Jacqueline - Task 7 (4)
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Module 7 Task: Problem Set
Name:____
Jacqueline C. Nduka
__________________________
In a study of environmental chemical exposure and childhood asthma, the exposed group
was comprised of 400 grade school children (asthma-free) living within a two-mile radius
of a chemical manufacturing plant.
These children received a physical examination at
baseline and then annually for two years to record the occurrence of asthma.
The
unexposed 600 grade school children (asthma-free) are randomly selected from three
surrounding counties where there are no manufacturing plants within 20 miles of their
residence.
These children also received a physical examination at baseline and then
annually for two years to record the occurrence of asthma.
At the end of the two-year
follow-up period, 200 of the exposed children developed asthma and 100 of the unexposed
children developed asthma.
Asthma
(D)
No Asthma
(D~)
Total
Live within a two-mile radius of a
chemical manufacturing plan
(E)
1. 200
2. 200
400
Do not live within a two-mile
radius of a chemical
manufacturing plan
(E~)
3. 100
4. 500
600
Total
300
700
1,000
5.
This study is a:
1
a.
Retrospective cohort study
b.
Cross-sectional study
c.
Prospective cohort study
d.
Case-control study
e.
Clinical trial
6.
Why?
This is a prospective cohort study because it involves following a group of initially
asthma-free grade school children (both exposed and unexposed) over time to
determine the development of asthma. The exposure (living within a two-mile
radius of a chemical manufacturing plant) is identified at the beginning, and the
occurrence of asthma is monitored prospectively.
7.
What is the risk of developing asthma in the exposed group of children?
8.
What is the risk of developing asthma in the unexposed group of children?
9.
What is the risk ratio?
10.
If the value of the risk ratio was 5.0, how would it be interpreted?
a.
Children living within a two-mile radius of a chemical manufacturing plant
are 5.0 times more likely to develop asthma than children living outside a
two-mile radius of a chemical manufacturing plant.
b.
The odds of living within a two-mile radius of a chemical manufacturing plant
are 5.0 times higher among those children with asthma than those children
without asthma.
2
c.
The odds of having asthma are 5.0 times higher among those children living
within a two-mile radius of a chemical manufacturing plant than those
children not living within a two-mile radius of a chemical manufacturing
plant.
d.
Children with asthma having a 5.0 risk of living within a two-mile radius of a
chemical manufacturing plant.
11.
Which observational study design is best for rare diseases?
Why?
(Choose from: Cohort study, Cross-sectional study, Case-control study, Ecologic
study, or Clinical trial)
The case-control study design is often considered the best for investigating rare
diseases. In a case-control study, individuals with the rare disease (cases) are
compared to individuals without the disease (controls). This design allows for
efficient investigation of the potential risk factors associated with the rare disease by
comparing the exposure history of cases to that of controls. Given that the disease is
rare, it's more practical to identify cases and then select appropriate controls to
study the potential causes or risk factors.
12.
Which observational study design is best for looking at multiple diseases? Why?
(Choose from: Cohort study, Cross-sectional study, Case-control study, Ecologic or
Clinical trial)
The cross-sectional study design is often most suitable for examining multiple
diseases simultaneously. In a cross-sectional study, data is collected from
participants at a single point in time or within a very short time frame. This design
allows for the assessment of the prevalence of various diseases or health conditions
within the studied population. It provides a snapshot of the population's health
status, making it efficient for analyzing the occurrence of multiple diseases
concurrently. However, it's important to note that cross-sectional studies provide a
snapshot and cannot establish causation or temporality of the diseases.
13.
Which observational study design is best for rare exposures? Why?
(Choose from: Cohort study, Cross-sectional study, Case-control study, Ecologic
study, or Clinical trial)
The case-control study design is the most suitable for investigating rare exposures.
This design involves identifying individuals with the specific outcome or condition
of interest (cases) and comparing their exposure history with that of individuals
without the outcome (controls). For rare exposures, this approach is efficient and
effective. By focusing on cases with the rare exposure and matching them with
appropriate controls, researchers can study the association between the infrequent
exposure and the outcome without the need for a large sample size. This targeted
selection makes it a cost-effective and powerful tool for understanding the impact of
rare exposures on specific health outcomes.
14.
Which observational study design is best for diseases with long latency periods?
Why?
(Choose from: Cohort study, Cross-sectional study, Case-control study,
Ecologic study, or Clinical trial)
3
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The cohort study design is the most effective observational study design for diseases
with long latency periods. Diseases with long latency periods often take years or
even decades to manifest after exposure to a particular risk factor. A cohort study
involves selecting a group of individuals based on their exposure to specific risk
factors and following them over an extended period to observe and analyze the
development of diseases or outcomes. This extended follow-up period is crucial for
capturing the prolonged incubation period associated with diseases with long
latency. Researchers can gather comprehensive data on exposures, lifestyle factors,
demographics, and other relevant variables at the beginning of the study and then
monitor the cohort over time. By assessing the incidence of the disease and
comparing it to the initial exposures, researchers can establish a clear and robust
association between the risk factor and the delayed development of the disease. The
cohort study design's ability to track and analyze individuals over a long duration
makes it the most suitable for understanding the delayed onset of diseases and
establishing causal relationships between risk factors and long-term health
outcomes.
15. Several researchers felt that a graduate degree increased one’s chances of
developing prostate enlargement. A study was designed to test this belief. The
investigators identified a group of 1,100 patients whose initial diagnosis on
admission to the hospital was prostate enlargement. A group of 2,000 patients
admitted to the hospital for non-prostate enlargement was ascertained as a control
group. Of the patients identified on admission, 1,015 patients with prostate
enlargement and 1,600 without prostate enlargement agreed to participate and
were included in the study. Then the patients of both groups were interviewed to
find out about their educational level. The interviewers did not know which patients
had prostate enlargement and which did not.
What type of study design is this?
Why?
(Choose from: Prospective cohort study, Retrospective cohort study, Historical
prospective cohort study, Cross-sectional study, Case-control study, Ecologic
study, or Clinical trial)
This study design is a type of cross-sectional study. A cross-sectional study collects
data from participants at a single point in time or within a very short period,
essentially providing a snapshot of a population or a specific group at that particular
moment. In this case, the researchers interviewed patients with and without
prostate enlargement to gather information about their educational level. The study
is cross-sectional because it assesses both exposure (educational level) and outcome
(prostate enlargement) simultaneously, without following the patients over time.
The design allows for the evaluation of the relationship between educational level
and prostate enlargement in a specific population at a specific point in time. The
selection of participants from those admitted to the hospital, both with and without
prostate enlargement, helps in comparing the educational levels between the two
groups and examining the hypothesis that a graduate degree might increase the
chances of developing prostate enlargement.
4
16.
A study was done to examine the hypothesis that exposure to laboratory animals
increases the risk of laboratory animal allergy (LAA). Two groups of workers
employed at GlaxoSmithKline (GSK), a pharmaceutical company in North Carolina
completed an in-person interview and questionnaire in 1991. Both groups were
similar in terms of major risk factors of LAA. During 15 years of follow-up, 185
incident cases of LAA were diagnosed in the group not exposed to laboratory
animals, so that a total of 142,140 person-years of follow-up time accrued. In the
group with exposure to laboratory animals, a total of 265 incident cases of LAA
occurred and 123,444 person-years accrued. Assume that the deaths were
uniformly distributed during the follow-up period and no other losses to follow-up
occurred.
What type of study design is this? Why?
(Choose from: Prospective cohort study, Retrospective cohort study, Historical
prospective cohort study, Cross-sectional study, Case-control study, Ecologic
study, or Clinical trial)
This study design is a type of retrospective cohort study. A retrospective cohort study
looks back in time to establish a relationship between exposure to a particular factor
and the occurrence of an outcome. In this case, the researchers initially identified
two groups of workers, one exposed to laboratory animals and the other not
exposed, and then looked back at their historical data from 1991. They assessed the
exposure to laboratory animals at the beginning of the study and followed the
participants for 15 years to observe the incidence of laboratory animal allergy
(LAA). The study examines the relationship between exposure (to laboratory
animals) and the subsequent development of LAA over the follow-up period. The
data collected during the 15 years allowed the researchers to calculate incidence
rates and person-years of follow-up for both groups, contributing to the
retrospective cohort study's methodology.
17. Prior research has shown that individuals who are small at birth are at increased
risk of ischemic heart disease (IHD) later in life.
One hypothesis to explain this
association is fetal adaptation to a suboptimum intrauterine environment. Therefore
a study was conducted to test whether pregnancy complications associated with low
birth weight are related to risk of subsequent IHD in the mother.
In 2005, routine
discharge data were used to identify all singleton first births in Scotland between
1981 and 1985. Linkage to the mothers' subsequent admissions and deaths
provided 20–24 years of follow-up.
What type of study design is this? Why?
(Choose from: Prospective cohort study, Retrospective cohort study, Historical
prospective cohort study, Cross-sectional study, Case-control study, Ecologic
study, or Clinical trial)
This study design is a type of retrospective cohort study. A retrospective cohort
study involves looking back at historical data to identify exposures or risk factors
and then analyzing the outcomes that occurred after those exposures. In this case,
the researchers identified a group of individuals (mothers) based on certain criteria
(singleton first births in Scotland between 1981 and 1985) and gathered data on
their pregnancy complications and birth outcomes. They then followed these
5
individuals over a 20–24 year period to observe the occurrence of ischemic heart
disease (IHD) later in life. The data from routine discharge records provided a
historical view of pregnancies and subsequent health outcomes, allowing the
researchers to analyze the relationship between pregnancy complications, low birth
weight, and the risk of IHD in the mothers.
18.
A study was conducted in order to better understand the influencing factors of HIV
infection among former commercial blood and plasma donors engaged in unsafe
blood donation practices in China. Data about influencing factors from the past 5
years was obtained from ten counties (districts) from six provinces using a national
blood and plasma donation database.
A representative sample of donors was
selected and data regarding
HIV/AIDS infection, incidence,
and death was collected
over the course of 5 years.
What type of study design is this? Why?
(Choose from: Prospective cohort study, Retrospective cohort study, Historical
prospective cohort study, Cross-sectional study, Case-control study, Ecologic
study, or Clinical trial)
This study design is a type of retrospective cohort study. A retrospective cohort
study involves looking back at historical data to identify exposures or risk factors
and then analyzing the outcomes that occurred after those exposures. In this case,
the researchers collected data from the past 5 years regarding influencing factors of
HIV infection among former commercial blood and plasma donors engaged in unsafe
donation practices in China. They selected a representative sample of donors from a
national blood and plasma donation database and gathered data on HIV/AIDS
infection, incidence, and death over the 5-year period. By analyzing this historical
data, the study aims to understand the relationship between unsafe blood donation
practices and HIV infection, making it a retrospective cohort study.
6
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