Methods: In this study, a total of 97 pediatric patients who were operated due to hypoplastic left heart syndrome and its variants between March 2011 and October 2018 were retrospectively analyzed. Thirty-two of the patients (28 males, 4 females; median age 5 days; range, 1 to 25 days) underwent Norwood Stage I operation (Group N), while the remaining 65 patients (44 males, 21 females; median age 6 days; range, 1 to 55 days) underwent a hybrid procedure (Group H). Both treatment strategies were compared.
Results: The median body weight in Group H was significantly lower and the number of patients with a low birth weight (<2,500 g) was significantly higher than Group N (p=0.002 and 0.004, respectively). The postoperative early mortality rate was similar between the groups. Univariate and multivariate analyses revealed that the need for preoperative mechanical ventilation was a significant factor for mortality (p=0.004 and 0.003, respectively). Syndromic appearance was also a significant factor the multivariate analysis (p=0.03). There was a statistically significant difference between the groups in terms of the inter-stage mortality rates (p=0.0045). Second-stage procedure was performed in 32 patients. The early mortality rate after the Glenn operation was 7.6%. Six patients died after comprehensive Stage II operation. Five patients underwent biventricular repair and 8 patients had third-stage fenestrated extracardiac Fontan operation (Group N, n=7 and Group H, n=1). The Kaplan-Meier survival curve demonstrated that Group N had a higher survival rate at both one and five years than Group H, although the difference was not statistically significant (p=0.15). Subgroup analysis showed that the Norwood procedure with Sano modification had the highest survival rate with 40% at five years.
Conclusion: Our study results show that patients undergoing the Norwood procedure have a more uneventful course of inter-stage period and Stage II and III, despite drawbacks early after Stage I procedure. Based on our experiences, we recommend performing the hybrid intervention in patients with a poor clinical condition and a body weight of <2,500 g.
To date, although no significant survival benefit of the hybrid approach over the conventional Norwood Stage I procedure has been reported, hybrid palliation is usually considered an appropriate alternative, particularly in high-risk patients with HLHS.[10,11] In this study, we present the outcomes of hybrid and Norwood Stage I procedures for the treatment of HLHS and its variants to shed light into the most optimal surgical strategy for the management of this difficult subset of patients.
Surgical and Interventional Techniques
Hybrid Stage Ia: Bilateral PA banding
Under general anesthesia, median sternotomy was
done. Right and left lobes of the thymus were separated
and left in situ. Upper half of the pericardium was
opened and hanged by two stay sutures. The bands
were fashioned by cutting a 2-mm ring from a 3.5-mm
expanded polytetrafluoroethylene (ePTFE) tube graft.
Without extensive dissection, right and left PAs were
encircled with a right-angle clamp. Bands were passed
around it and tightened with a 6/0 propylene suture.
They were, then, tacked to the local adventitia to
prevent distal migration. The target was an increase
in systemic systolic blood pressure by 10 mmHg and
fall in oxygen saturation by 10%. We always used
3.5-mm PTFE strips for all patients; however, we
arranged the tightness of the bands by taking deep or
swallow bites of sutures. Inotropic infusions (milrinone
0.5 ?g/kg/min and adrenaline 0.03 ?g/kg/min) were
initiated in advance in addition to prostaglandin E1
(PGE1) perfusion. In 11 patients, additional surgical
atrial septectomy was performed due to restricted
atrial septal communication. The PA and bicaval
cannulations were done. During normothermia, in
cases with aortic atresia, proximal main PA was
encircled and clamped. Atriotomy was performed on
a beating heart. Atrial septectomy was done. After
deairing, the PA clamp was removed and the patients
were weaned from CPB.
Hybrid Stage Ib: Ductus arteriosus stentingbr> A couple of days following PA banding, the patients were taken to the cardiac catheterization laboratory. The procedure was usually done under deep sedation without endotracheal intubation. A biplane angiography was usually preferred. After femoral venous access, the angiogram was done in two projections (lateral and right anterior oblique 40°) to delineate the anatomical details of the ductus arteriosus. The length and the narrowest part of the ductus were measured. A stent was selected larger than the narrowest part of the ductus and longer than the length of the ductus. In general, in patients with ductus-dependent systemic circulation, the ductus diameter was larger than those with pulmonary atresia. Therefore, peripheral stents (Omnilink® A bbott L aboratories, A bbott P ark, I L, USA) were often used for stenting. Ductus arteriosus was crossed with a delivery wire from the PA to the descending aorta. The stent was advanced through the femoral vein by means of the main PA into the ductus arteriosus. After confirming the correct location, the stent was deployed. Echocardiographic examination confirmed the correct implantation. After stent implantation, heparin infusion was continued in 15 U/kg/h for 24 h. Subsequently, acetylsalicylic acid was started at a dose of 5 mg/kg, until the second operation.
Hybrid Stage Ic: Atrial septal stenting
The femoral venous approach was used. The atrial
septum was crossed with a wire from the right atrium
to the left, and the wire was positioned in a pulmonary
vein. A balloon-expandable stent, which was usually
larger than 8 mm, was advanced through the long sheath
up to the atrial septum. The length of the stent was
usually shorter than the total atrial length. The stent
was, then, centralized. The sheath was withdrawn and
the stent was uncovered. After control angiograms and
echocardiographic examinations, the stent was implanted.
Comprehensive Norwood Stage II
Under general anesthesia, resternotomy was
performed. The aortic arch, brachiocephalic vessels,
ductus arteriosus, descending aorta, and PAs were all
dissected and encircled before beginning of CPB. In
cases in whom direct innominate artery cannulation
was not feasible, a 3.5-mm PTFE graft was anastomosed
to the innominate artery and used for arterial inflow.
Both caval veins were cannulated separately and CPB
was initiated. During moderate hypothermia (28°C),
the aortic arch was clamped distal to the innominate
artery. The left carotid and the left subclavian arteries
were clamped with temporary Yasargil neurovascular
mini-clips. A side clamp was applied to the descending
aorta 1-2 cm distal to the ductus arteriosus. Selective
cerebral and coronary perfusion was started with
40 to 50 mL/kg flow, while monitoring the right radial
artery pressure and near-infrared spectroscopy values.
While the heart was perfused, the descending aorta
was transected just below the ductal stent. The ductus
arteriosus was resected with its stent. The aortic arch
was longitudinally opened from the distal end to the
aortic arch clamp. Half of the descending aorta was
sutured to the distal aortic arch. The rest of the aortic
arch reconstruction was performed with a generous
patch of bovine pericardium, reaching the aortic arch
clamp. Both cavae were snared. The right atriotomy was performed, while the heart was still perfused. The
atrial septal stent was resected and atrial septectomy
was performed. The right atriotomy was closed leaving
a sump sucker in the atrium for decompression. The
main PA was divided below the PA bifurcation. Two
stay sutures were applied to the anterior and left lateral
edge of the main PA. Then, the aortic arch clamp is
was advanced toward the proximal innominate artery
to continue selective cerebral perfusion. Isothermic
blood cardioplegia was delivered to the ascending
aorta. After cardiac arrest was instituted, the aortic
arch incision was extended below to the proximal
ascending aorta paying attention to the coronary
orifices, and the incisions in the pulmonary root and
the aorta were adjusted to an appropriate height, which
would allow amalgamation of these roots without
kinking of the aortic root and risk for coronary
occlusion. The ascending aorta and the pulmonary root
were sutured. The remaining aortic reconstruction was
completed with the rest of the bovine pericardial patch.
After deairing procedure, all clamps were removed and
the whole body and heart perfusion were reinstituted.
Duration of cardiac arrest was usually around 15 min.
During rewarming, pulmonary bands were removed.
Narrowed pulmonary segments were either dilated or
patch reconstructed. Proximal opening of the PA was
closed primarily or with a small bovine pericardial
patch. The superior vena cava was divided at the right
atrial junction and anastomosed to the right PA in
an end-to-side fashion. The rest of the operation was
completed as usual, leaving the mediastinal and pleural
drains and temporary pacing wires. The sternum was
left open depending on the hemodynamic status of the
patient or surgeon"s preference.
Postoperative management and follow-up
After the first stage, general principles of the
intensive care unit management were the identical
between the groups. Typically, oxygen saturations
of 75 to 85% and a hematocrit level of 40 to
45% were targeted. Sedation was used to decrease
oxygen consumption. Balanced pulmonary and
systemic circulations were achieved with permissive
hypercapnia and low oxygen gas mixtures. All
patients received vasoactive agents including
milrinone, adrenaline, noradrenaline, and dopamine
depending on their hemodynamic status. Contrary
to the Norwood operations in which the patients
were kept sedated until the sternum was closed, we
attempted to extubate the patients after the hybrid
procedure as early as possible.
Follow-up was completed for all patients. After discharge following the first stage, echocardiographic examinations were performed at two-week intervals, whenever possible. All patients underwent heart catheterization and/or computed tomography angiography before Stage II and Stage III (Figures 1 and 2). Acetylsalicylic acid was the standard medicine after all stages for all patients.
Figure 1: An angiographic view before comprehensive Stage II procedure.
Figure 2: A computed tomography angiography view before comprehensive Stage II.
Statistical analysis
Statistical analysis was performed using the R
package version 3.5.2 (R Development Core Team,
IBM Corp., NY, USA). Descriptive data were expressed
in median (min-max) or number and frequency.
Normality for continuous variables was tested using the Shapiro-Wilk test. The Mann-Whitney U test was
used to compare the two groups in terms of continuous
variables. The chi-square test of independence was
used to examine relationships between categorical
variables. The Fisher"s exact test was used, when the
assumption of expected counts being at least 5 for
chi-square test of independence was not satisfied.
Univariate and multivariate logistic regression
analysis was used to analyze the relationship between
explanatory variables and binary outcomes. The
Kaplan-Meier survival probabilities were computed
and plotted to compare treatment groups in terms of
mortality risk. Survival curves were compared using
the log-rank test. A p value of <0.05 was considered
statistically significant.
Table 1: Baseline demographic and clinical characteristics of study population
The number of the patients who experienced sudden cardiac arrest and cardiopulmonary resuscitation in the early postoperative period was higher in Group H than Group N (n=20; 30.7% vs. n=3; 9.3%; p=0.028). Only two patients needed delayed sternal closure in Group H; however, three more patients had secondary sternal opening due to hemodynamic compromise (Table 2).
Table 2: Early postoperative outcomes after Stage I operations
Ductal stenting was unable to be performed in 12 patients due to low birth weight, unsuitable clinical condition, or early death. Three patients did not need ductal stenting, as no narrowing was detected in the patent ductus arteriosus, despite cessation of PGE1 infusion. Ductal stent migration occurred in three patients (5.6%) in the catheterization laboratory. Two of them underwent emergent Norwood conversion, but all died. Iliac artery perforation was observed in one (1.8%) patient causing immediate cardiac arrest and death, eventually. Four patients (7.5%) underwent second ductal stent implantation due to narrowing during follow-up.
Atrial septal intervention was performed in 10 patients (balloon atrial septostomy [BAS] n=5; atrial septal stenting n=5). One patient (20%) experienced atrial stent migration and emergent atrial septectomy, and stent removal was performed.
The ECMO support was done in two patients (3.0%) in Group H due to ECPR. Both were unable to be weaned off and died. Prolonged mechanical ventilation was needed in 27 patients (50%) in Group H. Causes of death in this group were sudden cardiac arrest in 11 (16.9%), low cardiac output in five (7.6%), cerebral hemorrhage in one (1.5%), aspiration in one (1.5%), and sepsis and MOF in nine patients (13.8%).
Both univariate and multivariate analyses revealed that the need for preoperative mechanical ventilation was a significant factor for postoperative death (p=0.004 and 0.003, respectively). Syndromic appearance was also a significant factor in the multivariate analysis (p=0.03). The prognosis of patients with the diagnosis of HLHC was 3.6 times better than the other patients (Tables 3 and 4).
Table 3: Univariate logistic regression analysis results for mortality after Stage I operations
Table 4: Multivariate logistic regression analysis results for mortality after Stage I operations
Inter-stage period
Between the first and second stage, three of the
remaining 17 patients (17.6%) required an additional
procedure in Group N due to recurrent aortic
coarctation. Two of them underwent balloon aortic
angioplasty successfully and one underwent surgical
coarctation repair with a separate left thoracotomy
incision. Nevertheless, 13 of the remaining 38 patients
(34.2%) needed an additional intervention in Group
H (p=0.22). Five of them underwent surgical atrial
septectomy due to atrial septal restriction and secondary
pulmonary venous hypertension. In seven of them,
Norwood conversion was performed due to suboptimal
hemodynamic condition such as inability to gain weight,
tachypnea, atrial septal restriction, ductal stent stenosis,
or retrograde aortic coarctation. Four patients underwent
ductal re-stenting due to ductal stent narrowing. There
were statistically significant differences between the groups in terms of inter-stage mortality (3/17, 17.6% in
Group N; 18/38, 47.3% in Group H) (p=0.0045). Most of
the deaths were sudden death at home or after additional
procedures in the hospital setting.
Second stage
Second-stage procedure was performed to
32 patients. The median age at the time of the second
procedure was 7.5 (range, 6 to 17) months. Thirteen
of them underwent bidirectional Glenn operation
in Group N. Three of them had additional aortic
patch replacement due to aneurysmal degeneration of
CorMatrix (small intestinal submucosa extracellular
matrix; CorMatrix Cardiovascular Inc., GA, USA)
patch (Figure 3).[12] One patient had additional tricuspid
valve annuloplasty. Fourteen of the patients (21.5%) in
Group H had comprehensive Stage II (Norwood+Glenn)
operation and five of the patients (7.6%) with the
diagnosis of HLHC in Group H underwent biventricular
repair. The details of these patients were published
elsewhere.[13] Early mortality after Glenn operation was
7.6% (n=1). This patient had also an aortic aneurysm
due to a degenerated CorMatrix patch, and aortic
patch replacement was also performed. Although early
postoperative period was uneventful, the patient had
sudden cardiac arrest on postoperative Day 1. The
patient died on postoperative Day 40 due to MOF,
despite successfully weaning from ECPR support.
Six patients (42.8%) died after comprehensive Stage II operation (p=0.06). Two of them (14.2%) experienced low cardiac output and died of MOF, despite ECMO support. One patient (7.1%) had sudden cardiac arrest on postoperative Day 2 and died, despite ECPR support. In three of them, vena cava superior (VCS) syndrome developed due to a high PA pressure. Left PA stent implantation was performed with some relief in two patients (14.2%). However, these patients died of sepsis after prolonged hospitalization. Another patient with VCS syndrome underwent Glenn take-down procedure and Sano shunt was performed. Perioperative ECMO support was needed and the patient died of cerebral hemorrhage. A total of four patients experienced VCS syndrome after comprehensive Stage II operation, while four patients needed left PA stent implantation.
Prolonged length of hospitalization (>30 days) was needed in two (15.3%) and eight (57.1%) patients in Group N and H, respectively (p=0.046).
Third stage
A total of eight patients underwent third-stage
fenestrated extracardiac Fontan operation. Seven
patients were in Group N and one patient was in Group
H. One patient (12.5%) in Group N died after operation.
Although ECMO support was provided due to low
cardiac output state in the early postoperative period,
the patient died of MOF during the ECMO support.
Other patients had an uneventful postoperative course
(Figure 4).
Figure 4: Summary of the patients" outcomes.
HLHC: Hypoplastic left heart complex.
The Kaplan-Meier actuarial survival probability of the groups are shown in Figure 5. Group N demonstrated better survival curve (37.5% at one year; 32.5% at five years vs. 20% at one year; 15% at five years, respectively), although the difference was not statistically significant (p=0.15). Subgroup analysis showed that the Norwood procedure with Sano modification had the highest survival curve (40% at five years) (Figure 6).
Figure 5: Kaplan-Meier actuarial survival probability of study groups.
Figure 6: Kaplan Meier actuarial survival probability of subgroups.
Although some centers reported up to 95% survival rates with hybrid interventions,[14] head-to-head studies comparing hybrid and Norwood approaches are limited. A recent multi-center study of the Congenital Heart Surgeons" Society (CHSS) compared hybrid and Norwood procedures in 564 patients.[15] Risk-adjusted four-year survival was higher after the Norwood with Sano modification than the Norwood with Blalock- Taussig (BT) shunt or hybrid (76% vs. 60% vs. 61%, respectively; p<0.001). Furthermore, for neonates with a lower birth weight (<2,000 g), an interaction between birth weight and hybrid resulted in a trend toward improved survival after hybrid, compared to the Norwood modifications. For propensity-matched neonates between hybrid and Norwood with BT shunt (88 pairs), four-year survival was similar (62% vs. 57%, respectively; p=0.58). For propensity-matched neonates between hybrid and Norwood with Sano modification (81 pairs), four-year survival was improved after the Norwood with Sano modification (59% vs. 75%, respectively; p=0.008).[15] In our study, however, we had no patient who underwent Norwood modifications below a body weight of 2,700 g, while there were 14 patients in the hybrid group below a body weight of 2,500 g (the smallest case was 1,500 g). Low-birthweight has been shown to be associated with high operative mortality after the Norwood modifications in many studies.[15-17] That is why we chose hybrid procedure for neonates below 2,500 g. We believe that hybrid procedure is the most optimal option and the only alternative for these patients. Due to the high rate of potential complications of ductal stenting in premature infants, we usually continue PGE1 infusion, until patients reach over 2,500 g.
Parallel to the CHSS study, our study demonstrated that the Norwood with Sano modification was associated with the most improved overall survival. A possible explanation can be related to the difference of coronary artery perfusion.[18] The greatest part of coronary artery perfusion occurs during diastole. Continuous, forward pulmonary artery flow through the BT shunt may cause diastolic run-off, which is associated with coronary artery insufficiency and decreased myocardial perfusion.[18,19] The physiology after the hybrid procedure is also similar to that after BT shunt. In contrast, the physiology after the Sano modification eliminates the possibility of diastolic run-off away from the coronary circulation, thereby, potentially resulting in better myocardial perfusion.[20] The results of the Pediatric Heart Network Single Ventricle Reconstruction Trial also support that the difference in coronary artery perfusion may be an important factor contributing to the early difference in survival rates between the Sano and BT shunt modifications (74% vs. 64%, respectively).[21]
The main advantages of hybrid procedure are avoidance of the adverse effects of CPB and deep hypothermic circulatory arrest or regional cerebral perfusion during the fragile neonatal period with shorter operation and hospitalization times and better potential neurological outcomes.[5-7] The disadvantages are, however, the concerns about the PA growth, risk for retrograde coarctation, difficulty in atrial septal manipulation, and increased inter-stage intervention rates.[8-10,15] Our hybrid procedure experience started with the patients in poor clinical condition. Initial promising results motivated us to use this strategy for all patients. Although the present study is the sum of the all patients with the initial learning period, we were unable to show any survival benefit in favor of hybrid strategy. Contrarily, management of the patients after hybrid intervention was much more difficult than the patients after the Norwood operation. Several patients experienced sudden death at home mostly after crying. We believe that hybrid patients need a very close follow-up (weekly, if applicable) and also home monitoring with oxygen saturation, respiratory rate, and weight gain measurements. In case of any suspicion, hospitalization, comprehensive examination and intervention, when necessary, should be performed.[22] In our study, we were unable to make properly these preventive follow-up programs due to the patients living other cities or scarcity of the resources.
Atrial septum is usually thick and its alignment may be different in patients with HLHS. That is why transcatheter BAS is usually ineffective in these cases.[1,5,14] We performed BAS in five patients with some success; however, the recurrent restriction rate was high. During the inter-stage period, we observed progressive residual or recurrent atrial septal restriction causing severe pulmonary venous hypertension, heart failure, and failure to thrive. Based on our experiences, inter-stage atrial septectomy has a high mortality rate. Atrial septal stent implantation was applied to these patients, due to the drawbacks of atrial septal manipulation. According to our limited experience in five patients, however, atrial stent implantation is not easy during catheterization laboratory and malposition and migration of stents are the main concerns. Similarly, one patient needed emergency surgery due to stent migration in our series. Due to the difficulty of atrial septal manipulation, we performed surgical atrial septectomy in 11 patients with a restricted atrial septum during bilateral banding procedure using a short period of CPB. Unfortunately, the subgroup analysis showed no survival benefit for this strategy, either.
According to our experience, comprehensive Stage II procedure has a high mortality and morbidity rate, mostly due to PA developmental problems or high residual PA pressures. In our study, left PAs usually had residual stenoses after de-banding. Compression of enlarged neoaortic roots might be an explanation. Intraoperative left PA stenting is a common practice during comprehensive Stage II operation.[14,15] We were unable to make any objective measurement of the branch PAs and make a comparison between the groups, but although Latus et al.[23] showed t hat the PA size was reduced (lower lobe index 135±74 vs. 161±62 mm2/m2, respectively; p=0.02) and the reintervention rate was significantly higher in the hybrid group, compared to the Norwood patients.
In our study, the patients who underwent the Norwood procedure had a more uneventful course of inter-stage period, Stage II and III, despite drawbacks early after Stage I procedure. We, therefore, quitted to perform hybrid procedure in patients who are good candidates for the Norwood operation. In our routine practice, we perform the hybrid intervention in patients with HLHS with a poor clinical condition or whose body weight is under <2,500 g.
We believe that hybrid strategy is very useful for patients who are candidates for further complex biventricular repairs. These patients usually need an extensive neonatal procedure with high mortality and morbidity or even difficult to decide for them whether biventricular repair may be performed. The hybrid procedure provides to avoid neonatal high-risk surgery in these patients and delays the difficult decision for biventricular repair to a later stage. Development of the left heart structures with time may also facilitate the decision and enhance the possibility of biventricular repair.[24,25] Besides, some concerns of hybrid procedure such as retrograde aortic coarctation, atrial septal defect restriction, and risk for coronary ischemia due to lack of the antegrade aortic flow usually do not exist in this group of patients.
The main limitations of the present study are its retrospective nature, relatively small sample size, and inclusion of the learning curve.
In conclusion, although our results are less prominent than current practice in developed countries, it has been improving with increased experience. However, more resources are still needed for hospital readmissions, hospitalizations, interventions, and home monitoring services. Based on our experiences, the Norwood with Sano modification had the highest survival rate and hybrid procedure may be reserved for patients with a low birth weight and poor clinical condition.
Acknowledgement
We thank Ozgur Asar for his invaluable statistical
assistance.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
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