University of Modena and Reggio Emilia, Cardiology Unit, Pulmonary Hypertension Program, Policlinico di Modena Hospital, Italy.
University of Modena and Reggio Emilia, Cardiology Unit, Pulmonary Hypertension Program, Policlinico di Modena Hospital, Italy.
Pulm Pharmacol Ther. 2018 Apr;49:147-151. doi: 10.1016/j.pupt.2017.06.005. Epub 2017 Jun 19.
Exogenous intravenous (IV) adenosine and epoprostenol are effective vasodilator agents, causing a substantial reduction in pulmonary vascular resistance in patients affected by idiopathic pulmonary arteriolar hypertension (PAH). Their action, in patients with PAH associated with other pathological conditions, is not well defined. In the present paper the authors retrospectively analyzed the acute hemodynamic effects of intravenous adenosine and epoprostenol in 30 consecutive patients (mean age: 58 ± 15 years; 21 females, and 9 males) affected by PAH associated with other pathological conditions, as determined by changes from baseline in systemic and pulmonary hemodynamic parameters. Acute IV administration of adenosine decreased pulmonary vascular resistance index (PVRI) by 3 Wood U/m (- 20%) compared to baseline (p = 0.02). We noted a slight, not significant, decrease in mean pulmonary artery pressure (mPAP) of 4 mmHg. Cardiac index (CI) increased by 0.5 L/min/m (15% increase respect to baseline; p = 0.03). The heart rate and mean systemic blood pressure (BP) did not change significantly. Acute IV administration of epoprostenol decreased PVRI by 6 mmHg (- 40%) respect to baseline (p < 0.0001). CI increased by 1.4 L/min/m (p < 0.0001); while mPAP decreased by 5 mmHg (nearly 10%) (p = 0.04). This decrease of mPAP was accompanied by a mean BP decrease of 11 mmHg compared to baseline (p = 0.003). Our results indicates that, in patients with PAH associated with other pathological conditions, adenosine is predominantly a positive inotropic agent; and epoprostenol a potent vasodilator of both pulmonary and systemic vessels, and a strong positive inotropic agent.
外源性静脉内(IV)腺苷和依前列醇是有效的血管扩张剂,可使特发性肺小动脉高压(PAH)患者的肺血管阻力显著降低。它们在伴有其他病理状况的 PAH 患者中的作用尚未明确。本文作者回顾性分析了 30 例连续 PAH 患者(平均年龄:58±15 岁;21 名女性,9 名男性)静脉内腺苷和依前列醇的急性血液动力学效应,其依据是全身和肺血流动力学参数从基线的变化。与基线相比,急性 IV 给予腺苷使肺血管阻力指数(PVRI)降低了 3 个伍德单位/米(降低 20%)(p=0.02)。我们注意到平均肺动脉压(mPAP)略有下降,但无统计学意义,降低了 4mmHg。心指数(CI)增加了 0.5L/min/m(比基线增加 15%;p=0.03)。心率和平均全身血压(BP)没有明显变化。急性 IV 给予依前列醇使 PVRI 降低了 6mmHg(降低 40%)(p<0.0001)。CI 增加了 1.4L/min/m(p<0.0001);而 mPAP 降低了 5mmHg(近 10%)(p=0.04)。与基线相比,mPAP 的这种降低伴随着平均 BP 降低 11mmHg(p=0.003)。我们的结果表明,在伴有其他病理状况的 PAH 患者中,腺苷主要是一种正性肌力药;而依前列醇是肺和全身血管的强效血管扩张剂,也是一种强正性肌力药。