Global Health Trials Group, Clinical Trials Unit, LSHTM, London, UK
Global Health Trials Group, Clinical Trials Unit, LSHTM, London, UK.
BMJ Open. 2023 Feb 22;13(2):e059982. doi: 10.1136/bmjopen-2021-059982.
HALT-IT was an international, randomised trial which assessed the effects of tranexamic acid (TXA) in 12 009 patients with gastrointestinal (GI) bleeding. The results found no evidence that TXA reduces death. It is widely accepted that results of trials should be interpreted in the context of other relevant evidence. We conducted a systematic review and individual patient data (IPD) meta-analysis to assess if the results of HALT-IT are compatible with evidence for TXA in other bleeding conditions.
Systematic review and IPD meta-analysis of randomised trials involving ≥5000 patients assessing TXA for bleeding. We searched our Antifibrinolytics Trials Register on 1 November 2022. Two authors extracted data and assessed risk of bias.
We used a one-stage model to analyse IPD in a regression model stratified by trial. We assessed heterogeneity of the effect of TXA on death within 24 hours and vascular occlusive events (VOEs).
We included IPD for 64 724 patients from four trials involving patients with traumatic, obstetric and GI bleeding. Risk of bias was low. There was no evidence for heterogeneity between trials for the effect of TXA on death or for the effect of TXA on VOEs. TXA reduced the odds of death by 16% (OR=0.84, 95% CI: 0.78 to 0.91, p<0.0001; p-heterogeneity=0.40). In patients treated within 3 hours of bleeding onset, TXA reduced the odds of death by 20% (0.80, 0.73 to 0.88, p<0.0001; p-heterogeneity=0.16). TXA did not increase the odds of VOEs (0.94, 0.81 to 1.08, p for effect=0.36; p-heterogeneity=0.27).
There is no evidence for statistical heterogeneity between trials assessing the effect of TXA on death or VOEs in different bleeding conditions. When the HALT-IT results are considered in the context of other evidence, a reduction in the risk of death cannot be discounted.
PROSPERO CRD42019128260.Cite Now.
HALT-IT 是一项国际性、随机试验,评估了在 12009 例胃肠道(GI)出血患者中使用氨甲环酸(TXA)的效果。结果并未发现 TXA 可降低死亡率。人们普遍认为,应根据其他相关证据来解释试验结果。我们进行了系统评价和个体患者数据(IPD)荟萃分析,以评估 HALT-IT 的结果是否与 TXA 在其他出血情况下的证据相符。
系统评价和 IPD 荟萃分析纳入了≥5000 例评估 TXA 用于出血的随机试验。我们于 2022 年 11 月 1 日检索了我们的抗纤维蛋白溶解剂试验登记处。两位作者提取数据并评估了偏倚风险。
我们使用单阶段模型,在按试验分层的回归模型中分析了 IPD。我们评估了 TXA 对 24 小时内死亡和血管闭塞性事件(VOE)的影响的异质性。
我们纳入了来自四项试验的 64724 例患者的 IPD,这些患者患有创伤性、产科和胃肠道出血。偏倚风险较低。TXA 对死亡和 VOE 的影响的试验间不存在异质性的证据。TXA 降低了 16%的死亡风险(OR=0.84,95%CI:0.78 至 0.91,p<0.0001;p 异质性=0.40)。在出血发作后 3 小时内接受治疗的患者中,TXA 降低了 20%的死亡风险(0.80,0.73 至 0.88,p<0.0001;p 异质性=0.16)。TXA 并未增加 VOE 的风险(0.94,0.81 至 1.08,p 效应=0.36;p 异质性=0.27)。
在评估 TXA 对不同出血情况下的死亡或 VOE 的影响的试验之间,没有证据表明存在统计学异质性。当将 HALT-IT 的结果置于其他证据的背景下考虑时,不能排除死亡风险降低的可能性。
PROSPERO CRD42019128260.