Disorder of Rhythm in Childreen

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    Disorder of Rhythm in

    Childreen

    By : Amy Fareena

    Mardiana KamalGroup 93

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    Normal Resting Heart Rate

    (in beats per minute)

    Newborn : 140-160

    1 year : 120

    5 years : 10010 years : 80-85

    15 years : 70-80

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    ArrhythmiaCardiac dysrhythmia (also knownas arrhythmia and irregular heartbeat) is group ofconditions in which there is abnormal electrical activity ofthe heartheart beat may be too fast (tachycardia) or too slow(bradycardia), and may be regular or irregular.

    Types of arrhythmia is children includes :

    -Long Q-T Syndrome (LQTS)

    - Premature Atrial Contraction (PAC) and PrematureVentricular Contraction (PVC)

    - Tachycardia

    -Sinus Tachycardia

    -Supraventricular Tachycardia- Wolff-Parkinson-White Syndrome

    -Ventricular Tachycardia

    -Bradycardia

    -Sick Sinus Syndrome

    -Complete Heart Block

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    Long Q-T Syndrome (LQTS)

    Prolong Q-T interval on ECG

    infrequent, hereditary disorder. May also

    occur in healthy people.

    usually affects children or young adults.

    Studies of otherwise healthy people with

    LQTS indicate that they had at least one

    episode of fainting by the age of 10. Themajority also had a family member with a

    long Q-T interval.

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    The Q-T interval represents the time for electrical activation and

    inactivation of the ventricles

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    Signs & Symptoms

    May be asymptomaticIf have symptoms, child may exhibit

    syncope and abnormal heartbeat

    Patients may show prolongation of the Q-Tinterval during physical exercise, intense

    emotion or when startled by a noise. They

    dont necessarily have a prolonged Q-T

    interval all the time. DiagnosisMay also result in deaf or may have

    congenital deafness

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    Diagnosis

    LQTS may be suspected if there is history

    of sudden death in the family or repeated &

    unexplained episodes of fainting.

    diagnosis is not easy since 2.5% of thehealthy population have prolonged QT

    interval, and 1015% of LQTS patients

    have a normal QT interval.

    LQTS "diagnostic score" may be used.

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    QTc (Defined as QT interval / square root of RR interval)>= 480 msec - 3 points

    460-470 msec - 2 points

    450 msec and male gender - 1 point

    Tordes de Pointes - 2 points

    T wave alternans - 1 point

    Notched T wave in at least 3 leads - 1 point

    Low heart rate for age (children) - 0.5 points

    Syncope (one cannot receive points both for syncope andtorsades de pointes)

    With stress - 2 pointsWithout stress - 1 point

    Congenital deafness - 0.5 points

    Family history (the same family member cannot be counted forLQTS and sudden death)

    Other family members with definite LQTS - 1 point

    Sudden death in immediate family (members before the age 30) - 0.5points

    four or more points, the probability is high for LQTS

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    Managements

    Arrhythmia prevention :- beta blockers

    - Na+ channel blockers (Mexiletin)

    - potassium supplimentsArrhythmia termination :

    - implantable cardioverter-defibrillator

    (ICD) on older patients & whenpatients have still experiencedsyncope even with beta blockerstherapy

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    Premature Atrial Contraction (PAC) and

    Premature Ventricular Contraction (PVC)

    Premature beats or extra beats most often cause

    irregular heart rhythmsThose that start in atria are called premature atrialcontractions or PAC

    Ventricle; Premature ventricular contractions or

    PVCPremature beats are very common in normalchildren and teenagers

    Premature heart beats may be perceived as askipped heart beat, a strong beat, or a feeling of

    suction in the chest. Of course the heart doesntreally skipped a beat, but actually, an extra beatcomes sooner than normal. Then there's usually apause that causes the next beat to be moreforceful

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    Usually no cause can be found and no specialtreatment is needed. The premature beats maydisappear later. Even if they continue, the child willstay well and won't need any restrictions.

    Occasionally premature beats may be caused bydisease or injury to the heart.

    So further test has to be done to make sure thechilds heart is functioning well because TAC cantrigger a more serious arrhythmia such as atrial

    flutter or atrial fibrillationOn ECG, PACs are characterized by anabnormally shaped P wave

    PVC; S-T is much shorter

    Several PVCs in a row becomes a formof ventricular tachycardia (VT), which is adangerous rapid heartbeat. This may also causechest pain, a faint feeling, fatigue, orhyperventilation after exercise symptomatic

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    Treatment for symptomatic PVCPVCs must be watched carefully, as theymay cause VT

    Pharmacological agents :

    - Antiarrhythmics: these agents alter the

    electrophysiologic mechanisms responsiblefor PVCs

    - Beta blockers

    -Calcium channel blockers

    Electrolytes replacement :

    - Magnesium supplements (e.g.magnesium citrate, orotate, Maalox, etc.)

    - Potassium supplements

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    Pediatric Tachycardia

    In children, the normal heart rate is

    age dependent, and the definition of

    tachycardia also varies according to

    age

    Tachycardia can be due to a

    physiologic response of the heart to

    noncardiac stimuli or to a truedysrhythmia

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    Cause

    Hyperdynamic cardiac activity :

    Increased heart rate and contractility arephysiologic responses to catecholamine

    release. Catecholamine release may occur withstress or anxiety, exercise, fever orinfection, pain, anemia, seizure,

    hypovolemia, hypoxia, drugs ormedications/stimulants, vasodilation (eg,anaphylaxis), hypoglycemia

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    True dysrhythmias :

    Supraventricular tachycardia (SVT)

    -Drug induced (eg, amphetamines, cocaine, caffeine,ephedrine, antihistamines, phenothiazines, antidepressants,tobacco, albuterol, theophylline, general anesthesia)

    -Wolff-Parkinson-White syndrome (WPW)

    -Hyperthyroidism

    -Congenital heart disease

    -Postoperative cardiac repair

    -Atrial ectopic tachycardia

    Atrial fibrillation or atrial flutterDrug induced

    Wolff-Parkinson-White syndrome (WPW)

    Postoperative cardiac repair

    Congenital or rheumatic mitral disease

    Hyperthyroidism

    Junctional ectopic tachycardia (JET) - Postoperative cardiacrepair

    Ventricular tachycardia (VT)

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    Causes of VT includes :

    -Drug induced (eg, tricyclics, phenothiazines, antiarrhythmics,chloral hydrate, organophosphates, hydrocarbons, digoxin,amphetamines, cocaine, arsenic)

    -Prolonged Q-T syndrome/torsades de pointes

    -Myocarditis

    -Rheumatic fever

    -Mitral valve prolapse

    -Cardiomyopathy

    -Myocardial ischemia

    -Postoperative cardiac repair-Hyperkalemia (peaked T waves, prolonged QRS and QT

    intervals)

    -Hypocalcemia (increased QT intervals secondary to ST-segment prolongation)

    -Hypokalemia (especially in association with digoxin use due toits synergistic effects on automaticity and conduction)

    -Hypomagnesemia (associated with hypocalcemia andhypokalemia)

    -Cardiac tumors

    -Arrhythmogenic right ventricular dysplasia

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    Signs&symptoms

    Chest pain, Palpitations, Syncope,

    Dizziness, Shortness of breath,

    Diaphoresis (for infantswhile

    feeding), cyanosis, Poor peripheralperfusion, Neurologic changes

    (mental status, motor/sensory

    deficits), Decrease in intake andoutput, Trauma, Pain, Fever, Cardiac

    gallop

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    Diagnosis

    Laboratory studies for tachycardia mayinclude the following:

    - Electrolyte levels - Particularly potassium,bicarbonate, calcium, and magnesium

    - Blood glucose level- Complete blood count

    - Toxicology screen

    - Arterial blood gas measurement

    - Thyroid function tests

    - Urine catecholamine metabolites(homovanillic and vanillylmandelic acid)

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    DDX

    Anemia, Chronic

    Atrial Fibrillation

    Atrial Flutter

    Hyperthyroidism, Thyroid Storm, and Graves DiseaseHypoglycemia

    Pediatrics, Bacteremia and Sepsis

    Pediatrics, Dehydration

    Pediatrics, Diabetic Ketoacidosis

    Torsade de Pointes

    Toxicity, AmphetamineToxicity, Anticholinergic

    Toxicity, Antidepressant

    Toxicity, Antihistamine

    Toxicity, Cocaine

    Toxicity, Cyclic Antidepressants

    Toxicity, Digitalis

    Toxicity, HallucinogenToxicity, Organophosphate and Carbamate

    Toxicity, Sympathomimetic

    Toxicity, Theophylline

    Toxicity, Thyroid Hormone

    Ventricular Tachycardia

    Wolff-Parkinson-White Syndrome

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    Treatment

    Antiarrhythmic agents Adenosine,

    Procainamide, Digoxin, Propanolol,

    Amiodarone, Lidocaine

    goals of pharmacotherapy are to

    reduce morbidity and prevent

    complications

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    Supraventricular Tachycardia

    The most common abnormal tachycardia inchildren

    also called paroxysmal atrial tachycardia (PAT) orparoxysmal supraventricular tachycardia (PSVT)

    The fast heart rate involves both atrial & ventricle.This isn't a life-threatening problem for mostchildren and adolescents. Treatment is onlyconsidered if episodes are prolonged or frequent.For many infants, SVT is a time-limited problem.Treatment with medications often stops after six to12 months.

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    SVT may occur in very young infants with

    otherwise-normal hearts. The heart rate is

    usually more than 220 beats a minute.Infants with an SVT episode may breathe

    faster than normal and seem fussy or

    sleepier than usual. This situation must be

    diagnosed and treated to return the heartrate to normal. Once the rhythm is normal,

    medication usually can prevent future

    episodes.

    Sometimes SVT can be detected while ababy is still in the womb. Then the mother

    may take medications to slow her baby's

    heart rate.

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    If an older infant or child has SVT, thechild may be aware of the rapid heartrate. This may be associated with

    palpitations, dizziness,lightheadedness, chest discomfort,upset stomach or weakness.

    Valsalva maneuver - children canlearn ways to slow down their heartrate using this method.

    Older children are more likely to havemore episodes of tachycardia.They're more likely to need prolongedtreatment. They also may need more

    diagnostic tests

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    cause

    Drug induced (eg, amphetamines, cocaine,caffeine, ephedrine, antihistamines,

    phenothiazines, antidepressants, tobacco,

    albuterol, theophylline, general anesthesia)

    Wolff-Parkinson-White syndrome (WPW)

    Hyperthyroidism

    Congenital heart disease

    Postoperative cardiac repairAtrial ectopic tachycardia

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    Signs & Symptoms

    Pounding heartShortness of breath

    Chest pain

    Rapid breathing

    Dizziness

    Loss of consciousness (in serious

    cases)

    Numbness of various body parts

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    Diagnosis

    ECG beat can be count and most have narrowQRS complex

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    Management

    Physical maneuver- activation of the parasympathetic

    nervous system by Valsalvamaneuver

    - other vagal maneuvers including:holding ones breath for a fewseconds, coughing, plunging the face

    into cold water,drinking a glass of icecold water, and standing on one'shead. Also Carotid sinus massage

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    Pharmacology

    - Adenosine, an ultra short acting AV

    nodal blocking agent, is indicated ifvagal maneuvers are not effective.

    - If this works, followup therapy

    with diltiazem, verapamil or metoprolol may be indicated.

    - SVT that does not involve the AV

    node may respond to other anti-arrhythmic drugs such

    as sotalol or amiodarone.

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    Cardioversion

    - Also called electrical countershock

    - If the patient is unstable or othertreatments have not been effective.

    - small catheter (a thin, flexible tube) is

    placed through the nostril into theesophagus. A small amount of

    electricity is sent through this catheter

    giving a small electrical shock to thechest wall. This is effective to stop the

    SVT.

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    Wolff-Parkinson-White syndrome

    congenital abnormality involving thepresence of abnormal conductive tissuebetween the atria and the ventricles inassociation with supraventricular

    tachycardia (SVT)involves preexcitation, which occursbecause of conduction of an atrial impulsenot by means of the normal conductionsystem, but via an extra atrioventricular(AV) muscular connection, termed asaccessory pathway (AP), that bypasses the

    AV node

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    Clinical Presentation

    Patients with Wolff-Parkinson-White(WPW) syndrome may present withanything from mild chest discomfort orpalpitations with or without syncope to

    severe cardiopulmonary compromise orcardiac arrest

    infant may frequently be irritable, may nottolerate feedings, or may demonstrateevidence of congestive heart failure

    verbal child with WPW syndrome usuallyreports chest pain, palpitations, orbreathing difficulty

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    DiagnosisClassic ECG

    short PR (< 120 ms) ,

    QRS >120 ms with a slurred onset of the QRS waveform

    producing a delta wave in the early part of QRS

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    Characteristic delta wave

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    Management

    Radio frequency ablation (RFA) -ablation of the accessory pathway[AP]

    antiarrhythmic drugs slowing APconduction, or

    AV blockers to slow AV nodal

    conduction ca+ channel blockers(verapamil, diltiazem)

    Beta blockers metoprolol, atenolol

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    Congenital complete heart block

    Third-degree congenital atrioventricular

    block (CAVB) is usually a complete heart

    block (ventricular impulses slower than and

    dissociated from the atrial rhythm) seen ina fetus or at an early age

    may be present at or even before birth

    2 types

    - isolated CAVB (structurally normal heart)

    - complex CAVB (congenital heart defects)

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    etiology

    CAVB with structural heart disease isconsidered to be caused by failure of the

    AV conduction system to develop duringheart development. This may be a result of

    increased distance between the AV nodeand the ventricular conduction tissues, aswhen associated with structural congenitalheart disease or damage related to the

    passage of maternal autoantibodiesBut for isolated CAVB, theres no clearetiology

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    Clinical presentationMother may be asymptomatic. But fetus inprenatal period usually presents withbradycardia or hydrops fetalis. Usually thisis found out by accident, or if siblings haveheart block (17% re-occurrence in family

    members)Newborns with congenital heart block maypresent with a hydropic appearance, maydevelop signs of low cardiac output orcardiac failure few hours or few days afterbirthIn older childern; pallor, mottling, lethargy,exercise intolerance, palpitations,dizziness, or syncope,

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    Diagnosis

    ECG long QT

    Children more than 7yrs old may be

    tested using stress test

    Chest radiography can reveal

    cardiomegaly and pleural effusions

    may also be identified during prenatal

    examinations, in the perinatal period,

    or during childhood or adulthood

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    Management

    Medications arent nessecary for children with thisdz

    Currently, medical care for children with completeheart block is focused on the optimal timing toplace a pacemaker.

    Pacemaker is to ensure positive outcome and toensure the child could live normaly because inserious cases (eg when syncope is present),sudden death may occur

    In emergency cases, chronotropic medications,with or without inotropic agents, may be helpful infetuses and newborns with hydrops fetalis,congestive heart failure, or low cardiac output

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    References

    http://www.heart.org/HEARTORG/Conditions/Arrhythmia/AboutArrhythmia/Types-of-Arrhythmia-in-Children_UCM_302023_Article.jsp#.TslBppWP_QB

    http://www.heart.org/HEARTORG/Conditions/Arrhythmia/AboutArrhythmia/AF-and-Children_UCM_423774_Article.jsp#.TskOzpWP_QA

    http://en.wikipedia.org/wiki/Cardiac_dysrhythmia

    http://en.wikipedia.org/wiki/Premature_atrial_contraction

    http://en.wikipedia.org/wiki/Premature_ventricular_contraction

    http://en.wikipedia.org/wiki/Long_QT_syndrome

    http://www.emedicinehealth.com/heart_rhythm_disorders/article_em.htm

    http://www.nlm.nih.gov/medlineplus/ency/article/003399.htm

    http://pediatrics.aappublications.org/content/96/1/122

    http://pediatrics.aappublications.org/content/26/3/402.short

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