SIC-IR Billing and Documentation (SIC-IR)
Surgical and Trauma Intensive Care Unit Documentation and Billing Improvements With Medical Informatics
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
An observational evaluation will be performed for all STICU patients over a three month time period.
- Data collected will be the outcome measures listed above (Number of ICD-9 codes at discharge, number of CPT codes at discharge, ext)
- 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.
- The SIC-IR billing module will be released on October 1st, 2007 after attending physician training on its use.
A prospective evaluation will be performed for all STICU patients over a three month time period
- Data collected will be the outcome measures listed above (Number of ICD-9 codes at discharge, number of CPT codes at discharge, ext)
- 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.
- After the 3 month prospective evaluation, the attending physicians will be given a survey to document their acceptance or rejection of the billing module.
- The observational and prospective documentation and billing data will be compared.
Study Type
Study Type
Enrollment (Actual)
Enrollment
Contacts and Locations
Study Locations
-
-
Ohio
-
Cleveland, Ohio, United States, 44109
- MetroHealth Medical Center
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Study Population
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
How is the study designed?
Design Details
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
Intervention / TreatmentIntervention / 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
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
Sponsor
Sponsor
Investigators
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
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
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.