Evidence map›Paper›PMID 34286479›Full record

ArticleCardiovascular engineering and technology2022

Characterizing Intracranial Hemodynamics in Sickle Cell Anemia: Impact of Patient-Specific Viscosity.

Sara B Keller, Jacob M Bumpus, J Christopher Gatenby, Elizabeth Yang, Adetola A Kassim, Carlton Dampier, John C Gore, Amanda K W Buck

Open access · greenAbstract read
In one paragraph

Article in Cardiovascular engineering and technology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Sara B KellerDepartment of Bioengineering, University of Washington, Seattle, WA, USA.
Jacob M BumpusDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.
J Christopher GatenbyDepartment of Radiology, University of Washington, Seattle, WA, USA.
Elizabeth YangCenter for Cancer and Blood Disorders, Pediatric Specialists of Virginia, Fairfax, VA, USA.
Adetola A KassimDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Carlton DampierDepartment of Pediatrics, Emory University and Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA, USA.
John C GoreDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.
Amanda K W BuckDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA. amanda.buck@vumc.org.ORCID 0000-0003-1042-6374
Vanderbilt University · USUniversity of Washington · USCenter for Cancer and Blood Disorders · USEmory University · USVanderbilt University Medical Center · US

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Postdoctoral Training in Biomedical MRI and MRST32EB001628 · NIBIB · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John C Gore · 2003 to 2026
$7.0M
NCATS NIH HHS UL1 TR002243NIBIB NIH HHS T32 EB001628
6 · The paper itself

Abstract

purposePediatric and adult patients with sickle cell anemia (SCA) are at increased risk of stroke and cerebrovascular accident. In the general adult population, there is a relationship between arterial hemodynamics and pathology; however, this relationship in SCA patients remains to be elucidated. The aim of this work was to characterize circle of Willis hemodynamics in patients with SCA and quantify the impact of viscosity choice on pathophysiologically-relevant hemodynamics measures.

methodsBased on measured vascular geometries, time-varying flow rates, and blood parameters, detailed patient-specific simulations of the circle of Willis were conducted for SCA patients (n = 6). Simulations quantified the impact of patient-specific and standard blood viscosities on wall shear stress (WSS).

resultsThese results demonstrated that use of a standard blood viscosity introduces large errors into the estimation of pathophysiologically-relevant hemodynamic parameters. Standard viscosity models overpredicted peak WSS by 55% and 49% for steady and pulsatile flow, respectively. Moreover, these results demonstrated non-uniform, spatial patterns of positive and negative WSS errors related to viscosity, and standard viscosity simulations overpredicted the time-averaged WSS by 32% (standard deviation = 7.1%). Finally, differences in shear rate demonstrated that the viscosity choice alters the simulated near-wall flow field, impacting hemodynamics measures.

conclusionsThis work presents simulations of circle of Willis arterial flow in SCA patients and demonstrates the importance and feasibility of using a patient-specific viscosity in these simulations. Accurately characterizing cerebrovascular hemodynamics in SCA populations has potential for elucidating the pathophysiology of large-vessel occlusion, aneurysms, and tissue damage in these patients.

Indexed as

Anemia, Sickle CellModels, CardiovascularAdultChildHemodynamicsHumansShear StrengthStress, MechanicalViscosityComputational fluid dynamics (CFD)HemodynamicsMedical imaging-based simulationsSickle cell anemia (SCA)Wall shear stress

Identifiers

PMID34286479
PMCPMC9030946
OpenAlexW3186299025

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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.