Evidence map›Paper›PMID 40399968›Full record

Observational studyCritical care (London, England)2025

Cerebral perfusion pressure targets after traumatic brain injury: a reappraisal.

Stefan Yu Bögli, Ihsane Olakorede, Erta Beqiri, Xuhang Chen, Andrea Lavinio, Peter Hutchinson, Peter Smielewski

Abstract readObservational Study
In one paragraph

Observational study in Critical care (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Trial
  2. Advances in Multimodality Monitoring in Traumatic Brain Injury.Current neurology and neuroscience reports · 2026
    Review
  3. Observational
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  10. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Stefan Yu BögliBrain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK. stefanyu.boegli@usz.ch.
Ihsane OlakoredeBrain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Erta BeqiriBrain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Xuhang ChenBrain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Andrea LavinioDivision of Anaesthesia, Department of Medicine, University of Cambridge, Cambridge, UK.
Peter HutchinsonDivision of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Peter SmielewskiBrain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Funding

National Institute for Health Research NIHR203312*Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 225270
6 · The paper itself

Abstract

introductionCerebral perfusion pressure (CPP) management is central to neurocritical care management after traumatic brain injury (TBI). While the Brain Trauma Foundation recommends a target of 60-70 mmHg, it is unclear whether this range reflects the lower limit or the optimal level, when viewed through the prism of cerebrovascular autoregulation. Autoregulation aims at stabilizing cerebral blood flow and can be estimated continuously using the pressure reactivity index (PRx). Personalized CPP targets can be derived from PRx including CPPopt (optimal CPP), LLA, and ULA (lower and upper limit of autoregulation). Emerging data suggests an asymmetric relationship around CPPopt, with more pronounced autoregulation deterioration with decreasing compared to increasing CPP. Based on the hypothesis that higher CPP levels may be less harmful than lower CPP levels, we aimed to reassess rigorously the prognostic value of the different CPP targets. MATERIAL AND

methodsWe analyzed 809 adult TBI patients admitted from 2002 to 2023 who underwent invasive intracranial pressure monitoring and had available 6-month outcomes. CPPopt, LLA, and ULA were estimated using previously published methodologies. Deviations of CPP from fixed or personalized targets were assessed describing the overall dose, the hourly dose and the percentage time spent outside of these targets and examined using Chi-squared tests, logistic regressions, heatmaps, ordinal analyses, and group-based trajectory modelling.

resultsOur data confirms an asymmetric CPP/PRx relationship with steeper increases in PRx with decreasing and only modest elevations with increasing CPP. Even small decreases below CPPopt were consistently linked to worse outcomes (OR 1.04 (CI 1.02-1.06) and 1.09 (CI 1.04-1.15) for hourly dose and percentage time spent below CPPopt, p < 0.001 and p = 0.001 respectively). The strength of association increased with further decreases in CPP away from CPPopt towards the LLA with OR of 1.11 (CI 1.07-1.14) and 1.26 (CI 1.18-1.35) for hourly dose and percentage time spent below LLA respectively (p < 0.001). Conversely, higher-than CPPopt levels generally showed no association to worse outcomes. Distinct trajectories in the relationship between CPPopt and LLA (introduced as the Lower Limit Margin) could be identified with worse outcomes in those with decreasing distance between these targets (Mortality of 18% vs. 45% for patients with increasing vs. decreasing lower limit margins, p = 0.003).

conclusionOur findings corroborate experimental work suggesting that TBI patients are more vulnerable to CPP reductions below as compared to elevations above personalized thresholds. The results highlight the need for individualized CPP management strategies that prioritize avoidance of lower CPP levels and suggest using CPPopt as the lower CPP limit.

Indexed as

Brain Injuries, TraumaticCerebrovascular CirculationIntracranial PressureAdultAgedCohort StudiesFemaleHemodynamic MonitoringHumansMaleMiddle AgedBlood pressure targetsCerebral perfusion pressureCerebrovascular autoregulationMultimodality monitoringTraumatic brain injury

Identifiers

PMID40399968
PMCPMC12096506

What OpenQuestion holds

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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.