Retrospective Chart Review Screening Algorithm to Assess the Prevalence of PNH-clones

Sponsor
AZ Delta (Other)
Overall Status
Completed
CT.gov ID
NCT05884060
Collaborator
Alexion (Industry)
568
1
46.4
12.3

Study Details

Study Description

Brief Summary

The present study is a non-interventional retrospective chart review study assessing the prevalence of PNH-clones in patients with PNH risk-factors aged ≥14 years and treated at our hospital. The objective of this study is to develop a PNH screening tool on the hospital Electronic Health Record (EHR) system. An algorithm defining PNH risk groups is developed.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Detailed Description

Paroxysmal Nocturnal Hemoglobinuria (PNH) is a life-threatening hematological disorder, but with an effective therapy. Prevalence is estimated between 1-5 per million people, often manifested by cardiovascular, gastrointestinal, neurological or haematological symptoms. Referral is therefore typically to several specialists, resulting in PNH underdiagnosis.

This chart review study consists primarily of developing an algorithm to identify a high-risk cohort of potential PNH patients who need treatment from all registered patients, with maximum ability to find relevant cases. Secondly, this cohort will be manually reviewed by clinicians for final screening. The challenge hence is maximizing the ability to find all relevant PNH patients yet limiting the number to ensure manual review is possible.

Study Design

Study Type:
Observational
Actual Enrollment :
568 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Retrospective Electronic Chart Review to Assess the Prevalence of PNH-clones Among Patients Identified With PNH Risk Factors
Actual Study Start Date :
Apr 20, 2018
Actual Primary Completion Date :
Mar 1, 2022
Actual Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
group 1

patients with evidence of haemolysis without obvious cause

Other: No intervention
No interventions

group 2

patients with evidence of bone marrow dysfunction (AA, MDS, unexplained cytopenia)

Other: No intervention
No interventions

group 3

patients with thrombosis

Other: No intervention
No interventions

group 4

patient group that needs to be eliminated from final high risk cohort: patients with cirrhosis, patients wit septic embolisms & embolisation

Other: No intervention
No interventions

Outcome Measures

Primary Outcome Measures

  1. PNH risk factors translation into query codes that can be interpreted by a computer system for analysis [2022]

    Three main PNH risk sub-cohorts were constructed, representing patients exhibiting PNH risk factors such as hemolytic anemia (group 1), bone marrow dysfunction (group 2) and thrombosis (group 3). To build these sub-cohorts, queries were created using a combination of structured and unstructured electronic health record (EHR) data, including lab results, diagnoses, medication, questionnaire data, text from medical and radiology reports, notes, and Internation Classification Codes (ICD-10). These sub-cohorts were validated by two hematologists who reviewed randomly selected patients, resulting in several iterations and query optimizations.

  2. Number of patients identified with high risk for PNH clone and per type of screening criteria by developing a computational screening algorithm [2022]

    A computational algorithm was employed for a retrospective EHR analysis, to identify high-risk cohorts of potential PNH patients who need treatment from all registered patients, with maximum ability to find relevant cases. Three main PNH risk sub-cohorts were constructed, representing patients exhibiting PNH risk factors such as hemolytic anemia (group 1), bone marrow dysfunction (group 2) and thrombosis (group 3). These sub-cohorts were validated by two hematologists who reviewed randomly selected patients, resulting in several iterations and query optimizations. Sub-cohorts were subsequently merged and refined into high risk cohorts that undergo further analysis and manual review. Two hematologists independently reviewed and rated medical records to achieve a manual risk stratification of the high risk cohorts.

Secondary Outcome Measures

  1. The number of patients at high risk for PNH, categorized by risk factor, across each medical department [2023]

    To increase awareness of PNH risk factors by medical departments that need to consider PNH lab testing

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patient ≥14 years of age

  • At least 1 record encoded in the General Hospital Delta (AZ Delta) patient database (HiX) between 20 April 2018 and 1 March 2022

  • A history or presence of at least one PNH risk factors identified following retrospective screening of electronic patient records

Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 AZ Delta Roeselare West-Vlaanderen Belgium 8800

Sponsors and Collaborators

  • AZ Delta
  • Alexion

Investigators

  • Principal Investigator: Dries Deeren, MD, AZ Delta

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
AZ Delta
ClinicalTrials.gov Identifier:
NCT05884060
Other Study ID Numbers:
  • B1172022000017
First Posted:
Jun 1, 2023
Last Update Posted:
Jun 2, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by AZ Delta
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 2, 2023