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A Bayesian network meta-analysis on the efficacy and safety of eighteen targeted drugs or drug combinations for pulmonary arterial hypertension

机译:贝叶斯网络荟萃分析对18种靶向药物或药物组合治疗肺动脉高压的有效性和安全性

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摘要

Pulmonary arterial hypertension (PAH) can be relieved by pharmacological interventions, especially the targeted drug, which is classified into endothelin receptor antagonist, phosphodiesterase 5 inhibitor, prostaglandin I2, soluble guanylate cyclase stimulator and selective non-prostanoid prostacyclin receptor agonist. To solve the contradictions existing in reported trials and provide a comprehensive guideline for clinical practice. PubMed, Embase, Cochrane library, and clinicaltrials.gov were searched. The basic information about the article, trial, arm, intervention, and the detailed data of outcome, including 6 minutes walking distance (6MWD) change, WHO functional class (FC) improvement, Borg dyspnea score (BDS) change, cardiac index (CI) change, mean pulmonary arterial pressure (mPAP) change, mean right arterial pressure (mRAP) change, pulmonary vascular resistance (PVR) change, clinical worsening, hospitalization, death, severe adverse events (SAEs), and withdrawal were extracted. The rank of treatments was estimated. 10,230 cases provided the firsthand comparison data about targeted drugs for treating PAH. For 6MWD, ambrisentan + tadalafil, vardenafil, and sildenafil + bosentan were better than others. Epoprostenol, macitentan, and sildenafil represented a greater WHO FC improvement. Vardenafil and treprostinil were better for BDS. So were bosentan + epoprostenol and bosentan alone for CI. Iloprost plus bosentan, bosentan + epoprostenol, and epoprostenol were better for mPAP. Iloprost plus bosentan, bosentan alone, and selexipag could reduce PVR. Sildenafil, epoprostenol, and vardenafil had the highest probability to reduce the incidence of death and withdrawal. To conclude, vardenafil and iloprost + bosentan showed relatively better performance in both efficacy and safety. However, the therapeutic choice should be made according to both the feature of each therapy and the individual condition.
机译:肺动脉高压(PAH)可通过药理学干预来缓解,尤其是靶向药物,可分为内皮素受体拮抗剂,磷酸二酯酶5抑制剂,前列腺素I2,可溶性鸟苷酸环化酶刺激剂和选择性非前列腺素前列腺素受体激动剂。解决现有试验中存在的矛盾并为临床实践提供全面指导。搜索PubMed,Embase,Cochrane库和Clinicaltrials.gov。有关文章,试验,手臂,干预的基本信息以及详细的结果数据,包括6分钟步行距离(6MWD)改变,WHO功能分类(FC)改善,Borg呼吸困难评分(BDS)改变,心脏指数(CI) )变化,平均肺动脉压(mPAP)变化,平均右动脉压(mRAP)变化,肺血管阻力(PVR)变化,临床恶化,住院,死亡,严重不良事件(SAEs)和停药被提取。估计治疗等级。 10,230例病例提供了有关治疗PAH的靶向药物的第一手对比数据。对于6MWD,安布生坦+他达拉非,伐地那非和西地那非+波生坦优于其他药物。 Epoprostenol,macitentan和sildenafil代表了更大的WHO FC改善。伐地那非和曲前列环素对BDS更好。因此,波生坦+泛烯醇和波生坦单独用于CI。伊洛前列素加波生坦,波生坦+异丁烯醇和e异丁烯醇对mPAP效果更好。伊洛前列素加波生坦,单独的波生坦和selexipag可以降低PVR。西地那非,依普司汀醇和伐地那非降低死亡和戒断的可能性最高。总之,伐地那非和伊洛前列素+波生坦在疗效和安全性方面均表现出相对较好的性能。但是,应根据每种疗法的特点和个人情况选择治疗方案。

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