Changes in Outcomes after Discharge from an Acute Hospital in Severe Traumatic Brain Injury
Neurological improvement occurs from the subacute to chronic phases in severe traumatic brain injury. We analyzed factors associated with improved neurological findings in the subacute phase, using data from the Japan Neurotrauma Data Bank (JNTDB). The subjects were 1345 patients registered in the J...
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Published in | Neurologia medico-chirurgica Vol. 62; no. 3; pp. 111 - 117 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Japan
The Japan Neurosurgical Society
01.01.2022
THE JAPAN NEUROSURGICAL SOCIETY Japan Science and Technology Agency |
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Online Access | Get full text |
ISSN | 0470-8105 1349-8029 1349-8029 |
DOI | 10.2176/nmc.oa.2021-0217 |
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Abstract | Neurological improvement occurs from the subacute to chronic phases in severe traumatic brain injury. We analyzed factors associated with improved neurological findings in the subacute phase, using data from the Japan Neurotrauma Data Bank (JNTDB). The subjects were 1345 patients registered in the JNTDB (Project 2015). Clinical improvement was evaluated by comparing the Glasgow Outcome Scale (GOS) at discharge and 6 months after injury. Of these patients, 157 with severe disability (SD) on the discharge GOS were examined to evaluate factors associated with neurological improvement in the subacute phase. Cases were defined as those with (group I) and without (group N) improvement: a change from SD at discharge to good recovery (GR) or moderate disability (MD) at 6 months after injury. Patient background, admission findings, treatment, and discharge destination were examined. In all patients, the favorable outcome (GR, MD) rate improved from 30.2% at discharge to 35.7% at 6 months after injury. Of SD cases at discharge, 44.6% had a favorable outcome at 6 months (group I). Patients in group I were significantly younger, and had a significantly lower D-dimer level in initial blood tests and a lower incidence of convulsions. In multivariate analysis, discharge to home was a significant factor associated with an improved outcome. Many SD cases at discharge ultimately showed neurological improvement, and the initial D-dimer level may be a predictor of such improvement. The environment after discharge from an acute care hospital may also contribute to an improved long-term prognosis. |
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AbstractList | Neurological improvement occurs from the subacute to chronic phases in severe traumatic brain injury. We analyzed factors associated with improved neurological findings in the subacute phase, using data from the Japan Neurotrauma Data Bank (JNTDB). The subjects were 1345 patients registered in the JNTDB (Project 2015). Clinical improvement was evaluated by comparing the Glasgow Outcome Scale (GOS) at discharge and 6 months after injury. Of these patients, 157 with severe disability (SD) on the discharge GOS were examined to evaluate factors associated with neurological improvement in the subacute phase. Cases were defined as those with (group I) and without (group N) improvement: a change from SD at discharge to good recovery (GR) or moderate disability (MD) at 6 months after injury. Patient background, admission findings, treatment, and discharge destination were examined. In all patients, the favorable outcome (GR, MD) rate improved from 30.2% at discharge to 35.7% at 6 months after injury. Of SD cases at discharge, 44.6% had a favorable outcome at 6 months (group I). Patients in group I were significantly younger, and had a significantly lower D-dimer level in initial blood tests and a lower incidence of convulsions. In multivariate analysis, discharge to home was a significant factor associated with an improved outcome. Many SD cases at discharge ultimately showed neurological improvement, and the initial D-dimer level may be a predictor of such improvement. The environment after discharge from an acute care hospital may also contribute to an improved long-term prognosis. [Abstract] Neurological improvement occurs from the subacute to chronic phases in severe traumatic brain injury. We analyzed factors associated with improved neurological findings in the subacute phase, using data from the Japan Neurotrauma Data Bank (JNTDB). The subjects were 1345 patients registered in the JNTDB (Project 2015). Clinical improvement was evaluated by comparing the Glasgow Outcome Scale (GOS) at discharge and 6 months after injury. Of these patients, 157 with severe disability (SD) on the discharge GOS were examined to evaluate factors associated with neurological improvement in the subacute phase. Cases were defined as those with (group I) and without (group N) improvement: a change from SD at discharge to good recovery (GR) or moderate disability (MD) at 6 months after injury. Patient background, admission findings, treatment, and discharge destination were examined. In all patients, the favorable outcome (GR, MD) rate improved from 30.2% at discharge to 35.7% at 6 months after injury. Of SD cases at discharge, 44.6% had a favorable outcome at 6 months (group I). Patients in group I were significantly younger, and had a significantly lower D-dimer level in initial blood tests and a lower incidence of convulsions. In multivariate analysis, discharge to home was a significant factor associated with an improved outcome. Many SD cases at discharge ultimately showed neurological improvement, and the initial D-dimer level may be a predictor of such improvement. The environment after discharge from an acute care hospital may also contribute to an improved long-term prognosis. |
ArticleNumber | oa.2021-0217 |
Author | SUEHIRO, Eiichi SUZUKI, Michiyasu KIYOHIRA, Miwa HAJI, Kohei The Japan Neurotrauma Data Bank Committee |
AuthorAffiliation | The Japan Neurotrauma Data Bank Committee, The Japan Society of Neurotraumatology |
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Cites_doi | 10.1016/j.apmr.2010.06.033 10.2176/nmc.oa.2018-0254 10.1016/j.nec.2016.06.001 10.2176/nmc.oa.2020-0030 10.3171/2015.6.JNS15674 10.2176/nmc.oa.2020-0071 10.1016/j.apmr.2012.10.041 10.1007/s11910-016-0654-5 10.1016/j.wneu.2012.06.026 10.1016/j.clineuro.2014.10.007 10.1212/WNL.0b013e3181e8e8cc 10.1089/neu.2018.6153 10.1089/neu.2011.1811 10.1080/02699050701727460 10.1089/neu.2017.5240 10.2176/nmc.46.567 10.1212/WNL.0b013e3181e8e8df 10.3171/2017.3.JNS162720 10.1016/j.wneu.2015.09.105 10.1089/neu.2017.5359 |
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References | 18) Sugimoto K, Suehiro E, Shinoyama M, et al.: D-dimer elevation as a blood biomarker for detection of structural disorder in mild traumatic brain injury. J Neurotrauma 34: 3245–3248, 2017 7) Wilkins TE, Beers SR, Borrasso AJ, et al.: Favorable functional recovery in severe traumatic brain injury survivors beyond six months. J Neurotrauma 36: 3158–3163, 2019 12) Sandsmark DK: Clinical outcomes after traumatic brain injury. Curr Neurol Neurosci Rep 16: 52, 2016 6) Whyte J, Nakase-Richardson R, Hammond FM, et al.: Functional outcomes in traumatic disorders of consciousness: 5-year outcomes from the National Institute on Disability and Rehabilitation Research Traumatic Brain Injury Model Systems. Arch Phys Med Rehabil 94: 1855–1860, 2013 10) Wilde EA, Whiteneck GG, Bogner J, et al.: Recommendations for the use of common outcome measures in traumatic brain injury research. Arch Phys Med Rehabil 91: 1650–1660.e17, 2010 1) Yokobori S, Yamaguchi M, Igarashi Y, et al.: Outcome and refractory factor of intensive treatment for geriatric traumatic brain injury: analysis of 1165 cases registered in the Japan Neurotrauma Data Bank. World Neurosurg 86: 127–133.e1, 2016 11) Walker WC, Stromberg KA, Marwitz JH, et al.: Predicting long-term global outcome after traumatic brain injury: development of a practical prognostic tool using the Traumatic Brain Injury Model Systems National Database. J Neurotrauma 35: 1587–1595, 2018 20) Raheja A, Sinha S, Samson N, et al.: Serum biomarkers as predictors of long-term outcome in severe traumatic brain injury: analysis from a randomized placebo-controlled Phase II clinical trial. J Neurosurg 125: 631–641, 2016 9) Nakamura N, Yamaura A, Shigemori M, et al.: Final report of the Japan Neurotrauma Data Bank project 1998–2001: 1,002 cases of traumatic brain injury. Neurol Med Chir (Tokyo) 46: 567–574, 2006 13) Andelic N, Bautz-Holter E, Ronning P, et al.: Does an early onset and continuous chain of rehabilitation improve the long-term functional outcome of patients with severe traumatic brain injury? J Neurotrauma 29: 66–74, 2012 19) Zimmermann LL, Diaz-Arrastia R, Vespa PM: Seizures and the role of anticonvulsants after traumatic brain injury. Neurosurg Clin N Am 27: 499–508, 2016 14) Estraneo A, Moretta P, Loreto V, Lanzillo B, Santoro L, Trojano L: Late recovery after traumatic, anoxic, or hemorrhagic long-lasting vegetative state. Neurology 75: 239–245, 2010 16) Suehiro E, Koizumi H, Fujiyama Y, Yoneda H, Suzuki M: Predictors of deterioration indicating a requirement for surgery in mild to moderate traumatic brain injury. Clin Neurol Neurosurg 127: 97–100, 2014 8) Dumont TM, Rughani AI, Goeckes T, Tranmer BI: Chronic subdural hematoma: a sentinel health event. World Neurosurg 80: 889–892, 2013 15) Luauté J, Maucort-Boulch D, Tell L, et al.: Long-term outcomes of chronic minimally conscious and vegetative states. Neurology 75: 246–252, 2010 17) Suehiro E, Fujiyama Y, Kiyohira M, Motoki Y, Nojima J, Suzuki M: Probability of soluble tissue factor release lead to the elevation of D-dimer as a biomarker for traumatic brain injury. Neurol Med Chir (Tokyo) 59: 63–67, 2019 3) Hiraizumi S, Shiomi N, Echigo T, et al.: Factors associated with poor outcomes in patients with mild or moderate acute subdural hematomas. Neurol Med Chir (Tokyo) 60: 402–410, 2020 5) Corral L, Ventura JL, Herrero JI, et al.: Improvement in GOS and GOSE scores 6 and 12 months after severe traumatic brain injury. Brain Inj 21: 1225–1231, 2007 2) Katsuki M, Kakizawa Y, Nishikawa A, et al.: Fifteen cases of endoscopic treatment of acute subdural hematoma with small craniotomy under local anesthesia: endoscopic hematoma removal reduces the intraoperative bleeding amount and the operative time compared with craniotomy in patients aged 70 or older. Neurol Med Chir (Tokyo) 60: 439–449, 2020 4) Vedantam A, Robertson CS, Gopinath SP: Clinical characteristics and temporal profile of recovery in patients with favorable outcomes at 6 months after severe traumatic brain injury. J Neurosurg 129: 234–240, 2018 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 10 |
References_xml | – reference: 17) Suehiro E, Fujiyama Y, Kiyohira M, Motoki Y, Nojima J, Suzuki M: Probability of soluble tissue factor release lead to the elevation of D-dimer as a biomarker for traumatic brain injury. Neurol Med Chir (Tokyo) 59: 63–67, 2019 – reference: 6) Whyte J, Nakase-Richardson R, Hammond FM, et al.: Functional outcomes in traumatic disorders of consciousness: 5-year outcomes from the National Institute on Disability and Rehabilitation Research Traumatic Brain Injury Model Systems. Arch Phys Med Rehabil 94: 1855–1860, 2013 – reference: 15) Luauté J, Maucort-Boulch D, Tell L, et al.: Long-term outcomes of chronic minimally conscious and vegetative states. Neurology 75: 246–252, 2010 – reference: 14) Estraneo A, Moretta P, Loreto V, Lanzillo B, Santoro L, Trojano L: Late recovery after traumatic, anoxic, or hemorrhagic long-lasting vegetative state. Neurology 75: 239–245, 2010 – reference: 16) Suehiro E, Koizumi H, Fujiyama Y, Yoneda H, Suzuki M: Predictors of deterioration indicating a requirement for surgery in mild to moderate traumatic brain injury. Clin Neurol Neurosurg 127: 97–100, 2014 – reference: 4) Vedantam A, Robertson CS, Gopinath SP: Clinical characteristics and temporal profile of recovery in patients with favorable outcomes at 6 months after severe traumatic brain injury. J Neurosurg 129: 234–240, 2018 – reference: 5) Corral L, Ventura JL, Herrero JI, et al.: Improvement in GOS and GOSE scores 6 and 12 months after severe traumatic brain injury. Brain Inj 21: 1225–1231, 2007 – reference: 12) Sandsmark DK: Clinical outcomes after traumatic brain injury. Curr Neurol Neurosci Rep 16: 52, 2016 – reference: 13) Andelic N, Bautz-Holter E, Ronning P, et al.: Does an early onset and continuous chain of rehabilitation improve the long-term functional outcome of patients with severe traumatic brain injury? J Neurotrauma 29: 66–74, 2012 – reference: 19) Zimmermann LL, Diaz-Arrastia R, Vespa PM: Seizures and the role of anticonvulsants after traumatic brain injury. Neurosurg Clin N Am 27: 499–508, 2016 – reference: 11) Walker WC, Stromberg KA, Marwitz JH, et al.: Predicting long-term global outcome after traumatic brain injury: development of a practical prognostic tool using the Traumatic Brain Injury Model Systems National Database. J Neurotrauma 35: 1587–1595, 2018 – reference: 9) Nakamura N, Yamaura A, Shigemori M, et al.: Final report of the Japan Neurotrauma Data Bank project 1998–2001: 1,002 cases of traumatic brain injury. Neurol Med Chir (Tokyo) 46: 567–574, 2006 – reference: 10) Wilde EA, Whiteneck GG, Bogner J, et al.: Recommendations for the use of common outcome measures in traumatic brain injury research. Arch Phys Med Rehabil 91: 1650–1660.e17, 2010 – reference: 20) Raheja A, Sinha S, Samson N, et al.: Serum biomarkers as predictors of long-term outcome in severe traumatic brain injury: analysis from a randomized placebo-controlled Phase II clinical trial. J Neurosurg 125: 631–641, 2016 – reference: 2) Katsuki M, Kakizawa Y, Nishikawa A, et al.: Fifteen cases of endoscopic treatment of acute subdural hematoma with small craniotomy under local anesthesia: endoscopic hematoma removal reduces the intraoperative bleeding amount and the operative time compared with craniotomy in patients aged 70 or older. Neurol Med Chir (Tokyo) 60: 439–449, 2020 – reference: 8) Dumont TM, Rughani AI, Goeckes T, Tranmer BI: Chronic subdural hematoma: a sentinel health event. World Neurosurg 80: 889–892, 2013 – reference: 3) Hiraizumi S, Shiomi N, Echigo T, et al.: Factors associated with poor outcomes in patients with mild or moderate acute subdural hematomas. Neurol Med Chir (Tokyo) 60: 402–410, 2020 – reference: 7) Wilkins TE, Beers SR, Borrasso AJ, et al.: Favorable functional recovery in severe traumatic brain injury survivors beyond six months. J Neurotrauma 36: 3158–3163, 2019 – reference: 1) Yokobori S, Yamaguchi M, Igarashi Y, et al.: Outcome and refractory factor of intensive treatment for geriatric traumatic brain injury: analysis of 1165 cases registered in the Japan Neurotrauma Data Bank. World Neurosurg 86: 127–133.e1, 2016 – reference: 18) Sugimoto K, Suehiro E, Shinoyama M, et al.: D-dimer elevation as a blood biomarker for detection of structural disorder in mild traumatic brain injury. 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Snippet | Neurological improvement occurs from the subacute to chronic phases in severe traumatic brain injury. We analyzed factors associated with improved neurological... [Abstract] Neurological improvement occurs from the subacute to chronic phases in severe traumatic brain injury. We analyzed factors associated with improved... |
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SubjectTerms | biomarker Brain Injuries Brain Injuries, Traumatic - complications Brain Injuries, Traumatic - diagnosis Brain Injuries, Traumatic - therapy Convulsions discharge destination Glasgow Outcome Scale Hospitals Humans Multivariate analysis Original outcome improvement Patient Discharge Patients rehabilitation Traumatic brain injury Treatment Outcome |
Title | Changes in Outcomes after Discharge from an Acute Hospital in Severe Traumatic Brain Injury |
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ispartofPNX | Neurologia medico-chirurgica, 2022, Vol.62(3), pp.111-117 |
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