General Flashcards

1
Q

In the absence of adverse features, regular narrow-complex tachyarrhythmia can be treated with:

A

vagal manouevres or adenosine In the absence of adverse features you should start with vagal manoeuvres: Carotid sinus massage or the Valsalva manoeuvre will terminate up to a quarter of episodes of paroxysmal SVT. An ECG (preferably multi-lead) should be recorded during each manoeuvre. If the rhythm is atrial flutter with 2:1 conduction, slowing of the ventricular response will often occur and reveal flutter waves, if this is the case seek expert help. If vagal manoeuvres do not terminate the arrhythmia or demonstrate underlying atrial flutter consider using adenosine. If vagal manoeuvres have been attempted and the arrhythmia persists (and it is not atrial flutter) give adenosine 6 mg IV as a very rapid bolus. Use a large cannula and a large (e.g. antecubital) vein. Remember to: check for contraindications such as asthma warn the patient that they will feel unwell and experience chest discomfort for a few seconds after the injection record the ECG continuously (preferably multi-lead) during the injection. If the ventricular rate slows transiently, but then speeds up again, look for atrial activity such as atrial flutter (or other atrial tachycardia) and treat accordingly. If there is no response to adenosine 6 mg, give a 12 mg bolus. If there is again no response give one further 12 mg bolus. Lack of response to adenosine will occur if the bolus is given too slowly or into a small peripheral vein.

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2
Q

Hyperkalaemia in cardiac arrest treatement

A
  • give 10 ml 10% calcium chloride IV by rapid bolus injection to antagonise the toxic effects of hyperkalaemia at the myocardial cell membrane
  • sodium bicarbonate: 50 mmol IV by rapid injection (if severe acidosis or renal failure)
  • glucose/insulin: 10 units short-acting insulin and 25 g glucose IV by rapid injection
  • consider haemodialysis: this may be an option for cardiac arrest induced by hyperkalaemia which is resistant to medical treatment. Several dialysis modes have been used safely and effectively in cardiac arrest, but this may only be available in specialist centres that offer acute renal replacement therapy in critically ill patients.
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3
Q

What is this?

A

Mobitz Type II AV block

There is a constant PR interval in the conducted beats but some of the P waves are not conducted (i.e. followed by QRS complexes), in this case producing 2:1 AV block. This may occur randomly, without any consistent pattern. People with Mobitz II AV block have an increased risk of progression to complete AV block and asystole.

2:1 AV block describes the situation in which only alternate P waves are followed by a QRS complex. 2:1 AV block may be due to Mobitz I or Mobitz II AV block and it may be difficult to distinguish which it is from the ECG appearance. If bundle branch block is present (broad QRS complexes) as well as 2:1 block, this is likely to be Mobitz II block.

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4
Q

If tachyarrythmia shows adverse features….

A

Synchronised DC shock (up to 3 attempts) If this does not work give… Amioderone 300mg IV (10-20 mins) Repeat shock Then give amioderone 900mg over 24 hours

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5
Q

Treatment of acute astma

A
  • Oxygen to maintain SpO2 94–98%. (CO2 retention is not usually aggravated by oxygen therapy in asthma).
  • Salbutamol 5mg or terbutaline 10mg via an oxygen-driven nebuliser.
  • Ipratropium bromide 0.5mg via an oxygen-driven nebuliser.
  • Prednisolone oral 40–50mg or hydrocortisone IV 100mg if unable to take oral.
  • No sedatives of any kind.
  • Repeat chest radiograph only if pneumothorax or consolidation are suspected or patient requires mechanical ventilation.

IF LIFE-THREATENING FEATURES ARE PRESENT:

  • Discuss with senior clinician and ICU team.
  • Consider IV magnesium sulphate 1.2–2g infusion over 20 minutes (unless already given).
  • Give nebulised beta2 agonist more frequently e.g. salbutamol 5mg up to every 15–30 minutes or (if special nebuliser available for continuous nebulisation) 10mg/hour.
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6
Q

Acute severe asthma

A

Features of acute severe asthma:

Peak expiratory flow (PEF) 33–50% of best (use % predicted if recent best unknown).

Can’t complete sentences in one breath.

Respiration >25breaths/minute.

Pulse >110beats/minute.

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7
Q

normocarbia

A

(PaCO2 4.7-6.0 kPa)

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8
Q

Life threating asthma

A

Any one of the following, in a patient with severe asthma:

  • Peak flow < 33% best or predicted;
  • Arterial oxygen saturation (SpO2) < 92%;
  • Partial arterial pressure of oxygen (PaO2) < 8 kPa;
  • Normal partial arterial pressure of carbon dioxide (PaCO2) (4.6–6.0 kPa);
  • Silent chest;
  • Cyanosis;
  • Poor respiratory effort;
  • Arrhythmia;
  • Exhaustion;
  • Altered conscious level;
  • Hypotension.

In these patients following senior advise would give amiopylinne. Loading dose is 5mg Kg IV over 20 mins unless already on on maintanace)

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9
Q

Unstable angina and NSTEMI treatment

A
  • Anti-thrombotic Aspirin
  • LMW heparin or fondaparinux
  • platelet inhibitor such as clopidogrel, prasugrel or ticagrelor
  • if very high risk: glycoprotein IIb/IIIa inhibitor
  • Pain relief
    • Nitrate
    • Morphine
  • Oxygen if patient is hypoxic
  • Myocardial protection Beta blocker
  • Coronary angiography/PCI in most patients
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10
Q

Adverse features

A

The following adverse features indicate that a patient is at risk of deterioration either wholly or partly because of their arrhythmia: Shock - features include: hypotension (systolic blood pressure <90 mmHg), pallor, sweating, cold extremities, confusion and impaired consciousness Syncope - transient loss of consciousness because of global reduction in blood flow to the brain Heart failure - features include: pulmonary oedema and/or raised jugular venous pressure (with or without peripheral oedema and liver enlargement) Myocardial ischaemia -features include: typical ischaemic chest pain and/or evidence of myocardial ischaemia on a 12-lead ECG

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11
Q

In patients with adverse features of a bradycardia?

A

Give Atropine 500 mcg IV.

If there is not a satisfactory response, this dose of atropine may be repeated (every 3-5 mins) up to a maximum total doses of 3 mg.

If atropine fails to provide a satisfactory response you should consider transcutaneous pacing. If this is not available immediately options for treatment using other drugs are listed in the algorithm.

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12
Q

Absolute contraindications to fibrinolytic therapy

A
  • Previous haemorrhagic stroke
  • Other stroke or CVA within six months
  • CNS damage or neoplasm
  • Active internal bleeding
  • Aortic dissection
  • Recent major surgery or trauma
  • Known bleeding disorder
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13
Q
A
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14
Q

What is this?

A

Agonal rhythm occurs in dying patients.

It is characterised by the presence of slow, irregular, wide ventricular complexes, often of varying morphology. These are unlikely to produce a pulse.

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15
Q

Which of the following drugs may be used for the treatment of sinus tachycardia?

A

Sinus tachycardia is not an arrhythmia. It is a common physiological response to stimuli such as exercise or anxiety. Do not attempt to treat sinus tachycardia with cardioversion or anti-arrhythmic drugs as treatment is directed at the underlying cause.

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16
Q

When bradycardia is so profound that it causes clinical cardiac arrest

A

percussion pacing may be used in preference to CPR because it may produce an adequate cardiac output with less trauma to the patient.

To perform percussion pacing:

  • With the side of a closed fist deliver repeated firm thumps to the praecordium just lateral to the lower left sternal edge.
  • Raise the hand about 20 cm above the chest for each thump.
  • If initial thumps do not produce a QRS complex try using slightly harder thumps and try moving the point of contact around the praecordium until a site is found that produces repeated ventricular stimulation.

If attempted percussion pacing does not achieve a cardiac output within a few seconds, start CPR.

17
Q

STEMI - further management

A

Anti-thrombotic therapy Beta blocker - (if no asthma - reduces risk of death) ACE inhibitor - (improves likely hood of developing LV failure) Coronary angiography and reperfusion strategies

18
Q

What is this?

A

Mobitz Type I AV block (also called Wenckebach AV block)

The PR interval shows progressive prolongation after each successive P wave until a P wave occurs without a resulting QRS complex. Often the cycle is then repeated.

The need for treatment is dictated by the effect of the arrhythmia on the patient and the risk of developing more severe AV block or asystole.

19
Q

Anaphylaxsis treatment

A

500micrograms IM adrenaline (1:1000),

oxygen, fluids and bronchodilators.

Antihistamines and hydrocortisone are second line drugs.

Chloraphenamine 10mg IM / slow IV

Hydrocortisone 200mg IM / slow IV

20
Q

In a stable patient with a broad-complex tachycardia which one of the following would be the recommended first-line treatment?

A

The appropriate choice is amiodarone 300 mg intravenously over 20-60 min. A 900 mg infusion of amiodarone over 24 h may be used after the initial 300 mg dose

21
Q

Patients with bradicardia who are at risk of asystole

A

recent asytole

mobitz II AV block

Complete Heart Block with broad QRS

Ventricular pause > 3 s

22
Q

Commonest cause of cardiac arrest and sudden cardiac death in adults

A

Coronary artery disease Other causes include structural heart disease and ‘electrical’ abnormalities

23
Q

What is this?

A

First-degree atrioventricular (AV) block is present when the PR interval is > 0.20 s and is a common finding. It represents a delay in conduction through the AV junction (the AV node and immediately adjacent myocardium).

First-degree AV block rarely causes any symptoms and as an isolated finding rarely requires treatment.

The normal PR interval is 0.12-0.20 s (or 3-5 small squares).

24
Q

In AF can treat with:

A

If the aim is to control a patient’s heart rate, the usual drug of choice is a beta blocker. Diltiazem may be used in patients in whom beta blockade is contraindicated (e.g. by asthma) or not tolerated. Digoxin may be used in patients with heart failure. Beta blockers, diltiazem and digoxin should be given orally in the first instance unless the patient has contraindications, is vomiting or is critically unwell. In these circumstances the IV route may be used. If the duration of atrial fibrillation is under 48 hours, and rhythm control is considered the appropriate strategy, chemical cardioversion may be appropriate. Drugs such as flecainide may be used but you should always seek expert help before using it. Do not use flecainide in the presence of heart failure, known left ventricular impairment, ischaemic heart disease, or a prolonged QT interval. Amiodarone (300 mg over 20-60 min followed by 900 mg over 24 h) may be used to attempt chemical cardioversion but is less often effective than drugs like flecainide and takes longer to work. Electrical cardioversion remains an option in this setting and will restore sinus rhythm in more patients than chemical cardioversion.

25
Q

Immediate treatment for all acute coronary syndromes

A
  • ABCDE approach
  • Aspirin 300 mg orally (crush/chew)
  • Nitrate (GTN spray or tablet)
  • Morphine
  • Oxygen if the patient is hypoxic
26
Q

hypoxaemic

A

PaO2 is <10 kPa

27
Q

STEMI (or acute MI with new LBBB) treatment

A
  • Emergency reperfusion therapy:
  • Percutaneous coronary intervention (PCI)
  • Fibrinolytic therapy only if no access to primary PCI Avoid delay - “Time is muscle”.
28
Q

What is this?

A

Third-degree atrioventricular block

Extreme bradycardia may sometimes precede cardiac arrest and this may be prevented by prompt and appropriate treatment.

In third-degree (complete) AV block, there is no relationship between P waves and QRS complexes; atrial and ventricular depolarisation arises independently from separate ‘pacemakers’. The site of the ‘pacemaker’ stimulating the ventricles will determine the ventricular rate and QRS width.

A pacemaker site in the AV node or proximal bundle of His may have an intrinsic rate of 40-50 min-1 or sometimes higher and will have a narrow QRS complex unless additional bundle branch block is present.

A pacemaker site in the distal His-Purkinje fibres or ventricular myocardium will produce broad QRS complexes, often have a rate of 30-40 min-1 or less, and is more likely to stop abruptly, resulting in asystole.

29
Q

Perform synchronised cardioversion

A

For a broad-complex tachycardia or atrial fibrillation, start with a 120-150 J biphasic shock and increase in increments if this fails to a maximum of three attempts. Atrial flutter and regular narrow-complex tachycardia will often be terminated by lower-energy shocks: start with 70-120 J biphasic. For patients who are in atrial fibrillation or atrial flutter, use anteroposterior self-adhesive pad positions when it is practical to do so.

30
Q

Anaphyalaxis is highly likely if all three of the following are present:

A
  1. sudden onset and rapid progression of symptoms
  2. life-threatening airway and/or breathing and/or circulation problems
  3. skin and/or mucosal changes (flushing, urticaria, angioedema).

Exposure to a known allergen for the patient helps to support the diagnosis.

The lack of any consistent clinical manifestation of anaphylaxis + a range of possible presentations can cause diagnostic difficulty. As a result, some patients have been given injections of adrenaline inappropriately for allergic reactions just involving the skin, or for vasovagal reactions or panic attacks.

Taking this information into account, you should admit Mr Jobbs for close observation. Antihistamines are prescribed to be taken if required.

31
Q

tricyclic antidepressant toxicity causes an ECG with:

A

Tachycardia with broad QRS complexes

32
Q

What is this?

A

This shows a 3:1 AV block, which is less common and is usually a form of Mobitz II AV block.

Immediate decisions about treatment of these rhythms will be determined by the effect of the resulting bradycardia on the patient. After identifying and providing any necessary immediate treatment, continue cardiac monitoring and arrange expert cardiological assessment.

33
Q

In a patient with a bradycardia and adverse features, who does not response to atropine:

A

transcutaneous pacing should be considered as an interim measure