Objectives To estimate the impact in the number of incident abortions due to the Dobbs v Jackson decision.
Methods We fit an interrupted time series model to annual incident abortions from 2004 to 2023 in the state of Colorado. In addition, we computed the proportion of residents that received abortive care from outside Colorado before and after the Dobbs v Jackson decision. Finally, we estimated the proportion of abortions over time stratified by gestation week of the mother.
Results We found that in the state of Colorado, after Dobbs v Jackson (compared to before): (1) an increase in non-resident incident abortions immediately after the decision (2) which is driven by residents in the states surrounding Colorado with the most restrictive abortion laws; the uptick in non-resident abortions has likely led to longer wait times, a higher burden on facilities, and (3) later gestation times for the mother.
Conclusions Shifts in abortion patterns in Colorado is evidence that the ramifications of Dobbs v Jackson extend beyond individual state borders, impacting both state-residents and non-residents seeking care. Policymakers must consider these findings in future reproductive legislation to ensure access to abortion in protective states, such as Colorado.
Public health implications This work underscores the immediate impact of healthcare legislation and the increased burden on healthcare services for states with more permissible abortion legislation.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityDe-identified data were collected from the CDPHE via a data request form and the Lehigh University Human Subjects Committee determined that no Institutional Review Board approval was necessary for this study. Data is available upon request from the Colorado Department of Public Health and Environment.
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