ArticleJACC. Case reports2026
Arteriopathy of the Internal Mammary Artery: Implications for Patients With Spontaneous Coronary Artery Dissection.
Article in JACC. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
backgroundSpontaneous coronary artery dissection (SCAD) is frequently associated with systemic arteriopathies, particularly fibromuscular dysplasia. Although extracoronary arterial screening is recommended, abnormalities of the internal mammary artery (IMA), the usual preferred conduit for coronary artery bypass grafting, is rarely described. CASE SUMMARY: We report 2 women with systemic arteriopathy and recurrent SCAD who had structural abnormalities of the IMA. The first had Loeys-Dietz syndrome and prior cervical artery dissections, presented with neck pain, and was found to have vertebral artery dissection and focal aneurysmal dilation and suspected dissection of the left IMA. The second had multifocal fibromuscular dysplasia involving renal, cervicocephalic, and thoracic arteries, and presented with recurrent SCAD myocardial infarction. Beaded irregularity of the left IMA was noted. Both patients were managed conservatively. DISCUSSION: These cases highlight under-recognized IMA involvement in patients with SCAD and systemic arteriopathy, raising considerations regarding conduit assessment when surgical revascularization is contemplated.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.