Hypopituitarism and pregnancy: clinical characteristics, management and pregnancy outcome


Por: Aulinas, A, Stantonyonge, N, Garcia-Patterson, A, Adelantado, JM, Medina, C, Espinos, JJ, Lopez, E, Webb, SM, Corcoy, R

Publicada: 1 abr 2022 Ahead of Print: 1 nov 2021
Resumen:
Purpose To describe the clinical characteristics, management and pregnancy outcome of women with prepregnancy hypopituitarism (HYPO) that received care at our center. Methods Retrospective study describing 12 pregnancies in women with prepregnancy HYPO (two or more pituitary hormonal deficiencies under replacement treatment) that received care during pregnancy at Hospital Santa Creu i Sant Pau. Clinical characteristics, management and pregnancy outcome were systematically collected. Results Average patients' age was 35 years and HYPO duration at the beginning of pregnancy was 19 years. The most frequent cause of HYPO was surgical treatment of a sellar mass (8 pregnancies). Eight pregnancies were in primigravid women and 10 required assisted reproductive techniques. The hormonal deficits before pregnancy were as follows: GH in 12 women, TSH in 10, gonadotropin in 9, ACTH in 5 and ADH in 2. All deficits were under hormonal substitution except for GH deficit in 4 pregnancies. During pregnancy, 4 new deficits were diagnosed. The dosage of replacement treatment for TSH, ACTH and ADH deficits was increased and GH was stopped. Average gestational age at birth was 40 weeks, gestational weight gain was excessive in 9 women, 8 patients required induction/elective delivery and cesarean section was performed in 6. Average birthweight was 3227 g. No major complications were observed. Five women were breastfeeding at discharge. Conclusions In this group of women with long-standing HYPO, with careful clinical management (including treatment of new-onset hormonal deficits) pregnancy outcome was satisfactory but with a high rate of excessive gestational weight gain and cesarean section.

Filiaciones:
Aulinas, A:
 ISCIII, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Unidad 747, Barcelona, Spain

 Univ Vic, Dept Med, Cent Univ Catalonia, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Inst Recerca, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Dept Endocrinol & Nutr, Barcelona, Spain

Stantonyonge, N:
 Hosp Santa Creu & Sant Pau, Dept Endocrinol & Nutr, Barcelona, Spain

 Univ Autonoma Barcelona, Dept Med, Barcelona, Spain

Garcia-Patterson, A:
 Hosp Santa Creu & Sant Pau, Inst Recerca, Barcelona, Spain

Adelantado, JM:
 Hosp Santa Creu & Sant Pau, Dept Gynecol & Obstet, Barcelona, Spain

Medina, C:
 Hosp Santa Creu & Sant Pau, Dept Gynecol & Obstet, Barcelona, Spain

Espinos, JJ:
 Hosp Santa Creu & Sant Pau, Dept Gynecol & Obstet, Barcelona, Spain

Lopez, E:
 Hosp Santa Creu & Sant Pau, Dept Pediat, Barcelona, Spain

Webb, SM:
 ISCIII, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Unidad 747, Barcelona, Spain

 Univ Autonoma Barcelona, Dept Med, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Inst Recerca, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Dept Endocrinol & Nutr, Barcelona, Spain

Corcoy, R:
 ISCIII, Ctr Invest Biomed Red Bioingn Biomat & Nanomed CI, Madrid, Spain

 Hosp Santa Creu & Sant Pau, Dept Endocrinol & Nutr, Barcelona, Spain

 Univ Autonoma Barcelona, Dept Med, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Inst Recerca, Barcelona, Spain
ISSN: 1386341X





Pituitary
Editorial
SPRINGER, ONE NEW YORK PLAZA, SUITE 4600, NEW YORK, NY, UNITED STATES, Estados Unidos America
Tipo de documento: Article
Volumen: 25 Número: 2
Páginas: 275-284
WOS Id: 000723997300001
ID de PubMed: 34846622
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