Statistical Rules of Thumb

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Edition: 2nd
Format: Paperback
Pub. Date: 2008-09-02
Publisher(s): Wiley-Interscience
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Summary

Statistical Rules of Thumb, Second Edition compiles simple rules that are widely applicable, robust, and elegant, and each captures key statistical concepts. This handbook provides a framework for considering statistical questions such as sample size and design of experiments. Explaining the justification for each rule, this book conveys the various possibilities that statisticians must think of when designing and conducting a study or analyzing its data. It provides a framework for considering such aspects of statistical work such as: randomness and statistical models; sample size; covariation; epidemiology; environmental studies; designing, conducting, and analyzing studies; words, tables, and graphs; and consulting. New rules of thumb are included such as: Sample size for ratios of means; Very non-significant P-values are very significant; Dichotomize continuous variables for odds ratio analysis; and Correlations need to be substantial to gain advantage in ANCOVA. Some rules have been revised for the new edition, i.e. sample size for relative risk and sample size for percentage change. In addition, the references have been completed updated and expanded. A related website www.vanbelle.org provides additional rules, author presentations and more.

Author Biography

GERALD van BELLE, PhD, is Professor in the Department of Biostatistics and the Department of Environmental and Occupational Health Sciences at the University of Washington. He is the author or coauthor of more than 130 journal articles and several books, including Biostatistics: A Methodology for the Health Sciences, also published by Wiley. A recipient of the 2003 Wiley Author of the Year Award (Mathematics and Statistics Section), Dr. van Belle is a Fellow of both the American Statistical Association and the American Association for the Advancement of Science.

Table of Contents

Preface to the Second Editionp. xiv
Preface to the First Editionp. xvi
Acronymsp. xix
The Basicsp. 1
Four Basic Questionsp. 2
Observation is Selectionp. 3
Replicate to Characterize Variabilityp. 4
Variability Occurs at Multiple Levelsp. 6
Invalid Selection is the Primary Threat to Valid Inferencep. 6
There is Variation in Strength of Inferencep. 7
Distinguish Randomized and Observational Studiesp. 8
Beware of Linear Modelsp. 10
Keep Models As Simple As Possible, But Not More Simplep. 12
Understand Omnibus Quantitiesp. 14
Do Not Multiply Probabilities More Than Necessaryp. 15
Use Two-sided p-Valuesp. 16
p-Values for Sample Size, Confidence Intervals for Resultsp. 18
At Least Twelve Observations for a Confidence Intervalp. 20
Estimate [plus or minus] Two Standard Errors is Remarkably Robustp. 22
Know the Unit of the Variablep. 23
Be Flexible About Scale of Measurement Determining Analysisp. 24
Be Eclectic and Ecumenical in Inferencep. 25
Sample Sizep. 27
Begin with a Basic Formula for Sample Size-Lehr's Equationp. 29
Calculating Sample Size Using the Coefficient of Variationp. 31
No Finite Population Correction for Survey Sample Sizep. 35
Standard Deviation and Sample Rangep. 36
Do Not Formulate a Study Solely in Terms of Effect Sizep. 37
Overlapping Confidence Intervals Do Not Imply Nonsignificancep. 38
Sample Size Calculation for the Poisson Distributionp. 40
Sample Size for Poisson With Background Ratep. 41
Sample Size Calculation for the Binomial Distributionp. 43
When Unequal Sample Sizes Matter; When They Don'tp. 45
Sample Size With Different Costs for the Two Samplesp. 47
The Rule of Threes for 95% Upper Bounds When There Are No Eventsp. 49
Sample Size Calculations Are Determined by the Analysisp. 50
Observational Studiesp. 53
The Model for an Observational Study is the Sample Surveyp. 54
Large Sample Size Does Not Guarantee Validityp. 55
Good Observational Studies Are Designedp. 56
To Establish Cause Effect Requires Longitudinal Datap. 57
Make Theories Elaborate to Establish Cause and Effectp. 58
The Hill Guidelines Are a Useful Guide to Show Cause Effectp. 60
Sensitivity Analyses Assess Model Uncertainty and Missing Datap. 61
Covariationp. 65
Assessing and Describing Covariationp. 67
Don't Summarize Regression Sampling Schemes with Correlationp. 68
Do Not Correlate Rates or Ratios Indiscriminatelyp. 70
Determining Sample Size to Estimate a Correlationp. 71
Pairing Data is not Always Goodp. 73
Go Beyond Correlation in Drawing Conclusionsp. 75
Agreement As Accuracy, Scale Differential, and Precisionp. 77
Assess Test Reliability by Means of Agreementp. 80
Range of the Predictor Variable and Regressionp. 82
Measuring Change: Width More Important than Numbersp. 84
Environmental Studiesp. 87
Begin with the Lognormal Distribution in Environmental Studiesp. 88
Differences Are More Symmetricalp. 90
Know the Sample Space for Statements of Riskp. 92
Beware of Pseudoreplicationp. 93
Think Beyond Simple Random Samplingp. 95
The Size of the Population and Small Effectsp. 96
Models of Small Effects Are Sensitive to Assumptionsp. 97
Distinguish Between Variability and Uncertaintyp. 99
Description of the Database is As Important as Its Datap. 100
Always Assess the Statistical Basis for an Environmental Standardp. 101
Measurement of a Standard and Policyp. 102
Parametric Analyses Make Maximum Use of the Datap. 104
Confidence, Prediction, and Tolerance Intervalsp. 106
Statistics and Risk Assessmentp. 108
Exposure Assessment is the Weak Link in Assessing Health Effects of Pollutantsp. 110
Assess the Errors in Calibration Due to Inverse Regressionp. 111
Epidemiologyp. 113
Start with the Poisson to Model Incidence or Prevalencep. 114
The Odds Ratio Approximates the Relative Risk Assuming the Disease is Rarep. 115
The Number of Events is Crucial in Estimating Sample Sizesp. 120
Use a Logarithmic Formulation to Calculate Sample Sizep. 122
Take No More than Four or Five Controls per Casep. 124
Obtain at Least Ten Subjects for Every Variable Investigatedp. 125
Begin with the Exponential Distribution to Model Time to Eventp. 127
Begin with Two Exponentials for Comparing Survival Timesp. 129
Be Wary of Surrogatesp. 131
Prevalence Dominates in Screening Rare Diseasesp. 134
Do Not Dichotomize Unless Absolutely Necessaryp. 138
Additive and Multiplicative Modelsp. 139
Evidence-Based Medicinep. 143
Strength of Evidencep. 144
Relevance of Information: POEM vs. DOEp. 148
Begin with Absolute Risk Reduction, then Follow with Relative Riskp. 149
The Number Needed to Treat (NNT) is Clinically Usefulp. 151
Variability in Response to Treatment Needs to be Consideredp. 153
Safety is the Weak Component of EBMp. 155
Intent to Treat is the Default Analysisp. 156
Use Prior Information but not Priorsp. 157
The Four Key Questions for Meta-analystsp. 158
Design, Conduct, and Analysisp. 163
Randomization Puts Systematic Effects into the Error Termp. 163
Blocking is the Key to Reducing Variabilityp. 165
Factorial Designs and Joint Effectsp. 166
High-Order Interactions Occur Rarelyp. 168
Balanced Designs Allow Easy Assessment of Joint Effectsp. 170
Analysis Follows Designp. 171
Independence, Equal Variance, and Normalityp. 173
Plan to Graph the Results of an Analysisp. 177
Distinguish Between Design Structure and Treatment Structurep. 179
Make Hierarchical Analyses the Default Analysisp. 181
Distinguish Between Nested and Crossed Designs-Not Always Easyp. 182
Plan for Missing Datap. 184
Address Multiple Comparisons Before Starting the Studyp. 186
Know Properties Preserved When Transforming Unitsp. 188
Consider Bootstrapping for Complex Relationshipsp. 191
Words, Tables, and Graphsp. 193
Use Text for a Few Numbers, Tables for Many Numbers, Graphs for Complex Relationshipsp. 193
Arrange Information in a Table to Drive Home the Messagep. 195
Always Graph the Datap. 198
Always Graph Results of an Analysis of Variancep. 199
Never Use a Pie Chartp. 203
Bar Graphs Waste Ink; They Don't Illuminate Complex Relationshipsp. 204
Stacked Bar Graphs Are Worse Than Bar Graphsp. 206
Three-Dimensional Bar Graphs Constitute Misdirected Artistryp. 209
Identify Cross-sectional and Longitudinal Patterns in Longitudinal Datap. 210
Use Rendering, Manipulation, and Linking in High-Dimensional Datap. 213
Consultingp. 217
Session Has Beginning, Middle, and Endp. 218
Ask Questionsp. 219
Make Distinctionsp. 220
Know Yourself, Know the Investigatorp. 222
Tailor Advice to the Level of the Investigatorp. 223
Use Units the Investigator is Comfortable Withp. 224
Agree on Assignment of Responsibilitiesp. 226
Any Basic Statistical Computing Package Will Dop. 227
Ethics Precedes, Guides, and Follows Consultationp. 228
Be Proactive in Statistical Consultingp. 230
Use the Web for Reference, Resource, and Educationp. 231
Listen to, and Heed the Advice of Experts in the Fieldp. 233
Epiloguep. 236
Referencesp. 239
Author Indexp. 255
Topic Indexp. 261
Table of Contents provided by Ingram. All Rights Reserved.

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