Evidence map›Paper›PMID 42272357›Full record

ArticleInternal medicine journal2026

Optimising hyperacute intracerebral haemorrhage management: factors influencing timely intervention.

Edmund Proper, Thanh Phan, Henry Ma, Michael Valente

Abstract read
In one paragraph

Article in Internal medicine journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Edmund ProperDepartment of Neurology, Monash Health, Clayton, Victoria, Australia.
Thanh PhanDepartment of Neurology, Monash Health, Clayton, Victoria, Australia.
Henry MaDepartment of Neurology, Monash Health, Clayton, Victoria, Australia.
Michael ValenteDepartment of Neurology, Monash Health, Clayton, Victoria, Australia.ORCID https://orcid.org/0000-0002-2692-6739

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBundled-care protocols, which include rapid lowering of blood pressure, have improved functional outcomes in patients with intracranial haemorrhage (ICH). Specifically, the intensive blood pressure reduction in acute cerebral hemmorhage trail (INTERACT) 3 trial aimed to achieve rapid lowering of systolic blood pressure (SBP) to 140 mmHg within an hour of arrival. We analyse factors that influenced the timely delivery of hyperacute ICH management.

aimWe aimed to identify the factors that delay the timely delivery of antihypertensive therapies for hyperacute ICH.

methodsA retrospective analysis of acute ICH patients admitted to Monash Health (January-December 2023) was performed to evaluate time to achieve SBP <140 mmHg. A Gamma regression model was used to assess the relationship of predictors, which included patient factors (age, GCS, admission SBP), process factors (times to antihypertensive medication, emergency department (ED) bed, computed tomography (CT) scan), and system factors (Code Stroke status, ED resuscitation bed assignment, care goals). Median times for antihypertensive medication delivery, neurosurgical review, neurosurgical intervention and anticoagulation reversal were calculated.

resultsOf 209 patients (median age 74 (IQR 63-84), GCS 14 (IQR 6-15), National Institute of Health Stroke Severity 13 (interquartile range (IQR) 4-27), admission SBP 160 mmHg (IQR 137.5-187)), 52% were treated as a Code Stroke. Median time to CT was 33 min (IQR 23-47.5) with Code Stroke versus 121 min (IQR 36-254) without. Patients who received non-palliative therapies (74%) achieved SBP < 140 in 193 min (IQR 91-552) and 25% achieved this in 60 min. Higher admission SBP, longer times to ED bed and absence of Code Stroke were associated with increased time to reach 140 mmHg SBP (P < 0.01). Other dependent variables did not reach significance.

conclusionSBP on arrival, delayed access to ED beds and Code Stroke activation were key factors associated with achieving early BP lowering. These findings underscore the need for protocolised, rapid-response systems to optimise ICH management.

Indexed as

Antihypertensive AgentsCerebral HemorrhageTime-to-TreatmentAgedAged, 80 and overBlood PressureDisease ManagementEmergency Service, HospitalFemaleHumansMaleMiddle AgedRetrospective StudiesTime FactorsTreatment DelayAntihypertensive Agentsanticoagulation reversalcode strokehyperacute treatmentintracerebral haemorrhageneurosurgical interventiontreatment delays

Identifiers

PMID42272357
PMCPMC13458217

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LicenceCC BY-NC-ND
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Registered trials

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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.