Abstract
Study Objective
To identify clinical features associated with primary ovarian insufficiency (POI)
and collect data on the evaluation and treatment received.
Design
Retrospective chart review. Data were abstracted on etiology of POI, history, laboratory
evaluation, imaging results, return for clinical care, and treatment plans.
Setting
Urban children's hospital in Cincinnati, Ohio.
Participants
Fifty female patients, age 11-26 years, with initial presentation of POI between January
1, 2006 and December 31, 2015.
Main Outcome Measures
Etiology of POI, bone mineral density (BMD), laboratory evaluation, and services utilized
at presentation.
Results
Three hundred thirty-one charts were reviewed, 71 with confirmed diagnosis of POI,
and 50 with sufficient data for inclusion. Among the 50, 21 (42%) had Turner syndrome,
18 (36%) remained idiopathic, and 11 (22%) had another condition (eg, autoimmune polyglandular
syndrome, galactosemia, etc). Thirty-six (72%) were karyotyped; in 14 (28%), 21-hydroxylase
antibodies were measured; 32 (64%) underwent dual-energy x-ray absorptiometry BMD
measures of lumbar spine. Eight of 50 patients (16%) reported fracture. Of these,
at presentation, 4 (50%) had low BMD, and 2 (25%) had slightly low BMD. On initial
spinal dual-energy x-ray absorptiometry, 9 of 32 (28%) had low BMD (Z-score ≤ −2.0)
and 7 of 32 (22%) were slightly low (−1.0 to −1.9). All started estrogen therapy within
2 years of presentation. In follow-up, only 2 patients (4%) saw a mental health consultant
for emotional support.
Conclusion
POI is a model of estrogen deficiency with most cases due to Turner syndrome or idiopathic
causes. At presentation, many had low BMD and few were seen for psychological support
as part of multidisciplinary care.
Key Words
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Article info
Publication history
Published online: August 03, 2017
Footnotes
The authors indicate no conflicts of interest.
Identification
Copyright
© 2017 North American Society for Pediatric and Adolescent Gynecology. Published by Elsevier Inc.