{"id":29726,"date":"2026-02-02T04:16:00","date_gmt":"2026-02-01T20:16:00","guid":{"rendered":"https:\/\/csccm.org.cn\/?p=29726"},"modified":"2026-02-02T05:35:46","modified_gmt":"2026-02-01T21:35:46","slug":"jama%e5%8f%91%e8%a1%a8%e8%ae%ba%e6%96%87%ef%bc%9a%e4%b8%a5%e9%87%8d%e5%bf%83%e6%ba%90%e6%80%a7%e4%bc%91%e5%85%8b%e6%82%a3%e8%80%85%e4%bd%bf%e7%94%a8%e5%b7%a6%e8%a5%bf%e5%ad%9f%e6%97%a6%e8%84%b1","status":"publish","type":"post","link":"https:\/\/csccm.org.cn\/?p=29726","title":{"rendered":"[JAMA\u53d1\u8868\u8bba\u6587]\uff1a\u4e25\u91cd\u5fc3\u6e90\u6027\u4f11\u514b\u60a3\u8005\u4f7f\u7528\u5de6\u897f\u5b5f\u65e6\u8131\u79bbECMO"},"content":{"rendered":"\n<p>Original Investigation<\/p>\n\n\n\n<p>Caring for the Critically Ill Patient<\/p>\n\n\n\n<h1 class=\"wp-block-heading\">Levosimendan to Facilitate Weaning From ECMO in Patients With Severe Cardiogenic Shock: The LEVOECMO Randomized Clinical Trial<\/h1>\n\n\n\n<h3 class=\"wp-block-heading\">Alain&nbsp;Combes,&nbsp;Ouriel&nbsp;Saura,&nbsp;Nicolas&nbsp;Nesseler,&nbsp;et al<\/h3>\n\n\n\n<h3 class=\"wp-block-heading\">JAMA Published Online:&nbsp;December&nbsp;1,&nbsp;2025<\/h3>\n\n\n\n<h3 class=\"wp-block-heading\">doi: 10.1001\/jama.2025.19843<\/h3>\n\n\n\n<p>Key Points<\/p>\n\n\n\n<p><strong>Question<\/strong>&nbsp;&nbsp;In patients with severe but potentially reversible cardiogenic shock who are receiving venoarterial extracorporeal membrane oxygenation (VA-ECMO), does early administration of levosimendan improve time to successful ECMO weaning within 30 days following randomization?<\/p>\n\n\n\n<p><strong>Findings<\/strong>&nbsp;&nbsp;In this double-blind, placebo-controlled randomized clinical trial that included 205 patients receiving VA-ECMO, successful ECMO weaning at day 30 occurred in 69 (68.3%) in the levosimendan group compared with 71 (68.3%) in the placebo group, a nonsignificant difference.<\/p>\n\n\n\n<p><strong>Meaning<\/strong>&nbsp;&nbsp;In patients with potentially reversible cardiogenic shock supported by VA-ECMO, levosimendan did not reduce the time to successful weaning from ECMO compared with placebo.<a><\/a><\/p>\n\n\n\n<p>Abstract<\/p>\n\n\n\n<p><strong>Importance<\/strong>&nbsp;&nbsp;Levosimendan may facilitate weaning from venoarterial extracorporeal membrane oxygenation (VA-ECMO) and improve survival, but supporting evidence remains limited.<\/p>\n\n\n\n<p><strong>Objective<\/strong>&nbsp;&nbsp;To assess whether early administration of levosimendan reduces the time to successful VA-ECMO weaning in patients with severe but potentially reversible cardiogenic shock.<\/p>\n\n\n\n<p><strong>Design, Setting, and Participants<\/strong>&nbsp;&nbsp;Randomized, double-blind, placebo-controlled trial conducted across 11 intensive care units (ICUs) in France. Between August 27, 2021, and September 10, 2024, 205 adult patients with acute cardiogenic shock who had started VA-ECMO in the preceding 48 hours were enrolled. Final follow-up was completed on November 10, 2024.<\/p>\n\n\n\n<p><strong>Interventions<\/strong>&nbsp;&nbsp;Patients were randomized in a 1:1 ratio to receive levosimendan, 0.15 \u03bcg\/kg per minute, to be increased to 0.20 \u03bcg\/kg per minute after 2 hours (n\u2009=\u2009101), or placebo (n\u2009=\u2009104).<\/p>\n\n\n\n<p><strong>Main Outcomes and Measures<\/strong>&nbsp;&nbsp;The primary outcome was time to successful ECMO weaning within 30 days following randomization. Secondary outcomes included ECMO-, mechanical ventilation\u2013, and organ failure\u2013free days, ICU and hospital lengths of stay, serious adverse events, and all-cause 30- and 60-day mortality.<\/p>\n\n\n\n<p><strong>Results<\/strong>\u00a0\u00a0Among the 205 randomized patients (median age, 58 [IQR, 50-67] years; 149 [72.7%] male), main cardiogenic shock etiologies were postcardiotomy (79 [38.5%]), acute myocardial infarction (56 [27.3%]), and myocarditis (28 [13.7%]). Treatment dose was increased to 0.20 \u00b1 0.01 \u03bcg\/kg per minute in 93% of patients receiving levosimendan and in 96% of those receiving placebo. Within 30 days, 69 of 101 patients (68.3%) had a successful ECMO weaning in the levosimendan group compared with 71 of 104 (68.3%) in the placebo group (risk difference, 0.0% [95% CI, \u221212.8% to 12.7%]; subdistribution hazard ratio, 1.02 [95% CI, 0.74-1.39];\u00a0<em>P<\/em>\u2009=\u2009.92). In the levosimendan and placebo groups, respectively, median ECMO duration (5 [IQR, 4-7] days vs 6 [IQR, 4-11] days;\u00a0<em>P<\/em>\u2009=\u2009.53), mean ICU length of stay (18 [SD, 15] days vs 19 [SD, 15] days;\u00a0<em>P<\/em>\u2009=\u2009.42), and 60-day mortality (27.7% vs 25.0%; risk difference, 2.7% [95% CI, \u22129.0% to 15.3%];\u00a0<em>P<\/em>\u2009=\u2009.78) did not differ significantly. Ventricular arrhythmias occurred more frequently with levosimendan (18 [17.8%] vs 9 [8.7%]; absolute risk difference, 9.2% [95% CI, 0.4%-18.1%]).<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087va_1766516491.21106.png?Expires=1770751632&amp;Signature=QFjrfhvajgZjAfyMBk-d8Rb1NB6Q2B8Jo6QnjGT-y-L~luqxeE9o1HfwOjcI5gR2GVS4T16DwdlK5VmWuMmWVc-RH4LO6oRPy40vL9EsthHU1-pwt5IVGQ0UZfgub2Ji1s9wdpvFxLx2yf2o7yVSIG44ui9PTYTOkH2tm-GDyZMqRxeKkyOWF1FNu8Aj7tsRdF49mxpQlbwExTwbDvBaGHF4kTPqaG9CLEJ3tBZa9~ZRYeoKAk5BUsesN-iOL48moe78h~MjvCbrXA-lRsxNQ4Pp2H7cMRJK93ZRXJO4iRf4yi-j8BvAMhtz2ZwpuTNQQj1E-s9j4KLXiXGL7jFmoQ__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087f1_1766516491.27106.png?Expires=1770751632&amp;Signature=WL04lhOhoUj7WdjC~A3byGbGJ~BHaQWkhKE7l~Vo6Ytm-FgqB7~O2IDXirhtKHfKZUfq3xX6zn-QsHEdkQDbhqqeJhyeW0EHvCtpqGM7DF6HU4An-w7c4JmrMnd~usLX-xLcaaTtmRDCNEpuPkR04GBk4H1l54qZVJTzPz3MwiLIgL7NhpFSX1eQ~mPSgnyQgHaq714uMKfticSWdvqUXk2~EDgWx7T2ZjVxjq~rS7rwYLJYs6pjWKCA7Ixt52bW425WzE~urCciIqEFa84cx4p4KORot~zGsEkrD-w0n2OiXcaLkU8gGrjTtKEnjTpWA6OWaiGJ7wJcbvSeJzYQRw__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087f2_1766516491.32213.png?Expires=1770751632&amp;Signature=f5~kggt7GgyAqf9iOctusbqwcgEo8ppbXxC7U~fi6zkHeGYgsATa6VFca7dnNn2d9McZfRYKcx~qxvBx6J4C48e-vzTzYctQl7inxuBZC9xJd-OewR5QqYGwwUiWu6NajaTJ8rFpcGptIe5u859ozXO8XIABBs7GX8QPvppeJXJWXaD4M2WMc-QTBl2TYZJqYYe0ahlJvtoWwAOxGT5ryVzZph0OK1KgBkugc-1NDHExyxnHYcKPvJjdIfzMvj6GT1YlBQVjV5hzKQqQFPa2F0iZlVTxqBVd47U6rqxCM9PqzaNJc27BbsO-Mu-~ThYTuhkpK7VN5YQR1txvRMdkSw__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087f3_1766516491.34325.png?Expires=1770751632&amp;Signature=ovhzE7HFTXw0GfmK3o7QaUZpvOqfiOz-G0x0KxcrMJLnK~5~xLdSr34PVXInPNmi-Ng5KjfKrglVGTJo8fZ1hrw73cG1yMdUOAqC799JegJJTNs0sWdJ142FRpZ7nHNxi0Y6Zv4kM4BksUkA5gPnpWwCwvBQfaa1n6njhkiSHg66k7ACkR6OnqXBtz~fz66zEfGeTAIhoq5vjj8bYNluQCprOuroC1prJKUCl0DkIoEVpy2akLiBF2Jp54yby-0ZKSXpRywFxl3kzDvmUf3lE4284SKtFMucR24CVukYESni-2-n9bt3RJVVo4e6Q6X9Q0FgrnglNlU~~PEr36MAzQ__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087t1_1766516491.28713.png?Expires=1770751632&amp;Signature=XwrDcwebZlTsbwJTZLaAcr19k4hPiZvBkqKsQMsqVIESlT32V9dqvPUNI1l~F41uTURErxlb3WcY3TdmtCtv1EsIfgDjY8cz5Y8QpbKxnXHCuQ1fB08qipf3FYgJdHcXiKzo0Hp6vvFtX2XHeRUgUQgAfEC2yEaeVUOLtOUiy9kuHGMNnt-Ija3XdzhwDJBvEHGMfAYoS5g4D81gelUthVEza~Vk0u3QaPY5qruAdxgImykg4W7yl8g~y7EJ2VsW76G9vSiUR6IYemQuHsQiTjHhIpc452L~PEipG5wc178P35e86dntp1Kd6V9ENzK9f1tBfa~h1AXwb2HioHS24w__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087t2_1766516491.31213.png?Expires=1770751632&amp;Signature=iV8ZUYycrWL7-BPtQh77cCyxNIeJGI9-3jrx6HJUSBWqtoh44NnOyHthQ91DjWCa~iU1lzb1mlzS~w3IB5EZGiZphtS8lrxiTqzB7OFTNd0r4bf7l3tJPihxQxQvXDAsO0ky7R56j385jy6CQigx8uXxWvQbN60Tw-y368kM9BJA-hbcj4FJyWf7lOrt-GRR49kElUiFTF5yQ9yavjlXuUHbZgtA11oFXP37VOE-SnnFUgvFWZFwA65gYQBY7muE17MyiQK-2N1X~1AjG2GxdoxEut4LYMCUcvPruEDwKHoNY1nvE5fYVoF8nFqAfgn5Gm9B9LnZhMnvwmIzrrnEAg__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/cdn.jamanetwork.com\/ama\/content_public\/journal\/jama\/939763\/joi250087t3_1766516491.33324.png?Expires=1770751632&amp;Signature=TNaGs7S0jAkbaL~X6HI3zOPWofCXDkmhybA7ZirNxYMmN2~Dgg4FhoxMm8tAti7yGfubDP1P5eptmTy5eSrkvMLeWjzQvTo56V2aOZEkY~pIz1XLS92XmJGApjwFUqjtPZU8cjoaFxWZul0AhttEcrstJ1AvopgoDsDASKX1-Sapz8Of-FVTq4KRS7-hgOftMaQ8fNX8vxGZxSipTLYrVShR-80WfvKcvjxpRXiYxwT-0T3Tptg293GM7o7wys6NajuHo8d8NRN4eEpTnh--p-I6ih9yhZU~giHCwQKGz5lUhNDN9OeikAqUfgmR6LCguRe7~nWjsYADGPqHIemkEw__&amp;Key-Pair-Id=APKAIE5G5CRDK6RD3PGA\" alt=\"\"\/><\/figure>\n\n\n\n<p><strong>Conclusions and Relevance<\/strong>&nbsp;&nbsp;Among patients with severe but potentially reversible cardiogenic shock supported by VA-ECMO, early levosimendan administration did not significantly reduce the time to successful weaning of ECMO compared with placebo.<\/p>\n\n\n\n<p><strong>Trial Registration<\/strong>&nbsp;&nbsp;ClinicalTrials.gov Identifier:&nbsp;<a href=\"https:\/\/www.clinicaltrials.gov\/study\/NCT04728932\">NCT04728932<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Original Investigation Caring for the Critically Ill Pa 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