1992
DOI: 10.1097/00006123-199202000-00002
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Delayed Brain Injury after Head Trauma

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Cited by 86 publications
(103 citation statements)
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“…There are variable data in the literature and different studies associated one or more of the following with TBI progression: Prothrombin time (PT) or INR, Partial thromboplastin time (PTT), thrombocytopenia, high fibrin degradation and low fibrinogen levels. [25][26][27][28][29][30] Fewer other studies reported no association between coagulopathy and bleeding progression in TBI. [31][32][33] This considerable variation is attributed to lack of consensus on TBI-coagulopathy definition, heterogeneity of patients involved, variable laboratory tests used in different studies and timing to perform these tests and CTs.…”
Section: Coagulopathy and Edhpmentioning
confidence: 98%
“…There are variable data in the literature and different studies associated one or more of the following with TBI progression: Prothrombin time (PT) or INR, Partial thromboplastin time (PTT), thrombocytopenia, high fibrin degradation and low fibrinogen levels. [25][26][27][28][29][30] Fewer other studies reported no association between coagulopathy and bleeding progression in TBI. [31][32][33] This considerable variation is attributed to lack of consensus on TBI-coagulopathy definition, heterogeneity of patients involved, variable laboratory tests used in different studies and timing to perform these tests and CTs.…”
Section: Coagulopathy and Edhpmentioning
confidence: 98%
“…3,9,10 In support of this concept, high levels of D-dimers, prolongation of clotting times, thrombocytopenia, and increased plasmin/anti-plasmin complexes correlate with increased mortality. 7,11,12 However, measures that attenuate the consumptive coagulopathy fail to reduce mortality and/or disability. 9,10 Thus, important gaps in our understanding of the pathophysiology and management of post-TBI bleeding persist 13,14 and there is continued need to examine other possible causes.…”
Section: Introductionmentioning
confidence: 99%
“…Abnormalities in admission PT, aPTT, INR, and fibrinogen degradation products have all been linked to increased morbidity and mortality in TBI patients [3,4,7,12,27,28,[32][33][34][35][36][37]. However, when we analyzed admission CCT values on 1924 of our highest-level trauma activations over 18 months, no statistically significant difference in the prevalence of coagulopathy based on these values was detected in TBI patients compared to non-TBI patients (Table 2).…”
Section: Discussionmentioning
confidence: 98%