ArticleJournal of cardiothoracic surgery2026
Endovascular treatment for spontaneous isolated dissection of superior mesenteric artery: a Single-centre prospective study.
Article in Journal of cardiothoracic surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03916965 (Prospective Observational Cohort Study in Patients With SIDSMA Treated With Stents), which is not on this map. Not yet cited in PubMed.
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Prospective Observational Cohort Study in Patients With SIDSMA Treated With Stents
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13 authors.
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Abstract
backgroundEndovascular stenting is a treatment option for spontaneous isolated dissection of superior mesenteric artery (SIDSMA). We aim to provide the prospective short-term data of the endovascular treatment for SIDSMA.
methodsOne hundred two patients were enrolled in the study between April 1, 2019, and March 12, 2021. The primary outcomes were primary patency and complete remodeling of SIDSMA in the first 12 months after endovascular stenting.
resultsThe participants had a mean age of 54.1 ± 7.7 years, and 95.1% were male. The most common symptom was abdominal pain. All patients underwent stent implantation, with a mean of 2.3 stents. The median follow-up duration was 38 (range 12–50) months. The primary patency rate was 100% at 1 month, 95.3% at 6 months, 92.9% at 12 months, and 92.9% at 36 months. All cases of restenosis occurred in the proximal portion of the superior mesenteric artery (SMA), with 83.3% (5/6) occurring within the initial 7 postoperative months. Two patients (2%) with severe stenosis required a second intervention. The complete remodeling rate was 56.9%, 73.6%, 75.9%, and 82.3% at 1, 6, 12, and 36 months, respectively. The symptom relief rate was 90.7% at 12 months and 94.6% at 36 months.
conclusionsEndovascular treatment for SIDSMA had satisfactory short-term primary patency and complete remodeling rates, with feasible symptom relief and a low dissection recurrence rate.
trial registrationThis prospective single-center study was approved by our center (clinical trial registration number: NCT03916965).
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