Stroke 2003

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Management of acute ischaemic stroke: new guidelines from the American Stroke Association and European Stroke Initiative The Lancet Neurology Volume 2 • Number 11 • November 2003

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Management of acute ischaemic stroke: new guidelines from the American Stroke Association and European Stroke Initiative

Transcript of Stroke 2003

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Management of acute ischaemic stroke: new guidelines from the American Stroke Association and European Stroke Initiative

The Lancet NeurologyVolume 2 • Number 11 •

November 2003

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Background

0·2% of the population each year Important cause of death and

Dependency 1/6 patients die in the first month

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Background

1/2 survivors are permanently disabled Despite best efforts to rehabilitate them and To prevent complications, recurrent stroke, And other serious vascular events

Early, and ongoing, management : Reduction of both case fatality and Long-term disability

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Recent developments Guidelines

Stroke Council of the American Stroke Association (ASA; Adams and co-Workers, Stroke 2003; 34: 1056–83)

European Stroke Initiative (EUSI; European Stroke Initiative Executive Committee and Writing Committee, Cerebrovasc Dis 2003; 16: 311–38)

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Recent developments Guidelines

Remarkably similar, even regarding Controversial issues

Evidence-based medicine and a major Step

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Recent developments Guidelines

ASA : Early diagnosis and management Of patients in the first 24–48 h of Ischaemic stroke EUSI :Primary and secondary stroke Prevention, rehabilitation, Improvement of public awareness of The symptoms of stroke, and the need For urgent medical attention after a Stroke

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Diagnosis

Clinical history and examination CT brain scan: most important to

Exclude non-vascular, structural, Intracranial lesions , brain ischaemia And haemorrhage

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Diagnosis

MRI :Contraindicated in metal implants, Cardiac pacemakers, or Claustrophobia ; and less widely Available, more costly, And less Reliable in identifying acute ICH MRI :Sensitive in the detection of brain Infarction

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Diagnosis

Further research : Diffusion and Perfusion MRI, magnetic resonance Spectroscopy, may be of additional help For the assessment of the risk to Benefit ratio for early reperfusion Therapy

Vascular imaging (ultrasound, CT Angiography, and magnetic resonance Angiography)

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Stroke-care delivery : Site

Stroke unit rather than a general Medical ward (level I)

Reduces the odds of death or Dependency : 22% (95% CI 11–32)

Monitoring in an intensive care setting Is not necessary

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Stroke-care delivery : Process

Specialised, organised, and Multidisciplinary(medical, nursing, Physiotherapy, occupational therapy, Speech therapy, and social work staff)

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General supportive care to maintain physiological homoeostasis

Despite the absence of reliable evidence For the effectiveness of interventions Aimed at the maintenance of Physiological homoeostasis

Airway support and ventilatory Assistance:reduced consciousness or a Compromised airway

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General supportive care to maintain physiological homoeostasis

Target O2 saturation: EUSI ≥92%; ASA ≥95%

Antipyretic agents : if the body Temperature is high (high temperature Defined as: EUSI ≥37·5°C; ASA no Temperature threshold stated)

Gradual lowering of high glucose concentrations : (target glucose : EUSI about 10 mmol/L; ASA <16·63 mmol/L) with normal Saline and insulin titration

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General supportive care to maintain physiological homoeostasis

Low blood glucose :rapidly corrected With intravenous dextrose bolus or Infusion of 10–20% glucose

Hypotonic solutions (NaCl 0·45% or Glucose 5%) should be avoided

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General supportive care to maintain physiological homoeostasis

Management of high BP is Highly controversial

Lowering of BP unless : >200–220 mm Hg systolic or >120 mm Hg diastolic in Ischaemic stroke ; >180/105 mm Hg in a patient with haemorrhagic stroke

Labetalol and sodium nitroprusside Avoidance of drugs such as sublingual

Nfedipine

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General supportive care to maintain physiological homoeostasis

ASA : nicardipine ASA : 10–15% reduction EUSI : intravenous urapidil,

Nitroglycerin, and oral captopril

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General supportive care to maintain physiological homoeostasis

EUSI : 180/100–105 mm Hg (previous HTN), and 160–180/90–100 mm Hg in Patients (without previous HTN)

Both : <180/110 mm Hg before Thrombolysis is potentially indicated

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Reperfusion of ischaemic brain

IV alteplase (0·9 mg/kg, at most 90 mg), With 10% as a bolus followed by an Infusion Lasting 60 min: selected Patients within 3h of Onset of ischaemic Stroke

Reduces the odds of death or Dependency at Final follow-up by 44%

110 people (50–170) from death or Dependency for every 1000 treated

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Reperfusion of ischaemic brain

people whose strokes are recognised on waking ?

Either streptokinase or ancrod (a defibrinating enzyme) >>> (x)

3 times, both the risk of symptomatic ICH (10% with alteplase vs 3% with placebo; absolute excess 62 per 1000 patients treated) and of fatal ICH within 7–10 days (4% vs 1%;25 per 1000 patients treated; level 1)

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Reperfusion of ischaemic brain

EUSI :intra-arterial treatment of acute Middle cerebral artery occlusion with Prourokinase in a 6 h time window : Improved outcome (level II)

ASA :more conservative,selected Patients,not approved by the FDA(no at Least two double-blind, placebo-Controlled, randomised trials )

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Reperfusion of ischaemic brain

Both :intra-arterial thrombolysis of Acute basilar artery occlusion is limited

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Protection of ischaemic brain cells

Currently, no agent with putative Neuroprotective effects (level I)

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Augmentation of cerebral blood flow

Isovolaemic haemodilution Increasing cerebral perfusion

pressure (eg, hypervolaemic haemodilution)

Both :not been established as useful

ASA :risk of serious neurological and Cardiovascular complications

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Prevention of early recurrent ischaemic stroke : Aspirin

Within 48 h unless thrombolytic therapy Is planned (withheld for 24 h )

160–300 mg/day reduced the odds of Recurrent stroke during the treatment Period by 13% and of death or Dependency at the end of follow-up by 5%

ASA : no recommendation of other Antiplatelet drugs in acute ischaemic stroke

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Prevention of early recurrent ischaemic stroke : Heparins

Do not recommend routine, urgent use Of heparin, low-molecular weight Heparin, or heparinoids after ischaemic Stroke

Risk of haemorrhagic transformation EUSI :cardiac sources with a high

risk Of re-embolism, arterial dissection, or High grade arterial stenosis before Surgery (level IV)

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Prevention of early recurrent ischaemic stroke : Heparins

ASA :more conservative, does not Recommend urgent anticoagulation for Patients with moderate-to-severe stroke Because of a high risk of serious Intracranial bleeding complications

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Revascularisation procedures

ASA :no definitive data about carotid Endarterectomy, extracranial–Intracranial arterial bypass, or Endovascular treatments (eg, stent, Angioplasty, clot removal, suction Thrombectomy, and thrombolysis Assisted by laser and power Doppler) Within the first few hours to days of Acute ischaemic stroke

EUSI :does not discuss these

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Prevention of complications : Medical complications

Not proven by randomised controlled Trials : but suggested by both that early Mobilisation is favoured to prevent Complications including aspiration Pneumonia, venous thromboembolism, Decubital ulcers (pressure sores), and Contractures

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Prevention of complications : Medical complications

Infections : appropriate antibiotics ; EUSI : NG tube feeding can’t prevent Aspiration pneumonia (level IV)

Venous thromboembolism : early rehydration And mobilisation, and graded external Compression stockings (level IV), and that Low dose subcutaneous heparin or low Molecular weight heparins should only be Used in patients at high risk of venous Thromboembolism (level II) by EUSI

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Prevention of complications : Medical complications

ASA : Subcutaneous anticoagulants to Prevent venous thromboembolism for All immobilised patients, or the use of Intermittent external graduated Compression stockings or aspirin for Patients who cannot receive Anticoagulants

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Prevention of complications : Neurological complications( Brain

oedema and high intracranial pressure )

Corticosteroids have no place in Cerebral oedema and may cause IICP (level 1)

Osmotherapy and hyperventilation : Condition is deteriorating secondary to High intracranial pressure, including Herniation syndromes (level IV)

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Prevention of complications : Neurological complications( Brain

oedema and high intracranial pressure )

External ventricular drainage or Ventriculostomy : treat IICP due to Hydrocephalus (level III)

Surgical decompression and evacuation Of large cerebellar infarctions that Compress the brainstem and cause Hydrocephalus is justified (level III)

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Prevention of complications : Neurological complications( Brain

oedema and high intracranial pressure )

Surgical decompression with evacuation Of a large hemispheric infarction can be A life-Saving measure but needs further Investigation

ASA :most survivors have severe Residual Neurological deficits (level III)

EUSI :survivors may have residual Neurological deficit that allows an Independent life (level III)

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Prevention of complications : Neurological complications( Seizures

)

Prophylactic use is not recommended (level IV)

Recurrent seizures should be treated

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Conclusion

Evidence-based, comprehensive, up-to-Date, and consistent overall

Accurate diagnosis, early reperfusion, Implementation of effective therapies to Minimise recurrent stroke and Complications, and maximised Rehabilitation : improve patient Outcome

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Conclusion

Minor disagreements and Inconsistencies between the ASA and EUSI :1.acute treatment of particular Patients with intra-arterial thrombolysis, Heparin, and craniectomy

2.Secondary prevention with clopidogrel as a Substitute for ticlopidine; and heparin Prophylaxis of venous thromboembolism Reflect different interpretations of unreliable (level III and level IV) evidence