Association of Digoxin With Interstage Mortality: Results From the Pediatric Heart Network Single Ventricle Reconstruction Trial Public Use Dataset.

BACKGROUND: Mortality for infants with single ventricle congenital heart disease remains as high as 8% to 12% during the interstage period, the time between discharge after the Norwood procedure and before the stage II palliation. The objective of our study was to determine the association between digoxin use and interstage mortality in these infants. METHODS AND
RESULTS: We conducted a retrospective cohort study using the Pediatric Heart Network Single Ventricle Reconstruction Trial public use dataset, which includes data on infants with single right ventricle congenital heart disease randomized to receive either a Blalock-Taussig shunt or right ventricle-to-pulmonary artery shunt during the Norwood procedure at 15 institutions in North America from 2005 to 2008. Parametric survival models were used to compare the risk of interstage mortality between those discharged to home on digoxin versus those discharged to home not on digoxin, adjusting for center volume, ascending aorta diameter, shunt type, and socioeconomic status. Of the 330 infants eligible for this study, 102 (31%) were discharged home on digoxin. Interstage mortality for those not on digoxin was 12.3%, compared to 2.9% among those on digoxin, with an adjusted hazard ratio of 3.5 (95% CI, 1.1-11.7; P=0.04). The number needed to treat to prevent 1 death was 11 patients. There were no differences in complications between the 2 groups during the interstage period.
CONCLUSIONS: Digoxin use in infants with single ventricle congenital heart disease is associated with significantly reduced interstage mortality.

Introduction

Although great strides have been made in the surgical and medical management of infants with single ventricle congenital heart disease, early mortality remains high. In the last decade, postoperative in‐hospital mortality after the Norwood procedure has ranged from 7% to 19%, and mortality before the stage II palliation among those discharged to home after the Norwood procedure has ranged from 2% to 12%.1, 2, 3, 4, 5, 6 This interstage period, the time between discharge to home after the Norwood procedure and the stage II operation, has been the focus of many efforts to reduce mortality. The effects of altering surgical options, such as use of the hybrid procedure7 and closer monitoring of infants with the use of home oxygen saturation or weight monitoring on interstage mortality, have been reported on.8 Though initial results have been promising, particularly in single‐center studies, sustainability of improved interstage mortality has not been demonstrated in multicenter studies.

Digoxin was traditionally a mainstay of treatment for heart failure (HF) in children.9, 10, 11, 12, 13 Over the last 2 decades, however, digoxin has lost favor with many pediatric cardiologists, with only 28% of patients in the National Pediatric Cardiology Quality Improvement Collaborative (NPC‐QIC) discharged home on the medicine.14 Reasons for the decreased use of digoxin include question about its mechanism of action, concerns about toxicity, and availability of other pharmacological options.15 However, it has recently been suggested that digoxin might play a role in reducing interstage mortality.16

The objective of our study was to evaluate the association of outpatient digoxin use with interstage mortality in infants with single ventricle congenital heart disease in a multicenter study using data from the Pediatric Heart Network Single Ventricle Reconstruction (SVR) trial. We hypothesized that the use of digoxin would be associated with reduced interstage mortality.

Methods

Data Source and Study Design

We performed a retrospective cohort study using data from the Pediatric Heart Network SVR Trial public use dataset (available at http://www.pediatricheartnetwork.org/ForResearchers/PHNPublicUseDatasets.aspx). The SVR trial has previously been well described.17 Briefly, the SVR trial enrolled infants in 2005–2008 with single ventricle congenital heart disease with a dominant morphologically right ventricle with the purpose of comparing outcomes for the Norwood procedure with the modified Blalock‐Taussig shunt (MBTS) versus the right ventricle‐to‐pulmonary artery shunt (RVPAS). Infants were randomized to either of the 2 surgical treatment options and followed until 14 months of age. Institutional review board approval and informed consent were obtained at participating institutions for the initial trial, and the public use dataset contains no personally identifiable information.

For our study, the primary aim was to compare the interstage mortality for infants in the SVR trial for those who were discharged to home on digoxin compared to those discharged to home without digoxin. Interstage mortality was defined as death before stage II palliation. The inclusion criterion was any patient discharged to home after the Norwood procedure before stage II palliation. In order to avoid the potential confounder for mortality attributable to arrhythmia, which may be collinear with digoxin treatment, we excluded all infants with a history of arrhythmia during their Norwood hospitalization. In the SVR trial, arrhythmias that required medication or other treatment during the Norwood hospitalization were recorded; these included atrial fibrillation, atrial flutter, supraventricular tachycardia, junctional ectopic tachycardia, ventricular tachycardia, and second‐ or third‐degree atrioventricular block. The secondary aim was to compare the occurrence of complications during the interstage period amongst the 2 groups.

Statistical Analysis

Descriptive statistics were calculated for all variables of interest and include medians and ranges or counts and percentages, when appropriate. Demographics and clinical characteristics (pre‐Norwood, during Norwood hospitalization, and after discharge for Norwood) were compared between patients on digoxin at Norwood discharge to those not on digoxin at discharge. Comparisons were made using chi‐square tests for categorical variables and Wilcoxon rank‐sum tests for continuous variables. When expected cell counts were small (<5), an exact test was used in place of the chi‐square test. The majority of patients died or received their stage II surgery within 6 months of their Norwood surgery, with less than 13% of the original sample size remaining at risk at 7 months. As a result, survival estimates were based on 6 months after Norwood surgery.

The time‐dependent outcome of interstage mortality after Norwood was parametrically modeled. Parametric probability estimates for the time‐dependent outcome were derived from a model based on multiple, overlapping phases of risk (available for use with the SAS system at https://www.lerner.ccf.org/qhs/software/hazard/documents/hazard.pdf). The HAZARD procedure uses maximum likelihood estimates to resolve risk distribution of time to event in up to 3 phases of risk (early, constant, and late). For the outcome of interstage mortality, an early‐phase model best described the data, given that the vast majority of the deaths occurred within 2 to 3 months after the Norwood procedure.

Variables potentially influencing the likelihood of interstage mortality and included in the adjusted model were chosen a priori from demographic and clinical variables previously identified in the literature, namely: center volume (enrolled <20 patients in SVR trial vs ≥20 patients); ascending aorta diameter (<0.3 cm preoperative measurement vs ≥0.3 cm); shunt type (MBTS vs RVPAS); and socioeconomic status (census block poverty level, as a continuous variable).2 Before multivariable modeling, mean imputation was used to reduce list‐wise deletion of patients with missing data. Mean imputation was used only when data were missing at random, and provided that no more than 5% of the data for a specific variable were missing (ie, for socioeconomic status only). Effects of digoxin use on the probability of interstage mortality are given as a hazard ratio (HR) with an associated 95% CI. Statistical analyses were performed using SAS software (version 9.4; SAS Institute Inc., Cary, NC), and statistical significance was assessed at the 0.05 level.

We performed additional analyses to examine the impact of some of our assumptions on our results. First, though the HAZARD procedure in SAS allows us to parametrically model early hazard of mortality, it does not allow for modeling of random effects such as individual center. Therefore, to examine the possible influence of clustering of patients within centers, we further compared the estimate for the effect of digoxin on interstage mortality using a shared frailty model with PHREG treating center effects as independent and identically distributed random variables. Second, to assess the impact that removing children with a history of arrhythmia may have had on our findings, we performed a sensitivity analysis using our multivariate model in which we (1) analyzed the association of digoxin with mortality in only those with tachyarrhythmia and (2) analyzed the association of digoxin with mortality in all patients, both those without any arrhythmia and those with any tachyarrhythmia. For these sensitivity analyses, we excluded those with a history of second‐ or third‐degree atrioventricular block, given that digoxin would be contraindicated in this population.

Results

Of 549 patients in the SVR trial, 330 met inclusion criteria for this study (Figure 1). Of these, 102 (31%) were discharged to home on digoxin after the Norwood procedure. Those discharged home on digoxin did not differ from those not on digoxin with regard to demographic, preoperative, or operative characteristics, but those discharged home on digoxin were more likely to have longer length of stay after the Norwood procedure and were more likely to be of a younger age at the time of stage II palliation (Table 1). There was wide variation with regard to use of digoxin by center, with use of digoxin at discharge ranging from 0% to 100% (Table 2). Of the 12 centers that discharged more than 0%, but less than 100%, of infants home on digoxin, interstage mortality was lower in the digoxin group at 10 centers.

Figure 1

Selection criteria. All patients enrolled in the Pediatric Heart Network Single Ventricle Reconstruction Trial were eligible for enrollment. Those who had a history of arrhythmia during hospitalization for the Norwood procedure, who did not survive to hospital discharge, or who remained in the hospital until their stage II operation were excluded.

Table 1

Demographics of Digoxin vs No Dgoxin Groups

Patient Characteristics	Digoxin (N=102)	No Digoxin (N=228)	P Value
	N (%) or Median (IQR)	N (%) or Median (IQR)
Sex, male	66 (64.7)	145 (63.6)	0.85
Race
White	82 (80.4)	175 (76.8)	0.46
Nonwhite	20 (19.6)	53 (23.2)
Hispanic	23 (22.5)	46 (20.4)	0.67
Birthweight, kg	3.07 (2.80–3.45)	3.20 (2.78–3.50)	0.51
Gestational age, weeks	39 (38–39)	38 (38–39)	0.58
Aortic atresia at screening	64 (62.7)	148 (64.9)	0.70
Age at Norwood, days	6 (4–8)	6 (4–8)	0.59
Norwood perfusion type
DHCA only	57 (56.4)	131 (58.0)
RCP only or RCP/DHCA time ≤10 min	25 (24.8)	51 (22.5%)	0.91
DHCA and RCP time >10 min	19 (18.8)	44 (19.5)
Number of complications post‐Norwood	2.0 (1.0–4.0)	2.0 (1.0–5.0)	0.85
Syndrome or genetic anomaly	26 (31.3)	52 (30.8)	0.93
Shunt type at end of Norwood
MBTS	44 (43.1)	102 (44.7)	0.79
RVPAS	58 (56.9)	126 (55.3)
Not on oral feeds at Norwood discharge	21 (20.6)	53 (23.3)	0.58
AVVR grade PRE Norwood
Mild/none	88 (86.3)	203 (89.0)	0.47
Moderate/severe	14 (13.7)	25 (11.0)
AVVR grade POST Norwood
Mild/none	80 (78.4)	184 (80.7)	0.63
Moderate/severe	22 (21.6)	44 (19.3)
Right ventricular fractional area change POST Norwood, N=314	0.36 (0.32–0.41)	0.36 (0.32–0.41)	0.60
Pre Norwood ascending aorta diameter, cm
<0.3	45 (45.5)	121 (54.3)	0.14
≥0.3	54 (54.5)	102 (45.7)
Mitral valve or aortic Aatresia at baseline	54 (52.9)	121 (53.3)	0.95
Census block poverty level (%)	8.3 (3.1–17.1)	8.9 (4.8–17.1)	0.14
Oxygen saturation at discharge	82 (80–85)	83 (80–86)	0.15
Postoperative length of stay, days	26 (19–40)	21 (15–33)	0.005*
Age at stage II palliation, days, N=289	148 (120–187)	163 (137–195)	0.005*
Center volume
Small (<20 patients)	18 (17.6)	60 (26.3)	0.09
Large (≥20 patients)	84 (82.4)	168 (73.7)

AVVR indicates atrioventricular valve regurgitation; DHCA, deep hypothermic circulatory arrest; MBTS, modified Blalock‐Taussig shunt; RCP, regional cerebral perfusion; RVPAS, right ventricle‐to‐pulmonary artery shunt.

Table 2

Percent of Infants Discharged to Home on Digoxin and Interstage Mortality by Center

Center	% on Digoxin	Interstage Mortality (%)
		On Digoxin	NOT on Digoxin
A	0.0	N/A	40.0
B	5.6	0	11.8
C	8.3	0	9.1
D	15.8	0	6.3
E	16.1	0	5.8
F	19.4	0	13.8
G	21.4	0	21.2
H	21.7	20	27.8
I	22.7	0	5.9
J	28.6	0	20.0
K	33.3	0	16.7
L	65.0	3.9	0
M	81.5	4.6	0
N	100.0	0	N/A
O	100.0	0	N/A

N/A indicates not applicable.

Overall, interstage mortality was significantly different between the 2 groups, with 28 of 228 (12.3%) of those not on digoxin dying before stage II palliation compared to 3 of 102 (2.9%) of those on digoxin (Figure 2). With an absolute risk reduction of 9.4%, the number needed to treat (1/absolute risk reduction) in order to prevent 1 interstage death in this population is 11 patients. After adjusting for center volume, ascending aorta diameter, shunt type, and socioeconomic status, those not on digoxin had an HR for interstage mortality of 3.5 (95% CI, 1.1–11.7; P=0.04) compared to those on digoxin (Table 3).

Figure 2

Parametric survival curve. This survival curves shows the interstage mortality for infants discharged to home after the Norwood procedure from 2005 to 2008 in the Pediatric Heart Network Single Ventricle Reconstruction Trial. Patients were censored at the time of the stage II operation or at 6 months of age, whichever occurred earlier. Those discharged to home not on digoxin had significantly higher mortality than those on digoxin (P=0.02). After adjusting for center volume, ascending aorta diameter, shunt type, and socioeconomic status, those not on digoxin had a hazard ratio for interstage mortality of 3.5 (95% CI, 1.1–11.7; P=0.04) compared to those on digoxin.

Table 3

Hazard Ratio for Interstage Mortality

Outcome	Group	Number of Deaths (%)	6‐Month Survival Rate (95% CI)	Hazard Ratioa
Interstage mortality	No Digoxin (N=228)	28 (12.3)	87.0% (84.2–94.1)	3.5 (1.1–11.7) P=0.04
	Digoxin (N=102)	3 (2.9)	96.7% (94.1–98.1)

Adjusted for center volume, ascending aorta diameter, shunt type, and socioeconomic status.

Our additional analyses yielded similar results to this primary analysis. In the shared frailty model with center as a random effect, the estimated hazard of mortality in those not on digoxin was 3.8 times that of those that were on digoxin (95% CI, 1.1–12.8; P=0.03). Moreover, the random effect for center was not statistically significant (P=0.15). In examination of the patients excluded on account of an arrhythmia, 91 had a tachyarrhythmia and survived to hospital discharge after the Norwood procedure. Of these, 50 were discharged to home on digoxin. Interstage mortality in the group not on digoxin was 17.1% (7 of 41) compared to 8.0% (4 of 50) for the group on digoxin (HR, 2.4; 95% CI, 0.7–8.3; P=0.17). When adding these patients to the original analyses, the overall estimated hazard for mortality for the group not on digoxin was 3.2 times that of the group on digoxin (95% CI, 1.4–7.2; P=0.005).

Overall, 52% of children experienced an adverse event during the interstage period. In the digoxin group, 56 of the 102 children experienced a total of 111 complications; among the children not on digoxin, 116 of the 228 infants had a total of 242 complications. There were no significant differences in the number of complications among any category (Table 4).

Table 4

Complications Among Those on Digoxin vs Those Not on Digoxin During the Interstage Period

Complication	Digoxin (%) (N=102)	No Digoxin (%) (N=228)	P Value
Arrhythmia	0 (0.0)	6 (2.6)	0.18
All other cardiac	15 (14.7)	31 (13.6)	0.79
Respiratory	25 (24.5)	44 (19.3)	0.28
Neurological	5 (4.9)	13 (5.7)	0.77
Gastrointestinal	15 (14.7)	28 (12.3)	0.55
Infectious	26 (25.5)	61 (26.8)	0.81
Renal	0 (0.0)	2 (0.9)	1.00
Hematologic/vascular	2 (2.0)	7 (3.1)	0.73
Other	0 (0.0)	8 (3.5)	0.06
Any complication	56 (54.9)	116 (50.9)	0.50

Discussion

In this large, multicenter cohort study of infants with single right ventricle congenital heart disease, we found the use of digoxin to be associated with significantly reduced interstage mortality. Those subjects not discharged on digoxin had a more than 3‐fold higher hazard of interstage mortality as compared to those prescribed the drug. For every 11 children treated with digoxin, 1 interstage death would be prevented. Given this potential benefit and the lack of difference between significant adverse events observed between the 2 cohorts, the routine use of digoxin should be considered during the interstage period.

Our findings are in agreement with the only other multicenter study, to our knowledge, to examine the association of digoxin with interstage mortality. In a study using data from the NPC‐QIC in June 2008 to July 2013, Brown et al. found that not being on digoxin at the time of discharge after the Norwood procedure conferred an increase in the absolute risk of interstage mortality of 11% and an adjusted odds ratio for interstage mortality of 2.9.16 We found similar results in our study, but by using survival analysis methods instead of logistic regression, our study accounted for the fact that there are varying durations of time at risk for each individual. Nevertheless, the fact that 2 separate independent multicenter studies with different time periods (minimal overlap of 6 months, during which the NPC‐QIC enrolled fewer than 10 patients) found similar results with similar effect sizes lends credence to the finding that digoxin may bestow a protective effect against interstage mortality for infants with single ventricle congenital heart disease.18

If digoxin may have such important effects on improving cardiac function and hemodynamics, why then is it not more commonly prescribed? Indeed, digoxin, the oldest drug available for treatment of HF, was formerly the mainstay of treatment for HF in both adults and children given its supposed effects on inotropy, chronotropy, and the sympathetic nervous system, although its demonstration in laboratory studies did not always translate to clinical improvement.19, 20, 21, 22, 23 However, in 1997, the Digitalis Investigation Group conducted a randomized, placebo‐controlled trial of 7800 adults and found no improvement in mortality.24 Digoxin use subsequently declined both among adults and children.25 With no proven benefit and concerns about toxicity, many advocated against its use in children.26

Episodes of digoxin toxicity were observed neither in our study nor in a recent randomized, double‐blind, multicenter study comparing the use of digoxin versus propranolol for treatment of supraventricular tachycardia.27 However, the risk of digoxin toxicity should not be ignored, particularly given that there is a decreased clearance of digoxin in children as compared to adults.28, 29 Although rare, digoxin toxicity is a well‐recognized entity in children, characterized by nausea, vomiting, anorexia, weakness, and atrioventricular block.10, 30

There are important limitations to our study. First, this was an observational study and participants were not randomized to receive digoxin. Whereas a randomized control trial would be ideal, this may not be feasible. With a recent baseline interstage mortality rate of 8%,31 a study would need to enroll 1000 infants with single ventricle who survived to Norwood discharge in order to have 80% power to detect a difference of 10% interstage mortality in the no digoxin group versus 5% in the digoxin group. Second, our analyses were all intention to treat. Though we know whether kids were discharged from the hospital to home on digoxin after the Norwood procedure, we do not know whether those on digoxin took the medicine or were continued on the medicine, nor do we know whether those not discharged to home on the medicine were later prescribed it as an outpatient. Regardless, the approach that we used did reflect real‐world conditions, and our findings can be used to dictate decision making at the time of discharge after the Norwood procedure. Third, we do not know what dosing regimen was used. The recommended dosing regimen for infants 1 month to 2 years of age is 10 to 15 μg/kg/day, although lower dosing may be needed for treatment of HF.15 Future research into the optimal dosing regimen for children during the interstage period is still needed. Finally, we do not have information regarding an indication for why a child was on digoxin. We excluded all children with a history of arrhythmia in our initial analyses, and children with single ventricle congenital heart disease typically have some degree of HF.21 In our experience, the choice of whether to treat a child with digoxin is driven by physician preference, but it may be possible that children treated with digoxin had some unmeasured variable that influenced the decision to treat them. We attempted to control for such factors, including effects of surgical center, and found no such associations in our study. Furthermore, we found similar effect sizes for digoxin in patients both with and without arrhythmia. Of note, if the choice was made to treat these children because they were felt to be in more‐severe HF and digoxin were to have no effect on mortality, one would expect their outcomes to be worse, not better.

Conclusions

In the Pediatric Heart Network SVR trial, infants with single right ventricle congenital heart disease who were not prescribed digoxin upon discharge after the Norwood procedure had greater than 3 times the hazards of interstage mortality as compared to those prescribed digoxin.

Disclosures

None.