COVID-19 Pandemic-related differences in the prevalence of genetic conditions and healthcare utilization and access for children with genetic conditions the United States.

Abstract

Purpose: to assess the pandemic-related differences in the prevalence of diagnosed genetic conditions (GC) in children (0-17 years) and their healthcare access and utilization in the US Methodology: Using the National Survey of Children's Health (NSCH) data, we compared pre-pandemic (2016-2019) and pandemic (2020-2022) prevalence estimates for diagnosed GC, healthcare utilization (HCU), and unmet health needs (UHN). The prevalence ratios (PR) of HCU and UHN during versus pre-pandemic for different groups were compared using interaction models, adjusted for age, sex, socioeconomic status, and race-ethnicity. Results: Pre-pandemic, GC prevalence was 3.55% rising to 4.51% during the pandemic [PR = 1.27 (1.18, 1.37), p < 0.001]. Pre-pandemic, children with GC had higher HCU [PR = 1.148 (1.129, 1.167), p < 0.001] and UHN [PR = 2.701 (2.225, 3.278), p < 0.001] as compared to children without GC. For children with GC, there was a decrease in HCU [PR = 0.954 (0.931, 0.978), p < 0.001], however, UHN was similar [PR = 1.112 (0.882, 1.402), p = 0.37] during versus pre-pandemic. Conclusion: The prevalence of diagnosed GC increased and disparities in UHN for children with GC persisted during the pandemic.

Competing Interest Statement

KV would like to disclose that she served as the Speakers Bureau of Global Blood Therapeutics for Oxbryta- a Sickle cell Modifying therapy till April 2022. There are no other conflicts of interest among the authors of this manuscript.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study used (or will use) ONLY openly available human data that were originally located at:https://www.census.gov/programs-surveys/nsch/data/datasets.html)

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the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

Comments (0)

No login
gif