Evidence map›Paper›PMID 39561739›Full record

Observational studyCerebrovascular diseases extra2025

Safety and Efficacy of Thrombectomy in Vietnamese Stroke Patients Selected through Perfusion Imaging with an Onset Time between 6 and 24 Hours.

Binh Nguyen Pham, Hang T Minh Tran, An Thai Thanh Nguyen, Huan Nguyen Pham, Anh Tuan Le Truong, Trung Quoc Nguyen, Huong Bich Thi Nguyen, Tri Quang Nguyen, Huy Quoc Do, Tra Vu Son Le and 5 more

Abstract readObservational Study
In one paragraph

Observational study in Cerebrovascular diseases extra, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Binh Nguyen PhamDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Hang T Minh TranPham Ngoc Thach University of Medicine, Ho Chi Minh City, Vietnam.
An Thai Thanh NguyenDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Huan Nguyen PhamLaboratory Department, Hung Vuong Hospital, Ho Chi Minh City, Vietnam.
Anh Tuan Le TruongDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Trung Quoc NguyenDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Huong Bich Thi NguyenDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Tri Quang NguyenDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Huy Quoc DoDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Tra Vu Son LeDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Vu Thanh TranDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.
Ryan Anh-Quang NguyenDepartment of Molecular and Cell Biology, University of California, Berkeley, California, USA.
Huy NguyenFaculty of Medicine, University of Debrecen, Debrecen, Hungary.
Thang Ba NguyenUniversity of Medicine and Pharmacy at HCMC, Ho Chi Minh City, Vietnam.
Thang Huy NguyenDepartment of Cerebrovascular Disease, People's Hospital 115, Ho Chi Minh City, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRecent trials have demonstrated the remarkable benefit of endovascular treatment (EVT) up to 24 h in patients with large vessel occlusion (LVO) and target mismatch profiles; however, benefits of late-window EVT in Vietnamese population remain poorly understood. This study aims to evaluate the real-world outcomes of EVT in acute ischemic stroke (AIS) patients selected using perfusion imaging within the 6-24-h window.

methodsThis is a prospective study of consecutive patients with anterior circulation LVO stroke who underwent EVT within 6-24 h after last known well between August 2022 and March 2024. Patients were selected based on the DAWN/DEFUSE-3 criteria (Perfusion-RAPID, iSchemaView). The primary outcome was the proportion of patients with functional independence at 90 days (modified Rankin Scale score of 0-2). The secondary outcomes were successful reperfusion defined by thrombolysis in cerebral infarction (TICI) ≥2b on the final procedure and subgroup analysis between good (hypoperfusion intensity ratio [HIR] <0.4) and poor collaterals (HIR ≥0.4) groups. Safety outcomes were mortality rate and symptomatic intracranial hemorrhage (sICH).

resultsOf 122 enrolled patients, 68% met inclusion criteria of DEFUSE-3 trial, 61% met DAWN trial criteria. Mean age was 66 years, median baseline NIHSS was 13, median time from stroke onset to hospital arrival was 12.55 h (9.50-16.48), and median infarct volume was 11.5 mL. The rate of functional independence at 90 days was 45.9%. Successful reperfusion (TICI score of ≥2b) was achieved by 83.6% of cases. The 90-day mortality rate was 10.7%; sICH was reported in 8 patients (6.6%). Patients with good collaterals had better functional outcome.

conclusionsThis real-world observational study suggests that late-window EVT may be safe and effective in eligible Vietnamese patients selected based on perfusion imaging, thus supporting its practical use in this patient population. HIR is a robust indicator of collateral status and could made it a valuable addition to stroke imaging workup in clinical setting.

Indexed as

Cerebrovascular CirculationDisability EvaluationFunctional StatusIschemic StrokePerfusion ImagingPredictive Value of TestsRecovery of FunctionThrombectomyTime-to-TreatmentAgedAged, 80 and overCollateral CirculationEndovascular ProceduresFemaleHumansIntracranial Hemorrhages6–24 hAcute ischemic strokeCollateralsEndovascular treatment of acute strokeHypoperfusion intensity ratioLate windowPerfusion imaging

Identifiers

PMID39561739
PMCPMC11666263

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.