Virginia 2026 Regular Session

Virginia House Bill HB1391

Introduced
1/21/26  
Refer
1/21/26  
Report Pass
2/10/26  
Report Pass
2/11/26  
Engrossed
2/16/26  
Refer
2/18/26  
Report Pass
2/26/26  
Report Pass
3/6/26  
Enrolled
3/30/26  
Chaptered
4/13/26  

Caption

An Act to amend the Code of Virginia by adding in Chapter 2 of Title 32.1 an article numbered 22.1, consisting of a section numbered 32.1-73.27:1, relating to Sickle Cell Coordinated Access Network established; report.

Impact

The implementation of HB1391 is expected to have significant implications on state healthcare laws. By introducing a structured network of sickle cell specialists, the bill promises to address a crucial gap in healthcare services for individuals affected by sickle cell disease. It mandates that healthcare providers will have access to telehealth consultations, ensuring timely assistance in managing pain and treatment protocols. This can notably enhance the quality of care, streamline communication among providers, and ultimately optimize health outcomes for patients with sickle cell conditions.

Summary

House Bill 1391, titled the Sickle Cell Coordinated Access Network, aims to establish a dedicated network within the Code of Virginia to facilitate healthcare support for individuals with sickle cell disease. The bill mandates the creation of a Sickle Cell Coordinated Access Network, which will provide real-time consultation from specialized healthcare professionals known as sickle cell specialists to healthcare providers throughout Virginia. This initiative is designed to improve the coordination and management of care for patients suffering from sickle cell disorders, thus enhancing healthcare outcomes for this population.

Sentiment

The sentiment surrounding HB1391 appears to be largely positive, as it addresses a specific health concern affecting a vulnerable segment of the population. Stakeholders, including healthcare practitioners and patient advocacy groups, likely view the establishment of a specialized network as a significant step towards improving healthcare disparities for those afflicted with sickle cell disease. However, as with most healthcare initiatives, there may be concerns regarding funding, integration with existing healthcare systems, and the execution of telehealth initiatives, which could call for further clarification and strategic planning.

Contention

While the bill seems to enjoy general support, potential contentions could arise regarding the operational aspects of the consultation network. Questions may involve the availability and accessibility of sickle cell specialists, the adequacy of telehealth infrastructure to meet demand, and the potential for increased costs in implementing the network across the state. Additionally, scrutiny may arise around how this network integrates with other existing healthcare services and the implications for patient outcomes in terms of access and quality of care.

Companion Bills

No companion bills found.

Previously Filed As

VA HB2593

Virginia College Access and Affordability Scholarship Fund; established, report.

VA SB835

Virginia College Opportunity Endowment and Fund; established, report.

VA HB2500

Florence Neal Cooper Smith Sickle Cell Research Endowment Fund; established.

VA HB1903

Virginia Health Workforce Development Authority; Virginia Nursing Workforce Center established; reporting and monitoring of health care workforce programs; residency slots; work group; report.

VA SB1183

Virginia Access to Justice Act; establishes public defender office in each judicial circuit.

VA HB1865

Virginia Access to Justice Act; establishes public defender office in each judicial circuit.

VA SB1287

Virginia Gaming Commission; established, penalties, report.

VA HB2498

Virginia Gaming Commission; established, penalties, report.

VA HB2757

Sickle cell disease; feasibility of Medicaid benefit and Medicaid Health Homes, report.

VA SB6004

Virginia Gaming Commerce Regulation Act; established, penalties, report.

Similar Bills

No similar bills found.