New Hampshire 2025 Regular Session

New Hampshire House Bill HB576

Introduced
1/16/25  
Refer
1/16/25  

Caption

Relative to tracking the number of ALS diagnoses in the state.

Impact

The introduction of this bill signifies a significant commitment to public health monitoring specifically targeted at ALS, aiming to improve data collection and possibly influence future health policies and resource allocation for ALS care. The bill's oversight will fall under the Department of Health and Human Services, which is responsible for developing a HIPAA-compliant surveillance system to handle sensitive patient information related to ALS diagnoses. The financial implications indicate a projected expenditure of around $861,000 within FY2026 to establish this system and employ dedicated IT personnel for management.

Summary

House Bill 576 aims to enhance the tracking of amyotrophic lateral sclerosis (ALS) diagnoses in the state by adding ALS to the list of critical health problems within the Critical Health Problems Reporting Act. This legislative action mandates healthcare facilities to report any diagnosed or confirmed ALS cases within a ten-day timeframe. The intent behind this bill is to create a systemic approach for monitoring ALS incidences which is expected to be higher than other reported critical diseases.

Sentiment

The general sentiment surrounding HB 576 appears to be supportive, particularly among health advocates and professionals who recognize the importance of improved tracking systems for combating ALS. While there may be occasional concerns about costs and data privacy, the primary focus remains on enhancing public health initiatives, which are largely welcomed by stakeholders in healthcare.

Contention

Some potential points of contention may arise regarding resource allocation and the long-term sustainability of funding for ALS tracking efforts. The absence of direct funding authorization within the bill may raise concerns among legislators about the financial viability of ongoing ALS surveillance initiatives. During discussions, stakeholders may stress the importance of ensuring that adequate support is in place not just for initial implementation, but for maintaining the system over time to ensure its efficacy and continued relevance.

Companion Bills

No companion bills found.

Previously Filed As

NH HB329

Establishing an ALS (Amyotrophic Lateral Sclerosis) registry in New Hampshire.

NH HB329

Establishing an ALS (Amyotrophic Lateral Sclerosis) registry in New Hampshire.

NH HB1662

Relative to restricting simultaneous employment of certain department of health and human services staff with adoption or child placement agencies.

NH HB1296

Relative to insurance coverage for diagnostic and supplemental breast examinations.

NH SB493

Relative to establishing municipal emergency disaster relief loan fund to aid municipalities in a natural disaster.

NH HB1363

Relative to allowing members of the general court to participate in the department of health and human services employee assistance program.

NH SB495

Relative to certification of alcohol and other drug use treatment facilities.

NH HB1466

Relative to providing disaster relief funding to municipalities after a natural disaster.

NH SB459

Establishing a committee to study the child protection act; establishing a right to submit evidence and testimony in family court proceedings; relative to wage garnishment with child support payments; and relative to parenting coordinators in high-conflict cases.

NH SB319

Relative to vaccine and pharmaceutical products purchased, promoted, or distributed by the state and its political subdivisions.

Similar Bills

No similar bills found.