OPB Flashcards

(85 cards)

1
Q

Breast cancer: Risk factors, classification, presentation, investigation

A

Risk factors:

  • Age 50+
  • History of benign breast disease (cystic disease, papilloma, radial scar)
  • Hyperplasia (atypical or proliferative)
  • FH
  • Previous breast cancer
  • Ionising radiation exposure
  • Nulliparous
  • Obesity

Classification:
By spread
- Early breast cancer (Size <5cm, no axillary lymphadenopathy)
- Locally advanced (Size >5cm, axillary lymphadenopathy
- Metastatic (spread beyond the breast and axilla)
By pathology
- Invasive (e.g. Ductal, lobular
- Non-invasive (DCIS, LCIS)

Presentation:
Symptoms: Lump, nipple discharge or eczema, skin changes/tethering, pain
Identified by screening programme

Investigation
“Triple assessment”:
- Clinical examination
-Imaging (US for <40. Mammogram + US for >40 or suspected cancer cases.)
- Histology (core biopsy first choice)
Staging:
- If early breast disease = CXR, SLNB, US liver, bloods
- If locally advanced= CT chest Bone scan

sentinel lymph node biopsy

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2
Q

Breast cancer: Management

A

TREATMENT BY DISEASE STAGE

Non-invasive breast cancer in situ i.e. DCIS : Breast conserving surgery +/- post-op radiotherapy

Neoadjuvant therapies

  • Older and ER+ve (Aromatase inhibitor)
  • Younger and ER -ve (Chemo)

Early invasive Breast cancer = Surgery (usually mastectomy) AND adjuvant therapy
Adjuvant therapy:
- ER+ and pre-menopausal (Goserelin + Tamoxifen)
-ER+ and post-menopausal (Aromatase inhibitor)
- HER+ (Trastuzumab + chemo/radiotherapy)

Metastatic breast cancer: Bisphosphonates (e.g. Weekly IV Zoledronate infusion) for bone mets, radiotherapy or systemic therapies for bone pain palliation, targeted therapies (e.g. Trastuzumab for HER2 +ve)

INDICATIONS FOR AXILLARY CLEARANCE
US of the axilla pre-treatment
1. Normal? SLNB –> Abnormal? Perform axillary clearance as 2nd operation
2.. Abnormal? Do Core biopsy –> Abnormal? Perform axillary clearance at 1st operation

RADIOTHERAPY
@ breast : For ALL WLE patients or women <50 on day for surgery as “boost”
@chest wall : after mastectomy
@ axilla and SCF : After axillary clearance

LONG TERM FOLLOW-UP SCHEDULE
Year 1 and 5 : Mammogram and Clinical examination
Year 10 : Mammogram (and clinical appointment if on endocrine treatment)
Years 2,3,4,6,7,8,9 : Mammogram only

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3
Q

Benign breast diseases

A

<25
Normal process: Breast development, ductal hyperplasia, lobular hyperplasia
Pathological: Fibroadenoma, juvenile hypertrophy

25-35
Normal process: Lactation, cyclical activity, epithelial turnover
Pathology: Galactocele, papilloma-duct discharge, cyclical mastalgia

35-55
Normal process: Lobular, ductal or stromal hyperplasia. Involution
Pathology: Atypical hyperplasia, macro cysts, duct ectasia, periductal mastitis, sclerosing lesions

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4
Q

Radial scar

A

What? Localised inflammatory reaction or ischaemia

Risk? 50% association with malignancy

Management? Send for triple assessment

Radial scar, or complex sclerosing lesion, is a rosette-like proliferative breast lesion. It is not related to surgical scarring.
View all
A radial scar is a growth that looks like a scar when the tissue is viewed under a microscope. It has a central core containing benign ducts. Growing out of this core are ducts and lobules that show evidence of unusual changes such as cysts and epithelial hyperplasia (overgrowth of their inner lining).

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5
Q

Gynaecomastia

Cx
Examination
Ix
Mx

A

Cause:

  • Drugs* (e.g. anti-androgen, hormonal drugs, infection medication, cardiac or anti-hypertensives, drugs of abuse, alcohol, cancer/chem drugs, psychoactive drugs)
  • Puberty
  • Old age
  • Tumours (lung, testicular, pituitary)
  • Liver disease

Examination

  • Breast tissue: Feels rubbery and firm. Cancer would be hard/firm. Tissue located concentrically around areola. Cancer tends to locate more peripherally
  • Liver exam
  • Spleen exam
  • Axillary lymph node examination

Investigations
If patient is 18-60 years with no obvious cause AND significant breast tissue –> Bloods (FBC, LFTs, Testosterone, LH, FSH, beta HCG, AFP, prolactin, U+Es)
If patient is >40 years –> Mammogram
If patient has discrete lesion –> US and core biopsy
If patient has abnormalities detected on examination –> Consider CXR and testicular exam

Management:
1st line: Reassure and address any underlying problem. Will resolve in a couple months
2nd line: 20mg OD tamoxifen for 6 months (consider aromatase inhibitor for older men)

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6
Q
Mastitis
Classification
Features
Referral criteria
Tx
A

CLASSIFCTION
Lactating: Due to staph aureus infection
Periductal mastitis: Peri areolar, smoking
- Risk of mammary duct fistula
Skin lesions: Epidermoid cysts, hydradinitis

FEATURES
Timing: Rapid
On examination:
• A red, swollen area on the breast (feels hot and tender on touch)
• Area of hardness on the breast
• A burning pain (continuous or during breastfeeding)
• Nipple discharge (white or blood stained)
• Flu-like symptoms

REFERRAL CRITERIA:
• Mastitis or breast inflammation unresponsive to one course of antibiotics
• Abscess or breast inflammation in patient over 35yrs

TREATMENT
1st line:
- Abscess present? Drain using LA.
- Antibiotics (neonatal/ lactating/ skin-associated –> Flucloxacillin. Non-lactating –> Co-amoxiclav)

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7
Q

Duct ectasia

A

What? An aberration of development and involution
Who? Women >50
Features: Nipple discharge (Cheesy /white), slit-like nipple retraction, doughy palpable mass
Management: Either conservative or surgical (Total duct excision)

Duct ectasia, also known as mammary duct ectasia, is a benign (non-cancerous) breast condition that occurs when a milk duct in the breast widens and its walls thicken. This can cause the duct to become blocked and lead to fluid build-up. It’s more common in women who are getting close to menopause

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8
Q

Duct papilloma

A

What? Development in lumen of mammary ducts
Age 35-55

Presentation? Bloody discharge

Risk? Rarely malignant

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9
Q

Phyllodes Tumour

A

What? Hypercellular stroma with atypia
Age? 35-50 years
Progression? Varied. May locally recur and metastasise
Treatment: Wide local excision (WLE) with clear margin or normal breast tissue

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10
Q

Hydradinitis Suppuritiva

A

What? Chronic inflammation of the axillary apocrine sweat glands
Presentation? Recurrent infections, abscesses, scar formation
Treatment: Antibiotics, drainage of abscesses, excision of the affected area

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11
Q

Mondor’s Disease

A

What? Self limiting, thrombophlebitis of the superficial vein on the breast and axilla
Presentation: Redness, pain and cord like thickening of the vein
Treatment: NSAIDs
Risk: Rare association with underlying malignancy

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12
Q

Breast screening

A

Who? All women aged 50-70. Women above 70 can arrange 3 yearly scan through their screening service

When? 3 yearly interval

What? Mammography, 2 views (craniocaudal “CC” and mediolateral oblique “MLO”). All films are reported twice

Follow-up:
If abnormal result, patient recalled for:
- Repeat mammographic views, including magnification
- Clinical examination
- US
- FNA/Core biopsy

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13
Q

Malignant hypercalcaemia

A

DDx for hypercalcaemia:

  • Severe hypercalcaemia
  • Primary or tertiary hyperparathyroidism
  • Thyrotoxicosis
  • Bone mets
  • Advanced solid tumours (lung, breast, multiple myeloma)
  • Thiazide diuretics
  • Vit D excess
  • Sarcoid

Presentation:

  • Bone pain /fracture
  • Polyuria + polydipsia
  • Abdo pain + constipation
  • Renal colic
  • Confusion / Coma
  • Fatigue

Investigations
Bloods: cCa, PO4, PTH, U+Es, Mg,
ECG: PR interval prolonged? QRS wide?

Management:
1ST - HYDRATION
If asymptomatic and cCa<3 –> Oral fluids, monitor and mobile
If symptomatic and cCa >3 –> 3L of 0.9% NaCl in 24hrs. Correct K and Mg as needed. Aim for UO for 150ml/hr. Once rehydrated, switch from thiazide diuretic to furosemide

2ND - BISPHOSPHONATES
If cCa still >3 after rehydration, then 4mg of zolandronate in 50ml salone or 5% dextrose over 15 mins. Monitor renal function, for hypocalcaema, PO4 and K. IF eGRF is <30 then use pamidronate.

3RD - MEDICATION REVEIW
Esp those medications that effect renal function e.g. NSAIDs, ACEIs, Diuretics

4TH - FOLLOW UP
Reassess U+Es 3-4 days later. If still not correct, consider rescue therapy.

Dialysis is an option if adequate hydration cannot be achieve due to renal or cardiac failure.

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14
Q

SVCO

A

Cause:

  • Intraluminal thrombus (e.g. DVT, central line, tumour in the vessel)
  • Extrinsic compression
  • Invasions

Presentation:
Onset = Insidious
Symptoms: Collateral vessel development, face and neck swelling, Dizziness/lethargy/syncope, conjunctical suffusion, SoB, headache, epistaxis
Signs: Non-pulsatile raised JVP, venous collaterals, arm oedema

Investigation
Non-acute to determine cause: CT, CXR, venogram and coag screen
If extrinsic compression, histology of mass using CT-guided FNA or biopsy or bronchoscopy

Management:
Immediate = ABCDE (including O2 and sit patient forwards)

Clot:

  • Local thrombolysis
  • Anti-coag → LMWH
  • Line removal

Extrinsic compression

  • ABC→ sit upright, O2
  • Steroids → dexamethasone
  • SVC stent insertion
  • Treat underlying tumour with with Chemo (SCLC, lymphoma) or Radiotherapy (solid tumour)
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15
Q

Malignant pericardial efffusion

A

Cause: *Lung cancer. Also breast cancer, lymphoma, oesophageal cancer, melanoma, leukaemia

Presentation
Acute: Rapid onset of dyspnoea, chest pain
Subacute: Asymptomatic, dyspnoea, chest discomfort, easily fatiguable

Investigations:
ECG: Low voltage QRS
US: Tamponade present?

Management. Depends if tamponade present..

  • With tamponade: URGENT pericardial drainage via percutaneous pericardiocentesis
  • Without tamponade: Pericardial fluid sampling / biopsy if needed. REFERRAL early to palliative care services. Prevention of reaccumulation either with prolonged catheter drainage OR create pericardial window
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16
Q

Neutropenic Sepsis

A

What?
Neutrophil count < 0.5 x 10^9 in a pt who is having anticancer treatment and has one of:
- temp higher than 37.5℃/ less than 36.5
- other signs/symptoms consistent w/ clinically significant sepsis

Cause:
Most at risk 7-21 days post-chemotherapy
Esp for patients receiving highly myelosuppressive therapies e.g. leukaemia or lymphoma patients

Scoring for risk of complications
MASCC 0-26 (High = low risk)
MASCC <21 or NEWS >=6 = “High risk”
MASCC >= 21 or NEW <6 = Standard risk

Investigations

  • Sepsis screen (Urine culture, blood culture, line culture, LP if indicated)
  • Bloods
  • Imaging (CXR, AXR, CT?)
  • Urine dip
  • Viral throat swab

Treatment
Immediate with 1 hour… (don’t want for FBC/culture)
- For HIGH risk patients = IV Tazocin AND gentamicin within 1 hour
- For STANDARD risk patients = IV Tazocin + specific cover if appropriate (e.g. Vancomycin for MRSA, Clarithromycin for atypical pneumonia)

Oral stepdown…
- Oral co-amoxiclav and ciprofloxacin

Granulocyte-Colony Stimulating Factor (GCSF)
Not routinely used
Indications:
	• Profound neutropenia (<0.1)
	• Prolonged neutropenia (>10 days)
	• Pneumonia
	• Hypotension
	• Multi-organ dysfunction
	• Uncontrolled primary disease
	• Invasive fungal infections
	• Age >65
	• Hospital inpatient at time of developing fever
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17
Q

Tumour Lysis Syndrome

A

What?
The rapid release for tumour cell contents into the blood after treatment.

Pathophysiology
Tumour cells release:
1. Potassium
2. Phosphorus
3. Uric acid
Phosphorus then sops up Ca, causing hypocalcaemia 

Cause:
Tumour feature: High burden, within rapidly dividing cells (e.g. high grade lymphoma, acute leukaemia), tumours v responsive to treatment
Patient features: Dehydrated, pre-existing kidney dysfunction

Presentation:

  • Cardiac arrhythmias/ palpitations and sudden death
  • Muscle cramps
  • Hallucinations, seizures, numbness
  • AKI features (dark urine, flank pain, reduced UO)
  • Fatigue, reduced appetite
  • Nausea +/- vomiting

Clinical diagnosis

  • Increased serum creatinine
  • Cardiac arrhymthia or sudden death
  • Seizure
Management
Acute:
• Calcium gluconate
• Fluid resuscitation
• Rasburicase (uric acid --> allantoin)
• Phosphate binder (e.g. al hydroxide)
Consider: Renal dialysis, sodium bicarbonate

Non-acute:
LOW RISK - Regular monitoring. Oral allopurinol

IMMEDIATE RISK e.g. large cell lymphoma, ALL, AML, CLL - Prechemo IV hydration + phosphate binder
+ allopurinol / rasburicase

HIGH RISK e.g. Burkitt’s lymphoma -
Prechemo IV hydration + phosphate binder + rasburicase + Loop diuretic

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18
Q

Malignancy spinal cord compression

A

Cause: Tumour growth, tumour mets (e.g. lung, breast, prostate and multiple myeloma) or vertebrae collapse

Presentation:
Symptoms: Neuropathic pain (“radicular and band-like”, sharp and shooting), paraparesis, paraplegia, paraesthesia, bladder/bowel disturbance
Progression: Pain then weakness then sensory/autonomic symptoms
Depends on level of lesion: above L1 → UMN signs in legs, below L1 → LMN in legs

Ix: MRI whole spine within 24hrs. If no history of cancer, obtain tissue biopsy

Scoring: Tokuhashi score to aid management decision.

Treatment:
1st line: Dex 16mg Oral / IV AND PPI. Radiotherapy asap
2nd line: Options…
- Surgery (if single area of compression from solid tumour? Consider circumferential decompression then radiotherapy)
- Chemotherapy (for lymphoma, teratoma, SCLC)
- Hormone therapy (for met prostate cancer)

Monitoring:

  • Glucose (for steroid induced diabetes)
  • Analgesia
  • Thromboprophylaxis
  • Physiotherapy
  • Spine stability
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19
Q

Aromatase Inhibitor: Letrozole

A

MoA: Inhibitors action of aromatase which normally catalyses the breakdown of androgens into oestrogen. Useful for ER+ve cancers as it decreases the amount of circulating oestrogen

Indication: 1st line for ER+ve breast cancer in post-menopausal women. Can be used as neo-adjuvant of adjuvant theraapy

Cautions:

  • If creatinine clearance is <10ml/min
  • If Susceptibility to osteoporosis
  • If severe hepatic impairment
  • Use contraception until fully postmenopausal

Contra-indications:

  • Pre-menopausal
  • Avoid if Breastfeeding or pregnant

Main side effects:

  • Arthralgia
  • Alopecia
  • Osteoporosis (require BMD before and during treatment)
  • Hot flushes
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20
Q

Trastuzumab (Herceptin)

A

MoA: Targets tumours positive for Human Epithelial growth factor Receptor 2 (HER2)

Indications:

  • Breast cancer HER2+ve: Either early or metastatic
  • Gastric cancer HER2+ve: Metastatic

Route: IV infusion or Sc injection

Contra-indications

  • Dyspnoea at rest
  • Cardiac disease (e.g. CAH, HTN history, uncontrolled arrhythmias, symptomatic heart failure_

Drug interactions

  • Live vaccines
  • Risk of cardiotoxicity with other cancer drugs e.g. Anthracyclines, pixanthrone and mitoxanthrone

SE

  • Common: Flue-like symptoms and diarrhoea
  • Risk of congestive heart failure
  • Pulmonary events e.g. interstitial lung dsiease
  • Hypersensitivity reaction

Monitoring
- Cardiac function before and during treatment

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21
Q

Rituximab

A

Class/MoA: Monoclonal antibody against B-lymphocytes by binding to CD20 on cell surface. Therefore this is an immunotherapy chemo drug

Indications: Haematological cancers (Stage III-IV follicular lymphoma, diffuse large B-cell NHL, CLL and maintenance therapy for NHL)

Route:
IV - NHL and CLL.
SC - CLL

CI

  • Severe HF
  • Infection
  • Live vaccines
  • Uncontrolled heart disease

SE
Myelosuppression**

Monitoring
Contraception to be taken during and post treatment
Look out for cytokine release syndrome

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22
Q

Capecitabine

A

MoA: Anti-metabolite that converts to Fluorouracil in tumour cells and then prevents de novo DNA synthesis

Indications:

  1. Rectal carcinoma (with radiotherapy)
  2. Stage III colorectal cancer (adjuvant post-surgery)
  3. Breast cancer (2nd line with docetaxel)
  4. Gastric cancer (with platinum based therapy)

Contra-indications:

  • G6PD inactivity
  • Pregnant or breastfeeding
  • Fluorouracil hypersensitivity
  • Severe hepatic or renal impairment

SE

  • Common: GI disorder, anorexia, diarrhoea, hand-foot syndrome, fatigue
  • Rare but life threatening: Steven johnson syndrome, cardiotoxicity, toxic epidermal necrosis, infertility

Dosage
Cycle of oral BD
*Risk of incorrect dosage

Monitoring

  • Plasma Ca levels
  • Eye disorders
  • Sever skin reactions
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23
Q

Goserelin

A

Moa / Class: GnRH analogue –> Inhibition of pituitary secretion of testosterone and oestradiol after 21 days

Route: SC every 28 days

Indications:

  • Prostate cancer (locally advanced or metastatic)
  • Breast cancers

Contra-indications:

  • Breastfeeding
  • Pregnancy
  • Undiagnosed vaginal bleeding

Monitoring:

  • Depression
  • QT prolongation
  • **Men in the 1st month: Worsened glucose tolerance, ureteric obstruction, spinal cord compression) ** GIVE FLUTAMIDE (Flutamide, a synthetic antiandrogen, can be used preemptively to attenuate the tumour flare through its antagonistic effects at androgen receptors.)

SE:

  • Hot flushes
  • Sweating
  • Gynaecomastia
  • Increased HF risk
  • SC site injury
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24
Q

Imatinib

A

MoA/Class: TKI (prevents cell proliferation by binding to BCR-ABL active site)

Route: Oral

Indications: CML, CLL or GIST (GI stromal tumour)

Contra-indications: Pregnancy, breastfeeding, HBV (risk of reactivation)

SE:
Generally well-tolerated BUT N/V, rash, oedema, diarrhoea and myelosuppression.
Rare but risk of infertility, tumour lysis syndrome and pericardial effusion

Monitoring:
For: GI bleeding, fluid retention
Regular FBC and LFTs

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25
Tamoxifen
MoA / Class: SERM (selective eostrogen receptor modular). Antagonises oestrogen at the hypothalamus and breast tissue. Partial agonist at the endometrium Dosage: Oral for 5 years. Menopausal review after 5 years. If still pre-menopausal, continue for further 5 years. If post-menopausal another 5 years of aromatase inhibitor or tamoxifen Indication: Breast cancer - 1st line for pre-menopausal women. 2nd line for post-menopausal women Male breast cancer Anovulatory infertility CI - Pregnancy - VTE risk - Acute polyphyria Interaction - Warfarin --> Increased bleeding risk - SSRI --> Reduced efficacy - Rifampicin --> Decreases exposire Side effects - Increases risk of endometrium cancer - VTE risk - Menstrual disturbance (e.g. ammenorrhoea, vaginal bleeding - Hot flushes
26
Chemotherapy side effects
Related to drug regime, including: - Myelosuppression and risk of neutropenic sepsis - Thromboembolism - Alopecia - GI toxicities - Neuropathy - Nephrotoxicity - Ototoxicity ``` Late effects - Cardiac toxicity - Cardiomyopathy - Congestive cardiac failure - Myocarditis - Infertility - Premature menopause - Oligospermia - Neuropathy - Renal impairment Carcinogenesis ```
27
Methotrexate
Action: Inhibits purine and pyrimidine synthesis i.e. An "antimetabolite" Indication: Inflammatory arthritis (esp RA), Psoriasis, ALL Route: Oral, IV, intra-arterial, IM or Intrathecal Contraindications: Active infection, immunodeficiency syndromes, significant pleural effusions Cautions: Photosensitivity, diarrhoea, blood disorder, peptic ulceration, pleural effusion or ascites accumulation Toxicity: - Bone marrow suppression (esp WCC and plt's) - GI toxicity - Pulmonary toxicity - Liver toxicity ``` Common side effects: Common: - Mucositis - Myelosuppression - Pneumonitis - Pulmonary fibrosis - Liver fibrosis ``` Consideration: - Contraception to be used during and 6 months post-treatment for men AND women. - Avoid in hepatic impairment - Avoid in renal impairement Drug interactions - .Trimethoprim and co-trimoxazole= Risk of marrow aplasia - Aspirin = At high dose reduces excretion and increases toxicity risk Monitoring requirements FBC, LFTs and renal function tests every 1-2 weeks until therapy stabilised. Then every 2-3 months. Must report all: - S/S of infection, esp sore throat - Blood disorder features e.g. sore throat, bruising and mouth ulcers - Liver toxicity signs e.g. N/V, abdo pain, dark urine - Respiratory effects e.g. SoB Counselling for patient Avoid self medications of aspirin or NSAIDs
28
Breast cancer referral guidelines
REFER people using a SUSPECTED cancer pathway referral (for an appointment within 2 weeks) for breast cancer if: • They are aged >=30 and have an unexplained breast lump with or without pain or • They are aged >=50 with any of the following symptoms in one nipple only: • Discharge • Retraction • Other changes of concern CONSIDER a SUSPECTED cancer pathway referral (for an appointment within 2 weeks) people: • With skin changes that suggest breast cancer or • Aged >=30 with an unexplained lump in the axilla CONSIDER NON-URGENT referral in people aged <30 with an unexplained breast lump with or without pain
29
DNACPR new additions to framework requirements
1. If a clinical DNACPR decision has been made, there should be a presumption of favour of sensitively informing the patient unless that conversation may cause then physical/mental harm OR the patient refuses the discussion OR the patient lacks capacity to engage 2. Subject to confidentiality decisions, those close to a patient who lacks capacity must be informed of any CPR decision without delay
30
When to discuss CPR
If the patient is likely to require CPR and illness risks rapid deterioration and it is unlikely to be successful in achieving sustainable life
31
Success of CPR and risks?
Success after CPR - Survival after cardiac arrest low ○ In hospital 15-20% ○ Out of hospital 5-10% Risks of CPR, even if "successful"? - Rib fractures - Hypoxic brain injury - Potential for distress, harm and suffering
32
An advance decision that CPR should not be attempted can be made if...
1. A patient makes a competent advance refusal | 2. CPR treatment would not be of overall benefit to the patient
33
What 4 medications are used for anticipatory care planning
1. Opioid for pain and/or breathlessness = Morphine sulphate injection 2. Anxiolytic sedative for anxiety/agitation/breathlessness = Midazolam injection 3. Anti-secretory for respiratory secretions = Hyoscine butylbromide injection ("Buscopan") 4. Anti-emetic for N/V =Levomepromazine inj
34
What are the components of the pain assessment
Patient characteristics Pain characteristics Drug responsiveness VAS (visual analogue scale)
35
WHO pain ladder
Step 1: Mild Pain Non-opioid i.e. Patacetamol OR NSAID +/- adjuvant ``` Step 2: Mild-mod pain Weak opioid (i.e. Codeine / co-codamol . tramadol) + Non-opioid +/- adjuvant ``` ``` Step 3: Mod-severe pain Strong opioid (1st line morphine) + Non-opioid +/- adjuvant ```
36
How is SC analgesia given?
Mode of administration: Given in CME T34 syringe pump over 24hrs Dose: Calculate 24hrs oral morphine dose and half for SC dose
37
What drugs can be given adjuvantly to analgesia
NSAIDs --> Bone mets, soft tissue infiltration, liver pain, inflammatory pain Steroids --> Raise ICP, nerve compression, liver pain, soft tissue infiltration Gabapentin --> Nerve pain Amitriptyline --> Nerve pain Carbamazepine (anti-convulsants) --> Nerve pain Bisphosphonates --> Malignant bone pain
38
1st line for intermittent anxiety and distress
SC midazolam SC 2-5mg 4hrly. If >3 doses given in 4 hours, seek advice. If 6 doses required in 24hrs, seek advice
39
Therapeutic options for persistent anxiety and distress
1st line: Midazolam SC 10mg to 20mg over 24 hours in a syringe pump + midazolam SC 5mg hourly, as required 2nd: Titrate midazolam SC 10-60mg over 24 hours in syringe pump + levomepromazine SC 6-12 hrly PRN (*QT prolongation risk). Stop any haloperidol (QT)
40
Causes of delirium
Drugs: Opioid toxicity, benzo, steroids, cancer treatments, substance abuse Cancer: Brain mets, para-neoplastic syndromes Infection: UTI, RTI Metabolic disturbances: Hyponatraemia, hypercalcaemia
41
Clinical features of delirium
Fluctuating symptoms Hallucinations Inattention Noctural agitation, daytime somnolence
42
Treatment of Delirium
1. General measures (good lighting, calm environment, familiar staff) 2. Treat cause 3. Antipsychotics (1st line Haloperidol oral or parenteral) 4. Add benzodiazepine if patient has marked distress (1st line SC midazolam)
43
Physiology of N/V
2 centres: VC and CTZ Input to CTZ: 1. Chemical triggers e.g. Drugs, metabolites, toxins 2. CN VIII Nucleus Inputs to VC 1. Higher centres 2. Autonomic nerves from stretch receptors 3. CN VIII Nucleus 4. CTZ Receptors CTZ = 5HT3 and D2 VC = Ach, H2, 5HT2 Outputs CTZ --> VC --> Vagus nerve + glossopharyngeal nerve + sympathetics
44
Reversible causes of N/V
Drugs: - CTZ stimulating i.e. opioids, antibiotics, digoxin, cytotoxics, SSRIs - Gastric stasis drugs e.g. opioids and TCAs - Gastric irritating drugs e.g. NSAIDs, Fe, Abx, tranexamic acid Constipation Hypercalcaemia Cough Gastric irritation Anxiety
45
Classes of anti-emetics and their side effects
Dopamine antagonists - Haloperidol, metoclopramide, domperidone (SE: Extrapyramidal) Antihistamine: Cyclizine (SE: Dry mouth, sedation) Phenothiazines: Levomepromazine (SE: Sedation, hypotension) 5HT3 antagonists: Granisetron, ondansetron (SE: Headaches, constipation)
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Drugs of choice in N/V management for the following causes: - Clinical toxicity / metabolic upset? - Motility disorders (gastroparesis)? - Intracranial disorders ? - Gastric / oesophageal irritation - Multifactorial
``` Clinical toxicity / metabolic upset - Dopamine receptor antagonist • E.g. Haloperidol, metoclopramide - ?Anti-serotoninergic (5HT3) •e.g "-setrons" ``` Motility disorders -Prokinetics I.e. dopamine antagonistse.g. metoclopramide or domperidone Intracranial disorders - Anticholinergics e.g. hyoscine hydrobromide - Antihistamines e..g cyclizine - Steroids - Levopromazine Gastric / oesophageal irritation - Antifungal / antiviral - Antacaid Multifactorial - Consider adding benzo
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Opioid and nausea
30% of patients will feel nausea on induction, with tolerance within 2 weeks
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Management of breathlessness in
Non-drug options: - PT / OT exercises - relaxation techniques - Bed positioning - O2 therapy in SpO2 <92% Pharmacological options 1st line Opioids (1st Morphine immediate release 2mg. If unable to take oral, then SC 1-2mg.) 2nd line Modified release PLUS 4 hourly equivalent dose immediate release) If anxiety or panic related? Anxiolytics (1st line SL Lorazepam) In terminal phase (final 48 to 72hrs) - syringe driver of midazolam and opioid
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Specific causes of breathlessness in palliative care
``` Pleural effusion Pulmonary embolism Large airways obstruction Lymphangitis carcinomatosa SCVO Resp infection Anaemia ```
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Cancer and Cachexia
What is cachexia: Wasting syndrome with loss of muscle and fat caused directly by tumour factors and/or indirectly by abnormal host response to tumour presence Features: - Weight loss - Anorexia - Fatigue - Muscle wasting - Aesthesia - Oedema - Anaemia Commonest cancers with cachexia - Gastric + colon - Pancreatic - NSCLC - Small cell lung cancer - Prostate Tx: -Early input from MDT
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What defines frequent use of breakthough?
>3 doses in 24hrs ? Seek specialist advice if patient still in mod-severe pain
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What to do if analgesia has persistent intolerable side effects?
Consider reducing dose and titrating more slowly OR adding adjuvant analgesia before changing opioid
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How to start and titrate immediate release oral morphine
In opioid naive: 2-5mg immediate release 4 hourly, titrating to effect. If patient has been on regular opioids: Prescribe 1/6-1/10 of 24 dose required for breakthrough.
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Paracetamol given at 1g QDS as part of WHO pain ladder Consider reducing paracetamol dose to 500mg four times daily when ...
Poor nutritional status Low body weight (< 50kg) Hepatic impairment and/or chronic alcohol abuse
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How to start and titrate modified release oral morphine
Prescribe 12 hourly or 24 hourly, 1/6to 1/10 of 24hour breakthrough dose. Allow 1 hour to take effect before taking breakthrough
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How to start and titrate morphine syringe pump
Titrate with immediate release oral morphine (start 5mg 4-hourly) and convert to modified release when stable → Divide 24h dose of immediate release by 2 Note: Higher SC infusion doses (>2ml in a single site) require consideration of alternative opioid e.g. diamorphine
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Preparation: Weak opioid for mild pain
``` 1st line CODEINE Most useful preparation as "co-codamol" • I.e. codeine + paracetamol • Dose as 30/500 = 30mg codeine with 500mg paracetamol • Codeine dose can range from 30-60mg QDS. If higher dose needed, switch to morphine • Side effects common ○ Nausea ○ Constipation ○ Drowsiness ``` Also: Tramadol, nefopam
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Preparation: Strong opioid for mod-severe pain 1st line
MORPHINE • Preparations: Oral (immediate or modified release), SC) injection and in a CME T34 syringe pump. • Half-life: 2-3.5hr • Duration of analgesia: 4-6 hrs • Renal impairment: Renally excreted, active metabolites – titrate morphine slowly and monitor carefully in stage 1 to 3 chronic kidney disease. Consider other opioids in stage 4 to 5 chronic kidney disease, dialysis patients. • Liver impairment: Consider low doses and slow titration DIAMORPHINE • Highly soluble opioid • Preparations: SC and CME T34 syringe driver • Used in high dose breakthrough injections (I.e. >180mg SC morphine in 24hrs) • Caution in renal and liver impairment
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Preparation: Strong opioid for mod-severe pain 2nd line
OXYCODONE • Preparations: Immediate and modified release via SC injection and CME T34 syringe pump • Limited SC dose due to lower concentration preparation • Avoid in moderate-severe liver impairment • In mild-moderate renal impairment: Titrate more slowly and monitor carefully. Avoid in stage 4-5 CKD FENTANYL • Indication: Stable pain if morphine not tolerated. Transdermal patches for cancer patients • Preparation: Patch lasting 72hrs, if SC or oral route unsuitable.SC or oral route unsuitable. • Limits: Dose cannot be quickly adjusted • Renal impairment: No initial dose reduced required, may accumulate over time • Liver impairment: Severe disease may require dose reduction • Do not initiate at end-of-life when oral route not available, long time until steady state reached
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Preparation: Strong opioid for mod-severe pain 3rd line **seek specialist advice**
ALFENTANIL • Duration: Short-acting • Preparation: SC or in CME T34 syringe pump • Indication: episodic or incidental pain, given SL or SC • Renal impairment: No dose reduction required. Good for dialysis patients. • Liver impairment: Reduce dose and titrate FENTANYL • Preparation: SL or Intranasal • Indication: Episodic / incidental pain
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Preparation: Strong opioid for mod-severe pain 4th line **specialist use only**
METHADONE • Indication: Complex pain • Challenge: Dosing difficult due to long half life • Renal impairment: No adjustment • Liver impairment: Leads to prolonged half-life
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Strong opioids for mod-severe pain?
1st line: Morphine, diamorphine 2nd line: Oxycodone, fentanyl 3rd line: Alfentanil, fentanyl 4th line: Methadone
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Opioid toxicity: Presentation and management
Presentation: - Persistent sedation - Subtle agitation - Shadows in peripheral visual field - Vivid cream - Auditory and visual hallucinations - Myoclonic jerks - Allodynia - Delirium - Confusion - Emergency: Pinpoint pupils and resp depressio Mangement: - Reduce opioid dose by 1/3 if pain controlled (consider switch opioid or adding adjuvant) - Ensure adequate hydration - Give haloperidol for aditiation - Naloxone for life-threatening resp depression
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Dose conversion: Oral codeine to oral morphine
Divide by 10
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Dose conversion: Oral morphine to SC morphine
Divide by 2
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Dose conversion: Oral morphine to IV morphine
Divide by 2 or 4
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Dose conversion: Oral morphine to SC diamorphine
Divide by 3
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Dose conversion: Oral morphine to oral oxycodone
Divide by 2
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What is the typical breakthrough dose?
1/10 to 1/6 of the 24hr
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If patient is opioid toxic OR frail OR elderly, reduce dose by up to ___% and re-titrate. If switching from 2nd line opioid back to morphine. then reduce dose by up to ___%
If patient is opioid toxic OR frail OR elderly, reduce dose by up to 30% and re-titrate. If switching from 2nd line opioid back to morphine. then reduce dose by up to 30%
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Features of a syringe driver?
What? Syringe driver. Delivers injectable drugs SC e.g. Opioids, benzodiazepines and anti-emetics Use? When patient NBM, losing consciousness or are vomiting / not absorbing via GIT How? Set to run over 24hrs. Up to three drugs can be mixed together (NB: Check compatibility charts). Takes a few hours to take effect. Dose? SC opioids are stronger, so require dose reduction via conversion charts
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Benzodiazepines used in palliative care
Midazolam MoA: Short acting Route: SC and buccal Use: SC for Agitation at end of life, spasticity / skeletal muscle spasm, severe breathlessness at end of life, alcohol withdrawal at end of life, 1st line delirium. SL for terminal haemorrhage Lorazepam MoA: Intermediate acting Route: SL or Oral Use: SL 1st line for anxiety/ breathlessness. Oral is 2nd line for delirium Diazepam MoA: Long acting Route: Oral and PR Use: Oral is 2nd line for delirium and 3rd line for anxiety/ breathlessness
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Colorectal Cancer
Causes/ Risk factors: - IBD - Age - Genetics (HNPCC, FAP) - Lifestyle: Smoking, low PA - Diet: Low fibre, low fruit and veg Presentation: Emergency: Obstruction, perforation, bleeding, localised pain Non-emergency: Altered bowel habit, rectal bleeding, colicky pain, unexplained anaemia, anorexia, malaise, flatulence Investigations: For symptomatic: DRE, Colonoscopy/sigmoidoscopy, contract radiography If confirmed cancer: CT CAP --> MDT Surveillance: IBD, HNPCC, FAP and previous cancers Management: Rectal cancer: Neoadjuvant treatment with radiotherapy or chemoradiotherapy All cancers: Adjuvant treatment with 5-FU IV or Oral pro-drug (e.g. capecitabine) Metastatic disease: Palliative chemo Bowel screening: - All men and women 50-75 (at 55 offer one of signmoidoscopy, 50-75 do home testing with FIT or FOB every 2 years)
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Tumour markers
``` Ca 125 - Ovarian AFP + LDH + Beta-HCG - Testicular Ca 19-9- Pancreatic cancer CEA - Colorectal cancer PSA- prostate AFP - Hepatocellular cancer and teratoma Ca 15-3 - Breast cancer ```
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Secondary lung cancer
Origins: Breast, kidney, uterus, ovary, testes and thyroid Pattern: Bilateral and multiple “cannonball” (commonly from renal cell cancer) Presentation: Breathlessness, haemoptysis and lobar collapse
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SCVO investigation and Mx
Ix: chest X-ray, followed by CT venography is required. Mx: Endovascular recanalisation and stent insertion is mots effective intervention.
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Different types of NSCLC
Squamous → ass w/ PTHrP secretion (hyperca), central Adenocarcinoma → peripheral, non-smokers, yng F Large cell → peripheral, poorly diff, poor prognosis Adenocarcinoma in situ
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Lung cancer
Pathology: 80% NSCLC (1/3 Squamous > 1/3 Adenocarcinoma> Large cell), 20% SCLC (from endocrine cells giving paraneoplastic syndrome--> Hyponatraemia due to ADH and Cushings due to ACTH) Presenting features: - Cough - Haemoptysis - Breathlessness - Pain, nerve entrapment - ? bronchial obstruction (Complete = atelectasis. Partial = monophonic or unilateral wheeze, predisposition to pneumonia. If in upper airways = Stridor) - Clubbing - Mediastinal spread - Mets (neuro, bone, liver, skin and gastric) - Pancoast tumour (Mostly in NSCLC) Referral: - Suspected cancer referral within 2 weeks if abnormal CXR or >40 with unexplained haemoptysis - Offer CXR within 2 weeks for lung Ca >40 if 2 of the following (1 if smoker): Cough, fatigue, SoB, chest pain, weight loss and appetite loss - Consider urgent CXR if >40 with any of the following: Recurrent / persistent chest infection, clubbing, lymphadenopathy, chest signs consistent with lunch cancer, thrombocytosis Investigations: CXR, Contract CT Chest, PET, biopsy for histology and FNA for cytology Investigations: - CXR → nodule, hilar enlargement, consolidation, collapse, pl effusion, bony secondaries - Cytology → sputum, pl fluid FNA/ biopsy → peripheral lesions/ lymph nodes Bronchoscopy → histology, assess operability CT w/ contrast → staging PET → staging in NSCLC Radionuclide bone scan → if suspect mets Lung function tests → assess for lobestomy ``` Management NSCLC: 1. Lobectomy: If medically fit and aim curative 2. Radical radiotherapy stage I, II, III Chem +/- for more advanced ``` SCLC: 1. Surgery: If limited stage disease (T1-2a) 2. Chemo +/- radiotherapy Palliation : Radiotherapy for bronchial obstruction / SVC obstruction / haemoptysis/ bone pain, palliative chemo Contraindications to surgery: SVC obs, FEV < 1.5, malignant pl effusion, vocal cord paralysis
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Pancoast's tumour
Tumour of pulmonary apex, v rare (5/100 lung ca) Most are NSCLC ``` Symptoms: - Horner’s syndrome - Weakness in hand = Pain in shoulder/ shoulder blade - Small muscle wasting of hands ``` Spread to: - Thoracic ribs - Brachial plexus - Blood vessels
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Male breast cancer
ER +ve >>> HER2 overexpression uncommon Management: 1st line: Mastectomy and SLNB/axillary clearance Post-mastectomy radiotherapy for T3/4 and involved lymph nodes Follow-up: Adjuvant tamoxifen is given to all men with ER+ve breast cancer for 5 years
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Fibroadenoma
Who? Common in 16-30 Px: Mobile, well-defined lump Ix: Core biopsy should be performed in lesions measuring more than 4cm in diameter. Mx:Only remove if growing/patient wish
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Periductal mastitis common in....
SMOKERS
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Breast cyst
Who? Common in 40-55 Px:Mobile, well-defined lump Ix: Triple assessment. Hallo sign imaging Mx: Aspiration if symptomatic
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Opioid to use in CKD
Alfentanil, buprenorphine and fentanyl
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Hiccups in palliative care -
chlorpromazine or haloperidol