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Maternal and fetal outcomes in multiparous women with Cystic Fibrosis.
Cohen-Cymberknoh, Malena; Ariel Dabby, Maya; Gindi Reiss, Bar; Melo Tanner, Joel; Pérez, Gema; Lechtzin, Noah; Polverino, Eva; Perez Miranda, Javier; Gramegna, Andrea; Aliberti, Stefano; Levine, Hagit; Mussaffi, Huda; Blau, Hanna; Prais, Dario; Mei-Zahav, Meir; Shteinberg, Michal; Livnat, Galit; Gur, Michal; Bentur, Lea; Downey, Damian G; Dagan, Adi; Golan-Tripto, Inbal; Aviram, Micha; Mondejar-Lopez, Pedro; Picard, Elie; Schwarz, Carsten; Jakubec, Petr; Kazmerski, Traci M; Amsalem, Hagai; Hochner Celnikier, Drorit; Kerem, Eitan; Reiter, Joel.
Afiliação
  • Cohen-Cymberknoh M; Pediatric Pulmonary Unit and Cystic Fibrosis Center, Hadassah Medical Center, Jerusalem, Israel; Faculty of Medicine, Hebrew University of Jerusalem, Israel. Electronic address: malena@hadassah.org.il.
  • Ariel Dabby M; Faculty of Medicine, Hebrew University of Jerusalem, Israel.
  • Gindi Reiss B; Safra Sheba Medical Center, Ramat-Gan, Israel.
  • Melo Tanner J; Instituto Nacional del Tórax, Santiago, Chile.
  • Pérez G; Pediatric Pulmonology and Cystic Fibrosis Unit, Hospital Exequiel González Cortés, Chile.
  • Lechtzin N; Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Polverino E; Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Perez Miranda J; Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Gramegna A; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Respiratory Unit and Cystic Fibrosis Center, Italy; Department Pathophysiology and Transplantation University of Milan, Italy.
  • Aliberti S; Department of Biomedical Sciences, Humanitas University, Milan, Italy; IRCCS Humanitas Research Hospital, Respiratory Unit, Milan, Italy.
  • Levine H; Graub CF Center, Schneider Children's Medical Center, Petach-Tikva and Sackler School of Medicine, Tel-Aviv University, Israel.
  • Mussaffi H; Graub CF Center, Schneider Children's Medical Center, Petach-Tikva and Sackler School of Medicine, Tel-Aviv University, Israel.
  • Blau H; Graub CF Center, Schneider Children's Medical Center, Petach-Tikva and Sackler School of Medicine, Tel-Aviv University, Israel.
  • Prais D; Graub CF Center, Schneider Children's Medical Center, Petach-Tikva and Sackler School of Medicine, Tel-Aviv University, Israel.
  • Mei-Zahav M; Graub CF Center, Schneider Children's Medical Center, Petach-Tikva and Sackler School of Medicine, Tel-Aviv University, Israel.
  • Shteinberg M; Pulmonology Institute and CF Center, Carmel Medical Center and the Technion- Israel Institute of Technology, Haifa, Israel.
  • Livnat G; Pulmonology Institute and CF Center, Carmel Medical Center and the Technion- Israel Institute of Technology, Haifa, Israel.
  • Gur M; Pediatric Pulmonary Institute and CF Center, Ruth Rappaport Children's Hospital, Rambam Medical Center and the Technion- Israel Institute of Technology, Haifa, Israel.
  • Bentur L; Pediatric Pulmonary Institute and CF Center, Ruth Rappaport Children's Hospital, Rambam Medical Center and the Technion- Israel Institute of Technology, Haifa, Israel.
  • Downey DG; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University, Belfast, Ireland.
  • Dagan A; Safra Sheba Medical Center, Ramat-Gan, Israel.
  • Golan-Tripto I; Pediatric Pulmonary Unit, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer Sheva, Israel.
  • Aviram M; Pediatric Pulmonary Unit, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer Sheva, Israel.
  • Mondejar-Lopez P; Pediatric Pulmonology and Cystic Fibrosis Unit, Hospital Clinico Universitario Virgen de la Arrixaca, Murcia, Spain.
  • Picard E; Pediatric Pulmonary Unit, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Schwarz C; Charite Hospital, Berlin, Germany.
  • Jakubec P; CF Center, University Hospital Olomouc and Faculty of Medicine, Palacky University, Olomouc, Czech Republic.
  • Kazmerski TM; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, USA; Center for Innovative Research on Gender Health Equity (CONVERGE), University of Pittsburgh, Pittsburgh, PA, USA.
  • Amsalem H; Department of Obstetrics and Gynecology, Mount Scopus, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
  • Hochner Celnikier D; Department of Obstetrics and Gynecology, Mount Scopus, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
  • Kerem E; Pediatric Pulmonary Unit and Cystic Fibrosis Center, Hadassah Medical Center, Jerusalem, Israel; Faculty of Medicine, Hebrew University of Jerusalem, Israel.
  • Reiter J; Pediatric Pulmonary Unit and Cystic Fibrosis Center, Hadassah Medical Center, Jerusalem, Israel; Faculty of Medicine, Hebrew University of Jerusalem, Israel.
Respir Med ; 228: 107654, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38735372
ABSTRACT

BACKGROUND:

Quality of life and survival in Cystic Fibrosis (CF) have improved dramatically, making family planning a feasible option. Maternal and perinatal outcomes in women with CF (wwCF) are similar to those seen in the general population. However, the effect of undergoing multiple pregnancies is unknown.

METHODS:

A multinational-multicenter retrospective cohort study. Data was obtained from 18 centers worldwide, anonymously, on wwCF 18-45 years old, including disease severity and outcome, as well as obstetric and newborn complications. Data were analyzed, within each individual patient to compare the outcomes of an initial pregnancy (1st or 2nd) with a multigravid pregnancy (≥3) as well as secondary analysis of grouped data to identify risk factors for disease progression or adverse neonatal outcomes. Three time periods were assessed - before, during, and after pregnancy.

RESULTS:

The study population included 141 wwCF of whom 41 (29%) had ≥3 pregnancies, "multiparous". Data were collected on 246 pregnancies, between 1973 and 2020, 69 (28%) were multiparous. A greater decline in ppFEV1 was seen in multiparous women, primarily in pancreatic insufficient (PI) wwCF and those with two severe (class I-III) mutations. Multigravid pregnancies were shorter, especially in wwCF over 30 years old, who had high rates of prematurity and newborn complications. There was no effect on pulmonary exacerbations or disease-related complications.

CONCLUSIONS:

Multiple pregnancies in wwCF are associated with accelerated respiratory deterioration and higher rates of preterm births. Therefore, strict follow-up by a multidisciplinary CF and obstetric team is needed in women who desire to carry multiple pregnancies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resultado da Gravidez / Fibrose Cística Limite: Adolescent / Adult / Female / Humans / Middle aged / Newborn / Pregnancy Idioma: En Revista: Respir Med Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resultado da Gravidez / Fibrose Cística Limite: Adolescent / Adult / Female / Humans / Middle aged / Newborn / Pregnancy Idioma: En Revista: Respir Med Ano de publicação: 2024 Tipo de documento: Article