ArticleFrontiers in neurology
Early pharmacological venous thromboembolism prophylaxis reduces lower limb deep vein thrombosis in surgical patients with severe hypertensive intracerebral hemorrhage: a retrospective cohort study.
Article in Frontiers in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: To investigate the efficacy and safety of early pharmacological prophylaxis for venous thromboembolism (VTE) on the incidence of lower extremity deep vein thrombosis (DVT) in patients undergoing surgery for severe hypertensive intracerebral hemorrhage (HICH). Methods: In this retrospective cohort study, 123 surgical patients with severe HICH admitted between September 2021 and February 2025 were included. Based on the initiation timing of VTE pharmacological prophylaxis (low-molecular-weight heparin calcium, LMWH), patients were categorized into an early group (prophylaxis initiated within <48 h after admission) and a late group (prophylaxis initiated at ≥48 h after admission). To compare the incidence of lower extremity deep vein thrombosis (DVT), intracranial rebleeding, and gastrointestinal bleeding within one week after prophylaxis initiation, as well as the 60-day mortality rate and 60-day modified Rankin Scale (mRS) score, between the two groups. Results: The VTE prophylaxis initiation times were (29.06 ± 4.44) hours and (70.27 ± 10.12) hours in the early and late groups, respectively. The incidence of lower extremity DVT was significantly lower in the early group compared to the late group (17.5% vs. 38.3%, Conclusion: For surgical patients with severe HICH, early postoperative (<48 h) pharmacological VTE prophylaxis was associated with a significantly reduced risk of lower extremity DVT, and no significant increases in intracranial rebleeding, gastrointestinal bleeding, or mortality were observed. However, given the limited sample size and number of events, these safety findings should be interpreted with caution.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.