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Current Management and Outcome of Pregnancies in Women With Adrenal Insufficiency: Experience from a Multicenter Survey
Univ Spital Zurich, Switzerland.
Univ Spital Zurich, Switzerland.
Mayo Clin, MN 55905 USA.
Endocrinol Charlottenburg, Germany.
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2020 (English)In: Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, E-ISSN 1945-7197, Vol. 105, no 8, p. E2853-E2863Article in journal (Refereed) Published
Abstract [en]

Context

Appropriate management of adrenal insufficiency (AI) in pregnancy can be challenging due to the rarity of the disease and lack of evidence-based recommendations to guide glucocorticoid and mineralocorticoid dosage adjustment.

Objective

Multicenter survey on current clinical approaches in managing AI during pregnancy.

Design

Retrospective anonymized data collection from 19 international centers from 2013 to 2019.

Setting and Patients

128 pregnancies in 113 women with different causes of AI: Addison disease (44%), secondary AI (25%), congenital adrenal hyperplasia (25%), and acquired AI due to bilateral adrenalectomy (6%).

Results

Hydrocortisone (HC) was the most commonly used glucocorticoid in 83% (97/117) of pregnancies. Glucocorticoid dosage was increased at any time during pregnancy in 73/128 (57%) of cases. In these cases, the difference in the daily dose of HC equivalent between baseline and the third trimester was 8.6 ± 5.4 (range 1-30) mg. Fludrocortisone dosage was increased in fewer cases (7/54 during the first trimester, 9/64 during the second trimester, and 9/62 cases during the third trimester). Overall, an adrenal crisis was reported in 9/128 (7%) pregnancies. Cesarean section was the most frequent mode of delivery at 58% (69/118). Fetal complications were reported in 3/120 (3%) and minor maternal complications in 15/120 (13%) pregnancies without fatal outcomes.

Conclusions

This survey confirms good maternal and fetal outcome in women with AI managed in specialized endocrine centers. An emphasis on careful endocrine follow-up and repeated patient education is likely to have reduced the risk of adrenal crisis and resulted in positive outcomes.

Place, publisher, year, edition, pages
Oxford University Press, 2020. Vol. 105, no 8, p. E2853-E2863
Keywords [en]
Addison disease; congenital adrenal hyperplasia; pregnancy; mineralocorticoid; glucocorticoid; adrenal crisis; miscarriage
National Category
Obstetrics, Gynecology and Reproductive Medicine
Identifiers
URN: urn:nbn:se:liu:diva-170003DOI: 10.1210/clinem/dgaa266ISI: 000565927300017PubMedID: 32424397Scopus ID: 2-s2.0-85087320992OAI: oai:DiVA.org:liu-170003DiVA, id: diva2:1470927
Note

Funding Agencies|Deutsche Forschungsgemeinschaft (DFG)German Research Foundation (DFG) [CRC/Transregio 205/1]; James A. Ruppe Career Development Award in Endocrinology; Catalyst Award for Advancing in Academics from Mayo Clinic; National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health (NIH) USA [K23DK121888]

Available from: 2020-09-26 Created: 2020-09-26 Last updated: 2020-10-09Bibliographically approved

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Wahlberg, Jeanette
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Division of Diagnostics and Specialist MedicineFaculty of Medicine and Health SciencesDepartment of Endocrinology
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