Connecticut Senate Bill SB00766

Connecticut 2025 Regular Session

• Introduced: 1/17/25
• Refer: 1/17/25

Caption

An Act Concerning Information Sharing Between The Office Of The Child Advocate And The Infant Mortality Review Committee Within The Department Of Public Health.

Impact

The implementation of SB00766 could significantly enhance the ability of the Infant Mortality Review Committee to identify trends and evaluate risk factors that contribute to infant mortality. By facilitating information sharing between critical health and advocacy bodies, the legislation aims to create a more collaborative approach in addressing public health concerns related to infants. It is expected that with better data access, more informed recommendations and policies can be developed to promote infant health and safety.

Summary

SB00766 is a legislative proposal aimed at improving the coordination of data between the Office of the Child Advocate and the Infant Mortality Review Committee within the Department of Public Health in Connecticut. The bill seeks to allow for the sharing of sensitive information related to infant mortality cases while ensuring that all confidentiality requirements are met. This initiative stems from a growing recognition of the need for comprehensive analysis and response strategies to address and decrease infant mortality rates in the state.

Contention

While the bill appears to have a broad objective of improving health outcomes, there may be concerns regarding the handling of sensitive data. The requirement to meet confidentiality guidelines could lead to debates about the adequacy of existing protections and the ethical implications of data sharing. Stakeholders, including health advocates and data privacy experts, may voice their opinions on how to balance the need for comprehensive data analysis with the rights of individuals to keep their health information private. Potential pushback may arise from those who fear that the sharing of information could breach confidentiality or complicate existing health data regulations.