Assessing the nitric oxide efficacy in bilateral lung transplantation
https://doi.org/10.23873/2074-0506-2022-14-2-132-141
Abstract
Background. One of the most frequent and severe complications in the early postoperative period in lung transplantation is primary graft dysfunction resulting from ischemia-reperfusion injury. There is evidence of the effectiveness of using inhaled nitric oxide in order to prevent such injury.
Objective. To assess the effectiveness of nitric oxide in the intra- and early postoperative period in bilateral lung transplantation.
Material and methods. We examined 43 patients who underwent bilateral lung transplantation at the N.V. Sklifosovsky Research Institute for Emergency Medicine in the period from 2012-2021. The patients were divided into two groups. The study group consisted of 23 patients, whose complex of treatment included the use of inhaled nitric oxide. Patients in the comparison group (n=20) received a standard therapy. The end points of the study were: the mechanical ventilation duration, the frequency of using extracorporeal membrane oxygenation and its duration, mortality, dynamics of oxygenation index, blood lactate level, pH, base deficiency.
Results. The use of inhaled nitric oxide therapy in patients in the intra- and early postoperative period during lung transplantation improved the ventilation-perfusion ratio, as evidenced by an increase in the oxygenation index by 1.1 times (p=0.128) and 1.3 times (p=0.026) at 48 and 72 hours after surgery, respectively. Meanwhile, the frequency of using extracorporeal membrane oxygenation during surgery was found to decrease by 1.2 times (p=0.033), and that after surgery decreased by 1.4 times (p=0.474); the mechanical ventilation duration decreased by 1.4 times (p=0.042); the duration of extracorporeal membrane oxygenation decreased by 1.6 times (p=0.028); mortality reduced by 8%.
Conclusion. The use of inhaled nitric oxide therapy for lung transplantation had a positive effect on the intra- and early postoperative period, as indicated by an improvement in blood gas parameters, a reduction in the frequency and duration of veno-arterial extracorporeal membrane oxygenation, and the duration of mechanical ventilation.
About the Authors
A. M. TalyzinRussian Federation
Alexey M. Talyzin, Chief of the Department for Anesthesiology and Intensive Care No 3
3 Bolshaya Sukharevskaya Sq., Moscow 129090
S. V. Zhuravel
Russian Federation
Sergey V. Zhuravel, Dr. Sci. (Med.), Head of the Scientific Anesthesiology Department
3 Bolshaya Sukharevskaya Sq., Moscow 129090
M. Sh. Khubutiya
Russian Federation
Mogeli Sh. Khubutiya, Academician of the Russian Academy of Sciences, Prof., Dr. Sci. (Med.), President; Head of the Department of Transplantology and Artificial Organs
3 Bolshaya Sukharevskaya Sq., Moscow 129090
20 Bldg. 1 Delegatskaya St., Moscow 127473
E. A. Tarabrin
Russian Federation
Evgeniy A. Tarabrin, Dr. Sci. (Med.), Head of the Scientific Department of Urgent Thoracoabdominal Surgery
3 Bolshaya Sukharevskaya Sq., Moscow 129090
N. K. Kuznetsova
Russian Federation
Natalya K. Kuznetsova, Cand. Sci. (Med.), Anesthesiologist-Intensive Care Physician, Leading Researcher of the Anesthesiology Department
3 Bolshaya Sukharevskaya Sq., Moscow 129090
References
1. Jin Z, Suen KC, Wang Z, Ma D. Review 2: Primary graft dysfunction after lung transplant–pathophysiology, clinical considerations and therapeutic targets. J Anesth. 2020;34(5):729–740. PMID: 32691226 https://doi.org/10.1007/s00540-020-02823-6
2. Meade MO, Granton JT, Matte-Martyn A, McRae K, Weaver B, Cripps P, et al. A randomized trial of inhaled nitric oxide to prevent ischemia–reperfusion injury after lung transplantation. Am J Respir Crit Care Med. 2003;167(11):14831489. PMID: 12770854 https://doi.org/10.1164/rccm.2203034
3. Yoon J, Salamanca-Padilla Y. Effect of left ventricular diastolic dysfunction on development of primary graft dysfunction after lung transplant. Curr Opin Anaesthesiol. 2020;33(1):10–16. PMID: 31789901 https://doi.org/10.1097/ACO.0000000000000811
4. Fiser SM, Tribble CG, Long SM, Kaza AK, Kern JA, Jones DR, et al. Ischemia-reperfusion injury after lung transplantation increases risk of late bronchiolitis obliterans syndrome. Ann Thorac Surg. 2002;73(4):1041-1047. PMID: 11996238 https://doi.org/10.1016/s0003-4975(01)03606-2
5. Golikov PP. Oksid azota v klinike neotlozhnykh zabolevaniy. Moscow: Medpraktika-M Publ.; 2004. (In Russ.).
6. Khubutiya MhS, Klychnikova EV, Tazina EV, Tarabrin TA, Pervakova EI, Romanov AA, et al. Dynamic changes in blood concentrations of nitrite/nitrate and methemoglobin in patients after lung transplantation during treatment with inhaled nitric oxide. Transplantologiya. The Russian Journal of Transplantation. 2014;(4):6–11. (In Russ.).
7. Naka Y, Chowdhury NC, Liao H, Roy DK, Oz MC, Michler RE, et al. Enhanced preservation of orthotopically transplanted rat lungs by nitro glycerin but not hydralazine: requirement for graft vascular homeostasis beyond harvest vasodilation. Circ Res. 1995;76(5):900–906. PMID: 7729008 https://doi.org/10.1161/01.res.76.5.900
8. Karamsetty MR, Klinger JR. NO: more than just a vasodilator in lung trans plantation. Am J Respir Cell Mol Biol. 2002;26(1):1–5. PMID: 11751196 https://doi.org/10.1165/ajrcmb.26.1.f223
9. Minamoto K, Pinsky DJ, Fujita T, Naka Y. Timing of nitric oxide donor supplementation determines endothelin-1 regulation and quality of lung preser vation for transplantation. Am J Respir Cell Mol Biol. 2002;26(1):14–21. PMID: 11751199 https://doi.org/10.1165/ajrcmb.26.1.4649
10. Lindemann S, Sharafi M, Spiecker M, Buerke M, Fisch A, Grosser T, et al. NO reduces PMN adhesion to human vascular endothelial cells due to downregulation of ICAM-1 mRNA and surface expression. Thromb Res. 2000;97(3):113–123. PMID: 10680642 https://doi.org/10.1016/s0049-3848(99)00162-0
11. Pinsky DJ, Naka Y, Chowdhury NC, Liao H, Oz MC, Michler RE, et al. The nitric oxide/cyclic GMP pathway in organ transplantation: critical role in successful lung preservation. Proc Natl Acad Sci USA. 1994;91(25):12086–12090. PMID: 7527550 https://doi.org/10.1073/pnas.91.25.12086
12. Liu M, Tremblay L, Cassivi SD, Bai XH, Mourgeon E, Pierre AF, et al. Alterations of nitric oxide synthase expression and activity during rat lung transplantation. Am J Physiol Lung Cell Mol Physiol. 2000;278(5):L1071-L1081. PMID: 10781440 https://doi.org/10.1152/ajplung.2000.278.5.L1071
13. Schutte H, Witzenrath M, Mayer K, Rosseau S, Seeger W, Grimminger F. Short-term “preconditioning” with inhaled nitric oxide protects rabbit lungs against ischemia-reperfusion injury. Transplantation. 2001;72(8):1363-1370. PMID: 11685104 https://doi.org/10.1097/00007890-200110270-00005
14. Tagawa T, Suda T, Daddi N, Kozower BD, Kanaan SA, Mohanakumar T, et al. Low-dose endobronchial gene transfer to ameliorate lung graft ischemia-reperfusion injury. J Thorac Cardiovasc Surg. 2002;123(4):795–802. PMID: 11986609 https://doi.org/10.1067/mtc.2002.119067
15. Thabut G, Brugiere O, Leseche G, Stern JB, Fradj K, Herve P, et al. Preventive effect of inhaled nitric oxide and pentoxifylline on ischemia/reperfusion injury after lung transplanta tion. Transplantation. 2001;71(9):1295-1300. PMID: 11397965 https://doi.org/10.1097/00007890-200105150-00019
16. Kawashima M, Bando T, Nakamura T, Isowa N, Liu M, Toyokuni S, et al. Cytoprotective effects of nitroglycerin in ischemia-reperfusion-induced lung injury. Am J Respir Crit Care Med. 2000;161(3 Pt 1):935–943. PMID: 10712346 https://doi.org/10.1164/ajrccm.161.3.9905003
17. Ardehali A, Laks H, Levine M, Shpiner R, Ross D, Watson LD, et al. A prospective trial of inhaled nitric oxide in clinical lung transplanta tion. Transplantation. 2001;72(1):112-115. PMID: 11468544 https://doi.org/10.1097/00007890-200107150-00022
18. Adatia I, Lillehei C, Arnold JH, Thompson JE, Palazzo R, Fackler JC, et al. Inhaled nitric oxide in the treatment of postoperative graft dysfunction after lung transplantation. Ann Tho rac Surg. 1994;57(5):1311–1318. PMID: 8179406 https://doi.org/10.1016/00034975(94)91382-x
19. Date H, Anastosios NT, Trulock EP, Pohl MS, Cooper JD, Patterson GA. Inhaled nitric oxide reduces human lung allograft dysfunction. J Thorac Cardiovasc Surg. 1996;111(5): 913–919. PMID: 8622313 https://doi.org/10.1016/s0022-5223(96)70364-1
20. Yerebakan C, Ugurlucan M, Bayraktar S, Bethea BT, Conte JV. Effects of inhaled nitric oxide following lung transplantation. J Card Surg. 2009;24(3):269–274. PMID: 19438780 https://doi.org/10.1111/j.1540-8191.2009.00833.x
21. Fessler J, Godement M, Pirracchio R, Marandon J-Y, Thes J, Sage E, et al. Inhaled nitric oxide dependency at the end of double-lung transplantation: a boosted propensity score cohort analysis. Transpl Int. 2019;32(3):244–256. PMID: 30449027 https://doi.org/10.1111/tri.13381
22. Kurilova OA, Zhuravel SV, Romanov AA, Marinin PN, Tsurova DKh, Kallagov TE, et al. Experience with application of extracorporeal membrane oxygenation in double lung transplantation. Russian Journal of Transplantology and Artificial Organs. 2014;16(2):66–74. (In Russ.). https://doi.org/10.15825/1995-1191-2014-2-66-74
23. Khubutiya MSh, Chuchalin AG, Tarabrin EA, Pervakova EI, Gasanov AM, Borovkova NV, et al. (compilers) Algoritm lecheniya pervichnoy disfunktsii legochnogo transplantata i zashchita donorskikh legkikh: metodicheskie rekomendatsii № 39. Moscow: NII SP im. N.V. Sklifosovskogo Publ.; 2017. (In Russ.).
Review
For citations:
Talyzin A.M., Zhuravel S.V., Khubutiya M.Sh., Tarabrin E.A., Kuznetsova N.K. Assessing the nitric oxide efficacy in bilateral lung transplantation. Transplantologiya. The Russian Journal of Transplantation. 2022;14(2):132-141. https://doi.org/10.23873/2074-0506-2022-14-2-132-141