Effects of lung recruitment maneuvers using mechanical ventilator on preterm hemodynamics

  • Adhi Teguh Perma Iskandar Cipto Mangunkusumo Hospital
  • Ahmad Kautsar Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Anisa Rahmadhany Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Risma Kerina Kaban Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Bambang Supriyatno Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Joedo Prihartono Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Dewi I. Santoso Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Tetty Yuniarti Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Najib Advani Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Mulyadi M. Djer Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
  • Fiolita I. Sutjipto Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta
Keywords: hemodynamic, Lung recruitment, mechanical ventilator

Abstract

Background Lung recruitment maneuvers (LRMs) are a strategy to gradually increase mean positive airway pressure (MAP) to expand the alveoli, leading to decreased pulmonary vascular resistance and increased cardiac output (CO). However, the hemodynamic impact of LRM using assist control volume guarantee (AC-VG) ventilator mode done in preterm infants born at 24 to 32 weeks’ gestation, especially in the first 72 hours of life, remains unknown.

Objective To determine the effect of LRM on right- and left cardiac ventricular output (RVO and LVO), ductus arteriosus (DA) diameter and its pulmonary hypertension (PH) flow pattern, as well as superior mesenteric artery (SMA) flow.

Method This randomized, controlled, single-blinded clinical trial was performed in 24-32-week preterm neonates with birth weights of >600 grams. Subjects were allocated by block randomization to the LRM and control groups, each containing 55 subjects. We measured RVO, LVO, DA diameter, PH flow pattern, and SMA resistive index (RI) at 1 and 72 hours after mechanical ventilation was applied. We analyzed for hemodynamic differences between the two groups.

Results During the initial 72 hours of mechanical ventilation, there were no significant differences between the control vs. LRM groups in mean changes of LVO [41.40 (SD 91.21) vs. 15.65 (SD 82.39) mL/kg/min, respectively; (P=0.138)] or mean changes of RVO [65.56 (SD 151.20) vs. 70.59 (SD 133.95) mL/kg/min, respectively; (P=0.859)]. Median DA diameter reduction was -0.08 [interquartile range (IQR) -0.55; 0.14] mm in the  control group and -0.10 (IQR -0.17 to -0.01) mm in the LRM group (P=0.481). Median SMA resistive index was 0.02 (IQR -0.16 to 0.24) vs. 0.01(IQR -0.20 to 0.10) in the control vs. LRM group, respectively. There was no difference in proportion of pulmonary hypertension flow pattern at 72 hours (25.4% vs. 20% in the control vs. LRM group, respectively) (P=0.495).

Conclusion When preterm infants of 24-32 weeks gestational age are placed on mechanical ventilation, LRM gives neither additional hemodynamic benefit nor harm compared to standard ventilator settings.

Author Biography

Najib Advani, Department of Child Health, Universitas Indonesia Medical School/Dr. Cipto Mangunkusumo Hospital, Jakarta

 

 

References

1. Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, Narwal R, et al. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications. Lancet. 2012;379:2162-72. DOI: https://doi.org/ 10.1016/S0140-6736(12)60820-4.
2. Kumar A, Vishnu BB. Epidemiology of respiratory distress of newborns. Indian J Pediatr. 1996;63:93-8. DOI: https://doi.org/10.1007/BF02823875.
3. Iskandar ATP, Kaban R, Djer MM. Heated, humidified high-flow nasal cannula vs. nasal CPAP in infants with moderate respiratory distress. Paediatr Indones. 2019;59:331-2. DOI: https://doi.org/10.14238/pi59.6.2019.331-9.
4. Wu TW, Azhibekov T, Seri I. Transitional hemodynamics in preterm neonates: clinical relevance. Pediatr Neonatol. 2016;57:7-18. DOI: https://doi.org/10.1016/j.pedneo.2015.07.002.
5. Castoldi F, Daniele I, Fontana P, Cavigioli F, Lupo E, Lista G. Lung recruitment maneuver during volume guarantee ventilation of preterm infants with acute respiratory distress syndrome. Am J Perinatol. 2011;28:521–8. DOI: https://doi.org/ 10.1055/s-0031-1272970.
6. Singhal R, Jain S, Chawla D, Guglani V. Accuracy of New Ballard Score in small-for-gestational age neonates. J. Trop. Pediatr. 2017;63:489–94. DOI: https://doi.org/ 10.1093/tropej/fmx055.
7. Nestaas E, Fugelseth D, Eriksen BH. Assessment of systemic blood flow and myocardial function in the neonatal period using ultrasound. In: Kleinman CS, Seri I, Polin RA, editors. Hemodynamics and cardiology. 3rd ed. Philadelphia: Elsevier; 2019. p. 191-5. ISBN: 9780323533669.
8. Bjorland PA, Ersdal HE, Haynes J, Ushakova A, Oymar K, Rettedal SI. Tidal volume and pressure delivered by NeoPuff T-piece resuscitator during resuscitation of term newborns. Resuscitation. 2022;170:222-9. DOI: https://doi.org/10.1016/j.resuscitation.2021.12.006
9. Carlo WA, Ambavalan N. Assisted ventilation. In: Fanaroff J, Fanaroff A, editors. Care of the high-risk neonate. 6th ed. Philadelphia: Saunders; 2013. p. 270-5. ISBN: 9781416040019.
10. Keszler M, Abubakar K. Physiologic principle. In: Goldsmith JP, Karotkin E, editors. Assisted ventilation of the neonate. 6th ed. Philadelphia: Saunders; 2017. p. 8-30. ISBN: 9780323392150.
11. Evans N, Kluckow M. Early determinants of right and left ventricular output in ventilated preterm infants. Arch Dis Child Fetal Neonatal Ed. 1996;74:F88-94. DOI: https://doi.org/ 10.1136/fn.74.2.f88.
12. Vrancken SL, van Heijst AF, de Boode WP. Neonatal hemodynamics: from developmental physiology to comprehensive monitoring. Front Pediatr. 2018;6:87. DOI: https://doi.org/ 10.3389/fped.2018.00087.
13. Lakshminrusimha S. The pulmonary circulation in neonatal respiratory failure. Clin Perinatal. 2012;39:655-83. DOI: https://doi.org/ 10.1016/j.clp.2012.06.006.
14. Hilman N, Kallapur SG, Jobe A. Physiology of transition from intrauterine to extrauterine life. Clin Perinatol. 2012;39:769-83. DOI: https://doi.org/ 10.1016/j.clp.2012.09.009..
15. De Waal K, Evans N, van der Lee J, van Kaam A. Effect of lung recruitment on pulmonary, systemic, and ductal blood flow in preterm infants. J Pediatr. 2009;154:651-5. DOI: https://doi.org/ 10.1016/j.jpeds.2009.01.012. .
16. Sehgal A, Ruoss JL, Stanford AH, Lakshminrusimha S, McNamara PJ. Hemodynamic consequences of respiratory interventions in preterm infants. J Perinatol. 2022;42:1153-60. DOI: https://doi.org/10.1038/s41372-022-01422-5.
17. Hermes-DeSantis ER, Clyman RI. Patent ductus arteriosus: pathophysiology and management. J Perinatol. 2006;26:14-8. DOI: https://doi.org/ 10.1038/sj.jp.7211465.
18. Clyman RI. Mechanisms regulating the ductus arteriosus. Biol Neonate. 2006;89:330-5. DOI: https://doi.org/ 10.1159/000092870.
19. Grasso C, Sciacca P, Giacchi V, Carpinato C, Mattia C, Palano GM, et al. Effects of sustained lung inflation, a lung recruitment maneuver in primary acute respiratory distress syndrome, in respiratory and cerebral outcomes in preterm infants. Early Hum Dev. 2015;91:71–5. DOI: https://doi.org/ 10.1016/j.earlhumdev.2014.12.002.
20. Wu R, Li S, Tian Z, Li N, Zheng G, Zhao Y, et al. Lung recruitment manoeuvre during proportional assist ventilation of preterm infants with acute respiratory distress syndrome. J Perinatol. 2014;34:524-7. DOI: https://doi.org/ 10.1038/jp.2014.53.
21. Stefano JL, Abbasi S, Pearlman SA, Spear ML, Esterly KL, Bhutani VK. Closure of the ductus arteriosus with indomethacin in ventilated neonates with respiratory distress syndrome. Effects on pulmonary compliance and ventilation. Am Rev Respir Dis. 1991;143:236-9. DOI: https://doi.org/ 10.1164/ajrccm/143.2.236.
22. Shimada S, Kasai T, Konishi M, Fujiwara T. Effects of patent ductus arteriosus on left ventricular output and organ blood flows in preterm infants with respiratory distress syndrome treated with surfactant. J Pediatr. 1994;125:270-7. DOI: https://doi.org/10.1016/s0022-3476(94)70210-1.
23. Martinho S, Adao R, Leite-Moreira AF, Bras-Silva C. Persistent pulmonary hypertension of the newborn: pathophysiological mechanisms and novel therapeutic approaches. Front Pediatr. 2020;8:342. DOI: https://doi.org/ 10.3389/fped.2020.00342.
24. Delaney C, Cornfield DN. Risk factors for persistent pulmonary hypertension of the newborn. Pulm Circ. 2012;2:15-20. DOI: https://doi.org/ 10.4103/2045-8932.94818.
25. McCurnin D, Clyman RI. Effects of patent ductus arteriosus on postprandial mesenteric perfusion in premature baboons. Pediatrics. 2008;122:1262-7. DOI: https://doi.org/ 10.1542/peds.2008-2045.
26. Ayoub D, Elmashad A, Rowisha M, Eltomey M, El Amrousy D. Hemodynamic effects of high-frequency oscillatory ventilation in preterm neonates with respiratory distress syndrome. Pediatr Pulm. 2021;56:424-32. DOI: https://doi.org/ 10.1002/ppul.25195.
Published
2023-06-28
How to Cite
1.
Perma Iskandar A, Kautsar A, Rahmadhany A, Kaban R, Supriyatno B, Prihartono J, Santoso D, Yuniarti T, Advani N, Djer M, Sutjipto F. Effects of lung recruitment maneuvers using mechanical ventilator on preterm hemodynamics. PI [Internet]. 28Jun.2023 [cited 1May2024];63(3):173-0. Available from: https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/3243
Section
Neonatology
Received 2022-11-16
Accepted 2023-01-05
Published 2023-06-28