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小剂量肾上腺素、苯海拉明和氢化可的松预防蛇伤后抗蛇毒血清急性不良反应的随机、双盲、安慰剂对照试验。

Low-dose adrenaline, promethazine, and hydrocortisone in the prevention of acute adverse reactions to antivenom following snakebite: a randomised, double-blind, placebo-controlled trial.

机构信息

Clinical Trials Unit, Faculty of Medicine, University of Kelaniya, Ragama, Sri Lanka.

出版信息

PLoS Med. 2011 May;8(5):e1000435. doi: 10.1371/journal.pmed.1000435. Epub 2011 May 10.

Abstract

BACKGROUND

Envenoming from snakebites is most effectively treated by antivenom. However, the antivenom available in South Asian countries commonly causes acute allergic reactions, anaphylactic reactions being particularly serious. We investigated whether adrenaline, promethazine, and hydrocortisone prevent such reactions in secondary referral hospitals in Sri Lanka by conducting a randomised, double-blind placebo-controlled trial.

METHODS AND FINDINGS

In total, 1,007 patients were randomized, using a 2 × 2 × 2 factorial design, in a double-blind, placebo-controlled trial of adrenaline (0.25 ml of a 1∶1,000 solution subcutaneously), promethazine (25 mg intravenously), and hydrocortisone (200 mg intravenously), each alone and in all possible combinations. The interventions, or matching placebo, were given immediately before infusion of antivenom. Patients were monitored for mild, moderate, or severe adverse reactions for at least 96 h. The prespecified primary end point was the effect of the interventions on the incidence of severe reactions up to and including 48 h after antivenom administration. In total, 752 (75%) patients had acute reactions to antivenom: 9% mild, 48% moderate, and 43% severe; 89% of the reactions occurred within 1 h; and 40% of all patients were given rescue medication (adrenaline, promethazine, and hydrocortisone) during the first hour. Compared with placebo, adrenaline significantly reduced severe reactions to antivenom by 43% (95% CI 25-67) at 1 h and by 38% (95% CI 26-49) up to and including 48 h after antivenom administration; hydrocortisone and promethazine did not. Adding hydrocortisone negated the benefit of adrenaline.

CONCLUSIONS

Pretreatment with low-dose adrenaline was safe and reduced the risk of acute severe reactions to snake antivenom. This may be of particular importance in countries where adverse reactions to antivenom are common, although the need to improve the quality of available antivenom cannot be overemphasized.

摘要

背景

蛇伤的治疗最有效的方法是使用抗蛇毒血清。然而,南亚国家使用的抗蛇毒血清通常会引起急性过敏反应,其中过敏性反应尤其严重。我们通过在斯里兰卡的二级转诊医院进行一项随机、双盲、安慰剂对照试验,研究肾上腺素、苯海拉明和氢化可的松是否能预防这种反应。

方法和发现

共有 1007 名患者参与了这项随机、双盲、安慰剂对照的试验,采用 2×2×2 析因设计,用皮下注射 1∶1000 的肾上腺素(0.25ml)、静脉注射苯海拉明(25mg)和静脉注射氢化可的松(200mg),单独和组合使用,每种干预措施或匹配的安慰剂在使用抗蛇毒血清前立即给予。患者在至少 96 小时内被监测轻度、中度或重度不良反应。主要终点是干预措施对抗蛇毒血清给药后 1 至 48 小时内严重反应发生率的影响。共有 752 名(75%)患者对抗蛇毒血清有急性反应:9%为轻度,48%为中度,43%为重度;89%的反应发生在 1 小时内;40%的患者在第一个小时内使用了急救药物(肾上腺素、苯海拉明和氢化可的松)。与安慰剂相比,肾上腺素在 1 小时时显著降低了 43%(95%CI 25-67)的严重反应发生率,在抗蛇毒血清给药后 1 至 48 小时内降低了 38%(95%CI 26-49);氢化可的松和苯海拉明没有。同时使用氢化可的松则消除了肾上腺素的益处。

结论

低剂量肾上腺素预处理是安全的,可降低蛇抗蛇毒血清引起的急性严重反应的风险。在抗蛇毒血清不良反应常见的国家,这可能尤其重要,尽管不能过分强调需要提高现有抗蛇毒血清的质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d95d/3091849/bfd154aa648b/pmed.1000435.g001.jpg

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