California 2019-2020 Regular Session

California Senate Bill SB452

Introduced
2/21/19  
Introduced
2/21/19  
Refer
3/7/19  
Refer
3/7/19  
Refer
4/11/19  
Refer
4/11/19  
Report Pass
4/25/19  
Report Pass
4/25/19  
Refer
4/25/19  
Report Pass
5/16/19  
Engrossed
5/23/19  
Refer
6/6/19  
Refer
6/6/19  
Report Pass
7/10/19  
Report Pass
7/10/19  
Refer
7/10/19  

Caption

Ken Maddy California Cancer Registry.

Impact

The introduction of SB 452 is significant as it not only mandates the notification of cancer patients regarding the registry but also clarifies the responsibility of healthcare providers in reporting cancer cases. By alleviating the requirement for facilities and physicians to ensure patients are informed about their reporting duties, the bill seeks to streamline the reporting process. Furthermore, it enhances transparency regarding the utilization of patient data, balancing the need for public health data collection with individual privacy concerns.

Summary

Senate Bill 452, known as the Ken Maddy California Cancer Registry bill, aims to enhance the framework for reporting cancer cases within California. This legislation modifies existing laws by requiring the State Department of Public Health to provide patients diagnosed with cancer or receiving cancer treatment with a brochure that explains their rights and the implications of the Ken Maddy Cancer Registry. The bill underscores the importance of informing patients about how their data is collected, its intended use, and their autonomy regarding participation in research studies.

Sentiment

The sentiment among legislators and health advocacy groups appears to be mixed. Supporters view the bill as a positive step towards keeping patients informed and engaged in their healthcare journey, while critics may argue that easing reporting obligations could lead to less oversight. There is a general recognition of the importance of cancer data for public health, but there are apprehensions about patient privacy and the handling of sensitive information.

Contention

Notable points of contention surrounding SB 452 include the adequacy of patient notification and protection of confidential information. Opponents may express concern that reducing the burden on reporting facilities could result in diminished patient awareness regarding the implications of the cancer registry. Additionally, the ongoing balance between effective data collection for public health purposes and stringent privacy standards remains a critical discussion point among stakeholders.

Companion Bills

No companion bills found.

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