Imaging prediction with ultrasound and MRI of long-term medical outcome in native liver survivor patients with biliary atresia after kasai portoenterostomy: a pilot study.
Biliary atresia
Kasai portoenterostomy
Long-term medical outcome prediction
Magnetic resonance imaging
Ultrasound
Journal
Abdominal radiology (New York)
ISSN: 2366-0058
Titre abrégé: Abdom Radiol (NY)
Pays: United States
ID NLM: 101674571
Informations de publication
Date de publication:
06 2021
06 2021
Historique:
received:
16
11
2020
accepted:
15
01
2021
revised:
07
01
2021
pubmed:
4
2
2021
medline:
22
6
2021
entrez:
3
2
2021
Statut:
ppublish
Résumé
To comparatively assess the role of abdominal ultrasound (US) and magnetic resonance imaging (MRI) in predicting long-term medical outcome in native liver survivor patients with biliary atresia (BA) after Kasai portoenterostomy (KP). Twenty-four retrospectively enrolled patients were divided in two groups according to clinical and laboratory data at initial evaluation after KP (median follow-up = 9.7 years; range = 5-25 years) as with ideal (Group 1; n = 15) or non-ideal (Group 2; n = 9) medical outcome. All patients were re-evaluated for a period of additional 4 years using clinical and laboratory indices. US and MRI studies were qualitatively analyzed assessing imaging signs suggestive of chronic liver disease (CLD). At re-evaluation, 6 patients (40%) of Group 1 changed their medical outcome in non-ideal (Group 1A); the other 9 patients (60%) remained stable (Group 1B); the mean time to change the medical outcome in non-ideal status at re-evaluation was 43.5 ± 2.3 months. The area under the ROC curve was 0.84 and 0.87 for US and MRI scores to predict long-term medical outcome with the best cut-off value score > 4 for both modalities (p = 0.89). In Group 2, 6 (67%) patients showed a clinical progression (Group 2A) with a mean time of 39.8 ± 3.8 months; in the other 3 (33%) patients, no clinical progression was observed (Group 2B). In BA patients with ideal medical outcome after KP, US and MRI may both predict long-term outcome. US, non-invasive and widely available technique, should be preferred.
Identifiants
pubmed: 33532908
doi: 10.1007/s00261-021-02958-4
pii: 10.1007/s00261-021-02958-4
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2595-2603Références
Hartley JL, Davenport M, Kelly DA (2009) Biliary atresia. Lancet 374:1704–1713. https://doi.org/10.1016/S0140-6736(09)60946-6
doi: 10.1016/S0140-6736(09)60946-6
pubmed: 19914515
Neto B, Borges-Dias M, Trindade E, et al (2018) Biliary Atresia - Clinical Series. GE - Port J Gastroenterol 25:68–73. https://doi.org/10.1159/000480708
doi: 10.1159/000480708
pubmed: 29662930
Govindarajan KK (2016) Biliary atresia: Where do we stand now? World J Hepatol 8:1593. https://doi.org/10.4254/wjh.v8.i36.1593
doi: 10.4254/wjh.v8.i36.1593
pubmed: 28083081
pmcid: 5192550
Feldman AG, Mack CL (2015) Biliary Atresia: Clinical Lessons Learned. J Pediatr Gastroenterol Nutr 61:167–75. https://doi.org/10.1097/MPG.0000000000000755
doi: 10.1097/MPG.0000000000000755
pubmed: 25658057
Baumann U, Ure B (2012) Biliary atresia. Clin Res Hepatol Gastroenterol 36:257–9. https://doi.org/10.1016/j.clinre.2012.03.017
doi: 10.1016/j.clinre.2012.03.017
pubmed: 22609296
Nio M, Wada M, Sasaki H, et al (2012) Risk factors affecting late-presenting liver failure in adult patients with biliary atresia. J Pediatr Surg 47:2179–2183. https://doi.org/10.1016/j.jpedsurg.2012.09.003
doi: 10.1016/j.jpedsurg.2012.09.003
pubmed: 23217872
Lee WS, Ong SY, Foo HW, et al (2017) Chronic liver disease is universal in children with biliary atresia living with native liver. World J Gastroenterol 23:7776–7784. https://doi.org/10.3748/wjg.v23.i43.7776
doi: 10.3748/wjg.v23.i43.7776
pubmed: 29209118
pmcid: 5703937
[8] Hadzić N, Davenport M, Tizzard S, et al (2003) Long-term survival following Kasai portoenterostomy: is chronic liver disease inevitable? J Pediatr Gastroenterol Nutr 37:430–3
doi: 10.1097/00005176-200310000-00006
Park CJ, Armenia SJ, Keung CH, et al (2019) Surgical modifications of the Kasai hepatoportoenterostomy minimize invasiveness without compromising short- and medium-term outcomes. J Pediatr Surg 54:537–542. https://doi.org/10.1016/j.jpedsurg.2018.06.028
doi: 10.1016/j.jpedsurg.2018.06.028
pubmed: 30041859
Li Y, Xiang B, Wu Y, et al (2018) Medium-term Outcome of Laparoscopic Kasai Portoenterostomy for Biliary Atresia With 49 Cases. J Pediatr Gastroenterol Nutr 66:857–860. https://doi.org/10.1097/MPG.0000000000001934
doi: 10.1097/MPG.0000000000001934
pubmed: 29470293
Jeon TY, Yoo S-Y, Kim JH, et al (2013) Serial ultrasound findings associated with early liver transplantation after Kasai portoenterostomy in biliary atresia. Clin Radiol 68:588–594. https://doi.org/10.1016/j.crad.2012.12.004
doi: 10.1016/j.crad.2012.12.004
pubmed: 23351775
Jancelewicz T, Barmherzig R, Chung CT-S, et al (2015) A screening algorithm for the efficient exclusion of biliary atresia in infants with cholestatic jaundice. J Pediatr Surg 50:363–370. https://doi.org/10.1016/j.jpedsurg.2014.08.014
doi: 10.1016/j.jpedsurg.2014.08.014
pubmed: 25746690
Serai SD, Trout AT, Sirlin CB (2017) Elastography to assess the stage of liver fibrosis in children: Concepts, opportunities, and challenges. Clin Liver Dis 9:5–10. https://doi.org/10.1002/cld.607
doi: 10.1002/cld.607
[14] Takahashi A, Hatakeyama S, Suzuki N, et al (1997) MRI findings in the liver in biliary atresia patients after the Kasai operation. Tohoku J Exp Med 181:193–202
doi: 10.1620/tjem.181.193
Takahashi A, Hatakeyama SI, Kuroiwa M, et al (2009) Time-course changes in the liver of biliary atresia patients on magnetic resonance imaging. Pediatr Int 51:66–70. https://doi.org/10.1111/j.1442-200X.2008.02657.x
doi: 10.1111/j.1442-200X.2008.02657.x
pubmed: 19371280
Mo YH, Jaw FS, Ho MC, et al (2011) Hepatic ADC value correlates with cirrhotic severity of patients with biliary atresia. Eur J Radiol 80:e253–e257. https://doi.org/10.1016/j.ejrad.2010.11.002
doi: 10.1016/j.ejrad.2010.11.002
pubmed: 21123015
Peng SSF, Jeng YM, Hsu WM, et al (2015) Hepatic ADC map as an adjunct to conventional abdominal MRI to evaluate hepatic fibrotic and clinical cirrhotic severity in biliary atresia patients. Eur Radiol 25:2992–3002. https://doi.org/10.1007/s00330-015-3716-1
doi: 10.1007/s00330-015-3716-1
pubmed: 25921590
Caruso M, Cuocolo R, Di Dato F, et al (2020) Ultrasound, shear-wave elastography, and magnetic resonance imaging in native liver survivor patients with biliary atresia after Kasai portoenterostomy: correlation with medical outcome after treatment. Acta radiol. https://doi.org/10.1016/j.jpeds.2014.05.038
doi: 10.1177/0284185120902379
pubmed: 32008344
Ng VL, Haber BH, Magee JC, et al (2014) Medical Status of 219 Children with Biliary Atresia Surviving Long-Term with Their Native Livers: Results from a North American Multicenter Consortium. J Pediatr 165:539-546.e2. https://doi.org/10.1016/j.jpeds.2014.05.038
doi: 10.1016/j.jpeds.2014.05.038
pubmed: 25015575
pmcid: 4144331
Konuş OL, Ozdemir A, Akkaya A, et al (1998) Normal liver, spleen, and kidney dimensions in neonates, infants, and children: evaluation with sonography. Am J Roentgenol 171:1693–1698. https://doi.org/10.2214/ajr.171.6.9843315
doi: 10.2214/ajr.171.6.9843315
Avni FE, Segers V, De Maertelaer V, et al (2002) The evaluation by magnetic resonance imaging of hepatic periportal fibrosis in infants with neonatal cholestasis: Preliminary report. J Pediatr Surg 37:1128–1133. https://doi.org/10.1053/jpsu.2002.34457
doi: 10.1053/jpsu.2002.34457
pubmed: 12149687
Ohhama Y, Shinkai M, Fujita S, et al (2000) Early prediction of long-term survival and the timing of liver transplantation after the Kasai operation. J Pediatr Surg 35:1031–1034. https://doi.org/10.1053/jpsu.2000.7765
doi: 10.1053/jpsu.2000.7765
pubmed: 10917290
Chiang LW, Lee CY, Krishnaswamy G, et al (2017) Seventeen years of Kasai portoenterostomy for biliary atresia in a single Southeast Asian paediatric centre. J Paediatr Child Health 53:412–415. https://doi.org/10.1111/jpc.13379
doi: 10.1111/jpc.13379
pubmed: 27859955
Shneider BL, Magee JC, Karpen SJ, et al (2016) Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia. J Pediatr 170:211-217.e2. https://doi.org/10.1016/j.jpeds.2015.11.058
doi: 10.1016/j.jpeds.2015.11.058
pubmed: 26725209
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. https://doi.org/10.1016/j.jpedsurg.2013.08.009
doi: 10.1016/j.jpedsurg.2013.08.009
pubmed: 24314173
Sasaki H, Tanaka H, Wada M, et al (2016) Analysis of the prognostic factors of long-term native liver survival in survivors of biliary atresia. Pediatr Surg Int 32:839–843. https://doi.org/10.1007/s00383-016-3934-x
doi: 10.1007/s00383-016-3934-x
pubmed: 27464487
Hahn SM, Kim S, Park KI, et al (2013) Clinical benefit of liver stiffness measurement at 3 months after Kasai hepatoportoenterostomy to predict the liver related events in biliary atresia. PLoS One 8:1–6. https://doi.org/10.1371/journal.pone.0080652
doi: 10.1371/journal.pone.0080652
Wu J-F, Lee C-S, Lin W-H, et al (2018) Transient elastography is useful in diagnosing biliary atresia and predicting prognosis after hepatoportoenterostomy. Hepatology 68:616–624. https://doi.org/10.1002/hep.29856
doi: 10.1002/hep.29856
pubmed: 29486516
Nio M, Wada M, Sasaki H, et al (2018) Using 99m Tc-DTPA galactosyl human serum albumin liver scintigraphy as a prognostic indicator in jaundice-free patients with biliary atresia. J Pediatr Surg 53:2412–2415. https://doi.org/10.1016/j.jpedsurg.2018.08.032
doi: 10.1016/j.jpedsurg.2018.08.032
pubmed: 30262199