Published on 16/03/2015 by admin
Filed under Dermatology
Last modified 22/04/2025
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Bethanee J. Schlosser and Ginat W. Mirowski
Evidence Levels: A Double-blind study B Clinical trial ≥ 20 subjects C Clinical trial < 20 subjects D Series ≥ 5 subjects E Anecdotal case reports
Vulvodynia is defined by the International Society for the Study of Vulvovaginal Disease as ‘vulvar discomfort, most often described as burning pain, occurring in the absence of relevant visible findings or a specific, clinically identifiable, neurologic disorder.’ Vulvodynia includes burning, stinging, irritation, and rawness, but does not indicate a specific etiology. Vulvodynia is a complex disorder of unknown etiology attributed to altered sensory perception and is a diagnosis of exclusion. Previous terms included burning vulva syndrome, vestibular adenitis, vulvar vestibulitis syndrome, dysesthetic vulvodynia, essential vulvodynia, and general or localized vulvar dysesthesia. Current classification divides vulvodynia into generalized and localized types which are subcategorized into provoked (requiring physical stimulus to elicit pain), unprovoked (pain in the absence of stimulus), and mixed (provoked and unprovoked).
A thorough examination and appropriate laboratory testing should be performed to exclude infections, dermatoses, and neoplasms. Neurologic conditions and referred pain from the genitourinary or gastrointestinal tracts should also be excluded. This chapter will focus on strategies for the management of vulvodynia.
Management should focus on excluding other etiologies of vulvar pain. Symptomatic relief is a priority. In addition to the physical discomfort, patients also find vulvodynia psychologically distressing and socially embarrassing. A multidisciplinary approach to the treatment of vulvodynia includes dermatology, gynecology, rehabilitation medicine, physical therapy, neurology, gastroenterology, urology, and others as indicated.
Once vulvodynia is diagnosed and all other potential etiologies of vulvar pain have been excluded, treatment options include topical anesthetics, antidepressants (tricyclics, selective serotonin reuptake inhibitors), anticonvulsants, and pelvic floor physical therapy. Relief may not be immediate, and the patient should be advised to undergo an adequate course of therapy before determining treatment failure. Surgical intervention (vestibulectomy) should be reserved for the treatment of refractory cases of localized vulvodynia.
Clinical visual and manual examination of the vulva, vagina, oral cavity, conjunctivae, total body skin, scalp, and nails
Clinical palpation of inguinal lymph nodes
Sensory testing for light touch and cotton swab evaluation of the vulva and vaginal vestibule
Normal saline wet mount of vaginal secretions (Trichomonas vaginalis, bacterial vaginosis, atrophic vaginitis)
pH assessment of vaginal secretions (bacterial vaginosis, atrophic vaginitis, inflammatory vaginitis)
Whiff test (bacterial vaginosis)
KOH microscopic examination (fungi, scabies infestation)
Microbiologic cultures (bacterial, fungal, viral)
Tape test, if perianal pruritus present (Enterobius vermicularis, pinworms)
Papanicolaou smear (in conjunction with gynecology)
Colposcopy of vulva (in conjunction with gynecology)
Biopsy, if lesion present
Blood glucose (recurrent candidiasis in diabetes mellitus)
Patch testing (allergic contact dermatitis)
Evaluation for the presence of primary or concomitant psychiatric disorders
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The article provides a practical approach to the evaluation of patients with vulvar symptoms including history, vulvar examination and associated diagnostic tests.
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Comprehensive review of medical and surgical interventions for treatment of vulvodynia.
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The article provides guidelines for the management of vulvodynia as recommended by the British Society for the Study of Vulval Disorders Guideline Group.
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A thorough review of the many etiologies for vulvar pain with specific focus on the pathogenesis, diagnosis, and treatment of vulvodynia.
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This review of the literature provides information on the diagnosis and treatment of vulvodynia.
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In a 12-week randomized, double-blinded, placebo-controlled trial, 133 women with vulvodynia were assigned to one of four treatment arms. Oral desipramine and topical lidocaine, as monotherapy or in combination, reduced provoked pain to the same degree as placebo. This suggests the importance of the placebo effect in the treatment of vulvodynia.
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A prospective cohort study of 209 women diagnosed with vulvodynia and treated initially with a tricyclic antidepressant (amitriptyline in 183 patients, desipramine in 23, and others in three). Of 83 women taking a tricyclic antidepressant at first follow-up (median 3.2 months), 59.3% improved by >50% versus 38% of women not taking a tricyclic antidepressant.
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Thirty-two women were treated with a tricyclic antidepressant and behavioral interventions: a complete response was recorded in 47% after 6 months.
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Sixty-one women with vulvar vestibulitis were instructed to place a cotton ball coated with 5% lidocaine ointment in the vestibule and apply the ointment to the affected areas nightly for an average of 7 weeks: 57% reported a 50% or greater reduction in pain with intercourse. Nearly two-thirds of the women who were unable to have intercourse prior to treatment reported the ability to have intercourse after treatment.
Harris G, Horowitz B, Borgida A. J Reprod Med 2007; 52: 103–6.
A retrospective chart review of 152 women diagnosed with generalized vulvodynia, treated with gabapentin as monotherapy and followed for at least 30 months; 64% experienced at least 80% resolution of symptoms; 32% did not have adequate resolution. Sleep disturbance was the only comorbidity found to negatively affect gabapentin efficacy. There was a trend towards a less favorable response to gabapentin in patients with longer periods of untreated vulvodynia.
Jerome L. Pain Res Manage 2007; 12: 212–14.
Case report of a 62-year-old woman with a 20-year history of vulvodynia recalcitrant to other medications who responded positively to pregabalin.
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A retrospective study of 51 patients with vulvodynia treated with gabapentin cream 2% to 6% three times daily for 8 weeks. 80% of patients showed at least 50% reduction in pain scores.
Gentilecore-Saulnier E, McLean L, Goldfinger C, Pukall CF, Chamberlain S. J Sex Med 2010; 7: 1003–22.
Eleven women with provoked vestibulodynia and 11 control subjects underwent pelvic floor muscle evaluation and therapy (eight sessions). Abnormal pelvic floor muscle function was noted at baseline in provoked vestibulodynia subjects. Following physical therapy, no difference in pelvic floor muscle function was noted between controls and provoked vestibulodynia subjects. Self-reported pain assessment was not included as an end-point.
Forth HL, Cramp MC, Drechsler WI. J Obstet Gynaecol 2009; 29: 423–9.
Fourteen patients with vulvodynia underwent physiotherapy treatment for 3 months. All patients self-reported reduction in vulvar pain.
McKay E, Kaufman RH, Doctor U, Berkova Z, Glazer H, Redko V. J Reprod Med 2001; 46: 337–42.
Twenty-nine patients performed biofeedback-assisted pelvic floor muscle rehabilitation exercises. Of the 29 women, 20 (69%) became sexually active and 24 (83%) reported negligible or mild pain. Five of the 29 did not show any significant improvement.
Danielsson I, Torstensson T, Brodda-Jansen G, Bohm-Starke N. Acta Obstet Gynecol Scand 2006; 85: 1360–7.
A prospective, randomized study of 46 women with vulvar vestibulitis treated with either electromyographic (EMG) biofeedback or topical lidocaine for 4 months. Both groups showed statistically significant improvements on vestibular pain measurements, sexual functioning, and psychosocial adjustment at 12 months’ follow-up. No differences were detected between the treatment groups. Compliance with EMG biofeedback training was low.
Walsh KE, Berman JR, Berman LA, Vierregger K. J Gend Specif Med 2001; 5: 21–7.
Thirty-four women were treated with 0.2% nitroglycerin cream applied directly to the skin of the affected area at least three times per week, 5 to 10 minutes prior to sexual relations. Nearly all reported a significant improvement in pain.
Danielsson I, Sjoberg I, Ostman C. Acta Obstet Gynecol Scand 2001; 80: 437–41.
Fourteen young women with vulvar vestibulitis were enrolled in the study, and 13 completed the acupuncture treatment a total of ten times. For evaluation, quality-of-life (QOL) assessments were made before starting the treatment and then at 1 week and 3 months post treatment. The treatment was well tolerated, and QOL measurements were all significantly higher both after the last acupuncture and at 3 months, compared to pretreatment measures.
Pelletier F, Parratte B, Penz S, Moreno JP, Aubin F, Humbert P. Br J Dermatol 2011; 164: 617–22.
Twenty women with provoked vestibulodynia were treated with botulinum toxin A injection (100 U divided between the bulbospongiosus muscles). Three and 6 months after injection, 80% of patients reported reduced pain and improved sexual function.
Petersen CD, Giraldi A, Lundvall L, Kristensen E. J Sex Med 2009; 6: 2523–37.
A randomized, double-blinded, placebo-controlled study of 64 women with vulvodynia evaluated injection of Botox or saline placebo. Both Botox and saline placebo injection resulted in significant reduction in visual analog pain scores, but no differences were noted between the two groups.
These authors do not recommend injection of botulinum toxin given these data.
Bornstein J, Tuma R, Farajun Y, Azran A, Zarfati D. J Pain 2010; 11: 1403–9.
A placebo-controlled trial of topical nifedipine in 30 patients with localized provoked vulvodynia showed no difference between the nifedipine group and placebo group in terms of patient self-report of pain.
Farajun Y, Zarfati D, Abramov L, Livoff A, Bornstein J. Obstet Gynecol 2012; 120: 565–72.
Enoxaparin (low molecular weight heparin) subcutaneous injection provided greater reduction in pain scores compared to saline injection in 40 patients with severe, localized, provoked vulvodynia. This novel medical therapy, though not risk-free, may be reasonable prior to undertaking vestibulectomy.
Harlow BL, Abenhaim HA, Vitonis AF, Harnack L. J Reprod Med 2008; 53: 171–8.
A population-based, case-control study of women with and without vulvodynia: 242 vulvodynia cases and 242 controls were assessed for dietary oxalate consumption in order to calculate the odds ratio for developing vulvodynia as a result of self-reported consumption of dietary oxalate. No differences were observed in oxalate consumption patterns between patients and controls. There was no increase in the risk of developing vulvodynia with increasing tertiles of estimated oxalate intake.
Shafik A. Eur J Obstet Gynecol Reprod Biol 1998; 80: 215–20.
Eleven women with vulvodynia ranging in age from 28 to 53 years had a significant increase in pudendal nerve terminal motor latency, and motor and sensory changes suggested a pudendal canal syndrome. Pudendal nerve block, as a diagnostic and therapeutic test, effected temporary pain relief. Pudendal nerve decompression was performed via a fasciotomy to release the pudendal nerve in the ischiorectal fossa. Vulvar pain disappeared in nine of the 11 patients. Stress urinary incontinence was relieved in four of six patients, anal reflex normalized in five of seven, and vulvar and perineal hypoesthesia in four of six.
Bergeron S, Binik YM, Khalife S, Pagidas K, Glazer HI, Meana M, et al. Pain 2001; 91: 297–306.
Seventy-eight women were randomly assigned to a 12-week trial of group cognitive behavioral therapy, EMG biofeedback, or vestibulectomy. After 6 months, completers of the study had statistically significant reductions on pain measures regardless of treatment assignment; the vestibulectomy group was slightly more successful than the two other groups.
Gaunt G, Good A, Stanhope CR. J Reprod Med 2003; 48: 591–5.
A retrospective chart review of 42 patients post vestibulectomy at the Mayo Clinic from 1992 to 2001. Thirty-eight (90%) had a significant improvement in their symptoms.
Pukall C, Kandyba K, Amsel R, Khalife S, Binik Y. J Sex Med 2007; 4: 417–25.
A case series of eight women with vulvar vestibulitis syndrome who underwent six hypnotherapy sessions. Pain and psychosexual questionnaires were administered at baseline and 1 and 6 months after treatment. Significant reductions in gynecologic examination pain and intercourse pain were noted. Overall sexual function and satisfaction increased after treatment. Patients reported satisfaction with treatment and rated the achieved pain reduction as average.
Nair A, Klapper A, Kushnerik V, Margulis I, Del Priore G. Obstet Gynecol 2008; 111: 545–7.
A postmenopausal woman with chronic vulvar and deep pelvic pain refractory to oral pain medications underwent spinal cord stimulator implantation. Ten months after surgery, the patient’s pain had improved by 80%.
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