Rosemarie Nagy, T. Hemmelgarn, Stephen Deptola, Brianna Hemmann
{"title":"评估新生儿重症监护室收治婴儿的初始依诺肝素剂量和抗因子 Xa 水平","authors":"Rosemarie Nagy, T. Hemmelgarn, Stephen Deptola, Brianna Hemmann","doi":"10.1159/000537797","DOIUrl":null,"url":null,"abstract":"Abstract Introduction Infants are at risk for thrombotic conditions due to multiple risk factors such as congenital heart defects and sepsis. According to the American College of Chest Physicians (ACCP) 2012 guidelines, enoxaparin may be given for thrombotic conditions at a dose of 1.5 mg/kg/dose every 12 h for patients less than 2 months of age and 1 mg/kg/dose every 12 h for those older than 2 months. Several studies have reported that infants typically require a higher initial dose of enoxaparin to reach therapeutic antifactor Xa levels than what is currently recommended. Methods This is a single-center retrospective case-control study of hospitalized infants less than 12 months of age who received treatment with enoxaparin while admitted to the neonatal intensive care unit (NICU) at a freestanding children’s hospital. The primary objective was the difference between the initial enoxaparin dose (mg/kg) compared to the enoxaparin dose in which the patient first achieved a therapeutic antifactor Xa level of 0.5–1.0 units/mL. Results A total of 56 infants were included in this study. The median enoxaparin dose at initiation was 1.5 mg/kg/dose, and the median enoxaparin dose at the first therapeutic antifactor Xa level was 1.9 mg/kg/dose (z = −12.7, p < 0.0001). There was no correlation between gestational age and weight with the enoxaparin dose required to reach a therapeutic antifactor Xa level. Conclusion Infants admitted to the NICU, specifically those less than 4 months of age, require higher initial enoxaparin dosing to reach therapeutic antifactor Xa levels than what is currently recommended.","PeriodicalId":101351,"journal":{"name":"Biomedicine hub","volume":"9 3","pages":"54 - 61"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of Initial Enoxaparin Dosing and Antifactor Xa Levels in Infants Admitted to the Neonatal Intensive Care Unit\",\"authors\":\"Rosemarie Nagy, T. Hemmelgarn, Stephen Deptola, Brianna Hemmann\",\"doi\":\"10.1159/000537797\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Introduction Infants are at risk for thrombotic conditions due to multiple risk factors such as congenital heart defects and sepsis. According to the American College of Chest Physicians (ACCP) 2012 guidelines, enoxaparin may be given for thrombotic conditions at a dose of 1.5 mg/kg/dose every 12 h for patients less than 2 months of age and 1 mg/kg/dose every 12 h for those older than 2 months. Several studies have reported that infants typically require a higher initial dose of enoxaparin to reach therapeutic antifactor Xa levels than what is currently recommended. Methods This is a single-center retrospective case-control study of hospitalized infants less than 12 months of age who received treatment with enoxaparin while admitted to the neonatal intensive care unit (NICU) at a freestanding children’s hospital. The primary objective was the difference between the initial enoxaparin dose (mg/kg) compared to the enoxaparin dose in which the patient first achieved a therapeutic antifactor Xa level of 0.5–1.0 units/mL. Results A total of 56 infants were included in this study. The median enoxaparin dose at initiation was 1.5 mg/kg/dose, and the median enoxaparin dose at the first therapeutic antifactor Xa level was 1.9 mg/kg/dose (z = −12.7, p < 0.0001). There was no correlation between gestational age and weight with the enoxaparin dose required to reach a therapeutic antifactor Xa level. Conclusion Infants admitted to the NICU, specifically those less than 4 months of age, require higher initial enoxaparin dosing to reach therapeutic antifactor Xa levels than what is currently recommended.\",\"PeriodicalId\":101351,\"journal\":{\"name\":\"Biomedicine hub\",\"volume\":\"9 3\",\"pages\":\"54 - 61\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomedicine hub\",\"FirstCategoryId\":\"0\",\"ListUrlMain\":\"https://doi.org/10.1159/000537797\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine hub","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1159/000537797","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
摘要 引言 由于先天性心脏缺陷和败血症等多种风险因素,婴儿有血栓形成的风险。根据美国胸科医师学会(ACCP)2012 年指南,对于年龄小于 2 个月的患者,可按 1.5 毫克/千克/剂量每 12 小时给药一次;对于年龄大于 2 个月的患者,可按 1 毫克/千克/剂量每 12 小时给药一次。有几项研究报告称,与目前推荐的剂量相比,婴儿通常需要更高的依诺肝素初始剂量才能达到治疗性抗因子 Xa 水平。方法 这是一项单中心回顾性病例对照研究,研究对象是在一家独立儿童医院新生儿重症监护室(NICU)住院期间接受依诺肝素治疗的 12 个月以下的住院婴儿。首要目标是初始依诺肝素剂量(毫克/千克)与患者首次达到 0.5-1.0 单位/毫升治疗抗因子 Xa 水平的依诺肝素剂量之间的差异。结果 本研究共纳入了 56 名婴儿。开始使用时依诺肝素剂量的中位数为 1.5 毫克/千克/剂量,首次达到治疗性抗因子 Xa 水平时依诺肝素剂量的中位数为 1.9 毫克/千克/剂量(z = -12.7,p < 0.0001)。胎龄和体重与达到治疗性抗因子 Xa 水平所需的依诺肝素剂量之间没有相关性。结论 与目前推荐的剂量相比,新生儿重症监护室收治的婴儿(尤其是 4 个月以下的婴儿)需要更高的初始依诺肝素剂量才能达到治疗性抗因子 Xa 水平。
Evaluation of Initial Enoxaparin Dosing and Antifactor Xa Levels in Infants Admitted to the Neonatal Intensive Care Unit
Abstract Introduction Infants are at risk for thrombotic conditions due to multiple risk factors such as congenital heart defects and sepsis. According to the American College of Chest Physicians (ACCP) 2012 guidelines, enoxaparin may be given for thrombotic conditions at a dose of 1.5 mg/kg/dose every 12 h for patients less than 2 months of age and 1 mg/kg/dose every 12 h for those older than 2 months. Several studies have reported that infants typically require a higher initial dose of enoxaparin to reach therapeutic antifactor Xa levels than what is currently recommended. Methods This is a single-center retrospective case-control study of hospitalized infants less than 12 months of age who received treatment with enoxaparin while admitted to the neonatal intensive care unit (NICU) at a freestanding children’s hospital. The primary objective was the difference between the initial enoxaparin dose (mg/kg) compared to the enoxaparin dose in which the patient first achieved a therapeutic antifactor Xa level of 0.5–1.0 units/mL. Results A total of 56 infants were included in this study. The median enoxaparin dose at initiation was 1.5 mg/kg/dose, and the median enoxaparin dose at the first therapeutic antifactor Xa level was 1.9 mg/kg/dose (z = −12.7, p < 0.0001). There was no correlation between gestational age and weight with the enoxaparin dose required to reach a therapeutic antifactor Xa level. Conclusion Infants admitted to the NICU, specifically those less than 4 months of age, require higher initial enoxaparin dosing to reach therapeutic antifactor Xa levels than what is currently recommended.