Midterm2 Flashcards

1
Q

What are Kochs postulates used for?

A

To prove the cause of an infectious disease

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2
Q

Kochs postulates

A

1) The same pathogen must be present in every case of the disease
2) The pathogen must be isolated from the disease host and grown in pure culture
3) the pathogen from the pure culture must cause the disease when it is inoculated into a healthy, susceptible laboratory animal.
4) The pathogen must be isolated from the inoculated animal and must be shown to be the original organism

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3
Q

Incidence

A

Describes the rate of development of a disease in a group over a period of time; new cases

(Number of persons develop a disease/ total number at risk)*unit time

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4
Q

Prevalence

A

♣ Count of the # of person w/ disease
- Is the most frequently used measure in epidemiology
♣ New and old cases
(# of persons w/ a disease/total # in grp

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5
Q

Morbidity rate

A

o incidence of illness (disease) in a population. It includes both fatal and nonfatal diseases; could refer to either prevalence or incidence

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6
Q

Mortality rate

A

Incidence of death in a population

♣ (# of persons dead/ total # in grp)x unit time

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7
Q

Case fatality rate

A

the number of confirmed cases that died of the disease

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8
Q

Sporadic disease:

A

disease that occurs only occasionally

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9
Q

Endemic disease

A

disease constantly present in a population

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10
Q

Epidemic disease

A

disease acquired by many people in a given area in a short time

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11
Q

Pandemic disease

A

worldwide epidemic

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12
Q

Acute disease

A

symptoms develop rapidly but the disease lasts only a short time

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13
Q

Chronic disease

A

symptoms develop slowly

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14
Q

Subacute disease

A

intermediate btw acute and chronic

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15
Q

Latent disease

A

causative agent is inactive for a time but then activates and produces symptoms

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16
Q

Herd immunity

A

immunity in most of a population

17
Q

Case definition

A

important and not trivial

18
Q

Local infection

A

pathogens are limited to a small area of the body

19
Q

Systemic (generalized) infection

A

an infection throughout the body

20
Q

Focal infection

A

systemic infection that began as a local infection

21
Q

Sepsis

A

Toxic inflammatory condition arising from the spread of microbes, especially bacteria or their toxins from a focus of infection

22
Q

Bacteremia

A

bacteria in the blood

23
Q

Septicemia

A

also known as blood poisoning growth of bacteria in the blood

24
Q

Toxemia

A

toxins in the blood

25
Q

Viremia

A

viruses in the blood

26
Q

Primary infection

A

acute infection that causes the initial illness

27
Q

Secondary infection

A

opportunistic infection after a primary infection

28
Q

Subclinical disease

A

no noticeable signs or symptoms

29
Q

Predisposing factors (make the body more susceptible to disease)

A
o	Gender
o	Inherited traits such as the sickle cell gene
o	Climate and weather
o	Fatigue
o	Age
o	Lifestyle 
o	Nutrition
o	Chemotherapy
30
Q
  • Development of Disease
A

o Incubation period: interval btw initial infection and first signs and symptoms
o Prodromal period: short period after incubation; early, mild symptoms
o Period of illness: disease is most severe
o Period of decline: signs and symptoms subside
o Period of convalescence: body returns to its pre-diseased state

31
Q

o Human reservoirs

A

♣ Carriers may have unapparent infections or latent diseases
♣ By vaccinating youre changing the dynamic of sideade and provide immunity for the community
♣ Influenza virus that are similar enough to humans can sometimes make that cross

32
Q

Animal reservoirs

A

Zoonoses are diseases transmitted from animals to humans

33
Q

Nonliving reservoirs

A

♣ Soil and water

Food

34
Q

Transmission

A

o Direct contact: requires close association btw the infected and a susceptible host
o Indirect contact: spreads to a host by a nonliving object called a fomite
o Droplet transmission: transmission via airborne droplets less than 1 meter (sneeze)
o Vehicle: transmission by an inaminate reservoir
♣ Waterborne, foodborne, airborne

35
Q

Healthcare-associated infections

A

o Acquired while receiving treatment in a health care facility
♣ Also known as nosocomial infections

36
Q

Emerging infectious diseases

A

diseases that are new, increasing in incidence, or show a potential to increase in the near futues

most zoonotic
of vital origin
likely vector borne

37
Q
  • Centers for Diesease control and prevention (CDC)
A

o Collects and analyzes epidemiological information in the US
o Morbidity and Mortality Weekly Report
o Notifiable infectious disease: diseases In which physicians are required to report ocurrence

38
Q

Molecular strain-typing techniques; when to use

A

♣ Simplicity – simpler to execute and simpler to trainpeople to use(e.coli in brazil 1 month v 6)
♣ High throughput – capacity of tet to process a large number of specimens simultaneously
♣ Cost- widespread use of molecular bio reagents reduced costs. PCR have all the same reagents except for primers
♣ Appropriateness –
• The capacity of a test to addres epidemiologic problems not possible to address by conventional methods
• If conventional test possible then no need
• Often DNA sequences allow unambiguous identification of new ingectious agents and evolution of these agents

39
Q

Molecular strain-typing techniques; how to select

A

♣ Typeabiliy: ability of a technique to generate an unambiguous result for an isolated test
♣ Reproducibility : ability to produce identical results
♣ Ease of interpretation: serve as stratum
♣ Ease of use: simplicity
♣ Stability: character us no subject to rapid evolution or lost from host
♣ Epidemiologic concordance: effectively group outbreak related strains
♣ Typing system concordance: molecular typing compares favorably with a previously validated test
♣ Validity: correctly predict or identify those who truy have the characteristics