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Welcome to the Vulvar Disorders
File
Patients all over the world
have used the information in The Vulvar Disorders File since
1992, when the Center for Current Researchone of the first
80 companies on the Internetwas founded. Our highly trained
researchers (all of whom hold Ph.D.s) have searched the advanced
medical database at the National Library of Medicine and compiled
a comprehensive collection of research descriptions on vulvar
disorders and their care.
As you will see, the following research descriptions detail the
findings published in the most respected journals in the field.
Because the research descriptions are written in medical terms,
most people will bring all or parts of the Vulvar Disorders File to their doctor
for further explanation and discussion. Often your doctor will
have access to full-text articles and other information that
could be useful in planning a successful course of treatment
and prevention. Note that the titles of the journals are abbreviated
according to the National Library of Medicine's format; your
doctor can provide the full title if you need it.
Thank you for accessing the Vulvar Disorders File. We truly hope the information
fosters better health.
Sincerely,
Gregory A. Fraser, Ph.D.
Director of Research
Important Note: The following information
is provided for your education. It should not be relied upon for
personal diagnosis or treatment. If you believe that a
particular therapy applies to you or someone you care about, be
sure to consult a doctor before trying it.
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Latest Research on
Vulvar Disorders
BJOG. 2008 Mar;115(4):509-14.
Life events in patients with vulvodynia.
Plante AF, Kamm MA.
Department of Gastroenterology, St Mark's Hospital, London, UK
OBJECTIVE: Vulval pain, in the absence of pathology, may have a psychological
basis that relates to life events. This study aimed to determine the nature of
such events. DESIGN: Structured questionnaire about patient's symptoms and
early-life events. SETTING: Private practice physiotherapist specialising in
pelvic floor disorders. POPULATION: Patients with vulvodynia as their primary
symptom and control patients being treated for urinary tract disorder or
post-childbirth routine physiotherapy who had no vulval pain on direct
questioning. METHODS: Questionnaire applied to consecutive patients referred for
treatment. Seventy-eight consecutive women presenting with vulvodynia (mean age
34 years, mean duration of symptoms 48 months) and 78 controls (mean age 39
years). MAIN OUTCOME MEASURES: Incidence of life events. RESULTS: A similar
proportion of both groups were married. Being in a new relationship (P < 0.04),
adverse current or previous relationships (39 versus 9%, P < or =
0.01), parental divorce (26 versus 9%, P < or = 0.001), history of termination
of pregnancy, and adverse childbirth experiences (P < 0.04) were more common in
patients than in controls. A history of sexual abuse was not more common in
patients with vulvodynia compared with controls (13 versus 10%, P = not
significant). Lack of libido was common in patients with vulvodynia (94 versus
29%, P < 0.0001). CONCLUSIONS: Adverse life experiences, including conflict, are
common in women with vulvodynia. These factors may be important in mediating the
genesis of pain through stress-related mechanisms. Sexual interest is diminished
in these women. Sexual abuse is not a factor in most of these women. These
findings have implications for treatment.
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Pain Physician. 2008 Mar;11(2):215-24.
Ultrasound-guided interventional procedures for patients with chronic pelvic
pain - a description of techniques and review of literature.
Peng PW, Tumber PS.
Department of Anesthesia and Pain Management, Toronto Western Hospital,
University of Toronto, Toronto, Ontario, Canada.
Chronic pelvic pain can present in various pain syndromes. In particular,
interventional procedure plays an important diagnostic and therapeutic role in 3
types of pelvic pain syndromes: pudendal neuralgia, piriformis syndrome, and
"border nerve" syndrome (ilioinguinal, iliohypogastric, and genitofemoral nerve
neuropathy). The objective of this review is to discuss the ultrasound-guided
approach of the interventional procedures commonly used for these 3 specific
chronic pelvic pain syndromes. Piriformis syndrome is an uncommon cause of
buttock and leg pain. Some treatment options include the injection of the
piriformis muscle with local anesthetic and steroids or the injection of
botulinum toxin. Various techniques for piriformis muscle injection have been
described. CT scan and EMG-guidance are not widely available to interventional
physicians, while fluoroscopy exposes the performers to radiation risk.
Ultrasound allows direct visualization and real-time injection of the piriformis muscle. Chronic neuropathic pain arising from the lesion or dysfunction
of the ilioinguinal nerve, iliohypograstric nerve, and genitofemoral nerve can
be diagnosed and treated by injection to the invloved nerves. However, the
existing techniques are confusing and contradictory. Ultrasonography allows
visualization of the nerves or the structures important in the identification of
the nerves and provides the opportunities for real-time injections. Pudendal
neuralgia commonly presents as chronic debilitating pain in the penis, scrotum,
labia, perineum, or anorectal region. A pudendal nerve block is crucial for the
diagnosis and treatment of pudendal neuralgia. The pudendal nerve is located
between the sacrospinous and sacrotuberous ligaments at the level of ischial
spine. Ultrasonography, but not the conventional fluoroscopy, allows
visualization of the nerve and the surrounding landmark structures.
Ultrasound-guided techniques offer many advantages over the conventio
nal techniques. The ultrasound machine is portable and is more readily available
to the pain specialist. It prevents patients and healthcare professionals from
the exposure to radiation during the procedure. Because it allows the
visualization of a wide variety of tissues, it potentially improves the accuracy
of the needle placement, as exemplified by various interventional procedures in
the pelvic regions aforementioned.
-----
J Reprod Med. 2008 Feb;53(2):102-10.
Influence of oral contraceptive use on the risk of adult-onset vulvodynia.
Harlow BL, Vitonis AF, Stewart EG.
Division of Epidemiology and Community Health, School of Public Health,
University of Minnesota, 1300 South 2nd Street, Suite 300, Minneapolis, MN
55454, USA. harlow@epi.umn.edu
OBJECTIVE: To examine the association of adult-onset vulvodynia with oral
contraceptive use. STUDY DESIGN: We conducted a population-based study of 177
women experiencing vulvar pain consistent with clinical criteria for vulvodynia
and community-matched controls. Analyses were repeated and validated in
clinically confirmed clinic-based and population-based cases and matched
controls. RESULTS: In our analyses of population-based cases and controls, oral
contraceptive use was associated with a nonsignificant, 30% increase in the risk
of vulvodynia (95% CI 0.7-2.3) and was highest among women whose first use
occurred before age 18 (OR = 2.5, 95% CI 1.1-5.8). These findings were similar
when restricted to clinically confirmed cases. CONCLUSION: These findings do not
support the strong associations observed in clinic-based studies. In our study,
clinically confirmed clinic-based cases, as compared to population-based cases,
were more often oral contraceptive users, earlier-age users and users for longer periods. Thus, observational studies using clinic-based
cases might not adequately represent oral contraceptive use in all women with
vulvodynia.
-----
Clin J Pain. 2008 Feb;24(2):155-71.
The treatment of provoked vestibulodynia: a critical review.
Landry T, Bergeron S, Dupuis MJ, Desrochers G.
Department of Sexology, Université du Québec à Montréal, Montreal, Canada.
landry.tina@courrier.uqam.ca
OBJECTIVE: To carry out a critical review of published studies concerning the
treatment of provoked vestibulodynia. METHODS: MEDLINE, PsycINFO, and Cochrane
were used to identify treatment studies published between January 1996 and
December 2006. All studies published in English that dealt specifically with the
treatment of provoked vestibulodynia were included in the review regardless of
their methodological quality. Thirty-eight treatment studies were thus examined
in the present paper. RESULTS: Since 1996, surgical treatment has received
somewhat less empirical attention. Nevertheless, it still boasts the best
success rates, which range from 61% to 94%. More studies have focused on medical
treatments, yielding success rates varying between 13% and 67%. Behavioral
treatments have been the least studied, although 35% to 83% of patients benefit
from them. Despite these interesting results, only 5 of the 38 treatment studies
reviewed are randomized clinical trials. Furthermore
, the majority of studies have several methodological weaknesses, such as the
absence of (1) control or placebo group, (2) double-blind evaluation, (3)
pretreatment pain evaluation, and (4) validated measures of pain and sexual
functioning. DISCUSSION: On the basis of the results of the reviewed prospective
studies and the randomized clinical trials, vestibulectomy is the most
efficacious treatment to date. Though some medical treatments seem little
effective, others appear promising and should be investigated further, as is the
case with behavioral treatments. Additional randomized clinical trials are
necessary to confirm the efficacy of surgery and validate nonsurgical treatments
for provoked vestibulodynia.
-----
Dermatol Online J. 2008 Jan 15;14(1):2.
Vulvodynia.
Ventolini G, Barhan SM.
Wright State University, USA.
Vulvodynia or vulvar pain syndrome is a chronic, heterogeneous, and
multifactorial disease with a high prevalence. This condition affects
Caucasians, African Americans, Africans and Hispanic women, particularly those
sexually active at child-bearing age. The etiology of this condition is complex
and remains elusive. An accurate diagnosis requires a comprehensive history,
physical examination and targeted diagnostic tests. Although many treatment
options have been utilized, a rational therapeutic strategy is still under
research. Psychological counseling and group support should be considered in all
cases.
-----
Obstet Gynecol. 2008 Jan;111(1):159-66.
Surgical and behavioral treatments for vestibulodynia: two-and-one-half year
follow-up and predictors of outcome.
Bergeron S, Khalifé S, Glazer HI, Binik YM.
Department of Sexology, Université du Québec à Montréal, Montréal, Québec,
Canada. bergeron.sophie@uqam.ca
OBJECTIVE: To estimate whether treatment gains for provoked vestibulodynia
participants randomly assigned to vestibulectomy, biofeedback, and
cognitive-behavioral therapy in a previous study would be maintained from the
last assessment-a 6-month follow-up-to the present 2.5-year follow-up. Although
all three treatments yielded significant improvements at 6-month follow-up,
vestibulectomy resulted in approximately twice the pain reduction as compared
with the two other treatments. A second goal of the present study was to
identify predictors of outcome. METHODS: In a university hospital, 51 of the 78
women from the original study were reassessed 2.5 years after the end of their
treatment. They completed 1) a gynecologic examination involving the cotton-swab
test, 2) a structured interview, and 3) validated pain and sexual functioning
measures. RESULTS: Results from the multivariate analysis of variance conducted
on the pain measures showed a significant time main effect (P<.05) and a significant treatment main effect (P<.01), indicating that participants
had less pain at the 2.5-year follow-up than at the previous 6-month follow-up.
Results from the multivariate analysis of variance conducted on sexual
functioning measures showed that participants remained unchanged between the
6-month and 2.5-year follow-up and that there were no group differences. Higher
pretreatment pain intensity predicted poorer outcomes at the 2.5-year follow-up
for vestibulectomy (P<.01), biofeedback (P<.05), and cognitive-behavioral
therapy (P<.01). Erotophobia also predicted a poorer outcome for vestibulectomy
(P<.001). CONCLUSION: Treatment gains were maintained at the 2.5-year follow-up.
Outcome was predicted by pretreatment pain and psychosexual factors. LEVEL OF
EVIDENCE: II.
-----
Medscape J Med. 2008 Jan 30;10(1):23.
The use of amielle vaginal trainers as adjuvant in the treatment of
vestibulodynia: an observational multicentric study.
Murina F, Bernorio R, Palmiotto R.
V. Buzzi Hospital, Milan, Italy Author's email: filippomurina@tin.it.
OBJECTIVE: To assess the effectiveness of a specific set of vaginal dilators (Amielle
Comfort) as a part of vestibulodynia therapy. STUDY DESIGN: Fifteen women
referred for vestibulodynia, localized vulvodynia, were advised to use vaginal
dilators (Amielle Comfort) accompanied by standardized instructions, after
previously receiving 1 or more therapies for the vestibulodynia. RESULTS: The
post-treatment Marinoff scale for dyspareunia significantly improved in patients
after vaginal dilator treatment compared with baseline values (2.2 +/- 0.4 vs
1.1 +/- 0.9; P < .01), and the Female Sexual Function Index scores were
significantly improved compared with the prestudy values (16.3 +/- 5.5 vs 25.3
+/- 7.5; P < .01). CONCLUSION: Among women with previous therapy for
vestibulodynia, vaginal dilator use was associated with improvement in symptoms.
Vaginal dilators can play an important role in overcoming pelvic floor muscular
responses that remain and sometimes increase after pain pe
rception has decreased.
-----
Am J Obstet Gynecol. 2008 Jan;198(1):41.e1-5. Epub 2007 Oct 22.
Multilevel local anesthetic nerve blockade for the treatment of vulvar
vestibulitis syndrome.
Rapkin AJ, McDonald JS, Morgan M.
Department of Obstetrics and Gynecology, David Geffen School of Medicine at UCLA
Los Angeles, CA, USA.
OBJECTIVE: Vulvar vestibulitis syndrome is a major cause of dyspareunia. This
pilot study was designed to evaluate a novel treatment approach. STUDY DESIGN:
This is a prospective study of 27 women with vulvar vestibulitis. The protocol
included 5 treatment sessions with caudal epidural, pudendal nerve block, and
vestibular infiltration of local anesthetic agents. RESULTS: There were
significant improvements in vestibular pain as determined by the
vulvalgesiometer, McGill pain questionnaire, self-report, and the Female Sexual
Functioning Inventory. CONCLUSION: Serial multilevel nerve blocks administered
for the treatment of vulvar vestibulitis is a conceptually neurophysiologically
based modality that may be effective and merits a placebo-controlled study.
-----
Obstet Gynecol Surv. 2007 Dec;62(12):812-9.
Vulvodynia: new thoughts on a devastating condition.
Gunter J.
Pelvic Pain and Vulvovaginal Disorders, Kaiser Northern California, OB/GYN, San
Francisco, California 94115, USA. jennifer.gunter@kp.org
Vulvodynia affects 3% to 15% of women; many suffer through years of misdiagnosis
and for those who receive care cures are uncommon. Little is known about the
etiology and a wide range of therapeutic options are available. With treatment
approximately 50% of women will report sustained improvement in pain scores of
50% or more, however, reasons for varied response rates are yet unknown. This
article will explore 3 factors that may contribute to inconsistent results with
therapy; the hypothesis that vulvodynia is a systemic disorder; the idea that
failure to address the psychological or emotional aspect or chronic pain may
affect outcome; and the concept that chronic vulvar pain, like headache, is not
a single condition but is a diverse group of disorders that produce the same
symptom. TARGET AUDIENCE: Obstetricians & Gynecologists, Family Physicians
LEARNING OBJECTIVES: After completion of this article, the reader should be able
to state that vulvodynia is a complex disorder, explain that no one treatment is
superior, relate that pathophysiology is important, and recall that
psychological aspects of chronic pain must be appreciated.
-----
Gynecol Oncol. 2007 Dec 21 [Epub ahead of print]
Comparison of outcome measures in patients with advanced squamous
cell carcinoma of the vulva treated with surgery or primary chemoradiation.
Landrum LM, Skaggs V, Gould N, Walker JL, McMeekin DS.
Department of Obstetrics and Gynecology, Section of Gynecologic Oncology,
University of Oklahoma Health Sciences Center, PO Box 26901, Williams Pavilion
2410, Oklahoma City, OK 73190, USA.
OBJECTIVE.: To review outcome measures including overall survival (OS),
progression free survival (PFS), and patterns of recurrence in patients with
advanced vulvar cancer managed by primary surgery (PS) or primary chemoradiation
(PCRT) as well as population characteristics for the two groups. METHODS.:
Patients diagnosed with stage III and IV squamous cell carcinoma of the vulva
from 1990 to 2006 were identified for retrospective analysis at a single
institution. Charts were abstracted for clinical and pathologic findings,
treatment modalities, complications, recurrence, and follow-up. Kaplan-Meier
method was used to determine PFS and OS. RESULTS.: Sixty-three patients with
stage III (n=47) and IV (n=16) carcinoma of the vulva were identified; 30
patients were treated with PS, and 33 patients had tumor that was unresectable
by vulvectomy and underwent PCRT. Patients treated with PCRT were younger (61
vs. 72 years; p=0.09), had less metastasis to lymph nodes (54% vs. 83%, p=0.01),
and larger tumors (6 vs. 3.5 cm, p=0.0001) compared to patients treated with PS.
Despite these differences, OS for the PS and PCRT groups was 69% and 76% (NS),
respectively, with median follow-up at 31 months. There were no differences in
PFS or recurrence rates between the two groups. By multivariate analysis, age
was the only significant predictor of OS or PFS. CONCLUSIONS.: Patients with
advanced vulvar cancer that are managed with PS tend to be older patients that
have smaller lesions but positive lymph nodes, whereas patients requiring PCRT
are younger and have larger volume disease but fewer lymph node metastases.
Despite these differences, patients treated with PS and PCRT have no differences
in OS, PFS, or recurrence rates. Age is the most powerful predictor of survival
when size, lymph node status, stage and treatment are accounted for.
-----
Obstet Gynecol Clin North Am. 2007 Dec;34(4):783-802.
Vulvo-vaginal cancers: risks, evaluation, prevention and early
detection.
Duong TH, Flowers LC.
Division of Gynecologic Specialties, Section of Urogynecology and Pelvic
Reconstructive Surgery, 69 Jessie Hill Jr. Drive SE. Glenn Building 4th floor,
Rm 402, Atlanta, GA 30303, USA.
Vulvar and vaginal cancers are rare and account for approximately 7% of cancers
of the female reproductive tract. Vulvar and vaginal neoplasia share similar
risk factors: human papillomavirus infection, previous cervical intraepithelial
neoplasia or cervical cancer, current smoking, sexual factors, and
immunosuppression. Several treatment options are available for patients with
documented histologic high-grade intraepithelial vulvar or vaginal neoplasia,
including excision, laser vaporization, and 5-fluorouracil. After treatment,
lifetime follow-up with cytology and colposcopy is recommended. With the
widespread use of the human papillomavirus vaccine, one half to two thirds of
vulvar and vaginal cancers may be prevented. Patient education regarding
reduction of risk factors for progression and close surveillance of at-risk
individuals may prevent the progression to invasive disease.
-----
Int Urogynecol J Pelvic Floor Dysfunct. 2007 Nov 24 [Epub ahead of print]
Painful bladder syndrome/interstitial cystitis and vulvodynia: a
clinical correlation.
Peters K, Girdler B, Carrico D, Ibrahim I, Diokno A.
Department of Urology, William Beaumont Hospital, Royal Oak, MI, USA, dcarrico@beaumonthospitals.com.
Vulvodynia affects 25% of women with painful bladder syndrome/interstitial
cystitis (PBS/IC). The objective of our study was to clinically evaluate the
association of PBS/IC and vulvodynia and possible contributing factors. To our
knowledge, this has not been reported. Seventy women with PBS/IC were evaluated
from December 2005 to December 2006 with a comprehensive history and exam. Two
groups were formed-those with vulvodynia and those without vulvodynia for
comparison. Of the women, 51.4% had vulvodynia and 48.6% did not have vulvodynia
using our operative definition. Average levator pain levels were significantly
greater in those with vulvodynia. There was no significant difference in the
total number of lifetime pelvic surgeries, history of sexually transmitted
infections (STIs), vaginitis, or abuse history between groups. The correlation
of vulvodynia and PBS/IC may have been underestimated. Research needs to explore
the link between precipitating factors, symptoms, and effective treatment
options for PBS/IC and vulvodynia.
-----
J Reprod Med. 2007 Oct;52(10):912-6.
Improvement in vulvar vestibulitis with montelukast.
Kamdar N, Fisher L, MacNeill C.
Department of Obstetrics and Gynecology, Pennsylvania State University College
of Medicine, Hershey, PA 17033, USA.
OBJECTIVE: To determine if montelukast treatment improves symptoms in patients
with vulvar vestibulitis. STUDY DESIGN: We administered montelukast to a series
of patients with vestibulitis seen at the Pennsylvania State University
Vulvodynia Clinic over a period of 2.5 years. We reviewed outcomes using a
scoring scheme to quantify signs and symptoms, before and after treatment, in 29
montelukast-treated subjects and 18 subjects in a comparison group treated with
standard therapies. RESULTS: Subjects treated with montelukast showed an average
of 52% in improvement in symptoms as compared to a 15% improvement in the
controls (p < 0.0001). CONCLUSION: Montelukast is a viable treatment option for
women with vulvar vestibulitis. This finding implies that leukotrienes have a
role in the pathophysiology of vulvar vestibulitis.
-----
Arch Sex Behav. 2007 Sep 18; [Epub ahead of print]
"If Sex Hurts, Am I Still a Woman?" The Subjective Experience of
Vulvodynia in Hetero-Sexual Women.
Ayling K, Ussher JM.
Gender, Culture and Health Research Unit: PsyHealth, School of Psychology,
University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW, 1797,
Australia, j.ussher@uws.edu.au.
Vulvodynia has recently been recognized as a significant health problem among
women, with a considerable proportion experiencing psychological distress and
sexual dysfunction for many years. This study used a material-discursive
framework and a qualitative methodology to investigate women's subjective
experience of vulvodynia within the context of a hetero-sexual relationship, and
their negotiation of coitus, commonly associated with vulvar pain. Seven women,
who had experienced vulvodynia between 2 and 10 years, took part in in-depth
interviews. Thematic decomposition drawing on a Foucauldian framework for
interpretation identified that six of the seven women took up subject positions
of "inadequate woman" and "inadequate partner," positioning themselves as
failures for experiencing pain during coitus, which they interpreted as
affecting their ability to satisfy their partners sexually, resulting in
feelings of shame, guilt, and a decreased desire for sexual contact. This was
interpreted in relation to dominant discourses of femininity and
hetero-sexuality, which conflate a woman's sexuality with her need to be
romantically attached to a man, position men as having a driven need for sex,
and uphold coitus as the organizing feature of hetero-sex. Only one woman
positioned herself as an "adequate woman/partner," associated with having
renegotiated the coital imperative and the male sex drive discourse within her
relationship. These positions, along with women's agentic attempts to resist
them, were discussed in relation to their impact on hetero-sexual women's
negotiation of vulvodynia. Implications for future research and vulvodynia
treatment regimes are also raised.
-----
Clin Obstet Gynecol. 2007 Sep;50(3):745-51.
Unique dermatologic aspects of the postmenopausal vulva.
Summers PR, Hunn J.
Department of Obstetrics and Gynecology, University of Utah School of Medicine,
Salt Lake City, Utah, USA. paul.summers@hsc.utah.edu
Aging and estrogen deficiency compromise the skin barrier's defense mechanisms,
resulting in greater microbial colonization of the skin. Susceptibility to
mechanical injury and chemical irritation also increases. Menopause blunts the
cell-mediated immune response to microbes and allergens. Healing after an insult
is delayed. Skin disorders such as lichen sclerosus or allergic dermatitis may
not be clinically obvious. A biopsy interpreted by a dermatopathologist is often
helpful. Some conditions require long-term use of topical steroid ointments, and
antimicrobial therapy. A compounding pharmacist may be necessary to find a base
for the topical cream that does not irritate.
-----
J Reprod Med. 2007 Jul;52(7):645-53.
Novel bioadhesive patch-type system for photodynamic vulvodynia
therapy after delivery of 5-aminolevulinic acid: preliminary evaluation.
Zawislak AA, McCarron PA, McCluggage WG, Donnelly RF, Price JH,
McClelland HR, Woolfson AD.
Department of Gynaecology, Belfast City Hospital; School of Pharmacy, Queen's
University Belfast, UK.
OBJECTIVE: To assess the applicability of photodynamic therapy (PDT) in the
management of vulvodynia whereby a novel, patch-type system, loaded with
5-aminolevulinic acid (ALA), was used to administer PDT to vulvar regions
displaying the characteristics of vulvodynia. STUDY DESIGN: Eleven patients
underwent PDT using a bioadhesive patch to deliver ALA over 4 hours. A nonlaser
light source delivered 100 J cm(-2) to the target area using red light of 630
nm. Fluorescence of protoporphyrin IX was observed under ultraviolet light
illumination, with no significant difference found between that produced after
the first and second applications of the patch. RESULTS: There was a significant
reduction (p= 0.0077) in overall symptoms after completion of treatment. No
significant alleviation (p = 0.1088) in pain during intercourse was observed
following treatment. Eight patients experienced a symptomatic response, while 3
exhibited no improvements in symptoms. No adverse reactions or worsening of
reported symptoms was reported. CONCLUSION: The results suggest that PDT is of
value in the management of vulvodynia, most probably as a viable option to
conventional approaches. Further studies involving larger numbers of patients
are required to confirm the efficacy of PDT in the management of vulvodynia.
-----
Gynecol Obstet Invest. 2007 Jul 27;64(4):180-186 [Epub ahead of print]
Pimecrolimus Cream 1% for Treatment of Vulvar Lichen Simplex
Chronicus: An Open-Label, Preliminary Trial.
Goldstein AT, Parneix-Spake A, McCormick CL, Burrows LJ.
Division of Gynecologic Specialties, Department of Gynecology and Obstetrics,
Johns Hopkins Medicine, Baltimore, Md., USA.
Background: To evaluate efficacy and safety of pimecrolimus cream 1% twice daily
for treatment of vulvar lichen simplex chronicus (LSC). Methods: Patients in
this 12-week, open-label study had biopsy-proven vulvar LSC. Inclusion criteria
were patient-reported Visual Analog Scale for Pruritus Relief >/=3 (VAS-PR, 0 cm
= no itching to 10 cm = severe itching) and Investigator's Global Assessment
>/=2 (IGA, 0 = no disease to 3 = severe disease). Safety was evaluated by
adverse event reports and pimecrolimus blood level measurements. Results: Twelve
women aged 25-53 years were enrolled. The median pruritus score (VAS-PR)
decreased from 6 (min. 4.9, max. 9.0) at baseline to 0 cm at week 4 (max. 4.2),
week 8 (max. 3.1) and week 12 (max. 2.1). Seven patients reported complete
resolution of pruritus by week 4. Median IGA decreased from 2.5 (min. 2, max. 3)
at baseline to 0 (min. 0, max. 2) at week 12. Erythema, excoriation, and
lichenification improved for all patients. Pimecrolimus blood concentration for
all samples was below the limit of quantification, 0.3 ng/ml. No adverse events
were reported. Conclusions: In this exploratory study, signs and symptoms of
vulvar LSC improved for all women and pimecrolimus cream showed a favorable
safety profile. Larger prospective studies are needed to further evaluate
pimecrolimus for treatment of vulvar LSC. Copyright (c) 2007 S. Karger AG,
Basel.
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Menopause. 2007 Jun 28; [Epub ahead of print]
Vulvar lichen sclerosus: effect of maintenance treatment with a
moisturizer on the course of the disease.
Simonart T, Lahaye M, Simonart JM.
From the 1Department of Dermatology, Erasme University Hospital; 2Department of
Gynaecology, Centre Medical des Champs Elysees; and 3private dermatological
practice, Brussels, Belgium.
OBJECTIVES:: Vulvar lichen sclerosus (LS) is an inflammatory disease of unknown
etiology that may result in significant discomfort and psychological distress in
postmenopausal women. One of the most troublesome features of LS is its
chronically relapsing nature. The aim of this study was to investigate the
effect of maintenance therapy with a moisturizer in preventing the risk of
relapse and progression of vulvar LS in postmenopausal women. DESIGN:: Between
January 1995 and January 2006, 34 postmenopausal women with vulvar LS were
included in a prospective open trial. The participants were treated with a
topical corticosteroid cream (0.1% betamethasone valerate) once daily for 1
month and then with maintenance therapy with a moisturizing cream alone once
daily. Follow-up visits were scheduled after 1 month and then twice per year
(median follow-up, 58 mo). RESULTS:: Overall the symptoms of all women improved
after therapy with a topical steroid. Twenty-four women (71%) became symptom
free, and 10 (29%) experienced partial response. Eighteen of the 24 women (75%)
who became symptom free and 6 of the 10 women (60%) who exhibited a partial
response reported no worsening of their symptoms while on therapy with a cold
cream alone. Total resolution of the clinical signs occurred in 6 of the 19
women with mild vulvar architectural changes. Partial resolution of clinical
signs was observed in 22 women (64%). No change was noticed in six (18%) women.
None of the participants experienced worsening of vulvar scarring. None of the
participants developed vulvar intraepithelial neoplasia or squamous cell
carcinoma during the follow-up period. There were no side effects. CONCLUSION::
Long-term maintenance therapy of vulvar LS with a moisturizing cream can
maintain the symptom relief induced by topical corticosteroids in women with
vulvar LS while being safe and inexpensive. This treatment may also be
associated with a reduction in topical corticosteroid use because more than half
of the women could eliminate corticosteroids altogether.
-----
J Reprod Med. 2007 May;52(5):379-84.
Is localized, provoked vulvodynia an inflammatory condition?
Eva LJ, Rolfe KJ, MacLean AB, Reid WM, Fong AC, Crow J, Perrett CW.
Department of Obstetrics and Gynecology, Royal Free and University College
Medical School, Royal Free Campus, London, UK.
OBJECTIVE: To perform a pilot study to investigate the relationship between
localized, provoked vulvodynia of the vestibule and inflammatory cytokine
expression. STUDY DESIGN: Women with a diagnosis of localized, provoked
vulvodynia had tissue samples taken for vulvar expression of Interleukin 1alpha
and 1beta and tumor necrosis factor alpha and compared to those of a control
group. RESULTS: The study group did not show a significant increase in
expression of inflammatory markers. CONCLUSION: There was no evidence in this
study that localized, provoked vulvodynia is an inflammatory condition, as
previously thought. This may be helpful in explaining why some women are
resistant to medical or antiinflammatory treatment and may allow treatment to be
prescribed more effectively.
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ScientificWorldJournal. 2006 Mar 7;6:2066-79.
Clinical holistic medicine: holistic sexology and acupressure
through the vagina (hippocratic pelvic massage).
Ventegodt S, Clausen B, Omar HA, Merrick J.
Many gynecological and sexological problems (like urine incontinence, chronic
pelvic pains, vulvodynia, and lack of lust, excitement, and orgasm) are
resistant to standard medical treatment. In our work at the Research Clinic for
Holistic Medicine in Copenhagen, we have found that vaginal acupressure, or
Hippocratic pelvic massage, can help some of these problems. Technically, it is
a very simple procedure as it corresponds to the explorative phase of the
standard pelvic examination, supplemented with the patient's report on the
feelings it provokes and the processing and integration of these feelings.
Sometimes it can be very difficult to control the emotions released by the
technique, i.e., regression to earlier traumas from childhood sexual abuse. This
review discusses the theory behind vaginal acupressure, ethical aspects, and
presentation of a case story. This procedure helped the patient to become
present in her pelvis and to integrate old traumas with painful emotions.
Holistic gynecology and sexology can help the patient to identify and let go of
negative feelings, beliefs, and attitudes related to sex, gender, sexual organs,
body, and soul at large. Shame, guilt, helplessness, fear, disgust, anxiety,
anger, hatred, and other strong feelings are almost always an important part of
a sexual or functional problem as these feelings are "held" by the tissue of the
pelvis and sexual organs. Acupressure through the vagina/pelvic massage must be
done with great care by an experienced physician, with a third person present,
after obtaining consent and the necessary trust of the patient. It must be
followed by conversational therapy and further holistic existential processing.
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J Reprod Med. 2007 Feb;52(2):107-10.
Vulvodynia as a possible somatization disorder. More than just an
opinion.
Mascherpa F, Bogliatto F, Lynch PJ, Micheletti L, Benedetto C.
Department of Gynecology and Obstetrics, University of Torino, Torino, Italy.
franco.mascherpa@virgilio.it
Vulvodynia, defined as vulvar pain, soreness or burning as opposed to pruritus,
is a common and important problem. Despite its high prevalence and associated
distress, the etiology, diagnosis and management of this disorder have not been
clearly delineated. On the basis of recent advances in psychosomatic medicine,
vulvodynia can be considered a somatiform disorder affecting the vulva.
Psychosomatic assessment is useful in patients with vulvodynia. This review
covered recent advances in psychosomatic medicine with reference to somatization
disorders and their application to vulvodynia. According to the literature,
vulvodynia shares some basic criteria by which functional pain disturbances are
defined. Thus, all patients with vulvodynia should undergo psychologic and
sexual evaluation since in some instances psychotherapy may offer the only
successful approach to the alleviation of vulvar pain.
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J Reprod Med. 2007 Feb;52(2):103-6.
Evaluation of gabapentin in the treatment of generalized
vulvodynia, unprovoked.
Harris G, Horowitz B, Borgida A.
Department of Obstetrics and Gynecology, University of Connecticut, Farmington,
USA. chazzanmlp@aol.com
OBJECTIVE: To determine the efficacy of gabapentin in the treatment of
generalized vulvodynia, unprovoked, to determine the most common presenting
symptoms in patients with this diagnosis, to evaluate the prevalence of
comorbidities in these patients and to determine the possibility of
comorbidities or specific presenting symptoms that decrease the efficacy of this
drug. STUDY DESIGN: The charts of all women seen in our facility with a
diagnosis of generalized vulvodynia between January 1, 2002, and September 30,
2004, were reviewed. A total of 601 charts were reviewed. Patients were included
in the study if they had a diagnosis of generalized vulvodynia, they were
treated with single-agent gabapentin, had follow-up for 30 months or more and
had adequately documented follow-up. RESULTS: A total of 152 patients were
included in the study. Ninety-eight (64%) patients treated with gabapentin had
resolution of at least 80% of their symptoms during the study period. Forty-nine
(32%) did not have adequate resolution. There was a high percentage of
comorbidities in patients with generalized vulvodynia. Sleep disturbance was the
only comorbidity that negatively affected the efficacy of gabapentin. In
addition, there appeared to be a trend toward a less favorable response in
patients with a longer period of untreated illness (p value not less than 0.05).
Side effects of gabapentin were few. Forty (26%) reported some side effects.
Fatigue was the most common complaint. Seventeen patients (11%) discontinued the
medication secondary to side effects. CONCLUSION: Gabapentin appears to be very
effective in the treatment of generalized vulvodynia, unprovoked. It has a very
low side effect profile. Certain patients may be less likely to benefit from
gabapentin, including those with the comorbidity of sleep disturbance. Patients
with symptoms of longer-standing generalized vulvodynia, unprovoked, may also be
less likely to benefit from this treatment.
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Am J Obstet Gynecol. 2007 Feb;196(2):128.e1-6.
Assessment of vulvodynia symptoms in a sample of US women: a
prevalence survey with a nested case control study.
Arnold LD, Bachmann GA, Rosen R, Rhoads GG.
Department of Epidemiology, School of Public Health, University of Medicine and
Dentistry of New Jersey, Piscataway, NJ, USA.
OBJECTIVE: Vulvodynia is a chronic pain syndrome of unknown origin with scant
data on frequency. This study assessed the prevalence of vulvodynia symptoms in
a sample of US women and compared health characteristics of symptomatic and
asymptomatic women. STUDY DESIGN: A phone survey contacted 2127 US households to
identify 100 symptomatic women, who were matched on age and time zone to 325
asymptomatic controls. Odds ratios (ORs) and logistic regression were used to
model associations between pain, medical conditions, and health care utilization
variables. RESULTS: Current vulvar pain of at least 6 months duration was
reported by 3.8% of respondents, with a 9.9% lifetime prevalence. Forty-five
percent of women with pain reported an adverse effect on their sexual life and
27% an adverse effect on their lifestyle. Cases more frequently reported
repeated urinary tract infections (OR, 6.15; 95% CI, 3.51-10.77) and yeast
infections (OR, 4.24; 95% CI, 2.47-7.28). Associations existed with chronic
fatigue syndrome (OR, 2.78; 95% CI, 1.33-6.19), fibromyalgia (OR, 2.15; 95% CI,
1.06-4.36), depression (OR, 2.99; 95% CI, 1.87-4.80), and irritable bowel
syndrome (OR, 1.86; 95% CI, 1.07-3.23). CONCLUSION: Lifetime chronic vulvar pain
was less prevalent in this national sample of women than previous data suggest
and was correlated with several comorbid chronic medical conditions and
substantial reduction in self-reported quality of life.
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J Reprod Med. 2007 Jan;52(1):63-71.
Vulvodynia. Development of a psychosexual profile.
Jantos M, Burns NR.
School of Psychology, University of Adelaide, Adelaide, South Australia.
marek.jantos@adelaide.edu.au
OBJECTIVE: To assess the psychosexual profile of vulvodynia patients, focusing
on the age at onset and age distribution, and to analyze the impact of
vulvodynia on the emotional, social and sexual well-being of this patient
population. STUDY DESIGN: A retrospective review was performed of patient files
consisting of questionnaires, psychometric tests, sexual history,
electromyographic assessments and clinical notes. RESULTS: The highest
prevalence of vulvodynia in this clinical sample occurred before the age of 25
years; 75% of the 744 patients were under the age of 34. A comparison of primary
and secondary vulvodynia patients showed the average age at symptom onset to be
19.1 years for primary cases and 25.0 years for secondary cases. There were
significant differences in duration of symptoms, age at first sexual intercourse
and number of sexual partners, even when controlling for age (p < 0.001).
Marriage provided an effective buffer against depression and anxiety.
CONCLUSION: Vulvodynia can have an early onset and affect social relationships.
Given the psychologic distress associated with vulvodynia, early diagnosis and
treatment of the medical aspects are essential, as is focusing on the
psychosexual implications of this pain syndrome.
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J Reprod Med. 2007 Jan;52(1):19-22.
A qualitative study of women with vulvodynia: II. Response to a
multidisciplinary approach to management.
Munday P, Buchan A, Ravenhill G, Wiggs A, Brooks F.
Watford Sexual Health Centre and Department of Physiotherapy, West Hertfordshire
Hospitals National Health Service Trust, and Centre for Research in Primary and
Community Care, University of Hertfordshire, Watford, UK. pat.munday@whht.nhs.uk
OBJECTIVE: To evaluate the response of a group of women with vulvodynia who were
participating in an integrated, multidisciplinary management program comprising
medical evaluation and treatment, psychotherapy, physiotherapy and dietary
advice. STUDY DESIGN: Retrospective, qualitative, in-depth interview study.
RESULTS: Twenty-seven of 29 women reported a significant benefit, and 9 who had
completed the program were pain free. All women appreciated the integrated
approach, and even those who were not completely pain free found that they were
able to manage their condition satisfactorily. CONCLUSION: Further evaluation of
this program is warranted to assess whether it would be helpfulfor other women
with this problem.
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Clin Infect Dis. 2007 Jan 15;44(2):213-9. Epub 2006 Dec 13.
A randomized trial of the duration of therapy with metronidazole
plus or minus azithromycin for treatment of symptomatic bacterial vaginosis.
Schwebke JR, Desmond RA.
Department of Medicine, University of Alabama at Birmingham, Birmingham, AL
35294, USA. schwebke@uab.edu
BACKGROUND: Bacterial vaginosis (BV) is the most common cause of vaginitis
worldwide. Currently recommended treatments have poor efficacy and are
associated with high rates of BV recurrence. We examined whether a longer
duration of treatment with metronidazole or combination therapy with
metronidazole and azithromycin would enhance the cure rates for BV. In addition,
we examined factors other than drug therapy associated with cure. METHODS: Women
with symptomatic BV (defined by a modified Amsel criteria) were enrolled in a
4-arm study that compared metronidazole for 7 days versus 14 days, plus or minus
azithromycin on days 1 and 3. Data regarding interim behaviors were also
obtained, as were vaginal specimens for Gram staining. RESULTS: At the first
follow-up visit (7 days after the completion of therapy), there was a
significant difference in cure rates among patients who received 7 days of
metronidazole therapy, compared with those who received 14 days of therapy,
combined across azithromycin therapy (P=.0003). There was no effect associated
with azithromycin therapy. There were no differences in cure rates between any
of the treatment groups at 21 days after completion of therapy. Abstinence or
protected sex, refraining from douching, and a lower baseline Nugent score for
the vaginal Gram stain were all significantly associated with cure. CONCLUSIONS:
Cure rates for BV were significantly improved by 14 days of metronidazole
treatment (compared with 7 days of treatment), but the effects were not
sustained, suggesting that relapse or reinfection occurred. Combination therapy
with the addition of azithromycin had no benefit. Lower baseline Nugent
scores--presumably reflecting less complex vaginal flora--were significantly
associated with cure, as was refraining from unprotected sex and from douching.
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J Low Genit Tract Dis. 2006 Oct;10(4):245-51.
Treatment of vulvodynia with tricyclic antidepressants: efficacy
and associated factors.
Reed BD, Caron AM, Gorenflo DW, Haefner HK.
Department of Family Medicine, University of Michigan, Ann Arbor, MI 48109-0708,
USA. barbr@umich.edu
OBJECTIVE: To determine the efficacy of tricyclic antidepressants (TCAs) as
treatment for vulvodynia, and to identify demographic factors and pain
characteristics associated with improvement. MATERIALS AND METHODS: Between
January 2001 and April 2004, women diagnosed with vulvodynia were offered TCA
therapy. The patients rated their worst recent pain on a 10-point scale at
baseline and at follow-up; improvement was classified as at least 50% reduction
in reported pain from baseline. RESULTS: Of 271 women diagnosed with vulvodynia,
209 (77.1%) were treated initially with a TCA (amitriptyline [n = 183],
desipramine [n = 23], and other tricyclic medications [n = 3]). One hundred
sixty-two (59.8%) of the women were followed up at a median period of 3.2 months
after their initial visit, including 122 women who had started on a TCA. Of 83
women taking a TCA at the first follow-up, 49 (59.3%) improved by more than 50%,
compared with 30 of 79 women not taking TCA at follow-up (improvement rate =
38.0%; p =.007; odds ratio = 2.35; 95% CI = 1.23-4.42). Multivariate analysis
indicated that age, severity of pain, diagnosis (localized vs generalized vulvar
pain), length of time with pain before treatment, age at menarche, use of oral
contraceptives, and the number of previous pregnancies were not associated with
the outcome; however, taking a TCA at the time of the first follow-up was
strongly associated with improvement (p <.001; odds ratio = 4.23; 95% CI =
1.98-9.01). Repeated analysis including only those women prescribed with
amitriptyline rather than any tricyclic revealed similar results. CONCLUSIONS:
Women with vulvodynia who were prescribed a TCA in general (or amitriptyline,
specifically) were more likely to have pain improvement compared with those
women not taking these medications at follow-up. Randomized, controlled studies
of TCAs versus other treatments are needed to clarify the overall effectiveness
of these drugs.
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J Chemother. 2006 Aug;18(4):409-14.
Topical kanamycin: an effective therapeutic option in aerobic
vaginitis.
Tempera G, Abbadessa G, Bonfiglio G, Cammarata E, Cianci A, Corsello S, Raimondi
A, Ettore G, Nicolosi D, Furneri PM.
Department of Microbiological and Gynecological Sciences, University of Catania,
Via Androne 81, 95124 Catania, Italy. tempera@unict.it
Eighty-one patients with clinical diagnosis of aerobic vaginitis (AV) were
included in the study. The patients were randomized for treatment, 45 with
kanamycin (100 mg vaginal ovules for 6 days, consecutively) and 36 with
meclocycline (35 mg vaginal ovules for 6 days, consecutively). The patients were
examined before starting the study, 1-2 days after treatment and 30 days after
the end of the study. At the first follow-up the patients showed different
levels of symptom reduction. Reduction in the presence of leukocytes, vaginal
mucosa burning and itching were statistically significant in the group treated
with kanamycin with respect to the group treated with meclocycline. Moreover,
there was also reduced isolation of Enterobacteriaeae (97%) in the group treated
with kanamycin versus those treated with meclocycline (76%). At the second
follow-up, vaginal homeostasis (normalization of pH and presence of
lactobacilli) was more evident in the kanamycin-treated group. In conclusion,
our data suggest that the topical use of kanamycin could be considered a
specific antibiotic for the therapy of this new pathology.
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