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Instructor Resource Chapter 10 Copyright © Scott B. Patten, 2015. Permission granted for classroom use with Epidemiology for Canadian Students: Principles,

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Presentation on theme: "Instructor Resource Chapter 10 Copyright © Scott B. Patten, 2015. Permission granted for classroom use with Epidemiology for Canadian Students: Principles,"— Presentation transcript:

1 Instructor Resource Chapter 10 Copyright © Scott B. Patten, 2015. Permission granted for classroom use with Epidemiology for Canadian Students: Principles, Methods & Critical Appraisal (Edmonton: Brush Education Inc. www.brusheducation.ca).

2 Chapter 10. Cross- sectional studies

3 Objectives Define cross-sectional studies. Differentiate between the potential descriptive and analytical goals of cross-sectional studies. Describe the following measures of association: prevalence differences, prevalence ratios, prevalence odds ratios, and specific types of linear equations. Explain how to interpret measures of association calculated from cross-sectional data. List strengths and weaknesses of cross-sectional studies.

4 Critical appraisal This chapter is our first examination of a specific study design. Identification of study designs is a key step in critical appraisal of research reports. Critical appraisal is more than just reading a study and intuitively trying to identify problems with it. Critical appraisal involves asking and answering a series of key questions. An early step in critical appraisal should be identification of the study design.

5 Strategies for classifying study design A common (but sometimes problematic) approach to classifying studies is based on the motivations of the investigators. This approach asks the question: did these investigators have descriptive or analytical goals? The problem is that studies can have mixed goals and motivations may not be clearly stated. A more reliable procedure for study-design classification is based on actual features of the study.

6 What is a cross-sectional study? Cross-sectional studies are studies in which all data are collected at a single point in time. Prevalence studies are usually cross-sectional.

7 What is a cross-sectional study? (continued) Obviously, no study can occur exactly in a single instant. A prevalence study may take months or even years to conduct. Conceptually, however, these studies take place at a point in time: the study design neither to looks back into the past (retrospectively), nor forward into the future (prospectively). Note that a cross-sectional study can look back in time with its questions (e.g., it may ask adults questions about abuse when they were children), but the design is neither retrospective nor prospective.

8 Examples of cross-sectional studies The Canadian Community Health Survey general health “iterations” specialized “iterations”: e.g., nutrition, aging

9 More examples See abstracts at: http://www.ncbi.nlm.nih.gov/pubmed/24044468 http://www.ncbi.nlm.nih.gov/pubmed/26001869 http://www.ncbi.nlm.nih.gov/pubmed/25935425 http://www.ncbi.nlm.nih.gov/pubmed/25929819

10 How cross-sectional studies look at associations For the next few slides, consider the classic 2 x 2 contingency table: DiseaseNo Disease Exposedab Nonexposedcd

11 Prevalence differences Key point: A prevalence difference is an example of a measure of association because it embodies a comparison between 2 simpler parameters, which are prevalence in exposed and nonexposed groups.

12 Prevalence ratios

13 Prevalence odds ratios

14 Specific types of linear equations

15 Strengths of the cross- sectional study design Cross-sectional studies: provide valuable snapshots of disease describe disease occurrence across multiple variables: they can examine multiple diseases and exposures are cost efficient: these studies are often relatively inexpensive and practical are invulnerable to attrition

16 Weaknesses of the cross- sectional study design Cross-sectional studies: lack causal inference: temporality is usually unclear provide no determination of risk are inefficient for rare diseases are insensitive to time-dependent frequency changes

17 End


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