Instructor Key with Performance
Summary
The 1st Hourly
Math 1107
Summer Term
2003
Please follow the
protocol and directions…
Protocol
You will use only the following
resources:
Your individual calculator;
Your individual tool-sheet (single 8.5 by 11 inch
sheet);
Your writing utensils;
Blank Paper (provided by me
);
This copy of the hourly.
Do not share these
resources with anyone
else.
Show
complete detail and work for full credit.
Follow case study solutions and sample hourly keys in presenting your
solutions.
Work all six
cases.
Using only one
side of the blank sheets provided, present your work. Do not write on both sides of the sheets provided, and
present your work only on these sheets.
Do not share information with
any other students during this hourly.
Sign and
Acknowledge:
I agree to follow this protocol.
Name (PRINTED)
Signature
Date
Cases were equally
weighted at 20 points per case, for a maximum total of 120 points for all six
cases.
Case One
Pair of
Dice
In this experiment we have a weird
pair of dice – they are telepathically linked so that they do not operate
independently. In fact, the dice produce the following face-pairs with the
following probabilities:
(d2face,d4face)
@
Pr{(d2face,d4face)}
|
1 |
2 |
1 |
(1,1) @
.10 |
(2,1) @
.10 |
2 |
(1,2) @
.10 |
(2,2) @
.20 |
3 |
(1,3) @
.05 |
(2,3) @
.20 |
4 |
(1,4) @
.15 |
(2,4) @
.10 |
In this experiment we toss this
weird pair of dice and note the resulting pair of faces. In each of the
following, show your intermediate steps and work. If a rule is specified, you
must use that rule for your computation.
Consider the SUM of the face
values within each pair of face values.
List the possible SUMS of face
values within the pairs,
(d2face,d4face)
@
Pr{(d2face,d4face)}
@ SUM=d2face+d4face |
1 |
2 |
1 |
(1,1)
@
.10 @ 2 |
(2,1)
@
.10 @ 3 |
2 |
(1,2)
@
.10 @ 3 |
(2,2)
@
.20 @ 4 |
3 |
(1,3)
@
.05 @ 4 |
(2,3)
@
.20 @ 5 |
4 |
(1,4)
@
.15 @ 5 |
(2,4)
@
.10 @ 6 |
Sum |
Corresponding Pairs as
(d2,d4) |
2 |
(1,1) |
3 |
(1,2),(2,1) |
4 |
(1,3),(2,2) |
5 |
(1,4),(2,3) |
6 |
(2,4) |
and compute the
probability for each value of SUM. Show full detail for full
credit.
Pr{ SUM=2 } = Pr{
(1,1) } = .10
Pr{ SUM=3 } = Pr{ (1,2) } + Pr{ (2,1) } = .10 + .10 =
.20
Pr{ SUM=4 } = Pr{ (1,3) } + Pr{ (2,2) } = .05 + .20 =
.25
Pr{ SUM=5 } = Pr{ (1,4) } + Pr{ (2,3) } = .15 + .20 =
.35
Pr{ SUM=6 } = Pr{
(2,4) } =
.10
This one went very
well, or not well at all. A few students ignored the model provided, and instead
used a fair model. Others did not use the SUM random variable, as
indicated.
Case
Two
Crohn’s disease is a chronic inflammation of the intestinal wall. Most often, lower areas of the small intestine (ileum) are involved, although any part of the digestive tract (from the mouth to the anus) may be involved. Most cases are noted between the ages of 14 and 25 years. In about 35% of cases, only the lower small intestine (ileum) is involved; in about 20% of cases, only the large intestine is involved and in about 45% of cases, both small and large intestines are involved.
Symptoms of Crohn’s disease include: chronic diarrhea, crampy abdominal pain, fever, suppressed appetite and weight loss.
Complications of Crohn’s disease include: intestinal obstructions, abnormal connections within the intestines, abnormal connections of the intestines and bladder, abnormal connections of the intestines and the skin surface, and intestinal infections. In children, symptoms may include joint inflammation, slow growth, fever and anemia.
Treatments of Crohn’s disease depend on the symptoms being treated. For infections, broad spectrum anti-biotics are employed. For inflammation, cortico-steriods are used, as well as other anti-inflammatories. Additionally, certain medications focus on the immune system for general symptom reduction, as well as keeping Crohn’s disease in remission. Cortico-steroids are used to provide relief for inflamed areas of the body. They lessen swelling, redness, itching, and allergic reactions.
Consider budesonide, which is an orally administered cortico-steroid that is released in the intestine, where it works locally and topically to decrease inflammation. Hopefully, patients taking budesonide experience fewer of the typical side effects associated with other cortico-steroids used to treat Crohn's Disease, such as prednisone or prednisolone tablets, because most of budesonide is not absorbed into the body.
Possible side effects of cortico-steroids include: lowered resistance to infections, persistent infections, decreased or blurred vision; frequent urination; increased thirst, abdominal or stomach pain or burning, headache; irregular heartbeat; menstrual problems; muscle cramps or pain; muscle weakness; nausea.
Sketch a comparative clinical trial for budesonide versus standard cortico-steroids in the treatment of intestinal inflammation in patients with Crohn’s disease.
Population and Disease of Interest: Patients with Crohn’s Disease (CD)
Treatments: Standard CS – Standard suite of corticosteroids
usually employed in the treatment of CD.
Budenoside – a hopefully kinder, gentler
corticosteroid.
Recruitment: Begin with human candidate volunteers. They
must meet all inclusion criteria, including having a diagnosis of CD, and they
must have none of the exclusion criteria. After screening out those volunteers
who do not have CD, or who meet one or more exclusion criteria, fully inform the
remaining volunteers of the risks and possible benefits of trial study
participation. Enroll those who give informed consent in the study. Those who
give such consent are aware of how the trial will be
conducted.
Assignment to Treatment: Randomly assign each volunteer to
either standard CS or to Budesonide. Double blinding
is employed, in that neither the study subjects nor the clinical workers know
the actual treatment assignment of individual
subjects.
Follow-up: Evaluate study subjects for intestinal
inflammation, as well as for the known side effects of these treatments. Also
track the occurrence of any other adverse events. Also track subjects for
significant toxicity, such as kidney or liver damage.
A number of
students did not present a clinical trial sketch as defined by course examples.
Some details were insufficient on random assignment and double blinding. A few
sharp students were very careful about informed consent and the possible ages of
the subject/volunteers. Error codes used in the scoring: RA=Random Assignment;
DB=Double Blinding; IC=Informed Consent.
Case
Three
Color Slot
Machine
Here is our slot machine – on each
trial, it produces a 4-color sequence, using the table
below:
Sequence* |
Probability |
GBRB |
.25 |
BBGG |
.10 |
GBBR |
.25 |
RGYB |
.10 |
BBYY |
.10 |
RRYY |
.10 |
YBGR |
.10 |
Total |
1.00 |
*
B-Blue, G-Green, R-Red, Y-Yellow, Sequence is
numbered as
1st to 4th , from left to
right: (1st 2nd 3rd
4th)
Compute the following
probabilities. In each of the following, show your intermediate steps and work.
If a rule is specified, you must use that rule for your
computation.
3.a) Pr{ Red Shows 3rd or 4th
}
Pr{ Red Shows 3rd or 4th } = Pr{
GBRB }+ Pr{ GBBR } + Pr{ YBGR } = .25 + .25 + .10 =
.60
3.b) Pr{ Red Shows and
Green Does Not Show }
Pr{ Red Shows and
Green Does Not Show } = Pr{ RRYY } = .10
3.c) Pr{ Blue Shows}
- Use the Complementary Rule.
Pr{ Blue Does Not
Show} = Pr{ RRYY } = .10
Pr{ Blue Shows } 1-
Pr{ Blue Does Not Show } = 1 - .10 = .90
A number of
students did not use the complementary rule in 3c, or got it backwards somehow.
Code used in 3.c: CR=Complementary Rule.
Case Four
We have a bowl containing the following colors and counts of balls (color@count):
Each trial of our experiment consists of five draws without replacement from the bowl. Compute the following conditional probabilities.
Compute these
directly.
This one went very
well or very badly. The idea was to do these directly, as in the example in
class.
4.a) Pr{ Yellow shows 2nd | Yellow shows 1st}
Pr{ Yellow shows
2nd | Yellow shows
1st} =
0 (Yellow available for 2nd draw) / 14 (Total For
2nd Draw) = 0
4.b) Pr{ Black shows 5th | Black shows 1st, Red shows 2nd, Blue shows 3rd, and Green shows 4th }
Color |
Total after 1st DWOR |
Total after 2nd DWOR |
Total after 3rd DWOR |
Total
after 4th
DWOR |
White |
1 |
1 |
1 |
1 |
Black |
1 |
1 |
1 |
1 |
Blue |
4 |
4 |
3 |
3 |
Green |
4 |
4 |
4 |
3 |
Red |
3 |
2 |
2 |
3 |
Yellow |
1 |
1 |
1 |
1 |
Total |
14 |
13 |
12 |
11 |
Pr{ Black shows
5th | Black shows 1st, Red shows 2nd, Blue
shows 3rd, and Green shows 4th } =
1/11
4.c) Pr{ Blue shows 3rd | Blue shows 1st, Blue shows 2nd }
Color |
Total after 1st DWOR |
Total
after 2nd
DWOR |
White |
1 |
1 |
Black |
2 |
2 |
Blue |
3 |
2 |
Green |
4 |
4 |
Red |
3 |
3 |
Yellow |
1 |
1 |
Total |
14 |
13 |
Pr{ Blue shows
3rd | Blue shows 1st, Blue shows 2nd } =
2/13
Case Five
Design Fault
Spot
In each of the following a brief description of a design is presented. Briefly identify faults present in the design. Use the information provided. Be brief and complete.
5.a) In a comparative clinical trial, treatment methods are compared in the treatment of Condition Z, which when left untreated leads to severe complications and possibly death. Suppose we have a new candidate treatment, and further suppose that a standard treatment for a similar (but different) disease is available. A comparative clinical trial is proposed that would compare these treatments in patients with condition Z.
The proposed trial would compare treatments
intended for two different diseases.
The comparative design would use an inappropriate treatment – the lack of
a standard treatment for CZ requires a
placebo.
5.b) A clinical trial of a new Hepatitis C treatment is designed as follows: subjects are screened for
Hepatitis C infection. Those who test positive for Hepatitis C infection are then told of their status, and are offered treatment for Hepatitis C at no cost, and are given no further information. Those who accept the free treatment offer are then randomly assigned to either a Placebo, or to the New Treatment Plan.
Informed consent
is not employed – the patients need to be fully informed of their Hepatitis C
Status, and then properly recruited into the study.
5.c) A sample
survey design targets a random sample of residents of metro
A
sample that systematically excludes rural
5.d) A random sample of parents of college/university first-year undergraduate students is surveyed about the study practices of their children. The survey questionnaire was properly written, and the sample of parents reasonably selected. The parents responded to questions about their children's study habits.
Parents
aren’t necessarily capable of giving accurate information of this type – direct
responses are generally preferred
to proxy responses.
As usual, this case went pretty
well.
Case
Six
Perfect Samples
Severity of cases of PuzKertin’s Syndrome (PKS) is
noted as: (F)atal, (S)evere, (Mo)derate, or
(Mi)ld. Suppose that severity probabilities for the population of PKS patients are: 15% Severe, 15% Moderate, 20% Mild and 50% Fatal.
6.a) Interpret each probability using the Long Run Argument. Be specific and complete for full credit.
In long
runs of draws with replacement from this population, approximately 20% of
sampled patients with PKS have mild cases.
In long
runs of draws with replacement from this population, approximately 15% of
sampled patients with PKS have moderate cases.
In long
runs of draws with replacement from this population, approximately 15% of
sampled patients with PKS have severe cases.
In long
runs of draws with replacement from this population, approximately 50% of
sampled patients with PKS have fatal cases.
6.b) Compute the perfect sample of n=150 PKS cases, and describe the relationship of this perfect sample to real samples of PKS cases. Show all work and detail for full credit.
Severity |
Probability |
Perfect
Count, n=150 |
Mild |
.20 |
.2*150=30 |
Moderate |
.15 |
.15*150=22.5 |
Severe |
.15 |
.15*150=22.5 |
Fatal |
.50 |
.50*150=75 |
Total |
1 |
1*150=150 |
Random samples of cases of PuzKertin’s Syndrome (PKS) yield approximately 30 mild
cases, 22 or23 moderate cases, 22 or 23 severe cases and 75 fatal cases.
For some reason, people got
parts 6.a. and 6.b. blurred together. The long run argument is a general
statement of how sample runs are governed by the model probabilities, while the
probabilities themselves apply directly and exactly to the entire population as
a whole. The perfect sample is a specific blueprint for a specific sample size
under a specific model, which real samples follow
approximately.
Be certain that you have worked all six (6)
cases.
first hourly score summaries summer term 2003 |
n |
min |
p10 |
p20 |
p25 |
p30 |
p40 |
p50 |
mean |
p60 |
p70 |
p75 |
p80 |
p90 |
max |
30 |
0 |
52.5 |
66.6667 |
71.6667 |
73.3333 |
81.25 |
84.5833 |
78.0833 |
87.9167 |
89.1667 |
89.1667 |
92.9167 |
97.5 |
97.5 |
The maximum absolute score
for the first hourly was 120 points. To get your percentage score, divide your
total by 120.
There were 30
scores.
The minimum score was
0%
Approximately 10% of scores
were at 52.5% or lower.
Approximately 20% of scores
were at 66.7% or lower.
Approximately 25% of scores
were at 71.7% or lower.
Approximately 30% of scores
were at 73.3% or lower.
Approximately 40% of scores
were at 81.3% or lower.
Approximately 50% of scores
were at 84.6%
or lower.
The average score was
approximately 78.1%.
Approximately 60% of scores
were at 87.9% or lower.
Approximately 70% of scores
were at 89.2% or lower.
Approximately 75% of scores
were at 89.2% or lower.
Approximately 80% of scores
were at 92.9% or lower.
There were four scores at
97.5%, these were the highest scores.
first hourly score summaries summer term 2003 |
tier |
scorehr1 |
count |
Percent |
tier five {“F”} |
<60% |
4 |
13.33 |
tier four {“D”} |
60%-69% |
2 |
6.67 |
tier three {“C”} |
70%-79% |
5 |
16.67 |
tier two {“B”} |
80%-89% |
12 |
40.00 |
tier one {“A”} |
90%-100% |
7 |
23.33 |
Do not interpret your
individual score as a grade. In this course, there is only one letter grade,
based on a weighted average of the hourlies and the
final. If this is your best in-class hourly, it will account for up to 40 points
of your course score. Otherwise, it will count for up to 20 points of your
course score.