S1E13: Hypertensive Emergencies - MISC
We’re back and this time, we’re turning the tables around and offering some tips and tricks to the youth!
Mohammed is joined by Barry and Karl, and they have gone back to school to re-live the trauma of final med exams while exploring hypertensive emergencies.
Those three need to be kept in check, so thankfully our Adult in the Room Dr Emer Kidney is on the case!
Dr Una Kennedy joins us again and sits down with Deirdre for a chat about looking after our wellbeing around exam time.
Callum is back with another great instalment of The Echo Chamber, where he chats with a future star of EM, Natalie Krakoski.
Right, let’s get to it!
Hypertensive Emergencies
Hypertension is a common referral to the ED. The most important role for the ED physician is to out-rule a hypertensive emergency.
Definitions
A hypertensive emergency is defined as a marked elevation in blood pressure associated with end-organ damage.
This may be indicated by a diastolic BP >125mmHg or hypertension with end-organ dysfunction.
What do we mean by end-organ dysfunction?
Hypertensive encephalopathy
Intracranial haemorrhage
Myocardial ischaemia/infarction
Aortic dissection
Acute heart failure
Eclampsia
Acute renal failure
Causes
Essential hypertension (most cases)
Secondary causes
Drugs
Cocaine
Amphetamines
CNS
Ischaemic or haemorrhagic stroke
Endocrinopathies
Hyperaldosteronism
Cushing’s syndrome
Hyperthyroidism
Phaeochromocytoma
Cardiac
Ischaemia
Renovascular
Renal artery stenosis
Aortic dissection
Non-compliance with anti-hypertensives
Investigations
Blood pressure!
Urinalysis - haematuria, proteinuria
Beta HCG (pre-eclampsia, eclampsia)
CXR
Pulmonary oedema,
Widened mediastinum
Cardiomegaly
ECG
Left ventricular hypertrophy
Ischaemia
Bloods
FBC and blood film
Microangiopathic haemolytic anaemia
Routine clinical chemistry (renal profile)
Glomerulonephritis
Nephrotic syndrome
Specific aetiologies need specific investigations!
CT Brain
Haemorrhage
Encephalopathy
PRES (Posterior Reversible Encephalopathy Syndrome)
Oedema (but MRI is more sensitive!)
POCUS in Hypertension
Lungs
Pulmonary oedema
Heart
Pericardial effusion
Dissection flap
Apical four chamber and suprasternal views needed
Aorta
Dissection flap
Renal arteries (if proficient!)
Eyes
Papilloedema
Management
The management of hypertension in the emergency department is somewhat controversial but here are the key take-home points. Firstly, don’t drop the blood pressure by too much too quickly. Aim for a reduction in blood pressure of 10-20% in the first hour. Beware of goose-chasing though. Don’t go chasing an arbitrary endpoint otherwise you risk causing harm to the patient!
If you remember nothing else as emergency medicine colleagues, medical students, interns or otherwise
DON’T USE AMLODIPINE!!!
Onset of action 6-12 hours
Tendency to prescribe another agent or another dose when it doesn’t work quickly which leads to dose stacking
Subsequent drastic reduction in blood pressure can cause huge harm including the possibility of a stroke
Bottom line: Do not treat hypertension in the emergency department in the absence of end-organ dysfunction - aim for slow reduction with the patient’s GP
Buuuuttttt….. that’s a lot of “Don’ts”, let’s move on to the “Do’s,” shall we?
Labetalol
Agent of choice
Beta-blocker, with selective alpha blocking properties
GTN
Venodilation vs arterial dilatation
Rapid onset and offset
Increases coronary flow - excellent in cardiac ischaemia and also commonly used in stroke with hypertension
May cause tachycardia
Sodium Nitroprusside
Short half-life (1-2 minutes)
Arterial dilatation vs venous
Rapid onset and offset
Adverse outcomes
Cyanide toxicity
Tachycardia
Coronary steal syndrome - promotes myocardial ischaemia
Can increase intracranial pressure
Phentolamine
Alpha blocker
Catecholamine-induced hypertension
Phaeochromocytoma
Ah the wonderful phaeochromocytoma… a solid option for every MCQ answer. But in truth, what is it?
A phaeochromocytoma is a tumour of the adrenal glands. In 85-90% of cases, these tumours are benign in nature.
Epidemiology
Usually affects 30-50yr olds
10% found in children
Rare: 0.05% of general population, 0.1-0.6% in hypertensive patients
Can affect all ages
1 in 3 can be genetic
Von Hippel-Lindau disease
Neurofibromatosis (I)
MEN type 2
Hereditary paraganglioma syndrome
Rule of 10’s
~10% are extra-adrenal
~10% are bilateral
~10% are malignant
~10% are found in children
~10% are familial
~10% are not associated with hypertension
~10% contain calcification
Presentation
Signs and Symptoms
Hypertension
Constipation
Dizziness
Nausea
Tremors
SOB
Palpitations
Headache
Pallor
Sweating
Abdominal pain
Vomiting
Weight loss
Anxiety
Pathophysiology
Catecholamine-secreting tumour
Derived from chromaffin cells
Triggers
Manual pressure
Massage
Beta-blockers
Physical activity
Emotional stress
Childbirth
Tyramine-rich foods (cheese, red wine, chocolate)
Diagnosis
The work-up for a phaeochromocytoma is extensive. We’ve popped a link to An Endocrine Society Clinical Practice Guideline published in the Journal of Clinical Endocrinology and Metabolism in 2014 for you to explore it further.
But pardon the pun… ESSENTIALLY
Biochemistry
Plasma free metanephrines
Urinary fractionated metanephrines (24hour collection)
Metanephrine is a metabolite of adrenaline and noradrenaline
Radiology
CT initially
MR more suitable for metastatic disease
Genetic testing
Recommended in all patients
Management
Symptomatic management of any end organ dysfunction
Removal of causative mass
Important to optimise patient’s physiology prior to surgery (alpha blockade)