eMedicine Specialties > Neurology > Neurological Emergencies
Subarachnoid Hemorrhage: Treatment & Medication
Updated: Dec 4, 2008
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
The patient with acute subarachnoid hemorrhage needs to be managed in an intensive care (ICU) setting, placed in a quiet room, and given mild sedation if agitated. The head end of the bed should be kept elevated at 30° to ensure optimal venous drainage. Blood pressure must be maintained with consideration of the patient's neurological status. Optimally, systolic blood pressure (SBP) of no more than 130-140 mm Hg should be the goal, unless clinical evidence of vasospasm is noted. Indwelling catheters include arterial line, central venous access, and Foley catheter. Seizure prophylaxis and calcium channel blockade are standard medical measures. Stool softeners are given to prevent Valsalva maneuvers with resultant peaks in SBP and ICP.
- Hydrocephalus
- Since acute hydrocephalus (HCP) is associated with lower preoperative grade and poorer prognosis, the clinician must carefully monitor the patient for early signs of acute HCP. The most reliable clinical measure is the patient's level of consciousness. Any change in the level of consciousness requires an emergent CT scan to evaluate ventricular size. An obtunded patient with dilated ventricles deserves an immediate ventriculostomy.
- Increased risk for rebleeding may be associated with ventriculostomy placement, along with known infectious risk; therefore, patients with dilated ventricles (but no compromise of level of consciousness) should be treated conservatively with close monitoring of mental status and prompt intervention in case their clinical status declines. Some have used serial LPs to monitor such patients.
- Ventriculostomy, when done correctly, is a relatively low-risk procedure that can result in dramatic and immediate clinical improvement in about two thirds of patients. If the patient's grade improves enough as a result of ventriculostomy, the patient may become a candidate for early surgery.
- When grading patients clinically, great care must be taken to note possibly reversible deficits related to HCP, which may be contributing to the patients' poor condition. According to a study of 47 patients with poor-grade aneurysm without CT evidence of irreversible brain destruction who underwent ventriculostomy, early control of the ICP and aggressive management appeared to be the appropriate treatment in this subset of patients.
- Vasospasm lethargy
- Lethargy with or without focal neurological deficit is vasospasm, until proven otherwise.
- Emergency CT must be performed to rule out other pathology.
- Swan-Ganz catheterization is indicated; hypertensive hypervolemic hemodilution (ie, triple H) management is used to target a pulmonary capillary wedge pressure (PCWP) of 14.
- The goal is to maximize cerebral blood flow (CBF) to areas of vasospasm to prevent or reverse neurological symptoms.
- Cardiac output and cardiac index should be monitored.
Surgical Care
- Surgical treatment involves clipping of the ruptured berry aneurysm. Endovascular treatment (ie, coiling) is an increasingly practiced alternative to surgical clipping. At many institutions, higher-grade patients and those with significant medical comorbidities tend to be treated by coiling as opposed to clipping. Posterior circulation aneurysms are preferentially treated by coiling because of the significant morbidity and mortality associated with surgical clipping.
- The large randomized prospective study ISAT found coiling to be significantly safer when comparing ruptured aneurysms that were deemed equally suitable candidates for either surgical or endovascular treatment. The incidence of rebleeding was slightly higher in the coiled group, but the endovascularly treated group did so much better overall that the study was stopped after reviewing the one-year outcome data. Partially because of the ISAT study, endovascular treatment is becoming the first-line treatment for many aneurysms.
- The data to establish long-term results of endovascular treatment are insufficient, however. In general, the incidence of recanalization is higher with coiling. Significant advances have been made in recent years with the introduction of new coated coils that either swell within the aneurysm or promote fibrous tissue formation and organization of the intraarterial clot.
- Other advances include the use of intracranial stents to promote coiling (especially in aneurysms with wide necks) and decrease inflow into the aneurysm in certain instances. The stents have also provided a novel approach to treating certain types of aneurysms that have historically been untreatable. At the moment, no long-term follow-up data exist to assess the efficacy of these new treatment modalities.
- The timing of surgery has been the subject of controversy for more than 40 years. Early surgery/coiling is generally recommended in patients with straightforward aneurysms of a favorable clinical grade. Poor-grade patients who fail to improve after stabilizing measures (including ventriculostomy placement), may not get treated in the acute period or may be preferentially treated by coiling.
The goals of early surgical/endovascular treatment are to prevent rebleeding and to institute triple H therapy (for vasospasm prevention). - Delayed surgery/coiling is recommended in patients with poor-grade aneurysms, those with medical complications, and those with giant or complicated aneurysms.
Consultations
- The neurosurgeon/neurointerventionalist must be involved early in the care of the patient with an aneurysmal subarachnoid hemorrhage.
- A clinician with critical care experience, pulmonologist, cardiologist, or anesthesiologist should manage the patient in the ICU.
Activity
Patients must be admitted to the ICU with strict bed rest until the etiology of hemorrhage is determined. Patients should not be allowed out of bed for any reason.
Medication
Therapeutic goals of subarachnoid hemorrhage are blood pressure control, prevention of seizures, treatment of nausea, management of ICP, prevention of vasospasm, control of pain, and maintenance of cerebral perfusion.
Calcium channel blocker
In specialized conducting and automatic cells in the heart, calcium is involved in the generation of the action potential. The calcium channel blockers inhibit movement of calcium ions across the cell membrane, depressing both impulse formation (automaticity) and conduction velocity.
Nimodipine (Nimotop)
For improvement of neurological impairments resulting from spasms following SAH caused by ruptured congenital intracranial aneurysm in patients who are in good postictal neurological condition.
While studies show benefit on severity of neurological deficits caused by cerebral vasospasm following SAH, no evidence exists that drug either prevents or relieves spasms of cerebral arteries. Thus, actual mechanism of action is unknown.
Adult
60 mg PO q4h x 21 d
Pediatric
Not established
Beta-blockers may slow cardiac conduction; cimetidine may increase level; may increase digitalis plasma levels
Documented hypersensitivity; ventricular dysfunction; hypotension—SBP <90 mm Hg; sick sinus syndrome; second- or third-degree AV block, except with pacemaker; digitalis toxicity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Rare elevations of LDH, alkaline phosphatase, and ALT levels may occur
Antiepileptic agents
These agents prevent seizure recurrence and terminate clinical and electrical seizure activity.
Phenytoin (Dilantin)
May act in motor cortex where may inhibit spread of seizure activity. Activity of brainstem centers responsible for tonic phase of grand mal seizures also may be inhibited.
Dose should be individualized. Administer larger dose before retiring if dose cannot be divided equally.
Adult
Loading dose: 500 mg (8-10 mg/kg) PO q6h x 2 doses; maintenance: 300 mg qhs; follow levels
Active seizure: 18 mg/kg IV loading dose; follow with half load if seizure not controlled (rate not to exceed 50 mg/min); maintenance dose is 100 mg IV q8h
Pro-drug, fosphenytoin, may be safer to use IV than phenytoin and is dosed by "phenytoin equivalents," in same way as above
Pediatric
15-20 mg/kg PO/IV loading dose once or in divided doses; follow by initial 5 mg/kg/d maintenance dose (range 4-8 mg/kg) PO/IV divided bid/tid
Amiodarone, benzodiazepines, chloramphenicol, cimetidine, fluconazole, isoniazid, metronidazole, miconazole, phenylbutazone, succinimides, sulfonamides, omeprazole, phenacemide, disulfiram, ethanol (acute ingestion), trimethoprim, and valproic acid may increase toxicity
Barbiturates, diazoxide, ethanol (chronic ingestion), rifampin, antacids, charcoal, carbamazepine, theophylline, and sucralfate may decrease effects
May decrease effects of acetaminophen, corticosteroids, warfarin, disopyramide, doxycycline, estrogens, haloperidol, amiodarone, carbamazepine, cardiac glycosides, quinidine, theophylline, methadone, metyrapone, mexiletine, oral contraceptives, valproic acid
Documented hypersensitivity; sinoatrial block; sinus bradycardia; second- or third-degree AV block; Adams-Stokes syndrome (slows cardiac conduction)
Pregnancy
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Precautions
Perform blood counts and LFTs; discontinue if skin rash appears; may cause hypotension and arrhythmias if rate of infusion exceeds 50 mg/min; may raise blood glucose levels
Phenobarbital (Barbita, Luminal, Solfoton)
Elevates seizure threshold, limits spread of seizure activity, sedative.
Adult
30 mg PO tid
Pediatric
3-6 mg/kg PO in divided doses
May decrease effects of chloramphenicol, digitoxin, corticosteroids, carbamazepine, theophylline, verapamil, metronidazole, and anticoagulants (patients whose coagulation parameters are stabilized on anticoagulants may require dosage adjustments if added to or withdrawn from their regimen); alcohol may produce additive CNS effects and death; chloramphenicol, valproic acid, and MAOIs may increase toxicity; rifampin may decrease effects; induction of microsomal enzymes may result in decreased effects of oral contraceptives in women (must use additional contraceptive methods to prevent unwanted pregnancy); menstrual irregularities also may occur
Documented hypersensitivity; severe respiratory disease; marked impairment of liver function; nephritis
Pregnancy
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Precautions
Avoid oversedation; routinely monitor patient's mental status; in prolonged therapy, evaluate hematopoietic, renal, hepatic, and other organ systems; caution in fever, hyperthyroidism, diabetes mellitus, and severe anemia since adverse reactions can occur; caution in myasthenia gravis and myxedema
Stool softeners
These agents prevent elevation of intracranial pressure associated with Valsalva maneuver.
Docusate sodium (Surfak, Colace, Dialose)
Anionic surfactant; for patients who should avoid straining during defecation. Allows incorporation of water and fat into stool causing stool to soften. Has minimal laxative effect.
Adult
100 mg PO tid
Pediatric
Not established
Decreases effects of warfarin and increases effects of phenolphthalein
Documented hypersensitivity; nausea, vomiting; acute abdominal pain
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Prolonged use of medication may result in electrolyte imbalance
Senna (Senokot, Ex-Lax, Senexon, Senna-Gen)
Anthraquinone stimulant hydrolyzed by colonic bacteria into active compound. More potent than cascara sagrada and produces considerably more abdominal pain. Usually produces action 8-12 h after administration.
Adult
17 mg tab, 2 tab qd, or 4 tab PO divided bid
Pediatric
<6 years: Not recommended
>6 years: Administer as in adults
Decreases effects of anticoagulants
Documented hypersensitivity; nausea, vomiting; GI bleeding; appendicitis; congestive heart failure; fecal impaction
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Excessive use may lead to electrolyte imbalance, osteomalacia, steatorrhea, cathartic colon
Antihypertensive agents
After SAH due to ruptured aneurysm, blood pressure must be maintained in a range that allows for sufficient cerebral perfusion yet limits the risk of rebleeding.
Nitroprusside (Nitropress)
Produces vasodilation in nonselective fashion via nitric oxide and increases inotropic activity of heart; causes only modest reflex tachycardia. Very potent, close monitoring necessary; short acting.
Adult
0.5 mcg/kg/min IV; use increments of 0.5 mcg/kg/min; titrate to desired blood pressure
Pediatric
Administer as in adults
Accelerated hypotensive effect may occur when administered concomitantly with other antihypertensive medications
Documented hypersensitivity; atrial fibrillation/flutter; IHSS; congenital (Leber) optic atrophy or tobacco amblyopia
Pregnancy
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Precautions
Caution in patients with increased ICP; renal or hepatic insufficiency may increase risk of cyanide toxicity; can worsen hypoxia in patients with COPD by causing mismatch in lungs; may cause high cyanide/thiocyanate levels and toxicity; protect drug from light (wrap in aluminum foil)
Labetalol (Trandate, Normodyne)
Blocks alpha-, beta1-, and beta2-adrenergic receptor sites, decreasing blood pressure.
Adult
20 mg slow IV over 2 min, closely monitor BP; titrate to desired BP; can provide additional IV injections of 40-80 mg over 10-min intervals to total dose of 300 mg
Pediatric
Suggested dose is 0.4-1 mg/kg/h IV; not to exceed 3 mg/kg/h
Decreases diuretic effects; cimetidine and hydralazine may increase bioavailability; phenytoin, phenobarbital, rifampin may decrease effects by inducing microsomal enzymes; increases toxicity of lithium and salicylates
Documented hypersensitivity; cardiogenic shock; severe CHF; pulmonary edema; bradycardia; AV block; COPD
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Discontinue if signs of liver dysfunction occur; may cause toxicity in older patients (eg, bradycardia, hypotension, prolonged AV conduction times, wide QRS complexes, seizures, altered mental status, rarely hypoglycemia)
More on Subarachnoid Hemorrhage |
| Overview: Subarachnoid Hemorrhage |
| Differential Diagnoses & Workup: Subarachnoid Hemorrhage |
Treatment & Medication: Subarachnoid Hemorrhage |
| Follow-up: Subarachnoid Hemorrhage |
| Multimedia: Subarachnoid Hemorrhage |
| References |
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References
Caplan LR. Subarachnoid hemorrhage. In: Stroke: A Clinical Approach. Boston: Butterworth-Heinemann; 1993:389-423.
Greenberg MS. SAH and aneurysms. In: Handbook of Neurosurgery. New York: Thieme Medical Publishers; 1999:711-52.
Jayaraman MV, Mayo-Smith WW, Tung GA, et al. Detection of intracranial aneurysms: multi-detector row CT angiography compared with DSA. Radiology. Feb 2004;230(2):510-8. [Medline].
Langer DJ, Zager EL, Flamm ES. Parasurgical management of aneurysmal subarachnoid hemorrhage. Neurologic and Neurosurgical Emergencies.
Le Roux PD, Winn HR. Management of the ruptured aneurysm. Neurosurg Clin N Am. Jul 1998;9(3):525-40. [Medline].
Liebenberg WA, Worth R, Firth GB, et al. Aneurysmal subarachnoid haemorrhage: guidance in making the correct diagnosis. Postgrad Med J. Jul 2005;81(957):470-3. [Medline].
Lin CL, Dumont AS, Lieu AS, et al. Characterization of perioperative seizures and epilepsy following aneurysmal subarachnoid hemorrhage. J Neurosurg. Dec 2003;99(6):978-85. [Medline].
Marden FA, Roy SS. Endovascular management of intracerebral and subarachnoid hemorrhage. Curr Treat Options Cardiovasc Med. Jul 2005;7(3):197-209. [Medline].
Molyneux A, Kerr R, Stratton I, et al. International Subarachnoid Aneurysm Trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: a randomised trial. Lancet. Oct 26 2002;360(9342):1267-74. [Medline].
Morris PG, Wilson JT, Dunn L. Anxiety and depression after spontaneous subarachnoid hemorrhage. Neurosurgery. Jan 2004;54(1):47-52; discussion 52-4. [Medline].
Ratcheson RA, Wirth FP. Ruptured cerebral aneurysms: perioperative management. In: Concepts in Neurosurgery. Baltimore: Williams & Wilkins; 1994.
Schievink WI. Intracranial aneurysms. N Engl J Med. Jan 2 1997;336(1):28-40. [Medline].
Further Reading
Keywords
subarachnoid hemorrhage, stroke, blood into the subarachnoid space, aneurysm rupture, arteriovenous malformations, berry aneurysm, mycotic aneurysm, ruptured aneurysm, saccular aneurysm, thunderclap headache, SAH, fibromuscular dysplasia, polycystic kidney disease, aortic coarctation, cerebral arteriovenous malformation, AVM, persistent carotid-basilar anastomosis, systemic lupus erythematosus, SLE, moyamoya disease, granulomatous angiitis, Marfan syndrome, Ehlers-Danlos syndrome, Osler-Weber-Rendu syndrome, pseudoxanthoma elasticum, Klippel-Trenaunay-Weber syndrome, atrial myxoma, choriocarcinoma
Treatment & Medication: Subarachnoid Hemorrhage