Controversies in Sexual Medicine Are Premature Ejaculation Symptoms Curable?
Transcription
Controversies in Sexual Medicine Are Premature Ejaculation Symptoms Curable?
© 2008 International Society for Sexual Medicine Controversies in Sexual Medicine Are Premature Ejaculation Symptoms Curable? Yoram Vardi, MD,* Chris G. McMahon, MBBS, FAChSHM,† Marcel D. Waldinger, MD, PhD,‡ Eusebio Rubio-Aurioles, MD, PhD,§ and David Rabinowitz, MD¶ *Department of Neuro-Urology, Rambam Medical Center, Haifa, Israel; †Australian Centre for Sexual Health, St. Leonards, NSW, Australia; ‡Department of Psychiatry and Neurosexology, HagaHospital Leyenburg, The Hague, the Netherlands; §Asociacion Mexicana para la Salud Sexual AC, Tlalpan, Mexico; ¶Psychiatric Outpatient Service, Rambam Medical Center, Haifa, Israel DOI: 10.1111/j.1743-6109.2008.00900.x ABSTRACT Introduction. While premature ejaculation (PE) is the most common sexual dysfunction in men under 40, there is currently no government-approved therapy for its treatment. Is a cure possible? Methods. Four experts in the area of PE and its treatment were asked to contribute their opinions. Main Outcome Measure. To provide food for thought, discussion, and possible further research in a poorly understood area of sexual medicine. Results. Differences among the different types of PE, and the ability to cure them are discussed. One expert examines the possible differences in lifelong and acquired PE as an explanation as to why treatment for the former does not carry over after termination of treatment whereas the latter can be treated successfully. The second and third experts break PE into four categories, explaining that those forms that are curable at present are not true PE or are based on anxiety. The last expert discusses the potential of a combined clinical and research platform to better understand the relative contributions of biological, behavioral, and couple factors to the disorder for potential curability. Conclusion. Improved understanding of the types of PE and their various etiologies and pathophysiologies would improve the potential for cure. Vardi Y, McMahon CG, Waldinger MD, Rubio-Aurioles E, and Rabinowitz D. Are premature ejaculation symptoms curable? J Sex Med 2008;5:1546–1551. Key Words. Premature Ejaculation; Cure; Treatment; Ejaculation Introduction P remature ejaculation (PE) is the most common sexual dysfunction in men younger than 40 years with significant adverse effects on their sexual and overall quality of life. Historically, this entity has been considered a psychological disorder, the treatment of which has received an increasing interest in recent years. The underlying pathophysiology of PE is not well understood, although both physiological and psychological 1546 components could contribute to the symptomatology. Traditional management continues to be psychotherapy, with techniques such as the “stopstart” and “squeeze” most commonly employed. However, evidence of their short-term efficacy is limited while support for their long-term benefit is lacking. The application of local anesthetics to the glans first described over 60 years ago continues to be used especially as an “over-the-counter” therapy. Over the years, a variety of centrally acting medications, especially antidepressants, J Sex Med 2008;5:1546–1551 Controversies in Sexual Medicine have been described as treatments for PE. At the present time, the selective serotonin re-uptake inhibitors, licensed for other indications, emerge as the most used agents to delay ejaculation. Currently, no medications licensed specifically for the treatment of PE are available. Nevertheless, none of the current “off-label” pharmacotherapeutic approaches are probably ideal therapy for these patients. In this month’s “Controversies in Sexual Medicine” section, four experts in the field deal with the curability of the present treatment modalities available for the treatment of premature ejaculatory symptoms. Yoram Vardi, MD PE is often described as one of the most common male sexual disorders based solely upon self-diagnosis by as many as 39% of men in the general community. However, most epidemiological studies are limited by their reliance upon self-diagnosis or application of the Diagnostic Statistical Manual of Mental Disorders-IV-Text revision (DSM-IV-TR) definition of PE, which is authority-based rather than evidence-based, and has no support from controlled clinical and/or epidemiological studies. Recently, an Ad Hoc Committee of International Society for Sexual Medicine was given the brief to develop a contemporary, evidence-based definition of PE and proposed that lifelong PE be defined as . . . “a male sexual dysfunction characterized by ejaculation which always or nearly always occurs prior to or within about one minute of vaginal penetration, and the inability to delay ejaculation on all or nearly all vaginal penetrations, and negative personal consequences, such as distress, bother, frustration and/or the avoidance of sexual intimacy” [1]. Based on this definition, the incidence of lifelong PE is likely to be much smaller, but despite achieving substantial insights into this condition with community-based stop-watch, normative intravaginal ejaculation latency time (IELT) studies has yet to be reliably determined [2]. The core symptoms of PE include early ejaculation and the inability to delay ejaculation, resulting in personal and interpersonal distress, bother, frustration and/or the avoidance of sexual intimacy. Cure of a medical illness refers to a completely effective treatment, which results in resolution of the underlying disease. Many treatments are not cures, and may merely provide temJ Sex Med 2008;5:1546–1551 porary relief from symptoms rather than removal of the underlying disease. The population of men with PE is heterogeneous and includes lifelong and acquired PE. Lifelong PE is characterized by early ejaculation from the first sexual encounters onward at nearly every intercourse within 30–60 seconds in the majority of cases (~90%) or within 1–2 minutes (~10%) of penetration, with nearly every or every sexual partner. Acquired PE differs in that sufferers develop early ejaculation at some point in their life, having previously had normal ejaculation experiences. Acquired PE may be due to psychological or relationship problems, erectile dysfunction (ED), prostatitis, or thyroid dysfunction. Animal psychopharmacological and human epidemiological studies suggest that IELT is probably a genetically determined biological variable, which may differ between populations and cultures, ranging from extremely rapid through average to slow ejaculation. In a normal population of rats, a Gaussian distribution biological continuum of ejaculation latency time has been demonstrated, suggesting that endophenotypes exist with regard to ejaculatory performance [3]. IELT is similarly distributed in humans and is positively skewed with a median IELT of 5.4 minutes and a range extending from 0.55 to 44.1 minutes [2]. Inherited hyposensitivity of the 5-HT2C and/or hypersensitivity of the 5-HT1A receptors have been suggested as a possible explanation of lifelong PE [4]. Men with lifelong PE, putative 5-HT2C receptor hyposensitivity and resultant low 5-HT neurotransmission may have their ejaculatory threshold genetically “set” at a lower point and ejaculate quickly and with minimal stimulation. Treatment with a selective serotonin reuptake inhibitor (SSRI) class drug activates the 5-HT2C receptor, elevates the ejaculatory threshold set-point, and delays ejaculation. Cessation of treatment results in the reestablishment of the fixed genetic setpoint within 5–7 days in men with lifelong PE. However, several human PE drug studies report that some men experience sustained improvement in IELT at up to 6 months follow-up following cessation of drug treatment [5–7]. McMahon reported that staged withdrawal of sertraline allowed 20 out of 29 patients (67%) to discontinue treatment after a mean treatment interval of 7.3 months, yet maintain improved ejaculatory latency and control [6]. Montorsi reported better but not 1547 Controversies in Sexual Medicine statistically significant improvement in ejaculatory control after the cessation of medication in men with acquired vs. lifelong PE [5]. Furthermore, McMahon reported that initial integrated treatment with a daily SSRI and use of rate-limiting ejaculatory control techniques with subsequent staged SSRI withdrawal resulted in sustained improvement in IELT and ejaculatory control in 68.2% of men with acquired PE compared to only 17.1% of men with lifelong PE [8]. He suggested that this variance in response may reflect the genetic and therefore fixed ejaculation set-point of lifelong PE and the down-regulated but modifiable set-point of acquired PE. The notion that acquired PE can be “cured” by successful treatment of the underlying etiology is logical but not well supported in the literature. Recent data demonstrate that almost half of men with ED also experience PE [9]. A recent systematic review of published data reported that phosphodiesterase type 5 inhibitors (PDE5is) alone or in combination with an SSRI may have a role in the management of acquired PE in men with comorbid ED by improving erectile function and reducing severity of PE [10]. Chronic prostatitis and chronic pelvic pain syndrome have been reported as causes of acquired PE [11,12]. Shamloul reported that prostatic inflammation was found in 64% and chronic bacterial prostatitis in 52% of patients with PE. El-Nashaar reported that 1 month of antibiotic treatment resulted in a marked improvement in PE symptoms in 83.9% of patients with a 2.6-fold increase in mean IELT compared to 1.4 in an untreated control group which was sustained at 4 months follow-up [13]. Sexual performance anxiety is reported as the most common cause of acquired PE although the causal link is speculative and is not supported by empirical evidence. Treatment success with cognitive behavioral therapy (CBT) is relatively good in the short term but convincing long-term treatment outcome data are lacking [14,15]. The lack of longitudinal CBT efficacy may reflect a failure of researchers to distinguish between CBT treatment responsive anxiety-based acquired PE and minimally responsive genetic lifelong PE and/or poor long-term patient compliance. The symptoms of PE will usually improve during pharmacological treatment especially when combined with CBT. Withdrawal of treatment is invariably associated with return of initial symp1548 toms in men with lifelong PE, the most common type of PE. However, treatment of the underlying etiology of acquired PE is likely to be associated with resolution of PE symptoms in a substantial proportion of sufferers although the data to support this are limited. Further research into this interesting aspect of the management of PE is required. Chris G. McMahon, MBBS, FAChSHM In 1970, Masters and Johnson wrote “The marital unit must be and is assured unequivocally that a complaint of premature ejaculation can be reversed successfully” [16] and “if there is full cooperation from the female partner and an inherent interest in pattern reversal, there is negligible chance of therapeutic failure to reverse the male’s rapid ejaculatory tendencies” [16]. We know that in those years it was not unusual to pose such statements without the support of medical scientific evidence. Today, in times of evidence-based medical research, no responsible physician would insist on his personal views without circumstantial evidence from published randomized clinical trials (RCTs). To answer the question posed in the abovementioned title, it remains essential to categorize the characteristics of PE and to elucidate the idea behind the medical concept of the curability of a disorder or dysfunction. A dysfunction may be considered “curable” if the symptoms do not reemerge after treatment. When symptoms of a dysfunction have disappeared under treatment but reemerge, such a treatment only temporarily suppressed the symptoms, without a definite cure of the dysfunction. We recently emphasized that PE is not a single well-distinguished dysfunction, but a cluster of symptoms that can be categorized into four subtypes, each with specific features, pathophysiologies, etiologies, and treatments [17]. Successful treatment has been argued to be dependent on the PE-subtype, its pathophysiology, and etiology [18]. For example, in premature-like ejaculatory dysfunction, a cluster of PE symptoms disclosing “complaints” of PE but with normal or even long IELTs, couple or individual therapy may result in a change of the subjective appreciation and perception of the male’s ejaculatory performance even when the durations of the ejaculation time have not been affected by the psychotherapy. In other J Sex Med 2008;5:1546–1551 Controversies in Sexual Medicine words, psychotherapy may have the capability to “cure” premature-like ejaculatory dysfunction just by altering a man’s perception. That means that the patient has been “cured” of his perception of suffering from PE. Another cluster of PE symptoms is called “acquired PE” that may occur in the case of hyperthyroidism. Thyreostatic treatment may lead to complete and lasting disappearance of PE symptoms meaning complete cure. In contrast to the aforementioned PE subtypes, there are no hard scientific data about the curability of lifelong PE. Lifelong PE, which is a cluster of PE symptoms characterized by IELTs of less than 1 minute in the majority of sexual encounters [19] associated with negative psychological consequences, can neither be cured by drug treatment nor psychotherapy. Although numerous well-controlled RCTs did show very strong efficacy of daily SSRIs and clomipramine in delaying ejaculation time, all symptoms will recur to the same extent and often within a few days of when treatment is stopped. In other words, drug treatment does not “cure” lifelong PE” but only diminishes its symptoms of objective very short IELTs. To be able to really cure lifelong PE, we need more neurobiological insights into its pathogenesis. These novelties may perhaps come from future genetic research. Marcel D. Waldinger, MD, PhD Are premature ejaculatory symptoms curable? Yes, many times. No, unfortunately most of the time. A straightforward answer to this question is not possible because the question assumes that PE is always the same sort of dysfunction. In my experience, this is not the case. There are very important differences between the man who develops PE in the course of the evolution of his ED, the man who experiences very high level of anxiety with his partner because of fear of losing her and this anxiety prompts a dramatic increase in the speed of ejaculation, the man who, after having a very restrictive education and never masturbated, really lacks knowledge of his own sexual response and sensations and hence cannot control his ejaculation, to mention just a few. I have seen patients whose PE is lifelong and meets the suggested 1 minute of IELT criteria who, through training with the traditional Seaman’s start-stop technique [20] and psychotherapy, overcome the symptoms and remain J Sex Med 2008;5:1546–1551 “cured” many years after. Also, I have seen patients for whom the benefit of the training and psychotherapy with various techniques is null. In a similar way, I have treated patients with SSRI medications who benefit from the effect to the point where the start-stop technique becomes useful and the control becomes possible even after suspending the medication, and patients for whom the benefit of medication is lost short after suspending the medication. The current system of classification of sexual dysfunction creates the illusion that one category of sexually dysfunctional individuals that share a diagnosis should have all the same pathophysiological mechanism and therefore the same treatment approaches should work. There is a clear need to develop classification systems that take into account the different etiological mechanisms. Not all men with PE share the same pathophysiology, and treatments should therefore be ideally directed toward these mechanisms. It is likely that some of the pathophysiologies included be more amendable or eliminable through interventions than others. In my experience, anxiety-related PE cases, and those (rare) cases where the learning process of ejaculatory control is defective, are the ones with more possibilities of cure. The classification proposed by Waldinger [17] is a significant advance in the need to differentiate between the various types of premature ejaculators; proposed categories are: lifelong, acquired, and two new ones: natural variable and PE-like syndromes. Some previous work by Metz and McCarthy [21] suggested an even longer list of nine types of PE according to the possible etiology: neurologic, secondary to physical (urologic) illness, secondary to trauma, secondary to drug side effect, psychological system PE, psychological distress PE, relationship distress PE, psychosexual skills-deficit PE, and a combined type. There is a need for more research that provides evidence for these proposed classifications, but the clinical experiences of many of us attest to a simple fact: there are many types of PE. It is likely and we all hope that the more we advance in the understanding of the various etiological mechanisms, the better we will become in predicting which patient has a realistic expectation for cure and which one will need chronic form of treatment. Eusebio Rubio-Aurioles, MD, PhD 1549 Controversies in Sexual Medicine Curability implies full recovery from symptoms and not requiring further treatment. No definitive position can be taken on the curability of PE in the absence of long-term follow-up studies. Relapse rates in the short- and long-term following treatment are unclear. The therapy of PE has been reviewed [22] and involves pharmacological, behavioral, and surgical strategies [23], including the use of selected serotonergic drugs, PDE5 inhibitors, topical applications, hyaluronic acid gel augmentation of the glans penis [24], and diverse sexological interventions, including directed genital stimulation [25]. All approaches impact on the symptom, varying, however, with subgroups that include primary vs. secondary PE, single young males, significant medical comorbidity, medication refusers, and negative intra-couple environments. Thus, diverse treatments applied to diverse populations increase the complexity of any long-term follow-up research strategy. If the jury is still out on PE curability, PE is best viewed as a manageable disorder. The optimal management approach is set out in the review [22] and involves pharmacological or behavioral approaches, the first choice varying with the primary or secondary subtypes and patient preferences, with the possibility of a combined approach as well. Medical and behavioral interventions are commonly thought of as alternatives to each other; it is proposed here that this is inherently problematic. In the mental health literature in general (e.g., [24]), studies commonly demonstrate the superiority of combined medical-behavioral interventions over single-paradigm interventions, a concept that has been explored in clinical and research work in PE, although in limited fashion [25]. The contours of a combined approach could include early medication intervention after diagnosis for rapid symptom control, early sexological assessment for multifactorial evaluation and intervention, and early educational counseling to achieve cognitive mastery (psychoeducation [25]) and an increased repertoire of relevant sexual skills. The latter can be provided by nursing staff (preferable male) after relatively simple training, possibly even in a small group setting. In principle, these modalities could be offered as an integrated package to all new cases as default mode, customized according to needs. This combined model permits a team approach and a relatively easily implemented clinical paradigm. It offers a short- and long-term research 1550 strategy comparing medical “treatment as usual” with and without behavioral and/or psychoeducational add-ons. It raises the important question as to the stability of treatment gains after medication weaning, as a function of add-on interventions. Long-term follow-up studies would help confirm or refute the validity of the combined approach. A combined package, as a clinical and research platform, may help to achieve a better understanding of the relative contributions of biological, behavioral, and couple factors to the disorder, and also help the fine-tuning of interventions. Ultimately, it may bring us closer to the question of curability. David Rabinowitz, MD References 1 International Society for Sexual Medicine. ISSM definition of premature ejaculation. 2007. Available at: http://www.issm.info/ (accessed December 22, 2007). 2 Waldinger MD, Quinn P, Dilleen M, Mundayat R, Schweitzer DH, Boolell M. A multinational population survey of intravaginal ejaculation latency time. J Sex Med 2005;2:492–7. 3 Pattij T, de Jong TR, Uitterdijk A, Waldinger MD, Veening JG, Cools AR, van der Graaf PH, Olivier B. Individual differences in male rat ejaculatory behaviour: Searching for models to study ejaculation disorders. Eur J Neurosci 2005;22:724–34. 4 Waldinger MD, Berendsen HH, Blok BF, Olivier B, Holstege G. Premature ejaculation and serotonergic antidepressants-induced delayed ejaculation: The involvement of the serotonergic system. Behav Brain Res 1998;92:111–8. 5 Montorsi F, Guazzoni L, Barbieri L, Rigatti P, Pizzini G, Miani A. Chlomipramine for premature ejaculation: A randomized, double blind placebo controlled study. Int J Imp Res 2004;6(1 suppl):Abstract D74. 6 McMahon CG. Treatment of premature ejaculation with sertraline hydrochloride: A single-blind placebo controlled crossover study. J Urol 1998; 159:1935–8. 7 Arafa M, Shamloul R. Efficacy of sertraline hydrochloride in treatment of premature ejaculation: A placebo-controlled study using a validated questionnaire. Int J Impot Res 2006;18:534–8. 8 McMahon CG. Long-term results of treatment of premature ejaculation with selective serotonin re-uptake inhibitors. Int J Imp Res 2002;14:S19. 9 Laumann EO, Nicolosi A, Glasser DB, Paik A, Gingell C, Moreira E, Wang T. Sexual problems J Sex Med 2008;5:1546–1551 Controversies in Sexual Medicine 10 11 12 13 14 15 16 among women and men aged 40–80 years: Prevalence and correlates identified in the global study of sexual attitudes and behaviors. Int J Impot Res 2005;17:39–57. McMahon CG, McMahon CN, Leow LJ, Winestock CG. Efficacy of type-5 phosphodiesterase inhibitors in the drug treatment of premature ejaculation: A systematic review. BJU Int 2006;98:259– 72. Gonen M, Kalkan M, Cenker A, Ozkardes H. Prevalence of premature ejaculation in Turkish men with chronic pelvic pain syndrome. J Androl 2005; 26:601–3. Shamloul R, el-Nashaar A. Chronic prostatitis in premature ejaculation: A cohort study in 153 men. J Sex Med 2006;3:150–4. El-Nashaar A, Shamloul R. Antibiotic treatment can delay ejaculation in patients with premature ejaculation and chronic bacterial prostatitis. J Sex Med 2007;4:491–6. McCarthy B. Cognitive-behavioural strategies and techniques in the treatment of early ejaculation. In: Leiblum SR, Rosen R, eds. Principles and practices of sex therapy: Update for the 1990’s. New York: Guilford Press; 1988:141–67. Hawton K, Catalan J, Martin P, Fagg J. Long-term outcome of sex therapy. Behav Res Ther 1986; 24:665–75. Masters WH, Johnson VE. Premature ejaculation. In: Masters WH, Johnson VE, eds. Human sexual J Sex Med 2008;5:1546–1551 17 18 19 20 21 22 23 24 25 inadequacy. Boston, MA: Little, Brown and Co.; 1970:101. Waldinger MD. Premature ejaculation: State of the art. Urol Clin North Am 2007;34:591–9. Waldinger MD. Premature ejaculation: Different pathophysiologies and etiologies determine its treatment. J Sex Marital Ther 2008;34:1–13. Waldinger MD, Hengeveld MW, Zwinderman AH, Olivier B. An empirical operationalization study of DSM-IV diagnostic criteria for premature ejaculation. Int J Psychiatry Clin Pract 1998;2:287–93. Semans JH. Premature ejaculation: A new approach. South Med J 1956;49:353–8. Metz ME, McCarthy BW. Coping with premature ejaculation. Oakland, CA: New Harbinger Publications; 2003. Sharlip ID. Guidelines for the diagnosis and management of premature ejaculation. J Sex Med 2006; 3:S309–17. Seftel AD. Effects of glans penis augmentation using hyaluronic acid gel for premature ejaculation. Urology 2005;173:2077. Roy-Burne PP, Craske MG, Stein MB, Sullivan G, Bystritsky A, Katon W, Golinelli D, Sherbourne CD. A randomized effectiveness trial of cognitivebehavioral therapy and medication for primary care panic disorder. Arch Gen Psychiatry 2005;62:290–8. Althof A. The psychology of premature ejaculation: Therapies and consequences. J Sex Med 2006;3: S324–31. 1551