» Articles » PMID: 31501792

Preoperative Alkaline Phosphatase is a Potential Predictor of Short-term Outcome of Surgery in Infants with Biliary Atresia

Overview
Specialty Gastroenterology
Date 2019 Sep 11
PMID 31501792
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Aim Of The Study: Biliary atresia (BA) is a fibro-inflammatory cholangiopathy of intra- and extrahepatic biliary radicles. The standard-of-care treatment is surgical restoration of bile flow by Kasai hepatoportoenterostomy (HPE). We aimed to identify the predictors of short-term outcome of the Kasai operation three months postoperatively.

Material And Methods: This retrospective study included 107 infants diagnosed with BA by intraoperative cholangiography. All underwent a Kasai operation. The surgical outcome was classified after 3 months post-operatively as successful (bilirubin ≤ 2 mg/dl) or failed (bilirubin > 2 mg/dl). The two groups were compared according to basic clinical, ultrasonographic and histopathological characteristics.

Results: Of the studied patients 29 (27.1%) had a successful outcome while 78 (72.9%) had failed Kasai HPE. Of the preoperative characteristics, lower age and lower serum alkaline phosphatase (ALP) were significantly associated with successful surgical outcome ( = 0.009 and < 0.0001, respectively). In addition, surgical type of BA affected the short-term outcome ( = 0.017), while there was no statistically significant difference regarding the other studied parameters between groups. Age of 69.5 days or less was predictive of successful outcome with 74.4% specificity but with low sensitivity (58.6%), and ALP at a cutoff level of 532.5 U/l or less was predictive of successful outcome with 75.9% sensitivity and 74.4% specificity.

Conclusions: Younger age at the time of surgery and lower ALP are good predictors for the short-term outcome of Kasai HPE with better performance of ALP. This may help to anticipate those who can benefit from surgical correction and those who should be given high priority for transplant referral.

Citing Articles

Combined Predictors of Long-Term Outcomes of Kasai Surgery in Infants with Biliary Atresia.

Degtyareva A, Isaeva M, Tumanova E, Filippova E, Sugak A, Razumovsky A Pediatr Gastroenterol Hepatol Nutr. 2024; 27(4):224-235.

PMID: 39035404 PMC: 11254651. DOI: 10.5223/pghn.2024.27.4.224.


Short- and long-term outcomes after Kasai operation for type III biliary atresia: Twenty years of experience in a single tertiary Egyptian center-A retrospective cohort study.

Gad E, Kamel Y, Salem T, Ali M, Sallam A Ann Med Surg (Lond). 2021; 62:302-314.

PMID: 33552489 PMC: 7847812. DOI: 10.1016/j.amsu.2021.01.052.


Predictors of Short-Term Outcome of Kasai Portoenterostomy for Biliary Atresia in Infants: a Single-Center Study.

Yassin N, El-Tagy G, Abdelhakeem O, Asem N, El-Karaksy H Pediatr Gastroenterol Hepatol Nutr. 2020; 23(3):266-275.

PMID: 32483548 PMC: 7231743. DOI: 10.5223/pghn.2020.23.3.266.

References
1.
Schoen B, Lee H, Sullivan K, Ricketts R . The Kasai portoenterostomy: when is it too late?. J Pediatr Surg. 2001; 36(1):97-9. DOI: 10.1053/jpsu.2001.20020. View

2.
Wiwanitkit V . High serum alkaline phosphatase levels, a study in 181 Thai adult hospitalized patients. BMC Fam Pract. 2001; 2:2. PMC: 55333. DOI: 10.1186/1471-2296-2-2. View

3.
Sangkhathat S, Patrapinyokul S, Tadtayathikom K, Osatakul S . Peri-operative factors predicting the outcome of hepatic porto-enterostomy in infants with biliary atresia. J Med Assoc Thai. 2003; 86(3):224-31. View

4.
Wildhaber B, Coran A, Drongowski R, Hirschl R, Geiger J, Lelli J . The Kasai portoenterostomy for biliary atresia: A review of a 27-year experience with 81 patients. J Pediatr Surg. 2003; 38(10):1480-5. DOI: 10.1016/s0022-3468(03)00499-8. View

5.
Giannini E, Testa R, Savarino V . Liver enzyme alteration: a guide for clinicians. CMAJ. 2005; 172(3):367-79. PMC: 545762. DOI: 10.1503/cmaj.1040752. View