Publication: Risk factors and complications of intracranial pressure monitoring with a fiberoptic device
dc.contributor.buuauthor | Bekar, Ahmet | |
dc.contributor.buuauthor | Doğan, Şeref | |
dc.contributor.buuauthor | Abaş, Faruk | |
dc.contributor.buuauthor | Caner, Burcu | |
dc.contributor.buuauthor | Korfalı, Gülşen | |
dc.contributor.buuauthor | Kocaeli, Hasan | |
dc.contributor.buuauthor | Yılmazlar, Selçuk | |
dc.contributor.buuauthor | Korfalı, Ender | |
dc.contributor.buuauthor | Caner, Burcu | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Anestezi ve Reanimasyon Ana Bilim Dalı | |
dc.contributor.department | Nöroşirürji Ana Bilim Dalı | |
dc.contributor.orcid | 0000-0003-3633-7919 | |
dc.contributor.researcherid | AAI-6531-2021 | |
dc.contributor.researcherid | AAH-5070-2021 | |
dc.contributor.scopusid | 7102693077 | |
dc.contributor.scopusid | 6603677218 | |
dc.contributor.scopusid | 8546184300 | |
dc.contributor.scopusid | 25027089000 | |
dc.contributor.scopusid | 6701462594 | |
dc.contributor.scopusid | 6603500567 | |
dc.contributor.scopusid | 6603059483 | |
dc.contributor.scopusid | 7004641343 | |
dc.date.accessioned | 2021-11-15T10:42:44Z | |
dc.date.available | 2021-11-15T10:42:44Z | |
dc.date.issued | 2009-02 | |
dc.description.abstract | We prospectively investigated the complications associated with intraparenchymal intracranial pressure (ICP) monitoring using the Camino intracranial pressure device. A fiberoptic ICP monitoring transducer was implanted in 631 patients. About half of the patients (n = 303) also received an external ventricular drainage set (EVDS). The durations (mean +/- SD) of ICP monitoring in patients without and with an EVDS were 6.5 +/- 4.4 and 7.3 +/- 5.1 days, respectively. Infection occurred in 6 patients with only an ICP transducer (6/328, 1.8%) and 24 patients with an EVDS also (24/303, 7.9%). The duration of monitoring had no effect on infection, whereas the use of an EVDS for more than 9 days increased infection risk by 5.11 times. Other complications included transducer disconnection (2.37%), epidural hematoma (0.47%), contusion (0.47%), defective probe (0.31%), broken transducer (0.31%), dislocation of the fixation screw (0.15%), and intraparenchymal hematoma (0.15%). In conclusion, intraparenchymal ICP monitoring systems can be safely used in patients who either have, or are at risk of developing, increased ICP. | |
dc.identifier.citation | Bekar, A. vd. (2009). "Risk factors and complications of intracranial pressure monitoring with a fiberoptic device". Journal of Clinical Neuroscience, 16(2), 236-240. | |
dc.identifier.endpage | 240 | |
dc.identifier.issn | 0967-5868 | |
dc.identifier.issue | 2 | |
dc.identifier.pubmed | 19071023 | |
dc.identifier.scopus | 2-s2.0-58149182696 | |
dc.identifier.startpage | 236 | |
dc.identifier.uri | https://doi.org/10.1016/j.jocn.2008.02.008 | |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0967586808001082 | |
dc.identifier.uri | http://hdl.handle.net/11452/22653 | |
dc.identifier.volume | 16 | |
dc.identifier.wos | 000264181900010 | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.relation.journal | Journal of Clinical Neuroscience | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Complications | |
dc.subject | Fiberoptic device | |
dc.subject | Intracranial pressure | |
dc.subject | Monitoring | |
dc.subject | Brain-tissue pressure | |
dc.subject | Head-injured patients | |
dc.subject | Clinical-evaluation | |
dc.subject | Infectious complications | |
dc.subject | Aggressive treatment | |
dc.subject | Experience | |
dc.subject | Duration | |
dc.subject | Neurosciences & neurology | |
dc.subject.emtree | Adolescent | |
dc.subject.emtree | Aged | |
dc.subject.emtree | Article | |
dc.subject.emtree | Child | |
dc.subject.emtree | Complication | |
dc.subject.emtree | Controlled study | |
dc.subject.emtree | Contusion | |
dc.subject.emtree | Device infection | |
dc.subject.emtree | Epidural hematoma | |
dc.subject.emtree | Female | |
dc.subject.emtree | Fiber optics | |
dc.subject.emtree | Human | |
dc.subject.emtree | Infection risk | |
dc.subject.emtree | Intracranial pressure monitoring | |
dc.subject.emtree | Major clinical study | |
dc.subject.emtree | Male | |
dc.subject.emtree | Medical instrumentation | |
dc.subject.emtree | Patient safety | |
dc.subject.emtree | Pressure transducer | |
dc.subject.emtree | Priority journal | |
dc.subject.emtree | Risk factor | |
dc.subject.emtree | Transducer | |
dc.subject.mesh | Adolescent | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Aged, 80 and over | |
dc.subject.mesh | Child | |
dc.subject.mesh | Child, preschool | |
dc.subject.mesh | Female | |
dc.subject.mesh | Glasgow coma scale | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Infant | |
dc.subject.mesh | Intracranial hypertension | |
dc.subject.mesh | Intracranial pressure | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle aged | |
dc.subject.mesh | Monitoring, physiologic | |
dc.subject.mesh | Optical fibers | |
dc.subject.mesh | Prospective studies | |
dc.subject.mesh | Retrospective studies | |
dc.subject.mesh | Risk factors | |
dc.subject.mesh | Statistics, nonparametric | |
dc.subject.mesh | Young adult | |
dc.subject.scopus | Ventriculostomy; Intracranial Pressure; Drain | |
dc.subject.wos | Clinical neurology | |
dc.subject.wos | Neurosciences | |
dc.title | Risk factors and complications of intracranial pressure monitoring with a fiberoptic device | |
dc.type | Article | |
dc.wos.quartile | Q4 (Neurosciences) | |
dc.wos.quartile | Q3 (Clinical neurology) | |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Nöroşirürji Ana Bilim Dalı | |
local.contributor.department | Tıp Fakültesi/Anestezi ve Reanimasyon Ana Bilim Dalı | |
local.indexed.at | Scopus | |
local.indexed.at | WOS |
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