case: diagnosis, management, complications or treatment side effects…? Do not go into detail in the
introduction but give the reader a clear idea of which aspects of case management you will be
describing.
Patient information: Remember that patient information is what can lead to patient identification
(which of course is to be avoided, even with informed consent from the patient). Therefore, include
patient information only if it is directly relevant to disease epidemiology and/or case management.
Wherever possible, take the additional precaution of de-identifying the information when this makes
sense (e.g. if describing an STI, instead of specifying: “a 26-year-old woman mother of three children
living in the Malawian town of Karonga”, say: “a young mother living in a resource-limited setting in
Malawi”.
Clinical Findings & Diagnostic assessment: a) relevant physical examination and other clinical findings;
b) diagnosis methods & challenges c) diagnostic reasoning including differential diagnosis d) prognostic
characteristics when applicable.
Therapeutic intervention & Outcome: a) types of intervention b) administration of intervention c)
changes in intervention with explanations d) adverse or unanticipated events.
Discussion: a) strengths and limitations of the approach to this case b) discussion of the relevant
medical literature (references) c) rationale for your conclusions
Conclusion: a) primary “take away” lesson from this Case Report, especially as concerns humanitarian
and resource-limited settings b) any suggestions for further research, public health policy, clinical
protocols…
Patient perspective: When available/relevant, it can be valuable to add the patient’s perspective. This
can include, when and where appropriate: subjective experience of symptoms (pain and discomfort),
previous treatments (traditional or other), self-medication or home remedies prior to presenting at
MSF, ideas on disease causality, adherence and patient education issues, day-to-day coping… etc.
Timeline: You may wish to include a timeline or table detailing case management. This can make your
report more understandable for the reader and also cut down your word count by including details
such as drug posology and specific dates in the timeline / chart. This in turn will give you the possibility
to make your Discussion longer and the Discussion can be the most interesting part of your Case
Report.
Informed Consent/Ethics approval: Here you should state that you have obtained written informed
consent, witnessed oral consent, or ethical approval for absence of informed consent (state why).
Conflict of interest statement: It is routine in medical journals to state any potential conflict of interest
you might have. For example, if your report is on snakebites and you are working for a pharmaceutical
company which produces anti-venoms.
Acknowledgements: Here you should acknowledge – with their consent – any persons who provided
assistance to you (review, editing,…) who does not qualify as a co-author.
Guarantor: It is becoming increasingly common for medical journals to ask that one of the authors be
named as the “guarantor”, as in the person who takes responsibility for the integrity and accuracy of
the report.