Conte J V, Gaine S P, Orens J B, Harris T, Rubin L J
Department of Surgery, The University of Maryland School of Medicine, Baltimore 21201, USA.
J Heart Lung Transplant. 1998 Jul;17(7):679-85.
Primary pulmonary hypertension (PPH) is a progressive disease with a median survival of less than 3 years from diagnosis. Medical management has typically consisted of anticoagulation and oral calcium channel blocking agents, whereas lung transplantation (LT) has been reserved for patients who are unresponsive to medical therapy. Continuous intravenous prostacyclin was introduced for patients who did not respond to calcium channel blockers and who would have required LT. We reviewed our experience with prostacyclin in LT candidates to study its effects on the timing and outcome of LT.
We retrospectively reviewed the clinic and hospital records of patients with PPH who were both treated with prostacyclin and evaluated for LT. Additional information was obtained from the pulmonary vascular disease and lung transplantation databases.
A total of 42 patients were identified who received prostacyclin for the treatment of PPH and were evaluated for LT. Thirty-seven patients were accepted as LT candidates, 22 at The University of Maryland Medical Center (UMMC), 15 at other LT programs. Overall, 70% (27/37) of LT candidates were removed from the LT waiting list or had listing for LT deferred because of clinical improvement. In patients listed for LT before initiation of prostacyclin therapy, 55% (12/22) were removed from the active waiting list for 27.2+/-17 months (range 8 to 60), and 92% (11/12) remain on the inactive status. In patients who received prostacyclin before listing for LT, listing for LT was deferred in 94% (14/15) for 17.4+/-9 months (range 6 to 33 months) because of clinical stability or improvement. In all, 93% of patients (39/42) experienced an improvement in 1 or more New York Heart Association functional class. The hemodynamic profiles of the eight patients removed from the active waiting list at UMMC demonstrated increases of 55%+/-18% in cardiac output, and decreases of 14.3%+/-4.9% in mean pulmonary artery pressure and 36%+/-8.3% in total pulmonary resistance (p < 0.05). The 1-year survival rate for LT after prostacyclin therapy was 88% (7/8) at UMMC and 60% (3/5) at the other centers.
We conclude that prostacyclin therapy is an effective means of delaying, possibly indefinitely, the need for LT in patients with PPH and that excellent results can be obtained when LT is performed after prostacyclin therapy. Consideration should be given to initiating prostacyclin therapy in all patients whose conditions do not respond to conventional therapy before proceeding with transplantation.
原发性肺动脉高压(PPH)是一种进行性疾病,自诊断起中位生存期不足3年。药物治疗通常包括抗凝和口服钙通道阻滞剂,而肺移植(LT)则适用于对药物治疗无反应的患者。对于对钙通道阻滞剂无反应且原本需要进行肺移植的患者,引入了持续静脉输注前列环素治疗。我们回顾了我们在前列环素治疗肺移植候选患者方面的经验,以研究其对肺移植时机和结果的影响。
我们回顾性分析了接受前列环素治疗并接受肺移植评估的PPH患者的临床和医院记录。从肺血管疾病和肺移植数据库中获取了其他信息。
共确定42例接受前列环素治疗PPH并接受肺移植评估的患者。37例患者被列为肺移植候选者,其中22例在马里兰大学医学中心(UMMC),15例在其他肺移植项目。总体而言,70%(27/37)的肺移植候选者因临床改善而从肺移植等待名单中移除或推迟列入肺移植名单。在前列环素治疗开始前列入肺移植名单的患者中,55%(12/22)从活跃等待名单中移除27.2±17个月(范围8至60个月),92%(11/12)仍处于非活跃状态。在列入肺移植名单前接受前列环素治疗的患者中,94%(14/15)因临床稳定或改善而将肺移植列入推迟17.4±9个月(范围6至33个月)。总体而言,93%的患者(39/42)纽约心脏协会功能分级有1项或更多项得到改善。从UMMC活跃等待名单中移除的8例患者的血流动力学参数显示心输出量增加55%±18%,平均肺动脉压降低14.3%±4.9%,总肺阻力降低36%±8.3%(p<0.05)。前列环素治疗后肺移植的1年生存率在UMMC为88%(7/8),在其他中心为60%(3/5)。
我们得出结论,前列环素治疗是一种有效手段,可推迟(可能无限期)PPH患者对肺移植的需求,并且在前列环素治疗后进行肺移植可取得优异结果。在进行移植前,对于所有对传统治疗无反应的患者,应考虑启动前列环素治疗。