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CMS Sacral Nerve Stimulation For Urinary Incontinence Form


sacral nerve stimulation for urinary incontinence

Indications

(648319) Is the procedure intended for the treatment of urinary urge incontinence, urgency-frequency syndrome, or urinary retention? 
(648320) Has the patient been refractory to documented behavioral, pharmacologic, and/or surgical corrective therapy? 
(648321) Is the patient an appropriate surgical candidate such that implantation with anesthesia can occur? 
(648322) Has the patient had a successful test stimulation demonstrating a 50% or greater improvement? 
(648323) Is the patient able to record voiding diary data adequately? 

YesNoN/A
YesNoN/A
YesNoN/A

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Effective Date

01/01/2002

Last Reviewed

NA

Original Document

  Reference



Effective January 1, 2002, sacral nerve stimulation is covered for the treatment of urinary urge incontinence, urgency-frequency syndrome, and urinary retention. Sacral nerve stimulation involves both a temporary test stimulation to determine if an implantable stimulator would be effective and a permanent implantation in appropriate candidates. Both the test and the permanent implantation are covered.

The following limitations for coverage apply to all three indications:

  • Patient must be refractory to conventional therapy (documented behavioral, pharmacologic and/or surgical corrective therapy) and be an appropriate surgical candidate such that implantation with anesthesia can occur.
  • Patients with stress incontinence, urinary obstruction, and specific neurologic diseases (e.g., diabetes with peripheral nerve involvement) which are associated with secondary manifestations of the above three indications are excluded.
  • Patient must have had a successful test stimulation in order to support subsequent implantation. Before a patient is eligible for permanent implantation, he/she must demonstrate a 50% or greater improvement through test stimulation. Improvement is measured through voiding diaries.
  • Patient must be able to demonstrate adequate ability to record voiding diary data such that clinical results of the implant procedure can be properly evaluated.