Skip to content

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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04726202
Enrollment
1200
Registered
2021-01-27
Start date
2019-06-01
Completion date
2020-01-31
Last updated
2021-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diagnosis-Related Groups, Healthcare Common Procedure Coding System

Keywords

DRG, Diagnosis-Related Groups, ICD, reimbursement

Brief summary

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.

Interventions

Coding of cases follows the standard procedures established at the hospital

OTHERprecoding

Standard coding will be reviewed by dedicated physicians and corrected or extended if necessary. Coding will compared to the written OP report for consistency. Dedicated physician visits patients daily (in addition to routine visits). Dedicated physicians review discharge report and will make changes and additions. DRG coding will be adapted to results from visits and discharge report.

Sponsors

Thomas Steffen
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
reimbursement per day at hospital8 monthstotal reimbursement per arm divided by the total stay of the patients in the arm in days

Secondary

MeasureTime frameDescription
Length of hospital stay8 monthslength of hopital stay in full days including entry and discharge day
Total reimbursement per case8 monthsreimbursement in Swiss Francs per case
case mix index per case8 monthsFinancial department will provide the cost weight/case mix index per case
Severity of perioperative complications8 monthscomplications during hospitalisation will be graded according to the Clavian-Dindo scale. In case of multiple complications the highest grade will be taken.
readmission rate8 monthsRate of case related readmissions

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026