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Registry Technology

Quentry for SRS® is customized software developed by Brainlab to extract data from DICOM RT images and treatment plans, significantly reducing the administrative effort and mitigating data integrity challenges. Quentry for SRS® standardizes the collection of data in everyday practice, creating real world evidence on:

  • The characteristics of the patients who receive SRS treatments
  • Treatment locations, disease diagnoses and lesion descriptions
  • Treatment planning and delivery information, including volumetric and dosimetry data and the equipment used to treat the patient
  • Information on disease progression and lesion response to treatment
  • Patient-reported and observational outcomes data
  • Overall survival

Quality Measures

The SRS Registry contains a wide array of information that supports measures in various quality domains including Care Coordination, Patient Safety, Functional Outcomes, Guideline Adherence, Patient-Focused Episodes of Care, Peer Review, Quality Assurance and Treatment Success.

SRS Registry Process

The SRS registry focuses on measures that matter most to patients in addition to objective measures derived from imaging studies and clinical data. The registry continues to develop primary and secondary outcomes measures to gauge objective response rates and lesion response to treatment utilizing the registry’s robust technology platform.

About Neuropoint

NeuroPoint Alliance, Inc. (NPA) is a not-for-profit corporation created to coordinate a variety of national projects involving the acquisition, analysis, and reporting of clinical data, using online technologies.

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NeuroPoint Alliance, Inc
5550 Meadowbrook Industrial Ct.
Rolling Meadows, IL 60008-3852
847.378.0500
info@neuropoint.org

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