onco emergencies Flashcards
tumour lysis syndrome
rapid lysis of tumour cells releases intracellular components
results in Hyperuricemia Hyperkalemia Hyperphosphatemia AKI (uric acid and/or calcium phosphate crystals in the renal tubules) Hypocalcemia
RFs tumor types
patient specific RFs
for tumor lysis syndrome
o Large tumour burden o Extensive marrow involvement o ALL o Burkitt lymphoma o High chemosensitivity o High proliferation rate
pt specific RFS o Renal impairment Pretreatment hyperuricaemia Hypovolemia/ Pretreatment diuretic use Pretreatment LDH high Urinary tract obstruction from tumor o Pre-existing metabolic abnormalities are associated with TLS
Sx and signs of tumour lysis
present 3-7 days post chemo Symptoms o Nausea o Diarrhoea o Anorexia o Lethargy o Seizures o Altered mental status o Muscle cramps
Signs o Fluid overload o Haematuria o Tetany & paraesthesia o Weakness o Bronchospasm o Arrhythmias Peaked T waves, QTc derangement Primary presentation of malignancy ‘Spontaneous tumor lysis’ o AKI
Ix for TLS
Urea and electrolytes Metabolic abnormalities: Hyperkalaemia, Hyperphosphatemia, Hyperuricaemia, Hypocalcaemia o Urine dip followed by MC&S o Full blood count o Serum lactate o Basic metabolic panel o Phosphorus o High Lactate dehydrogenase o ECG
define neutropenic sepsis
responsible pathogens
Patient undergoing systemic anticancer treatment (SACT)
Temp >38
Neutrophil count < 0.5 x 10 9 per litre or lower
- reaches its lowest level 5 to 10 days after the last dose of chemotherapy
gram +ve cocci; indwelling plastic catheters promote colonisation
- staph aureus, staph epidermidis, enterococcus and streptococcus
fungal candida
Sx of neutropenic sepsis
signs
Fever Symptoms related to a specific system cough, shortness of breath Drowsy Confused
signs - Febrile Tachycardic and hypotensive Drowsy Impaired MMSE Signs of infection? Don’t forget: Hickmann/Picc Line Skin wounds/ soft tissue Mouth
Ix of neutropenic sepsis
Blood tests: FBC (with differential) U&Es/Renal profile LFTs (including albumin) Lactate CRP
Cultures:
- Blood – central and peripheral
- Urine
Swabs:
Lines
Wounds
ABG
imaging
CXR
AXR
CT/MRI
DDx
malig related fever
chemo related fever
PE
Mx of neutropenic sepsis
- empirical IV ABx within one hour
- > TAZOCIN
- fluid resuscitation
- consider catheterisation
- if risk is low switch to oral ABx
- GCSF on profoundly septic/neutropenic
pathophysiology of malignant spinal cord compression
Usually caused by the collapse or compression of a vertebral
body that contains metastatic disease (arterial seeding)
10% by direct tumour (paraspinal mass) extension into the
vertebral column
Compression of cord initially causes oedema, venous congestion
and demyelination which are reversible
Prolonged compression vascular injury, cord necrosis and
permanent damage
BLT and kosher pickle
Ix
MRI whole spine
signs and Sx of malignant spinal cord compression
back pain first and prolonged spinal or radicular pain - exarcerbated by straight leg raising, coughing, sneezing or straining - limb weakness - sensory level - bladder and anal sphincter dysfunction diminishing performance status
examination of MSCC
- Acute onset; flaccid paralysis
Progressing over time - Spasticity (increased tone, clonus and hyperreflexia in limbs below
level of MSCC
Plantar reflexes up going (not cauda equina)
Sensory loss with well defined dermatonal level
Palpable bladder (urinary retention)
Ix full spinal MRI
if a pt comes with MSCC
Local pathway for rapid diagnosis, treatment,
rehabilitation and on-going care
Educate high risk patients
Pain suggestive of spinal mets; MRI within 1 week
Signs MSCC; MRI within 24 hours
Admit
Bed rest with log-rolling
Dexamethasone 16mg + PPI (unless ?lymphoma)
Adequate analgesia
Treatment within 24 hours of diagnosis
Mx of MSCC
Steroids improve functional outcome stat dex 16mg then 8mg BD til the imaging
> 48hr no motor function; best supportive care, 1# RT for pain
SURGERY - relieves compression, removes tumour, stabilises spine
- Continence preserved
- Reduced pain
- Greater degree of mobility
preserved
Treatment of choice if fit and good prognosis (>3/12)
balloon kyphoplasty
Good nursing care; care re pressure areas Analgesia Laxatives Bladder care Monitor BMs VTE prophylaxis Physiotherapy Occupational therapy
prognostic indicators of MSCC
Multiple myeloma, lymphoma, or breast, prostate or renal cancers Good motor function at presentation Good performance status Limited comorbidity Single-level spinal disease Absence of visceral metastasis Long interval from primary diagnosis Also for biopsy or stabilisation
Radiotherapy for MSCC
- Majority (extensive disease and poor physiological
reserve)
Delivered within 24 hour of confirmation
Relieves compression of the spine and nerve roots by causing cell death in the rapidly dividing tumour tissue
Relieves pain
Stabilises neurological deficit
Life expectancy often measured in months
what is SVCO
- Obstruction of blood flow through the SVC
Compression or occlusion of SVC
causes SCLC/lymphoma lymphoma post RT fibrosis TB
symptoms and signs of SVCO
Sx - Breathlessness (50%) Swelling of face and neck (40%) Trunk and arm swelling Headache - worse in the mornings - visual disturbance - Hallucinations - pulseless jugular venous distension A sensation of choking A feeling of head fullness
Lethargy Chest pain Cough Dysphagia Cognitive dysfunction
Seizures
Signs Thoracic vein distension (65%) Neck vein distension (55%) Facial oedema (55%) Increased RR (40%) Plethora 15% Cyanosis 15% Arm oedema 10% Advanced stages Laryngeal stridor Drowsy Coma and death
Ix of SVCO
Mx
URGENT CXR - mass - mediastinum or mass lesion in the lung CT with contrast Extensive collateralization Intraluminal thrombus of SVC Evidence of extrinsic compression
Mx
initial -> sit pt up -> OXYGEN & stat dose of dexamethasone steroids
acute stent - if not radio or chemo sensitive
chemotherapy - used for SCLC lymphoma and teratoma
radiotherapy
hypercalcaemia
- Most common in SCC (lung, H&N, kidney, cervix)
Also seen in breast cancer and multiple myeloma
Tumour secretion parathyroid hormone-related peptide (PTHrP)
(80%) increased bone resorption and renal reabsorption
prognosis Most patients who develop hypercalcaemia have disseminated disease Many die in < 3/12 52 days for solid organ malignancy 362 days for haematological malignancy
features of hypercalcaemia
Ix
Mx
nausea and vomiting, anorexia
thirst
polydipsia, polyuria, lethargy, renal failure, acute pancreatitis
bone pain, abdominal pain, constipation, confusion and weakness.
ECG - short QT interval
Ix
ionised calcium
Mx
rehydration
Rehydration first: at least 24 hours of normal saline
Bisphosphonates:
e.g. 60-90mg pamidronate IV or IV zolendronic acid 4mg SYMPTOMATIC SEVERE
Can cause renal failure so must make sure properly
rehydrated first
Takes up to a week to work
(Denosumab 120mg SC for refractory hypercalcaemia)
Systemic treatment of malignancy
Mx of tumour lysis
o Hydration
Dextrose containing IV fluids at twice the maintenance rate. Keep urine-specific gravity <1.010 and urine output >100 mL/m2/hr.
o Hyperkalaemia- check ECG
IV calcium gluconate, insulin/dextrose infusion and nebulised salbutamol. Cardiac monitoring advised on this
o Hyperphosphatemia
Dietary restriction. Phosphate binders may be used. In severe cases, patients may require hemofiltration
o Hyperuricaemia
Allopurinol inhibits xanthine oxidase to prevent formation of uric acid and should only be given PO.
Rasburicase (synthetic uricase) concerts uric acid to more soluble allantoin. Use in high risk especially if uric acid >7.5 mg/dl. Don’t use if know G6PD as may result in methemoglobinemia
o Monitor potassium, calcium, phosphorus, uric acid and urinalysis closely
o Prophylaxis
May take the form of oral hydration, IV hydration, allopurinol and rasburicase
o Haemofiltration
Intractable fluid overload
Refractory hyperkalaemia
Hyperphosphataemia-induced symptomatic hypocalcaemia
High calcium-phosphate product
what is leukostasis
high white cell count, respiratory failure, intracranial haemorrhage and early death
occurs in pts with AML and ALL
high fever and papilloedema? retinal vein bulging, retinal haemorrhage and focal neurological deficits
thrombocytopenia
Mx of leukostasis
Rapid cytoreduction is the initial treatment, ideally with induction chemotherapy, which can dramatically reduce the white cell count within 24 hours.
prophylaxis with allopurinol or raburicase high risk of tumour lysis syndrome
SIADH
tumor cellls may secrete ADH esp small cell lung cancer
pt present with hyponatraemia
asymptomatic may cause
Depression and lethargy.
Irritability and other behavioural changes.
Muscle cramps.
Seizures.
Depressed consciousness leading to coma.
Neurological signs (such as impaired deep tendon reflexes and pseudobulbar palsy).