Dementia_Rajib
Dementia
A group of thinking and social symptoms that
interferes with daily functioning.
Presented By : Rajib Barua
Key points :
Impairment of multiple domains of cognitive functions:
Memory impairment – (Must)
1. New material learning
2. Forget previous learning
With at least one of the following cognitive disturbance:
1. Aphasia : Language disturbance
2. Apraxia : Impaired ability to carry out motor activities despit
intact motor function
3. Agnosia: Failure to recognize/ identify familiar object
despite intact sensory function
4. Disturbance in executive functions
Significant impairment of social & occupational functioning decline
from previous level
Presented By : Rajib Barua
Types Of Dementia
Presented By : Rajib Barua
The global “prevalence” of
dementia
• 46.8 million people worldwide
are living with dementia in 2015.
• This number will almost double
every 20 years.
• Reaching 74.7 million in 2030 and
131.5 million in 2050.
• These new estimates are 12-13%
higher than those made for the
World Alzheimer Report 2009.
Ref : www.alz.co.uk/worldreport2015
Presented By : Rajib Barua
“Prevalence” in Bangladesh
According to the study of
Alzheimer Society of Bangladesh :
• There are about 4,60,000 people
with dementia in Bangladesh in
2015.
• While the number will rise to
8,34,000 in 2030 and
21,93,000 in 2050 respectively.
Ref : http://alzheimerbd.com/dementia-
statistics/
Presented By : Rajib Barua
Risk Factors
Presented By : Rajib Barua
Alzheimer’s Dementia (AD)
Alzheimer's is the most
common form of dementia,
a general term for memory
loss and other intellectual
abilities serious enough to
interfere with daily life.
Alzheimer's disease accounts
for 60 to 80 percent of
dementia cases.
Ref:
http://www.alz.org/alzheimers_disease_wha
t_is_alzheimers.asp
Presented By : Rajib Barua
1. Recent memory loss that affects job
skills.
2. Difficulty performing familiar tasks.
3. Problem with language.
4. Disorientation of time and place.
5. Poor or decreased judgment.
6. Problem with abstract thinking.
7. Misplacing things.
8. Changes in personality.
9. Changes in mood or behavior.
10. Loss of initiative.
“10 warning signs” of
Alzheimer’s Disease
Presented By : Rajib Barua
Memory, Language & Judgment centre
of human brain.
Presented By : Rajib Barua
Healthy brain
Vs
Alzheimer's brain
Presented By : Rajib Barua
What a normal brain loses in AD?
The cholinergic deficit in AD underlies the
clinical symptom :
Progressive loss of Cholinergic neurons
Progressive decrease in available Ach*.
Impairment in ADL*, behavior & cognition.
*Ach = Acetylcholine
*ADL = Activity of daily living
Presented By : Rajib Barua
Strategies for Medical Treatment
of Dementia
• Prevention of disease
• Delay of onset
• Slow rate of progression
• Treat primary symptoms (cognitive)
• Treat secondary symptoms (behavioural)
Presented By : Rajib Barua
Management of Dementia
• Supportive treatment
(Non-pharmacological)
• Treatment of complications
& co-morbidities
• Symptomatic treatment
Presented By : Rajib Barua
Supportive treatment
(Non-pharmacological)
• Advice, support and a sensible
explanation are important for the
caregiver.
• Reduce excessive stimulation.
• Divide tasks into small, simple
steps; allow ample time.
• Eliminate caffeine and alcohol.
• Take their concern seriously.
Presented By : Rajib Barua
Treatment of complications
and co-morbidities
Like AD other diseases rise with advancing age :-
• Hypertension
• Diabetes mellitus
• IHD
• Heart failure
• Arthritis
• Infections
Presented By : Rajib Barua
Symptomatic treatment
Symptomatic treatment of mild to moderate forms of
Alzheimer's dementia is “Cholinesterase inhibitor”.
• It increases acetylcholine in the brain, &
• Slowing down of the disease's progression.
Presented By : Rajib Barua
Overview of AChE inhibitors
– Obsolete because, very short lasting (half life 30 mints)
necessitating frequent oral administration
– Potentially serious dose-limiting S/E
– Again S/E; 50% of the patients treated with tacrine
discontinued treatment because of adverse events especially
hepatotoxicity.
Oldest (probably most extensively tested):
“Physostigmine”
In the past : “Tacrine”
Presented By : Rajib Barua
Overview of AChE inhibitors
(cont’d.)
– Launched in the USA in January 1997 and in the UK in March
1997
– Modest benefits in terms of cognition
– Most common S/E are similar to those seen with tacrine
– Launched in the USA in April 2000; received approval for use in
60 countries including all member states of EU and USA
– Improvements were seen in cognition, ADL & severity of
dementia
– Dose of 6-12 mg/day
– Lower risk of adverse effects
Recent past : “Donepezil”
Recent : “Rivastigmine”
Presented By : Rajib Barua
What is “Rivastigmine” ?
• Rivastigmine is Acetyl Cholinesterase (AChE) as well as Butyl
Cholinesterase (BChE) inhibitor.
• Rivastigmine treats Alzheimer’s disease as well as other
dementias.
Presented By : Rajib Barua
Cholinergic function in AD:
from pathology to therapy – summary
• In AD brains BuChE activity increases significantly; BuChE as well
as AChE regulates ACh levels.
• Dual AChE/BuChE inhibition may result in cholinergic function
being effectively maintained along the continuum of AD.
• Rivastigmine is a dual AChE/BuChE inhibitor.
• Inhibition of CSF AChE and BuChE with Rivastigmine correlates
with clinical benefits in AD patients.
Ref : Perry et al.,1978, 1984;Giacobini, 1997, Cutler et al; 1998, Costa et al., 1999
Presented By : Rajib Barua
What is Exelon?
• Exelon is rivastigmine.
• Exelon is Acetyl Cholinesterase (AChE) as well as (BChE)
inhibitor.
• Exelon treats Alzheimer’s dementia as well as other dementias.
Rivastigmine Brand :-
HISTORY :
Rivastigmine was developed by Marta Weinstock-Rosin of the
Department of Pharmacology at the Hebrew University of Jerusalem
and sold to Novartis by Yissum for commercial development.
It is a semi-synthetic derivative of physostigmine.
It has been available in capsule and liquid formulations since 1997.
In 2006, it became the first product approved globally for the
treatment of mild to moderate dementia associated with Parkinson's disease
and in 2007 the rivastigmine transdermal patch became the first
patch treatment for dementia.
Ref : https://en.wikipedia.org/wiki/Rivastigmine
Presented By : Rajib Barua
Available Dosage Forms
CapsuleCapsule Transdermal PatchTransdermal Patch
1.5 mg =
3.0 mg =
4.5 mg =
6.0 mg =
Exelon Patch 5 cm2
= 4.6 mg/24 h
Exelon Patch 10 cm2
=9.5 mg/24 h
Presented By : Rajib Barua
Aim to achieve maximum tolerated individual
dose
 Start with 1.5mg, BID.
 Increase by 3mg/day at intervals of minimum 02 weeks, up to
maximum 12mg/day.
 Omit dose(s) in response to adverse events.
 Reduce dose if problems persist.
Exelon Capsule Dosage Guideline
Presented By : Rajib Barua
Exelon Patch Dosage Guideline
1. “Exelon Patch is once daily”.
2. Target dose is Exelon Patch-10
(9.5mg/ 24h).
3. Only one patch should be worn
at a time.
4. Patch should be replaced by a
new one after 24 hours.
5. It is recommended that location
for new patch be rotated.
Presented By : Rajib Barua
Exelon Patch:
How Delicately it is made
Coloured backing layer
Acrylic (drug) matrix
Silicone (adhesive) matrix
Release liner
(peeled off just before patch application)
Designed with new generation matrix technology
Presented By : Rajib Barua
Exelon Patch:
How drug is Delivered Across the Skin
Epidermis
Patch
Dermis
Subcutis
Blood Vessels
Presented By : Rajib Barua
Dosage Guideline for newly
diagnosed patient
Exelon
4.6 mg/24 h
Patch
Exelon
9.5 mg/24 h
Patch
Starting
dose
Target
dose
4 weeks
One-step dose
increase
Exelon Patch-5 Exelon Patch-10
Presented By : Rajib Barua
Algorithm for Starting or Switching to
Exelon Patch
< 6 mg/day*
Start on Exelon
4.6 mg/24 hours patch
4weeks
Switch directly to target
dose Exelon 9.5 mg/24 hours patch
Is the patient already receiving oral Exelon?
NO YES
What dose of oral Exelon is the patient receiving?
Increase to Exelon
9.5 mg/24 hours patch
6–12 mg/day*
Presented By : Rajib Barua
Smooth and continuous drug
delivery over 24 hours
Graphic representation (not ‘real’ data) Imbimbo 2001
Increased
side effects
Poor activity
“Optimal
therapeutic
window”
Druglevelintheblood
Peak
Oral Dose
Trough
Patch
Time
Presented By : Rajib Barua
Exelon Patch: How to apply
1. The patch should be
removed from the pouch,
2. Remove one side of the
protective liner,
3. Place the patch at the
selected application site,
4. Remove the other side of
the protective liner,
5. Press the patch firmly into
place for 20–30 seconds.
Presented By : Rajib Barua
Exelon Patch: Where to apply
• Exelon Patch can be applied to:
– Upper or lower back
– Upper arm
– Chest
• When replacing the patch, the
new patch should be applied to a
different spot of skin.
– Do not use the same spot
more than once every 14 days
• Normal daily activities, such as
bathing are permitted.
Presented By : Rajib Barua
Advantage of Exelon Patch
Presented By : Rajib Barua
1. Easy to apply.
2. Reduce patients’ pill burden.
3. Reduce care giver’s distress.
4. Achieve optimal therapeutic dose.
5. Dramatically improved GI Tolerability.
6. Ensures Continuous & Consistent drug
delivery that results fewer side effects &
Improved efficacy.
Conclusion : The time to act
Presented By : Rajib Barua
• Promoting a dementia-friendly society.
• National public health and social care priority.
• Improving public and professional attitudes and
understanding of dementia.
• Investing to improve care and services for
dementia affected people.
• Priority given to dementia in the
public health research agenda.
““Love them while they are with you”Love them while they are with you”
Dementia_Rajib

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Dementia_Rajib

  • 2. Dementia A group of thinking and social symptoms that interferes with daily functioning. Presented By : Rajib Barua
  • 3. Key points : Impairment of multiple domains of cognitive functions: Memory impairment – (Must) 1. New material learning 2. Forget previous learning With at least one of the following cognitive disturbance: 1. Aphasia : Language disturbance 2. Apraxia : Impaired ability to carry out motor activities despit intact motor function 3. Agnosia: Failure to recognize/ identify familiar object despite intact sensory function 4. Disturbance in executive functions Significant impairment of social & occupational functioning decline from previous level Presented By : Rajib Barua
  • 4. Types Of Dementia Presented By : Rajib Barua
  • 5. The global “prevalence” of dementia • 46.8 million people worldwide are living with dementia in 2015. • This number will almost double every 20 years. • Reaching 74.7 million in 2030 and 131.5 million in 2050. • These new estimates are 12-13% higher than those made for the World Alzheimer Report 2009. Ref : www.alz.co.uk/worldreport2015 Presented By : Rajib Barua
  • 6. “Prevalence” in Bangladesh According to the study of Alzheimer Society of Bangladesh : • There are about 4,60,000 people with dementia in Bangladesh in 2015. • While the number will rise to 8,34,000 in 2030 and 21,93,000 in 2050 respectively. Ref : http://alzheimerbd.com/dementia- statistics/ Presented By : Rajib Barua
  • 8. Alzheimer’s Dementia (AD) Alzheimer's is the most common form of dementia, a general term for memory loss and other intellectual abilities serious enough to interfere with daily life. Alzheimer's disease accounts for 60 to 80 percent of dementia cases. Ref: http://www.alz.org/alzheimers_disease_wha t_is_alzheimers.asp Presented By : Rajib Barua
  • 9. 1. Recent memory loss that affects job skills. 2. Difficulty performing familiar tasks. 3. Problem with language. 4. Disorientation of time and place. 5. Poor or decreased judgment. 6. Problem with abstract thinking. 7. Misplacing things. 8. Changes in personality. 9. Changes in mood or behavior. 10. Loss of initiative. “10 warning signs” of Alzheimer’s Disease Presented By : Rajib Barua
  • 10. Memory, Language & Judgment centre of human brain. Presented By : Rajib Barua
  • 12. What a normal brain loses in AD? The cholinergic deficit in AD underlies the clinical symptom : Progressive loss of Cholinergic neurons Progressive decrease in available Ach*. Impairment in ADL*, behavior & cognition. *Ach = Acetylcholine *ADL = Activity of daily living Presented By : Rajib Barua
  • 13. Strategies for Medical Treatment of Dementia • Prevention of disease • Delay of onset • Slow rate of progression • Treat primary symptoms (cognitive) • Treat secondary symptoms (behavioural) Presented By : Rajib Barua
  • 14. Management of Dementia • Supportive treatment (Non-pharmacological) • Treatment of complications & co-morbidities • Symptomatic treatment Presented By : Rajib Barua
  • 15. Supportive treatment (Non-pharmacological) • Advice, support and a sensible explanation are important for the caregiver. • Reduce excessive stimulation. • Divide tasks into small, simple steps; allow ample time. • Eliminate caffeine and alcohol. • Take their concern seriously. Presented By : Rajib Barua
  • 16. Treatment of complications and co-morbidities Like AD other diseases rise with advancing age :- • Hypertension • Diabetes mellitus • IHD • Heart failure • Arthritis • Infections Presented By : Rajib Barua
  • 17. Symptomatic treatment Symptomatic treatment of mild to moderate forms of Alzheimer's dementia is “Cholinesterase inhibitor”. • It increases acetylcholine in the brain, & • Slowing down of the disease's progression. Presented By : Rajib Barua
  • 18. Overview of AChE inhibitors – Obsolete because, very short lasting (half life 30 mints) necessitating frequent oral administration – Potentially serious dose-limiting S/E – Again S/E; 50% of the patients treated with tacrine discontinued treatment because of adverse events especially hepatotoxicity. Oldest (probably most extensively tested): “Physostigmine” In the past : “Tacrine” Presented By : Rajib Barua
  • 19. Overview of AChE inhibitors (cont’d.) – Launched in the USA in January 1997 and in the UK in March 1997 – Modest benefits in terms of cognition – Most common S/E are similar to those seen with tacrine – Launched in the USA in April 2000; received approval for use in 60 countries including all member states of EU and USA – Improvements were seen in cognition, ADL & severity of dementia – Dose of 6-12 mg/day – Lower risk of adverse effects Recent past : “Donepezil” Recent : “Rivastigmine” Presented By : Rajib Barua
  • 20. What is “Rivastigmine” ? • Rivastigmine is Acetyl Cholinesterase (AChE) as well as Butyl Cholinesterase (BChE) inhibitor. • Rivastigmine treats Alzheimer’s disease as well as other dementias. Presented By : Rajib Barua
  • 21. Cholinergic function in AD: from pathology to therapy – summary • In AD brains BuChE activity increases significantly; BuChE as well as AChE regulates ACh levels. • Dual AChE/BuChE inhibition may result in cholinergic function being effectively maintained along the continuum of AD. • Rivastigmine is a dual AChE/BuChE inhibitor. • Inhibition of CSF AChE and BuChE with Rivastigmine correlates with clinical benefits in AD patients. Ref : Perry et al.,1978, 1984;Giacobini, 1997, Cutler et al; 1998, Costa et al., 1999 Presented By : Rajib Barua
  • 22. What is Exelon? • Exelon is rivastigmine. • Exelon is Acetyl Cholinesterase (AChE) as well as (BChE) inhibitor. • Exelon treats Alzheimer’s dementia as well as other dementias. Rivastigmine Brand :- HISTORY : Rivastigmine was developed by Marta Weinstock-Rosin of the Department of Pharmacology at the Hebrew University of Jerusalem and sold to Novartis by Yissum for commercial development. It is a semi-synthetic derivative of physostigmine. It has been available in capsule and liquid formulations since 1997. In 2006, it became the first product approved globally for the treatment of mild to moderate dementia associated with Parkinson's disease and in 2007 the rivastigmine transdermal patch became the first patch treatment for dementia. Ref : https://en.wikipedia.org/wiki/Rivastigmine Presented By : Rajib Barua
  • 23. Available Dosage Forms CapsuleCapsule Transdermal PatchTransdermal Patch 1.5 mg = 3.0 mg = 4.5 mg = 6.0 mg = Exelon Patch 5 cm2 = 4.6 mg/24 h Exelon Patch 10 cm2 =9.5 mg/24 h Presented By : Rajib Barua
  • 24. Aim to achieve maximum tolerated individual dose  Start with 1.5mg, BID.  Increase by 3mg/day at intervals of minimum 02 weeks, up to maximum 12mg/day.  Omit dose(s) in response to adverse events.  Reduce dose if problems persist. Exelon Capsule Dosage Guideline Presented By : Rajib Barua
  • 25. Exelon Patch Dosage Guideline 1. “Exelon Patch is once daily”. 2. Target dose is Exelon Patch-10 (9.5mg/ 24h). 3. Only one patch should be worn at a time. 4. Patch should be replaced by a new one after 24 hours. 5. It is recommended that location for new patch be rotated. Presented By : Rajib Barua
  • 26. Exelon Patch: How Delicately it is made Coloured backing layer Acrylic (drug) matrix Silicone (adhesive) matrix Release liner (peeled off just before patch application) Designed with new generation matrix technology Presented By : Rajib Barua
  • 27. Exelon Patch: How drug is Delivered Across the Skin Epidermis Patch Dermis Subcutis Blood Vessels Presented By : Rajib Barua
  • 28. Dosage Guideline for newly diagnosed patient Exelon 4.6 mg/24 h Patch Exelon 9.5 mg/24 h Patch Starting dose Target dose 4 weeks One-step dose increase Exelon Patch-5 Exelon Patch-10 Presented By : Rajib Barua
  • 29. Algorithm for Starting or Switching to Exelon Patch < 6 mg/day* Start on Exelon 4.6 mg/24 hours patch 4weeks Switch directly to target dose Exelon 9.5 mg/24 hours patch Is the patient already receiving oral Exelon? NO YES What dose of oral Exelon is the patient receiving? Increase to Exelon 9.5 mg/24 hours patch 6–12 mg/day* Presented By : Rajib Barua
  • 30. Smooth and continuous drug delivery over 24 hours Graphic representation (not ‘real’ data) Imbimbo 2001 Increased side effects Poor activity “Optimal therapeutic window” Druglevelintheblood Peak Oral Dose Trough Patch Time Presented By : Rajib Barua
  • 31. Exelon Patch: How to apply 1. The patch should be removed from the pouch, 2. Remove one side of the protective liner, 3. Place the patch at the selected application site, 4. Remove the other side of the protective liner, 5. Press the patch firmly into place for 20–30 seconds. Presented By : Rajib Barua
  • 32. Exelon Patch: Where to apply • Exelon Patch can be applied to: – Upper or lower back – Upper arm – Chest • When replacing the patch, the new patch should be applied to a different spot of skin. – Do not use the same spot more than once every 14 days • Normal daily activities, such as bathing are permitted. Presented By : Rajib Barua
  • 33. Advantage of Exelon Patch Presented By : Rajib Barua 1. Easy to apply. 2. Reduce patients’ pill burden. 3. Reduce care giver’s distress. 4. Achieve optimal therapeutic dose. 5. Dramatically improved GI Tolerability. 6. Ensures Continuous & Consistent drug delivery that results fewer side effects & Improved efficacy.
  • 34. Conclusion : The time to act Presented By : Rajib Barua • Promoting a dementia-friendly society. • National public health and social care priority. • Improving public and professional attitudes and understanding of dementia. • Investing to improve care and services for dementia affected people. • Priority given to dementia in the public health research agenda.
  • 35. ““Love them while they are with you”Love them while they are with you”