sudden death Flashcards

(56 cards)

1
Q

what is sudden death

A

natural, rapid, unexpected

not trauma, toxicity, poison or chronic illness

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2
Q

causes of sudden death

A

heart +/- vessels
non cardiac vessels (eg stroke or aneurysm)
pulmonary system (PE)
CNS (rare seizures in epilepsy)

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3
Q

what is sudden cardiac death

A

sudden death due to cardiovascular/coronary vessels

most due to arrhythmias

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4
Q

what are the direct causes of sudden cardiac death

A

coronary obstruction
infarct
embolism
arrhythmia/dysrhythmia

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5
Q

what disorders lead to risks for sudden cardiac death

A

CHD/ low LVEF
structural heart disease-also dev/genetic structural pathologies
primary arrhythmia

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6
Q

what is a cardiac arrest

A

a sudden stop in effective blood circulation due to failure of the heart to contract effectively or at all

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7
Q

is a cardiac arrest the same as a MI or HF

A

No
Can result from AMI (blood flow to heart muscle impaired)
AMI - heart cont pumping but less effectively
HF - circulation substandard, still pumping and sustaining life

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8
Q

what is arrhythmia and dysrhythmia

A

same thing - a variation in the normal beating pattern or rhythm of the heart
usually due to disorganisation of electrical signals running through the heart
can be fast, slow, abnormal

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9
Q

what are the electrical causes of arrhythmia

A

primary or arrhythmogenic.
ion channels and electrical issues at cellular level
extra conduction pathways at the organ level

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10
Q

what are the structural causes of arrhythmia

A

unusual shape or size of cardiac tissue so changes signal pathway, can lead to delays that interfere with conduction cycle

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11
Q

what are the ischaemic causes of arrhythmia

A

hypoxia makes heart tissue electrically unstable

effectively changes signal pathway, leading to delays interfering with conduction cycle

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12
Q

what are the causes of primary arrhythmia

A
unstable myocardium (damage, hypoxia eg AF)
Ion channels (channelopathies, long QT syndrome)
Accessory conduction pathways
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13
Q

what is cardiomyopathy

A

heart size, shape or thickness is (structure and function) abnormal (not CAD, hypertension, heart valves and HD present at birth)

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14
Q

what are the consequences of cardiomyopathy

A

risk of pumping dysfunction or low output HF

conduction abnormalities

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15
Q

what are the types of cardiomyopathy

A

dilated (eccentric)

hypertrophic (concentric)

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16
Q

what developmental defect is associated with a higher risk of sudden death

A

tetralogy of fallot

associated with higher risk even after childhood surgery

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17
Q

what do you need to have for an arrhythmia

A

trigger and substrate

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18
Q

what is a trigger

A

brief event required to initiate a period of arrhythmia
precipitating event
eg extrasystole or atrial flutter (extra firing)

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19
Q

what is a substrate

A

ongoing, underlying tissue instability that increases triggers or allows for maintenance/amplifications of dysrhythmias

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20
Q

what can substrates be

A

predisposing factor
electrical (eg genetic or pharmacological issues with ion channels or electrolytes) or structural defect (eg fibrosis or inflammation caused by IHD)

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21
Q

what is a R on T (ECG phenomenon)

A

type of potential trigger for arrhythmias
on ECG - premature QRS on previous T wave
T wave is a vulnerable period (repolarisation of ventricular AP, refractory period ending)
Resulting QRS= premature ventricular contraction

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22
Q

what is a pacemaker

A

implanted electronic device - electrodes to stimulate heart
consistently applies impulses for each heart beat
mostly used for bradyarrhythmias and heart block

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23
Q

what is an Implantable Cardioverter Defibrillator (ICD)

A

same as pacemaker but only applies electrical impulses when V arrhythmias detected to protect from fast or uncontrolled rhythms

24
Q

what are indications for implanting an ICD

A

cardiac arrest due to ventricular fibrillation
symptomatic HF with low LVEF (LOHF after MI)
cardiomyopathies - eg dilated
congenital
channelopathies

25
what are antiarrhythmic drugs
usually affect ion channel activity or sympathetic drive eg amiodarone, beta blockers, digoxin for AF mostly for supraventricular arrhythmias (atria or AV node)
26
what is reperfusion injury
tissue damage caused when blood supply returns to the tissue after a period of ischaemia or hypoxia can lead to electrical irregularities & risk
27
what causes reperfusion injury
the restoration of circulation results in inflammation and oxidative damage
28
what are preventative treatments for reperfusion injury
cooling immunosuppression oxygen radical scavengers
29
how can syncope be distinguished from seizure
both loss of consciousness may have no symptoms when not occurring Syncope registered by Holter monitor (24 hr ECG) Seizure registered by EEG (brain imaging is also important) seizures associated with stiffness/unusual posture seizures tip and syncope crumple convulsive syncope can feature both
30
what is vasovagal syncope
``` Vagal increase (& symp decrease) - vasodilatation and low heart rate Triggered centrally (ie brain) not at level of heart most common form of syncope, common in young adults and is recurrent ```
31
what is exertion syncope
Neurocardiogenic origin | Benign
32
what is index case
the initial patient in the population of an epidemiological investigation
33
what is the proband
In medical genetics, the index case is the case of the original patient that stimulates investigation of other members of the family
34
what is the number needed to treat
Statistical measurement of the impact of a medicine or therapy Average number of patients who need to be treated to prevent one additional bad outcome 
35
can arrhythmia be detected
genetic screening
36
what is penetrance
proportion of individuals carrying a particular variant (or allele) of a gene that also expresses an associated trait (the phenotype)
37
what is incomplete or reduced penetrance
do not express trait even though they carry the allele channelopathies can vary from patient to patient phenotypes of disease can differ most diseases are polygenic
38
what is the epidemiology of sudden cardiac death
50% all cardiac death more male peak 45-75y/o majority related to coronary disease
39
what are the mechanisms of arrhythmias
``` substrate (structure or elec) ectopic activity (early after depolarisation, short coupling interval, delayed after depolarisation) re-entry wave break ```
40
what is re-entry
reconduction through an area of unidirectional conduction block circuit larger, refractory period abnormal, zone of slow conduction - allow for repolarisation
41
how can IHD contribute to arrhythmias
acute ischaemia | ventricular remodelling - scar formation, myocardial fibrous, coupling, dilatation, poor function
42
how does an infarction affect the heart
zone of infarction to injury to ischaemia which spreads
43
what can cause dilated cardiomyopathy
``` idiopathic viral alcohol drugs autoimmune ```
44
what is the pathophysiology of dilated cardiomyopathy
``` myocardial fibrosis neurohumoral activation increased sympathetic tone electrolyte disturbances = ectopy, re-entry, VT/VF ```
45
what is hypertrophic cardiomyopathy
most common cause of SCD in young athletes autosomal dominant, incomplete penetrance mutation of cardiac muscle sarcomere genes commonly beta-myosin or troponin-T LV outflow obstruction, anterior motion of mitral valve, asymmetrical septal hypertrophy
46
what are symptoms of hypertrophic cardiomyopathy
``` asymptomatic exertion chest pain/dyspnoea exertion syncope palpitations mechanism of SCD unclear ```
47
what is arrhythmogenic RV cardiomyopathy
30-50% familial multi-genomic replace RV myocardium with fibro-fatty tissue RV hypertrophy and dilation VT/VF due to re-entry around interstitial fibrosis
48
what are the symptoms of ARVC
asymptomatic exertional syncope atrial arrhythmias common epsilon wave on ECG
49
what are other structural causes of SCD
aortic stenosis mitral stenosis mitral valve prolapse congenital heart disease (anomalous coronary arteries, Epstein's anomaly, complex like tetralogy)
50
what are primary arrhythmias
non ischaemic structurally normal heart syndromes include - long QT, WPW, Brugada, primary VT/VF
51
what is WPW
``` Wolff-Parkinson-White accessory pathway from atria to ventricle atrial arrhythmia ventricular pre-excitation VTVF clues on resting ECG ```
52
what is Brugada
``` channelopathy mostly SCN5A - fast-type sodium channel reduce conduction velocities particularly affects RVOT prone to VT arising from RVOT ```
53
How can SCD be treated
identify those at risk preventative treatment - underlying cause, avoid precipitants, anti-arrhythmic meds, ICDs family screening if appropriate
54
what are the types of ICDs
S-ICD - subcutaneous, on breastbone | Transverse ICD - intravascular, tip of lead in contact with right V
55
how are patients selected for an ICD
``` Cardiac arrest survivors VT with haemodynamic compromise high risk - CAD, poor LV function, broad QRS Some HCM, long QT, Brugada, ARVC Congenital HD ```
56
What are ICD indications for HCM
``` survived cardiac arrest one or more of VF/spontaneous sustained VT Unexplained syncope LV wall thickness over 30mm spontaneous NSVT abnormal exercise BP family history of premature sudden death ```