UMEM Educational Pearls - Cardiology

Title: Chagas Heart Disease

Category: Cardiology

Keywords: Chagas Disease, AV Block (PubMed Search)

Posted: 10/13/2012 by Semhar Tewelde, MD (Updated: 10/14/2012)
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Etiological agent is the parasite Trypanosoma cruzi

Chagas is one of the most common causes of AV block worldwide
 
Most frequent & important manifestation is chronic panmyocarditis resulting in dilated cardiomyopathy
 
RBBB with or w/out left anterior fascicular block is the most common conduction defect
 
Other characteristic ECG abnormalities include atrial and ventricular extrasystoles, intraventricular and/or AV conduction disturbances, and primary ST-T wave changes
 

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Title: Autoantibody-associated Congenital Heart Block

Category: Cardiology

Keywords: Autoantibody-associated Congenital Heart Block, neonatal lupus, CHB (PubMed Search)

Posted: 10/7/2012 by Semhar Tewelde, MD
Click here to contact Semhar Tewelde, MD

Autoantibody-associated congenital heart block (CHB), also know as neonatal lupus, is responsible for the majority (~60-90%) of CHB

This is secondary to maternal antibodies that cross the placenta and may disappear postnatal

Neonatal lupus can result in diffuse myocardial disease both with and without conduction disturbances, structural defects, and electrophysiologic anomalies

Overall mortality is up to 30%, with 15% mortality before 3 months of age

More than 65% of surviving newborns require pacemakers

Maternal screening and fetal echocardiography has allowed routine prenatal diagnosis 

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Title: Heyde s Syndrome

Category: Cardiology

Keywords: Heyde s Syndrome, aortic stenosis, angiodysplasia (PubMed Search)

Posted: 9/30/2012 by Semhar Tewelde, MD (Updated: 11/21/2024)
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Aortic valve (AV) stenosis associated with gastrointestinal angiodysplasia

Proteolysis of Von Willebrand (type 2A) as it passes through the stenotic valve is one culprit of bleeding

Hemostatic abnormalities e.g. GI bleed are often corrected after AV replacement

Valve replacement is only recommended for cardiac symptoms

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Title: Brugada Syndrome

Category: Cardiology

Keywords: Brugada syndrome (PubMed Search)

Posted: 9/23/2012 by Semhar Tewelde, MD
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Autosomal dominant inherited arrhythmic disorder characterized by mutation in sodium-channels
Arrhythmic events are often observed at rest or while asleep, resulting in VF and SCD
Diagnostic criteria consists of 2 parts: (1) ECG abnormalities (2) clinical characteristics
A. ECG abnormalities: incomplete or complete RBBB in right precordial leads (V1-V2) w/
    Type I coved-type ST segment elevation and negative T wave 
    Type II saddle-back ST segment elevation followed by a positive or biphasic T wave 
    Type III ST segment elevation without meeting criteria for type I or II variants
B. Clinical characteristics: hx of VT/ VF, family hx of SCD or abnormal ECG, agonal respirations during sleep, or inducible VT/VF during EP study

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Title: blood pressure and organ perfusion

Category: Cardiology

Keywords: mean arterial pressure, blood pressure (PubMed Search)

Posted: 9/9/2012 by Amal Mattu, MD (Updated: 11/21/2024)
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Which patient has a better blood pressure, the patient with a blood pressure of 110/40 or the patient with a blood pressure of 90/60?

 

Mean arterial pressure (MAP) is generally considered to be the organ perfusion pressure in an individual. Because MAP requires an inconvenient calculation, we've all been taught...misled perhaps...into focusing on systolic blood pressure (SBP) as a marker of how well-perfused a patient is, and we tend to ignore the diastolic blood pressure (DBP).

 

It's important to remember, however, that we spend most of our lives in diastole, not systole. As a result, our organs spend more time being perfused during diastole than systole. The MAP takes this into account: MAP = (SBP + DBP + DBP)/3. DBP is more important than SBP!

 

So which patient is perfusing his vital organs better, the one with a BP of 110/40 or the one with a BP of 90/60? Do the MAP calculation...90/60 is better than 110/40!

 

Pay more attention to those diastolic BPs!



Title: Lyme Carditis

Category: Cardiology

Keywords: Lyme disease, Lyme carditis, AV block (PubMed Search)

Posted: 9/2/2012 by Semhar Tewelde, MD
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Lyme disease is the most prevalent arthropod zoonosis in the Northern hemisphere

Lyme carditis (LC), first reported in 1980, occurs in 1.5–10% of untreated adults in USA
 
Symptoms develop on average within a month after the onset of erythema migrans
 
Symptoms range from asymptomatic to dyspnea, syncope, chest pain, and fluctuating degrees of atrioventricular block
 
Temporary pacing is usually necessary in approximately 30% 
 
Prognosis is favorable and complete recovery occurs in more than 90% 
 
Tx typically consists of three weeks of oral or parenteral antibiotics after continuous cardiac monitoring in any symptomatic patients 

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Title: Arrhythmogenic right ventricular dysplasia

Category: Cardiology

Keywords: ARVD, ARVC, cardiomyopathy, triangle of dysplasia, ICD (PubMed Search)

Posted: 8/26/2012 by Semhar Tewelde, MD
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Arrhythmogenic right ventricular dysplasia (ARVD) is a heritable form of cardiomyopathy, characterized by the replacement of myocytes with adipose and fibrous tissue leading to arrhythmias, right ventricular failure, and sudden cardiac death (SCD)

The areas of the myocardium most affected are localized to the the inflow tract, outflow tract, and apex of the right ventricle (triangle of dysplasia)
 
Most common symptoms are palpitations, syncope, and SCD in 27, 26, and 23% of patients, respectively

ECG findings include T-wave inversions in V1–V3 (85% ), epsilon waves (in 33%), as well as a QRS duration >110 ms in V1-V3 (64%)

Dx is based on a combination of characteristics family history, ECG/arrhythmia, cardiac imaging (MRI/Echo), and endomyocardial biopsy 
 
ARVD patients are at high risk for sudden cardiac death and often recommended ICD placement

 

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Title: Negative T waves

Category: Cardiology

Keywords: T wave inversions, negative T waves, ACS, PE (PubMed Search)

Posted: 8/19/2012 by Semhar Tewelde, MD
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Pulmonary P waves (S1Q3T3 pattern + clockwise rotation) are specific for PE, but not sensitive.
This study examines if an ECG can discriminate between ACS vs. PE
- 40 patients with PE & 87 patients with ACS 
- All had negative T waves in the precordial leads (V1-V4) on the admission ECG
The PE group had negative T waves commonly present in leads II, III, aVF, V1, V2, but less frequent in leads I, aVL, and V5 to V6 (p <0.05).
The ACS group had negative T waves in leads III and V1 in 1% compared with 88% of patients with PE (p <0.001).
Sensitivity, specificity, positive predictive value, and negative predictive value for Dx of PE were 88%, 99%, 97%, and 95%, respectively.
Negative T waves in both leads III and V1 may suggest PE can be differentiated from ACS in patients with negative T waves in the precordial leads.

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Title: Hypertrophic Cardiomyopathy

Category: Cardiology

Keywords: hypertrophic cardiomyopathy (PubMed Search)

Posted: 8/12/2012 by Semhar Tewelde, MD
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Hypertrophic cardiomyopathy (HCM) is characterized by left ventricular hypertrophy (typically asymmetric) that occurs in the absence of pressure overload or storage/infiltrative disease.

HCM demonstrates remarkable diversity in disease course, age of onset, pattern and extent of LVH, degree of obstruction, and risk for sudden cardiac death.

Exertional dyspnea and chest pain are the most common symptoms, presumably related to diastolic dysfunction, obstructive physiology, and ischemia.
 
First line therapy is medical treatment with beta or calcium channel blockers used to prolong diastolic filling and blunt dynamic intra-cavitary gradients.
 
Medically refractory symptoms are caused by severe obstruction from systolic anterior motion of the mitral valve; these patients are candidates for invasive septal reduction therapy with surgical myectomy or alcohol septal ablation.  

Patients with HCM are at increased risk for sudden death, annual rate of SCD is ~1%. ICDs are recommended for all patients with prior arrest/sustained ventricular tachycardia (class I recommendation).

 

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Title: Takotsubo Cardiomyopathy

Category: Cardiology

Keywords: takotsubo cardiomyopathy, stress cardiomyopathy, broken-heart syndrome (PubMed Search)

Posted: 8/5/2012 by Semhar Tewelde, MD
Click here to contact Semhar Tewelde, MD

Takotsubo cardiomyopathy a.k.a. stress cardiomyopathy is an acute reversible disorder characterized by left ventricular (LV) dysfunction most commonly affecting postmenopausal women

The LV adopts the shape of an octopus trap (“takotsubo”) describing the narrow neck and broad base globular form during systole

Symptoms include precordial chest pain, dyspnea, or heart failure presenting with pulmonary edema mimicking ACS

Mayo Clinic Diagnostic Criteria

 - Suspicion of AMI based on symptoms and STEMI on ECG

 - Transient hypokinesia or akinesia of the middle and apical regions of LV

 - Functional hyperkinesia of the basal region of LV

 - Normal coronary arteries (luminal narrowing <50%)

 - Absence of recent head injury, ICH, HCOM, myocarditis, or pheochromocytoma

Treatment is symptomatic and determined based on complications during the acute phase; occasionally requiring IABP or ECMO

Prognosis is better than those with ACS, however initial LVEF is similar to those seen with ischemic heart disease 

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Title: Yamaguchi Cardiomyopathy

Category: Cardiology

Keywords: yamaguchi cardiomyopathy, apical hypertrophic cardiomyopathy, hypertrophic cardiomyopathy (PubMed Search)

Posted: 7/29/2012 by Semhar Tewelde, MD
Click here to contact Semhar Tewelde, MD

Yamaguchi Cardiomyopathy

Yamaguchi cardiomyopathy a.k.a. apical hypertrophic cardiomyopathy (AHCM) was first described 1976 in Japanese patients.

AHCM is a variant of hypertrophic cardiomyopathy that is nonobstructive with predominant involvement of the apex of the heart.

AHCM is frequently misdiagnosed as ACS or STEMI since the typical ECG abnormalities include giant inverted T waves or ST elevation in the mid precordial leads, however coronaries are characteristically clean on cardiac catheterization.

Echocardiography classically used to diagnosis HCM may frequently miss AHCM because hypertrophy is only localized to the apex.

Nuclear magnetic resonance imaging or angiography reveals the pathognomonic "ace of spades" configuration of the left ventricle with systolic obliteration of the apical region.

Unlike HCM sudden cardiac death is very uncommon.

 

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Title: Atrial Fibrillation

Category: Cardiology

Keywords: Atrial fibrillation, a fib (PubMed Search)

Posted: 7/15/2012 by Semhar Tewelde, MD (Updated: 11/21/2024)
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Atrial fibrillation is most commonly associated with cardiovascular disease    

Non cardiac causes: pulmonary disease/PE, hyperthyroidism, sympathomimetics, drugs/ETOH

AFFIRM & RACE trials compared outcomes of a fib patients treated w/ rate vs. rhythm control

    - No significant difference in survival between groups

Risk of thromboembolic CVA

   - Rhythm control = Rate control + anticoagulation

New data challenges the need for strict heart rate control

   - Resting heart rate should be <110 bpm

Use CHADS2 score to identify who requires anticoagulation based on %risk of emboli 

   - Chronic heart failure, HTN, Age>75, DM, Stroke/TIA 

  

 

 

 

                                           

 

 

 

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Title: cocaine effects on the heart

Category: Cardiology

Keywords: cocaine (PubMed Search)

Posted: 7/1/2012 by Amal Mattu, MD (Updated: 11/21/2024)
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[Pearls provided by Dr. Semhar Tewelde]

Cocaine...
1. causes systolic and diastolic dysfunction, arrhythmias, and atherosclerosis even in young users with relatively few cardiac risk factors, typically TIMI risk score <1

2. decreases myocardial contractility and ejection fraction by blocking sodium and potassium channels within the myocardium

3. prolongs the PR, QRS, and QT intervals on the ECG

4. users have a higher overall incidence of MI (odds ratio 3.8 to 6.9)

5. -induced chest pain is associated with acute MI in approx. 6% of cases

6. increases the risk of MI by 24-fold in the first hour after use

7. contributes to approx. 1 of every 4 MIs  between 18 and 45 years of age

 

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Title: Sgarbossa Criteria

Category: Cardiology

Keywords: Sgarbossa Criteria, MI, LBBB (PubMed Search)

Posted: 6/24/2012 by Semhar Tewelde, MD (Updated: 7/15/2012)
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Sgarbossa et al, initially identified patients with MI and left bunde branch block (LBBB) from the GUSTO trial; these ECGs were compared to the ECGs of patients with chronic CAD and LBBB

LBBB is defined by 3 criteria QRS >125msec, V1- QS or rS, and R wave peak time 60ms with no q wave in leads I, V5, V6

After a criteria to identify MI with LBBB was estabilshed it was tested on patients presenting with chest pain and 
The study resulted in Sgarbossa criteria; 3 independent predictors of MI in setting of LBBB
1.) ST segment concordance of 1mm any lead (greatest odd ratio, i.e. most specific)
2.) ST depression 1mm V1- V3
3.) Excessive ST discordance greater than 5mm (lowest odds ratio)

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Title: chest pain HPI and predictors of ACS

Category: Cardiology

Keywords: chest pain, acute coronary syndrome, history of present illness, predictor (PubMed Search)

Posted: 6/17/2012 by Amal Mattu, MD (Updated: 11/21/2024)
Click here to contact Amal Mattu, MD

For patients presenting to the ED with chest pain,  we've been taught that “classic” or “typical” presentations for ACS (chest pressure with radiation to the left neck/jaw/shoulder/arm, dyspnea, diaphoresis, nausea, vomiting, lightheadedness) are most worrisome. Yet, many of the patients that present with typical symptoms end up having negative workups for ACS. What are the symptoms that truly predict ACS? Three major studies have demonstrated that the best predictors of ACS in patients presenting to the ED with chest pain are (not necessarily ranked in order):
1. chest pain that radiates to the arms, especially if the pain radiates bilaterally or to the right arm
2. chest pain associated with diaphoresis
3. chest pain associated with vomiting
4. chest pain associated with exertion

The description of the chest pain (e.g. "pressure" or "squeezing," etc.), the dyspnea, nausea, lightheadedness, and pain at rest were, surprisingly, not helpful at predicting ACS.

The simple takehome point is the following: always ask your patient with chest pain if the pain radiates, if there was associated diaphoresis, if there was associated vomiting, and if the pain is associated with exertion. If the answers to any of these 4 questions is "yes," think twice before labeling the patient with a non-ACS diagnosis.

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Title: new uses for therapeutic hypothermia

Category: Cardiology

Keywords: hypothermia, cardiogenic shock (PubMed Search)

Posted: 6/10/2012 by Amal Mattu, MD (Updated: 11/21/2024)
Click here to contact Amal Mattu, MD

 

[pearl provided by Dr. Semhar Tewelde]
 
Therapeutic Hypothermia... Broadening its use beyond cardiac arrest survivors
 

New studies are utilizing mild therapeutic hypothermia as a treatment option in cardiogenic shock. These studies have reported improved circulatory support, an increase in systemic vascular resistance, and reduction in vasopressor use which ultimately may result in lower cardiac oxygen consumption. The preliminary results suggest that mild therapeutic hypothermia could be a therapeutic option in hemodynamically unstable patients independent of current recommendations which support its use in cardiac arrest survivors.

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Title: Myocarditis part II

Category: Cardiology

Keywords: myocarditis (PubMed Search)

Posted: 6/3/2012 by Amal Mattu, MD (Updated: 11/21/2024)
Click here to contact Amal Mattu, MD

[Pearl provided by Dr. Semhar Tewelde]
 
The diagnosis of myocarditis is complex. The ECG is a widely used screening tool despite low sensitivity; findings vary from nonspecific T-wave and ST-segment changes to ST-segment elevation mimicking an acute myocardial infarction.

Cardiac biomarkers lack specificity, but may help to confirm the diagnosis of myocarditis; higher levels of troponin T have been shown to be of prognostic value by predicting M&M.
 
Cardiovascular magnetic resonance (CMR) has evolved as a noninvasive and valuable clinical tool for the diagnosis of myocarditis. The initial changes in myocardial tissue during the first phase of myocardial inflammation represents an attractive target for successful CMR-based imaging diagnosis. The gold standard is endomyocardial biopsy (EMB). The Dallas criteria defines acute myocarditis by lymphocytic infiltrates associated w/ necrosis.

The prognosis ranges from full recovery, development of dilated cardiomyopathy, or death.
 
Tx strategies remain limited to standard heart failure therapy and supportive therapy. Immunomodulating and immunosuppressive therapy have been effective, particularly in a single-center trial (TIMIC study) in chronic virus-negative inflammatory cardiomyopathy. Immunosuppression therapy is also beneficial for acute giant cell myocarditis, sarcoidosis, and autoimmune diseases, such as lupus carditis.
 
 

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Title: myocarditis part I

Category: Cardiology

Keywords: myocarditis (PubMed Search)

Posted: 5/27/2012 by Amal Mattu, MD (Updated: 11/21/2024)
Click here to contact Amal Mattu, MD

[pearl provided by Dr. Semhar Tewelde]

Myocarditis is an under-diagnosed cardiac disease resulting from a broad range of infectious, immune, and toxic etiologies

Symptoms range from asymptomatic, dyspnea (most commonly) and chest pain, to presentations with signs of myocardial infarction, pericardial effusion with cardiac tamponade, to devastating illness with cardiogenic shock
Etiologies to consider 
        Bacteria (tuberculosis, strep pneumonia, chlamydia, legionella, mycoplasma)
        Fungi (candida, aspergillosis, actinomyces, crypotococcus)
        Helminthic (trichinella, echinococcus)
        Protozoal (toxoplasma, trypanosoma)
        Viral (adeno, echo, parvo, entero e.g., coxsackie, HSV, CMV, EBV, HIV)
        Rickettsial (coxiellia,  rickettsia)
        Spirochetes (borrelia, treponema, leptospirosis) 
        Autoimmune diseases (celiac, churg-strauss, crohn's/UC, dermatomyositis, giant cell, 
        lupus, RA, sarcoidosis, kawasaki)
        Toxic reactions to drug (amphetamines, anthracyclines, catecholamines, cocaine, phenytoin)
        Others (ethanol, copper, iron, radiotherapy, thyroid storm)

 

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Title: Peripartum cardiomyopathy part II

Category: Cardiology

Keywords: peripartum cardiomypathy, cardiomyopathy (PubMed Search)

Posted: 5/20/2012 by Amal Mattu, MD
Click here to contact Amal Mattu, MD

[This week's cardiology pearl provided by Dr. Semhar Tewelde]

PPCM is diagnosed  by echocardiography and increasingly confirmed and complemented with cardiac MRI after the ddx has been ruled-out i.e. pregnancy associated myocardial infarction, valvular heart disease, unrecognized congenital heart disease, hypertensive emergency, amniotic fluid or pulmonary embolism, or pre-eclampsia
 
PPCM has no histological classification and the role of routine endomyocardial biopsy (EMB) is controversial and remains unclear
 
Tx includes management of acute heart failure: non-invasive ventilatory/mechanical ventilation, diuretics, vasodilators (nitroglycerine/nitroprusside), inotropes (dobutamine/milrinone), pressors (dopamine), heparin, mechanical circulatory support (IABP, ECMO, LVAD), and finally cardiac transplant 
PPCM has a mortality rate as high as 30%
 
 

 

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Title: peripartum cardiomyopathy

Category: Cardiology

Keywords: peripartum, cardiomyopathy (PubMed Search)

Posted: 5/13/2012 by Amal Mattu, MD
Click here to contact Amal Mattu, MD

[pearl provided by Dr. Semhar Tewelde]

Peripartum cardiomyopathy (PPCM) is a relatively rare idiopathic form of heart failure that occurs during the last months of pregnancy or the first months after delivery

By definition, the LV ejection fraction (LVEF) is generally <45% and dilated
LV diastolic assessment often reveals a restrictive pattern, indicating elevated LV filling pressure
Risk factors associated with PPCM  include multiparity, twin pregnancy, extremes of reproductive age, and prolonged tocolysis
The most common presenting symptoms in PPCM include dyspnea, peripheral edema, and fatigue
The ECG typically  demonstrate sinus rhythm or sinus tachycardia
Left bundle branch block develops in up to 50% of cases and based on studies on long term outcomes in patients with systolic heart failure, may serve as a predictor of mortality
  
 

 

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