The CARE checklist is a 13-item reporting guideline for case reports, published by Gagnier and colleagues in 2013. The name is formed from CAse REport. It specifies what the write-up of a single patient's clinical episode must contain for it to be usable by another clinician, and two of its items are unusual among reporting guidelines: a timeline of the episode, and the patient's own perspective on their experience.
Case reports occupy a peculiar position in research. They are the most accessible form of publication, often a clinician's first, and simultaneously the form most likely to be rejected, usually for a reason that has nothing to do with writing quality. The commonest fatal problem is that the case has no takeaway. A report that describes an unusual event and stops has documented something without teaching anything, and rarity by itself is not a contribution.
What makes a case worth reporting
Before the checklist, the judgement. A case earns publication when it changes something a reader might do. In practice that means one of a small number of things:
- An unexpected presentation of a common condition, such that a clinician might otherwise miss it.
- An adverse or unexpected effect of a drug, device or procedure, particularly one not in the existing literature.
- A diagnostic pitfall, where the obvious interpretation of findings was wrong and there was a way to tell.
- A management approach that worked where standard treatment had failed, or a novel application of an existing treatment.
- A genuinely rare condition described in enough detail to help with recognition, which is the weakest of the five and needs the most careful framing.
If your case does not fit one of these, the honest options are to write it up as an educational piece rather than a research report, or to combine it with similar cases into a case series, which supports a slightly stronger claim. Our healthcare case study service handles both routes.
The 13 items
Described in our own words. The authoritative wording and the checklist file sit with the guideline and are indexed on the guideline library EQUATOR maintains.
- Title. That the article is a case report, with the phenomenon of greatest interest named, whether a symptom, diagnosis, intervention or outcome.
- Key words. Two to five words capturing the key elements of the case.
- Abstract. The background of why this case is unusual, the main symptoms and important clinical findings, the main diagnoses and interventions and outcomes, and the conclusion including the primary lesson.
- Introduction. Brief background summarising why this case is unusual, with references.
- Patient information. De-identified demographic details, the primary concerns and symptoms, and relevant medical, family and psychosocial history including diet, lifestyle, genetic information and any past interventions with outcomes.
- Clinical findings. The relevant physical examination and other clinical findings.
- Timeline. The episode organised as a chronology, which is usually best given as a figure or table.
- Diagnostic assessment. The diagnostic methods used including examination, laboratory testing and imaging; the diagnostic challenges encountered; the diagnostic reasoning including the differential diagnoses considered; and any prognostic characteristics.
- Therapeutic intervention. The types of intervention, whether pharmacological, surgical, preventive or self-care, and their administration including dose, strength, duration and frequency, with any changes and the rationale.
- Follow-up and outcomes. The clinician and patient-assessed outcomes, the results of any follow-up testing, the extent of adherence and tolerability, and any adverse or unanticipated events.
- Discussion. The strengths and limitations of the management of this case, the relevant medical literature, the rationale for conclusions including any assessment of cause and effect, and the primary lesson to be drawn.
- Patient perspective. The patient sharing their own experience or perspective on the care they received, wherever possible.
- Informed consent. A statement that the patient gave informed consent for publication, with the document available if requested.