Disease Detectives Flashcards

1
Q

asymptomatic

A

Showing no signs or symptoms, although can be carrier of disease

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2
Q

cluster

A

An aggregation of cases over a particular period closely grouped in time and space, regardless of whether the number is more than the expected number

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3
Q

elimination

A

Reduction to zero of a disease in a defined geographical area due to deliberate efforts. This requires continued intervention measures.

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4
Q

endemic disease

A

Present at a continuous level throughout a population/geographic area; constant presence of an agent/health condition within a given geographic area/population; refers to the usual prevalence of an agent/condition.

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5
Q

epidemic

A

Large numbers of people over a wide geographical area are affected.

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6
Q

etiology

A

Study of the cause of a disease.

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7
Q

fomite

A

A physical object that serves to transmit an infectious agent from person to person. An example of this is lice on a comb. The comb is the fomite and the lice are the agent that can make your hair itch.

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8
Q

latrogenic

A

An illness that is caused by medication or a physician.

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9
Q

incubation period

A

Time in between when a person comes into contact with a pathogen and when they first show symptoms or signs of disease.

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10
Q

index case

A

First patient in an epidemiological study (also known as patient zero or primary case).

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11
Q

morbidity

A

rate of disease in a population

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12
Q

mortality

A

rate of death in a population

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13
Q

nosocomial disease

A

An infection that is acquired in a hospital

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14
Q

outbreak

A

More cases of a particular disease than expected in a given area or among a specialized group of people over a particular period of time.

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15
Q

pandemic

A

An epidemic occurring over several countries or continents and affecting a large proportion of the population.

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16
Q

plague

A

A serious, potentially life-threatening infectious disease that is usually transmitted to humans by the bites of rodent fleas. It was one of the scourges of our early history. There are three major forms of the disease: bubonic, septicemic, and pneumonic.

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17
Q

risk

A

The probability that an individual will be affected by, or die from, an illness or injury within a stated time or age span. Risk of illness is generally considered to be the same as the Incidence (see below) and the terms are used interchangeably. Age-span is not usually a consideration in this usage. Risk of death from a particular illness is expressed as the Case Fatality Rate (Number deaths due to a disease/Number with the disease) or the Cause-specific Mortality Rate (Number deaths due to a disease/Number in population). Age span is a more common consideration in this last usage.

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18
Q

surveillance

A

The systematic and ongoing collection, analysis, interpretation, and dissemination of health data. The purpose of public health surveillance is to gain knowledge of the patterns of disease, injury, and other health problems in a community so that we can work towards their prevention and control.

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19
Q

symptomatic

A

showing symptoms or signs of injury

20
Q

vector

A

An animal that transmits disease but is not the cause of the disease itself. For example, a mosquito is a vector for malaria.

21
Q

zoonosis

A

An infectious disease that is transmissible from animals to humans.

22
Q

incidence (of illness)

A

he number of new instances of disease in a population over a given time period. It is expressed as “X cases/Y population/ Z time”.

23
Q

prevalence

A

the number of affected persons in the population at any given point in time. It is expressed as “X cases/Y population”. There are two major ways in which prevalence is measured: period prevalence and point prevalence

24
Q

point prevelance

A

snapshot of the population and its rate of a certain disease at a point in time

25
Q

period prevalence

A

tracks the prevalence over a certain duration

26
Q

13 steps to investigating an outbreak

A
  1. Prepare for field work - Research and Supplies, Official Arrangements, Safety Protocols, and Contacts
  2. Establish the Existence of an Outbreak - Consider Severity, Potential for Spread, Public Concern, and Availability of Resources
  3. Verify the Diagnosis - Verify Procedures and Eliminate Experimental Error (and Other Errors/Biases, for That Matter)
  4. Construct a Working Case Definition
  5. Find Cases Systematically and Record Information - Time: Tables, Epi Curves; Place: Geographical Extent of Disease & Spot Map; Identify By Demographic Information or Exposures to Risk Factor
  6. Describe and Orient the Data in Terms of Person, Place, and Time - Descriptive Epidemiology
  7. Develop Hypotheses (Agent/Host/Environment Triad) = Chain of Transmission
  8. Evaluate Hypotheses - Analytical Studies (MUST Have a Control Group)
  9. Refine Hypotheses if Necessary
  10. Compare and Reconcile with Laboratory and/or Environmental Studies
  11. Implement Control and Prevention Measures (ASAP!)
  12. Initiate or Maintain Surveillance - Monitor Implementation: Track New Cases, Check the Outbreak’s Spread Outside Targeted Area, Control and Change if Needed
  13. Communicate Findings - Reports, To Important People and Public
27
Q

passive surveillance

A

Diseases are reported by healthcare providers. This type of surveillance, though simple and inexpensive, is often limited by incomplete reporting and quality variation in reporting

28
Q

active surveillance

A

Health agencies contact health provers seeking reports. This ensures more complete reporting of conditions. Active surveillance is often used with a specific epidemiological investigation or during an outbreak

29
Q

syndromic suveillance

A

The syndrome of the disease is monitored as a proxy for the disease. The syndrome must be infrequent and severe enough to warrant investigation of each identified case, and must be unique. This form of surveillance is often used when timeliness is key, diagnosis is difficult or time-consuming, or when detecting and defining the scope of an outbreak.

30
Q

sentinel surveillance

A

Professionals selected to represent a specific geographic area or group report health events to health agencies. This is used when high-quality data can’t be obtained through passive surveillance. It involves monitoring trends or key health indicators and a limited network of reporting sites. Advantages include being able to implement intervention earlier and not being as reliant on doctors to diagnose disease. One downside to sentinel surveillance is that it’s not as effective for detecting rare diseases or diseases that occur the outside the catchment areas of the sentinel sites.

31
Q

Hill’s Criteria for Causation

A
  1. Strength of Association - relationship is clear and risk estimate is high
  2. Consistency - observation of association must be repeatable in different populations at different times
  3. Specificity - a single cause produces a specific effect
  4. Alternative Explanations - consideration of multiple hypotheses before making conclusions about whether an association is causal or not
  5. Temporality - cause/exposure must precede the effect/outcome
  6. Dose-Response Relationship - an increasing amount of exposure increases the risk
  7. Biological Plausibility - the association agrees with currently accepted understanding of biological and pathological processes
  8. Experimental Evidence - the condition can be altered, either prevented or accelerated, by an appropriate experimental process
  9. Coherence - the association should be compatible with existing theory and knowledge, including knowledge of past cases and epidemiological studies
32
Q

convalescent carriers

A

Humans are also capable of spreading disease following a period of illness, typically thinking themselves cured of the disease

33
Q

incubatory carrier

A

When an individual transmits pathogens immediately following infection but prior to developing symptoms

34
Q

chronic carrier

A

Someone who can transmit a disease for a long period of time

35
Q

genetic carrier

A

has inherited a disease trait but shows no symptoms

36
Q

transient/temporary carrier

A

Someone who can transmit an infectious disease for a short amount of time

37
Q

advantages of Trial study design

A

most scientifically sound, best measure of exposure

38
Q

disadvantages of trial study design

A

time consuming, unethical for harmful exposures, most expensive

39
Q

advantages for cohort study design

A

Most Accurate Observational Study
Good Measure of Exposure
Correct Time Sequence
Good for Rare Exposures
Easy Risk Calculation

40
Q

disadvantages for cohort study design

A

Time Consuming
Expensive
Bad for Rare Diseases
Possible Loss of Follow-up

41
Q

advantages for case-control study design

A

Can Study Rare Diseases
Relatively Less Expensive and Relatively Fast
Good for Rare Diseases
Good for Long Latency Periods

42
Q

disadvantages of case-control study design

A

Possible Time-Order Confusion
Error in Recalling Exposure
Only 1 outcome

43
Q

advantages of cross-sectional study

A

Fastest
Least Expensive
Good for More Than 1 Outcome

44
Q

disadvantages of cross-sectional study design

A

Possible Time-Order Confusion
Least Confidence in Findings

45
Q
A