Kaltungo Snakebite Research Hospital, Gombe State, Nigeria.
Department of Community Medicine, Federal Teaching Hospital, Gombe, Nigeria.
Am J Trop Med Hyg. 2024 Aug 6;111(4):904-910. doi: 10.4269/ajtmh.24-0222. Print 2024 Oct 2.
In an open randomized controlled trial, we compared one vial (10 mL) to two vials (20 mL) of EchiTAb-plus-ICP (EPI) antivenom among children with systemic carpet viper (Echis romani) envenoming of moderate severity in northeastern Nigeria. Systemic envenoming, presenting with incoagulable blood, was diagnosed using the 20-minute whole blood clotting test (20WBCT). Eligible patients with positive 20WBCT whose guardians assented were recruited and randomly allocated to receive either one vial or two vials of EPI administered either as a bolus or as a slow continuous infusion. The primary outcome was permanent restoration of blood coagulability 6 hours after the start of treatment, assessed by the 20WBCT and repeated at 6, 12, 24, and 48 hours after treatment. Secondary outcomes were the incidences of early adverse reactions to antivenom treatment. Initial doses permanently restored blood coagulability at 6 hours in 34/39 (87.2%) of those treated with one vial and 39/41 (95.1%) of those treated with two vials of EPI (P = 0.258). However, the proportion with permanent restoration of clotting at 6 hours among patients randomized to bolus administration was 41 of 42 (97.6%) patients compared with 32 of 38 (84.2%) patients randomized to slow infusion of EPI antivenom (P = 0.049); however, the difference was not sustained through the remaining time points. There was no difference in early adverse reactions between those treated with the two different doses or modes of delivery. We conclude that the one-vial dose compared favorably to two vials of EPI antivenom with regards to effectiveness and safety among children with carpet viper envenoming of moderate severity in Nigeria.
在一项开放性、随机对照试验中,我们比较了在尼日利亚东北部中重度系统性地毯毒蛇(Echis romani)咬伤的儿童中,使用一(10 毫升)瓶和两(20 毫升)瓶 EchiTAb-plus-ICP(EPI)抗蛇毒血清的效果。系统性中毒表现为血液不可凝固,通过 20 分钟全血凝固试验(20WBCT)进行诊断。对于 20WBCT 阳性且监护人同意的合格患者进行招募,并随机分配接受一(10 毫升)瓶或两(20 毫升)瓶 EPI,以推注或缓慢持续输注的方式给药。主要结局是治疗开始后 6 小时内永久性恢复血液凝固能力,通过 20WBCT 评估,并在治疗后 6、12、24 和 48 小时重复评估。次要结局是抗蛇毒血清治疗的早期不良反应发生率。一(10 毫升)瓶组有 34/39(87.2%)例患者,两(20 毫升)瓶组有 39/41(95.1%)例患者在 6 小时内永久性恢复凝血功能,两组间差异无统计学意义(P=0.258)。然而,与接受 EPI 抗蛇毒血清缓慢输注的患者(32/38,84.2%)相比,接受推注的患者中 6 小时内永久性恢复凝血功能的比例为 42/42(97.6%)(P=0.049);然而,这种差异在其余时间点并未持续存在。两种不同剂量或给药方式之间的早期不良反应发生率无差异。我们得出结论,在尼日利亚中重度系统性地毯毒蛇咬伤的儿童中,与两(20 毫升)瓶 EPI 抗蛇毒血清相比,一(10 毫升)瓶剂量在有效性和安全性方面具有优势。