{"id":22215,"date":"2022-08-31T05:08:00","date_gmt":"2022-08-30T21:08:00","guid":{"rendered":"http:\/\/csccm.org.cn\/?p=22215"},"modified":"2022-08-31T05:48:02","modified_gmt":"2022-08-30T21:48:02","slug":"nejm%e5%8f%91%e8%a1%a8%e8%ae%ba%e6%96%87%ef%bc%9aepo%e6%b2%bb%e7%96%97%e6%96%b0%e7%94%9f%e5%84%bf%e7%bc%ba%e8%a1%80%e7%bc%ba%e6%b0%a7%e6%80%a7%e8%84%91%e7%97%85","status":"publish","type":"post","link":"https:\/\/csccm.org.cn\/?p=22215","title":{"rendered":"[NEJM\u53d1\u8868\u8bba\u6587]\uff1aEPO\u6cbb\u7597\u65b0\u751f\u513f\u7f3a\u8840\u7f3a\u6c27\u6027\u8111\u75c5"},"content":{"rendered":"\n<p><a href=\"https:\/\/www.nejm.org\/medical-articles\/original-article\" class=\"\">ORIGINAL ARTICLE<\/a><\/p>\n\n\n\n<h1 class=\"wp-block-heading\">Trial of Erythropoietin for Hypoxic\u2013Ischemic Encephalopathy in Newborns<\/h1>\n\n\n\n<h3 class=\"wp-block-heading\">Yvonne W. Wu, Bryan A. Comstock, Fernando F. Gonzalez,\u00a0et al<\/h3>\n\n\n\n<h3 class=\"wp-block-heading\">N Engl J Med 2022; 387:148-159<br \/>DOI: 10.1056\/NEJMoa2119660<\/h3>\n\n\n\n<h2 class=\"wp-block-heading\">Abstract<\/h2>\n\n\n\n<h2 class=\"wp-block-heading\">BACKGROUND<\/h2>\n\n\n\n<p>Neonatal hypoxic\u2013ischemic encephalopathy is an important cause of death as well as long-term disability in survivors. Erythropoietin has been hypothesized to have neuroprotective effects in infants with hypoxic\u2013ischemic encephalopathy, but its effects on neurodevelopmental outcomes when given in conjunction with therapeutic hypothermia are unknown.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">METHODS<\/h2>\n\n\n\n<p><img decoding=\"async\" loading=\"lazy\" srcset=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xsmall\/nejmoa2119660_f0.jpeg 150w, https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_small\/nejmoa2119660_f0.jpeg 300w, https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_medium\/nejmoa2119660_f0.jpeg 800w\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_medium\/nejmoa2119660_f0.jpeg\" width=\"300\" height=\"400\"\/><\/p>\n\n\n\n<p>In a multicenter, double-blind, randomized, placebo-controlled trial, we assigned 501 infants born at 36 weeks or more of gestation with moderate or severe hypoxic\u2013ischemic encephalopathy to receive erythropoietin or placebo, in conjunction with standard therapeutic hypothermia. Erythropoietin (1000 U per kilogram of body weight) or saline placebo was administered intravenously within 26 hours after birth, as well as at 2, 3, 4, and 7 days of age. The primary outcome was death or neurodevelopmental impairment at 22 to 36 months of age. Neurodevelopmental impairment was defined as cerebral palsy, a Gross Motor Function Classification System level of at least 1 (on a scale of 0 [normal] to 5 [most impaired]), or a cognitive score of less than 90 (which corresponds to 0.67 SD below the mean, with higher scores indicating better performance) on the Bayley Scales of Infant and Toddler Development, third edition.<a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa2119660#\"><\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\">RESULTS<\/h2>\n\n\n\n<p>Of 500 infants in the modified intention-to-treat analysis, 257 received erythropoietin and 243 received placebo. The incidence of death or neurodevelopmental impairment was 52.5% in the erythropoietin group and 49.5% in the placebo group (relative risk, 1.03; 95% confidence interval [CI], 0.86 to 1.24; P=0.74). The mean number of serious adverse events per child was higher in the erythropoietin group than in the placebo group (0.86 vs. 0.67; relative risk, 1.26; 95% CI, 1.01 to 1.57).<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xlarge\/nejmoa2119660_f0.jpeg\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xlarge\/nejmoa2119660_f1.jpeg\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xlarge\/nejmoa2119660_t1.jpeg\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xlarge\/nejmoa2119660_f2.jpeg\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xlarge\/nejmoa2119660_t2.jpeg\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.nejm.org\/na101\/home\/literatum\/publisher\/mms\/journals\/content\/nejm\/2022\/nejm_2022.387.issue-2\/nejmoa2119660\/20220711\/images\/img_xlarge\/nejmoa2119660_f3.jpeg\" alt=\"\"\/><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">CONCLUSIONS<\/h2>\n\n\n\n<p>The administration of erythropoietin to newborns undergoing therapeutic hypothermia for hypoxic\u2013ischemic encephalopathy did not result in a lower risk of death or neurodevelopmental impairment than placebo and was associated with a higher rate of serious adverse events. (Funded by the National Institute of Neurological Disorders and Stroke; ClinicalTrials.gov number,&nbsp;<a href=\"http:\/\/clinicaltrials.gov\/show\/NCT02811263\" target=\"_blank\" rel=\"noreferrer noopener\">NCT02811263. opens in new tab<\/a>.)<\/p>\n","protected":false},"excerpt":{"rendered":"<p>ORIGINAL ARTICLE Trial of Erythropoietin for Hypoxic\u2013Is [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[32,23],"tags":[],"_links":{"self":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts\/22215"}],"collection":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=22215"}],"version-history":[{"count":1,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts\/22215\/revisions"}],"predecessor-version":[{"id":22216,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts\/22215\/revisions\/22216"}],"wp:attachment":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=22215"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=22215"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=22215"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}