Automated ICD Coding of Primary Diagnosis Based on Machine Learning
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04817423 |
|
Recruitment Status :
Active, not recruiting
First Posted : March 26, 2021
Last Update Posted : March 26, 2021
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment |
|---|---|
| Cardiovascular Diseases | Other: No intervention |
The accuracy and productivity of ICD coding has always been a concern of clinical practice. Errors of ICD codes may result in claim denials and missed revenue. However, ICD coding process is complex, time-consuming and error-prone. More experienced coders are in need, but there is an increasing lack of supply. Automated ICD coding has potential to facilitate clinical coders for improved efficiency and quality. Model performance of related studies is still far below coders and both the accuracy and interpretability need to be improved in great demand. Besides, studies in Chinese corpus are not sufficient.
In this study, the investigators will implement automated ICD coding study based on inpatient' data collected from electronic medical records from Fuwai Hospital, the world's largest medical center for cardiovascular disease. Feature engineering and machine learning methods will be used to develop classification models with good performance, interpretability and practicability for ICD codes of primary diagnosis.
| Study Type : | Observational |
| Estimated Enrollment : | 74880 participants |
| Observational Model: | Other |
| Time Perspective: | Retrospective |
| Official Title: | Automated ICD Coding of Primary Diagnosis Based on Machine Learning |
| Actual Study Start Date : | March 1, 2021 |
| Estimated Primary Completion Date : | April 2021 |
| Estimated Study Completion Date : | April 2021 |
| Group/Cohort | Intervention/treatment |
|---|---|
|
Model training and test group
Data set will be split into training group and test group, where training group will be used for model building, and test group for subsequent evaluation and verification.
|
Other: No intervention
No intervention |
- ICD code of primary diagnosis [ Time Frame: At the end of enrollment ]Each admission will be a sample in this study. The ICD code of primary diagnosis assigned by medical coders for each admission will be collected as the primary outcome.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Admissions in Fuwai Hospital, from January 1, 2019, to December 31, 2020
Exclusion Criteria:
- Admissions stayed in nephrology department, Fuwai Hospital
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04817423
| China | |
| Fuwai Hospital | |
| Beijing, China | |
| Principal Investigator: | Wei Zhao, PhD | China National Center for Cardiovascular Diseases |
| Responsible Party: | China National Center for Cardiovascular Diseases |
| ClinicalTrials.gov Identifier: | NCT04817423 |
| Other Study ID Numbers: |
2021-1425 |
| First Posted: | March 26, 2021 Key Record Dates |
| Last Update Posted: | March 26, 2021 |
| Last Verified: | March 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Cardiovascular Diseases |

