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脓毒性休克患者的活化蛋白 C:连续病例系列。

Activated protein C in patients with septic shock: a consecutive case series.

机构信息

Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.

出版信息

Int J Clin Pharm. 2012 Feb;34(1):23-6. doi: 10.1007/s11096-011-9588-9. Epub 2011 Nov 27.

Abstract

BACKGROUND

The recommendation to restrict the use of activated protein C (APC) to patients with severe sepsis and the highest risk of death originates from large trials that were subject to major exclusion criteria.

OBJECTIVE

To investigate the effect of APC on prognosis in 'real world' patients.

METHOD

Consecutive case series at tertiary care hospital including 63 adults with septic shock and multi-organ failure treated with APC (24 mcg/kg/h) for up to 96 h in addition to standard care.

RESULTS

Median APACHE score was 35 (quartiles, 29-41), mean number of failing organs was 4 (quartiles, 4-5), and overall 30-day mortality was 48%. Independent predictors of 30-day mortality risk were the number of failing organs and number of antibiotics given. Risk of dying was significantly lower if compared with the mortality rates expected per APACHE II score category (P for trend per 5-point increment <0.001). This association was most prominent in patients with an APACHE II score of 30-44. Intracranial or major bleeding during APC treatment did not occur.

CONCLUSION

These findings support the view that targeting APC treatment to patients with septic shock and a very high risk is a sound and safe approach. However, due to lack of consistent evidence from randomized studies APC was recently removed from the market.

摘要

背景

限制活化蛋白 C (APC) 仅用于严重脓毒症和死亡风险最高的患者的建议源于受到重大排除标准限制的大型试验。

目的

研究 APC 对“真实世界”患者预后的影响。

方法

在三级护理医院进行连续病例系列研究,纳入 63 例脓毒性休克和多器官衰竭患者,在标准治疗的基础上加用 APC(24 mcg/kg/h)治疗,最长 96 小时。

结果

中位急性生理与慢性健康评分(APACHE)为 35 分(四分位距,29-41 分),衰竭器官的平均数量为 4 个(四分位距,4-5 个),总体 30 天死亡率为 48%。30 天死亡率的独立预测因素是衰竭器官的数量和使用的抗生素数量。与每个急性生理与慢性健康评分(APACHE)Ⅱ评分类别预期的死亡率相比,死亡风险显著降低(趋势 P 值每增加 5 分<0.001)。这种关联在急性生理与慢性健康评分 30-44 分的患者中最为显著。在 APC 治疗期间未发生颅内或重大出血。

结论

这些发现支持这样一种观点,即针对脓毒性休克和极高风险患者靶向 APC 治疗是一种合理且安全的方法。然而,由于缺乏来自随机研究的一致证据,APC 最近已从市场上撤出。

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