Oncological Emergencies Flashcards

(39 cards)

1
Q

What are the 3 main criteria for diagnosing neutropenic sepsis?

A

Patient undergoing anticancer treatment
Neutrophils <0.5x10˄9/L
Temperature >38

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2
Q

How many days after chemotherapy does neutropenic sepsis tend to occur?

A

7-14 days

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3
Q

Give 4 risk factors for neutropenic sepsis

A
Active chemotherapy
Extensive field radiotherapy 
Haematological malignancy
Infection risk increased ie. increased exposure to pathogens 
Autoimmune predisposition
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4
Q

Give 3 examples of pathogens that commonly are the cause of neutropenic sepsis

A
80% are endogenous flora
Staph. aureus
Staph. epidermidis
Enterococcus
Streptococcus
MRSA
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5
Q

How does neutropenic sepsis present?

A
Tachycardia
Hypotension 
Tachypnoea
Fever
Drowsy
Confused
Sx related to site of infection eg. cough, painful line
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6
Q

What scoring system is used to score neutropenic sepsis?

A

MASCC

Score out of 26, if >21 then low risk

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7
Q

What investigations will be done for a patient with neutropenic sepsis?

A
FBC
U+Es
LFTs
Lactate
CRP
Blood culture
Urine culture
Sputum culture
Line/wound swab
ABG
Imaging --> CXr, AXr, CAP CT
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8
Q

How is neutropenic sepsis managed?

A

Empirical IV broad spectrum Abx within the hour –> Tazocin or Meropenem
IV fluids –> 0.9% saline 500ml over 1 hour
Catheterise
Escalate to senior

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9
Q

What other longer term management can be given to patients with neutropenic sepsis?

A

Granulocyte Colony Stimulating Factor (GCSF) makes bone marrow produce WBCs

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10
Q

How can neutropenic sepsis be prevented?

A

Patient education
Antibiotic prophylaxis
Decrease dose of further chemotherapy cycles

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11
Q

Describe the pathophysiology of metastatic spinal cord compression

A

Caused by the collapse or compression of a vertebral body that contains metastatic disease or the growth of a primary tumour. This results in compression of the spinal cord.

Over time this leads to vascular injury, cord necrosis and permanent damage .

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12
Q

Which cancers commonly metastasise to bone?

A
Breast
Prostate
Lung 
Myeloma 
Lymphoma
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13
Q

What are the clinical features of metastatic spinal cord compression?

A
Back pain --> radicular, prolonged, exacerbated by straight leg raise, coughing, sneezing or straining. 
 Limb weakness
Sensory loss (dermatomal) 
Bladder and anal sphincter dysfunction
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14
Q

Describe the features of cauda equina

A
Bilateral sciatica 
Impotence
Bladder dysfunction 
Saddle anaesthesia 
Loss of anal tone
Weakness of gluteal muscles
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15
Q

What is the main investigation needed in metastatic spinal cord compression?

A

MRI Spine within 24 hours

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16
Q

How is metastatic spinal cord compression managed conservatively?

A
Bed rest with log-rolling 
Bladder care 
Physiotherapy 
OT 
VTE prophylaxis
17
Q

How is metastatic spinal cord compression managed medically?

A

Dexamethasone 16mg + PPI protection
Analgesia
Laxatives

18
Q

How is metastatic spinal cord compression managed surgically?

A

Surgery –> relieves compression, removes tumour, stabilises spine

19
Q

How is metastatic spinal cord compression managed palliatively?

20
Q

What is the pathophysiology of superior vena cava obstruction?

A

Obstruction of blood through the SVC causing occlusion which leads to reduced venous return to the heart.

21
Q

Give 2 causes of extrinsic superior vena cava obstruction?

A

Right sided lung tumour

Superior mediastinal lymphadenopathy –> lymphoma, thymoma, germ cell tumour

22
Q

Give 2 causes of intrinsic superior vena cava obstruction?

A

Thrombosis
Foreign body (central venous catheter)
Tumour

23
Q

Give 4 features of superior vena cava obstruction

A
Shortness of breath 
Swelling of face, neck and arm 
Choking sensation 
Headache 
Lethargy 
Cough 
Chest pain 
Dysphagia 
Distended neck and chest wall veins
24
Q

What investigations are required in superior vena cava obstruction?

A

Chest x-ray
CT chest with contrast (urgent)
Angiography

25
How is acute superior vena cava obstruction managed?
Sit patient up IV access 100% O2 Dexamethasone 8mg BD
26
How is stable superior vena cava obstruction managed?
Chemotherapy Radiotherapy Stent
27
What cancers are commonly associated with malignant hypercalcaemia?
``` Breast Squamous cell lung cancer Prostate Lymphoma Myeloma Leukaemias ```
28
What are the 3 main pathological mechanisms of malignant hypercalcaemia?
Tumour secretion of parathyroid hormone related peptide Osteolytic metastases with local cytokine release Tumour production of vitamin D metabolites
29
Give some clinical features of malignant hypercalcaemia
``` *Very non-specific* Fatigue Drowsiness Anorexia Dehydration Weakness Depression Seizures Nausea Vomiting Polyuria Postural hypotension Constipation ```
30
What investigations are required in diagnosing malignant hypercalcaemia?
``` FBC U+Es Ca2+ (corrected) PTH/PTHrP Phosphate Myeloma screen ECG ```
31
How is malignant hypercalcaemia managed?
Rehydration --> 0.9% saline 3-6L in 24 hours Monitor U+Es Bisphosphonates --> 30-60 mg Pamidronate IV over 24 hours Treat underlying malignancy
32
Describe the pathophysiology of Tumour Lysis Syndrome
Massive lysis of rapidly proliferating tumour cells resulting in the release of intracellular contents into the circulation. Occurs 3-7 days after chemotherapy
33
What cancers are commonly associated with Tumour Lysis Syndrome?
``` High grade lymphoma ALL Myeloma Germ cell tumour Breast cancer ```
34
Give 5 metabolic abnormalities associated with Tumour Lysis Syndrome
``` Hyperuricemia Hyperkalemia Hyperphosphatemia Hypocalcaemia Hypomagnesaemia ``` Leads to metabolic acidosis
35
What 3 characteristics of a tumour are most likely to predispose to Tumour Lysis Syndrome?
Large tumour Large tumour burden High proliferation rate
36
Give 5 clinical features of Tumour Lysis Syndrome
``` N+V Diarrohea Flank pain Arrythmias Lethargy Confusion Haematuria Syncope Hallucinations Seizures Oedema Oliguria Coma Muscle cramps Heart failure Anorexia ```
37
What investigations will be carried out to diagnose Tumour Lysis Syndrome?
``` FBC U+Es Ca2+ Phosphate Magnesium Urate ABG ECG LDH --> tumour burden assessment ```
38
How is Tumour Lysis Syndrome managed?
Urgent correction of hyperkalaemia (with calcium gluconate, insulin) Monitor fluid balance via U+Es Need for haemodyalysis
39
How is Tumour Lysis Syndrome prevented?
Identify high risk patients early Keep well hydrated Low risk --> allopurinol 300mg PO od High risk --> rasburicase 200 micrograms/kg OD