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Impact of Semi-automated Proposal and Optimization of Diagnoses and Surgical Procedures for Precoding: a Randomized Controlled Trial

T

Thomas Steffen

Status

Completed

Conditions

Healthcare Common Procedure Coding System
Diagnosis-Related Groups

Treatments

Other: precoding
Other: Standard procedure

Study type

Observational

Funder types

Other

Identifiers

NCT04726202
Chir201902

Details and patient eligibility

About

The hypothesis of present study is that the daily monitoring and optimization of DRG coding is associated with higher reimbursement. Therefore, the primary objective is to determine if the daily monitoring and optimization of DRG coding of individual cases leads to better proceeds per day.

Enrollment

1,200 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients undergoing surgery as inpatients (at least one night stay)
  • treated at the Kantonsspital St. Gallen, St. Gallen site

Exclusion criteria

  • surgery as outpatients
  • surgery at the Rorschach and Flawil sites
  • patients operated on by the Department of Surgery, but hospitalized at another department of the hospital

Trial design

1,200 participants in 2 patient groups

Control arm
Description:
standard procedure of coding at hospital
Treatment:
Other: Standard procedure
Precoding arm
Description:
Coding of the standard procedure will be reviewed and corrected
Treatment:
Other: precoding

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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