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Randomized trialNew England Journal of Medicine

Mechanical Thrombectomy 24 to 72 Hours after Large-Vessel Ischemic Stroke

First online Oct 23, 2026On EM Weekly Oct 28, 2026Discovered Oct 28, 2026AI-generated Not yet human-reviewed

Summary

LATE-MT randomized 336 patients in China with anterior-circulation large-vessel occlusion, imaging-identified salvageable tissue, and presentation 24 to 72 hours after onset or last-known-well to thrombectomy plus medical care or medical care alone. At a median 38.5 hours to randomization, thrombectomy improved the 90-day modified Rankin scale distribution (common OR for better functional outcome 1.74, 95% CI 1.19-2.55). Symptomatic intracranial hemorrhage occurred in 4.8% versus 0%, and 90-day case fatality was 6.0% versus 1.8%.

Why it matters

This is randomized evidence that selected patients with salvageable tissue may benefit from thrombectomy beyond the current 24-hour evidence window. It supports urgent thrombectomy-center discussion for carefully selected very-late presenters, but does not establish universal treatment beyond 24 hours.

Study at a glance

Design
Randomized trial
Population
Adults with anterior-circulation large-vessel occlusion ischemic stroke, imaging-identified salvageable tissue, and presentation 24 to 72 hours after symptom onset or last-known-well.
Sample size
336
Intervention
Endovascular thrombectomy plus standard medical care.
Comparator
Standard medical care alone.
Primary endpoint
Distribution of modified Rankin scale scores at 90 days.

Main findings

  • Common OR for a better 90-day functional outcome was 1.74 (95% CI 1.19-2.55) with thrombectomy.
  • Median time from onset or last-known-well to randomization was 38.5 hours.
  • Symptomatic intracranial hemorrhage occurred in 4.8% with thrombectomy versus 0% with medical care alone.
  • Ninety-day case fatality was 6.0% versus 1.8%, respectively.

Limitations

The trial was open-label, conducted at comprehensive stroke centers in China, and required favorable imaging selection. The higher symptomatic hemorrhage and mortality signals, plus uncertain external validity, warrant caution pending replication and guideline integration.

Read the primary source

Full text: Abstract available; full text paywalled.

Original source

DOI: 10.1056/NEJMoa2609362

PMID: 42929656

Source retrieved Oct 28, 2026. Abstract reviewed; full text unavailable. Primary PubMed record and DOI metadata were verified.

Corrections & review history

No corrections recorded. Human review: not yet human-reviewed.