Professional Documents
Culture Documents
1 in
6 MILLION 1 IN 6 EVERY 6
WORLDWIDE, NEARLY
6 MILLION PEOPLE DIE
WORLDWIDE, 1 IN 6
PEOPLE ON AVERAGE WILL
SECONDS
EVERY 6 SECONDS,
EACH YEAR FROM A SUFFER A STROKE IN
SOMEONE DIES FROM
STROKE1,2 THEIR LIFETIME1
A STROKE1,2
PENUMBRA
(SALVAGEABLE
BRAIN AREA)2
ISCHAEMIC CORE
(BRAIN TISSUE
DESTINED TO DIE)2
EMERGENCY EMERGENCY
GENERAL PUBLIC STROKE UNIT
CALL CENTRE MEDICAL SERVICES
RECOGNISE STROKE SYMPTOMS IDENTIFY STROKE SYMPTOMS PROMPT EVALUATION & IMMEDIATE TRIAGE,
STABILISATION ASSESSMENT AND IMAGING
REACT APPROPRIATELY PRIORITY DISPATCH OF EMS
PRIORITY TRANSFER TO STROKE MULTIDISCIPLINARY STROKE
FACILITIES TEAM
PRE-NOTIFICATION OF ACCURATE DIAGNOSIS
HOSPITAL
TREAT APPROPRIATELY
Recombinant tissue plasminogen activator (rTPA) is the only FDA-approved for ischemic
stroke drug. However, rTPA’s narrow therapeutic window, its application to less than 5% of
stroke patients.
developing a safe and effective anti-stroke therapeutic agent will fulfill an unmet need and
have the potential significant.
POOR RECOGNITION OF SIGNS AND SYMPTOMS
INAPPROPRIATE OR DELAYED MEDICAL ASSISTANCE2
Barriers to Providing Prehospital Care
to Ischemic Stroke Patients
Kota semarang merintis Ambulance Hebat !!!
AVOIDANCE OR DELAYED DISPATCH OF EMS2
Emergency
Diagnose stroke Choose hospital Pre-notify team
transport
1. POOR TRIAGE AND INACCURATE EARLY ASSESSMENT3,4
1. Diagnosing stroke
Choose hospital
• Choose most appropriate hospital that can provide the patients with
recanalization therapy, and stroke unit care
Do as much as possible before hospital arrival
Oxygen saturation Blood pressure IV access Glucose test Pre-admit patient
Leaving as little as
possible to be done
after hospital arrival
https://www.laerdal.com/us/item/15-1043
4 key actions to reduce DTN Time
1. AMBULANCE
PRE- 2. DIRECT TO CT 3. POC TESTING 4. TREAT AT CT
NOTIFICATION
1. Pre-notification
BENEFITS HOW?
ACUTE TREATMENT
AIMED AT PREVENTING OTHER CAUSES OF DEATH IN THE
FIRST 24 HOURS
POST-ACUTE TREATMENT
AIMED AT PREVENTING RECURRENT STROKE AS WELL
AS OTHER CAUSES OF DEATH AND DISABILITY FROM
24 HOURS ONWARDS
Priority bloods in the hyper acute phase
LABORATORY TESTS TO CONSIDER IN ALL PATIENTS INCLUDE:
• Point of care: Blood glucose and international • Complete Blood Count (with Platelet count)
normalized ratio (INR)
• Electrolytes panel (Renal function studies)
• Hypoglycemia may cause focal signs and
symptoms that mimic stroke, and hyperglycemia • Cardiac markers: TP
is associated with unfavorable outcomes. • Coagulation tests: prothrombin time (PT),
activated partial thromboplastin time (aPTT), TT
or ECT
BECAUSE TIME IS CRITICAL, FIBRINOLYTIC THERAPY SHOULD NOT BE DELAYED WHILE AWAITING THE RESULTS OF THE PT,
APTT, OR PLATELET COUNT UNLESS:
THE PATIENT HAS RECEIVED OTHER ANTICOAGULANTS (DIRECT THROMBIN INHIBITORS OR DIRECT FACTOR XA INHIBITORS).
THE ONLY LABORATORY RESULTS REQUIRED IN ALL PATIENTS BEFORE FIBRINOLYTIC THERAPY IS INITIATED IS A GLUCOSE DETERMINATION AND INR;
USE OF FINGER-STICK MEASUREMENT DEVICES IS ACCEPTABLE.
Jauch EC, Saver JL, Adams HP, Jr., et al. Guidelines for the early management of patients with acute ischemic
stroke: a guideline for healthcare professionals from the American Heart Association/ American Stroke
Association. Stroke. 2013;44:870-947.
3. Treat at CT
BENEFITS HOW?
During the acute phase the patient is still at risk from the cerebral
infarction as a result the neurological status needs to be
monitored closely for deterioration of symptoms.
The focus now starts shifting to reducing the risk of death as a
result of cardiac or respiratory causes.
Thrombolysis of acute ischaemic stroke ESO recommendations
2008 guidelines
▪ In patients admitted within 3 hours of stroke onset brain CT should be obtained to guide routine
thrombolysis treatment with rt-PA (Class I, Level A)
• Intravenous rtPA (0.9 mg/kg BW, maximum 90 mg), with 10% of the dose given as a
bolus followed by a 60-minute infusion, is recommended within 3 hours of onset of
ischaemic stroke (Class I, Level A)
• Intravenous rtPA may be of benefit also for acute ischaemic stroke beyond 3 hours
after onset (Class I, Level B) but is not recommended for routine clinical practice.
• The use of multimodal imaging criteria may be useful for patient selection (Class III,
Level C)
The major focus in this phase is on reducing the risk of mortality by focussing on
respiratory and cardiac complications as well as preventing recurring stroke.
This can be achieved through:
• Continuous cardiac monitoring
• A simplified stroke unit protocol that intensively monitors Fever, Sugar and
Swallowing to identify and treat respiratory disease and sepsis
• Intensive screening for causes of the stroke and treatment to prevent
recurrent stroke.
INTERVENTION: FESS PROTOCOLS