IMC 3.0 Flashcards
? is the MC type of cardiomyopathy
Dx is confirmed w/ Echo findings of ?
How is severity and prognosis evaluated
Dilated after injury/damage leads to dilation all chambers
LV dilation, thinning
Global dysfunction
RV dysfunction
? defines the category of dilated cardiomyopathy
What characterizes this condition
What 3 nutritional diseases can cause this
LV enlargement
Dec myocardial contractility- systolic dysfunction
Thiamine/Selenium/Carnitine deficiency
? cardiac abnormalities can cause dilated cardiomyopathy
Define Quebec beer drinker cardiomyopathy
What can be seen on PE
Prolonged tachycardia
PVCs >15% of beats
Frequent RV pacing
Cobalt exposure induced dilated cardiomyopathy
MR TR Megaly JVD S3
What EKG findings are seen in dilated cardiomyopathy
What may be seen on CXR
What abnormal breathing pattern may be seen in advanced HF cases
LBBB
Arrhythmia
Sinus tach
Balloon heart:
Megaly, Effusions R>L
Cheyne Stokes breathing
Dilated cardiomyopathy Pts experiencing need ? lab drawn
Why
What is a non-invasive method to measure EF and monitor wall motion?
This method has fallen out of favor to ? test
BNP
Establish prognosis and disease severity
Radionuclide ventriculography
Cardiac MRI
What is the preferred diagnostic study for RV dysplasia in dilated cardiomyopathy
When is a biopsy most useful
What medication will be added to LAB Tx if increased contractility is needed
Cardiac MRI
Transplant rejections
Digitalis
How is dilated cardiomyopathy Tx
What is the next step if still Sxs
CCBs need to be avoided except for during ?
All diabetics w/ dilated cardiomyopathy need to be on ? med if ?
ACEI/BB/Loop diuretic
Add aldosterone antagonist
ARNI instead of ACEI/ARB
Afib/flutter
EF <40%, put on mineral corticoid antagonist
When/why would dilated cardiomyopathy Pt be placed on Ivabradine
What med is second line to Ivabradine
Why is this second line med used more often anyway?
Resting HR >70bpm,
LVEF <35% and
Chronic, stable HF
Digoxin
Decreases recurrent hospitalizations
Ventricular rate control in Afib
What medication combo is used in AfAm Pts w/ dilated cardiomyopathy that is usually avoided in this population?
When do dilated cardiomyopathy Pts need to have cardiac synchronization
When would an ICD implant be considered
Hydralazine-nitrate for abnormal NO utilization
Biventricular pacing if:
Significant MR and QRS >150msec
ASx ischemic cardiomyopathy
LVEF <30% on medical therapy
>40 days post-MI
? therapy is avoided all together in dilated cardiomyopathy Txs?
? adverse event is more common in dilated cardiomyopathy populations?
All Pts w/ AFib need Tx w/ ?
ImmSuppression
Arterial/pulmonary emboli
DOACs
Warfarin if MS
What 2 etiologies of dilated cardiomyopathy have better prognosis?
What 3 etiologies have poor prognosis?
When do Pts need to be referred
Peripartum
Stress induced
HIV
Infiltrative
Doxorubicin therapy
New/worsening Sxs
Continued Sxs and LVEF <35% for ICD consideration
Re-synchronization- if QRS >150msec and LBBB
The Sxs of HOCM are primarily related to ? and primarily include ?
What is the definition of HOCM
What causes the LV outflow tract to become obstructed?
Diastolic dysfunction; chest pain and dyspnea
LVH w/out press/vol overload
LV >1.5cm thick on echo
Septal block during systole
Anterior MV leaflet pulls inward
What is the end result of the cardiac hypertrophy during HOCM?
What causes HOCM
How is HOCM differentiated from Athletic Heart
Inc LV diastolic pressure
Autosomal dom mutation of sarcomeres:
myosin heavy chains
Ca regulation proteins
No diastolic dysfunction in athletes
What HOCM variety is more common in Asians
HOCM in older adults d/t HTN has ? distinct identifier
Initial Sx may be syncope which occurs d/t ?
Apical hypertrophy
Sigmoid interventricular septum w/ knob of cardiac muscle below AV
Dec diastolic filling
Tachycardia increases LV obstruction
? is a long term consequence and poor prognosis of HOCM
What PE findings may be seen
HOCM murmur needs to be differentiated from ? murmur
Afib from inc LA pressures
Bisferiens carotid pulse Apical lift Triple apical impulse S4 Inc A wave d/t dec RV compliance (a- atrial contraction, absent in afib)
AS
? EKG finding is nearly universal in HOCM Pts w/ Sxs
What other EKG finding may be noted
Echo is needed for Dx to differentiate HOCM from ? other inherited Dx
LVH
Septal dagger q-waves
Ventricular Noncompaction- trabeculation that partially fills LV
How is a HOCM Dx made and confirmed
? vascular anomaly may occur in these Pts
How is this Tx
What is avoided
Echo, catheterization
Arterial bridging- squeezing of coronary in systole
Initial Tx= BB
Verapamil/Diltiazem
Digoxin- inc contraction worsens obstruction
What Tx may help prevent hypertrophy/obstruction progression in HOCM
What Pts are best managed w/ implantable ICD
What Pts are eligible for ICD consideration
Dual chamber pacing
Malignant ventricular arrhythmia and/or unexplained syncope w/ +FamHx
Wall thickness of 30mm
Sudden death 1* relative
Unexplained syncope <6mon
What surgical Tx is avail to HOCM for severe/resistant Sxs
What procedure is done if MR is present
What non-surgical Tx is available
Myotomy-myomectomy
Alfieri stitch: ant/post leaflets together
Alcohol ablation via LCA
How are pregnant Pts w/ HOCM managed
What are the 6 high RFs for HOCM
When do these Pts need to be referred
Maintain BB regiment
1- personal Hx ventricular arrhythmia/survived death
2- FamHx sudden death
3- unexplained syncope
4- documented unstained V-tach
5- LV thickness of 30mm or >
6- SBP doesn’t dec by 20mm during treadmill stress test
Syncope has occured
Any 6 RFs
Difficult to control Sxs
Define Restrictive Cardiomyopathy
What other condition is usually present
Half of these cases are caused by but the ? is the MC cause in the world and US
Non-compliant ventricles that resist diastolic filling w/ preserved contractility, leading to RHF/diastolic HF
P-HTN
Half- idiopathic
World: tropical endomyocardial fibrosis
US: amyloidosis
What is the MC type of amyloid to cause Restrictive Cardiomyopathy
What causes familial amyloidosis in elderly AfAm
Restrictive Cardiomyopathy must be differentiated from ? Dx
Light chain- AL
Mutated transthyretin during production in liver
Constrictive pericarditis-
no ventricular interaction accentuated w/ inspiration
Inc pulm arterial pressure
Elevated BNP
What PE findings suggest Pts has amyloidosis infiltrates
What EKG combo is suggestive of a Restrictive Cardiomyopathy Dx
What is the non-invasive modality of choice to Dx transthyretin amyloidosis
Periorbital purpura
Thick tongue
Hepatomegaly
Low voltage + LVH
Tech-pyrophosphate (bone scan) to detect myocardial amyloid deposits
What is a useful screening test for Restrictive Cardiomyopathy
Biopsies from ? locations can confirm but not r/o systemic involvement
How is Restrictive Cardiomyopathy Tx
Cardiac MRI- abnormal texture
Rectal
Abdominal fat
Gingival biopsy
ACEI
BB/Verapamil
Loop/Tzd/Aldosterone antagonists
Tafamidis- transthyretin amyloidosis