Objective: We aimed to assess the association of right ventricular acceleration during isovolumic contraction (RVIVA) to functional recovery after device closure of patent ductus arteriosus (PDA).

Methods: 84(7.5+6.8year; 49 female ) patients who underwent device closure of PDA were evaluated with conventional and tissue Doppler echocardiography pre closure, at 24hours and at 6months post closure to assess RVIVA, myocardial performance index (MPI). Brain natreuretic peptide (BNP) was assessed pre closure and 6months post closure

Results: RVIVA was significantly decreased in children with PDA, while other conventional Echo Doppler parameters were comparable to controls. Following closure of PDA, RVIVA was significantly increased (P<0.001). These changes were correlated with significant decrease in LVMPI, BNP and sPAP (P <0 .001, for all). At 6month of follow-up the BNP markedly decreased with significant improvement of LVMPI in 78 (92.9) patients. With multivariate analysis, RV IVA were the strongest predictors of functional recovery (r= 0.582, P<0.001 and r=- -0.518; P<0.001). ROC sowed that RVIVA >2.4m/s was the best cutoff value in predicting functional recovery after percutaneous closure of PDA.

Conclusion: Measurement of RVIVA in patients with PDA specially those presented late are important to differentiate high- and low-risk groups in terms of prognosis.. RVIVA might be considered a useful indicator for functional recovery after device closure of PDA

Keywords: isovolumetric acceleration, pulmonary stiffness, patent ductus arteriosus

In patients with patent ducts arteriosus, cardiovascular system is generally exposed to much overload and subsequently several complications as congestive heart failure, pulmonary hypertension and infective endocarditis. These complications depend on the size of the defect and the timing of intervention.¹ It is important to close PDA to prevent occurrence of these complications.² Today percutaneous transcatheter closure method is the first choice for PDA closure, mostly utilizing Amplatzer Duct Occluder. Right ventricular echocardiographic indices before and after PDA closure are scarcely studied. Right ventricular systolic function can be determined with assessment of tricuspid annular motion utilizing pulsed-wave Doppler tissue imaging.^3‒5 Why…. Pauliks et al.,³ and Turhan et al.,⁴ reported that IVA assessment seems to be a more reliable and sensitive for predicting cardiac function than tissue Doppler imaging (TDI)-derived peak systolic velocity. Tissue Doppler echocardiography (TDE) derived myocardial performance index (MPI) is a widely accepted parameter for quantitative assessment of myocardial function,⁵ and it is more sensitive for global myocardial function than separately assessing systolic and diastolic function.⁶

We hypothesized right ventricular dysfunction may occur as well in patients with PDA and early identification of these changes may improve evaluation of cardiac function and timing of interventions. The purpose of this study was to evaluate the right ventricular isovolumic acceleration in children with patent ductus arteriosus and its relation to functional recovery after transcatheter closure of the PDA

84 consecutive patients, with hemodynamically significant PDA, were included in a prospective study. Inclusion criteria for percutaneous closure of PDA were children with PDA, who the murmur was significantly auscultated, had bounding pulse, and their body weight ≥ 6kg, and the duct size less than 12mm. Exclusion criteria: PDA not suitable for percutaneous closure, irreversible pulmonary vascular disease (pulmonary vascular resistance index i.e. PVRI > 7 WU.m²), and other associated significant congenital heart disease. Informed consent was obtained from the patients’ or their parents. The study was approved from the faculty ethical committee. Forty two healthy subjects with age and sex matched were recruited as control group.

Echocardiographic studies

Echocardiography was performed in all patients in the left lateral decubitus position with standard views using a Vivid 5 machine (GE Vingmed, Horten, Norway). Left atrial systolic dimension and LV internal dimensions and wall thicknesses were measured from two dimensional guided M-mode tracings obtained at the mid chordal level in the parasternal long-axis view according to the criteria of the American Society of Echocardiography.^7‒9 Mitral inflow velocities were obtained by pulsed-wave Doppler in the apical 4-chamber view with the sample volume placed at the tips of the mitral valve leaflets. The peak early (E) and late (A) diastolic mitral inflow velocities, deceleration time, E/A ratio, and isovolumic relaxation time were measured and averaged over three cardiac cycles. Color tissue Doppler imaging was performed from the apical 4-chamber view using a 2.5-MHz transducer and frame rates of >80/sec and the images were digitized. Derivation and analysis of TDI-derived velocity profiles were performed offline using commercial computer software (Echopac, GE Vingmed). Myocardial velocity profiles of the basal septal and lateral mitral annulus were obtained by placing a 6-mm sample volume at the junction of the mitral annulus with the septum and lateral myocardial wall. Myocardial velocities of the lateral tricuspid annulus were obtained similarly by placing the sample volume at the junction of the tricuspid valve annulus and right ventricular free wall. The ratio of peak early diastolic mitral inflow velocity by pulsed wave Doppler to peak early diastolic mitral annular velocity by TDI was calculated as a measure of LV filling pressure. The MPI of LV obtained by TDE, defined as the sum of the isovulumetric relaxation time and isovolumetric contraction time divided by ejection time. Doppler measurements were made at a recording rate of 100 mm/s. Myocardial isovolumic acceleration was measured by dividing the peak velocity bythe time interval from the onset of the wave (zero-crossing) during isovolumic contraction to the peak velocity of this wave as previously described.¹⁰

Cardiac catheterization

A hemodynamic study was performed first: Right and left heart cardiac catheterization was performed. Mean pulmonary artery pressure was obtained by the data of right heart catheterization. Data from right and left heart catheterization were obtained and with the use of Fick" principle, the systemic flow (Qs), pulmonary flow (Qp) and pulmonary vascular resistance (PVR) were calculated. The PVR was calculated using the formula: PVR = (MPAP - PCWP)/Qp. After sizing, PDA percutaneous closures of PDA were performed with all children under general anesthesia, by standard technique utilizing a loading catheter, a Mullin delivery sheath and a delivery cable. Amplatzer type (Cocoon) ductal occluder device (Vascular Innovations Co. Ltd., Bankok, Thailand) was used in all subjects. After device deployment, echocardiographic assessment was done for the device position, and descending thoracic aortic and left pulmonary artery velocity. The ductal occluder device was released after excluding the significant residual shunt and obstruction in aorta and/or left pulmonary artery.

Brain natreuretic peptide measurement

The blood samples were collected by veni-puncture into EDTA tubes kept at room temperature and analyzed within 4hours of sampling usingthe Triage BNP assay (Biosite diagnostics. The BNP assay was as andwich immuno- assay that consisted of a disposable device to which 250mL of EDTA-anticoagulated whole blood or plasma was added. The Triage meter was used to measure the BNP concentration by detecting a fluorescent signal that reflected the amount of BNP in the sample. The upper limit of the normal lab reference for BNP was 42pg/ml.¹¹

Follow-up

Patients underwent serial follow-up examinations at 24hours, 3, 6, and 12months, and then yearly after the procedure. Follow-up studies included clinical examination, ECG, and transthoracic echocardiogram. BNP was assessed during follow-up only at 6months.

Statistics

The SPSS software (Statistical Package for the Social Sciences, Version 21.0, SSPS Inc., Chicago, IL, USA) was used to analyze the obtained data of the study. Continuous variables were expressed as mean ± S.D. and categorical variables were expressed as percentages. The Pearson correlation analysis was used to estimate the correlations between LV functional recovery assessed by (MPI and BNP) and PAS, RVIVA. A linear regression-stepwise analysis model was performed to test the effects of PAS, and RVIA on left ventricular functional recovery assessed by (MPI and BNP). ROC curve analysis was used to determine the best cutoff values of RVIVA and PAS in predicting functional recovery after device closure of PDA

The study included 84 patients. The mean age was 7.5 + 6.8year (49 female and 35 male) and 42 matched healthy subjects were studies as a control group. Table 1 shows the basic characteristics characteristics of the study population. Left atrial volume index, E/E' ratio, LV-MPI, sPAP and BNP levels were significantly higher in patients with PDA compared to controls. On the other hand LVIVA, RVIVA were significantly lower in children with PDA. The catheterization data of children with PDA are represented in Table 2.

Table 3 shows that Left atrial volume index, E/E' ratio, LV-MPI, LVIVA, RVIVA were significantly improved at 6 months of follow-up after device closure of PDA. LV-MPI was significantly decreased at 6months of follow-up compared to pre-closure and at 24hours post-closure (P<0.001 for all). The BNP levels as well were significantly decreased at 6months post-closure of PDA compared to both pre-closure and at 24hours post-closure (P<0.001 for both).

The results showed that RVIVA tends to improve 24hours after closure (P<0.05), and continued to increase to be comparable to normal at 6months of follow-up (P<0.002). In contrast, the other right ventricular echocardiographic parameters (S', TAPSE, FAS%,), didn't changed significantly either early or late at 6months of follow-up (P>0.05 for all).

At the 6-month follow-up, 78 patients showed complete functional recovery (LV-MPI and BNP levels came back to values comparable to control subjects). However, 6 patients did not show complete functional recovery. (MPI>0.49 ± 0.08 versus 0.35+0.06 and BNP103+15 versus 53+9' P<0.001). The pre-closure RVIVA was significantly lower and E/E' were significantly higher in patients without complete recovery compared to those with complete recovery (Table 4).

Table 6 shows a significant correlation of RVIVA to LVIVA, E/E" ratio, LAVI, baseline sPAP in children with patent ductus arteriosus. With ROC analysis the results demonstrated that RVIVA with a cutoff value of >2.4 m/s (AUC=0.95) predicts functional recovery after device closure of PDA with a sensitivity of 86% and specificity of 96% (Table 6).

We observed significantly lowering of IVA at the time of diagnosis of patent ductus arteriosus, that correlated with sPAP and serum levels of BNP.At 6months postclosure of PDA, we found that RVIVA had normalized compared to the values from preclosure and at one month after closure. This normalization of RVIVA was associated with normalization of LVIVA, significant decrease in sPAP and decrease in BNP at 6months postclosure. The RVIVA with a cut-off value of > 2.4m/s2 was an independent predictors of functional recovery after device closure of PDA.

Subclinical right ventricular dysfunction may occur early in patients with PDA and may affect the clinical course of the disease even after closure. However, no much studies had investigated right ventricular function in patients with PDA. With significant systemic-to-pulmonary shunt, the LV volume load and right ventricular pressure load increase simultaneously. After closure of PDA, the PAP remains suspended at a high level, due to longer period of recovery of pulmonary endothelial injury, pulmonary in situ thrombosis, and LV failure.^12,13 Right ventricle is usually the victim of the different diseases affecting cardiovascular system, as it is more compliant, more thin walled and less muscular and usually forgetting in there clinical practice¹⁴ Moreover Right ventricle dysfunction has a significant impact on the patients symptoms in addition to it’s a valuable indicator of the severity and chronicity of pulmonary hypertension.¹⁵

Echocardiographic parameters have been reported to assess the RV function, namely, TAPSE, 2D RV FAC, 2D RV EF, TDI, ratio of RV transverse diameter to left ventricular transverse diameter (RVETD/LVETD), and Sm. These parameters, however are load dependent and unreliable when RA pressure is elevated.¹⁶ On the other hand, IVA can detect minimal changes in myocardial function, even the changes in the preload and afterload within the physiological. IVA was the most strong pre and after load independent compared to tissue Doppler derived peak systolic velocities, strain and strain rate.¹⁷

Tugcu et al.,¹⁸ reported that spite of normal pulmonary and systemic pressure in patients with obstructive sleep apnea syndrome, IVA was the only parameter that changed significantly during right ventricular functional assessment. This may be related to subclinical RV dysfunction. We analyzed the effect of percutaneous device closure of PDA on RVIVA and other RV function parameters. There were significant rise in RV-IVA, decrease in pulmonary artery pressure. These changes were significantly associated with significant reduction in BNP and improvement of left ventricular function at 6 months of follow-up. Pauliks et al.,¹⁹ demonstrated that IVA was significantly improved after defect closure in patients with atrial septal defect.

We observed little significant difference in FAC and TAPSE in patients with PDA and controls. Moreover these parameters did not changes significantly after closure of PDA or even after 6month of follow-up. On the other hand both RV-IVA showed a highly significant difference. Based on this information, the significant recovery in the right ventricular IVA values may help explain the improved ejection fraction and significant decrease in BNP. Moreover these observation provide that right ventricular IVA assessment seems to be a more sensitive technique to assess early changes and follow-up of right ventricular function.

Measurement of RVIVA in patients with PDA specially those presented late are important to differentiate high- and low-risk groups in terms of prognosis. In our study, we assessed right ventricular function in children with PDA utilizing RVIVA, RVEF, PAP, TAPSE, and MPI), and reached the conclusion that tissue Doppler RVIVA was an independent predictors for functional recovery after percutaneous closure of patent ductus arteriosus.

None.

Author declares there are no conflicts of interest.

None.

1. Samánek M. “Children with congenital heart disease: probability of natural survival,” Pediatr Cardiol. 1992;13(3):152‒158.
2. Eerola A, Jokinen, E, Boldt T, et al. Serum Levels of Natriuretic Peptides in Children before and after Treatment for an Atrial Septal Defect, a Patent Ductus Arteriosus, and a Coarctation of the Aorta-A Prospective Study. Int J Pediatr. 2010;2010:674575.
3. Pauliks LB, Chan K, Chang D, et al. Regional myocardial velocities and isovolumic contraction acceleration before and after device closure of atrial septal defects: A color tissue Doppler study. Am Heart J . 2005;150(2):294‒301.
4. Turhan S, Tulunay C, Cin M, et al. Effects of Thyroxine Therapy on Right Ventricular Systolic and Diastolic Function in Patients with Subclinical Hypothyroidism: A Study by Pulsed Wave Tissue Doppler Imaging. J Clin Endocrinol Metab. 2006;91(9):3490‒3493.
5. Tei C, Ling LH, Hodge DO, et al. New index of combined systolic and diastolic myocardial performance: a simple and reproducible measure of cardiac function-a study in normals and dilated cardiomyopathy. J Cardiol. 1995;26(6):357‒366.
6. Tei C, Dujardin KS, Hodge DO, et al. Doppler echocardiographic index for assessment of global right ventricular function. J Am Soc Echocardiogr . 1996;9(6):838‒847.
7. Schiller NB, Shah PM, Crawford M, et al. Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms. J Am Soc Echocardiogr. 1989;2(5):358‒367.
8. Devereux RB, Alonso DR, Lutas EM, et al. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol. 1986;57(6):450‒458.
9. Teichholz LE, Kreulen T, Herman MV, et al. Problems in echocardiographic volume determinations: echocardiographic angiographic correlations in the presence of absence of asynergy. Am J Cardiol . 1976;37(1):7‒11.
10. Vogel M, Schmidt MR, Kristiansen SB, et al. Validation of myocardial acceleration during isovolumic contraction as a novel noninvasive index of right ventricular contractility: comparison with ventricular pressure-volume relations in an animal model. Circulation. 2002;105(14):1693‒1699.
11. Yandle TG, Richards AM, Gilbert A, et al. Assay of brain natriuretic peptide (BNP) in human plasma: evidence for high molecular weight BNP as a major plasma component in heart failure. J Clin Endocrinol Metab . 1993;76(4):832‒888.
12. Jeong YH, Yun TJ, Song JM, et al. Left ventricular remodeling and change of systolic function after closure of patent ductus arteriosus in adults: device and surgical closure. Am Heart J . 2007;154(3):436‒440.
13. Voelkel NF, Quaife RA, Leinwand LA, et al. Right Ventricular Function and Failure: Report of a National Heart, Lung, and Blood Institute Working Group on Cellular and Molecular Mechanisms of Right Heart Failure. Circulation. 2006;114(17):1883‒1891.
14. Chin KM, Kim NH, Rubin J. The Right Ventricle in Pulmonary Hypertension. Coron Artery Dis. 2005;16(1):13‒18.
15. McLaughlin VV, Sitbon O, Badesch DB, et al. Survival with First-Line Bosentan in Patients with Primary Pulmonary Hypertension. The European Respiratory Journal. 2005;25:244‒249.
16. Rudski LG, Lai WW, AfilaloJ, et al. Guidelines for the Echocardiographic Assessment of the Right Heart in Adults: A Report from the American Society of Echocardiography Endorsed by the European Association of Echocardiography, a Registered Branch of the European Society of Cardiology, and the Canadian Society of Echocardiography. J Am Soc Echocardiogr. 2010;23(7):685‒713.
17. Vogel M, Cheung MM, Li J, et al. Noninvasive Assessment of Left Ventricular Force-Frequency Relationships Using Tissue Doppler-Derived Isovolumic Acceleration: Validation in an Animal Model. Circulation. 2003;107(12):1647‒1652.
18. Tugcu A, Yildirimtürk O, Tayyareci Y, et al. Evaluation of subclinical right ventricular dysfunction in obstructive sleep apnea patients using velocity vector imaging. Circ J. 2010;74(2):312‒319.
19. Pauliks LB, Chan KC, Chang D, et al. Regional myocardial velocities and isovolumetric contraction acceleration before and after device closure of atrial septal defects: a color tissue Doppler study. Am Heart J . 2005;150(2):294‒301.