Dementia: its effects on patients, family and carers Flashcards

1
Q

Identify the main types of dementia.

A
  • AD
  • Frontotemporal Dementia
  • Vascular Dementia
  • Lewy Body dementia
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2
Q

Which of men or women are more at risk of dementia ?

A

WOMEN

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3
Q

Define dementia.

A

Progressive:

  • Cognitive/Intellectual function loss (concentrating, planning, organising, memory, visuospatial skills, orientation, language/comm problems)
  • Loss in ability to do day to day activities
  • Changes in personality and social behaviour (mood)
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4
Q

Identify the main features of ‘early’ AD.

A
Forgetful
Mislaying items
Struggle to find words
Slower cognitive capacity
Confusion/losing track of day
Poor judgement, hard to make plans/decision
Judging distance/seeing objects in 3D
Lose interest
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5
Q

Identify the main features of ‘moderate’ AD.

A
More forgetful
Fail to recognise people
Time/place/events/getting lost
Need help w/ personal care
Diff in daily activities
Behaviour changes
Safety
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6
Q

Identify the main features of ‘late’ AD.

A

(usually total dependency)

Unaware of time/place
Confusion/ comprehension
Not recognise familiar faces
Behaviour changes
Mobility problems
Increased need in self care
Incontinence 
Need assistance in eating
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7
Q

Describe the role of caregivers in the early stage.

A

• Caregivers become aware of their caregiving role (often as a result of diagnosis)
• Provide emotional support following diagnosis and when
the person is depressed or anxious
• Prompt and remind the person about events, tasks and
other things to help them maintain involvement and
independence
• Provide assistance with instrumental activities (e.g.
personal finances, shopping)

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8
Q

Describe the role of caregivers in the middle stage.

A

Use communication strategies to aid
understanding
• Provide help with carrying out personal care
• Provide help with other activities of daily living
such as food preparation, dressing appropriately
• Respond to and manage behavioural disturbance
and inappropriate behaviour.

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9
Q

Describe the role of caregivers in the late stage.

A

• Provide care, support and supervision around the
clock
• Provide full assistance with eating and drinking
• Provide full physical care (bathing, toileting,
dressing, mobilizing)
• Manage behavioural problems.

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10
Q

How many people in the UK live with dementia ?

A

850 K

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11
Q

Which of M or W are more likely to develop dementia ?

A

Women

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12
Q

Identify the main people/organisations which ‘care’ for people with dementia.

A
  • Primary family caregivers
  • Family members, relative and friends
  • Neighbours and community
  • Local and national governments, and NGOs
  • International organisations
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13
Q

Identify the main consequences of caregiving.

A

• A second patient in the making
• Needs of primary caregiver are crucial in the long-term care of the patient
• Consequences for psychological, physical health, quality of life
– Depression/anxiety
– Lower quality of life/wellbeing
– Worse health outcomes: e.g., obesity, higher metabolic risk, higher levels of stress hormones, compromised immune system, cognitive decline, less preventive health behaviours
– Sleep problems
– Social isolations
– Family conflict
– Financial strain (providing dementia care can be full time job)
– Sense of loss/grief
– Guild/resentment/anger
– Role strain (trying to manage multiple caring duties)

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14
Q

Identify barriers to diagnosis of dementia and receipt of good quality care.

A

Public and professional knowledge and attitudes are a barrier:

-Stigma of dementia prevents discussion
\+
-False belief: normal part of aging
\+
-False belief: nothing can be done
 = Inactivity in seeking and offering help
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15
Q

Identify sources of support for dementia patients.

A

• Social services department of local authority/council
• Community psychiatric nurse –> For long-term care plan
• Physiotherapist: issues around mobility
• Occupational therapy:
– Helps with reminiscing and how to make a life story book – Recommending suitable exercise/changes around home
– Assist with personal care training
– Improving safety at home
– Info support on accessing other support
– Advising carers

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