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Managing Increased Intracranial Pressure Introduction • The cranium is a rigid compartment. • Contains the brain, vessels and cerebrospinal fluid. • Can not expand after closure of the skull sutures. • It’s ability to accommodate volume changes is limited. Cranial Contents Monroe-Kellie Doctrine Monroe-Kellie Doctrine Presentation • Headache. • Visual Symptoms. • Vomiting. • Altered level of consciousness. • Papilledema. Etiology • Space occupying lesions. • Trauma. • Hydrocephalus. • Meningitis. • Bleeding. • Idiopathic intracranial hypertension. Effect on Cerebral Perfusion • Normal blood flow to the grey matter is 75 ml/100 gm/min, and 45 ml/100 gm/min. • Ischemia ensues at 20 ml/100 gm/min. • Irreversible damage at 10 ml/100gm/min. • Cerebral Perfusion Pressure is the most significant measure of blood flow. Effect on Cerebral Perfusion • CPP: the effective blood pressure gradient across the brain. • Calculated as: CPP= MAP-ICP. *CPP: cerebral perfusion pressure, MAP: mean arterial pressure, ICP: intracranial pressure. • Increased ICP decreases CPP, leading to ischemia. Cerebral Autoregulation • The ability of the brain to maintain blood flow across a wide range of CPPs. • Increases in CPP cause vasoconstriction and vice versa. • CO2 tension controls autoregulation. • Hyperventilation leads to decreased CO2 tension leading to vasoconstriction. Cerebral Auto regulation Failure of Autoregulation • Autoregulation is limited to CPPs ranging from 50-150 mmHg. • Failure of autoregulation occurs when CPP exceeds 150 mmHg. • Blood flow increases and leads to vasogenic edema. • Hypotension may contribute to worsening of the process. (CPP=MAPICP). Monitoring ICP • ICP is the most important indicator of morbidity and mortality. • Indicated in patients presenting with head trauma and spontaneous subarachnoid hemorrhage, as well as a GCS score between 3-8 and abnormal CT scans. • Two main techniques of monitoring: intraventricular and intraparenchymal. Monitoring ICP ICP waveforms ICP Waveforms Treatment • Aims at decreasing ICP and optimizing perfusion to brain tissue. • Utilizes auto regulatory mechanisms to achieve the required balance. • Several targets of therapy lead to synergistic effect on ICP. Non-pharmacological Head Elevation • Rapid, easy and effective. o • Keeping the head elevated at 30-45 . • Uses the force of gravity to promote venous drainage. • Head must be forward facing. • Contraindicated in hypovolemic patients. Head Elevation Hyperventilation • Leads to decreased blood flow to the brain by vasoconstriction. • Rapidly decreases ICP. • Target Pco2: 30-35 mmHg. • Sustained hyperventilation may lead to ischemia. • Target: Cerebral blood volume. Hyperventilation Hypothermia • Core temperature target of 32-35o for a few days. • Controversial, but more centers are starting to embrace it. • High incidence of manageable complications. • Efficacious. • Eurotherm3235 trial currently underway. Hypothermia Hyperbaric Oxygen • Class I evidence suggests decreased mortality. • Class IV evidence suggest acute decrease in ICP. • Functional outcome controversial. Hyperbaric Oxygen Summary of Non- Pharmacologic Management Pharmacologic Management Sedation • Intubation indicated when the patient is unable to protect airway or breath spontaneously. • Propofol is the agent of choice due to short action and effect on brain metabolism. Target: decreasing cerebral metabolism. Sedation Mannitol • Osmotic agent most commonly used in high ICP. • Effect is two-fold: 1- Creation of osmotic gradient which increases intravascular volume, leading to vasoconstriction. 2- Cumulative osmotic gradient causes interstitial fluid to enter vasculature leading to decreased edema. Mannitol • Given in boluses of 0.25 g to 1 g/kg at 4 to 6-hour intervals. • Most useful in the initial 48 to 72 hours. • Monitoring of kidney functions, urine osmolality and electrolytes needed. Mannitol Hypertonic Saline Therapy • Emerging as an effective alternative to mannitol. • Similar efficacy and mechanism of action. • May be used beyond 72 hours. • Superior to mannitol in hypovolemia and hypotension. Hypertonic Saline Therapy • Boluses of 30 ml of 23.4% hypertonic saline • Infused over 15 minutes through a central line. • Sustained use may lead to electrolyte imbalances. Hypertonic Saline Therapy Barbiturate Coma • Controversial. • Drug of choice is Thiopental. • Requires intensive monitoring of vitals signs. • May lead to hypotension. Barbiturate Coma Opioids • Conflicting evidence, mostly due to use along with other ICP lowering agents. • Used alone, they are thought to increase ICP and CBF. • Fentanyl most commonly used, with remifentanyl emerging as a substitute. Opioids Corticosteroids • Evidence against use. • May increase mortality. • Some agents have shown promising results. Corticosteroids Progesterone Therapy • Potentially neuroprotective, with very weak evidence on outcome. • No effect on ICP, possible better functional outcome. Progesterone Therapy Summary of Pharmacological Therapy Summary of Pharmacological Therapy Surgical Management CSF Drainage • Decreases CSF volume. • Allows for ICP monitoring. CSF Drainage Decompressive Craniectomy • Bifrontal craniectomy or hemicraniectomy including the frontal temporal and parietal bones. • Cancels the Monroe-Kellie Doctrine and allows the brain to expand. • Evacuation of an underlying hematoma if present. • Remains controversial due to lack of class I evidence. Decompressive Craniotomy References 1- Sekhar L, Abdulrauf S, Ellenbogen R. Principles of Neurological Surgery [monograph on the Internet]. Philadelphia, PA: Saunders; 2012. [cited December 30, 2014]. Available from: Discovery eBooks. 2- Qureshi A, Wilson D, Traystman R. Treatment of elevated intracranial pressure in experimental intracerebral hemorrhage: comparison between mannitol and hypertonic saline. Neurosurgery [serial on the Internet]. (1999, May), [cited December 30, 2014]; 44(5): 1055-1063. Available from: MEDLINE Complete. 3-Meyer M, Megyesi J, Teasell R, et al. Acute management of acquired brain injury part I: An evidence-based review of non-pharmacological interventions. Brain Injury [serial online]. May 2010;24(5):694-705. Available from: Academic Search Complete, Ipswich, MA. Accessed December 30, 2014. 4-Meyer M, Megyesi J, Teasell R, et al. Acute management of acquired brain injury part II: An evidence-based review of pharmacological interventions. Brain Injury [serial online]. May 2010;24(5):706-721. Available from: Academic Search Complete, Ipswich, MA. Accessed December 30, 2014. 5- Thomé C. Intracranial pressure and hypothermia. Critical Care 2012;16(Suppl 2):A23. doi:10.1186/cc11281.