The following guidelines are recommended for BP control in acute ICH [level of evidence (LOE) : III, Grade of Recommendation (GOR) : B] (Table 1).

1) For systolic BP (SBP) >200 mm Hg or mean arterial pressure (MAP) >150 mm Hg, measure BP every 5 minutes, and lower BP aggressively with intravenous antihypertensives.

2) For SBP >180 mm Hg or MAP >130 mm Hg with (suspected) ICP elevation, maintain cerebral perfusion pressure (CPP) at 60-80 mm Hg, and lower BP with intravenous antihypertensives (bolus or infusion).

3) For SBP >180 mm Hg or MAP >130 mm Hg without evidence of ICP elevation, clinically evaluate the patient every 15 minutes, and control BP with intravenous antihypertensives (bolus or infusion) to maintain a MAP of 110 mm Hg or SBP/diastolic BP (DBP) of 160/90 mm Hg.

American Heart Association/American Stroke Association (AHA/ASA, USA)52)

1) Until ongoing clinical trials of BP intervention for ICH are completed, physicians must manage BP based on the present incomplete efficacy evidence. Current suggested recommendations for target BPs in various situations are listed below and may be considered (Class IIb; LOE C)

i. If SBP is >200 mm Hg or MAP is >150 mm Hg, then consider aggressive reduction of BP with continuous intravenous infusion, with frequent BP monitoring every 5 minutes.

ii. If SBP is >180 mm Hg or MAP is >130 mm Hg and there is the possibility of elevated ICP, then consider monitoring ICP and reducing BP using intermittent or continuous intravenous medications while maintaining a CPP of ≥60 mm Hg.

iii. If SBP is >180 mm Hg or MAP is >130 mm Hg and there is no evidence of elevated ICP, then consider a modest reduction of BP (e.g., a MAP of 110 mm Hg or a target BP of 160/90 mm Hg) using intermittent or continuous intravenous medications to control BP and clinically reexamine the patient every 15 minutes.

2) In patients presenting with a SBP of 150 to 220 mm Hg, acute lowering of SBP to 140 mm Hg is probably safe (Class IIa; LOE B) (new recommendation).

The previous recommendations on BP management in patients with acute ICH were mainly based on small observational studies. An anecdotal report showed that an admission SBP >200 mm Hg was associated with hematoma expansion on follow up CT scan. Therefore, a SBP <200 mm Hg was initially recommended as a BP goal38). However, lowering BP may not always be safe because the majority of patients have a history of hypertension (HT). Considering that the autoregulation curve is shifted toward the higher ranges of BP in patients with HT, there is a safety concern regarding the acute reduction of BP. Therefore, a modest recommendation was made in the previous guidelines for safety reasons. An Initial practice guideline suggested that a SBP <180-185 mm Hg with a DBP <105-110 mm Hg was recommended in patients with a history of HT, while a SBP <160-170 mm Hg with a DBP <95-100 mm Hg was recommended in those without a history of HT13). Those recommendations were rephrased in terms of MAP, and a MAP < 130 mm Hg was suggested in the 1999 and 2007 American Stroke Association (ASA) guidelines10,11).

After the ASA ICH guideline in 2007, three major clinical trials were published, which focused on the relationship between acute BP reduction and clinical outcome. In 2008, Intensive blood pressure reduction in acute cerebral hemorrhage Trial (IN-TERACT) result came out3). Included patients had acute spontaneous ICH diagnosed by CT within 6 hours of onset, an elevated SBP (150 to 220 mm Hg), and no definite indication or contraindication to BP control. They were randomly assigned to early intensive BP lowering (a target SBP of 140 mm Hg; n=203) or standard guideline-based BP management (a target SBP of 180 mm Hg; n=201). While the mean proportional hematoma growth after 24 hours was lower in the intensive group compared to the standard treatment group [13.7% vs. 36.3%, absolute difference 22.6%, 95% confidence interval (CI) 0.6-44.5%; p=0.04], intensive BP-lowering did not increase the risks of adverse events, but failed to improve clinical outcomes at 90 days. Although intensive BP reduction may be safe, the absolute difference in hematoma volume between the two groups was only 1.7 mL, which raised the question regarding the effectiveness of intensive BP reduction from a practical standpoint. In addition, the majority of patients (85% of the intensive group, and 95% of the conventional group) were treated with diuretics or vasodilators, which were not commonly used for controlling BP in usual practice. Despite these limitations, intensive BP reduction may be safely tried in patients with acute ICH.

Another study reflecting a real practice pattern came out in 20105). The Antihypertensive Treatment of Acute Cerebral Hemorrhage (ATACH) trial also included patients with acute ICH within 6 hours from symptom onset if they had an elevated SBP ≥170 mm Hg. Patients were randomly allocated into three tiers of SBP goals (170 to 200 mm Hg, n=18 ; 140 to 170 mm Hg, n=20; or 110 to 140 mm Hg, n=22), and SBPs were controlled with intravenous nicardipine infusion. Primary outcomes were treatment feasibility and safety up to 72 hours. Serious adverse events were observed in one subject (5%) in tier two (SBP 140 to 170 mm Hg) and in three subjects (14%) in tier three (SBP 110 to 140 mm Hg). However, the safety stopping rule was not activated in any of the tiers. Therefore, controlling BP with nicardipine may be safe5). In order to explore its clinical utility, a phase 3 clinical trial is currently underway (ATACH-II)65).

Recently, the result of the INTERACT II, a phase 3 trial, was published2). A total of 2839 patients with acute ICH within 6 hours from symptom onset were randomized to two BP goals (a target SBP <140 mm Hg within 1 hour vs. SBP <180 mm Hg) if their SBP was between 150 mm Hg and 220 mm Hg. The antihypertensive drugs were chosen at the discretion of the treating physicians. The primary outcome was a combined endpoint of death and major disability (mRS 3 to 6) at 3 months. The intensive treatment group had a tendency for less death or major disability (52.0%) compared to those in the guideline group (55.6%) (odds ratio with intensive treatment, 0.87; 95% CI, 0.75 to 1.01; p=0.06), which failed to reach statistical significance. However, secondary outcome with the ordinal analysis on the mRS showed a significantly lower mRS with intensive treatment (odds ratio for greater disability, 0.87; 95% CI, 0.77 to 1.00; p=0.04). Safety outcome was not different between the two groups. The main mechanism for the improv-ed outcomes with rapid intensive BP reduction is still unclear because there were no significant absolute or relative changes in hematoma growth between the two treatment groups. The hematoma volume difference between the groups was very small (adjusted mean volume, 1.4 mL).

The major safety concern regarding acute BP reduction is the potential for aggravation of ischemic injury due to the possible existence of perihematomal penumbra. In order to clarify this issue, a randomized open-label study with blinded evaluation was carried out14). The included patients were >18 years of age with acute spontaneous ICH within 24 hours after onset, and had a SBP greater than 150 mm Hg. Patients were randomized to an SBP target of <150 mm Hg (n=39) or <180 mm Hg (n=36) and underwent a CT perfusion scan to compare the difference in relative cerebral blood flow (rCBF) between the two treatment groups. There was no relationship between the BP change and perihematomal rCBF in both treatment groups suggesting the safety of acute BP reduction in patients with ICH.

Based on these results, rapid BP reduction to a SBP <140 mm Hg in patients with acute ICH is probably safe, and may be beneficial in terms of improving functional outcome.

1. The suggested BP targets in patients with acute ICH are described below (LOE III, GOR B). Drugs that can be used for BP control in spontaneous ICH are shown in Table 2 (revised recommendation).

1) If the SBP is >200 mm Hg or MAP is >150 mm Hg, then consider aggressive BP reduction with a continuous intravenous infusion of drugs, with frequent BP monitoring every 5 minutes.

2) If the SBP is >180 mm Hg or MAP is >130 mm Hg and there is any possibility of an ICP elevation, then consider ICP monitoring and reducing BP using an intermittent or continuous intravenous infusion while maintaining a CPP (MAP-ICP) of 50-70 mm Hg.

3) If the SBP is >180 mm Hg or MAP is >130 mm Hg and there is no evidence of an ICP elevation, then consider a modest reduction of BP using an intermittent or continuous intravenous infusion (MAP of 110 mm Hg for a BP of 160/90 mm Hg) and clinically reexamine the patient every 15 minutes.

2. In patients with acute ICH, when the SBP is measured between 150 and 220 mm Hg, the SBP may be safely lowered to 140 mm Hg within 1 hour (LOE Ib, GOR A) (new Recommendation).

1. Treatment and monitoring at the intensive care unit (ICU) is recommended in acute hemorrhage patients because of the need for ICP elevation monitoring, BP control, intubation, and mechanical ventilation (LOE III, GOR B).

2. To control an elevated ICP, a gradual treatment should be considered. The patient's head should be elevated by about 30° to start with. Limited use of analgesics and/or sedatives may be considered in patients with pain and/or unstable conditions (LOE IV, GOR C).

3. A more aggressive ICP control includes the use of mannitol and hypertonic saline solution, CSF drainage via a ventricular catheter, neuromuscular blockade, and hyperventilation. In general, maintaining a CPP ≥70 mm Hg is recommended along with the close monitoring of the ICP and blood pressure (LOE IV, GOR C).

1. People with ICH should be monitored by specialists in neurosurgical or stroke care for deterioration in function and referred immediately for brain imaging when necessary [Royal College of Physicians (RCP), UK 2008, LOE consensus].

2. Patients with a Glasgow Coma Scale (GCS) score of ≤8, those with clinical evidence of transtentorial herniation, or those with significant intraventricular hemorrhage (IVH) or hydrocephalus could be considered for ICP monitoring and treatment. A CPP of 50 to 70 mm Hg may be reasonable to maintain depending on the status of cerebral autoregulation (AHA/ASA, USA 2010 : Class IIb; LOE C).

3. Ventricular drainage as a treatment for hydrocephalus is reasonable in patients with a decreased level of consciousness (AHA/ASA, USA 2010 : Class IIa; LOE B).

4. Corticosteroid should not be used for the treatment of primary ICH [Scottish Intercollegiate Guidelines Network (SIGN) 2008 : LOE 1++, GOR B].

5. Intravenous mannitol should not be used routinely for the treatment of raised intracranial pressure in patients with primary ICH (SIGN 2008 : LOE 1+, GOR B).

An accurate ICP measurement is the first step in managing patients with ICP elevation. Intraparenchymal monitor may better reflect perihematomal ICPs, representing a more accurate hemodynamic status in the perilesional area which is vulnerable to secondary injury. ICP measured by ventricular catheter (VC) represents global ICP, which is regarded as a gold standard. Given that VC can be used to drain cerebrospinal fluid or intraventricular hemorrhage, ICP measurement via VC is preferred in patients with concomitant IVH. The procedural complication rate is reported to be as high as 3% to 4% including procedural hemorrhage and catheter related infection24).

The frequency and risk factors for ICP crisis in patients with ICH remains to be elucidated. In small randomized studies, an initial ICP, measured at the time of VC insertion, was not directly associated with the IVH volume or parenchymal ICH volume79). Moreover, the mean daily ICP was not correlated with hemorrhage burden79). Although the existence of IVH per se does not mean an ICP crisis, the presence of IVH is considered to be associated with poor prognostic factors, probably mediated by hydrocephalus. In the International Surgical Trial in Intracerebral Haemorrhage (STICH) trial, 377 (42%) out of 902 patients had IVH, and a total of 208 (23% among the study patients; 55% of the patients with IVH) developed hydrocephalus. Favorable functional outcomes at 6 months occurred in 15% and 31% of the patients with and without IVH (p<0.00001), respectively, suggesting an association between the presence of IVH and functional outcome44). Moreover, if hydrocephalus is combined in patients with IVH, the percentage of favorable outcomes drops from 20% to 12% (p<0.031). Therefore, the presence of hydrocephalus is considered as an important prognostic factor7). In addition, the presence of IVH is accepted as an important prognostic factor to predict mortality at 1 month and functional recovery at 12 months, which is reflected in the ICH score17,27,28). Therefore, ICP measurement is necessary, especially in patients who have IVH or hydrocephalus, and the insertion of VC may be considered when their mental status deteriorates as hydrocephalus develops.

The indications of ICP monitoring is still unclear, but it may be tried in ICH patients with significant severity (GCS score of 3 to 8), based on the TBI guideline in 20088,57). ICP monitoring is needed in patients with huge supratentorial lesions because those patients are at high risk for transtentorial herniation with secondary brainstem compression4,64). Therefore, patients with clinical signs of transtentorial herniation may be a good candidate for ICP monitoring.

If ICP can be measured, CPP can be calculated from the difference between MAP and ICP. It is still debatable regarding which ranges of CPP should be pursued in patients with ICH. The AHA/ASA ICH guideline in 2007 suggested that CPP should be maintained greater than 70 mm Hg, and the target level was lowered to a CPP of 50 to 70 mm Hg in 201052). Those recommendations are adapted from the 2007 TBI guideline from the brain trauma foundation. It recommended that a CPP lower than 50 mm Hg should be avoided (Level III) and not be maintained greater than 70 mm Hg (Level II)9). The lower limit of CPP (>50 mm Hg) is based on a small study. In patients with severe TBI with a depressed CPP level around 32 mm Hg, if the CPP was elevated up to 68 mm Hg with the proper use of pressors, the partial brain tissue oxygen pressure (PbtO2) improved. Based on the fact that the PbtO2 level is associated with a poor functional outcome, a low CPP should be avoided as well39). Moreover, in a small observational study using microdialysis, when the CPP dropped below 50 mm Hg, the lactate/pyruvate ratio surged, reflecting a metabolic crisis and anaerobic shift of brain glucose metabolism61). Taken together, a CPP less than 50 mm Hg should be avoided9). The upper range of the CPP at 70 mm Hg is also based on studies in patients with severe TBI66). Severe TBI patients were randomized to either a CPP >70 mm Hg or a CPP 50-70 mm Hg, and the frequency of sustained jugular venous desaturation (JvSO2) <50% more than 10 minutes, was less in patients with higher CPP goals (CPP >70 mm Hg), while the functional outcome was not different. However, the development of acute respiratory difficulty syndrome was 5 times more frequent in the higher CPP group because of prolonged use of pressors with high fluid therapy66). Therefore, a CPP >70 mm Hg is not routinely recommended in patients with TBI9). However, no studies have been performed in patients with ICH targeting CPP ranges, and the recommendations on CPP ranges were extrapolated from a TBI guideline. A small study using comatose ICH patients showed that a CPP >80 mm Hg may be beneficial in terms of maintaining better brain tissue oxygenation, which needs to be confirmed in large numbers of patients41). Therefore, it is still unclear which CPP goal should be suggested in patients with ICH.

A variety of methods have been tried in lowering ICPs, including hyperventilation, osmotic agents (mannitol and hypertonic saline) and therapeutic hypothermia. Based on a study comparing the effectiveness of osmotic agents on ICP management using equi-osmolar doses, mannitol is considered to be equivalent to hypertonic saline. However, recent meta-analysis suggests that hypertonic saline has a tendency for better ICP control31). In refractory cases, therapeutic hypothermia (targeting body temperature down to 33 to 35℃) may be tried to manage an ICP crisis. The effect of hypothermia on ICP lowering is considered to be comparable to osmotic therapy67). Although some reports suggest that therapeutic hypothermia may decrease perihematomal edema, systemic infection including pneumonia is one of the common adverse events. Therefore, use of therapeutic hypothermia in ICH patients should be individualized42).

1. It is recommended that patients with acute ICH are treated in the intensive care unit for the monitoring of the ICP and BP and possible need for mechanical ventilation or intubation (LOE III, GOR B) (revised recommendation).

2. Patients with a GCS score of ≤8, those with clinical evidence of transtentorial herniation, or those with significant IVH or hydrocephalus should be considered for ICP monitoring and treatment (LOE III, GOR B) (new recommendation).

3. Ventricular drainage as a treatment for hydrocephalus is reasonable in patients with a decreased level of consciousness (LOE III, GOR B) (new recommendation).

4. To control an elevated ICP, a gradual treatment should be considered. The patient's head should be elevated by approximately 30°. Limited use of analgesics and/or sedatives may be considered in patients with pain and/or unstable conditions (LOE IV, GOR C).

5. For more aggressive ICP control, the use of mannitol and hypertonic saline solution, neuromuscular blockade, hyperventilation, or therapeutic hypothermia may be tried (LOE IV, GOR C) (Revised Recommendation)

1. Post-cerebral hemorrhage seizures should warrant the use of proper anticonvulsants (LOE Ib, GOR A).

2. A short-term use of anticonvulsants immediately following a lobar hemorrhage may decrease the risk of early seizures and is recommended (LOE IIa, GOR B).

3. Anticonvulsants used in cerebral hemorrhage should be gradually discontinued if no recurrence is observed. In the case of recurrence, chronic therapy may be considered (LOE IV, GOR C).

The incidence of seizure after ICH is highly variable depending on the study population or the definition of seizure. However, clinical seizure is reported to be as high as 5% to 19% in patients with ICH within one week after onset1,16,19,63). Moreover, electrographic seizure is four times more common than clinical seizure16,75). In addition, 39% of patients who had electrographic seizures actually have a non-convulsive status epilepticus.

The risk factors for the development of seizures after ICH are as follows : lobar in location1,19), involvement of the cortex19), and hematoma expansion16). Although seizure is believed to be associated with rapid aggravation of mass effect and neurologic deterioration in patients with ICH, the causal relationship is questionable75). Even with the development of seizures, its direct effect on poor neurologic outcome or mortality is not clear16,19).

Recently, a secondary analysis was performed using a placebo group from the Cerebral Hematoma and NXY Treatment (CHA-NT) trial, which showed that the odds for poor neurologic outcome at 90 days (mRS 5 or 6) was 6.8 in patients with prophylactic treatment using antiepileptic drugs (95% CI 2.2-21.3), sug-gesting the harmful effect of the prophylactic use of antiepileptic drugs46). However, the majority (78%) of patients was treated with phenytoin; hence; it is not clear whether a new generation antiepileptic drugs have similar safety concerns.

In a recent randomized trial, valproic acid (VPA) prophylaxis (n=36) did not prevent the occurrence of seizures compared to the placebo (n=36) in patients with spontaneous ICH22). However, the VPA treated group did not show a poor neurologic outcome. Therefore, it is still not clear whether the use of antiepileptic drug, except for phenytoin, is associated with a poor neurologic outcome.

In summary, the development of clinical seizure after ICH is probably not a cause of neurologic deterioration in patients with ICH. Moreover, the prophylactic use of antiepileptic drugs in ICH may be associated with a poor outcome, although it is still unclear whether other new generation drugs have similar safety concerns. Therefore, the prophylactic use of antiepileptic drugs without considering individual seizure risk is discouraged. However, if clinical seizure develops, it is reasonable to treat convulsive seizures with the appropriate antiepileptic drugs.

1. Clinical seizures should be treated with the appropriate antiepileptic drugs (LOE Ib, GOR A) (revised recommendation).

2. If the patient's mental status is depressed out of proportion to the degree of brain injury, EEG monitoring (continuous EEG, more preferably) is needed to exclude the possibility of electrographic seizures. Patients who are found to have electrographic seizures on the EEG should be treated with antiepileptic drugs (LOE III, GOR B) (new recommendation).

3. The prophylactic use of antiepileptic drugs should be individualized based on the seizure risk, and potential harmful effects of antiepileptic drugs. The use of antiepileptic drugs in all patients without considering seizure risk is not recommended (LOE IIa, GOR B) (new recommendation).

1) Surgery is not indicated for patients with a small amount of hematoma less than 10 ml or with mild neurologic deficits (Grade D). There is no evidence for clot removal in patients with a level of consciousness of 300 on the Japan Coma Scale III (Grade C2).

2) Putaminal hemorrhage : Surgery should be considered for putaminal hemorrhage with moderate neurologic deficits or a high grade of compression due to hematoma over 30 mL (Grade C1). Especially, stereotactic clot removal is recommended in a case accompanied by a level of consciousness of 20-30 on the Japan Coma Scale II (Grade B).

3) Thalamic hemorrhage : There is no evidence for clot removal as an acute management (Grade C2). For severe ventricular enlargement as a result of ventricular rupture, ventricular drainage may be considered (Grade C1).

4) Subcortical hemorrhage : Surgery may be considered for a hematoma located 1 cm or less in depth from the cortical surface (Grade C1). A craniotomy is recommend as a surgical method (Grade C1).

5) Cerebellar hemorrhage : Surgery is indicated when there is neurologic deterioration or hydrocephalus due to compression of the brain stem in the case of a cerebellar hemorrhage 3 cm or longer in maximal diameter (Grade C1).

6) Brain stem hemorrhage : There is no evidence for clot removal in the acute stage of brain stem hemorrhage (Grade C2). Ventricular drainage may be considered when ventricular hemorrhage, as a result of brain stem hemorrhage, is the main lesion with enlarged ventricles (Grade C1).

7) IVH in adults : Evaluation of the cause of IVH is desirable when a vascular abnormality is suspected (Grade C1). Ventricular drainage should be considered when acute hydrocephalus is suspected (Grade C1).

1) Consider a craniotomy if there is deterioration in consciousness (from a GCS level of between 12 and 9 to 8 or lower), if the ICH is superficial (the clot is subcortical ≤1 cm from the surface and does not reach the deep basal ganglia) or if it is located in the cerebellum (Level C recommendation).

2) Deep-seated haematomas do not benefit from a craniotomy. Stereotaxic aspiration may be considered, especially if mass effect is present (Class IV evidence).

3) External ventricular drainage (EVD) for hydrocephalus can be ventricular or via the lumbar route if it is a communicating type of hydrocephalus. Lumbar drainage is definitely contra-indicated with all types of obstructive hydrocephalus or if the aetiology is in doubt (Class IV evidence).

4) Intraventricular thrombolysis trials may be considered if an EVD becomes necessary but not in infants (Class IV evidence).

The result of a large multicenter trial, the STICH trial44), which randomized 1033 patients from 107 centers over an 8-year period, beginning in 1995, was published in 2005. The inclusion criteria were 1) randomization within 72 hours and operation within 96 hours of ictus, 2) a clot over 2 cm in diameter, and 3) GCS score of 5 or more. Randomization was done to either early surgery or initial medical management if the neurosurgeon was not sure of the benefit of surgery. The primary end point of this study was the extended Glasgow Outcome Scale (GOS) at 6 months, and the secondary end point was the mortality, mRS and BI at 6 months. Five hundred six patients were randomized to surgery and 530 to medical therapy, with groups being well matched for all known variables. In an intention-to-treat analysis, surgery within 96 hours of ictus was associated with a statistically insignificant absolute benefit of 2.3% (95% CI-3.2% to 7.7%) in a 6-month prognosis-dichotomized extended GOS. The mortality [absolute benefit 1.2% (-4.9% to 7.2%)], mRS [absolute benefit 4.7% (-1.2% to 10.5%)], and BI [absolute benefit 4.1% (-1.4% to 9.5%)] showed similar statistically insignificant trends in favor of surgery. However, 26% of the medical arm ultimately crossed over to surgery because of rebleeding or neurological deterioration, and a craniotomy was performed in 85% of those crossed-over subjects. In contrast, only 75% of the patients in the primary surgical arm underwent a craniotomy, with the others being treated with less invasive surgical techniques. Ninety-three percent of the patients were available for analysis at 6 months. In addition, several subgroup analyses were performed using the age, GCS, location and amount of hematoma, distance from cortical surface, surgical method, severity of hemiplegia or aphasia, additional fibrinolytic therapy, and participating countries, which failed to show any statistically significant differences between the subgroups. However, the subgroup analysis identified that those subjects with a GCS score of 9 to 12, and those with a lobar hemorrhage with clots <1 cm from the surface may have been helped by an early craniotomy, although this did not reach statistical significance. The STICH II trial45) started from a subgroup analysis of STICH I, which suggested benefits of early surgery for patients with a superficial lobar ICH, relative to the initial medical treatment. The STICH II included 601 patients who had a spontaneous lobar ICH with 10 to 100 mL on the CT (1 cm or less from the cortical surface of the brain), were within 48 hours of ictus, and had a best motor score with a GCS score of 5 or 6, and a best eye score of 2 or more. They were randomly assigned to early surgery or initial medical treatment. Of these patients, 291 assigned to undergo early hematoma evacuation within 12 hours of randomization, and 286 assigned to initial medical treatment were included in this analysis. The primary outcome was a prognosis-based favorable or unfavorable outcome dichotomized from the extended GOS at 6 months after randomization. Overall, 59% of the patients in the early surgery group had an unfavorable outcome at 6 months, compared with 62% of the initial medical treatment group, which was, however, statistically insignificant. Mortality, the secondary outcome, showed a reduction in the early surgery group, but this finding was also statistically insignificant. However, the subgroup analyses revealed a significant 51% relative benefit of early surgery for patients with an initial poor prognosis with a GCS score of 9-12. The STICH II concluded that early surgery did not increase mortality or morbidity at 6 months and might have a small but clinically relevant survival advantage for patients with primary superficial ICH without IVH. However, there was a large crossover in the initial medical treatment group. In STICH II, 62 (21%) of 291 patients initially assigned to medical treatment later deteriorated and underwent surgery. Although this group of crossovers had generally poor outcomes, the delayed surgery could have prevented mortality and masked the benefits of early surgery in this kind of intention-to-treat analysis.

Other small randomized controlled trials (RCTs) regarding the negative results of surgical treatment for primary ICH have also been reported30,51,80). They did not show significant improvement in the prognosis after surgical treatment for primary ICH in their RCTs for supratentorial ICH. Teernstra et al.71) also did not provide reasonable evidence for the advantage of surgical treatment for supratentorial ICH in their meta-analysis of 9 RCTs including STICH. In contrast, a randomized study including 108 patients with supratentorial subcortical or putaminal ICH >30 mL in volume assigned to craniotomy or medical management within 8 hours of onset showed a better outcome (good recovery or moderate disability on the GCS score at 1 year) in those treated with surgery62). However, this study showed no difference in the overall survival and had the limitation of having a small ICH volume in the patients. However, recently, individual patient data subgroup meta-analysis of surgery for spontaneous supratentorial ICH has been published23). This study included 2186 cases from 8 studies. Improved outcome with surgery was reported if surgery was undertaken within 8 hours of ictus, or the volume of hematoma was 20 to 50 mL, or the GCS score was between 9 and 12 in this meta-analysis. In addition, there was weaker evidence that more superficial hematomas with no IVH might also be beneficial23).

Nonrandomized clinical studies have consistently reported good outcomes for surgically treated patients with a cerebellar ICH larger than 3 cm in diameter or those with brainstem compression or hydrocephalus, whereas similar patients treated medically resulted in bad outcomes18,36,40,53,69,73). Moreover, EVD alone instead of hematoma evacuation is not generally recommended, especially in patients with compressed cisterns73). Surgical evacuation of thalamic and pontine ICH has been known to be limited33,35,53).

The timing of the operation remains controversial. Clinical studies have reported wide variability in the timing of the surgery, ranging from within 4 hours up to 96 hours from the onset of symptoms to the time of the operation44,51,62,80). In a retrospective study, Kaneko et al.34) reported on the surgical results of 100 putaminal ICHs within 7 hours of symptom onset among which sixty were within 3 hours of onset. Seven (7%) had died, whereas 15 (15%) had fully recovered, and 35 (35%) were living independently at home at 6 months after the surgery. However, subsequent randomized trials in which surgery was performed within 12 hours of onset showed mixed results51,62,80). The main flaw of early surgery was an increased risk of rebleeding which was noted in the small trial of subjects randomized within 4 hours of onset50). Trials that randomized patients into surgery within 24 hours70), 48 hours6,30), 72 hours72,76), and 96 hours44) have also shown no clear benefit for surgery compared with the initial medical management.

The rationales for minimally invasive surgery for primary ICH are 1) possibility for earlier evacuation in the clinical setting, 2) less operation time, 3) reduced trauma to the surrounding brain tissue, especially for deep seated ICH, and 4) performance under local anesthesia. In contrast, the disadvantages are 1) potential rebleeding due to the use of fibrinolytics, and 2) increased risk of infections related to prolonged indwelling catheters. The techniques for minimally invasive clot removal include stereotactic aspiration with or without thrombolytic or fibrinolytic clot lysis and endoscopic aspiration.

In their randomized study of 490 patients with putaminal ICH and moderate degree of neurological status, Hattori et al.26) reported that stereotactic evacuation of the hematoma resulted in a lower mortality rate and better recovery to functional independence in patients with neurological Grade 3 (eyes are closed but open to strong stimuli). More recently, Wang et al.76) reported on the results of a multicenter, randomized control clinical trial comprised 465 cases of hemorrhage in the basal ganglion from 42 hospitals in China. Three hundred and seventy-seven patients with basal ganglia ICH were randomized to minimally invasive craniopuncture therapy (n=195) or conservative control treatment (n=182). They evaluated neurological impairment on the 14th day after treatment, activities of daily living at the end of the 3rd month and the case fatality within 3 months. Improvement of neurological function in the minimally invasive craniopuncture group was significantly better than that in the control group on the 14th day. At 3 months, there was a significant difference between the two groups in the score for activities of daily living. The proportion of dependent survival patients (mRs >2) in the craniopuncture group (40.9%) was significantly lower than that in the conservative group (63.0%) at the end of the 3rd month. There was no significant difference in the cumulative fatality rates within 3 months between the two groups (6.7% in the craniopuncture group and 8.8% in the conservative group). Along with these randomized studies, a number of nonrandomized studies using the stereotactic aspiration reported aspiration rates ranging from 30% to 90% of the initial hematoma6,12,32,37) and rebleeding rates comparable to those seen with conventional craniotomy ranging from 0% to 10%6,12,32,37,59,60).

For the Stereotactic Treatment of ICH by means of a Plasminogen Activator (SICHPA), the multicenter randomized controlled trial (n=71 patients) tried the utility of stereotactic infusion of 5000 IU of urokinase every 6 hours for a maximum of 48 hours within 72 hours of ictus72). The inclusion criteria were 45 years or older, the amount of clot ≥10 mL, a Glasgow Eye Motor score between 2 and 10, at least one pupil reactive to light, and a normal coagulative status (corrected if necessary). Primary end points were death and the degree of functional handicap (measured with mRS) at 6 months. Overall, the mortality at 6 months was 57% ; this included 56% in the surgical group and 59% in the nonsurgical group. A significant reduction in ICH volume was achieved by the surgery (10% to 20%). Logistic regression analysis indicated the possibility of efficacy for surgical treatment, but this was not statistically significant (odds ratio, 0.23). The odds ratio of mortality combined with the mRS 5 at 180 days was also not statistically significant (odds ratio, 0.52). Since urokinase became unavailable in the United States because of reports of potential viral contamination during pharmacological preparation in 1999, tPA has been used in the treatment of ICH10,71). Vespa et al.74) published the phase-2 safety trial for frameless stereotactic aspiration and thrombolysis for 28 patients with ICH in the deep basal ganglia and internal capsule with a volume >5 mL. After a confirmatory CT scan to localize the catheter, 1 mg of recombinant tPA was injected into the center of the hematoma, permitted to bathe the clot for 30 minutes, and then drained into a closed circuit collection system. tPA was infused every 8 hours for 48 hours. They concluded that frameless stereotactic aspiration and thrombolysis of deep spontaneous ICH was a safe therapy that was associated with a reduction in the ICH volume, the early improvement in the National Institute of Health Stroke Scale (NIHSS) and potentially could be used to improve the outcome. Given these results, Minimally Invasive Stereotactic Surgery with rtPA for ICH Evacuation (MISTIE) study, a multicenter, randomized, controlled and stratified study comparing the administration of tPA into the clot cavity versus conventional medical treatment has recently been launched, and preliminary positive results have been published, reporting that the average clot reduction in the acute treatment phase for the surgery arm was 46% (versus the medical arm 4%) and that recorded adverse events were within safety limits, including a 30-day mortality of 8%, symptomatic rebleeding of 8%, and bacterial ventriculitis of 0%49).

The MISTIE phase II trial was designed and was done from 2005 to 2012 to find the safety and efficacy of using minimally invasive surgery with recombinant tPA. In the presentation at the International Stroke Conference 2013 reporting the results of MISTIE II, the authors reported that minimally invasive surgery with recombinant tPA showed 14% improvement in the group with a mRS 0-2, 38 fewer days for the hospital stay, savings of $44000 USD per patient, and 14% less subjects in long-term care for 365 days compared to the medical management group (unpublished yet). The MISTIE II investigators also reported that hematoma evacuation was associated with a significant reduction in perihematomal edema, one of the major causes for secondary neurologic exacerbation after ICH, and that perihematomal edema does not seem to be exacerbated by recombinant tPA54).

A controlled randomized study of endoscopic evacuation versus medical treatment was performed in 100 patients with spontaneous supratentorial intracerebral (subcortical, putaminal, and thalamic) hematomas6). The inclusion criteria for this study were 1) patients' age between 30 and 80 years, 2) a hematoma volume of more than 10 mL, 3) the presence of neurological or consciousness impairment, 4) the appropriateness of surgery from a medical and anesthesiological point of view, and 5) the initiation of treatment within 48 hours after hemorrhage. Endoscopic hematoma removal could lower mortality in the patients with a hematoma volume ≥ 50 mL, and improve functional recovery in surgical patients with hematomas smaller than 50 mL. These effects from surgery in this study were limited to patients aged ≤60 years in a preoperatively alert or somnolent state and with a lobar hematoma. A larger volume study will clarify the benefit of endoscopic aspiration of the hematoma in patients with supratentorial ICH. Another prospective randomized study for spontaneous basal ganglia hemorrhage was performed to evaluate the safety, neurological outcomes, and cost-effectiveness of three surgical procedures : endoscopic aspiration versus stereotactic aspiration versus craniotomy15). Ninety non-comatose patients with basal ganglia ICH were randomized into three groups. In this study, both endoscopic aspiration and stereotactic aspiration showed lower complication rates and lower mortality at 3 months and better neurologic outcomes at 6 months after surgery. However, the delayed time for stereotactic aspiration was usually longer than that of endoscopic surgery. Endoscopic surgery was more cost-effective than craniotomy using functional independence manner and BI.

A meta-analysis of high-quality RCTs regarding minimally invasive surgery (stereotactic aspiration or endoscopic surgery) for spontaneous supratentorial ICH has been recently published78). This study with 1955 patients from 12 high-quality randomized controlled trials concluded that patients with supratentorial ICH might benefit more from minimally invasive surgery than from other treatment options. The most beneficial subgroups were both sexes, 30 to 80 years of age with a superficial hematoma, a GCS score of ≥9, a hematoma volume between 25 mL and 40 mL, and within 72 hours after onset of symptoms78).

IVH coincides with ICH in 40% of patients with primary ICH25). IVH is comprised of primary IVH, which is confined to the ventricles, and secondary IVH which is an extension of an ICH due to hypertensive ICH or vascular malformation in the basal ganglia and the thalamus20,25). Conventional management of IVH is the use of an EVD to remove blood clots in the ventricles and to treat obstructive hydrocephalus. Theoretically, EVD via VC can be helpful to drain blood and cerebrospinal fluid from the clotted ventricles, but an EVD alone is often inadequate for an IVH because the catheter becomes occluded with blood clots, and it takes so much time for blood clots to be clearly reduced that a longer indwelling of the catheter does not prevent inflammatory reactions caused by the breakdown of blood clots in the ventricles, which often leads to communicating hydrocephalus29). Thus, the administration of fibrinolytic agents through a VC has attracted a lot of attention recently. Several reports from animal studies and clinical series suggested that intraventricular administration of fibrinolytic agents, including urokinase, streptokinase, and recombinant tPA, may reduce morbidity and mortality by accelerating blood clearance in IVH21,43,55,56,58,62). The Clot Lysis, Evaluating Accelerated Resolution of IVH (CLEAR-IVH) Trial, prospectively was designed to evaluate the safety and efficacy of using 1.0 mg injections of recombinant tPA through an EVD every 8 hours up to 9 doses to accelerate lysis and evacuation of the IVH, and is still ongoing48). In the preliminary report published in 2008, the average clot reduction after the acute treatment phase was 46%, and the 30-day mortality rate was 8%, while symptomatic rebleeding occurred in 4%, and bacterial ventriculitis in 0%48).