维生素K在危重儿童凝血障碍中的应用。

Q2 Medicine Hospital practice (1995) Pub Date : 2023-12-01 Epub Date: 2024-01-10 DOI:10.1080/21548331.2023.2277679
Christina J Smith, Ryan Valencia, Caroline M Sierra, Merrick Lopez
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引用次数: 0

摘要

目的:凝血障碍与重症监护室(ICU)儿童死亡率增加有关。维生素K缺乏性凝血病的推荐治疗方法是服用维生素K。本研究的目的是评估维生素K治疗危重儿童凝血障碍的疗效,并确定维生素K剂量与凝血酶原时间(PT)和国际标准化比值(INR)变化之间的关系。方法:这项回顾性队列研究回顾了≤17岁患者的电子病历 2013年1月至2021年1月在儿科重症监护室接受维生素K治疗的患者。接受维生素K拮抗剂治疗的患者被排除在外。有效性数据包括维生素K给药后PT/INR的变化。安全性数据包括超敏反应或过敏反应的发生率。结果:共有310名患者(中位年龄6.8岁) 年,范围22 第177天 年)接受维生素K。中位数为3剂(范围1-8)和0.14 mg/kg/剂量(范围0.09-0.22 mg/kg),最常见的是静脉注射(892/949,94%)。大多数患者(304/310,98%)至少有一个维生素K缺乏的危险因素。服用维生素K前,平均PT/INR为21.5/2.1,下降了4.4(SD = 9.0,95%置信区间16.011至18.015,p p 结论:维生素K治疗危重儿童维生素K缺乏性凝血病是有效和安全的。需要进一步的研究来确定维生素K剂量与PT/INR变化之间的关系。
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The use of vitamin K for coagulopathy in critically ill children.

Objectives: Coagulopathy is associated with increased mortality in children in the intensive care unit (ICU). Recommended management of vitamin K-deficient coagulopathy is vitamin K administration. The goal of this study was to evaluate vitamin K administration for coagulopathy in critically ill children and determine a relationship between vitamin K dose and change in prothrombin time (PT) and international normalized ratio (INR).

Methods: This retrospective cohort study reviewed electronic medical records of patients ≤17 years who received vitamin K for acute coagulopathy in the pediatric ICU from January 2013 to January 2021. Patients receiving vitamin K antagonists were excluded. Effectiveness data included change in PT/INR after vitamin K administration. Safety data included incidence of hypersensitivity or anaphylaxis.

Results: A total of 310 patients (median age 6.8 years, range 22 days-17.7 years) received vitamin K. A median of three doses (range 1-8) and 0.14 mg/kg per dose (range 0.09-0.22 mg/kg) were given, most frequently intravenously (892/949, 94%). Most patients (304/310, 98%) had at least one risk factor for vitamin K deficiency. Mean PT/INR was 21.5/2.1 prior to vitamin K administration, which decreased by 4.4 (SD = 9.0, 95% CI 16.011 to 18.015, p < 0.001) and 0.5 (SD = 1.0, 95% CI 1.490 to 1.705, p < 0.001) to means of 17.0 and 1.6, respectively, after the first vitamin K dose. No linear relationship was found between vitamin K dose and change in PT/INR. No hypersensitivity or anaphylaxis occurred following vitamin K administration; 27% (84/310) of patients died.

Conclusions: Administration of vitamin K is effective and safe for the management of vitamin K-deficient coagulopathy in critically ill pediatric patients. Further study is needed to determine a relationship between vitamin K dose and change in PT/INR.

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来源期刊
Hospital practice (1995)
Hospital practice (1995) Medicine-Medicine (all)
CiteScore
2.80
自引率
0.00%
发文量
54
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