Preserved Continence Does NOT Guarantee Intact Sexual Sensation After Sphincter Surgery
Internal anal sphincter (IAS) pressure for continence and sexual signaling are anatomically and functionally distinct—preserved continence after lateral internal sphincterotomy and trans-sphincteric fistulotomy does not indicate intact sexual sensation. 1
Why These Functions Are Separate
Different Mechanisms of Dysfunction
- Sexual dysfunction after LIS is primarily neuropathic and myofascial, involving altered sensations and dysesthesia rather than structural sphincter damage 1
- Continence depends on IAS resting tone (responsible for most anal sphincter resting pressure) and external anal sphincter (EAS) voluntary contraction 2
- Patients with sexual dysfunction typically have intact continence with altered sensations rather than mechanical problems 1, 3
The IAS Role in Continence vs. Sensation
- The IAS is responsible for most of anal sphincter resting tone and should be identified and reapproximated during repair 2
- LIS causes a significant decline in resting anal pressure (from 138 ± 28 mmHg pre-op to 110 ± 18 mmHg at 12 months), yet patients remain continent 4
- Fistulotomy significantly decreases maximum resting pressure (85.9 ± 20.4 to 60.2 ± 18.4 mmHg) without necessarily affecting continence in most patients 5
The Real Problem: Pelvic Floor Muscle Tension
Pathophysiology of Post-Surgical Sexual Dysfunction
- Pelvic floor muscle tension commonly develops after anorectal surgery and contributes to altered sensations during sexual activity 1, 3
- Protective guarding patterns that developed during the painful fissure period persist even after surgery 3, 6
- This creates a neuropathic pain syndrome rather than a mechanical sphincter failure 1
Treatment Algorithm for Your Patient
First-Line Conservative Management
- Initiate specialized pelvic floor physical therapy 2-3 times weekly focusing on internal and external myofascial release 1, 3, 6
- Apply topical lidocaine 5% ointment to affected areas for neuropathic pain management 1, 3, 6
- Implement gradual desensitization exercises guided by a physical therapist 1, 6
- Use warm sitz baths to promote muscle relaxation and reduce symptoms 1, 6
- Perform muscle coordination retraining to reduce protective guarding patterns 1, 6
Advanced Biofeedback Therapy
- Incorporate an anorectal probe with rectal balloon during pelvic-floor physical therapy to provide real-time feedback on dynamic changes 6
- Serial rectal balloon inflation training enhances sensory perception through operant-conditioning principles 6
- A typical rehabilitation program consists of 8-10 weekly sessions supplemented with home exercises 6
- Biofeedback therapy improves symptoms in more than 70% of patients with pelvic floor dysfunction 6
Expected Timeline
- The dysesthesia and altered sensations typically improve significantly over 6-12 months with appropriate pelvic floor therapy and neuropathic pain management 3, 6
Critical Pitfalls to Avoid
Do NOT Pursue Additional Surgery
- Additional surgical interventions should not be pursued for post-LIS sexual dysfunction, as this would likely worsen the neuropathic component rather than improve it 1, 3, 6
- Manual anal dilatation should be avoided entirely, as it carries a 30% temporary and 10% permanent incontinence rate 1, 3
Recognize the Distinction
- The distinction between sexual dysfunction after LIS being typically neuropathic/myofascial rather than mechanical sphincter failure should be recognized, requiring physical therapy rather than surgical revision 1
- Your patient's preserved continence actually confirms that the sexual dysfunction is neuropathic/myofascial rather than structural 1, 3
What This Means for Future Patients
Consider Botulinum Toxin Instead
- Botulinum toxin injection represents a safe alternative to LIS, achieving 75-95% cure rates with no risk of permanent incontinence or sexual dysfunction 2, 1, 3
- The mechanism involves temporary paresis of the anal sphincter through reversible sphincter relaxation without permanent damage 1
- Botulinum toxin should be considered after 8 weeks of failed topical therapy 1