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Referral Patterns and Factors Influencing Age at Admission of Infants with Cholestasis in India

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Abstract

Objectives

To define the recognition, age at admission, referral time and referral pattern of neonatal cholestasis in India.

Methods

This prospective, observational study was conducted from February 2015 through March 2016 in the Pediatric gastroenterology unit of JIPMER, Pondicherry in infants with cholestasis < 6 mo of age.

Results

Among 64 infants, median age of admission was 52 d (IQR 28–63 d). Fifty of sixty four infants (78.1%) came with parent-reported cholestasis-related symptoms of either jaundice alone (57.8%) or bleeding manifestations (20.3%). In 21.9% infants, jaundice was detected by physicians at a median age of 45 d (IQR 38.5–53.2 d). Two infants had intracranial bleed. Only 34% infants with pale stools were identified by the mother. The median healthcare-seeking time was 5.5 d (IQR 2.5–12 d). Among infants presenting to primary healthcare physicians (PHPs) with cholestasis-related symptoms, median time to referral was 5 d (IQR 2.5–12 d). The first point of healthcare contact in 54.7% was a PHP; 17.1% PHPs had reassured the parents. Herbal preparations were prescribed by 14.3%. Only 11.8% of those with jaundice as the only problem were given vitamin K before referral. Biliary atresia (BA) was missed in neonatal intensive care units in 9 cases.

Conclusions

The above issues need to be accounted for before evaluating or implementing screening strategies in India.

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References

  1. Howard ER, Mowat AP. Extrahepatic biliary atresia. Recent developments in management. Arch Dis Child. 1977;52:825–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Mieli-Vergani G, Portman B, Howard ER, Mowat AP. Late referral for biliary atresia--missed opportunities for effective surgery. Lancet. 1989;333:421–3.

    Article  Google Scholar 

  3. Karmarkar SJ, Oak SN, Ramadwar RH, Deshmukh SS. Biliary atresia: need for an “Indian effort”. Indian Pediatr. 1992;29:791–2.

  4. Matsui A, Ishikawa T. Identification of infants with biliary atresia in Japan. Lancet. 1994;343:925.

    Article  CAS  PubMed  Google Scholar 

  5. Mowat AP, Davidson LL, Dick MC. Earlier identification of biliary atresia and hepatobiliary disease: selective screening in the third week of life. Arch Dis Child. 1995;72:90–2.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Yachha SK, Khanduri A, Kumar M, et al. Neonatal cholestasis syndrome: an appraisal at a tertiary center. Indian Pediatr. 1996;33:729–34.

    CAS  PubMed  Google Scholar 

  7. Yachha SK, Mohindra S. Neonatal cholestasis syndrome: Indian scene. Indian J Pediatr. 1999;66:S94–6.

    CAS  PubMed  Google Scholar 

  8. Matthai J, Paul S. Evaluation of cholestatic jaundice in infants. Indian Pediatr. 2001;38:893–8.

    CAS  PubMed  Google Scholar 

  9. Yachha SK, Sharma A. Neonatal cholestasis in India. Indian Pediatr. 2005;42:491–2.

    CAS  PubMed  Google Scholar 

  10. Chen SM, Chang MH, Du JC, et al; Taiwan Infant Stool Color Card Study Group. Screening for biliary atresia by infant stool color card in Taiwan. Pediatrics. 2006;117:1147–54.

  11. Lee WS. Pre-admission consultation and late referral in infants with neonatal cholestasis. J Paediatr Child Health. 2008;44:57–61.

    PubMed  Google Scholar 

  12. Akiyama T, Yamauchi Y. Use of near infrared reflectance spectroscopy in the screening for biliary atresia. J Pediatr Surg. 1994;29:645–7.

    Article  CAS  PubMed  Google Scholar 

  13. Matsui A, Kasano Y, Yamauchi Y, et al. Direct enzymatic assay of urinary sulfated bile acids to replace serum bilirubin testing for selective screening of neonatal cholestasis. J Pediatr. 1996;129:306–8.

    Article  CAS  PubMed  Google Scholar 

  14. Mushtaq I, Logan S, Morris M, et al. Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry. BMJ. 1999;319:471–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Matsui A, Dodoriki M. Screening for biliary atresia. Lancet. 1995;345:1181–2.

    Article  CAS  PubMed  Google Scholar 

  16. Lien T-H, Chang M-H, Wu J-F, et al; Taiwan Infant Stool Color Card Study Group. Effects of the infant stool color card screening program on 5-year outcome of biliary atresia in Taiwan. Hepatology. 2011;53:202–8.

  17. Wang KS. Newborn screening for biliary atresia. Pediatrics. 2015;136:1663–9.

    Article  Google Scholar 

  18. Gu YH, Yokoyama K, Mizuta K, et al. Stool color card screening for early detection of biliary atresia and long-term native liver survival: a 19-year cohort study in Japan. J Pediatr. 2015;166:897–902.e1.

    Article  PubMed  Google Scholar 

  19. Lee M, Chen SC, Yang HY, Huang JH, Yeung CY, Lee HC. Infant stool color card screening helps reduce the hospitalization rate and mortality of biliary atresia: a 14-year nationwide cohort study in Taiwan. Medicine (Baltimore). 2016;95:e3166.

    Article  Google Scholar 

  20. Zhou K, Lin N, Xiao Y, et al. Elevated bile acids in newborns with biliary atresia (BA). PLoS One. 2012;7:e49270.

  21. Schreiber RA, Barker CC, Roberts EA, et al; Canadian Pediatric Hepatology Research Group. Biliary atresia: the Canadian experience. J Pediatr. 2007;151:659–65,665.e1.

    Article  PubMed  Google Scholar 

  22. Serinet MO, Wildhaber BE, Broué P, et al. Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Pediatrics. 2009;123:1280–6.

    Article  PubMed  Google Scholar 

  23. Martin LR, Davenport M, Dhawan A. Skin colour: a barrier to early referral of infants with biliary atresia in the UK. Arch Dis Child. 2012;97:1102–3.

    Article  PubMed  Google Scholar 

  24. Witt M, Lindeboom J, Wijnja C, et al. Early detection of neonatal cholestasis: inadequate assessment of stool color by parents and primary healthcare doctors. Eur J Pediatr Surg. 2016;26:67–73.

    PubMed  Google Scholar 

  25. Children’s Liver Disease Foundation - Family Services. August 2016. Available at: http://www.childliverdisease.org/What-we-do/Family-Services. Accessed on 23rd August 2016.

  26. Akiyama H, Okamura Y, Nagashima T, Yokoi A, Muraji T, Uetani Y. Intracranial hemorrhage and vitamin K deficiency associated with biliary atresia: summary of 15 cases and review of the literature. Pediatr Neurosurg. 2006;42:362–7.

    Article  PubMed  Google Scholar 

  27. Alatas FS, Hayashida M, Matsuura T, Saeki I, Yanagi Y, Taguchi T. Intracranial hemorrhage associated with vitamin K-deficiency bleeding in patients with biliary atresia: focus on long-term outcomes. J Pediatr Gastroenterol Nutr. 2012;54:552–7.

    Article  CAS  PubMed  Google Scholar 

  28. Fawaz R, Baumann U, Ekong U, et al. Guideline for the evaluation of cholestatic jaundice in infants: joint recommendations of the north American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition. J Pediatr Gastroenterol Nutr. 2017;64:154–68.

  29. Moyer V, Freese DK, Whitington PF, et al; North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Guideline for the evaluation of cholestatic jaundice in infants: recommendations of the north American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr. 2004;39:115–28.

  30. Bakshi B, Sutcliffe A, Akindolie M, et al. How reliably can paediatric professionals identify pale stool from cholestatic newborns? Arch Dis Child Fetal Neonatal Ed. 2012;97:385–7.

    Article  Google Scholar 

  31. Bhatia V, Bavdekar A, Matthai J, et al. Management of neonatal cholestasis: consensus statement of the pediatric gastroenterology chapter of Indian Academy of Pediatrics. Indian Pediatr. 2014;51:203–10.

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Contributions

GM: Collected the data; BJ: Conceptualized and designed the study, analysed the data and prepared the manuscript. All authors contributed to the manuscript and approved the final manuscript. BJ will act as guarantor for the paper.

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Correspondence to Barath Jagadisan.

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Ethical Clearance

The study had been approved by the institute ethic committee that complies with International standards and is registered with the Government of India (JIP/IEC/2014/8/418).

Conflict of Interest

None.

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None.

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Mathiyazhagan, G., Jagadisan, B. Referral Patterns and Factors Influencing Age at Admission of Infants with Cholestasis in India. Indian J Pediatr 84, 591–596 (2017). https://doi.org/10.1007/s12098-017-2342-0

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  • DOI: https://doi.org/10.1007/s12098-017-2342-0

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