03534nas a2200541 4500000000100000008004100001653001100042653001100053653000900064653002400073653000900097653001600106653002600122653001700148653002400165653001900189653002400208653002200232653000900254653002400263653002800287653003100315653002200346653002400368100001900392700001600411700001700427700001700444700002000461700002100481700001900502700002800521700001300549700001600562700001800578700002000596700001700616700001400633700001700647700001300664700001400677700002200691245015800713300001400871490000700885520208600892022001402978 2016 d10aFemale10aHumans10aAged10aDouble-Blind Method10aMale10aMiddle Aged10aDisability Evaluation10aHypertension10aProspective Studies10aBlood Pressure10aCerebral Hemorrhage10aAged, 80 and over10aRisk10aFibrinolytic Agents10aAntihypertensive Agents10aEarly Medical Intervention10aPreoperative Care10aStatistics as Topic1 aAnderson Craig1 aHeeley Emma1 aHuang Yining1 aWang Jiguang1 aStapf Christian1 aDelcourt Candice1 aArima Hisatomi1 aINTERACT2 Investigators1 aWang Xia1 aChalmers J.1 aLavados Pablo1 aLindley Richard1 aSandset Else1 aSong Lili1 aChen Guofeng1 aYang Jie1 aWu Guojun1 aRobinson Thompson00aEarly blood pressure lowering in patients with intracerebral haemorrhage and prior use of antithrombotic agents: pooled analysis of the INTERACT studies. a1330-13350 v873 a

OBJECTIVE: Antithrombotic agents increase risks of intracerebral haemorrhage (ICH) and associated adverse outcomes. We determined differential effects of early blood pressure (BP) lowering in patients with/without antithrombotic-associated ICH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT1 and 2).

DESIGN: Post hoc pooled analyses of the INTERACT studies-international, multicentre, prospective, open, blinded end point trials of patients with ICH (<6 h) and elevated systolic BP (SBP 150-180 mm Hg) randomly assigned to intensive (target SBP <140 mm Hg) or guideline-based (SBP <180 mm Hg) BP management. Associations of antithrombotic use and (1) death or dependency (modified Rankin scale scores 3-6) were analysed using logistic regression, and (2) of increased haematoma+intraventricular haemorrhage volume (IVH) with/without intraventricular haemorrhage (IVH) over 24 h were estimated in analyses of covariance.

RESULTS: In all, 3184 patients were included in these analyses. Antithrombotic-associated ICH (364 patients, 11%) was not associated with a significantly increased risk of death or dependency (OR 1.38, 95% CI 0.93 to 2.04). There was no heterogeneity in the BP-lowering treatment effect on death or dependency. Among 1309 patients who underwent follow-up CT after 24 h, absolute increase in haematoma±IVH volume was larger (5.2/5.0 mL) in those with compared to those without prior antithrombotics (2.2/0.9 mL; p=0.022/0.031). Intensive BP lowering reduced haematoma±IVH growth by 4.7/7.1 mL in patients on antithrombotics versus 1.3/1.4 mL in those without, although these differences did not reach statistical significance (p homogeneity=0.104/0.059).

CONCLUSIONS: In patients with ICH, prior antithrombotic therapy is associated with greater haematoma growth, which may be reduced by early intensive BP-lowering treatment.

TRIAL REGISTRATION NUMBER: NCT00226096, NCT00716079.

 a1468-330X