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Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature

Authors :
Andreas Ebbehoj
Eleonora P M Corssmit
Jan Calissendorff
Thera P. Links
Özer Makay
Maximilien Rappaport
Petr Vlĕek
Tushar Bandgar
Catharina Larsson
Elena N. Grineva
Luigi Petramala
Ravinder Kaur
Viacheslav I. Egorov
Hartmut P. H. Neumann
Heather Wachtel
Tobias Else
Francesca Boaretto
Xiao-Ping Qi
Henri J L M Timmers
Anna Roslyakova
M. Umit Ugurlu
Ronald M. Lechan
Anand Vaidya
Kornelia Hasse-Lazar
Claudio E. Kater
Esben Søndergaard
Zhi-xian Yu
Rene Eduardo Diaz
Mohammad Hassan Murad
Ruth T Casey
Debbie L. Cohen
Roman Petrov
Lucinda Gruber
C Christofer Juhlin
Claudio Letizia
Maria Adelaide Albergaria Pereira
Inna Stepanovna Kudlai
Bernadette Jenner
Sergiy Cherenko
Lauren Fishbein
William F. Young
Ya-Sheng Huang
Marina Y. Yukina
Scott A Akker
Andrey Y Kovalenko
Uma Kaimal Saikia
Minghao Li
Silvia Rizzati
Stefania Zovato
Xu-dong Fang
Nelson Wohllk
Charis Eng
Mariola Pęczkowska
Martin Fassnacht
Sanjeet Kumar Jaiswal
Oliver Gimm
Gianluca Donatini
Milan Jovanovic
Robin P.F Dullaart
Ilgin Yildirim Simsir
Helen Simpson
Maciej Robaczyk
Marcin Barczyński
Steven G. Waguespack
Katharina Langton
Martin K. Walz
Paul Skierczynski
Alfonso Massimiliano Ferrara
Dipti Sarma
Irina Bancos
Vishnu Garla
Birke Bausch
Maria João Bugalho
Merav Fraenkel
Joanne Ngeow Yuen Yie
Flavia A Costa-Barbosa
Giuseppe Opocher
Camilo Jimenez
Tada Kunavisarut
Larry J. Prokop
Lawrence S Kirschner
Longfei Liu
Feyza Erenler
Elisa Taschin
Valentina Morelli
Per Løgstrup Poulsen
Marcus Quinkler
Natalia Valeryevna Khudiakova
Åse Krogh Rasmussen
Volha Vasilkova
Nicola Tufton
Nikita V. Ivanov
William Drake
Maryna Bobryk
Eric Jonasch
Swati Ramteke-Jadhav
Aviva Cohn
Diane Donegan
Sarka Dvorakova
Elizabeth J. Atkinson
Dmitry Beltsevich
Emma Hodson
Uliana Tsoy
Nino Zavrashvili
Jochen Seufert
Zulfiya Shafigullina
Xin He
Utku E Soyaltin
Nicole M. Iñiguez-Ariza
Timo Deutschbein
Francesca Schiavi
Mark Sherlock
Stefan Zschiedrich
Jes Sloth Mathiesen
Bonita Bennett
Anna Riester
Nalini S. Shah
Giovanni Barbon
Julie A Miller
Source :
Bancos, I, Atkinson, E J, Eng, C, Young, W F, Neumann, H P H & International Pheochromocytoma and Pregnancy Study Group 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes & Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6, Lancet Diabetes & Endocrinology, 9, 1, pp. 13-21, Bancos, I, Atkinson, E, Eng, C, Young, W F, Neumann, H P H, International Pheochromocytoma and Pregnancy Study Group & Robaczyk, M G 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes and Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6, Lancet Diabetes & Endocrinology, 9, 13-21, Lancet Diabetes Endocrinol
Publication Year :
2021

Abstract

Contains fulltext : 245825.pdf (Publisher’s version ) (Closed access) BACKGROUND: Phaeochromocytoma or paraganglioma (collectively known as PPGL) in pregnant women can lead to severe complications and death due to associated catecholamine excess. We aimed to identify factors associated with maternal and fetal outcomes in women with PPGL during pregnancy. METHODS: We did a multicentre, retrospective study of patients with PPGL and pregnancy between Jan 1, 1980, and Dec 31, 2019, in the International Pheochromocytoma and Pregnancy Registry and a systematic review of studies published between Jan 1, 2005, and Dec 27, 2019 reporting on at least five cases. The inclusion criteria were pregnancy after 1980 and PPGL before or during pregnancy or within 12 months post partum. Eligible patients from the retrospective study and systematic review were included in the analysis. Outcomes of interest were maternal or fetal death and maternal severe cardiovascular complications of catecholamine excess. Potential variables associated with these outcomes were evaluated by logistic regression. FINDINGS: The systematic review identified seven studies (reporting on 63 pregnancies in 55 patients) that met the eligibility criteria and were of adequate quality. A further 197 pregnancies in 186 patients were identified in the International Pheochromocytoma and Pregnancy Registry. After excluding 11 pregnancies due to potential overlap, the final cohort included 249 pregnancies in 232 patients with PPGL. The diagnosis of PPGL was made before pregnancy in 37 (15%) pregnancies, during pregnancy in 134 (54%), and after delivery in 78 (31%). Of 144 patients evaluated for genetic predisposition for phaeochromocytoma, 95 (66%) were positive. Unrecognised PPGL during pregnancy (odds ratio 27·0; 95% CI 3·5-3473·1), abdominal or pelvic tumour location (11·3; 1·5-1440·5), and catecholamine excess at least ten-times the upper limit of the normal range (4·7; 1·8-13·8) were associated with adverse outcomes. For patients diagnosed during pregnancy, α-adrenergic blockade therapy was associated with fewer adverse outcomes (3·6; 1·1-13·2 for no α-adrenergic blockade vs α-adrenergic blockade), whereas surgery during pregnancy was not associated with better outcomes (0·9; 0·3-3·9 for no surgery vs surgery). INTERPRETATION: Unrecognised and untreated PPGL was associated with a substantially higher risk of either maternal or fetal complications. Appropriate case detection and counselling for premenopausal women at risk for PPGL could prevent adverse pregnancy-related outcomes. FUNDING: US National Institutes of Health.

Details

ISSN :
22138587
Volume :
9
Database :
OpenAIRE
Journal :
Lancet Diabetes & Endocrinology
Accession number :
edsair.doi.dedup.....b5323c7add8c398d2a79180450e78b9b
Full Text :
https://doi.org/10.1016/S2213-8587(20)30363-6