardiographic assessmentof valve
stenosis, European Journal of Echocardiography 2009
ECHO EVALUATION OF AORTIC STENOSIS
RCC
LCCNCC
DIASTOLE
SYSTOLE
59. ECHO EVALUATION OF AORTIC STENOSIS
B. Determine the aortic valve area by
Continuity Equation
EAE/ASE recommendations for Echocardiographic assessmentof valve
stenosis, European Journal of Echocardiography 2009
60. ECHO EVALUATION OF AORTIC STENOSIS
C. Determine the transaortic jet velocity
• measured using continuous-wave (CW) Doppler
Valvular Hear Disease, Chapter 63, Braunwarld’s HeartDisease10th Edition 2014
61. ECHO EVALUATION OF AORTIC STENOSIS
EAE/ASE recommendations for Echocardiographic assessmentof valve
stenosis, European Journal of Echocardiography 2009
84. PSEUDOSEVERE AORTIC STENOSIS
will exhibit an increase in the AVA
little change in transvalvular gradient in
response to the increase in transvalvular flow
rate
85. TRUE SEVERE AORTIC STENOSIS
• will have no or minimal increase in AVA
• marked increase in gradient when flow is increased
87. ParadoxicalLow flow Low gradient AS
• Elderly female
• Associatedwith HTN, DM
EchoCharacteristics
• Severely thickened and calcified AV
• AVA < 1.0; MVG <40mmHg
• EF ≥ 50%
• Small LV cavity size (LVEDD
<47mm, LVEDV <55mL
• RWT of >0.5
• Impaired global longitudinal strain
<15%
• SV index of <35mL/m2 ASE’s Comprehensive Echocardiography 2nd ed , 2016
88.
89. ECHO EVALUATION OF AORTIC STENOSIS
Hemodynamic Progression
• annual decrease in valve area : 0.12 cm2/year
• annual increase in jet velocity of 0.32 m/sec/year
Follow-up Echo
• every year: severe AS
• every 1 to 2 years for moderate AS
• every 3 to 5 years for mild AS.
Valvular Hear Disease, Chapter 63, Braunwarld’s HeartDisease10th Edition 2014