Cancer complications / emergencies Flashcards

1
Q

Malignant bowel obstruction - state the following:
- 2 cancers it’s more likely to happen with
- Pathophysiology
- Presentation
- Investigations
- Management

A

2 cancers it’s more likely to happen with:
- Bowel
- Ovarian

Pathophysiology:
- Mechanical obstruction (partial or complete) of bowel lumen +/- failure of peristalsis

Presentation:
- N&V +/- faeculant
- Abdominal pain
- Abdominal fullness / distension
- Reduced / absent bowel sounds
- Bowels not opened

Investigations:
- Plain abdominal x-ray (identify site of obstruction)
- CT (mechanical vs peristalsis)
- MRI (distinguishing benign vs malignant bowel obstruction in known malignancy)

Management:
- Haloperidol (antiemetic)
- Hyoscine butylbromide aka. Buscopan (reduce peristalsis, secretions and antiemetic)
- Dexamethasone (reduce oedema, secretions and antiemetic)
If peristalsis failure…Metoclopramide (prokinetic) and analgesia

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2
Q

Malignant hypercalcaemia - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
** Oncological emergency **
- Complications which occurs in 20-30% of patients with cancer
- Increased osteoclast activity, more calcium resorption from bone

Presentation:
- N&V
- Renal stones
- Abdominal pain
- Constipation
- Depression
- Altered mental state / confusion
- Polydipsia
- Polyuria

Investigations:
- Bone profile bloods
- ECG (cardiac arrhythmias)
- Consider skeletal survey if multiple myeloma or bone mets suspected

Management:
Stop any calcium supplements, thiazide diuretics or nephrotoxic drugs
If mild / asymptomatic…
- Encourage oral intake / IV fluids
- Recheck corrected calcium after 24 hrs
If moderate/severe or persistent with fluids…
- IV fluids = 3 litres over 24 hours
- After 24 hours of fluids, IV Zoledronic acid (Bisphosphates)

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3
Q

Malignant ascites - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Accumulation of fluid in the peritoneal cavity
- Can be caused by peritoneal deposits or by liver mets leading to functional cirrhosis

Presentation:
- N&V
- Abdominal distension
- Abdomianl pain / discomfort
- SOB
- Early satiety
- Weight loss / progression of cancer signs
- Shifting dullness on percussion

Investigations:
- Ascitic fluid for cytology (cell count, culture, albumin, glucose etc.)
- CT to help identify underlying cause of ascites
- Blood tests (FBC, U&Es, LFTs, coagulation screen)

Management:
- Consider treatment of underlying cause e.g. chemotherapy to debulk ovarian tumour
- Ascitic drainage (paracentesis)

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4
Q

State the 3 main mechanisms by which malignancy can cause hypercalcaemia

A
  1. Osteolytic metastases (commonly in breast cancer)
  2. Tumour secretion of parathyroid hormone-related protein (PTHrP) (common in SSC of lung, head or neck and renal and ovarian cancer)
  3. Tumour secretion of 1,25-dihydroxyvitamin D (calcitriol) (common in Hodgkin lymphoma)
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5
Q

State the 2 main mechanisms by which malignancy can cause ascites

A
  1. Peritoneal deposits from ovarian / urological cancers leading to blockage of lymphatic drainage and increased vascular permeability
  2. Cancers with extensive liver metastases which may result in functional cirrhosis and portal hypertension
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6
Q

Outline how malignant pleural effusion presents, how it is investigated and managed

A

Common complication of thoracic and extrathoracic malignancies and is associated with high mortality

Presentation:
- Incidental finding on chest x-ray
- SOB
- Dull chest pain
- Constitutional symptoms e.g. WL

Investigation:
- Chest x-ray / CT / USS
- Thoracentesis and pleural fluid Analysis (generally exudative)

Management:
Overall poor prognosis, median survival = 3-12 months
If asymptomatic, may monitor without intervention
- Therapeutic thoracentesis (<1.5L)
- If recurrent, pleurodesis / indwelling pleural catheter

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7
Q

Malignant spinal cord compression - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
** Oncological emergency **
- Compression of the spinal cord / cauda equina
- Occurs by direct pressure or vertebral collapse
- First cancer presentation in approximately 20% of cancer patients

Presentation:
- New/severe back pain
- Leg weakness
- Bilateral sciatica
- Urinary retention / incontinence
- Faecal incontinence
- Saddle anaesthesia

Investigations:
- Whole spine MRI within 24 hours of arrival

Management:
- Lie flat and bed rest (limit movement)
- High dose steroids (16mg Dexamethasone) and PPI
- Analgesia
- Liaise with orthopaedics/neurosurgeons (consider surgery debulking / radiotherapy)

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8
Q

Malignant raised ICP - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
** Oncological emergency **
- Increased intracranial pressure
- Caused by either space occupying tumour or obstructive hydrocephalus (sometimes other causes e.g. abscess)

Presentation:
- Headache
- N&V
- Double / blurred vision
- Papilloedema
- Hypertension and bradycardia
- Seizures
- Reduced conscious level

Investigations:
- Urgent MRI brain / CT head

Management:
- Sit upright
- High dose steroids (16mg Dexamethasone) and PPI
- Consider IV Mannitol
- Analgesia
- Antiemetics e.g. Prochlorperazine, Haloperidol
- Consider definitive therapy e.g. surgery / radiotherapy

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9
Q

Outline how palliative malignant raised ICP is managed (not for surgery / radiotherapy)

A
  • Dexamethasone long-term
  • Analgesia (may need very high doses)
  • Antiemetics e.g. Prochlorperazine, Haloperidol
  • Consider sedation e.g. Benzodiazepines
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10
Q

Malignant-related seizures - state the following:
- Pathophysiology
- Management

A

Pathophysiology:
- Seizures are common for patients with brain tumours (up to 65%)
- Temporary surge of abnormal electrical activity, can present in many ways depending on area of brain affected

Management:
- Make area safe (put something under head, remove glasses etc.)
- Anticonvulsants (class depend on the type of seizure), but either IV Lorazepam or buccal Midazolam
- If unresolving, additional IV Lorazepam

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11
Q

Malignant superior vena cava obstruction - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
** Oncological emergency **
- Nearly always caused by malignancy

Presentation:
- Facial / neck / arm swelling
- Thoracic and neck veins distention
- Non-pulsatile JVP
- Central/peripheral cyanosis
- Dyspnoea
- Tachypnoea
- Cough
- Stridor (laryngeal oedema) and hoarse voice
- Chest pain
- Headaches and/or confusion

Investigations:
- FBC, clotting, U&Es
- CTPA (tumour extent, site of occlusion, any thrombus)

Management:
- Sit upright
- Oxygen
- High dose steroids (oedema) and PPI
- Analgesia as required
- Anticoagulation if thrombotic cause found
- Liaise with oncology for resolving underlying cause (stent / chemotherapy / radiotherapy)

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12
Q

Neutropenic sepsis - state the following:
- Pathophysiology
- When is most likely to occur after chemotherapy
- Presentation
- Investigations
- Management

A

Pathophysiology
** Oncological emergency **
- Potentially life-threatening complication of neutropenia
- Patients will a low neutrophil count are more susceptible to infections and sepsis
- Suspect in patients who have known neutropenic or chemotherapy within the last 6 weeks

When is most likely to occur after chemotherapy:
- 7-10 days post-chemotherapy

Presentation:
May appear well
- Fever or low temperature
- Shivering and sweating
- Feeling confused
- Sore throat / cough
- Rashes and swelling
- Diarrhoea
- UTI symptoms
- Flu-like symptoms
- Meningitis symptoms

Investigations:
- Bloods (urgent FBC, U&E, LFTs, CRP, glucose, lactate)
- Blood cultures (peripheral and central line)
- MRSA screen
If symptomatic = looking for source of infection…
- MSSU/CSU if symptomatic
- Stool culture if diarrhoea
- Wound swabs if breaks in skin
- Sputum if available
- Chest x-ray if clinically indicated

Management:
- IV Tazocin 4.5g stat dose (Meropenem second line) within 1 HOUR
- IV fluids
- Oxygen as required
- Measure fluid balance

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13
Q

Outline the criteria for when to suspect neutropenic sepsis

A

In a patient with a neutrophil count of < 0.5 x 109/L or undergoing recent chemotherapy…

Temperature:
>38°C
OR temperature >37.5°C on 2 occasions 30 minutes apart
OR temperature <36°C

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14
Q

State some risk factors for neutropenic sepsis (in addition to recent chemo)

A
  • Duration of neutropenia
  • Indwelling vascular line / devices
  • Comorbidities
  • Elderly
  • Other cancer therapies/treatments
  • Malnutrition
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15
Q

Tumour lysis syndrome - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
** Oncological emergency **
- When tumour cells break down, they release large amounts of cell contents into the bloodstream
- Tumour lysis syndrome occurs when this overload of cell content is more than the body can cope with
- Leads to metabolic disturbances of hyperkalaemia, hyperuricemia, hyperphosphatemia and hypocalcaemia
- Can occur spontaneously or in response to therapy

Presentation:
= Metabolic disturbances (increased K+, increased uric acid, increased phosphorus, decreased calcium)
- Urinary problems (renal damage) dysuria or oliguria
- Gout/joint swelling
- Symptoms of hypocalcaemia e.g. abdominal pain, weakness, N&V, muscle cramps, seizures
- Cardiac arrhythmias (hyperkalaemia)

Investigations:
- Baseline bloods (identify metabolic disturbance)
- ECG to check for cardiac abnormalities

Management:
Risk based approach
- Ongoing monitoring - 6 hourly until stable
- Give IV fluids and strict input / output monitoring
- Allopurinol or Rasburicase
Most patients = Allopurinol (xanthine oxidase inhibitor)
Medium-high risk patients e.g. high-grade lymphoma and leukaemia = Rasburicase (urate oxidase inhibitor)

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16
Q

State the 4 main metabolic disturbances seen in tumour lysis syndrome

A

Hyperkalaemia (K)
Hyperuricaemia (uric acid)
Hyperphosphataemia (phosphate)
.
Hypocalcaemia (can be caused by hyperphosphataemia)

17
Q

What 2 drugs can be used in the management of tumour lysis syndrome and how they work

A
  1. Allopurinol
    Xanthine oxidase inhibitor = stops uric acid production
  2. Rasburicase
    Urate oxidase inhibitor = stops uric acid being processed further
    Given to medium-high risk patients e.g. high-grade lymphoma and leukaemia
18
Q

State some complications of tumour lysis syndrome if left untreated

A

Complications related to metabolic disturbances:
- Renal damage / AKI (hyperuricaemia)
- Cardiac arrhythmias (hyperkalaemia)
- Seizures (hypocalcaemia)
- Death

19
Q

State characteristics of some cancers which increases the likelihood of tumour lysis syndrome

A
  • Large cancer mass
  • Highly proliferative cancer
  • Very responsive to treatment
  • High-grade B-cell lymphoid malignancies (e.g. Burkitt’s lymphoma
  • Acute leukaemias e.g. AML and ALL
20
Q

State what parameters are required for tumour lysis syndrome to be classed both laboratory or clinically (Cairo-Bishop definition)

A

Laboratory parameters needed:
- 2 or more of the following metabolic abnormalities: hyperuricaemia, hyperphosphataemia, hyperkalaemia, or hypocalcaemia

Clinical parameters needed:
- Laboratory confirmation above
- 1 or more of the following clinical manifestations: AKI, cardiac arrhythmia, seizure, or sudden death

21
Q

Immune related colitis - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Common immune related adverse event (associated with immune checkpoint inhibitors) from immunotherapy
- Typically occurs 1-2 months after the 2nd/3rd dose of treatment

Presentation:
Mild = < 4 stools / day over baseline
Moderate = 4-6 stools / day over baseline + abdominal pain + mucus in stool
Severe = > 7 stools / day over baseline + abdominal pain + dehydration + fever + blood in stool + limiting ADL

Investigations:
- Baseline bloods (FBC, U&E, LFTs, TFTs, cortisol & CRP)
- Stool microscopy and culture (C. diff)
- Faecal calprotectin
- Abdominal x-ray if mod-severe

Management:
- Fluid balance
- Encourage fluids / IV fluids
- Prednisolone if moderate (Methylprednisolone if severe)
- Consider omitting next dose of immunotherapy
- Consider Infliximab if severe

22
Q

Mucositis (complication of chemotherapy) - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Inflammation or mucosa, anywhere from mouth to anus
- Occurs from chemotherapy or radiotherapy killing rapidly dividing cells, which include the mucous lining
- Common in radiotherapy for head and neck cancers
- Can be serious, stop the patient from eating and drinking and lead to weight loss, risk of local and systemic infection
- Can stop subsequent radiotherapy session (poor cancer outcomes)

Presentation:
- Painful or sore mouth / gums / tongue
- Inflammation
- Difficulty swallowing / eating & drinking talking
- Xerostomia, mild burning, or pain when eating food
- Soft, whitish patches or pus in the mouth or on the tongue
- Diarrhoea

Investigations:
- Urgent FBC, U&Es, LFT, CRP, Lactate
- Blood Cultures
- Stool sample if diarrhoea (check for infective cause)
- Fungal culture if candida suspected

Management:
- Encourage oral hygiene
- Oral analgesics e.g. Paracetamol or Ibuprofen
- Local anaesthetic spray e.g. Difflam
- Mouthwashes e.g. Chlorhexidine
- Loperamide if not infectious on stool sample
- Dietician input: ensure food charts, weights
- Analgesia / syringe drivers if severe