About

Founded by Sepsis Alliance and governed by its stakeholders, the National Sepsis Registry Initiative (NSRI) is an independent, consensus-driven, multi-stakeholder initiative to create a National Sepsis Registry.

Each year, sepsis kills more than 270,000 people in the United States. For hospitalized patients with sepsis, more than one in five either die in the hospital or are discharged to hospice care. Another 1.4 million Americans survive sepsis each year, and many face months and years of difficult recovery. Sepsis also has a disproportionate impact on people and communities of color.

We can do better.

But we can’t make progress until we know the key symptoms and signs of who gets sepsis, and which treatments are the most effective, and how to do a better job helping survivors.

By building on current state and local efforts, and linking existing but unconnected data sources and repositories, a National Sepsis Registry will provide patients, doctors and researchers the critical information needed to improve sepsis diagnosis, treatment, innovation, and equity.

Founder

Founding Partners

Founding Advisers

Steven Q. Simpson, MD

Steven Q. Simpson, MD

Senior Medical Advisor

Karin Molander, MD, FACEP

Karin Molander, MD, FACEP

Chair, Board of Directors

NSRI Core Team

Jon Glaudemans

Jon Glaudemans

NSRI Director

Samantha Gilman

Samantha Gilman

NSRI Program Director

Greggory Briddick

Greggory Briddick

Advisor

Julie Cantor-Weinberg

Julie Cantor-Weinberg

Advisor

Paul Epner

Paul Epner

Advisor

Thomas Heyman

Thomas Heyman

Sepsis Alliance Liaison

Cindy Hou

Cindy Hou

Advisor

Joel Kallich

Joel Kallich

Advisor

Jasmine Moore

Jasmine Moore

Advisor

Sandra Newman

Sandra Newman

Advisor

Get in Touch. Get Involved.

We are seeking interested experts and organizations to guide and support creation of a National Sepsis Registry. We have a variety of workgroups and Advisory Boards where we need your help.

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