Literature DB >> 32060243

Management of Infants with Congenital Adrenal Hyperplasia.

Aashima Dabas1, Pallavi Vats1, Rajni Sharma2, Preeti Singh3, Anju Seth3, Vandana Jain2, Prerna Batra4, Neerja Gupta2, Ravindra Kumar5, Madhulika Kabra2, Seema Kapoor1, Sangeeta Yadav6.   

Abstract

Treatment of congenital adrenal hyperplasia (CAH) requires lifelong replacement of glucocorticoids with regular follow up to manage associated morbidities. The current review focuses on follow-up and management of infants diagnosed with classical CAH pertinent to Indian context. Early initiation of oral hydrocortisone in divided doses is recommended after diagnosis in newborn period, infancy and childhood. Fludrocortisone is recommended for all infants with classical CAH. All infants should be monitored as per protocol for disease and treatment related complications. The role of prenatal steroids to pregnant women with previous history of CAH affected infant for prevention of virilization of female fetus is controversial.

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Year:  2020        PMID: 32060243

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  1 in total

1.  Exploring Dried Blood Spot Cortisol Concentrations as an Alternative for Monitoring Pediatric Adrenal Insufficiency Patients: A Model-Based Analysis.

Authors:  Viktoria Stachanow; Uta Neumann; Oliver Blankenstein; Davide Bindellini; Johanna Melin; Richard Ross; Martin J Whitaker; Wilhelm Huisinga; Robin Michelet; Charlotte Kloft
Journal:  Front Pharmacol       Date:  2022-03-17       Impact factor: 5.810

  1 in total

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