This document provides information on the management of stroke. It defines stroke and transient ischemic attack (TIA). It describes the different types of stroke and outlines the rationale for developing a stroke acute care pathway. The pathway includes components for TIA management, administration of thrombolysis for ischemic stroke patients within 3 hours of onset, organized inpatient care in a stroke unit, neurointervention, and stroke surgery. It provides details on each component, including evidence-based guidelines and levels of evidence. The goal is to establish an efficient system to rapidly diagnose and treat stroke patients according to best practices to improve outcomes.
an updated account on management of TIA, Ischemic and hemorrhagic stroke in Sri Lanka. This is based on American Stroke Association and NICE guidelines.
an updated account on management of TIA, Ischemic and hemorrhagic stroke in Sri Lanka. This is based on American Stroke Association and NICE guidelines.
Presentation by Dr Jason Wu - resident in Critical Care at TWH, for the critical care journal club report findings of a paper by Kaukonen KM, et al. N Engl J Med. 2015 & update from the recent SMACC conference in Chicago #FOAMed #SMACC (http://www.ncbi.nlm.nih.gov/m/pubmed/25776936/)
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
Presentation by Dr Jason Wu - resident in Critical Care at TWH, for the critical care journal club report findings of a paper by Kaukonen KM, et al. N Engl J Med. 2015 & update from the recent SMACC conference in Chicago #FOAMed #SMACC (http://www.ncbi.nlm.nih.gov/m/pubmed/25776936/)
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
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2. STROKE ACUTE CARE PATHWAY
DEFINITIONS
1.WHO
A NEUROLOGICAL DEFICIT OF
• Sudden onset
• With focal rather than global dysfunction
• In which, after adequate investigations, symptoms are presumed to
be of non-traumatic vascular origin
• and last for >24 hours
2. NINDS 2005
• When the blood supply to part of the brain is suddenly interrupted or when
a blood vessel in the brain bursts
3.TIA-neurological deficit of vascular origin lasts from few minutes to
hours and resolves within 24 hours
4. STROKE ACUTE CARE PATHWAY
WHY?
MAJOR GLOBAL PUBLIC HEALTH CONCERN
MAIN CAUSE OF DISABILITY IN ADULTS
SECOND COMMONEST CAUSE OF DEATH (WHO 2003)
FIFTY PERCENT ARE DEPENDENT DAILY ACTIVITIES
AMONG THE TOP 4 CAUSES OF DEATH IN ASEAN COUNTRIES
IN MALAYSIA, 4TH COMMON CAUSE OF DEATH AFTER SEPTICAEMIA, HEART
DISEASE AND CANCER
There are no study reports of either organized stroke care or analysis of outcome in
stroke patients, from Malaysia
5. STROKE ACUTE CARE PATHWAY
CHANGING TRENDS….
• Stroke is a preventable and treatable disease
• More effective evidence based primary and secondary prevention
strategies
• Evidence of interventions that are effective soon after the onset of symptoms
• Understanding of the care processes that contribute to a better outcome has
improved
6. EVIDENCE BASED PATHWAY
• ISCHEMIC STROKE IN ADULTS
• TRANSIENT ISCHEMIC ATTACKS-TIA
• HEMORRHAGIC STROKE IN ADULTS
• STROKE IN CHILDREN
• ANEURYSMAL RUPTURE
• AVM BLEED
8. STROKE FLOW
Acute Care Pathway
MODIFICATIONS
5 COMPONENTS:
1. TIA PATHWAY
2. STROKE – THROMBOLYSIS- ER TO ICU PATHWAY
3. STROKE UNIT CARE
4. NEUROINTERVENTION IN STROKE PATHWAY
5. STROKE SURGERY PATHWAY
9. Suspected TIA
EXCLUDE HYPOGLYCEMIA
HISTORY
AND
FAST
+
_
CONSIDER ALTERNATIVE
DIAGNOSIS
ROSIER TO
ESTABLISH DX TIA
START ASPIRIN 300MG/DAY
TO GO HOME
SPECIALIST ASSESSMENT &
INVESTIGATION IN 1 WEEK
ASSESS RISK OF STROKE
ABCD2
ABCD2<4 ABCD2>4
START ASPIRIN 300MG/DAY
ADMIT STROKE UNIT FOR
SPECIALIST ASSESSMENT
& INVESTIGATION IN 24 HRS
CAROTID IMAGING
if the patient is a
candidate for carotid intervention
BRAIN IMAGING WITH
MRI WITH DWI
NO
BEST MEDICALTREATMENT
Eg.Control of blood pressure, anti-
platelet drugs and cholesterol lowering
through diet and drugs and lifestyle
changes smoking cessation,
exercise regimen etc.)
YES
Level of
symptomatic
carotid stenosis
ECST
<70-99%
CAROTID ENDARTERECTOMY
>70-99%
STROKE PATHWAY ALGORITHM
TIA
ANGIOPLASTY & STENTING
OR
BEST MEDICAL
TREATMENT
COMPLETELY RESOLVED
NO STROKE PATHWAY
10. TIA Acute Care Pathway
• Use the Face–Arm–Speech Test (FAST)
Three simple checks can help you recognise whether someone has
had a stroke or mini-stroke (transient ischemic attack – TIA).
F -Facial weakness: Can the person smile? Has their mouth or an
eye drooped?
A -Arm weakness: Can the person raise both arms?
S -Speech problems: Can the person speak clearly and
understand what you say?
T -Test all three signs.
REFERENCE : NICE CLINICAL GUIDELINES- STROKE
EVIDENCE LEVEL 1 B
11. Recognition Of Stroke In ER (ROSIER)
YES NO
Has there been loss of consciousness or syncope? -1 0
Has there been a seizure? -1 0
Asymmetric facial weakness? 1 0
Asymmetric hand weakness? 1 0
Asymmetric leg weakness? 1 0
Speech disturbance? 1 0
Visual field disturbance? 1 0
Total score
--------------------------------------------------------------------------------------------------------------------------------------------
If total score >0 stroke likely
if total score –2, -1 or 0 stroke unlikely
NB : EXCLUDE HYPOGLYCEMIA
REFERENCE : NICE CLINICAL GUIDELINES- STROKE
EVIDENCE LEVEL 1B
12. TIA ABCD2 Score
Symptom Score
Age > 60 years 1 point
Blood pressure > 140/80 1 point
Clinical (neurological
deficit)
2 points for hemiparesis
1 point for speech problem without
weakness
Duration 2 points for >60 minutes
1 point for 10-60 min
Diabetes 1 point
Maximal score is 7.
REFERENCE: Rothwell et al, Lancet. 2007;369:283-92
EVIDENCE LEVEL 3
13. TIA
• People who have had a suspected TIA who are at lower risk of stroke
ABCD2 score of 3 or below: should have
• aspirin (300 mg daily) started immediately
• specialist assessment and investigation as soon as possible, but
definitely within 1 week of onset of symptoms
• measures for secondary prevention introduced as soon as the diagnosis
is confirmed, including discussion of individual risk
NB: People who have had a TIA but who present late (more than 1 week
after their last symptom has resolved) should be treated as though they are
at lower risk of stroke.
REFERENCE : NICE CLINICAL GUIDELINES- STROKE
14. TIA
• People who have had a suspected TIA who are at high risk of stroke
TIAs with ABCD2 score ≥ 4 or above should have:
• aspirin (300 mg daily) started immediately
• specialist assessment and investigation within 24 hours of onset of symptoms
• measures for secondary prevention introduced as soon as the diagnosis is
confirmed, including discussion of individual risk
•TIAS with a score of 5 or greater to be admitted for
immediate Ix and Tx (within 24 h).
REFERENCE : NICE CLINICAL GUIDELINES- STROKE
EVIDENCE LEVEL 3
15. Carotid Endarterectomy
Pooled Reanalysis of ECST and NASCET data
Almost 6000 patients
For patients with 50% or higher stenosis, the number of patients
needed to undergo surgery (ie, number needed to treat) to prevent one
ipsilateral stroke in 5 years was
• 9 for men versus 36 for women
• 5 for age 75 years or older versus 18 for younger than 65 years
• 5 for those randomized within 2 weeks after their last ischaemic event,
versus 125 for patients randomized after more than 12 weeks.
Benefit from surgery was greatest in men, patients aged 75 years or older,
and those randomized within 2 weeks after their last ischemic event,
and fell rapidly with increasing delay.
REFERENCE : Lancet 2004;363:915-924
EVIDENCE LEVEL 1 ++
16. SUSPECTED STROKE
Exclude hypoglycaemia
STROKE MIMICS
-VE
+VE
Establish a diagnosis rapidly
using a validated tool,
- ROSIER
Consider alternative diagnosis
(stroke remains a possible
diagnosis)
Assessment for IMMEDIATE
brain scanning
Face Arm
Speech Test (FAST)
to screen
YES
NO
MRI
PATHWAY ALGORITHM- I
STROKE
INDICATIONS FOR
rTPA
ADMIT TO
STROKE UNIT*
for
SPECIALIST CARE
THROMBOLYSE
IV r TPA
YES
<3HRS
NO
Scan as soon as
possible (within24 hours)
DEPARTMENT OF
NEUROANAESTHESIA
& INTENSIVE CARE *
REFER TO INTERVENTIONAL NEURORADIOLOGY
• I A r TPA
• MERCI
YES > 3HRS
ICU STROKE PATHWAY
*GENERAL CARE
NEUROPROTECTION
Rx of COMPLICATION OF r TPA
NEUROSURGERY REFERRAL
*MULTIDISCIPLINARY
SPECIALIST STROKE
TEAM
NIHSS Score
17. ACUTE CARE PATHWAY
• STROKE UNIT
• Organised inpatient (stroke unit) care for stroke
The Cochrane Database of Systematic Reviews
Organised inpatient (stroke unit) care for stroke:
• Organised stroke unit care is a form of care provided in hospital by nurses,
doctors and therapists who specialise in looking after stroke patients and work
as a co-ordinated team.
• This review of 31 trials, involving 6936 participants, showed that patients who
receive this care are more likely to survive their stroke, return home and become
independent in looking after themselves. A variety of different types of stroke
unit have been developed.
• The best results appear to come from those which are based in a dedicated
ward.
OUTCOME:
EVIDENCE LEVEL : 2+ A
RCT= 304 : 1+
LENGTH OF STAY:
COCHRANE REVIEW: 1++
18. STROKE Acute Care Pathway
Administration of rTPA
‘CLOT BUSTER’
Main eligibility criteria
FOR IV INFUSION
Treatment given within 3hrs)
Intracranial bleeding excluded
Age <80
Early major infarction excluded (parenchyma hypo-attenuation or brain
swelling >1/3rd MCA territory)
NIHSS SCORE <22
MRS ≥ 2
BP < 185/110
Not on warfarin or heparin, platelets and coagulation normal
Treatment given by a specially trained physician
Facilities for close monitoring
19. RECOMMENDATIONS:
STROKE UNIT
• Every hospital should have a stroke unit
• A stroke should be managed by a multidisciplinary stroke
team
• An efficient referral and rehabilitation system to be
established for the success of a stroke unit
• Stroke units significantly reduce death, dependency,
institutionalisation and length of hospital stay.
OUTCOME:
EVIDENCE LEVEL : 2+ A
RCT= 304 : 1+
LENGTH OF STAY:
COCHRANE REVIEW: 1++
20. Patient Admitted in
STROKE UNIT
TYPE OF STROKE
ISCHEMIC HEMORRHAGIC
surgical referral
for Decompression
indicated ?
REFER IMMEDIATELY
YES
INDICATIONS FOR
EVACUATION OF HEMATOMA / VENTRICULO
STOMY/ BOTH
INDICATION S FOR
DECOMPRESSIVE
CRANIECTOMY(1)
CONTINUE MEDICAL
TREATMENT
NO
YES
CONSIDER SURGICAL
INTERVENTION
NO
YES
DECOMPRESS AS
EARLY AS POSSIBLE
1. DECIMAL TRIAL
2. STICH II TRIAL
3. MISTIE TRIAL
EVACUATION BY
CRANIOTOMY (2)
EVACUATION BY MINIMAL
INVASIVE TECHNIQUES(3)
VENTRICULOSTOMY/
EVD
Medical treatment prior to discharge:
• cholesterol lowering
• BP control
• dietary advice
• antiplatelet treatment
• lifestyle advice. CLOSURE
PATHWAY ALGORITHM - II
STROKE - SURGERY
WITH / WITHOUT
HYDROCEPHALUS
NEUROREHAB
21. STROKE SURGERY
HEMORRHAGIC
A. Lobar hemorrhage
1.STICH Trial -Mendelow AD et al.Lancet 2005, RCT,
-No difference in outcome in stable patients
-Surgery Outcome better than conservative RX in progressive
Neurological deterioration.
Evidence Level 1++
B. Basal ganglia Hemorrhage
1..Endoscopy Evacuation better than conservative treatment,
Vol.> 50cc, age < 50 years
Evidence Level 1+
C. Cerebellar Hemorrhage with obstructive hydrocephalus
Surgical Emergency
22. Stroke Surgery
Surgical Treatment Of Intracerebral Hemorrhage
The International STICH Trial
• Spontaneous ICH < 72 hrs
• GCS > 5, Diameter > 2cm
• Age > 14 yrs R
• Craniotomy/Evacuation
• 500 patients
• Conservative Med Control
• 500 patients
Design
• •83 Centers
• •Goal: 1000 patients
• •Inclusion: Supratentorial hemorrhage only, uncertainty on need to operate
• •Exclusions: severe pre-ICH disability or systemic disease, IVH, BGH
• •Outcome: GOS, BI, RS at 6 months
• •Funding: UK Stroke Association, UK Medical Research Council
• •Coordinating Center: Dept Neurosurgery, Newcastle upon Tyne, UK
David Mendelow, MD
The Lancet Feb 2005
23. UROKINASE OR TPA
INSTILATION AND
ASPIRATION
THROMBOLYSIS WITH
UK / TPA AND
MINIMAL INVASIVE
EVACUATION- PHASE II
24. STROKE SURGERY
ISCHEMIC
People with middle cerebral artery (MCA) infarction who meet all of the criteria below
should be considered for decompressive hemicraniectomy.
• They should be referred within24 hours of onset of symptoms and
• treated within a maximum of 48 hours:
• aged 60 years or under
• clinical deficits suggestive of infarction in the territory of the MCA with a score on the
• National Institute of Health Stroke Scale (NIHSS) of above 15
• decrease in the level of consciousness to give a score of 1 or more on item 1a of the
NIHSS
• signs on MRI of an infarct of at least 50% of the MCA territory, with or without
additional
• infarction in the territory of the anterior or posterior cerebral artery on the same side, or
• infarct volume greater than 145 cm3 as shown on diffusion-weighted MRI.
• DECIMAL TRIAL- RCT - Stroke. 2007;38:2506.)
• EVIDENCE LEVEL 1+
25. DECIMAL TRIAL-RESULT
Decompressive Craniectomy in Malignant MCA infarction
• Thirty-eight patients from 7 stroke centers had been enrolled in the
DECIMAL trial when it was prematurely stopped on recommendation
from the data safety monitoring committee. On the basis of interim
data, the data safety monitoring committee recommended first, to
stop the trial, mainly because of slow recruitment and a high
difference in mortality between the 2 groups, and
• second, to organize a pooled analysis of the individual data from
DECIMAL and the 2 other ongoing European randomized trials of
decompressive craniectomy in malignant MCA infarction (DESTINY
and HAMLET).
26. STROKE PATHWAYS
RESOURCES:
1.National clinical guidelines for stroke
Clinical Effectiveness& Evaluation Unit
ROYAL COLLEGE OF PHYSICIANS
2. STROKE
National clinical guideline for diagnosis
and initial management of acute stroke and
transient ischaemic attack
ROYAL COLLEGE OF PHYSICIANS
3. Stroke:
Diagnosis and initial management of acute stroke and transient ischaemic attack (TIA)
National Institute of clinical Excellence and Health clinical guideline (NICE)
32. STROKE ACUTE CARE
STROKE UNIT
MULTIDISCIPLINARY TEAM
INTENSIVE CARE
PREHOSPITAL
CARE
NEURO REHABILITATION
HOW?
EARLY DETECTION
RAPID DISPATCH EVIDENCE BASED
PATHWAY
PHYSICAL THERAPY
OCCUPATIONAL THERAPY
SPEECH AND LANGUAGE THERAPY
PSYCHOLOGY
IDENTIFY
RISK FACTORS
CHRONIC CARE