Intracerebral Hemorrhage: Perihemorrhagic Edema and Secondary Hematoma Expansion: From Bench Work to Ongoing Controversies
- 1Department of Neurology, University of Kansas Medical Center, Kansas City, KS, USA
- 2Department of Anesthesiology, University of Kansas Medical Center, Kansas City, KS, USA
Intracerebral hemorrhage (ICH) is a medical emergency, which often leads to severe disability and death. ICH-related poor outcomes are due to primary injury causing structural damage and mass effect and secondary injury in the perihemorrhagic region over several days to weeks. Secondary injury after ICH can be due to hematoma expansion (HE) or a consequence of repair pathway along the continuum of neuroinflammation, neuronal death, and perihemorrhagic edema (PHE). This review article is focused on PHE and HE and will cover the animal studies, related human studies, and clinical trials relating to these mechanisms of secondary brain injury in ICH patients.
Intracerebral hemorrhage (ICH) is a medical emergency, which often leads to severe disability and death (1). ICH-related poor outcome is due to the combined effect of primary injury and secondary injury. In the primary injury, the hematoma cleaves or dissects neuronal tissue over several hours leading to the presenting symptoms. The loss of neurons within the hematoma is extensive; although some islands of preserved neurons may exist (2). Hematoma expansion (HE) stops due to tamponade effect of the surrounding tissue or clotting at the parent vessel. Due to the rapid onset, the primary injury of ICH is difficult to treat. The best way to minimize the injury from primary insult would be the preventative measures in high-risk individuals and early access to care once symptoms start. Primary injury is followed by secondary injury in the perihemorrhagic region over several days to weeks and provides a longer treatment window than the primary injury. In survivors of ICH, the total extent of remodeled brain tissue may exceed the volume of the initial hematoma. This excess volume of remodeling serves as an evidence of secondary injury. There are multiple factors that contribute to secondary injury after ICH, some of which may occur concurrently or in sequence. Secondary injury after ICH can be separated into two major types: rebleeding causing HE and the consequences of repair pathways along the continuum of neuroinflammation and neuronal death, including perihemorrhagic edema (PHE), elevated intracranial pressure (ICP), hydrocephalus, and brain atrophy. This review article is focused on PHE and HE, and will cover the animal studies, related human studies, and the clinical trials relating to these mechanisms of secondary brain injury in ICH patients. Although numerous animal studies have shown promising targets for therapy to reduce PHE and HE, we currently do not have any approved therapy for either. Practice guidelines published by the American Heart Association/American Stroke Association (AHA/ASA) in 2015 did not recommend any current therapy for PHE or HE (1).
Perihemorrhagic edema is often seen in ICH patients and causes mass effect on adjacent brain structures, elevation in ICP, hydrocephalus, or brain herniation often leading to clinical deterioration. The extent of PHE after ICH is variable and is governed by several mechanisms including the early effects of the Starling oncotic forces and the late effects of cell breakdown, neuroinflammation, and disruption of the blood–brain barrier (BBB). The early PHE occurs without disruption of the BBB (3, 4). PHE starts within 3 h of ICH onset and grows fastest in the first 3 days. PHE continues to grow for 7 days in rats (5) and for as long as 3 weeks in humans with peak between 2 and 3 weeks (4). Absolute PHE volume is linked to hematoma volume, low systolic blood pressure (BP), and high admission hematocrit (4). Admission partial thromboplastin time, baseline hematoma volume, history of hypertension, and earlier time from hematoma onset to CT are associated with higher relative PHE, defined as PHE per hematoma volume (4). PHE growth is associated with decline in neurological examination during hospitalization (6). Absolute, relative, and rate of increase in PHE are all related to death or dependency at 90 days (4, 7, 8). PHE-associated effect on clinical outcomes may be dependent on hematoma volume, as shown in three previous studies where PHE in setting of moderate size hematoma volume around 30 cc was associated with poor outcomes (9–11). Hematoma location in basal ganglion was also found to be associated with an increase in PHE-related adverse outcomes (10). The formation of post-ICH brain edema is related to direct clot retraction releasing serum, which causes hydrostatic pressure leading to early edema in the first 72 h (12). Delayed edema is secondary to neuroinflammation and oxidative stress (13) from a cascade of reactions triggered by red blood cell lysis, thrombin production, complement activation, and neuroinflammation, which in turn causes damage to the BBB (14–16). NXY-059, a free radical scavenger, was studied in comparison to placebo in 607 patients and showed no benefit on HE, PHE, or clinical outcomes (17). The animal studies done so far have helped to delineate these mechanisms and provided some data for therapeutic targets.
Treatment of Perihemorrhagic Edema
Targeting Direct Clot-Related Hydrostatic Pressure
Direct effect of clot-related hydrostatic pressure can be minimized using clot removal and/or osmotherapy. We present here the bench to bedside studies supporting each of these two treatment options.
Animal magnetic resonance imaging (MRI) studies have found that PHE corresponds to reduced perfusion in the perihemorrhagic area (18, 19), but does not represent cytotoxic edema. Hematoma evacuation in study animals led to normalization of this reduced perfusion (18, 20). The non-cytotoxic nature of PHE is further supported by the lack of effect of reductions in BP and cerebral blood flow (CBF) on the extent of PHE in a study of ICH patients (21). Furthermore, PHE occurs in cadaveric models of ICH in the absence of any blood flow (22). Surgical removal of ICH hematoma improves CBF on the ipsilateral side as shown in a single-photon-emission computed tomography (SPECT) study (23). Based on supportive data from animal studies, the role of surgery in ICH was explored in humans. Unfortunately, two large multicenter surgical trials in ICH patients failed to show any benefit of surgery over medical therapy (24, 25). Mean time to surgery in these trials was more than 24 h, which may have affected the possible benefit from surgery in these studies. Data from rabbit studies suggest that early surgery within 6–12 h might be of maximum benefit with lower glutamate levels, less BBB permeability, and less brain edema (26). Since large studies did not find any role for open surgery in ICH management, the role of minimally invasive surgery is currently being explored. In a rat study, recombinant tissue plasminogen activator (rt-PA) was found to be safe after ICH (27). In a phase-II ICH trial investigating hematoma evacuation using minimally invasive surgery and intra-lesional rt-PA (MISTIE-II), there was significant reduction in PHE in the minimally invasive surgical group with no ill effects of rt-PA (28). MISTIE-III trial is in underway to investigate the effect of hematoma reduction using minimally invasive surgery and intra-lesional rt-PA on long-term patient outcomes. MISTIE-III promises to be an important ICH trial and will further improve our understanding about ICH management (29). Large volume hematoma and PHE may lead to severe mass effect including uncal herniation and death. Decompressive hemicraniectomy is sometimes used in clinical practice as a life saving measure. In a retrospective case series, clot evacuation with decompressive hemicraniectomy for large ICH was associated with a favorable outcome in 29% patients (30). Decompressive hemicraniectomy trials with (31) and without (32) hematoma evacuation are currently enrolling patients to study the effect of surgery versus medical therapy in ICH patients. Although animal studies suggest reduced CBF in the perihemorrhagic region with improvement following surgery, the role of surgery still needs to be established in humans. Currently, the AHA/ASA guidelines do not recommend surgery for all ICH patients. The guidelines do recommend urgent sub-occipital craniectomy for cerebellar ICH patients with neurological decline, brainstem compression, or obstructive hydrocephalus (1).
Mannitol is a commonly used osmotherapy agent for cerebral edema. The effect of mannitol on ICH-related edema and patient outcome is controversial. In rat studies, mannitol did not cause any change in the brain water content suggesting lack of its effect in ICH-related edema (33). However, a transcranial Doppler study showed that a single bolus of 100 mg mannitol in ICH patients led to higher mean flow velocity and lower pulsatility index suggesting reduced edema on the affected side (34). In two studies, mannitol was found to be safe in ICH patients, although had no clinical response (35, 36). However, Sansing et al. showed that mannitol had no effect on PHE but was related to adverse discharge outcome (37). Although one study showed transient clinical improvement with mannitol, it failed to show any improvement on computed tomography (CT) (38). A systematic review reported only two small trials about the use of mannitol in ICH and concluded that there was not enough evidence to suggest either benefit or harm with mannitol (39).
Hypertonic saline is another common mode of osmotherapy for PHE. In an ICH dog study, basal ganglia ICH was related to higher perilesional pressures, and administration of 23.4% hypertonic saline bolus led to reduction in intraparenchymal pressure; this effect was sustained for 3 h (40). An experimental dog study of ICH-induced transtentorial herniation found elevation in ICP with preservation of cerebral perfusion pressure due to concomitant arterial hypertension. Transtentorial herniation was accompanied by reduction in regional CBF in brainstem and bilateral gray/white matter. A bolus of 23.4% hypertonic saline reversed the effect of transtentorial herniation on ICP and restored CBF and cerebral oxygen consumption. The reduction in ICP after a single hypertonic saline bolus lasted 30 min (41). In a retrospective study of herniating ICH patients, two-thirds of the patients had reversal of herniation after a bolus of 30–60 ml of 23.4% hypertonic saline (42). Herniation reversal is associated with a good functional outcome in 25% patients (43). In two retrospective studies of 78 ICH patients and 132 historical controls, continuous 3% saline infusion with goal serum sodium concentration of 145–155 mmol/l and osmolality of 310–320 mOsm/kg led to less PHE on day 14, less ICP elevation, and reduced mortality with similar safety profile (cardiac arrhythmias, acute heart failure, pulmonary edema, and acute renal failure) (44). Another retrospective study also failed to show any higher risk of acute kidney injury with the use of hypertonic saline in ICH patients (45).
The effectiveness of hypertonic saline in reducing ICP and reversing herniation syndromes has been compared to the effectiveness of mannitol. In an experimental dog study with ICH in left basal ganglia, use of hypertonic saline [3% NaCl (5.3 ml/kg) or 23.4% NaCl (0.7 ml/kg)] caused reduction in ICP immediately and at 15 min. Mannitol (1 gm/kg) led to an immediate reduction in ICP, but this effect did not persist at 15 min. Only 3% NaCl caused a persistent reduction in ICP at 120 min (46). In humans, 20% ICH patients did not respond adequately (change in sodium ≤5 mEq/l) to sustained mannitol infusion (47). Although animal studies and retrospective studies suggest benefit of hyperosmolar therapy in reversing transtentorial herniation and reducing ICP, this effect needs to be proved in RCTs.
Targeting ICH-Related Neuroinflammation and Oxidative Stress
Numerous animal studies have investigated the effect of clot lysis and the cascade of reactions that follow. The result of this cascade is neuroinflammation and the consequent late stages of PHE (48). We present here a few animal studies and corresponding human studies, which have investigated some of the targets to reduce neuroinflammation-induced PHE. Hemoglobin released from hematoma lysis leads to iron deposition, glutamate deposition (49), free radical production, and antioxidase deactivation causing activation of matrix metalloproteinases-9 (MMP-9). MMP-9 plays an important role in BBB disruption, PHE, apoptosis, and neuronal death. Inflammation involving microglia activation and leukocyte infiltrations; and possible mitochondrial dysfunction also contribute to this oxidative stress (13). However, the role of BBB disruption in the formation of PHE has not been clearly defined in human studies. BBB disruption has been disputed as a cause of PHE by at least one group of authors (50). If BBB disruption does contribute to perihematomal edema formation, it is most likely a late effect. MMP-9 has been found to be elevated in ICH patients and is associated with HE and clinical decline (51, 52).
Hypothermia was noted to be effective for treating brain edema and BBB disruption in animal studies. It involves upregulation of tight junction proteins and the suppression of inflammatory cytokines [interleukin 1β (IL-1β) and tumor necrosis factor α (TNF-α)] (53, 54). Hypothermia further reduces the expression of MMP-9 and apoptosis (55). In addition, elevated ambient temperature has deleterious effect on PHE. Elevated ambient temperature in patients in intensive BP reduction in acute cerebral hemorrhage trial (INTERACT) was found to be associated with worsening PHE (56) consistent with prior animal studies (57, 58). A meta-analysis of animal studies found hypothermia to be ineffective in reducing brain edema (48) contrary to a human study of ICH patients (12 experimental versus 25 control) where hypothermia up to 35°C showed more reduction in edema in the experimental group (59). A phase-II hypothermia trial in ICH is exploring role of hypothermia (32–34°C) in improving edema and patient outcomes (60). Although there is conflicting data in the animal studies, the role of hypothermia in reducing the PHE or improving patient outcomes warrants future studies.
Hemoglobin degradation leading to iron deposition contributes to PHE. In animal models, heme diffused rapidly through perivascular spaces and induced heme oxygenase-1 enzyme that led to accumulation of ferritin and hemosiderin; generation of free radicals; neuronal injury; and BBB disruption (61). In a rat study, ferrous iron was found to cause brain injury, making this a potential target for chelation therapy (62). Lipocalin-2, a siderophore-binding protein, present in astrocytes, microglia, neurons, and endothelial cells, is involved in cellular iron transport and neuroinflammation. Lipocalin-2 plays an active role in iron toxicity after ICH with ferritin upregulation in ipsilateral basal ganglia, microglial activation, more brain swelling, brain atrophy, and neurological deficits (63). In ICH rat studies, brain pathology showed iron overload and upregulation of iron-handling proteins (transferrin, transferrin receptor, and ferritin) (64). In human studies of ICH patients, high serum ferritin (65–67), low serum iron, and low transferrin were correlated with high hematoma volume, early PHE, and poor outcome at 90 days (68). Another study suggested that the effect of ferritin on poor clinical outcomes is not a direct cause and effect but a marker of iron-related PHE, which in turn causes a direct effect on patient outcomes (69). In an MRI study in ICH patients, increased iron deposition in the hematoma and the contralateral globus pallidus was associated with increased PHE suggesting iron overload in the brain may contribute to PHE (70).
In rat and piglet studies, deferoxamine, an iron chelator, reduced ferritin upregulation, hematoma lysis, hematoma cavity size, neuronal death, and neurological deficits (71–74). The iron chelator enters the perifocal reactive zone via the disrupted BBB (61). A phase-I study of 20 patients found deferoxamine (7–62 mg/kg/day) to be safe in ICH patients (75). A controlled study of 42 patients showed slowing of hematoma absorption and reduction in PHE using deferoxamine without any clinical benefit (76). Currently, two controlled trials are ongoing to study the effect of deferoxamine on PHE and long-term clinical outcomes (77, 78).
Minocycline is another iron chelator, MMP-9 inhibitor, and anti-inflammatory drug, which has reduced iron-related neuronal injury in animals along with reducing PHE, neuronal death, improving BBB, and improving neurobehavioral outcomes (79–83). A combined phase-I and phase-II study is currently recruiting 24 ICH patients to test the safety and pharmacokinetics of minocycline and to simultaneously test its effect on blood biomarkers (84). Animal and early human studies support a toxic role of iron in ICH-related neuroinflammation and oxidative damage. Ongoing clinical trials will explore the role of iron chelation on PHE and patient outcomes.
Statins are inhibitors of 3-hydroxy-3-methyl-glutaryl-coenzyme-A (HMG-CoA) reductase and are commonly used medications for dyslipidemia. In animal studies, statins showed less neuronal tissue loss and inflammation; increased cell proliferation, angiogenesis, and synaptogenesis in the perihemorrhagic zone with better functional outcomes (85–87). Statins’ neuroprotective actions may be explained by their ability to induce expression of vascular endothelial growth factor (VEGF), brain-derived neurotrophic factor (BDNF), and nerve growth factor (NGF) (88) to reduce activated microglia, MMP-9 (89), and cytokine-mediated inflammation (less TNF-α and higher interleukin-10 levels) (90, 91). Statins also reduce BBB dysfunction, edema, tissue loss, and improve CBF in the perihemorrhagic zone (92, 93). Combination of granulocyte-colony stimulating factor (G-CSF) and statins further enhance their neuroprotective capacity with less cell apoptosis than with either agents alone (94). Combination of statins and deferoxamine showed a greater effect on PHE and hematoma volume than either agent alone (95). Unlike animal studies, statin use in humans has been linked to increased PHE volume in ICH patients with no effect on CBF (96). One study of 303 ICH patients with 71 statin users showed higher initial and final hematoma volume in statin users (97). Conversely, a pilot study of 18 patients showed a possible protective role of rosuvastatin in ICH patients with lower mortality; however, after adjustment for disease severity, the hazards ratio was not significant (HR 0.20; 95% CI 0.02–1.67) (98). A meta-analysis of 17 studies with 3455 ICH patients exposed to statins showed a significant risk reduction of mortality (OR 0.73; 95% CI 0.54–0.97) (99). Three studies assessed the effect of statin discontinuation following ICH and noted a trend toward reduction in mortality risk with continuation of statins (OR 0.14; 95% CI 0.1–0.20) (99–102). Animal studies suggesting a beneficial role of statins in reducing neuroinflammation and retrospective human studies showing conflicting results set the stage for a large phase-III trial to explore the potential benefit of continuing statins in ICH patients who were receiving statins prior to ICH onset.
Animal studies demonstrate that elevated glutamate after ICH contributes to BBB breakdown, neuronal death, and brain edema via stimulating N-methyl-d-aspartate (NMDA) receptors (49). A meta-analysis of animal studies did not show any benefit of glutamate receptor antagonists (Amantadine, Memantine, and YM872) on PHE (48). However, the effect of memantine has been consistently positive. Memantine, an FDA-approved NMDA antagonist for Alzheimer’s disease, showed benefit for ICH in animal studies with reduced hematoma growth, reduced inflammation with low MMP-9 level, less apoptosis, and better functional recovery (103). A similar effect was seen along with reduced PHE in another study with the combination of memantine and celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor. The effect of this combination on PHE was better than the use of single agent (104). A single-centered RCT of 64 ICH patients confirmed the beneficial effect of memantine with better modified Rankin score and Barthel index at 90 days (105). With supportive data from animal studies and a single-centered RCT in humans, there is enough preliminary data to support a large multicenter RCT to confirm these findings. There are currently no registered trials looking at role of memantine in ICH.
Animal models with ICH have shown that celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, has anti-inflammatory, antioxidant, and neuroprotective effects. Celecoxib use was associated with reduced brain edema, prostaglandin E2 level, perihematomal cell death, and better neurobehavioral recovery (106). As mentioned earlier, celecoxib in combination with memantine was associated with less apoptosis, less inflammation, reduced hematoma volume and brain edema, and better functional recovery. The effect was greater than each drug alone (104). In a retrospective study of ICH patients, celecoxib (400 mg/day) for ≥7 days significantly reduced the hematoma volume and PHE as compared to controls, without any difference in adverse events (107). These findings were further confirmed in multicenter RCT of 44 ICH patients where celecoxib 400 mg twice a day was given for 14 days (108). To confirm the findings of animal studies and a single small RCT, a larger trial is needed to show the effect of celecoxib on clinical outcomes in ICH patients.
Animal studies showed that PHE results from inflammatory response with perilesional infiltration of neutrophils and macrophages, activation of microglia, ICAM-1 immunoreactivity, and leakage of BBB (109, 110). A sphingosine-1-phosphate receptor (S1PR) modulator, fingolimod was found to have mixed results in animal studies varying from no effect on PHE or clinical outcomes (111) to reduced edema with better neurobehavioral recovery (112–114). The positive effect from fingolimod is due to reduction in lymphocytes, markers of inflammation [intercellular adhesion molecule-1 (ICAM-1), interferon-γ, and interleukin-17], apoptosis, and brain atrophy (112–114). In a human study of 23 patients, fingolimod use was associated with less inflammation (reduced ICAM-1, lymphocytes, natural killer cells, and MMP-9 levels) and positive effect on BBB (115). In a phase-II study, fingolimod use within 72 h of ICH onset was associated with less PHE and improvement in clinical outcomes at 3 months without any increase in side effects (116). Fingolimod use is limited due to its potential for cardiotoxicity. RP101075, a selective S1PR1 agonist, has less potential for cardiotoxicity, yet, it retains the ability to reduce cerebral edema in mice. RP101075 results in less cytokine expression, higher BBB integrity, less infiltration of lymphocytes, neutrophils, and microglia, and less cell death (117). Human studies with RP101075 are awaited. Although animal studies and a phase-II human study suggest a possible beneficial role of fingolimod, a phase-III study is needed to confirm these findings.
A rat study has shown that induced hyperglycemia leads to more cell death in perihemorrhagic region and more global edema (118). Another animal study found a correlation between perilesional hyperglycemia and PHE and suggested a possible role for hyperglycemia in BBB breakdown (119). A post hoc exploratory analysis of the antihypertensive treatment of acute cerebral hemorrhage (ATACH) trial found a trend toward worsening of PHE with hyperglycemia, but it was not statistically significant (relative risk 1.25; CI 0.73–2.13) (120). Another retrospective study did not find any relationship between hyperglycemia and PHE in ICH patients (121). Supporting data from animal studies and conflicting results from two small human studies point toward need for more data to understand role of hyperglycemia on PHE in ICH patients before future trials can be planned. AHA/ASA guidelines recommend avoiding hypoglycemia or hyperglycemia in ICH patients (1).
Current AHA/ASA guidelines do not recommend routine use of any anti-inflammatory agents in ICH patients (1).
About one-third of the ICH patients have HE within 3 h and one-sixth in the first 6 h causing early neurological decline and increasing the risk of long-term poor outcomes (1, 122). HE may be related to prior antithrombotic use, computed tomography angiography (CTA) spot sign (123), heterogeneous hematoma density, irregular hematoma shape (124), platelet dysfunction, and higher BP (1). Currently, there are no approved therapies for reducing HE. We will discuss some potential methods of reducing HE for which we have basic science research, or clinical evidence, regarding their potential application at the bedside.
Treatment of Hematoma Expansion
Activated Recombinant Factor VII
An animal study found hematoma reduction in experimental ICH rats with use of activated recombinant factor VII (rFVIIa) (125). In humans, an open-label uncontrolled study found benefit of rFVIIa in controlling ICH in patients with hemophilia A or B (126). The benefit of rFVIIa in hemophilia triggered interest for its use in ICH patients without hemophilia and a phase-II safety study of 48 patients found it to be safe with adverse events (rash, vomiting, fever, ECG T-wave inversion, and deep venous thrombosis) in 12.5% patients (122). This safety study led to a RCT of 399 patients, which found reduction in hematoma volume with rFVIIa as compared to placebo (11–16 versus 29%). Hematoma growth was reduced by 3–6 ml depending on the rFVIIa dose (40–160 μg/kg). Poor outcome including mortality was reduced at 90 days, despite rFVIIa-related serious adverse events in 2.3% patients (myocardial or cerebral infarction) (127). A follow-up efficacy study of 841 patients again showed reduction in HE with rFVIIa as compared to placebo (11–18 versus 26%). However, in this larger study, there was an excess in arterial thrombotic events and there was no overall clinical benefit, while the trend was toward greater death and disability in the treatment group with rFVIIa as compared to placebo (26–29 versus 24%) (128).
Few studies have explored the potential benefit of rFVIIa during the perioperative management for ICH patients. Use of rFVIIa (40–90 μg/kg) prior to hematoma evacuation in 15 patients with mean preoperative ICH volume of 60 ml was found to be safe with good outcome in 73% patients (129). In another placebo-controlled open-label study, rFVIIa was used during hematoma evacuation (100 μg/kg) with no difference in postoperative hematoma volume and adverse events (130). It remains to be seen how rFVIIa would find a place in ICH management knowing that animal and phase-III studies have shown that it reduces HE. The clinical benefit would have to outweigh the side effect of arterial thrombosis and the right dose and clinical setting would need to be narrowly defined. Currently, AHA/ASA and neurocritical care society (NCS) guidelines recommend against use of rFVIIa in ICH patients (1, 131).
Oral anticoagulation (OAC) is a common risk factor for ICH associated with higher rate of HE and poor clinical outcomes. In a rat study, higher INR was associated with higher hematoma volume. OAC-related hematoma enlargement occurred in the first 3 h of ICH onset (132). Interestingly, warfarin also reduced the cell death and MMP-9 levels; however, HE was out of proportion than this positive effect (133). Warfarin-related HE has been confirmed in several human studies (134–137). Following warfarin-related ICH, warfarin is held and emergent reversal of the warfarin effect is needed. A meta-analysis comparing agents: prothrombin complex concentrate (PCC) and fresh frozen plasma (FFP) for warfarin reversal included five RCTs and eight observational studies. PCC use was associated with significant normalization of INR, shorter time to INR correction, lower risk of posttransfusion volume overload, and less mortality without any added risk of thromboembolism (138). A RCT of PCC versus FFP in ICH patients is currently recruiting patients (139). Supporting animal studies and phase-III studies have led to NCS recommendations of administering PCC with intravenous vitamin K over FFP and vitamin K combination for warfarin reversal for ICH patients (131).
Newer Anticoagulants Reversal
In large RCTs of anticoagulation after atrial fibrillation, direct thrombin inhibitors (dabigatran) and direct factor Xa inhibitors (apixaban, rivaroxaban) were associated with lower annual rate of hemorrhagic stroke when compared to warfarin (140), which made them the agents of choice for secondary stroke prevention in atrial fibrillation patients. Their main limiting factor was non-availability of a reversal agent in case of hemorrhage. There was uncertainty around the effect of these medications on ICH volume. An animal study using dabigatran etexilate did not find any significant change in ICH volume when compared to placebo (141). In humans, most cases of newer anticoagulants (NOAC)-related ICH has reported hematoma size less than 30 cc with very low risk for HE (136, 142–144). Need for reversal agents for these agents led to research on Idarucizumab, an antibody fragment, which is currently food and drug administration (FDA) approved. It was studied in 90 patients (51 patients with acute serious bleeding) taking dabigatran and was found to normalize the abnormal thrombin and ecarin clotting time in more than 80% patients within minutes resulting in normal hemostasis within 11.4 h. There were 5.6% patients with thrombotic events over the next 30 days (145). In a rat study, Idarucizumab was associated with reduced mortality (146). Andexanet alfa, a recombinant modified human factor Xa decoy protein, was evaluated in 67 patients with acute major gastrointestinal or intracranial bleeding while on factor Xa inhibitor. Anti-factor Xa activity decreased consistently for 2 h by more than 80% from baseline. Clinical hemostasis was achieved in 79% patients within 12 h; however, there were 18% patients with thrombotic events during the 30-day follow-up (147). Andexanet alfa is not yet approved by FDA. Future trials may help us understand if this change in hemostasis using these novel medications will translate into better clinical outcome.
Another important issue in ICH patients requiring anticoagulation for atrial fibrillation or mechanical heart valve is the timing of resumption of anticoagulation after ICH. There is no previous RCT answering this question and a phase-II study is currently recruiting patients to compare the safety of apixaban versus antiplatelet agents or no antiplatelet/anticoagulation agent in atrial fibrillation patients after ICH (148). Current NCS guidelines recommend using activated charcoal and PCC if needed for direct factor Xa inhibitor-related ICH. They recommend use of Idarucizumab for dabigatran-related ICH, which is supported by animal and current human studies (131).
Elderly patients with ICH are often taking antiplatelet agents prior to admission. An experimental rat study did not find any significant change in hematoma volume or neurological deficits between rats that were pretreated with antiplatelet agent before ICH versus those who were not pretreated (149). However, in humans, prior antiplatelet agent use has been associated with higher risk of HE and poor outcome, with aspirin having the lowest risk as compared to clopidogrel or ticlopidine (135, 150). In a pilot study of 14 ICH patients, desmopressin use was found to be safe and resulted in improvement of platelet function warranting larger studies to confirm these findings (151). A recently completed European randomized, open-label, and phase-III trial studying platelet transfusion versus standard care after acute ICH with prior antiplatelet therapy (PATCH) found two times higher odds of death or dependence at 3 months in patients receiving platelet transfusion (152). It remains to be seen if findings from the PATCH trial will be validated in another blinded RCT in a continent other than Europe. A larger RCT is awaited to study the efficacy of desmopressin on ICH patient outcomes. Despite conflicting data from the animal study and early human studies, current NCS guidelines recommend using a dose of desmopressin (0.4 mcg/kg IV) in ICH patients on antiplatelet agents prior to admission and platelet transfusion only in patients scheduled to undergo neurosurgery (131).
Hypertension is common in ICH patients with two-thirds of patients having systolic BP more than 140 mm Hg at presentation (153). A rat study found acute BP elevation in either normotensive or hypertensive rats after ICH, which is associated with higher HE, more brain swelling, and worse neurological deficits (154, 155). Since acute ICH leads to activation of the adrenergic system, the role of antiadrenergic agents needs to be explored. There are conflicting data about the effect of beta-blockade on clinical outcomes following ICH. Inpatient use of antiadrenergic medications (beta-blockers or clonidine) in 303 patients was associated with less PHE and better clinical outcome after controlling for hematoma volume and BP (156). This protective effect of antiadrenergic medications was confirmed by another study of 138 ICH patients where in-hospital atenolol use was associated with less mortality, systemic inflammatory response, and pneumonia (157). This protective effect of antiadrenergic medications was challenged by a large cohort study from Denmark with 11,779 ICH patients who showed no benefit of preadmission beta blockers over long-term mortality (158). A US study of 426 ICH patients did not find any class-specific benefit of beta-blockers over other antihypertensives (159).
Another area of interest in ICH is intense BP control defined as less than 140/90 mm Hg. ATACH-II, a recent RCT studying role of intensive BP control versus standard BP management in ICH patients found a trend toward less HE (≥33%) in the intensive BP arm (18.9 versus 24.4%, p = 0.09) (160). Another similar trial also showed a trend toward less absolute hematoma volume change in the intensive arm as compared to standard BP management (3.1 versus 4.9 ml, p = 0.09) (161). However, both these trials failed to show any benefit in clinical outcomes with intensive BP control. A pooled analysis of five RCTs also showed no benefit of aggressive BP lowering on patient outcomes or HE (162). A new open-label, dose-escalating study of glyceryl trinitrate transdermal patch in ICH patients is underway, to study the effect of BP control in the first 2 h of symptom onset by starting medication via the emergency medical services (163). Although animal studies suggested possible role of BP control in reducing HE in ICH patients, failed phase-III RCTs do not support it. There is probably some role of BP control on HE; however, the right BP target and timing to achieve it needs further evaluation. AHA/ASA guidelines suggest that acute systolic BP lowering to 140 mm Hg is safe and can be effective for improving functional outcomes (1). It remains to be seen if these guidelines would change after the recently published ATACH II trial.
Tranexamic acid is an antifibrinolytic agent, which acts by inhibiting conversion of plasminogen to plasmin. In an experimental rat ICH study, combination of plasminogen and thrombin was noted to cause significant neuronal damage, which was prevented by tranexamic acid (164). A RCT including 30 ICH patients found that tranexamic acid group had no significant hematoma growth as compared to control (165). Another pilot study showed that two patients per month can be enrolled to study the effect of tranexamic acid on ICH patients (166). Animal studies and positive pilot studies support the ongoing two phase-II studies to explore the benefit of tranexamic acid for ICH patients (167, 168). Lack of strong evidence explains why tranexamic acid is missing in the current ICH guidelines from AHA/ASA (1).
In addition to its possible benefit in reducing PHE, memantine has been purported to have some role in preventing HE. In a rat study, memantine use was associated with reduction in tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), MMP-9, and HE (103). In a study of 186 ICH patients, elevated MMP-9 was independently associated with the risk of HE (OR 15.65, 95% CI: 5.30–46.15) (52). Another rat study with a combination therapy with memantine and celecoxib showed a reduction in cerebral inflammation, apoptosis, hematoma volume, and better functional recovery (104). A single-centered RCT of 64 ICH patients confirmed the beneficial effect to memantine in humans on outcomes, but they did not study its effect on HE (105). The effect of memantine on HE and clinical outcomes in animals would need further evidence in humans to achieve clinical utility. There are currently no registered trials looking at the role of memantine in ICH; memantine is not listed in the current AHA/ASA guidelines (1).
A rat study found that hyperglycemia via its interaction with plasma kallikrein, leads to HE via inhibition of collagen-induced platelet aggregation (169). Another animal study found protective role of 17-beta estradiol in preventing hyperglycemia-induced harmful effect on HE. A post hoc exploratory analysis of ATACH trial found a statistically significant worsening of HE with hyperglycemia (120). Hyperglycemia associated HE worsening was also seen in another retrospective study, but the association was not statistically significant (121). Prospective cohort studies are needed to understand the association between hypoglycemia and HE. As mentioned previously, AHA/ASA guidelines recommend avoiding hypoglycemia or hyperglycemia in ICH patients (1).
Despite extensive animal data supporting numerous therapeutic targets to prevent morbidity and mortality in ICH, very few studies have made the journey from bench to bedside. Failures of recent ICH trials have given us an opportunity to rethink the paradigms of the management for ICH patients. What are the critical steps in improving the outcomes of these patients? Is early hematoma evacuation using minimally invasive surgery crucial to minimizing injury by preventing the cascade of secondary injury? Is the need for critical care (reversal of antiplatelet agents and anticoagulation agents, BP control, hyperglycemia control, cerebral edema management, venous thromboembolism prevention) the key to prevention of secondary injury? Is it the use of anti-inflammatory agents like statins and Fingolimod? Or is there some other, yet undetermined, factor? An MRI animal study suggests that mortality may be determined less by hematoma volume than by the invasion of internal capsule suggesting an anatomically more eloquent basis for clinical deterioration (170). Patient selection may be the key as not everyone would benefit from either surgery or medical therapy, possibly depending on damage to an eloquent area or pathway during the primary injury.
MM: first draft preparation, literature review, critical review of manuscript, and revision after peer review. AL: second draft preparation, literature review, and critical review of manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: intracerebral hemorrhage, secondary brain injury, perihemorrhagic edema, hematoma expansion
Citation: Mittal MK and LacKamp A (2016) Intracerebral Hemorrhage: Perihemorrhagic Edema and Secondary Hematoma Expansion: From Bench Work to Ongoing Controversies. Front. Neurol. 7:210. doi: 10.3389/fneur.2016.00210
Received: 22 September 2016; Accepted: 08 November 2016;
Published: 21 November 2016
Edited by:Michael L. James, Duke University, USA
Reviewed by:Laurel Jean Cherian, Rush University, USA
Ryan Matthew Martin, University of California Davis, USA
Copyright: © 2016 Mittal and LacKamp. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Manoj K. Mittal, email@example.com