Section 1

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Infectious diseases cause __ % of deaths worldwide

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Cards (401)

Section 1

(50 cards)

Infectious diseases cause __ % of deaths worldwide

Front

20%

Back

Reservoir

Front

can be human, animal, or non living

Back

John Snow

Front

Physician and skeptic of miasma theory of cholera. Mapped cases of Cholera in London showing clusters around broad st. Persuaded Soho council to remove pump handle. Cases dropped. Water delivered from polluted section of Thames.

Back

Confirmed case

Front

an infected person. Definitely infected or diseased. Cases that are lab confirmed. Requires lab testing.

Back

Who wrote Airs, Water, and Places about disease causes?

Front

Hippocrates

Back

Host

Front

Organism infected by an agent. Whether and how badly they are infected depends on multiple factors. Example: age, sex, race, previous diseease, etc.

Back

Miasma

Front

A noxious form of bad air that causes epidemics. Poisonous vapor filled with rotting organic matter. Commonly used to explain diseases with crowding. Among main arguments for early public health.

Back

Host/natural reservoir for dengue

Front

Humans

Back

Agent

Front

The infecting organism. Depends on biologic properties, prevention, characteristics of agent.

Back

animal reservoirs (zoonoses)

Front

Diseases that occur primarily in wild or domestic animals that can be transmitted to humans

Back

When were statistics developed to set stage for epi investigations?

Front

Early and mid 1800s

Back

Escape mechanism

Front

properties of an agent that allow it to evade or escape the immune system

Back

Nutritional prevention for agents

Front

Lack of food Access

Back

Ignatz Semelweiss

Front

Hungarian physician Observed wards at a hospital had 3x mortality of midwife wards. Puerperal fever

Back

What did ancient Greece think caused disease?

Front

Hippocrates attributed illness to characteristics of environment: climate soil water. Or human behavior: nutrition lifestyle. If illness has natural cause, should have natural cure in herbs and foods etc.

Back

Probable case

Front

Clinical features consistent with symptoms associated with pathogen

Back

What lead to the discovery of germ theory?

Front

Microscope invention Pasteur germ theory experiments Koch causative agents for infectious disease

Back

Who conducted experiments supporting germ theory

Front

Louis Pasteur 1800s

Back

Characteristics of agents that affect infectivity

Front

escape mechanism

Back

Point source outbreak

Front

Limited to one place and time Everyone exposed at same point in time. Represents distribution of incubation period

Back

Natural reservoir

Front

the long-term host of a pathogen of an infectious disease. Can be a source of disease outbreaks.

Back

Vector for west nile virus

Front

Mosquito

Back

What is infectious disease epidemiology?

Front

Causes are infectious agents which live on or in a larger organism. For infecting organisms to survive, they must eventually leave their host and cause infectious elsewhere. For transmissible or communicable diseases.

Back

Koch's Postulates

Front

1) the microorganism must be present in every case of the disease but absent from healthy individuals 2) the suspected microorganism must be isolated and grown in a pure culture from each case 3) Reinoculation in another host causes disease 4) the same microorganism must be isolated again from the new host

Back

Germ Theory

Front

the theory that infectious diseases are caused by certain microbes

Back

When was the golden era of bacteriology?

Front

Beginning in 1850s

Back

Chemical prevention of agents

Front

Poison Alcohol Smoke

Back

Possible case

Front

suggestive clinical signs but not fit case definition. plot on curve but may not be infected. Have some epi criteria for case definition

Back

Epidemiologic triangle

Front

agent, host, environment framework to understand risk factors for disease. Maps out how disease spreads in human populations

Back

Host/ Natural reservoir for west nile virus

Front

Bird

Back

What did epidemiologic studies do in 17th and 18th centuries?

Front

Mortality trends Fatality rates

Back

Pandemic

Front

Epidemic that is spread through human populations across a large region or worldwide

Back

What are the public health implications of infectious disease epidemiology?

Front

Future incidence is a function of current prevalence/ dependency. Cases are risk factors for future cases- which is not true for chronic cases. Prevent transmission, acquisition, progression of disease.

Back

Non living reservoirs

Front

water, food, soil

Back

Physical prevention for agents

Front

Trauma Radiation Fire

Back

What did Robert Koch do?

Front

1800s 1900s Identified cause of TB, cholera, anthrax. First link to specific micro organism to a specific disease- anthrax. Created 4 criteria to establish relationships between microbe and disease.

Back

Biologic properties of an agent

Front

Is it a bacteria or a virus?

Back

Vector

Front

Any organism that transmits disease from host to host. Must be living. Usually a mosquito or a tick.

Back

How are reservoirs different from vectors?

Front

Vectors are agents of disease transmission. Reservoirs are continuing sources of outbreaks. Many diseases have multiple hosts and vectors

Back

Epidemic

Front

Occurrence of disease in a given human population during a specific period of time in which new cases substantially exceed what is expected

Back

Where was miasma theory developed?

Front

Europe, india, china

Back

Environment

Front

Medium in which hosts and agents interact. Influence how we are infected and transmit disease. Example: seasonality in flu

Back

What can epidemiology do?

Front

Studies shape policy decisions and evidence based practice by identifying risk factors for disease and targets for preventive healthcare

Back

Infection

Front

Being invaded by a pathogen May or may not lead to disease

Back

Targets for prevention in infectious disease epidemiology

Front

1. Prevent acquisition and progression of disease. 2. Prevent transmission.

Back

Who invented the microscope?

Front

1683 Anton van Leeuwenhoek

Back

Disease vs infection

Front

Disease is Infected and symptomatic

Back

When did cholera epidemic in Soho occur?

Front

1854

Back

What is epidemiology?

Front

The study of distribution and determinants of disease and other health related states or events: WHO

Back

Puerperal fever

Front

common in mid 19th centure hospitals Mortality 10%-35%

Back

Section 2

(50 cards)

Types of incidence

Front

Cumulative incidence Incidence rate

Back

Alternate epidemiologic triangle

Front

Have a natural reservoir as well as another. Share the agent.

Back

Why do we measure burden of disease?

Front

to describe risk and determinants of disease

Back

Risk ratio formula

Front

[a/(a+b)]/[c/(c+d)] Cumulative incidence of disease in exposed/ CI of diseased in unexposed

Back

Incidence

Front

Estimates the risk of acquiring a disease. The number of new cases or events that occur or develop in a defined population at risk during a specified time interval (cumulative) or as a function of follow up time (rate)

Back

Is prevalence a proportion or a rate?

Front

A proportion. It is expressed as a percent or number. .183% or 1.83 per 1,000

Back

How to interpret odds ratio

Front

over 1: may be associated with developing disease 1: no association under 1: exposure may be protective 1.3= the odds of getting x illness was 1.3 times higher among people with exposure

Back

Types of prevalence

Front

point prevalence period prevalence

Back

When do we need to calculate an incidence rate?

Front

when population is dynamic. number of people who acquire disease relative to total population is large. need to account for drop outs or loss to follow up

Back

Period prevalence

Front

Count individuals who have and or develop disease over a period of time

Back

Experimental studies

Front

studies in which the independent variables are directly manipulated and the effects on the dependent variable are examined. RCT

Back

How to interpret risk ratio

Front

over 1: may be associated with developing disease 1: no association under 1: exposure may be protective 1.3= those who ate nanaimo had a 1.3 times increased risk of developing food poisoning compared to those who didnt

Back

Analytic sample

Front

Subset of the study population in any given analysis

Back

Interpretation of incidence rate ratio

Front

over 1: may be associated with developing disease 1: no association under 1: exposure may be protective

Back

Rate

Front

a/t Ratio where time is included in the denominator #new cases per 1000 person days of follow up

Back

Pathogens with human reservoir

Front

anything with H suggests a human in the natural reservoir. HIV, HPV

Back

Ratio

Front

a/b or a:b Fraction represented by one quantity to another Measles sex ratio (M:F)

Back

Risk Ratio

Front

The risk of developing a disease relative to exposure to a certain risk factor. A ratio of the probability of disease developing in exposed versus unexposed group. Can be calculated in studies that estimate incidence- cohorts and RCT.

Back

Prevalence formula

Front

number of existing cases at a specific time or interval /number of people in population at a time or interval

Back

systematic review and meta-analysis

Front

Collects all previous studies on the topic and statistically combines their results

Back

Point prevalence

Front

Count individuals who have disease at one point in time

Back

Why do we measure disease?

Front

To determine who is at highest risk. Understand etiology of disease. Measure intensity or degree of infection. Prioritize resources.

Back

case series

Front

involves a small group of patients with a similar diagnosis

Back

Prevalence

Front

The proportion of individuals in a defined population who have the disease at a specific time or interval. Measures the burden of a disease in a population.

Back

Goal of infectious disease epidemiology

Front

to control transmission of disease

Back

Target population

Front

the group of individuals whom we want to infer about . the population that findings are generalized to

Back

Case-control study

Front

A type of epidemiologic study where a group of individuals with the diseases, referred to as cases, are compared to individuals without the disease, referred to as controls

Back

Vector for dengue

Front

mosquito. There is no human to human transmission.

Back

Spillover effect

Front

An event where virus jumps into another triad. Ex. bats infect other primates

Back

Attack rate formula

Front

Number of persons infected/total number of exposed susceptible people during the outbreak

Back

Count measures

Front

a. Number of occurrences # cases of measles

Back

Proportion

Front

a/a+b Ratio where numerator is included in the denominator #of measles cases/total residents

Back

Example alternate epi triangle: ebola

Front

Natural host is fruit bat, environment is jungle, agent is ebola. Alternate host is human, environment is city.

Back

Study population

Front

individuals in the source population who contribute data to the study

Back

What is another name for risk ratio?

Front

Relative risk

Back

Attack rate

Front

Cumulative incidence of infection in a group of exposed and susceptible hosts Measured from the beginning to the end of an outbreak "of those who were exposed, __% were infected over the course of the outbreak"

Back

Odds ratio formula

Front

ad/bc

Back

Types of observational studies

Front

Case report, case series, ecological study, cohort study, case control study

Back

ecologic study

Front

a study in which the units of analysis are populations or groups of people rather than individuals

Back

prevalence ratio (PR)

Front

(a/a+b)/ (c/c+d)

Back

Why do we use measures of association

Front

to compare the risk of disease associated with certain exposures to the risk of disease in absence of exposure. identify risk factors (association) causal relationships Consider them in terms of probability (p values, CI)

Back

Source population

Front

Subset of the target population that can be enumerated and studied

Back

Cumulative incidence formula

Front

Number of new cases of disease during a specified time/ number of people in population at risk at beginning of same time interval expressed as ___ per ___ 0.04 is 4 per 100 4% over period of time. Example 4% over a 5 year period.

Back

Odds ratio

Front

a probability statement about the association between a particular disease and a specific risk factor

Back

Incidence rate formula

Front

number of new cases of disease during specified time/ number of people in population at risk during the same time interval x time units Denominator is also called person time at risk "0.133 per person month at risk" "13.3 per 100 person months"

Back

Incidence rate ratio

Front

incidence rate in exposed/incidence rate in unexposed

Back

Measures of disease frequency

Front

incidence, prevalence

Back

cohort study

Front

A type of epidemiologic study where a group of exposed individuals (individuals who have been exposed to the potential risk factor) and a group of non-exposed individuals are followed over time to determine the incidence of disease

Back

Does association imply causation?

Front

No can be useful to suggest causality, but need evidence to prove it

Back

Case reports

Front

accounts of a single occurrence of a noteworthy health-related incident or small collection of such events

Back

Section 3

(50 cards)

Organisms with soil reservoir

Front

Histoplasma capsulatum Clostridium tetani Clostridium botulinum

Back

Airborne transmission

Front

Inhalation of contaminated air. Infection spread by particles that remain infectious when suspended in air etc. measles

Back

How are viral infections classified

Front

DNA virus RNA virus

Back

Disease

Front

Abnormal state associated with clinical signs, symptoms, and atypical laboratory findings

Back

Progression axis of infectious disease

Front

Exposure Infection Disease- clinical sx Cure or death or chronic infection

Back

Epidemiologist classification of disease

Front

Population Risk Factor Transmission Route Reservoir

Back

What measure of association do you use for a cohort study?

Front

Incidence Relative risk

Back

Top infectious disease causes of death

Front

Lower resp infection Diarrhea disease Tuberculosis

Back

When is knowledge of latency and incubation period critical?

Front

For contact tracing and quarantining of exposed people

Back

Vectorborne transmission

Front

Dependent on biology of vector and infectivity of organism

Back

Latent

Front

State in which the agent is non replicating and generally non infectious

Back

Incubation period

Front

Time from exposure resulting in infection until onset of disease

Back

Indirect contact

Front

through infected fomite, blood, or body fluid

Back

Infection

Front

Agent invades host tissue

Back

How are prion infections classified

Front

Protiens

Back

Latency period

Front

Pre infectiousness period Time from exposure to infectiousness

Back

Is period prevalence a rate?

Front

No, time is defined outside of proportion.

Back

Colonization

Front

Agent persists on a host without infection

Back

How is sepsis classified

Front

Disseminated

Back

How is prevalence ratio interpreted?

Front

pr=3 the prevalence of infection among those who were exposed is 3 times that of the prevalence among non exposed

Back

Prevalence Ratio

Front

[a/(a+b)]/[c/(c+d)] Prevalence of exposed/ Prevalence of unexposed Used in cross sectional studies Ratio of burden in a cross sectional study

Back

Contact transmission

Front

requires direct or indirect contact Ex. MRSA

Back

How are diarrheal diseases classified

Front

Secretory Invasive

Back

What measure of association do you use in a case control study

Front

Odds Ratio

Back

Is attack rate a rate?

Front

NO

Back

Food or waterborne transmission

Front

Ingestion of contaminated food

Back

Physician Classification of Disease

Front

Clinical symptoms Diagnosis Prognosis Pathophysiology Treatment Care

Back

In a cross sectional study, what is more reliable, OR or Prev Ratio?

Front

Prevalence Ratio

Back

Transmission axis of infectious disease

Front

Exposure Pre infectious infection Post infectious

Back

When does an odds ratio approximate the prevalence ratio?

Front

A cross sectional study. It is okay when the overall prevalence of disease is low.

Back

Organism with human reservoir

Front

Treponema pallidum Gonorrhea HIV Hep B Hep C Shigella S typhi

Back

Organism with animal reservoir

Front

Rabies Yersinia pestis Leptospira Nontyphoid salmonella Brucella

Back

How are cardiovascular infections classified

Front

Endocarditis Myocarditis Vasculitis

Back

spillover effect

Front

WHen an animal or human becomes infected with a virus through contact with the reservoir host.

Back

How are respiratory diseases classified

Front

Upper resp lower resp

Back

How are CNS infections classified

Front

Meningitis (bacterial v aseptic) Encephalitis Abscess

Back

Microbiologist classification of disease

Front

Isolation Identification Growth Virulence Pathogenicity

Back

Perinatal transmission

Front

Similar to contact infection; however, the contact may occur in utero during pregnancy or at the time of delivery

Back

zoonoses

Front

Diseases transmitted from animals to humans

Back

Direct contact

Front

skin or sexual contact with an infected individual

Back

When are OR, RR,and PR similar?

Front

When prevalence is low.

Back

What measure of association do you use for RCT

Front

Incidence Relative Risk

Back

What measure of association do you use in a cross sectional study?

Front

Prevalence Prevalence ratio

Back

What does prevalence measure?

Front

The burden of disease

Back

Is time in denominator of period prevalence?

Front

No, it sits outside

Back

How are bacterial infections classifed

Front

gram negative gram positive

Back

How are parasitic infections classified

Front

Protozoa Helminths Trematodes Cestodes

Back

When is quarantine most effective?

Front

When latency period is shorter than the incubation period

Back

How are fungal infections classified

Front

Disseminated Localized

Back

Organism with water as reservoir

Front

Legionella Pseudomonas aeruginosa Mycobacterium marinum

Back

Section 4

(50 cards)

Reproductive number of HIV AIDS

Front

2-5`

Back

Infectious period

Front

period from onset of infectiousness to end of infectiousness

Back

Transmission route for diphtheria

Front

saliva

Back

Key measures of virulence

Front

Ratio of cases of serious disease to those infected Case fatality rate

Back

Reproductive number of polio

Front

5-7

Back

What is the incubation period for CJD

Front

Unknown to over 60 years

Back

What is the incubation period for SARS

Front

1 to 10 days

Back

Transmission route for mumps

Front

Airborne droplet

Back

Rt

Front

Repro number t is index of time after initial index case after population is no longer completely susceptible

Back

Reproductive number of mumps

Front

4-7

Back

Transmission route for polio

Front

Fecal oral

Back

VIrulence

Front

Severity of disease after infection occurs

Back

Key measures of infectivity

Front

Incidence rate Attack rate

Back

Herd immunity

Front

Collective immunity Entire population, including those not immunized, that is protected against disease when a critical number of people have been immunized

Back

Transmission route for pertussis

Front

airborne droplet

Back

False positive

Front

Alpha error Type 1 error Test positive but not diseased

Back

Reproductive number of flu

Front

1-3

Back

What is the incubation period for mumps

Front

14 to 18 days

Back

Reproductive number of diphtheria

Front

6-7

Back

Is the case-fatality rate a rate, a proportion or a ratio?

Front

proportion

Back

What is the incubation period for cholera

Front

1 to 3 days

Back

Transmission route for Measles

Front

Airborne

Back

Individual immunity

Front

individuals who acquire immunity are protected against disease

Back

Transmission route for flu

Front

Airborne

Back

Infectivity

Front

Ability of an agent to cause infection in a susceptible host

Back

R0 > 1

Front

Infection will spread in the population Initial period of exponential growth

Back

Pathogenicity

Front

The ability of an agent to cause disease

Back

Immunogenicity

Front

Ability of an organism to produce an immune response in the host after infection which protects against reinfection with same or similar organism

Back

Illness rate

Front

# diseased/ #infected

Back

What type of infections do virulent agents cause

Front

Severe disease

Back

R0=1

Front

Infection will reach an endemic phase

Back

Immunogenicity toward hep c

Front

Poor

Back

What is the incubation period for rabies

Front

1 to 3 months

Back

Key measure of pathogenicity

Front

illness rate

Back

WHen is case fatality used

Front

with discrete, time limited events Outbreaks

Back

Immunogenicity of humans toward hep b

Front

Excellent

Back

Transmission route for HIV AIDS

Front

sexual parenteral

Back

R

Front

Reproductive number after population is no longer completely susceptible

Back

When is an agent pathogenic

Front

if it can cause disease

Back

What is the incubation period for influenza

Front

1 to 3 days

Back

Does virulence change?

Front

Yes as our ability to control and treat disease improves

Back

What is the incubation period for HIV

Front

2 to 4 weeks 3 to 20 years

Back

What is the incubation period for chicken pox

Front

14-16 days

Back

How is case fatality rate different from mortality rate

Front

mortality rate is a rate

Back

What type of infections do agents with low pathogenicity cause

Front

Asymptomatic or clinically inapparent

Back

Reproductive number of measles

Front

12-18

Back

Reproductive number of pertussis

Front

12-17

Back

Reproductive Number

Front

R0 The expected number of secondary cases produced by a single infection in a completely susceptible pipulation

Back

Case fatality rate

Front

proportion of deaths within a designated population of cases over the course of the disease Time is implied or described separately

Back

R0<1

Front

Infection will die out in the population

Back

Section 5

(50 cards)

Herd immunity threshold of measles

Front

83 to 94%

Back

Transmission serial interval

Front

Amount of time elapsed between infection from one generation to the next. Also called the generation time

Back

Beta

Front

Risk of transmission per contact

Back

Herd immunity threshold of mumps

Front

75 to 86%

Back

Index case

Front

the first case in a defined outbreak or epidemic that is recognized by public health authorities

Back

Primary case

Front

Person who first brings a disease into a group of people. Often determined in retrospect or unknown

Back

Specificity calculation

Front

true negative/(true negative + false positive)

Back

When might excess cases not indicate an outbreak

Front

change in reporting change in case definition increased awareness improved diagnosis

Back

Carrier

Front

Infectious, asymptomatic persons

Back

Specificity

Front

Probability a test correctly classifies individuals without disease as negative If everyone without disease tests negative, has 100% specificity

Back

Most common study design in outbreaks

Front

Case control if population is large or disease is rare descriptive case series

Back

Two ways odds ratios are interpreted

Front

1. Ratio of the odds of disease among exposed to odds among unexposed 2. Ratio of odds of exposure among diseased to odds among non diseased

Back

Naturally resistant

Front

not able to become infected because of genetic constitution

Back

Herd immunity threshold of flu

Front

Over 60%

Back

Contact

Front

An individual who has been exposed to a source of infection and who thus may be infected

Back

When is field epidemiology conducted

Front

in real time

Back

Does R0 have dimensions

Front

No

Back

Herd immunity threshold of Polio

Front

80% to 86%

Back

Two steps to communicate outbreak findings

Front

Brief public health officers Write a report with future investigations

Back

Field epidemiology

Front

The application of epi methods in non clinical settings to respond to unexpected health problems

Back

Clinical onset serial interval

Front

The average time between symptom onset in a primary case and secondary cases

Back

Critical vaccination threshold

Front

V=1- 1/r0 Missing vaccine efficacy

Back

D

Front

Duration of infectiousness per same unit time

Back

WHen do we calculate an effective Ro

Front

Also called R or Rt After initial index case and entire population isnt susceptible

Back

Sensitivity

Front

The probability that a test correctly classifies individuals with disease as positive If everyone with disease tests positive, test had 100% sensitivity

Back

Epidemic curve

Front

histogram of the number of cases against the time disease onset. Used to measure and track disease

Back

R0 calculation

Front

R0=BCD Mean number of secondary infections being transmitted by a primary case

Back

How is clinical onset serial interval derived

Front

from retrospective analysis of symptom onset times between primary and secondary case

Back

Propagated source outbreak

Front

multiple peaks. usually person to person transmission usually airborne

Back

False negative

Front

Beta error Type 2 error Diseased but tests negative

Back

Steps in an outbreak investigation

Front

1. prepare for field work 2. establish the existence of an outbreak 3. verify the diagnosis 4. choose study design 5. collect risk factor info 6. collect lab specimen 7. environmental investigation 8. make and test hypothesis 9. implement control and prevention measures 10. communicate findings

Back

Estimation of transmission serial interval

Front

Latency period + half of infectious period

Back

ARI cause ___ % of hospitalizations among children

Front

20 to 40

Back

3 assumptions of R0

Front

Population is completely susceptible ( number of susceptible people , S, should be much greater than number of infected people ) Population is constant N Population is well mixed/ homogenous

Back

Identify and count cases

Front

Case define Define population at risk Plot epi curve

Back

Secondary Case

Front

Cases who were infected by primary case. Same disease or strain.

Back

C

Front

Number of susceptible contacts per unit time

Back

Herd immunity threshold of Diphtheria

Front

80 to 85%

Back

Case

Front

An infected individual

Back

Extended source outbreak

Front

continuous or ongoing outbreak People exposed over time Etc. LD

Back

When is high sensitivity important

Front

When disease is severe

Back

Susceptible

Front

Able to become infected if exposed

Back

How is risk information collected

Front

questionnaires clinical data public health surveillance reporting systems

Back

Outbreak control measures

Front

Food recall Advisory to carriers Correct health procedures Prophylaxis Education

Back

Outbreak

Front

occurrence of disease that is greater than would be expected at a particular time and a particular place

Back

Sensitivity formula

Front

true positive/(true positive + false negative)

Back

Preparing for field work

Front

Build a team and identify responsibilities Implement regular readings Plan for early communication Research what is known about disease

Back

Acute respiratory infection

Front

Group of diseases that invlude pneumonia, influenza, tb, respiratory syncytical virus Leading cause of morbidity and mortality

Back

What are the 3 factors that determine reproductive number

Front

1. risk of transmission (infectiousness) 2. Number of susceptible people an index case comes in contact with 3. Average duration of infectivity

Back

Confirming an outbreak

Front

does observed cases exceed expected

Back

Section 6

(50 cards)

Routine infection control practices

Front

minimum level of precautions used with all patients all times handwashing gloves masks gowns eye protection

Back

When would the clinical onset serial interval be the same value as the transmission serial interval

Front

If transmission of infection occurs at the same time as disease onset if disease onset occurs halfway through the infectious period

Back

When to wear gowns

Front

during procedures or patient care when in contact with blood, body fluid, secretion, excretion Definite: contact As needed: for standard, droplet, airborne

Back

Is negative pressure room needed with droplet spread?

Front

No

Back

URI viruses

Front

Rhinovirus Coronavirus Flu Parainfluenza virus RSV Herpesvirus Adenovirus Bocavirus Coxsackivirus

Back

Secondary resistance

Front

develops during therapy Inappropriate treatment or nonadherence

Back

MDR TB

Front

Multidrug resistant Caused by bacteria resistant to standard TB drugs isoniazid and rifampin

Back

Bacterial respiratory infections of LRI

Front

Legionella S. pneumoniae

Back

Primary drug resistance

Front

caused by person to person transmission of drug resistant organisms

Back

% of patients that complete home TB treatment

Front

61%

Back

Contact precautions

Front

single room cohort room separation 3 ft PPE gown and gloves Clean hospital rooms daily with disinfectant

Back

Classification of bacterial respiratory infections of LRI

Front

Community acquired Hospital acquired Ayptical

Back

URI

Front

Of the nasal cavity, pharynx, larynx Common cold tonsillitis acute sinusitis

Back

XDR TB

Front

extensively drug resistant resistant to isoniazid, rifampin, fluoroquinolones and more than one of 3 second line injectable drugs

Back

LRI

Front

Of the trachea, primary bronchi, lungs Bronchitis Pneumonia

Back

How many cases of flu each year

Front

3 to 5 million

Back

Acquisition of tb

Front

Inhalation travel to alveoli Bacilli ingested by alveolar macrophages which may spread to other tissues

Back

LRI viruses

Front

Influenza Parainfluenza RSV Adenovirus Bocavirus Metapneumovirus

Back

AIIR

Front

airborne infection isolation room Ventilation >12 exchanges per hour mechanical or natural ventilation Air circulated through HEPA filter Negative air pressure

Back

Natural reservoir of TB

Front

disease tissue of human and other warm blooded animals

Back

ARI cause ____% of all deaths among children under 5

Front

18

Back

secondary bacterial pneumonia

Front

common in elderly or immunocompromised. Other bacteria invade the lungs bc immune system poor. Mort in all years. Underlying all morb and mort for disease.

Back

Primary flu viral pneumonia

Front

seen most often in pandemic years rapid progression to resp distress high mortality in all age groups

Back

Airborne precautions

Front

Airborne infection isolation room AIIR Minimal pt movement Surgical mask on patient not in AIIR

Back

First line TB drugs

Front

Isoniazid Rifampin Pyrazinamide Ethambutol Rifabutine Rifapentine

Back

Is drug resistant TB transmitted differently?

Front

No just more severe

Back

When to wear mask or eye protection

Front

procedures likely to generate splashes or sprays As needed for all types

Back

Pathogenesis of TB

Front

2 to 8 weeks of macrophages ingesting and surrounding bacilli. Cells form a barrier shell called a granuloma. If immune system doesnt work, bacilli multiply

Back

Classification of ARI

Front

Upper respiratory infection (URI) Lower respiratory infection

Back

Bacterial respiratory infections of URI

Front

Streptococcus pyogenes Haemophilus influenza

Back

primary viral pneumonia

Front

virus colonizes in lungs and makes pneumonia. Usually in pandemic situations. Rapid progression. Can have high mort in all, even young adults. Usually 1 or 2 days after symptom onset

Back

Infectious period of flu

Front

less than 1 day only 5% of cases infectious for over 3 days

Back

Two main types of infection control practices

Front

1. routine/ standard precaution 2. transmission based

Back

Transmission of TB

Front

Small droplet Expelled when cough, sneeze, speak, sing Close contact Risk factors differ for infection and disease

Back

Risk factors for community acquired pneumonia

Front

COPD Alcoholism Lung abcess HIV Travel IDU Etc

Back

Incubation period of flu

Front

1 to 4 days

Back

Clinical presentation of flu

Front

High abrupt fever malaise myalgia headache cough prostration

Back

Generation time of flu

Front

latency period times half infectious period 1.6+0.5*1 2 days

Back

What is attact rate of flu during pandemic years

Front

30%

Back

When to wear gloves

Front

contact with blood, body fluid, secretion, mucous membranes, wounds, contaminated items Definite: contact As needed: standard, droplet, airborne

Back

When are private patient rooms suggested

Front

Definitely for droplet, contact, airborne

Back

Droplet procautions

Front

Single room Cohort rooms Pt separation by 3 ft Surgical mask on pt Don PPE mask upon room entry

Back

Mask v respirator

Front

masks protect from splashes, body fluids, inhalation of droplets respirators needed for airborne or aerosolized pathogens

Back

Droplet transmission

Front

infections spread by large droplets generated by cough, sneezes etc. flu

Back

PPE

Front

Personal protective equipment Gloves Gowns Mask

Back

Second line TB drugs

Front

Streptomycin Cycloserine P-aminosalicylic acid Ethionamide Amikacin/kanamycin Capreomycin Levofloxacin Moxifloxacin Gatifloxacin

Back

% of patients who complete DOT

Front

86-90%

Back

Secondary bacterial pneumonia

Front

more common in elderly or immunocompromised patients cause of mortality in all epidemics

Back

Cold weather and ARI

Front

Inhalation of cool air, cool body, cold stressor cause suppression of immune responses vasoconstriction and limitation of leukocytes decreased muscociliary activity Spending more time indoors

Back

Latency period of flu

Front

1 to 2 days

Back

Section 7

(50 cards)

Who should get flu vaccine

Front

all pts 6 months old or greater unless pt has life threatening allergy to the vaccine or one of its ingredients

Back

Surveillance systems

Front

networks of people and activities that maintain the processes

Back

Flu like illnesses

Front

parainfluenza viruses rhinoviruses

Back

Attributes of surveillance

Front

PPV Sensitivity Timeliness Representativeness Data quality Simplicity Flexibility Acceptability

Back

Types of flu

Front

A B C

Back

Active surveillance

Front

organization conducting the surveillance collects data actively

Back

NA

Front

Neuraminidase in flu virus allows for viral release from host epithelial cell important for pathogenisis, immune protection, antiviral target

Back

World flu patterns

Front

less seasonality in tropical regions multiple strains circulate at once, first in tropical regions

Back

Antigen

Front

Substance or molecule that is capable of stimulating an immune response

Back

What should surveillance systems have

Front

Have processes and methodologies to keep sensitive data private have no barriers to info flow guide services and programs capitalize on natural experiences

Back

1918 flu pandemic

Front

500 million infected 10 to 20% mortality 50 to 100 million deaths

Back

Objectives of surveillance

Front

1. monitor occurrence 2. Provide useful info for appropriate timely ix 3. Provide indication of success of ix

Back

IIV

Front

inactivated influenza vaccine shot Cant cause flu soreness

Back

Flu classifications

Front

influenza flu like illness haemophilus influenzae bacterium

Back

Case defintions

Front

for surveillance balance sensitivity, specificity, simplicity costs, ftimeliness Probably, sus, confirmed Dependent on context and current needs Change over time for emerging infectious disease

Back

How flu is named

Front

virus type geographic region strain number year of isolation subtype

Back

Acceptability

Front

does effort yield info that is useful to people who need it

Back

Notifiable diseases

Front

national diseases that SHOULD be reported to cdc by states and jurisdictions without personal identifiers used for monitoring diseased, nationwide aggregates, identify at risk groups, forming policy

Back

Primary objective of surveillance

Front

monitor occurrence of disease over time where and when problems occur who is affected

Back

Seasonality of flu

Front

low humidity ,cold weather increase transmissibility Viral shedding greater at low temperature Droplets are more stable at low humidity

Back

HA

Front

hemagglutinin is part of flu virus that is an attachment protein important for pathogenisis, immune protection, antiviral targets

Back

Flexibility

Front

can the system readily adapt to new circumstances or changing needs

Back

Surveillance cycle

Front

Data collection Data integration Analysis and interpretation Surveillance Products Action* Dissemination

Back

Simplicity

Front

can data be accessed easily

Back

Notifiable v reportable disease

Front

not mutually exclusive can change reporting from care provider to state. notification from state to cdc or who

Back

Predictor of flu severity

Front

primary site of infection where HA protein binds

Back

LAIV

Front

Live attenuated influenza vaccine mist does infect host cells but doesnt cause disease easy to administer less effective

Back

Population based surveillance

Front

seeks to capture all occurrences or a representative sample in a defined geographic area Used to calculate incidence and prevalence includes reporting systems

Back

Flu C

Front

mild illness

Back

Timeliness

Front

how promptly does info flow thru cycle of surveillance

Back

Positive predictive value

Front

PPV = TP / (TP + FP) To what extent are reported cases really cases dependent on accuracy of test and disease prevalence

Back

Flu vaccine production

Front

3 or 4 A and B strains selected vaccine made in eggs 9 months

Back

Triple A surveillance cycle

Front

Assess- data generation, reporting Analyze- and interpret Action- decision

Back

Antigenetic drift

Front

minor antigen changes through mutations causes annual epidemics changes in HA or NA lead to no antibody protection

Back

Flu B

Front

exclusively in humans and seals

Back

Flu A

Front

causes pandemics. most virulent

Back

Two types of flu vaccine

Front

IIV LAiV

Back

Flu treatment

Front

antivirals that inhibit NA activity zanamivir oseltamivir 70 to 90% effective prophylacically must be taken within 48 hours of onset reduces severity and duration

Back

Antigenetic shift

Front

major genetic changes through reassortment common with viruses with segmented genomes coinfection

Back

Flu mortality rate

Front

0.1%

Back

When can antigenetic shift cause pandemics

Front

variant retains ability to replicate in humans is efficiently transmitted between humans has new surface antigens that evade existing antibodies

Back

Efficacy of flu shot

Front

50 to 80%

Back

Representativeness

Front

do events detected represent all persons in target pop

Back

Reportable diseases

Front

diseases of public health importance that MUST be reported to state or territorial jurisdictions by law allows contact tracing and partner notification Each state has own laws and lists

Back

Flu surveillance

Front

1. viral surveillance network- weekly numbers of lab confirmed in hospitals 2.mort surveillance of 122 cities weeky reporting % of deaths 3. flu associated peds deaths weekly 4. outpt services - 1800 sites weekly 5. geographic dist of flu activity

Back

Flu transmission

Front

person to person close contact droplet, contact, airborne transmission

Back

Non population based surveillance

Front

Active passive enhanced passive sentinel post marketing syndromic

Back

Data quality

Front

how complete are data

Back

Surveillance

Front

ongoing and systematic collection, collation, analysis and interpretation of health data and dissemination of results to those who need to know to avoid and prevent infections or epidemics

Back

How many flu deaths each year

Front

250k to 500k

Back

Section 8

(50 cards)

Horizontal HAi reduction

Front

reduce risk of a broad range of infections that are not pathogen specific includes -standard precaution -universal decolonization -universal gloving -cleaning

Back

Is latency period the same length as the preinfectious period?

Front

Ues

Back

How many HAi deaths each year

Front

75000

Back

Most common HAi

Front

Pneumonia GI (cdif) Surgical site Bloodstream infection UTI

Back

Norovirus and Sapovirus

Front

Noro is highly contagious Infectious dose is 18 particles 60% of all GI illness fecal oral or droplet stable and survives freezing and heating to 140 F Not killed by 70% alcohol

Back

Can an odds ratio be used to interpret findings from cohort study?

Front

Yes

Back

Total cost of HAi

Front

over 9 billion

Back

How does length of incubation period and latency impact quarantine?

Front

If incubation period is shorter than latent period, people start showing symptoms before they are infectious which makes quarantine effective

Back

BRFSS

Front

phone survey starting in 1993 Behavioral risk factor surveillance states collect data, send to cdc

Back

Source of contact HAI

Front

Other pt Visitor Hospital staff Reusable equipment non mobile equipment Catheter Drain

Back

How to reduce risk of cdif

Front

sensitive detection enhanced cleaning isolation hand hygiene

Back

Most common HAI pathogens

Front

Cdif Staph Ecoli

Back

How are HAI reported

Front

THrough CMS website

Back

What is a practical definition for generation time

Front

time separating onset of symptoms of infector and infectee

Back

What is best measure of association for case control study

Front

Odds ratio

Back

Case fatality rate

Front

percentage of population that dies from a specific disease

Back

Syndromic surveillance

Front

surveillance of health related data preceding diagnosis with a sufficiently strong signal to warrant future response Used for early detection of outbreak, monitor trends, confirm outbreaks uses existing health data in real time to provide immediate analysis ex. OTC sales, internet searches

Back

Vaccine effectiveness in outbreak

Front

1- attack rate vac/ attack rate unvac

Back

Bundles

Front

Grouping of evidence based best practices that individually improve care, but when applied together result in greater improvement

Back

How many HAI in US each year

Front

720000 4% hospitalized patients 25% device related

Back

What does latent TB lack?

Front

Sensitivity

Back

Do vaccines only protect those immunized?

Front

No

Back

What is most likely reduced with DOT?

Front

Secondary drug resistance

Back

post marketing surveillance

Front

monitor safety of drug or device after it is released to the market

Back

Contact tracing

Front

the identification and diagnosis of people who may have come into contact with an infected person

Back

HAi

Front

Hospital acquired infection

Back

What are primary risk factors for cdif infection?

Front

Recent antibiotic exposure contamination of environment

Back

Passive surveillance

Front

data supplied to health departments based on established rules and regulations usually undercount

Back

Rare disease assumption

Front

assumption that OR approximates RR

Back

What is the purpose of statistical tests that evaluate associations?

Front

determine if the findings are due to chance alone

Back

Is a respirator needed to protect HCW from droplets?

Front

no

Back

Limitations of sentinel surveillance

Front

not effective for rare disease wont id outside of catchment areas cant directly estimate prevalence and incidence

Back

Source of airborne hAI

Front

Other patients Visitors Hospital spread Environment Can be large droplets or airborne

Back

Why is generation time difficult to measure?

Front

Cant find precise moment of infection

Back

Are magnitude of effect size and statistical significance equivalent?

Front

No

Back

When to use soap and water

Front

hands visibly soiled or dirty, contaminated with blood or body fluid after using bathroom

Back

Does the disease incubation period impact R0?

Front

no

Back

When does a zoonotic infection occur

Front

When a virus, bacteria, fungus, or parasite crosses species to infect humans

Back

Where do HAI microbes come from

Front

Potable water (LD) Air Contact Self

Back

How would you calculate generation time assuming equal transmissibility during the infectious period?

Front

Generation time= latency period+ infectious period/2

Back

Vaccine effectiveness in case control

Front

1-OR

Back

Strengths of sentinel surveillance

Front

signal trends id outbreaks monitor changes in disease burden

Back

Vertical HAI reduction strategies

Front

Reduce risk of infection for specific pathogens -active screening -contact precautions -vaccination

Back

What criteria do epis use to classify disease

Front

reservoir of organism means of transmission

Back

What most impacts R0?

Front

Infectivity

Back

What is best measure when calculating how many people have disease over 2 years

Front

period prevalence

Back

Enhanced passive surveillance

Front

active follow up once a case is reported involves contact tracing for diseases like TB, STI, Ebola, to prevent transmission

Back

Sentinel Surveillance

Front

reporting of disease cases by select institutions or individuals useful when need high quality data not from passive system involves limited networks

Back

When to use purell

Front

not visibly soiled before and after pt contact after direct contact after touching equipment

Back

Vaccine effectiveness in prospective cohort

Front

1-hazard rate 1-relative risk 1- CI vac/ CI unvac

Back

Section 9

(1 card)

Vaccine effectiveness in cross sectional study

Front

1- prevalence vac/prevalence unvac

Back