Literature DB >> 31194685

The spectrum of pediatric adrenal insufficiency: insights from 34 years of experience.

Mara Ventura1,2, Joana Serra-Caetano3, Rita Cardoso3, Isabel Dinis3, Miguel Melo1,4, Francisco Carrilho1, Alice Mirante3.   

Abstract

Background Adrenal insufficiency (AI) is a life-threatening disease characterized by deficient production of glucocorticoids and/or mineralocorticoids. It is caused by primary or secondary/tertiary adrenal failure. Prompt diagnosis and management are essential and may even be life-saving. Methods We retrospectively collected clinical, laboratory and radiological data from AI patients observed over 34 years (1984-2017) in a pediatric endocrinology department of a tertiary care hospital. Results Seventy AI patients were identified: 59% with primary adrenal insufficiency (PAI) and 41% with central adrenal insufficiency (CAI). PAI patients were diagnosed at 1.5 ± 4.4 years and followed for 11.6 ± 6.2 years; 85% had classical congenital adrenal hyperplasia (CAH) and 7% had autoimmune PAI. At presentation, 73% had hyponatremia and more than half had mucocutaneous hyperpigmentation, asthenia, anorexia, weight loss, nausea and vomiting. All the patients were treated with hydrocortisone and 90% were also on fludrocortisone. Regarding CAI patients, they were diagnosed at 5.4 ± 5.0 years and they were followed for 9.6 ± 6.4 years; craniopharyngioma was present in 31% of the cases and 14% had pituitary hypoplasia. Besides corticotropin, thyrotropin (93%), growth hormone (63%) and antidiuretic hormone (52%) were the most common hormone insufficiencies. The most frequent manifestations were hypoglycemia (34.5%), nausea/vomiting (27.6%) and infectious diseases (27.6%); all the patients were treated with hydrocortisone. Conclusions Despite medical advances, the diagnosis and management of AI remains a challenge, particularly in the pediatric population. Raising awareness and knowledge in medical teams and population about the disease is of crucial importance to improve clinical outcomes and to reduce disease morbidity/mortality.

Entities:  

Keywords:  Addison’s disease; central adrenal insufficiency; pediatric adrenal insufficiency; primary adrenal insufficiency; secondary adrenal insufficiency

Mesh:

Substances:

Year:  2019        PMID: 31194685     DOI: 10.1515/jpem-2019-0030

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  4 in total

Review 1.  Adrenal insufficiency.

Authors:  Stefanie Hahner; Richard J Ross; Wiebke Arlt; Irina Bancos; Stephanie Burger-Stritt; David J Torpy; Eystein S Husebye; Marcus Quinkler
Journal:  Nat Rev Dis Primers       Date:  2021-03-11       Impact factor: 52.329

2.  Long-Term Follow-Up of Three Family Members with a Novel NNT Pathogenic Variant Causing Primary Adrenal Insufficiency.

Authors:  Tjasa Krasovec; Jaka Sikonja; Mojca Zerjav Tansek; Marusa Debeljak; Sasa Ilovar; Katarina Trebusak Podkrajsek; Sara Bertok; Tine Tesovnik; Jernej Kovac; Jasna Suput Omladic; Michaela F Hartmann; Stefan A Wudy; Magdalena Avbelj Stefanija; Tadej Battelino; Primoz Kotnik; Urh Groselj
Journal:  Genes (Basel)       Date:  2022-04-20       Impact factor: 4.141

Review 3.  Adrenal crises in adolescents and young adults.

Authors:  R Louise Rushworth; Georgina L Chrisp; Suzannah Bownes; David J Torpy; Henrik Falhammar
Journal:  Endocrine       Date:  2022-05-18       Impact factor: 3.925

4.  Trends in hospital admissions for adrenal insufficiency in adolescents and young adults in the 21st century.

Authors:  Georgina L Chrisp; Maria Quartararo; David J Torpy; Henrik Falhammar; R Louise Rushworth
Journal:  Front Endocrinol (Lausanne)       Date:  2022-09-20       Impact factor: 6.055

  4 in total

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