Transcatheter uterine artery embolization (UAE) for treatment of fibroids was first reported by Ravina in 1995. The continuous advance in the field of vascular Interventional Radiology has facilitated UAE, through the development of low profile catheters and particulate emboli such as polyvinyl alcohol particles (PVA), PVA microspheres and tris-acryl gelatine microspheres (TAGM). Prospective randomized studies such as the EMMY and REST trial that compare UAE with hysterectomy have proven scientifically that there is a place for UAE in the treatment of women with symptomatic fibroids. The QOL 5 years after hysterectomy or embolization is equal. Several registries and non-randomized trials have supported these findings. The trials have shown that UAE should be offered to women with symptomatic fibroids causing menorrhagia, as an alternative to hysterectomy (Level 1). The present document provides quality assurance guidelines regarding UAE for the treatment of symptomatic uterine fibroids.
Purpose: To investigate the effect of renal denervation (RDN) on blood pressure and renal function in refractory hypertension after renal artery recanalization and optimal medical therapy.
Percutaneous renal sympathetic denervation (RDN) is a very promising treatment strategy adopted to supplement antihypertensive therapy in patients with resistant hypertension. Despite the widespread performance of this procedure, serious complications during the procedure have not yet been reported. We report a case of transient renal artery stenosis during RDN complicated by late stenosis.
Patients with arterial hypertension responding suboptimally to drug treatment (i.e., those with resistant hypertension) represent a sizable group and a clinical challenge. Building upon prior favorable evidence for surgical renal sympathetic denervation and experimental data underlying the detrimental impact of the sympathetic nervous system on blood pressure control, transcatheter renal sympathetic denervation (TRSD) has been recently introduced into clinical practice. This procedure has been demonstrated safe and effective in reducing systolic and diastolic blood pressure in patients with resistant hypertension based on non-blinded randomized clinical trials, observational studies, and anecdotal cases. This evidence has led to approval of the devices in Europe and other countries, but not yet in the US, India, or Japan. Indeed, thousands of patients have already been treated with this procedure, with apparently satisfactory outcomes.
Purpose: To assess the displacement of the aorta and its visceral branch ostia after insertion of a rigid system including a stiff guidewire and endograft delivery system during endovascular aneurysm repair (EVAR).
Purpose: To describe a simple and quick technique for converting a Zenith bifurcated stent-graft to an aortouni-iliac device for emergency treatment of hemorrhage when a suitable marketed stent-graft is not readily available.
Purpose: To evaluate the impact of renal chimney grafts on anatomical suitability for endovascular aneurysm repair (EVAR) in ruptured abdominal aortic aneurysm (rAAA).
Purpose: To retrospectively review all patients undergoing late open conversion (LOC) after endovascular aneurysm repair (EVAR) in order to identify any clinical or technical predictors of poor outcome.
Purpose: To compare the vascular response after paclitaxel-coated nitinol drug-eluting stent (Zilver PTX) implantation for superficial femoral artery lesions after 6 and 12 months using optical coherence tomography (OCT).
Purpose: To test the ability of a drug-eluting balloon (DEB) to reduce recurrent in-stent restenosis (ISR) in diabetic patients with femoropopliteal stents.
Purpose: To evaluate the safety and feasibility of using drug-eluting balloons (DEBs) in the treatment of infrainguinal bypass graft stenoses.
Purpose: To report long-term outcomes of endovascular therapy (EVT) for aortoiliac bifurcation lesions.
Purpose: To compare the patency rates and clinical outcomes of balloon angioplasty vs. nitinol stent placement for patients with short (≤150 mm) as compared to long (>150 mm) femoropopliteal (FP) occlusive lesions.
Purpose: To assess the extent of early recoil in patients with critical limb ischemia (CLI) undergoing conventional tibial balloon angioplasty.
Purpose: To evaluate the performance of the Turbo Elite laser catheter in combination with the Turbo-Booster guiding catheter for the treatment of femoropopliteal in-stent restenosis (ISR).
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