This document discusses several diseases of the circulatory system including plague, viral hemorrhagic fevers like Ebola and Marburg, and infectious mononucleosis. It provides details on the causative agents, symptoms, transmission, treatment and prevention of these diseases. Plague is caused by the bacterium Yersinia pestis and is transmitted via flea bites. Ebola and Marburg are viral hemorrhagic fevers transmitted through direct contact with body fluids. Infectious mononucleosis or "kissing disease" is caused by the Epstein-Barr virus and is most commonly spread through saliva.
Pertussis : Highly contagious respiratory infection caused by Bordetella pertussis
Outbreaks first described in 16th century
Bordetella pertussis isolated in 1906
Estimated >300,000 deaths annually worldwide
Before the availability of pertussis vaccine in the 1940s, public health experts reported more than 200,000 cases of pertussis annually.
Since widespread use of the vaccine began, incidence has decreased more than 75% compared with the pre-vaccine era.
In 2012, the last peak year, CDC reported 48,277 cases of pertussis.
Extremely contagious-attack rate 100%
Immunity is never complete
Protection begins to wane in 3-5 yrs after vaccination
Pertussis : Highly contagious respiratory infection caused by Bordetella pertussis
Outbreaks first described in 16th century
Bordetella pertussis isolated in 1906
Estimated >300,000 deaths annually worldwide
Before the availability of pertussis vaccine in the 1940s, public health experts reported more than 200,000 cases of pertussis annually.
Since widespread use of the vaccine began, incidence has decreased more than 75% compared with the pre-vaccine era.
In 2012, the last peak year, CDC reported 48,277 cases of pertussis.
Extremely contagious-attack rate 100%
Immunity is never complete
Protection begins to wane in 3-5 yrs after vaccination
Diptheria (Whooping cough) and PertussisPinky Rathee
Pertussis also known as whooping cough, is a highly contagious respiratory disease.
It is known for uncontrolled, violent coughing which often makes it hard to breath.
It is a serious bacterial infection caused by corynebacterium diptheriae that affects the mucous membranes of the throat and nose
Diphtheria is an infection caused by the bacterium Corynebacterium diphtheriae. Diphtheria causes a thick covering in the back of the throat. It can lead to difficulty breathing, heart failure, paralysis, and even death. CDC recommends vaccines for infants, children, teens and adults to prevent diphtheria. The presentation consists of basic concepts regarding the bacteria and its infection. It has explanation in detail about signs and symptoms of Diptheria
Diptheria (Whooping cough) and PertussisPinky Rathee
Pertussis also known as whooping cough, is a highly contagious respiratory disease.
It is known for uncontrolled, violent coughing which often makes it hard to breath.
It is a serious bacterial infection caused by corynebacterium diptheriae that affects the mucous membranes of the throat and nose
Diphtheria is an infection caused by the bacterium Corynebacterium diphtheriae. Diphtheria causes a thick covering in the back of the throat. It can lead to difficulty breathing, heart failure, paralysis, and even death. CDC recommends vaccines for infants, children, teens and adults to prevent diphtheria. The presentation consists of basic concepts regarding the bacteria and its infection. It has explanation in detail about signs and symptoms of Diptheria
• Gross anatomy:
– Components of the lymphatic system: lymphatic plexuses, lymphatics, lymphoid tissue
– Plan of the lymphatic system: Superficial lymphatic vessels, deep lymphatic vessels, lymph nodes, lymph trunks, cysterna chyli, lymph ducts: right lymph duct and thoracic duct.
– Lymphatic drainage of the lower limb
• Superficial inguinal lymph nodes: arrangement and drainage area.
• Deep inguinal lymph nodes: arrangement and drainage area. The popliteal lymph nodes
– Lymphatic drainage of the upper limb
• Superficial and deep lymphatics. Supratrochlear and infraclavicular lymph nodes.
• Axillary lymph nodes: arrangement and drainage area.
– Plan of the lymphatic drainage of the head and neck: deep cervical lymph nodes, inner and outer circle of lymph nodes.
• Deep cervical lymph nodes: location of the upper and lower groups, jugulodigastric node, jugulo-omohyoid, supraclavicular lymph nodes. Drainage area and efferent vessels.
• The outer circle of lymph nodes: submental, submandibular, buccal, mandibular, parotid, mastoid, occipital: location, drainage area and efferent vessels.
• The inner circle of lymph nodes: pretracheal, paratracheal and retropharyndeal.
• The tonsils and Waldeyer’s ring.
– Lymphatic drainage of the thorax:
• Lymph nodes of the chest wall: Parasternal, intercostal, and phrenic
• Lymph nodes of the mediastinum: Nodes around the division of the trachea and the main bronchi, anterior and posterior mediastinal nodes.
– Plan of lymphatic drainage of the abdomen: lumbar and intestinal lymph trunks.
• Pre-aortic lymph nodes: mesenteric, celiac, superior and inferior mesenteric lymph nodes.
• Para-aortic lymph nodes.
• MALT & Peyer’s patches.
– Lymphatic drainage in the pelvis: External and internal iliac lymph nodes, lymph nodes in fascial sheaths, sacral and common iliac lymph nodes.
• Applied anatomy
• Functional and clinical importance of the lymphatic system; Virchow’s lymph nodes; Retropharyngeal abscess; Clinical applications of enlarged thoracic lymph nodes: involvement of left recurrent laryngeal nerve and phrenic nerve. Pressure on the esophagus. Carinal lymph nodes and bronchoscopy; Communications of lymphatics between thorax and abdomen.
• Radiographic anatomy:
– Lymphangiogrms.
• Surface anatomy of palpable lymph node groups: superficial inguinal, axillary, infraclavicular, outer circle of crevical lymph nodes, deep cervical lymph nodes.
Pseudorabies is an acute, frequently fatal disease with a worldwide distribution that affects swine primarily and other domestic and wild animals incidentally. The pseudorabies virus has emerged as a significant pathogen in the USA since the 1960s, probably because of the increase in confinement swine housing or perhaps because of the emergence of more virulent strains. Clinical signs in nonporcine animals are similar to those of rabies, hence the name “mad itch” (pigs do not display this sign). Pseudorabies is a reportable disease and has been successfully eradicated from the vast majority of the USA.
Leptospirosis is a worldwide public health problem. In humid tropical and subtropical areas, where most developing
countries are found, it is a greater problem than in those with a temperate climate. The magnitude of the problem in
tropical and subtropical regions can be largely attributed to climatic and environmental conditions but also to the
great likelihood of contact with a Leptospira-contaminated environment caused by, for example, local agricultural
practices and poor housing and waste disposal, all of which give rise to many sources of infection. In countries with
temperate climates, in addition to locally acquired leptospirosis, the disease may also be acquired by travellers
abroad, and particularly by those visiting the tropics.
Leptospirosis is a potentially serious but treatable disease. Its symptoms may mimic those of a number of other
unrelated infections such as influenza, meningitis, hepatitis, dengue or viral haemorrhagic fevers. Some of these
infections, in particular dengue, may give rise to large epidemics, and cases of leptospirosis that occur during such
epidemics may be overlooked. For this reason, it is important to distinguish leptospirosis from dengue and viral
haemorrhagic fevers, etc. in patients acquiring infections in countries where these diseases are endemic. At present,
this is still difficult, but new developments may reduce the technical problems in the near future. It is necessary,
therefore, to increase awareness and knowledge of leptospirosis as a public health threat.
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.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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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
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
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
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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
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
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.
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
3. an acute, often severe zoonosis
infectious disease caused by Yersinia pestis
symptoms depend on the concentrated areas of
infection in each person
Lymph nodes = BUBONIC
PLAGUE
Blood vessels =
SEPTICEMIC PLAGUE
Lungs = PULMONARY PLAGUE
12. bubonic septicemic pneumonic
PORTAL OF ENTRY
Any site of the
body bitten by
the vector (flea)
PORTAL OF EXIT
PORTAL OF ENTRY
PORTAL OF EXIT
PORTAL OF ENTRY
PORTAL OF EXIT
Eyes, nose, and
mouth (Highly
contagious)
Eyes, nose, and
mouth
Eyes, nose, and
mouth (Highly
contagious)
Breaks in the skin,
nose, mouth
Breaks in the skin,
nose, mouth
14. bubonic septicemic pneumonic
Bites from flea vectors
Bites or scratches from
infected animals, such
as cats
Direct contact with
infected animal
carcasses, such as
rodents (especially
marmots), rabbits,
hares, carnivores (eg,
wild cats, coyotes), and
goats
1º Bites from flea
vectors where Y pestis
is inserted directly into
bloodstream
- no discernable bubo
present
2º Develops as a
complication of
bubonic or 1º
pneumonic plague -
when Y pestis enters
the bloodstream
1º Inhalation of respiratory
droplets from infected
animals such as cats
Inhalation of respiratory
droplets from a person with
primary or secondary
pneumonic plague
Handling Y pestis cultures in
the laboratory setting
2º Bubonic and 1° septicemic
spread plague bacilli
hematogenously to the lungs
16. bubonic
Signs symptoms
Incubation Period: 2-6 Days Fever
Headache
Abdominal pain
Cough
Pain/tenderness at
regional lymph
nodes enlarge to
become “buboes”
malaise
Presence buboes in
groin, axilla,
cervical area
Ulcer or skin lesions
at site of flea bite
Skin rash
Rapid pulse
Hypotension
Vomiting
Severe exhaustion
Intestinal
discomfort
17. septicemic
Signs symptoms
Incubation Period: 2-6 Days Fever
Nausea
Vomiting
Diarrhea
Patchy bilateral
infiltrates (Chest
x-ray)
Prostration
Hemorrhagic changes
in skin called
“purpuric lesions”
Disseminated
intravascular
coagulation (DIC)
Extremity gangrene
Sepsis
Altered mental status
Abdominal pain
21. diagnosis
Lymph node aspirate affected bubo should contain numerous organisms that can be
evaluated microscopically and by culture
Blood cultures
smears taken from suspected plague patients early in the course of
illness are usually negative in microscopic examination but may be
positive by culture
CSF (cerebrospinal fluid)a test to look at the fluid that surrounds the brain and spinal cord;
gram stain of CSF may show plague bacilli; Limulus test of CSF
demonstrates the presence of endotoxin
Immunodiagnostic tests
Observation of typical appearance (Bipolar-staining bacilli that resemble safety pins) in
Gram-stained or Wright-Giemsa-stained sputum
Gram stain of sputum often reveals Y pestis
Biochemical Tests
uses an antigen-antibody reaction as their primary means of
detection
22. treatment
In a contained casualty setting, parenteral antibiotic
therapy, especially streptomycin or gentamycin, is
suggested.
In a mass casualty setting, intravenous or
intramuscular therapy may not be possible, so oral
therapy, preferably with doxycycline (or tetracycline)
or ciprofloxacin, should be administered.
Patients with pneumonic plague will suffer from
complications and therefore require substantial
advanced medical supportive care.
Preferred
Streptomycin
Gentamycin
alternative
Alternative Doxycycline
Ciprofloxacin
Chloramphenicol
23. Prevention and
control
Reduce rodent habitat
in homes, work
places, and
recreational areas
remove brush, rock piles, junk, cluttered
firewood, and possible rodent food supplies,
such as pet and wild animal food.
Make your home and buildings rodent-proof!!!
24. Prevention and
control
Wear gloves,
protective masks,
when handling or
skinning potentially
infected animals
To prevent contact between skin and the plague bacteria
25. Prevention and
control
Use of Repellants
during activities such
as camping, hiking, or
working outdoors
It is suggested to use products containing DEET and permethrin
26. Prevention and
control
wash your hands
regularly and avoid
touching your eyes,
nose, and mouth
28. Viruses of four distinct families
ARENAVIRIDA
E
BUNYAVIRIDA
E
FILOVIRIDAE FLAVIVIRIDAE
JUNIN
CRIMEAN-CONGO
H.F.
EBOLA
KYASANUR
FOREST
DISEASE
MACHUPO HANTAVIRUS MARBURG OMSK H.F.
SABIA
RIGT VALLEY
FEVER
YELLOW
FEVER
GUANARITO DENGUE
LASSA
29. Severe multi-system syndrome (multiple organs affected).
Vascular system is damaged and body loses the ability to
regulate itself
Accompanied by hemorrhaging
Many VHF viruses cause life threatening diseases
Most have no established treatment or cure.
30. Features of these Viruses
RNA Viruses, covered in lipid coating
Humans are not natural reservoir, but
can transmit virus
Viruses are restricted to areas of their
host species
31. mARBURG
ZOONOTIC 1st recognize in 1967 when
simultaneous outbreaks occurred in
Marburg and Frankfurt, Germany, and
in Belgrade, Yugoslavia.
Bats have been
implicated for this virus
The area to which the
virus is native is
unknown ,
but it is believed to include parts
of Uganda, Western Kenya, and
Zimbabwe
Original people who became
ill had been exposed to the
tissues of African green monkeys, which
were imported from Uganda for research.
Rousettus aegyptiacus
Egyptian rousettes
(bat)
Bat, Human and Non-human primates
destroyed by gamma and UV
radiation, lipid solvents, and
bleach
32. Portal of entry Portal of exit
Respiratory Tract
Eyes
Skin
Respiratory Tract
Eyes
Skin
The investigation for the entry of exit of the
causative agent is still under research. But some
suggests that the entry of MAV is dependent on
NPC1, a cholesterol transporter to enter and
replicate.
33. transmission
The animal host to the Marburg Virus is unknown, and so is the
way that the animal transmits the disease to humans
People who have been exposed to infected monkeys or their
body fluids have become infected in the past.
Disease is easily transmitted between humans.
Direct contact with an infected person, or exposure to their
body fluids, are both ways by which the disease is transmitted.
34. SIGNS SYMPTOM
S Incubation period of 5-10 days
Maculopapular rash
Most prominent on the trunk (chest and back)
Jaundice
Inflammation of the pancreas
Severe weight loss
Delirium
Shock
Liver failure
Massive hemorrhaging
Multi-organ dysfunction.
Fever
Chills
Headache
Myalgia
Nausea
Vomiting
Chest pain
Abdominal pain
Diarrhea
35. diagnosis
Many of the signs and symptoms of Marburg hemorrhagic fever
are similar to those of other infectious diseases, such as malaria or
typhoid fever, diagnosis of the disease can be difficult, especially if
only a single case is involved
Readily diagnosed by:
To confirm a case of Marburg hemorrhagic
fever within a few days of the onset of
symptoms:
Antigen-capture enzyme-linked
immunosorbent assay (ELISA) testing
virus isolation
IgM-capture ELISA
polymerase chain reaction (PCR)
Test appropriate for testing persons later in
the course of disease or after recovery:
The IgG-capture ELISA
Immunohistochemistry
virus isolation
polymerase chain reaction (PCR)
36. treatment
A specific treatment for this disease is unknown
Isolation and quarantine
Quick containment
No standard treatment
Use of heparin (which blocks clotting) to prevent the consumption of clotting factors
Fresh-frozen plasma and other preparations to replace the blood proteins important in clotting
Supportive therapy, which includes balancing the patient’s fluids and electrolytes,
maintaining their oxygen status and blood pressure, and treating them for complicating
infections.
37. Prevention and control
Still no established preventive measures for the transmission of disease
Use of barrier nursing techniques to prevent direct physical contact with the patient
Use of protective clothing
wearing of protective gowns, gloves, and masks
Proper disposal of all needles, equipments, and patient excretions
38. ebola
Has 4 types
Ebola-Zaire
Ebola-Sudan
Ebola-Ivory Coast
Ebola Reston
zoonotic
Named after the river in
congo (zaire) – first
outbreak - where 88% of the
people died
Sporadic
appearance
Fatal in humans and
other non-human
primates
Natural reservoir remains unknown
destroyed by gamma and
Originated in africa
UV radiation, lipid
solvents, and bleach
40. transmission
Intimate contact Direct contact with the blood or
Aerosol transmission
secretions of an infected person
Nosicomial transmission
• contact with objects, such as needles, that
are contaminated with secretions or blood.
• reuse of needles and syringes
• exposure to infectious tissues, excretions,
and hospital wastes
Common among primates
41. SIGNS SYMPTOM
S Incubation period of 2-21 days
Arthritic pain and backache
Chills
Diarrhea
Fatigue
Fever
Headache
Malaise
Nausea
Sore throat
Vomiting
Bleeding from eyes, ears, and nose
Gastrointestinal bleeding
Eye inflammation (conjunctivitis)
Genital swelling (labia and scrotum)
Increased feeling of pain in skin
Rash over the entire body that often
contains blood (hemorrhagic)
Roof of mouth looks red
Seizures, coma, delirium
Impaired kidney and liver
Internal and external bleeding
43. diagnosis
It is initially difficult to diagnose Ebola
clinically because many of the
symptoms are nonspecific
RT-PCR and ELISA Polymerase Chain Reaction
Enzyme-linked immunosorbent assays (ELISA)
IgM response most useful in diagnosis of recent infections in
surviving patients.
somewhat delayed and expected only in the
early convalescent sera IgG response
44. treatment
there is no specific treatment or cure for Ebola HF
Isolation and quarantine
Quick containment
No standard treatment
Mechanical ventilation
Renal dialysis
Anti-seizure therapy
Supportive therapy
• balancing the patient’s fluids
and electrolytes
• maintaining oxygen status and
blood pressure
• Treatment of infection
complications
47. Epstein- Barr Virus
human herpesvirus 4 Herpesviridae family
double stranded linear DNA core
core surrounded
by a
nucleocapsid
envelope contains glycoproteins
affects B- lymphocytes
48. Portal of
entry and Exit
TONSILS
transmission
(bodily fluids, especially saliva, can also spread through blood and semen
during sexual contact, blood transfusions, and organ transplantations)
50. SIGNS SYMPTOM
S Incubation Period: 4-6 weeks
swollen lymph
nodes
enlargement of
liver or spleen
skin rash
Jaundice
pharyngitis/
tonsilitis
sore throat
fever
constant
fatigue
sore muscles
abdominal
pain
loss of appetite
nausea or
vomiting
headaches
51. diagnosis
Heterophil Antibody/
Monospot Test
- detects a type of antibody (heterophil antibody) that
forms during certain infections
- looks for antibodies that possess the unique ability to
cause clumping of red cells
- presence of heterophil antibodies indicates a mono
infection. complete blood cell count
EBV Antibody Test
Blood sample is mixed with a substance that
attaches to antibodies against EBV
Davidson Differential Slide Test
52. diagnosis
Mono- Plus Test Clumping of horse red blood cells by mono antibodies
presumed to be in a person's serum
53. treatment
Corticosteroids
fever reducing medications
may be prescribed in rare cases of airway obstruction,
hemolytic anemia (an autoimmune process in which red
blood cells are destroyed), severe thrombocytopenia (a
decrease in platelets, which are clotting components in
the blood), and complications involving the heart and
nerves
drinking fluids to stay hydrated
medications to treat pain, and other symptoms
bed rest
54. Prevention and control
Avoid sharing drinks, food, or personal
items, like toothbrushes, with people
who have EBV infection.
Avoid kissing with people who have
EBV infection.
Wash hands at all time
55. Diseases of the
Circulatory
System
Casipe, Kimberly
Chua, Charlean Lou
Espinosa, Karl Elvis
Sodusta, Patrick Jason
Editor's Notes
There are 3 biovars of Y. pestis, each named for the pandemic that it is thought to have caused
They are named based on their ability to convert nitrate to nitrite and ferment glycerol
(survival in air increases its threat and aids in its dispersal as a potential bioterrorism weapon.
Image: Wayson stain of blood shows the characteristic bipolar “safety pin” appearance of Yersinia pestis. From CDC.
1. Flea feeds on blood with y. pestis
2. enters the midgut and multiplies
3. clump of y. pestis blocks the foregut
4. because of the clump present in the foregut, during the fleas next meal, blood cannot enter the midgut thus flea gets very hungry
5. flea bites vigorously and injects the contents of its midgut into the next wound
6. only blocked fleas effectively transmit plague to mammals.
7.while growing inside the flea, the bacteria loses its antiphagocytic capsular layer (F1) and so many of the pathogenic organisms are phagocytosed and killed by mammalian leukocyte
8.. Howevernot all are killed, Those that are ingested by neutrophils appears to be readily killed, but cbacteria within macrophages are able to survive
9. macrophages provide protection. Giving time to the bacteria to resynthesize their protective F1 capsular layer and other irulence antigens. The ability of Y. pestis to survive and grow in macrophages is critical to the early pathogenesis of pague
10. The bacteria within the macrophages are then transported to the local draining lymph node.
11. the massive filtration of the phagocytic cells within the nodes cause them to become hot and swollen and hemorrhagic giving rise to buboes.
12. within the bubo, undergoing unknown mechanism , the bacteria escapes from the macrophages and adopt an extracellular lifestule where they further grow and replicate.
13. The newly formed protective capsular layer of the bacteria helps resist phagocytosis by the leukocytes.
14. Eventually, the infection can now sppill out into the bloodstream, leading to involvement of the liver, spleen, and the lungs (eading to second degree septicemic and pneumonic development).
First degree septicemic plague
1, flea inserts directly into the bloodstream causing migration of Y. pestis to organs
First degree pneumonic plague
inhaled Y. pestis bacili would eneter into the lungs
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
There are 3 biovars of Y. pestis, each named for the pandemic that it is thought to have caused
They are named based on their ability to convert nitrate to nitrite and ferment glycerol
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.
Infection Control
The use of standard precautions is appropriate for managing plague patients who do not have respiratory infections.
In past epidemics, patient-to-patient transmission only seemed to occur after close contact, often for prolonged periods, with a patient that coughed bloody sputum. It is extremely rare for patients in the early stage of pneumonic plague to transmit the infection to others.
Bubonic: Standard and contact precautions if any open wounds.
Pneumonic: Standard and respiratory droplet precautions. (Note: Available evidence indicates that person-to-person spread of pneumonic plague is via respiratory droplets, not fine aerosols or droplet nuclei.)
Septicemic: Standard precautions.
Pneumonic plague patients are no longer infective after 24 to 48 hours of antibiotic treatment, because the sputum no longer contains live bacilli. However, they may still be ill and continue demonstrating signs of pneumonia.
Infection Control
When individual isolation of suspected plague patients is not possible, they should be cohorted away from other hospital patients, and managed under respiratory droplet precautions until no longer considered to be contagious.
Although quick diagnosis and appropriate antibiotic treatment is imperative in preventing the spread of disease throughout the community, isolation of contacts and/or quarantine may increase in importance for outbreak control.
The bodies of persons who have died from plague should be handled with standard infection control precautions
Occupational Exposures – Hospital and Laboratory
Medical staff or laboratory workers accidentally exposed to infectious materials via needle sticks, cuts, or abrasions should immediately wash the area with a nonabrasive soap and water and follow the standard policy of their institution regarding workplace exposures.
When eye exposure occurs, the eye should be flushed with copious amounts of water or eye wash solution for at least 15 minutes.
In addition, postexposure antimicrobial prophylaxis with doxycycline or ciprofloxacin should be started immediately and continued for 7 days.
Laboratory workers who handle cultures should be alerted to the possibility of Y. pestis and take precautions to avoid aerosolization of cultures or other infectious materials.