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Abstract Details

Admission Coagulopathies on Viscoelastic Hemostatic Assays Predict Infection after Intracerebral Hemorrhage
Neuro Trauma and Critical Care
P9 - Poster Session 9 (5:00 PM-6:00 PM)
18-002
To assess whether viscoelastic hemostatic assay (VHA) coagulation parameters relate to infection risk after ICH.

Infection is common after spontaneous intracerebral hemorrhage (ICH) and contributes to morbidity. VHA differences have been appreciated in infected patients within non-ICH populations. Here, we investigate the relationship between baseline coagulopathy in patients admitted for ICH and risk for subsequent infection.

Consecutively admitted spontaneous ICH patients were enrolled in a single-center prospective observational cohort-study and underwent viscoelastic hemostatic assay (Rotational Thromboelastometry: ROTEM) testing at admission. Patients with death or withdrawal of care within 24 hours were excluded. The primary exposure variables were ROTEM measurements of clot strength (maximum clot firmness: MCF). The primary outcome was any infection (pneumonia, bacteremia, urinary tract infection, C. Difficile colitis, ventriculitis, cellulitis) within 30 days of admission, with specific infections defined by clinical diagnostic criteria. Regression models assessed relationships of ROTEM parameters with infection, adjusted for baseline severity via ICH Score.

Of 73 patients assessed, 35(48%) experienced infection within 30 days of admission, with most frequent diagnoses being urinary tract infection (32%) and pneumonia (29%). Patients with and without infection had similar baseline stroke severity (ICH Score median [IQR] 2[1–3] vs 2[1–3], p=0.08). Logistic regression showed that greater fibrinogen assay clot strength (FIBTEM MCF) was associated with infection (adjusted OR 1.08[1.02–1.15], p=0.01). When defined as a binary exposure variable, FIBTEM MCF above the reference level (>24 mm) similarly related to increased odds of infection (adjusted OR 3.5[1.2–11.7], p=0.03).

Our findings suggest that hypercoagulable features related to elevated fibrinogen contribution to clotting are detectable on VHAs and may predict infection risk after ICH. Future work is needed to assess the generalizability and underlying mechanisms of these associations, and to determine whether VHAs can provide risk stratification strategies or insights into preventative treatment approaches for post-ICH infectious complications.

Authors/Disclosures
Laura Sieh
PRESENTER
Ms. Sieh has nothing to disclose.
Emma S. Peasley (Yale School of Medicine) Miss Peasley has nothing to disclose.
Shivani Ghoshal, MD (Columbia University Medical Center) Dr. Ghoshal has nothing to disclose.
Sachin Agarwal, MD, MPH (Columbia University Med Center) Dr. Agarwal has nothing to disclose.
Soojin Park, MD Dr. Park has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Neurocritical Care. The institution of Dr. Park has received research support from National Institutes of Health.
Jan Claassen, MD, PhD (Columbia University College of Physicians & Surgeons) Dr. Claassen has stock in iCE Neurosystems. The institution of Dr. Claassen has received research support from NINDS. The institution of Dr. Claassen has received research support from McDonnel Foundation. Dr. Claassen has received publishing royalties from a publication relating to health care. Dr. Claassen has received publishing royalties from a publication relating to health care.
David J. Roh, MD (Columbia University Medical Center) Dr. Roh has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Portola Pharmaceuticals.