Department of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Department of Cardiology, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12203, Berlin, Germany.
Clin Res Cardiol. 2019 Mar;108(3):290-297. doi: 10.1007/s00392-018-1355-7. Epub 2018 Aug 18.
Right ventricular (RV) dysfunction predicts adverse outcome in peripartum cardiomyopathy (PPCM). We recently demonstrated beneficial effects associated with the prolactin release inhibitor bromocriptine at different doses when added to standard heart failure therapy in PPCM. Here, we evaluated for the first time the therapeutic potential of bromocriptine particularly in PPCM patients with RV involvement.
In this study, 40 patients with PPCM were included, of whom 24 patients had reduced RV ejection fraction (RVEF < 45%). We examined the effect of short-term (1W: bromocriptine, 2.5 mg, 7 days, n = 10) compared with long-term bromocriptine treatment (8W: 5 mg for 2 weeks followed by 2.5 mg for another 6 weeks, n = 14) in addition to guideline-based heart failure therapy in patients with an initial RVEF < 45% on the following outcomes: (1) change from baseline (Δ delta) in RVEF, (2) change from baseline in left ventricular EF (LVEF), and (3) rate of patients with full LV recovery (LVEF ≥ 50%) and (4) rate of patients with full RV recovery (RVEF ≥ 55%) at 6-month follow-up as assessed by cardiac magnetic resonance imaging.
Reduced RVEF at initial presentation was associated with a lower rate of full cardiac recovery at 6-month follow-up (patients with RV dysfunction: 58% vs. patients with normal RV function: 81%; p = 0.027). RVEF increased from 38 ± 7 to 53 ± 11% with a delta-RVEF of + 15 ± 12% in the 1W group, and from 35 ± 9 to 58 ± 7% with a Δ RVEF of + 23 ± 10% in the 8W group (Δ RVEF 1W vs 8W: p = 0.118). LVEF increased from 25 ± 8 to 46 ± 12% with a Δ LVEF of + 21 ± 11% in the 1W group, and from 22 ± 6 to 49 ± 10% with a Δ LVEF of + 27 ± 9% in the 8W group (Δ LVEF 1W vs 8W: p = 0.211). Full LV recovery was present in 50% of the 1W group and in 64% of the 8W group (p = 0.678). Full RV recovery was observed in 40% of the 1W group and in 79% of the 8W group (p = 0.092).
Despite overall worse outcome in patients with RV dysfunction at baseline, bromocriptine treatment in PPCM patients with RV involvement was associated with a high rate of full RV and LV recovery, although no significant differences were observed between the short-term and long-term bromocriptine treatment regime. These findings suggest that bromocriptine in addition to standard heart failure therapy may be also effective in PPCM patients with biventricular impairment.
右心室(RV)功能障碍可预测围产期心肌病(PPCM)的不良预后。我们最近证明了在 PPCM 中,与标准心力衰竭治疗联合使用不同剂量的催乳素释放抑制剂溴隐亭会产生有益的效果。在这里,我们首次评估了溴隐亭在 RV 受累的 PPCM 患者中的治疗潜力。
本研究纳入了 40 名 PPCM 患者,其中 24 名患者的 RV 射血分数(RVEF < 45%)降低。我们比较了短期(1 周:溴隐亭 2.5mg,7 天,n = 10)与长期(8 周:5mg 持续 2 周,然后再用 2.5mg 持续 6 周,n = 14)溴隐亭治疗联合标准心力衰竭治疗对初始 RVEF < 45%的患者的以下结局的影响:(1)RVEF 的基线变化(Δ delta),(2)左心室 EF(LVEF)的基线变化,以及(3)6 个月随访时完全左心室恢复(LVEF ≥ 50%)的患者比例和(4)完全 RV 恢复(RVEF ≥ 55%)的患者比例,通过心脏磁共振成像评估。
初始表现时 RV 功能降低与 6 个月随访时完全心脏恢复的比例较低相关(RV 功能障碍患者:58%;RV 功能正常患者:81%;p = 0.027)。1 周组 RVEF 从 38 ± 7%增加到 53 ± 11%,Δ RVEF 为+ 15 ± 12%,8 周组从 35 ± 9%增加到 58 ± 7%,Δ RVEF 为+ 23 ± 10%(Δ RVEF 1W 与 8W:p = 0.118)。LVEF 从 25 ± 8%增加到 46 ± 12%,Δ LVEF 为+ 21 ± 11%,8 周组从 22 ± 6%增加到 49 ± 10%,Δ LVEF 为+ 27 ± 9%(Δ LVEF 1W 与 8W:p = 0.211)。1 周组中有 50%的患者完全恢复左心室功能,8 周组中有 64%的患者完全恢复左心室功能(p = 0.678)。1 周组中有 40%的患者完全恢复 RV 功能,8 周组中有 79%的患者完全恢复 RV 功能(p = 0.092)。
尽管基线时 RV 功能障碍患者的总体预后较差,但在 RV 受累的 PPCM 患者中,溴隐亭治疗与 RV 和 LV 完全恢复的高比例相关,尽管短期和长期溴隐亭治疗方案之间没有观察到显著差异。这些发现表明,除了标准心力衰竭治疗外,溴隐亭可能对伴有双心室损害的 PPCM 患者也有效。