Al-Naamani Nadine, Espitia H Gaudalupe, Velazquez-Moreno Hugo, Macuil-Chazaro Benjamin, Serrano-Lopez Arturo, Vega-Barrientos Ricardo S, Hill Nicholas S, Preston Ioana R
Pulmonary, Critical Care and Sleep Division, Tufts Medical Center, 800 Washington Street, Box 257, Boston, MA, 02111, USA.
Tufts Clinical and Translational Science Institute, Boston, MA, USA.
Lung. 2016 Apr;194(2):315-23. doi: 10.1007/s00408-016-9842-y. Epub 2016 Jan 9.
Chronic thromboembolic pulmonary hypertension (CTEPH) is characterized by precapillary pulmonary hypertension secondary to vaso-occlusive pulmonary vasculopathy and is classified as Pulmonary Hypertension Group 4. The aim of this study is to report the clinical experience of CTEPH in Mexico.
Consecutive patients diagnosed with CTEPH were identified from the Registro de Pacientes con Hipertension Pulmonar del Instituto de Seguridad y Servicio Social de los Trabajadores del Estado (REPHPISSSTE) registry between January 2009 and February 2014. Right heart catheterization was not routinely performed prior to August 2010 in the work-up of CTEPH.
We identified 50 patients with CTEPH; their median age was 63 years and 58 % were female. Patients had multiple associated co-morbidities and moderate hemodynamic impairment. All patients were treated with anticoagulation. Despite surgical evaluation for pulmonary endarterectomy (PEA), only one patient underwent PEA given the lack of infrastructure for post-operative care and lack of insurance for this procedure. Most of the patients were treated with sildenafil, bosentan, or both, with increasing use of rivaroxaban and sildenafil in recent years. The overall survival of the cohort was similar to that reported in other international registries, despite the limitations of care imposed by drug availability and surgical feasibility.
This is the first report on the CTEPH experience in Mexico. It highlights the similarity of patients in the REPHPISSSTE registry to those in international registries as well as the challenges that clinicians face in a resource-limited setting.
慢性血栓栓塞性肺动脉高压(CTEPH)的特征是继发于血管闭塞性肺血管病的毛细血管前肺动脉高压,被归类为肺动脉高压第4组。本研究的目的是报告墨西哥CTEPH的临床经验。
从2009年1月至2014年2月的墨西哥国家工人社会保障和服务研究所肺动脉高压患者登记处(REPHPISSSTE)中识别出连续诊断为CTEPH的患者。在2010年8月之前,CTEPH检查中未常规进行右心导管检查。
我们识别出50例CTEPH患者;他们的中位年龄为63岁,58%为女性。患者有多种合并症和中度血流动力学损害。所有患者均接受抗凝治疗。尽管对肺动脉内膜剥脱术(PEA)进行了手术评估,但由于缺乏术后护理基础设施和该手术的保险,只有1例患者接受了PEA。大多数患者接受了西地那非、波生坦或两者治疗,近年来利伐沙班和西地那非的使用有所增加。尽管药物可及性和手术可行性对治疗有限制,但该队列的总体生存率与其他国际登记处报告的相似。
这是关于墨西哥CTEPH经验的首份报告。它突出了REPHPISSSTE登记处患者与国际登记处患者的相似性,以及临床医生在资源有限环境中面临的挑战。