Combination Therapy in Pulmonary Arterial Hypertension: Single Centre Long-term Experience.

G. Taçoy, A. Çengel, Yakup Alsancak, Serkan Ünlü, Sedat Türkoğlu
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引用次数: 1

Abstract

Background Pulmonary arterial hypertension (PAH) is a progressive disease of the pulmonary vascular bed and causes right heart failure and death. Combination therapy which targets three different pathways is necessary due to the progressive nature of the disease. In patients with PAH, there are two approaches in combination therapy: "first-line up-front" and "sequential add-on" treatment. In "firstline up-front" treatment, patients receive double or triple drug therapy from the start. In the "sequential add-on" approach, a single drug is initially started and then according to the patient's requirements, a second or third drug is added. There is insufficient evidence about the efficiency and safety of treatment approaches. In this study, we aimed to evaluate the treatment approach in patients with PAH at a tertiary centre. Methods Pulmonary arterial hypertension was diagnosed according to clinical, echocardiographic and right heart catheterization findings. The patients received bosentan, sildenafil and iloprost treatment in accordance with guidelines recommendations. Clinical worsening in patients was defined as death, requirement of hospitalization for PAH, a 15% decline in the six-minute walk test (6MWT) distance, deterioration in functional capacity, and symptoms and findings of right heart failure. Results At the end of the follow-up period, clinical and echocardiographic findings, brain natriuretic peptide (BNP) levels and oxygen saturation were similar between patients who completed the study with monotherapy and with combination therapy. The follow-up period was significantly longer in patients who required combination treatment. Two patients (6.9%) died and four patients (13.8%) were hospitalized due to recurrent symptoms and findings of right heart failure. At the end of follow-up, 10 patients (34.5%) completed the study with a single drug, 15 patients (51.7%) with two drugs and four patients (13.8%) with three drugs. Conclusion In this study, combination therapy was given to patients as "sequential add-on therapy". At the end of the follow-up period, monotherapy was sufficient in 34.5% of patients of the study group and in eight patients, sildenafil or prostaglandin analogues were added; a total of 15 patients (48.4%) completed the study under dual therapy. Four patients (12.9%) received combination therapy with three drugs.
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肺动脉高压的联合治疗:单中心长期经验。
肺动脉高压(PAH)是一种进行性肺血管床疾病,可导致右心衰和死亡。由于疾病的进行性,针对三种不同途径的联合治疗是必要的。在PAH患者中,有两种联合治疗方法:“一线前期”和“顺序附加”治疗。在“一线预先”治疗中,患者从一开始就接受双重或三重药物治疗。在“顺序加药”方法中,最初使用一种药物,然后根据患者的要求添加第二或第三种药物。关于治疗方法的有效性和安全性的证据不足。在这项研究中,我们旨在评估在三级中心治疗多环芳烃患者的方法。方法根据临床、超声心动图及右心导管检查结果诊断肺动脉高压。患者按照指南建议接受波生坦、西地那非和伊洛前列治疗。患者的临床恶化被定义为死亡、因PAH需要住院、6分钟步行试验(6MWT)距离下降15%、功能能力恶化以及右心衰的症状和表现。结果随访结束时,单药组和联合用药组患者的临床和超声心动图表现、脑钠肽(BNP)水平和血氧饱和度相似。需要联合治疗的患者随访时间明显更长。2例患者(6.9%)死亡,4例患者(13.8%)因复发症状和右心衰住院。随访结束时,单药组10例(34.5%),双药组15例(51.7%),三药组4例(13.8%)。结论本研究以“序贯补充治疗”的方式对患者进行联合治疗。在随访期结束时,研究组中34.5%的患者单药治疗是足够的,8例患者添加了西地那非或前列腺素类似物;共有15名患者(48.4%)在双重治疗下完成了研究。4例患者(12.9%)接受三种药物联合治疗。
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