SIC-IR Billing and Documentation (SIC-IR)

February 26, 2008 updated by: MetroHealth Medical Center

Surgical and Trauma Intensive Care Unit Documentation and Billing Improvements With Medical Informatics

Accurate documentation in the patient medical record is critical to ensure proper diagnosis coding and subsequent hospital reimbursement. Multiple studies have demonstrated that clinicians often omit diagnoses which may result in insurance company denials and significant delays in payment. In addition, omitting diagnoses decreases the severity of patient illness which is often used as a risk adjustment tool to compare institution and physician outcomes. Medical informatics has been used to help improve accurate diagnosis documentation as well as improve billing efficiency. We plan to utilize a medical informatics program called SIC-IR (Surgical Intensive Care - Infection Registry) to improve documentation and attending billing efficiency within the surgical and trauma intensive care unit (STICU). We propose a six month study: a three month observational evaluation of current billing procedures followed by a three month prospective evaluation using a newly created SIC-IR billing module. The outcome measures will include the number of ICD-9 and CPT codes at discharge per patient, severity of patient illness based on documentation, STICU charges, number of insurance company denials, DRG relative weights, as well as a qualitative assessment of attending physician use of the electronic billing module. The observational and prospective patient populations will be compared for total patient-days in the STICU, ventilator-days, antibiotic-days, infectious complications per patient, and injury severity score (trauma patients only) to ensure the populations are similar and only the documentation and billing changes can account for our measured outcomes. We hypothesize that the SIC-IR billing module will increase the number of patient ICD-9 and CPT codes at discharge, increase severity of STICU patient illness via accurate documentation, increase total STICU charges, decrease insurance company denials, and be an efficient and well accepted electronic medical application.

Study Overview

Detailed Description

  1. An observational evaluation will be performed for all STICU patients over a three month time period.

    1. Data collected will be the outcome measures listed above (Number of ICD-9 codes at discharge, number of CPT codes at discharge, ext)
    2. In addition the total number of STICU patient-days, ventilator-days, central line-days, confirmed infectious complications, injury severity scores for trauma patients, and antibiotic-days will be collected over the three month period. This will serve as a way to ensure the observational and prospective populations are not different, and only the documentation and billing methods changed.
  2. The SIC-IR billing module will be released on October 1st, 2007 after attending physician training on its use.
  3. A prospective evaluation will be performed for all STICU patients over a three month time period

    1. Data collected will be the outcome measures listed above (Number of ICD-9 codes at discharge, number of CPT codes at discharge, ext)
    2. In addition the total number of STICU patient-days, ventilator-days, central line-days, confirmed infectious complications, injury severity scores for trauma patients, and antibiotic-days will be collected over the three month period. This will serve as a way to ensure the observational and prospective populations are not different, and only the documentation and billing methods changed.
  4. After the 3 month prospective evaluation, the attending physicians will be given a survey to document their acceptance or rejection of the billing module.
  5. The observational and prospective documentation and billing data will be compared.

Study Type

Observational

Enrollment (Actual)

814

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ohio
      • Cleveland, Ohio, United States, 44109
        • MetroHealth Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Study Population

All surgical and trauma intensive care unit patients addmitted to our reional Level I trauma center

Description

Inclusion Criteria:

  • consecutive patients admitted to the surgical and trauma intensive care unit a a single level one trauma center care for by the surgical intensivist

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
1
Observational evaluation of current billing and documentation practices
2
Use of SIC-IR Billing Module
Medical informatic application designed to help with billing and documentation within the surgical and trauma intensive care unit

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of ICD-9 codes at discharge (per patient)
Time Frame: 6 months
6 months
Number of STICU specific ICD-9 codes at discharge (per patient)
Time Frame: 6 months
6 months
Number of CPT codes at discharge (per patient)
Time Frame: 6 months
6 months
Number of STICU specific CPT codes at discharge (per patient)
Time Frame: 6 months
6 months
Number of specific evaluation and management codes used (per patient)
Time Frame: 6 months
6 months
Total STICU charges at discharge (per patient)
Time Frame: 6 months
6 months
Number of denied insurance claims (per month)
Time Frame: 6 months
6 months
Estimated patient survival based on documentation (illness severity) (per patient)
Time Frame: 6 months
6 months
DGR relative weight at discharge (per patient)
Time Frame: 6 months
6 months
Qualitative assessment of attending approval of the SIC-IR module
Time Frame: 6 months
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Joseph F Golob, MD, MetroHealth Medical Center
  • Principal Investigator: Jeffrey A Claridge, MD, MetroHealth Medical Center
  • Study Director: Adam MA Fadlalla, PhD, Cleveland State University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2007

Primary Completion (Actual)

December 1, 2007

Study Completion (Actual)

December 1, 2007

Study Registration Dates

First Submitted

September 13, 2007

First Submitted That Met QC Criteria

September 13, 2007

First Posted (Estimate)

September 14, 2007

Study Record Updates

Last Update Posted (Estimate)

February 27, 2008

Last Update Submitted That Met QC Criteria

February 26, 2008

Last Verified

February 1, 2008

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • IRB07-00922

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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