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Evaluation of a Claims-based Algorithm for the Identification of Transthyretin-mediated Amyloidosis (ATTR) Amyloidosis in Medical Records

Primary Purpose

Transthyretin Amyloidosis

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Computer algorithm for ATTR
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Transthyretin Amyloidosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Identified by the ATTR diagnostic algorithm and matched by Yale's list of potential subjects defined as:

    1. subjects within the claims dataset that are predicted to be at risk of having ATTR who are also being managed within YNHHS
    2. patients who need to be contacted and offered additional clinical evaluation to determine whether they have a diagnosis of ATTR (non-hereditary or Hereditary ATTR amyloidosis).

      Exclusion Criteria:

  • Patients who have opted out of research in the Epic system will be excluded entirely from the study
  • Patients who are pregnant or who may become pregnant

Sites / Locations

  • Yale New Haven Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Computer algorithm for ATTR

Arm Description

Patients will be evaluated for the identification of ATTR Amyloidosis through a claims-based algorithm

Outcomes

Primary Outcome Measures

Diagnostic performance of algorithm in identifying patients with ATTR amyloidosis
Potential thresholds for defining diagnostic positivity based on the calculated algorithmic scores will be explored and the corresponding positive predictive value (PPV) will serve as indicator for the diagnostic performance. Negative predictive values (NPV) may be explored if the actual distribution of score data will allow for it.

Secondary Outcome Measures

Proportion of diagnosed patients
The proportion or rate of patients who were previously undiagnosed of ATTR Amyloidosis

Full Information

First Posted
September 24, 2020
Last Updated
September 12, 2023
Sponsor
Yale University
Collaborators
Alnylam Pharmaceuticals Inc
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1. Study Identification

Unique Protocol Identification Number
NCT04569903
Brief Title
Evaluation of a Claims-based Algorithm for the Identification of Transthyretin-mediated Amyloidosis (ATTR) Amyloidosis in Medical Records
Official Title
Evaluation of a Claims-based Algorithm for the Identification of ATTR Amyloidosis in Medical Records
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 2023 (Anticipated)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
February 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
Alnylam Pharmaceuticals Inc

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary objective of this study is to evaluate the diagnostic performance of an algorithm in identifying patients with ATTR amyloidosis.
Detailed Description
A screening strategy to identify ATTR in the large background population of patients with one or more common ATTR manifestations, would be of significant clinical value. In addition, novel ATTR therapies have been recently made available or are currently in development in late-stage clinical trials. As early diagnosis and treatment is expected to achieve better outcomes, this makes the development and validation of an easily implemented, rapid and electronically-enabled diagnostic algorithm especially important. A medical and pharmacy claims-based algorithm was developed to potentially identify patients at risk of having ATTR. The goal of this study is to evaluate the ability of the algorithm to identify patients with ATTR by performing diagnostic clinical work up in patients that the algorithm identifies in a large dataset of patients at Yale. The primary objective of this study is to evaluate the diagnostic performance of the algorithm in identifying patients with ATTR amyloidosis. The secondary objective of this study is to estimate the clinical benefit of the algorithm, as measured by the added diagnostic value, i.e. the proportion or rate of patients who were previously undiagnosed. The total obtained prevalence will be assessed and informally compared to the referral-based prevalence of ATTR amyloidosis patients at Yale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Transthyretin Amyloidosis

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Computer algorithm for ATTR
Arm Type
Experimental
Arm Description
Patients will be evaluated for the identification of ATTR Amyloidosis through a claims-based algorithm
Intervention Type
Device
Intervention Name(s)
Computer algorithm for ATTR
Intervention Description
Patients will be evaluated for the identification of ATTR Amyloidosis through a claims-based algorithm
Primary Outcome Measure Information:
Title
Diagnostic performance of algorithm in identifying patients with ATTR amyloidosis
Description
Potential thresholds for defining diagnostic positivity based on the calculated algorithmic scores will be explored and the corresponding positive predictive value (PPV) will serve as indicator for the diagnostic performance. Negative predictive values (NPV) may be explored if the actual distribution of score data will allow for it.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Proportion of diagnosed patients
Description
The proportion or rate of patients who were previously undiagnosed of ATTR Amyloidosis
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Identified by the ATTR diagnostic algorithm and matched by Yale's list of potential subjects defined as: subjects within the claims dataset that are predicted to be at risk of having ATTR who are also being managed within YNHHS patients who need to be contacted and offered additional clinical evaluation to determine whether they have a diagnosis of ATTR (non-hereditary or Hereditary ATTR amyloidosis). Exclusion Criteria: Patients who have opted out of research in the Epic system will be excluded entirely from the study Patients who are pregnant or who may become pregnant
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cinthia S De Freitas, RN, BSN
Phone
(203)785-6315
Email
cinthia.defreitas@yale.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edward Miller, MD
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale New Haven Hospital
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06520
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Edward Miller, MD

12. IPD Sharing Statement

Learn more about this trial

Evaluation of a Claims-based Algorithm for the Identification of Transthyretin-mediated Amyloidosis (ATTR) Amyloidosis in Medical Records

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