section name header

Information

Editors

AnttiLindgren
TimoKoivisto
JuhaE.Jääskeläinen

Intracranial Aneurysm and Subarachnoid Haemorrhage (SAH)

Essentials

  • Subarachnoid haemorrhage (SAH) should be suspected however slight the symptoms, and the diagnosis confirmed with an urgent CT scan.
  • The patient should be transferred without delay to an appropriate hospital for neurosurgical treatment, relevant intensive care and cerebral angiography.
  • A ruptured intracranial aneurysm must be closed (microsurgical clipping or an endovascular approach) during the acute phase to prevent rebleeding.
  • Patients with SAH often have sequelae in the form of neurological, psychiatric and psychosocial problems.

In general

  • An aneurysm is almost always a saccular pouch in a branch of the large cerebral arteries in the region of the circle of Willis.
  • The aneurysm is located on the brain surface in the cerebrospinal fluid space and primarily bleeds into this space (subarachnoid haemorrhage).
  • A patient who survives a primary bleed is immediately at risk of a new bleed because there is a threat that the brittle thrombus that obstructs the bleeding site may yield.
  • SAH may damage the brain by, e.g.
    • acute damage (bleed into the parenchyma, acute hydrocephalus, increased intracranial pressure, brain ischaemia)
    • subacute ischaemic brain damage (”vasospasm”)
    • late damage (communicating hydrocephalus).
  • An inflammatory reaction may develop in the aneurysm wall, leading to rupture.

Epidemiology

  • The lifetime incidence of intracranial aneurysms in the general population is 2-3%.
  • In Finland (population 5.5 million), about 100 000 individuals have unruptured intracranial aneurysms, the majority of which will never cause any symptoms (median diameter only 4 mm) and will not be detected.
  • About 40% of the patients die of the sequelae of the bleed within 12 months.
  • In Finland, the median diameter of ruptured aneurysms is 7 mm.
  • Large size and irregular shape of the aneurysm increase the bleeding risk.
  • The prevalence of SAH is focused on the working-age population (median age 55 years), unlike in cerebral infarction and haemorrhage.
  • Particularly young patients diagnosed with aneurysm may develop new aneurysms during long-term follow-up.
  • Acquired risk factors include
    • age
    • smoking (45% of unruptured and 42% of ruptured patients at the time of diagnosis)
    • excessive alcohol intake
    • hypertension (73% of unruptured and 63% of ruptured patients).
  • Congenital risk factors include
    • family history of aneurysms (28% of unruptured and 14% of ruptured patients)
    • polycystic kidney disease (1% of all SAH cases).
  • The concordance of monozygotic twins in relation to SAH is low.

Signs and symptoms

  • The characteristic symptom of SAH is a sudden explosive, severe and relentless headache which
    • is often associated with nausea and vomiting, nuchal rigidity and photosensitivity
    • may be associated with localising symptoms (limb paralysis, speech difficulties, diplopia)
    • may be associated with convulsions and loss of consciousness.
  • The bleed only last for a few seconds but the blood released to the CSF circulation irritates the meninges and causes headache that may last up to several days.
  • On presentation the patient's condition may range from being alert and orientated to deeply unconscious.
  • A patient with mild symptoms may seek medical appointment several days after the event.
  • Up to one third of patients have had an earlier, usually initially undiagnosed, premonitory minor leak (”a sentinel bleed”) with few symptoms.
  • SAH in a patient known to have migraines, or whose symptoms are mild, might remain undiagnosed at the first appointment.

SAH and other causes of blood in the cerebrospinal fluid

  • Primary SAH
    • Ruptured intracranial aneurysm (80%)
    • Perimesencephalic haemorrhage (10%) - good prognosis and quick recovery
    • Bleed from an arteriovenous or other blood vessel malformation (5%)
    • Spinal SAH (rare)
    • No site of bleeding identified by neuroradiology (15%)
      • Angiography is usually repeated within one week - an aneurysm that has bled may then become visible, although in the initial examination it did not fill with contrast medium.
  • Secondary SAH
    • Spontaneous intracerebral haemorrhage (ICH) may bleed into the ventricles of the brain and the cerebrospinal fluid space.
  • Even mild brain contusion may be the cause of blood in the cerebrospinal fluid.
    • In an acute brain injury, lumbar puncture is contraindicated and of no benefit.
  • Other causes:
    • Any condition with bleeding diathesis and anticoagulant treatment
    • Vascular diseases
    • Inflammatory diseases
    • CNS tumours (rarely)
  • Lumbar puncture induced bleeding
    • Lumbar puncture is technically difficult and a small vein may be punctured Lumbar Puncture

Detecting SAH by CT scanning

  • SAH should be diagnosed or excluded by emergency CT scanning.
  • In a CT scan, an acute bleed will show up as light areas in the cerebrospinal fluid spaces in the sellar region, Sylvian fissure, interhemispheric spaces or the posterior cranial fossa.
    • Blood may also be noted in the ventricles.
  • The bleeding may extend to the brain parenchyma or under the dura mater.
  • A normal CT scan does not exclude SAH - particularly if several days or weeks have lapsed from the bleed.
  • A lumbar puncture should be carried out if SAH is clinically possible but the CT scan result is negative.
  • Spectroscopic (degradation products of haemoglobin) or cytological analysis of cerebrospinal fluid (siderophages) may reveal a previous SAH.

Treatment in the acute phase and transfer of the patient

  • Clinical suspicion of SAH will indicate an immediate referral to a hospital for CT scanning.
  • If SAH is confirmed, a neurosurgical unit is to be consulted immediately.
    • A patient with SAH should be admitted to a neurointensive care unit. The patient must not be treated on a general ward.
    • The neurosurgeon on call should be contacted by telephone, and the CT images sent to him/her electronically.
    • The patient should be transferred immediately (especially in the case of a large haematoma, poor general condition, hydrocephalus) to the neurosurgical unit and neurointensive care.
    • Brief (72-hour) antifibrinolytic therapy Antifibrinolytic Therapy for Aneurysmal Subarachnoid Haemorrhage (tranexamic acid) initiated immediately after the bleeding may prevent hyperacute rebleeding for sufficiently long to allow closure of the ruptured aneurysm.
  • Medical care during transfer should be discussed with the accident and emergency doctor or the doctor responsible for the intensive care unit at the receiving hospital, particularly if the patient's conscious level is affected or is deteriorating.
    • The escort must have sufficient skills in emergency medical care.
    • Optimal airway management
  • Aneurysm(s) must be identified or excluded with four-vessel angiography at the neurosurgical unit.
    • CT angiography is the examination of choice.
    • Catheter angiography (digital subtraction angiography DSA), if indicated
  • Symptomatic drug treatment
    • Blood pressure
    • Headache
    • Nausea
    • Epileptic seizures

Acute treatment of an aneurysm Endovascular Coiling Versus Neurosurgical Clipping for Aneurysmal Subarachnoid Haemorrhage, Antiplatelet Therapy for Aneurysmal Subarachnoid Haemorrhage, Endothelin Receptor Antagonists for Subarachnoid Hemorrhage

  • A ruptured aneurysm must be occluded on the next day by the latest, in order to prevent a rebleed.
  • The anatomy of the aneurysm and the experience of the treatment team will define the choice between surgical or intravascular treatment.
  • Microsurgical clipping of the neck of the aneurysm via a craniotomy:
    • +: more secure than endovascular treatment
    • -: invasive
    • -: risk of ischaemic damage to the brain
  • Closing of the aneurysmal sac with coils, a stent and other material via an endovascular route:
    • +: less invasive
    • -: not suitable for all aneurysms
    • -: risk of ischaemic damage to the brain
    • -: requires angiographic follow-up to ensure the firm closing of the aneurysm
  • An intracerebral or subdural haematoma may warrant immediate evacuation.
  • Hydrocephalus may require ventriculostomy and the insertion of a ventricular shunt.
  • SAH is an acute systemic illness requiring neurointensive care.
  • SAH puts strain on the heart and lungs and may be associated with electrolyte imbalances.
  • Drug therapy (nimodipine) may be used in an attempt to prevent the emergence of delayed ischaemic brain damage Calcium Antagonists for Aneurysmal Subarachnoid Haemorrhage.

Long-term prognosis of SAH

  • The Kuopio Intracranial Aneurysm Database http://www.uef.fi/ns maintained by the University of Eastern Finland (UEF) and Neurosurgery of NeuroCenter, Kuopio University Hospital (KUH) in Kuopio, Finland, includes data of 4 500 patients living in Central and Eastern Finland. Data collection was started in 1980.
    • 27% of the SAH patients admitted to the Kuopio University Hospital died of their disease within 12 months.
      • Risk factors included unconsciousness, high age, intracerebral haemorrhage, intraventricular haemorrhage, acute hydrocephalus
      • Mortality was 92% among patients who were unconscious and responded to pain with extension at arrival.
      • Mortality was as low as 3.5% among patients who were fully conscious and in good condition at arrival.
    • In long-term follow-up after 12 months there still was a clear over-mortality among the SAH survivors as compared to the general population.
    • The risk of hydrocephalus requiring placement of a shunt was 18%.
    • The risk of epilepsy was 13%.
      • Risk factors included acute onset, poor condition at arrival, intracerebral haemorrhage.
    • The risk of depression is about 29%.
  • Vitreous haemorrhage (Terson syndrome) may occur during the acute phase with a subsequent effect on the patient's eyesight.
  • The psychological and socio-economical well-being of those suffering from sequelae of SAH has not been properly researched.
    • Of patients living independently after recovery from SAH, 67% report of fatigue, 32% of anxiety and 23% of depression.

Screening of relatives

  • Cerebral aneurysm belongs to multifactorial illnesses that typically accumulate to varying extent in a family.
  • 18% of patients have a family history of aneurysms.
    • For the moment there is no genetic test to assess the aneurysm risk (except for polycystic kidney disease).
    • A clinical geneticist may be consulted if required for providing information and for relieving anxiety.
  • Screening of family members (siblings, children, parents)
    • If two first-degree family members have a history of an unruptured aneurysm or aneurysmatic SAH
    • The primary imaging method being MR angiography.

Treatment of unruptured aneurysm

  • An unruptured aneurysm will not close on its own.
  • The number of patients referred for treatment evaluation is significant because
    • 28% of patients with SAH are found to have additional, unruptured aneurysms
    • the screening of families with a history of aneurysms is increasing
    • aneurysms are found in brain imaging carried out for other reasons.
  • A team of specialists will consider the expected benefit of prophylactic closing of the aneurysm. Aspects relevant for the decision include the patient's life expectancy, other illnesses, the size of the aneurysm and its location in the arterial tree of the brain, irregularity of its shape, growth during follow-up, psychological factors, etc.
  • Being aware of an unruptured aneurysm may cause the patient a mental burden that is difficult to bear without closing the aneurysm.

Prophylactic treatment

  • Cessation of smoking
  • Treatment of hypertension
    • 73% of unruptured and 63% of ruptured patients used antihypertensive medication before the aneurysm diagnosis or thereafter
    • 10% have secondary hypertension, which should be taken into account if conventional pharmacotherapy is not effective.
  • Avoidance of excessive alcohol consumption
  • No specific prophylactic treatment exists as either to prevent the generation, growth or rupture of intracranial aneurysms.

    References

    • Vlak MH, Algra A, Brandenburg R ym. Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis. Lancet Neurol 2011;10(7):626-36. [PubMed]
    • Huttunen T, von und zu Fraunberg M, Frösen J et al. Saccular intracranial aneurysm disease: distribution of site, size, and age suggests different etiologies for aneurysm formation and rupture in 316 familial and 1454 sporadic eastern Finnish patients. Neurosurgery 2010;66(4):631-8; discussion 638. [PubMed]
    • Korja M, Lehto H, Juvela S ym. Incidence of subarachnoid hemorrhage is decreasing together with decreasing smoking rates. Neurology 2016;87(11):1118-23. [PubMed]
    • Karamanakos PN, von Und Zu Fraunberg M, Bendel S et al. Risk factors for three phases of 12-month mortality in 1657 patients from a defined population after acute aneurysmal subarachnoid hemorrhage. World Neurosurg 2012;78(6):631-9. [PubMed]
    • Lindgren AE, Kurki MI, Riihinen A et al. Hypertension predisposes to the formation of saccular intracranial aneurysms in 467 unruptured and 1053 ruptured patients in Eastern Finland. Ann Med 2014;46(3):169-76. [PubMed]
    • Lindgren AE, Räisänen S, Björkman J et al. De Novo Aneurysm Formation in Carriers of Saccular Intracranial Aneurysm Disease in Eastern Finland. Stroke 2016;47(5):1213-8. [PubMed]
    • Korja M, Silventoinen K, Laatikainen T et al. Risk factors and their combined effects on the incidence rate of subarachnoid hemorrhage--a population-based cohort study. PLoS One 2013;8(9):e73760. [PubMed]
    • Lindgren AE, Kurki MI, Riihinen A et al. Hypertension predisposes to the formation of saccular intracranial aneurysms in 467 unruptured and 1053 ruptured patients in Eastern Finland. Ann Med 2014;46(3):169-76. [PubMed]
    • Korja M, Silventoinen K, McCarron P et al. Genetic epidemiology of spontaneous subarachnoid hemorrhage: Nordic Twin Study. Stroke 2010;41(11):2458-62. [PubMed]
    • Kurki MI, Gaál EI, Kettunen J et al. High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms. PLoS Genet 2014;10(1):e1004134. [PubMed]
    • Juvela S. Minor leak before rupture of an intracranial aneurysm and subarachnoid hemorrhage of unknown etiology. Neurosurgery 1992 Jan;30(1):7-11. [PubMed]
    • Steiner T, Juvela S, Unterberg A et al. European Stroke Organization guidelines for the management of intracranial aneurysms and subarachnoid haemorrhage. Cerebrovasc Dis 2013;35(2):93-112. [PubMed]
    • Hillman J, Fridriksson S, Nilsson O et al. Immediate administration of tranexamic acid and reduced incidence of early rebleeding after aneurysmal subarachnoid hemorrhage: a prospective randomized study. J Neurosurg 2002;97(4):771-8. [PubMed]
    • Lindgren A, Vergouwen MD, van der Schaaf I ym. Endovascular coiling versus neurosurgical clipping for people with aneurysmal subarachnoid haemorrhage. Cochrane Database Syst Rev 2018;8():CD003085. [PubMed]
    • Lindgren A, Burt S, Bragan Turner E ym. Hospital case-volume is associated with case-fatality after aneurysmal subarachnoid hemorrhage. Int J Stroke 2018;():1747493018790073. [PubMed]
    • Stroke GOAL Group, Dr Foster Global Comparators Project, Dr Foster Ltd in association with the Dr Foster Unit at Imperial College London .. Outcome After Clipping and Coiling for Aneurysmal Subarachnoid Hemorrhage in Clinical Practice in Europe, USA, and Australia. Neurosurgery 2018;():. [PubMed]
    • Huttunen T, von und Zu Fraunberg M, Koivisto T et al. Long-term excess mortality of 244 familial and 1502 sporadic one-year survivors of aneurysmal subarachnoid hemorrhage compared with a matched Eastern Finnish catchment population. Neurosurgery 2011;68(1):20-7. [PubMed]
    • Huttunen J, Kurki MI, von Und Zu Fraunberg M et al. Epilepsy after aneurysmal subarachnoid hemorrhage: A population-based, long-term follow-up study. Neurology 2015;84(22):2229-37. [PubMed]
    • Huttunen J, Lindgren A, Kurki MI ym. Antidepressant Use After Aneurysmal Subarachnoid Hemorrhage: A Population-Based Case-Control Study. Stroke 2016;47(9):2242-8. [PubMed]
    • Koskela E, Setälä K, Kivisaari R et al. Visual field findings after a ruptured intracranial aneurysm. Acta Neurochir (Wien) 2014;156(7):1273-9. [PubMed]
    • Passier PE, Visser-Meily JM, Rinkel GJ et al. Determinants of health-related quality of life after aneurysmal subarachnoid hemorrhage: a systematic review. Qual Life Res 2013;22(5):1027-43. [PubMed]
    • Greving JP, Wermer MJ, Brown RD Jr ym. Development of the PHASES score for prediction of risk of rupture of intracranial aneurysms: a pooled analysis of six prospective cohort studies. Lancet Neurol 2014;13(1):59-66. [PubMed]
    • Backes D, Rinkel GJE, Greving JP ym. ELAPSS score for prediction of risk of growth of unruptured intracranial aneurysms. Neurology 2017;88(17):1600-1606. [PubMed]
    • Etminan N, Brown RD Jr, Beseoglu K ym. The unruptured intracranial aneurysm treatment score: a multidisciplinary consensus. Neurology 2015;85(10):881-9. [PubMed]

Related Keywords

ATC Code:

B02AA02

C08CA06

Primary/Secondary Keywords