Clinical Oncology SC019: Palliative And Hospice Care: Adding Life To Years Flashcards

1
Q

Palliative care

A
WHO:
- Approach that improves QoL of patients and their families facing the problem associated with ***life-threatening illness, through ***prevention + ***relief of suffering by means of ***early identification + impeccable assessment + treatment of pain and other problems
—> ***Physical
—> ***Psychosocial
—> ***Spiritual

Palliative care:

  • Affirms life and regards dying as a ***normal practice
  • Neither hastens nor postpones death
  • Provides ***relief from pain and other distressing symptoms
  • Integrates the **psychological and **spiritual aspects of care
  • Offers ***holistic care
  • Offers a support system to help patients live as active as possible until a death
  • Offers a support system to help the ***families of patients cope during the patient’s illnesses and in their own bereavement
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2
Q

Essential components of Palliative care

A
  1. Control of symptoms
  2. Effective communication
  3. Rehabilitation
  4. Continuity of care
  5. Terminal care
  6. Support in bereavement
  7. Education (Patients + Family)
  8. Research
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3
Q

Palliative care vs End-of-life care

A
Palliative Care:
- At ***any point of a chronic disease
- Can still seek for ***curative treatment (e.g. Palliative chemo / target therapy for metastatic CA lung)
- Goal:
—> Provide comfort, QoL
—> Support to patients and families

End of life care/ Hospice care:

  • ***Part of palliative care
  • A specific type of care at the **last stage of life (usually **<6 months)
  • Provides comfort ***without a curative intent
  • ***No curative options available / patient has chosen not to pursue curative or aggressive treatment
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4
Q

Who needs palliative care

A
  1. Cancer patients (good condition until disease progress —> condition drops rapidly)
  2. Chronic organ failure (multiple exacerbations / recovery before death)
    - Heart failure
    - Respiratory disease
    - Liver disease
    - Renal disease
  3. Frailty related illness (start with poor initial condition, gradual deterioration)
    - Advanced dementia
    - Parkinson’s disease
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5
Q

Who should provide palliative care

A
  1. Primary palliative care clinicians
    - Provide basic management of physical + psychological symptoms
    - Discuss **goals of care with the patient
    - Discuss **
    end-of-life care / ***DNACPR
  2. Secondary + Tertiary palliative care
    - Physical / Psychological symptom **assessment + management
    - **
    Complicated, refractory symptoms/ distress
    - **Conflict resolution
    - **
    Futility issues
    - Work alongside the patient’s primary clinician
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6
Q

Multidisciplinary team

A
  1. Physicians
  2. Nurses (Palliative, Home care nurses)
  3. Therapists (OT, PT)
  4. Social workers
  5. Pharmacists
  6. Home health aides
  7. Spiritual counselors
  8. Volunteers
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7
Q

When should palliative care be provided?

A

Conventional model:
Anti-cancer treatment
—> Not work
—> ***Abrupt change to Palliative / Hospice care

Problems:

  1. Persistent, unattended symptoms + ***distress in the phase of active treatment
  2. Patients and families: ***less time for preparation of deterioration
  3. Patients and families may refuse the “abrupt” referral to palliative care service —> feel abandoned

Current model:

  • **Early integration of palliative care into oncology practice
  • Anti-cancer treatment + Palliative care (ongoing at the same time, add more palliative care component as anti-cancer treatment less effective / condition deteriorate)

Advantages:

  1. Maintain / Improve ***QoL
  2. Reduce depression + anxiety
  3. Reduce ***invasiveness of end-of-life care
  4. Reduce symptom ***intensity (e.g. less pain)
  5. Does ***NOT compromise anti-cancer intensity
  6. Reduce ***over-treatment at end-of-life period (50% reduction of IV chemo exposure within 60 days of death)
  7. Better understanding of treatment nature but less anxiety and depression
  8. Improve ***overall survival
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8
Q

Benefits of Palliative care

A
  1. Improves communication between patients, caregivers, healthcare providers
  2. Addresses needs of caregivers as they cope with + care for a loved one with a serious illness
  3. Improves patients and family satisfaction with care
  4. Improves QoL while reducing costs
  5. Enables patients to remain comfortable by preventing + relieving pain / suffering
  6. Allows patients to maintain connections to family and friends
  7. Foster vitality and independence in patients

Importance to Society:
- Higher patient’s satisfaction, Less admission —> Lower health care cost

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9
Q

4 Main aspects in Palliative care

A

Focus on Disease ***as well as QoL

QoL:

  1. Physical
  2. Psychological
  3. Social
  4. Spiritual

Means:

  1. Identification
    - symptoms
    - functional status
    - needs
  2. Assessment
    - performance status
    - physical, psychological, social, spiritual
  3. Treatment
    - management
    —> constantly re-assess / monitor —> treatment again

—> **ONLY proceed with investigations / assessments that would **change the management plan (e.g. End stag CA lung: checking CEA / PET scan)

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10
Q
  1. Physical
A

Functional assessment: **Palliative performance scale
1. Ambulation
2. Activity + Evidence of disease
3. Self-care
4. Intake
5. Conscious level
—> **
<70% —> worry if patient can still continue on anti-cancer treatment

Identification of S/S:
1. Pain
2. Chest symptoms: dyspnea, cough, haemoptysis
3. GI symptoms: vomiting, colic
4. Pelvic symptoms: fistula, discharge /
bleeding (PV / PR)
5. CNS symptoms: focal (e.g. seizures) / delirium
6. MSK: local wound management, bedsore
7. Systemic: insomnia, cachexia, fatigue
8. Treatment-associated SE
—> by ***History taking: OPQRSTUV (understanding, value (i.e. what’s his goal), significance of pain to him e.g. cannot walk)

Assessment of pain:

  1. Site
  2. Pain rating scale

Treatment:

  1. Pharmacological
    - Analgesic
  2. Non-pharmacological
    - Heat
    - Cold application
    - Massage therapy
    - Physical therapy
    - Transcutaneous electrical nerve stimulation
    - Spinal cord stimulation
    - Aromatherapy
    - Guided imagery
    - Laughter
    - Music
    - Biofeedback
    - Self-hypnosis
    - Acupuncture
    - CBT
Reassessment:
1. Treatment SE
- Opioid
—> N+V
—> Constipation
—> Drowsiness
—> Delirium
—> Xerostomia
—> Sweating
  • TCA
    —> Anticholinergic effects (dry mouth, constipation, blurred vision, urinary retention, dizziness, tachycardia, memory impairment)
    —> Cardiac (arrhythmias, QT prolongation)
    —> Sedation
    —> Weight gain
- Gabapentin / Pregabalin
—> Dizziness (usually in morning ∵ given nocte)
—> Drowsiness
—> Peripheral edema
—> Dry mouth
  1. Treatment efficacy
    - Pain score: compare with last assessment (2-3 days after escalation of dose)
    - Functional: improvement in general condition
  2. Any change in pattern
    - breakthrough pain
    - change of site of pain
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11
Q

WHO recommendations on Analgesic use

A
  1. By mouth
    - oral administration of medication is an **effective, **convenient, **inexpensive method of medicating patients
    - should be used wherever possible
    - medicines are easy to **
    titrate
  2. By the clock
    - for **persistent pain
    - additional doses as needed
    - aim: **
    prevent (rather than react to pain)
    - allow ***continuous pain relief by maintaining a constant level of drug in body —> prevent pain from recurring
  3. By ladder
    - non-opioid —> weak opioid —> strong opioid
    - validated + effective method of ensuring therapy for pain
    - administered according to severity of pain + drug suitability
  4. On individual basis
    - ***individualise pain management
    - different patients will require different dosages / intervention to achieve good pain relief
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12
Q

WHO pain ladder

A
  1. Non-opioid (+/- Adjuvant)
    - Paracetamol
    - NSAID (generally avoided ∵ cause gastritis, renal impairment esp. long-term treatment)
    —> other options: Celebrex (Celecoxib), Arcoxia (Etoricoxib))
  2. Weak opioid + Non-opioid (+/- Adjuvant)
    - Codeine
    - Dihydrocodeine
    - Tramadol
  3. Strong opioid + Non-opioid (+/- Adjuvant)
    - Morphine
    - Methadone
    - Fentanyl
    - Hydromorphone
    - Oxycodone
    —> Start with low dose morphine elixir: 2.5-5mg Q2-4 hourly
    —> titrate against pain reported on the 1-10 scale
    —> after 2-3 days add the total daily dose, divide it in two and administer as long-acting morphine sulphate tablets Q12 hourly

Adjuvant treatment:

  1. Somatic pain
    - NSAIDs
    - Bisphosphonates (for metastatic bone pain)
    - RT (for metastatic bone pain)
  2. Neuropathic pain
    - Anticonvulsant: Gabapentin, Pregabalin
    - Antidepressant: Nortriptyline (TCA, significant sedation), Venlafaxine (SNRI), Duloxetine (SNRI), SSRI
  3. Visceral pain
    - Corticosteroids (Dexamethasone) (useful for hepatic capsular pain)

(Other uses of Dexamethasone:

  • Cerebral edema
  • Brain metastasis
  • Spinal cord compression
  • SVCO
  • Anti-emetic
  • Appetite stimulant
  • Adrenal insufficiency)
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13
Q
  1. Psychological
A
  1. Anxiety (6-39%)
  2. Depression (~25%)
  3. Coping skills / Adjustment disorder
  4. Mood / Affection
  5. Suicidal ideation / Hasten death
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14
Q

Anxiety / Depression

A

Identification:

  • present with somatic symptoms e.g. dyspnea, ***insomnia, tremor, palpitations
  • irritability, depressed mood, lack of hope, feeling of worthlessness

Assessment:
1. Screening tool
- **Hospital and Depression scale (HADS)
- **
Brief Edinburgh Depression scale (BEDS)
—> assess pre-morbid personality + previous psychiatry history
—> medications used
—> any use of stimulated drugs, excessive alcohol / withdrawal of the drugs
—> review of family + social history

Treatment:
1. Pharmacological
- BDZ
—> Diazepam PO (more sedative effect)
—> Lorazepam PO/SL (more anxiolytic effect)
—> Midazolam SC/IV (emergency sedation / end-of-life)

  • Antidepressants
    —> SSRI (Sertraline, TCA)
    —> SNRI
  1. Non-pharmacological
    - CBT
    - Relaxation techniques
    - Various complementary therapies (e.g. massage, acupuncture)
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15
Q
  1. Social
A
  1. Financial support
  2. Family dynamics
  3. Community care plan
    - old age home
    - hospice care
    - day care centre
  4. Home care plan
    - home care
    - clean + tidy
    - safety at home (OT to help in putting equipment)
    - wheelchair
    - home catering service
  5. Volunteer service
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16
Q
  1. Spiritual
A

Spiritual care:
- Provides appropriate support in order for
people to express their **thoughts + feelings in regard to their spirituality
- Belief and religion
- Not only dignity / comfort but human rights and **
deeply held values

Even amongst patients and carers for whom religion plays a relatively small part in their life when they are well
—> questions of meaning, purpose + hope can take on a larger profile during times of illness

Assessment (***FICA):

  1. Faith
    - have religious faith?
    - what gives you life meaning / purpose?
  2. Importance
    - how important is faith / beliefs to you?
  3. Community
    - part of community that offers you support e.g. church?
  4. Assist
    - how can we assist?
    - any things need to aware of e.g. prayer times / diet?
    - can we contact anyone?
    - how can we best support?

Support:

  1. Help from Chaplains
  2. Particular ceremony for their particular religion
  3. Special arrangement in burial / cremation
  4. Must have clear guidance esp. in hospital setting
    - e.g. no candles burning close to oxygen cylinders
    - carers staying with patients and regulations of hospital
17
Q

Communication

A
  • Effective symptom control is impossible without effective communication
  • Fundamental to good palliative care
  • Always a two-way activity, requiring sensitivity, empathy + ***active listening
  • Communication in palliative care is necessary to achieve an accurate assessment of patient’ physical, emotional and psychosocial needs
18
Q

Breaking bad news (10 steps)

A
  1. Preparation
    - know all facts before meeting
    - prepare ALL NOTES (e.g. scan, clinical notes)
    - prepare the setting: ensure comfort and privacy
    - minimise risk of interruption
  2. What does the patient know / want to know?
    - ask patient to give a brief narrative of events
  3. Give a warning shot
    - “I am afraid it is rather serious” —> ***Pause
  4. Allow denial
  5. Explain + Check understanding
    - use simple language + diagrams if needed
  6. Is more information wanted?
    - ask patient / carer “would you want to know more?”
  7. Listen to concerns
    - ask what they worry / bother them most at the moment?
  8. Encourage ventilation of feelings
    - show empathy
  9. Summary + Plan
    - summarise concerns, plan treatment + foster hope
  10. Offer availability
19
Q

Summary

A
  • Basic palliative care skills is essential to all clinical practitioners
  • Good palliative care improves QoL of patients + their families
  • It can carry long positive impact on bereaved families
  • Consider early referral to specialist palliative care service for patients in life-threatening diseases