Garekar Swati, Meeran Talha, Dhake Shyam, Malankar Dhananjay
Division of Pediatric Cardiology, Fortis Hospital, Mulund, Mumbai, 400078 India.
Division of Advanced Heart Failure, Cardiac Transplant and Pulmonary Hypertension, Fortis Hospital, Mulund, Mumbai, 400078 India.
Indian J Thorac Cardiovasc Surg. 2021 Jan;37(1):89-92. doi: 10.1007/s12055-020-00993-2. Epub 2020 Aug 7.
Idiopathic pulmonary hypertension has a predictably morbid natural history with an absence of a uniformly successful treatment strategy. We describe our palliative surgical strategy in a symptomatic teenager. A 16-year-old girl, with a recent diagnosis of severe suprasystemic pulmonary hypertension, with severe right ventricular dysfunction, presented with syncope and World Health Organization functional class 4 symptoms. Blood and imaging work up revealed changes suggestive of pulmonary veno-occlusive disease. She failed to improve with oral pulmonary vasodilators and was listed for heart and lung transplant. Pending the transplant, a 10-mm handmade valved tube graft was placed between descending thoracic aorta and the proximal left pulmonary artery, on cardiopulmonary bypass. She had an uneventful recovery period with an early improvement in her symptoms. She was discharged home on aspirin and oral pulmonary vasodilators. At last follow up, 4 months post procedure, her functional capacity and right ventricular function had improved. The valved Potts shunt proved to be helpful in improving her symptomatology and as a bridge to transplant.
特发性肺动脉高压具有可预测的不良自然病史,且缺乏统一成功的治疗策略。我们描述了对一名有症状青少年的姑息性手术策略。一名16岁女孩,近期诊断为严重的系统性高血压,伴有严重的右心室功能障碍,出现晕厥及世界卫生组织功能分级为4级的症状。血液和影像学检查发现提示肺静脉闭塞性疾病的改变。她口服肺血管扩张剂后病情未改善,被列入心肺移植名单。在等待移植期间,在体外循环下,将一根10毫米的手工带瓣管道移植到胸降主动脉与左肺动脉近端之间。她恢复过程顺利,症状早期有所改善。她出院回家时服用阿司匹林和口服肺血管扩张剂。在术后4个月的最后一次随访中,她的功能能力和右心室功能有所改善。带瓣的波特分流术被证明有助于改善她的症状,并作为移植的桥梁。