Evidence map›Paper›PMID 40624381›Full record

Observational studyNeurosurgical review2025

Increased bleeding risk with bridging and early anticoagulation in traumatic brain injury patients with intracranial hemorrhage and mechanical heart valves.

Sophie Samuel, Eman Alnosair

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Neurosurgical review, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Sophie SamuelDepartment of Pharmacy, Memorial Hermann-Texas Medical Center, 6411 Fannin Street, Houston, TX, 77030, USA. Sophie.samuel@memorialhermann.org.
Eman AlnosairPeaceHealth Sacred Heart Medical Center Riverbend, Springfield, OR, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of bridging anticoagulation with unfractionated heparin (UFH) in traumatic brain injury (TBI) patients with mechanical heart valves (MHV) remains uncertain. While bridging has traditionally been used to reduce thromboembolic risk, emerging evidence suggests it may increase bleeding complications without clear benefit. This study evaluates the impact of bridging and anticoagulation resumption timing on clinical outcomes.

methodsA retrospective observational study was conducted at Memorial Hermann–Texas Medical Center, including 44 adult patients with MHV and acute TBI previously on warfarin. Patients were categorized into bridging (n = 22) and non-bridging (n = 22) groups. Anticoagulation resumption was also compared between early (< 14 days, n = 37) and delayed (> 14 days, n = 7) initiation groups. The primary outcome was hematoma expansion leading to clinical deterioration or death. Secondary outcomes included thromboembolic events, extracranial bleeding, and anticoagulation-related laboratory abnormalities.

resultsHematoma expansion was more frequent in the bridging group (27.3%) compared to the non-bridging group (13.6%), and four bridging patients (18.2%) required blood transfusions. Thromboembolic events occurred in one bridging (4.5%) and two non-bridging patients (9.1%). Among those who resumed anticoagulation within 14 days, four experienced hematoma expansion and four had extracranial bleeding, whereas none in the delayed resumption group (> 14 days) had these complications. Laboratory findings showed higher supratherapeutic INR (> 3.5) and PTT (> 90) in the bridging group.

conclusionBleeding complications were more frequent in the bridging group, while thromboembolic events were slightly more common in the non-bridging group. Early anticoagulation resumption (< 14 days) appeared to carry a higher complication rate, whereas delaying beyond 14 days was associated with fewer observed events. These findings should be interpreted cautiously given the small sample size.

Indexed as

AnticoagulantsBrain Injuries, TraumaticHeart Valve ProsthesisHemorrhageIntracranial HemorrhagesAdultAgedAnticoagulation BridgeFemaleHeparinHumansMaleMiddle AgedRetrospective StudiesThromboembolismTreatment OutcomeAnticoagulantsHeparinWarfarinAnticoagulationBridging complicationsMechanical heart valveTraumatic brain injury

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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.