Most Common Medications That Cause Erectile Dysfunction – Current smoking is significantly associated with ED and smoking cessation has a beneficial effect on erectile function recovery.

Men with metabolic syndrome should be advised to make lifestyle changes to reduce the risk of cardiovascular events and ED.

Most Common Medications That Cause Erectile Dysfunction

Most Common Medications That Cause Erectile Dysfunction

The five-question International Index of Erectile Function (IIEF-5) allows rapid clinical assessment of ED and can measure the effectiveness of ED treatments (see https:///afp/2010/0201/p305.html#afp20100201p305-t3). Other diagnostic options include a single-question self-assessment (Table 1).

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Impotence is the inability to get an erection strong enough for satisfactory sexual activity. How would you describe yourself?

ED has vascular, neurologic, psychological, and hormonal causes. Conditions commonly associated with ED include diabetes mellitus, hypertension, hyperlipidemia, obesity, testosterone deficiency, and prostate cancer treatment (Table 2).

Antidepressants are a common cause, particularly the selective serotonin reuptake inhibitors citalopram (Celexa), fluoxetine (Prozac), paroxetine (Paxil), and sertraline (Zoloft), and the serotonin-norepinephrine reuptake inhibitor venlafaxine. Bupropion (Wellbutrin), mirtazapine (Remeron), and fluvoxamine are less likely to cause ED.

Hormones and hormone-active agents (eg, 5-alpha-reductase inhibitors, androgen receptor blockers, androgen synthesis inhibitors, corticosteroids, estrogens, gonadotropin-releasing hormone analogs, progesterones)

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ED has been linked to increased fasting serum glucose levels, diabetes, hypertension, and abdominal obesity, as well as increased risk of cardiovascular disease (CVD) and each component of the metabolic syndrome (eTable A).

Men <40 mg per dL (1.04 mmol per L); Women <50 mg per dL (1.29 mmol per L)

The adipose tissue enzyme aromatase, prevalent in obese men, converts testosterone to estradiol, an important cause of hypogonadism.

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Patients with diabetes are three times more likely to develop ED, and longer duration of diabetes is strongly associated with ED.

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Metabolic syndrome was associated with a 2.6-fold increase in the incidence of ED, and fasting blood glucose level was the component associated with the highest risk of ED.

About one in 50 men aged 40 to 59 without ED have undiagnosed diabetes, but it rises to one in 10 in those with ED.

ED and CVD share similar risk factors, including aging, hypertension, dyslipidemia, smoking, obesity, and diabetes. ED increases the risk of CVD, coronary artery disease (CAD), stroke, and all-cause mortality and is probably an independent risk factor for CVD.

ED typically occurs two to five years before CAD, providing a potential window during which men with ED can make lifestyle changes to prevent CAD.

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Men with ED have an increased risk of angina, myocardial infarction, stroke, transient ischemic attack, congestive heart failure, and cardiac arrhythmia compared with men without ED.

ED has a positive predictive value for the development of CVD equal to or greater than smoking, hyperlipidemia, or a family history of myocardial infarction.

In one study, the incidence of CAD in men younger than 40 years of age with ED was seven times that of the control population.

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ED is a useful marker for predicting cardiovascular risk, particularly in young adults and minorities, for whom global risk assessment calculators may underestimate actual risk.

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Use of the IIEF-5 during CVD risk assessment is also recommended, as a diagnosis of ED may help identify men at increased CVD risk.

Medical and surgical history, sexual history, drug and other substance use, and assessment of mental and relationship health are critical components of the patient history. Important parts of the physical examination include measurement of blood pressure, body mass index, and waist circumference to assess abdominal obesity; a genital exam; and assessment of male secondary sex characteristics.

A1C or fasting glucose level can be used to predict diabetes. A lipid panel can assess hyperlipidemia. A thyroid-stimulating hormone level is recommended for men with signs or symptoms of hypothyroidism.

Routine measurement of testosterone levels is controversial. As part of the Choice Wisely campaign, the American Urological Association recommends that doctors not prescribe testosterone to men with ED who have normal testosterone levels. A diagnosis of hypogonadism should be based on more than just an abnormal laboratory test result.

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A morning total testosterone measurement may be considered in men with small testes, absence of male secondary sex characteristics, significantly low libido, or a history of inadequate response to phosphodiesterase-5 (PDE-5) inhibitors; If the initial result is abnormal, the test should be repeated in a few months. Free testosterone levels vary widely among laboratories and are not uniformly recommended for screening. However, even when hypogonadism is clinically suspected, when the morning total testosterone level is repeatedly normal, bioavailable testosterone or free testosterone may account for the effects of sex hormone-binding globulin levels on testosterone activity. Follicle-stimulating hormone, luteinizing hormone, sex hormone-binding globulin, estradiol, and prolactin levels help differentiate between primary and secondary causes of testicular hypogonadism.

Regular exercise, weight loss in obese or overweight men, and better control of diabetes, hypertension, and hyperlipidemia are recommended. Weight loss may improve low testosterone levels, although the extent of benefit in ED is unclear.

Smoking cessation is highly recommended. Compared to men who had never smoked, the risk of ED was increased by 51% in current smokers and 20% in former smokers.

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Sexual stimulation is necessary to produce an erection; A PDE-5 inhibitor helps maintain erectile function by enhancing the vasodilatory effects of endogenous nitric oxide. Currently in the U.S. for the treatment of ED. Four PDE-5 inhibitors have been approved by the Food and Drug Administration (FDA) with similar efficacy and safety profiles: avanafil (Stendra), sildenafil (Viagra), tadalafil (Cialis), and vardenafil (Levitra). Table 4 summarizes these drugs.

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All are effective within an hour of dosing and are usually used on an as-needed basis. If the patient has recently eaten a fatty meal, especially for sildenafil and vardenafil, the effects may be delayed or reduced.

PDE-5 inhibitors are ineffective in some men, especially those with severe ED. Headache, flushing and dyspepsia are common adverse effects.

PDE-5 inhibitors are contraindicated in men using nitroglycerin or other nitrates because of the risk of catastrophic low blood pressure. Tadalafil has a longer half-life, which allows men to take the drug 12 hours before sex, or at a lower dose, once daily; However, the negative effects are also long lasting. Vardenafil is available as a 10-mg orally disintegrating tablet. Sildenafil is the only commonly available PDE-5 inhibitor; Generic formulations of other agents are expected to be available from 2017 to 2019. Insurance coverage for these medications is limited and prescriptions may require prior authorization.

Second-line treatments for ED include alprostadil (Cavarject) and vacuum devices. These treatments can be used to establish an erection before sexual stimulation. They should be avoided in men who receive anticoagulants or have sickle cell disease or other bleeding or clotting disorders.

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Alprostadil causes penile vasodilation by relaxing arterial smooth muscle; It is available in injectable and intraurethral forms and can be used in combination with PDE-5 inhibitors. Injection alprostadil is given intracavernosally on one side of the penis. Intra-urethral alprostadil is a dissolving capsule that is inserted into the urethra with an applicator.

The lowest effective dose should be used and the patient should be instructed on the correct technique by performing a test dose in the doctor’s office. Fear of needles or pain may limit patient acceptance of alprostadil. Patients should be warned to seek emergency urological treatment if erection lasts four hours or longer. Penile fibrosis is another adverse effect; In one study, persistent fibrotic changes occurred in 4.9% of patients using intracavernosal alprostadil for four years.

A similar ED treatment not approved by the FDA is intracavernosal injection of a mixture of alprostadil, papaverine, and phentolamine.

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Vacuum devices consist of a tube placed over the penis and sealed at the base with lubricant (Figure 3).

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The vacuum pump removes air from the tube, drawing blood into the penis and creating an erection. A constricting ring is slipped from the base of the tube onto the penis to maintain an erection. To avoid ischemic damage, the constricting ring should not generally be left in place for more than 30 minutes. Vacuum devices are cumbersome, require several minutes to produce an erection, can lead to bending at the base of the penis with the ring in place, and can make an erect penis feel cold or cold due to limited blood flow. However, success and satisfaction rates are very high.

Vacuum devices can be used in combination with an oral PDE-5 inhibitor or alprostadil for men who have not had success with single-component therapy. These devices are also useful in men receiving daily nitroglycerin or other chronic nitrate therapy, in whom PDE-5 inhibitors are contraindicated. Patients can obtain vacuum devices at medical supply companies by presenting a doctor’s prescription. Insurance coverage varies.

Surgically implanted penile prostheses are a third-line treatment option for ED when other treatments are ineffective. Semirigid malleable prostheses are simple and easy to implant, but difficult to hide because the penis is always erect. Inflatable prostheses typically consist of two tubes that replace the corpora cavernosa, plus a pump in the scrotum and an intra-abdominal reservoir (eFigure A). Mechanical failure or infection may require removal

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