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1.
Catheter Cardiovasc Interv ; 68(2): 193-8, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16810700

ABSTRACT

OBJECTIVES: To evaluate whether double balloon pulmonary valvuloplasty (DBPV) with the Multi-Track system (MTS) may help to simplify the procedure. BACKGROUND: DBPV is usually required for patients with pulmonary valve stenosis with large annulus. However, it needs two venous accesses and can be technically demanding. METHODS: From 07/03, 20 consecutive patients (19 +/- 10 yrs) with typical pulmonary valve stenosis underwent DBPV using the MTS (G1). The results were compared with those achieved by conventional DBPV performed in a matched historical group of 28 patients (21 +/- 11 yrs; P = NS) (G2). RESULTS: MTS balloons were easily advanced through the skin and inflated across the valve. Similar results were observed in regards to residual gradients (12 +/- 11 vs 14 +/- 10 mm Hg; P = NS) and right ventricular to systemic pressures (0.35 +/- 0.22 vs 0.37 +/- 0.26; P = NS). Procedure and fluoroscopic times were significant lower in G1 (78 +/- 24 vs 126 +/- 28; 15 +/- 12 vs 25 +/- 8 min, respectively; both P < 0.001). There was no major complication. Median follow-up was 1.8 yr for G1 and 5 yr for G2 (P = 0.037). At the last visit, peak instantaneous gradient across the right ventricular outflow tract by echocardiography was a mean 22 +/- 10 mm Hg for G1 and 25 +/- 9 mm Hg for G2 (P = NS). No patient had severe pulmonary insufficiency or required reintervention. CONCLUSIONS: The use of the MTS helped to expedite the procedure providing satisfactory midterm clinical outcomes, similar to those observed with the conventional DBPV technique.


Subject(s)
Catheterization/methods , Pulmonary Valve Stenosis/therapy , Adolescent , Adult , Catheterization/instrumentation , Feasibility Studies , Female , Humans , Male , Treatment Outcome
2.
Rev Bras Cardiol ; 14(02): 126-132, abr/mai/jun 2006. ilus, tab
Article in Portuguese | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1066267

ABSTRACT

Na última década, o fechamento percutâneo da comunicação interatrial tipo ostium secundum (CIA) emergiu como ótima alternativa terapêutica. Adultos com CIA representam um grupo de risco para o tratamento cirurgico devido a maior incidência de complicações que em crianças. Método: Neste estudo, comparamos a segurança e eficácia entre os dois métodos terapêuticos em pacientes >40 anos. Os pacientes foram alocados nos Grupos: Grupo I (GI) - percutâneo: 29 pacientes; Grupo II (GII) - cirúrgico: 20 pacientes, de acordo com a disponibilidade do uso de próteses e preferência do médico d referência e seguidos prospectivamente em um período de tempo contemporâneo. Resultados: Não houve diferença estatística entre os grupos em relação à idade, peso, Qp/Qs, pressão média da artéria pulmonar, pressão diastólica final do ventrículo esquerdo e prevalência de arritmias...


Subject(s)
Cardiac Catheterization , Heart Septal Defects, Atrial
3.
Catheter Cardiovasc Interv ; 68: 193-198, 2006.
Article in English | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1061838

ABSTRACT

the Multi-Track system (MTS) may help to simplify the procedure. Background: DBPV


is usually required for patients with pulmonary valve stenosis with large annulus. However,


it needs two venous accesses and can be technically demanding. Methods: From


07/03, 20 consecutive patients (19 6 10 yrs) with typical pulmonary valve stenosis


underwent DBPV using the MTS (G1). The results were compared with those achieved


by conventional DBPV performed in a matched historical group of 28 patients (21 6


11 yrs; P = NS) (G2). Results: MTS balloons were easily advanced through the skin and


inflated across the valve. Similar results were observed in regards to residual gradients


(12 6 11 vs 14 6 10 mm Hg; P = NS) and right ventricular to systemic pressures (0.35


6 0.22 vs 0.37 6 0.26; P = NS). Procedure and fluoroscopic times were significant


lower in G1 (78 6 24 vs 126 6 28; 15 6 12 vs 25 6 8 min, respectively; both P < 0.001).


There was no major complication. Median follow-up was 1.8 yr for G1 and 5 yr for G2


(P = 0.037). At the last visit, peak instantaneous gradient across the right ventricular


outflow tract by echocardiography was a mean 22 6 10 mm Hg for G1 and 25 6 9 mm


Hg for G2 (P = NS). No patient had severe pulmonary insufficiency or required reintervention.


Conclusions: The use of the MTS helped to expedite the procedure providing


satisfactory midterm clinical outcomes, similar to those observed with the conventional


Subject(s)
Heart Defects, Congenital , Pulmonary Valve Stenosis , Ultrasonography, Interventional
4.
Revista Brasileira de Cardiologia Intensiva ; 13(3): 231-239, jul.ago.set 2005. tab
Article in Portuguese | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1067294

ABSTRACT

A hipertensão arterial pulmonar (HAP) secundária a cardiopatias congênitas é uma enfarmidade comum em nosso meio devida a referências tardias para o tratamento. Nos pacientes com HAP, a avaliação hemodinâmica é um método importante para definir a reversibilidade do qudro e a indicação operatória. Neste artigo, revisamos os principais aspectos sobre a avaliação hemodinâmica da HAP na sala de cateterismo, discutindo os conceitos importantes para o cardiolodiasta (pediátrico e de adultos), intensivista ecocardiografista, cirurgião cardíaco e , principalmente, para o cardiologista invasivo (hemodinamicista).


Subject(s)
Infant, Newborn , Infant , Adult , Middle Aged , Humans , Heart Defects, Congenital , Hypertension, Pulmonary/congenital , Nitric Oxide/therapeutic use
5.
Catheter Cardiovasc Interv ; 61(3): 403-10, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14988905

ABSTRACT

Percutaneous closure of perimembranous ventricular septal defects (VSDs) has been feasible, safe, and effective with the new Amplatzer membranous septal occluder. We report further experience with this device with emphasis on morphological aspects of the VSDs and technical issues. Ten patients (median age and weight, 14 years and 34.5 kg, respectively) with volume-overloaded left ventricles underwent closure under general anesthesia and transesophageal guidance (TEE). The VSD diameter was 7.1 +/- 4.0 mm by angiography and 7.8 +/- 3.7 mm by TEE. Three patients had defects associated with aneurysm-like formations (two with multiple exit holes), four had defects shrouded by extensive tricuspid valve tissue, two had defects with little or no tricuspid valve involvement, and one had a right aortic cusp prolapse with trivial aortic regurgitation. Implantation was successful in all patients, although in two the initial device had to be changed for a larger one. Kinkings in the delivery sheath, inability to position the sheath near the left ventricular apex, and device prolapse through the VSD prompted modifications in the standard technique of implantation. Device orientation was excellent except in one case. Nine patients had complete occlusion within 1-3 months. Device-related aortic or tricuspid insufficiency, arrhythmias, and embolization were not observed. Two patients had slight gradients across the left ventricular outflow tract, normalizing after 3 months. The Amplatzer membranous septal occluder was suitable to close a wide range of perimembranous VSD sizes and morphologies with good short-term outcomes. Longer follow-up is required.


Subject(s)
Heart Septal Defects, Ventricular/therapy , Adolescent , Anesthesia, General , Echocardiography, Transesophageal , Humans , Prostheses and Implants , Radiography, Interventional
6.
Catheter. cardiovasc. interv ; 61: 1-8, 2004. ilus
Article in English | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1061878

ABSTRACT

Percutaneous closure of perimembranous ventricular septal defects (VSDs) has beenfeasible, safe, and effective with the new Amplatzer membranous septal occluder. Wereport further experience with this device with emphasis on morphological aspects of theVSDs and technical issues. Ten patients (median age and weight, 14 years and 34.5 kg,respectively) with volume-overloaded left ventricles underwent closure under generalanesthesia and transesophageal guidance (TEE). The VSD diameter was 7.1 4.0 mm byangiography and 7.8 3.7 mm by TEE. Three patients had defects associated withaneurysm-like formations (two with multiple exit holes), four had defects shrouded byextensive tricuspid valve tissue, two had defects with little or no tricuspid valve involvement,and one had a right aortic cusp prolapse with trivial aortic regurgitation. Implantationwas successful in all patients, although in two the initial device had to be changedfor a larger one. Kinkings in the delivery sheath, inability to position the sheath near theleft ventricular apex, and device prolapse through the VSD prompted modifications in thestandard technique of implantation. Device orientation was excellent except in one case.Nine patients had complete occlusion within 1–3 months. Device-related aortic or tricuspidinsufficiency, arrhythmias, and embolization were not observed. Two patients hadslight gradients across the left ventricular outflow tract, normalizing after 3 months. TheAmplatzer membranous septal occluder was suitable to close a wide range of perimembranousVSD sizes and morphologies with good short-term outcomes. Longer follow-upis required.


Subject(s)
Arrhythmias, Cardiac , Heart Septal Defects , Heart Ventricles
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