Skip to main content
Log in

Prognostic values of serum bilirubin at 7th day post-Kasai for survival with native livers in patients with biliary atresia

  • Original Article
  • Published:
Pediatric Surgery International Aims and scope Submit manuscript

Abstract

Background

Biliary atresia (BA) is a serious liver disease with uncertain prognosis. The objective of this study was to investigate prognostic values of the >20 % decrease in serum total bilirubin (TB) at 7th day post-op regarding early outcome and 5-year survival with native liver in BA.

Methods

Biliary atresia patients undergoing Kasai operation between 2000 and 2014 were reviewed. The ratio of serum TB at 7th day post-op to pre-op TB levels (TB7/TB0) was calculated for every patient. TB7/TB0 ratio of <0.8 indicated the >20 % decrease in serum TB. At 6th month following Kasai operation, outcome of BA patients were categorized into good outcome (TB < 2 mg % or clinically jaundice free) and poor outcome (TB > 2 mg % or clinically jaundice). For outcome analysis, logistic regression was used. For survival analysis, Cox regression was applied.

Results

There were 133 BA patients (M:F = 68:65) undergoing Kasai operation. Median age at surgery was 79 days. BA patients with TB7/TB0 ratio of <0.8 were found in 38 %. Outcome at 6-month post-op could be evaluated in 126 patients (good: poor = 68:58). The 1-, 3- and 5-year survival rates with native livers were 85, 70 and 65 %, respectively. The median overall survival with native livers was 164 months. Median follow-up time was 87 months. Logistic regression showed that gender and age at operation were not significant factors impacting on early outcome (p > 0.05). However, TB7/TB0 ratio of <0.8 was an independent factor for good outcome (Odds ratio = 3.0, p = 0.006). Cox regression analysis demonstrated that 5-year survival rate was significantly correlated with TB7/TB0 ratio of <0.8 (HR = 0.46, 95 % CI 0.23–0.91, p = 0.025) and outcome at 6th month post-op (HR = 0.05, 95 % CI 0.01–0.15, p < 0.001).

Conclusions

The >20 % decrease in serum TB at 7th day post-Kasai is a predictor for good outcome. BA patients with TB7/TB0 of <0.8 had 5-year survival with native livers significantly higher than those with the ratio of >0.8.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Kasai M (1983) Advances in treatment of biliary atresia. Jpn J Surg 13:265–276

    Article  CAS  PubMed  Google Scholar 

  2. Kelly DA, Davenport M (2007) Current management of biliary atresia. Arch Dis Child 92:1132–1135

    Article  PubMed  PubMed Central  Google Scholar 

  3. Schreiber RA, Barker CC, Roberts EA et al (2007) Biliary atresia: the Canadian experience. J Pediatr 151:659–665

    Article  PubMed  Google Scholar 

  4. Sookpotarom P, Vejchapipat P, Chittmittrapap S et al (2006) Short-term results of Kasai operation for biliary atresia: experience from one institution. Asian J Surg 29:188–192

    Article  PubMed  Google Scholar 

  5. Nio M, Wada M, Sasaki H, Tanaka H (2015) Effects of age at Kasai portoenterostomy on the surgical outcome: a review of the literature. Surg Today 45:813–818

    Article  PubMed  Google Scholar 

  6. Nio M, Sasaki H, Wada M, Kazama T, Nishi K, Tanaka H (2010) Impact of age at Kasai operation on short- and long-term outcomes of type III biliary atresia at a single institution. J Pediatr Surg 45:2361–2363

    Article  PubMed  Google Scholar 

  7. Rodeck B, Becker AC, Gratz KF, Petersen C (2007) Early predictors of success of Kasai operation in children with biliary atresia. Eur J Pediatr Surg 17:308–312

    Article  CAS  PubMed  Google Scholar 

  8. Goda T, Kawahara H, Kubota A et al (2013) The most reliable early predictors of outcome in patients with biliary atresia after Kasai’s operation. J Pediatr Surg 48:2373–2377

    Article  PubMed  Google Scholar 

  9. Koga H, Wada M, Nakamura H et al (2013) Factors influencing jaundice-free survival with the native liver in post-portoenterostomy biliary atresia patients: results from a single institution. J Pediatr Surg 48:2368–2372

    Article  PubMed  Google Scholar 

  10. Chung PH, Wong KK, Tam PK (2015) Predictors for failure after Kasai operation. J Pediatr Surg 50:293–296

    Article  PubMed  Google Scholar 

  11. Suominen JS, Lampela H, Heikkila P, Lohi J, Jalanko H, Pakarinen MP (2015) APRi predicts native liver survival by reflecting portal fibrogenesis and hepatic neovascularization at the time of portoenterostomy in biliary atresia. J Pediatr Surg 50:1528–1531

    Article  PubMed  Google Scholar 

  12. Vejchapipat P, Passakonnirin R, Sookpotarom P, Chittmittrapap S, Poovorawan Y (2007) High-dose steroids do not improve early outcome in biliary atresia. J Pediatr Surg 42:2102–2105

    Article  PubMed  Google Scholar 

  13. Laurent J, Gauthier F, Bernard O et al (1990) Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years. Gastroenterology 99:1793–1797

    CAS  PubMed  Google Scholar 

  14. Otte JB, de Ville de Goyet J, R Reding et al (1994) Sequential treatment of biliary atresia with Kasai portoenterostomy and liver transplantation: a review. Hepatology 20:41S–48S

    CAS  PubMed  Google Scholar 

  15. Kasai M, Mochizuki I, Ohkohchi N, Chiba T, Ohi R (1989) Surgical limitation for biliary atresia: indication for liver transplantation. J Pediatr Surg 24:851–854

    Article  CAS  PubMed  Google Scholar 

  16. Chardot C, Carton M, Spire-Bendelac N et al (2001) Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia? J Pediatr 138:224–228

    Article  CAS  PubMed  Google Scholar 

  17. Chardot C, Carton M, Spire-Bendelac N, Le Pommelet C, Golmard JL, Auvert B (1999) Prognosis of biliary atresia in the era of liver transplantation: French national study from 1986 to 1996. Hepatology 30:606–611

    Article  CAS  PubMed  Google Scholar 

  18. Serinet MO, Wildhaber BE, Broue P et al (2009) Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Pediatrics 123:1280–1286

    Article  PubMed  Google Scholar 

  19. Superina R, Magee JC, Brandt ML et al (2011) The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg 254:577–585

    Article  PubMed  PubMed Central  Google Scholar 

  20. Shneider BL, Brown MB, Haber B et al (2006) A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. J Pediatr 148:467–474

    Article  PubMed  Google Scholar 

  21. Baruah RR, Bhatnagar V, Agarwala S, Gupta SD (2015) Correlation of pre- and post-operative liver function, duct diameter at porta hepatis, and portal fibrosis with surgical outcomes in biliary atresia. J Indian Assoc Pediatr Surg 20:184–188

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Paisarn Vejchapipat.

Ethics declarations

Conflict of interest

The authors declare that the authors have no conflict of interest.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chusilp, S., Sookpotarom, P., Tepmalai, K. et al. Prognostic values of serum bilirubin at 7th day post-Kasai for survival with native livers in patients with biliary atresia. Pediatr Surg Int 32, 927–931 (2016). https://doi.org/10.1007/s00383-016-3951-9

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00383-016-3951-9

Keywords

Navigation