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Clinical Research Unit Seminar UAB Ophthalmology

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Coming Attractions???? Tips from the start. Not all papers are created equally. A paper can be in a respected journal and still have serious flaws. ... – PowerPoint PPT presentation

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Title: Clinical Research Unit Seminar UAB Ophthalmology


1
Clinical Research Unit SeminarUAB Ophthalmology
  • How to Read a Paper
  • Assessing the Methodological Quality of Published
    Papers
  • October 15, 2003
  • Gerald McGwin, MS, PhD
  • Cynthia Owsley, MSPH, PhD

2
  • Coming Attractions????

3
Tips from the start
  • Not all papers are created equally.
  • A paper can be in a respected journal and still
    have serious flaws.
  • Famous clinicians are not necessarily good
    scientists.
  • Just because a government agency funds the
    research does not mean that it should be
    uncritically accepted.

4
Approach
  • Introduction
  • Methods
  • Results
  • Discussion/Comment

5
Approach
  • Introduction
  • Methods
  • Results
  • Discussion/Comment

6
Introduction
  • Does the Introduction succinctly describe the
    clinical question of interest?
  • What is the problem? (e.g., physiologically,
    structurally, biochemically, genetically)
  • Prevalence of problem.
  • Person, place and time.
  • What is the public health issue?
  • Vision impairment/blindness/mortality.
  • Health-related quality of life.
  • Ocular pain discomfort.
  • Why is our current understanding of issue
    inadequate?
  • How do previous studies inform the issue?

7
Introduction Things to Watch For
  • Is the ophthalmic condition or disorder
    adequately defined?
  • Is the reader told key information on the
    conditions scope and treatment options?
  • Is the answer to the question already known?
  • Does the author incorporate the results of
    previous studies in framing the question?
  • Beware of straw men used to motivate a topic.
  • Clinically, does anyone care about this issue?
  • If not, why should they?
  • After youve read the Introduction, and youre
    not relatively clear on these issues, the paper
    probably has a serious problem.

8
Approach
  • Introduction
  • Methods
  • Results
  • Discussion/Comment

9
Methods
  • Nitty gritty
  • Provides important information about validity
  • Setting
  • Design
  • Sample size calculation
  • Data collection procedures
  • Analysis

10
Collection of Data
  • Context? (Why)
  • Objectives? (Specific hypothesis)
  • Primary exposure/condition of interest?
  • Causes, prevents or treats outcome
  • Accurately defined and measured?
    (misclassification)
  • Primary outcome of interest?
  • Accurately defined and measured?
    (misclassification)

11
Collection of Data
  • Type of study?
  • Experimental, cohort, case-control,
    cross-sectional, ecologic)
  • Could there have been bias?
  • Subject selection
  • Sample size
  • Recall, interviewer, LTF, misclassification
  • What provisions made to minimize bias?
  • Were they sufficient?

12
Analysis of Data
  • Methods to control confounding bias?
  • Measures of association?
  • Measures of statistical stability?

13
Approach
  • Introduction
  • Methods
  • Results
  • Discussion/Comment

14
Results
  • Population Characteristics
  • Balance (randomized studies)
  • Generalizability
  • Findings
  • Text, Tables and Figures
  • Read the legends!

15
Approach
  • Introduction
  • Methods
  • Results
  • Discussion/Comment

16
Discussion
  • Are the results discussed in the context of the
    question posed in the Introduction?
  • Is there mention of how these findings fit with
    similar studies?
  • If different, how so and potential reasons why.
  • What are the clinical implications?
  • For expectations on progression/prognosis.
  • For treatment options.
  • For prevention.
  • Are the strengths and limitations of the study
    addressed?
  • What questions remain unanswered?
  • Directions for future research.

17
Discussion Things to Watch For
  • Discussion section should not be a simple
    re-statement of the results.
  • Over generalization.
  • Unaddressed confounding factors and biases not
    frankly acknowledged.
  • Clinical significance is overblown or not
    mentioned.
  • Make note of any proprietary interests.
  • Not a death blow, but do notice.

18
Future Seminars
  • Please suggest other topics youd like to hear
    about in the CRU seminar.
  • E-mail us at CRU_at_uab.edu with your ideas.
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