TY - JOUR
T1 - Prognostic significance of delayed intraventricular haemorrhage in the INTERACT studies
AU - Moullaali, Tom J.
AU - Sato, Shoichiro
AU - Wang, Xia
AU - Rabinstein, Alejandro A.
AU - Arima, Hisatomi
AU - Carcel, Cheryl
AU - Chen, Guofang
AU - Robinson, Thompson
AU - Heeley, Emma
AU - Chan, Edward
AU - Delcourt, Candice
AU - Stapf, Christian
AU - Cordonnier, Charlotte
AU - Lindley, Richard I.
AU - Chalmers, John
AU - Anderson, Craig S.
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Background and purpose Intraventricular extension of intracerebral haemorrhage (ICH) predicts poor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined. We determined the prognostic significance of dIVH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT 1 and 2). Methods Pooled analyses of the INTERACT CT substudies - international, multicentre, prospective, open, blinded end point, randomised controlled trials of patients with acute spontaneous ICH and elevated systolic blood pressure (SBP) - randomly assigned to intensive (<140 mm Hg) or guideline-based (<180 mm Hg) SBP management. Participants had blinded central analyses of baseline and 24 h CTs, with dIVH defined as new intraventricular haemorrhage (IVH) on the latter scan. Outcomes of death and major disability were defined by modified Rankin Scale scores at 90 days. Results There were 349 (27%) of 1310 patients with baseline IVH, and 107 (11%) of 961 initially IVH-free patients who developed dIVH. Significant associations of dIVH were prior warfarin anticoagulation, high (≥15) baseline National Institutes of Health Stroke Scale score, larger (≥15 mL) ICH volume, greater ICH growth and higher achieved SBP over 24 h. Compared with those who were IVH-free, dIVH had greater odds of 90-day death or major disability versus initial IVH (adjusted ORs 2.84 (95% CI 1.52 to 5.28) and 1.87 (1.36 to 2.56), respectively (p trend <0.0001)). Conclusions Although linked to factors determining greater ICH growth including poor SBP control, dIVH is independently associated with poor outcome in acute small to moderate-size ICH. Trial registration numbers NCT00226096 and NCT00716079.
AB - Background and purpose Intraventricular extension of intracerebral haemorrhage (ICH) predicts poor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined. We determined the prognostic significance of dIVH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT 1 and 2). Methods Pooled analyses of the INTERACT CT substudies - international, multicentre, prospective, open, blinded end point, randomised controlled trials of patients with acute spontaneous ICH and elevated systolic blood pressure (SBP) - randomly assigned to intensive (<140 mm Hg) or guideline-based (<180 mm Hg) SBP management. Participants had blinded central analyses of baseline and 24 h CTs, with dIVH defined as new intraventricular haemorrhage (IVH) on the latter scan. Outcomes of death and major disability were defined by modified Rankin Scale scores at 90 days. Results There were 349 (27%) of 1310 patients with baseline IVH, and 107 (11%) of 961 initially IVH-free patients who developed dIVH. Significant associations of dIVH were prior warfarin anticoagulation, high (≥15) baseline National Institutes of Health Stroke Scale score, larger (≥15 mL) ICH volume, greater ICH growth and higher achieved SBP over 24 h. Compared with those who were IVH-free, dIVH had greater odds of 90-day death or major disability versus initial IVH (adjusted ORs 2.84 (95% CI 1.52 to 5.28) and 1.87 (1.36 to 2.56), respectively (p trend <0.0001)). Conclusions Although linked to factors determining greater ICH growth including poor SBP control, dIVH is independently associated with poor outcome in acute small to moderate-size ICH. Trial registration numbers NCT00226096 and NCT00716079.
UR - http://www.scopus.com/inward/record.url?scp=85017035349&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/NHMRC/358395
UR - http://purl.org/au-research/grants/NHMRC/571281
UR - http://purl.org/au-research/grants/NHMRC/512402
UR - http://purl.org/au-research/grants/NHMRC/1004170
U2 - 10.1136/jnnp-2015-311562
DO - 10.1136/jnnp-2015-311562
M3 - Article
C2 - 26746184
AN - SCOPUS:85017035349
VL - 88
SP - 19
EP - 24
JO - Journal of Neurology, Neurosurgery & Psychiatry
JF - Journal of Neurology, Neurosurgery & Psychiatry
SN - 1468-330X
ER -