@article{23197, keywords = {Female, Humans, Aged, Male, Middle Aged, Severity of Illness Index, Stroke, Age Factors, Brain Ischemia, Aged, 80 and over, Administration, Intravenous, Outcome Assessment (Health Care), Fibrinolytic Agents, Tissue Plasminogen Activator, Asian Continental Ancestry Group}, author = {Woodward Mark and Anderson Craig and Lavados Pablo and Arima Hisatomi and Li Qiang and Wang Xia and Chalmers J. and Olavarría Verónica and Billot Laurent and Demchuk Andrew and Lindley Richard and Robinson Thompson and Lee Tsong-Hai and Pandian Jeyaraj and Bath Philip and Kim Jong and Parsons Mark and Pontes-Neto Octavio and Ricci Stefano and Sharma Vijay and Wang Ji-Guang and Broderick Joseph and Donnan Geoffrey and Martins Sheila and Thang Nguyen and Enhanced Control of Hypertension and Thrombolysis Stroke Study (ENCHANTED) Investigators}, title = {Low-Dose vs Standard-Dose Alteplase for Patients With Acute Ischemic Stroke: Secondary Analysis of the ENCHANTED Randomized Clinical Trial.}, abstract = {

Importance: A lower dose of intravenous alteplase appears to be a safer treatment option than the standard dose, reducing the risk of symptomatic intracerebral hemorrhage. There is uncertainty, however, over how this effect translates into an overall clinical benefit for patients with acute ischemic stroke (AIS).

Objective: To assess whether older, Asian, or severely affected patients with AIS who are considered at high risk of thrombolysis may benefit more from low-dose rather than standard-dose alteplase treatment.

Design, Setting, and Participants: This study is a prespecified secondary analysis of the Enhanced Control of Hypertension and Thrombolysis Stroke Study (ENCHANTED), an international, randomized, open-label, blinded, end-point clinical trial of low-dose vs standard-dose intravenous alteplase for patients with AIS. From March 1, 2012, to August 31, 2015, a total of 3310 patients who had a clinical diagnosis of AIS as confirmed by brain imaging and who fulfilled the local criteria for thrombolysis treatment were included in the alteplase-dose arms. Patients were randomly assigned to receive low-dose (0.6 mg/kg; 15% as bolus and 85% as infusion over 1 hour) or standard-dose (0.9 mg/kg; 10% as bolus and 90% as infusion over 1 hour) alteplase. Of the 3310 randomized patients, 13 patients were excluded for missing consent, mistaken randomization, and duplicate randomization numbers. This secondary analysis was conducted between May 1, 2016, and April 28, 2017.

Main Outcomes and Measures: The primary end point was a poor outcome defined by the combination of death and any disability as scored by the modified Rankin Scale (scores range from 2 to 6, with the highest score indicating death) at 90 days.

Results: Of the 3297 patients included in the analysis, 1248 (37.9%) were women, and the mean (SD) age was 67 (13) years. No significant differences in the treatment effects were observed between low- and standard-dose alteplase for poor outcomes (death or disability) by age, ethnicity, or severity (all P > .37 for interaction). Similarly, the treatment effects of low- vs standard-dose alteplase on function outcome (ordinal shift of the modified Rankin Scale) in Asians (odds ratio, 1.05; 95% CI, 0.90-1.22) was consistent with non-Asians (odds ratio, 0.93; 95% CI, 0.76-1.14) (P = .32 for interaction). There were generally consistent reductions in rates of symptomatic intracerebral hemorrhage with low-dose alteplase, although this reduction was not statistically significant by age, ethnicity, or severity.

Conclusions and Relevance: This analysis found that the effects of low-dose alteplase were not clearly superior to the effects of standard-dose alteplase on death or disability in key demographic subgroups of patients with AIS. Further investigation is required to identify patients with AIS who may benefit from low-dose alteplase.

Trial Registration: clinicaltrials.gov Identifier: NCT01422616.

}, year = {2017}, journal = {JAMA Neurol}, volume = {74}, pages = {1328-1335}, issn = {2168-6157}, doi = {10.1001/jamaneurol.2017.2286}, language = {eng}, }