The slides are from a keynote presentation delivered by ASTMH Secretary-Treasurer David R. Hill, MD, DTM&H, FRCP, FFTM, FASTMH at the 2013 Annual Conference of New Zealand Society of Travel Medicine in Wellington, NZ, 3 August - 4 August.
Arthropods form a major group of disease vectors with mosquitoes, flies, sand flies, lice, fleas, ticks and mites transmitting a huge number of diseases.
Many such vectors are haematophagous, which feed on blood at some or all stages of their lives.
Arthropods form a major group of disease vectors with mosquitoes, flies, sand flies, lice, fleas, ticks and mites transmitting a huge number of diseases.
Many such vectors are haematophagous, which feed on blood at some or all stages of their lives.
Monkeypox is a rare zoonosis caused by monkeypox virus. This disease is similar to smallpox disease but with lesser severity. This disease is common among Africans. It can be prevented by avoiding contact with contaminated animal and human fluids as well as respiratory droplets. It require a multidisciplinary approach to achieve cure and prevention.
Arthropods form a major group of disease vectors with mosquitoes, flies, sand flies, lice, fleas, ticks and mites transmitting a huge number of diseases.
A viral infection spread by a particular species of mosquito.Yellow fever is spread by a species of mosquito common to areas of Africa and South America. Vaccination is recommended before travelling to certain areas.
Zoonoses (Greek “zoon” = animal) are the diseases or infections that are naturally transmissible from vertebrate animals to humans. This group of infections constitutes significant burdens on global public health. The World Health Organisation (WHO) estimates that 25% of the total 57 million annual deaths that occur globally are caused by microbes with a major proportion occurring in the developing world (Chugh, 2008). Of total identified 1,415 species of infectious organisms known to be pathogenic to humans (including 217 viruses and prions, 538 bacteria and rickettsia, 307 fungi, 66 protozoa and 287 helminths), zoonotic agents constitute 868 (61%), with humans serving as the primary reservoir for only 3% of them. Of the 175 diseases considered to be emerging, 132 (75%) are zoonotic in origin (Taylor et al., 2001). In low income countries, established and emerging zoonoses make up 26 % of the DALYs (Disability-adjusted life year) lost to infectious disease and 10 % of the total DALYs lost. In contrast, in high income countries it represent < 1 % of DALYs lost to infectious disease and only 0.02 % of the total disease burden (Grace et al., 2012).
Vectors are living organisms that can transmit infectious diseases between humans or from animals to humans. Vector-borne diseases are infections transmitted by the bite of infected arthropod species, such as mosquitoes, ticks, triatomine bugs, flies, fleas, sandflies, and blackflies (Confalonieri et al., 2007). Among these mosquitoes are the best known disease transmission vectors for many of the fatal and diseases of economic burden. Vector-borne diseases account for 17% of the estimated global burden of all infectious diseases (CDC, 2014). Every year > 1 billion people are infected and > 1 million people die from vector-borne diseases including malaria, dengue, schistosomiasis, leishmaniasis, yellow fever, lymphatic filariasis, Japanese encephalitis and onchocerciasis. One sixth of the illness and disability suffered worldwide is due to vector-borne diseases with more than half the world’s population currently estimated to be at risk of these diseases. Global trade, rapid international travel, unsustainable urbanization, environmental changes such as climate change and emerging insecticidal and drug resistances, are causing vectors and vector-borne diseases to spread beyond borders (WHO, 2014).
Monkeypox is a rare zoonosis caused by monkeypox virus. This disease is similar to smallpox disease but with lesser severity. This disease is common among Africans. It can be prevented by avoiding contact with contaminated animal and human fluids as well as respiratory droplets. It require a multidisciplinary approach to achieve cure and prevention.
Arthropods form a major group of disease vectors with mosquitoes, flies, sand flies, lice, fleas, ticks and mites transmitting a huge number of diseases.
A viral infection spread by a particular species of mosquito.Yellow fever is spread by a species of mosquito common to areas of Africa and South America. Vaccination is recommended before travelling to certain areas.
Zoonoses (Greek “zoon” = animal) are the diseases or infections that are naturally transmissible from vertebrate animals to humans. This group of infections constitutes significant burdens on global public health. The World Health Organisation (WHO) estimates that 25% of the total 57 million annual deaths that occur globally are caused by microbes with a major proportion occurring in the developing world (Chugh, 2008). Of total identified 1,415 species of infectious organisms known to be pathogenic to humans (including 217 viruses and prions, 538 bacteria and rickettsia, 307 fungi, 66 protozoa and 287 helminths), zoonotic agents constitute 868 (61%), with humans serving as the primary reservoir for only 3% of them. Of the 175 diseases considered to be emerging, 132 (75%) are zoonotic in origin (Taylor et al., 2001). In low income countries, established and emerging zoonoses make up 26 % of the DALYs (Disability-adjusted life year) lost to infectious disease and 10 % of the total DALYs lost. In contrast, in high income countries it represent < 1 % of DALYs lost to infectious disease and only 0.02 % of the total disease burden (Grace et al., 2012).
Vectors are living organisms that can transmit infectious diseases between humans or from animals to humans. Vector-borne diseases are infections transmitted by the bite of infected arthropod species, such as mosquitoes, ticks, triatomine bugs, flies, fleas, sandflies, and blackflies (Confalonieri et al., 2007). Among these mosquitoes are the best known disease transmission vectors for many of the fatal and diseases of economic burden. Vector-borne diseases account for 17% of the estimated global burden of all infectious diseases (CDC, 2014). Every year > 1 billion people are infected and > 1 million people die from vector-borne diseases including malaria, dengue, schistosomiasis, leishmaniasis, yellow fever, lymphatic filariasis, Japanese encephalitis and onchocerciasis. One sixth of the illness and disability suffered worldwide is due to vector-borne diseases with more than half the world’s population currently estimated to be at risk of these diseases. Global trade, rapid international travel, unsustainable urbanization, environmental changes such as climate change and emerging insecticidal and drug resistances, are causing vectors and vector-borne diseases to spread beyond borders (WHO, 2014).
Revisión de Fiebre Amarilla que trasciende desde la historia milenaria de esta enfermedad, nos da un enfoque amplio de su concepto, características epidemiológicas, criterios clínicos de aproximación diagnóstica y terapeútica.
Recombinant Expression and Purification of Aedes aegypti Midgut Serine Protea...Kamille Parungao
The Aedes aegypti mosquito is a major vector of blood-borne pathogens, such as the Dengue, Chikungunya, yellow fever, and Zika viruses. This poster discusses the recombinant expression and purification of a late-phase trypsin- like protease, Aedes aegypti serine protease VII (AaSPVII).
A introduction on Viral vaccine for medical students.Although most attenuated vaccines are viral, some are bacterial in nature. Examples include the viral diseases yellow fever, measles, rubella, and mumps, and the bacterial disease typhoid.
A description about Aedes aegypti, a primary vector for yellow fever and dengue fever. To know more about the mosquito in general, check out my "Mosquito" slide.
TEDx Manchester: AI & The Future of WorkVolker Hirsch
TEDx Manchester talk on artificial intelligence (AI) and how the ascent of AI and robotics impacts our future work environments.
The video of the talk is now also available here: https://youtu.be/dRw4d2Si8LA
***For the visually or hearing impaired, this Government of Canada presentation can be made available in an accessible format upon request. Please contact the Lyme Disease Conference Secretariat at maladie_lyme_disease@phac-aspc.gc.ca to request a copy.***
Presentations given at the Conference to Develop a Federal Framework on Lyme Disease are the property of the author, unless otherwise cited. If you reference the author's work, you must give the author credit by naming the author and their work as well as the place and date it was presented.
For more information, contact the Lyme Disease Conference Secretariat at maladie_lyme_disease@phac-aspc.gc.ca
slides on emporiatrics for indian travellers,i was not able to find a decent slide so i compiled the epidemologicl data for various diseases hope u guys find it useful
Presentation by Bernard Bett at the 14th conference of the International Society for Veterinary Epidemiology and Economics (ISVEE), Merida, Yucatan, Mexico, 3-7 November 2015.
Presentation bumpsa 2015-symposium - effect of global travel on health _ the ...Gordon Takop Nchanji
The aim of the presentation was to create awareness about the interaction between health and travel. Here, particular emphasis is on infectious diseases. Read and digest. Comments are welcomed.
Dengue Fever Epidemiology and Control in the Caribbean: A Status Report (2012)rsmahabir
The epidemiology of Dengue fever in the English speaking Caribbean over the last two decades is reviewed. Dengue cases reported to the World Health Organization, Pan American Health Organization, Caribbean Epidemiology Centre and in recent published papers were collated and analysed to determine the incidence and geographical distribution among the various countries. Dengue fever was observed among most Caribbean countries with various intensities of transmission. During 2010 all four dengue serotypes were found co-circulating within the Caribbean islands with crude fatality rates of 6 in Barbados, 4 in Jamaica, 3 in the Bahamas and 2 in Dominica. Similar numbers of males and females from the 20-39 age group were found with DHF but the 10-19 age group shows a slight increase in disease levels. Overall more males were reported with DF/DHF than females. The results show significant (P<0.002) increases in the number of DF/DHF cases and in Ae. aegypti indices during the rainy season compared to the dry season. Little data is available on the density of the Aedes aegypti population in the Caribbean region, and most information comes from Jamaica and Trinidad and Tobago.
View the slides of a tribute to the late Alan Magill by ASTMH Past President Christopher V. Plowe, MD, MPH, FASTMH, during WRAIR's inaugural Magill Symposium on June 23 in Silver Spring, MD.
Slides from President-Elect Patricia F. Walker, MD DTM&H, FASTMH, keynote adress to the 6th Annual North American Refugee Health Conference , June 12, 2016 in Niagara Falls, NY: “Refugee Healthcare: Imagining our Future.”
Presentation delivered by ASTMH Executive Director Karen A. Goraleski for the National Center for Emerging and Zoonotic Infectious Diseases (NCEZID) Lecture Series at the Centers for Disease Control and Prevention
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
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
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.
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
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
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.
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.
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
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
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
1. Yellow Fever: Risk Mapping
Wellington, August 2013
David R Hill MD DTM&H FRCP FFTM FASTMH
Professor of Medical Sciences
Director, Global Public Health
Frank H Netter MD School of Medicine
Quinnipiac University
2. Assessing Geographic Risk of Yellow Fever
• Defining disease risk in travellers
• Goals, rationale and process
• Outcomes: new categories of risk
• Specific country examples
• Implications: travel medicine & IHR (2005)
• Implementation
3. • For relatively high incidence disease we combine:
global epidemiology of disease
imported cases / # travellers / destination / time
Defining Disease Risk for Travel
4. Defining Disease Risk: Malaria
US Civilian Travellers, 2008
Mali S, et al. MMWR
59(SS-7):1, 2010
Travellers Visiting Friends and Relatives:
3.7 x risk to West Africa Smith AD, et al. BMJ 337:a120, 2008
5. • Enteric fever imported to UK:
93% of cases from South Asia
Defining Disease Risk: Enteric fever
UK Travellers
Country
Rate*
VFR
Rate Non-
VFR
India 28.8 3.3
Pakistan 26.4 8.2
Bangladesh 36.9 10.5
* Rate of S. Typhi and S. Paratyphi A/100,000 visits
Lawrence J, Jones J. Enhanced enteric fever surveillance.
UK Public Health England, 2008.
6. • For low volume disease we take into account:
global epidemiology (geography of risk)
severity of disease
case reporting becomes anecdotal
• Polio, Japanese encephalitis, yellow fever
• Define risk based on geography and exposure
Defining Disease Risk for Travel
Base prevention on sensible,
‘evidence-based’ measures
7. Imported Yellow Fever Cases: 1970-2013
Country Year Case Outcome Vaccinated?
Senegal 1979 42, M Death No
Senegal 1979 25, M Death No
Guinea-Bissau 1985 27, F Survived No
West Africa 1988 37, F Survived Yes
Brazil 1996 53, M Death No
Brazil 1996 42, M Death No
Cote d’Ivoire 1999 40, M Death No
Venezuela 1999 48, M Death No
The Gambia 2001 47, F Death No
Brazil 2002 47, M Death No
8. 2011 WHO Yellow Fever
Vaccination Maps
Vaccination recommended
Vaccination usually not recommended
Not recommended
9. Historical Determination of YF Risk
• Clinical case reports
– severe illness, foreigners,
coastal ports, rivers and railways
– non-specific: e.g. confused with
malaria, hepatitis, leptospirosis
• Serosurveys: mouse protection
assay (1931)
• Viscerotomies in persons dying
with a febrile illness; mostly in
S. America
10. Yellow Fever Epidemiology: Africa
Sawyer WA. Harvey Lectures. 66-92, 1936.
Human Cases: 1920-1934 Human Serology: 1930-1934
11. Yellow Fever Endemic Regions, 1945
UN Relief and Rehabilitation Administration. Epidemiol Inf Bull. 1:687, 1945.
South America Africa
12. • Response to:
– recognition of serious adverse events
– changing epidemiology of yellow fever
• Goals:
– more accurate definition of risk areas
– unify risk maps between CDC & WHO
– transparency of recommendations
– inform country policy around IHR (2005)
WHO Consultation on Yellow Fever Risk, 2008
Jentes E, et al. Lancet Infect Dis. 11:622, 2011
Curr Infect Dis Rep 14:246, 2012
13. Evidence Used for Risk Mapping
• Human and non-human primates: cases,
clusters and outbreaks
• Human serology prior to YF vaccination;
most data generated in 1950s and earlier
• Vegetation and altitude
• Vector distribution
17. • Endemic
• Transitional
• Low potential (risk)
for exposure
• No risk
Yellow Fever Consultation
Creation of New Categories of Risk
18. Yellow Fever Risk Classification
Risk
Classification
Examples
Criteria for Risk
YF vectors
and NHP
present?
Human or
NHP YF
cases?
Serosurvey
evidence?
Endemic Nigeria Yes Repeatedly High levels
Transitional Paraguay Yes
Reported at
long intervals
Present
Low potential
for exposure
Tanzania Yes None Low levels
No New Zealand Yes / No None No
19. Use of Elevation Data: Bolivia
Areas below 2,300 m, determined from
global digital elevation model (GTOPO30 )
Areas below 2,300 m classified endemic
Altitude limit of 2,300 m
20. Use of Vegetation Data: Niger
Barren or sparsely vegetated areas
as determined from normalized
difference vegetation index (NDVI)
Areas classified as endemic
21. Peru:
no risk: coastal, south of La
Libertad, Andes above 2,300 m
low potential: Tumbes,
Lambayeque, and parts of
Piura and Cajamarca
transitional: eastern Piura state
endemic: remainder of country
New Yellow Fever Risk Maps
22. Kenya:
low potential: North
Eastern zone, Coastal
zone and Nairobi
endemic: remainder of
country
New Yellow Fever Risk Maps
24. Zambia
low potential: North
West and Western
provinces
no risk: remainder
of country
New Yellow Fever Risk Maps
25. Special Considerations
• Examined high volume destinations, in attempt to
avoid vaccinating many travelers unnecessarily
• Low potential for exposure:
port cities in South America
Cartagena, Baranquilla, Port of Spain
Nairobi
• No risk:
transit of 12 h or less in international airports
Inca Trail (Peru)
26. Yellow Fever Risk Mapping:
Shift from risk maps to vaccination maps
• Vaccination recommended
– endemic
– transitional
• Vaccination generally not recommended
– low potential for exposure (low risk)
– exceptions: prolonged, often rural,
extensive mosquito exposure
• Vaccination not recommended
– no risk
28. Implications for IHR (2005)
Low risk countries
Low potential for exposure
Thus, low risk countries will never appear in Annex 1
29. IHR (2005): Annex 1B, 2f
Afghanistan, Australia, & India require YF vaccine
from travellers arriving from countries with a (low) risk
of YF transmission; e.g. historically from Tanzania,
Eritrea, Zambia.
South Africa considers ‘low potential’ as risk and
requires vaccine of travelers from Tanzania &
Zambia, including those in transit.
30. 2011 WHO Yellow Fever
Vaccination Maps
Vaccination recommended
Vaccination usually not recommended
Not recommended
32. Conclusions
• Robust process using best available evidence
• Transparency in decision making
• Attempts at ‘shrinking’ risk map
• Achieved globally agreed risk categorization
• Implications for travel medicine practitioners
• Implications for Annex 1 (ITH) under IHR (2005)
• Continuous review of model and epidemiology