Abstract
Purpose
We assessed the effect of high partial pressure of arterial carbon dioxide (PaCO2) due to pneumoperitoneum (PP) on growth (height/weight) and development (gross/fine motor function, receptive/expressive communication, and social interaction), by comparing outcome after portoenterostomy (PE) for biliary atresia (BA) using laparoscopic PE (LPE: n = 13) and open PE (OPE: n = 13) cases performed between 2005 and 2014.
Methods
Our PE is based on Kasai’s original PE. All data were collated prospectively.
Results
Differences in duration of follow-up (LPE: 38.8 months; OPE: 38.1 months), jaundice clearance (LPE: 12/13 = 92.3 %; OPE: 9/13 = 69.2 %), survival with the native liver (LPE: 10/13 = 76.9 %; OPE: 9/13 = 69.2 %), incidence of cholangitis, hypersplenism, and incidence of esophageal varices were not significant. Mean intraoperative PaCO2 was significantly higher in LPE (LPE: 50.1 mmHg; OPE: 40.7 mmHg, p < 0.05). Liver function impairment was not statistically different, although LPE results were slightly worse. There was no overall delay in growth observed, although height/weight gain was more consistent in LPE. The pattern of developmental delay observed was similar for LPE and OPE suggesting that developmental delay is not PE-related; in other words, PP is not implicated in developmental delay.
Conclusions
PP during LPE would appear to have no adverse effects on overall growth/development and liver function in BA patients.
Similar content being viewed by others
References
Laje P, Clark FH, Friedman JR et al (2010) Increased susceptibility to liver damage from pneumoperitoneum in a murine model of biliary atresia. J Pediatr Surg 45:1791–1796
Ure BM, Kuebler JF, Schukfeh N et al (2011) Survival with the native liver after laparoscopic versus conventional Kasai portoenterostomy in infants with biliary atresia: a prospective trial. Ann Surg 253:826–830
Tan M, Xu FF, Peng JS et al (2003) Changes in the level of serum liver enzymes after laparoscopic surgery. World J Gastroenterol 9:364–367
Saber AA, Laraja RD, Nalbandian HI et al (2000) Changes in liver function tests after laparoscopic cholecystectomy: not so rare, not always ominous. Am Surg 66:699–702
Nguyen NT, Braley S, Fleming NW et al (2003) Comparison of postoperative hepatic function after laparoscopic versus open gastric bypass. Am J Surg 186:40–44
Morino M, Giraudo G, Festa V (1998) Alterations in hepatic function during laparoscopic surgery. An experimental clinical study. Surg Endosc 12:968–972
Guven HE, Oral S (2007) Liver enzyme alterations after laparoscopic cholecystectomy. J Gastrointestin Liver Dis 16:391–394
Sahin DA, Haliloglu B, Sahin FK et al (2007) Stepwise rising CO2 insufflation as an ischemic preconditioning method. J Lap Surg Tech 17:726–729
Bickel A, Drobot A, Aviram M et al (2007) Validation and reduction of the oxidative stress following laparoscopic operations: a prospective randomized controlled study. Ann Surg 246:31–35
Jaeschke H, Lemasters JJ (2003) Apoptosis versus oncotic necrosis in hepatic ischemia/reperfusion injury. Gastroenterology 125:1246–1257
Mogilner JG, Bitterman H, Hayari L et al (2008) Effect of elevated intra-abdominal pressure and hyperoxia on portal vein blood flow, hepatocyte proliferation and apoptosis in a rat model. Eur J Pediatr Surg 18:380–386
Jesch NK, Vieten G, Tschering T et al (2005) Mini-laparotomy and full laparotomy but not laparoscopy alter hepatic macrophage populations in a rat model. Surg Endosc 19:804–810
Kuebler JF, Kos M, Jesch NK et al (2007) Carbon dioxide suppresses macrophage superoxide anion production independent of extracellular pH and mitochondrial activity. J Pediatr Surg 42:244–248
Shimotakahara A, Kuebler JF, Vieten G et al (2008) Carbon dioxide directly suppresses spontaneous migration, chemotaxis, and free radical production of human neutrophils. Surg Endosc 22:1813–1817
Nakamura Y (2010) Maternal and child health handbook in Japan. Jpn Med Assoc J 53:259–265
Wada M, Nakamura H, Koga H et al (2014) Experience of treating biliary atresia with three types of portoenterostomy at a single institution: extended, modified Kasai, and laparoscopic modified Kasai. Pediatr Surg Int 30:863–870
Kasai M (1974) Treatment of biliary atresia with special reference to hepatic portoenterostomy and its modification. Prog Pediatr Surg 6:5–52
Nakamura H, Koga H, Wada M et al (2012) Reappraising the portoenterostomy procedure according to sound physiologic/anatomic principles enhances postoperative jaundice clearance in biliary atresia. Pediatr Surg Int 28:205–209
Davenport M (2012) Biliary atresia: clinical aspects. Semin Pediatr Surg 21:175–184
Aspelund G, Ling SC, Ng V et al (2007) A role for laparoscopic approach in the treatment of biliary atresia and choledochal cysts. J Pediatr Surg 42:869–872
Esteves E, Clemente Neto E, Ottaiano Neto M et al (2002) Laparoscopic Kasai portoenterostomy for biliary atresia. Pediatr Surg Int 18:737–740
Lee H, Hirose S, Bratton B et al (2004) Initial experience with complex laparoscopic biliary surgery in children: biliary atresia and choledochal cyst. J Pediatr Surg 39:804–807
Martinez-Ferro M, Esteves E, Laje P (2005) Laparoscopic treatment of biliary atresia and choledochal cyst. Semin Pediatr Surg 14:206–215
Koga H, Miyano G, Takahashi T et al (2011) Laparoscopic portoenterostomy for uncorrectable biliary atresia using Kasai’s original technique. J Laparoendosc Adv Surg Tech A 21:291–294
Yamataka A, Lane GJ, Cazares J (2012) Laparoscopic surgery for biliary atresia and choledochal cyst. Semin Pediatr Surg 21:201–210
Chan KW, Lee KH, Mou JW et al (2011) The outcome of laparoscopic portoenterostomy for biliary atresia in children. Pediatr Surg Int 27:671–674
Chan KW, Lee KH, Wong HY et al (2014) From laparoscopic to open Kasai portoenterostomy: the outcome after reintroduction of open Kasai portoenterostomy in infant with biliary atresia. Pediatr Surg Int 30:605–608
Sefr R, Puszkailer K, Jagos F (2003) Randomized trial of different intraabdominal pressures and acid-base balance alterations during laparoscopic cholecystectomy. Surg Endosc 17:947–950
Koivusalo AM, Kellokumpu I, Ristkari S et al (1997) Splanchnic and renal deterioration during and after laparoscopic cholecystectomy: a comparison of the carbon dioxide pneumoperitoneum and the abdominal wall lift method. Anesth Analg 85:886–891
Galizia G, Prizio G, Lieto E et al (2001) Hemodynamic and pulmonary changes during open, carbon dioxide pneumoperitoneum and abdominal wall-lifting cholecystectomy. A prospective, randomized study. Surg Endosc 15:477–483
Ure BM, Suempelmann R, Metzelder MM et al (2007) Physiological responses to endoscopic surgery in children. Semin Pediatr Surg 16:217–223
Richter S, Olinger A, Hildebrandt U et al (2001) Loss of physiologic hepatic blood flow control (“hepatic arterial buffer response”) during CO2-pneumoperitoneum in the rat. Anesth Analg 93:872–877
Kirsch AJ, Hensle TW, Chang DT et al (1994) Renal effects of CO2 insufflation: oliguria and acute renal dysfunction in a rat pneumoperitoneum model. Urology 43:453–459
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Nakamura, H., Koga, H., Okazaki, T. et al. Does pneumoperitoneum adversely affect growth, development and liver function in biliary atresia patients after laparoscopic portoenterostomy?. Pediatr Surg Int 31, 45–51 (2015). https://doi.org/10.1007/s00383-014-3625-4
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00383-014-3625-4