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Impact of the 2018 revised Pregnancy Prevention Programme by the European Medicines Agency on the use of oral retinoids in females of childbearing age in Denmark, Italy, Netherlands, and Spain: an interrupted time series analysis.
Durán, Carlos E; Riera-Arnau, Judit; Abtahi, Shahab; Pajouheshnia, Romin; Hoxhaj, Vjola; Gamba, Magdalena; Alsina, Ema; Martin-Perez, Mar; Garcia-Poza, Patricia; Llorente-Garcia, Ana; Gonzalez-Bermejo, Diana; Ibánez, Luisa; Sabaté, Mònica; Vidal, Xavier; Ballarín, Elena; Sanfélix-Gimeno, Gabriel; Rodríguez-Bernal, Clara; Peiró, Salvador; García-Sempere, Aníbal; Sanchez-Saez, Francisco; Ientile, Valentina; Ingrasciotta, Ylenia; Guarneri, Claudio; Tanaglia, Matilde; Tari, Michele; Herings, Ron; Houben, Eline; Swart-Polinder, Karin; Holthuis, Emily; Huerta, Consuelo; Gini, Rosa; Roberto, Giuseppe; Bartolini, Claudia; Paoletti, Olga; Limoncella, Giorgio; Girardi, Anna; Hyeraci, Giulia; Andersen, Morten; Kristiansen, Sarah Brøgger; Hallgreen, Christine Erikstrup; Klungel, Olaf; Sturkenboom, Miriam.
Afiliação
  • Durán CE; Julius Center for Health Sciences and Primary Care, Department of Data Science and Biostatistics, University Medical Center Utrecht, Utrecht, Netherlands.
  • Riera-Arnau J; Julius Center for Health Sciences and Primary Care, Department of Data Science and Biostatistics, University Medical Center Utrecht, Utrecht, Netherlands.
  • Abtahi S; Department of Clinical Pharmacology, Vall Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Pajouheshnia R; Division of Pharmacoepidemiology and Clinical Pharmacology, Faculty of Science, Utrecht Institute for Pharmaceutical Sciences, Universiteit Utrecht, Utrecht, Netherlands.
  • Hoxhaj V; Division of Pharmacoepidemiology and Clinical Pharmacology, Faculty of Science, Utrecht Institute for Pharmaceutical Sciences, Universiteit Utrecht, Utrecht, Netherlands.
  • Gamba M; Julius Center for Health Sciences and Primary Care, Department of Data Science and Biostatistics, University Medical Center Utrecht, Utrecht, Netherlands.
  • Alsina E; Division of Pharmacoepidemiology and Clinical Pharmacology, Faculty of Science, Utrecht Institute for Pharmaceutical Sciences, Universiteit Utrecht, Utrecht, Netherlands.
  • Martin-Perez M; Julius Center for Health Sciences and Primary Care, Department of Data Science and Biostatistics, University Medical Center Utrecht, Utrecht, Netherlands.
  • Garcia-Poza P; Agencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.
  • Llorente-Garcia A; Agencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.
  • Gonzalez-Bermejo D; Agencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.
  • Ibánez L; Agencia Española de Medicamentos y Productos Sanitarios, Madrid, Spain.
  • Sabaté M; Department of Clinical Pharmacology, Vall Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Vidal X; Department of Clinical Pharmacology, Vall Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Ballarín E; Department of Clinical Pharmacology, Vall Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Sanfélix-Gimeno G; Department of Clinical Pharmacology, Vall Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Rodríguez-Bernal C; The Foundation for the Promotion of Health and Biomedical Research of Valencia Region, Health Services Research Unit (FISABIO - HSRU), Valencia, Spain.
  • Peiró S; The Foundation for the Promotion of Health and Biomedical Research of Valencia Region, Health Services Research Unit (FISABIO - HSRU), Valencia, Spain.
  • García-Sempere A; The Foundation for the Promotion of Health and Biomedical Research of Valencia Region, Health Services Research Unit (FISABIO - HSRU), Valencia, Spain.
  • Sanchez-Saez F; The Foundation for the Promotion of Health and Biomedical Research of Valencia Region, Health Services Research Unit (FISABIO - HSRU), Valencia, Spain.
  • Ientile V; The Foundation for the Promotion of Health and Biomedical Research of Valencia Region, Health Services Research Unit (FISABIO - HSRU), Valencia, Spain.
  • Ingrasciotta Y; Department of Biomedical and Dental Sciences and Morpho-functional Imaging, University of Messina, Messina, Italy.
  • Guarneri C; Section of Pharmacology, Department of Diagnostics and Public Health, University of Verona, Verona, Italy.
  • Tanaglia M; Department of Biomedical and Dental Sciences and Morpho-functional Imaging, University of Messina, Messina, Italy.
  • Tari M; Section of Pharmacology, Department of Diagnostics and Public Health, University of Verona, Verona, Italy.
  • Herings R; Caserta Local Health Unit, Caserta, Italy.
  • Houben E; PHARMO Institute, Utrecht, Netherlands.
  • Swart-Polinder K; PHARMO Institute, Utrecht, Netherlands.
  • Holthuis E; PHARMO Institute, Utrecht, Netherlands.
  • Huerta C; PHARMO Institute, Utrecht, Netherlands.
  • Gini R; Department of Public Health and Maternal and Child Health, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
  • Roberto G; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Bartolini C; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Paoletti O; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Limoncella G; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Girardi A; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Hyeraci G; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Andersen M; Agenzia Regionale di Sanità Della Toscana (ARS), Florence, Italy.
  • Kristiansen SB; Pharmacovigilance Research Center, Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Hallgreen CE; Pharmacovigilance Research Center, Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Klungel O; Copenhagen Centre for Regulatory Science, Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Sturkenboom M; Division of Pharmacoepidemiology and Clinical Pharmacology, Faculty of Science, Utrecht Institute for Pharmaceutical Sciences, Universiteit Utrecht, Utrecht, Netherlands.
Front Pharmacol ; 14: 1207976, 2023.
Article em En | MEDLINE | ID: mdl-37663263
ABSTRACT

Background:

In March 2018, the European pregnancy prevention programme for oral retinoids was updated as part of risk minimisation measures (RMM), emphasising their contraindication in pregnant women.

Objective:

To measure the impact of the 2018 revision of the RMMs in Europe by assessing the utilisation patterns of isotretinoin, alitretinoin and acitretin, contraceptive measures, pregnancy testing, discontinuation, and pregnancy occurrence concomitantly with a retinoid prescription.

Methods:

An interrupted time series (ITS) analysis to compare level and trend changes after the risk minimisation measures implementation was conducted on a cohort of females of childbearing age (12-55 years of age) from January 2010 to December 2020, derived from six electronic health data sources in four countries Denmark, Netherlands, Spain, and Italy. Monthly utilisation figures (incidence rates [IR], prevalence rates [PR] and proportions) of oral retinoids were calculated, as well as discontinuation rates, contraception coverage, pregnancy testing, and rates of exposed pregnancies to oral retinoids, before and after the 2018 RMMs.

Results:

From 10,714,182 females of child-bearing age, 88,992 used an oral retinoid at any point during the study period (mean age 18.9-22.2 years old). We found non-significant level and trend changes in incidence or prevalence of retinoid use in females of child-bearing age after the 2018 RMMs. The reason of discontinuation was unknown in >95% of cases. Contraception use showed a significant increase trend in Spain; for other databases this information was limited. Pregnancy testing was hardly recorded thus was not possible to model ITS analyses. After the 2018 RMM, rates of pregnancy occurrence during retinoid use, and start of a retinoid during a pregnancy varied from 0.0 to 0.4, and from 0.2 to 0.8, respectively.

Conclusion:

This study shows a limited impact of the 2018 RMMs on oral retinoids utilisation patterns among females of child-bearing age in four European countries. Pregnancies still occur during retinoid use, and oral retinoids are still prescribed to pregnant women. Contraception and pregnancy testing information was limited in most databases. Regulators, policymakers, prescribers, and researchers must rethink implementation strategies to avoid any pregnancy becoming temporarily related to retinoid use.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Pharmacol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Pharmacol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda