C02: Bradycardia Flashcards

1
Q

What HR is considered bradycardia, per BCEHS CPGs?

A

less than 50bpm
if your patient is symptomatic at a rate of 50 or more, consider other causes

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2
Q

What are “symptomatic findings” in the context of bradycardia?

A
  • Use CHADS
  • Chest pain (ischemic)
  • Hypotension
  • Acute heart failure (pulmonary edema)
  • Decresed LOC
  • Shock
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3
Q

What are the two primary goals in the management of symptomatic bradycardia?

A
  1. Optimize hemodynamics!
  2. Identify and treat the underlying cause
    remember: resuscitate before you differentiate!
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4
Q

Describe the most appropriate care for a patient with a HR of 42, orthostatic pre-syncope, and mild dyspnea. All other findings are unremarkable

A
  • Supportive care and transport
  • The patient does not meet CHADS criteria for requiring pre-hospital management of bradycardia (orthostatic pre-syncope is not DLOC, and mild dyspnea is not the same as acute CHF)
  • Investigate for causes of bradycardia and provide ongoing monitoring
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5
Q

Describe the role of atropine in patients with 1st, 2nd, and 3rd degree heart block

A
  • 1st-degree: atropine is the treatment of choice
  • 2nd and 3rd degree: atropine is less likely to be successful, but SHOULD still be attempted if appropriate.
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6
Q

You repond to a patient who presents with DLOC, chest pain, and hypotension. Their HR is 34BPM. While performing your physical exam you note a large surgical scar on their chest, and they inform you they had a heart transplant 3 years previous. Which medication is specifically contraindicated in this patient population?

A

atropine!
Atropine is ineffective and potentially harmful in patients who have had a heart transplant.

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7
Q

You are treating a 120kg patient for symptomatic bradycardia. After adminstering a 0.6mg dose of atropine, you note that their HR is paradoxically slowing and they complain of worsening symptoms. What should you do next?

A

Administer additional atropine! Paradoxical bradycardia is an adverse effect of atropine when given too slowly or in too low of a dose. You should immediately give more atropine to reverse the effect.

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8
Q

What is the preferred pharmacological therapy for patients with symptomatic bradycardia and marked hemodynamic instability? (i.e. they are peri-arrest)

A

Epinephrine
* Consider push-dose epinephrine (10mcg IV push) as a bridge to epinephrine infusion (2-10mcg/minute)

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9
Q

Describe the components and pathophysiology of BRASH syndnrome

A
  • Bradycardia
  • Renal failure
  • AV nodal blockers (CCB or BB)
  • Shock/hypotension
  • Hyperkalemia
  • BRASH syndrome describes a vicious cycle of cascading cardiorenal failure in patients who are taking AV Nodal blockers
  • Bradycardia leads to poor renal perfusion, leading to decresed excretion of potassium and worsening bradycardia.
  • AV Nodal blockers inhibit normal compensation, and synergize with increased potassium, leading to worsening shock, decreased renal perfusion, and a positive feedback loop culminating in death
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10
Q

Describe common, field-reversible causes of bradycardia

A
  • Remember this or your patients will D.I.E.
  • Drugs (CCBs, B-blockers, Digoxin, Amiodarone)
  • Ischemia (Especially Inferior or RV infarct)
  • Electrolytes (hyperkalemia)
  • Also consider hypoxia and increased vagal tone, especially in pediatric patients
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11
Q

Should you correct bradycardia in a patient with signs of myocardial infarction?

A
  • Only if they are significantly hypotensive (i.e. peri-arrest)
  • In the setting of myocardial infarction, bradycardia is often compensatory and somewhat beneficial. Be cautious of initiating rate-specific therapies as these may increase myocardial oxygen demand and extend the margins of infarct.
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12
Q

Describe atropine dosing in symptomatic bradycardia

A
  • 0.6mg IV/IO push. Repeat PRN to a maximum dose of 0.04mg/kg (approx. 3mg in most patients)
  • Be sure to give as a RAPID push. If paradoxical bradycardia develops, give additional atropine
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13
Q

What three pharmacological interventions are indicated specifcally in the setting of hyperkalemia? Include dosages

A
  • Calcium Chloride: 1g IV push, may repeat at 5 minute intervals
  • Sodium Bicarbonate: 1 mEq/kg IV/IO slow push. May repeat 0.5 mEq/kg IV/IO slow push every 10-15 minutes as required
  • Salbutamol: 10-20mg via nebulizer or 400mcg via MDI PRN
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14
Q

Describe how epinephrine is given as an infusion for symptomatic bradycardia (i.e. what is the indication, how is it prepared, what equipment is used, what are the drip rates)

A
  • Used in settings of symptomatic bradycardia refractory to atropine or in peri-arrest settings
  • 2-10mcg/minute infusion
  • add 1mg epinephrine to a 250mL bag with a 60gtts/mL drip set. 1gtt/second = 4mcg/minute (adjust accordingly, so 1gtt/2sec=2mcg/mL, etc.)
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15
Q

Which electrodes must be placed on a patient prior to initiating transcutaneous pacing?

A
  • The limb leads
  • Therapy electrodes (the “pads”)
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16
Q

What is appropriate positioning of the therapy electrodes for transcutaneous pacing?

A

either anterolateral or anterior-posterior is acceptable

17
Q

What is the preferred agent for sedation when providing transcutaneous pacing?

A

ketamine (0.1-0.5mg/kg IV/IO)

18
Q

What steps can be taken to confirm the effectiveness of transcutaneous pacing?

A
  • identification of electrical capture
  • identification of mechanical capture (palpate a pulse)
  • positive waveform on the SpO2 pleth
  • Improvement in blood pressure
19
Q

Does the LP15 default to demand pacing, continuous pacing, or overdrive pacing?

A

demand pacing

20
Q

What is the indication for transcutaneous pacing in bradycardic patients?

A

Symptomatic bradycardia unresponsive to atropine and epinephrine infusions
attempt pharmacological inteventions FIRST

21
Q

You respond to a patient with DLOC and bradycardia. On assessment, you find them to be GCS=E3V4M6, BP=108/60, SpO2=97%, skin is cool and dry. You obtain the following 12-lead ecg. Describe management for this patient.

A
  • This is a symptomatic bradycardia in context of 3rd degree AV block. The patient is symptomatic with signs of instability, but does not appear peri-arrest.
  • First-line treatment is atropine, which should be attempted even if it has a low chance of success in 3rd-degree block.
  • Epinephrine infusion may be attempted if patient is refractory to atropine.
  • If patient does not respond to epinephrine infusion, consider procedural sedation and transcutaneous pacing.
  • As with all cases of bradycardia, investigate and treat causes
22
Q

You respond to a 72YO patient with DLOC. On arrival you find them to be GCS=E2V3M5, BP=68/40, HR=29BPM, SpO2=91% RA with poor pleth. Skin is ashen and diaphoretic. The patient has a history of HTN and palpitations, and was recently prescribed amiodarone for management of atrial fibrillation with RVR. What is the likely cause of their symptoms?

A

BRASH syndrome

23
Q

You respond to a 72YO patient with DLOC. On arrival you find them to be GCS=E2V3M5, BP=68/40, HR=29BPM, SpO2=91% RA with poor pleth. Skin is ashen and diaphoretic. The patient has a history of HTN and palpitations, and was recently prescribed amiodarone for management of atrial fibrillation with RVR.

How should you treat this patient?

A
  • This patient is peri-arrest! They are likely experiencing BRASH syndrome and will continue to decline without imminent intervention
  • Epinephrine is the first line therapy. Consider push-dose epinephrine as a bridge to an epinephrine infusion
  • If the patient is refractory to epinephrine, begin transcutaneous pacing (consider PSA first)
  • Acquire a 12-lead ecg. If ECG changes consistent with hyperkalemia are present, consider calcium chloride, sodium bicarbonate, and salbutamol.