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Patient informed consent: not required.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical approval"}},{"value":"The manuscript\u2019s corresponding author (Koji Matsuo) affirms that the manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained. The National Inpatient Sample is developed for the Healthcare Cost and Utilization Project that is sponsored by the Agency for Healthcare Research and Quality, and the program is the source of the de-identified data used; race and ethnicity was grouped by the program; and the program has not verified and is not responsible for the statistical validity of the data analysis or the conclusions derived by the study team.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Transparency"}},{"value":"In this nationwide cross-sectional study, increasing trends of full-term labor induction for low-risk pregnancy may have stopped during the COVID-19 pandemic in the U.S.; labor induction was associated with cesarean delivery and other measured adverse outcomes.","order":5,"name":"Ethics","group":{"name":"EthicsHeading","label":"Tweetable statement"}}],"article-number":"12689"}}