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Akinci et al. Vessel Plus 2021;5:56  https://dx.doi.org/10.20517/2574-1209.2021.20  Page 9 of 20



 diltiazem,   patients                              patients  (4-6) at   outcome   outcome
 uradipil                                                     three     event     event
                                                              months
                                                              post
                                                              randomiza
                                                              tion
 Neutral  ATACH  ICH   SBP ≥ 170 6 h  Nicardipin 90 ± 15   Cohort 1: 18 patients, target SBP of 170-200 mmHg   Treatment  Rates   Rates
 [54,58]
 ,   patients  e  days  Cohort 2: 20 patients, target SBP of 140-170 mmHg   failure,   were 21%  were 31%
 2010   Cohort 3: 22 patients, target SBP of 110-140 mmHg     neurologic  for     for
 Mean time from symtom onset to initiating treatment was 3.94 h, 4.13 h and 4.44 h,   deteriorati hematom hematom
 respectively and the goals were achieved in 90% of the patients by 2 h  ons within  a   a
                                                              24 h, and  expansion  expansion
                                                              SAE       and 35%   and 48%
                                                              within 72  for poor   for poor
                                                              h         three-    three-
                                                                        month     month
                                                                        outcome   outcome

 Neutral   ENOS  Ischemic   SBP 140-  48 h  Transder  90 days  GTN group: 310 patients   Mortality  Median   Median
 [64,65]
 but,   ,   or   220  mal   No GTN group: 319 patients        rate and   mRS      mRS
 secondar  2015   hemorrha  glyceryl   Time from onset to treatment was 25.2 ± 13.1 h in the GTN group, 25.1 ± 12.9 h in the no GTN  mRS at 3   grade of 3  grade of 3
 gic stroke
                                                              months
 group
                                                                                  (IQR 2)
 trinitrate
                                                                        (IQR 2)
 y analysis   patients  Baseline BP was 172/93 mmHg and significantly lower in GTN group (-7.5/-4.2 mmHg) on   post
 supporte  day 1                                              randomiza
 d                                                            tion
 Arguing/  RIGHT-  Ischemic   SBP ≥ 120 4 h  Transder  90 days  GTN group: 74 patients   mRS at 90  Mean   Mean
 [73]
 against  2  , 2019  or   mal   Sham group: 71 patients       days post  mRS      mRS
 hemorrha  glyceryl   Median SBP was 176 ± 27 mmHg, mean time from onset to treatment was 74 (45-110) min,   randomiza grade of   grade of
 gic stroke   trinitrate  BP was lower in the GTN group by admission to hospital (mean, -4.4/-3.5 mmHg)  tion  4.9 (± 1.4) 4.3 (± 1.6)
 patients
 ATACH: Antihypertensive Treatment of Acute Cerebral Hemorrhage; BP: blood pressure; CBF: cerebral blood flow; CT: computerized tomography; ENOS: efficacy of nitric oxide in stroke; ICH: intracerebral
 hemorrhage; ICH ADAPT: intracerebral hemorrhage acutely decreasing arterial pressure trial; INTERACT: Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trial; IQR: interquartile range; MAP:
 mean arterial pressure; MMP-9: matrix metalloproteinase-9; mRS: modified Rankin scale; NIHSS: National Institutes of Health Stroke Scale; RIGHT: Rapid Intervention with Glyceryl Trinitrate in Hypertensive Stroke
 Trial; SAE: serious adverse event; SBP: systolic blood pressure.



 [52]
 Koch et al. , 2008
 Koch et al.  investigated the feasibility and safety of aggressive BP lowering in this prospective, randomized, single-center study. They used MAP instead of
 [52]
 SBP in line with AHA guidelines at the time of the study. Forty-two patients with ICH, within 8 h of onset, with elevated MAP (≥ 110 mmHg) were
 randomized to standard treatment (target MAP 110-130 mmHg, n = 21) or aggressive treatment (target MAP < 110 mmHg). Baseline characteristics were
 similar except that the ICH and edema volumes were larger in the aggressive BP group. IV labetalol, nicardipine, or sodium nitroprussid was used and target
 BP was obtained within 87.1 ± 59.6 min in the standard treatment group and 163.5 ± 163.8 min in the aggressive BP treatment group. No significant differences

 were found between two groups in terms of hematoma and edema growth, early neurological deterioration, and clinical outcome at 90 days.
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