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SB 2400

HOSPICE DATA COLLECTION

104th Regular Session Introduced by Bill Cunningham

Illinois SB 2400 requires hospice providers to collect and report standardized data to state health authorities for quality monitoring and regulatory oversight purposes.

Rule 2-10 Committee/3rd Reading Deadline Established As May 15, 2026
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Bill Summary · SB 2400

Legislative bill overview

SB 2400 establishes new data collection and reporting requirements for hospice providers operating in Illinois. The bill mandates that hospice facilities gather and submit specified metrics to state health authorities, creating standardized oversight mechanisms for end-of-life care services.

Why is this important

Hospice data collection enables state regulators to monitor quality metrics, identify underperforming providers, and protect vulnerable populations receiving end-of-life care. This information can inform policy decisions, guide consumer choice, and potentially reveal patterns of inadequate service or financial exploitation.

Potential points of contention

  • Administrative burden: Hospice providers, particularly smaller organizations, may face significant compliance costs and staffing requirements to collect and report data, potentially affecting care delivery resources
  • Data scope and privacy: Questions remain about what specific metrics will be collected, how patient privacy will be protected, and whether certain sensitive information could inadvertently identify individuals or breach confidentiality
  • Regulatory clarity: The bill's current early stage leaves ambiguity about enforcement mechanisms, penalties for non-compliance, and how collected data will be used or made publicly accessible

Compiled from official sources — confirm details with the bill’s official record.

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