Carlo Uran

Dr. Carlo Uran

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Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 July 2020 in Monaldi Archives for Chest Disease
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CUCarlo Uran
Carlo Uran
GCGiacomo Di Chiara
Giacomo Di Chiara
BBBiagio Bosco
Biagio Bosco
DDDomenico D'ANdrea
Domenico D'ANdrea
PIPietro Iodice
Pietro Iodice
We report the case of a 40-year-old man, transferred from another hospital to our ICU because of acute coronary syndrome. Coronarography did not show coronary stenosis. Twenty-four hours monitoring EKG allowed diagnosis of Prinzmetal angina and appropriate therapy was administered. Six months after discharge due recurrence of symptoms, ranolazine was added to therapy. After one year the patient is symptoms free.

9 September 2021 in Monaldi Archives for Chest Disease
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CUCarlo Uran
Carlo Uran
Ranolazine derives from piperazine and has been approved as a drug for the therapy of chronic stable angina. It acts by selectively inhibiting the late sodium inward current. Moreover, ranolazine has other metabolic features which makes it effective in other diseases as well as coronary artery ones. In this paper I make an updated review of all possible therapeutic roles of ranolazine: through cardiology and beyond.

23 April 2026 in Journal of Clinical Medicine
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FZFrancesco Zanon
Francesco Zanon
CUCarlo Uran
Carlo Uran
VBVincenzo Bonfantino
Vincenzo Bonfantino
NBNatale Di Belardino
Natale Di Belardino
ALAntonio Lupo
Antonio Lupo
FNFranco Noventa
Franco Noventa
Background/Objectives: Heart failure (HF) is associated with substantial morbidity, impaired quality of life (QOL), and reduced functional capacity. In selected patients with symptomatic HF despite Optimal Medical Therapy (OMT), Cardiac Contractility Modulation (CCM) may be a therapeutic option. Identifying patients most likely to benefit from CCM remains an unmet need. The Predict-CCM study aims to evaluate long-term clinical and objective outcomes after CCM therapy and to assess the predictive value of pre-implant low-dose dobutamine stress echocardiography (LDDSE). Methods and Results: Predict-CCM is an independent, non-profit, multicenter, observational cohort study conducted in Italy, with both retrospective and prospective enrollment. The primary endpoint is the proportion of subjects with a clinical response to CCM at 12 months, defined as a ≥1-class reduction in NYHA class. Secondary clinical endpoints include reductions in HF-related hospitalizations, changes in QOL assessed by the Minnesota Living with Heart Failure Questionnaire (MLHFQ), and changes in NT-proBNP levels from baseline to follow-up. Outcomes will be evaluated in the overall cohort and in two subcohorts stratified by pre-implant LDDSE response: (1) reduction in left ventricular end systolic volume (LVESV) ≥ 15% (DeltaLVESV ≥ 15%); and (2) reduction in LVESV < 15% (DeltaLVESV < 15%). Assuming a 70% clinical response rate at 12 months, the estimated sample size is 120 patients. The study was approved by the Ethics Committee in March 2025. Enrollment will continue for 2 years, with a 12-month follow-up period after implant for each subject. Conclusions: This study may provide new criteria for patient selection and outcome assessment in CCM therapy. Left ventricular contractile reserve assessed by stress echocardiography may be a promising predictor of response.

5 March 2021 in Monaldi Archives for Chest Disease
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CUCarlo Uran
Carlo Uran
AGAngela Giojelli
Angela Giojelli
Aortic diseases cover a large spectrum of conditions, such as aortic aneurysm and acute aortic syndromes (i.e., dissections, intramural hematoma, penetrating atherosclerotic ulcer, traumatic aortic injuries, and pseudoaneurysms), genetic diseases (e.g., Marfan syndrome) and congenital abnormalities, such as coarctation of the aorta. These conditions may have an acute presentation; thus, if the acute aortic syndrome is the first sign of the disease, the prognosis is extremely poor. Prompt diagnosis and timely therapy are therefore mandatory. In this paper, we discuss a deceptive symptom of painless aortic dissection and its physiopathology. Furthermore, we briefly review the literature and discuss the management of diagnostic tools.

17 October 2026 in Clinical Autonomic Research
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CUCarlo Uran
Carlo Uran

28 October 2026 in Preprints.org
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CUCarlo Uran
Carlo Uran
AUAmbra Uccello
Ambra Uccello
Background: Reel syndrome, rotation of the generator on its transverse axis with coiling of the lead, is a rare cause of cardiac implantable electronic device failure. While described for transvenous systems, it is exceptionally rare in subcutaneous ICDs (S-ICD). Case presentation: A 63-year-old woman with dilated cardiomyopathy and S-ICD implanted in 2022 for secondary prevention in a standard subcutaneous pocket presented with a shock during exertion. Remote monitoring (LATITUDE) had not been activated. Device interrogation showed an inappropriate 80J shock due to myopotential oversensing after caudal retraction of the lead. Chest X-ray documented Reel syndrome with proximal coiling around the can and distal tip retracted to the subcostal region, >10 cm from the manubrio-sternal junction, with horizontalization of the shock coil, incompatible with effective defibrillation. Management: The system was explanted and a new S-ICD re-implanted using the intermuscular two-incision technique in the virtual space between serratus anterior and latissimus dorsi. The procedure was performed under ultrasound-guided serratus anterior plane block combined with parasternal block. The generator was anchored to the fascia with non-absorbable sutures. Defibrillation test was effective at 40J. Remote monitoring was activated. Conclusion: To our knowledge, this is one of the few documented cases of Reel syndrome in S-ICD with both radiographic and stored electrogram evidence of inappropriate 80J shock, rescued with intermuscular two-incision technique under ultrasound-guided serratus anterior plane block. Intermuscular fixation with non-absorbable sutures, combined with regional anesthesia and systematic remote monitoring, ensures device stability and maintains continuous defibrillation protection.