New Hampshire 2022 Regular Session

New Hampshire House Bill HB1606

Introduced
12/22/21  
Refer
12/22/21  
Report Pass
3/8/22  
Engrossed
3/22/22  
Refer
3/22/22  
Report Pass
4/20/22  
Report Pass
4/28/22  
Enrolled
6/15/22  
Chaptered
6/29/22  

Caption

Relative to administration of the state immunization registry.

Impact

If passed, this legislation would significantly alter the operational framework of the state immunization registry, transitioning it from a presumptive default of inclusivity to one that prioritizes individual consent. This new system aims to strengthen patient autonomy and trust in healthcare systems, potentially increasing public willingness to share immunization information for public health tracking. However, implementing this opt-in system may come with logistical challenges and costs associated with developing a suitable information management framework.

Summary

House Bill 1606 aims to amend the administration of the state immunization registry by instituting an opt-in system. Under this bill, individuals or their guardians must explicitly consent to have their information, such as immunization records, included in the registry. This change seeks to enhance patient privacy and control over personal health data by requiring that no individual's information can be recorded without their permission.

Sentiment

The sentiment surrounding HB 1606 appears to be generally positive among proponents who emphasize the importance of personal consent and privacy in healthcare. They argue that this legislation is a necessary step toward safeguarding patient data. However, there may be concerns expressed by some healthcare officials regarding the practicality of managing an opt-in system, especially if it complicates immunization tracking efforts that are fundamental to public health initiatives.

Contention

One of the main points of contention regarding HB 1606 is the financial implications of transitioning to an opt-in system. The estimated cost of implementing the necessary changes to the immunization registry is projected to be around $42 million spread over four years. Critics might highlight these costs as a concern, especially amidst ongoing discussions about public health funding. Additionally, there are worries that requiring explicit consent could hinder the ability of health officials to efficiently monitor immunization rates and respond to public health crises.

Companion Bills

No companion bills found.

Previously Filed As

NH HB679

Relative to immunization requirements.

NH HB358

Relative to exemption from immunization requirements on the basis of religious belief.

NH SB0096

Pharmacist administration of immunizations.

NH SB75

Providing health insurance carriers access to the state immunization registry and making an appropriation therefor.

NH HB357

Relative to the department of health and human services' rulemaking authority regarding immunization requirements.

NH HB1219

(New Title) relative to immunization requirements in foster family homes and relative to financial eligibility for the Medicare savings program.

NH HB772

Relating to the immunization data included in and excluded from the immunization registry.

NH SB46

Relating to the immunization data included in and excluded from the immunization registry.

NH A1016

Requires automatic registration with New Jersey Immunization Information System upon administration of vaccine for certain persons who consent to registration.

NH S2987

Requires automatic registration with New Jersey Immunization Information System upon administration of vaccine for certain persons who consent to registration.

Similar Bills

NJ A1155

Establishes State Parkinson's disease registry.

OH SB236

Enact the Suicide Self-Defense Act

NJ A1016

Requires automatic registration with New Jersey Immunization Information System upon administration of vaccine for certain persons who consent to registration.

NJ S2987

Requires automatic registration with New Jersey Immunization Information System upon administration of vaccine for certain persons who consent to registration.

NJ A3853

Establishes State Parkinson's disease registry and awareness campaign.

TX HB772

Relating to the immunization data included in and excluded from the immunization registry.

TX SB46

Relating to the immunization data included in and excluded from the immunization registry.

LA HB541

Establishes a registry for individuals and entities that provide caregiving services (EN NO IMPACT See Note)