JAMA Cardiology (jama-cardiology)
Journal positioning
JAMA Cardiology is a JAMA Network specialty journal for cardiovascular clinical
research relevant to the practice of cardiology and cardiovascular medicine. It favors
rigorous, practice-relevant work — randomized cardiovascular trials, large outcomes and
registry analyses, prevention and risk-factor studies, and cardiac imaging studies tied
to clinical outcomes — with JAMA's emphasis on hard endpoints, absolute risk, and
direct relevance to patient care. Mechanistic bench cardiology, small physiology
studies with surrogate-only readouts, and imaging-technique papers with no outcome link
are a weak fit. This skill is a fit / venue-selection / re-framing aid; it is not
clinical or regulatory advice and does not replace the journal's current instructions
for authors. Before submitting, re-check the live JAMA Cardiology author instructions.
When to trigger
- The author names JAMA Cardiology for a cardiovascular clinical, outcomes, or
imaging-outcome study and wants a fit/framing check.
- A cardiovascular study must be re-framed around a hard clinical endpoint (MACE,
mortality, hospitalization) for a practicing-cardiology audience.
- The author is choosing between JAMA Cardiology, JAMA, and a cardiology-society
journal.
- The author needs the journal's reporting-guideline, registration, and desk-reject
expectations for cardiovascular work.
Scope & topic fit
- Randomized cardiovascular trials (drug, device, procedural, or strategy) with
clinically meaningful endpoints, including pragmatic and de-implementation designs.
- Large outcomes, registry, and claims analyses on cardiovascular events, heart
failure, arrhythmia, and structural/interventional outcomes.
- Cardiovascular prevention, risk-factor, lipid, hypertension, and population
cardiovascular-health studies.
- Cardiac imaging (echo, CMR, CCT, nuclear) studies where the contribution is a
clinical-outcome or prognostic association, not a pure imaging technique.
- Cardiovascular biomarker and risk-prediction studies validated against outcomes.
- Systematic reviews and meta-analyses answering a focused cardiovascular question.
Method & evidence bar
- Trials must be adequately powered with a prespecified primary endpoint, ideally a
hard clinical outcome or validated composite (with the composite components reported);
surrogate-only endpoints need strong justification.
- The applicable reporting guideline and checklist are required: CONSORT for trials
(with device/procedure extensions where relevant), STROBE for observational studies,
PRISMA for systematic reviews; risk-model work should follow TRIPOD-style reporting.
- Trials require prospective registration; registration number, protocol, and
statistical-analysis plan are expected, including for device and procedural trials.
- Effect estimates need absolute and relative measures, confidence intervals, adequate
follow-up, and adjudicated endpoints where feasible.
- Registry/observational claims must address confounding by indication, immortal-time
bias, and missing data; causal language must match the design.
- Risk-prediction and biomarker claims need internal and ideally external validation,
calibration, and discrimination metrics.
Structure & house style
- JAMA Network format with a structured abstract and a Key Points box; re-check current
article types (Original Investigation, Brief Report, Research Letter, etc.) and limits
on the live guide.
- The introduction frames a focused, practice-relevant cardiovascular question; the
discussion states the clinical implication and absolute benefit/harm plainly.
- Tables/figures follow JAMA Network statistical-reporting standards; CONSORT/STROBE
flow diagrams, event-free survival curves with numbers at risk, and adjudicated-event
tables are expected where applicable.
- Supplements carry the protocol, SAP, endpoint definitions, and additional analyses.
Official-submission checklist
- Before giving submission-ready advice, read
../../resources/source-basis.md and
../../resources/official-source-map.md; start from the ICMJE and JAMA Network
anchors, then cite the current JAMA Cardiology page you checked.
- Search the live site for "JAMA Cardiology instructions for authors" and follow the
current version.
- Re-check article types and word/reference/table limits, structured-abstract and Key
Points format, and the JAMA Network statistical-reporting requirements.
- Confirm trial registration, the reporting checklist (CONSORT/STROBE/PRISMA), the
data-sharing statement, and protocol/SAP submission.
- Re-check IRB/ethics and consent statements, ICMJE authorship and conflict-of-interest
disclosure (device/industry ties scrutinized), funding, and AI-use disclosure.
- If the live official instructions conflict with this skill, the official instructions
win.
Pre-submission self-check
Common desk-reject triggers
- Underpowered trials or surrogate-only physiology studies framed as practice-relevant.
- Imaging-technique papers with no clinical-outcome or prognostic link.
- Registry/observational analyses with confounding by indication or immortal-time bias and overstated causal claims.
- Risk models or biomarkers without validation, calibration, or discrimination reporting.
- Missing trial registration, protocol, endpoint adjudication, or the required reporting checklist.
- Mechanistic/basic cardiology better served by a cardiovascular-science journal.
Re-routing decision
- Broadly practice-changing, top-tier cardiovascular trial → general medicine (
jama / NEJM / The Lancet in the natural-science bundle).
- General internal-medicine relevance over cardiology specialty →
jama-internal-medicine.
- Cardiac imaging with an imaging-method core over clinical outcome →
radiology.
- Cerebrovascular/stroke-specific cardiovascular focus →
stroke.
- Surgical/perioperative cardiac focus →
jama-surgery.
Output format
[Fit] High / Medium / Low (one-line reason)
[Target] JAMA Cardiology
[Specialty tags] <2–3 closest cardiovascular topics>
[Study design / reporting guideline] <RCT-CONSORT / cohort-STROBE / model-TRIPOD / review-PRISMA>
[Method/evidence] <does power, endpoint, registration, and validation clear the bar?>
[Top risk] <the single most likely reason for rejection>
[Official items to re-check] <article type / registration / checklist / endpoint adjudication / ethics / disclosures>
[Re-route suggestion] <if not a fit, a better-matched venue>