Psychotherapy and Pharmacotherapy for Sexual Dysfunctions

Author(s):  
Emmanuelle Duterte ◽  
Taylor Segraves ◽  
Stanley Althof

Well-controlled (Type 1 and Type 2) investigations have demonstrated the efficacy of psychological interventions for erectile dysfunctions. However, when the oral agent sildenafil was approved by the Food and Drug Administration in 1998, its introduction was nothing short of dramatic. Sildenafil is a phosphodiesterase Type 5 inhibitor (PDE 5) that enhances the man’s ability to achieve a natural erection given adequate psychic and physical stimulation. Unlike other interventions, such as self-injection, transurethral, or vacuum therapy, sildenafil does not induce erection irrespective of the man’s degree of arousal. Although myths abound, sildenafil does not improve libido, promote spontaneous erections, or increase the size of the penis. The efficacy of sildenafil has been demonstrated in Type 1 multiple double-blind, placebo-controlled, multicenter studies. A large number of placebo-controlled, double-blind studies have demonstrated that fluoxetine, sertraline, clomipramine, and paroxetine can be used to delay ejaculatory latency in men with rapid ejaculation. Since the early 1970s, an array of individual, conjoint, and group therapy approaches employing behavioral strategies such as stop-start or squeeze techniques have evolved as the psychological treatments of choice for rapid ejaculation, although the impressive initial posttreatment success rates, ranging from 60 to 95%, are not necessarily sustainable; three years after treatment, success rates dwindle to 25%.

2014 ◽  
Vol 104 (5) ◽  
pp. 479-485 ◽  
Author(s):  
Warren S. Joseph ◽  
Tracey C. Vlahovic ◽  
Radhakrishnan Pillai ◽  
Jason T. Olin

Background Efinaconazole 10% solution is a new triazole antifungal agent developed for the topical treatment of onychomycosis. This article reviews the pooled results of the two pivotal clinical trials of this drug that have been performed in the United States, Canada, and Japan. Methods The two studies of 1,655 patients were both double-blind, vehicle-controlled, parallel-group, randomized, multicenter studies designed to determine the efficacy and safety of efinaconazole 10% solution in the treatment of mild-to-moderate onychomycosis of the toenails caused by dermatophytes. Treatment was provided once daily for 48 weeks, and the primary end point was at week 52. Results The combined results show a 56% mycologic cure rate compared with 17% for vehicle at week 52. Clinical treatment success was achieved in 43% of patients treated with efinaconazole 10% solution at follow-up (week 52). Clinical treatment success was achieved in 47% of patients. As expected for a topical agent, the use of efinaconazole 10% solution was found to be safe, with mild, transient irritation at the site of application reported as the most common adverse event. Conclusions The efficacy and safety profile of efinaconazole 10% solution suggests that it may represent an important advance in the topical treatment of onychomycosis. Further studies will help us better understand the role of this agent for the treatment of this widespread podiatric medical condition.


CNS Spectrums ◽  
2003 ◽  
Vol 8 (3) ◽  
pp. 194-202 ◽  
Author(s):  
H. George Nurnberg ◽  
Paula L. Hensley

AbstractSexual dysfunction related to antidepressants, particularly serotonin reuptake inhibitors is a major cause of premature treatment discontinuation. This places patients at increased risk for recurrence, relapse, chronicity, and mortality (eg, suicide). The clinical assessment requires a comprehensive evaluation of sexual function, including libido, arousal, orgasm, and resolution prior to affective disorder, disturbances associated with the emergence of depression, and changes or dysfunctions associated with antidepressant treatment. Other factors to be included for evaluating sexual dysfunction include inquiry for concurrent medical conditions, somatic treatments, lifestyle risk factors, and response to antidepressants. Current treatment approaches to antidepressant-associated sexual dysfunction have relied on open-label reports, literature reviews, and clinical wisdom. Without double-blind, placebo-controlled studies to support them, too much non-evidence-based treatment may be offered to patients. Advances into nonadrenergic-noncholinergic novel signal transduction, specifically phosphodiesterase type-5 inhibitors, offer new opportunities for developing evidence-based treatments for this side effect and improving depression disease management outcomes.


2006 ◽  
Vol 175 (4S) ◽  
pp. 387-387 ◽  
Author(s):  
Trinity J. Bivalacqua ◽  
Hunter C. Champion ◽  
Warren Mason ◽  
Arthur L. Burnett

Sign in / Sign up

Export Citation Format

Share Document