Tenecteplase versus alteplase in stroke thrombolysis : An individual patient data meta-analysis of randomized controlled trials
© 2016 World Stroke Organization..
BACKGROUND: Tenecteplase, a modified plasminogen activator with higher fibrin specificity and longer half-life, may have advantages over alteplase in acute ischemic stroke thrombolysis.
AIMS: We undertook an individual patient data meta-analysis of randomized controlled trials that compared alteplase with tenecteplase in acute stroke.
METHODS: Eligible studies were identified by a MEDLINE search, and individual patient data were acquired. We compared clinical outcomes including modified Rankin Scale at three months, early neurological improvement at 24 h, intracerebral hemorrhage, symptomatic intracerebral hemorrhage, and mortality at three months between all dose tiers of tenecteplase and alteplase.
RESULTS: Three relevant studies (Haley et al., Parsons et al., and ATTEST) included 291 patients and investigated three doses of tenecteplase (0.1, 0.25, 0.4 mg/kg). There were no differences between any dose of tenecteplase and alteplase for either efficacy or safety end points. Tenecteplase 0.25 mg/kg had the greatest odds to achieve early neurological improvement (OR [95%CI] 3.3 [1.5, 7.2], p = 0.093), excellent functional outcome (modified Rankin Scale 0-1) at three months (OR [95%CI] 1.9 [0.8, 4.4], p = 0.28), with reduced odds of intracerebral hemorrhage (OR [95%CI] 0.6 [0.2, 1.8], P = 0.43) compared with alteplase. Only 19 patients were treated with tenecteplase 0.4 mg/kg, which showed increased odds of symptomatic intracerebral hemorrhage compared with alteplase (OR [95% CI] 6.2 [0.7, 56.3]).
CONCLUSIONS: While no significant differences between tenecteplase and alteplase were found, point estimates suggest potentially greater efficacy of 0.25 and 0.1 mg/kg doses with no difference in symptomatic intracerebral hemorrhage, and potentially higher symptomatic intracerebral hemorrhage risk with the 0.4 mg/kg dose. Further investigation of 0.25 mg/kg tenecteplase is warranted.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2016 |
---|---|
Erschienen: |
2016 |
Enthalten in: |
Zur Gesamtaufnahme - volume:11 |
---|---|
Enthalten in: |
International journal of stroke : official journal of the International Stroke Society - 11(2016), 5 vom: 15. Juli, Seite 534-43 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Huang, Xuya [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 02.10.2017 Date Revised 31.03.2022 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1177/1747493016641112 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM259115509 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM259115509 | ||
003 | DE-627 | ||
005 | 20231224190504.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2016 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1177/1747493016641112 |2 doi | |
028 | 5 | 2 | |a pubmed24n0863.xml |
035 | |a (DE-627)NLM259115509 | ||
035 | |a (NLM)27048693 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Huang, Xuya |e verfasserin |4 aut | |
245 | 1 | 0 | |a Tenecteplase versus alteplase in stroke thrombolysis |b An individual patient data meta-analysis of randomized controlled trials |
264 | 1 | |c 2016 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 02.10.2017 | ||
500 | |a Date Revised 31.03.2022 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2016 World Stroke Organization. | ||
520 | |a BACKGROUND: Tenecteplase, a modified plasminogen activator with higher fibrin specificity and longer half-life, may have advantages over alteplase in acute ischemic stroke thrombolysis | ||
520 | |a AIMS: We undertook an individual patient data meta-analysis of randomized controlled trials that compared alteplase with tenecteplase in acute stroke | ||
520 | |a METHODS: Eligible studies were identified by a MEDLINE search, and individual patient data were acquired. We compared clinical outcomes including modified Rankin Scale at three months, early neurological improvement at 24 h, intracerebral hemorrhage, symptomatic intracerebral hemorrhage, and mortality at three months between all dose tiers of tenecteplase and alteplase | ||
520 | |a RESULTS: Three relevant studies (Haley et al., Parsons et al., and ATTEST) included 291 patients and investigated three doses of tenecteplase (0.1, 0.25, 0.4 mg/kg). There were no differences between any dose of tenecteplase and alteplase for either efficacy or safety end points. Tenecteplase 0.25 mg/kg had the greatest odds to achieve early neurological improvement (OR [95%CI] 3.3 [1.5, 7.2], p = 0.093), excellent functional outcome (modified Rankin Scale 0-1) at three months (OR [95%CI] 1.9 [0.8, 4.4], p = 0.28), with reduced odds of intracerebral hemorrhage (OR [95%CI] 0.6 [0.2, 1.8], P = 0.43) compared with alteplase. Only 19 patients were treated with tenecteplase 0.4 mg/kg, which showed increased odds of symptomatic intracerebral hemorrhage compared with alteplase (OR [95% CI] 6.2 [0.7, 56.3]) | ||
520 | |a CONCLUSIONS: While no significant differences between tenecteplase and alteplase were found, point estimates suggest potentially greater efficacy of 0.25 and 0.1 mg/kg doses with no difference in symptomatic intracerebral hemorrhage, and potentially higher symptomatic intracerebral hemorrhage risk with the 0.4 mg/kg dose. Further investigation of 0.25 mg/kg tenecteplase is warranted | ||
650 | 4 | |a Comparative Study | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Meta-Analysis | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Acute stroke therapy | |
650 | 4 | |a alteplase | |
650 | 4 | |a intracerebral hemorrhage | |
650 | 4 | |a meta-analysis | |
650 | 4 | |a tenecteplase | |
650 | 4 | |a thrombolysis | |
650 | 7 | |a Fibrinolytic Agents |2 NLM | |
650 | 7 | |a Tissue Plasminogen Activator |2 NLM | |
650 | 7 | |a EC 3.4.21.68 |2 NLM | |
700 | 1 | |a MacIsaac, Rachael |e verfasserin |4 aut | |
700 | 1 | |a Thompson, John Lp |e verfasserin |4 aut | |
700 | 1 | |a Levin, Bruce |e verfasserin |4 aut | |
700 | 1 | |a Buchsbaum, Richard |e verfasserin |4 aut | |
700 | 1 | |a Haley, E Clarke |c Jr |e verfasserin |4 aut | |
700 | 1 | |a Levi, Christopher |e verfasserin |4 aut | |
700 | 1 | |a Campbell, Bruce |e verfasserin |4 aut | |
700 | 1 | |a Bladin, Christopher |e verfasserin |4 aut | |
700 | 1 | |a Parsons, Mark |e verfasserin |4 aut | |
700 | 1 | |a Muir, Keith W |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t International journal of stroke : official journal of the International Stroke Society |d 2006 |g 11(2016), 5 vom: 15. Juli, Seite 534-43 |w (DE-627)NLM181612585 |x 1747-4949 |7 nnns |
773 | 1 | 8 | |g volume:11 |g year:2016 |g number:5 |g day:15 |g month:07 |g pages:534-43 |
856 | 4 | 0 | |u http://dx.doi.org/10.1177/1747493016641112 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 11 |j 2016 |e 5 |b 15 |c 07 |h 534-43 |