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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 generic viagra online paypal 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 generic viagra online paypal 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 generic viagra online paypal 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, viagra tablets in walgreens 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), 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, buy viagra gel online 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 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.

45 However, combination therapy was also associated with significantly more side effects, which is consistent with the poor tolerability of non-selective beta blockers.

Despite several studies that have evaluated the use of sildenafil, vardenafil, or tadalafil, substantial data to support the efficacy of these agents in

men

with PE, who do not have coexisting ED, is lacking.

Other currently available agents that have received attention or have limited data for the treatment of PE include tramadol and alpha adrenergic antagonists such as alfuzosin and terazosin. Finally, clinical research focused on topical preparations that have novel

delivery

formulations, such as a lidocaine/prilocaine metered dose aerosolized spray continue to receive attention because they have demonstrated efficacy and are well tolerated by most patients.

The prompt recognition and management of underlying organic, neurogenic, and psychogenic conditions associated with ED are necessary to improve treatment-related outcomes. Phosphodiesterase inhibitors have now replaced older agents such as alprostadil, phentolamine, and papaverine for the first-line treatment of ED.

The convenience of these oral dosage forms, which have been available for the past decade, has also generated the willingness of more men to seek earlier treatment for their symptoms. Although premature ejaculation remains one of

the

most common sexual disorders, the lack of FDA-approved treatments has proven to be a significant challenge for the management of this condition.

Despite this obstacle, several agents are currently recommended by the AUA for the treatment of PE such as SSRIs, TCAs, and topical lidocaine/prilocaine. Several investigational drugs for the management of ED and PE are also in various phases of development.

Douglass is assistant clinical professor, Northeastern

University

School of Pharmacy, Adult Internal Medicine, Boston Medical Center, Mass. Lin is a urologist at Massachusetts Bay Urologic Associates, Dorchester Center, Mass. Disclosure Information: The authors report no financial disclosures as related to products discussed in this article. Management of erectile dysfunction: diagnosis and treatment guideline.

Feldman, HA, Goldstein I, Hatzichristou DG, Krane RJ, McKinlay JB. Impotence and its medical and psychosocial correlates: results of the Massachusetts Male Aging Study.

The worldwide prevalence and epidemiology of erectile dysfunction.

Montague DK, Jarow J, Broderick GA, et al; AUA Erectile Dysfunction Guideline Update Panel.

AUA guideline on the pharmacologic management of premature ejaculation.

An evidence-based definition of lifelong premature ejaculation: report of the International Society for Sexual Medicine Ad Hoc Committee for the Definition of Premature Ejaculation. Molecular mechanisms for the regulation of penile smooth muscle contractility. Current concepts in the evaluation and management of erectile dysfunction.

Diagnosis and management of erectile dysfunction in the primary care setting. Clinical guidelines panel on erectile dysfunction: summary report on the treatment of organic erectile dysfunction. The contribution of common medical conditions and drug exposures to erectile dysfunction in adult males.

Montague DK, Jarow JP, Broderick GA, et al; Erectile Dysfunction Guideline Update Panel.

Chapter 1: The management of erectile dysfunction: an AUA update.

Chapter 3: Detailed outcomes analyses of treatments for erectile dysfunction. Management of erectile dysfunction: diagnosis and treatment guideline [AUA website]. Phosphodiesterase inhibitors for erectile dysfunction in patients with diabetes mellitus.

Management of sexual dysfunction in patients with cardiovascular disease: recommendations of The Princeton Consensus Panel. Sexual dysfunction and cardiac risk (the Second Princeton Consensus Conference). Vision disorders and phosphodiesterase type 5 inhibitors: a review of the evidence to date.

Intracavernous prostaglandin E1 in erectile dysfunction.

Urciuoli

R, Cantisani TA, Carlini M, Giuglietti M, Botti FM.

Prostaglandin E1 for treatment of erectile dysfunction. Intracavernosal versus intraurethral alprostadil: a prospective generic viagra online paypal randomized study.

Intracavernous alprostadil alfadex is more efficacious, better tolerated, and preferred over intraurethral alprostadil plus optional actis: a comparative, randomized, crossover, multicenter study.

Effects of testosterone replacement in hypogonadal men. Testosterone supplementation for erectile dysfunction: results of a meta-analysis.

Testosterone use in men with sexual dysfunction: a systematic review and meta-analysis of randomized placebo-controlled trials. Risks of testosterone-replacement therapy and recommendations for monitoring. Long-term survival of inflatable penile prostheses: single surgical group experience with 2,384 first-time implants spanning two decades.

Looking to the future for erectile dysfunction therapies. Novel phosphodiesterase-5 (PDE5) inhibitors in the alleviation of erectile dysfunction due to diabetes and ageing-induced oxidative stress. A review of current progress in gene and stem cell therapy for erectile dysfunction. Melman A, Bar-Chama N, McCullough A, Davies K, Christ G.

Plasmid-based gene transfer for treatment of erectile dysfunction and overactive bladder: results of a phase I trial. Melman A, Davies K, McCullough A, Bar-Chama N, Christ G. Long-term safety follow-up of a phase 1 trial for gene transfer therapy of ED with hMaxi-K.

Identifying and treating premature ejaculation: importance of the sexual history. The pharmacological treatment of premature ejaculation. Development and validation of a premature ejaculation diagnostic tool. Efficacy and safety of fluoxetine, sertraline and clomipramine in patients with premature ejaculation: a double-blind, placebo controlled study. 'Up and coming' treatments for premature ejaculation: progress towards an approved therapy. Once-daily high-dose pindolol for paroxetine-refractory premature ejaculation: a double-blind, placebo-controlled and randomized study. Efficacy of type-5 phosphodiesterase inhibitors in the drug treatment of premature ejaculation: a systematic review. Although it may feel uncomfortable to take that first step and see a doctor, there

are

many treatments available today that can restore erectile function, allowing patients to return to sexual activity.

Conservative treatment often begins with pills (such as “the blue pill,” Viagra and Cialis) and penile injections.

But, what happens if pills and injections don’t work for

you

?

At The Institute for Advanced Reconstruction, we may be able to restore erectile function by performing a minimally invasive nerve transfer procedure.

Erectile dysfunction (ED), also known as impotence, is a common male sexual dysfunction defined as an inability to achieve or sustain an erection. If you are affected by ED, know that you are not alone.

It is estimated that one in every ten men will suffer from long-term ED at some point during his lifetime.

ED is often a symptom of another underlying condition.

Male sexual arousal is a complex process that involves the brain, hormones, emotions, nerves, muscles and blood vessels.

Erectile dysfunction can result from a problem with any of these.

Some of the common causes of ED include: Heart Disease High Cholesterol Obesity Certain Prescription Medications Trauma Treatments for Prostate Cancer. Clogged blood vessels (atherosclerosis) Diabetes Emotional Disorders (Stress, Anxiety, Depression) Alcoholism or Substance Abuse Surgeries in the Pelvic Region.

A common treatment option used for complete remission of localized prostate cancer is a radical prostatectomy.

Unfortunately, this operation carries a risk of postoperative complications including ED.

Although great advances have been made in surgical techniques and devices, the prevalence of ED after prostatectomy

remains

a major postoperative complication. The effects of radiotherapy for the treatment of prostate cancer can also contribute to ED. 40% of men report ED symptoms after radiotherapy, and half of all men use erectile aids thereafter. What is our treatment approach for Erectile Dysfunction?

At The Institute for Advanced Reconstruction, we believe that patients should explore all conservative ED treatment methods before considering surgery. As mentioned above, many men with ED will experience improvements when taking medications such as

Viagra

and Cialis. These medications improve blood flow to the penis and make developing an erection easier.

Penile injections and penis pumps may also be used to achieve an erection in men with erectile dysfunction.

When pills and injections don’t work, a penile prosthesis may be considered. Implantation of a penile implant may require complex surgery and is irreversible. If the implant is removed, other treatment for ED will not be successful. Before proceeding with a penile prosthesis, we offer patients a minimally invasive nerve transfer procedure to permanently

restore

erectile function.

What are the causes of Erectile Dysfunction that we treat?

The procedure that we offer at The Institute for Advanced Reconstruction addresses erectile dysfunction caused by nerve damage or interruption.

We may be able to treat erectile dysfunction resulting from a prostatectomy, prostate radiation, pelvic surgery, pelvic trauma or diabetes.

In addition, we may be able to treat idiopathic erectile dysfunction (unknown cause).

At The Institute for Advanced Reconstruction, we perform a genitofemoral to cavernous nerve transfer to restore erectile function (see figures).

A “nerve transfer” is a standard surgical technique that utilizes a healthy, functioning nerve, connecting it to an unhealthy,

injured

nerve, in order to restore the function in the injured nerve. This minimally invasive procedure is usually performed on an outpatient basis.

Patients are often able to return to work within one week.

Full recovery from this surgery usually takes around six weeks.

Following the procedure, nerve regeneration is expected to occur in less than a year before the desired erection is possible, but each case is unique. The standard of treatment for ED often focuses on short-term solutions however; our surgical option offers a long-term solution to ED.

You may be a candidate if you… Are over 18 years old and otherwise healthy Have a history of spontaneous erectile function prior to prostatectomy, prostate radiation, pelvic surgery, trauma or diabetes Experienced a loss of erectile function after prostatectomy, prostate radiation, pelvic surgery, trauma or being diagnosed with diabetes Are within 18 months of the onset of

Erectile

Dysfunction symptoms Are willing and capable to proceed with surgery and follow-up appropriately Are free from tobacco use, alcoholism and other forms of substance abuse. Please contact The Institute for Advanced Reconstruction if you are interested in learning more about this procedure. Erectile function recovery rate after radical prostatectomy: a meta-analysis.

Sexual rehabilitation and cancer survivorship: a state of art review of current literature and management strategies in male sexual dysfunction among prostate cancer survivors. Penile rehabilitation after radical prostatectomy: what the evidence really says. Prediction of erectile function following treatment for prostate cancer.

Men now have a new option to treat erectile dysfunction. Food and Drug Administration has approved the new drug Stendra to treat the illness that causes problems in the sex lives of 30 million men.

It is the first erectile dysfunction drug in a decade. And its reacts faster than other drugs on the market meaning men may be able to add spontaneity back into the bedroom.

Men take the drug, which increases blood flow to the penis, as needed 30 minutes before engaging in sex. They'll still have to take some precautions like when taking other drugs on the market. For example, Stendra can't be taken with nitrates, such as those used to treat chest pain, because it can cause a sudden drop in blood pressure, the FDA said. Remember the movie Something's Gotta Give, when the doctor told Jack Nicholson's character he should be truthful about taking Viagra because it might cause a heart attack when mixed with other medications? Erection problems often occur as men get older and are more common in men with HIV. There may be physical or psychological causes, or a combination of the two.

There can be drug-drug interactions between erectile dysfunction drugs and anti-HIV medications. While many men struggle with erectile dysfunction, it is more common in men living with HIV.

There may be physical or psychological causes, or more frequently a combination of the two. Factors such as dealing with a new diagnosis, stigma, and anxiety about passing on HIV may impact upon your ability to get hard or stay hard. Physical causes may include older age, diabetes, heart disease, taking certain types of HIV medication and how long

you

have taken these medications. Sexual wellbeing is an important part of your overall health and problems in this area can have an impact on how you feel about yourself.

Help is available from healthcare professionals if you are struggling with erectile dysfunction. Having sexual problems may also indicate that there are other areas of your physical and psychological health that need to be attended to. Erectile dysfunction (or impotence) is when you cannot get or keep an erection that enables you to have sex. Most men are sometimes unable to have an erection, perhaps caused by drinking too much alcohol, using recreational drugs, anxiety or tiredness. Occasional problems are not necessarily a cause for concern, but ongoing erectile dysfunction should be investigated by a doctor.

It is one form of male sexual dysfunction, which also includes problems ejaculating and reduced sexual desire or satisfaction.

Erectile dysfunction often affects men as they get older. It is also more common in men with HIV than in the general population, although it has been difficult to estimate how many men with HIV are affected.

Research suggests that around 40 to 60% of men with HIV may have some degree of erectile dysfunction.

Erectile dysfunction has various physical and psychological causes. It is often associated with conditions that affect blood flow in the penis, including diabetes, high cholesterol, high blood pressure, cigarette smoking, obesity and heart disease. Other factors commonly linked to erectile dysfunction include older age, low testosterone levels, alcohol or drug use, anxiety and depression.

It is important to consider both the physical and the psychological reasons behind sexual problems.

If you have experienced impotence in the past, you generic viagra online paypal may fear not being able to get an erection during sex. Your anxiety around sexual performance may add to an existing physical cause and worsen the problem.

Physical causes of erectile dysfunction in men with HIV.

In addition to the factors mentioned above, there are specific factors that are important if you are living with HIV.

These include having lived with HIV for a longer time, a lower CD4 cell count when you were first diagnosed and possibly taking certain HIV medications (see below). If you have both HIV and hepatitis C, or suffer from body fat redistribution (lipodystrophy), you may be more likely to have difficulties getting an erection.

Many men with HIV have low testosterone levels (hypogonadism).

This can be difficult to diagnose because some symptoms (such as loss of vitality, low sexual desire, low bone mineral density and loss of muscle mass) are less specific and can occur in men with HIV who have normal testosterone levels. It is important for your doctor to investigate whether this could be the cause of your impotence. Chronic illness, HIV replication, antiretroviral medications,

lipodystrophy

, metabolic syndrome, other co-morbidities and co-infections can contribute to low testosterone levels in people living with HIV. A feeling of unease, such as worry or fear, which can be mild or severe.

Anxiety disorders are conditions in which anxiety dominates a person’s life or is experienced in particular situations.



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