FDA授权，飞利浦超声可诊断新冠患者并发症！

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                    <section data-role="paragraph" data-color="rgb(182, 228, 253)" data-custom="rgb(182, 228, 253)"><section><section><section><section powered-by="gulangu"><section><section><section><section powered-by="gulangu"><section><section><section><section powered-by="gulangu"><section><section><section><section powered-by="gulangu"><section><section><section><section><p><p><img src="image/20201014/86b79d371e9862b01189f0252a03b2cd_1.jpg" /></p></p></section><section><section><span><strong></strong></span></section><p><span>医疗器械媒体报道先锋</span></p><p><span>分享专业医疗器械知识</span></p></section><section><section><section><span>关注</span></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section></section><section data-tools="gulangu" data-id="97917"><section><section><section data-bgless="spin" data-bgopacity="30%"><br  /></section><p><span>日前，飞利浦医疗发布了2020年第一季度财报，总销售额为42亿欧元(约45.6亿美元)，可比销售额下降2％，三大业务板块中，健康个护领域下滑最多，诊断&amp;治疗领域中的图像引导治疗降幅较大，从数据上来看，受新冠疫情影响，飞利浦医疗Q1收入大幅下跌。</span></p><p><br  /></p><p><span>新冠疫情带来的负面影响在第一季度逐渐增加，1月下旬开始，影响到飞利浦在中国以及亚太地区的业务；3月起，影响扩大到飞利浦在全球其他地区的业务。预计飞利浦的所有业务区域都将在整个第二季度受到影响，这将导致健康个护的业务收入急剧下降，而诊断&amp;治疗收入则出现会接近10%(high-single-digit)的大幅下降。</span></p><p><br  /></p><p><p><img src="image/20201014/133c8f426bbf9540e8f02505f80d4f30_2.jpg" /></p></p><p><br  /></p><p><span>好在，互联护理业务的大幅增长能够为飞利浦医疗抵消一部分负面影响，同时，其他主要业务领域也在疫情之下寻求新的契机。据外媒报道，近日FDA刚刚通过了一项决议，允许飞利浦医疗旗下获得510（K）认证的超声产品参与诊断因新冠肺炎导致的心肺并发症。这几乎涵盖了飞利浦医疗旗下的所有超声产品系列，包括EPIQ系列、Affiniti系列、Lumify、CX50和Sparq及QLAB高级定量软件等产品。</span></p><p><br  /></p><p><p><img src="image/20201014/489ec45cbe68097e5c6df7c964490643_3.jpg" /></p></p><p><br  /></p><p><span>我国一般以CT图像+核酸检测的为新冠肺炎诊断的金标准，但超声的便捷性在抗疫工作中也是至关重要的，对于快速为呼吸困难的患者诊断有着得天独厚的优势，尤其是如飞利浦医疗<span>Lumify</span>手持超声这类便携式设备，能够大大降低病人的转运成本，降低病毒传播的可能性。</span></p><p><br  /></p><p><p><img src="image/20201014/49066715dfd5dea0386ac9f0b3f3498b_4.jpg" /></p></p><p><br  /></p><p><span>此外，飞利浦还为Lumify 提供远程医疗的配套系统，与手机或平板电脑配合使用，能够共享超声成像数据并与其他医生远程通信（包含语音及视频通话），以此来缓解医务人员紧张的状况。</span></p><p><br  /></p><p><p><img src="image/20201014/33edda936c9ac2c83571691d242029a9_5.jpg" /></p></p><section data-bgless="spin" data-bgopacity="30%"><br  /></section><section data-bgless="spin" data-bgopacity="30%"><span>除了超声产品，飞利浦医疗一款用于检测住院的新冠肺炎患者情况的生物传感器BX100也得到了FDA的首肯，并获得了下一代无线可穿戴生物传感器的CE标志。</span></section><section data-bgless="spin" data-bgopacity="30%"><span><br  /></span></section><p><p><img src="image/20201014/402e617c391630d355ed8c83fb6863bb_6.jpg" /></p></p><p><span>BX100</span><br  /></p><section data-bgless="spin" data-bgopacity="30%"><br  /></section><section data-bgless="spin" data-bgopacity="30%"><span>BX100能够在患者病情恶化检测解决方案中加强临床监测，降低临床医生检测风险，从而使他们能够更早进行干预，并帮助改善较低视力护理领域的护理。这款轻便的一次性生物传感器是一款5天一次性可穿戴贴片，可与可扩展集线器集成，用于监控多个房间的多个患者。该设备内置于移动查看和通知的现有临床工作流程中，无需清洁或充电。</span></section><section data-bgless="spin" data-bgopacity="30%"><span><br  /></span></section><section data-bgless="spin" data-bgopacity="30%"><strong><span>结语：</span></strong><span>可以看出，虽然业务因新冠疫情的影响而受到重创，但飞利浦医疗正在进行积极的调整，希望让疫情成为公司再发展的跳板，而全球几乎每一家医疗器械公司都有类似的计划或举动，不知这次疫情，究竟会不会成为一次医疗器械行业大洗牌的契机？<br  /></span></section><section data-bgless="spin" data-bgopacity="30%"><br  /></section></section></section></section><section data-role="outer" label="Powered by gulangu"><section data-role="paragraph" data-color="#757576"><section data-role="paragraph"><section><section><section data-brushtype="text"><strong>相关阅读</strong></section></section></section><section><section><br  /></section></section><section data-width="100%"><section><section><section><section data-width="100%"><section data-tools="gulangu" data-id="87578" data-color="#6aa9ad" data-custom="#59c3f9"><section><p><img src="image/20201014/2aac877ff9233ba5a66e7a5ff3a4febf_7.gif" /></p></section><section data-brushtype="text">戳一下，更有料！</section></section><section 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