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Objectives: We investigated COVID-19 vaccine safety in pregnant and breastfeeding women with autoimmune diseases (AID) in the COVID-19 Vaccination in Autoimmune Diseases (COVAD) study.
Methods: Delayed-onset (>7 days) vaccine-related adverse events (AE), disease flares (DF), and AID-related treatment modifications were analyzed upon diagnosis of AID versus healthy controls (HC) and the pregnancy/breastfeeding status at the time of at least one dose of vaccine.
Results: Among the 9201 participants to the self-administered online survey, 6787 (73.8%) were women. Forty pregnant and 52 breastfeeding patients with AID were identified, of whom the majority had received at least one dose of COVID-19 vaccine (100% and 96.2%, respectively). AE were reported significantly more frequently in pregnant than in non-pregnant patients (overall AE 45% vs 26%, p= 0.01; minor AE 40% vs 25.9%, p= 0.03; major AE 17.5% vs 4.6%, p< 0.01), but no difference was found in comparison with pregnant HC. No difference was observed between breastfeeding patients and HC with respect to AE. Post-vaccination DF were reported by 17.5% of pregnant and 20% of breastfeeding patients, and by 18.3% of age- and disease-matched non-pregnant and non-breastfeeding patients (n = 262). All pregnant/breastfeeding patients who experienced a DF were managed with glucocorticoids; 28.6% and 20% of them required initiation or change in immunosuppressants, respectively.
Conclusion: This study provides reassuring insights into the safety of COVID-19 vaccines administered to women with AID during the gestational and post-partum periods, helping overcome hesitant attitudes, as the benefits for the mother and the fetus by passive immunization appear to outweigh potential risks.
COVID-19 vaccine safety during pregnancy and breastfeeding in women with autoimmune diseases: results from the COVAD study
Laura Andreoli;Daniele Lini;Karen Schreiber;Ioannis Parodis;Parikshit Sen;R Naveen;Jessica Day;Mrudula Joshi;Kshitij Jagtap;Arvind Nune;Elena Nikiphorou;Vishwesh Agarwal;Sreoshy Saha;Ai Lyn Tan;Samuel Katsuyuki Shinjo;Nelly Ziade;Tsvetelina Velikova;Marcin Milchert;Abraham Edgar Gracia-Ramos;Lorenzo Cavagna;Masataka Kuwana;Johannes Knitza;Ashima Makol;Aarat Patel;John D Pauling;Chris Wincup;Bhupen Barman;Erick Adrian Zamora Tehozol;Jorge Rojas Serrano;Ignacio García-De La Torre;Iris J Colunga-Pedraza;Javier Merayo-Chalico;Okwara Celestine Chibuzo;Wanruchada Katchamart;Phonpen Akarawatcharangura Goo;Russka Shumnalieva;Yi-Ming Chen;Leonardo Santos Hoff;Lina El Kibbi;Hussein Halabi;Binit Vaidya;Syahrul Sazliyana Shaharir;A T M Tanveer Hasan;Dzifa Dey;Carlos Enrique Toro Gutiérrez;Carlo V Caballero-Uribe;James B Lilleker;Babur Salim;Tamer Gheita;Tulika Chatterjee;Miguel A Saavedra;Oliver Distler;COVAD study group;Gabriela Arredondo;Hector Chinoy;Vikas Agarwal;Rohit Aggarwal;Latika Gupta Collaborators COVAD study group: Zoltán Griger;Sinan Kardes;Melinda Nagy Vince;Yogesh Preet Singh;Rajiv Ranjan;Avinash Jain;Sapan C Pandya;Rakesh Kumar Pilania;Aman Sharma;Manesh Manoj M;Vikas Gupta;Chengappa G Kavadichanda;Pradeepta Sekhar Patro;Sajal Ajmani;Sanat Phatak;Rudra Prosad Goswami;Abhra Chandra Chowdhury;Ashish Jacob Mathew;Padnamabha Shenoy;Ajay Asranna;Keerthi Talari Bommakanti;Anuj Shukla;Arunkumar R Pande;Kunal Chandwar;Akanksha Ghodke;Hiya Boro;Zoha Zahid Fazal;Binit Vaidya;Döndü Üsküdar Cansu;Reşit Yıldırım;Armen Yuri Gasparyan;Nicoletta Del Papa;Gianluca Sambataro;Atzeni Fabiola;Marcello Govoni;Simone Parisi;Elena Bartoloni Bocci;Gian Domenico Sebastiani;Enrico Fusaro;Marco Sebastiani;Luca Quartuccio;Franco Franceschini;Pier Paolo Sainaghi;Giovanni Orsolini;Rossella De Angelis;Maria Giovanna Danieli;Vincenzo Venerito;Silvia Grignaschi;Alessandro Giollo;Alessia Alunno;Florenzo Iannone;Marco Fornaro;Lisa S Traboco;Suryo Anggoro Kusumo Wibowo;Jesús Loarce-Martos;Sergio Prieto-González;Raquel Aranega Gonzalez;Akira Yoshida;Ran Nakashima;Shinji Sato;Naoki Kimura;Yuko Kaneko;Takahisa Gono;Stylianos Tomaras;Fabian Nikolai Proft;Marie-Therese Holzer;Margarita Aleksandrovna Gromova;Or Aharonov;Zoltán Griger;Ihsane Hmamouchi;Imane El Bouchti;Zineb Baba;Margherita Giannini;François Maurier;Julien Campagne;Alain Meyer;Daman Langguth;Vidya Limaye;Merrilee Needham;Nilesh Srivastav;Marie Hudson;Océane Landon-Cardinal;Wilmer Gerardo Rojas Zuleta;Álvaro Arbeláez;Javier Cajas;José António Pereira Silva;João Eurico Fonseca;Olena Zimba;Doskaliuk Bohdana;Uyi Ima-Edomwonyi;Ibukunoluwa Dedeke;Emorinken Airenakho;Nwankwo Henry Madu;Abubakar Yerima;Hakeem Olaosebikan;Becky A;Oruma Devi Koussougbo;Elisa Palalane;Ho So;Manuel Francisco Ugarte-Gil;Lyn Chinchay;José Proaño Bernaola;Victorio Pimentel;Hanan Mohammed Fathi;Reem Hamdy A Mohammed;Ghita Harifi;Yurilís Fuentes-Silva;Karoll Cabriza;Jonathan Losanto;Nelly Colaman;Antonio Cachafeiro-Vilar;Generoso Guerra Bautista;Enrique Julio Giraldo Ho;Lilith Stange Nunez;Cristian Vergara M;Jossiell Then Báez;Hugo Alonzo;Carlos Benito Santiago Pastelin;Rodrigo García Salinas;Alejandro Quiñónez Obiols;Nilmo Chávez;Andrea Bran Ordóñez;Gil Alberto Reyes Llerena;Radames Sierra-Zorita;Dina Arrieta;Eduardo Romero Hidalgo;Ricardo Saenz;Idania Escalante M;Wendy Calapaqui;Ivonne Quezada
2023-01-01
Abstract
Objectives: We investigated COVID-19 vaccine safety in pregnant and breastfeeding women with autoimmune diseases (AID) in the COVID-19 Vaccination in Autoimmune Diseases (COVAD) study.
Methods: Delayed-onset (>7 days) vaccine-related adverse events (AE), disease flares (DF), and AID-related treatment modifications were analyzed upon diagnosis of AID versus healthy controls (HC) and the pregnancy/breastfeeding status at the time of at least one dose of vaccine.
Results: Among the 9201 participants to the self-administered online survey, 6787 (73.8%) were women. Forty pregnant and 52 breastfeeding patients with AID were identified, of whom the majority had received at least one dose of COVID-19 vaccine (100% and 96.2%, respectively). AE were reported significantly more frequently in pregnant than in non-pregnant patients (overall AE 45% vs 26%, p= 0.01; minor AE 40% vs 25.9%, p= 0.03; major AE 17.5% vs 4.6%, p< 0.01), but no difference was found in comparison with pregnant HC. No difference was observed between breastfeeding patients and HC with respect to AE. Post-vaccination DF were reported by 17.5% of pregnant and 20% of breastfeeding patients, and by 18.3% of age- and disease-matched non-pregnant and non-breastfeeding patients (n = 262). All pregnant/breastfeeding patients who experienced a DF were managed with glucocorticoids; 28.6% and 20% of them required initiation or change in immunosuppressants, respectively.
Conclusion: This study provides reassuring insights into the safety of COVID-19 vaccines administered to women with AID during the gestational and post-partum periods, helping overcome hesitant attitudes, as the benefits for the mother and the fetus by passive immunization appear to outweigh potential risks.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/581785
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simulazione ASN
Il report seguente simula gli indicatori relativi alla propria produzione scientifica in relazione alle soglie ASN 2023-2025 del proprio SC/SSD. Si ricorda che il superamento dei valori soglia (almeno 2 su 3) è requisito necessario ma non sufficiente al conseguimento dell'abilitazione. La simulazione si basa sui dati IRIS e sugli indicatori bibliometrici alla data indicata e non tiene conto di eventuali periodi di congedo obbligatorio, che in sede di domanda ASN danno diritto a incrementi percentuali dei valori. La simulazione può differire dall'esito di un’eventuale domanda ASN sia per errori di catalogazione e/o dati mancanti in IRIS, sia per la variabilità dei dati bibliometrici nel tempo. Si consideri che Anvur calcola i valori degli indicatori all'ultima data utile per la presentazione delle domande.
La presente simulazione è stata realizzata sulla base delle specifiche raccolte sul tavolo ER del Focus Group IRIS coordinato dall’Università di Modena e Reggio Emilia e delle regole riportate nel DM 589/2018 e allegata Tabella A. Cineca, l’Università di Modena e Reggio Emilia e il Focus Group IRIS non si assumono alcuna responsabilità in merito all’uso che il diretto interessato o terzi faranno della simulazione. Si specifica inoltre che la simulazione contiene calcoli effettuati con dati e algoritmi di pubblico dominio e deve quindi essere considerata come un mero ausilio al calcolo svolgibile manualmente o con strumenti equivalenti.