Madani Michael M
Cardiovascular and Thoracic Surgery, University of California San Diego, La Jolla, CA, USA.
Pulm Circ. 2021 May 24;11(2):20458940211007372. doi: 10.1177/20458940211007372. eCollection 2021 Apr-Jun.
Pulmonary endarterectomy is the treatment of choice for patients with operable chronic thromboembolic pulmonary hypertension (CTEPH) as it is potentially curative. In expert centers that conduct > 50 pulmonary endarterectomy procedures per year, peri- and post-surgical mortality rates are very low and long-term outcomes are excellent, with three-year post-operative survival of > 80%. Therapeutic decisions in CTEPH are based largely on the location of the arterial obstruction, with pulmonary endarterectomy for obstructions in main, lobar, and segmental vessels, and balloon pulmonary angioplasty and medical therapy for small-vessel disease. Medical therapy is also an option for patients with persistent/recurrent pulmonary hypertension after pulmonary endarterectomy or balloon pulmonary angioplasty. With increasing surgical experience and improvements in instruments and procedures, an increasing number of patients are now considered operable who would previously have been inoperable, including some patients with subsegmental disease. At our University (University of California San Diego), around 200 pulmonary endarterectomy procedures are performed every year and several advances have been developed, including resection of more distal disease, availability of pulmonary endarterectomy to patients previously considered to be at too high risk for surgery, improved management of post-pulmonary endarterectomy complications, and minimally invasive pulmonary endarterectomy. Pulmonary endarterectomy can be combined with other treatment modalities, including balloon pulmonary angioplasty, medical therapy for persistent/recurrent pulmonary hypertension after pulmonary endarterectomy, and medical therapy or balloon pulmonary angioplasty as bridging therapy before surgery. Data on these combinations are, however, limited. Combination treatment should therefore be considered on an individual patient basis. In the future, however, multimodal therapy with pulmonary endarterectomy, balloon pulmonary angioplasty, and/or medical therapy is likely to be an important treatment option for many patients.
肺动脉内膜剥脱术是可手术治疗的慢性血栓栓塞性肺动脉高压(CTEPH)患者的首选治疗方法,因为它具有潜在的治愈性。在每年进行超过50例肺动脉内膜剥脱术的专家中心,围手术期和术后死亡率非常低,长期预后良好,术后三年生存率超过80%。CTEPH的治疗决策很大程度上基于动脉阻塞的位置,对于主、叶和段血管的阻塞采用肺动脉内膜剥脱术,对于小血管疾病则采用球囊肺动脉成形术和药物治疗。对于肺动脉内膜剥脱术或球囊肺动脉成形术后持续/复发肺动脉高压的患者,药物治疗也是一种选择。随着手术经验的增加以及器械和手术方法的改进,现在越来越多以前被认为无法手术的患者被认为可以进行手术,包括一些亚段疾病患者。在我们大学(加利福尼亚大学圣地亚哥分校),每年大约进行200例肺动脉内膜剥脱术,并且取得了一些进展,包括切除更远端的病变、使以前被认为手术风险过高的患者能够接受肺动脉内膜剥脱术、改善肺动脉内膜剥脱术后并发症的管理以及微创肺动脉内膜剥脱术。肺动脉内膜剥脱术可以与其他治疗方式联合使用,包括球囊肺动脉成形术、肺动脉内膜剥脱术后持续/复发肺动脉高压的药物治疗以及术前作为桥接治疗的药物治疗或球囊肺动脉成形术。然而,关于这些联合治疗的数据有限。因此,应根据个体患者情况考虑联合治疗。然而,未来肺动脉内膜剥脱术、球囊肺动脉成形术和/或药物治疗的多模式治疗可能会成为许多患者的重要治疗选择。