Perihematomal edema as predictor of outcome.

Intracerebral hemorrhage (ICH) is the most serious form of stroke, with over two-thirds of patients either dying or left permanently disabled from the condition. It is well recognized that the location, initial volume at presentation, and subsequent degree of growth of the hematoma of ICH are critical determinants of the prognosis, for which early intensive blood pressure (BP) lowering[1] and targeted surgical decompression[2] offer the best opportunities to benefit the patient. As perihematomal edema, a component of ICH, contributes to the resulting mortality and morbidity, it lends itself to being an additional therapeutic target in this disease. However, it is a complex process that involves several pathophysiological mechanisms, ranging from the hydrostatic pressure of the hematoma to subsequent toxic effects of breakdown products resulting from coagulation cascade activation and erythrocyte lysis as part of the natural process of hematoma resolution.[3] Thus, although perihematoma edema and hematoma volumes are strongly correlated, there is less conclusive evidence regarding role of perihematomal edema itself as being an independent prognostic factor over and above the hematoma.

The article by Gupta et al. provides further support for the hematoma being the pivotal prognostic determining factor in ICH, but it also suggests that relative perihematomal edema is a good prognostic sign.[4] These latter findings are somewhat counter-intuitive, as they imply that patients with greater cerebral edema response to the underlying hematoma have a better outcome. However, it could also imply that patients with early cessation of hemorrhage, or clot retraction, relative to the surrounding edema, have better outcomes. There is some support for this hypothesis in a study showing that baseline relative perihematomal edema (<20 hours of onset) was strongly associated with improved functional outcome (odds ratio [OR] 0.79 per 10% increase; P = 0.02) but not mortality.[5] However, another study indicates that relative perihematomal edema at presentation predicts early neurological deterioration (OR 22.6, P = 0.009),[6] while other studies found that relative edema at 48-72 hours had no relation with either early neurologic deterioration[7] or death/dependency at 90 days.[8]

Methodological differences in definitions, case selection, timing and measures of outcome likely contribute to the discrepancies in results across studies. It is quite plausible, though, that the etiology and significance of, and thus therapeutic approach toward, perihematomal edema will differ over the course of ICH. Early after the onset of ICH, the degree of perihematomal edema follows closely with the volume of hematoma, as it is directly related to extraversation of serum from the pressure of the hematoma. In which case, reduction (even decompression) of hematoma is the most direct therapeutic approach. Beyond 72 hours, though, perihematomal edema has a strong component of toxicity from the iron, thrombin, and other blood products, as well as local natural reactive inflammation. While subsidiary analysis of the INTERACT2 trial will likely shed light on any benefits of effective control of BP beyond the first 24 hours, other therapeutic approaches at this time that are under investigation include the use of iron chelation with deferroxamine.[9]

Current treatment of perihematoma edema is directed at managing raised intracranial pressure (ICP), and especially if there is hydrocephalus. The principles of managing ICP in ICH are borrowed from experience in traumatic brain injury where there is a strong emphasis on maintaining adequate cerebral perfusion pressure according to the status of cerebral autoregulation, although there is much controversy over the use of ICP monitoring at all, let alone by what is the most appropriate location site in the brain.[10] ICH patients with a Glasgow Coma Scale score of 8 or less, evidence of transtentorial herniation, significant intraventricular hemorrhage or hydrocephalus, should be considered for ICP monitoring and aggressive treatment. Further research is required to better elucidate the prognostic significance of perihematoma edema in ICH and to translate the mechanistic data into the clinical domain.