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1.
Indian Pediatr ; 2020 Feb; 57(2): 143-157
Artículo | IMSEAR | ID: sea-199479

RESUMEN

ustification: A number of guidelines are available for management of congenital heart diseases from infancy to adult life. However,these guidelines are for patients living in high income countries. Separate guidelines, applicable to Indian children, are required whenrecommending an intervention for congenital heart diseases, as often these patients present late in the course of the disease and mayhave co-existing morbidities and malnutrition. Process: Guidelines emerged following expert deliberations at the National ConsensusMeeting on Management of Congenital Heart Diseases in India, held on 10th and 11th of August 2018 at the All India Institute of MedicalSciences, New Delhi. The meeting was supported by Children’s HeartLink, a non-governmental organization based in Minnesota, USA.Objectives: To frame evidence based guidelines for (i) indications and optimal timing of intervention in common congenital heartdiseases; (ii) follow-up protocols for patients who have undergone cardiac surgery/catheter interventions for congenital heart diseases.Recommendations: Evidence based recommendations are provided for indications and timing of intervention in common congenitalheart diseases, including left-to-right shunts (atrial septal defect, ventricular septal defect, atrioventricular septal defect, patent ductusarteriosus and others), obstructive lesions (pulmonary stenosis, aortic stenosis and coarctation of aorta) and cyanotic congenital heartdiseases (tetralogy of Fallot, transposition of great arteries, univentricular hearts, total anomalous pulmonary venous connection, Ebsteinanomaly and others). In addition, protocols for follow-up of post surgical patients are also described, disease wise.

2.
Indian Heart J ; 2019 May; 71(3): 207-223
Artículo | IMSEAR | ID: sea-191691

RESUMEN

Introduction A number of guidelines are available for management of congenital heart diseases from infancy to adult life. However, these guidelines are for patients living in high-income countries. Separate guidelines, applicable to Indian children, are required when recommending an intervention for congenital heart diseases, as often these patients present late in the course of the disease and may have co-existing morbidities and malnutrition. Process Guidelines emerged following expert deliberations at the National Consensus Meeting on Management of Congenital Heart Diseases in India, held on the 10th and 11th of August, 2018 at the All India Institute of Medical Sciences. Objectives The aim of the study was to frame evidence-based guidelines for (i) indications and optimal timing of intervention in common congenital heart diseases and (ii) follow-up protocols for patients who have undergone cardiac surgery/catheter interventions for congenital heart diseases. Recommendations Evidence-based recommendations are provided for indications and timing of intervention in common congenital heart diseases, including left-to-right shunts, obstructive lesions, and cyanotic congenital heart diseases. In addition, protocols for follow-up of postsurgical patients are also described.

3.
4.
Indian Pediatr ; 2016 Oct; 53(10): 933-934
Artículo en Inglés | IMSEAR | ID: sea-179301
5.
Indian Pediatr ; 2013 September; 50(9): 885
Artículo en Inglés | IMSEAR | ID: sea-169981
6.
Indian Pediatr ; 2004 Oct; 41(10): 1048-50
Artículo en Inglés | IMSEAR | ID: sea-13727

RESUMEN

We describe case report of a 45 days old male baby with neonatal lupus erythematosus, who presented with 3rd degree congenital heart block and depigmented skin lesions on face and upper part of body. Diagnosis of the baby was confirmed by anti nuclear levels and skin biopsy.


Asunto(s)
Anticuerpos Antinucleares/análisis , Bloqueo Cardíaco/congénito , Humanos , Lactante , Lupus Eritematoso Cutáneo/complicaciones , Masculino , Pigmentación de la Piel/inmunología
7.
Indian Pediatr ; 2004 Feb; 41(2): 185-7
Artículo en Inglés | IMSEAR | ID: sea-15713

RESUMEN

Congenital afibrinogenemia/hypofibrinogenemia is an extremely rare coagulation disorder. We describe a case of congenital hypofibrinogenemia in a 6-year female child, who presented with recurrent ecchymotic spots with no frank bleeding.


Asunto(s)
Afibrinogenemia/complicaciones , Trastornos de la Coagulación Sanguínea/congénito , Niño , Terapia Combinada , Femenino , Hemorragia/etiología , Humanos , India , Pronóstico , Recurrencia , Índice de Severidad de la Enfermedad
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