Laboratorial evolution of multifactorial cholestasis in pediatric patients

Authors

DOI:

https://doi.org/10.11606/issn.1679-9836.v98i5p309-314

Keywords:

Cholestasis, Jaundice, neonatal, Infant, newborn

Abstract

Introduction: In the immature liver of the newborn (RN) neonatal cholestasis can occurs in association with several risk factors, with no underlying pathology. This condition is called transient multifactorial neonatal cholestasis. Prematurity, intrauterine growth restriction or situations that lead to increased oxidative stress (ischemia, hemodynamic compromise, infections, surgical interventions, food pause, intravenous nutrition and drugs) are related to its genesis. Objective: to assess the evolution of neonatal cholestasis in the multifactorial period, as well as to verify the mean changes in liver enzymes such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), and canalicular, gammaglutamyltransferase (GGT) and direct bilirubin (BD), comparing the duration of cholestasis in patients who used ursodeoxycholic acid with the time of evolution of those who did not, in order to better characterize this clinical condition and to draw the attention of the health professional about its transient nature, thus avoiding the request for more specific, expensive, and unnecessary exams. Methods: A cross-sectional study with 32 patients from zero to 90 days who presented with neonatal multifactorial cholestasis, accompanied in the ambulatory of pediatric hepatology of IMIP, from August 2016 to August 2017. Data were collected through medical records. The analysis of the data was performed using software “R” v.3.3.1. Results: The majority of the patients were male (59.38%). The mean age of onset of cholestasis was 35.5 days, and the mean age of onset was 171 days. The mean duration of cholestasis was 135.8 days. The mean BD value of the onset and end of cholestasis was 6.05 and 0.29 mg/dL, respectively. In relation to liver and canalicular enzymes, the mean values of AST, ALT and GGT at baseline were 194.7, 123.8 and 387.9 U/L, and the mean values of 69.1, 56.0 and 121.6U/L, respectively. Only 11 patients used ursodeoxycholic acid (UDCA). The mean duration of cholestasis in this group was 114.1 days. Those who did not use the UDCA, 21 patients, presented cholestatic jaundice for a mean time of 147.1 days. Conclusion: In view of the results obtained with the retrospective analysis of patients with a diagnosis of multifactorial cholestasis, the transient and benign nature of this clinical condition is noted, with a mean duration of cholestasis around 136 days of life and with an important decrease in liver enzyme levels after resolution of the condition

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Author Biographies

  • Lígia Patrícia de Carvalho Batista Éboli, Instituto de Medicina Integral Prof. Fernando Figueira (IMIP)/Faculdade Pernambucana de Saúde (FPS)

    Hepatologista pediatra no Instituto de Medicina Integral Prof. Fernando Figueira (IMIP) e da Unidade de Transplante de Fígado do Hospital Universitário Oswaldo Cruz. Gastroenterologista e hepatologista pediatra da clínica Real Hepato do Real Hospital Português e Tutora do curso de medicina da Faculdade Pernambucana de Saúde (FPS), Recife, PE.

  • Marianne Fernanda de Melo Duarte, Faculdade Pernambucana de Saúde (FPS)

    Acadêmica de Medicina da Faculdade Pernambucana de Saúde (FPS), Recife, PE.

  • Luciana Maria Marques de Albuquerque, Faculdade Pernambucana de Saúde (FPS)

    Acadêmica de Medicina da Faculdade Pernambucana de Saúde (FPS), Recife, PE.

  • Thaysa Amaral França, Faculdade Pernambucana de Saúde (FPS)

    Acadêmica de Medicina da Faculdade Pernambucana de Saúde (FPS), Recife, PE.

  • Raquel Nogueira Cordeiro, Faculdade Pernambucana de Saúde (FPS)

    Acadêmica de Medicina da Faculdade Pernambucana de Saúde (FPS), Recife, PE.

  • Diego Laurentino Lima, Hospital dos Servidores do Estado de Pernambuco (HSE)

    Cirurgião Geral. Pesquisador. Professor da disciplina de Prática Hospitalar da Universidade Católica de Pernambuco. Mestrando de Ciências da Saúde da Universidade de Pernambuco, Recife, Brasil.

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Published

2019-10-15

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Section

Artigos/Articles

How to Cite

Éboli, L. P. de C. B., Duarte, M. F. de M., Albuquerque, L. M. M. de, França, T. A., Cordeiro, R. N., & Lima, D. L. (2019). Laboratorial evolution of multifactorial cholestasis in pediatric patients. Revista De Medicina, 98(5), 309-314. https://doi.org/10.11606/issn.1679-9836.v98i5p309-314