Doble salida del ventrículo derecho Survival rates Escrito por el personal de Mayo Clinic With treatment, long-term survival is high for many children with DORV. Studies have reported survival rates above 85%. There is no single survival rate for all types of DORV. The outlook depends on: The structure of your child's heart. The size of the ventricles and how well they work. The type of DORV. The type of repair. Survival rates describe groups of people and cannot predict what may happen for one child. In a study from Norway, 89.5% of children were alive five years after treatment. The same percentage of children were still alive 10 years after treatment. In a 2025 study of 1,135 people who had surgery for DORV, 96.3% were alive at five years, 93% at 10 years and 92.7% at 15 years. The need for another surgery increased over time. A 2024 study from several hospitals followed 81 children after a two-ventricle repair. At 10 years, 86% were alive. The outlook varied depending on the structure of the heart and how complex the repair was. Talk with your child's care team about what the survival statistics mean for your child and what to expect over time. Solicite una consulta Síntomas y causas Dec. 07, 2024 Comparte en: FacebookTwitter Living with defectos cardíacos congénitos en los niños? Connect with others like you for support and answers to your questions in the Transplants support group on Mayo Clinic Connect, a patient community. Transplants Discussions Anyone waiting for liver transplant and diagnosed with liver cancer? 56 Replies Thu, Sep 10, 2026 chevron-right Snapshots of hope: Life on the other side of transplant. 129 Replies Sun, Aug 16, 2026 chevron-right SPK (simultaneous pancreas and kidney) transplants 78 Replies Wed, Aug 12, 2026 chevron-right See more discussions Mostrar referencias Kliegman RM, et al., eds. Cyanotic congenital heart disease: Lesions associated with decreased pulmonary blood flow. In: Nelson Textbook of Pediatrics. 22nd ed. Elsevier; 2025. https://www.clinicalkey.com. Accessed Sept. 8, 2024. Libby P, et al., eds. Congenital heart disease in the adolescent and adult. In: Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine. 12th ed. Elsevier; 2022. https://www.clinicalkey.com. Accessed Sept. 8, 2024. Townsend CM Jr, et al. Congenital heart disease. In: Sabiston Textbook of Surgery: The Biological Basis of Modern Surgical Practice. 21st ed. Elsevier; 2022. https://www.clinicalkey.com. Accessed Sept. 8, 2024. Priya S, et al. Imaging spectrum of double-outlet right ventricle on multislice computed tomography. Journal of Thoracic Imaging. 2019; doi:10.1097/RTI.0000000000000396. Adam A, et al., eds. Congenital heart disease: General principles and imaging. In Grainger & Allison's Diagnostic Radiology. 7th ed. Elsevier; 2021. https://www.clinicalkey.com. Accessed Sept. 8, 2024. Stout KK, et al. 2018 AHA/ACC guideline for the management of adults with congenital heart disease: A report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2019; doi:10.1161/CIR.0000000000000603. What are congenital heart defects? National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov/health/health-topics/topics/chd. Accessed Sept. 8, 2024. Double outlet right ventricle. Merck Manual Professional Version. https://www.merckmanuals.com/professional/pediatrics/congenital-cardiovascular-anomalies/double-outlet-right-ventricle. Accessed Oct. 5, 2024. Bolin EH, et al. Maternal smoking and congenital heart defects, National Birth Defects Prevention Study, 1997-2011. Journal of Pediatrics. 2022; doi: 10.1016/j.jpeds.2021.09.005. Yoo S-J, et al. 3D printing in surgical management of double outlet right ventricle. Frontiers in Pediatrics. 2018; doi:10.3389/fped.2017.00289. Defectos cardíacos congénitos en los niñosSíntomasycausasDiagnósticoytratamientoMédicosydepartamentosAtención enMayoClinic Doble salida del ventrículo derechoSolicite una Consulta CON-20359709 Enfermedades y afecciones Defectos cardíacos congénitos en los niños