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1.
Ann Pediatr Cardiol ; 15(2): 121-127, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36246746

RESUMO

Background: Balloon angioplasty (BA) for aortic coarctation in neonates and infants remains controversial due to high recurrence rate and vascular complications. Aim: This study aimed to determine the safety and outcome of percutaneous treatment of coarctation in neonates and infants and to share the initial experience of strategy of prepartial dilatation with high-pressure noncomplaint balloon before final targeted dilatation using low-pressure compliant balloon. Materials and Methods: Retrospective analysis of records of all neonates and infants aged <6 months who underwent BA either using only low-pressure balloon (Group A) or those with prepartial dilatation using high-pressure noncomplaint balloon followed by low-pressure compliant balloon (Group B) between July 2017 and February 2020 was performed. Demographic, clinical, echocardiographic, interventional, and follow-up data were collected for all. Results: A total of 51 patients (41.2% neonates) were included in the study. Median age was 1 month 14 days (60.8% girls) and mean weight was 3.6 ± 1.5 kg. The mean peak trans-coarctation gradient was 53 ± 12 (34-80) mmHg. The final pressure gradient dropped to <10 mmHg in all cases of Group B and only in 26.3% (5) patients of Group A (P < 0.001). Recoarctation rate was 25.5% (13) overall and was significantly higher in Group A patients (P < 0.001), in those with borderline/mildly hypoplastic arch (P = 0.04) and in those with postprocedure gradient between 10 and 20 mmHg (P = 0.02). Median time to re-coarctation was significantly delayed in Group B (P < 0.001). There were no major complications or mortality in either group. Conclusions: BA in neonates and young infants has an excellent short and mid-term safety and efficacy. The recoarctation rate is significantly reduced as well as delayed with prepartial dilatation using high-pressure noncompliant balloon.

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3.
BMJ Case Rep ; 20162016 Mar 04.
Artigo em Inglês | MEDLINE | ID: mdl-26944369

RESUMO

Invasive aspergillosis is a severe fungal infection that primarily affects immunocompromised patients. We report a case of invasive aspergillosis presenting as a febrile respiratory infection with a cardiac mass in an immunocompetent patient. Excision of the intracardiac mass followed by histopathological examination confirmed the diagnosis. The patient was managed with voriconazole, to which he responded well. Rare occurrence of an intracardiac mass with systemic aspergillosis in an immunocompetent host is discussed in this case report.


Assuntos
Aspergilose/diagnóstico , Cardiopatias/diagnóstico por imagem , Cardiopatias/microbiologia , Administração Intravenosa , Antifúngicos/administração & dosagem , Aspergilose/tratamento farmacológico , Aspergilose/microbiologia , Aspergilose/cirurgia , Aspergillus fumigatus/isolamento & purificação , Diagnóstico Diferencial , Ecocardiografia/métodos , Cardiopatias/tratamento farmacológico , Cardiopatias/imunologia , Humanos , Imunocompetência , Masculino , Infecções Respiratórias/diagnóstico , Infecções Respiratórias/imunologia , Infecções Respiratórias/microbiologia , Resultado do Tratamento , Voriconazol/administração & dosagem , Adulto Jovem
4.
Asian Cardiovasc Thorac Ann ; 24(2): 195-7, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25281764

RESUMO

Management of vascular ring is always a matter of great concern. There is limited literature on management of carbon dioxide retention in mechanically ventilated patients with vascular rings due to double aortic arch, while awaiting corrective cardiac surgery. A 29-day-old girl with complete duplicated double aortic arch, left descending aorta, and a left patent ductus arteriosus, had severe upper respiratory tract obstruction with carbon dioxide retention. She was managed successfully by endotracheal tube manipulation.


Assuntos
Obstrução das Vias Respiratórias/terapia , Aorta Torácica/anormalidades , Tubos Torácicos , Intubação Intratraqueal/instrumentação , Stents , Estenose Traqueal/terapia , Malformações Vasculares/complicações , Adulto , Obstrução das Vias Respiratórias/diagnóstico , Obstrução das Vias Respiratórias/etiologia , Obstrução das Vias Respiratórias/fisiopatologia , Aorta Torácica/diagnóstico por imagem , Aorta Torácica/cirurgia , Aortografia/métodos , Permeabilidade do Canal Arterial/complicações , Permeabilidade do Canal Arterial/diagnóstico , Desenho de Equipamento , Feminino , Humanos , Respiração Artificial , Tomografia Computadorizada por Raios X , Estenose Traqueal/diagnóstico , Estenose Traqueal/etiologia , Estenose Traqueal/fisiopatologia , Resultado do Tratamento , Malformações Vasculares/diagnóstico , Malformações Vasculares/cirurgia
5.
Artigo | IMSEAR | ID: sea-188687

RESUMO

Background: Transcatheter device closure of ostium secundum atrial septal defect is a safe & effective intervention in older children, & is usually done under transesophageal echocardiography guidance. However, the procedure under transthoracic echocardiography guidance, especially in smaller children, is done only at few centers, the data of which is scarce. Methods: A prospective study was undertaken to assess the mid-term efficacy and outcome of transcatheter device closure of ostium secundum atrial septal defect under transthoracic echocardiographic guidance, in children <15 Kg. Results: Eighty three children with ostium secundum atrial septal defect were included in the study. Median age of the study population was 3.5 years (1.9-5.6 years), and median weight of 11.6 Kg (7.6 - 14.9 Kg). The primary and secondary procedural success rates were 94% and 96.4% respectively. Post procedure patients were followed up for 12-30 months. Device related major complications were encountered in 4 (4.8%) cases. The total occlusion rates of the defect at 24 hours, 1 month and 3 months post procedure were 94%, 98.8% and 100% respectively. Conclusion: The transcatheter device closure of ostium secundum atrial septal defect under transthoracic echocardiography guidance, in children <15 Kg, has a high short and mid-term safety and efficacy.

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