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7篇 您的检索式:作者名="Massimo Chessa"
    题名 作者 年代 出处 被引量
1Early and late complications associated with transcatheter occlusion of secundum atrial septal defect显示文摘Massimo Chessa Mario Carminati Gianfranco Butera Roberta Margherita Bini Manuela Drago Luca Rosti Alessandro Giamberti Giuseppe Pomè Eduardo Bossone Alessandro Frigiola 2002Journal of the American College of Cardiology2002,,6:2
2Management of patients with patent foramen ovale and cryptogenic stroke: A collaborative, multidisciplinary, position paper显示文摘Christian Pristipino Gian Paolo Anzola Luigi Ballerini Antonio Bartorelli Moreno Cecconi Massimo Chessa Andrea Donti Achille Gaspardone Giuseppe Neri Eustaquio Onorato Gualtiero Palareti Serena Rakar Gianluca Rigatelli Gennaro Santoro Danilo Toni Gian Pao 2013Cathet Cardiovasc Intervent2013,,1:1
3Transcatheter Closure of Perimembranous Ventricular Septal Defects显示文摘Gianfranco Butera Mario Carminati Massimo Chessa Luciane Piazza Angelo Micheletti Diana Gabriella Negura Raul Abella Alessandro Giamberti Alessandro Frigiola 2007Journal of the American College of Cardiology2007,,12:1
4Treatment of isolated secundum atrial septal defects: Impact of age and defect morphology in 1,013 consecutive patients显示文摘Gianfranco Butera Enrico Romagnoli Mario Carminati Massimo Chessa Luciane Piazza Diana Negura Alessandro Giamberti Raul Abella Giuseppe Pomè Claudia Condoluci Alessandro Frigiola 2008American Heart Journal2008,,4:1
5Congenital Absence of Pericardium:The Largest Systematic Review in the Field on 247 Worldwide Cases(1977-Now)显示文摘Background:Congenital absence of pericardium(CAP),also known as pericardial agenesis,represents an uncommon cardiac abnormality and mostly incidental finding.It can be subdivided into complete and partial(left or right-sided)forms.Because of its infrequency,just case reports and a few case series have been released so far.This paper represents the largest systematic review in the field.Nine features(age at diagnosis,type,gender,clinical presentation,electrocardiography,imaging(ultrasounds,CT/MRI),concomitant cardiac defects,and outcome)were analysed.Methods:The electronic database PubMed was investigated from its establishment up to July 15th,2023.Just case reports and case series were included.Animal studies,papers that were not in English,Spanish,and Italian,and those manuscripts not reporting at least seven of the nine analysed features.were ruled out.The analysed data were reported mostly in terms of percentage.Results:One hundred eighty studies were included encompassing 247 patients.More than half of reviewed CAP cases were in males(63.2%).The mean age at diagnosis was 31.8±19.3 years;a range of 32 weeks of gestation-81 years).23.5%of the patients did not report any symptoms.The most common clinical presentations were chest pain(35.2%)and dyspnoea(29.2%).The most commonly seen ECG changes were right axis deviation(28.7%)and right bundle branch block(23.9%).CAP was suspected or diagnosed by echocardiography in 20.1%of cases.The diagnosis was made by CT and/or MRI in 61.9%of cases.CAP was left-sided in 71.2%,complete in 23.1%,and right-sided in 5.7%.A concomitant congenital heart defect was found in 22.7%,especially in the form of atrial septal defect(6.5%)and patency of ductus arteriosus(2.8%).The pericardial repair was required in 12.9% of the incomplete forms of the disease.Never did the complete form require surgical correction.The outcome appeared favourable in the vast majority of cases,with just 18 deaths(7.3%).Discussion:The main limitation of this systematic review is that it is based just on case reports and case series,due to the lack of large studies on CAP.However,it represents the largest analysis in the field.Due to the rarity of CAP establishing an International Registry is recommended.Pier Paolo Bassareo Aurelio Secinaro Paolo Ciliberti Massimo Chessa Marco Alfonso Perrone Kevin Patrick Walsh Colin Joseph Mcmahon 2023Congenital Heart Disease2023,18,6:0
6Percutaneous pulmonary valve implantation in a single artery branch: A preliminary experience显示文摘To describe preliminary experience of percutaneous pulmonary valve implantation, in a single pulmonary branch position. Two procedures in 2 patients from a single center are described, where implantation of percutaneous valves within a single pulmonary artery branch was technically successful. The procedural indication was pulmonary valve regurgitation and/or residual stenosis. The 2 patients were symptomatic. An Edwards Sapien? valve(Patient 1), and a Medtronic Melody? valve(Patient 2) were implanted. Both pts were discharged with an excellent valve function. In this report it is underlined that this modality is technically feasible and may be considered an option in patients with congenital heart defect under special circumstances.Massimo Chessa Gianfranco Butera Luca Giugno Angelo Micheletti Diana G Negura Mario Carminati 2015World Journal of Cardiology2015,7,10:0
7Multimodal Imaging with 3D-Holograms for Preoperative Planning in Pediatric Cardiac Surgery:A Unique Case Report显示文摘Multimodal imaging,including augmented or mixed reality,transforms the physicians’interaction with clinical imaging,allowing more accurate data interpretation,better spatial resolution,and depth perception of the patient’s anatomy.We successfully overlay 3D holographic visualization to magnetic resonance imaging images for preoperative decision making of a complex case of cardiac tumour in a 7-year-old girl.Federica Caldaroni Massimo Chessa Alessandro Varrica Alessandro Giamberti 2022Congenital Heart Disease2022,17,4:0
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