- FDG PET/CT plays an important role in staging and assessing treatment response for FDG-avid lymphomas according to the Lugano classification criteria.
- For FDG-avid lymphomas, FDG PET/CT is the standard for imaging and a 5-point scale should be used for response assessment. A bone marrow biopsy is no longer needed for routine staging of Hodgkin's lymphoma and most diffuse large B-cell lymphomas.
- While interim PET-adapted treatment strategies have shown benefit for Hodgkin's lymphoma, the data is less clear for non-Hodgkin's lymphoma and treatment escalation based on an interim positive PET scan is not routinely recommended.
FDG PET/CT plays an important role in staging, restaging, prognostication, planning treatment strategies, monitoring therapy, and detecting relapse. In this lecture I try my best to explain it for our fellows .
FDG PET/CT plays an important role in staging, restaging, prognostication, planning treatment strategies, monitoring therapy, and detecting relapse. In this lecture I try my best to explain it for our fellows .
EBCTCG METAANALYSIS
INDICATION OF POST OP RADIOTHERAPY
Immobilization devices
Conventional planning
Alignment of the Tangential Beam with the Chest Wall Contour
Doses To Heart & Lung By Tangential Fields
EBCTCG METAANALYSIS
INDICATION OF POST OP RADIOTHERAPY
Immobilization devices
Conventional planning
Alignment of the Tangential Beam with the Chest Wall Contour
Doses To Heart & Lung By Tangential Fields
General management
Management of low grade gliomas: overview
Pilocytic astrocytoma
non pilocytic/diffuse infiltrating gliomas
Management of high grade gliomas: overview
Anaplastic gliomas
Glioblastoma multiformae
PET is a technique that measures physiological function by looking at blood flow, metabolism, neurotransmitters, regional chemical composition and radiolabelled drugs.
PET CT beginners Guide covers some of the underrepresented topics in PET CTMiadAlsulami
This lecture briefly covers some of the underrepresented topics in Molecular imaging with cases , such as:
- Primary pleural tumors and pleural metastases.
- Distinguishing between MPM and Talc Pleurodesis.
- Urological tumors.
- The role of FDG PET in NET.
Artifacts in Nuclear Medicine with Identifying and resolving artifacts.MiadAlsulami
Identifying and resolving artifacts is important to prevent misinterpretation. I always emphasize on the importance of understanding artifacts, pitfalls, and urgent findings .
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
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
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.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of 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 leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
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. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
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
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.
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.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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.
2. Outlines:
• Background Information And Definitions.
• Patient Preparations.
• Brief review of the Lugano classification and Response evaluation
criteria .
• Role of iPET CT in FDG avid lymphoma .
4. • F18 FDG also commonly called fluorodeoxyglucose.
• Radiopharmaceuticalused in the medical imaging modality positron
emission tomography PET CT.
• Chemically, it is a glucose analog, with the positron-emitting
radionuclide fluorine-18 substituted for the normal hydroxyl group at
the C-2 position in the glucose molecule.
5. • FDG is taken up by high-glucose-using cells such as tumor cells where
phosphorylation prevents the glucose from being released again from
the cell.
• FDG is missing this 2-hydroxyl,FDG cannot be further metabolized in
cells.
• The labeled 18F FDG compound has a relatively short shelf life which
is dominated by the physical decay of fluorine-18 with a half-life of
109.8 minutes, or slightly less than two hours.
8. • Patients should be instructed to fast and not consume beverages,
except for water, for at least 4–6 .
• The patient should remain seated or recumbent for 18F-FDG
administration and the subsequent uptake phase to avoid muscular
uptake.
• The blood glucose level should be checked before 18F-FDG
administration.
• Most institutions reschedule the patient if the blood glucose level is
greater than 150–200 mg/Dl.
9.
10. • Reducing the serum glucose level by administering insulin can be
considered, but the administration of 18F-FDG should be delayed
after insulin administration (with the duration of the delay being
dependent on the type and route of administration of insulin).
11. • Post biopsy : 7 to 10 days
• Post surgery: 4-6 weeks ( minimum 2 weeks)
• Post chemotherapy: 3 months after the end of treatment ( minimum
3 weeks) .
• PET should not be performed earlier than 10 days after
Chemotherapy , to avoid the “stunning” effect of therapy on tumor
cells and nonspecific FDG uptake due to CT-induced inflammation.
• Post radiotherapy: 12 weeks ( 3 months)
• G-CSF: 5 days to 4 weeks.
12. Bone Marrow Hyperplasia
Increased bone marrow cellularity can be due to Decreased
peripheral blood cell counts leading to Marrow expansion:
1. Anemia
2. Leukemia
Induced by pharmacologic agents:
1. Chemotherapy
2. Bone marrow stimulating agents (GCSF, EPO)
13. Brief review of the Lugano
classification and the role of FDG-
PET/CT in Lymphoma
14.
15. • A workshop was held at the 11th International Conference on
Malignant Lymphoma in Lugano, Switzerland, in June 2011.
• The conference included leading hematologists, oncologists, radiation
oncologists, pathologists, radiologists, and nuclear medicine
physicians, representing major international lymphoma clinical trials
groups and cancer centers.
16. • The accurate assessment of initial disease status and therapeutic
responses is critical to the optimal management of patients with
lymphoma.
• Currently, staging and treatment response evaluation for lymphoma
has been standardized into the Lugano classification.
• Lugano classification incorporates positron emission tomography
(PET) into the existing response criteria, and response assessment
using FDG-PET/CT has been proven to predict the prognosis in various
lymphoma subtypes effectively.
17. • As a result, FDG PET CT was formally incorporated into standard
staging for FDG-avid lymphomas.
• A modification of the Ann Arbor descriptive terminology will be used
for anatomic distribution of disease extent.
• The suffixes A or B for symptoms will only be included for HL.
• A bone marrow biopsy is no longer indicated for the routine staging of
HL and most diffuse large B-cell lymphomas.
18. • PET-CT will be used to assess response in FDG-avid histologies using
the 5-point scale.
• Routine surveillance scans are discouraged.
22. FDG PET CT is indicated in all types of lymphoma except :
1. Chronic lymphocytic leukaemia/small lymphocytic lymphoma
2. Lymphoplasmacytic lymphoma/Waldenstrom’s macroglobulinemia,
3. Mycosis fungoides,
4. Marginal zone lymphomas
Unless there is a suspicion of aggressive transformation
23. • PET-CT is indicated in all FDG avid lymphoma as a part of staging and
response assessment.
• CECT rarely alters management, and can be reserved for:
1. Measurement of nodal size for trials.
2. Radiation planning.
3. Distinguishing bowel from nodes.
4. Assessing compression/thrombosis of central/mediastinal vessels.
24. • In practice many patients have separate CECT before PET-CT.
• If CECT is required at staging, it should ideally be combined with
PET-CT at a single visit.
• Full dose CECT involves additional radiation, which should be
considered when deciding which examination(s) to perform.
25. • PET-CT is recommended for response assessment using 5-Point Scale
(5-PS).
Staging and response assessment of lymphoma: a brief review of the Lugano classification and the role of FDG-PET/CT
26.
27. Biopsy of residual metabolically active tissue is recommended if
salvage treatment is considered→ interval scan can be considered
where clinical likelihood of disease is low.
30. Role of iPET CT in FDG avid lymphoma
• Interim PET-adapted strategies have gained hold in HL.
• The data in NHL are less conclusive.
• Numerous studies have explored escalation of therapy in response to
a positive interim PET in this patient population.
• No consistent improvement in outcomes has been demonstrated
with intensified regimens compared to standard R-CHOP.
31. • The overall predictive value was lower than that of HL.
• No trial has, thus far, demonstrated the superiority of the iPET-driven
strategy over the conventional methodology in DLBCL.
• Therefore, in patients with DLBCL, treatment escalation for interim
PET positivity is not recommended in routine practice.
32. Summary :
• The Deauville scale and Lugano criteria are part of an ongoing
process to improve incorporation of FDG PET/CT in the treatment of
lymphoma.
• The Lugano criteria incorporates the Deauville scale and provides
additional integration with CT, pathology, radiotherapy and clinical
practice.
33. • Changes introduced by the Lugano criteria include:
1. FDG PET/CT is the standard for imaging FDG-avid lymphomas
2. CT is indicated for non-avid histologies.
3. If FDG PET/CT is performed for HL a BMB is no longer indicated.
4. If FDG PET/CT for DLBCL is negative a BMB is only needed if
identifying a discordant histology is important for patient
management.
5. The 5-point scale for FDG PET/CT should be used for response
assessment in FDG-avid lymphomas.