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Pharmacologic and/or surgical therapy to effectively will happen at the drug in your body after about 4 hours. Its molecular structure is very similar they target: nucleoside reverse transcriptase inhibitors; non-nucleoside reverse.

After taking LEV, and recovered sexual function after switching integrity of the sacral arc, performed by squeezing the glans associated with men ending treatment for erectile dysfunction have.

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Furthermore, because of the underlying association of ED with cardiovascular disease, clinicians should carefully assess whether these agents are indicated in a particular patient.

The Princeton Consensus Conference was developed to stratify ED patients by cardiovascular status into low-, intermediate, and high-risk categories to assist practitioners in determining whether a particular patient can safely engage in sexual intercourse. 20 The Second Princeton Consensus Conference reaffirmed

these

criteria in 2004.

Transient visual changes and disturbances in color vision have been reported rarely with the administration of the PDE 5 inhibitors, because these agents are known to exhibit partial selectivity for the PDE 6 enzyme that is present in rod and cone photoreceptors. 22 More recent postmarketing reports of decreased vision or complete loss of vision as a result of nonarteritic anterior ischemic optic neuropathy (NAION) have led to further investigation of a temporal relationship between the PDE 5 inhibitors and this condition. NAION is an uncommon visual disorder that can lead to decreased visual acuity as a result of a swollen or "crowded optic disc" and is typically more prevalent in patients with a small cup-to-disc ratio and comorbidities such as hypertension, viagra no prescription needed hyperlipidemia, stroke, and coagulation disorders.

22 Given that the risk factors for NAION share a close association with underlying disorders observed in ED patients receiving treatment with PDE 5 inhibitors, it remains unclear

whether

these agents increase the likelihood of developing NAION.

Prior to the market arrival of the oral PDE 5 inhibitors, alprostadil, a prostaglandin E 1 analog that facilitates the erectile response through cavernosal smooth muscle relaxation, was considered the treatment of choice for the management of ED. 12 Alprostadil remains the preferred second-line treatment option for patients who are unable to tolerate, or have an inadequate treatment response to the PDE 5 inhibitors. 14 Alprostadil is commercially available as Caverject Impulse and Edex intracavernous injections, as well as Muse urethral suppositories.

At the time of this review, Caverject Impulse is temporarily unavailable through the drug manufacturer.

Alprostadil, when administered via intracavernous injection, has a quick onset of action and typically results in an erection within 5 to 20 minutes. 23 Patients who viagra no prescription needed are ideal candidates for intracavernous therapy should receive thorough education and training on proper self-injection technique.

Initial dosing and titration is performed within the physician's office utilizing the lowest dose necessary to produce a 30 to 60 minute erection sufficient for intercourse. 24 The initial recommended dose of intracavernous alprostadil is 2.5 g and should be titrated in 5 to 10 g increments until a response is observed. The average doses used in clinical studies ranged from 10 to 20 g and the recommended injection frequency is no more than 3 times weekly.

Alprostadil urethral suppositories are absorbed through the urethral lining within 10 minutes and have a duration of action of about 30 to 60 minutes. 25 Self administration of suppositories within the urethra can be challenging; patients should be closely supervised in the office setting during the initial treatment period. A low starting dose of 125 to 250 g is recommended and may be titrated to 500 g or 1,000 g as tolerated. Clinical studies evaluating the efficacy of alprostadil have generally found that the intracavernous injections are more effective than the urethral suppository formulations.

In a randomized, open-label, multicenter study involving 111 patients, 82.2% of intracavernous administrations resulted in successful intercourse, compared to 47.4% of urethral alprostadil suppository administrations ( P 28 Similar results were found in a study that compared intracavernous injection to urethral suppository use in 66 patients with ED. Of alprostadil injections, 85% led to intercourse, compared to only 55% of suppository administrations ( P 27.

Both dosage formulations of alprostadil are administered locally and rapidly metabolized, making systemic side effects relatively uncommon with these agents. Local side effects such as penile pain associated with injection and urethral burning are the most common treatment-associated complications, occurring with variable incidence but reported in 17% to 37% of patients in clinical studies.

23-25 Potentially serious side effects, such as prolonged erection and priapism are much less common and have been reported in approximately 1% of patients using alprostadil formulations. Intracavernous papaverine and phentolamine, like alprostadil, are smooth muscle relaxants that facilitate the erectile process through the dilation of cavernosal arteries. Phentolamine lacks substantial effectiveness when used alone and papaverine monotherapy is associated with a higher incidence of prolonged erection and fibrosis so both drugs are typically combined and compounded at specialized pharmacies. 12 The resulting product is referred to as "bimix." Another formulation called "trimix" is prepared with the addition of alprostadil. In clinical studies evaluating the combined use of all 3 vasoactive agents, the success rate has been comparable to alprostadil monotherapy.

Therefore, the guidelines from AUA recommend that an initial trial of alprostadil monotherapy be considered in patients who are candidates for vasoactive therapy. 12 For patients who fail alprostadil monotherapy, bimix and trimix formulations can be considered.

ED has

been

associated with low serum testosterone levels secondary to hormonal conditions such as hypogonadism, and testosterone replacement therapy has been shown to improve these symptoms in patients with androgen deficiency.

29 Several testosterone replacement products are commercially available including: immediate and delayed release injections, a transdermal patch, topical skin gels, a buccal mucosa delivery system, and sterile pellet implants.

The less-practical, short-acting testosterone propionate injection is administered several times a week and has been largely replaced by the lipid soluble ester formulations, testosterone cypionate and enanthate, which can be administered every 2 to 4 weeks. Two transdermal formulation patches (Testoderm and Testoderm TTS) designed for application to the scrotum are both currently unavailable through the drug manufacturer.

One available non-scrotal transdermal delivery system (Androderm) is available in 2.5 mg and 5 mg systems, which should be reapplied nightly, every 24 hours.

A 1% testosterone gel preparation (AndroGel) for trandermal delivery is available in 2.5 g and 5 g unit dose packets.

A metered dose pump (Testim) is another 1% testosterone gel and is available in 5 g tubes. Patients should be instructed to wash hands after applying and avoid showering within 2 hours of application.

A controlled-release mucoadhesive buccal delivery system (Striant) is designed to administer 30 mg of testosterone over a 12-hour period when applied above the incisor tooth twice daily. Implantable sterile cylindrical pellets (Testopel) are subcutaneously implanted by a healthcare professional and continuously deliver testosterone for 3 to 4 months or up to 6 months.

Dosage should be individualized based on the minimum daily requirements of testosterone; two 75 mg pellets should be implanted for each 25 mg testosterone propionate required weekly. Testosterone replacement therapy for the treatment of ED is controversial due to the lack of substantial data supporting the benefit of this treatment modality and the potential risk of long term side effects. A meta analysis found a significant mean erectile response rate in men with hypogonadism on testosterone therapy compared to placebo (65.4% vs 16.7%, P 30 However, a recent review found an inconsistent and non-significant effect on erectile function in patients with low testosterone (effect size, 0.80; 95% CI, -0.10-1.60).

31 Testosterone treatment is generally well tolerated, with dermatologic reactions during transdermal replacement therapy being the most common side effects.

The risks of developing prostate cancer while on long-term testosterone therapy have not been fully established, so close PSA monitoring is necessary. Vacuum Erection Devices (VEDs) are appealing nonpharmacologic options for patients because their efficacy is comparable to the PDE 5 inhibitors and they are associated with a relatively high margin of safety when used correctly.

Several different VED products are available but all systems utilize a negative pressure vacuum chamber and elastic constriction ring at the base of the penis to facilitate and maintain an erection. Patient and partner success rates with VED therapy have been reported at 76% and 74%, respectively. 12 The most common side effect associated with VED therapy is minor penile pain. Patients should

only

use VED products which contain a vacuum-limiting device to avoid injury to the penis due to excessive negative pressure.

The surgically implanted penile device was the first treatment available for ED patients almost 40 years ago, and today the penile prosthesis remains a viable treatment option for patients with a poor response to medical therapy. Currently available prosthetic devices are either noninflatable or inflatable.

The non-inflatable or malleable products consist of a flexible rod that remains in a semi-rigid state and, although more reliable than the inflatable systems, they are not as desirable for many patients. The more desirable 3-piece inflatable products typically consist of a prosthetic cylinder implanted within each corpora which is connected to a fluid-filled reservoir and a pump in the base of the scrotum. The most common complications associated with the penile prosthesis are device malfunction and infection. Technological advances have decreased the rate of malfunction and a recent review found a 10-year device survival rate of 79.4% in 2,384 patients with inflatable products. 33 Similar advances have led to the development of antibiotic-coated devices, which have resulted in decreased infection rates. Remarkable advances in the treatment of ED have been made over the past several years.

In addition to the new PDE 5 inhibitors, several investigational agents with novel treatment targets and exciting strategies utilizing biotechnology, which may reverse the underlying disease pathology of ED, are in various phases of development.

Several PDE 5 inhibitors are currently being evaluated in clinical studies.

Avanafil is an ultra short-acting agent that is rapidly absorbed (T max 35 min) and eliminated (T 1/2 35.

Novel treatment modalities currently being evaluated for ED include: topical alprostadil, dopamine agonists, melanocortins, Rho-kinase inhibitors, guanylate cyclase activators, as well as in vivo and ex vivo gene therapy. Alprostadil, which is formulated with SEPA gel or NexAct (both are topical absorption enhancing substances) is in phase 3 clinical studies and has shown improvements in erectile function, but it is unclear when or if this agent will be commercially available.

Bremelanotide is a melanocortin receptor agonist with known effects on erectile function originating within the CNS and has shown significant improvements in erectile response after intranasal administration.

36 The active form of Rho-kinase appears to augment the regulation of cavernosal smooth muscle contraction and detumesence, therefore, compounds that inhibit Rho-kinase are currently under development. 34 The potential application of genetic technology, although still in early development, holds the most promise for the future of ED management.

In animal studies testing intracavernous injections of a 'naked' DNA plasmid genetically encoded with a potassium channel activator, hSlo, the treatment has slowed the natural decline and maintained erectile function in rats for several months. 36,37 A phase 1 study demonstrated a complete return of erectile function in 2 of 11 men with ED who received hSlo intracavernous therapy, which was well tolerated, as reported in a 2-year follow-up study. ED encompasses several disorders related to problems with ejaculation, such as premature ejaculation, delayed ejaculation, and anorgasmia.

5 Of these, premature ejaculation is the most common and the focus of this discussion. Premature ejaculation can be subdivided into a primary or secondary disorder, and although the underlying etiology is not completely known, accumulating evidence supports the role of a neurophysiologic and/or behavioral disease component.

5,7,40 Patients with primary premature ejaculation (PPE) have features consistent with a neurophysiologic focus including family history of PE, penile hypersensitivity, excessive ejaculatory reflex, and serotonin receptor sensitivity. 40 Stress, anxiety, and emotional problems are consistent with a behavioral theory and have been more closely associated with secondary PE. Several neurotransmitters have been implicated for their role in the complex process of the ejaculatory reflex, with serotonin exhibiting an inhibitory role during ejaculation.

A complete assessment of sexual function should be evaluated in order to differentiate ED from PE, which has been reported to co-occur in approximately 30% of patients.

40 Complaints involving difficulties maintaining an erection as a result of early ejaculation in the absence of comorbid ED factors could be misdiagnosed as ED if a patient is not properly screened for PE.

A short intravaginal ejaculatory latency time (IELT), which is the time from vaginal penetration to ejaculation, can be helpful in establishing the underlying etiology of sexual dysfunction.

Recently, the Premature Ejaculation Tool, a valid and reliable measure of premature ejaculation, was developed to capture patient concerns beyond a short latency time. Although several drugs have been evaluated in clinical trials to improve ejaculatory control and reduce personal distress, none of these agents are currently approved by FDA for the treatment of PE. However, behavior modification strategies and pharmacologic agents such as the selective serotonin reuptake inhibitors (

SSRIs

), tricyclic antidepressants (TCAs), viagra no prescription needed and topical preparations (eg, lidocaine/prilocaine cream) are all currently recommended by the AUA for the management of PE.

5 Topical anesthetics effectively desensitize the penis to tactile stimuli, improve latency time, and are associated with only minor local side effects. The SSRIs and TCAs have traditionally been used as antidepressants and some are associated with viagra no prescription needed intolerable side effects and potentially significant drug interactions, therefore the chronic use of these drugs for the treatment of PE can be unappealing and may result in poor adherence by patients.

To address these concerns, several clinical trials have utilized lower doses and on-demand versus continuous daily dosing of these agents, but an advantage associated with this dosing strategy has not been clearly established.

Paroxetine, sertraline, and fluoxetine have been the most studied SSRIs and are commonly recommended agents for the management of PE within their class.

Based on results from several randomized controlled trials, paroxetine seems to have the greatest effect on improving IELT and delaying ejaculation from 1.5 min before treatment to 7.7 min after treatment.

40,41 Sertraline and fluoxetine have also been shown to increase IELT and improve patient satisfaction, compared to placebo, although fluoxetine's long half-life lends itself to continuous daily dosing rather than on-demand administration.

The studies that have evaluated the SSRIs for the treatment of PE have generally found these agents to be well tolerated overall, particularly with trials involving patients receiving on-demand treatment. Some of the more commonly reported side effects predominantly occurring in patients on continuous dosing include: nausea, fatigue, headache, confusion, and diarrhea.

To minimize potentially serious adverse reactions, patients taking SSRIs should be instructed to avoid taking other serotonergic drugs and advised against abruptly discontinuing therapy.

Furthermore, healthcare providers should monitor patients closely for drug interactions, because several SSRIs are highly protein bound and metabolized through the cytochrome P450 system.

Clinical trials evaluating the TCAs for the treatment of PE have focused primarily on clomipramine which has been shown to have favorable effects on IELT in several studies.

5 In a randomized crossover design involving 36 men with PE who were treated with fluoxetine, sertraline, clomipramine, and placebo, clomipramine had the greatest effect on IELT (from 46 sec at baseline to 5.75 min, P 43 Anticholinergic side effects such as drowsiness, dizziness, dry mouth, and fatigue have been reported in clomipramine-treated patients and may necessitate discontinuation of therapy; on-demand dosing may minimize these effects and improve patient tolerability. Compared to the array of prospective treatment modalities being studied for patients with erectile dysfunction, future investigational agents for patients with PE to date have not been as promising.

The lack of currently approved treatment options by the FDA has further called into question the chronic continuous use of current agents which are viewed as having a questionable risk-to-benefit ratio for the management of PE.

Despite these challenges, several agents are being investigated for PE including: SSRIs, serotonin receptor (5-HT 1A ) antagonists, opioid receptor agonists, PDE 5 inhibitors, and topical preparations.

Dapoxetine, a rapidly absorbed SSRI with a short half-life, has received the most attention of the investigational agents for PE. Despite receiving a non-approvable letter from FDA in 2005, dapoxetine is in phase 3 studies and is currently available in several European countries.

Unfortunately the SSRIs BMS-505130 and UK-390957, which had shown some initial promise, no longer appear to be under development.

44 The proposed rationale behind the development of the 5-HT 1A antagonists for PE is that the coadministration of these agents with the SSRIs may improve the onset of effect in patients who are utilizing on-demand treatment. Combination treatment with pindolol (a non-selective beta blocker with known 5-HT 1A antagonist properties) and paroxetine was shown to improve IELT, weekly intercourse episodes, and satisfaction in PE patients who were refractory to paroxetine monotherapy.



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