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Table of Contents   
ORIGINAL ARTICLE  
Year : 2021  |  Volume : 14  |  Issue : 3  |  Page : 350-355
Effect of change in tidal volume on left to right shunt across ventricular septal defect in children – A pilot study


1 Department of Cardiac Anaesthesia, CNC, All India Institute of Medical Sciences, New Delhi, India
2 Department of Cardiology, Cardiothoracic Centre, CNC, All India Institute of Medical Sciences, New Delhi, India

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Date of Submission01-Jan-2021
Date of Decision08-Jun-2021
Date of Acceptance17-Jul-2021
Date of Web Publication21-Aug-2021
 

   Abstract 


Background : Pulmonary vascular resistance, an important determinant of shunting across ventricular septal defects (VSD), rises at both extremes of lung volume.
Aims : We sought to determine the effect of changes in tidal volumes (VT) on pulmonary blood flow (Qp), systemic blood flow (Qs), and shunt (Qp/Qs) in children with VSD.
Setting : Single-center teaching hospital.
Design : Prospective observational study.
Methods : Thirty children with a mean age of 11.8 ± 5 months undergoing surgical closure of VSD were studied. Hemodynamics and shunt-related parameters were assessed using transthoracic echocardiography measured at three different VT i.e. 10, 8, and 6-ml/kg keeping the minute ventilation constant.
Results : Reduction in VT from 10 to 8 to 6 ml/kg led to a reduction in gradient across VSD measuring 23.5, 20 and 13 mmHg respectively (P < 0.001). Similarly, right ventricluar outflow tract (RVOT) diameter, RVOT velocity time integral, Qp (57.3 ± 18.1, 50.6 ± 16.9, 39.9 ± 14.7 mL; P < 0.001), Qs (24.1 ± 10.4, 20.0 ± 8.7, 15.3 ± 6.9 mL; P < 0.001) and peak airway pressure (17.2 ± 1.5, 15.8 ± 1.3, 14.5 ± 1.2 cmHg; P < 0.001) showed progressive decline with decreasing VT from 10 to 8 to 6 ml/kg, respectively. However, Qp/Qs (2.4 ± 0.4, 2.6 ± 0.4, 2.6 ± 0.4) demonstrated a minor increasing trend.
Conclusion : Lower VT reduces the gradient across VSD, the pulmonary blood flow, and the peak airway pressure. Hence, ventilation with lower VT and higher respiratory rate maintaining adequate minute ventilation might be preferable in children with VSD. Further studies are required to confirm the findings of this pilot study.

Keywords: Peak airway pressure, shunt (Qp/Qs), tidal volume, transthoracic echocardiography, ventilatory setting, ventricular septal defect

How to cite this article:
Pathak P, Das S, Gupta SK, Hasija S, Choudhury A, Gharde P, Makhija N, Chauhan S. Effect of change in tidal volume on left to right shunt across ventricular septal defect in children – A pilot study. Ann Pediatr Card 2021;14:350-5

How to cite this URL:
Pathak P, Das S, Gupta SK, Hasija S, Choudhury A, Gharde P, Makhija N, Chauhan S. Effect of change in tidal volume on left to right shunt across ventricular septal defect in children – A pilot study. Ann Pediatr Card [serial online] 2021 [cited 2021 Dec 2];14:350-5. Available from: https://www.annalspc.com/text.asp?2021/14/3/350/324179





   Introduction Top


Ventricular septal defect (VSD) is the most common congenital heart disease (CHD),[1] with isolated VSD constituting 20% of all CHD.[2],[3] The magnitude and direction of the shunt across VSD depend upon the size of the defect and pulmonary vascular resistance (PVR) compared to systemic vascular resistance.[4],[5] In patients with moderate and large VSD, increased pulmonary blood flow (Qp) results in left ventricular volume overload and pulmonary hypertension.[6]

Children with moderate and large VSD usually present with congestive heart failure and are routinely treated with diuretics, digoxin, and after-load reduction.[4],[7] As part of their management, especially in the perioperative period, they may require mechanical ventilatory support.[5] The increased Qp generates higher resistance and lower compliance in the lungs and leads to high peak airway pressure (Paw), hypercarbia, and hypoxemia.[8],[9],[10] In patients on ventilation, PVR rises at both upper and lower limits of tidal volume (VT).[11] During inspiration, lung inflation above the functional residual capacity (FRC) causes alveolar distension which in turn results in compression of alveolar vessels. Lower limits of VT produce atelectasis, collapse of the lung, increase in dead space ventilation, hypercarbia, hypoxia, and intrapulmonary shunting.

Mechanical ventilation before initiation of cardiopulmonary bypass (CPB) is aimed at optimizing oxygenation and removal of CO2, while avoiding barotrauma to the lungs. The ideal method of ventilation with better control of Qp is still not determined. The ventilation strategies have mostly focused on parameters influencing PVR, but the effect of VT on PVR and shunt flow is not well studied. Therefore, in this prospective observational study, we planned to evaluate the effect of changes in VT on VSD shunt-related parameters by echocardiography during preoperative mechanical ventilation.


   Methods Top


After obtaining institutional ethics committee approval and informed consent from parents or guardians of all participants, we prospectively enrolled 33 children younger than 3 years with isolated VSD who were scheduled for an elective surgical closure. Patients with concomitant CHDs were excluded from the study.

Anesthesia management

Patients were premedicated with syrup Triclofos sodium 30 mg/kg orally 1-hour before induction of anesthesia. In the operating room, 5-lead electrocardiography, pulse oximetry and noninvasive blood pressure were monitored. Anesthesia was induced with ketamine 2 mg/kg, fentanyl 3 mcg/kg and rocuronium 0.6 mg/kg. After intubation, ventilation was initiated with FiO2 (Fractional inspiratory oxygen concentration) of 0.5 by the ventilator (Datex-Ohmeda, Avance) and VT of 10 ml/kg of ideal body weight calculated by Mclaren method.[12] Anesthesia was maintained with sevoflurane, intermittent boluses of 0.1 mg/kg vecuronium, 2 mcg/kg fentanyl, and 50 mcg/kg midazolam. Invasive monitoring included femoral arterial pressure and right atrial pressure. Drugs were repeated during CPB. After the completion of the surgery, patients were managed in the cardiac intensive care unit as per hospital protocols.

All patients were ventilated on volume-controlled ventilation mode with VT of 10 ml/kg body weight with Paw pressure limitation of 30 cmH2O. A FiO2 of 0.5, I: E of 1:1.5 and positive end-expiratory pressure of zero were set to maintain an end-tidal CO2 (ETCO2) between 35 and 45 mmHg and SPO2 >95%. The respiratory rate was adjusted accordingly to keep the minute ventilation (MV) within the normal range. The normal range of MV was calculated by multiplying VT of 10 ml/kg with respiratory rate per minute adjusted to maintain the desired ETCO2. After initially setting the VT at 10 ml/Kg, it was changed to 8 ml/Kg and 6 ml/Kg with simultaneous adjustment of the respiratory rate to maintain a constant MV. Patients were ventilated with one set of VT for 5 min before transthoracic echocardiography (TTE) assessment was performed. The data acquired at these settings were designated VT10, VT8, and VT6, respectively.

Echocardiography examination

The echocardiographic examination was performed using a pediatric transthoracic probe of 8 or 12 MHz on an iE33 echocardiography machine (Philips; Bothell, WA, USA) to obtain the images. An independant experienced echocardiographer performed a comprehensive TTE in all patients. Echocardiography was performed following induction of anesthesia and before surgical incision under stable hemodynamic conditions. In parasternal long-axis view, VSD size [Figure 1], peak gradient across the VSD and diameter of the left ventricular outflow tract (LVOT) at the level of aortic valve were recorded.[13] In the parasternal short axis-aortic valve view, diameter of the right ventricular outflow tract (RVOT) and velocity-time integral (VTI) at the level of pulmonary annulus were calculated. Apical 5 chamber view was used to measure VTI at the level of LVOT [Figure 2]. Images were stored for offline analysis. Qp/Qs was calculated using the continuity equation: [13]
Figure 1: Parasternal short axis-aortic valve level view showing right ventricular outflow tract (RVOT), pulmonary valve and pulmonary artery. Velocity time integral at RVOT was taken at pulmonary valve level using pulse wave (PW) Doppler

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Figure 2: Apical 5 chamber (A5C) view showing left ventricular outflow tract (LVOT), aortic valve and ascending aorta. Velocity time integral at LVOT was taken at the aortic valve level using pulse wave Doppler

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Qp/Qs = Stroke Volume (SV) Right heart/SV Left heart = RVOT diameter × VTIRVOT/LVOT diameter × VTILVOT

Statistical analysis

Quantitative variables were expressed in mean ± standard deviation (SD) or median as applicable. Categorical data were expressed as frequency (percentage). A multiple-time point comparison was done using repeated measures ANOVA followed by post hoc pairwise comparisons, if significant, using paired t-test with Bonferroni correction. Statistical analysis was performed using the R console (RStudio IDE, 250 Northern Ave, Boston, MA 02210). A P < 0.05 was considered statistically significant.

Sample size

An arbitrary sample size of 30 was taken for this proof-of-concept study. A retrospective statistical analysis of the study, considering the difference in mean gradient across VSD from VT of 10 ml/Kg to 6 ml/Kg with SD of 12.5 and specified level of significance (alpha value) of 0.017 for three VT settings, the power of the study emerged to be 96% using the online version of nMaster 2.0 software, Department of Biostatistics, CMC, Vellore, Tamil Nadu, India.[14]


   Results Top


Out of the 33 patients, we excluded 3-patients from the analysis-one patient had very high Paw at 10 ml/kg VT and in the other two patients, ETCO2 and SpO2 could not be maintained within the desired range. Baseline demographic and hemodynamic characteristics of the patients are summarized in [Table 1] and [Table 2]. The mean age of the patients was 11.83 ± 5.5 months with 19 (63%) boys. The mean VSD diameter was 0.76 ± 0.13 cm.
Table 1: Baseline patient characteristics (n=30)

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Table 2: Patients hemodynamic characteristics

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Hemodynamic and respiratory parameters like HR, systolic and diastolic blood pressure, SpO2 were comparable in all the three VT settings [Table 2]. There was gradual reduction in the Paw when VT was changed from 10 to 8–6 ml/Kg. Echocardiographic parameters like gradient across the VSD, RVOT diameter, RVOT-VTI, LVOT-VTI, Qp, Qs, and Qp/Qs had significant statistical differences using repeated measures ANOVA [Table 3]. On further analysis, it was evident that there was a graded reduction in gradient from 23.5 (range 10, 51) to 20 (range 8, 50) and 13 (range 4, 44) mmHg, when VT was reduced from 10 ml-8 ml-6 ml/Kg, respectively [Table 3]. Qp and Qs demonstrated a decreasing trend, whereas the Qp/Qs demonstrated an increasing trend (2.4 ± 0.4, 2.6 ± 0.4, and 2.6 ± 0.4) [Figure 3]. Post hoc analysis of the variables showed statistical significant differences on the application of pairwise comparisons using Wilcoxon signed-rank test with Bonferroni correction.
Table 3: Patients echocardiographic characteristics

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Figure 3: Showing the gradual and simultaneous reduction in Gradient across VSD, Pulmonary flow (Qp), RVTI (velocity time integral at right ventricular outflow tract), RVOT D (right ventricular outflow tract diameter) and paw (peak airway pressure) when the VT changed from 10 ml/kg

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   Discussion Top


Moderate and large VSDs usually present with tachypnea, growth retardation, recurrent chest infections, and heart failure. Mechanical ventilation plays a crucial role in the ventilatory support in some of these patients presenting with acute heart failure or for pre- and peri-operatve optimization. Ventilatory strategies described have emphasized the need of eliminating factors that increase Qp, such as hyperventilation and higher oxygen administration. Higher VT like 12–14 ml/kg produces high Paw, inflated lungs, reduction in venous return to heart, rise in stroke volume variation, and increase in PVR, which reduces Qp.[15] High Paw produces barotrauma to alveoli making ventilation difficult with repeated alarms thus leading to suboptimal VT and hypercarbia. Besides, the resultant reduction in venous return with higher VT may reduce the stroke volume and more inflation of lungs may interfere with the operative field.

A study by Li et al .[16] evaluated the effect of changing VT on left to right shunt-related echocardiographic parameters in patients undergoing VSD repair. A prospective study,[13] estimated left to right shunt in patients with isolated VSD using Doppler echocardiography and oximetry by cardiac catheterization. They found that the Doppler method gives the estimation of Qp/Qs with greater accuracy and enables the demonstration of the size of VSD by calculating shunt magnitude.[13] We followed the same principles of assessment of various shunt parameters by Doppler interrogation.

Our study demonstrates that the decrease in the VT settings from 10 ml/kg to 8 ml/kg and 6 ml/kg keeping the MV constant, produces a significant decrease in the Qp as reflected by significant decrease in RVOT-VTI. There was a gradual reduction in the Paw when VT changed from 10 ml-8 ml-6 ml. Gradient across VSD and RVOT decreased along with the reduction in VT. A simultaneous fall in LVOT VTI led to reduction in Qs. The reduction in Qs was more than the reduction in Qp making Qp/Qs higher at lower VT settings.

The main determinants of shunt flow across a VSD are the size of the defect, pulmonary vascular bed, the pressure difference between RV and LV, and relative resistance between pulmonary and systemic circulations.[4] The increased Qp has an important role in producing higher resistance and low compliance to the lungs.[17] The altered lung dynamics create difficulty during artificial ventilation till the closure of VSD.

Another prospective study[18] compared the pre- and post-surgery lung functions in infants with increased Qp and evaluated the correlation between FRC, airway resistance, and lung compliance. They studied 30 pediatric patients and followed them postoperatively for 6 months. They found that infants with increased Qp had decreased pulmonary compliance, higher airway resistance, and FRC, which improved significantly after the surgical repair. These alterations in lung mechanics showed a strong correlation with the amount of pulmonary vascular enlargement and the severity of pulmonary hypertension. The result of this study stimulated us to find out the ventilator strategies for the patients with CHD having increased Qp as they pose difficulties in managing ventilation.

Li et al.[16] compared the VTI of left to right shunt in the pulmonary artery and descending aorta (DA) by manipulating the ventilation parameters for pediatric patients with VT 10, 8, and 6 ml/kg. The effect on cerebral oxygen saturation (rScO2) was noted by the alteration in VT. They had similar objectives as our study to determine the ventilation strategy with the ideal range of PaCO2 which could provide optimal Qp/Qs with an adequate oxygen supply for children with the left to right shunt. They maintained a higher PaCO2 to raise the PVR, which was achieved by VT of 6 ml/kg that had decreased the left to right shunt after anesthesia and a favorable VTIPA/VTIDA associated with an improvement in cerebral perfusion. Li et al. managed a range of PaCO2 40–50 mmHg, which has a significant impact on PVR. They detected reduction in VTIPA/VTIDA measured by transesophageal echocardiography when the VT was altered from 10 to 8–6 ml/kg.

Our study was different from Li et al. in the principle that we demonstrated the direct effect of VT change on Qp/Qs by maintaining a constant MV. We have used TTE to calculate different hemodynamic parameters with the changes in VT. We observed decrease in gradient across VSD, RVOT diameter, RVOT VTI, Qp, LVOT VTI, and Qs. However, we detected a slight increasing trend in Qp/Qs ratio at lower VT. The reduction in the LVOT VTI and Qs was attributable to the decreased return of blood to the left side of the heart at lower VT. The higher reduction in Qs compared to Qp might be the probable rationale for increasing the trend in the Qp/Qs. However, the reduction in Qs had no significant alteration in BP, HR, and clinical outcome at 3 settings of VT.

The present study finding proposes for a lower VT like 6–8 ml/kg and a higher respiratory rate for maintaining constant MV when mechanical ventilation is required in the preoperative and intraoperative period for VSD or L-R shunt patients. This method will reduce the Qp. The lungs will be prevented from barotrauma and hyper-inflation caused by high Paw while ventilating at higher VT. Our study was one of the preliminary studies of its kind with clinical importance. It will guide researchers to conduct further study in this field to substantiate the findings.

Limitations of the study

A single echocardiographer had acquired all the readings, hence some intra-observer bias might not be ruled out. Examination by 2 echocardiographers might have been better. The fall in Paw at lower VT might be possible, but we cannot differentiate between reduction in lung volume from the reduction in Qp or VT. A higher time interval between two settings of VT perhaps might have a better stabilization of respiratory parameters. It was not practical to get arterial blood gas with every change in VT, hence PaCO2, PaO2, and SaO2 values were not examined during the changes in VT.


   Conclusions Top


To conclude, reduction in VT from 10 ml/kg to 8 ml/kg and 6 ml/kg with adequate MV decreases the Qp besides reducing Paw and resultant barotrauma. We, therefore, propose the use of lower VT and higher respiratory rate with adequate MV as the preferred ventilatory strategy in pediatric patients having VSD with left to right shunt.

Acknowledgment

The authors sincerely thank Mrs. Nilima for conducting the statistical analysis.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

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Mavroudis C, Backer CL, Jacobs JL. Ventricular septal defect. In: Mavroudis C, Backer CL, editors. Pediatric Cardiac Surgery. 3rd ed. Philadelphia: Mosby; 2003. p. 298-20.  Back to cited text no. 1
    
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Backer CL, Eltayeb O, Mongé MC, Mazwi ML, Costello JM. Shunt lesions part I: Patent ductus arteriosus, atrial septal defect, ventricular septal defect, and atrioventricular septal defect. Pediatr Crit Care Med 2016;17 8 Suppl 1:S302-9.  Back to cited text no. 5
    
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Diller GP, Gatzoulis MA. Pulmonary vascular disease in adults with congenital heart disease. Circulation 2007;115:1039-50.  Back to cited text no. 6
    
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Morris K, Beghetti M, Petros A, Adatia I, Bohn D. Comparison of hyperventilation and inhaled nitric oxide for pulmonary hypertension after repair of congenital heart disease. Crit Care Med 2000;28:2974-8.  Back to cited text no. 9
    
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Hakim TS, Michel RP, Chang HK. Effect of lung inflation on pulmonary vascular resistance by arterial and venous occlusion. J Appl Physiol Respir Environ Exerc Physiol 1982;53:1110-5.  Back to cited text no. 11
    
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McLaren DS, Read WW. Classification of nutritional status in early childhood. Lancet 1972;2:146-8.  Back to cited text no. 12
    
13.
Mahmood M, Haque SS, Siddique MA, Ahmed CM, Hossain Z. Doppler evaluation of left to right shunt (Qp/Qs) in patients with isolated ventricular septal defect (Vsd). Mymensingh Med J 2007;16:181-6.  Back to cited text no. 13
    
14.
Sample Size Calculation. Available from: https://www.cmc-biostatistics.ac.in ' nmaster 2.0. [Last accessed on 2021 Jul 28].  Back to cited text no. 14
    
15.
Kang WS, Kim JY, Woo NS, Yoon TG. The influence of different mechanical ventilator settings of peak inspiratory pressure on stroke volume variation in pediatric cardiac surgery patients. Korean J Anesthesiol 2014;66:358-63.  Back to cited text no. 15
    
16.
Li P, Zeng J, Wei W, Lin J. The effects of ventilation on left-to-right shunt and regional cerebral oxygen saturation: A self-controlled trial. BMC Anesthesiol 2019;19:178-84.  Back to cited text no. 16
    
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Yau KI, Fang LJ, Wu MH. Lung mechanics in infants with left-to-right shunt congenital heart disease. Pediatr Pulmonol 1996;21:42-7.  Back to cited text no. 17
    
18.
Agha H, El Heinady F, El Falaky M, Sobih A. Pulmonary functions before and after pediatric cardiac surgery. Pediatr Cardiol 2014;35:542-9.  Back to cited text no. 18
    

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Correspondence Address:
Dr. Sambhunath Das
Department of Cardiac Anaesthesia, Room No. 7, 7th Floor, Cardiothoracic Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110 029
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.apc_1_21

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    Figures

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    Tables

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