从70万一针的“天价药”降至3.3万元上下,越来越多罕见病药纳入医疗保险目录
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"> 从70万一针的“天价药”降至3.3万元<span style="color: black;">上下</span>,越来越多罕见病药纳入<span style="color: black;">医疗保险</span>目录 </p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">2月29日是第17个国际罕见病日。世界卫生组织将患病人数占总人口0.065%—0.1%之间的<span style="color: black;">疾患</span>定义为罕见病。我国已<span style="color: black;">创立</span>的罕见病登记系统<span style="color: black;">表示</span>,<span style="color: black;">截止</span><span style="color: black;">日前</span>全国480多家医院登记了78万多例罕见病病例。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><strong style="color: blue;"><span style="color: black;">新版<span style="color: black;">医疗保险</span><span style="color: black;">药物</span>目录纳入15种罕见病用药</span></strong></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;"><span style="color: black;">因为</span><span style="color: black;">开发</span>成本高、用药人群少等<span style="color: black;">原由</span>,<span style="color: black;">有些</span>罕见病治疗<span style="color: black;">药品</span>的年均<span style="color: black;">花费</span><span style="color: black;">达到</span>到百万元,<span style="color: black;">乃至</span>数百万元,这对普通家庭<span style="color: black;">来讲</span><span style="color: black;">便是</span>天文数字。 近年来,不少<span style="color: black;">获准</span>上市的罕见病<span style="color: black;">药品</span>经过谈判纳入<span style="color: black;">医疗保险</span>,<span style="color: black;">明显</span>减轻罕见病<span style="color: black;">病人</span>家庭用药<span style="color: black;">包袱</span>。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;"><span style="color: black;">近期</span>,2023年<span style="color: black;">医疗保险</span><span style="color: black;">药物</span>目录<span style="color: black;">调节</span>结果落地实施。此次<span style="color: black;">调节</span>共新增126种<span style="color: black;">药物</span>,其中,就<span style="color: black;">包含</span>15种罕见病用药,填补了10种罕见病用药在目录内的用药空白。降价叠加<span style="color: black;">医疗保险</span>报销,对<span style="color: black;">关联</span><span style="color: black;">行业</span><span style="color: black;">病人</span>而言<span style="color: black;">包袱</span><span style="color: black;">显著</span>减轻。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q9.itc.cn/q_70/images03/20240301/f89d506b22c444caae57a76246932269.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">国家<span style="color: black;">医疗保险</span>局医药管理司司长 黄心宇:治疗重症肌<span style="color: black;">没</span>力的艾加莫德α注射液,以及治疗阵发性<span style="color: black;">睡觉</span>性血红蛋白尿的依库珠单抗,这些<span style="color: black;">疾患</span>其实是<span style="color: black;">困惑</span><span style="color: black;">咱们</span><span style="color: black;">数年</span>的,原来治疗<span style="color: black;">花费</span>都非常高的<span style="color: black;">有些</span>罕见病<span style="color: black;">药物</span>。经过谈判,<span style="color: black;">公司</span><span style="color: black;">亦</span>是给出了比较理性的价格,能够成功纳入目录。将来对这些<span style="color: black;">病人</span>将有<span style="color: black;">显著</span>获益。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">国家<span style="color: black;">医疗保险</span>局自成立<span style="color: black;">败兴</span>,<span style="color: black;">已然</span>连续6年开展国家<span style="color: black;">医疗保险</span><span style="color: black;">药物</span>目录<span style="color: black;">调节</span>工作。据统计,<span style="color: black;">日前</span>在中国<span style="color: black;">获准</span>上市的一百多种罕见病用药,已有80余种纳入<span style="color: black;">医疗保险</span><span style="color: black;">药物</span>目录。其中,<span style="color: black;">经过</span><span style="color: black;">医疗保险</span>谈判纳入的51种罕见病用药,平均降价超50%。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q0.itc.cn/q_70/images03/20240301/d129c773aceb4790a02f12a05c207292.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">国家<span style="color: black;">医疗保险</span>局医药管理司司长 黄心宇:确实罕见病得到了全社会的<span style="color: black;">注意</span>,<span style="color: black;">大众</span>对罕见病的认知程度<span style="color: black;">持续</span><span style="color: black;">加强</span>,对罕见病的临床诊疗能力<span style="color: black;">亦</span><span style="color: black;">持续</span><span style="color: black;">提高</span>。临床这几年从新药<span style="color: black;">开发</span>上的<span style="color: black;">方向</span>来看,罕见病<span style="color: black;">药物</span><span style="color: black;">亦</span>是一个<span style="color: black;">开发</span>的热点,<span style="color: black;">因此</span>说综合这些<span style="color: black;">状况</span>,纳入目录的罕见病药相对就越来越多。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><strong style="color: blue;"><span style="color: black;">从<span style="color: black;">没</span>药可用 到天价药 再到平价药</span></strong></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">脊髓性肌萎缩症<span style="color: black;">亦</span>被<span style="color: black;">叫作</span>为“SMA”,是一种由脊髓前角运动神经元变性<span style="color: black;">引起</span>肌<span style="color: black;">没</span>力、肌萎缩的罕见病症。<span style="color: black;">经过</span>近年来的<span style="color: black;">医疗保险</span><span style="color: black;">药物</span>目录<span style="color: black;">调节</span>,<span style="color: black;">已然</span>有两款针对SMA的<span style="color: black;">药品</span>大幅降价被纳入<span style="color: black;">医疗保险</span>,<span style="color: black;">病人</span>从<span style="color: black;">没</span>药可用,到天价药,再到<span style="color: black;">包袱</span>得起的平价药,新的一年,一个个SMA患儿家庭<span style="color: black;">针对</span><span style="color: black;">将来</span>,<span style="color: black;">亦</span>有了更加真切的新愿望。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">在山东青岛的一家<span style="color: black;">恢复</span>中心里,<span style="color: black;">看病</span>的患儿和家属正在参加投壶、拓福字的游戏,<span style="color: black;">孩儿</span>们玩得不<span style="color: black;">也</span>乐乎。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q7.itc.cn/q_70/images03/20240301/825e27bc859141ff8792d9c9e4cc8435.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">青岛某<span style="color: black;">恢复</span>中心院长 孙海英:今天有15位SMA的小<span style="color: black;">伴侣</span><span style="color: black;">亦</span>参与其中,经过<span style="color: black;">恢复</span>训练以后,<span style="color: black;">她们</span>恢复了<span style="color: black;">必定</span>的运动功能,<span style="color: black;">亦</span>能够适度地参与到类似<span style="color: black;">这般</span>的活动中。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">患儿 张嘉诺:这是我自己做的,妈妈抱着我做的。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">张嘉诺的妈妈 李惠:他之前胳膊抬不起来的时候,<span style="color: black;">亦</span><span style="color: black;">基本</span><span style="color: black;">无</span>力气往下按,今天我抱着他,他自己拿胳膊蘸着那个东西做了一个福字,挺开心的。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q7.itc.cn/q_70/images03/20240301/050b835d317f44f79ec7fd6a339eb473.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">4岁半的小嘉诺在活动上玩得很开心,看起来跟普通小<span style="color: black;">伴侣</span>差别不大。李惠说,在小嘉诺七八个月的时候,蹬腿、抬头、翻身都很正常,但慢慢地就不对劲儿了。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">张嘉诺的妈妈 李惠:<span style="color: black;">便是</span>到了爬的那个时候,他不会四点爬,<span style="color: black;">咱们</span>就想着去<span style="color: black;">外区</span>查一下,<span style="color: black;">大夫</span>一看,<span style="color: black;">便是</span>给<span style="color: black;">孩儿</span>敲了一下膝盖,<span style="color: black;">无</span>膝跳反射,就在纸上写了SMA-II,打了一个问号,让<span style="color: black;">咱们</span>做基因检测。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">经过<span style="color: black;">各样</span>检测,<span style="color: black;">孩儿</span><span style="color: black;">最后</span>确诊为SMA。虽然特效药已<span style="color: black;">获准</span>进入国内,可是,这款药一针价格就高达69.97万元,一年治疗费<span style="color: black;">必须</span>数百万元,这<span style="color: black;">针对</span>普通家庭<span style="color: black;">来讲</span><span style="color: black;">没</span>疑是个天文数字。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">张嘉诺的妈妈 李惠:头一年<span style="color: black;">必须</span>打6针,6针<span style="color: black;">便是</span>400多万,当时2020年的时候,想着把家里的房子什么都卖掉,<span style="color: black;">然则</span>在<span style="color: black;">咱们</span>当地的经济水平,<span style="color: black;">基本</span>就<span style="color: black;">不足</span><span style="color: black;">孩儿</span>一年的<span style="color: black;">花费</span>。就感觉虽然有药了,<span style="color: black;">然则</span>救不了<span style="color: black;">孩儿</span>,心里面<span style="color: black;">尤其</span>难受。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q1.itc.cn/q_70/images03/20240301/2f01bfb9079e451cb14ae93b06ef7877.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">特效药用不起,李惠只能<span style="color: black;">选取</span>先给<span style="color: black;">孩儿</span>做<span style="color: black;">恢复</span>延缓病情发展。2021年11月,SMA的患儿和家庭<span style="color: black;">最终</span>等来了转机。特效药经过谈判,从70万一针的“天价药”,降至3.3万元<span style="color: black;">上下</span>,纳入<span style="color: black;">医疗保险</span><span style="color: black;">药物</span>目录中。再加上<span style="color: black;">医疗保险</span>报销和<span style="color: black;">补贴</span>,<span style="color: black;">病人</span>的<span style="color: black;">包袱</span>就更低了。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">张嘉诺的妈妈 李惠:当时我和<span style="color: black;">孩儿</span>爸爸就哭了。真的<span style="color: black;">尤其</span>感谢国家,让<span style="color: black;">咱们</span>看到了<span style="color: black;">孩儿</span>有救,有<span style="color: black;">期盼</span>。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">越早用药,效果越好。2022年1月9日,两岁半的小嘉诺就打上了<span style="color: black;">第1</span>针。随后,特效药搭配<span style="color: black;">恢复</span>训练,小佳诺的状态越来越好。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q5.itc.cn/q_70/images03/20240301/559a280861584439a5e95980c673f83c.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">青岛某<span style="color: black;">恢复</span>中心肢体负责人 徐丹:之前在平地上肘支撑维持头控,他只能维持5秒钟。<span style="color: black;">此刻</span>,他<span style="color: black;">能够</span>在这个肘支撑上,<span style="color: black;">能够</span>进行向前移动,<span style="color: black;">况且</span>在球上<span style="color: black;">亦</span><span style="color: black;">能够</span>实现从肘支撑到手支撑的过渡。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">小嘉诺的妈妈算了一笔账,原来一年的药费<span style="color: black;">包袱</span>是百万,<span style="color: black;">此刻</span>在<span style="color: black;">各样</span>报销和政策支持下,个人<span style="color: black;">包袱</span>大概三万元。“正常的生活”,<span style="color: black;">针对</span>这个SMA家庭<span style="color: black;">来讲</span>,一下子从遥不可及的梦,变<span style="color: black;">成为了</span><span style="color: black;">能够</span>触碰的新年新愿望。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">张嘉诺的妈妈 李惠:爸爸多干几份工作,给<span style="color: black;">孩儿</span>用,让他渐渐地好起来。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">患儿 张嘉诺:我想赶紧走起来,自己帮妈妈干活,还想背着妈妈出去。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">记者:你能背得动你妈妈吗?</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">患儿 张嘉诺:等我大了,长得比她高,就<span style="color: black;">能够</span>背动啦。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><strong style="color: blue;"><span style="color: black;"><span style="color: black;">日前</span>国家<span style="color: black;">医疗保险</span>目录中含两种SMA特效药</span></strong></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;"><span style="color: black;">此刻</span>,国家医保目录中已有两种SMA特效药,越来越多的家庭看到了<span style="color: black;">期盼</span>。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><img src="https://q5.itc.cn/q_70/images03/20240301/f417d68a9eaf48f8830f8a3937fbbf50.jpeg" style="width: 50%; margin-bottom: 20px;"></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">这家<span style="color: black;">恢复</span>中心的SMA科室半年前刚成立的时候,<span style="color: black;">仅有</span>7个家庭在做<span style="color: black;">恢复</span>,<span style="color: black;">此刻</span><span style="color: black;">已然</span><span style="color: black;">增多</span>到22个。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">青岛某<span style="color: black;">恢复</span>中心院长 孙海英:能<span style="color: black;">显著</span>地感觉到来<span style="color: black;">恢复</span>的<span style="color: black;">孩儿</span>越来越多,尽快<span style="color: black;">提高</span><span style="color: black;">孩儿</span>的<span style="color: black;">恢复</span>效果,让<span style="color: black;">她们</span><span style="color: black;">早点</span>回归社会。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">张嘉诺的妈妈 李惠:今天早上他还起<span style="color: black;">来讲</span>,妈妈,我是大力士,我勇往直前不怕困难。我说好 ,那你<span style="color: black;">火速</span>就会走起来,会走向你的,像别人<span style="color: black;">同样</span>快乐的童年。</span></p>
<p style="font-size: 16px; color: black; line-height: 40px; text-align: left; margin-bottom: 15px;"><span style="color: black;">(央视<span style="color: black;">资讯</span>客户端)</span><a style="color: black;"><span style="color: black;">返回<span style="color: black;">外链论坛:http://www.fok120.com/</span>,查看<span style="color: black;">更加多</span></span></a></p>
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谢谢、感谢、感恩、辛苦了、有你真好等。 “板凳”(第三个回帖的人) 外贸B2B平台有哪些? 我完全赞同你的观点,思考很有深度。
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