Volume 23, Issue 12, Pages 1313-1333 (December 2004)

14 of 27

FULL TEXT

FULL-TEXT PDF (233 KB)

International Society for Heart and Lung Transplantation: Practice guidelines for management of heart failure in children

Refers to erratum:

Erratum
The Journal of Heart and Lung Transplantation
September 2009 (Vol. 28, Issue 9, Page 987)
Full Text | Full-Text PDF (54 KB)

Article Outline

• Introduction

• The need for pediatric guidelines

• Levels of evidence and strength of recommendations

• Definitions and classification

• Definition of heart failure

• NYHA classification

• Ross classification

• Other scoring systems

• Staging system

• Chronic heart failure in the biventricular circulation

• Introduction

• Left ventricular systolic dysfunction

• Digitalis

• Clinical data in adult patients with HF

• Clinical data in pediatric patients

• Diuretics

• Clinical data in adult patients

• Clinical data in pediatric patients

• Angiotensin converting enzyme inhibitors and angiotensin receptor blockers

• Clinical data in adult patients

• Clinical data in pediatric patients

• β adrenergic blockers

• General remarks

• Clinical data in adult patients

• Clinical data in pediatric patients

• Therapeutic recommendations: No structural disease

• Therapeutic recommendations: Volume or pressure overload conditions

• Left ventricular diastolic dysfunction

• Overview

• Diuretics

• Clinical data

• Ace inhibitors and angiotensin receptor blockers

• Clinical data in adult patients

• Clinical data in pediatric patients

• Calcium channel blockers

• Clinical data in adult patients

• Clinical data in pediatric patients

• β blockers

• Clinical data

• Nitrates

• Clinical data

• Therapeutic recommendations

• The systemic right ventricle

• Overview

• Clinical data

• Special considerations

• Therapeutic recommendations

• Chronic heart failure in the univentricular circulation

• Overview

• Diagnostic approach

• Diuretics

• Digoxin

• Ace inhibitors

• β blockers

• Therapeutic recommendations

• Acute heart failure

• Pharmacologic support

• Mechanical support

• Overview

• Risks and benefits

• Therapeutic recommendations

• Electrophysiology considerations

• Overview

• Pharmacotherapy

• Acute arrhythmia management

• Chronic arrhythmia management

• Therapeutic recommendations

• Device therapy

• Pediatric ICD and resynchronization experience

• Special considerations in structural heart disease

• Therapeutic recommendations

• References

• Copyright

Introduction

The need for pediatric guidelines

Heart failure (HF) in the United States is well recognized as a major public health problem, with over 900,000 hospital admissions annually in the United States, and greater than 250,000 deaths per year. The great majority of heart failure occurs in adults. In children, the scope of the problem is less well defined, but recent data from the Pediatric Cardiomyopathy Registry suggest an annual incidence of 1.13 cases of cardiomyopathy per 100,000 children.1 While some of this represents asymptomatic disease, the burden of disease overall is nonetheless quite high. In the Pediatric Cardiomyopathy Registry, the majority of children with cardiomyopathy also had HF, with mortality rates of 13.6% at 2 years in dilated forms of cardiomyopathy.

The etiology of heart failure differs greatly between children and adults. Children in the Pediatric Cardiomyopathy Registry had a recognizable syndrome or genetic diagnosis in 27% of cases, with an additional 5% of cases due to myocarditis. Furthermore, a large percentage of children with end-stage HF (between 25% and 75%, depending upon the age group) have an underlying diagnosis of congenital heart disease.2 In contrast to adult patients, ischemic heart disease is rare in children.

There is a large, and rapidly growing literature addressing HF treatment for adult patients, with a much smaller literature concerning HF therapy in children. Excellent guidelines for adult patients have recently been published, but given the significant differences between adult and pediatric patients with HF, there is little reason to believe that these guidelines are directly applicable to children.3 Accordingly, in this document we have attempted to summarize the relevant literature and synthesize management guidelines for children with HF. The document that follows has been prepared in a consensus fashion, with input from pediatric cardiologists at multiple sites throughout the United States and Canada.

Levels of evidence and strength of recommendations

Each recommendation in this document is ranked with regard to the level of supporting evidence:

•Level A recommendations are based upon multiple randomized clinical trials.

•Level B are based upon a single randomized trial or multiple non-randomized trials.

•Level C are based primarily upon expert consensus opinion.

The level of evidence upon which a recommendation is based, differs from the strength of the recommendation. A given recommendation may be based upon randomized trials yet still be controversial. Other forms of therapy, which are based solely upon expert consensus, may be strongly recommended.

Recommendations in this document adhere to the format of guidelines previously published by the American College of Cardiology (ACC) and American Heart Association (AHA).

•Class I: Conditions for which there is general agreement that a given therapy is useful and effective.

•Class II: Conditions for which there is conflicting evidence or a divergence of opinion concerning the usefulness and effectiveness of a therapy.

•Class IIa: Weight of evidence/opinion favors usefulness/effectiveness.

•Class IIb: Weight of evidence/opinion is less in favor of usefulness/effectiveness.

•Class III: Conditions for which there is general agreement that a therapy is not useful and (in some cases) may be harmful.

Definitions and classification

Definition of heart failure

Heart failure is a complex clinical syndrome, with multiple etiologies and diverse clinical manifestations. Many definitions have been offered, but we prefer that set forth by Arnold Katz, which not only describes the clinical aspects of HF, but also reflects a growing understanding of the cellular processes which accompany this condition:4

“…heart failure is a clinical syndrome in which heart disease reduces cardiac output, increases venous pressures, and is accompanied by molecular abnormalities that cause progressive deterioration of the failing heart and premature myocardial cell death.”

It is important to note that at present, this definition is not clinically applicable as a diagnostic roadmap. In fact, there is no gold standard diagnostic approach to HF. Rather, the recognition of HF depends on a thorough characterization of the patient from a clinical, hemodynamic, and – increasingly – neurohumoral perspective. In specific cases, the weight of the diagnosis may stem from elements of the medical history, while in other cases, echocardiography or cardiac catheterization may provide essential data. Perturbations in circulating hormones such as the natriuretic peptides are coming to play a substantial role in the diagnosis of HF in the adult population, but are less widely used for this purpose in children.

Additionally, there is often ambiguity concerning the use of the term HF for children with uncorrected structural lesions resulting in left to right shunting with preserved systolic function. In this manuscript, we do not address the clinical issues posed by such patients, which are very different from HF associated with myocyte dysfunction.

NYHA classification

The New York Heart Association (NYHA) classification is widely used for grading HF in adult patients because of its simplicity in providing a practical assessment of functional limitation. It is an ordinal scale defined by the degree to which symptoms of HF limit a patient’s physical activity. However, the applicability to younger children and infants is limited.

Ross classification

The Ross Classification was developed for grading HF in infants and younger children (Table 1).5 In 1994 the Ross Classification was adopted by the Canadian Cardiovascular Society as their official system for grading HF in children,6 and the system is currently used in the national Cardiomyopathy Registry and in a multicenter study of carvedilol. A direct correlation between the Ross class and plasma norepinephrine concentrations5 and an inverse relationship between the Ross class and β-receptor density support the validity of the Ross classification system.7

Table 1.

Ross Classification


	Class	Interpretation
	I	Asymptomatic
	II	Mild tachypnea or diaphoresis with feeding in infants. Dyspnea on exertion in older children.
	III	Marked tachypnea or diaphoresis with feeding in infants. Prolonged feeding times with growth failure due to heart failure. In older children, marked dyspnea on exertion.
	IV	Symptoms such as tachypnea, retractions, grunting, or diaphoresis at rest.

Other scoring systems

Several other scoring systems have been proposed for grading HF in children. One such system developed for infants has a 12-point scale based on variables assigned by 4 pediatric cardiologists blinded to the patient’s diagnosis.8 These variables were: quantity and duration of feeding, respiratory rate and pattern, heart rate, peripheral perfusion, presence of a diastolic filling sound, and degree of hepatomegaly. Another recently proposed system is the New York University Pediatric Heart Failure Index.9 In this system, a total score from 0 to 30 is obtained by adding together points based on physiologic indicators and the patient’s specific medical regimen. Items scored are signs and symptoms, HF medications, and ventricular pathophysiology. None of these systems have been validated in large numbers of children nor tested against biological markers of HF or exercise capabilities.10 Ohuchi and colleagues have recently published a detailed analysis of the relationship between changes in neurohumoral indices and clinical status of children and young adults with congenital heart disease.11

Staging system

Both the NYHA and Ross HF scales concentrate on current symptomatology. Neither of these scales discriminates well among patients with early stages of disease, nor between stable and decompensated stages of illness. Overt HF symptoms occur late in the disease process, indicating a failure of compensatory mechanisms. The ACC/AHA 2002 HF guidelines therefore advocate a HF classification schema that addresses these deficiencies and complements the NYHA scale.12 The ACC/AHA staging identifies patients at risk for HF who require early intervention to prolong the symptom-free state; it also delineates patients who require aggressive management of symptoms once they become manifest.

The system advocated by the ACC/AHA for HF staging in adults can be readily applied to infants and children as well, with minor modifications as shown in Table 2.12 The writing committee of this document has adopted this nomenclature due to the advantages enumerated above.

Table 2.

Proposed Heart Failure Staging for Infants and Children*


	Stage	Interpretation
	A	Patients with increased risk of developing HF, but who have normal cardiac function and no evidence of cardiac chamber volume overload. Examples: previous exposure to cardiotoxic agents, family history of heritable cardiomyopathy, univentricular heart, congenitally corrected transposition of the great arteries.
	B	Patients with abnormal cardiac morphology or cardiac function, with no symptoms of HF, past or present. Examples: aortic insufficiency with LV enlargement, history of anthracycline with decreased LV systolic function.
	C	Patients with underlying structural or functional heart disease, and past or current symptoms of HF.
	D	Patients with end-stage HF requiring continous infusion of intropic agents, mechanical circulatory support, cardiac transplantation or hospice care.

HF, heart failure; LV, left ventricular.

Chronic heart failure in the biventricular circulation

Introduction

The spectrum of etiologies for HF in children is considerable, and a discussion of the diagnostic approach to children with HF is beyond the scope of this manuscript. This topic has been addressed thoroughly in a number of excellent publications, to which the reader is referred for further detail.13, 14, 15

HF in children may develop from myocyte dysfunction (such as is seen in idiopathic cardiomyopathy, or post-operative forms of cardiac dysfunction), or on the basis of congenital disorders resulting in volume or pressure overload. In the current era, both volume loading and pressure loading are typically – but not invariably – addressed surgically or in the catheterization laboratory.

Chronic volume overload associated with mitral or aortic insufficiency may be well tolerated for a prolonged period of time. In contrast to adult patients, mitral valve replacement for infants and children is often delayed because of technical difficulties inherent to the patient size and anticoagulation requirements. Limited data suggest that although early ventricular dysfunction after surgery is common after correction of chronic mitral insufficiency in children, left ventricular function frequently normalizes over time.16, 17

Left ventricular systolic dysfunction

Pharmacotherapy.

Digitalis

Clinical data in adult patients with HF

Digoxin improves symptoms in adults with HF.18 However, despite large study cohorts, digoxin has not been shown to improve survival in HF. Adams and colleagues have recently shown that low doses of digoxin are as effective as higher doses in preventing further HF, and may reduce the incidence of side effects and toxicity, especially when other medications are instituted which can increase digoxin levels.19 In one recent post-hoc analysis of the DIG trial, higher serum digoxin levels were associated with increased mortality in men with HF, independent of glomerular filtration rate.20

Clinical data in pediatric patients

Although only scant pediatric data are available, digoxin is widely used to treat HF in infants and children. Recommendations can only be extrapolated from those for adult patients with left ventricular systolic dysfunction and HF.

Diuretics

Clinical data in adult patients

Few data are available concerning the appropriate use of diuretics, but their use is widespread. Current guidelines in adult patients recommend the use of diuretics in all patients with HF and fluid retention in order to achieve a euvolemic state.

Spironolactone, specifically, has been shown to improve survival in adults with advanced HF.21 This does not appear to represent a diuretic effect, but rather is specifically due to blockade of aldosterone; the benefit has also been demonstrated with another aldosterone antagonist, eplerenone.22 The activation of the renin-aldosterone-angiotensin system (RAAS) is thought to be critical in the pathogenesis of HF, and interruption of the RAAS is a foundation of modern HF therapy.23 Although this is primarily accomplished in current management by administration of ACE inhibitors, spironolactone has an additive effect in adults with severe HF.

Clinical data in pediatric patients

No published clinical studies are available concerning the effectiveness of diuretics in reducing mortality or improving symptoms in pediatric patients.

Angiotensin converting enzyme inhibitors and angiotensin receptor blockers

Clinical data in adult patients

HF is associated with chronic activation of the RAAS and increased sympathetic drive.24 These alterations, which may be beneficial acutely, contribute to the progression of HF over time. Increased adrenergic tone increases afterload and myocardial oxygen demand. Angiotensin II is a vasoconstrictor which causes myocyte hypertrophy and fibrosis as well as aldosterone secretion. Increased concentrations of both aldosterone and angiotensin II are associated with a poor outcome in HF patients.25 The efficacy of ACE inhibitor therapy in HF is related to disruption of the activation of the renin-angiotensin axis and to decreased cardiac adrenergic drive.23, 24, 26

Multiple large clinical trials have shown that therapy with ACE inhibitors improves symptoms and survival in adult patients (primarily middle-aged men) with HF, and reduces the rate of disease progression in asymptomatic patients.27, 28, 29, 30 In the majority of trials, ACE inhibitors were well tolerated. Symptomatic hypotension can occur; careful uptitration of these agents and adjustment of diuretic dosages is necessary. Cough, which is often associated with pulmonary edema, is present more frequently in patients treated with ACE inhibitors.28

A frequent observation in the literature evaluating treatment of patients with HF concerns the underutilization of ACE inhibitors. On the one hand, only a minority of eligible adults receives an ACE inhibitor.31 Of equal importance, those patients who are treated with ACE inhibitors are often treated with doses considerably lower than the doses for which efficacy has been established in clinical trials.31 Although there is some controversy regarding appropriate dosing of ACE inhibitors for HF, most studies suggest a more robust response to higher doses of ACE inhibitors when hemodynamics, symptoms or neurohumoral profiles are considered.32, 33, 34, 35 The ATLAS trial compared the effects of low and high dose lisinopril on the morbidity and mortality of 3164 subjects with NYHA class II-IV.35 No survival benefit was seen from high dose therapy as compared to low dose, but high dose therapy reduced the composite outcome of death or hospitalization by 12%, and reduced hospitalization by 13%. Although dizziness, hyperkalemia and hypotension were all more common in the high dose group, these side effects did not require withdrawal from therapy more commonly than in the lower dose group. The ATLAS trial confirmed that certain benefits of ACE inhibition are greater at higher doses, and that these agents are clinically tolerated at higher doses. It is also noteworthy that the effect on symptoms was not associated with dose level, suggesting that titration of ACE inhibitors according to clinical endpoints is not a viable strategy.

Data concerning administration of ACE inhibitors to patients with structural heart disease is understandably limited. However, the beneficial effects of ACE inhibition on LV volume, dimensions, mass index, wall stress and reduction in the volume-loaded ventricle have been demonstrated for adult patients with aortic regurgitation.36

There are important differences between the ACE inhibitors and the angiotensin receptor blockers (ARB’s). The ARB’s are competitive antagonists for the angiotensin II receptor that is responsible for mediating all the known actions of angiotensin II. ARB’s block the cell surface receptor37 for angiotensin, rather than acting through blockade of angiotensin converting enzyme. Unlike ACE inhibitors, ARB’s do not inhibit bradykinin breakdown, which has been implicated in causing the troublesome cough that is a prominent side effect of ACE inhibitors. ARB’s are not nephrotoxic, affording these drugs a theoretical advantage over ACE inhibitors.

Despite these mechanistic differences, trials in adult patients with HF have not shown any important differences in hemodynamic effects, efficacy and safety between ARB’s and ACE inhibitors.38, 39 Currently ARB’s are recommended in adults intolerant to ACE inhibitors. The addition of ARB’s to ACE inhibitor therapy may increase efficacy40 and is often recommended in adult HF patients intolerant to β-blockade.

Clinical data in pediatric patients

Although ACE inhibitors have been used in the pediatric population for two decades, relatively few studies concerning the administration of ACE inhibitors to children with HF are available. Numerous small observational studies have shown that ACE inhibitors benefit children with HF caused by systemic ventricular systolic dysfunction.41, 42, 43, 44, 45, 46 Effects on mortality have not been described, with the exception of one retrospective report, in which survival was improved by administration of ACE inhibitors during the first year of treatment but not subsequently.46

The use of ACE inhibitors in patients with structural heart disease is less well understood. However, a single controlled study in children with preserved ventricular function and volume-overloaded ventricles from valvar insufficiency showed a reduction in both LV volume overload as well as hypertrophy in the ACE inhibitor treated group over an average of 3 years of follow-up.47

No safety or efficacy data regarding the use of ARB in children with HF are available. There is very limited experience with ARB therapy for pediatric patients with hypertension.48

β adrenergic blockers

General remarks

Initial compensatory mechanisms in the failing heart include activation of the sympathetic nervous system and increased levels of circulating catecholamines. In the long term the increased levels of catecholamines, particularly norepinephrine, contribute to the progression of HF through multiple mechanisms, including myocardial fibrosis and apoptosis, peripheral vasoconstriction, and salt/water retention by the kidneys.49, 50, 51 The rationale for the use of adrenergic antagonists in HF is to antagonize the deleterious effects of sympathetic activation on the myocardium.

The risks associated with the use of beta-blockers include hypotension and worsening HF.52, 53, 54, 55 Usually these symptoms occur in the first 48 hours after initiation of treatment or at the time of up-titration of the drug. Fluid retention may cause an increase in symptoms56, 57, 58 and adjustment in diuretic dosage may be needed. Bradycardia is seen with the use of β-blockers, is usually asymptomatic, but may require dose reduction if there is associated hypotension.52 β-blockers are contraindicated in patients with severe bradycardia, sick sinus syndrome and second or third degree heart block, unless a pacemaker is in place. β-blockers are also contraindicated in patients with bronchial asthma and in patients with cardiogenic shock.

Clinical data in adult patients

Metoprolol was the first β-blocker studied in placebo-controlled trials in patients with HF. Early studies failed to show a statistically significant decrease in the risk of death or listing for transplantation.59, 60 Eventually, in a trial involving 3991 patients with ischemic and non-ischemic cardiomyopathy and mild to moderate CHF, administration of metoprolol reduced mortality by 34%, which was statistically significant.61 In addition to metoprolol, carvedilol has been studied extensively in adult patients with HF resulting from left ventricular dysfunction. Several placebo-controlled trials have shown that carvedilol therapy decreases the risk of clinical progression of HF and decreases all-cause mortality.62, 63, 64 Of particular interest, the COPERNICUS study (Carvedilol Prospective Randomized Cumulative Survival Trial)65 evaluated the effects of carvedilol in 2289 patients with severe HF from either ischemic or non-ischemic cardiomyopathy. Patients treated with carvedilol had a 24% reduction in combined risk of death and hospitalization for any reason and a 35% reduction in mortality, showing that even these severely compromised patients benefited from carvedilol therapy.

Clinical data in pediatric patients

The reported use of β-blockers in children with HF is very limited, and no large placebo-controlled trials are available.

In a multi-institutional experience Shaddy, et al. reviewed the results with metoprolol in 15 children with cardiomyopathy of different etiologies.66 Metoprolol was started at 0.2–0.4 mg/kg/day and slowly increased to a maximum dose of 1.1 mg/kg/day. There was no significant difference in ejection fraction on conventional therapy from the time of diagnosis to the time when metoprolol was started, but after a mean of 23 months on metoprolol there was a statistically significant and clinically important increase in ejection fraction from 27% to 41%.

The experience with carvedilol in pediatric patients with HF is similarly limited. Bruns, et al.53 reviewed the use of carvedilol in 46 infants and children with cardiomyopathy (80%) or congenital heart disease (20%) at 6 centers. Patients were on standard treatment with digoxin, diuretics, and ACE inhibitors for at least three months before the start of β-blocker therapy. Carvedilol was initiated at an average dose of 0.08 mg/Kg/day and titrated to a mean maximum dose of 0.92 mg/kg/day. After 3 months of therapy, modified NYHA class improved in 67% of patients and worsened in 11%. Shortening fraction improved slightly, from 16.2% to 19.0%. Side effects, mainly dizziness, hypotension, and headache, occurred in 54% of patients and were well tolerated overall.

In a single center study Rusconi, et al.54 reviewed the results in 24 pediatric patients with dilated cardiomyopathy. Carvedilol was added to standard treatment at a mean of 14 months after the diagnosis of cardiomyopathy was made, with an average maximum dose of 1.0 mg/kg/day. Adverse effects occurred in 5 patients. The medication was tolerated in 22 patients. The mean left ventricular ejection fraction improved from 25% to 42% (p<0.001). The NYHA class improved in 15 patients, 1 patient died and 3 were transplanted. Lower doses of carvedilol may also be effective, as suggested by Azeka and colleagues.67 In this study of 22 children with DCM, improvement of both ejection fraction and clinical status was seen at 6 months with treatment dose of 0.2 mg/kg day of carvedilol, which was tolerated in all patients.

Therapeutic recommendations: No structural disease

Recommendation 1: The underlying cause of new-onset ventricular dysfunction (HF Stages B, C or D) should be evaluated thoroughly in all patients. The evaluation may include metabolic and genetic evaluation in selected cases, as indicated by the available history and physical findings. Invasive assessment, including myocardial biopsy, may be considered in selected cases. In infants, particular care should be paid to the exclusion of coronary artery anomalies and other anatomic causes. (Level of Evidence C; Strength of Recommendation I)

Recommendation 2: Screening of first-degree relatives should be considered in patients with new-onset ventricular dysfunction due to DCM (HF Stages B, C or D). (Level of Evidence C; Strength of Recommendation I)

Recommendation 3: Patients with fluid retention associated with ventricular dysfunction (HF stage C) should be treated with diuretics to achieve a euvolemic state using clinical criteria of fluid status and cardiac output. (Level of Evidence C; Strength of Recommendation I)

Recommendation 4: Digoxin is not currently recommended for patients with asymptomatic forms of left ventricular dysfunction (HF Stage B) because this agent did not alter survival in large trials of adult patients with HF. (Level of Evidence C; Strength of Recommendation IIb)

Recommendation 5: Digoxin should be employed for patients with ventricular dysfunction, and symptoms of HF (HF Stage C), for the purpose of relieving symptoms. Lower doses of digoxin are preferred for this purpose. (Level of Evidence B; Strength of Recommendation I)

Recommendation 6: For the treatment of moderate or severe degrees of left ventricular dysfunction with or without symptoms (HF Stage B and C), ACE inhibitors should be routinely employed unless there is a specific contraindication. These medications should be started at low doses, and should be up-titrated to a maximum tolerated safe dose. Uptitration may require a reduction in the dose of diuretics. (Level of Evidence B; Strength of Recommendation I)

Recommendation 7: For the treatment of decompensated left ventricular dysfunction (HF Stage D), the use of ACE inhibitors as initial therapy is not recommended. (Level of Evidence C; Strength of Recommendation IIb)

Recommendation 8: Patients who have an indication for ACE inhibitors therapy, but are intolerant of ACE inhibitors should be considered for ARB therapy. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 9: Given the limited information available concerning the efficacy and safety of β agonist receptor blockade in infants and children with HF, no recommendation is made concerning the use of this therapy for patients with left ventricular dysfunction (HF Stage B or C). If a decision is made to initiate β-blocker therapy, consultation or co-management with a heart failure or heart transplantation referral center may be desirable. (Level of Evidence B; Strength of Recommendation IIa)

Recommendation 10: Use of β-blocker therapy is not indicated for patients in HF Stage D. (Level of Evidence C; Strength of Recommendation IIb)

Therapeutic recommendations: Volume or pressure overload conditions

Recommendation 11: In all cases of HF associated with structural heart disease (HF Stage B, C or D), consideration should be given to surgical repair of significant lesions, as the long-term outlook may be more favorable than with medical management alone. (Level of Evidence C; Strength of Recommendation I)

Recommendation 12: In pressure-induced left ventricular hypertrophy, with normal myocardial function, ACE inhibitors are not recommended in the absence of a non-cardiac indication such as hypertension. (Level of Evidence C; Strength of Recommendation III)

Left ventricular diastolic dysfunction

Overview

Diastolic dysfunction is a syndrome characterized by impaired filling of one or both ventricles.68, 69 Diastolic heart failure refers to a clinical syndrome of HF with preserved systolic function.70, 71, 72 Diastolic dysfunction is the sole or primary cause of HF in as many as 1/3 of adult patients with HF.12, 70, 71, 72, 73, 74 No published estimates of the prevalence of diastolic dysfunction in the pediatric population are available.

There are 2 fundamental types of diastolic abnormality: impaired ventricular relaxation (affecting early diastole), and increased myocardial stiffness (affecting late diastolic filling).70 The hemodynamic consequences of diastolic dysfunction include increased ventricular filling pressures leading to elevation in atrial and venous pressures, and in the case of left ventricular dysfunction, leading also to an increase in pulmonary arterial pressure.

Conditions that cause diastolic dysfunction are varied and include pericardial as well as myocardial etiologies.75, 76, 77, 78 Of note, patients with chronic diastolic dysfunction are at risk for sudden death, as well as for developing pulmonary hypertension, which further complicates treatment and limits survival.75, 76, 77, 78

Pharmacotherapy.

There are no large-scale, randomized controlled trials of diastolic HF therapy in the adult or pediatric population.70, 71

Diuretics

Clinical data

Diuretics are the first line of therapy for diastolic dysfunction. Diuretics reduce pulmonary congestion and relieve symptoms such as orthopnea, cough and dyspnea. Injudicious or excessive use will reduce preload and result in diminished cardiac output.73, 74, 75

Ace inhibitors and angiotensin receptor blockers

Clinical data in adult patients

Therapy with ACE inhibitors may benefit some forms of diastolic dysfunction as tissue ACE levels are increased in models of hypertrophy,70, 79, 80 and angiotensin II is known to induce myocyte hypertrophy as well as fibrosis. ACE inhibitors may be employed to obtain regression of left ventricular hypertrophy, reverse vascular hypertrophy and fibrosis, and improve endothelial function. Theoretically, ACE inhibitors and perhaps angiotensin receptor blockers may be a reasonable treatment option.70

In the PRESERVE study, enalapril had moderately beneficial and statistically indistinguishable effects on regression of left ventricular hypertrophy compared with nifedipine.81 There are currently no mortality data to support the use of ACE inhibitors for patients with chronic HF and preserved ejection fraction in the absence of another indication for ACE inhibitors therapy (such as hypertension).

Limited experience in the adult population demonstrates improved exercise tolerance with ARB therapy in patients with diastolic dysfunction.82

Clinical data in pediatric patients

Captopril was deleterious in 1 small study with 4 pediatric patients with restrictive cardiomyopathy who demonstrated systemic hypotension without an improvement in cardiac output.41

Calcium channel blockers

Clinical data in adult patients

Much of the literature regarding calcium channel blockers is in the elderly population and in patients with hypertrophic cardiomyopathy. There are no prospective randomized trials. Benefit may be achieved by cardiac slowing, prolonging filling time, and improving myocardial relaxation.73, 79 Prolonged administration of calcium channel blockers may lead to regression of left ventricular hypertrophy.81 Calcium channel blockers may also directly improve ventricular relaxation or compliance, but there are few data to indicate that this is a clinically important effect.74

When compared to enalapril, nifedipine had moderately beneficial and statistically indistinguishable effects on regression of left ventricular hypertrophy compared with enalapril.81 Some patients may deteriorate after administration of calcium channel blockers; this is likely the result of a decrease in afterload.73

Clinical data in pediatric patients

There are no data on the use of calcium channel blockers for the treatment of diastolic dysfunction in children.

β blockers

Clinical data

Use of β-blockers has been reported for diastolic dysfunction in elderly patients with hypertrophic cardiomyopathy but no prospective randomized study has been performed. The rationale for use includes reduced heart rate leading to a prolonged filling time and relief of cardiac ischemia.73, 74 It is recognized that some patients deteriorate with institution of β blockade.73 β-blockers are proposed to directly improve diastolic dysfunction by augmenting ventricular relaxation or improving compliance, but there are few data to indicate that these agents exert a clinically important effect by this mechanism.

Nitrates

Clinical data

Nitric oxide or drugs that enhance NO release (sodium nitroprusside, nitroglycerin) improve diastolic dysfunction when administered locally to the coronary arteries.69, 83 Systemic use of nitrates may result in decreased systemic venous preload, increased pulmonary venous filling, reduced systemic afterload, hypotension and clinical deterioration.73 Patients with chronic restrictive disease may have typical or atypical anginal pain, which may respond to nitrate therapy.

Therapeutic recommendations

Recommendation 13: Clinical management of diastolic dysfunction should address symptoms and attempt to address the underlying cause of the diastolic dysfunction, if known. This should include a careful evaluation for pericardial disease, and coronary insufficiency with attendant myocardial ischemia. Systemic hypertension, if present, should be controlled aggressively. (Level of Evidence C; Strength of Recommendation I)

Recommendation 14: Fluid management to control symptoms remains a cornerstone in the management of symptomatic diastolic dysfunction (HF Stage C). Diuretics can be very useful to control symptoms but must be used cautiously as cardiac output depends on the elevated filling pressures. Renal function should be followed closely with care taken not to over-diurese a patient. Finally, sodium and fluid restriction may be helpful in controlling symptoms. (Level of Evidence C; Strength of Recommendation I)

Recommendation 15: Patients with marked atrial dilatation due to diastolic dysfunction (HF stage B or C) have a propensity for the formation of thrombi and prophylactic anticoagulation may be considered in this setting. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 16: Atrial arrhythmias are not infrequent in patients with diastolic dysfunction due to atrial enlargement. However, atrial contribution to ventricular filling is particularly important for this group of patients (HF Stage B and C). Therefore, efforts should be made to maintain sinus rhythm by use of antiarrhythmic therapy and pacemaker therapy. (Level of Evidence C; Strength of Recommendation I)

Recommendation 17: Asymptomatic diastolic dysfunction (HF Stage B) should be followed closely, but does not require pharmacotherapy. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 18: Treatment with agents which reduce afterload, such as ACE inhibitors, β blockers, calcium channel blockers and nitrates, should be cautiously undertaken with close monitoring. Abrupt decreases in afterload in patients with restrictive or constrictive disease may be deleterious. (Level of Evidence C; Strength of Recommendation IIb)

Recommendation 19: Patients with diastolic dysfunction that is refractory to optimal medical/surgical management should be evaluated for heart transplantation as they are at high risk of developing secondary pulmonary hypertension, and of sudden death (HF Stage C). (Level of Evidence B; Strength of Recommendation I)

The systemic right ventricle

Overview

The morphologic right ventricle (RV) is connected to the aorta and is thus the systemic ventricle in 2 main groups of patients with biventricular circulation: patients born with d-transposition of the great arteries who were treated with atrial baffle surgery (Mustard or Senning repair) and patients born with congenitally-corrected transposition of the great arteries. RV dysfunction has been described in both these groups of patients and may lead to HF. Although RV performance at rest is often normal,84 exercise ability is often limited in patients who have undergone atrial baffle surgery because of both chronotropic incompetence and limited stroke volume reserve.85, 86, 87, 88, 89, 90, 91, 92

The mechanism of systemic right ventricular dysfunction is poorly understood. Various theories include: (a) a sub-optimal myocardial fiber arrangement and mechanics in the right ventricle, (b) adverse pattern and reduced heterogeneity of ventricular strain, (c) tricuspid insufficiency and, (d) myocardial fibrosis secondary to prolonged hypoxemia during infancy while awaiting atrial baffle surgery.93 Perfusion defects with associated wall motion abnormalities have been described using single photon emission computed tomography,94, 95, 96 suggesting a role for chronic subendocardial ischemia.

The clinical course in patients with congenitally-corrected transposition of the great arteries is often determined by associated structural (ventricular septal defect, pulmonary stenosis) or electrophysiologic abnormalities (AV block). Although there are reports of patients without such abnormalities whose right ventricles have continued to function normally well into adulthood, systemic RV dysfunction and HF occur with increasing prevalence with advancing age. By 45 years of age, 25% of patients without and 67% of patients with associated lesions have HF.97

There is a limited surgical experience with conversion of the atrial baffle to a systemic left ventricle (“double-switch”), with baffle takedown accompanied by arterial switch procedure. Early results indicate that surgery is feasible, but surgical risk may be substantial for this approach, and the long-term results are not known.98 A similar procedure has been performed in small numbers of patients with corrected transposition, although again, long-term outcomes are not yet defined.

Pharmacotherapy.

Clinical data

Data specifically addressing the medical therapy of systemic right ventricular dysfunction are exceptionally scanty. Administration of ACE inhibitors to 14 survivors of the Mustard operation did not affect exercise tolerance or right ventricular ejection fraction.99 However, selected patients did show benefit. In the absence of more specific data, the management guidelines below are based on clinical experience and the effectiveness of these regimens in adult patients with systemic LV failure.

Special considerations

Although β-blockers are now considered an important part of HF therapy in adult patients with cardiomyopathy, specific problems may be encountered in administration of these agents to patients with a systemic RV. These difficulties relate to the high prevalence of sinus node dysfunction in survivors of atrial baffle repair and AV node dysfunction in patients with congenitally corrected transposition of the great arteries. The administration of β-blockers in these patients may be particularly problematic, and may result in symptomatic bradycardia and exacerbation of HF.

Therapeutic recommendations

Recommendation 20: Patients with a right ventricle in the systemic position are at risk of developing systemic ventricular dysfunction (HF Stage A) and should undergo periodic evaluation of ventricular function. (Level of Evidence B; Strength of Recommendation I)

Recommendation 21: Patients with fluid retention associated with systemic right ventricular dysfunction (HF stage C) should be treated with diuretics to achieve a euvolemic state. In patients receiving chronic diuretic therapy, electrolyte balance and renal function should be evaluated periodically. (Level of Evidence C; Strength of Recommendation I)

Recommendation 22: Digoxin should be employed for patients with symptomatic systemic RV dysfunction (HF Stage C), for the purpose of relieving symptoms. Digoxin is not currently recommended for patients with asymptomatic systemic right ventricular dysfunction (HF Stage B). (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 23: For the treatment of asymptomatic systemic right ventricular dysfunction (HF Stage B), ACE inhibitors should be routinely employed unless there is a specific contraindication. These medications should be employed at standard doses. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 24: For the treatment of symptomatic systemic right ventricular dysfunction (HF Stage C), ACE inhibitors should be routinely employed, as above. (Level of Evidence C; Strength of Recommendation I)

Recommendation 25: Patients who have an indication for ACE inhibitors therapy, but are intolerant of ACE inhibitors should be considered for ARB therapy. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 26: Consideration of surgical revision of the tricuspid valve should be given where both systemic right ventricular dysfunction and severe tricuspid valve regurgitation are present, particularly when the regurgitation is due to an intrinsic abnormality of the tricuspid valve (HF Stage B and C). (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 27: Anatomic revision (“double-switch”) or cardiac transplantation should be considered for patients with advanced systemic right ventricular failure (HF Stage C) that is refractory to medical therapy. (Level of Evidence C; Strength of Recommendation IIa)

Chronic heart failure in the univentricular circulation

Overview

For most patients with single ventricle anatomy, surgical management is the primary treatment path, and may include a variety of early palliative procedures followed by bi-directional Glenn (superior cavopulmonary connection, SCPC), and ultimately the Fontan procedure (total cavopulmonary connection, TCPC). Early palliation with complete mixing of systemic and pulmonary venous flow requires that ventricular output must be maintained at a level that is 2 to 3 times normal.100, 101 This chronic volume overload places the myocardium at considerable risk.100 Ventricular anatomic type and the specifics of early management are important determinants of ventricular outcome after the SCPC or TCPC. In particular, patients with a prior aortopulmonary shunt typically have larger postoperative ventricular size than those with a prior pulmonary artery band.102 In some series,102 systemic left ventricles are more dilated than systemic right ventricles at the time of volume-unloading surgery, although other reports have found no difference in size or function between morphologically single right or left ventricles.103 The durability of the systemic right ventricle is in question, with reports suggesting this may104, 105, 106 or may not107 be a problem. In one series, early postoperative survival was better in patients with a morphologic left ventricle but by 6 months after completion of the Fontan procedure, ventricular morphology did not influence survival.107

In patients who have completed the bi-directional Glenn or Fontan palliation, the manifestations of HF do not include the typical symptoms that occur in patients with 2 ventricles. After SCPC, TCPC, or Fontan palliation, systemic venous pressure is by necessity higher than pulmonary. These patients experience peripheral edema, pleural and pericardial effusions, cyanosis, and symptoms related to reduced cardiac output such as chronic fatigue, loss of appetite, and extreme exercise intolerance. These symptoms can clearly be related to factors other than myocardial dysfunction, many of which are common in this patient population. The basic physiology of the post-Fontan circulation is not intrinsically distinguishable from HF: activation of the renin-angiotensin system is usual if not universal, neurohumoral activation does not correlate with hemodynamic variables, and increased levels of catecholamines do not track well with severity of symptoms.108, 109

Reduction in exercise capacity may be helpful in making this distinction; however exercise performance in children with successful or optimal Fontan palliation may be quantitatively identical to that in children with mild HF.110 Reduced exercise capacity may in part be explained by diminished resting stroke volume and stroke volume reserve111 compared with normal hearts. The impact of reduced stroke volume in patients who have had the Fontan operation is compounded by chronotropic incompetence, with most series reporting maximum achieved heart rate to be about 75% of the age-predicted normal value,112, 113, 114 and in some series,115, 116 though not all,117 peak heart rate correlates with the percent of predicted VO2max that is achieved. Exercise-induced hypoxia may also be a limiting factor. Arterial saturation typically falls during exercise in Fontan patients113, 118 and correlates with exercise capacity.116 The cause of the exercise-related hypoxia is not clear. Vital capacity and functional residual capacity are reduced,119 consistent with a restrictive pattern of pulmonary abnormality.114 Adult patients after Fontan have been reported to have sufficient restriction so as to manifest severely diminished maximum ventilation with secondary reduction in aerobic capacity.114

The role of ventricular dysfunction and myocardial insufficiency in limiting exercise capacity in these patients remains unclear. This highlights the importance of identifying other potentially treatable sources of exercise intolerance before classifying the patient as having cardiogenic HF.

Diagnostic approach

In patients who have previously undergone Fontan-type repair, thorough evaluation and management of circulatory insufficiency is essential. Significant systemic or pulmonary venous obstruction is unlikely to be tolerated. Valve regurgitation is common and may be progressive, causing persistent volume overload, and is associated with a poorer outcome.105

Atrial arrhythmias increase in frequency with age120 and may be associated with tachycardia-induced ventricular dysfunction. Chronotropic incompetence may be more poorly tolerated than in other forms of heart disease.121 Residual right-to-left shunts may augment during exercise, severely limiting exercise capacity. In general, invasive hemodynamic investigation is needed both to document that myocardial dysfunction is primarily responsible and that other potentially treatable contributing factors are not present.

Pharmacotherapy.

Diuretics

Use of diuretics is common in the early post-operative period and in many instances becomes a permanent component of therapy, even in the absence of specific findings that clearly point to fluid overload. Peripheral edema, pleural and pericardial effusions, and other evidence of elevated systemic venous pressure occur frequently and often respond favorably to diuretics. However, the absence of a pulmonary pumping chamber renders the Fontan circulation particularly vulnerable to an inability to maintain an adequate systemic ventricular preload. Reduction of systemic venous pressure through diuresis reduces systemic ventricular preload in a more direct fashion than in patients with a biventricular circulation. Although the beneficial use of diuretics for HF invariably represents a balancing act with regard to maintenance of cardiac output, the margin of safety is far narrower in these patients and requires a greater degree of vigilance with regard to electrolyte disturbances, pre-renal azotemia, and exacerbation of exercise intolerance.

Digoxin

Digoxin is in common use for post-Fontan patients despite the absence of specific evidence of safety or benefit in this setting. There are no theoretical concerns that would make this population more or less likely to benefit from this agent than other groups with ventricular dysfunction.

Ace inhibitors

In patients with single ventricles, activation of the RAAS contributes to the increased vascular resistance that typically occurs after the Fontan procedure, and a favorable response to ACE inhibitors or ARB might therefore be anticipated.108 However, in a study of Fontan patients who did not have HF, administration of enalapril for 6 weeks did not alter systemic resistance, resting cardiac index, or exercise capacity.122, 123 Although these agents were well tolerated, and clinical experience confirms that ACE inhibitors can be safely administered to patients who have had the Fontan operation, the efficacy and risks of long-term ACE inhibitor therapy in this setting are not known.

β blockers

The utility of β-blockers in patients after Fontan-type operations is unknown. Specific clinical data in this population are absent. There is a reasonable probability that β-blocker therapy may impair exercise tolerance in these patients because of the pervasive finding of chronotropic incompetence in post-Fontan patients and the generally adverse impact of β-blocker therapy on VO2max.

Therapeutic recommendations

Recommendation 28: In patients with a univentricular circulation who undergo deterioration in clinical status (HF Stage B and C), consideration should be given to invasive assessment of hemodynamics, due to the heightened sensitivity of this group to elevations of filling pressure. (Level of Evidence C; Strength of Recommendation I)

Recommendation 29: A clinical decision as to the severity or presence of HF symptoms in patients with a univentricular circulation must include consideration of the patient’s prior status and underlying anatomic defects. Longitudinal evaluation is of great importance in this regard. (Level of Evidence C; Strength of Recommendation I)

Recommendation 30: Maintenance of atrioventricular synchrony should be a priority in the management of patients with a univentricular circulation and HF (HF Stages B and C). (Level of Evidence C; Strength of Recommendation I)

Recommendation 31: Patients with fluid retention associated with systemic ventricular dysfunction in a univentricular circulation (HF stage C) should be treated with diuretics to achieve a euvolemic state. In patients receiving chronic diuretic therapy, electrolyte balance and renal function should be periodically evaluated. (Level of Evidence C; Strength of Recommendation I)

Recommendation 32: Digoxin should be employed for patients with systemic ventricular dysfunction in a univentricular circulation (HF Stage C), for the purpose of relieving symptoms. Digoxin is not currently recommended for patients with asymptomatic systemic ventricular dysfunction in a univentricular circulation (HF Stage B). (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 33: For patients with a univentricular circulation after SCPC or TCPC, in whom systolic function is normal (HF Stage A), ACE inhibitors should not be employed routinely. (Level of Evidence C; Strength of Recommendation III).

Recommendation 34: For the treatment of asymptomatic systemic ventricular dysfunction in a univentricular circulation after SCPC or TCPC (HF Stage B), ACE inhibitors should be employed unless there is a specific contraindication. These medications should be employed at standard doses (Level of Evidence C; Strength of Recommendation IIa).

Recommendation 35: For the treatment of symptomatic systemic ventricular dysfunction in a univentricular circulation after SCPC or TCPC (HF Stage C), ACE inhibitors should be employed, as above. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 36: Use of β-blocker therapy is not routinely recommended for patients with systemic ventricular dysfunction in a univentricular circulation after SCPC or TCPC (HF Stage B and C). (Level of Evidence C; Strength of Recommendation IIb)

Acute heart failure

Pharmacologic support

In adult studies, it has been recognized that inotropes may be required in the management of refractory acute HF exacerbations that are accompanied by hypoperfusion and hypotension.124 Currently available inotropic agents increase contractility through a common pathway of increasing intracellular levels of cyclic adenylate monophosphate (cAMP). Increased cytoplasmic levels of cAMP cause increased calcium release from the sarcoplasmic reticulum and increased contractile force generation by the contractile apparatus. Increases in cAMP occur by two different mechanisms: β-adrenergic-mediated stimulation (increased production) or phosphodiesterase III (PDE III) inhibition (decreased degradation).125

The catecholamines are the most potent positive inotropic agents available; however, effects are not limited to inotropy. They also possess chronotropic properties and complex effects on vascular beds of the various organs of the body. Consequently, the choice of an agent may depend as much on the state of the circulation as it does on the myocardium.

Amrinone and milrinone belong to a class of nonglycoside, nonsympathomimetic inotropic agents (phosphodiesterase III inhibitors). Intravenous administration of amrinone or milrinone increases cardiac output and reduces cardiac filling pressures, pulmonary vascular resistance, and systemic vascular resistance with minimal effect on the heart rate and systemic blood pressure of adult patients.126 These drugs are particularly useful in the treatment of cardiogenic shock because they increase contractility and reduce afterload by peripheral vasodilatation without a consistent increase in myocardial oxygen consumption. Milrinone has been well studied in the pediatric population.126, 127, 128 A recently completed randomized, controlled trial demonstrated that milrinone infusion reduced the incidence of low cardiac output following cardiac surgery.129

Both of these agents require careful bolus dosing prior to initiating an infusion – a rapid infusion of the bolus dose may cause hypotension. An alternative approach, which may be preferred in unstable patients, is to begin infusion without an initial bolus.130 Since both of these drugs have relatively long half-lives, they should be used cautiously in the presence of significant hypotension. However, recent data indicate that the half-life of milrinone may be shorter than originally extrapolated from adult data.129

Nesiritide, a recombinant B-type natriuretic peptide, is the first new drug approved by the U.S. Food and Drug Administration in 14 years for the treatment of acutely decompensated HF in adults. Endogenous B-type natriuretic peptide is a cardiac hormone produced by the failing heart to counteract the maladaptive hemodynamic, neural, and hormonal compensations associated with the syndrome of CHF. Nesiritide is identical to the naturally occurring peptide, and like this peptide, Nesiritide reduces preload and afterload, leading to increases in cardiac index without reflex tachycardia or direct inotropic effect, increased diuresis and natriuresis, and suppression of the renin-angiotensin-aldosterone axis and sympathetic system. In a large randomized controlled clinical trial of 489 patients, nesiritide was found to be faster and more effective than IV nitroglycerin plus standard care at improving hemodynamic and symptomatology in patients with acutely decompensated CHF who have dyspnea at rest.131, 132, 133 Because of its unique mechanism of action and greater safety compared to both standard inotropic therapy with dobutamine and vasodilator therapy with nitroglycerin, the availability of nesiritide may alter the current algorithms for CHF management. However, no pediatric data are currently available.

Infants and children with low blood pressure and adequate cardiac function after cardiac surgery refractory to standard cardiopressors respond well to the pressor action of exogenous vasopressin and permit withdrawal or significant lowering of epinephrine dose. In a study of 11 children with vasodilatory shock after cardiac surgery, all 9 children with adequate cardiac function improved with vasopressin and survived; the 2 patients that received vasopressin in the setting of poor cardiac function died, despite transient improvement in blood pressure.134 Plasma vasopressin levels were decreased before treatment in 3 patients in whom blood levels were tested indicating that deficiency of the hormone may contribute to this hypotensive condition.

Mechanical support

Overview

Mechanical circulatory support has become an important addition to the treatment armamentarium for the infant or child with acutely decompensated HF and low cardiac output unresponsive to pharmacologic maneuvers. Options for mechanical circulatory support include total heart-lung bypass (Extracorporeal Membrane Oxygenation [ECMO]), or more limited cardiac support with a left ventricular assist device (LVAD), right ventricular assist device (RVAD), or intra-aortic balloon pump (IABP). In pediatric patients, most experience has been with ECMO, primarily because size limitations have generally precluded extensive use of other modalities. However, with the development of smaller ventricular assist devices (primarily in Europe) and the adaptation of existing devices, mechanical ventricular assistance has been applied to infants as young as 5 days of age.135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145 The choice of modality in a given patient will depend on the specific pathophysiology of HF in that patient, on the availability of support devices and on the expertise of the child’s physicians.

Risks and benefits

Mechanical assist in children can be life saving in low cardiac output situations where there is a reversible underlying abnormality that would benefit from short-term cardiac support.146 Mechanical support maintains end-organ function and reduces myocardial oxygen requirements during a critical period of recovery from a cardiac insult. Preliminary evidence indicates that cardiac remodeling, on both a structural and molecular level, occurs during mechanical support. Studies with small number of patients have demonstrated rates of survival to hospital discharge ranging from 25 to 65%.147, 148, 149, 150 Ibrahim and colleagues reviewed a 10-year experience in 96 cardiac patients requiring ECMO (67 patients) or ventricular assist devices (29 patients).147 Of these patients, 40% and 41%, respectively, survived to hospital discharge. The use of mechanical support in patients with single ventricle physiology has been associated in some studies with a poorer outcome, although recent data from Jaggers et al. and others support the use of ECMO after Norwood palliation.151 Overall hospital survival in the 35 patients in that series was 61%.151

Mechanical assist can also be used a bridge to transplant when cardiac recovery is not expected.152 In this case, mechanical support extends the period over which a patient can wait for a donor organ. End-organ function may be preserved, or perturbations in function may reverse with improved perfusion, thus improving transplant suitability and outcome.153

Therapeutic recommendations

Recommendation 37: Institution of mechanical cardiac support should be considered in patients without structural congenital heart disease, who manifest acute low cardiac output or who have intractable arrhythmias during a presumably temporary condition that is refractory to medical therapy (HF Stage D) such as myocarditis, septic shock, or acute rejection following cardiac transplantation. (Level of Evidence C; Strength of Recommendation I)

Recommendation 38: Institution of mechanical cardiac support should be considered in patients with or without structural congenital heart disease, who have acute decompensation of end-stage HF, primarily as a bridge to cardiac transplantation (HF Stage D). (Level of Evidence B; Strength of Recommendation I)

Recommendation 39: Institution of mechanical cardiac support may be considered in patients who have experienced cardiac arrest, hypoxia with pulmonary hypertension, or severe ventricular dysfunction with low cardiac output after surgery for congenital heart disease, including “rescue” of patients who fail to wean from cardiopulmonary bypass or who have myocarditis (HF Stage D). However, the outcomes in this group are less satisfactory than for other indications for mechanical support. (Level of Evidence B; Strength of Recommendation IIa)

Recommendation 40: Mechanical cardiac support is not indicated in those cases in which there is evidence of a severe and irreversible defect (e.g. catastrophic intracranial hemorrhage, or advanced multisystem organ failure). However, in practice, the determination of the severity and/or irreversibility of the associated condition may be difficult to determine, so the decision concerning eligibility for mechanical support is a difficult clinical judgment. (Level of Evidence C; Strength of Recommendation IIb)

Electrophysiology considerations

Overview

Arrhythmia is a major cause of morbidity and mortality in pediatric patients with end-stage HF.154, 155, 156, 157, 158, 159, 160, 161 Myocardial scars and stretching associated with pressure or volume overload, previous heart surgery or intrinsic myocardial disease provide a ripe substrate for arrhythmogenesis.162, 163 Multiple triggers for arrhythmia are prevalent in patients with HF and include electrolyte imbalance, blood gas and pH abnormalities, ischemia and administration of potentially pro-arrhythmic drugs such as digoxin, positive inotropes, phosphodiesterase inhibitors and anti-arrhythmic drugs themselves.164, 165 Although it is controversial whether ventricular arrhythmias are independent risk factors for sudden death in this population, sustained tachycardia may cause hemodynamic collapse, and complex non-sustained ventricular ectopy reflects potential electrical instability of the myocardium.157 Atrial arrhythmias may also impair cardiac output and aggravate HF by eliminating the atrial contribution to filling and/or causing a rapid ventricular response.

In patients with dilated cardiomyopathy, between 50 and 63% of those patients who die have ventricular arrhythmias at presentation.154, 155 In pediatric patients awaiting transplantation, 62% had life-threatening arrhythmias, most commonly ventricular tachycardia.166 Arrhythmia management is an important component in the overall care of the pediatric patient with HF.

Treatment can be broken down into the management of acute arrhythmias causing hemodynamic collapse and chronic arrhythmias requiring long-term suppression because they lead to impaired cardiac performance or may pose a significant risk factor for sudden death.

Pharmacotherapy

Acute arrhythmia management

Arrhythmias likely to require acute treatment in patients with HF include atrial tachyarrhythmias with a rapid ventricular rate, paroxysmal supraventricular tachycardia, junctional ectopic tachycardia and sustained ventricular tachycardia. Synchronized DC cardioversion/defibrillation should be considered for treatment of either supraventricular or ventricular arrhythmias if hemodynamic collapse is imminent.167, 168

Atrial tachycardia, flutter or fibrillation can be initially managed by controlling the ventricular rate with AV nodal blocking agents. For rate control, digoxin is not likely to be useful primarily because of its delayed onset of action. Intravenous diltiazem is a reasonable first choice, but hypotension is a major concern in a setting of impaired ventricular function. An intravenous β-blocker, such as esmolol can be useful in decreasing the ventricular rate but hypotension is likely to preclude its use.

The treatment of the atrial rhythm itself includes intravenous amiodarone, procainamide or ibutilide. However, side effects such as hypotension and torsade de pointes occur frequently and elective cardioversion is often preferable. There is very little experience using IV ibutilide for the acute conversion of atrial flutter or fibrillation in pediatric patients with significant myocardial dysfunction. Paroxysmal supraventricular tachycardia is best treated with intravenous adenosine, but a longer acting agent such as procainamide or amiodarone may be necessary for control of recurrent episodes.

Junctional ectopic tachycardia responds best to IV amiodarone and to minimizing the dose of any intravenous inotropes or phosphodiesterase inhibitors. The pharmacologic treatments for ventricular tachycardia, include intravenous lidocaine, amiodarone and procainamide.169, 170 Lidocaine is the first line drug because of its rapid onset of action and limited toxicity if drug levels are kept in the therapeutic range. If this is unsuccessful, either intravenous amiodarone or procainamide can be utilized, but amiodarone is preferable because of a lower incidence of hypotension and tendency for arrhythmia aggravation.

Chronic arrhythmia management

Chronic drug suppression of arrhythmias in patients with HF can be very problematic. For atrial arrhythmias, many drugs have been shown to have a modest success rate including those in the category of IA, IC and III. However, amiodarone stands out as the most appropriate drug because of its somewhat higher success rate and lesser tendency for pro-arrhythmia.171, 172 For ventricular tachycardias, the superiority of amiodarone over the other drugs is even more evident. This medication is usually well tolerated, even in patients with very poor contractility. The major limiting factor in the short-term is bradycardia and hypotension, while longer use requires monitoring for thyroid and liver dysfunction as well as pulmonary interstitial disease.

As an alternative to pharmacotherapy in the setting of chronic atrial arrhythmias, ablation therapy can be considered. The safety of radiofrequency or surgical ablation is well established, and there are significant data attesting to its efficacy.172, 173, 174 Triedman and colleagues report a 73% procedural success rate for radiofrequency ablation, with approximately 50% success at 1 year, for a mixed population including Fontan and Mustard patients.172 In a population of Fontan patients, short-term control of atrial tachycardia was achieved in 14/15 patients using a modified RA maze intraoperatively, with no recurrences after 43 months of follow-up.173

Therapeutic recommendations

Recommendation 41: In patients with significant arrhythmias in the setting of HF associated with structural heart disease (HF Stages B, C or D), consideration should be given to surgical repair of important uncorrected or residual defects, as this is likely to be essential to achieve adequate rhythm control. (Level of Evidence C; Strength of Recommendation I)

Recommendation 42: In patients with significant arrhythmias in the setting of HF associated with structural heart disease (HF Stages B, C or D), consideration should be given to improving or optimizing the medical treatment for HF and correcting aggravating factors such as electrolyte abnormalities, as this is likely to be a key determinant of the successful control of arrhythmias. (Level of Evidence C; Strength of Recommendation I)

Recommendation 43: In patients with significant arrhythmias in the setting of HF associated with structural heart disease (HF Stages B, C or D), maintenance of atrio-ventricular synchrony is of great importance in optimizing hemodynamics, and management of intra-atrial arrhythmias should be oriented towards restoration of sinus rhythm rather than on ventricular rate control alone. (Level of Evidence C; Strength of Recommendation I)

Recommendation 44: In patients with impaired ventricular function (HF Stages B, C or D), many forms of tachycardia can precipitate acute hemodynamic collapse, and many of the available pharmacotherapies can precipitate hypotension. Therefore, consideration should be given to early utilization of electrical cardioversion/defibrillation for treatment of both atrial and ventricular tachycardias. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 45: For acute treatment of clinically significant junctional ectopic tachycardia, the first line of therapy should usually be amiodarone because of its superior efficacy as compared to alternative medications. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 46: For chronic suppression of atrial arrhythmias in children with HF (HF Stages B, C or D), the first line of therapy should usually be amiodarone because of its superior efficacy as compared to alternative medications. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 47: Patients with potentially significant atrioventricular tachycardias who are scheduled to undergo completion of the Fontan procedure, should be considered for definitive ablation therapy, prior to the Fontan surgery, to reduce the risk of serious arrhythmia during the postoperative period and beyond. Ablation, in these circumstances, might be accomplished by transcatheter technique or by intra-operative Maze procedure. (Level of Evidence C; Strength of Recommendation IIa)

Device therapy

Pediatric ICD and resynchronization experience

The development of the ICD has improved survival in the adult HF population.175 Recent multicenter trials in adult HF patients have shown that ICD therapy is more beneficial than antiarrhythmics in both ischemic and idiopathic cardiomyopathies.176, 177 Data from Bocker and colleagues suggest that ICD therapy prolongs life in NYHA classes I—III, with greatest initial benefit in class II and III but longest benefit in class I.178 However no multicenter prospective trials of ICD therapy in children with any heart disease have been performed.

In a study of the use of defibrillator therapy in adult patients awaiting cardiac transplant, 71% received appropriate discharge with no inappropriate discharges.179 In a multicenter retrospective review of ICD therapy in pediatric patients awaiting heart transplantation, 45% of the patients had appropriate discharges with an inappropriate discharge rate of 27%. Freedom from appropriate discharge at 100 days was 63%.180

In pediatric practice it appears that ICD are commonly used in older HF patients with missed sudden death episodes, but not as commonly used in younger patients, or those with syncope.181 This may be due to the higher rate of complications and the technical difficulties associated with placing ICD in the pediatric population. Berul and colleagues found a significantly higher complication and infection rate when comparing a pediatric group of ICD recipients to an adult group.182 However, this issue may be diminishing with the development of newer leadless ICD systems for smaller children.183

In adult patients with HF associated with LV dysfunction and left bundle branch block, LV resynchronization has proven valuable in improving hemodynamics and clinical status, which is thought to be the result of improved mechanical efficiency within the left ventricle.184, 185, 186, 187 This therapy has not been validated in children, but Dubin and colleagues have shown that resynchronization of the right ventricle in patients with right ventricular dysfunction can produce favorable hemodynamic changes in an acute setting.188 In addition, Janousek et al have shown improved blood pressure in patients with acute heart failure following repair of congenital heart disease, by combining atrioventricular optimization with ventricular resynchronization of the right ventricle.189 While these results are intriguing, their implications are not yet clear.

Special considerations in structural heart disease

Patients with structural heart disease offer unique challenges in arrhythmia management that may not need to be considered when treating the patient with dilated cardiomyopathy alone. The negative inotropic properties of anti-arrhythmic therapy may be accentuated in patients with congenital heart disease such as those with single ventricle physiology, multiple ventricular scars, or significant dysfunction of either the atrioventricular or semilunar valves. A second area of concern is that patients with significant ventricular dysfunction may require an elevated heart rate to help maintain an adequate cardiac output. Antiarrhythmic medications may lead to a relative bradycardia, and impair cardiac output. This is compounded in patients with congenital heart disease who have underlying sinus or atrioventricular node dysfunction.

There are also issues encountered with the use of device therapy in patients with congenital heart disease that are not seen in those with structurally normal hearts. The use of transvenous pacing and defibrillator leads is impossible in some forms of palliated congenital heart disease. Patients who have undergone superior vena cava to pulmonary artery anastomosis have no access to the heart from above. In patients who have undergone a Fontan procedure there is typically no direct venous access to the heart. Transvenous pacing and defibrillator leads are contraindicated in patients with residual right to left shunting such as seen in Eisenmenger’s syndrome. The inability to use transvenous systems in these patients necessitates the placement of epicardial systems with their risks of morbidity and mortality in a hemodynamically compromised patient.

Although ventricular arrhythmias are the most worrisome type of arrhythmias seen in patients with HF, supraventricular arrhythmias also can lead to significant hemodynamic compromise. Patients with significant myocardial dysfunction will be compromised with relatively modest increases in their heart rates and are at risk for the rhythm to degenerate into a life threatening arrhythmia. In a study by Rosenthal et al. of 96 patients listed for cardiac transplantation, 2 of 5 patients with SVT degenerated into ventricular fibrillation.166 Atrial tachyarrhythmias are frequently seen in patients with congenital heart disease that have had atrial level surgery such as Fontan, Senning, or Mustard procedures.

Ventricular arrhythmias are common in patients with HF. It is well known that patients who have undergone surgery for congenital heart disease will often develop ventricular arrhythmias from scars and suture lines in the heart. Although there would seem to be an increased preponderance of these arrhythmias in patients with congenital heart disease and HF, Rosenthal and colleagues found that of 8 pre-transplant patients with VT only 1 had congenital heart disease.166 In the same study one patient with congenital heart disease developed VF.

Therapeutic recommendations

Recommendation 48: At this time, clinical criteria for ICD placement in children are in flux and are not well defined. ICD placement may be considered as a bridge to cardiac transplantation in selected patients with advanced HF (HF Stage C and D), on a case-by-case basis. (Level of Evidence C; Strength of Recommendation IIa)

Recommendation 49: In patients with structural heart disease, particularly including those with a univentricular circulation, pacemaker implantation should be considered as possible adjunctive therapy, to maintain atrioventricular synchrony and chronotropic competence, and to permit administration of other pharmacotherapies that are needed for treatment of HF. (Level of Evidence C; Strength of Recommendation IIa)

References

1. 1 Lipshultz SE , Sleeper LA , Towbin JA , et al. The incidence of pediatric cardiomyopathy in two regions of the United States . N Engl J Med . 2003;348:1647–1655 . CrossRef

2. 2 Boucek MM , Edwards LB , Keck BM , et al. The Registry of the International Society for Heart and Lung Transplantation (Sixth Official Pediatric Report–2003) . J Heart Lung Transplant . 2003;22:636–652 . Full Text | Full-Text PDF (1066 KB) | CrossRef

3. 3 Heart Failure Society of America (HFSA) practice guidelines . HFSA guidelines for management of patients with heart failure caused by left ventricular systolic dysfunction-pharmacological approaches . J Card Fail . 1999;5:357–382 . Full-Text PDF (2817 KB) | CrossRef

4. 4 Katz AM . Heart Failure Pathophysiology, Molecular Biology and Clinical Management . Philadelphia, Pa: Lippincott, Williams & Wilkins; 2000; .

5. 5 Ross RD , Daniels SR , Schwartz DC , Hannon DW , Shukla R , Kaplan S . Plasma norepinephrine levels in infants and children with congestive heart failure . Am J Cardiol . 1987;59:911–914 . MEDLINE | CrossRef

6. 6 Johnstone DE , Abdulla A , Arnold JM , et al. Diagnosis and management of heart failure. Canadian Cardiovascular Society . Can J Cardiol . 1994;10:613–631 35–54 .

7. 7 Wu JR , Chang HR , Huang TY , Chiang CH , Chen SS . Reduction in lymphocyte beta-adrenergic receptor density in infants and children with heart failure secondary to congenital heart disease . Am J Cardiol . 1996;77:170–174 . Abstract | Full-Text PDF (557 KB) | CrossRef

8. 8 Ross RD , Bollinger RO , Pinsky WW . Grading the severity of congestive heart failure in infants . Pediatr Cardiol . 1992;13:72–75 . MEDLINE | CrossRef

9. 9 Connolly D , Rutkowski M , Auslender M , Artman M . The New York University Pediatric Heart Failure Index (a new method of quantifying chronic heart failure severity in children) . J Pediatr . 2001;138:644–648 . Abstract | Full Text | Full-Text PDF (87 KB) | CrossRef

10. 10 Ross RD . Grading the graders of congestive heart failure in children . J Pediatr . 2001;138:618–620 . Full Text | Full-Text PDF (44 KB) | CrossRef

11. 11 Ohuchi H , Takasugi H , Ohashi H , et al. Stratification of pediatric heart failure on the basis of neurohormonal and cardiac autonomic nervous activities in patients with congenital heart disease . Circulation . 2003;108:2368–2376 . CrossRef

12. 12 Hunt SA , Baker DW , Chin MH , et al. ACC/AHA guidelines for the evaluation and management of chronic heart failure in the adult: executive summary. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to revise the 1995 Guidelines for the Evaluation and Management of Heart Failure) . J Am Coll Cardiol . 2001;38:2101–2113 . Full Text | Full-Text PDF (184 KB) | CrossRef

13. 13 Bonnet D , de Lonlay P , Gautier I , et al. Efficiency of metabolic screening in childhood cardiomyopathies . Eur Heart J . 1998;19:790–793 . CrossRef

14. 14 Schwartz ML , Cox GF , Lin AE , et al. Clinical approach to genetic cardiomyopathy in children . Circulation . 1996;94:2021–2038 . MEDLINE

15. 15 Kohlschutter A , Hausdorf G . Primary (genetic) cardiomyopathies in infancy. A survey of possible disorders and guidelines for diagnosis . Eur J Pediatr . 1986;145:454–459 . MEDLINE | CrossRef

16. 16 Krishnan US , Gersony WM , Berman-Rosenzweig E , Apfel HD . Late left ventricular function after surgery for children with chronic symptomatic mitral regurgitation . Circulation . 1997;96:4280–4285 . MEDLINE

17. 17 Skudicky D , Essop MR , Sareli P . Time-related changes in left ventricular function after double valve replacement for combined aortic and mitral regurgitation in a young rheumatic population. Predictors of postoperative left ventricular performance and role of chordal preservation . Circulation . 1997;95:899–904 . MEDLINE

18. 18 Packer M , Gheorghiade M , Young JB , et al. Withdrawal of digoxin from patients with chronic heart failure treated with angiotensin-converting-enzyme inhibitors. RADIANCE Study . N Engl J Med . 1993;329:1–7 . MEDLINE | CrossRef

19. 19 Adams KF , Gheorghiade M , Uretsky BF , Patterson JH , Schwartz TA , Young JB . Clinical benefits of low serum digoxin concentrations in heart failure . J Am Coll Cardiol . 2002;39:946–953 . Abstract | Full Text | Full-Text PDF (223 KB) | CrossRef

20. 20 Rathore SS , Curtis JP , Wang Y , Bristow MR , Krumholz HM . Association of serum digoxin concentration and outcomes in patients with heart failure . Jama . 2003;289:871–878 . MEDLINE | CrossRef

21. 21 Pitt B , Zannad F , Remme WJ , et al. The effect of spironolactone on morbidity and mortality in patients with severe heart failure. Randomized Aldactone Evaluation Study Investigators . N Engl J Med . 1999;341:709–717 . MEDLINE | CrossRef

22. 22 Pitt B , Remme W , Zannad F , et al. Eplerenone, a selective aldosterone blocker, in patients with left ventricular dysfunction after myocardial infarction . N Engl J Med . 2003;348:1309–1321 . CrossRef

23. 23 Brunner-La Rocca HP , Vaddadi G , Esler MD . Recent insight into therapy of congestive heart failure (focus on ACE inhibition and angiotensin-II antagonism) . J Am Coll Cardiol . 1999;33:1163–1173 . Abstract | Full Text | Full-Text PDF (216 KB) | CrossRef

24. 24 Braunwald E , Bristow MR . Congestive heart failure (fifty years of progress) . Circulation . 2000;102:IV14–IV23 .

25. 25 Swedberg K , Eneroth P , Kjekshus J , Wilhelmsen L CONSENSUS Trial Study Group . Hormones regulating cardiovascular function in patients with severe congestive heart failure and their relation to mortality . Circulation . 1990;82:1730–1736 . MEDLINE

26. 26 Gilbert EM , Sandoval A , Larrabee P , Renlund DG , O’Connell JB , Bristow MR . Lisinopril lowers cardiac adrenergic drive and increases beta-receptor density in the failing human heart . Circulation . 1993;88:472–480 . MEDLINE

27. 27 The CONSENSUS Trial Study Group . Effects of enalapril on mortality in severe congestive heart failure. Results of the Cooperative North Scandinavian Enalapril Survival Study (CONSENSUS) . N Engl J Med . 1987;316:1429–1435 . MEDLINE

28. 28 Cohn JN , Johnson G , Ziesche S , et al. A comparison of enalapril with hydralazine-isosorbide dinitrate in the treatment of chronic congestive heart failure . N Engl J Med . 1991;325:303–310 . MEDLINE

29. 29 Effect of enalapril on survival in patients with reduced left ventricular ejection fractions and congestive heart failure. The SOLVD Investigators . N Engl J Med . 1991;325:293–302 . MEDLINE

30. 30 Effect of enalapril on mortality and the development of heart failure in asymptomatic patients with reduced left ventricular ejection fractions. The SOLVD Investigattors . N Engl J Med . 1992;327:685–691 . MEDLINE

31. 31 Packer M . Do angiotensin-converting enzyme inhibitors prolong life in patients with heart failure treated in clinical practice . J Am Coll Cardiol . 1996;28:1323–1327 . Abstract | Full-Text PDF (517 KB) | CrossRef

32. 32 Uretsky BF , Shaver JA , Liang CS , et al. Modulation of hemodynamic effects with a converting enzyme inhibitor (acute hemodynamic dose-response relationship of a new angiotensin converting enzyme inhibitor, lisinopril, with observations on long-term clinical, functional, and biochemical responses) . Am Heart J . 1988;116:480–488 . MEDLINE | CrossRef

33. 33 Pacher R , Globits S , Bergler-Klein J , et al. Clinical and neurohumoral response of patients with severe congestive heart failure treated with two different captopril dosages . Eur Heart J . 1993;14:273–278 .

34. 34 Riegger GA . Effects of quinapril on exercise tolerance in patients with mild to moderate heart failure . Eur Heart J . 1991;12:705–711 .

35. 35 Packer M , Poole-Wilson PA , Armstrong PW , et al. ATLAS Study Group Comparative effects of low and high doses of the angiotensin-converting enzyme inhibitor, lisinopril, on morbidity and mortality in chronic heart failure . Circulation . 1999;100:2312–2318 . MEDLINE

36. 36 Lin M , Chiang HT , Lin SL , et al. Vasodilator therapy in chronic asymptomatic aortic regurgitation (enalapril versus hydralazine therapy) . J Am Coll Cardiol . 1994;24:1046–1053 . MEDLINE

37. 37 Pitt B , Konstam MA . Overview of angiotensin II-receptor antagonists . Am J Cardiol . 1998;82:47S–49S . Full Text | Full-Text PDF (70 KB) | CrossRef

38. 38 Pitt B , Segal R , Martinez FA , et al. Randomised trial of losartan versus captopril in patients over 65 with heart failure (Evaluation of Losartan in the Elderly Study, ELITE) . Lancet . 1997;349:747–752 . Abstract | Full Text | Full-Text PDF (89 KB) | CrossRef

39. 39 Pitt B , Poole-Wilson P , Segal R , et al. Effects of losartan versus captopril on mortality in patients with symptomatic heart failure (rationale, design, and baseline characteristics of patients in the Losartan Heart Failure Survival Study—ELITE II) . J Card Fail . 1999;5:146–154 . Abstract | Full-Text PDF (914 KB) | CrossRef

40. 40 Hamroff G , Katz SD , Mancini D , et al. Addition of angiotensin II receptor blockade to maximal angiotensin-converting enzyme inhibition improves exercise capacity in patients with severe congestive heart failure . Circulation . 1999;99:990–992 .

41. 41 Bengur AR , Beekman RH , Rocchini AP , Crowley DC , Schork MA , Rosenthal A . Acute hemodynamic effects of captopril in children with a congestive or restrictive cardiomyopathy . Circulation . 1991;83:523–527 . MEDLINE

42. 42 Leversha AM , Wilson NJ , Clarkson PM , Calder AL , Ramage MC , Neutze JM . Efficacy and dosage of enalapril in congenital and acquired heart disease . Arch Dis Child . 1994;70:35–39 . CrossRef

43. 43 Seguchi M , Nakazawa M , Momma K . Effect of enalapril on infants and children with congestive heart failure . Cardiol Young . 1992;2:14–19 .

44. 44 Stern H , Weil J , Genz T , Vogt W , Buhlmeyer K . Captopril in children with dilated cardiomyopathy (acute and long-term effects in a prospective study of hemodynamic and hormonal effects) . Pediatr Cardiol . 1990;11:22–28 . MEDLINE | CrossRef

45. 45 Schiffman H , Gawlik L , Wessel A . Treatment effects of captopril in neonates, infants and young children with congestive heart failure . Z Kardiol . 1996;85:709 .

46. 46 Lewis AB , Chabot M . The effect of treatment with angiotensin-converting enzyme inhibitors on survival of pediatric patients with dilated cardiomyopathy . Pediatr Cardiol . 1993;14:9–12 . MEDLINE

47. 47 Mori Y , Nakazawa M , Tomimatsu H , Momma K . Long-term effect of angiotensin-converting enzyme inhibitor in volume overloaded heart during growth (a controlled pilot study) . J Am Coll Cardiol . 2000;36:270–275 . Abstract | Full Text | Full-Text PDF (204 KB) | CrossRef

48. 48 Marino MR , Vachharajani NN . Pharmacokinetics of irbesartan are not altered in special populations . J Cardiovasc Pharmacol . 2002;40:112–122 . MEDLINE | CrossRef

49. 49 Smith KM , Macmillan JB , McGrath JC . Investigation of alpha1-adrenoceptor subtypes mediating vasoconstriction in rabbit cutaneous resistance arteries . Br J Pharmacol . 1997;122:825–832 . MEDLINE | CrossRef

50. 50 Elhawary AM , Pang CC . Alpha 1b-adrenoceptors mediate renal tubular sodium and water reabsorption in the rat . Br J Pharmacol . 1994;111:819–824 . MEDLINE

51. 51 Communal C , Singh K , Pimentel DR , Colucci WS . Norepinephrine stimulates apoptosis in adult rat ventricular myocytes by activation of the beta-adrenergic pathway . Circulation . 1998;98:1329–1334 . MEDLINE

52. 52 Packer M . Current role of beta-adrenergic blockers in the management of chronic heart failure . Am J Med . 2001;110(Suppl 7A):81S–94S .

53. 53 Bruns LA , Chrisant MK , Lamour JM , et al. Carvedilol as therapy in pediatric heart failure (an initial multicenter experience) . J Pediatr . 2001;138:505–511 . Abstract | Full Text | Full-Text PDF (82 KB) | CrossRef

54. 54 Rusconi P , Gomez-Marin O , Rossique-Gonzalez M , et al. Carvedilol in children with cardiomyopathy (3 years experience in a single institution) . J Heart Lung Transplant . 2003; in press .

55. 55 Packer M , Bristow MR , Cohn JN , et al. U.S. Carvedilol Heart Failure Study Group The effect of carvedilol on morbidity and mortality in patients with chronic heart failure . N Engl J Med . 1996;334:1349–1355 . MEDLINE | CrossRef

56. 56 Waagstein F , Caidahl K , Wallentin I , Bergh CH , Hjalmarson A . Long-term beta-blockade in dilated cardiomyopathy. Effects of short- and long-term metoprolol treatment followed by withdrawal and readministration of metoprolol . Circulation . 1989;80:551–563 . MEDLINE

57. 57 Epstein SE , Braunwald E . The effect of beta adrenergic blockade on patterns of urinary sodium excretion. Studies in normal subjects and in patients with heart disease . Ann Intern Med . 1966;65:20–27 . MEDLINE

58. 58 Weil JV , Chidsey CA . Plasma volume expansion resulting from interference with adrenergic function in normal man . Circulation . 1968;37:54–61 . MEDLINE

59. 59 Waagstein F , Bristow MR , Swedberg K , et al. Metoprolol in Dilated Cardiomyopathy (MDC) Trial Study Group Beneficial effects of metoprolol in idiopathic dilated cardiomyopathy . Lancet . 1993;342:1441–1446 . Abstract | CrossRef

60. 60 Effects of metoprolol CR in patients with ischemic and dilated cardiomyopathy (the randomized evaluation of strategies for left ventricular dysfunction pilot study) . Circulation . 2000;101:378–384 .

61. 61 Hjalmarson A , Goldstein S , Fagerberg B , et al. MERIT-HF Study Group Effects of controlled-release metoprolol on total mortality, hospitalizations, and well-being in patients with heart failure (the Metoprolol CR/XL Randomized Intervention Trial in congestive heart failure (MERIT-HF)) . Jama . 2000;283:1295–1302 . MEDLINE | CrossRef

62. 62 Colucci WS , Packer M , Bristow MR , et al. US Carvedilol Heart Failure Study Group Carvedilol inhibits clinical progression in patients with mild symptoms of heart failure . Circulation . 1996;94:2800–2806 . MEDLINE

63. 63 Packer M , Colucci WS , Sackner-Bernstein JD , et al. Double-blind, placebo-controlled study of the effects of carvedilol in patients with moderate to severe heart failure. The PRECISE Trial. Prospective Randomized Evaluation of Carvedilol on Symptoms and Exercise . Circulation . 1996;94:2793–2799 . MEDLINE

64. 64 Bristow MR , Gilbert EM , Abraham WT , et al. Carvedilol produces dose-related improvements in left ventricular function and survival in subjects with chronic heart failure. MOCHA Investigators . Circulation . 1996;94:2807–2816 . MEDLINE

65. 65 Packer M , Coats AJ , Fowler MB , et al. Effect of carvedilol on survival in severe chronic heart failure . N Engl J Med . 2001;344:1651–1658 . MEDLINE | CrossRef

66. 66 Shaddy RE , Tani LY , Gidding SS , et al. Beta-blocker treatment of dilated cardiomyopathy with congestive heart failure in children (a multi-institutional experience) . J Heart Lung Transplant . 1999;18:269–274 . Abstract | Full Text | Full-Text PDF (119 KB) | CrossRef

67. 67 Azeka E , Franchini Ramires JA , Valler C , Alcides Bocchi E . Delisting of infants and children from the heart transplantation waiting list after carvedilol treatment . J Am Coll Cardiol . 2002;40:2034–2038 . Abstract | Full Text | Full-Text PDF (95 KB) | CrossRef

68. 68 Grossman W . Diastolic dysfunction in congestive heart failure . N Engl J Med . 1991;325:1557–1564 . MEDLINE

69. 69 Grossman W . Defining diastolic dysfunction . Circulation . 2000;101:2020–2021 .

70. 70 Sweitzer NK , Stevenson LW . Diastolic heart failure (miles to go before we sleep) . Am J Med . 2000;109:683–685 . Full Text | Full-Text PDF (49 KB) | CrossRef

71. 71 Vasan RS , Benjamin EJ , Levy D . Prevalence, clinical features and prognosis of diastolic heart failure (an epidemiologic perspective) . J Am Coll Cardiol . 1995;26:1565–1574 . Abstract | Full-Text PDF (1039 KB) | CrossRef

72. 72 Vasan RS , Levy D . Defining diastolic heart failure (a call for standardized diagnostic criteria) . Circulation . 2000;101:2118–2121 .

73. 73 Tardif JC , Rouleau JL . Diastolic dysfunction . Can J Cardiol . 1996;12:389–398 .

74. 74 Guidelines for the evaluation and management of heart failure. Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on Evaluation and Management of Heart Failure) . Circulation . 1995;92:2764–2784 . MEDLINE

75. 75 Lewis AB . Clinical profile and outcome of restrictive cardiomyopathy in children . Am Heart J . 1992;123:1589–1593 . MEDLINE | CrossRef

76. 76 Rivenes SM , Kearney DL , Smith EO , Towbin JA , Denfield SW . Sudden death and cardiovascular collapse in children with restrictive cardiomyopathy . Circulation . 2000;102:876–882 .

77. 77 Kushwaha SS , Fallon JT , Fuster V . Restrictive cardiomyopathy . N Engl J Med . 1997;336:267–276 . MEDLINE | CrossRef

78. 78 Chen SC , Balfour IC , Jureidini S . Clinical spectrum of restrictive cardiomyopathy in children . J Heart Lung Transplant . 2001;20:90–92 . Abstract | Full Text | Full-Text PDF (95 KB) | CrossRef

79. 79 Lee RT , Lord CP , Plappert T , Sutton MS . Effects of nifedipine on transmitral Doppler blood flow velocity profile in patients with concentric left ventricular hypertrophy . Am Heart J . 1990;119:1130–1136 . MEDLINE | CrossRef

80. 80 Lorell BH , Grossman W . Cardiac hypertrophy (the consequences for diastole) . J Am Coll Cardiol . 1987;9:1189–1193 . MEDLINE

81. 81 Devereux RB , Palmieri V , Sharpe N , et al. Effects of once-daily angiotensin-converting enzyme inhibition and calcium channel blockade-based antihypertensive treatment regimens on left ventricular hypertrophy and diastolic filling in hypertension (the prospective randomized enalapril study evaluating regression of ventricular enlargement (preserve) trial) . Circulation . 2001;104:1248–1254 . CrossRef

82. 82 Warner JG , Metzger DC , Kitzman DW , Wesley DJ , Little WC . Losartan improves exercise tolerance in patients with diastolic dysfunction and a hypertensive response to exercise . J Am Coll Cardiol . 1999;33:1567–1572 . Abstract | Full Text | Full-Text PDF (206 KB) | CrossRef

83. 83 Paulus WJ , Vantrimpont PJ , Shah AM . Acute effects of nitric oxide on left ventricular relaxation and diastolic distensibility in humans. Assessment by bicoronary sodium nitroprusside infusion . Circulation . 1994;89:2070–2078 . MEDLINE

84. 84 Redington AN , Rigby ML , Shinebourne EA , Oldershaw PJ . Changes in the pressure-volume relation of the right ventricle when its loading conditions are modified . Br Heart J . 1990;63:45–49 . MEDLINE | CrossRef

85. 85 Hagler DJ , Ritter DG , Mair DD , et al. Right and left ventricular function after the Mustard procedure in transposition of the great arteries . Am J Cardiol . 1979;44:276–283 . MEDLINE | CrossRef

86. 86 Benson LN , Bonet J , McLaughlin P , et al. Assessment of right ventricular function during supine bicycle exercise after Mustard’s operation . Circulation . 1982;65:1052–1059 . MEDLINE

87. 87 Murphy JH , Barlai-Kovach MM , Mathews RA , et al. Rest and exercise right and left ventricular function late after the Mustard operation (assessment by radionuclide ventriculography) . Am J Cardiol . 1983;51:1520–1526 . MEDLINE | CrossRef

88. 88 Mathews RA , Fricker FJ , Beerman LB , et al. Exercise studies after the Mustard operation in transposition of the great arteries . Am J Cardiol . 1983;51:1526–1529 . MEDLINE | CrossRef

89. 89 Ensing GJ , Heise CT , Driscoll DJ . Cardiovascular response to exercise after the Mustard operation for simple and complex transposition of the great vessels . Am J Cardiol . 1988;62:617–622 . MEDLINE | CrossRef

90. 90 Paridon SM , Humes RA , Pinsky WW . The role of chronotropic impairment during exercise after the Mustard operation . J Am Coll Cardiol . 1991;17:729–732 . MEDLINE

91. 91 Reybrouck T , Gewillig M , Dumoulin M , van der Hauwaert LG . Cardiorespiratory exercise performance after Senning operation for transposition of the great arteries . Br Heart J . 1993;70:175–179 . MEDLINE | CrossRef

92. 92 Matthys D , De Wolf D , Verhaaren H . Lack of increase in stroke volume during exercise in asymptomatic adolescents in sinus rhythm after intraatrial repair for simple transposition of the great arteries . Am J Cardiol . 1996;78:595–596 . Abstract | Full-Text PDF (226 KB) | CrossRef

93. 93 Fogel MA , Weinberg PM , Fellows KE , Hoffman EA . A study in ventricular-ventricular interaction. Single right ventricles compared with systemic right ventricles in a dual-chamber circulation . Circulation . 1995;92:219–230 . MEDLINE

94. 94 Millane T , Bernard EJ , Jaeggi E , et al. Role of ischemia and infarction in late right ventricular dysfunction after atrial repair of transposition of the great arteries . J Am Coll Cardiol . 2000;35:1661–1668 . Abstract | Full Text | Full-Text PDF (923 KB) | CrossRef

95. 95 Lubiszewska B , Gosiewska E , Hoffman P , et al. Myocardial perfusion and function of the systemic right ventricle in patients after atrial switch procedure for complete transposition (long-term follow-up) . J Am Coll Cardiol . 2000;36:1365–1370 . Abstract | Full Text | Full-Text PDF (631 KB) | CrossRef

96. 96 Singh TP , Humes RA , Muzik O , Kottamasu S , Karpawich PP , Di Carli MF . Myocardial flow reserve in patients with a systemic right ventricle after atrial switch repair . J Am Coll Cardiol . 2001;37:2120–2125 . Abstract | Full Text | Full-Text PDF (220 KB) | CrossRef

97. 97 Graham TP , Bernard YD , Mellen BG , et al. Long-term outcome in congenitally corrected transposition of the great arteries (a multi-institutional study) . J Am Coll Cardiol . 2000;36:255–261 . Abstract | Full Text | Full-Text PDF (273 KB) | CrossRef

98. 98 Imamura M , Drummond-Webb JJ , Murphy DJ , et al. Results of the double switch operation in the current era . Ann Thorac Surg . 2000;70:100–105 . MEDLINE | CrossRef

99. 99 Hechter SJ , Fredriksen PM , Liu P , et al. Angiotensin-converting enzyme inhibitors in adults after the Mustard procedure . Am J Cardiol . 2001;87:660–663 A11 . Full Text | Full-Text PDF (240 KB) | CrossRef

100. 100 Sluysmans T , Sanders SP , van der Velde M , et al. Natural history and patterns of recovery of contractile function in single left ventricle after Fontan operation . Circulation . 1992;86:1753–1761 . MEDLINE

101. 101 Tanoue Y , Sese A , Ueno Y , Joh K , Hijii T . Bidirectional Glenn procedure improves the mechanical efficiency of a total cavopulmonary connection in high-risk fontan candidates . Circulation . 2001;103:2176–2180 .

102. 102 Berman NB , Kimball TR . Systemic ventricular size and performance before and after bidirectional cavopulmonary anastomosis . J Pediatr . 1993;122:S63–S67 . Abstract | Full-Text PDF (363 KB) | CrossRef

103. 103 Graham TP , Johns JA . Pre-operative assessment of ventricular function in patients considered for Fontan procedure . Herz . 1992;17:213–219 . MEDLINE

104. 104 Matsuda H , Kawashima Y , Kishimoto H , et al. Problems in the modified Fontan operation for univentricular heart of the right ventricular type . Circulation . 1987;76:III45–III52 . MEDLINE

105. 105 Uemura H , Yagihara T , Kawashima Y , et al. What factors affect ventricular performance after a Fontan-type operation . J Thorac Cardiovasc Surg . 1995;110:405–415 . Abstract | Full Text | Full-Text PDF (1021 KB) | CrossRef

106. 106 Mahle WT , Coon PD , Wernovsky G , Rychik J . Quantitative echocardiographic assessment of the performance of the functionally single right ventricle after the Fontan operation . Cardiol Young . 2001;11:399–406 . MEDLINE | CrossRef

107. 107 Julsrud PR , Weigel TJ , Van Son JA , et al. Influence of ventricular morphology on outcome after the Fontan procedure . Am J Cardiol . 2000;86:319–323 . Abstract | Full Text | Full-Text PDF (115 KB) | CrossRef

108. 108 Hjortdal VE , Stenbog EV , Ravn HB , et al. Neurohormonal activation late after cavopulmonary connection . Heart . 2000;83:439–443 .

109. 109 Mainwaring RD , Lamberti JJ , Moore JW , Billman GF , Nelson JC . Comparison of the hormonal response after bidirectional Glenn and Fontan procedures . Ann Thorac Surg . 1994;57:59–63 discussion 64 . MEDLINE

110. 110 Buheitel G , Hofbeck M , Gerling S , Koch A , Singer H . Similarities and differences in the exercise performance of patients after a modified Fontan procedure compared to patients with complete transposition following a Senning operation . Cardiol Young . 2000;10:201–207 . MEDLINE

111. 111 Miyairi T , Kawauchi M , Takamoto S , Morizuki O , Furuse A . Oxygen utilization and hemodynamic response during exercise in children after Fontan procedure . Jpn Heart J . 1998;39:659–669 . MEDLINE

112. 112 Chua TP , Iserin L , Somerville J , Coats AJ . Effects of chronic hypoxemia on chemosensitivity in patients with univentricular heart . J Am Coll Cardiol . 1997;30:1827–1834 . Abstract | Full Text | Full-Text PDF (188 KB) | CrossRef

113. 113 Durongpisitkul K , Driscoll DJ , Mahoney DW , et al. Cardiorespiratory response to exercise after modified Fontan operation (determinants of performance) . J Am Coll Cardiol . 1997;29:785–790 . Abstract | Full Text | Full-Text PDF (242 KB) | CrossRef

114. 114 Fredriksen PM , Therrien J , Veldtman G , Warsi MA , et al. Lung function and aerobic capacity in adult patients following modified Fontan procedure . Heart . 2001;85:295–299 .

115. 115 Ohuchi H , Tasato H , Sugiyama H , Arakaki Y , Kamiya T . Responses of plasma norepinephrine and heart rate during exercise in patients after Fontan operation and patients with residual right ventricular outflow tract obstruction after definitive reconstruction . Pediatr Cardiol . 1998;19:408–413 . MEDLINE | CrossRef

116. 116 Ohuchi H , Yasuda K , Hasegawa S , Miyazaki A , et al. Influence of ventricular morphology on aerobic exercise capacity in patients after the Fontan operation . J Am Coll Cardiol . 2001;37:1967–1974 . Abstract | Full Text | Full-Text PDF (259 KB) | CrossRef

117. 117 Ohuchi H , Hasegawa S , Yasuda K , Yamada O , Ono Y , Echigo S . Severely impaired cardiac autonomic nervous activity after the Fontan operation . Circulation . 2001;104:1513–1518 . CrossRef

118. 118 Iserin L , Chua TP , Chambers J , Coats AJ , Somerville J . Dyspnoea and exercise intolerance during cardiopulmonary exercise testing in patients with univentricular heart. The effects of chronic hypoxaemia and Fontan procedure . Eur Heart J . 1997;18:1350–1356 .

119. 119 Ohuchi H , Arakaki Y , Hiraumi Y , Tasato H , Kamiya T . Cardiorespiratory response during exercise in patients with cyanotic congenital heart disease with and without a Fontan operation and in patients with congestive heart failure . Int J Cardiol . 1998;66:241–251 . Abstract | Full Text | Full-Text PDF (199 KB) | CrossRef

120. 120 Ghai A , Harris L , Harrison DA , Webb GD , Siu SC . Outcomes of late atrial tachyarrhythmias in adults after the Fontan operation . J Am Coll Cardiol . 2001;37:585–592 . Abstract | Full Text | Full-Text PDF (194 KB) | CrossRef

121. 121 Cohen MI , Rhodes LA , Wernovsky G , Gaynor JW , Spray TL , Rychik J . Atrial pacing (an alternative treatment for protein-losing enteropathy after the Fontan operation) . J Thorac Cardiovasc Surg . 2001;121:582–583 . Abstract | Full Text | Full-Text PDF (41 KB) | CrossRef

122. 122 Kouatli AA , Garcia JA , Zellers TM , Weinstein EM , Mahony L . Enalapril does not enhance exercise capacity in patients after Fontan procedure . Circulation . 1997;96:1507–1512 . MEDLINE

123. 123 Mahle WT , Wernovsky G , Bridges ND , Linton AB , Paridon SM . Impact of early ventricular unloading on exercise performance in preadolescents with single ventricle Fontan physiology . J Am Coll Cardiol . 1999;34:1637–1643 . Abstract | Full Text | Full-Text PDF (196 KB) | CrossRef

124. 124 Felker GM , O’Connor CM . Inotropic therapy for heart failure (an evidence-based approach) . Am Heart J . 2001;142:393–401 . Abstract | Full Text | Full-Text PDF (84 KB) | CrossRef

125. 125 Lowes BD , Simon MA , Tsvetkova TO , Bristow MR . Inotropes in the beta-blocker era . Clin Cardiol . 2000;23:III11–III16 . MEDLINE | CrossRef

126. 126 Wessel DL . Managing low cardiac output syndrome after congenital heart surgery . Crit Care Med . 2001;29:S220–S230 . MEDLINE | CrossRef

127. 127 Tabbutt S . Heart failure in pediatric septic shock (utilizing inotropic support) . Crit Care Med . 2001;29:S231–S236 . MEDLINE | CrossRef

128. 128 Chang AC , Atz AM , Wernovsky G , Burke RP , Wessel DL . Milrinone (systemic and pulmonary hemodynamic effects in neonates after cardiac surgery) . Crit Care Med . 1995;23:1907–1914 . MEDLINE | CrossRef

129. 129 Hoffman TM , Wernovsky G , Atz AM , et al. Prophylactic intravenous use of milrinone after cardiac operation in pediatrics (PRIMACORP) study. Prophylactic Intravenous Use of Milrinone After Cardiac Operation in Pediatrics . Am Heart J . 2002;143:15–21 . Abstract | Full Text | Full-Text PDF (104 KB) | CrossRef

130. 130 Baruch L , Patacsil P , Hameed A , Pina I , Loh E . Pharmacodynamic effects of milrinone with and without a bolus loading infusion . Am Heart J . 2001;141:266–273 . Abstract | Full Text | Full-Text PDF (115 KB) | CrossRef

131. 131 SoRelle R . Cardiovascular news. VMAC . Circulation . 2000;102:E9050–E9051 .

132. 132 Colucci WS , Elkayam U , Horton DP , et al. Nesiritide Study Group Intravenous nesiritide, a natriuretic peptide, in the treatment of decompensated congestive heart failure . N Engl J Med . 2000;343:246–253 . MEDLINE | CrossRef

133. 133 Colucci WS . Nesiritide for the treatment of decompensated heart failure . J Card Fail . 2001;7:92–100 . Abstract | Full Text | Full-Text PDF (176 KB) | CrossRef

134. 134 Rosenzweig EB , Starc TJ , Chen JM , et al. Intravenous arginine-vasopressin in children with vasodilatory shock after cardiac surgery . Circulation . 1999;100:II182–II186 . MEDLINE

135. 135 Reinhartz O , Keith FM , El-Banayosy A , et al. Multicenter experience with the thoratec ventricular assist device in children and adolescents . J Heart Lung Transplant . 2001;20:439–448 . Abstract | Full Text | Full-Text PDF (419 KB) | CrossRef

136. 136 Hetzer R , Loebe M , Potapov EV , et al. Circulatory support with pneumatic paracorporeal ventricular assist device in infants and children . Ann Thorac Surg . 1998;66:1498–1506 . MEDLINE | CrossRef

137. 137 Weyand M , Kececioglu D , Kehl HG , et al. Neonatal mechanical bridging to total orthotopic heart transplantation . Ann Thorac Surg . 1998;66:519–522 . MEDLINE | CrossRef

138. 138 Konertz W , Hotz H , Schneider M , Redlin M , Reul H . Clinical experience with the MEDOS HIA-VAD system in infants and children (a preliminary report) . Ann Thorac Surg . 1997;63:1138–1144 . MEDLINE | CrossRef

139. 139 Stiller B , Dahnert I , Weng YG , Hennig E , Hetzer R , Lange PE . Children may survive severe myocarditis with prolonged use of biventricular assist devices . Heart . 1999;82:237–240 . MEDLINE

140. 140 Sidiropoulos A , Hotz H , Konertz W . Pediatric circulatory support . J Heart Lung Transplant . 1998;17:1172–1176 . MEDLINE

141. 141 del Nido PJ , Duncan BW , Mayer JE , Wessel DL , LaPierre RA , Jonas RA . Left ventricular assist device improves survival in children with left ventricular dysfunction after repair of anomalous origin of the left coronary artery from the pulmonary artery . Ann Thorac Surg . 1999;67:169–172 . MEDLINE | CrossRef

142. 142 Thuys CA , Mullaly RJ , Horton SB , et al. Centrifugal ventricular assist in children under 6 kg . Eur J Cardiothorac Surg . 1998;13:130–134 . Abstract | Full Text | Full-Text PDF (81 KB) | CrossRef

143. 143 Williams MR , Quaegebeur JM , Hsu DT , Addonizio LJ , Kichuk MR , Oz MC . Biventricular assist device as a bridge to transplantation in a pediatric patient . Ann Thorac Surg . 1996;62:578–580 . MEDLINE | CrossRef

144. 144 Helman DN , Addonizio LJ , Morales DL , et al. Implantable left ventricular assist devices can successfully bridge adolescent patients to transplant . J Heart Lung Transplant . 2000;19:121–126 . Abstract | Full Text | Full-Text PDF (126 KB) | CrossRef

145. 145 Goldstein DJ . Worldwide experience with the MicroMed DeBakey Ventricular Assist Device as a bridge to transplantation . Circulation . 2003;108(Suppl 1):II272–II277 .

146. 146 Khan A , Gazzaniga AB . Mechanical circulatory assistance in paediatric patients with cardiac failure . Cardiovasc Surg . 1996;4:43–49 . MEDLINE | CrossRef

147. 147 Ibrahim AE , Duncan BW , Blume ED , Jonas RA . Long-term follow-up of pediatric cardiac patients requiring mechanical circulatory support . Ann Thorac Surg . 2000;69:186–192 . MEDLINE | CrossRef

148. 148 Kulik TJ , Moler FW , Palmisano JM , et al. Outcome-associated factors in pediatric patients treated with extracorporeal membrane oxygenator after cardiac surgery . Circulation . 1996;94:II63–II68 . MEDLINE

149. 149 Mehta U , Laks H , Sadeghi A , et al. Extracorporeal membrane oxygenation for cardiac support in pediatric patients . Am Surg . 2000;66:879–886 . MEDLINE

150. 150 Pizarro C , Davis DA , Healy RM , Kerins PJ , Norwood WI . Is there a role for extracorporeal life support after stage I Norwood . Eur J Cardiothorac Surg . 2001;19:294–301 . Abstract | Full Text | Full-Text PDF (177 KB) | CrossRef

151. 151 Jaggers JJ , Forbess JM , Shah AS , et al. Extracorporeal membrane oxygenation for infant postcardiotomy support (significance of shunt management) . Ann Thorac Surg . 2000;69:1476–1483 . MEDLINE | CrossRef

152. 152 Kirshbom PM , Bridges ND , Myung RJ , Gaynor JW , Clark BJ , Spray TL . Use of extracorporeal membrane oxygenation in pediatric thoracic organ transplantation . J Thorac Cardiovasc Surg . 2002;123:130–136 . Abstract | Full Text | Full-Text PDF (71 KB) | CrossRef

153. 153 Burnett CM , Duncan JM , Frazier OH , Sweeney MS , Vega JD , Radovancevic B . Improved multiorgan function after prolonged univentricular support . Ann Thorac Surg . 1993;55:65–71 discussion 71 . MEDLINE

154. 154 Burch M , Siddiqi SA , Celermajer DS , Scott C , Bull C , Deanfield JE . Dilated cardiomyopathy in children (determinants of outcome) . Br Heart J . 1994;72:246–250 . MEDLINE | CrossRef

155. 155 Lewis AB , Chabot M . Outcome of infants and children with dilated cardiomyopathy . Am J Cardiol . 1991;68:365–369 . MEDLINE | CrossRef

156. 156 Griffin ML , Hernandez A , Martin TC , et al. Dilated cardiomyopathy in infants and children . J Am Coll Cardiol . 1988;11:139–144 . MEDLINE

157. 157 Friedman RA , Moak JP , Garson A . Clinical course of idiopathic dilated cardiomyopathy in children . J Am Coll Cardiol . 1991;18:152–156 . MEDLINE

158. 158 Muller G , Ulmer HE , Hagel KJ , Wolf D . Cardiac dysrhythmias in children with idiopathic dilated or hypertrophic cardiomyopathy . Pediatr Cardiol . 1995;16:56–60 . MEDLINE | CrossRef

159. 159 Duster MC , Bink-Boelkens MT , Wampler D , Gillette PC , McNamara DG , Cooley DA . Long-term follow-up of dysrhythmias following the Mustard procedure . Am Heart J . 1985;109:1323–1326 . MEDLINE | CrossRef

160. 160 Hayes CJ , Gersony WM . Arrhythmias after the Mustard operation for transposition of the great arteries (a long-term study) . J Am Coll Cardiol . 1986;7:133–137 . MEDLINE

161. 161 Garson A , Bink-Boelkens M , Hesslein PS , et al. Atrial flutter in the young (a collaborative study of 380 cases) . J Am Coll Cardiol . 1985;6:871–878 . MEDLINE

162. 162 Sullivan ID , Presbitero P , Gooch VM , Aruta E , Deanfield JE . Is ventricular arrhythmia in repaired tetralogy of Fallot an effect of operation or a consequence of the course of the disease? A prospective study . Br Heart J . 1987;58:40–44 . MEDLINE | CrossRef

163. 163 Deanfield JE , Ho SY , Anderson RH , McKenna WJ , Allwork SP , Hallidie-Smith KA . Late sudden death after repair of tetralogy of Fallot (a clinicopathologic study) . Circulation . 1983;67:626–631 . MEDLINE

164. 164 Wiles HB , Gillette PC , Harley RA , Upshur JK . Cardiomyopathy and myocarditis in children with ventricular ectopic rhythm . J Am Coll Cardiol . 1992;20:359–362 . MEDLINE

165. 165 Dyckner T , Wester PO . Potassium/magnesium depletion in patients with cardiovascular disease . Am J Med . 1987;82:11–17 . Abstract | Full-Text PDF (721 KB) | CrossRef

166. 166 Rosenthal DN , Dubin AM , Chin C , Falco D , Gamberg P , Bernstein D . Outcome while awaiting heart transplantation in children (a comparison of congenital heart disease and cardiomyopathy) . J Heart Lung Transplant . 2000;19:751–755 . Abstract | Full Text | Full-Text PDF (114 KB) | CrossRef

167. 167 Bossaert L , Van Hoeyweghen R The Cerebral Resuscitation Study Group . Bystander cardiopulmonary resuscitation (CPR) in out-of-hospital cardiac arrest . Resuscitation . 1989;17(Suppl):S55–S69 discussion S199–206 . CrossRef

168. 168 Nichol G , Stiell IG , Laupacis A , Pham B , De Maio VJ , Wells GA . A cumulative meta-analysis of the effectiveness of defibrillator-capable emergency medical services for victims of out-of-hospital cardiac arrest . Ann Emerg Med . 1999;34:517–525 . Abstract | Full-Text PDF (871 KB) | CrossRef

169. 169 Perry JC , Knilans TK , Marlow D , Denfield SW , Fenrich AL , Friedman RA . Intravenous amiodarone for life-threatening tachyarrhythmias in children and young adults . J Am Coll Cardiol . 1993;22:95–98 . MEDLINE

170. 170 Figa FH , Gow RM , Hamilton RM , Freedom RM . Clinical efficacy and safety of intravenous Amiodarone in infants and children . Am J Cardiol . 1994;74:573–577 . MEDLINE | CrossRef

171. 171 Coumel P , Fidelle J . Amiodarone in the treatment of cardiac arrhythmias in children (one hundred thirty-five cases) . Am Heart J . 1980;100:1063–1069 . MEDLINE | CrossRef

172. 172 Triedman JK , Bergau DM , Saul JP , Epstein MR , Walsh EP . Efficacy of radiofrequency ablation for control of intraatrial reentrant tachycardia in patients with congenital heart disease . J Am Coll Cardiol . 1997;30:1032–1038 . Abstract | Full Text | Full-Text PDF (274 KB) | CrossRef

173. 173 Deal BJ , Mavroudis C , Backer CL , Buck SH , Johnsrude C . Comparison of anatomic isthmus block with the modified right atrial maze procedure for late atrial tachycardia in Fontan patients . Circulation . 2002;106:575–579 . CrossRef

174. 174 Deal BJ , Mavroudis C , Backer CL , Johnsrude CL , Rocchini AP . Impact of arrhythmia circuit cryoablation during Fontan conversion for refractory atrial tachycardia . Am J Cardiol . 1999;83:563–568 . Abstract | Full Text | Full-Text PDF (165 KB) | CrossRef

175. 175 Fogoros RN . The effect of the implantable cardioverter defibrillator on sudden death and on total survival . Pacing Clin Electrophysiol . 1993;16:506–510 . MEDLINE | CrossRef

176. 176 Moss AJ , Hall WJ , Cannom DS , et al. Improved survival with an implanted defibrillator in patients with coronary disease at high risk for ventricular arrhythmia. Multicenter Automatic Defibrillator Implantation Trial Investigators . N Engl J Med . 1996;335:1933–1940 . MEDLINE | CrossRef

177. 177 A comparison of antiarrhythmic-drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias. The Antiarrhythmics versus Implantable Defibrillators (AVID) Investigators . N Engl J Med . 1997;337:1576–1583 . MEDLINE | CrossRef

178. 178 Bocker D , Bansch D , Heinecke A , et al. Potential benefit from implantable cardioverter-defibrillator therapy in patients with and without heart failure . Circulation . 1998;98:1636–1643 . MEDLINE

179. 179 Lorga-Filho A , Geelen P , Vanderheyden M , et al. Early benefit of implantable cardioverter defibrillator therapy in patients waiting for cardiac transplantation . Pacing Clin Electrophysiol . 1998;21:1747–1750 . MEDLINE | CrossRef

180. 180 Dubin A , Berul CI , Bevilacqua LM , et al. The use of implantable cardioverter defibrillators in pediatric patients awaiting heart transplantaion . J Card Fail . 2003; in press .

181. 181 Dubin AM , Van Hare GF , Collins KK , Bernstein D , Rosenthal DN . Survey of current practices in use of amiodarone and implantable cardioverter defibrillators in pediatric patients with end-stage heart failure . Am J Cardiol . 2001;88:809–810 . Full Text | Full-Text PDF (52 KB) | CrossRef

182. 182 Link MS , Hill SL , Cliff DL , et al. Comparison of frequency of complications of implantable cardioverter-defibrillators in children versus adults . Am J Cardiol . 1999;83:263–266 A5–6 . Full Text | Full-Text PDF (274 KB) | CrossRef

183. 183 Berul CI , Triedman JK , Forbess J , et al. Minimally invasive cardioverter defibrillator implantation for children (an animal model and pediatric case report) . Pacing Clin Electrophysiol . 2001;24:1789–1794 . MEDLINE

184. 184 Abraham WT , Fisher WG , Smith AL , et al. Cardiac resynchronization in chronic heart failure . N Engl J Med . 2002;346:1845–1853 . CrossRef

185. 185 Cazeau S , Leclercq C , Lavergne T , et al. Effects of multisite biventricular pacing in patients with heart failure and intraventricular conduction delay . N Engl J Med . 2001;344:873–880 . MEDLINE | CrossRef

186. 186 Nelson GS , Berger RD , Fetics BJ , et al. Left ventricular or biventricular pacing improves cardiac function at diminished energy cost in patients with dilated cardiomyopathy and left bundle-branch block . Circulation . 2000;102:3053–3059 .

187. 187 Nelson GS . In: Erratum in (Circulation) . 103:2001;p. 476 .

188. 188 Dubin AM , Feinstein JA , Reddy VM , Hanley FL , Van Hare GF , Rosenthal DN . Electrical resynchronization (a novel therapy for the failing right ventricle) . Circulation . 2003;107:2287–2289 . CrossRef

189. 189 Janousek J , Vojtovic P , Hucin B , et al. Resynchronization pacing is a useful adjunct to the management of acute heart failure after surgery for congenital heart defects . Am J Cardiol . 2001;88:145–152 . Abstract | Full Text | Full-Text PDF (889 KB) | CrossRef

a International Society for Heart and Lung Transplantation, Addison, Texas

Reprint requests: David Rosenthal, MD, (W) 725 Welch Road, room 1751, Stanford, California 94304, Telephone: 650 497-8676, Fax: 650 497-8422.

PII: S1053-2498(04)00200-1

doi:10.1016/j.healun.2004.03.018

14 of 27