Improved Outcomes in ICH Achieved with Investigational Minimally Invasive Surgery

Summary

Intracranial hemorrhage (ICH) remains the only untreatable form of stroke. In clinical trials, no benefit has been found with open surgery compared with medical therapy in reducing ICH volume in patients with stable supratentorial large hematomas. The invasiveness and risk of open surgery, particularly for deeper ICHs, and the impact on quality of life are concerns. Minimally invasive surgical (MIS) approaches (endoscopic, thrombolytic), but not open surgery, were shown to have some benefit in ICH [Prasad K et al. Cochrane Database Syst Rev 2008]. This article discusses the MISTIE technique, which is the farthest along of the MIS approaches under investigation.

  • Ischemia
  • Interventional Techniques & Devices
  • Ischemia
  • Neurology
  • Interventional Techniques & Devices

Intracranial hemorrhage (ICH) remains the only untreatable form of stroke. An ICH volume >20 to 30 mL predicts poor outcomes [Broderick JP et al. Stroke 1993]. In clinical trials, no benefit has been found with open surgery compared with medical therapy in reducing ICH volume in patients with stable supratentorial large hematomas. The invasiveness and risk of open surgery, particularly for deeper ICHs, and the impact on quality of life are concerns.

Minimally invasive surgical (MIS) approaches (endoscopic, thrombolytic), but not open surgery, were shown to have some benefit in ICH [Prasad K et al. Cochrane Database Syst Rev 2008]. The MISTIE technique is the farthest along of the MIS approaches under investigation, said Issam Awad, MD, University of Chicago, Chicago, Illinois, USA.

The feasibility of this technique was shown by a 70% reduction in ICH volume after 4 days of treatment in the Minimally Invasive Surgery Plus rt-PA for Intracerebral Hemorrhage Evacuation trial [MISTIE; NCT00224770]. This Phase 2 trial of patients with >20 cc supratentorial ICH without underlying structural vascular abnormalities compared best medical care with the MISTIE intervention including direct delivery of recombinant tissue plasminogen activator (rt-PA) at progressively larger doses at 8-hour intervals. Imaging-guided catheter placement within the center of the clot is followed by clot aspiration using a rigid cannula.

An association between ideal catheter placement and outcomes was found in the MISTIE trial, and allows for achieving generalizable results said Dr. Awad. The ideal “hot dog in the bun” placement along the axis and within the center of the clot was associated with less residual hematoma than the “eccentric catheter” placement.

At 180 days, achieving an ICH volume <20 mL was associated with good outcomes, while the poor outcomes were associated with poor catheter placement.

The MISTIE procedure did not increase mortality or vegetative survival at 180 days, and a smaller proportion of these patients were in long-term care facilities. For the good outcomes strata of the prespecified mRS score, there was an absolute 11% improvement. These benefits were further improved at 360 days. The hospital length of stay was dramatically shorter with MISTIE, resulting in a 35% reduction in total costs. Subgroup analyses showed the MISTIE intervention was effective for deep and lobar sites and across the Glasgow Coma Scale. Also, MISTIE was equally as effective whether patients were treated within the first 36 hours or the second 36 hours, showing the rush to surgery is not as important as stabilizing the hematoma, said Dr. Awad.

The mechanism of the benefit seen in MISTIE appears to be reduction of clot burden, perhaps saving tissue at risk, and preventing secondary injury from occurring over subsequent days, he stated. Despite the benefits seen in MISTIE, two unanswered questions are whether MIS spares tissue and the amount of clot removal that is sufficient. These may be answered in the Phase 3 Minimally Invasive Surgery Plus Rt-PA for ICH Evacuation Phase III trial [MISTIE III; NCT01827046], which enrolled its first of 500 patients in December 2013 and has a similar study protocol.

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