2020
DOI: 10.1016/j.jcjq.2019.11.007
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Implementation of a Prophylactic Anticoagulation Guideline for Patients with Traumatic Brain Injury

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Cited by 9 publications
(13 citation statements)
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“…Patients with high-risk TBI without progression on repeat imaging can have VTE prophylaxis safely initiated at 72 hours 50 . Adherence with the modified Berne-Norwood criteria is associated with a significant reduction in VTE events for TBI patients without added risk of TBI progression 44,51,52 …”
Section: Protocol Rationale and Goalsmentioning
confidence: 99%
See 1 more Smart Citation
“…Patients with high-risk TBI without progression on repeat imaging can have VTE prophylaxis safely initiated at 72 hours 50 . Adherence with the modified Berne-Norwood criteria is associated with a significant reduction in VTE events for TBI patients without added risk of TBI progression 44,51,52 …”
Section: Protocol Rationale and Goalsmentioning
confidence: 99%
“…50 Adherence with the modified Berne-Norwood criteria is associated with a significant reduction in VTE events for TBI patients without added risk of TBI progression. 44,51,52 Many trauma centers follow the Brain Injury Guidelines (BIG) in which repeat CT head is not routinely done in BIG 1 and 2 injuries and is done at 6 hours after the initial head CT in BIG 3 patients. 53 Initiation of VTE chemical prophylaxis in the low-risk BIG 1 and 2 may be prudent 24 hours to 48 hours after injury if neurologic examination remains stable.…”
Section: Vte Pharmacologic Prophylaxis For Tbimentioning
confidence: 99%
“…None of the studies were randomized trials. Studies by Haut et al, 15 Engels et al, 16 and Tignanelli et al 17 were retrospective, whereas the study by Burns et al 18 had both retrospective and prospective components. Burns et al studied 134 acute spinal cord injury patients in six VA hospitals in the United States.…”
Section: Resultsmentioning
confidence: 99%
“…Ultimately, the CPG adhered to a “middle of the road” approach by instituting universal prophylactic weight-based anticoagulation for all patients. Similar to anticoagulation CPGs for other disease processes [ 19 ], we incorporated a risk stratification model, whereby the intensity of anticoagulation was increased to moderate intensity (0.5 mg/kg BID enoxaparin or low intensity heparin infusion in case of renal failure) for patients with a history of thrombosis, cancer, admission to the intensive care unit (ICU), or D-dimer >10 times the upper limit of normal. The CPG is a “living” framework, and has since undergone several iterations of modifications (upstratification of patients with a prior history of deep venous thrombosis or cancer, and ICU patients, and exclusion of pregnant patients) based on evolution of the evidence.…”
Section: Methodsmentioning
confidence: 99%