1. Managerial Epidemiology
Managerial Epidemiology1. Managerial Epidemiology: What is the cost-effectiveness
analysis and what is it used for in healthcare and public health? Provide an example
study.2. Qualitative, Quantitative (Cause-Effect): You are the Chief Operating Officer of a
hospital. The Human Resources Director reports to you. Two of your valued Directors have
a random drug screening for controlled substances with a group of hospital cohorts, and the
result comes up as positive for heroine. Your experience with epidemiology and your
understanding of cause-effect makes you skeptical of these general screening results. You
request that the specimens be sent out to a specialty lab for confirmatory testing with gas
chromatography specific for heroine. The results of the confirmatory testing show that both
Directors are negative (0 mg/dl) for all control substances, including heroine. A further
investigation revealed that both Directors attended a morning meeting the day of the
random test and had eaten poppy seed muffins. You do research and find that poppy seed
muffins produce a byproduct in the body that mimics opiates/heroine in a
screening.Discuss why these results occurred , i.e., the two very different results between a
screening, and the confirmatory test in terms of a) qualitative and b) quantitative testing, c)
specificity, d) reliability.(Points : 10)3. Research Methods: Why is the randomized clinical
trial (RCT) research considered the “ gold standard” in clinical epidemiology
research? What is an IRB and why is it requirement when performing research with human
beings? (Points : 10)4. Decision Making: Clinical epidemiology research should be based
on empirical evident. Define empirical evidence and what it means in decision making in
both private and public health decision making in regard to interventions, i.e., the
implementation of medical testing, processes or public health programs. (Points :
10)5. Risk Factor Research: Why is the Framingham Heart Study a pivotal research
program in healthcare today? What are some of the milestones the study has given to
clinical epidemiology? (Points : 10)6. NOTE: Essay Question is in 2 parts. This is Part 1 to
be completed and then go , to Part 2 and complete it.Case #2 of 2: (50 pts) Cost/Benefit
literature review for vaginal birth after cesarean (VBAC)A client had a cesarean delivery in a
hospital setting for breech presentation with her first pregnancy. She is pregnant again and
after exploring her delivery options, has decided she wants to attempt a vaginal birth after
cesarean (VBAC). She has had an uncomplicated pregnancy this time and the fetus is not
breech. The same OB-GYN will be assisting in her delivery. The OB-GYN performs a
systematic review of the literature to assess the benefits and harms of VBAC versus repeat
cesarean delivery.Part 1 of 2: Researching Empirical Evidence1. What kinds and sources of
2. data does the OB-GYN need to review in order to make a rational clinical planning
decision?2. Which types of studies available on this topic would be the most useful in
clinical decision making?3. What types of studies would you want to exclude?4. Why
would there be a lack of randomized clinical trials (RCT’ s) available to aIDress this clinical
question?(Points : 20)7. NOTE: This is Part 2 of the final essay question: The last essay
question requires you to do a 2×2 table in aIDition to calculations. The tables may be done
by copying the table from the question directly into your answer and then filling the table
out.Case: Calculating OIDs RatioIn planning for her delivery, the client reads about birthing
centers and asks the midwife if it is safe to have a VBAC in a freestanding birthing center.
The midwife reviews the data from national studies of VBACs in birthing centers compared
to VBACs in hospital settings and obtains the following statistics to aid her in clinical
decision making:N= 1913 Birthing Center based VBAC Rates• 87% delivered vaginally•
24% of women were transferred to the hospital prior to delivery• There were 25 women
who experienced a serious adverse outcome (of which 6 were uterine rupture)• There
were 7 perinatal deaths (0.5%)• There were 15 infants with low apgar scores (below 7)
after 5 minutes of life (1.0%)N= 1913 Hospital based VBAC Rates (Control)• 76% delivered
vaginally• There were 32 women who experienced a serious adverse outcome (of which 15
were uterine ruptures)• There were 3 perinatal deaths• There were 2 infants with low
apgar scores (less than 7) after 5 minutes of life(Part 2 of 2): Construct the following for 1
and 2 and answer question 31. Construct a 2 x 2 table, calculate, and interpret the oIDs ratio
of women who suffered a serious adverse outcome from attempting a VBAC delivery in
order to estimate the relative risk to a mother delivering VBAC in midwifery based
freestanding birthing centers. Cases are those with a serious outcome, controls are those
without. The exposure is treatment in a birthing center. The not exposed group is treatment
in a hospital.Exposure Cases ControlsBirthing CenterHospital2. Construct a 2 x 2 table,
calculate, and interpret the oIDs ratio of infants who suffered a serious adverse outcome
(including death) from attempting a VBAC delivery in order to estimate the relative risk to
an infant delivered VBAC in midwifery based freestandingCases Controls3. What does the
midwife conclude regarding the safety to mother and baby by attempting a VBAC in
midwifery based birthing centers? What clinically is the best decision for this client and her
unborn baby?(Points : 30)8. Case 1 of 2 (50 Pts): Cost-Effectiveness Analysis (CEA): In
Wu et al. (2006) researchers performed an analysis to evaluate the cost-effectiveness of
doing stool DNA testing in aIDition to other types of traditional screenings, i.e., fecal occult
blood testing annually, flexible sigmoidoscopy or colonoscopy, every 5 and 10 years for
colorectal cancer in countries where colon cancer prevalence is low. Also, evaluated was
the cost/benefit of doing no screenings (Wu, 2006).The subjects were people 50 to 75 years
of age in Taiwan. The researchers used the annual cost of $13,000 per life-year saved
(which is roughly the per capita GNP of) as the ceiling ratio for assessing whether DNA
testing was cost-effective (Wu, 2006).Simulated results for screening strategies to prevent
Colon Rectal Cancer (CRC)Variable Screening StrategyNo Screening DNA (3yrs) DNA
(5yrs) DNA (10yrs) Occult Blood Flexible Sigmoid. (5yrs) Colonoscopy (10 yrs)a.
Total cases of CRC, n 2,917 2,435 2,654 2,710 2,129 2,253 1,780b. CRC deaths,
n 1,729 1,345 1,467 1,574 1,059 1,328 1,077c. Perforation deaths,
3. n 0 3 2 1 5 3 12e. Reduction in CRC incidence, % 0 17 9 7 27 23 39f.
Reduction in CRC mortality, % 0 22 15 9 39 23 39g. Life expectancy,
year 15.7337 15.7476 15.7434 15.74 15.7584 15.7477 15.759h. Total costs,
thousand $ 22,022 35,637 31,077 26,856 19,824 24,909 21,843i. Incremental
life-year saved, year 0 1,390 970 626 2,464 1,383 2,530j. Incremental cost,
thousand $ 0 13,615 9,054 4,834 -2,198 2,887 -180k. Incremental cost ($)/life-
years saved compared with no
screening 0 9,794 9,335 7,717 Dominant ‡ 2,087 Dominant †* Values obtain
from a cohort of 100,000 persons 50 years of age who were followed for 25 years.† The
other screening strategy is more effective and less costly than stool DNA testing strategy.‡
The screening is more effective and less costly than No Screening.Adapted from: Wu et al.
BMC Cancer 2006 6:136 doi:10.1186/1471-2407-6-136_____________Reference:Wu, Grace
HM. Wang, Yi-Ming . Yen, Amy MF. Wong, Jau-Min Lai, Hsin-Chih Warwick, Jane and Chen,
Tony HH. (2006) Cost-effectiveness analysis of colorectal cancer screening with stool DNA
testing in intermediate-incidence countries. BMC Cancer 2006, 6:136 doi:10.1186/1471-
2407-6-136QUESTIONS: In your own words and1) From the research results shown in the
chart above, which type of screening had the highest and which had the lowest reduction in
colon-rectal cancer mortality?2) How do you interpret the findings (Conclusion) in regard
to the A-K results in regard to the cost/effectives of doing DNA-testing at 3 years, 5 years,
10 years, or not doing DNA tests at all?ORDER TODAY YOUR PAPER WITH SIMILAR
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