Risk of anti-TNF therapy on pregnancy, breastfeeding, live vaccines and related information in patients with inflammatory bowel disease: Real-world data from a nationwide study.

Anti-TNF therapy Breastfeeding Inflammatory bowel disease Live vaccines Pregnancy

Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
ISSN: 1878-3562
Titre abrégé: Dig Liver Dis
Pays: Netherlands
ID NLM: 100958385

Informations de publication

Date de publication:
08 Jul 2024
Historique:
received: 05 03 2024
revised: 06 06 2024
accepted: 12 06 2024
medline: 10 7 2024
pubmed: 10 7 2024
entrez: 9 7 2024
Statut: aheadofprint

Résumé

Anti-TNF are usually maintained during pregnancy in patients with inflammatory bowel disease (IBD) but safety is still a concern for them. To provide data on management of anti-TNF agents during pregnancy, safety of live vaccines (BCG-MMR-rotavirus) and breastfeeding in newborns and dedicated information delivered to IBD women. We performed an observational study in 25 centers from 2016 to 2018. We administered questionnaires to women with IBD receiving anti-TNF during pregnancy with newborn follow-up ≥ one year. Of 153 patients, 52 % maintained anti-TNF during the third trimester. Anti-TNF was shortly resumed in 79 % (58/73) after delivery. The rate of breastfeeding was 44 % (68/153) without any complication; 38 % of the mothers denied to breastfeed based on physician's advice. 26 % (34/129) of the newborns received live vaccines before 6 months-old (BCG:30 %; MMR:63 %; Rotavirus:8 %) and only 3 complications occurred (local BCGitis=1, fever=2). Information concerning anti-TNF during pregnancy/post-partum was delivered to 92 % of the patients, mainly by a gastroenterologist (97 %) who discussed with the obstetrician or the paediatrician in only 48 % and 25 %. In IBD patients, maintaining anti-TNF during pregnancy and breastfeeding is safe. Accidental live vaccines before 6 months did not lead to significant adverse events. The communication about these questions remains to improve.

Sections du résumé

BACKGROUND BACKGROUND
Anti-TNF are usually maintained during pregnancy in patients with inflammatory bowel disease (IBD) but safety is still a concern for them.
AIMS OBJECTIVE
To provide data on management of anti-TNF agents during pregnancy, safety of live vaccines (BCG-MMR-rotavirus) and breastfeeding in newborns and dedicated information delivered to IBD women.
METHODS METHODS
We performed an observational study in 25 centers from 2016 to 2018. We administered questionnaires to women with IBD receiving anti-TNF during pregnancy with newborn follow-up ≥ one year.
RESULTS RESULTS
Of 153 patients, 52 % maintained anti-TNF during the third trimester. Anti-TNF was shortly resumed in 79 % (58/73) after delivery. The rate of breastfeeding was 44 % (68/153) without any complication; 38 % of the mothers denied to breastfeed based on physician's advice. 26 % (34/129) of the newborns received live vaccines before 6 months-old (BCG:30 %; MMR:63 %; Rotavirus:8 %) and only 3 complications occurred (local BCGitis=1, fever=2). Information concerning anti-TNF during pregnancy/post-partum was delivered to 92 % of the patients, mainly by a gastroenterologist (97 %) who discussed with the obstetrician or the paediatrician in only 48 % and 25 %.
CONCLUSION CONCLUSIONS
In IBD patients, maintaining anti-TNF during pregnancy and breastfeeding is safe. Accidental live vaccines before 6 months did not lead to significant adverse events. The communication about these questions remains to improve.

Identifiants

pubmed: 38981787
pii: S1590-8658(24)00822-3
doi: 10.1016/j.dld.2024.06.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest Romain Altwegg received board or lectures fees from Abbvie, Janssen, Pfizer, Takeda. Vered Abitbol received lecture fees from Biogen Amgen Sandoz Mylan Pfizer Takeda Janssen, Gilead, Tillots. Laurent Peyrin-Biroulet received consulting fees from Merck, Abbvie, Janssen, Genentech. Ferring, Norgine, Tillots, Vifor, Shire, Therakos, Pharmacosmos, Pilège, BMS, UCB-Pharma. Hospira, Celltrion, Takeda, Biogaran, Boerhinger-Ingelheim, Lilly, Pfizer, and HAC-Pharma. This author also received lecture fees from Merck, Abbvie, Takeda, Janssen Cilag, Ferring. Norgine, Tillots, Vifor, Therakos, HAC-Pharma, and Mitsubishi. No conflicts of interest are claimed by the remaining authors.

Auteurs

S Bendaoud (S)

Department of Gastroenterology, Hôpital Diaconesses-Croix Saint-Simon, Paris, France.

S Nahon (S)

Department of Gastroenterology, Montfermeil, France.

L Beaugerie (L)

Department of Gastroenterology, Saint Antoine hospital, Paris, France.

J M Gornet (JM)

Department of Gastroenterology, Saint Louis hospital, Paris, France.

P Wils (P)

Department of Gastroenterology, Claude Huriez hospital, University of Lille 2, Lille, France; Inserm, CHU Lille, U1286- INFINITE- Institute for Translational Research in Inflammation, University of Lille, F-59000 Lille, France.

A Amiot (A)

Department of Gastroenterology, Kremlin Bicêtre Hospital, Kremlin-Bicêtre, France.

L Peyrin-Biroulet (L)

Department of Gastroenterology, Nancy, France.

V Abitbol (V)

Department of Gastroenterology, Cochin Hospital, Paris, France.

X Hébuterne (X)

Department of Gastroenterology, Nice, France.

R Altwegg (R)

Department of Gastroenterology, Montpellier, France.

I Rosa (I)

Department of Gastroenterology, Créteil, France.

M Amil (M)

Department of Gastroenterology, Vendée La Roche Sur Yon, France.

F Heluwaert (F)

Department of Gastroenterology, Hôpital Annecy Genevois, France.

L Plastaras (L)

Department of Gastroenterology, Colmar, France.

C Stefanescu (C)

Department of Gastroenterology, Neuilly-sur-Seine, France.

V Quentin (V)

Department of Gastroenterology, Saint Brieuc, France.

M Antoni (M)

Department of Gastroenterology, Orange, France.

K Bideau (K)

Department of Gastroenterology, Quimper, France.

M Boualit (M)

Department of Gastroenterology, Valenciennes, France.

E Cuillerier (E)

Department of Gastroenterology, Dreux, France.

C Locher (C)

Department of Gastroenterology, Meaux, France.

F Skinazi (F)

Department of Gastroenterology, Delafontaine, Saint Denis, France.

A Boureille (A)

Department of Gastroenterology, Nantes, France.

A Buisson (A)

Department of Gastroenterology, Clermont Ferrand, France.

M Simon (M)

Department of Gastroenterology, Institut Mutualiste Montsouris, Paris, France. Electronic address: marion.simon3@free.fr.

Classifications MeSH