Description

Book Synopsis

Essential Statistics for the Pharmaceutical Sciences is targeted at all those involved in research in pharmacology, pharmacy or other areas of pharmaceutical science; everybody from undergraduate project students to experienced researchers should find the material they need.

This book will guide all those who are not specialist statisticians in using sound statistical principles throughout the whole journey of a research project - designing the work, selecting appropriate statistical methodology and correctly interpreting the results. It deliberately avoids detailed calculation methodology. Its key features are friendliness and clarity. All methods are illustrated with realistic examples from within pharmaceutical science.

This edition now includes expanded coverage of some of the topics included in the first edition and adds some new topics relevant to pharmaceutical research.

  • a clear, accessible introduction to the key statistical techniques used

    Table of Contents

    Preface xiii

    Statistical packages xix

    About the website xxi

    PART 1 PRESENTING DATA 1

    1 Data types 3

    1.1 Does it really matter? 3

    1.2 Interval scale data 4

    1.3 Ordinal scale data 4

    1.4 Nominal scale data 5

    1.5 Structure of this book 6

    1.6 Chapter summary 6

    2 Data presentation 7

    2.1 Numerical tables 8

    2.2 Bar charts and histograms 9

    2.3 Pie charts 14

    2.4 Scatter plots 16

    2.5 Pictorial symbols 21

    2.6 Chapter summary 22

    PART 2 INTERVAL]SCALE DATA 23

    3 Descriptive statistics for interval scale data 25

    3.1 Summarising data sets 25

    3.2 Indicators of central tendency: Mean, median and mode 26

    3.3 Describing variability – standard deviation and coefficient of variation 33

    3.4 Quartiles – Another way to describe data 36

    3.5 Describing ordinal data 40

    3.6 Using computer packages to generate descriptive statistics 43

    3.7 Chapter summary 45

    4 The normal distribution 47

    4.1 What is a normal distribution? 47

    4.2 Identifying data that are not normally distributed 48

    4.3 Proportions of individuals within 1SD or 2SD of the mean 52

    4.4 Skewness and kurtosis 54

    4.5 Chapter summary 57

    4.6 Appendix: Power, sample size and the problem of attempting to test for a normal distribution 58

    5 Sampling from populations: The standard error of the mean 63

    5.1 Samples and populations 63

    5.2 From sample to population 65

    5.3 Types of sampling error 65

    5.4 What factors control the extent of random sampling error when estimating a population mean? 68

    5.5 Estimating likely sampling error – The SEM 70

    5.6 Offsetting sample size against SD 74

    5.7 Chapter summary 75

    6 95% Confidence interval for the mean and data transformation 77

    6.1 What is a confidence interval? 78

    6.2 How wide should the interval be? 78

    6.3 What do we mean by ‘95%’ confidence? 79

    6.4 Calculating the interval width 80

    6.5 A long series of samples and 95% C.I.s 81

    6.6 How sensitive is the width of the C.I. to changes in the SD, the sample size or the required level of confidence? 82

    6.7 Two statements 85

    6.8 One]sided 95% C.I.s 85

    6.9 The 95% C.I. for the difference between two treatments 88

    6.10 The need for data to follow a normal distribution and data transformation 90

    6.11 Chapter summary 94

    7 The two]sample t]test (1): Introducing hypothesis tests 95

    7.1 The two]sample t]test – an example of an hypothesis test 96

    7.2 Significance 103

    7.3 The risk of a false positive finding 104

    7.4 What aspects of the data will influence whether or not we obtain a significant outcome? 106

    7.5 Requirements for applying a two]sample t]test 108

    7.6 Performing and reporting the test 109

    7.7 Chapter summary 110

    8 The two]sample t]test (2): The dreaded P value 111

    8.1 Measuring how significant a result is 111

    8.2 P values 112

    8.3 Two ways to define significance? 113

    8.4 Obtaining the P value 113

    8.5 P values or 95% confidence intervals? 114

    8.6 Chapter summary 115

    9 The two]sample t]test (3): False negatives, power and necessary sample sizes 117

    9.1 What else could possibly go wrong? 118

    9.2 Power 119

    9.3 Calculating necessary sample size 122

    9.4 Chapter summary 130

    10 The two]sample t]test (4): Statistical significance, practical significance and equivalence 131

    10.1 Practical significance – Is the difference big enough to matter? 131

    10.2 Equivalence testing 135

    10.3 Non]inferiority testing 139

    10.4 P values are less informative and can be positively misleading 141

    10.5 Setting equivalence limits prior to experimentation 143

    10.6 Chapter summary 144

    11 The two]sample t]test (5): One]sided testing 145

    11.1 Looking for a change in a specified direction 146

    11.2 Protection against false positives 148

    11.3 Temptation! 149

    11.4 Using a computer package to carry out a one]sided test 153

    11.5 Chapter summary 153

    12 What does a statistically significant result really tell us? 155

    12.1 Interpreting statistical significance 155

    12.2 Starting from extreme scepticism 159

    12.3 Bayesian statistics 160

    12.4 Chapter summary 161

    13 The paired t]test: Comparing two related sets of measurements 163

    13.1 Paired data 163

    13.2 We could analyse the data by a two]sample t]test 165

    13.3 Using a paired t]test instead 165

    13.4 Performing a paired t]test 166

    13.5 What determines whether a paired t]test will be significant? 169

    13.6 Greater power of the paired t]test 170

    13.7 Applicability of the test 170

    13.8 Choice of experimental design 171

    13.9 Requirement for applying a paired t]test 172

    13.10 Sample sizes, practical significance and one]sided tests 173

    13.11 Summarising the differences between paired and two]sample t]tests 175

    13.12 Chapter summary 175

    14 Analyses of variance: Going beyond t]tests 177

    14.1 Extending the complexity of experimental designs 177

    14.2 One]way analysis of variance 178

    14.3 T wo]way analysis of variance 188

    14.4 Fixed and random factors 198

    14.5 Multi]factorial experiments 204

    14.6 Chapter summary 204

    15 Correlation and regression – Relationships between measured values 207

    15.1 Correlation analysis 208

    15.2 Regression analysis 218

    15.3 Multiple regression 225

    15.4 Chapter summary 235

    16 Analysis of covariance 237

    16.1 A clinical trial where ANCOVA would be appropriate 238

    16.2 General interpretation of ANCOVA results 239

    16.3 Analysis of the COPD trial results 241

    16.4 Advantages of ANCOVA over a simple two]sample t]test 244

    16.5 Chapter summary 249

    PART 3 NOMINAL]SCALE DATA 251

    17 D escribing categorised data and the goodness of fit chi]square test 253

    17.1 Descriptive statistics 254

    17.2 Testing whether the population proportion might credibly be some pre]determined figure 258

    17.3 Chapter summary 264

    18 Contingency chi]square, Fisher’s and McNemar’s tests 265

    18.1 Using the contingency chi]square test to compare observed proportions 266

    18.2 Extent of change in proportion with an expulsion – Clinically significant? 270

    18.3 Larger tables – Attendance at diabetic clinics 270

    18.4 Planning experimental size 273

    18.5 Fisher’s exact test 275

    18.6 McNemar’s test 277

    18.7 Chapter summary 279

    18.8 Appendix 280

    19 Relative risk, odds ratio and number needed to treat 283

    19.1 Measures of treatment effect – relative risk, odds ratio and number needed to treat 283

    19.2 Similarity between relative risk and odds ratio 287

    19.3 Interpreting the various measures 288

    19.4 95% confidence intervals for measures of effect size 289

    19.5 Chapter summary 293

    20 Logistic regression 295

    20.1 Modelling a binary outcome 295

    20.2 Additional predictors and the problem of confounding 304

    20.3 Analysis by computer package 307

    20.4 Extending logistic regression beyond dichotomous outcomes 308

    20.5 Chapter summary 309

    20.6 Appendix 309

    PART 4 ORDINAL]SCALE DATA 311

    21 Ordinal and non]normally distributed data: Transformations and non]parametric tests 313

    21.1 Transforming data to a normal distribution 314

    21.2 The Mann–Whitney test – a non]parametric method 318

    21.3 Dealing with ordinal data 323

    21.4 Other non]parametric methods 325

    21.5 Chapter summary 333

    21.6 Appendix 334

    PART 5 OTHER TOPICS 337

    22 Measures of agreement 339

    22.1 Answers to several questions 340

    22.2 Several answers to one question – do they agree? 344

    22.3 Chapter summary 358

    23 Survival analysis 361

    23.1 What special problems arise with survival data? 362

    23.2 Kaplan–Meier survival estimation 363

    23.3 Declining sample sizes in survival studies 369

    23.4 Precision of sampling estimates of survival 369

    23.5 Indicators of survival 371

    23.6 Testing for differences in survival 374

    23.7 Chapter summary 383

    24 Multiple testing 385

    24.1 What is it and why is it a problem? 385

    24.2 Where does multiple testing arise? 386

    24.3 Methods to avoid false positives 388

    24.4 The role of scientific journals 392

    24.5 Chapter summary 393

    25 Questionnaires 395

    25.1 Types of questions 396

    25.2 Sample sizes and low return rates 398

    25.3 Analysing the results 399

    25.4 Problem number two: Confounded questionnaire data 401

    25.5 Problem number three: Multiple testing with questionnaire data 401

    25.6 Chapter summary 403

    Index 405

Essential Statistics for the Pharmaceutical

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    Order before 4pm today for delivery by Tue 30 Jun 2026.

    A Hardback by Philip Rowe

    Out of stock


      View other formats and editions of Essential Statistics for the Pharmaceutical by Philip Rowe

      Publisher: John Wiley and Sons Ltd
      Publication Date: 02/10/2015
      ISBN13: 9781118913383, 978-1118913383
      ISBN10: 1118913388

      Description

      Book Synopsis

      Essential Statistics for the Pharmaceutical Sciences is targeted at all those involved in research in pharmacology, pharmacy or other areas of pharmaceutical science; everybody from undergraduate project students to experienced researchers should find the material they need.

      This book will guide all those who are not specialist statisticians in using sound statistical principles throughout the whole journey of a research project - designing the work, selecting appropriate statistical methodology and correctly interpreting the results. It deliberately avoids detailed calculation methodology. Its key features are friendliness and clarity. All methods are illustrated with realistic examples from within pharmaceutical science.

      This edition now includes expanded coverage of some of the topics included in the first edition and adds some new topics relevant to pharmaceutical research.

      • a clear, accessible introduction to the key statistical techniques used

        Table of Contents

        Preface xiii

        Statistical packages xix

        About the website xxi

        PART 1 PRESENTING DATA 1

        1 Data types 3

        1.1 Does it really matter? 3

        1.2 Interval scale data 4

        1.3 Ordinal scale data 4

        1.4 Nominal scale data 5

        1.5 Structure of this book 6

        1.6 Chapter summary 6

        2 Data presentation 7

        2.1 Numerical tables 8

        2.2 Bar charts and histograms 9

        2.3 Pie charts 14

        2.4 Scatter plots 16

        2.5 Pictorial symbols 21

        2.6 Chapter summary 22

        PART 2 INTERVAL]SCALE DATA 23

        3 Descriptive statistics for interval scale data 25

        3.1 Summarising data sets 25

        3.2 Indicators of central tendency: Mean, median and mode 26

        3.3 Describing variability – standard deviation and coefficient of variation 33

        3.4 Quartiles – Another way to describe data 36

        3.5 Describing ordinal data 40

        3.6 Using computer packages to generate descriptive statistics 43

        3.7 Chapter summary 45

        4 The normal distribution 47

        4.1 What is a normal distribution? 47

        4.2 Identifying data that are not normally distributed 48

        4.3 Proportions of individuals within 1SD or 2SD of the mean 52

        4.4 Skewness and kurtosis 54

        4.5 Chapter summary 57

        4.6 Appendix: Power, sample size and the problem of attempting to test for a normal distribution 58

        5 Sampling from populations: The standard error of the mean 63

        5.1 Samples and populations 63

        5.2 From sample to population 65

        5.3 Types of sampling error 65

        5.4 What factors control the extent of random sampling error when estimating a population mean? 68

        5.5 Estimating likely sampling error – The SEM 70

        5.6 Offsetting sample size against SD 74

        5.7 Chapter summary 75

        6 95% Confidence interval for the mean and data transformation 77

        6.1 What is a confidence interval? 78

        6.2 How wide should the interval be? 78

        6.3 What do we mean by ‘95%’ confidence? 79

        6.4 Calculating the interval width 80

        6.5 A long series of samples and 95% C.I.s 81

        6.6 How sensitive is the width of the C.I. to changes in the SD, the sample size or the required level of confidence? 82

        6.7 Two statements 85

        6.8 One]sided 95% C.I.s 85

        6.9 The 95% C.I. for the difference between two treatments 88

        6.10 The need for data to follow a normal distribution and data transformation 90

        6.11 Chapter summary 94

        7 The two]sample t]test (1): Introducing hypothesis tests 95

        7.1 The two]sample t]test – an example of an hypothesis test 96

        7.2 Significance 103

        7.3 The risk of a false positive finding 104

        7.4 What aspects of the data will influence whether or not we obtain a significant outcome? 106

        7.5 Requirements for applying a two]sample t]test 108

        7.6 Performing and reporting the test 109

        7.7 Chapter summary 110

        8 The two]sample t]test (2): The dreaded P value 111

        8.1 Measuring how significant a result is 111

        8.2 P values 112

        8.3 Two ways to define significance? 113

        8.4 Obtaining the P value 113

        8.5 P values or 95% confidence intervals? 114

        8.6 Chapter summary 115

        9 The two]sample t]test (3): False negatives, power and necessary sample sizes 117

        9.1 What else could possibly go wrong? 118

        9.2 Power 119

        9.3 Calculating necessary sample size 122

        9.4 Chapter summary 130

        10 The two]sample t]test (4): Statistical significance, practical significance and equivalence 131

        10.1 Practical significance – Is the difference big enough to matter? 131

        10.2 Equivalence testing 135

        10.3 Non]inferiority testing 139

        10.4 P values are less informative and can be positively misleading 141

        10.5 Setting equivalence limits prior to experimentation 143

        10.6 Chapter summary 144

        11 The two]sample t]test (5): One]sided testing 145

        11.1 Looking for a change in a specified direction 146

        11.2 Protection against false positives 148

        11.3 Temptation! 149

        11.4 Using a computer package to carry out a one]sided test 153

        11.5 Chapter summary 153

        12 What does a statistically significant result really tell us? 155

        12.1 Interpreting statistical significance 155

        12.2 Starting from extreme scepticism 159

        12.3 Bayesian statistics 160

        12.4 Chapter summary 161

        13 The paired t]test: Comparing two related sets of measurements 163

        13.1 Paired data 163

        13.2 We could analyse the data by a two]sample t]test 165

        13.3 Using a paired t]test instead 165

        13.4 Performing a paired t]test 166

        13.5 What determines whether a paired t]test will be significant? 169

        13.6 Greater power of the paired t]test 170

        13.7 Applicability of the test 170

        13.8 Choice of experimental design 171

        13.9 Requirement for applying a paired t]test 172

        13.10 Sample sizes, practical significance and one]sided tests 173

        13.11 Summarising the differences between paired and two]sample t]tests 175

        13.12 Chapter summary 175

        14 Analyses of variance: Going beyond t]tests 177

        14.1 Extending the complexity of experimental designs 177

        14.2 One]way analysis of variance 178

        14.3 T wo]way analysis of variance 188

        14.4 Fixed and random factors 198

        14.5 Multi]factorial experiments 204

        14.6 Chapter summary 204

        15 Correlation and regression – Relationships between measured values 207

        15.1 Correlation analysis 208

        15.2 Regression analysis 218

        15.3 Multiple regression 225

        15.4 Chapter summary 235

        16 Analysis of covariance 237

        16.1 A clinical trial where ANCOVA would be appropriate 238

        16.2 General interpretation of ANCOVA results 239

        16.3 Analysis of the COPD trial results 241

        16.4 Advantages of ANCOVA over a simple two]sample t]test 244

        16.5 Chapter summary 249

        PART 3 NOMINAL]SCALE DATA 251

        17 D escribing categorised data and the goodness of fit chi]square test 253

        17.1 Descriptive statistics 254

        17.2 Testing whether the population proportion might credibly be some pre]determined figure 258

        17.3 Chapter summary 264

        18 Contingency chi]square, Fisher’s and McNemar’s tests 265

        18.1 Using the contingency chi]square test to compare observed proportions 266

        18.2 Extent of change in proportion with an expulsion – Clinically significant? 270

        18.3 Larger tables – Attendance at diabetic clinics 270

        18.4 Planning experimental size 273

        18.5 Fisher’s exact test 275

        18.6 McNemar’s test 277

        18.7 Chapter summary 279

        18.8 Appendix 280

        19 Relative risk, odds ratio and number needed to treat 283

        19.1 Measures of treatment effect – relative risk, odds ratio and number needed to treat 283

        19.2 Similarity between relative risk and odds ratio 287

        19.3 Interpreting the various measures 288

        19.4 95% confidence intervals for measures of effect size 289

        19.5 Chapter summary 293

        20 Logistic regression 295

        20.1 Modelling a binary outcome 295

        20.2 Additional predictors and the problem of confounding 304

        20.3 Analysis by computer package 307

        20.4 Extending logistic regression beyond dichotomous outcomes 308

        20.5 Chapter summary 309

        20.6 Appendix 309

        PART 4 ORDINAL]SCALE DATA 311

        21 Ordinal and non]normally distributed data: Transformations and non]parametric tests 313

        21.1 Transforming data to a normal distribution 314

        21.2 The Mann–Whitney test – a non]parametric method 318

        21.3 Dealing with ordinal data 323

        21.4 Other non]parametric methods 325

        21.5 Chapter summary 333

        21.6 Appendix 334

        PART 5 OTHER TOPICS 337

        22 Measures of agreement 339

        22.1 Answers to several questions 340

        22.2 Several answers to one question – do they agree? 344

        22.3 Chapter summary 358

        23 Survival analysis 361

        23.1 What special problems arise with survival data? 362

        23.2 Kaplan–Meier survival estimation 363

        23.3 Declining sample sizes in survival studies 369

        23.4 Precision of sampling estimates of survival 369

        23.5 Indicators of survival 371

        23.6 Testing for differences in survival 374

        23.7 Chapter summary 383

        24 Multiple testing 385

        24.1 What is it and why is it a problem? 385

        24.2 Where does multiple testing arise? 386

        24.3 Methods to avoid false positives 388

        24.4 The role of scientific journals 392

        24.5 Chapter summary 393

        25 Questionnaires 395

        25.1 Types of questions 396

        25.2 Sample sizes and low return rates 398

        25.3 Analysing the results 399

        25.4 Problem number two: Confounded questionnaire data 401

        25.5 Problem number three: Multiple testing with questionnaire data 401

        25.6 Chapter summary 403

        Index 405

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