24 research outputs found
Tranexamic acid for hyperacute primary IntraCerebral Haemorrhage (TICH-2): an international randomised, placebo-controlled, phase 3 superiority trial
BackgroundTranexamic acid (TXA) reduces death due to bleeding after trauma and post-partum haemorrhage. The aim was to assess if tranexamic acid reduces haematoma expansion and improves outcome in adults with stroke due to intracerebral 6 haemorrhage (ICH). MethodsWe undertook an international, randomised placebo-controlled trial in adults with intracerebral haemorrhage. Participants received 1g intravenous tranexamic acid bolus followed by an 8 hour 1g infusion, or matching placebo, within 8 hours of symptom onset. The primary outcome was functional status at day 90, measured by shift in the modified Rankin Scale (mRS), using ordinal logistic regression, with adjustment for stratification and minimisation criteria. All analyses were performed on an intention to treat basis. This trial is registered as ISRCTN93732214.FindingsWe recruited 2,325 participants (TXA 1161, placebo 1164) from 124 hospitals in 12 countries between 2013 and 2017. Treatment groups were well balanced at baseline. The primary outcome was determined for 2307 (99·2%) participants. There was no statistically significant difference between the groups for the primary outcome of functional status at day 90 (adjusted odds ratio [aOR] 0·88, 95% CI 0·76-1·03, p=0·11). Although there were fewer deaths by day 7 in the TXA group (aOR 0·73, 95% CI 0·53-0·99, p=0·0406), there was no difference in case fatality at 90 days (adjusted hazard ratio 0·92, 95% CI 0·77 to 1·10, p =0·37). There were fewer serious adverse events after TXA vs. placebo by days 2 (p=0·0272), 7 (p=0·0200) and 90 (p=0·0393).InterpretationThere was no significant difference in functional status 90 days after intracerebral haemorrhage with tranexamic acid, despite a reduction in early deaths and serious adverse events. Larger randomised trials are needed to confirm or refute a clinically significant treatment effect
Pragmatic guidance for IPD systematic reviews and meta-analyses of intervention effects based on randomised trials.
<p>Pragmatic guidance for IPD systematic reviews and meta-analyses of intervention effects based on randomised trials.</p
Relative risks and p values for the interaction between treatment and categorical covariates using one and two-stage models.
<p>The two-stage model with fixed-effect replicating the analysis of <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0046042#pone.0046042-Askie1" target="_blank">[29]</a>. One-stage models were consistent whether treatment effects were fixed or random.</p
Forest plot of relative risks of developing pre-eclampsia (fixed-effect inverse variance model based on two-stage analysis replicating the analysis of [<b>29</b>]).
<p>Q(df = 23) = 31.19, p = 0.12, I<sup>2</sup> = 26.3.</p
Tradeoffs between analytical, computational and statistical complexity, ability to minimise potential bias and provide insights into treatment-covariate interactions.
<p>Tradeoffs between analytical, computational and statistical complexity, ability to minimise potential bias and provide insights into treatment-covariate interactions.</p
Relative risk and p value for treatment-covariate interactions for continuous covariates.
<p>Relative risk and p value for treatment-covariate interactions for continuous covariates.</p
Comparison of one-stage models including interaction between antiplatelets and presence of a high-risk factor.
<p>Comparison of one-stage models including interaction between antiplatelets and presence of a high-risk factor.</p
Maternal secondary outcomes<sup>*</sup>.
<p>Maternal secondary outcomes<sup><a href="http://www.plosmedicine.org/article/info:doi/10.1371/journal.pmed.1002398#t008fn002" target="_blank">*</a></sup>.</p