Page 135 - Read Online
P. 135

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.
   130   131   132   133   134   135   136   137   138   139   140