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Stroke Treatment Gets Boost From New Clot Retrievers

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Trials Are Major Steps Forward

Despite modest sample sizes, the "carefully done" SWIFT and TREVO 2 trials begin to answer the call for high-level evidence about the efficacy and safety of mechanical clot retrieval devices in acute ischemic stroke, Dr. Philip B. Gorelick wrote in an editorial accompanying the Lancet articles.

"It will be interesting to learn, on the basis of future non-primary analyses, whether collateral flow patterns or clot characteristics elucidate propensity for treatment response," he said (Lancet 2012 Aug. 26 [doi: 10.1016/S0140-6736(12)61302-6]).

He also stated that the "mechanistic basis for superiority" of these next-generation devices might relate to retention of structural integrity of the clot and vessel wall during the procedure.

"Future randomized trials of these and other, newer devices will need to take into account comparison or complementary treatment with rt-PA [recombinant tissue plasminogen activator], or with newer-generation thrombolytics such as desmoteplase and tenecteplase," he said.

Meanwhile, SWIFT and TREVO 2 represent major steps forward, and pave the way for new treatment options, as well as for further validation by additional study, he said.

Dr. Gorelick is with the Hauenstein Neuroscience Center and Michigan State University College of Human Medicine in Grand Rapids. He disclosed that he receives remuneration as co-director of the clinical coordinating center for the DIAS trial that involves desmoteplase.


 

FROM THE LANCET

As for how the Solitaire and Trevo devices compare with each other, no conclusions can be drawn from SWIFT and TREVO 2 because the two studies used different definitions of reperfusion and good neurological outcomes. However, the devices, both of which have been cleared for general use in the United States and Europe, appear to have a similar or better safety profile than the Merci retriever, and the results thus far suggest that "significant improvement could be forthcoming in stroke patients for whom drug treatment is ineffective," according to a Lancet press statement.

The SWIFT trial was funded by Covidien/ev3, the maker of the Solitaire device. TREVO 2 was funded by Stryker Neurological, the maker of Trevo. Many of the investigators disclosed conflicts of interest involving Covidien/ev3 Neurovascular or Stryker Neurological, as well as other manufacturers of endovascular therapies for stroke.

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