2017
DOI: 10.1016/j.pmr.2016.12.004
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Management of Medical Complications During the Rehabilitation of Moderate-Severe Traumatic Brain Injury

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Cited by 8 publications
(9 citation statements)
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“…A sustained ICP > 20 -25 mmHg is considered pathologically significant due to the high correlation between an elevated ICP and mortality [19]. Recent studies have reported that IVH, SAH, age, DC, GCS score, Fisher score, and CSF infection could be risk factors for PTH development [18,20]. These previous findings represented the observational data for our study.…”
supporting
confidence: 52%
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“…A sustained ICP > 20 -25 mmHg is considered pathologically significant due to the high correlation between an elevated ICP and mortality [19]. Recent studies have reported that IVH, SAH, age, DC, GCS score, Fisher score, and CSF infection could be risk factors for PTH development [18,20]. These previous findings represented the observational data for our study.…”
supporting
confidence: 52%
“…Despite advances in first aid capability and intensive care management, the reported mortality rates for severe TBI remain high (27%–46%) [ 15 17 ]. PTH can develop either in the acute or recovery stage of TBI at a reported rate of 0.7%–51.4% [ 18 ], and it often affects the outcome, rehabilitation, and quality of life of patients with TBI. ICP elevation is a significant cause of death and long-term disability resulting from head injuries and other intracranial pathological conditions.…”
Section: Discussionmentioning
confidence: 99%
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“…Les lésions cérébrales touchent également les réseaux moteurs entrainant des troubles de la régulation tonique et du contrôle moteur volontaire (Barat & Mazaux, 1986;Schultz & Bellamkonda, 2017;Weimar, Ziegler, König, 2002). La motricité volontaire comme outil de la connaissance de soi, subit des limitations.…”
Section: L'altération De La Perception Du Corps Vivantunclassified
“…Motor, cognitive, behavioural and personality deficits, which may occur following TBI, can be disabling. Some potential common complications, especially after moderate-severe TBI include posttraumatic seizures (PTS) and epilepsy, hydrocephalus, paroxysmal sympathetic hyperactivity, spasticity, agitation, neuroendocrine dysfunction, heterotrophic ossification, venous thromboembolism, sleep disturbances and cranial nerve dysfunction [ 5 , 7 – 10 ]. The reported incidence of posttraumatic seizures and epilepsy vary between 4–53% [ 10 ].…”
Section: Introductionmentioning
confidence: 99%