Methods: Thirty three patients who underwent neosinus creation with pericardial patching due to the right ventricular outflow tract stenosis in our clinic between January 2000 and December 2012 were retrospectively analyzed. The mean follow-up was 4.7 years (range, 1 to 10 years) postoperatively for 28 patients as assessed by echocardiographic findings.
Results: The mean duration of cardiopulmonary bypass and cross-clamp were 112.8±23 and 66.9±9.4 min, respectively. Postoperatively three patients required inotropic support in the intensive care unit. One patient who was operated for Fallot’s tetralogy died due to pneumonia and sepsis following reintubation on postoperative day three. The remaining patients were discharged after an average duration of 8.1±1 days. No patients required reoperation during the follow-up. Twenty-five patients were in New York Heart Association (NYHA) Functional Classification class 1, while three were in NHYA class 2. Echocardiographic examination showed grade 2 pulmonary insufficiency in one patient and grade 1 in six patients with a mean gradient of 21±3 mmHg.
Conclusion: Our study findings suggest that creation of pulmonary neosinus with pericardial patching is a safe surgical technique with a lower perioperative mortality rate. The mid-term results of this technique are encouraging, which can be considered as an alternative treatment modality for the right ventricular outflow tract reconstruction.
Table 1: Clinical profile of the patients
Surgical technique
Following general anesthesia and a midsternal
incision, cardiopulmonary bypass (CPB) was
commenced with aortic and double venous cannulation.
Cardiac arrest was achieved with standard cardioplegia.
After the placement of the aortic cross-clamp, the
repair procedure was performed primarily through a
right atriotomy for those patients with accompanying
defects (atrial or ventricular septal defect). Then, the
pulmonary artery was severed vertically 2 cm distal
to the annulus, and the commissure and leaflets
(particularly the anterior leaflet) of the pulmonary
valve were evaluated with regard to their feasibility for reconstruction. A total of 45 patients were considered
for this procedure, and it was performed on 33 via a
small pulmonary annulus and commissural fusion.
In addition, patients with pulmonary hypoplasia who
needed a transannular patch underwent a pulmonary
neosinus operation. In this procedure, the incision was
extended to the anterior pulmonary sinus and RVOT.
The anterior leaflet was then divided into two parts
using an incision extending from the middle portion of
the anterior leaflet to the free margin without damaging
the commissure. However, a commissurotomy was
performed where there was commissural fusion.
Next, the hypertrophic fibrous bands and infundibular
muscles of the RVOT were resected, and a pericardial
patch was prepared with a Z value between 0 and 2.
This was then sutured to the right and left side of the
anterior leaflet using 4/0 polypropylene sutures, and
valve reconstruction was accomplished to obtain
pulmonary valve coaptation using the pericardial
patch at the free margin of the anterior leaflet together
with the two remaining rudimentary leaflets. The
free margin of the pericardial patch was supported
with 6/0 PTFE sutures in order to reduce the risk
of early postoperative prolapsus. Following this, the
remaining part of the patch attached to the anterior
leaflet was closed via a pulmonary arteriotomy to
widen the pulmonary artery. The RVOT stenosis was
then repaired and widened using a second pericardial
patch.[8,9] After the termination of CPB and assessment
of the valve coaptation with control transesophageal
echocardiography (TEE), the surgery was completed.
Table 2: Operative data (n=33)
Clinically significant pulmonary insufficiency has been reported to occur in 84% of the patients with RVOT stenosis who underwent the application of a transannular patch, whereas only 17% suffered from this complication when pulmonary valve augmentation with a pericardial patch was performed.[12] For patients whose RVOT stenosis is amenable to patch techniques (transannular or non-transannular), the durability is higher than with homografts. In addition, valve insufficiency or stenosis can develop in the early stages of homograft replacement.[6] Furthermore, Kaza et al.[1] found that the proportion of patients who did not require a reoperation was 88.9% in the non-transannular group compared with 63% in the transannular group.[1]
Although biological monoleaflets are able to prevent pulmonary insufficiency in the short term, they become non-functional in less than a year. This has led to the development of alternative techniques such as a pericardial patch, PTFE grafting with a thickness of 0.1 mm, allograft pulmonary valve tissue, and the creation of a monocusp in the RVOT.[4]
Porcine heterografts become calcified within three to five years while Dacron grafts show pseudointimal thickening, particularly when the diameter is small. In contrast, aortic and pulmonary allografts are associated with excellent short-term results for the reconstruction of RVOT stenoses, and pulmonary allografts are also more stable due to the preservation of pulmonary valve structure.[4] Porcine-valved Dacron conduit were used in the past for RVOT reconstruction, but allografts preserved with cryopreservation were introduced after the mid-1980’s after advances in cryopreservation techniques.[4]
We found no significant differences in the survival rates between pulmonary or aortic allografts at 25 years. According to Homann et al.[3] 30% of the allograft and 70% of the xenograft patients required a reoperation within 10 years. Furthermore, in the first five to six years after the procedure, no differences in durability were observed between the two groups. Since a reoperation is required due to growth, xenografts are preferred for newborns.[3] On the other hand, the limited availability of allografts is still a major issue. Trileaflet Contegra conduits with a natural sinus structure produced from heterologous bovine jugulary veins (Medtronic Inc., Minneapolis, MN, USA) have been reported to yield similar results at seven years;[10] therefore, this valve might be preferable, especially for infants and neonates, because of the lower regurgitation rates and freedom from significant gradients.[10]
When valvular homografts and xenografts are used, the conduit structure is usually disturbed in the majority of the cases due to the growth potential of the patient. Furthermore, augmentation of the pulmonary valve with autologous pericardial tissue for the treatment of pulmonary stenosis is associated with a reduced risk of pulmonary valve insufficiency postoperatively. This technique allows for the preservation of the natural function of the leaflets as well as the retension of the growth potential due to the use of native pericardial tissue.[11] Another option involves the use of the autologous pericardium for valvular reconstruction. This provides adequate tissue thickness and resistance, and the tissue compatibility is higher than with a bovine pericardium and synthetic patches.
The primary objective of the surgical treatment of RVOT stenosis is to create a functional pulmonary valve. A technique reported by Yılmaz et al.[8] in which the commissural structures are preserved and extended into the anterior leaflet for this purpose has been associated with good valvular motility, coaptation, and positive results in the short term. In this technique in which the pulmonary annulus and leaflet are extended simultaneously using a pericardial patch, the native commissural structures are preserved and RVOT reconstruction is accomplished using autologous pericardial tissue. Moreover, the preservation of the commissural structures is also associated with the preservation of the physiological movement of the leaflets that have been reconstructed. Additionally, the infundibular functions are preserved due to less extensive surgical muscular resection and a smaller incision. The reconstructed leaflets then become a part of the right ventricle wall and move optimally during systole and diastole without causing obstruction.[8]
Creating a monoleaflet using a PTFE patch has been associated with normal valvular functions for the initial two to three years postoperatively without recurrent valvular gradient formation. However, in these patients, regurgitation developed in conjunction with RVOT stenosis.[4] The surgical technique that we used involved the expansion of the pericardial patch together with an increase in the size of the annulus, thus aiding the coaptation process. Thus far, no cases of significant pulmonary failure have been observed postoperatively. All of our study participants were adult patients with limited growth potential. Hence, the real value of our approach is more likely to be evident in a pediatric population. Although positive short-term results have been reported by Liu et al.[11] who used this same procedure on children, the long-term results need to be evaluated to judge what role that this procedure will have with this age group.
The monocusp technique has been associated with positive results for the first one to three years after the surgery, and the beneficial effects may even last up to 10 years in some cases. Although no RVOT gradient has been reported in these patients, pulmonary insufficiency upon the development of RVOT stenosis may occur. When a reoperation is required due to allograft dysfunction in the pulmonary valve, the PTFE monocusp technique may be preferred because it achieved better results compared with patients without a valve, and it does not result in recurrent obstruction.[4]
There is no difference between allografts and xenografts in terms of graft patency in the first postoperative five to six years; however, after 10 years, xenografts show signs of degeneration due to calcification and sclerosis[3] An early sign of a dysfunctional graft is tricuspid insufficiency.[3]
In addition to the patch used in the expansion of the pulmonary valve, the patch employed during the closure of the ventriculotomy can also affect long-term patency.[6] In our technique, the pericardial patch used for the pulmonary valve reconstruction has the same width as the pericardial patch used for the repair of the pulmonary annulus. Furthermore, the reconstructed leaflet is in the form of a native valve, with the level of the reconstructed valve being the same as that of the posterior leaflet or annulus. Expanding the pulmonary artery from the pulmonary annular level with a quadrangular pericardial patch helps achieve valve coaptation by creating a spacious neosinus,[8] and creating a new valsalva sinus via a second pericardial patch prevents regurgitation by helping ensure that coaptation occurs.
The main limitations of this study were the short follow-up duration, the small sample size, and a patient group comprised solely of young adults.
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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