Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
World J Pediatr Congenit Heart Surg ; 14(4): 500-502, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-37006129

RESUMO

Early and long-term outcomes in patients with pulmonary atresia-intact ventricular septum undergoing staged univentricular palliations have been known to be adversely affected by the presence of right ventricle-dependent coronary circulation. We describe a surgical technique to circumvent the coronary insufficiency caused by acute decompression of the right heart.


Assuntos
Atresia Pulmonar , Septo Interventricular , Humanos , Ventrículos do Coração/cirurgia , Resultado do Tratamento , Ponte Cardiopulmonar , Atresia Pulmonar/cirurgia , Septo Interventricular/cirurgia , Perfusão , Circulação Coronária , Descompressão
2.
World J Pediatr Congenit Heart Surg ; 14(2): 134-140, 2023 03.
Artigo em Inglês | MEDLINE | ID: mdl-36788380

RESUMO

Background: Reimplantation of the left pulmonary artery (LPA) and slide tracheoplasty has been our standard approach of care for patients with pulmonary artery sling (PAS) and tracheal stenosis. We present our experience, with emphasis on tracheal arborization and hypoplastic lungs; and their impact on long-term outcome of children with PAS and tracheal stenosis. Methods: It is a retrospective comparative study. Data were classified and analyzed based on the type of tracheobronchial arborization and normal versus hypoplastic lungs. Results: Seventy-five children operated between January 1994 and December 2019 (67 with normal lungs and 8 with lung hypoplasia/agenesis) were included. Patients with hypoplastic lungs had higher rates of preoperative ventilation (87.5%), postoperative ventilation (10 vs 8 days, P = .621), and mortality (50% vs 9%, P = .009) compared with those with normal lungs. Nineteen patients had tracheal bronchus (TB) variety and 30 patients had congenital long-segment tracheal stenosis (CLSTS) variety of tracheobronchial arborization. Endoscopic intervention was needed in 47.4% of patients with TB type and 60% with CLSTS type. CLSTS patients had higher rates of preoperative ventilation (60% vs 47.4%, P = .386), longer periods of postoperative ventilation (13 vs 6.5 days, P = .006), and ICU stay (15 vs 11 days, P = .714) compared with TB type. Conclusion: Surgical repair of PAS with tracheal stenosis has good long-term outcomes. All variations of tracheal anatomy can be managed with slide tracheoplasty. Persistence of airway problems requires intervention during follow-up as tracheal stenosis continues to be the Achilles heel.


Assuntos
Broncopatias , Cardiopatias Congênitas , Estenose Traqueal , Malformações Vasculares , Criança , Humanos , Lactente , Estenose Traqueal/cirurgia , Estenose Traqueal/congênito , Artéria Pulmonar/cirurgia , Artéria Pulmonar/anormalidades , Estudos Retrospectivos , Resultado do Tratamento , Traqueia/cirurgia , Cardiopatias Congênitas/cirurgia , Pulmão
3.
Ann Thorac Surg ; 113(3): 884-888, 2022 03.
Artigo em Inglês | MEDLINE | ID: mdl-33607054

RESUMO

BACKGROUND: Pulmonary artery sling (PAS) is usually associated with long-segment congenital tracheal stenosis (LSCTS). This combination of abnormalities can also be associated with lung hypoplasia abnormalities (hypoplasia, aplasia, or agenesis). This study analyzed the association of lung hypoplasia abnormalities with combined PAS and LSCTS and its influence on its surgical outcomes. METHODS: All patients (0 to 18 years) who underwent surgical procedures for both PAS and LSCTS from 1995 to 2019 were analyzed retrospectively for mortality, ventilation days, and intensive care unit days by dividing them into those with normal lungs (group 1) and hypoplastic lungs (group 2). RESULTS: Included were 75 patients (30 girls [40%]), who were a median age of 5.7 months (interquartile range [IQR], 2.9-13.3 months), median weight of 5.5 kg (IQR, 4.1-7.9 kg), and had a median follow-up of 99.8 months (IQR, 54.5-152.0 months); of these, 8 patients (10.7%) had hypoplastic right lung, comprising hypoplasia in 7 (87.5%), aplasia in 1 (12.5%), and agenesis in 0 (0%). There was a significant difference in mortality (group 1, 9.0%; group 2, 50%; P = .007) but no significant difference in median ventilation days (group 1, 9.0; group 2, 9.0; P = .89) or in median intensive care unit days (group 1, 14.0; group 2, 11.5; P = .44). CONCLUSIONS: Lung hypoplasia associated with PAS and LSCTS is usually right-sided. As a result of severe airway obstruction and single-lung physiology, there is a high requirement of preoperative cardiorespiratory support and a significant association with adverse surgical outcomes.


Assuntos
Anormalidades Múltiplas , Cardiopatias Congênitas , Pneumopatias , Anormalidades do Sistema Respiratório , Estenose Traqueal , Malformações Vasculares , Anormalidades Múltiplas/cirurgia , Constrição Patológica , Feminino , Cardiopatias Congênitas/cirurgia , Humanos , Lactente , Pulmão/anormalidades , Pneumopatias/complicações , Artéria Pulmonar/cirurgia , Estudos Retrospectivos , Traqueia/anormalidades , Estenose Traqueal/congênito , Estenose Traqueal/cirurgia , Resultado do Tratamento , Malformações Vasculares/complicações
4.
Front Cardiovasc Med ; 8: 760523, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-35141288

RESUMO

BACKGROUND: Vascular rings are rare congenital abnormalities of the aortic arch. There are many embryological variants including a double aortic arch. In symptomatic children, division of ring and release of airway structures may be sufficient. Persistence of symptoms can be related to an anterior angle formed between the two arches. The aim of this study is to evaluate the clinical efficacy in improving symptoms and on changing this angle at the primary surgery. METHODS: All children who had surgery for double aortic arch between 2005 and 2020, were studied. Relevant factors were analyzed for persistent symptoms including anatomical substrates and surgical details. RESULTS: A total of 87 out of 224 children had surgery for a double aortic arch. At presentation, airway symptoms (n = 74/87) were more common than esophageal symptoms (n = 27/87). Early onset symptoms within 1 year were seen in 49 children. In addition to division of one arch, surgical steps also included realigning the anterior left arch, thereby eliminating the acute angle in 36 children (after 2014). After surgery, symptom relief within 12 months following surgery was seen in 64% of children (56 out of 87) but in 27 out of 36 children (75%) with additional surgical modification, as against 29 out of 51 (57%) in those with division of the arch. Symptoms persisted beyond 1 year needing reintervention in eight children. CONCLUSION: Anterior arch angulation plays an important role in double aortic arch by causing a "nutcracker" phenomenon. Repair in double aortic arch should consider this aspect and include modification of surgical steps by realigning the corresponding aortic arch branches and an anterior pexy in selected cases.

5.
Semin Thorac Cardiovasc Surg ; 31(3): 571-572, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31005577

RESUMO

Rerouting of persistent left superior vena cava is necessary in correction of certain congenital cardiac conditions. Techniques previously described involve either an "intracardiac" baffle or an "extracardiac" connection between the left superior vena cava and the right atrium or its appendage or the right superior vena cava. We present a modification of the extracardiac technique, utilizing flaps of right and left atrial appendages in construction of the extra-anatomic tube. Using this technique in 7 patients, we obtained a tension-free, oblique anastomosis with vascular tissue circumferentially and potentially preserving growth.


Assuntos
Apêndice Atrial/cirurgia , Procedimentos Cirúrgicos Cardíacos , Cardiopatias Congênitas/cirurgia , Retalhos Cirúrgicos , Veia Cava Superior/cirurgia , Procedimentos Cirúrgicos Cardíacos/efeitos adversos , Cardiopatias Congênitas/diagnóstico por imagem , Cardiopatias Congênitas/fisiopatologia , Humanos , Resultado do Tratamento , Veia Cava Superior/anormalidades , Veia Cava Superior/diagnóstico por imagem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...