Lange Tobias J, Baron Miriam, Seiler Isabella, Arzt Michael, Pfeifer Michael
Department of Internal Medicine II, Division of Pneumology, University Medical Center Regensburg, Regensburg, Germany.
Cardiovasc Ther. 2014 Oct;32(5):202-8. doi: 10.1111/1755-5922.12084.
Pulmonary hypertension (PH) can occur in patients with lung disease and worsen prognosis. Endothelin receptor antagonists, phosphodiesterase 5-inhibitors, and prostacyclin analogs, referred to as targeted therapy, have not been shown in a limited number of controlled clinical studies to improve exercise capacity in these patients. Possibly targeted therapy could be of benefit in patients with severe PH due to lung disease, but this subgroup is not well studied.
To analyze influence of PH severity and use of targeted therapy on exercise capacity and survival in patients with PH due to lung disease.
Consecutive patients with PH (mean pulmonary artery pressure ≥25 mmHg at rest) due to lung disease diagnosed by right heart catheterization between 1/2005 and 9/2011 were retrospectively included. Severe PH was defined as mean pulmonary artery pressure ≥35 mmHg. Patients were followed until 4/2012 for exercise capacity, survival, and targeted therapy use.
Patients with severe PH (n = 40) received significantly more often targeted therapy compared to the 32 patients with less severe PH (65% vs. 25%, P = 0.001). Survival was not significantly different between these groups (P = 0.310). Patients on targeted therapy were older, more often female, and had worse hemodynamic impairment, but significantly higher estimated 1-, 3-, and 5-year survival rates compared to untreated patients (97%, 81%, and 75% vs. 83%, 54%, and 19%, respectively; P = 0.002). This effect was mainly driven by the patients with severe PH, in whom the survival advantage was statistically significant on subgroup analysis (HR 0.182, P = 0.002). Exercise capacity was not significantly altered in any patient group.
Patients with severe PH due to lung disease may have a survival benefit from targeted therapy compared to untreated patients with less severe PH. Prospective clinical trials utilizing targeted therapy and long-term endpoints are justified in this patient group.
肺动脉高压(PH)可发生于肺部疾病患者,并使预后恶化。内皮素受体拮抗剂、磷酸二酯酶5抑制剂和前列环素类似物,即所谓的靶向治疗,在少数对照临床研究中尚未显示能改善这些患者的运动能力。对于因肺部疾病导致的重度PH患者,靶向治疗可能有益,但该亚组患者尚未得到充分研究。
分析PH严重程度和靶向治疗的使用对因肺部疾病导致PH患者的运动能力和生存的影响。
回顾性纳入2005年1月至2011年9月期间经右心导管检查诊断为因肺部疾病导致PH(静息时平均肺动脉压≥25 mmHg)的连续患者。重度PH定义为平均肺动脉压≥35 mmHg。对患者进行随访直至2012年4月,观察其运动能力、生存情况及靶向治疗的使用情况。
与32例轻度PH患者相比,40例重度PH患者接受靶向治疗的频率显著更高(65%对25%,P = 0.001)。两组患者的生存率无显著差异(P = 0.310)。接受靶向治疗的患者年龄更大,女性更多,血流动力学损害更严重,但与未治疗患者相比,估计的1年、3年和5年生存率显著更高(分别为97%、81%和75%对83%、54%和19%;P = 0.002)。这种效应主要由重度PH患者驱动,在亚组分析中,其生存优势具有统计学意义(HR 0.182,P = 0.002)。任何患者组的运动能力均无显著改变。
与未治疗的轻度PH患者相比,因肺部疾病导致重度PH的患者可能从靶向治疗中获得生存益处。在该患者群体中进行利用靶向治疗和长期终点的前瞻性临床试验是合理的。