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Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008
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Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

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Page 1: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

ObservationalStudy Designs

andConfounding

Michael A. Kohn, MD, MPP

26 August 2008

Page 2: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Outline

• Single Sentence Study Description

• REVIEW Observational study designs

• Definition of a confounder

• Coping with Confounding

• Examples of observational designs (“Name that Design”) and approaches to the problem of confounding

Page 3: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Single-Sentence Study Description

“The [cute acronym] study is a [DESIGN] study of the association between [predictor] and [outcome] in [study population].”

Exercise for section today: Present your study with a sentence like this.

Page 4: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Study Design

• Not just a matter of semantics

• Weaknesses and strengths associated with each study design

• Different measures of disease association

• Worth getting right or at least thinking about

Page 5: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Study Designs

• Experimental-- Randomized controlled trial (next week)• Observational (today’s topic)-- Cohort -- Double Cohort (risk-no risk; exposure-no

exposure)-- Cross-sectional-- Case-control

Page 6: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Experimental vs. Observational• Predictor = intervention (treatment or therapy):

-- experiment (randomized controlled trial)*

-- observational study

• Predictor = exposure or risk factor:

-- observational study

*Not all treatments require RCTs to prove effectiveness.

Page 7: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

OBSERVATIONAL STUDIES

• Usually the only option if the predictor is a potentially harmful exposure or risk factor

• Even if the predictor is an intervention, an RCT may not be feasible

• Confounding always an issue

• Many observational studies also qualify as secondary data analysis

• More intellectually interesting than RCTs?

Page 8: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Note on Figures

The schematics of observational study designs that follow assume that you are studying the association between a risk factor and development of a disease.

• Predictor = Risk Factor

• Outcome = Disease

Page 9: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cohort Study

Page 10: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cohort Studies

• Determine predictor status on all patients in a single population (defined by something other than the predictor). Exclude any patients who already have the outcome.

• Follow patients over time and attempt to determine outcome in all subjects

• Can identify individuals lost to follow up• Can measure overall incidence of outcome in

the population (e.g., cases/person-year)• Measure of disease association is the relative

risk (RR) or relative hazard (RH)

Page 11: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Double Cohort Study

Page 12: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Double Cohort (Exposure-No Exposure) Studies

• Sample study subjects based on predictor status.

• Attempt to determine outcome in all subjects over time

• Can identify individuals lost to follow up• Cannot measure overall incidence of outcome in

the population (e.g., cases/person-year)• Measure of disease association is the relative

risk (RR) or relative hazard (RH)

Page 13: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cohort Studies: Sampling Frame vs. Time Frame

Time Frame: All cohort studies are longitudinal (follow patients over time).

Sampling Frame:Double cohort study -- samples on predictor

status, i.e. there are separate predictor-positive and predictor-negative samples.

Cohort study -- starts with a cross-sectional sample (a population defined by something other than the predictor variable).

Page 14: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cohort Studies: Prospective vs. Retrospective

Prospective – Predictor status collected as part of this study

Retrospective – Predictor status collected by someone else in the past (another study, medical records, etc.)

It’s a cohort study if you follow predictor-positive and predictor-negative subjects over time for development of the outcome and if you can identify the subjects lost to follow up. Don’t worry too much about retrospective vs. prospective!

Page 15: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Case-Control Study

Page 16: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Case-Control Study• Separately sample subjects with the outcome (cases)

and without the outcome (controls)• Attempt to determine predictor status on all subjects in

both outcome groups• Cannot identify individuals lost to follow up (no such

thing as “lost to follow up”, since by definition outcome status is known)

• Cannot calculate prevalence (or incidence) of outcome• Measure of disease association is the Odds Ratio (OR)• Trying to replicate a nested case control study in which

the cases and controls come from the same cohort.

Page 17: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Nested Case-Control Study

Page 18: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cross-Sectional Study

Page 19: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cross-Sectional Study• Attempt to determine predictor and outcome

status on all patients in a single population (defined by something other than predictor and outcome).

• Cannot identify individuals lost to follow up (no such thing as “lost to follow up”)

• Can calculate prevalence but not incidence• Measure of disease association is the Relative

Prevalence (RP).• Time frame is the same as for a case-control

study; both discussed in Hulley, Chapter 8

Page 20: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Cohort Studies Start with a Cross-Sectional Study

Eliminate subjects who already have disease

Page 21: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Causal Association Between Predictor and Outcome

• Does predictor cause outcome?

• For now, not interested in studies of diagnostic/prognostic tests. (Test result does not cause outcome. See Ch. 12.)*

• Not interested in descriptive studies.

*How many of you are doing studies of diagnostic/prognostic tests?

Page 22: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Errors in Causal Inference

• Conclude that predictor causes outcome when, in truth, it doesn’t (false positive study)

• Fail to conclude that predictor causes outcome when, in truth, it does (false negative study)

Page 23: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Sources of Error

• Chance

• Bias

• Confounding

Page 24: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Sources of Error: Confounding

Association between predictor and outcome is “real” – but not causal.

Page 25: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Confounding In Observational Studies of a Treatment

Predictor = Treatment

Page 26: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Sources of Error: Confounding

Treatment Outcome

ConfounderReduces RiskAssociation or

Looks Good

Cause

Falsely conclude that treatment improves outcomes

Page 27: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Confounding: Vitamin E

Vitamin E Fewer CAD events

Diet, Exercise, Health Awareness?

True CauseAssociation

False Cause

Cause

Page 28: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Confounding: Suppression or Confounding by Indication

Treatment Outcome

SuppressorWorsensAssociation

Improves

Cause

Falsely conclude that treatment does not improve or even worsens outcome

Appears to Worsen

Page 29: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Confounding by Indication : Diuretic Therapy

Diuretics CVD Mortality

Severity of Disease

IncreasesAssociation

Decreases

Cause

Falsely concluded that diuretics increased CVD mortality

Warram JH, et al. Excess mortality associated with diuretic therapy in diabetes mellitus. Arch Intern Med 1991;151(7):1350-6. Turnbull, F., et al. (2005). "Effects of different blood pressure-lowering regimens on major cardiovascular events in individuals with and without diabetes mellitus.” Arch Intern Med 165(12): 1410-9.

Appears to Worsen

Page 30: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Intermediates

An intermediate on the causal pathway between predictor and outcome will look like a confounder.

A cohort study of HIV-infected pregnant women shows an association between protease inhibitor-based HAART and low birth weight.

Should we control for maternal weight gain during pregnancy?

Page 31: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

IS IT THIS?

PI-Based HAART Low Birth Weight

Low maternal weight gain

True CauseAssociation

False Cause

Cause

Page 32: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

OR THIS?

PI-Based HAART Low Birth Weight

Low maternal weight gain

CauseCause

Page 33: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Coping with ConfoundingDesign Phase

• Specification

• Matching

• Instrumental Variable– Associated with the predictor of interest but

not independently associated with the outcome

– Look for association between instrumental variable and outcome

Page 34: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Assessing the Importance of Confounding

• Alternative Outcome – Caused by confounders but not by the primary

predictor – If still associated with the primary predictor,

confounding is a problem

• Alternative Predictor– Associated with same confounders as main predictor

but not thought to cause the outcome– If still associated with the outcome, confounding is a

problem

Page 35: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Coping with ConfoundingAnalysis Phase*

• Stratification

• Statistical Adjustment

• Propensity Scores

*Have to measure potential confounders

Page 36: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Examples

Name that observational study design

Address issue of confounding

Page 37: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

AZT Prophylaxis after Needlestick in Health Care Workers

The proportion receiving AZT prophylaxis was compared between health care workers who sero-converted after a needlestick and health care workers who did not seroconvert after a needlestick.

Cardo et al. N Engl J Med 1997;337(21):1485-90.

DESIGN?

Page 38: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

AZT Prophylaxis after Needlestick in Health Care Workers

Cardo et al. N Engl J Med 1997;337(21):1485-90.

Seroconversion

Yes No

AZTYes 9 (27%) 247 (36%)

No 24 432

33 679

OR = 0.66

(95% CI 0.26 - 1.5)

Confounding?

Page 39: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Suppression: AZT after Needlestick

AZTHIV Sero-conversion

Deep Stick, Visible Blood on Needle

IncreasesAssociation

Decreases

Cause

Unadjusted analysis showed statistically insignificant effect of AZT in reducing

seroconversion

Appears to Increase

Page 40: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

AZT Prophylaxis after Needlestick in Health Care Workers

Logistic Regression Model Adjusting for Deep Stick, Visible Blood on Device

Cardo et al. N Engl J Med 1997;337(21):1485-90.

MVOR = 0.14

(95% CI 0.03-0.47)

Page 41: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Enhancing Causal Inference

Statistical Adjustment

(Multivariable Modeling)

Katz, M. H. (2006). Multivariable analysis : a practical guide for clinicians. Cambridge ; New York, Cambridge University Press.

Page 42: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Effect of Flu Vaccination on All-Cause Mortality During the Flu Season

The study population included almost 300,000 subjects at least 65 years old, of whom about 58% were vaccinated. Among vaccinated and unvaccinated subjects, 1.2% and 2.0% respectively died during the flu season.

Nichol et al. N Engl J Med. Apr 3 2003;348(14):1322-1332.

Pooled computerized data from 3 large managed care organizations.

Study Design?

Page 43: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Effect of Flu Vaccination on All-Cause Mortality During the Flu Season

Could confounding explain the association between flu vaccination and decreased risk of death during the flu season?

Page 44: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Effect of Flu Vaccination on All-Cause Mortality During the Flu Season

“Healthy Vaccinee Bias”

Flu Vaccination Death During Flu Season

Better health, better health care, other confounders

DecreasesAssociation

False Effect

Cause

Page 45: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Effect of Flu Vaccination on All-Cause Mortality During the Flu Season

How might you assess the importance of confounding?

Page 46: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

If worried about confounding, measure another outcome that could be caused by the confounder but NOT by the predictor of interest. If there is NO association between the predictor of interest and the alternative, causally unrelated outcome, then the relationship between the primary predictor and the outcome is more likely to be causal.

Enhancing Causal InferenceMeasure Alternative Outcome

Page 47: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Effect of Flu Vaccination on All-Cause Mortality During the Flu Season

Flu Vaccination Death During Summer Months

Better health care, other confounders

DecreasesAssociation

Should Not Affect

Cause

If the association of flu vaccination and decreased mortality during the flu season were due to confounding, then vaccination should also appear to reduce death during the summer months.

Appears to Decrease

Page 48: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

“Our analysis for evidence of a healthy-vaccinee bias was negative; during the two noninfluenza periods for which we had information, vaccinated and unvaccinated persons had similar risks of hospitalization”

Effect of Flu Vaccination on All-Cause Mortality During the Flu Season

Nichol, K. L., J. D. Nordin, et al. (2007). "Effectiveness of influenza vaccine in the community-dwelling elderly." N Engl J Med 357(14): 1373-81.

Time Period

Adjusted Odds Ratio

95% CI

6/ – 9/1999 1.0 0.78 - 1.28

6/ – 9/2000 0.94 0.74 - 1.19

Page 49: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Health Professionals Follow-up Study

• In 1986, 39,910 male dentists, veterinarians, pharmacists, optometrists, and podiatrists filled out a questionnaire including information about Vitamin E intake (the predictor)

• In 1988 and 1990, vital status was determined and those who were still alive were re-contacted to see if they had developed coronary artery disease (the outcome). Death/disease rates were lower in those who took Vitamin E.

Rimm, E. B., M. J. Stampfer, et al. (1993). "Vitamin E consumption and the risk of coronary heart disease in men." N Engl J Med 328(20): 1450-6.

Design?

Page 50: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Health Professionals Follow-up Study

Vit E – med. intake (IU/day)

6.4 8.5 11.2 25.2 419

Multivariate Odds Ratio

1.0 (Ref)

0.90 0.82 0.77 0.64

Page 51: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Confounding: Vitamin E

Vitamin E Fewer CAD events

Diet, Exercise, Health Awareness?

True CauseAssociation

False Cause

Cause

Page 52: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Health Professionals Follow-up Study

Vit E – med. intake (IU/day)

6.4 8.5 11.2 25.2 419

Multivariate Odds Ratio

1.0 (Ref)

0.90 0.82 0.77 0.64

Vit C – med. intake (mg/day)

92 149 218 392 1,162

Multivariate Odds Ratio

1.0 (Ref)

1.02 1.15 1.02 0.89

Page 53: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

If worried about confounding, measure another predictor that is associated with the same confounders. If this second predictor is NOT associated with the primary outcome, then the relationship between the primary predictor and the outcome is more likely to be causal.

Enhancing Causal InferenceMeasure Alternative Predictor

Page 54: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Confounding: Alternative Predictor

Vitamin C Fewer CAD events

Diet, Exercise, Health Awareness?

True CauseAssociation

False Cause

Cause

If the confounding accounted for the benefits of Vitamin E, then Vitamin C should also appear beneficial.

Page 55: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Randomized Trials “Trump” Observational Results

Combined results of 7 large-scale randomized trials of the effectiveness vitamin E in the treatment and prevention of cardiovascular disease “provide strong support for a lack of statistically significant or clinically important effects of vitamin E on cardiovascular disease.”

Eidelman, R. S., D. Hollar, et al. (2004). "Randomized trials of vitamin E in the treatment and prevention of cardiovascular disease." Arch Intern Med 164(14): 1552-6.

Page 56: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Year of Visit and Provision of Analgesia in ED Patients with RLQ Pain

• Subjects: Patients presenting to the SFGH ED with RLQ pain in 1998 and 2003

• Predictor: Year of presentation

• Outcome: Receipt of parenteral analgesia

Neighbor ML, Baird C*, Kohn MA. Changing Opioid Use for Right Lower Quadrant Abdominal Pain in the ED. Acad Emerg Med 2005; 12(12): 1216-20.. *UCSF MSIII

Page 57: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Year of Visit and Provision of Analgesia in ED Patients with RLQ Pain

Analgesia

Year Yes No Total Prevalence

2003 72 65 137 53%

1998 43 144 187 23%

Relative Prevalence = 2.3

Design?

Page 58: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Year of Visit and Provision of Analgesia in ED Patients with RLQ Pain

1. Patients who get abdominal CTs are much more likely to get analgesia (59% vs. 22%)

2. CTs were much more common in 2003 than in 1998 (56% vs 20%)

Is the increase in analgesia rates between 1998 and 2003 wholly explained by increased CT scanning?

Page 59: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Year of Visit and Provision of Analgesia in ED Patients with RLQ Pain

CT YES CT NO

Year Analg No Analg Total Prev Year Analg No Analg Total Prev.

2003 47 30 77 61% 2003 25 35 60 42%

1998 21 17 38 55% 1998 22 127 149 15%

Prev. Ratio 1.1

Prev. Ratio 2.8

Page 60: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Year of Visit and Provision of Analgesia in ED Patients with RLQ Pain

Is the increase in analgesia rates between 1998 and 2003 wholly explained by increased CT scanning?

NO. In the group that did not receive CTs, analgesia rate was almost 3x higher in 2003 than in 1998.

Page 61: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Enhancing Causal Inference

Stratification

DCR 3rd Ed. Chapter 9 pp. 137.

Also, Appendix 9A

Smoking as a confounder of the relationship between coffee drinking and MI.

Page 62: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

JIFeeBabies born at Kaiser with neonatal

hyperbilirubinemia (Bili > 25) are compared with randomly selected “controls” from the same birth cohort.

Outcome measure is IQ and neurologic status at age 5 years.

No difference in IQ or fraction with neurologic disability between the “case” and “control” groups.

Newman, T. B., P. Liljestrand, et al. (2006). "Outcomes among newborns with total serum bilirubin levels of 25 mg per deciliter or more." N Engl J Med 354(18): 1889-900.

Design?

Page 63: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

RRISK(Reproductive Risk Factors for

Incontinence at Kaiser)

• Random sample of 2100 women aged 40-69 yo

• Interview, self report, diaries to determine whether they have the outcome, urinary incontinence.

• Chart abstraction of L&D/surgical records to establish predictor status

Design?

Page 64: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

RRISK

*There is a longitudinal element in this study, and it was funded with an R01 by the NIDDK as a “retrospective cohort study.”

Can you identify losses to follow up? (e.g., patients who had surgical procedures in the past but for whom outcome status cannot be determined)

Page 65: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

HIV Tropism and Rapid Progression*

Is HIV CXCR4 (as opposed to CCR5) tropism a predictor of rapid progression in acutely infected HIV patients?

Molecular tropism assay is “high end” and labor-intensive. Have funding to perform a total of 80 assays.

UCSF OPTIONS cohort follows patients acutely infected with HIV. Has banked serum from near time of acute infection.

* Vivek Jain’s Project

Page 66: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Identify the 40 patients with the most rapid progression (Group 1) and randomly select 40 others from the UCSF Options cohort (Group 2).

Run the tropism assay on banked serum for these 80 patients and compare results between Group 1 and Group 2.

HIV Tropism and Rapid Progression (continued)

Design?

Page 67: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Screening Sigmoidoscopy and Risk of Death from Colon Cancer

Compared rates of previous sigmoidoscopy in patients who had died of colon cancer (of the rectum and distal colon) with sigmoidoscopy rate in patients who had not died of colon cancer. Sigmoidoscopy rates were lower in the group of patients who died of cancer.

Selby JV, et al. N Engl J Med 1992;326(10):653-7.

Design?

Page 68: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Screening Sigmoidoscopy and Risk of Death from Colon Cancer

Selby JV, et al. N Engl J Med 1992;326(10):653-7.

The authors did a second comparison between patients who died of proximal colon cancers and patients who did not die of proximal colon cancers. Sigmoidoscopy rates were the same in both. (See Hulley, Ch 12, page 195.)

Confounding?

Page 69: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Enhancing Causal InferenceMeasure Alternative Outcome

If worried about confounding, measure another outcome that could be caused by the confounder but NOT by the predictor of interest. If there is NO association between the predictor of interest and the alternative, causally unrelated outcome, then the relationship between the predictor and the primary outcome is more likely to be causal.

Page 70: Observational Study Designs and Confounding Michael A. Kohn, MD, MPP 26 August 2008.

Sigmoidoscopy and Death from Colon CA

Screening sigmoidoscopy

Death from Proximal Colon CA

Better health care, other confounders

DecreasesAssociation

Should Not Affect

Cause

If the association of sigmoidoscopy and decreased colon cancer death were due to confounding, then sigmoidoscopy should also appear to reduce cancers beyond the reach of the sigmoidoscope

Appears to Decrease