Davis
SNP, Bergeron S, Binik YM, and Lambert B.
Article first published online: 12
SEP 2013 DOI: 10.1111/jsm.12309
The
Journal of Sexual Medicine
Introduction
Provoked vestibulodynia (PVD) is a
prevalent genital pain syndrome that has been assumed to be chronic, with
little spontaneous remission. Despite this assumption, there is a dearth of
empirical evidence regarding the progression of PVD in a natural setting.
Although many treatments are available, there is no single treatment that has
demonstrated efficacy above others.
Aims
The aims of this secondary analysis
of a prospective study were to (i) assess changes over a 2-year period in pain,
depressive symptoms, and sexual outcomes in women with PVD; and (ii) examine
changes based on treatment(s) type.Methods Participants completed questionnaire packages at Time 1 and a follow-up package 2 years later.
Main Outcome Measures Visual analog scale of genital pain, Global Measure of Sexual Satisfaction, Female Sexual Function Index, Beck Depression Inventory, Dyadic Adjustment Scale, and sexual intercourse attempts over the past month.
Results
Two hundred thirty-nine women with
PVD completed both time one and two questionnaires. For the sample as a whole,
there was significant improvement over 2 years on pain ratings, sexual
satisfaction, sexual function, and depressive symptoms. The most commonly
received treatments were physical therapy, sex/psychotherapy, and medical
treatment, although 41.0% did not undergo any treatment. Women receiving no
treatment also improved significantly on pain ratings. No single treatment type
predicted better outcome for any variable except depressive symptoms, in which
women who underwent surgery were more likely to improve.
Discussion
These results suggest that PVD may
significantly reduce in severity over time. Participants demonstrated
clinically significant pain improvement, even when they did not receive
treatment. Furthermore, the only single treatment type predicting better
outcomes was surgery, and only for depressive symptoms, accounting for only
2.3% of the variance. These data do not demonstrate the superiority of any one
treatment and underscore the need to have control groups in PVD treatment
trials, otherwise improvements may simply be the result of natural progression.
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