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Modifications of medical treatment and outcome after percutaneous correction of secondary mitral regurgitation

机译:二次二尖瓣重新改变后经皮校正后的医疗与结果

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Aims The optimization of guideline‐directed medical therapy (GDMT) in reduced ejection fraction heart failure (HFrEF) is associated with improved survival and can reduce the severity of secondary mitral regurgitation (SMR). Highest tolerated doses should be achieved before percutaneous mitral valve repair (pMVR) and drugs titration further pursued after procedure. The degree of GDMT titration in patients with HFrEF and SMR treated with pMVR remains unexplored. We sought to evaluate the adherence to GDMT in HFrEF in patients undergoing pMVR and to explore the association between changes in GDMT post‐pMVR and prognosis. Methods and results We included all the patients with HFrEF and SMR?≥?3?+?treated with pMVR between 2012 and 2019 and with available follow‐up. GDMT, comprehensive of dosages, was systematically recorded. The study endpoint was a composite of death and heart transplantation. Among 133 patients successfully treated, 121 were included (67?±?12?years old, 77% male patients). Treatment rates of angiotensin‐converting enzyme inhibitors/angiotensin receptor blockers/angiotensin receptor neprilysin inhibitor (ACEIs/ARBs/ARNI), beta‐blockers, and mineralcorticoid receptor antagonist at baseline and follow‐up were 73% and 79%, 85% and 84%, 70% and 70%, respectively. At baseline, 33% and 32% of patients were using 50% of the target dose of ACEI/ARB/ARNI and beta‐blockers. At follow‐up (median time 4?months), 33% of patients unchanged, 34% uptitrated, and 33% of patients downtitrated GDMT. Downtitration of GDMT was independently associated with higher risk of death/heart transplantation (hazard ratio: 2.542, 95%confidence interval: 1.377–4.694, P?=?0.003). Conclusions Guideline‐directed medical therapy is frequently underdosed in HFrEF patients with SMR undergoing pMVR. Downtitration of medications after procedure is associated with poor prognosis.
机译:旨在在减少的喷射分数心力衰竭(HFREF)中的指导指导医疗治疗(GDMT)的优化与改善的存活相关,并且可以降低次级二尖瓣流动的严重程度(SMR)。在进行经皮二尖瓣修复(PMVR)和术后进一步追求的药物滴定之前,应达到最高耐受剂量。用PMVR处理的HFREF和SMR患者GDMT滴定程度仍未探索。我们试图在接受PMVR的患者中评估HFREF中GDMT的依从性,并探讨GDMT后PMVR和预后变化之间的关联。方法和结果我们包括所有HFREF和SMR的患者?≥?3?+?在2012年和2019年间在2012年和2019年之间进行PMVR处理。全面的剂量GDMT进行了系统地记录。研究终点是死亡和心脏移植的复合物。在成功治疗的133名患者中,包括121名(67?±12?12?岁,77%男性患者)。基线和随访中的血管紧张素转化酶抑制剂/血管紧张素受体阻滞剂/血管紧张素受体阻滞剂/血管紧张素受体阻滞剂/血管紧张素受体嵌入剂抑制剂(Aceis / ARB / ARNI),β-阻滞剂和含有聚菌的拮抗剂为73%和79%,85%和84 %,70%和70%。在基线,33%和32%的患者使用αcei/ arb / arni和β-嵌体的目标剂量的> 50%。在随访(中位数4?月),33%的患者未改变,上升34%,33%的患者患者占额外的GDMT。 GDMT的押韵与较高的死亡/心脏移植风险(危害比率:2.542,95%置信区间:1.377-4.694,P?= 0.003)。结论在HFREF患者中经常被患者进行指导指导的医疗疗法。程序后的药物衰退与预后差有关。
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