View Clinical Trial (Medical Research Study)
Day Zero Urinary Catheter Removal in General Thoracic Surgery Patients Receiving Thoracic Epidural Analgesia: Recatheterization Rates and Urinary Tract Infection Occurrences
| City: |
|
Chattanooga |
| State: |
|
Tennessee |
| Zip Code: |
|
37404 |
| Conditions: |
|
Postoperative Retention of Urine - Postoperative Urinary Tract Infection |
| Purpose: |
|
Current standard of practice in study institution dictates day of surgery urinary catheter
removal in general thoracic surgery patients receiving thoracic epidural analgesia. The
investigators hypothesize that this practice results in low recatheterization rates
secondary to urinary retention and low urinary tract infection rates.
|
| Study Summary: |
|
Study Design A prospective study design will be utilized as data will be collected in a
prospective manner and standard of care/current practice will be unaltered in the patient
population.
Sampling will include all patients that meet the eligibility criteria from March 01, 2011
until August 01, 2011 with a goal of forty-five patients.
Data Collection Protocol
1. The patient will be interviewed and given information regarding participation in the
study by Principal Investigator and/or research team prior to surgery. Informed
Consent Forms will be collected by Principal Investigator and/or research team.
Principal Investigator and/or research team will collect all data on Data Collection
Sheet.
2. Thoracic epidural will be placed by the anesthesiologist in pre-op per standard
protocol.
- Location of epidural will be documented by Principal Investigator and/or research
team on Data Collection Sheet. (See Appendix 1)
3. Prior to surgery, if indicated, an indwelling urinary bladder catheter will be placed
per pre-operative protocol.
4. Post-operative documentation of time, type and settings for epidural infusion will be
documented on Data Collection Sheet.
5. Post-op eligible patients admitted to cardiothoracic step-down unit will be placed on
the following protocol:
- Thoracic Epidural will be managed by the anesthesia group.
- Any change in prescription or dosing will be documented on the Data
Collection Sheet.
- If urinary catheter present, will be discontinued at midnight day of surgery, Day
Zero; the time of discontinuation will be noted on the Data Collection Sheet.
- If micturition occurs, amount and time will be documented on Data Collection
Sheet.
- If no spontaneous void by 0800 post-operative day (POD) 1, bladder scanning
will be initiated.
- If ≥ 400 cc per bladder scanner, the thoracic surgeon, surgeon's nurse or the
Principal Investigator will not notified.
- Any ordered interventions, the response and re- evaluation will be noted on Data
Collection Sheet.
- Urinary retention will be defined as > 400 cc and recatheterization (either
intermittent or indwelling) will occur.
6. Data will only be collected during current surgery hospitalization.
|
| Criteria: |
|
Inclusion Criteria:
- All general thoracic surgery patients with a thoracic epidural catheter.
Exclusion Criteria:
- Men > 65 years old
- History of urologic procedure
- Known benign prostatic hyperplasia
- Admission to intensive care units
- History of urinary retention
- Foreign speaking patient
- Pregnant women and those less than 18 years old
|
| NCT ID: |
|
NCT01309529 |
| Primary Contact: |
|
Principal Investigator
Laurel Rhyne, ACNP-BC
Memorial Hospital-Thoracic Program
Tiffany E Potter, BSN
Phone: 4223-495-7848
Email: tiffany_potter@memorial.org
|
| Backup Contact: |
|
Email: laurel_rhyne@memorial.org
Laurel Rhyne, ACNP-BC
Phone: 423-495-7834
|
| Location Contact: |
|
Chattanooga, Tennessee 37404
United States
Potter
Email: tiffany_potter@memorial.org
Site Status: Recruiting |
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
May 21, 2013 |
| Modifications to this listing: |
|
Only selected fields are shown, please use the link
below to view all information about this clinical trial. |
|
Click to view Full Listing
|