1. Treadmill testing (TMT) is used to detect myocardial ischemia by stressing the cardiovascular system during exercise and observing the physiological responses.
2. During TMT, increases in heart rate, blood pressure, cardiac output and oxygen consumption are measured along with ECG changes to detect ischemia.
3. Abnormal responses that may indicate ischemia include ST segment depression, elevated systolic blood pressure, chest pain, and failure to reach target heart rate.
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.
Various coronary physiological measurements can be made in the cardiac catheterization laboratory using sensor-tipped guidewires; they include the measurement of poststenotic absolute coronary flow reserve, the relative coronary flow reserve, and the pressure-derived fractional flow reserve of the myocardium. Ambiguity regarding abnormal microcirculation has been reduced or eliminated with measurements of relative coronary flow reserve and fractional flow reserve. The role of microvascular flow impairment can be separately determined with coronary flow velocity reserve measurements. In addition to lesion assessment before and after intervention, emerging applications of coronary physiology include the determination of physiological responses to new pharmacological agents, such as glycoprotein IIb/IIIa blockers, in patients with acute myocardial infarction. Measurements of coronary physiology in the catheterization laboratory provide objective data that complement angiography for clinical decision-making
Repolarization ST wave Abnormalities
Precise guide for Allied Health Science Students especially cardiac specialty students, DGNM, B.Sc Nursing & M.Sc Nursing Students regarding Repolarization ST wave Abnormalities.
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.
Various coronary physiological measurements can be made in the cardiac catheterization laboratory using sensor-tipped guidewires; they include the measurement of poststenotic absolute coronary flow reserve, the relative coronary flow reserve, and the pressure-derived fractional flow reserve of the myocardium. Ambiguity regarding abnormal microcirculation has been reduced or eliminated with measurements of relative coronary flow reserve and fractional flow reserve. The role of microvascular flow impairment can be separately determined with coronary flow velocity reserve measurements. In addition to lesion assessment before and after intervention, emerging applications of coronary physiology include the determination of physiological responses to new pharmacological agents, such as glycoprotein IIb/IIIa blockers, in patients with acute myocardial infarction. Measurements of coronary physiology in the catheterization laboratory provide objective data that complement angiography for clinical decision-making
Repolarization ST wave Abnormalities
Precise guide for Allied Health Science Students especially cardiac specialty students, DGNM, B.Sc Nursing & M.Sc Nursing Students regarding Repolarization ST wave Abnormalities.
Cardiovascular response to exercise stress enables assessment of cardiovascular reserve.
Helps to identify patients with compensated disease with normal resting hemodynamics
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
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
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
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.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
2. • To detect presence of myocardial infarction
secondary to CAD
• To predict the prognosis
3. TMT
• Exercising muscles need energy to contract
and relax.
• Energy is derived from oxidative metabolism
to generate ATP.
• Energy requirement at rest or active state can
be estimated from measurement of
TOTAL BODY O2 UPTAKE = Vo2
4. TMT
• Fick equation demonstrates that
Vo2 = CO x Perip. O2 extractn (A-V o2difference)
• Vo2 expressed in multiples of resting o2
requirements ( Metabolic equivalents METs )
• 1 MET = basal resting energy expenditure
= 3.5mL o2 / kg body wt / mt
5. • Eg. 5 MET activity requires 5 times the energy
required at rest.
• Vo2 max = peak o2 uptake achieved during
highest level of exercise .
• Dep on age, sex, heridity, exercise habits, cvs
status
6. • During exercise,
• CO increases 4-6 times the resting levels
• HR- 2to 3 fold increase.
• SV plateaus at 50-60% of vo2 max
• O2 extraction at periphery can increase 3 fold
• Max A-V o2 difference has a physiologic limit
15-17mlo2 / 100ml blood
7. Vo2 Peak
• During tmt , pts are prompted to exercise not
until they reach vo2 max
• but rather to the vo2 that is attained during
symptom limited , maximum tolerated
exercise
• – this level is termed as vo2 peak
8. • Myocardial ischemia = demand supply mismatch
of o2 blood
• Many factors influence this delicate balance
• TMT is performed to stress these relationships
and observe the physiologic responses
• To assess the devolepment of ischemia
• And to evaluate at what level of myocardial o2
demand and physical activity ( work rate )
ischaemia occurs.
12. Myocardial Oxygen Demand
• Indirectly measured as the Double Product or
rate pressure product
• “Double Product” = HR x SBP
• Reliable index of myocardial o2 demand
Increases to more than 20,000 on exercise
16. ENERGY REQ ACTIVITY
1 MET TAKING CARE OF SELF
WALKING INDOORS
WALK AT 2-3 mph
4 METS LIGHT WORK AROUND THE HOUSE
WALKING AT 3-4 mph
>4-<10 METS CLIMB 1 FLIGHT OF STAIRS/UP HILL
WALK>4 mph, SHORT RUNNING
SCRUBBING FLOOR,MOVING
FURNITURE
>10 METS RUNNING> 6-7 mph
HEAVY LABOUR
SWIMMING,FOOTBALL
17.
18. Calculation of METs on the Treadmill
• METs = Speed x [0.1 + (Grade x 1.8)] +
3.5
3.5
• Calculated automatically by Device
19.
20. Patient Assessment
• Withhold cardiac medications on the day of
study to better assess ischemic response
• If taking medications , to evaluate the effects
on HR, BP, Symptoms and ischemia during
exercise
• If ICD ; Peak HR < 10 beats/min below the
programmed heart rate threshold for
antitachycardia pacing & defibrillation
21. Contraindications to Exercise Testing
Absolute
• A/c MI (< 2 d)
• High-risk unstable angina
• Uncontrolled cardiac arrhythmias causing symptoms with
hemodynamic compromise
• Symptomatic severe AS
• Decompensated heart failure
• Acute pulmonary embolus or infarction
• A/c myocarditis or pericarditis
• Physical disability
22. Contraindications to Exercise Testing
Relative
• LMCA stenosis
• Mod- AS + symptoms
• CHB
• Tachyarrhythmias with FVR
• HOCM with sev. Resting gradient
• Mental or physical impairment leading to
inability to exercise adequately
23. • Rate of major complications (MI/ hospitaliation)
• <1-5 per 10,000 tests
• Recent MI, low EF, exertion induced myocard
ischemia & serious ventric. Arrythmias = Highest
risk
• Death < 0.5 per 10,000 tests
24.
25. Pretest Probability
• Based on the pat's h/o ( age, gender, chest pain ),
phy ex and initial testing, and the clinician's
experience.
• Typical or definite angina →pretest probability
high
26.
27. The Bruce protocol
• 1949 by Robert A. Bruce,
considered the “father of
exercise physiology”.
• Published as a standardized
protocol in 1963.
• gold-standard for detection
of myocardial ischemia when
risk stratification is
necessary.
28.
29.
30.
31.
32. Normal Response to Stress Testing
• Heart rate increases
• Blood pressure increases
• Cardiac output increases
• Total peripheral resistance decreases
• Dysrhythmias – isolated unifocal PVC’s and
PAC’s (suppressed at increased heart rate)
• Oxygen consumption increases
33. Exercise capacity
• Strong predictor of mortality & Non fatal
cardiovascular outcome in both men &
women with or without CAD
• Predicted METS = 18-(0.15x age)
• Predicted METS = 14.7- (0.13x age)
34.
35. MHR
• HR max = 220 – age
• HR max = 208 – (0.7 x age)
• HR max = 206 – (0.88 x age)
• HR max = 164 – (0.7 x age)
36. Abnormal Response
to Stress Testing
• Heart rate fails to rise above 120 or unable to
attain THR of 85% of max
• SBP shows a drop
• Physically unable to complete test
• Marked hypertension, >260/115
• Chest Pain and/or unusual shortness of breath
37. Chronotropic incompetence
• inability of the heart to increase its rate to meet
the demand placed on it
• Independent predictor of mortality
• < 85 % of age predicted MHR = incomplete study
• Chronotopic index
[(HR max- HR rest )x 100 ]/[(220-age)- HR rest]
• < 80 % = CI
• <62 % = CI (B blocker)
38. HR recovery
• < 12beats / min after 1 min with post exercise
cool down
• < 18 beats / min after 1 min with complete
cessation of movement
• < 45 beats / min after 2 min.
• Associated with increase in mortality
indepently , in both asymptomatic and in ppl
with established heart disease
39. Exaggerated systolic pressure response
• > 210 mm hg ; > 190 mm hg
• Not an indication to terminate the test
• May indicate future development of
hypertension or adverse cardiac events
40. Excercise induced hypotension
• Systolic pressure during exercise < resting
pressure
• 20 mm hg fall in BP after an initial rise
• Reason to terminate the test
• More predictive of poor prognosis & multiple
vessel CAD
• Cardiomyopathy, LVOT obstruction,
hypovolumia, hypertensive medications
41. Low systolic peak
• Rise in BP to 140mm hg
• Overall rise less than 10 mm hg
– Severe CAD
– Worse cardiovascular outcome in persons with
and without CAD
42. Normal Response of ECG
to Stress Testing
• ECG Changes
– QRS complex ↓ in size
– PR,QRS,QT shorten
– J point ↓, resulting in up sloping of ST segment
– ST segment returns to baseline by 80
milliseconds
– PR segment may down slope(Inf leads– baseline
PQ junction)
– R amplitude may decr at rates > 130
– P ampl ↑
– T wave decreases
45. • ST 60 -- HR > 130/min
• ST 80 -- HR ≤ 130/min
46. ST-Segment Changes on the Exercise ECG
ST DEPRESSION:
• Measurements made on 3 consecutive ECG complexes
• ST level is measured rel to the P-Q junction
• When J-point is depressed rel to P-Q junction at baseline:
– Net diff from the rest J junction - amount of deviation
• When the J-point is ↑ rel to P-Q junction at baseline and
becomes ↓ isoel with exercise:
– Mag of ST dep - P-Q junction and not the resting J point
47. Abnormal and Borderline ST-Segment Depression
• ABNORMAL:
– 1.0 mm or > horizontal or downsloping ST dep at
80 msec after J point on 3 consecutive ECG complexes
• BORDERLINE:
– 0.5 to 1.0 mm horizontal or downsloping ST dep at
80 msec after J point on 3 consecutive ECG complexes
– 1.5 mm or > upsloping ST dep at 80 msec after J
point on 3 consecutive ECG complexes
51. ECG Patterns Indicative of Myocardial Ischaemia
ECG Patterns Not Indicative of Myocardial Ischaemia
52. • In lead V4 , the
exercise ECG result is
abnormal early in the
test, reaching 0.3 mV
(3 mm) of horizontal
ST segment
depression at the end
of exercise.
• severe ischemic
response.
53. •The J point at peak exertion is
depressed 2.5 mm, the ST
segment slope is 1.5 mV/sec,
and the ST segment level at 80
msec after the J point is
depressed 1.6 mm.
• “slow upsloping” ST segment
at peak exercise indicates an
ischemic pattern in patients
with a high coronary disease
prevalence pretest.
•typical ischemic pattern is
seen at 3 minutes of the
recovery phase when the ST
segment is horizontal and 5
minutes after exertion when
the ST segment is
downsloping.
54. • abnormal at 9:30 minutes
ES test and resolves in the
immediate recovery phase.
•pattern in which the ST
segment becomes
abnormal only at high
exercise workloads and
returns to baseline in the
immediate recovery phase
may indicate a false-positive
result in an asymptomatic
individual without
atherosclerotic risk factors.
55. LEAD aVR
• 1mm or greater ST elevation – significant
predictor of LMCA, Proximal LAD or
multivessel CAD
• As an isolated marker, high sensitivity,
moderate specificity & high –ve predictive
value
56. CHANGES IN QRS
• Exercise induced BBB are rare < 0.5% or less
• If EI LBBB occurs @ HR > 125, CAD is unlikely
• IF EI LBBB occurs @ lower heart rates => death
& major cardiac events
• EI RBBB no risk