Epidemiology Flashcards

1
Q

Fill in the blanks: ‘Epidemiology is the study of the __________ and ___________ of disease frequency in human/animal populations and the application of this study to control health problems.’

A

(Distribution and determinants)

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2
Q

What are determinants of disease?

A

(Factors that cause some individuals to acquire disease and/or factors that prevent some individuals from getting disease → aka EXPOSURES)

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3
Q

What is the term for a testable statement that tries to explain a set of observations and can be tentatively rejected/not rejected through scientific research?

A

(Hypothesis)

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4
Q

What is the difference in the use/purpose of descriptive and scientific/analytical studies?

A

(Descriptive - describe patterns of disease; scientific - search for disease causes and prevention)

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5
Q

What is the limitation of descriptive epidemiology?

A

(It cannot identify the causes of disease)

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6
Q

What is the term for the resistance to spread of contagious disease within a population if a high proportion are immune?

A

(Herd immunity)

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7
Q

How is herd immunity accomplished? Three answers.

A

(Natural exposure, controlled exposure, or vaccination)

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8
Q

The key to excluding pathogens is to remember what characteristic about them?

A

(How they spread)

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9
Q

How long is the suggested quarantine or isolation period?

A

(45 days (I’m adding this because it’s intuitive, for isolation with a known disease, the isolation period will depend on the disease present so 45 days is likely a catch all but not perfect for every disease)

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10
Q

When vaccines are non-existent or poorly effective for a certain disease, what becomes your best option?

A

(Premunization aka controlled exposure)

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11
Q

Long term stress increases or decreases your resistance to bacterial, parasitic, and viral pathogens. Give an answer for each category.

A

(Bacterial - increases; parasitic - increases; viral - decreases)

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12
Q

How is scrapie controlled in sheep populations?

A

(You destroy genetically susceptible sheep in affected flocks (so bloodline related sheep of scrapie positive animals) or those possessing scrapie-susceptible PrP alleles; this is a good example of using genetics to control disease)

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13
Q

How is scrapie controlled in goat populations?

A

(Goats that are exposed to scrapie positive sheep are destroyed)

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14
Q

(T/F) The inclusion of coccidiostats in poultry feed are meant to rid the population of coccidian infections entirely.

A

(F, they are meant to limit coccidial replication and allow time for immunity to develop, then you can pull the coccidiostats prior to going to market and the birds will not get sick)

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15
Q

Besides treating the sickness associated with leptospirosis in dogs, what is the other purpose of leptospirosis treatment?

A

(Eliminates shedding to reduce the likelihood of spread to naive animals and people)

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16
Q

Water chlorination and/or access to clean drinking water is important for the prevention of what parasite in backyard chicken flocks?

A

(Trichomoniasis)

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17
Q

What nutritional control of disease is utilized in shelter dogs to help control diarrhea?

A

(The administration of pre and probiotics at the time of admission)

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18
Q

What nutritional control of disease is utilized in backyard chickens to prevent trichomoniasis?

A

(Providing access to clean and/or chlorinated water as pigeons carrying Trichomonas gallinae contaminate water supplies)

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19
Q

Give two examples of using immunity to control disease spread.

A

(1. FMD ring vaccinations prevent spread beyond the infected zone due to host resistance; 2. rabies vaccination of urban domestic animals creates a buffer against sylvatic rabies crossing over to urban areas, 3. providing colostrum and pre/post weaning IBR/BVD/PI-3/BRSV vaccinations to reduce susceptibility to 2ndry M. haemolytica infections)

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20
Q

What is the first step in containing a disease outbreak?

A

(Inform the owner of your concerns; this should be done before contacting authorities)

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21
Q

What is the first step in eliminating infectious agents from the environment (truck bed, housing, etc.)?

A

(Removal of gross organic material)

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22
Q

Does low or high stress increase an animals’ susceptibility to bacterial and parasitic pathogens?

A

(Low stress)

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23
Q

Does low or high stress increase an animals’ susceptibility to viral pathogens?

A

(High stress)

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24
Q

Although intense genetic selection produces uniformity in phenotypes especially in relation to desirable production characteristics, it also reduces survivability by altering what other characteristic of the animals?

A

(Disease resistance → decreases it)

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25
Q

What is the difference between a fixed and dynamic population?

A

(Fixed populations are associated with permanent membership to that population i.e. veterans of the vietnam war; dynamic populations are associated with transient membership to that population i.e. graduate students)

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26
Q

Why is it important to distinguish between your study population being fixed versus dynamic?

A

(It will guide you to the appropriate measures of disease frequency and study designs)

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27
Q

What is the term for the measurement of disease in which the numerator is a subset of the denominator?

A

(Proportion)

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28
Q

What is the key difference between a ratio and a proportion?

A

(In a ratio, the numbers used do not need to be related to each other whereas with a proportion, the numbers must be related, specifically the numerator is a subset of the denominator)

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29
Q

With which measure of disease (ratio, proportion, or rate) is time an intrinsic part of the denominator?

A

(A rate)

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30
Q

What is prevalence?

A

(Prevalence measures the presence of existing cases of disease in a population during a specified time period → proportion of population who have the disease)

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31
Q

Who are included in your numerator and denominator when calculating prevalence?

A

(Numerator - all current existing cases of the disease you are studying; denominator - the total population including healthy and sick)

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32
Q

You have been observing a group of 118 veterinary students for lack of motivation for the month prior to winter break. During the first week, 23 students expressed a lack of motivation. During the second week, 64 students expressed a lack of motivation. During the third week, 87 students expressed a lack of motivation. During the fourth week, 31 students expressed a lack of motivation. What was the prevalence of lack of motivation during the third week (in english that a child would understand)?

A

(73% of the veterinary students were experiencing a lack of motivation during the third week of the month prior to winter break → since you are canceling out the units of time, you must include it in words with your answer)

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33
Q

Who is excluded from the denominator when calculating incidence?

A

(People who are not at risk for the disease being measured → when measuring uterine cancer cases, individuals of the male sex are not included; this includes individuals who are already sick as they cannot be considered a ‘new’ case)

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34
Q

Would you use the prevalence or incidence of a disease to assess the burden of the disease for the use of administration and planning, i.e. allocating resources appropriately?

A

(Prevalence)

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35
Q

Would you use prevalence or incidence of a disease to evaluate treatments for a certain disease?

A

(Incidence, will tell you if the treatments are working, so you’d be looking for their state to change from diseased to non-diseased)

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36
Q

How do prevalence and incidence differ in terms of what they are measuring?

A

(Prevalence - existing disease; incidence - new disease)

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37
Q

What is the measurement of the occurrence of new cases of disease in a population during a specified time period?

A

(Cumulative incidence)

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38
Q

What does an incidence rate measure?

A

(Incidence rate measures the speed at which new cases of disease occur in a population)

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39
Q

Between cumulative incidence and incidence rate, which takes into account when disease occurs in the population followed?

A

(Incidence rate)

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40
Q

What is the appropriate population type and follow up length that cumulative incidence can be used to measure disease?

A

(Fixed populations with a short follow up or no loss to follow up)

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41
Q

What is person-time?

A

(The amount of time each person at risk for a disease is under observation; their accrual time ends when they are no longer at risk or the observation period ends)

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42
Q

What is the formula for prevalence in relation to incidence rate?

A

(Prevalence (P) is approximately equal to incidence rate (IR) multiplied by the average duration of disease (D) → P ~= IR * D)

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43
Q

(Dr. P q) Which type of disease frequency is expressed in the following statement: Percentage of nursing home residents who contracted influenza during the course of an outbreak (January 1-20, 2017).

A

(Cumulative incidence)

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44
Q

(Dr. P q) Which type of disease frequency is expressed in the following statement: Percentage of potential army recruits rejected at intake exam because of poor vision.

A

(Prevalence)

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45
Q

(Dr. P q) Which type of disease frequency is expressed in the following statement: Number of colds diagnosed in 1,000 person-years within an elementary school.

A

(Incidence rate)

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46
Q

(Dr. P q) Which type of disease frequency is expressed in the following statement: Percent of live-born infants with a cardiac malformation among 100,000 live-births.

A

(Prevalence)

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47
Q

(Dr. P q) A population of 100 healthy men was followed for the development of prostate cancer. Twenty men developed prostate cancer after being followed for 5 years. Another 10 men were followed for 1 year and then were lost to follow up. The remaining 70 men were followed for 10 years and never developed prostate cancer. Calculate the number of person-years of observation accrued by this population.

A

(810 person years; can check slide 71 of the measures of disease ppt if confused)

48
Q

(Dr. P q) (T/F) Only the population at risk contributes to the denominator of cumulative incidence.

A

(T)

49
Q

(Dr. P q) (T/F) When calculating the incidence rate of disease, it is necessary to follow subjects for the same amount of time.

A

(F)

50
Q

(Dr. P q) (T/F) If the incidence rate of a very serious disease is 75/100,000 person-years and the prevalence of disease in the population is 25/100,000 people, then the average duration of this disease must be 3 years.

A

(F, should be ⅓ year)

51
Q

(Dr. P q) (T/F) All other things being equal, when a treatment is developed that prolongs the life of people with a disease, the prevalence of the disease will increase over time.

A

(T)

52
Q

Does the sensitivity or specificity of a test represent the true negative rate of a diagnostic test?

A

(Specificity)

53
Q

(T/F) If a test is not precise, it cannot be accurate.

A

(T)

54
Q

(T/F) A test can be precise but that does not guarantee accuracy.

A

(T → consistently wrong)

55
Q

Compare and contrast true and apparent prevalence.

A

(True prevalence uses the gold standard positive cases (necropsy, bacterial culture, etc.) while the apparent prevalence uses the new test positive cases (which may include false positives))

56
Q

What test results/portions of the population (i.e. true positives, both true and false negatives, entire population, etc.) would you use for your numerator and denominator when trying to assess the true prevalence of disease in that sample population?

A

(Numerator is gold standard test positives (true positives and false negatives), denominator is entire population → you are calculating the proportion of all animals sampled that truly have the disease)

57
Q

What test results/portions of the population (i.e. true positives, both true and false negatives, entire population, etc.) would you use for your numerator and denominator when trying to assess the apparent prevalence of disease in that sample population?

A

(Numerator is true and false positives (all test positives) , denominator is entire population → you are calculating the proportion of animals sampled that appear to be infected based on the positive results from the new test)

58
Q

What test results/portions of the population (i.e. true positives, both true and false negatives, entire population, etc.) would you use for your numerator and denominator when you want to find the proportion of all animals tested that were correctly classified by the test kit?

A

(You are seeking accuracy, numerator would be true positives and true negatives, denominator would be entire population)

59
Q

What values need to be included in your numerator and denominator to calculate sensitivity?

A

(Numerator → true positives; denominator → all gold standard positives (so true positives plus false negatives))

60
Q

What values need to be included in your numerator and denominator to calculate specificity?

A

(Numerator → true negatives; denominator → all gold standard negatives (so true negatives plus false positives))

61
Q

What values need to be included in your numerator and denominator to calculate the positive predictive value of a test?

A

(Numerator → true positives; denominator → all test positives (so true positives plus false positives))

62
Q

What values need to be included in your numerator and denominator to calculate the negative predictive value of a test?

A

(Numerator → true negatives; denominator → all test negatives (so true negatives plus false negatives))

63
Q

If you are seeking the probability that a test subject with a positive test result is truly diseased, what value would you look at?

A

(Positive predictive value of the test; if you were seeking negative/truly undiseased → negative predictive value)

64
Q

If you are seeking the proportion of truly uninfected animals that test negative using a test kit, what value would you look at?

A

(Specificity; if you wanted positive instead → sensitivity)

65
Q

(T/F) As the prevalence of a disease falls, that will innately decrease your positive predictive value of a test and increase your negative predictive value of a test.

A

(T)

66
Q

Will your negative predictive value be higher or lower as sensitivity increases?

A

(Higher, as there are fewer false negatives/higher sensitivity your negative predictive value with be higher)

67
Q

What will result from a lower specificity, an increased or decreased positive predictive value?

A

(Decreased positive predictive value → lower specificity means more false positives and that results in a decreased positive predictive value)

68
Q

Describe sequential testing, the steps involved and what you are avoiding with each step.

A

(Start with a highly sensitive test, this avoids false negatives; test all those who tested positive with the highly sensitive test with a highly specific test, this avoids false positives; at the end you should end up with a population of close to if not 100% certainly positive individuals)

69
Q

Does parallel or series concurrent testing increase specificity of a test?

A

(Series → animal declared diseased only if it tests positive on both tests run; parallel = increased sensitivity → animal declared diseased if it tests positive on one or both tests)

70
Q

Who determines important requirements for animals entering different states?

A

(The state veterinarian aka chief state agricultural animal health officer)

71
Q

You are seeking a subject matter expert in zoonotic diseases, who would you turn to in your state?

A

(Your state public health veterinarian)

72
Q

What government sector contains the chief veterinary office for animal health for the United States, who is also the U.S. delegate for the WHOA?

A

(The USDA, specifically APHIS and more specifically the Veterinary Services → the head of the VS or the ‘deputy administrator’ is the CVO and WHOA delegate)

73
Q

Which subsector of the USDA protects consumers by ensuring that meat, poultry, and processed egg products are safe, wholesome, and accurately labeled?

A

(FSIS/Food Safety and Inspection Service)

74
Q

Who is the global authority on animal health that sets standards as opposed to laws?

A

(World Organization for Animal Health/WHOA)

75
Q

Is colostrum an example of passive or active immunity?

A

(Passive)

76
Q

Are vaccinations a form of passive or active immunity?

A

(Active)

77
Q

Is obtaining a disease and living a form of passive or active immunity?

A

(Active)

78
Q

With which type of vaccines is the cellular response variable?

A

(Inactivated/killed vaccines)

79
Q

Adjuvants are necessary for which type of vaccines?

A

(Inactivated/killed vaccines)

80
Q

Which vaccine type gets the best response but also has a chance of causing true disease?

A

(Modified live)

81
Q

What effect do intranasal vaccines have on pathogen shedding?

A

(Reduces it (if the shedding is related to the mucus membranes))

82
Q

Where are intramuscular vaccines administered in cattle?

A

(Cervical muscles always)

83
Q

Which side of a dog is the rabies vaccine administered?

A

(The right)

84
Q

Which side of a dog is the lepto vaccine administered?

A

(The left)

85
Q

How does perigestational vaccination differ in multiparous and primiparous dams?

A

(Multiparous dams are vaccinated at 3-4 weeks preparturition while primiparous dams are vaccinated at 6 and 3 weeks preparturition)

86
Q

For active immunity, how many weeks prior to an exposure event should an animal be vaccinated?

A

(3 weeks prior)

87
Q

You should be suspicious of a reportable disease when the morbidity and mortality are low/high (choose one).

A

(High)

88
Q

What types of skin lesions/conditions would make you suspicious of a reportable disease? Three answers.

A

(Vesicular, pox, or lumpy skin lesions/conditions)

89
Q

What level of response to treatment would make you suspicious of a reportable disease?

A

(Poor or no response to treatment)

90
Q

Avian diseases with what characteristics would make you suspicious of a reportable disease? Two answers.

A

(Avian disease with acute deaths and/or CNS signs)

91
Q

What are the three ‘epidemiologic investigation 101’ questions that you should ask once you have determined a disease outbreak has occurred?

A

(Where did the disease come from, what management factors allowed it to spread, and where did it go from here)

92
Q

Once a potential FAD is reported, who shows up and within what time period?

A

(A trained foreign animal disease diagnostician will be sent to the premises within 24 hours)

93
Q

To obtain the incidence risk ratio for a set of data, you need to divide the incidence risk of disease in the exposed by the incidence risk of disease in the unexposed, how do you get those values?

A

(You divide the exposed with disease by the total of exposed for incidence risk of disease in exposed; you divide the unexposed with disease by the total of unexposed for incidence risk of disease in the unexposed)

94
Q

What is the incidence risk ratio if I tell you that the risk of lack of motivation in veterinary students without iPads was 6 times greater than the risk of lack of motivation in veterinary students with iPads?

A

(The RR would be 6, I know this is kinda a dumb question but interpretations are important)

95
Q

What measure of strength will provide an estimate of how many times more likely exposed individuals will be diseased compared to non-exposed individuals?

A

(Incidence risk/rate ratio)

96
Q

(T/F) The risk ratio, the relative risk, and the incidence risk/rate ratio all mean the same thing.

A

(T)

97
Q

How do the odds ratio calculations differ for cohort and case-control studies?

A

(For cohort studies, you are comparing the odds of disease in the exposed versus unexposed where for case-control studies, you are comparing the odds of exposure in the diseased versus undiseased)

98
Q

How do you calculate the incidence risk of disease in the exposed that is attributable to the exposure?

A

(Subtract the incidence risk of the unexposed from the incidence risk of the exposed, this will give you attributable risk)

99
Q

How do you calculate the attributable fraction, which is the proportion of disease in the exposed that is due to the exposure?

A

(Incidence risk of exposed minus incidence risk of unexposed divided by the incidence risk of exposed)

100
Q

How do you calculate population attributable risk?

A

(Subtract the incidence risk of unexposed from the total incidence risk)

101
Q

What do you need to divide the population attributable risk by to get the population attributable fraction?

A

(The total incidence risk)

102
Q

A well built clinical research question has four architectural components, what are those components? (Hint: PICO).

A

(Patient or population, intervention (aka exposure), comparison intervention, and outcome)

103
Q

If you are starting a study in which you do not assign the exposures, you are utilizing comparison groups, and you start with the outcome and then search for exposure, what type of study design are you creating?

A

(Case-control study; if you were to instead go from exposure to outcome that would be a cohort)

104
Q

What is the term for bias that can occur if people who agree to take part in a study are different from the source population you want to study?

A

(Selection bias)

105
Q

What is the term for bias that can occur if study participants are placed into the wrong exposure or disease category?

A

(Misclassification or measurement error/bias → most common form and can be present in all types of studies)

106
Q

Of a differential or non-differential misclassification error, which will bias towards a null value only?

A

(Non-differential, differential will bias towards or away from a null value)

107
Q

What is the term for the bias that can occur if people with a disease remember/report their exposure differently than people without said disease?

A

(Recall bias)

108
Q

What is the term for the bias that can occur if there is a systematic difference in soliciting, recording, or interpreting information?

A

(Interviewer bias)

109
Q

What is the term for the branch of biology that deals with the relationships of organisms to one another and to their physical surroundings?

A

(Ecology)

110
Q

What is the term for the complex of living organisms, their physical environment, and all their interrelationships in a particular unit of space?

A

(Ecosystems)

111
Q

(T/F) Biodiversity can be used as an indicator of ecosystem health.

A

(T)

112
Q

Who is the global authority of species extinction risk?

A

(The International Union for Conservation of Nature/IUCN)

113
Q

What is the term for the study of underlying principles that influence the spatial and temporal patterns of diseases?

A

(Disease ecology)

114
Q

An emerging infectious disease is one that either has appeared in a population for the first time or what other scenario?

A

(One that may have existed previously but is rapidly increasing in incidence or geographic range)

115
Q

The drivers of disease emergence include ecological, social, and what other category of conditions that facilitate disease emergence and transmission?

A

(Economic)

116
Q

What is the main difference between surveillance and monitoring in terms of action?

A

(Surveillance implies an action will be performed based on the information collected whereas monitoring does not)