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SYMPOSIUM RECOMMENDATIONS FOR STROKE MANAGEMENT

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Title: SYMPOSIUM RECOMMENDATIONS FOR STROKE MANAGEMENT


1
- SYMPOSIUMRECOMMENDATIONS FOR STROKE
MANAGEMENT
European Federation of Neurological
Societies EFNS Copenhagn 2000
2
RECOMMENDATIONS FOR STROKE MANAGEMENT
  • Part 1 Organizing Modern Stroke Care Tom
    Skyhoj Olsen, Copenhagn (DEN)
  • Part 2 Risk Factors and Primary
    Prevention Julien Bogousslavsky, Lausanne
    (SUI)
  • Part 3 Acute Stroke Care - General
    Therapy Markku Kaste, Helsinki (FIN)
  • Part 4 Acute Stroke Care - Specific
    Therapy Werner Hacke, Heidelberg (GER)
  • Part 5 Rehabilitation and Secondary
    Prevention Jean-Marc Orgogozo, Bordeaux (FRA)

3
RECOMMENDATIONS FOR STROKE MANAGEMENT
  • Part 1 Organizing Modern Stroke Care Tom
    Skyhoj Olsen, Copenhagn (DEN)

4
RECOMMENDATIONS FOR STROKE MANAGEMENT
  • Part 2 Risk Factors and Primary
    Prevention Julien Bogousslavsky, Lausanne
    (SUI)

5
RECOMMENDATIONS FOR STROKE MANAGEMENT
  • Part 3 Acute Stroke Care - General
    Therapy Markku Kaste, Helsinki (FIN)

6
RECOMMENDATIONS FOR STROKE MANAGEMENT
  • Part 4 Acute Stroke Care - Specific
    Therapy Werner Hacke, Heidelberg (GER)

7
RECOMMENDATIONS FOR STROKE MANAGEMENT
  • Part 5 Rehabilitation and Secondary
    Prevention Jean-Marc Orgogozo, Bordeaux (FRA)

8
Definitions of Levels of Evidencemodified from
Adams et al. 1994
  • Level I Highest Level of Evidence
  • Sources a) Primary endpoint of double blind RCT
    with adequate sample size
  • b) Meta-analysis of qualitatively outstanding
    RCTs
  • Level II Intermediate Level of Evidence
  • Sources a) Randomised not blinded trials
  • b) Small randomised trials
  • c) Predefined secondary endpoints of large
    RCTs
  • Level III Lower Level of Evidence
  • Sources a) Prospective case series with
    concurrent or historical control
  • b) Post hoc analyses of large RCTs
  • Level IV Undetermined Level of Evidence
  • Sources a) Small uncontrolled case series
  • b) General agreement despite lack of evidence

9
Acute Stroke Care-Emergency Diagnostic Tests
  • Differentiation between different types of stroke
  • Ruling out other brain diseases
  • Assessing the underlying cause of brain ischemia
  • Providing a basis for physiological monitoring of
    the stroke patient
  • Identifying concurrent diseases or complications
    associated with stroke

10
Emergency Diagnostic Tests
  • Cranial computed tomography (CCT)
  • distinguishes reliably between hemorrhagic and
    ischemic stroke
  • early signs of ischemia detected as early as 2 h
    after stroke onset
  • identifies hemorrhages almost immediately
  • detects SAH in the majority of cases
  • helps to identify other neurological diseases
    (e.g. neoplasms)

11
Emergency Diagnostic Tests
  • Magnetic resonance imaging (MRI)
  • only helpful in centres using modern MRI
    techniques
  • diffusion- and perfusion-weighted MRI may help to
    differentiate between infarcted tissue and tissue
    at risk

12
Emergency Diagnostic Tests
  • Electrocardiogram
  • high incidence of heart involvement in stroke
    patients
  • coincidence of stroke and myocardial infarction
  • ischemic stroke may cause arrhythmias
  • detection of atrial fibrillation as a possible
    cause of embolic stroke

13
Emergency Diagnostic Tests
  • Ultrasound studies
  • cw/pw- Doppler and/or duplex sonography of the
    extracranial cervical and the basal intracranial
    arteries
  • identification of vessel stenosis, occlusion,
    state of collaterals, or recanalisation
  • transesophageal echocardiography to screen for
    cardiogenic emboli (not in the ER but recommended
    within the first 24 h after stroke onset)

14
Emergency Diagnostic Tests
  • Laboratory tests
  • hematology
  • clotting parameters
  • electrolytes
  • renal and hepatic chemistry
  • cardiac enzymes
  • basic parameters of infection

15
Emergency Diagnostic Tests
  • EUSI Recommendations
  • 1. CCT is the most important diagnostic tool in
    patients with suspected stroke (Level IV)
  • 2.Early evaluation of physiological parameters,
    blood chemistry and hematology, and cardiac
    function (ECG, pulsoximetry, chest x-ray) is
    recommended in the management of acute stroke
    patients

16
Emergency Diagnostic Tests
  • EUSI Recommendations
  • 3. Cardiac and Neurological ultrasound should be
    readily available (Level IV)

17
Acute Stroke Care-General Management
  • EUSI-recommendations include
  • Pulmonary and airway care
  • Blood pressure
  • Body temperature
  • Glucose metabolism
  • Fluid and electrolyte management

18
General Management
  • Monitoring of vital and neurological functions
  • continuous monitoring
  • heart rate
  • O2 saturation
  • discontinuous monitoring
  • Blood pressure (e.g. automatic inflatable
    sphygmomanometry)
  • Clinical Vigilance / GCS, pupils
  • Neurological (e.g. NIH and Scandinavian stroke
    scale)

19
General treatment
  • Pulmonary function and airway protection
  • Adequate oxygenation important for preservation
    of the penumbra
  • Improved blood oxygenation by administration of gt
    2 l O2 (SO2 -guided)
  • Risk for aspiration in patients with
    pseudobulbar/bulbar paralysis and reduced
    vigilance side positioning, consider
    tracheotomia
  • Consider hypoventilation by pathological
    respiration pattern
  • Risk of airway obstruction (vomiting,
    oropharyngeal muscular hypotonia) mechanical
    airway protection

20
General treatment
  • Blood pressure (BP)
  • elevated in most of the patients with acute
    stroke
  • Flow in the critical penumbra passively dependent
    on the mean arterial pressure
  • Sufficient post-stenotic flow requires high blood
    pressure

21
General treatment
  • Blood pressure
  • There are no controlled, randomised studies
    guiding BP management
  • Recommended target BP in patients with prior
    hypertension 180 / 100-105 mmHg
  • Recommended target BP in previously normotonic
    patients 160-180 / 90-100 mmHg
  • Avoid and treat hypotension or drastic reductions
    in BP

22
General treatment
  • Blood pressure
  • Indications for immediate antihypertensive
    therapy in acute stroke
  • Non-ischemic cause for stroke
  • Cardiac insufficiency
  • Aortic dissection
  • Acute renal failure
  • Hypertensive encephalopathy

23
General treatment
  • Body temperature
  • Facts
  • Fever negatively influences neurological outcome
    after stroke
  • Experimentally, fever increases infarct size
  • Many patients with acute stroke develop a febrile
    infection after stroke
  • Although no controlled trial supporting treatment
    of an elevated temperature, consider to treat
    fever when the body temperature reaches 37.5C
    rectally

24
General treatment
  • Glucose metabolism
  • Facts
  • Pre-existent diabetic metabolic derangement can
    be worsened
  • High glucose levels in the acute phase of stroke
    may increase the size of the infarction and
    reduce functional outcome
  • Hypoglycemia worsens outcome as well
  • Hypoglycemia can mimic an acute ischemic
    infarction

25
General treatment
  • Fluid and electrolyte management
  • Serious electrolyte abnormalities are rare after
    ischemic stroke but frequent after ICH and SAH
  • Balanced electrolyte and fluid status are
    important to avoid
  • plasma volume contraction
  • raised hematocrit
  • impaired rheologic properties

26
General treatment
  • EUSI Recommendations
  • 1. Neurological status and vital functions should
    be monitored
  • 2. Glucose and body temperature should be
    monitored and corrected, if elevated (Level III)
  • 3. Do not treat hypertension in patients with
    ischemic stroke, if they do not have critically
    elevated BP levels (Level III)

27
General treatment
  • EUSI Recommendations
  • 4. Secure airways and supply oxygen to patients
    with severe acute stroke (Level IV)
  • 5. Monitoring and correction of electrolyte and
    fluid disturbances are advised (Level IV)

28
Acute Stroke Care-Specific Treatment
  • EUSI-recommendations include
  • Acute anti-thrombotic therapy
  • Thrombolytic therapy
  • Defibrinogenating enzymes
  • ASA
  • Neuroprotection
  • Treatment of elevated ICP and brain edema
  • Medical treatment
  • Surgical treatment

29
Thrombolytic Therapy
  • IV-Thrombolysis (rtPA)
  • Facts (NINDS Pt. 1 2, ECASS I II, ATLANTIS)
  • 3h time window approved in USA, CDN, MEX, I.V.
    0.9mg/kg, max 90mg
  • Not yet approved in Europe
  • Efficacy signal beyond 3h (meta-analysis)
  • IV-Thrombolysis (SK)
  • Facts (MAST-I, MAST-E, AST)
  • Although some efficacy signal in early time
    windwow, SK currently abandoned

30
Thrombolytic Therapy
  • IA-Thrombolysis (rtPA, UK)
  • Facts
  • Only cases and some prospective uncontrolled case
    series
  • IA-Thrombolysis (rPUK)
  • Facts (PROACT I and II)
  • Efficacy proven in small RCT, 6h window,
  • Not approved, PROACT III?

31
Thrombolytic Therapy
  • EUSI Recommendations (for centers offering
    thrombolysis)
  • 1. I.V. rtPA (0.9mg/kg max 90mg, 10 bolus,
    followed by 60 min infusion) is recommended
    within 3 hours after stroke onset (Level I)
  • 2. The benefit from the use of I.V. rtPA beyond 3
    hours is smaller, but present in selected
    patients (Level I)
  • 3. I.V. rtPA is not recommended when time of
    onset is uncertain

32
Thrombolytic Therapy
  • EUSI Recommendations (for centers offering
    thrombolysis)
  • 4. I.V. SK outside of the setting of acontrolled
    clinical trial is dangerous and not indicated for
    the management of persons with ischemic stroke
    (Level I)
  • 5. Intra-arterial treatment of acute M1 occlusion
    in a 6 h time window using rPUK results in a
    significantly improved outcome (Level II)
  • 3. Acute BA-occlusion may be treted with I.A,
    therapy in selected centers (Level IV)

33
Defibrinogenating Therapy
  • ANCROD
  • Treatment of acute ischemic stroke with I.V.
    Ancrod in a 3 h time window results in
    significantly improved outcome (primary endpoint
    only (STAT)
  • Futility analysis of 6 h trial (ESTAT) led to
    premature termination of the trial

34
Defibrinogenating Therapy
  • EUSI Recommendation
  • 1. Ancrod given in a 3 h time window
    significantly improves outcome after acute
    ischemic stroke (Level II)

35
Platelet Inhibitors
  • ASA
  • only substance tested in acute (lt48 h) stroke
    (IST, CAST)
  • CT not required for randomisation
  • small but significant reduction of mortality and
    recurrence of stroke in combined analysis of both
    trials

36
Platelet Inhibitors
  • EUSI-recommendation
  • 1. Aspirin 100-300 mg/day may be given to an
    unselected stroke population (Level II)

37
Therapeutic Anticoagulation
  • Unfractionated heparin
  • no formal trial available testing standard I.V.
    heparin
  • IST showed no benefit for sc heparin treated
    patients, increased risk of ICH
  • Low molecular weight heparins
  • Postive effect seen in small pilot trial (Kay
    1995) was not found in subsequent trial (fisBIS)
  • Heparinoid (Orgaran)
  • TOAST trial negative

38
Therapeutic Antioagulation
  • EUSI-recommendation
  • 1. There is no recommendation for the general use
    of heparin, low molecular weight heparines or
    heparinoids after ischemic stroke (Level I)
  • 2. Full dose heparin may be used in selected
    indications such as AF, other cardiac sources
    with high risk of re-embolism, arterial
    dissection, or high grade arterial stenosis
    (Level IV)
  • 3. Administration for DVT-prophylaxis see general
    treatment

39
Neuroprotection
  • Up to now, not a single neuroprotective substance
    has been shown to influence outcome after stroke.
  • Currently there is no recommendation to treat
    patients with neuroprotective drugs after
    ischaemic stroke (Level I)

40
Elevated Intracranial Pressure and Brain Edema
Treatment
  • Medical therapy
  • Basic management
  • Head positioning lt30
  • Pain relief and sedation
  • Normothermia
  • Osmotic agents
  • Glycerol
  • Mannitol
  • Hypertonic saline
  • Barbiturates, hyperventilation and THAM-buffer

41
Elevated Intracranial Pressure and Brain Edema
Treatment
  • Surgical Therapy
  • Ventricular drainage
  • Posterior fossa space occupying infarction
  • Thalamic infarction (rare)
  • Decompressive surgery
  • Posterior fossa space occupying infarctian
  • Malignant MCA/hemispheric infarction
  • Encouraging reduction of mortality with decent
    outcome i prospective case series
  • RCT (HEADFIRST) starts recruiting

42
Elevated Intracranial Pressure and Brain Edema
Treatment
  • EUSI-recommendations
  • 1. Osmotherapy is recommended for patients whose
    condition is deteriorating secondary to increased
    ICP, including those with herniation syndromes
    (Level III)
  • 2. Surgical decompression of large cerebellar
    infarctions that compress the brainstem is
    justified (Level III)
  • 3.Surgical decompression of large hemispheric
    infarction can be life-saving (Level III)

43
Stroke Units
  • Definition
  • Hospital or part of a hospital that (nearly)
    exclusively takes care of stroke patients
  • Specialised staff with multidisciplinary approach
    to treatment and care
  • Core disciplines medical treatment, nursing,
    physiotherapy, occupational therapy, speech and
    language therapy, social work

44
Stroke Units
  • Facts (Stroke Unit Trialists Collaboration)
  • Acute treatment in a stroke unit results in
    significant reduction in mortality, death,
    dependence, or need of institutional care in
    comparison to a general medical ward

45
Stroke Units
  • Types of stroke units
  • 1. Acute stroke unit
  • acute treatment lt 1 week (2-3 days)
  • 2. Combined acute and rehabilitation stroke unit
  • acute phase reha for several weeks / months
  • 3. Rehabilitation stroke unit
  • admission after 1to 2 weeks after stroke onset
  • 4. Mobile stroke team
  • offers stroke care and treatment on a variety of
    wards

46
Stroke Units
  • EUSI Recommendations
  • 1. Stroke patients should be treated in
    specialised stroke units (Level I)

47
Rehabilitation
  • Early rehabilitation
  • 40 of stroke patients need active reha services
  • active rehabilitation should start as soon as
    possible
  • if the patient is unconscious, rehabilitation is
    passive to prevent contractions and other
    immobilisation-associated complications

48
Rehabilitation
  • Rehabilitation programs
  • - Assessment for the degree of disability
    (motor, cognitive, sensory, visual)
  • - Assessment of the ability to respond to
    rehabilitation (financial burden, chances to
    return to social activities and work and to live
    alone, need of help)
  • - adaptation of the intensity of the
    rehabilitation to status and the degree of
    disability

49
Rehabilitation
  • Rehabilitation programs
  • - daily documentation of the patients progress
  • - teaching and involvement of the patient and
    his family members
  • - home visitation as early as possible (smoothing
    the transit, increasing motivation)
  • - planning the transfer to a specialised
    rehabilitation hospital if a longer reha period
    is expected

50
Rehabilitation
  • ideal multidisciplinary stroke team for adequate
    rehabilitation
  • - stroke physician and nurses experienced in
    stroke management
  • - physiotherapist, speech therapist and
    occupational therapist trained in stroke
    rehabilitation
  • - neuropsychologist and social worker accustomed
    to stroke rehabilitation

51
Rehabilitation
  • EUSI Recommendations
  • 1. Rehabilitation should be initiated early after
    stroke (Level I)
  • 2. Every patient should have access to evaluation
    for rehabilitation (Level III)
  • 3. Rehabilitation services should be provided by
    a multidisciplinary team (Level III)

52
Primary Prevention
  • Conditions and lifestyle factors identified as a
    risk for stroke
  • arterial hypertension
  • myocardial infarction
  • atrial fibrillation
  • diabetes mellitus
  • elevated cholesterol levels
  • carotid artery disease
  • smoking
  • alcohol use
  • physical activity

53
Primary Prevention
  • Hypertension
  • Facts
  • most prevalent and modifiable risk factor for
    stroke
  • significant reduction of stroke incidence with a
    decrease of 5 mmHg in diastolic BP or teatment of
    isolated systolic BP elevation

54
Primary Prevention
  • Diabetes mellitus
  • Facts
  • independent risk factor for ischemic stroke
  • strict control of blood glucose not established
    for stroke prevention
  • elevated blood glucose at stroke onset worsens
    mortality and functional outcome

55
Primary Prevention
  • Hypercholesterolemia
  • Facts
  • no strong association between serum cholesterol
    levels and stroke
  • reduction in the relative risk of stroke with
    pravastatin therapy
  • reduction of stroke mortality by statin therapy
    controversial

56
Primary Prevention
  • Cigarette smoking
  • Facts (Cohort studies)
  • independent risk factor for ischemic stroke in
    men and women
  • 6-fold risk compared to non-smokers
  • 50 risk reduction by stop of smoking

57
Primary Prevention
  • Alcohol consumption
  • decreased risk by moderate consumption (men
    20-30 mg/die)
  • increased risk for both ischemic and hemorrhagic
    stroke by heavy alcohol consumption

58
Primary Prevention
  • Physical activity
  • Facts
  • vigorous exercise is associated with a decreased
    risk of stroke
  • this effect may be mediated by reduction in body
    weight, BP, cholesterol and increased glucose
    tolerance

59
Primary Prevention
  • Antithrombotic drugs
  • Facts
  • trend to higher incidence of disabling strokes
    (hemorrhagic) by aspirin ingestion (325-500
    mg/die) in males
  • no risk alteration in women
  • risk reduction in MI for both men and women

60
Primary Prevention
  • EUSI-recommendations
  • 1. BP measurement should be an essential
    component of regular health care visits BP
    should be lowered to normal (140/85 mmHg) values
    by means of life-style and/or pharmacological
    treatment (Level I)
  • 2. Although strict control of glucose or high
    cholesterol levels has not been proven to be
    associated with a decreased risk of stroke, it
    should be encouraged because of benefits in terms
    of other diseases (Level III)

61
Primary Prevention
  • EUSI-recommendations
  • 3. In coronary patients, treatment with
    simvastatin or pravastatin clearly reduces the
    risk of stroke (Level II). Statins should be
    prescribed in patients with CHD and high or
    moderate cholesterol levels the benefits of
    statins probably extend to patients with stroke
    and high cholesterol levels.
  • 4. Cigarette smoking should be discouraged (Level
    II)

62
Primary Prevention
  • EUSI-recommendations
  • 5. Heavy use of alcohol should be avoided,
    while moderate consumption may be permitted
    (Level II)
  • 6. Regular physical activity is recommended
    (Level II)
  • 7. There is no scientific support for prescribing
    aspirin to reduce the risk of stroke in
    asymptomatic patients (Level I) however, aspirin
    may reduce the risk of MI (Level I)

63
Primary Prevention
  • Atrial fibrillation (AF)
  • Facts
  • average stroke rate of 5 per year
  • warfarin reduces the rate of ischemic strokes by
    25
  • anticoagulation with an INR of 2.0 to 3.0 reduces
    the rate of ischemic and hemorrhagic events by
    80 when compared to below 2.0, where
    non-significant reduction in thromboembolic
    events is seen
  • unacceptable risk for bleeding complications with
    an INR gt 5.0

64
Primary Prevention
  • Atrial fibrillation
  • Facts
  • aspirin (300 mg) achieves a pooled risk reduction
    of 21
  • aspirin is less efficacious than warfarin
  • patients less than 65 years of age with lone AF
    are at low risk, whereas patients older than 65
    years are at moderate risk for embolic stroke

65
Primary Prevention
  • Atrial fibrillation EUSI-recommendations
  • 1. Long-term oral anticoagulation therapy (target
    INR 2.5 range 2.0 - 3.0) should be considered
    for all AF patients who are at high risk for
    stroke (Level I)
  • 2. Patients aged less than 65 years with no
    cardiovascular disease or patients who are unable
    to receive anticoagulants should be offered 300
    mg aspirin per day (Level I)

66
Primary Prevention
  • Atrial fibrillation EUSI-recommendations
  • 3. Although not yet established by randomised
    studies, patients over 65 years of age without
    risk factors could be offered both AC and aspirin
    300 mg/ day (Level III)
  • 4. Although not yet established by randomised
    studies, patients over 75 years of age, warfarin
    may be used with a lower INR (target INR of 2.0
    range 1.6. - 2.5) to decrease the risk of
    hemorrhage (Level III)

67
Primary Prevention
  • Asymptomatic carotid artery stenosis
  • CEA is still a matter of controversy
  • 5-year relative risk reduction by CEA for carotid
    artery stenosis gt65 of 50 (absolute reduction
    about 6)
  • absolute risk reduction by medical treatment of
    11/ 5 years

68
Secondary Prevention
  • Antithrombotic drugs
  • Aspirin Facts
  • 25 risk reduction
  • optimal dose still matter of debate
  • no proven advantage by low (lt 160 mg) versus
    medium (160 - 325) or high (500 - 1500 mg) doses

69
Secondary Prevention
  • Antithrombotic drugs
  • Dipyridamole aspirin
  • ESPS II risk reduction of stroke with a
    combination is significantly higher (37) than
    with aspirin alone

70
Secondary Prevention
  • Antithrombotic drugs
  • Clopidogrel
  • CAPRIE Clopidogrel is slightly but significantly
    more effective than medium-dose aspirin

71
Secondary Prevention
  • EUSI-recommendations
  • 1. Low- or medium-dose ASA (50-325 mg) should be
    given as first-choice agent to reduce stroke
    recurrence (Level I).
  • 2. Alternatively, where available, the
    combination of ASA (25 mg) and dipyridamole (200
    mg) twice daily may be given as first choice
    (Level I)

72
Secondary Prevention
  • EUSI-recommendations
  • 3. Clopidogrel is slightly more effective than
    aspirin (Level I). It may be prescribed as
    first-choice or when aspirin is not tolerated or
    efficacious, and in special indications, such as
    in high-risk patients (Level III)

73
Secondary Prevention
  • EUSI-recommendations
  • 4. Patients starting treatment with
    thienopyridine derivatives should receive
    clopidogrel instead of ticlopidine since it has
    fewer side-effects (Level I)
  • patients who have already been treated with
    ticlopidine for a long time should be maintained
    on this regimen because the most severe
    side-effects (neutropenia and rash) appear at the
    beginning of treatment

74
Secondary Prevention
  • EUSI-recommendations
  • 5. Patients who do not tolerate both ASA or
    clopidogrel may be treated with dipyridamol ret
    2x200 mg daily (Level I)

75
Secondary Prevention
  • Anticoagulation after thromboembolic stroke
  • Facts (EAFT)
  • oral anticoagulation with an INR of 2 - 3 reduces
    the risk of recurrent stroke in patients with AF
  • Oral anticoagulation is well established for
    other causes of embolism such as mechanical
    prosthetic valve replacement, rheumatic valvular
    heart disease, ventricular aneurysm,
    cardiomyopathy, or PFO

76
Secondary Prevention
  • EUSI-recommendation
  • 1. Oral anticoagulation (INR 2.0 - 3.0) is
    indicated after stroke associated with
    AF (Level I)
  • 2. Patients with mechanical prosthetic valves
    should receive long-term anticoagulation therapy
    with a target INR between 3.0 and 4.0 (Level III)

77
Secondary Prevention
  • EUSI-recommendation
  • 3. Patients with proven cardioembolic stroke
    should be anticoagulated if the risk of
    recurrence is high, with a target INR between
    2.0 and 3.0 (Level III)

78
Secondary Prevention
  • Carotid Endarterectomy (CEA)
  • Facts (NASCET, ECST)
  • surgery is efficacious for symptomatic patients
    with ipsilateral carotid stenosis gt 70
  • if perioperative complications exceed 2.5 , the
    benefit of CEA will diminish if it approaches
    10, the benefit will vanish entirely
  • there is also some risk reduction in male
    patients with 50 - 69 stenosis of the
    ipsilateral carotid artery

79
Secondary Prevention
  • Percutaneous Transluminal Angioplasty (PTA)
  • Advantages
  • short hospital stay
  • avoidance of general anesthesia and surgical
    incision
  • ability to treat surgically inaccessible sites
  • PTA and stenting as most effective means of
    treating restenosis after CEA
  • preliminary results of controlled
    trialscomparable procedural risks compared to CEA

80
Secondary Prevention
  • EUSI-recommendations
  • 1. CEA is indicated in symptomatic patients with
    stenosis of 70 - 90. This is valid only for
    centres with a perioperative complication rate
    (all strokes and death) lt 6 (Level I)

81
Secondary Prevention
  • EUSI-recommendations
  • 2. CEA may be indicated in some patients with
    stenosis of 50 - 59 without a severe neurologic
    deficit. This is valid only for centres with a
    perioperative complication rate of lt 6. Males
    with recent hemispheric symptoms are the subgroup
    of patients most likely to benefit from surgery
    (Level I)

82
Secondary Prevention
  • EUSI-recommendations
  • 3. CEA is not recommended for symptomatic
    patients with stenosis lt 50 (Level I)
  • 4. CEA should not be performed in centres not
    exhibiting equally low complication rates like
    NASCET or ECST.

83
Secondary Prevention
  • EUSI-recommendations
  • 5. CEA may be indicated for some patients with
    stenosis between 60 and 99. Only patients with a
    low surgical risk (lt3) and a life expectancy of
    at least 5 years are likely to benefit from
    surgery (Level II)

84
Primary Prevention
  • EUSI-recommendations
  • 6. Surgery for asymptomatic carotid stenosis is
    not generally recommended (Level II).
  • 7. It may be recommended in individual patients
    if the surgical risk is low

85
Secondary Prevention
  • EUSI-recommendations
  • 8. Carotid PTA with or without stenting may be
    performed in patients with
    contra-indications to CEA (Level IV)
  • 9. Carotid PTA with or without stenting may be
    indicated in patients with stenosis at
    surgically inaccessible sites (Level IV)
  • 10. Carotid PTA and stenting may be indicated in
    patients with re-stenosis after initial CEA
    (Level IV)
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