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The original Article has been corrected.","order":6,"name":"change_details","label":"Change Details","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}},{"value":"French law (in accordance with Articles L1122-1 and L1122-1-1 of the French Public Health Code) requires that participation in research of this nature (non-interventional epidemiological study) be offered to patients after they have been individually informed in writing, with the physician seeking the patient\u2019s opposition to participation, and ensuring traceability of the absence of opposition (\u201cnon-objection form\u201d). The law does not require written traceability to be directly ensured by the patient. These procedures have been implemented for this study (PGL.EXPO-1-ClinicalTrials.gov Identifier: NCT04481152) after approval by a committee for the protection of persons, in accordance with the law (Protection of Persons Committee of Ile-de-France X, Ref: 34-2020). It also received a favorable opinion from the French data protection authority, the Commission Nationale Informatique et Libert\u00e9s (CNIL) (Ref: MLD\/MFI\/AR2114411). More specifically, before being included in the study, the patient receives a written information. The investigator orally explains to the patient the content of this information note, which consists of presenting the study, explaining its objectives and answering any questions the patient may have. The patient\u2019s consent is given orally to the investigator, following the various items of information provided by the investigator, i.e. \u201cinformed consent\u201d, who attests to this on the information note by indicating the following 4 items of information: patient\u2019s surname\/first name\/identifier in the research; opposition expressed, date of issue of information, signature of person responsible for information.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics and legal aspects"}}],"article-number":"22716"}}