TY - JOUR
T1 - Evolution of practice during the interventional management of stroke III trial and implications for ongoing trials
AU - Interventional Management of Stroke III Investigators
AU - Broderick, Joseph P.
AU - Palesch, Yuko Y.
AU - Demchuk, Andrew M.
AU - Yeatts, Sharon D.
AU - Khatri, Pooja
AU - Hill, Michael D.
AU - Jauch, Edward C.
AU - Jovin, Tudor G.
AU - Yan, Bernard
AU - Von Kummer, Rüdiger
AU - Molina, Carlos A.
AU - Goyal, Mayank
AU - Mazighi, Mikael
AU - Schonewille, Wouter J.
AU - Engelter, Stefan T.
AU - Anderson, Craig
AU - Spilker, Judith
AU - Carrozzella, Janice
AU - Janis, L. Scott
AU - Foster, Lydia D.
AU - Tomsick, Thomas A.
N1 - Publisher Copyright:
© 2014 American Heart Association, Inc.
PY - 2014/12/11
Y1 - 2014/12/11
N2 - Background and Purpose - We explored changes in the patient population and practice of endovascular therapy during the course of the Interventional Management of Stroke (IMS) III Trial.Methods - Changes in baseline characteristics, use of baseline CT angiography, treatment times and specifics, and outcomes were compared between the first 4 protocols and the fifth and final protocol.Results - Compared with subjects treated in the first 4 protocol versions (n=610), subjects treated in fifth and final protocol (n=46) were older (75 versus 68 years, P<0.0002) and less likely to have a pretreatment Rankin of 0 (76% versus 89%, P=0.01), were more likely to have a pretreatment CT angiography (65% versus 45%, P=0.009), had quicker median times in the endovascular arm from onset to start of intra-arterial therapy (209 versus 250 minutes, P=0.002) and to reperfusion (269 versus 344 minutes, P<0.0001), had a higher mean dose of total tissue-type plasminogen activator in the endovascular arm (74.0 versus 63.7 mg, P<0.0001), and were less likely to receive intra-arterial tissue-type plasminogen activator as part of the endovascular procedure (16% versus 44%, P=0.015). There were no significant differences in functional and safety outcomes between subjects treated in the 2 treatments arms in either the first 4 protocols or fifth protocol although the small sample size in the fifth protocol provided limited power.Conclusions - Endovascular technology and diagnostic approaches to acute stroke patients changed substantially during the IMS III Trial. Efforts to decrease the time to delivery of endovascular therapy were successful.
AB - Background and Purpose - We explored changes in the patient population and practice of endovascular therapy during the course of the Interventional Management of Stroke (IMS) III Trial.Methods - Changes in baseline characteristics, use of baseline CT angiography, treatment times and specifics, and outcomes were compared between the first 4 protocols and the fifth and final protocol.Results - Compared with subjects treated in the first 4 protocol versions (n=610), subjects treated in fifth and final protocol (n=46) were older (75 versus 68 years, P<0.0002) and less likely to have a pretreatment Rankin of 0 (76% versus 89%, P=0.01), were more likely to have a pretreatment CT angiography (65% versus 45%, P=0.009), had quicker median times in the endovascular arm from onset to start of intra-arterial therapy (209 versus 250 minutes, P=0.002) and to reperfusion (269 versus 344 minutes, P<0.0001), had a higher mean dose of total tissue-type plasminogen activator in the endovascular arm (74.0 versus 63.7 mg, P<0.0001), and were less likely to receive intra-arterial tissue-type plasminogen activator as part of the endovascular procedure (16% versus 44%, P=0.015). There were no significant differences in functional and safety outcomes between subjects treated in the 2 treatments arms in either the first 4 protocols or fifth protocol although the small sample size in the fifth protocol provided limited power.Conclusions - Endovascular technology and diagnostic approaches to acute stroke patients changed substantially during the IMS III Trial. Efforts to decrease the time to delivery of endovascular therapy were successful.
KW - Clinical trial
KW - Therapeutic thrombolysis
KW - Tissue-type plasminogen activator
UR - https://www.scopus.com/pages/publications/84922480613
U2 - 10.1161/STROKEAHA.114.005952
DO - 10.1161/STROKEAHA.114.005952
M3 - Artículo
C2 - 25325911
AN - SCOPUS:84922480613
SN - 0039-2499
VL - 45
SP - 3606
EP - 3611
JO - Stroke
JF - Stroke
IS - 12
ER -