Voiding Trial Orders
A standard voiding trial should include removal of the Foley catheter, measurement of post-void residual after spontaneous voiding, and specific criteria for passing the trial based on voided volume relative to total bladder volume.
Components of Voiding Trial Orders
Pre-Trial Preparation
- Ensure adequate hydration prior to the trial
- Document baseline urinary symptoms
- Consider initiating alpha-blockers (e.g., alfuzosin 10mg daily) at least 3 days before the trial for patients with urinary hesitancy 1
Catheter Removal Protocol
- Remove Foley catheter on postoperative day 1 for most patients 2
- Two main techniques for catheter removal:
Monitoring Protocol
- Instruct patient to void when feeling the urge
- Measure and record:
Criteria for Passing Voiding Trial
- Voided volume ≥ two-thirds (66%) of total bladder volume (voided volume + PVR) 3
- OR voided volume > 50% of instilled volume (for back-fill method) 4
- OR force of urinary stream ≥ 5 on a scale of 0-10 4
- PVR < 100-150cc (clinically acceptable threshold)
Failed Voiding Trial Management
- If initial trial fails:
Post-Trial Monitoring
- Monitor for symptoms of urinary retention or incomplete emptying
- Consider second voiding trial within 3 hours after passing initial trial to confirm sustained voiding ability 5
- Document final PVR before discharge
Special Considerations
Risk Factors for Failed Voiding Trial
- Higher Charlson comorbidity index 6
- Low maximum flow rate on preoperative uroflowmetry (< 15 cc/second) 5
- Non-detrusor contraction voiding pattern 6
- Nocturia 6
Location Options for Catheter Removal
- Both home and office catheter removal show similar patient satisfaction rates (95% satisfaction) 4
- Home catheter removal may be associated with lower rates of urinary tract infection (8.3% vs 26.3%) 4
Follow-Up Recommendations
- Schedule follow-up within 1-2 weeks after successful voiding trial
- Perform post-void residual measurement at follow-up visit 2
- Monitor for symptoms of urinary tract infection, which occur more frequently in patients who fail initial voiding trials (20% vs 6%) 6
Documentation Requirements
- Document voiding trial technique used
- Record voided volumes and post-void residuals
- Note criteria used to determine success or failure
- Document patient education regarding signs/symptoms requiring medical attention
This structured approach to voiding trials provides clear criteria for success while accounting for individual patient factors that may affect voiding function.