Cardiology Flashcards

(79 cards)

1
Q

Cardiac Causes of Clubbing

A

Subacute infective endocarditis

Cyanotic congenital heart disease

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2
Q

Outline causes of left sided heart failure

A

HTN (most common)
IHD
Cardiomyopathy
Myocarditis
Valvular disorders e.g. aortic stenosis

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3
Q

What is Congestive Cardiac Failure?

A

When there is evidence of biventricular failure (both RVF and LVF)

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4
Q

NYHA Classification of Heart Failure

A

I = No effect on normal activities

II = Can walk 100m on flat without SoB

III = SoB on minimal exertion, normal at rest

IV = SoB at rest

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5
Q

Management of Heart Failure

A

CONSERVATIVE
- MDT approach, heart failure team
- Exercise training
- Modifiable risk factors (CVD) e.g. stop smoking

MEDICAL
- Diuretics
- ACEIs/ARBS (affect prognosis)
- Beta blockers
- K+-sparing diuretics if NYHA > III
- Digoxin
- Entresto (sacubitril-valsartan) if NYHA III/IV with reduced ejection fraction already on ACEI/ARB

SURGICAL/INTERVENTIONAL
- Biventricular pacing
—- Indicated if wide QRS and LVEF<35%

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6
Q

What is S1?

A

Sound of mitral and tricuspid valves closing

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7
Q

What is S2?

A

Sound of aortic and pulmonary valves closing

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8
Q

Differentials for a systolic murmur

A

Aortic stenosis (Ejection systolic)
Mitral regurgitation (Pansystolic)
— Mitral Valve prolapse (mid click or late systolic)
Pulmonary stenosis
Tricuspid stenosis
ASD
VSD (pansystolic)
HOCM (ejection systolic)

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9
Q

Differentials for a Diastolic Murmur

A

Aortic regurgitation (early)
Mitral Stenosis (mid-diastolic)
Pulmonary regurgitation
Tricuspid Stenosis

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10
Q

Which murmurs are loudest during inspiration?

A

Right sided murmurs (Tricuspid and pulmonary) due to increased blood flow across these valves during inspiration (increased venous return)

{RILE = Right Inspiration, Left Expiration}

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11
Q

Outline the pros and cons of Biological vs Mechanical Valves

A

BIOLOGICAL
- Usually bovine/porcine
- Do NOT require anticoagulation long term
- Higher risk of structural deterioration over time (esp aortic valves)
- Usually offered to older patients
—– AV >65, MV > 70

MECHANICAL
- More durable
- Low failure rate
- Require long term anticoagulation
- Valve of choice in <60s

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12
Q

Outline the INR targets for metallic valves

A

Aortic - INR 2.0-3.0

Mitral - INR 2.5-3.5

Multiple Valves - INR 2.5-3.5

Concurrent AF - INR 2.5-3.5

{MV requires higher INR target as associated with increased thromboembolism risk - ?due to lower flow rates across MV compared to AV}

RIGHT SIDED VALVES DO NOT GET MECHANICAL VALVES

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13
Q

Causes of Aortic Stenosis

A

Degenerative calcific aortic valve (common in elderly)
Congenital bicuspid valve
Rheumatic heart disease

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14
Q

Features of Aortic Stenosis

A

Syncope
Angina (due to reduced diastolic coronary perfusion time)
Dyspnoea

Slow-rising pulse (anacrotic)
Narrow pulse pressure
Ejection systolic, radiating to carotids, loudest in expiration

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15
Q

Features of Severe Aortic Stenosis

A

Soft/absent S2
Syncope
Slow-rising pulse
Quieter the murmur, the more severe

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16
Q

Potential complications of Aortic Stenosis

A

Concurrent mitral regurgitation
Heart failure
Infective endocarditis
Injury due to syncope
AV block (due to invasion of calcium from valve into His-Purkinje system)

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17
Q

Echocardiogram features of Aortic Stenosis

A

Valve area < 1.5cm2
- SEVERE if <1cm

Pressure gradient across valve > 20
- SEVERE if >40mmHg

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18
Q

Outline how you would investigate a patient with a new murmur?

A

ABCDE

Set of observations
ECG

Bloods
- Routine (FBC, U&Es, LFTs, inflam)

CXR
- Exclude features of heart failure

Echocardiogram (Key investigation)
- Investigating for valve disorder

Coronary angiogram
- Exclude coronary artery disease; if present, could undergo CABG at same time as valve repair/replacement

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19
Q

Indications for Surgical Intervention for Aortic Stenosis

A

Symptomatic AS

Asymptomatic and gradient >40mmHg AND….
- Evidence of LVSD (EF<45%)
- Valve area < 0.6
- LVH > 15mm
- Abnormal exercise response e.g. hypotension during exercise
- Ventricular tachycardias

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20
Q

How often should asymptomatic patients with mild-moderate AS be followed up?

A

6-12 monthly follow up with echocardiograms

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21
Q

What is a TAVI?

A

Transcatheter Aortic Valve Implantation

This is a surgical intervention for Aortic Stenosis

Indicated for patients with severe AS who are:
>75 years old
<75 years old but not a candidate for open heart surgery (e.g. due to pulmonary HTN, severe LVSD)

CONTRAINDICATED IF:
- Evidence of Peripheral vascular disease (access issue)
- Evidence of severe coronary artery disease

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22
Q

Potential Complications of TAVI procedure

A

Failure
Conduction abnormality - may require PPM
Damage to vasculature/surrounding structures
Stroke
MI

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23
Q

What is Heydes Disease?

A

Association between Aortic Valve Stenosis & Angiodysplasia (particularly colonic)

Mild form of von Willebrand disease due to sheer stresses around aortic valve = increase in vW factor breakdown

= consider in patients with SoBOE, anaemia and ejection systolic murmur

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24
Q

Outline the differences between Aortic Stenosis and Aortic Sclerosis

A

STENOSIS
= valve narrowing
- ECG may show LVH
- Ejection systolic murmur, radiating to carotids

SCLEROSIS
= valve thickening
- Usually normal ECG
- Ejection systolic murmur, non radiating

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25
Outline some causes of Aortic Regurgitation
Bicuspid AV Ankylosing Spondylitis (and other seronegative arthropathies) Luetic heart disease (syphilis) Dissection Rheumatic heart disease Infective endocarditis Connective Tissues Disease e.g. Marfan's, Pseudoxanthoma Elasticum {Usually due to disease of AV cusps or aortic root dilatation}
26
Features of Aortic Regurgitation
Fatigue Angina Dyspnoea Wide pulse pressure Collapsing pulse Early diastolic murmur, increased on expiration and on leaning forwards
27
Eponymous Signs of Aortic Regurgitation
Austin Flint Murmur - Mid-diastolic murmur (due to partial closure of anterior MV cusps in severe AR) Corrigan's Pulse - visible distension and collapse of the bilateral carotid arteries - A.k.a collapsing pulse De Musset Sign - Head bobbing with each heart beat Mueller Sign - Pulsatile Uvula Quincke Sign - Exaggerated capillary pulsation of nail bed Traube Sign - "Pistol shot" noise over femoral artery Waterhammer Pulse - Collapsing pulse (e.g. radial)
28
Causes of a Collapsing Pulse
Aortic Regurgitation PDA Hyperkinetic states e.g. anaemia, exercise, thyrotoxicosis
29
Features of Severe AR
Wide pulse pressure Short murmur - this is a sign of increase volume of regurgitant blood (tap running as opposed to bucket of water being turned upside down) Features of left ventricular failure
30
Indications for surgical intervention for Aortic Regurgitation
Symptomatic AR Dilated heart EF<50% Regurgitant fraction >50%
31
Causes of Absent Radial Pulse
Coarctation of Aorta Congenital (usually bilateral) Trauma (previous arterial line or coronary angio) Cervical Rib Arterial embolisation (AF)
32
Causes of Mitral Regurgitation
Calcific degeneration of valve (common in elderly) Rheumatic heart disease MV prolapse Infective endocarditis Connective Tissue disease e.g. Marfan's Post MI (e.g. papillary muscle rupture)
33
Features of Mitral Regurgitation
AF! Features of heart failure Features of pulmonary HTN (e.g. P2 thrill, left parasternal heave) Displaced apex {All of above also features of severe MR!} Pansystolic murmur, radiates to axilla, increased on expiration
34
What ECG findings may you see in MR?
AF LVH P-mitrale (= bifid p wave, secondary to left atrial enlargement)
35
Indications for surgical intervention in MR
LV dysfunction (EF < 60%) New onset AF New onset pulmonary HTN Severely symptomatic Sudden onset MR e.g. post MI
36
True or False: MV replacement is preferred over MV repair
FALSE Subvalvular apparatus disconnection can occur in replacement --> this can lead to a reduction of LVEF by 20%
37
What is Mitral Valve Prolapse?
Common condition (1-2%) in which one or both of the cusps of the mitral valve prolapse into the left atrium during systole Usually idiopathic Associated with - Congenital heart disease - Cardiomyopathy - Turner's syndrome - Marfan's syndrome - Other CTD e.g. Ehler Danlos, osteogenesis imperfecta and pseudoxanthoma elasticum - Wolf Parkinson White - Long QT syndrome - PKD (25% of APKD have valvular disorder) Mid-systolic "click" or late systolic murmur
38
Which condition is more likely to have AF associated with it? Mitral Stenosis or Mitral Regurgitation?
Mitral Stenosis
39
Causes of Mitral Stenosis
Rheumatic heart disease (>90%) - 40% of patients with rheumatic MS ahve multivalvular disease Degenerative calcification Congenital (RARE) Infective Endocarditis
40
Features of Mitral Stenosis
AF Malar Flush Hoarse voice (=Ortner's syndrome) - Compression of left recurrent laryngeal nerve by enlarged LA/pulm artery Features of RVF Features of pulm HTN e.g. P2 thrill, left parasternal heave Apex non displaced, tapping Loud S1, opening snap Mid-diastolic murmur (loudest in expiration and in left lateral position)
41
Features of severe Mitral Stenosis
AF Pulmonary HTN RVF Short gap between S2 and opening snap Long mid diastolic murmur Mitral Valve Are < 1.0cm2
42
When would you consider giving warfarin to a patient with Mitral Stenosis?
1) If they have concurrent AF 2) If their left atrium > 55mm (increased risk of thrombus formation)
43
Indication for surgical intervention in Mitral Stenosis
Severe MS (MVA < 1.0cm2) Symptomatic - NHYA > II
44
Outline examples of surgical intervention for Mitral Stenosis
Percutaneous Balloon Mitral Valvuloplasty - Indicated in symptomatic (NHYA>II) or MVA < 1.0 AND favourable morphology (Wilkin's Score <8) - in abscence of Left atrial thrombus or mod/severe mitral regurg MV Repair/Replacement - Indicated if PBMV not suitable or have concurrent coronary artery disease and would likely require CABG MV Valvotomy - if have had previous failed PBMV
45
Management of Mitral Stenosis in Pregnancy
If severe MS - Advise to avoid getting pregnant prior to any intervention Asymptomatic patients often present in 2nd trimester with symptoms due to increased HR and intravascular volume which occurs in pregnancy If develops severe MS and NHYA III/IV during pregnancy = PBMV
46
Outline causes of tricuspid regurgitation
Most cases are secondary to pulmonary HTN PRIMARY - Rheumatic heart disease - Infective Endocarditis - Ebstein's congenital anomaly SECONDARY - Functional TR e.g. RV dilation secondary to chronic LVF - RV infarction - Pulmonary HTN - Carcinoid syndrome
47
Features of tricuspid regurgitation
Often asymptomatic Raised JVP - CW wave - "Ear wiggling" Pulsatile liver Pansystolic murmur, loudest on inspiration Left parasternal heave
48
Outline the management of tricuspid regurgitation
If primary TR with no pulmonary HTN = Monitor If functional TR = 1) Correct cause of RV overload 2) Diuretics and vasodilators Last resort = Balloon valvuloplasty/TVR
49
Outline causes of Pulmonary Stenosis
5% of all congenital heart disease Almost always congenital (maternal rubella!) Carcinoid syndrome
50
Indications for Pacing
Symptomatic sinus bradycardia (<40bpm) e.g. syncope Complete AV block (even if asympto) Advanced or symptomatic 2nd degree AV block Exercise induced 2nd or 3rd degree AV block Neuromuscular disease with AV block e.g. myotonic dystrophy
51
What is diastolic dysfunction? Outline some causes of this
Diastolic dysfunction = HFpEF LV relaxation during diastole and filling is impaired CAUSES - HTN - IHD - Diabetes - HOCM - RCM - Infiltrative disease e.g. sarcoid, amyloid, haemochromatosis - Constrictive pericarditis
52
What is HOCM?
Hypertrophic Obstructive Cardiomyopathy Ventricular wall thickening and stiffening --> LVH, septal hypertrophy & LVOT obstruction and reduced compliance --> reduced cardiac output 1 in 500 Autosomal dominant - most common defect = MHY 6 gene Pansystolic murmur
53
What features would you expect to see on echocardiogram of a patient with HOCM?
MR SAM ASH Mitral Regurgitation Systolic anterior motion of anterior MV leaflet Asymmetric hypertrophy
54
Which medications must you AVOID in HOCM?
Positive Inotropes e.g. ACE inhibitors and nitrates {Any medication that causes afterload reduction, peripheral vasodilation, intravascular volume depletion, or positive inotropy can worsen the dynamic left ventricular outflow tract obstruction}
55
Outline the management of HOCM
MDT approach MEDICAL (ABCD) - Amiodarone (prevent ventricular arrhythmias) - Beta blockers (to reduce HR and contractility = reduce myocardial oxygen demand) - CCB (verapamil) - Diuretics SURGICAL - ICD if at risk of sudden death - Percutaneous Alcohol Septal Ablation (PASA) if evidence of LVOT obstruction and symptomatic despite medical Rx (CAUTION - risk of arrhythmogenic scar!) - Surgical myomectomy Genetic counselling/screening
56
Features of HOCM which suggest increase risk of sudden cardiac death?
Syncope (esp if exertional) FHx of sudden death in 1st degree relative Abnormal BP response during exercise VT LVOT pressure gradient >50mmHg at rest LV wall > 30mm
57
Outline causes of Restrictive Cardiomyopathy
Endomyocardial firbosis Loeffler's endocarditis (Eosinophils) Haemochromatosis Amyloidosis Sarcoidosis Radiation Scleroderma Fabry's disease
58
Outline causes of Constrictive Pericarditis
CARDIAC RIND C - CTD e.g. SLE A - Aortic aneurysm R - Radiation D - Drugs e.g. hydralazine, clozapine I - Infections e.g. TB A - Acute Renal Failure (Uraemia) C - Cardiac infarction (first 48 hours) R - Rheumatic fever I - Injury (haemopericardium) N - Neoplasms D - Dressler's syndrome (2-6 weeks post MI)
59
Outline examples of common causative organisms of Infective Endocarditis
3/4 caused by strep or staph infections Strep Viridans - URTI, dental damage Strep Pneumoniae/Pyogenes Staph Aureus Staph Epidermis Strep Bovis (colorectal cancer) Enterococcus Faecalis HACEK group = slow growing, gram negative Coxiella Burnetti "Q Fever" Yeasts & Fungi
60
Outline Duke's Criteria
Diagnostic of IE if - 2 x Major - 1x Major, 3 x Minor - 5x Minor MAJOR CRITERIA 1) Positive blood cultures 2) Evidence of endocardial involvement (characteristic echo findings e.g. vegetations) MINOR CRITERIA 1) Serological evidence of acute infection with organism consistent with IE 2) Vascular embolic phenomena e.g. Janeway lesions 3) Immunological phenomena e.g. glomerulonephritis, Osler's nodes, Roth's spots 4) Fever > 38 5) Predisposing condition e.g. valvular disease, IVDU 6) Suggestive echo findings
61
How would you investigate for Infective Endocarditis?
ECG Urinalysis - ?proteinuria ?haematuria ECG Multiple blood cultures - at least 3 sets CXR Echocardiogram - TOE best esp if small vegetations, ?abscess or prosthetic valves
62
How would you manage a patient with Infective Endocarditis?
MDT approach - cardiologists, microbiologists, ?cardiothoracic surgeons, vascular access team Antibiotics (guided by microbiology team) May need to refer to surgeons for valve replacement/surgical intervention
63
What are some of the indications for surgical intervention for Infective Endocarditis?
Aortic abscess (prolonged PR) Septal perforation Persistent infection e.g. fever > 10 days Persistent mobile vegetations > 10mm Recurrent emboli Severe valvular incompetence e.g. AR/MR Heart failure refractory to treatment Resistant/fungal infections
64
Can you give some examples of "stigmata of Infective Endocarditis"?
Janeway lesions Splinter haemorrhages Conjunctival haemorrhages Osler's nodes Roth spots Clubbing (subacute IE)
65
What is Marfan's Syndrome?
Autosomal dominant connective tissue disorder Defect in fibrillin-1 gene on chromosone 15 - Complete penetrance but variable phenotypes Diagnosed using Ghent Criteria (major criteria in at least 2 different systems) CARDIOVASCULAR FEATURES - Ascending Aorta Dilatation - Aortic dissection - MV prolapse (minor) OCULAR - Ectopic lentis SKELETAL - Pectus carinatum/excavatum - Arm span/Height ratio > 1.05 - Hypermobility - Scoliosis - Pes planus - High arched palate (minor) RESP - Spontaneous pneumothoraces (minor) SKIN - Skin striae - Recurrent/incisional herniae
66
Outline the management of Marfan's Syndrome from a cardiology perspective
MDT approach Genetic counselling/family screening Yearly echocardiogram due to risk of aortic dilatation and dissection Beta blockers (can reduce rate of Aortic dilatation) Indications for Aortic Root Repair - Symptomatic AR - Meets criteria for aortic regurg surgery - Dilation of Aortic root > 45mm - Aortic root growth > 1cm/year
67
Outline examples of Acyanotic Congenital Heart Disease
= "Left to Right" ASD VSD PDA Coarctation of Aorta
68
Outline examples of Cyanotic Congenital Heart Disease
"5 T's of Congenital Heart disease" = "Right to Left" 1) Tetralogy of Fallot 2) Transposition of the Great Vessels 3) Total anomalous pulmonary venous connection 4) Truncus arteriosus 5) Tricuspid atresia
69
What is Eisenmenger's ?
This is a reversal of a left-to-right shunt in a congenital defect, secondary to pulmonary HTN This occurs due to remodelling of pulmonary vasculature --> increases pulmonary resistance --> reversal of blood flow --> right-to-left shunt
70
What is Kartagener's Syndrome?
Rare autosomal recessive condition Dysmotility of dynein arm of cilia = 1) Dextrocardia/Situs invertus 2) Bronchiectasis 3) Infertility in men
71
Outline possible complications of an Atrial Septal Defect
50% mortality by 50 Paradoxical emboli (risk of stroke) AF Features of RV overload/RVF Pulmonary HTN --> Eisenmenger's Infective endocarditis
72
Indications for surgical closure of an ASD
Symptomatic Paradoxical emboli Evidence of significant shunt If evidence of pulmonary HTN, closure will only be offered if evidence of reversibility on vasodilator testing
73
Indications for surgical closure of VSD
Significant shunting Endocarditis Significant AR due to prolapse of leaflets throughout defect Acute septal rupture due to MI If other cardiac surgery planned
74
What is Tetralogy of Fallot?
Commonest form of cyanotic congenital heart disease Typically presents in first months of life PROV = Pulmonary stenosis RVH Overriding aorta VSD Severity of RVOT obstruction! Some associated conditions e.g. DiGeorge syndrome (cleft palate), Poland Syndrome (unilateral pectoral hypoplasia) Look for Blalock-Taussig scars
75
Possible complications following ToF surgical repair
Pulmonary regurgitation AR or Aortic Root dilatation (due to distortion during VSD repair) Infective endocarditis Residual VSD Arrhythmias
76
Coarctation of the Aorta
Congenital condition of narrowing of aorta (usually where ductus arteriosus inserts into aortic arch) Classified according to location with ductus arteriosus e.g. pre-ductal, post-ductal FEATURES - Intermittent claudication of lower limbs - LVF - Uncontrolled HTN --> headache - Chest pain (increased risk of coronary artery disease) - Underdeveloped lower body/left arm (if preductal) - Raised BP in arms compared to legs (>20mmg difference) - Delayed radio-fem or RR - Continuous systolic-diastolic murmur (best heard between scapulae)
77
Conditions associated with coarctation of the aorta
Bicuspid AV VSD Mitral valve prolapse PDA Aortic dissection Turner's syndrome Neurofibromatosis type 1 Marfan's SAH (berry aneurysms in circle of willis in 5%)
78
Management of coarctation of aorta
AVOID extreme isometric exercise e.g. weight lifting (risk of aortic dissection) Treat hypertension Manage Cardiac RFs Primary percutaneous endovascular stenting (if suitable)
79
Outline risks associated with valve replacement
Risk related to operation Risk related to anticoagulation Infective endocarditis