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Circulation. 2006;114:I-594-I-599
doi: 10.1161/CIRCULATIONAHA.105.001438
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(Circulation. 2006;114:I-594 – I-599.)
© 2006 American Heart Association, Inc.


Surgery for Valvular Heart Disease

Homograft Valved Right Ventricle to Pulmonary Artery Conduit as a Modification of the Norwood Procedure

Olaf Reinhartz, MD; V. Mohan Reddy, MD; Edwin Petrossian, MD; Malcolm MacDonald, MD; John J. Lamberti, MD; Stephen J. Roth, MD, MPH; Gail E. Wright, MD; Stanton B. Perry, MD; Sam Suleman, BS; Frank L. Hanley, MD

From the Divisions of Pediatric Cardiothoracic Surgery and Pediatric Cardiology, Stanford University School of Medicine, Stanford, Calif.

Correspondence to Olaf Reinhartz, Cardiothoracic Surgery, Stanford University, 300 Pasteur Drive, Stanford, CA 94305. E-mail orx{at}stanford.edu


*    Abstract
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*Abstract
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Background— The use of a right ventricle to pulmonary artery (RV-PA) conduit in the Norwood procedure has been proposed to increase postoperative hemodynamic stability. A valve within the conduit should further decrease RV volume load. We report our clinical experience with this modification.

Methods and Results— From February 2002 through August 2005, we performed 88 consecutive Norwood procedures using RV-PA conduits. We used composite valved conduits made from cryopreserved homograft and polytetrafluoroethylene (PTFE) in 66 cases (54 pulmonary, 12 aortic homografts), other valved conduits in 14, and unvalved PTFE in 8 cases. Hospital survival was 88.6% overall and increased to 93.1% after the initial year. Early interventions were required in 18 patients (16 for cyanosis). Prestage II cardiac catheterization was performed at a mean age of 126 days. Mean Qp/Qs was 1, with mean aortic saturation 71%, mean O2 extraction 24%, and mean right ventricular end-diastolic pressure 9 mm Hg. Patient weight, use of an aortic homograft valve in the conduit, stage I palliation within the first year of our experience, and low O2 extraction and high transpulmonary gradient prestage II were risk factors for overall death. Early interventions were more frequent in aortic valve conduits compared with all other conduits.

Conclusions— The valved RV-PA conduit was associated with low early mortality after the Norwood procedure. The majority of these patients had normal cardiac output and well-maintained RV function. There may be a higher risk for early conduit interventions and death when aortic valve homografts are used in the RV-PA conduit.


Key Words: congenital • heart defects • surgery • survival


*    Introduction
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*Introduction
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Over the past few years, the use of a conduit from the right ventricle to the pulmonary artery (RV-PA) as an alternative to the modified Blalock-Taussig (BT) shunt in the stage I Norwood procedure has gained popularity.1 Some groups reported decreased surgical and/or interstage mortality using this modification,2–4 whereas others did not find any difference.5 The RV-PA conduit is thought to favorably change some aspects of the poststage I hemodynamics. It is proposed to lead to more reliable coronary flow by way of increased diastolic aortic pressures, because it limits pulmonary blood flow to systole. It may possibly also result in reduced ventricular volume load, through secondary mechanisms.6–11 Potential concerns are earlier onset of postoperative cyanosis and the possibility of ventricular dysfunction and dysrhythmias over time caused by the RV infundibulotomy.12

Two of the early reports from Japan about the RV-PA conduit modification described integrating a valve into the pathway. Kishimoto made a bicuspid valve from xenopericardium,13 and Murakami used a valved saphenous vein homograft.14 Eliminating diastolic regurgitation into the right ventricle should further reduce volume load and increase hemodynamic efficiency. We have considered these potential advantages and recently pursued a routine policy of using valved composite conduits in all our stage I Norwood palliations.


*    Methods
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up arrowIntroduction
*Methods
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Study Design
We provide a retrospective analysis of all patients undergoing stage I Norwood palliation between January 2002 and August 2005 by the 6-surgeon Stanford pediatric cardiac surgery group. Procedures were performed at Lucille Packard Children’s Hospital (Stanford, Calif), Children’s Hospital of Central California (Madera, Calif), and Children’s Hospital and Research Center Oakland (Oakland, Calif). All data were collected from existing sources (patient files and clinical databases). The study was approved by the Stanford Administrative Panel on Human Subjects. The authors had full access to the data and take responsibility for their integrity. All authors have read and agree to the manuscript as written.

Operative Technique
Details of the operative management were consistent across the time period and between surgeons. For stage I surgery, cardiopulmonary bypass was established by cannulation of the innominate artery and right atrial appendage. Patients were cooled to 18°C and perfusion was maintained at a minimum of 30 mL/kg per minute. A brief period of sucker bypass was used during the atrial septectomy. No deep hypothermic circulatory arrest was employed.

Arch reconstruction was performed using a pulmonary artery homograft patch. In the majority of patients, a composite conduit was fashioned from polytetrafluoroethylene (PTFE) tubing and an aortic or pulmonary homograft valve (if available) before sternotomy and inserted between a right ventricular infundibulotomy and the pulmonary artery bifurcation on the left side of the neoaorta (Figure 1). Patient weight generally determined the choice of PTFE diameter: <2 kg, 4 mm; 2 to 3.5 kg, 5 mm; >3.5 kg, 6 mm. The sternum was routinely closed in a delayed fashion. For stage II palliation, patients underwent a bidirectional Glenn procedure, which was performed without cardiopulmonary bypass utilizing a passive superior-vena-cava to right-atrium shunt whenever feasible.


Figure 1001438
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Figure 1. Surgical anatomy of the RV-PA conduit. Surgical techniques used are described in Methods.

Definitions
Surgical or early mortality was defined as death after stage I Norwood palliation within 30 days or before hospital discharge. If patients were transferred back to referring centers, the date of transfer was considered to be the time of discharge. Interstage mortality was defined as death between discharge after stage I and time of stage II palliation. Early intervention for cyanosis was defined as any surgical or transcatheter intervention required urgently for cyanosis before planned evaluation for stage II.

Statistical Analysis
Descriptive data are presented as means±standard deviations of the mean. For Kaplan-Meier survival analysis, a composite endpoint of any failure of the procedure resulting in either death or transplant was used. Univariate risk analysis for categorical variables was performed producing odds ratios with 95% confidence intervals. Student t test was used for univariate analysis of continuous variables. P≤0.05 was considered significant. Multivariate analysis of risk factors was performed using logistic regression. Statistical analyses were conducted with Stata 8.0 (StataCorp LP, College Station, Tex).


*    Results
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*Results
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Patient Population
Eighty-eight consecutive patients (56 male, 32 female) with hypoplastic left heart syndrome or variants of single ventricle with aortic arch obstruction underwent stage I palliation within the time period. Mean age was 6.0±4.3 days and mean weight was 3.1±0.5 kg. Table 1 provides a list of the morphological cardiac diagnoses as well as concomitant noncardiac diagnoses. Preoperative echocardiographic RV function was qualitatively assessed as normal in 80 patients, mildly decreased in 4, and moderately decreased in 4. Three patients had more than mild tricuspid regurgitation. Seven patients with severely restrictive atrial septal defects underwent emergent preoperative balloon septostomy or stent placement.


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TABLE 1. Spectrum of Cardiac Diagnoses and Comorbidities

RV-PA Conduits
When small aortic or pulmonary homografts were not available, other valved or occasionally nonvalved conduits were used between the RV and the PA. A list of all conduits used is provided in Table 2.


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TABLE 2. Type of RV-PA Conduits Used and Homograft Diameter

Survival and Follow-Up
Complete follow-up information was available for all patients. Survival in the first 30 days was 94.3%. It was increased to 98.6% after 2002. Survival to discharge was 88.6% overall and increased to 93.1% after 2002. Of the patients discharged, 5 died before stage II palliation, for an interstage mortality of 7%.

A bidirectional Glenn procedure was performed in 64 patients at a mean age of 151 days; 64% of Glenn procedures could be performed without cardiopulmonary bypass. In those who underwent bypass, 10 tricuspid valve repairs and 11 pulmonary artery augmentations were performed concomitantly. Hospital survival after stage II was 97%. Two patients died late after stage II, 1 suddenly at home and 1 from fungal sepsis after readmission for pneumonia. Two others required cardiac transplantation late after Glenn surgery at ages 9 and 21 months for severe right ventricular dysfunction. One patient had a biventricular repair instead of a Glenn procedure (aortic atresia with multiple ventricular septal defects). Another patient was considered not to be a candidate for stage II palliation because of severe neurologic dysfunction related to cri-du-chat syndrome; this patient died from progressive cyanosis.

The incidence of recurrent aortic coarctation was 14%. Seven patients required balloon dilatations of the aortic arch and 2 others surgical patch augmentation.

Figure 2 shows Kaplan-Meier estimated survival for the entire patient cohort. Mean follow-up was 15 months (2.5 to 40 months). Estimated 1-year survival was 73.4% and estimated 2-year survival 70.8%.


Figure 2001438
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Figure 2. Kaplan-Meier estimated freedom from death or transplant for the entire cohort. The number of available observations is provided for selected 10-month time intervals.

Conduit Interventions Before Stage II Palliation
Eighteen patients (20%) required early unplanned interventions to the RV-PA conduit before the bidirectional Glenn procedure. Sixteen of these interventions were performed for early cyanosis and included 11 stent placements, 3 balloon dilations, 1 RV myectomy, and 1 PTFE graft exchange (from 4 mm to 5 mm). Two interventions were indicated for pulmonary overcirculation and included 1 placement of a covered stent in the conduit and 1 surgical conduit banding.

Evaluation Before Stage II
Cardiac catheterization was performed in all stage II candidates. The hemodynamic data are provided in Table 3. On echocardiography at the time of prestage II evaluation, RV function was moderately decreased in 8% of patients and severely decreased in none. At this time, moderate tricuspid regurgitation was present in 16% of patients and severe tricuspid regurgitation in 2% (all patients with valved conduits). All others had mild tricuspid regurgitation or none.


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TABLE 3. Hemodynamics Before Bidirectional Glenn

Risk Analysis for Death
Several preoperative, operative, and postoperative variables were analyzed for their predictive value for both early and overall death (Table 4). Of the preoperative factors, only patient weight <2.5 kg was a significant predictor for late death. Of the operative factors, stage I procedure during the first year was a significant predictor for both early and overall death. Homograft size was not a significant risk factor. However, the use of an aortic valve was a significant predictor for overall death, but not for early death. Neither the operating surgeon nor the hospital site (not in table) was a predictor for death. Of the postoperative risk factors, mechanical support was a significant predictor for early death.


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TABLE 4. Analysis of Risk Factors for Death

Prestage II Predictors for Death
We analyzed hemodynamic variables obtained at the pre-Glenn catheterization for their predictive value for death at any time after stage II palliation. Variables that were significant or approached significance are listed in Table 5.


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TABLE 5. Pre-Glenn Catheterization Predictors for Death

Risk Analysis for Types of Conduits Used
Because the use of an aortic valve in the RV-PA conduit was determined to be a predictor for overall death in the univariate analysis, we performed logistic regression to rule out confounding risk factors. Even after adjusting for other variables that had been significant in the univariate analysis, aortic valve was still a significant predictor for overall death when compared with pulmonary valve or all other groups combined (Table 6).


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TABLE 6. Multivariate Risk Analysis (Logistic Regression) of Valves Used in the RV-PA Conduit

We also compared the 4 main groups of conduits used with regard to different complications (Table 7). There was a substantially higher rate of early interventions for cyanosis in the aortic valve group than in all others, but it was not statistically significant. There were no differences between conduits for low aortic saturations at the pre-Glenn evaluation or for the need for pulmonary artery augmentations. All conduits without a valve (PTFE only) were moderately or severely insufficient by echocardiogram, compared with one-quarter of the pulmonary valves and cryoveins. All aortic valves remained competent until stage II.


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TABLE 7. Comparison of Types of Conduits Used


*    Discussion
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up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
*Discussion
down arrowReferences
 
Our study adds to the growing literature on RV-PA conduits as Norwood stage I modification. It is the largest series of RV-PA conduits reported to date. In our analysis, we did not focus on the physiological and hemodynamic effects of the RV-PA conduit, because these have been described in detail in previous studies.6–9,15 Instead, we report clinical outcome data and analyze risk factors for death in our series. Furthermore, we focus on our specific technical modification, which is the incorporation of a homograft valve into the RV-PA conduit.

For the purpose of discussion, we divided mortality after Norwood palliation into three distinct time periods: early, interstage, and late.

Early Mortality
Early surgical mortality during the hospitalization after stage I surgery can often be attributed to one of the following problems: (1) technical shortcomings leading to hemodynamic instability and low cardiac output, which typically occurs intraoperatively and/or within the first few postoperative days; (2) complications in the intensive care unit such as infection or iatrogenic adverse events; and (3) organ failure caused by severe pre-existing noncardiac conditions. In many instances, death is related to a combination of these factors. A reduction in this early mortality can therefore be achieved either through: (1) improvements in surgical technique that increase early hemodynamic stability; (2) improvements in ICU management; and (3) exclusion of certain high-risk patients. The RV-PA conduit is believed by some to be such a technical improvement. Therefore, it has been proposed to lead to reduced early mortality in some studies when compared with BT shunt cohorts.2,3 However, because these studies use historical cohorts as controls, other factors may also contribute to improved outcomes.

The only published report comparing contemporaneous groups of BT shunt and RV-PA conduit patients did not find differences in outcomes between the 2 techniques.5 However, that study also has some limitations, in that it is retrospective, and bias between individual surgeons and a difference in risk profile between the groups cannot be excluded. Only a large, prospective, randomized trial might be able to answer this question. A prospective, randomized trial sponsored by the National Institute of Health to compare these 2 techniques has, in fact, been initiated.

In our risk analysis, patient weight was the only significant preoperative predictor of early mortality. The fact that other variables such as restrictive atrial septal defects, small ascending aorta, or severe comorbidities did not predict death as they have in other studies5,16–18 could suggest that some high-risk patients survive with an RV-PA conduit who would otherwise die early because of additive risk factors. At some institutions, this modification is being performed primarily on patients deemed at "high risk" for a Norwood with a modified BT shunt. Although we continue to use the valved RV-PA conduit for all patients, this series certainly supports using the RV-PA conduit in patients previously considered high-risk anatomic candidates for a Norwood. Further evaluation is warranted over time, however, because this study may not be sufficiently large to assess each of these factors independently.

Interstage Mortality
The second distinct time period is referred to as the "interstage" period. Stage I palliated patients appear to have a uniquely high risk for death during this time period, and the cause of death remains largely unknown.19,20 It has been proposed to be preventable by a home surveillance program.21 There has been some evidence that the RV-PA conduit might decrease interstage death, both in individual studies5,22 and in a recent metaanalysis.4 Again, a prospective trial should help to determine if the risk of death is reduced.

In our series, we were not able to identify risk factors for interstage death because of the small number of events.

Late Mortality
During the third time period, the "late death" period beginning after stage II palliation, chronic right ventricular failure is the predominant cause of death or transplantation. Because of the requirement for long term follow-up, this time period is obviously the most difficult one to analyze and will take additional time. There is theoretical concern that the ventriculotomy for the RV-PA conduit may lead to an increased risk of late RV failure and, therefore, increased late mortality. This effect could outweigh a lower early and interstage mortality. There is not sufficient follow-up yet to address this question. However, the results of our study, with its limited follow-up, do not suggest a high rate of ventricular dysfunction.

Our risk analysis reveals transpulmonary gradient as the strongest risk factor for death after Glenn surgery, with pulmonary artery pressure being borderline significant. This emphasizes the importance of a normal low-resistance pulmonary vascular bed in these patients. We observed this in the majority of patients, as shown by a low mean pulmonary artery pressure. The second strongest risk factor for death was high oxygen extraction, which serves as a marker for low cardiac output. Patients with high oxygen extraction may benefit from afterload reduction, as suggested in previous publications.23

Shunt Interventions
Tabbutt et al have described a significantly increased rate of early interventions, both surgical and transcatheter, and most often to relieve conduit obstruction, in RV-PA conduit patients when compared with BT shunt patients (32% versus 17%).5 Even though several of our patients required interventions, our intervention rate of 20% is comparable to the rate for BT shunt cases as reported by Tabbutt. Our lower intervention rate could be related to technical differences such as a more adequate infundibular muscle resection and/or to the homograft leading to less distortion at the pulmonary anastomosis site. Homograft tissue is more pliable than PTFE and more "forgiving" if conduit length is not perfectly adjusted.

Differential Risk of Conduits Used
Somewhat surprisingly, we found the use of an aortic homograft valve in the conduit versus a pulmonary valve or all other conduit materials to be significantly associated with late death. In conjunction with the finding of an increased rate of early interventions in the aortic valve group, one could conclude that aortic valves lead to earlier conduit narrowing. A possible mechanism for this could be early calcification as has been noted when valved aortic homograft is used for other indications, such as repair of pulmonary atresia.24 Therefore, it would be an inferior conduit material and not recommended. However, the results in this analysis are not conclusive. We used far fewer aortic than pulmonary homografts, limiting the statistical power of the analysis. If aortic valve is a risk factor for death, and this risk is largely caused by early interventions, then one would expect that early intervention would be a risk factor for death. However, our analysis did not lead to this result. Finally, not all deaths in the aortic valve group were clearly attributable to early cyanosis or were sudden in nature. Still, some suspicion remains, and we will have to follow our patients carefully, particularly when aortic homografts are used.

Valved Versus Nonvalved Conduits
Because of small patient numbers, our study cannot determine survival differences between patients with conduits containing valves and those with nonvalved grafts. However, not surprisingly, we could show that nonvalved conduits lead to a higher rate of "pulmonary" insufficiency by color Doppler echocardiography. In this retrospective study, we did not quantify regurgitant fractions. Echocardiography is limited in its ability to measure regurgitation quantitatively. To evaluate the differences between valved and nonvalved conduits, one would have to design a prospective study comparing both groups, preferably using magnetic resonance imaging, at different time intervals and assess RV function, ventricular volumes, and regurgitant fraction from the conduit. We are currently debating the feasibility of such a study.

Conclusions
Our preliminary experience with valved RV-PA conduits in the stage I Norwood procedure shows low early mortality, with well-maintained RV function in most patients. This encourages us to continue to use this modification. There is a potential concern with using aortic valve conduits because of an observed higher risk for early conduit interventions and death. More data and longer follow-up are needed to address this issue.


*    Acknowledgments
 
We are indebted to Meredith Milet, Children’s Hospital and Research Center Oakland, for providing the statistical analysis of this data.

Disclosures

None.


*    Footnotes
 
Presented at the American Heart Association Scientific Sessions, Dallas, Tex, November 13–16, 2005.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
up arrowDiscussion
*References
 
1. Pearl JM. Right ventricular-pulmonary artery connection in stage 1 palliation of hypoplastic left heart syndrome. J Thorac Cardiovasc Surg. 2003; 126: 1268–1270.[Free Full Text]

2. Pizarro C, Malec E, Maher KO, Januszewska K, Gidding SS, Murdison KA, Baffa JM, Norwood WI. Right ventricle to pulmonary artery conduit improves outcome after stage I Norwood for hypoplastic left heart syndrome. Circulation. 2003; 108 (Suppl 1): II155–II160.

3. Sano S, Ishino K, Kado H, Shiokawa Y, Sakamoto K, Yokota M, Kawada M. Outcome of right ventricle-to-pulmonary artery shunt in first-stage palliation of hypoplastic left heart syndrome: a multi-institutional study. Ann Thorac Surg. 2004; 78: 1951–1957;discussion 1957–1958.

4. Cua CL, Thiagarajan RR, Taeed R, Hoffman TM, Lai L, Hayes J, Laussen PC, Feltes TF. Improved interstage mortality with the modified Norwood procedure: a meta-analysis. Ann Thorac Surg. 2005; 80: 44–49.[Abstract/Free Full Text]

5. Tabbutt S, Dominguez TE, Ravishankar C, Marino BS, Gruber PJ, Wernovsky G, Gaynor JW, Nicolson SC, Spray TL. Outcomes after the stage I reconstruction comparing the right ventricular to pulmonary artery conduit with the modified Blalock Taussig shunt. Ann Thorac Surg. 2005; 80: 1582–1590;discussion 1590–1591.

6. Azakie A, Martinez D, Sapru A, Fineman J, Teitel D, Karl TR. Impact of right ventricle to pulmonary artery conduit on outcome of the modified Norwood procedure. Ann Thorac Surg. 2004; 77: 1727–1733.[Abstract/Free Full Text]

7. Mahle WT, Cuadrado AR, Tam VK. Early experience with a modified Norwood procedure using right ventricle to pulmonary artery conduit. Ann Thorac Surg. 2003; 76: 1084–1088;discussion 1089.[Free Full Text]

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9. Bradley SM, Simsic JM, McQuinn TC, Habib DM, Shirali GS, Atz AM. Hemodynamic status after the Norwood procedure: A comparison of right ventricle-to-pulmonary artery connection versus modified Blalock-Taussig shunt. Ann Thorac Surg. 2004; 78: 933–941.[Abstract/Free Full Text]

10. Malec E, Januszewska K, Kolcz J, Mroczek T. Right ventricle-to-pulmonary artery shunt versus modified Blalock-Taussig shunt in the Norwood procedure for hypoplastic left heart syndrome—influence on early and late haemodynamic status. Eur J Cardiothorac Surg. May 2003; 23: 728–733;discussion 733–734.

11. Takabayashi S, Kado H, Shiokawa Y, Fukae K, Nakano T. Comparison of hemodynamics between Norwood procedure and systemic-to-pulmonary artery shunt for single right ventricle patients. Eur J Cardiothorac Surg. 2005; 27: 968–974.[Abstract/Free Full Text]

12. Tanoue Y, Kado H, Shiokawa Y, Fusazaki N, Ishikawa S. Midterm ventricular performance after Norwood procedure with right ventricular-pulmonary artery conduit. Ann Thorac Surg. 2004; 78: 1965–1971;discussion 1971.[Free Full Text]

13. Kishimoto H, Kawahira Y, Kawata H, Miura T, Iwai S, Mori T. The modified Norwood palliation on a beating heart. J Thorac Cardiovasc Surg. 1999; 118: 1130–1132.[Free Full Text]

14. Murakami A, Takamoto S, Takaoka T, Kobayashi J, Maeda K, Takayama H, Motomura N, Murakawa T, Ono M. Saphenous vein homograft containing a valve as a right ventricle-pulmonary artery conduit in the modified Norwood operation. J Thorac Cardiovasc Surg. 2002; 124: 1041–1042.[Free Full Text]

15. Pizarro C, Norwood WI. Right ventricle to pulmonary artery conduit has a favorable impact on postoperative physiology after Stage I Norwood: preliminary results. Eur J Cardiothorac Surg. 2003; 23: 991–995.[Abstract/Free Full Text]

16. Ashburn DA, McCrindle BW, Tchervenkov CI, Jacobs ML, Lofland GK, Bove EL, Spray TL, Williams WG, Blackstone EH. Outcomes after the Norwood operation in neonates with critical aortic stenosis or aortic valve atresia. J Thorac Cardiovasc Surg. 2003; 125: 1070–1082.[Abstract/Free Full Text]

17. Daebritz SH, Nollert GD, Zurakowski D, Khalil PN, Lang P, del Nido PJ, Mayer JE, Jr., Jonas RA. Results of Norwood stage I operation: comparison of hypoplastic left heart syndrome with other malformations. J Thorac Cardiovasc Surg. 2000; 119: 358–367.[Abstract/Free Full Text]

18. Forbess JM, Cook N, Roth SJ, Serraf A, Mayer JE, Jr., Jonas RA. Ten-year institutional experience with palliative surgery for hypoplastic left heart syndrome. Risk factors related to stage I mortality. Circulation. 1995; 92 (9 Suppl): II262–II266.

19. Mahle WT, Spray TL, Gaynor JW, Clark BJ, 3rd. Unexpected death after reconstructive surgery for hypoplastic left heart syndrome. Ann Thorac Surg. 2001; 71: 61–65.[Abstract/Free Full Text]

20. Wright GE, Crowley DC, Charpie JR, Ohye RG, Bove EL, Kulik TJ. High systemic vascular resistance and sudden cardiovascular collapse in recovering Norwood patients. Ann Thorac Surg. 2004; 77: 48–52.[Abstract/Free Full Text]

21. Ghanayem NS, Hoffman GM, Mussatto KA, Cava JR, Frommelt PC, Rudd NA, Steltzer MM, Bevandic SM, Frisbee SS, Jaquiss RD, Litwin SB, Tweddell JS. Home surveillance program prevents interstage mortality after the Norwood procedure. J Thorac Cardiovasc Surg. 2003; 126: 1367–1377.[Abstract/Free Full Text]

22. Pizarro C, Mroczek T, Malec E, Norwood WI. Right ventricle to pulmonary artery conduit reduces interim mortality after stage 1 Norwood for hypoplastic left heart syndrome. Ann Thorac Surg. 2004; 78: 1959–1963;discussion 1963–1964.

23. Tweddell JS, Hoffman GM, Mussatto KA, Fedderly RT, Berger S, Jaquiss RD, Ghanayem NS, Frisbee SJ, Litwin SB. Improved survival of patients undergoing palliation of hypoplastic left heart syndrome: lessons learned from 115 consecutive patients. Circulation. 2002; 106 (12 Suppl 1): I82–I89.

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