Methods: Seventy-six patients (34 males, 42 females; mean age 11.4±5.8 years; range 7 to 18 years) underwent pulmonary valve replacement for pulmonary insufficiency following right ventricle outflow tract reconstruction between January 2009 and September 2016. Surgical indications were symptoms including exercise intolerance or arrhythmias which are attributed to the right ventricular volume overload or dysfunction with or without branch pulmonary artery stenosis in 54 symptomatic patients with chronic pulmonary insufficiency. Surgical indication was made according to magnetic resonance imaging in 22 asymptomatic patients.
Results: The mean follow-up was 60±19 (range 17 to 108) months. There was no early and late mortality. The mean right ventricular ejection fraction value in symptomatic patients increased in the postoperative period, although it did not reach statistical significance. There was a decline in the right ventricular area index, right ventricular volume index, and tricuspid annulus measurements, compared to preoperative values. Compared to the symptomatic patients, the increase in the right ventricular ejection fraction and the decline in the right ventricular area index, right ventricular volume index, and tricuspid annulus was less prominent in asymptomatic patients, indicating no statistically significant difference.
Conclusion: Pulmonary valve replacement can be performed with low morbidity and mortality rates. To relief the right ventricle function, the operation should be performed before the irreversible changes in the right ventricular volumes and functions occur.
In all patients, either symptomatic or asymptomatic, the pre- and postoperative ECHO examinations included the right ventricular area index (RVAI) and right ventricular volume index (RVVI) normalized according to body surface area and right ventricular ejection fraction (RVEF) were calculated with the Simpsons method.
All patients were anticoagulated with oral warfarin for three months with the international normalized ratio (INR) values kept between 2 and 2.5. The warfarin treatment was replaced with 5 m/kg/day of acetylsalicylic acid at the end of the third month. All data were collected through the patient reports and directly from patients through telephone calls.
Surgical procedure
Median sternotomy was performed and
cardiopulmonary bypass was achieved through
aortic and bicaval cannulation. The operations were
performed on beating heart in 49 patients in whom
there were no intracardiac defects such as atrial septal
defect (ASD) or ventricular septal defect (VSD).
Eleven patients with residual VSD, seven patients with
ASD, and nine patients in whom reconstruction of the
pulmonary artery branches were needed underwent
PVR operations under cardioplegic arrest. All of these
residual defects were closed during PVR operation. The
transanular patch used for the RVOTR or the conduits
were incised vertically. The pulmonary arteriotomies
were performed according to the right ventricular
or pulmonary artery branch reconstructions planned
preoperatively. The incision was advanced to left
pulmonary artery, or to the origin of both pulmonary
branches according to the reconstruction plan. The
largest possible biological valve was chosen (stented
bovine pericardial valve-Biocor) considering the age
and weight of the patient. The valve was implanted in
the right ventricular outflow. The valve was covered
with pericardial xenograft. Pulmonary artery plasty
was performed in six patients to left pulmonary artery
and in three patients to both pulmonary arteries.
Statistical analysis
Statistical analysis was performed using the PASW
version 18.0 software (SPSS Inc., Chicago, IL, USA).
Data were expressed in mean ± standard deviation (SD)
or frequency (%) as appropriate. Comparisons between
independent groups were performed using the Mann-
Whitney U test. A p value of <0.05 was considered
statically significant.
Table 1: Patient demographics (n=76)
ECHO and MRI measurements
The perioperative RVEF, area and volume
index measurements, and tricuspid valve annulus
measurements of symptomatic and asymptomatic
patients are shown on Table 2. The mean RVEF
value in symptomatic patients increased in the
postoperative term, although this result was not
statistically significant. There was a decline in the
RVAI, RVVI, and tricuspid annulus measurements,
compared to preoperative values. Compared to the symptomatic patients, the increase in the RVEF and
the decrease in the RVAI, RVVI, and tricuspid annulus
was less prominent in asymptomatic patients, although
this difference was not statistically significant. The
mean preoperative pulmonary valve annulus was
calculated as 21.4±2.8 mm. High-grade pulmonary
valve insufficiency was detected in all patients via
ECHO. In 22 asymptomatic patients who were operated
according to the MRI results, the calculated RV-EDVL
and RV-ESVI were 154±7.1 mL/m2 and 83±4.7 mL/m2,
respectively.
Procedural data
The cardiopulmonary bypass and cross-clamp times
were 110±41.5 and 61±39.5 min, respectively. The
mean procedural time was 4.7±1.2 hours in patients
with a transannular patch and 5.1±1.8 hours in patients
with conduits, indicating no significant difference. The
mean size of the implanted valve was 27.6±1.9 mm.
In addition to PVR, VSD closure in 11 patients,
ASD closure in seven patients, and pulmonary artery
reconstruction in nine patients were performed.
Follow-up
The mean follow-up was 60±19 (range 17-108)
months. There was no early mortality and late mortality.
In the ECHO measurements, the mean gradient in the
pulmonary valve was calculated as 19±14 mmHg,
there was no pulmonary insufficiency. There was no
need for reoperation due to implanted valve-related
problems. The functional capacity of the symptomatic
patients increased significantly (all reached NYHA
Class I). No arrhythmia was detected using ECG or
Holter measurements.
The length of intensive care unit and in hospital stays were 1.7±0.9 and 5.9±3.4 days in symptomatic patients, respectively and 2.1±1.6 and 7.1±2.9 days in asymptomatic patients, respectively, indicating no significant difference. Among nine patients who had pulmonary artery reconstruction, three patients developed diaphragm paralysis and one patient developed recurrent nerve paralysis.
In the past, TOF procedure-related pulmonary valve insufficiency was believed to be harmless to the cardiac functions in the postoperative period; however, with the use of innovative screening methods such as cardiac MRI, it is now widely accepted that chronic pulmonary valve insufficiency deteriorates the right ventricular functions.[5] Gatzoulis et al.[5] demonstrated that pulmonary valve insufficiency caused right ventricular dilatation and dysfunction, intolerance to exercise, newly developing arrhythmias, and even sudden death over time. It is a common belief that pulmonary valve replacement leads to improvement in the right ventricular functions, decrease in the ventricular volumes, and increase in functional capacity.[6,7]
The pulmonary valve replacement procedure is performed with low mortality. Lee et al.[8] reported 98% of 10-year-survival after the procedure. There was no mortality in our cohort in the early postoperative period or during three-year-follow up. In the literature, two-thirds of the PVR patients either needed reintervention or developed structural changes in the valve after 10 years; this was five times faster in children compared to the adults due to metabolism and growth rate.[9,10] The need for reintervention may partially be avoided using larger-size valve implants as in our patients.
There are contradictory reports about the effects of PVR on the right ventricular functions, volumes, QRS duration, and arrhythmias. Several authors showed fast recovery of the right ventricular functions and volumes along with a significant decline in the QRS duration and in the rate of arrhythmias,[8] whereas some others did not.[11,12] In our study, we observed postoperative decrease in the right ventricular volumes and QRS duration along with improved right ventricular functions, compared to the preoperative results in the symptomatic patients, although the difference was not statistically significant. Pulmonary valve replacement is usually performed much later in asymptomatic patients, compared to symptomatic patients; therefore, the beneficial changes in the right ventricular volumes, QRS duration, and right ventricular functions were less prominent in asymptomatic patients. The intensive care unit and hospital stay lengths were also longer in the asymptomatic group; however, this difference was not statistically significant. This can be associated with the preoperative condition of the symptomatic patients that they underwent operation before right ventricular dilatation developed, in other words, before irreversible changes in the right ventricular developed. The procedural times were also longer in the patients in whom conduit was used instead of a transannular patch in the RVOTR. This may be related to the adhesion of the conduit to the neighboring tissues.
In addition, transcatheter PVR is reported as a new alternative method to conventional surgery.[13] Prosthetic valve migration, guidewire-related pulmonary artery branch or tricuspid valve injury, and stent fractures are among the reported complications of this new technique.[14]
On the other hand, in all of our patients, the effects of PVR on the right ventricular functions were shown using ECHO, but not with MRI. In none of the patients, implanted valve-related reoperation was needed in the mid-term follow-up; however longer follow-up is essential to identify the actual reintervention need in PVR patients.
In conclusion, pulmonary valve replacement can be performed with low morbidity and mortality rates. To relief the right ventricle function, the operation should be performed before the irreversible changes in the right ventricular volumes and functions occur.
We believe that larger implant sizes may diminish the need for reoperations.
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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