This document discusses H1N1 influenza, also known as swine flu. It provides information on:
- The 2009 H1N1 pandemic which was declared by the WHO.
- Symptoms, transmission, treatment and prevention of H1N1 influenza. Key points are that it is highly contagious and spreads through coughing/sneezing. Oseltamivir is an effective antiviral treatment.
- Those at higher risk include children, pregnant women, elderly, and those with underlying health conditions. Complications can include pneumonia. Vaccination is the best prevention.
Hello friends i am BSc Nursing intern.This presentation of mine covers almost each and every aspect related to swine flu.Hope it will help you to increase your knowledge regarding the topic.Looking forward to your feedback.Thank you
Hello friends i am BSc Nursing intern.This presentation of mine covers almost each and every aspect related to swine flu.Hope it will help you to increase your knowledge regarding the topic.Looking forward to your feedback.Thank you
What is influenza ,ethology ,types ,presentations signs and symptoms ,epidemic influenza ,laboratory investigations , management , the WHO guidelines in dealing with cases and contact
This ppt contains all information about epidemiology of Diptheria. It is useful for students of medical field learning preventive and social medicine, Swasthavritta (Ayurved), nursing and everyone who is interested in knowing about it.
Swine flu is a respiratory disease. It is caused by the influenza viruses that infect the respiratory tract of pigs. It can lead to symptoms such as a barking cough, decreased appetite, nasal secretions, and listless behaviour; the virus can be transmitted to humans. The Swine flu vaccination or H1N1 vaccination is crucial to provide immunity against swine flu.
This ppt contains all information about epidemiology of mumps. It is useful for students of medical field learning preventive and social medicine, Swasthavritta (Ayurved), nursing and everyone who is interested in knowing about it.
Dr. Sachin Verma is a young, diligent and dynamic physician. He did his graduation from IGMC Shimla and MD in Internal Medicine from GSVM Medical College Kanpur. Then he did his Fellowship in Intensive Care Medicine (FICM) from Apollo Hospital Delhi. He has done fellowship in infectious diseases by Infectious Disease Society of America (IDSA). He has also done FCCS course and is certified Advance Cardiac Life support (ACLS) and Basic Life Support (BLS) provider by American Heart Association. He has also done a course in Cardiology by American College of Cardiology and a course in Diabetology by International Diabetes Centre. He specializes in the management of Infections, Multiorgan Dysfunctions and Critically ill patients and has many publications and presentations in various national conferences under his belt. He is currently working in NABH Approved Ivy super-specialty Hospital Mohali as Consultant Intensivists and Physician.
What is influenza ,ethology ,types ,presentations signs and symptoms ,epidemic influenza ,laboratory investigations , management , the WHO guidelines in dealing with cases and contact
This ppt contains all information about epidemiology of Diptheria. It is useful for students of medical field learning preventive and social medicine, Swasthavritta (Ayurved), nursing and everyone who is interested in knowing about it.
Swine flu is a respiratory disease. It is caused by the influenza viruses that infect the respiratory tract of pigs. It can lead to symptoms such as a barking cough, decreased appetite, nasal secretions, and listless behaviour; the virus can be transmitted to humans. The Swine flu vaccination or H1N1 vaccination is crucial to provide immunity against swine flu.
This ppt contains all information about epidemiology of mumps. It is useful for students of medical field learning preventive and social medicine, Swasthavritta (Ayurved), nursing and everyone who is interested in knowing about it.
Dr. Sachin Verma is a young, diligent and dynamic physician. He did his graduation from IGMC Shimla and MD in Internal Medicine from GSVM Medical College Kanpur. Then he did his Fellowship in Intensive Care Medicine (FICM) from Apollo Hospital Delhi. He has done fellowship in infectious diseases by Infectious Disease Society of America (IDSA). He has also done FCCS course and is certified Advance Cardiac Life support (ACLS) and Basic Life Support (BLS) provider by American Heart Association. He has also done a course in Cardiology by American College of Cardiology and a course in Diabetology by International Diabetes Centre. He specializes in the management of Infections, Multiorgan Dysfunctions and Critically ill patients and has many publications and presentations in various national conferences under his belt. He is currently working in NABH Approved Ivy super-specialty Hospital Mohali as Consultant Intensivists and Physician.
Coronavirus is the largest known RNA virus responsible for a range of respiratory illnesses in man. 7 Known coronaviruses have been identified with 4 causing mild infections and 3 severe diseases. The severe diseases are SARS, MERS and COVID-19
There is presently an ongoing epidemic of the disease in China which has gradually spread across the continent.
Content & references in part including multimedia content (illustrations, videos) might be taken from the public domain, by no means, aiming at copyrights infringement. All intellectual property rights reserved with the owners.
Lecture by Dr. Naji Aoun, Infectious diseases specialist, Hotel Dieu, held at Le Bristol Hotel, Sept. 28, 2009 under the sponsorship of LIONS Midtown Club and Hoffmann-La Roche
- 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
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!
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.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
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
Title: Sense of Taste
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 structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
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
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.
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.
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.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
3. INTRODUCTION
• Influenza is a serious respiratory illness of humans.
• Influenza pandemics have been associated with high
morbidity and mortality worldwide.
• Influenza A(H1N1) virus is a subtype of influenza A
virus and the most common cause of influenza(flu)
in humans.
• In 2009, the WHO declared the new strain of swine
origin H1N1 as a pandemic which is often referred as
“swine flu”.
4. What is Influenza (“flu”)?
• It is an acute
respiratory illness
caused by influenza
virus
• It infects the nose,
throat and lungs
• It is highly contagious
and spreads rapidly
from person to person
http://www.cdc.gov/flu/about/disease/
6. 80 to 120 nm
Lipid bilayer
16 types H1-H16
9 types N1- N9
Surface
antigens
Relevant parts of the virus
Subtypes of type A - depend on H & N antigens and are many.
Type B & C - not many subtype variations
H & N antigens of Influenza virus A change every year.
Neuraminidase (NA)
Haemaglutinin (HA)
http://emedicine.medscape.com/article/219557-overview#a0101
8. The Novel 2009 H1N1 Virus
• Quadruple reassortment virus from pigs (North
American and Eurasian), Avian and human
2009 H1N1
virus
Replicates in the lungs more efficiently
9.
10.
11. How does it spread ?
Flu viruses spread mainly from
person to person through
coughing, sneezing, or talking to
someone with the flu.
Direct
contamination
The virus is transmitted by
respiratory aerosols (droplets)
loaded with virus that is expelled
during coughing & sneezing.
Respiratory
aerosols
(loaded with
virus)
Gets
infected
People with flu can spread it to
others up to about 6 feet away.
http://www.cdc.gov/flu/about/disease/spread.htm
12. How does it spread ?
People may also catch flu by touching their mouth
or nose after touching something with the virus on
it, such as doorknobs, tables, or an infected
person’s dirty hand.
Indirect
contamination
Infected
person
Gets
infectedhttp://www.cdc.gov/flu/about/disease/spread.htm
13. Source: Bean B, et al. JID 1982;146:47-51
Survival of Influenza Virus
Surfaces and Affect of Humidity & Temperature*
• Hard non-porous surfaces 24-48 hours
▫ Plastic, stainless steel
Recoverable for > 24 hours
Transferable to hands up to 24 hours
• Cloth, paper & tissue
▫ Recoverable for 8-12 hours
▫ Transferable to hands 15 minutes
• Viable on hands <5 minutes only at high viral titers
▫ Potential for indirect contact transmission
*Humidity 35-40%, Temperature 28C (82 F)
14. How long can a person with the flu
spread the virus to other people?
Most people may be
able to spread the flu
from 1 day before
showing symptoms
to 5 to 7 days after
symptoms begin.
Some people, especially
young children and
people with weakened
immune systems, might
be able to infect others
for an even longer time.
Some persons can
be infected with
the flu virus but
have no symptoms.
During this time,
those persons may
still spread the
virus to others.
Symptoms start 1 to
4 days after the
virus enters the
body.
15.
16. What are the signs and symptoms?
http://www.cdc.gov/flu/about/disease/symptoms.htm
17. >
38°C Any
2
SIGNS AND SYMPTOMS:
Lab tests not easily available & diagnosis is
clinical
If fever is accompanied with
any of these 2 signs and
symptoms, then diagnosis is
confirmed in 70% of cases
during the influenza season
18. Signs and symptoms
Two less common signs of the flu include:
Not everyone who
is sick with flu will
have all the signs
of the flu at the
same time.
It’s important to
note that not
everyone with flu
will have a fever.
These signs are more
common in children
than adults.
19. Case Definitions
A suspected case of Pandemic influenza A (H1N1)
virus infection is defined as a person with acute febrile
respiratory illness (fever ≥ 38 0 C) with onset.:
• within 7 days of close contact with a person who is a
confirmed case of pandemic influenza A (H1N1) virus
infection, or
• within 7 days of travel to community where there are one
or more confirmed pandemic influenza A(H1N1) cases,
or
• resides in a community where there are one or more
confirmed pandemic influenza cases.
20. Case Definitions
A probable case of Pandemic influenza A (H1N1)
virus infection is defined as a person with an acute
febrile respiratory illness who:
• is positive for influenza A, but unsubtypable for H1 and
H3 by influenza RT-PCR or reagents used to detect
seasonal influenza virus infection, or
• is positive for influenza A by an influenza rapid test or an
influenza immunofluorescence assay (IFA) plus meets
criteria for a suspected case
• individual with a clinically compatible illness who died of
an unexplained acute respiratory –illness who is
considered to be epidemiologically linked to a probable
or confirmed case.
21. Case Definitions
• A confirmed case of pandemic influenza A
(H1N1) virus infection is defined as a person with an
acute febrile respiratory illness with laboratory
confirmed pandemic influenza A (H1N1) virus
infection at WHO approved laboratories by one or
more of the following tests:
• Real Time PCR
• viral culture
• Four-fold rise in pandemic influenza A (H1N1) virus
specific neutralizing antibodies.
22. WHO IS AT RISK?????
EVERYONE IS AT RISK
• Children, Pregnant women, The elderly
(over 65)
• Those with chronic disease and underlying
health conditions
• Healthcare professionals
23. • Asthma
• Neurological and neurodevelopmental conditions
(cerebral palsy, epilepsy stroke, mental retardation,
moderate to severe developmental delay, muscular
dystrophy, or spinal cord injury)
• Chronic lung disease (chronic obstructive pulmonary
disease [COPD] and cystic fibrosis)
• Heart disease (congenital heart disease, congestive heart
failure and coronary artery disease)
• Blood disorders (sickle cell disease)
• Endocrine disorders (diabetes mellitus)
• Kidney disorders
• Liver disorders
• Metabolic disorders (inherited metabolic and
mitochondrial disorders)
• Weakened immune system due to disease or
medication (people with HIV or AIDS/cancer/those on
chronic steroids)
• People younger than 19 years of age who are
receiving long-term aspirin therapy
• People who are morbidly obese (Body Mass Index
(BMI) of 40 or greater)
25. “Emergency warning signs” in children
In infants
Also look for these warning signs: being unable to eat, having no tears
when crying, and having far fewer wet diapers than normal.
26. What are its complications?
Most people who get influenza will recover in a few days to less
than two weeks, but some people may develop complications like:
Some people are more likely to get flu complications that
result in being hospitalized & occasionally result in death.
The flu can make chronic health problems worse.
Bacterial
pneumonia
For example, people with asthma may experience
asthma attacks while they have the flu, and people
with chronic congestive heart failure may have
worsening of this condition that is triggered by the
flu.
Bronchitis
Sinus/ear
infections
Dehydration
http://www.cdc.gov/flu/about/disease/symptoms.htm
27. DIAGNOSIS
Confirmation of Pandemic influenza A(H1N1)
infection is through:
• Real time RT PCR or
• Isolation of the virus in culture or
• Four-fold rise in virus specific neutralizing
antibodies.
28. • For confirmation of diagnosis, clinical specimens such as
nasopharyngeal swab, throat swab, nasal swab, wash or
aspirate, and tracheal aspirate (for intubated patients) are to
be obtained.
• The sample should be collected by a trained physician /
microbiologist preferably before administration of the anti-
viral drug.
• Keep specimens at 4°C in viral transport media until
transported for testing.
• The samples should be transported to designated laboratories
with in 24 hours.
• If they cannot be transported then it needs to b stored at -
70°C.
• Paired blood samples at an interval of 14 days for serological
testing should also be collected.
29. RT- PCR
• The Human Influenza Virus Real-Time RT-PCR is an
in vitro laboratory diagnostic test for direct molecular
identification of influenza isolates is a rapid and
powerful technique.
• Can provide results within 4 hours.
• It is the only in vitro diagnostic test for influenza that is
cleared by the FDA for use with lower respiratory tract.
• The RT-PCR allows template viral RNA to be reverse
transcribed producing complementary DNA(cDNA)
which can then be amplified and detected
.
30. The kit utilizes a 3-module design and can:
• Identify and distinguish between influenza A and B
viruses,
• Classify influenza A viruses by subtype, and
• Detect Pandemic influenza A (H1N1) 2009 strain
31.
32. TREATMENT
The guiding principles are:
• Early implementation of infection control precautions
to minimize nosocomical / household spread of
disease
• Prompt treatment to prevent severe illness & death.
• Early identification and follow up of persons at risk.
33. Guidelines on categorization of Seasonal
Influenza A H1N1 cases during screening for
home isolation, testing, treatment and
hospitalization (Revised on 11.02.2015)
• In order to prevent and contain outbreak of
Influenza-A H1N1 virus for screening, testing and
isolation following guidelines are to be followed:
• At first all individuals seeking consultations for flu
like symptoms should be screened at healthcare
facilities both Government and private or examined
by a doctor and these will be categorized as
34. Category- A
• Patients with mild fever plus cough / sore throat
with or without bodyache, headache, diarrhoea and
vomiting will be categorized as Category-A.
• They do not require Oseltamivir and should be
treated for the symptoms mentioned above. The patients
should be monitored for their progress and reassessed at
24 to 48 hours by the doctor.
• No testing of the patient for H1N1 is required.
• Patients should confine themselves at home and avoid
mixing up with public and high risk members in the
family.
35. Category-B
(i) In addition to all the signs and symptoms mentioned under Category-A, if the
patient has high grade fever and severe sore throat, may require home
isolation and Oseltamivir;
(ii) In addition to all the signs and symptoms mentioned under Category-A,
individuals having one or more of the following high risk conditions shall
be treated with Oseltamivir:
• Children with mild illness but with predisposing risk factors.
• Pregnant women;
• Persons aged 65 years or older;
• Patients with lung diseases, heart disease, liver disease kidney disease, blood
disorders, diabetes, neurological disorders, cancer and HIV/AIDS;
• Patients on long term cortisone therapy.
No tests for H1N1 is required for Category-B (i) and (ii).
All patients of Category-B (i) and (ii) should confine themselves at home and
avoid mixing with public and high risk members in the family.
Broad Spectrum antibiotics as per the Guideline for Community-acquired
pneumonia (CAP) may be prescribed.
36. Category-C
In addition to the above signs and symptoms of Category-A and
B, if the patient has one or more of the following:
• Breathlessness, chest pain, drowsiness, fall in blood pressure,
sputum mixed with blood, bluish discolouration of nails;
• Children with influenza like illness who had a severe disease
as manifested by the red flag signs (Somnolence, high and
persistent fever, inability to feed well, convulsions, shortness
of breath, difficulty in breathing, etc).
• Worsening of underlying chronic conditions.
All these patients mentioned above in Category-C require
testing, immediate hospitalization and treatment.
37. How does one manage influenza?
Treatment1 Prevention1
Drugs (antivirals)
• Antivirals
(chemoprophylaxis)
• Good health habits
• Vaccines
Adamantanes
• Amantadine
• Rimantadine
Neuraminidase Inhibitors (NAIs)
• Zanamivir
• Oseltamivir
• Peramivir
• Laninamivir
Vaccination is the most effective measure
at preventing influenza and its severe
outcomes.2
2. http://www.apaci.asia/influenza/burden-of-influenza-a-benefit-of-vaccination
Everyone 6 months of age and older
should get a flu vaccine every season
(CDC)3
3. http://www.cdc.gov/flu/protect/keyfacts.htm
1.http://www.who.int/mediacentre/factsheets/fs211/en/ last accessed on 19th January 2014
40. Adverse reactions:
• Oseltamivir is generally well tolerated
• Gastrointestinal side effects (transient nausea, vomiting)
may increase with increasing doses, particularly above 300
mg/day.
• Occasionally it may cause bronchitis, insomnia and
vertigo.
• Less commonly angina, pseudo membranous colitis and
peritonsillar abscess have also been reported.
•There have been rare reports of anaphylaxis and skin
rashes
41. Commencement within 12 h of symptom onset reduced
illness duration by 3.1 days (compared to 48 hrs treatment)
Early treatment with oseltamivir is
better!
Journal of Antimicrobial Chemotherapy 2003; 51: 123-129
42. Timely oseltamivir administration has a beneficial
effect on outcomes in hospitalized adults
Chest 2011; 140(4):1025–1032
Time from onset of symptoms to oseltamivir administration (+ 1-day
increase) was independently associated with a prolonged duration of the
fever, prolonged LOS, more-often need for mechanical ventilation, and
higher mortality
43. Oseltamivir reduces complications and antibiotic use in
influenza infected patients in healthy and high-risk patients
Risk for pneumonia approximately 50% lower than among those
persons receiving a placebo and 34% lower among patients at risk
for complications Arch Int Med 2003;163:1667-72
44. Benefits of oseltamivir in high-risk population with
chronic respiratory diseases* or cardiac disease
*chronic bronchitis, obstructive emphysema, bronchial asthma or
bronchiectasis
Oseltamivir given within 48 hours of symptom onset
significantly reduced:
• Duration of influenza symptoms by 36.8%
• Severity by 43.1%
• Duration of fever by 45.2%
• Time to return to baseline health status by 5 days
A decrease in the incidence of secondary complications
and antibiotic use, without increasing the total medical
cost noted.
Curr Med Res Opin. 2006 Jan;22(1):75-82.
45. Reduction in hospitalizations by 59% with
early oseltamivir treatment
1. Arch Int Med 2003;163:1667-72
0.7% vs 1.7%1
46. 2. The Lancet Infectious Diseases 2014; 14 (2): 109–118
1. http://www.cdc.gov/flu/news/flu-antiviral-benefits.htm
•Overall flu symptoms reduced by one day compared with placebo
(3 days versus 4 days)
•Reduced amount of live virus that was isolated from respiratory
specimens by 12% to 50% compared with placebo regardless of
whether treatment started before or after 2 days since illness
onset.
Oseltamivir treatment within 5 days of symptom onset; Crowded, low-income, urban
community in Bangladesh, (mostly children< 5 years)2
Treatment not to be delayed while awaiting diagnostic test results, nor
should it be withheld in patients with indications for therapy who present
>48 after the onset of symptoms3
3. Int. J. Pharm. Sci. Rev. Res., 2014: 25(2), Article No. 48:
252-258
47. Dose of Zanamivir - Treatment
Adults and children > 5 years
• 5 mg capsules to be inhaled
• 2 inhalations twice a day with DPI
• 2 doses on first day at least 2 hours apart
• Subsequently 12 hours apart
Warning
Generally not recommended for patients with asthma/COPD
Occasionally bronchospasm has been reported. Keep
bronchodilator ready
48. Significant benefits with administration of
zanamivir within 48 hours
Rapid reduction of the viral load observed. The mean area under the
curve for viral load during the first 48 h of treatment was 8.48 log10 vRNA copies/ml
x h lower in the zanamivir group compared with placebo2
Meta-analysis of 7 trials showed:1
• 31% reduction of antibiotic prescription in zanamivir
• Lower incidence of complications (13% vs 18%)
• Fewer nights of sleep disturbance (median 2 nights vs 3 nights)
in asthma or COPD patients
• Reduced the incidence of complications (requiring antibiotics
and a change in respiratory medication) compared with placebo
by 58%
1. Clin Drug Invest 2000 Nov; 20 (5): 337-349
2. Scand J Infect Dis. 2003;35(1):52-8.
49. • Patients with signs of tachypnea, dyspnea, respiratory
distress and oxygen saturation less than 90 per cent
should be supplemented with oxygen therapy.
• Types of oxygen devices depend on the severity of
hypoxic conditions which can be started from oxygen
cannula, simple mask, partial re-breathing mask (mask
with reservoir bag) and non re-breathing mask. In
children, oxygen hood or head boxes can be used.
• Patients with severe pneumonia and acute respiratory
failure (SpO2 < 90% and PaO2 <60 mmHg with oxygen
therapy) must be supported with mechanical ventilation.
Invasive mechanical ventilation is preferred choice.
50.
51. PREVENTION
If you get sick…
• Stay home if you’re
sick for 7 days
after your
symptoms
begin or until
you’ve been
symptom-free
for 24 hours,
whichever is
longer..
52.
53. PERSONAL PROTECTION EQUIPMENTS
PPE reduces the risk of infection if used correctly. It
includes:
• Gloves (nonsterile),
• Mask (high-efficiency mask) / Three layered surgical
mask,
• Long-sleeved cuffed gown,
• Protective eyewear (goggles/visors/face shields),
• Cap (may be used in high risk situations where there may
be increased
aerosols),
• Plastic apron if splashing of blood, body fluids, excretions
and secretions is
anticipated.
54. How are vaccines helpful in
preventing flu?
• The best way to prevent the flu is by getting a flu
vaccine each year.
• Levels of protective antibody against influenza
viruses can decline over the course of a year, so
even people who got a flu vaccine last year
should get vaccinated again this year to ensure
that they are optimally protected.
• About two weeks after vaccination, antibodies
develop that protect against influenza virus
infection.
• Flu vaccines will not protect against flu-like
illnesses caused by non-influenza viruses.
55. When should one get vaccinated?
• To allow time for production of protective
antibody levels, vaccination should
optimally occur before onset of influenza
activity in the community.
• Vaccination also should continue to be
offered throughout the influenza season.
56. Seasonal Influenza A (H1N1): Guidelines for
Vaccination of Health Care Workers (Updated on
14th February 2015)
• World Health Organization recommends vaccination of high risk
groups with Seasonal Influenza Vaccination.
• Health Care Workers working in casualty/ emergency
department of identified hospitals treating Influenza cases.
• Heath Care Workers working in ICU and Isolation Wards
managing influenza patients.
• Health Care Workers identified to work in screening centres
that would be set up for categorization of patients during Seasonal
Influenza outbreak.
• Health Care workers treating/managing the High Risk Group
• Laboratory personnel working in virological laboratories testing
Influenza samples.
• Rapid Response Team members identified to investigate
outbreaks of Influenza.
• Drivers and staff of vehicles/ambulances involved in transfer
of Influenza patients.
57. • The vaccine should be used every year.
• Influenza vaccination is most effective when circulating
viruses are well-matched with vaccine viruses.
• Even with appropriate matching, efficacy of vaccine may be
about 70% to 80%, especially in geriatric age group.
• In case the locally circulating virus is different from vaccine
virus recommended by WHO, it may not be effective at all.
• Hence, vaccine should not give a false sense of security.
Considering the risk perspective, the preventive modality of
infection prevention and control practices like use of PPEs
should be strictly adhered to.
• The available vaccine takes about 2-3 weeks for
development of immunity. The use of chemoprophylaxis
during this period may be considered.
58. MAJOR ISSUES
• Underutilization of vaccines
• Questionable efficacy of current vaccines
on 2014-2015 influenza virus
• Differences in perceptions/concepts for
influenza control
• Limited medical care and treatment delay
Editor's Notes
What are pandemics? Pandemics are when a new influenza A emerges to which most or many of the population have no immunity. The result usually from an animal influenza combining some of its genes with a human influenza. To be a pandemic strain an influenza A virus needs to have three or four characteristics. They need to be able to infect humans, to cause disease in humans and to spread from human to human quite easily. An additional criteria that is often applied is that many or most of the population should be non-immune to the new virus.
Note this animated slide was first developed by the National Institute of Infectious Disease in Japan and we are grateful to them and especially Masato Tashiro for letting us use it.
Affects of humidity on infectivity influenza, Loosli et al, 1943