Published online December 1, 2005
PEDIATRICS Vol. 116 No. 6 December 2005, pp. 1339-1345 (doi:10.1542/peds.2004-2697)
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Impact of Cardiac Rehabilitation on the Exercise Function of Children With Serious Congenital Heart Disease

Jonathan Rhodes, MD, Tracy J. Curran, MS, Laurel Camil, MS, Nicole Rabideau, MS, David R. Fulton, MD, Naomi S. Gauthier, MD, Kimberlee Gauvreau, ScD and Kathy J. Jenkins, MD, MPH

From the Department of Pediatric Cardiology, Children’s Hospital, Boston, Massachusetts


    ABSTRACT
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Objectives. The exercise capacity of children with congenital heart disease (CHD) is often depressed. This depression is thought to be attributable to (1) residual hemodynamic defects and (2) deconditioning secondary to physical inactivity. We hypothesized that this latter component would be ameliorated by a formal cardiac rehabilitation program designed specifically for children. The objective of this study was to characterize the effect of a cardiac rehabilitation program on the exercise performance of children with CHD and to define the physiologic mechanisms that might account for any improvements that are observed.

Methods. Nineteen patients with CHD who were referred for exercise testing and found to have a peak oxygen consumption (VO2) and/or peak work rate <80% of predicted were enrolled in the study. Sixteen patients (11 Fontan patients, 5 with other CHD) completed the program and had postrehabilitation exercise tests, results of which were compared with the prerehabilitation studies.

Results. Improvements were found in 15 of 16 patients. Peak VO2 rose from 26.4 ± 9.1 to 30.7 ± 9.2 mL/kg per min; peak work rate from 93 ± 32 to 106 ± 34 W, and the ventilatory anaerobic threshold from 14.2 ± 4.8 to 17.4 ± 4.5 mL/kg per min. The peak heart rate and peak respiratory exchange ratio did not change, suggesting that the improvements were not attributable merely to an increased effort. In contrast, the peak oxygen pulse rose significantly, from 7.6 ± 2.8 to 9.7 ± 4.1 mL/beat, an improvement that can be attributed only to an increase in stroke volume and/or oxygen extraction at peak exercise. No patient experienced rehabilitation-related complications.

Conclusion. Cardiac rehabilitation can improve the exercise performance of children with CHD. This improvement is mediated by an increase in stroke volume and/or oxygen extraction during exercise. Routine use of formal cardiac rehabilitation may greatly reduce the morbidity of complex CHD.


Key Words: congenital heart defects • exercise • cardiac rehabilitation

Abbreviations: CHD, congenital heart disease • VO2, oxygen consumption • VAT, ventilatory anaerobic threshold • {Delta}VE/{Delta}VCO2, slope of the minute ventilation versus carbon dioxide production relationship below the respiratory compensation point • MVV, maximal voluntary ventilation • FEV1, the forced expiratory volume in the first second • RER, the ratio of carbon dioxide production over oxygen consumption • FVC, forced vital capacity

Over the past 2 decades, medical and surgical advances have dramatically increased the survival rates of patients with congenital heart disease (CHD). Survival into adulthood is now expected for even the most complex malformations. However, despite excellent surgical outcomes, the exercise capacity of children who have had heart surgery is often depressed.114 Undoubtedly, residual hemodynamic defects are partly responsible for the poor exercise capacity. However, we believe that many of these children are often (inappropriately) considered to be excessively fragile and may be unduly restricted from participation in physical activities.15 We suspect that the inactivity and consequent deconditioning that results from the imposed restrictions exacerbate whatever exercise intolerance the children might experience as a result of residual cardiovascular disease. A formal cardiac rehabilitation program might be expected to reverse partially the effects of inactivity and deconditioning and thereby improve exercise function, as well as allow children to initiate exercise in a safe environment.

Data from adult cardiac patients have shown that many benefits may be derived from a supervised cardiac rehabilitation program. These benefits include improvement in lipid profiles, decrease in obesity, and improvement in exercise capacity. Adult cardiac rehabilitation programs have also been shown to produce significant reductions in hospitalization costs and overall cardiac morbidity and mortality.16,17

Only limited data are available concerning the effect of cardiac rehabilitation on pediatric patients with CHD. Past studies have included small numbers of patients and have had mixed results. In those studies that have detected an improvement in exercise function, the mechanisms that were responsible for the observed improvements have not been elucidated.15,1825 We therefore undertook this study to characterize more clearly the effect of a 12-week pediatric cardiac rehabilitation program on the exercise performance and cardiopulmonary function of children with CHD and to define the physiologic mechanisms that account for any improvements that may be observed.


    METHODS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
For this pilot project, we sought to enroll children who we believed would be most likely to benefit from cardiac rehabilitation and for whom exercise would pose a low risk. To accomplish this goal, our entry criteria included (1) age 8 to 17 years; (2) a nontrivial congenital heart defect of severity sufficient to have potentially caused a degree of activity restriction to be imposed on the patient by his or her doctors, parents, teachers, coaches, etc; consequently, all patients had to have had at least 1 surgical or interventional catheterization procedure and/or have a significant residual hemodynamic defect; (3) abnormal exercise function, characterized by a peak work rate and/or peak oxygen consumption (VO2) <80% of predicted on a standard progressive bicycle ergometry test that was performed at the Children’s Hospital exercise physiology laboratory within the last 6 months; and (4) a commitment to attend and participate reliably in rehabilitation sessions.

Out of concern for the safety of the patients, those who developed during their exercise tests abnormalities (eg, exercise-induced arrhythmias, ST depression, hypertension, hypotension, cardiac chest pain, or systemic desaturation <80%) that could pose a health risk during exercise were excluded from the study. In addition, patients with the following conditions were excluded:

Recruitment
During the 6 months before the initiation of the rehabilitation program, 188 patients aged 6 to 17 years completed exercise tests with expiratory gas analysis in our laboratory. Of these, 71 did not have a congenital heart defect of severity sufficient to be included in the study, and 33 were excluded because they had a peak VO2 and peak work rate >80% predicted. An additional 16 were excluded on account of 1 or more of the exclusion criteria. The remaining 68 patients were contacted by mail and asked to participate in the study. Nineteen of these patients agreed to participate in the study; geographic factors (ie, living a great distance from the facility in which the rehabilitation program was located) were the primary reasons that precluded the participation of the other 49 patients. The clinical characteristics of the respondents who did participate were similar to those of the respondents who did not participate. Three patients elected to withdraw from the program within the first 3 weeks. The remaining 16 patients completed the 12-week program and are the subject of this report. All patients were at least 6 months post their last surgical or interventional catheterization procedure, and no patient had an additional procedure during the course of the study.

This study was approved by the Committee on Clinical Investigation at Children’s Hospital. All parents signed consent forms, and all children gave their assent before enrolling in the study.

Rehabilitation Program
Rehabilitation sessions were conducted for 1 hour twice a week for 12 weeks. They were conducted in a 30' x 15'-room at a suburban satellite clinic facility. The sessions were staffed by a pediatric cardiologist (J.R.) and 1 or 2 exercise physiologists (T.J.C., L.C., and N.R.) who led the sessions, participated in the activities, and monitored the patients. The patients were divided by age into 2 groups (8- to 13-year-olds and 13- to 17-year-olds). Each session began with 5 to 10 minutes of stretching exercises, followed by ~45 minutes of aerobic and light weight/resistance exercises. Activities included aerobic dance, step aerobics, calisthenics (sit-ups, crunches, jumping jacks, push-ups, etc), kick boxing, and jumping rope. When the weather permitted, outdoor games such as capture the flag and relay races were conducted. Resistance exercises were performed with 3- and 5-lb barbells, light elastic bands, and cords. Games, rubber balls, music, and simple, age-appropriate prizes (eg, baseball cards) were incorporated into the activities to promote enthusiasm and motivation. Attempts were also made to vary activities and to accommodate to the moment-to-moment desires of the patients to optimize participation and interest. The last 5 to 10 minutes of each session were devoted to cooling down and stretching. Patients were also encouraged to exercise at home on at least 2 additional occasions per week. This message was reinforced at each rehabilitation session, but a specific home exercise program was not prescribed and compliance was not monitored.

Heart rate was checked (manually) at the start of each session and on 2 or 3 additional occasions during each session. The patients were encouraged to exercise at an intensity sufficient to raise their heart rates to levels equal to that associated with the ventilatory anaerobic threshold (VAT; as determined on their baseline exercise tests). At each session, the patients also rated the intensity of exercise using the Borg rate of perceived exertion score.26 As a safety precaution, oxygen, a pulse oximeter, and an external defibrillator were available at each rehabilitation session. At the last rehabilitation session, all participants were awarded a certificate of attendance and a pedometer.

Exercise Tests
The patients performed progressive, symptom-limited exercise tests using a stationary, upright cycle ergometer with a continuous graded workload adjusted for each patient according to the methods of Wasserman et al.27 Electrocardiographic monitoring and breath-by-breath expiratory gas analysis were performed with a Medical Graphics exercise testing system (Medical Graphics Corp, St Paul, MN). As mentioned previously, all patients had undergone exercise testing as part of clinical care, within 6 months before the start of the rehabilitation program. Within 2 weeks of the end of the 12-week rehabilitation program, all patients performed a second progressive bicycle ergometry exercise test with expiratory gas analysis, using a ramp rate identical to that used for the prerehabilitation test. A monetary award was issued to each patient at the time of the postrehabilitation exercise test.

Predicted values were calculated on the basis of regression equations that take into account age, gender, and size.28 The VAT was determined by the V-slope method.29 The slope of the minute ventilation versus carbon dioxide production relationship below the respiratory compensation point ({Delta}VE/{Delta}VCO2) was calculated as previously described.30

Spirometric measurements were obtained on every patient before each exercise test. The maximal voluntary ventilation (MVV) was estimated by multiplying the forced expiratory volume in the first second (FEV1) by 40.31 The breathing reserve was calculated from the following equation: Breathing Reserve (%) = 100 x (MVV – peak VE)/MVV.

Statistical Analysis
Student’s paired t test was used to compare continuous variables, and McNemar’s test was used to compare dichotomous variables before and after rehabilitation. The relationships between indexes of exercise performance and other continuous variables were evaluated using Pearson’s correlation coefficient.


    RESULTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
The demographic and clinical features of the patients are summarized in Table 1. Eleven of the patients had had Fontan procedures, and all but 3 patients were maintained on at least 1 cardiac medication. On preparticipation questionnaires, 11 of 16 patients indicated that their physical activities were limited on account of concern about their heart problems. The participants attended a mean of 18.2 ± 3.8 (range: 10–22) of the 24 sessions. They achieved their target heart rates at 92.3 ± 4.1% of the sessions and reported Borg RPE scores of 15.1 ± 3.0. No patient experienced a rehabilitation-related complication during the study. On no occasion was it necessary to use the aforementioned safety equipment.


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TABLE 1. Clinical Characteristics

 
Effect of the Cardiac Rehabilitation Program on Peak Exercise
Before the rehabilitation program, the patients’ peak VO2, work rate, heart rate, and oxygen pulse (the amount of oxygen consumed per heart beat, an index equal to stroke volume times oxygen extraction32) were abnormally low (Table 2). After rehabilitation, there was a significant increase in peak VO2 and peak work rate. One or both of these parameters increased in 15 of 16 patients (Fig 1). The improved exercise function was not attributable solely to somatic growth, because absolute values as well as weight normalized, and percentage of predicted values for each parameter also increased. Furthermore, the patients’ peak respiratory exchange ratio (RER; the ratio of VCO2 over VO2; the magnitude of the peak RER roughly reflects the effort expended by the patient at peak exercise.33,34) and peak heart rate on the postrehabilitation study did not differ from prerehabilitation values, indicating that the improvements in exercise performance were not attributable to an increased effort. The improvements in exercise function, however, were almost without exception accompanied by a significant increase in peak oxygen pulse (Fig 2).


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TABLE 2. Effect of Cardiac Rehabilitation on Peak Exercise Parameters

 

Figure 1
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Fig 1. Effect of cardiac rehabilitation on peak oxygen consumption. Peak oxygen consumption rose in 15 of 16 patients after cardiac rehabilitation. Pre, before rehabilitation; post, after rehabilitation.

 

Figure 2
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Fig 2. Changes in peak oxygen pulse after cardiac rehabilitation. The peak oxygen pulse declined in the 1 patient whose peak oxygen consumption declined. It fell slightly in 1 other patient and rose in the remaining 14 patients.

 
The peak exercise systolic blood pressure was not affected by cardiac rehabilitation. However, the patients’ peak exercise diastolic blood pressure was significantly higher after cardiac rehabilitation.

As would be expected, the increase in peak VO2 after rehabilitation was associated with comparable increases in peak VCO2 and VE. The increase in VE was mediated by a rise in the tidal volume at peak exercise (when expressed in liters). When expressed as a percentage of the resting forced vital capacity (FVC), the tidal volume also increased (P = .06). The respiratory rate at peak exercise did not differ significantly from prerehabilitation values. The rise in VE at peak exercise resulted in a statistically insignificant decline in the breathing reserve. Moreover, the patients’ breathing reserve remained substantial after the rehabilitation program. Cardiac rehabilitation had no effect on peak exercise oxygen saturation.

Improvements in peak exercise function were observed in all 11 Fontan patients. The only patient whose peak exercise function did not improve after the rehabilitation program was an 11-year-old boy with severe pulmonary regurgitation after transannular repair of double-outlet right ventricle with pulmonary stenosis.

Impact of Cardiac Rehabilitation on Submaximal Exercise Function
The effect of cardiac rehabilitation on the patients’ cardiopulmonary function at the VAT was similar to that observed at peak exercise. After rehabilitation, the VO2 and the work rate at the VAT rose significantly. These changes were associated with a concomitant increase in the oxygen pulse; the heart rate at the VAT did not change. Neither the ventilatory equivalents for oxygen and carbon dioxide at the VAT nor the {Delta}VE/{Delta}VCO2 (indices that reflect the efficiency of gas exchange during exercise) was affected by the rehabilitation program (Table 3).


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TABLE 3. Effect of Cardiac Rehabilitation on Submaximal Exercise Parameters

 
Low-grade atrial and/or ventricular ectopy developed in 8 of 16 patients during the prerehabilitation exercise test. Ectopy was not detected during the postrehabilitation exercise test in 5 of these patients. None of the patients without ectopy on the prerehabilitation study subsequently developed ectopy on the postrehabilitation study (P = .06 by McNemar’s test).

Impact of Cardiac Rehabilitation on Measurements at Rest
Between the times of the pre–and post–cardiac rehabilitation exercise tests, small but statistically significant increases in body weight and height were observed. The FVC and FEV1 also increased slightly. These increases were attributed to the patients’ somatic growth, as there was no change in the percentage of predicted FVC and FEV1. Statistically significant changes were also not observed in the patients’ body mass index, FEV1/FVC, resting oxygen saturation, or blood pressures (Table 4).


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TABLE 4. Effect of Cardiac Rehabilitation on Measurements at Rest

 
Correlates of the Improvement in Peak Exercise Function
The improvement in percentage of predicted peak VO2 correlated strongly with the improvement in percentage of predicted peak oxygen pulse (r = 0.75; P < .001). Pre–post rehabilitation changes in peak VO2 did not correlate with age, baseline exercise function, Borg RPE score, or attendance. Although the patients’ {Delta}VE/{Delta}VCO2 correlated negatively with their peak VO2, changes in the {Delta}VE/{Delta}VCO2 from pre–to postrehabilitation tests were not associated with the corresponding changes in peak VO2.


    DISCUSSION
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
This study demonstrates that the exercise function of many patients with palliated CHD can be significantly improved by a 12-week cardiac rehabilitation program. In this series, the improvement seems to have been mediated by an increase in the oxygen pulse during exercise. Because the oxygen pulse is the product of stroke volume and oxygen extraction, an increased oxygen pulse could result from improvements in either or both of these parameters. Studies in adults indeed have found that an increase in oxygen extraction is 1 mechanism by which exercise function is enhanced by cardiac rehabilitation.35 Past studies, in children and adults, have also demonstrated that exercise training can enhance (and that inactivity can have a deleterious effect on) the stroke volume and cardiac output response to exercise.16,36 The significant increase in our patients’ peak-exercise diastolic blood pressure after cardiac rehabilitation is consistent with a rehabilitation-induced augmentation of the cardiac output (and because the heart rate was unchanged, the stroke volume) at peak exercise and suggests that this second mechanism was at least partially responsible for the observed improvement in exercise function.

The improvements in exercise capacity and cardiovascular function achieved by the patients of this study we believe are related to and underscore the important bidirectional nature of the interaction between the cardiovascular system and the skeletal muscles. Although the cardiovascular system provides the blood flow necessary to accommodate the metabolic requirements of the skeletal muscles during exercise, the pumping action of the skeletal muscles in turn helps to maintain ventricular preload. This pumping action makes an important contribution to the normal increase in cardiac output during exercise.37 We speculate that the improvements identified in this and other studies are related, at least in part, to a rehabilitation-induced increase in the strength, mass, and pumping capacity of the skeletal muscles.

We believe that this interaction between the skeletal muscles and the cardiovascular system is an important clinical concept that may not be fully appreciated. An implication of this interaction is that interventions that address only 1 component of the skeletal muscle–cardiovascular unit may have a limited impact on exercise capacity, unless they are combined with programs that are designed to improve the function of the other component. This phenomenon probably explains the common observation that surgical and/or interventional catheterization procedures that achieve dramatic hemodynamic results often, in the short term, have a relatively minor impact on exercise function.3,13,21,3842 In our opinion, these observations and the results of our study provide strong arguments for the incorporation of cardiac rehabilitation into the care of many patients with CHD. Indeed, the improvements achieved in this study equal or exceed those obtained with many other medical or surgical interventions. Furthermore, no adverse events were encountered in conjunction with our rehabilitation program, suggesting that, in this class of patients, the risks associated with cardiac rehabilitation are low and the risk:benefit ratio for this form of therapy is favorable.

In light of recent studies that have identified the {Delta}VE/{Delta}VCO2 to be a strong predictor of mortality in patients with heart failure,30,43 an important correlate of exercise function in patients who have undergone surgical repair of tetralogy of Fallot,9,44 and to be elevated after the Fontan procedure,45 it is interesting to note that rehabilitation had no effect on this parameter and that the rehabilitation-related rise in peak VO2 did not correlate with concurrent changes in {Delta}VE/{Delta}VCO2. Furthermore, rehabilitation seemed to have no effect on other indices of pulmonary function, such as baseline spirometric measurements or the ventilatory equivalents for oxygen or carbon dioxide at the VAT. Indeed, our data point primarily to an improvement in cardiovascular function as the source for the rehabilitation-related improvement in exercise performance.

The results of this study compare favorably with most previous studies of cardiac rehabilitation in children. Bradley et al19 studied the effect of a 12-week rehabilitation program on the exercise function of 11 patients with CHD (9 of whom completed the program) and found improvements in peak VO2 and endurance time comparable to those attained in our series. However, these investigators noted a significant increase in heart rate on the postrehabilitation exercise test but did not report their patients’ RER before and after rehabilitation. It therefore was unclear whether the effect that they observed was in fact attributable to an increased effort rather than an objective improvement in exercise function. They also did not detect a significant increase in their patients’ VE, which, in the absence of an (implausible) improvement in the lungs’ efficiency of gas exchange, seems to be incompatible with the observed increase in peak VO2. Balfour et al18 reported data from 6 patients who had CHD and completed a 3-month rehabilitation program. They also found improvements similar to those achieved in our study. However, their study was small, was plagued by a high dropout rate, and included patients with a relatively low acuity of disease. They also did not provide data regarding the patients’ heart rate and RER. Neither of these studies provided insights into the mechanisms by which the patients’ exercise function might have improved.

Other investigators have reported more modest improvements after cardiac rehabilitation. Goldberg et al,20 in a study of 26 patients with repaired tetralogy of Fallot or ventricular septal defects, found that a 6-week home exercise program using stationary bicycles improved peak work capacity but had no effect on peak VO2. Ruttenberg et al23 studied 12 patients with a variety of congenital heart defects and found that a 9-week program based on a jogging and walking regimen improved treadmill endurance time but did not improve peak VO2. Similarly, Fredriksen et al25 found that 55 patients who had a wide spectrum of congenital heart defects and participated in a training program that introduced them to a variety of sports and other physical activities achieved a small (<5%) improvement in endurance time and no improvement in peak VO2 normalized for body weight. Minamisawa et al,22 in a study of 11 children and young adults who had had Fontan procedures, found that a 2- to 3-month home exercise program produced only small (~7%) improvements in peak VO2 and peak work rate. They did not detect a significant change in oxygen pulse or respiratory function.

We believe that the favorable outcomes obtained in our study are related to the flexibility of our program, the use of age-appropriate incentives, the low patient:staff ratio, the opportunity for prompt feedback and encouragement, and the high priority that was placed on pursuing activities that accommodated the individual needs/desires of our patients. We also believe that our patients were motivated by the opportunity to exercise in a child-oriented environment, with children their own age and carrying similar diagnoses. In our opinion, cardiac rehabilitation facilities should incorporate these features into their pediatric programs to maximize the likelihood that patients will be properly motivated and derive optimal benefit from their rehabilitation sessions.

Limitations
This study examined only the immediate impact of cardiac rehabilitation on children with CHD. Additional studies are necessary to determine whether the benefits identified in this study are sustained over an extended period of time and whether they produce improved activity levels and lifestyles. The number of patients who were involved in this study was also relatively small. Although sufficient to provide persuasive data regarding the benefits of cardiac rehabilitation in children, the study was not large enough to characterize definitively the risks associated with this form of therapy. Additional studies are also needed to establish the optimal design, duration, and intensity of a pediatric cardiac rehabilitation program.

It must also be noted that the patients in this study were a highly selected group. The results of this study therefore may not be applicable to patients with milder degrees of disability or to patients with medical conditions that were excluded from this study.


    CONCLUSION
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
This study has demonstrated that a 12-week, semiweekly cardiac rehabilitation program with encouragement of additional home exercise can significantly improve the exercise performance of children with serious CHD. This improvement seems to be mediated by an increase in stroke volume and/or oxygen extraction during exercise. Routine use of formal cardiac rehabilitation may reduce the morbidity of complex CHD.


    ACKNOWLEDGMENTS
 
This study was supported by a grant from the Deborah Munroe Noonan Memorial Fund and by the Pediatric Heart Network (5U01 HL068285).


    FOOTNOTES
 
Accepted Feb 14, 2005.

Reprint requests to (J.R.) Department of Cardiology, 300 Longwood Ave, Boston, MA 02115. E-mail: jonathan.rhodes{at}cardio.chboston.org

No conflict of interest declared.


    REFERENCES
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 

  1. Ben Shachar G, Fuhrman BP, Wang Y, et al. Rest and exercise hemodynamics after the Fontan procedure. Circulation. 1982;65 :1043 –1048[Abstract/Free Full Text]
  2. Driscoll DJ, Danielson GK, Puga FJ, et al. Exercise tolerance and cardiorespiratory response to exercise after the Fontan operation for tricuspid atresia or functional single ventricle. J Am Coll Cardiol. 1986;7 :1087 –1094[Abstract]
  3. Duffie ER, Adams FA. The use of the working capacity test in the evaluation of children with congenital heart disease. Pediatrics. 1963;757 –768
  4. Grant GP, Mansell AL, Garofano RP, et al. Cardiorespiratory response to exercise after the Fontan procedure for tricuspid atresia. Pediatr Res. 1988;24 :1 –5[ISI][Medline]
  5. James FW, Kaplan S, Schwartz DC, et al. Response to exercise in patients after total surgical correction of tetralogy of Fallot. Circulation. 1976;54 :671 –679[Abstract/Free Full Text]
  6. Jonsson H, Ivert T, Jonasson R, et al. Work capacity and central hemodynamics thirteen to twenty-six years after repair of tetralogy of Fallot. J Thorac Cardiovasc Surg. 1995;110 :416 –426[Abstract/Free Full Text]
  7. Meijboom F, Szatmari A, Deckers JW, et al. Cardiac status and health-related quality of life in the long term after surgical repair of tetralogy of Fallot in infancy and childhood. J Thorac Cardiovasc Surg. 1995;110 :t-91
  8. Mocellin R, Bastanier C, Hofacker W, et al. Exercise performance in children and adolescents after surgical repair of tetralogy of Fallot. Eur J Cardiol. 1976;4 :367 –374[Medline]
  9. Rhodes J, Dave A, Pulling MC, et al. Effect of pulmonary artery stenoses on the cardiopulmonary response to exercise following repair of tetralogy of Fallot. Am J Cardiol. 1998;81 :1217 –1219[CrossRef][ISI][Medline]
  10. Rowe SA, Zahka KG, Manolio TA, et al. Lung function and pulmonary regurgitation limit exercise capacity in postoperative tetralogy of Fallot. J Am Coll Cardiol. 1991;17 :461 –466[Abstract]
  11. Strieder DJ, Aziz K, Zaver AG, et al. Exercise tolerance after repair of tetralogy of Fallot. Ann Thorac Surg. 1975;19 :397 –405[Abstract]
  12. Wessel HU, Cunningham WJ, Paul MH, et al. Exercise performance in tetralogy of Fallot after intracardiac repair. J Thorac Cardiovasc Surg. 1980;80 :582 –593[Abstract]
  13. Goldberg SJ, Mendes F, Hurwitz R. Maximal exercise capability of children as a function of specific cardiac defects. Am J Cardiol. 1969;23 :349 –353[CrossRef][ISI][Medline]
  14. Rhodes J, Garofano RP, Bowman FO Jr, et al. Effect of right ventricular anatomy on the cardiopulmonary response to exercise. Implications for the Fontan procedure. Circulation. 1990;81 :1811 –1817[Abstract/Free Full Text]
  15. Linde LM. Psychiatric aspects of congenital heart disease. Psychiatr Clin North Am. 1982;5 :399 –406[ISI][Medline]
  16. Ades PA, Coello CE. Effects of exercise and cardiac rehabilitation on cardiovascular outcomes. Med Clin North Am. 2000;84 :251 –265[CrossRef][ISI][Medline]
  17. Lavie CJ, Milani RV. Benefits of cardiac rehabilitation and exercise training. Chest. 2000;117 :5 –7[Free Full Text]
  18. Balfour IC, Drimmer AM, Nouri S, et al. Pediatric cardiac rehabilitation. Am J Dis Child. 1991;145 :627 –630[Abstract]
  19. Bradley LM, Galioto FM Jr, Vaccaro P, et al. Effect of intense aerobic training on exercise performance in children after surgical repair of tetralogy of Fallot or complete transposition of the great arteries. Am J Cardiol. 1985;56 :816 –818[CrossRef][ISI][Medline]
  20. Goldberg B, Fripp RR, Lister G, et al. Effect of physical training on exercise performance of children following surgical repair of congenital heart disease. Pediatrics. 1981;68 :691 –699[Abstract/Free Full Text]
  21. Longmuir PE, Turner JA, Rowe RD, et al. Postoperative exercise rehabilitation benefits children with congenital heart disease. Clin Invest Med. 1985;8 :232 –238[ISI][Medline]
  22. Minamisawa S, Nakazawa M, Momma K, et al. Effect of aerobic training on exercise performance in patients after the Fontan operation. Am J Cardiol. 2001;88 :695 –698[CrossRef][ISI][Medline]
  23. Ruttenberg HD, Adams TD, Orsmond GS, et al. Effects of exercise training on aerobic fitness in children after open heart surgery. Pediatr Cardiol. 1983;4 :19 –24[CrossRef][ISI][Medline]
  24. Washington RL. Cardiac rehabilitation programmes in children. Sports Med. 1992;14 :164 –170[ISI][Medline]
  25. Fredriksen PM, Kahrs N, Blaasvaer S, et al. Effect of physical training in children and adolescents with congenital heart disease. Cardiol Young. 2000;10 :107 –114[ISI][Medline]
  26. Borg G. Perceived exertion as an indicator of somatic stress. Scand J Rehabil Med. 1970;2 :92 –98[Medline]
  27. Wasserman K, Hansen JE, Sue DY, et al. Principles of Exercise Testing and Interpretation. 3rd ed. Philadelphia, PA: Lippincott; 1999
  28. Jones NL. Clinical Exercise Testing. Philadelphia, PA: WB Saunders; 1997:243
  29. Beaver WL, Wasserman K, Whipp BJ. A new method for detecting anaerobic threshold by gas exchange. J Appl Physiol. 1986;60 :2020 –2027[Abstract/Free Full Text]
  30. Chua TP, Ponikowski P, Harrington D, et al. Clinical correlates and prognostic significance of the ventilatory response to exercise in chronic heart failure. J Am Coll Cardiol. 1997;29 :1585 –1590[Abstract]
  31. Campbell SC. A comparison of the maximum voluntary ventilation with the forced expiratory volume in one second: an assessment of subject cooperation. J Occup Med. 1982;24 :531 –533[ISI][Medline]
  32. Jones NL. Clinical Exercise Testing. 4th ed. Philadelphia, PA: WB Saunders; 1997
  33. Wasserman K. The Dickinson W. Richards lecture. New concepts in assessing cardiovascular function. Circulation. 1988;78 :1060 –1071[Abstract/Free Full Text]
  34. Wasserman K. Determinants and detection of anaerobic threshold and consequences of exercise above it. Circulation. 1987;76 (suppl VI):VI-29–VI-39
  35. Dubach P, Myers J, Dziekan G, et al. Effect of high intensity exercise training on central hemodynamic responses to exercise in men with reduced left ventricular function. J Am Coll Cardiol. 1997;29 :1591 –1598[Abstract]
  36. Eriksson BO, Koch G. Effect of physical training on hemodynamic response during submaximal and maximal exercise in 11–13-year old boys. Acta Physiol Scand. 1973;87 :27 –39[ISI][Medline]
  37. Braunwald E, Sonnenblick EH, Ross J Jr, et al. An analysis of the cardiac response to exercise. Circ Res. 1967;XXII(suppl 1) :I-44 –I-58
  38. Barber G, Danielson GK, Puga FJ, et al. Pulmonary atresia with ventricular septal defect: preoperative and postoperative responses to exercise. J Am Coll Cardiol. 1986;7 :630 –638[Abstract]
  39. Helber U, Baumann R, Seboldt H, et al. Atrial septal defect in adults: cardiopulmonary exercise capacity before and 4 months and 10 years after defect closure. J Am Coll Cardiol. 1997;29 :1345 –1350[Abstract]
  40. Jonsson B, Lee SJ. Haemodynamic effects of exercise in isolated pulmonary stenosis before and after surgery. Br Heart J. 1968;30 :60 –66[Free Full Text]
  41. Matthys D. Pre- and postoperative exercise testing of the child with atrial septal defect. Pediatr Cardiol. 1999;20 :22 –25[CrossRef][ISI][Medline]
  42. Rhodes J, Patel H, Hijazi ZM. Effect of transcatheter closure of atrial septal defect on the cardiopulmonary response to exercise. Am J Cardiol. 2002;90 :803 –806[CrossRef][ISI][Medline]
  43. Ponikowski P, Francis DP, Piepoli MF, et al. Enhanced ventilatory response to exercise in patients with chronic heart failure and preserved exercise tolerance: marker of abnormal cardiorespiratory reflex control and predictor of poor prognosis. Circulation. 2001;103 :967 –972[Abstract/Free Full Text]
  44. Clark AL, Gatzoulis MA, Redington AN. Ventilatory responses to exercise in adults after repair of tetralogy of Fallot. Br Heart J. 1995;73 :445 –449[Abstract/Free Full Text]
  45. Troutman WB, Barstow TJ, Galindo AJ, et al. Abnormal dynamic cardiorespiratory responses to exercise in pediatric patients after Fontan procedure. J Am Coll Cardiol. 1998;31 :668 –673[Abstract/Free Full Text]

PEDIATRICS (ISSN 1098-4275). ©2005 by the American Academy of Pediatrics




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