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1.
Chinese Journal of Cardiology ; (12): 476-480, 2023.
Article in Chinese | WPRIM | ID: wpr-984678

ABSTRACT

Objective: To assess the safety and efficacy of transcatheter fenestration closure following Fontan procedure with an atrial septal occluder. Methods: This is a retrospective study. The study sample consists of all consecutive patients who underwent closure of a fenestrated Fontan baffle at Shanghai Children's Medical Center Affiliated to Shanghai Jiaotong University School of Medicine between June 2002 and December 2019. The indications of Fontan fenestration closure included that normal ventricular function, targeted drugs for pulmonary hypertension and positive inotropic drugs were not required prior the procedure; and the Fontan circuit pressure was less than 16 mmHg (1 mmHg=0.133 kPa) and no more than a 2 mmHg increase during test occlusion of the fenestration. Electrocardiogram and echocardiography were reviewed at 24 hours, 1, 3, 6 months and annually thereafter post procedure. Follow-up information including clinical events and complications related to Fontan procedure was recorded. Results: A total of 11 patients, including 6 males and 5 females, aged (8.9±3.7) years old were included. The types of Fontan were extracardiac conduits (7 cases) and intra-atrial duct (4 cases). The interval between percutaneous fenestration closure and the Fontan procedure was (5.1±2.9) years. One patient reported recurrent headache after Fontan procedure. Successful fenestration occlusion with atrial septal occluder was achieved in all patients. Compared with prior closure, Fontan circuit pressure ((12.72±1.90) mmHg vs. (12.36±1.63) mmHg, P<0.05), and aortic oxygen saturation ((95.11±3.11)% vs. (86.35±7.26)%, P<0.01) were increased. There were no procedural complications. At a median follow-up of (3.8±1.2) years, there was no residual leak and evidence of stenosis within the Fontan circuit in all patient. No complication was observed during follow-up. One patient with preoperative headache did not have recurrent headache after closure. Conclusions: If the Fontan pressure is acceptable by test occlusion during the catheterization procedure, Fontan fenestration could be occluded with the atrial septum defect device. It is a safe and effective procedure, and could be used for occlusion of Fontan fenestration with varying sizes and morphologies.


Subject(s)
Child , Male , Female , Humans , Child, Preschool , Septal Occluder Device , Retrospective Studies , Atrial Fibrillation , Cardiac Catheterization/methods , China , Fontan Procedure/methods , Treatment Outcome
2.
Int. j. cardiovasc. sci. (Impr.) ; 34(5): 523-530, Sept.-Oct. 2021. tab, graf
Article in English | LILACS | ID: biblio-1340048

ABSTRACT

Abstract Background: Fontan circulation can be associated with significant morbidity, especially Protein-Losing Enteropathy (PLE). Echocardiographic parameters can provide valuable diagnostic information about a patient's risk of developing PLE after Fontan surgery. Objectives: To describe echocardiographic/ultrasonographic parameters associated with PLE in patients after Fontan surgery through a systematic review with meta-analysis. Methods: A literature search was performed in electronic databases to identify relevant studies about echocardiographic parameters and PLE prediction in children after Fontan surgery. The search terms used were: "echocardiography", "ultrasonography", "Fontan," and "protein-losing enteropathy". A p < 0.05 was considered statistically significant. Results: A total of 653 abstracts were obtained from electronic databases and bibliographic references. From these, six articles met criteria to be included in the qualitative analysis and three in the quantitative (meta-analysis). The resistance index in the superior mesenteric artery was described in three studies, and the quantitative analysis showed statistical significance (p < 0.001). Other echocardiographic and ultrasonographic parameters were also described, albeit in single studies not allowing a meta-analysis. Conclusion: This systematic review with meta-analysis identified echocardiographic and ultrasonographic parameters related to PLE in patients with Fontan physiology. Vascular ultrasonography seems to play a prominent role in this aspect, but additional studies are needed to increase the degree of evidence.


Subject(s)
Humans , Male , Female , Protein-Losing Enteropathies/diagnostic imaging , Fontan Procedure/methods , Echocardiography/methods , Ultrasonography/methods , Fontan Procedure/adverse effects
3.
Arq. bras. cardiol ; 112(2): 130-135, Feb. 2019. tab, graf
Article in English | LILACS | ID: biblio-983830

ABSTRACT

Abstract Background: The Fontan-Kreutzer procedure (FK) was widely performed in the past, but in the long-term generated many complications resulting in univentricular circulation failure. The conversion to total cavopulmonary connection (TCPC) is one of the options for treatment. Objective: To evaluate the results of conversion from FK to TCPC. Methods: A retrospective review of medical records for patients who underwent the conversion of FK to TCPC in the period of 1985 to 2016. Significance p < 0,05. Results: Fontan-type operations were performed in 420 patients during this period: TCPC was performed in 320, lateral tunnel technique in 82, and FK in 18. Ten cases from the FK group were elected to conversion to TCPC. All patients submitted to Fontan Conversion were included in this study. In nine patients the indication was due to uncontrolled arrhythmia and in one, due to protein-losing enteropathy. Death was observed in the first two cases. The average intensive care unit (ICU) length of stay (LOS) was 13 days, and the average hospital LOS was 37 days. A functional class by New York Heart Association (NYHA) improvement was observed in 80% of the patients in NYHA I or II. Fifty-seven percent of conversions due to arrhythmias had improvement of arrhythmias; four cases are cured. Conclusions: The conversion is a complex procedure and requires an experienced tertiary hospital to be performed. The conversion has improved the NYHA functional class despite an unsatisfactory resolution of the arrhythmia.


Resumo Fundamento: O procedimento de Fontan-Kreutzer (FK) foi amplamente realizado no passado, mas a longo prazo gerou muitas complicações, resultando em falha na circulação univentricular. A conversão para conexão cavopulmonar total (CCPT) é uma das opções de tratamento. Objetivo: Avaliar os resultados da conversão de FK para CCPT. Métodos: Revisão retrospectiva de prontuários de pacientes submetidos à conversão de FK para CCPT no período de 1985 a 2016. Significância p < 0,05. Resultados: Operações do tipo Fontan foram realizadas em 420 pacientes durante este período: CCPT foi realizada em 320, técnica de túnel lateral em 82 e FK em 18. Dez casos do grupo FK foram eleitos para conversão em CCPT. Todos os pacientes submetidos à conversão de Fontan foram incluídos neste estudo. Em nove pacientes, a indicação deveu-se a arritmia não controlada e em um devido à enteropatia perdedora de proteínas. A morte foi observada nos dois primeiros casos. O tempo médio de internação na unidade de terapia intensiva (UTI) foi de 13 dias e o tempo médio de internação hospitalar foi de 37 dias. Uma classe funcional pela melhora da New York Heart Association (NYHA) foi observada em 80% dos pacientes em NYHA I ou II. Cinquenta e sete por cento das conversões devido a arritmias tiveram melhora das arritmias; quatro casos foram curados. Conclusões: A conversão é um procedimento complexo e requer que um hospital terciário experiente seja realizado. A conversão melhorou a classe funcional da NYHA, apesar de uma resolução insatisfatória da arritmia.


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Young Adult , Heart Bypass, Right/methods , Fontan Procedure/methods , Univentricular Heart/surgery , Heart Failure/surgery , Arrhythmias, Cardiac/surgery , Arrhythmias, Cardiac/mortality , Time Factors , Retrospective Studies , Treatment Outcome , Statistics, Nonparametric , Heart Bypass, Right/mortality , Fontan Procedure/adverse effects , Fontan Procedure/mortality , Coronary Circulation , Kaplan-Meier Estimate , Univentricular Heart/mortality , Heart Failure/mortality , Length of Stay
4.
Rev. bras. cir. cardiovasc ; 33(4): 353-361, July-Aug. 2018. tab, graf
Article in English | LILACS | ID: biblio-958436

ABSTRACT

Abstract Objective: Ebstein's anomaly remains a relatively ignored disease. Lying in the 'No Man's land' between congenital and valve surgeons, it largely remains inadequately studied. We report our short-term results of treating it as a 'one and a half ventricle heart' and propose that the true tricuspid annulus (TTA) 'Z' score be used as an objective criterion for estimation of 'functional' right ventricle (RV). Methods: 22 consecutive patients undergoing surgery for Ebstein's anomaly were studied. Echocardiography was performed to assess the type and severity of the disease, tricuspid annular dimension and its 'Z' score. Patients were operated by a modification of the cone repair, with addition of annuloplasty, bidirectional cavopulmonary shunt (BCPS) and right reduction atrioplasty to provide a comprehensive repair. TTA 'Z' score was correlated later with postplication indexed residual RV volume. Results: There was one (4.5%) early and no late postoperative death. There was a significant reduction in tricuspid regurgitation grading (3.40±0.65 to 1.22±0.42, P<0.001). Residual RV volume reduced to 71.96±3.8% of the expected volume and there was a significant negative correlation (rho −0.83) between TTA 'Z' score and indexed residual RV volume. During the follow-up of 20.54±7.62 months, the functional class improved from 2.59±0.7 to 1.34±0.52 (P<0.001). Conclusion: In Ebstein's anomaly, a higher TTA 'Z' score correlates with a lower postplication indexed residual RV volume. Hence, a complete trileaflet repair with offloading of RV by BCPS (when the TTA 'Z' score is >2) is recommended. The short-term outcomes of our technique are promising.


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Adult , Young Adult , Tricuspid Valve/surgery , Fontan Procedure/methods , Ebstein Anomaly/surgery , Cardiac Valve Annuloplasty/methods , Heart Ventricles/surgery , Postoperative Complications , Tricuspid Valve/diagnostic imaging , Echocardiography , Follow-Up Studies , Fontan Procedure/mortality , Recovery of Function , Ebstein Anomaly/mortality , Ebstein Anomaly/diagnostic imaging , Cardiac Valve Annuloplasty/mortality , Heart Ventricles/physiopathology , Medical Illustration
6.
Rev. chil. pediatr ; 87(5): 366-372, oct. 2016. graf, tab
Article in Spanish | LILACS | ID: biblio-830165

ABSTRACT

Introducción: Durante los últimos años múltiples pacientes con diagnóstico de corazón univentricular han sido tratados quirúrgicamente en nuestra institución mediante una anastomosis cavopulmonar total, de acuerdo al protocolo de corrección quirúrgica por etapas. Objetivo: Evaluar los resultados postoperatorios y la sobrevida de pacientes con síndrome de hipoplasia de corazón izquierdo (SHCI) sometidos a la operación de Fontan en comparación con pacientes con otras formas de corazón univentricular. Pacientes y método: Ciento dos pacientes fueron sometidos a la operación de Fontan entre abril de 1996 y marzo de 2014, 25 con SHCI (grupo I) y 77 con otras formas de corazón univentricular (grupo II). Se analizó la sobrevida, variables demográficas, estudio hemodinámico, morbimortalidad quirúrgica, ventilación mecánica, uso de drenajes, estancia postoperatoria, score de isótropos, necesidad de marcapasos y necesidad de revertir el Fontan take down. Resultados: La mortalidad perioperatoria fue del 4% (n = 1) para el grupo I y del 7,8% (n = 6) para el grupo II (p = 0,451). La única diferencia encontrada fue la estancia hospitalaria, siendo de 17 días (6-47) para el grupo I y 12 (5-103) para el grupo II(p = 0,017). El seguimiento promedio fue de 4,24 ± 2,08 años para el grupo I y de 8,7 ± 4,67 para el grupo II. La sobrevida a 8 años para ambos grupos fue de 88% y de 81% a 10 años para el grupo II. Conclusiones: La cirugía de Fontan tuvo una mortalidad similar en pacientes con SHCI en comparación con aquellos con otras formas de corazón univentricular, mientras que el primer grupo tuvo una mayor estancia hospitalaria. La sobrevida a largo plazo fue similar para ambos grupos.


Introduction: During the last few years, numerous patients with univentricular heart disease have been treated surgically with total cavopulmonary anastomosis according to a staged surgery protocol in our institution. Objective: To evaluate the perioperative outcomes and survival of patients with hypoplastic left heart syndrome (HLHS) after the Fontan procedure and compare them with other types of univentricular heart disease. Patients and method: A total of 102 patients underwent a Fontan procedure between April 1996 and March 2014, 25 with HLHS (group I), and 77 patients with other types of univentricular heart disease (group II). Groups survival, demographics, hemodinamic studies, morbimortality, mechanical ventilation, surgical drains, post-operative stay, isotopes score, pacemaker use, and requiriment of Fontan takedown were analyzed. Results: Intraoperative mortality was 4% (n = 1) for group I, and 7.8% (n = 6) for group II (P = .451). A difference was only found in hospital length of stay (LOS), being 17 days (6-47) for group I and 12 days (5-103) for group II (P = .017). Mean follow-up was 4.24 ± 2.08 years for group I, and 8.7 ± 4.67 for group II. Survival rate at 8 years for both groups was 88%, and 81% at 10 years for group II. Conclusions: The Fontan procedure had similar mortality, but longer LOS, in patients with HLHS compared to those with another types of single ventricle anatomy. Long term survival was comparable between both groups.


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Young Adult , Hypoplastic Left Heart Syndrome/surgery , Fontan Procedure/methods , Heart Defects, Congenital/surgery , Time Factors , Survival Rate , Retrospective Studies , Follow-Up Studies , Treatment Outcome , Hospital Mortality , Hypoplastic Left Heart Syndrome/mortality , Heart Defects, Congenital/physiopathology , Heart Defects, Congenital/mortality , Intraoperative Complications/epidemiology
7.
Rev. Soc. Cardiol. Estado de Säo Paulo ; 25(3): 147-155, jul.-set. 2015. tab
Article in Portuguese | LILACS | ID: lil-788856

ABSTRACT

O avanço no tratamento das cardiopatias tem permitido um progressivo número de mulheres com doenças cardíacas congênitas alcançarem a idade reprodutiva e a gravidez. Assim, o conhecimento sobre as modificações fisiológicas do ciclo gravídico-puerperal e sua interface com as lesões cardiacas estruturais é fundamental para a adequada conduta em portadoras de cardiopatia congênita durante a gestação. Neste artigo, discutiremos os fatores de prognóstico materno-fetal, as principais complicações, os cuidados obstétricos durante a gestação, parto e puerpério e o planejamento familiar da mulher com cardiopatia congênita.


Advances in the treatment of congenital heart defects has led to a gradually increase in the number of women with congenital heart defects reaching reproductive age and pregnancy. Thus, a knowledge of the physiological changes of the pregnant-puerperal cycle, and their interface with structural heart defects, is essential for adequate conduct in patients with congenital heart disease during pregnancy. In this article, we discusses thefactors of maternal-fetal prognosis, the main complications, the obstetric care provided during pregnancy, labor and puerperium, and family planning for women with congenital heart defects.


Subject(s)
Humans , Female , Adult , Heart Defects, Congenital/mortality , Heart Defects, Congenital/therapy , Prenatal Care/methods , Risk Factors , Pregnancy , Parturition , Fetal Development , Heredity , Familial Primary Pulmonary Hypertension , Maternal Mortality , Women , Fontan Procedure/methods
8.
Rev. bras. cir. cardiovasc ; 30(4): 497-500, July-Aug. 2015. tab, graf
Article in English | LILACS | ID: lil-763165

ABSTRACT

AbstractThe Glenn operation involving anastomosis of the superior vena cava to the pulmonary artery has been performed for palliative operations of many cyanotic congenital heart diseases in addition to the single ventricle since the 1960s. The classic procedure is done via median sternotomy and cardiopulmonary bypass. The benefits of this procedure without the use of cardiopulmonary bypass remain mixed within reported series. Cases using this approach and off-pump technique together in Latin-America have not yet been reported in the scientific literature.


ResumoA operação de Glenn envolvendo anastomose da veia cava superior à artéria pulmonar foi realizada como procedimento paliativo de muitas doenças cardíacas congênitas cianóticas, além do ventrículo único desde os anos 1960. O procedimento clássico é feito por esternotomia mediana e circulação extracorpórea. Os benefícios deste procedimento sem o uso de circulação extracorpórea permanecem incertos dentro da série relatada. Casos utilizando conjuntamente esta abordagem e a técnica sem circulação extracorpórea na América Latina ainda não foram relatados na literatura científica.


Subject(s)
Humans , Infant , Male , Fontan Procedure/methods , Pulmonary Artery/surgery , Thoracotomy/methods , Vena Cava, Superior/surgery , Anastomosis, Surgical/methods , Extracorporeal Circulation , Latin America , Medical Illustration , Photography , Pulmonary Atresia/surgery
9.
Rev. cuba. pediatr ; 86(4): 413-422, oct.-dic. 2014. tab, ilus
Article in Spanish | LILACS, CUMED | ID: lil-730316

ABSTRACT

INTRODU: la enteropatía perdedora de proteínas puede aparecer en la evolución de los pacientes con corazón univentricular que sobreviven a la derivación cavopulmonar total. Una vez que se diagnostica, la mortalidad es alta. OBJETIVO: identificar los posibles factores de riesgo de esta complicación. MÉTODOS: se realizó un estudio de cohorte prospectivo de la evolución en 74 pacientes con derivación cavopulmonar total, intervenidos en el Cardiocentro Pediátrico "William Soler", desde enero de 1992 hasta enero de 2011. RESULTADOS: el tiempo promedio de evolución fue de 8 años. Sufrió enteropatía perdedora de proteínas 8,1 % de los pacientes. Se presentó con mayor frecuencia en los operados con la técnica intratrial, en los operados con más de 6 años de edad, y en quienes sufrieron derrames pleurales persistentes en el posoperatorio inmediato. Se encontró relación significativa entre la enteropatía y la disfunción ventricular posoperatoria, con RR= 11,45 (IC: 95 %: 2,37 a 55,16). El análisis multivariado identificó a la disfunción ventricular como factor de riesgo. CONCLUSIÓN: la detección de disfunción ventricular en la evolución del paciente con derivación cavopulmonar debe orientar el tratamiento, en aras de evitar la aparición de enteropatía perdedora de proteínas.


INTRODUCTION: protein-losing enteropathy may occur in the progression of patients with univentricular heart, who survived total cavopulmonary shunt. Once diagnosed, the mortality rate of the condition is high. ONJECTIVE: to identify the possible risk factor of this complication. METHODS: a prospective cohort study of the progression of 74 patients with total cavopulmonary shunt was conducted from January 1992 through January 2011. They had been operated on at "William Soler" pediatric cardiac center. RESULTS: the average time of progression was 8 years. In this group, 8.1 % of patients suffered protein-losing enteropathy that was more frequently seen in patients operated on by the intraatrial technique, aged over 6 years and in those suffering persistent pleural effusion in the immediate postoperative period. Significant statistical relation was found between enteropathy and postoperative ventricular dysfunction with RR= 11.45 (CI: 95 %: 2.37 to 55.16). The multivariate analysis showed that the ventricular dysfunction was a risk factor. CONCLUSIONS: Detection of the ventricular dysfunction in the progression of a patient with cavopulmonary shunt should guide the treatment to avoid occurrence of protein-losing enteropathy.


Subject(s)
Humans , Protein-Losing Enteropathies/complications , Protein-Losing Enteropathies/etiology , Protein-Losing Enteropathies/prevention & control , Ventricular Dysfunction/prevention & control , Fontan Procedure/adverse effects , Fontan Procedure/methods , Prospective Studies , Cohort Studies
10.
Rev. bras. cir. cardiovasc ; 29(4): 595-605, Oct-Dec/2014. tab, graf
Article in Portuguese | LILACS | ID: lil-741722

ABSTRACT

Objetivo: Comparar a eficácia do AAS e da Varfarina na profilaxia da trombose em pacientes submetidos a operação cavopulmonar total. Avaliar se fatores de coagulação (VII, VIII e Proteína C), dados clínicos, fenestração ou fatores hemodinâmicos, interferem na trombose no pós-operatório. Métodos: Estudo prospectivo e randomizado de 30 pacientes, randomizados em Grupo I (Varfarina) e Grupo II (AAS), submetidos à derivação cavopulmonar total com tubo extracardíaco, entre 2008 e 2011, com seguimento de dois anos. Foram realizadas consultas clínicas que avaliavam efeitos colaterais e aderência. Realizado ecocardiograma transesofágico no pós-operatório imediato, 3, 6,12 e 24 meses; angiotomografia aos 6, 12 e 24 meses de pós-operatório para avaliação de alterações na parede interna do tubo ou trombos e cintilografia pulmonar, para avaliar possível TEP. Resultados: Dois óbitos no grupo I; 33,3% dos pacientes apresentaram trombo (46,7% no Grupo II). A ocorrência prévia de trombo e baixos níveis de proteína C da coagulação foram os únicos fatores que influenciaram no tempo livre de trombo (P=0,035 e 0,047). Avaliação angiotomográfica: 35,7% dos pacientes do grupo II tinham atapeteamento maior que 2 mm (P=0,082). Cintilografia: dois pacientes apresentaram TEP no grupo II. Cinco pacientes tiveram dificuldade de aderência, 4 no grupo I com INR variando de 1 a 6,4. Conclusão: A ocorrência prévia de trombo é um fator de risco para trombose no pós-operatório. Pacientes em uso de AAS tendem a depósito de material na parede do tubo. O número reduzido da amostra não permitiu concluir qual a droga mais eficaz na prevenção da trombose na população estudada. .


Objective: To compare the efficacy of aspirin and warfarin for prophylaxis of thrombosis in patients undergoing total cavopulmonary anastomosis. Evaluate whether coagulation factors (VII, VIII and protein C), clinical data, fenestration or hemodynamic factors, interfere with postoperative thrombosis. Methods: A prospective, randomized study of 30 patients, randomized into Group I (Warfarin) and Group II (AAS), underwent total cavopulmonary shunt with extracardiac conduit, between 2008 and 2011, with follow-up by clinical visits to evaluate side effects and adhesion. Performed transesophageal echocardiography in post operatory time, 3, 6,12 and 24 months; angiotomography at 6, 12 and 24 months to evaluate changes in the internal tube wall or thrombi and pulmonary scintigraphy to evaluate possible PTE. Results: Two deaths in group I; 33.3% of patients had thrombus (46.7% in Group II). The previous occurrence of thrombus and low levels of coagulation protein C were the only factors that influenced the time free of thrombus (P=0.035 and 0.047). Angiotomographic evaluation: 35.7% in group II presented material accumulation greater than 2 mm (P=0.082). Scintigraphy: two patients had PTE in group II. Five patients had difficulty to comply with the treatment, 4 in group I with INR ranging from 1 to 6.4. Conclusion: The previous occurrence of thrombus is a risk factor for thrombosis in the postoperative period. Patients using AAS tend to deposit material in the tube wall. The small sample size did not allow to conclude which is the most effective drug in the prevention of thrombosis in this population. .


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Male , Anticoagulants/therapeutic use , Aspirin/therapeutic use , Fontan Procedure/methods , Platelet Aggregation Inhibitors/therapeutic use , Thrombosis/prevention & control , Warfarin/therapeutic use , Echocardiography , Fontan Procedure/adverse effects , Fontan Procedure/mortality , Kaplan-Meier Estimate , Prospective Studies , Postoperative Complications/drug therapy , Postoperative Complications/prevention & control , Pulmonary Embolism/prevention & control , Pulmonary Embolism , Radionuclide Imaging , Statistics, Nonparametric , Time Factors , Tomography, X-Ray Computed , Treatment Outcome , Thrombosis/drug therapy , Thrombosis/mortality , Ventricular Dysfunction/physiopathology
11.
Article in English | IMSEAR | ID: sea-162163

ABSTRACT

In Fontan patients, reduced exercise capacity due to diminished cardiac output is a common finding with important prognostic implications. Beneficial effects have been shown for sildenafil treatment and regular exercise, but data comparing both strategies is scarce. We report on a female patient with Fontan circulation who underwent repeated cardiopulmonary exercise tests with either placebo or a single dose of 50mg sildenafil before and after 6months of supervised aerobic and resistance exercise. At baseline, V O2peak was 29.1ml/min/kg, and a marked increase to 32.8ml/min/kg was observed after administration of sildenafil. After the training period, V O2peak was 34.5ml/kg/min in the placebo test, and no further increase by sildenafil was possible (33.7ml/kg/min). Similar results were observed for exercise capacity at the ventilatory anaerobic threshold. In summary, this Fontan patient showed that regular exercise might use up and probably exceed the acute sildenafil effects on exercise capacity. Exercise should be considered as a primary treatment strategy within secondary prevention and rehabilitation after the Fontan procedure.


Subject(s)
Exercise Tolerance/drug effects , Female , Fontan Procedure/methods , Heart Defects, Congenital/drug therapy , Heart Defects, Congenital/epidemiology , Heart Defects, Congenital/rehabilitation , Heart Defects, Congenital/surgery , Heart Ventricles/abnormalities , Heart Ventricles/surgery , Humans , Piperazines/administration & dosage , Purines/administration & dosage , Sulfonamides/administration & dosage , Young Adult
14.
Rev. cuba. pediatr ; 85(3): 346-355, jul.-set. 2013.
Article in Spanish | LILACS | ID: lil-687736

ABSTRACT

Introducción: la atresia tricuspídea es la cardiopatía congénita cianótica que motiva mayor indicación de cirugía univentricular. El tratamiento quirúrgico consiste en separar las circulaciones sistémica y pulmonar a través de una derivación cavopulmonar total (proceder de Fontan). Objetivo: comparar la evolución posoperatoria del proceder de Fontan entre enero de 1990 y diciembre de 2010 en relación con el diagnóstico morfológico. Métodos: se ordenaron en 2 grupos de estudio (AT: atresia tricuspídea y No AT: con diagnóstico diferente a atresia tricuspídea). Las variables cualitativas y cuantitativas se analizaron a través de las pruebas chi cuadrado y t de student para un nivel de significación £ 0,05. Resultados: presentaron atresia tricuspídea 31 pacientes y 61 no atresia tricuspídea. En el posoperatorio 68 pacientes presentaron complicaciones, 23 con atresia tricúspidea (74,2 por ciento) y 45 con diagnóstico diferente a atresia tricuspídea (73,7 por ciento). Treinta pacientes presentaron efusiones pleurales persistentes durante el posoperatorio, 11 (35,5 por ciento) y 19 (31,4 por ciento) para la atresia tricúspidea y con diagnóstico diferente a atresia tricuspídea respectivamente. Fallecieron 18 enfermos, sin diferencia significativa entre ambos grupos. Durante el seguimiento, la causa de morbilidad más frecuentes fue por capacidad funcional disminuida de forma moderada o grave, en 13 pacientes con atresia tricúspidea (44,8 `por ciento) y en 20 (44,4 por ciento) en el otro grupo (p= 1). Conclusiones: el proceder de Fontan es una opción quirúrgica que permite la supervivencia de los pacientes con corazón univentricular asociada a morbilidad posoperatoria a largo plazo. El diagnóstico morfológico de atresia tricuspídea no se relaciona con la morbilidad y mortalidad


Introduction: tricuspid atresia is the cyanotic congenital heart disease that more frequently involves the indication of univentricular heart surgery. The surgical treatment consists of separating the systemic circulation from the pulmonary one through total cavopulmonary shunt (Fontan procedure). Objective: to compare the evolution of Fontan procedure postoperatively from January 1990 to December 2010 with the morphological diagnosis. Methods: the children were divided into 2 study groups (Triscupid atresia and Triscupid atresia-free with diagnosis different from that of tricuspid atresia). Chi square and Student's tests helped to analyze qualitative and quantitative variables for significance level £ 0.05. Results: tricuspid atresia was observed in 31 patients and 61 tricuspid atresia-free. In the postoperative period, 68 patients suffered complications, 23 with tricuspid atresia (74.2 percent) and 45 diagnosed with a disease other than tricuspid atresia (73.7 percent). Thirty patients had persistent pleural effusions during the postoperative period, 11 (35.5 percent) and 19 (31.4) in the tricuspid atresia group and in the tricuspid atresia-free group respectively. Eighteen patients died and no significant association was found in neither of the groups. During the follow-up, the most frequent cause of morbidity was reduced functional capacity either moderate or severe in 13 patients with tricuspid atresia (44.8 percent) and in 20 children (44.4 percent)from the other group (p= 1). Conclusions: Fontan procedure is a surgical option that allows the survival of patients with univentricular heart associated to long-term postoperative morbidity. The morphological diagnosis of tricuspid atresia is not related to morbility and mortality


Subject(s)
Humans , Tricuspid Atresia/surgery , Tricuspid Atresia/mortality , Fontan Procedure/methods , Disease-Free Survival
15.
Rev. Soc. Cardiol. Estado de Säo Paulo ; 21(4): 24-30, out.-dez. 2011. tab
Article in Portuguese | LILACS | ID: lil-619507

ABSTRACT

A operação de Fontan, descrita para o coração univentricular anatômico e funcional, originalmente para a atresia tricúspide em 1971, constitui-se na técnica paliativa hoje mais empregada na cardiologia pediátrica, em vista da mudança substancial da história natural dessas anomalias, em especial proporcionada após a modificação da técnica original para a cavopulmonar em 1988 por deLevall. No entanto, o “princípio Fontan” persiste e não se observa nele uma fisiologia ideal, dada a ausência de cavidade ventricular em conexão com a circulação pulmonar, e, por isso, o sistema hemodinâmico é pouco eficiente. Assim, observa-se que o débito cardíaco é diminuído e a pressão venosa sistêmica aumentada e, desses fatores, surgem complicações difíceis de serem evitadas a longo prazo. Constituem-se em causas de piora da qualidade de vida e até de morte, dependentes da disfunção hepática, anormalidades da coagulação sanguínea, enteropatia perdedora de proteínas, bronquite plástica, disfunção cardíaca, arritmias cardíacas, principalmente supraventriculares, tromboembolismo, hipoxemia e, daí, o surgimento de inúmeras outras consequências orgânicas. Essas alterações foram minimizadas com a técnica cavopulmonar, no entanto, necessitam de profilaxia mais cuidadosa ainda pela obediência rigorosa aos critérios de indicação da operação estabelecidos por Choussat, nos idos de 1977. Como principais, figuram presença de ritmo sinusal, função ventricular normal, desenvolvimento adequado da árvore arterial pulmonar, pressão média pulmonar menor que 15 mm Hg e resistência vascular pulmonar menor que 2 UW, além da boa função das valvas atrioventriculares. Em vista dos progressos diagnósticos, terapêuticos e cirúrgicos, portadores da operação de Fontan evoluem para a idade adulta com maior frequência, mas se constituem na causa principal da necessidade de transplante cardíaco dentre todas as cardiopatias congênitas nesta faixa etária.


Subject(s)
Humans , Heart Defects, Congenital/surgery , Heart Defects, Congenital/complications , Clinical Medicine/methods , Fontan Procedure/methods , Fontan Procedure , Heart Transplantation/methods , Heart Ventricles/abnormalities , Death, Sudden , Heart Failure/complications , Tachycardia/complications
16.
Rev. bras. cardiol. invasiva ; 19(3): 317-326, set. 2011. tab, ilus
Article in Portuguese | LILACS, SES-SP | ID: lil-607270

ABSTRACT

Introdução: A fenestração na cirurgia de Fontan (CF) melhora o resultado imediato no pós-operatório, por descompressão do circuito venoso-pulmonar e aumento do débito cardíaco, a despeito da dessaturação arterial de oxigênio e do risco de embolia paradoxal. Geralmente as fenestrações são ocluídas percutaneamente no seguimento a médio prazo. Este estudo teve como objetivo relatar a experiência institucional na oclusão percutânea da fenestração. Métodos: Estudo descritivo longitudinal, observacional, retrospectivo, de uma coorte não-consecutiva de pacientes. O procedimento foi realizado sob anestesia geral com a ajuda de ecocardiograma transesofágico. O teste de oclusão da fenestração com cateter Bermann angiográfico foi realizado antes da intervenção. Diferentes técnicas e dispositivos foram empregados para a oclusão da fenestração. Resultados: Entre abril de 2004 e dezembro de 2010, 12 pacientes (média de idade, 103,1 ± 88,6 meses; peso, 29,9 ± 12,7 kg) submetidos a CF (10 tubos extracardíacos, 2 túneis intra-atriais) foram tratados 44,1 ± 26,7 meses após a CF. Um paciente não tolerou o teste de oclusão com o balão, sendo contraindicado o procedimento. As próteses utilizadas foram: HelexTM (4 pacientes), AmplatzerTM (2 pacientes), Cardia AtriaseptTM (2 pacientes), FigullaTM (1 paciente), CeraTM (1 paciente), e 1 stent coberto Cheatham-PlatinumTM. Após a oclusão da fenestração, a saturação de oxigênio aumentou significativamente (82,1 ± 6,5% para 95,2 ± 3,2%), sem aumento significativo da pressão venosa central (12,4 ± 2,6 mmHg para 14,5 ± 2,3 mmHg) nem queda do débito cardíaco. Após o procedimento foi observado shunt residual imediato em 5 pacientes, que desapareceu antes da alta. Conclusões: A oclusão percutânea das fenestrações após CF pode ser realizada com várias opções de próteses e técnicas, sendo um procedimento seguro e efetivo e que resulta em normalização dos níveis de saturação.


BACKGROUND: Surgical fenestrations improve the early postoperative outcomes of the Fontan operation (FO) as a result of reduced systemic venous congestion and increased cardiac output, in spite of mild systemic desaturation and risk of paradoxical embolization. Generally, these fenestrations are occluded in the midterm follow-up. This study was aimed at reporting our experience with the percutaneous occlusion of Fontan fenestrations. METHODS: Longitudinal descriptive, observational, retrospective study of a non-consecutive cohort of patients. The procedure was performed under general anesthesia with the guidance of the transesophageal echocardiogram. A fenestration occlusion test was performed prior to the intervention using a Bermann angiographic catheter. Different techniques and devices were used to occlude fenestrations. RESULTS: From April 2004 to December 2010, 12 patients (mean age 103.1 ± 88.6 months; weight 29.9 ± 12.7 kg) undergoing FO (10 extracardiac conduits, 2 intra-atrial tunnels) were treated 44.1 ± 26.7 months after the operation. One patient failed the balloon occlusion test and the procedure was contraindicated. The following devices were used: HelexTM (4 patients), AmplatzerTM (2 patients), Cardia AtriaseptTM (2 patients), FigullaTM (1 patient), CeraTM (1 patient) and 1 covered Cheatham-PlatinumTM stent. After fenestration closure there was a significant increase in oxygen saturation (82.1 ± 6.5% to 95.2 ± 3.2%), without a significant increase in central venous pressures (12.4 ± 2.6 mmHg to 14.5 ± 2.3 mmHg) or reduction of cardiac output. Immediate residual shunt was observed in 5 patients, which disappeared before discharge. CONCLUSIONS: Percutaneous occlusion of Fontan fenestrations can be performed safely and effectively using a variety of techniques and devices resulting in normalization of systemic saturation levels.


Subject(s)
Humans , Male , Female , Prostheses and Implants , Angioplasty/methods , Angioplasty , Heart Defects, Congenital/surgery , Stents , Fontan Procedure/methods , Fontan Procedure , Catheterization/methods , Catheterization , Echocardiography/methods , Echocardiography
17.
Arq. bras. cardiol ; 97(1): e4-e7, jul. 2011. ilus
Article in Portuguese | LILACS | ID: lil-597673

ABSTRACT

Apesar dos avanços na cirurgia de Fontan, obstruções nos condutos extracardíacos podem ocorrer e causar deterioração clínica. Relatamos dois casos em que foram realizados implante de stent para correção de estenose na cirurgia de Fontan. Ascite era o sinal clínico comum; um paciente tinha enteropatia perdedora de proteínas.Todos os procedimentos obtiveram sucesso angiográfico e clínico.


Despite advances in Fontan surgery, obstruction in extracardiac ducts may occur and cause clinical deterioration. We report two cases of stent implantation for correction of stenosis in the Fontan surgery. Ascites was a common clinical sign; a patient was protein losing enteropathy. All procedures were angiographically and clinically successful.


Pese a los avances en la cirugía de Fontan, obstrucciones en los conductos extracardíacos pueden producirse y ocasionar deterioro clínico. Relatamos dos casos en que se llevaron a cabo implante de stent para la corrección de estenosis en la cirugía de Fontan. Ascitis era o el signo clínico común; un paciente tenía enteropatía perdedora de proteínas. Todos los procedimientos obtuvieron éxito angiográfico y clínico.


Subject(s)
Child , Female , Humans , Male , Fontan Procedure/adverse effects , Pulmonary Artery/surgery , Stents , Ascites/etiology , Constriction, Pathologic/surgery , Fontan Procedure/methods , Protein-Losing Enteropathies/etiology , Treatment Outcome , Vena Cava, Inferior/surgery
19.
Rev. bras. cir. cardiovasc ; 24(4): 463-469, out.-dez. 2009. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-540747

ABSTRACT

Objetivo: Estudos recentes de fluxo com modelos experimentais de anastomoses cavopulmonares totais (ACPTs) baseados em ressonância magnética e angiografia demonstram que este é um procedimento bem estabelecido para o tratamento de várias cardiopatias, mas o melhor arranjo espacial continua controverso. Nosso intuito é apresentar os resultados imediatos com três diferentes técnicas de ACPTs. Métodos: Ensaio clínico de ACPTs realizadas no período de janeiro de 2005 a julho de 2008 com 40 pacientes, com idade média de 6,4 ± 3,2 anos, com Glenn prévio. Os pacientes foram divididos em três grupos, dependendo da técnica cirúrgica empregada: Grupo 1 (G1) - túnel lateral; Grupo 2 (G2) - conduto extracardíaco; Grupo 3 (G3) - conduto intracardíaco dirigido para o ramo esquerdo de artéria pulmonar, todos com fenestração. Foram avaliadas variáveis pré e pós-operatórias. Resultados: Foram incluídos 11 pacientes no G1, 10 no G2 e 19 no G3. As variáveis pré-operatórias foram semelhantes nos três grupos (P>0,05). A mortalidade foi maior nos Grupos 1 e 2 (9,1 por cento e 10,0 por cento, respectivamente), comparadas ao Grupo 3 (zero), porém sem significância estatística (P=0,3841). Efusão pleural foi ausente no Grupo 3, diferença significativa (P=0,0128) em relação aos outros grupos (40,0 por cento e 33,3 por cento). A mediana do tempo de hospitalização pós-operatória foi menor no Grupo 3 (8 dias), em relação aos grupos 1 e 2 (18 e 13 dias, respectivamente) (P=0,0164). Conclusão: A técnica de conduto intracardíaco foi associada a menor morbidade pós-operatória, sendo a opção atual do nosso serviço na anastomose cavopulmonar total.


Objectives: Recent experimental flow studies based on angiography and magnetic resonance have shown that total cavopulmonary anastomosis (TCPA) is a valid concept for surgical treatment of many congenital heart defects, but there is not agreement of the best surgical arrangement. Our purpose is to analyze the immediate results with three different techniques of TCPA. Methods: We sought to analyze retrospectively all TCPA realized from January 2005 to July 2008; there were 40 patients, all with previous Glenn anastomosis, with mean age of 6.4 ± 3.2 years. Three different techniques were employed: Group 1 (G1) lateral tunnel, Group 2 (G2) extracardiac conduits, Group 3 (G3) intracardiac conduit directed to the left pulmonary artery. All patients had a fenestration done. Results: G1 had 11 patients, G2 10 patients and G3 19 patients. Preoperative data were similar in the 3 groups (P>0.05). Surgical mortality was higher in Groups 1 and 2 (9.1 percent and 10 percent) compared to Group 3 (0 percent) but there was no statistical significance (P=0.3841). Pleural effusion was absent in Group 3 (0 percent), which was statistically significant in relation to the other groups (P=0.0128). The hospitalization time was also significantly lower in G3 (8 days) in relation to G1 (18 days) and G2 (13 days) (P=0.0164). Conclusion Intracardiac TCPA was associated with lower postoperative morbidity and is currently our preferred technique.


Subject(s)
Child , Female , Humans , Male , Fontan Procedure , Fontan Procedure/adverse effects , Fontan Procedure/methods , Fontan Procedure/mortality , Pleural Effusion/etiology , Statistics, Nonparametric , Time Factors
20.
RELAMPA, Rev. Lat.-Am. Marcapasso Arritm ; 22(1): 35-39, jan.-mar. 2009. ilus
Article in Portuguese | LILACS | ID: lil-516435

ABSTRACT

A presença de ritmo não sinusal e arritmias características da doença sinusal é indício de mau prognóstico em pacientes com circulação de Fontan. O objetivo deste artigo é descrever o uso de algoritmo para minimizar o estímulo ventricular em um paciente pediátrico. Uma criança de oito anos, com cardiopatia cianótica complexa e circulação de Fontan, apresentou taquicardia ventricular (32% dos batimentos) mediada por bradicardia e disfunção ventricular...


Subject(s)
Humans , Male , Heart Defects, Congenital , Pacemaker, Artificial , Pulmonary Artery , Echocardiography , Fontan Procedure/methods
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