This resource was developed by the ASHP New Practitioners Forum Clinical Practice Advisory Group, which is providing members the opportunity to share
resources that might assist in professional endeavors. ASHP is not responsible for, and does not officially endorse this resource, and further expressly
disclaims any and all liability for damages of any kind arising out of the use, reference to, or reliance upon any information contained in the resource. No
guarantee is provided that the content is correct, accurate, complete, up-to-date, or owned by the individual who posted it.
Copyright © 2020, American Society of Health-System Pharmacists, Inc. All rights reserved.
Example Journal Club Template
Background and Overview
Study Citation
Cite your article here using proper format.
Purpose/Background
Give a brief summary about why this study is important. You can also provide a
short background on the drug, disease state, or procedure that is being
evaluated. In addition, relevant literature on the subject can be discussed.
Study Objective
The objective, study aim or goal, should be clearly stated in the article and
copied directly so as not to change the meaning here.
Historical Context
What other related trials have been done prior to this study? Discuss any other
relevant literature on the subject here. Be sure to cite these below in the
reference list.
Methods
Study Design
Things to consider*:
Retrospective vs. prospective
Randomization
Blinding
Case control vs. RCT vs. meta-analysis
Superiority vs. non-inferiority
Multicenter vs. single site
*This is not an all-inclusive list.
Funding
Disclose funding and consider potential conflicts of interest.
Population
Inclusion Criteria
Exclusion Criteria
List the major and
noteworthy inclusion
criteria.
List the major and noteworthy exclusion criteria.
Give consideration to if exclusions are appropriate.
The reason does not need to be included here,
though should be a point of discussion.
This resource was developed by the ASHP New Practitioners Forum Clinical Practice Advisory Group, which is providing members the opportunity to share
resources that might assist in professional endeavors. ASHP is not responsible for, and does not officially endorse this resource, and further expressly
disclaims any and all liability for damages of any kind arising out of the use, reference to, or reliance upon any information contained in the resource. No
guarantee is provided that the content is correct, accurate, complete, up-to-date, or owned by the individual who posted it.
Copyright © 2020, American Society of Health-System Pharmacists, Inc. All rights reserved.
Interventions or Study
Procedures
Describe the interventions performed in the trial. Was it active-controlled? What
was the dose of the medication(s) used? How often were they administered?
Was there a washout period for study drugs? Was there an enrollment period to
determine adherence? How were study participants randomized (i.e. 1:1, 1:2:1,
etc.)? How long was the intervention period? What was the median follow-up
time-frame? Was the follow-up period similar between the groups?
Outcomes
Primary outcome/endpoint:
Secondary outcomes/endpoints:
Statistical Analysis
What statistical tests were used for each set of data? You should evaluate if
these tests were appropriate for your discussion, though you don’t need to
include the appropriateness of the tests here.
Did the study include a sample size calculation?
Results
Study Sample
Sample Size
Baseline Characteristics
How many participants
were enrolled in the study
and in each arm?
Are they well matched between treatment groups?
Are there any noteworthy characteristics of this
sample that stand out to you?
Results
You may include tables and/or bullet points to describe and summarize
the main results.
Be sure to include how many patients dropped out of the study and
why.
Be sure to include the results of the primary and secondary endpoints,
statistical significance (e.g. p-value, confidence interval, etc.). Consider
directing the audience to a specific table/figure within the article if
available.
Consider also including number needed to treat (NNT) or number
needed to harm (NNH).
Address noteworthy adverse event rates (if applicable).
Summary
What were the key takeaways from the trial? The key takeaways should
not include any interpretation of the results. Interpretation of the results
This resource was developed by the ASHP New Practitioners Forum Clinical Practice Advisory Group, which is providing members the opportunity to share
resources that might assist in professional endeavors. ASHP is not responsible for, and does not officially endorse this resource, and further expressly
disclaims any and all liability for damages of any kind arising out of the use, reference to, or reliance upon any information contained in the resource. No
guarantee is provided that the content is correct, accurate, complete, up-to-date, or owned by the individual who posted it.
Copyright © 2020, American Society of Health-System Pharmacists, Inc. All rights reserved.
will be included in the discussion & conclusions.
Discussion and Conclusions
Evaluation of Study
Quality
Strengths of the Study
Limitations of the Study
List them here. Examples:
large sample size, external
validity, etc.
What could be improved about the study design?
What about the trial weakens its overall impact?
(e.g. internal/external validity, statistical vs. clinical
significance, inclusion/exclusion criteria
appropriateness)
Author’s Discussion and
Conclusion
Summarize the author’s conclusion from the article.
Personal Discussion and
Conclusion
Write out your conclusions. You may reference other articles and how
findings from those might play a role in interpreting this study.
Application to Patient
Care
How will you use this information in practice (consider your practice site
specifically)?
References:
1. [citation for the study your journal club is focused on]
This resource was developed by the ASHP New Practitioners Forum Clinical Practice Advisory Group, which is providing members the opportunity to share
resources that might assist in professional endeavors. ASHP is not responsible for, and does not officially endorse this resource, and further expressly
disclaims any and all liability for damages of any kind arising out of the use, reference to, or reliance upon any information contained in the resource. No
guarantee is provided that the content is correct, accurate, complete, up-to-date, or owned by the individual who posted it.
Copyright © 2020, American Society of Health-System Pharmacists, Inc. All rights reserved.
Questions to Consider for your Presentation:
Background & Overview
What are the current guideline recommendations for this particular disease state or topic?
If applicable, how do we stratify the severity of disease being studied (i.e. A1C for patients with
diabetes, CKD stages, COPD GOLD classifications, etc.)?
If this is a new therapy, what is the biological rationale for why it might be useful for a particular disease
state?
Methods
How do the inclusion/exclusion criteria limit the population you can apply the results to?
Were the patients appropriately randomized to their treatment groups? Was there stratification in the
process?
Did the authors include a power analysis? Did enrollment achieve desired power?
Was everyone (patients, physicians, study personnel, etc.) blinded to treatments?
Was this an active controlled trial? If yes, does the active control depict the standard of care? Was it
appropriately dosed?
Was the method used to study the primary outcome appropriate? For example, if a study is assessing
agitation, was the chosen behavioral scale appropriate and validated? Have other studies assessing
similar outcomes used it?
Results
How do the baseline characteristics of the population in the study compare to the disease state being
studied?
Did exclusion criteria eliminate outliers and patients who may be at increased harm?
For statistically significant results, how does the NNH compare to the NNT? Are they similar, or are the
two significantly different from each other?
Are these results clinically significant?
Was the trial long enough to detect a difference?
Are the potential treatment benefits worth the potential harm and costs?
This resource was developed by the ASHP New Practitioners Forum Clinical Practice Advisory Group, which is providing members the opportunity to share
resources that might assist in professional endeavors. ASHP is not responsible for, and does not officially endorse this resource, and further expressly
disclaims any and all liability for damages of any kind arising out of the use, reference to, or reliance upon any information contained in the resource. No
guarantee is provided that the content is correct, accurate, complete, up-to-date, or owned by the individual who posted it.
Copyright © 2020, American Society of Health-System Pharmacists, Inc. All rights reserved.
Discussion
For your personal conclusions, would you change guideline recommendations based on the study? If so,
how? Will this study change how you practice?
Would it be feasible/appropriate to apply the study to your specific institution?
What additional limitations would you note besides the limitations described in the study?
Is the population in the study similar to patients in your practice?
Was there any bias present in the study? Who funded the study and what was the sponsor's role in the
study?
How would you apply this to your practice?