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10.1097/MD.0000000000006667

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suck abstract from ncbi


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pmid28471961
      Medicine+(Baltimore) 2017 ; 96 (18 ): e6667
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  • Efficacy and safety of desmoteplase in acute ischemic stroke patients: A systematic review and meta-analysis #MMPMID28471961
  • Li X ; Ling L ; Li C ; Ma Q
  • Medicine (Baltimore) 2017[May]; 96 (18 ): e6667 PMID28471961 show ga
  • BACKGROUND: Pending results from double-blind, multicenter, parallel-group, randomized trials, the benefit and safety of the novel plasminogen activator, desmoteplase remain undetermined. The aim of this meta-analysis was to help evaluate desmoteplase's efficacy and safety. METHODS: A thorough search was performed of the Cochrane Library, PubMed, and Embase from the inception of electronic data to March 2017, and double-blind, multicenter, parallel-group, randomized trials were chosen. We conducted a meta-analysis of studies investigating intravenous desmoteplase treatment of acute ischemic stroke patients 3 to 9 hours after symptom onset. Asymptomatic intracerebral hemorrhage, good clinical outcome at 90 days, and reperfusion 4 to 8 hours posttreatment were variables assessing efficacy; symptomatic intracerebral hemorrhage and death rates were measures of safety. RESULTS: Six trials involving 1071 patients thrombolyzed >3 hours postonset were included (600 received intravenous desmoteplase, 471 placebo). Desmoteplase was associated with increased reperfusion (odds ratio [OR] 1.57; 95% confidence interval [CI], 1.10-2.24; P?=?.01 vs control) and showed a tendency to increase asymptomatic intracerebral hemorrhage (OR 1.25; 95% CI, 0.97-1.62; P?=?.09 vs control), whereas there was no increase in symptomatic intracerebral hemorrhage and death rate with desmoteplase. However, there was no difference in the clinical response at 90 days (OR 1.14; 95% CI, 0.88-1.49; P?=?.31 vs control). Subgroup analysis showed that desmoteplase 90??g/kg (OR 1.53; 95% CI, 1.07-2.21; P?=?.02 vs control) and 125??g/kg (OR 4.07; 95% CI, 1.16-14.24; P?=?.03 vs control) were associated with an increase in reperfusion. Also, we found desmoteplase 90??g/kg showed a tendency to increase asymptomatic intracerebral hemorrhage (OR 1.25; 95% CI, 0.95-1.63; P?=?.11 vs control). CONCLUSION: Intravenous desmoteplase is associated with a favorable reperfusion efficacy and acceptable safety in ischemic stroke treatment >3 hours after symptom onset. Well-designed randomized controlled trials with larger patient cohorts and a moderate dose of drugs are needed to further evaluate the true efficacy of desmoteplase in stroke patients. TRIAL REGISTRATION: URL: http://www.crd.york.ac.uk/PROSPERO; PROSPERO registration number: CRD42016037667).
  • |Administration, Intravenous [MESH]
  • |Brain Ischemia/*drug therapy [MESH]
  • |Fibrinolytic Agents/*administration & dosage/adverse effects [MESH]
  • |Humans [MESH]
  • |Plasminogen Activators/*administration & dosage/adverse effects [MESH]
  • |Randomized Controlled Trials as Topic [MESH]


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