| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
From the Center for Sexual Function, Lahey Clinic, Burlington, Massachusetts.
| Correspondence to: Andre Guay, MD, Director, Center for Sexual Function/Endocrinology, Lahey Clinic Northshore, One Essex Center Dr, Peabody, MA 01960 (e-mail: andre.t.guay{at}lahey.org). |
An important point to keep in mind is the specialty that controls the sexual function clinic. Although the same complete evaluation can be done by any interested specialty, the focus for referrals might be different. A clinic in a urology department might have a higher percentage of men with penile fibrosis or ED after radical prostatectomy. A clinic that is a secondary referral center will generally see a more severely affected population. A sexual clinic managed by someone in internal medicine or a clinic receiving referrals primarily from internists or primary care physicians will see a different mix of patients (Slag et al, 1983; Guay et al, 1999). In this instance, the majority of cases will have medical disease etiologies. In any clinic, there are a large number of patients who will have both medical and psychological aspects to their ED problem. In our evaluation of 990 consecutive consultations, the percentage of men with mixed ED was 28.2% (Guay et al, 1999).
The following discussion will highlight the causes of the ED and how a practitioner might be able to optimize therapy by paying attention to the various etiologies. It is also recognized that men prefer oral therapy for ED, when possible. Because sildenafil has been recognized as the definitive first-line drug, some emphasis will be given to methods of optimizing treatment with this drug. The same will undoubtedly hold true for other phosphodiasterase inhibitors that will follow.
Progression of Ideas in ED![]()
During the 1950s and 1960s, ED (or impotence, as it was referred to then)
was separated into psychogenic and organic causes, with vague relationships to
specific etiologies. As more research developed in the 1970s, the organic or
medical components began to be outlined a little more specifically
(Carrier et al, 1994). It was
recognized that medications played a part in the problem. Also, neurological,
hormonal, and vascular causes were recognized. Vascular flow in the penis was
investigated, and a difference between arteriogenic and venogenic causes was
appreciated (Lue and Donatucci,
1994; Sharlip,
1994). Hormonal factors were being noticed as early as the early
1980s (Spark et al, 1980,
1984). In the late 1980s and
into the 1990s, penile physiology and erectile pathophysiology moved into the
biochemical sphere as endothelial function and neurotransmitters were being
identified and studied, especially nitric oxide
(Rajfer et al, 1992;
Pickard et al, 1995). All
these factors have to be considered in outlining the oftentimes multiplicity
of causes of ED in order to better plan a treatment regimen.
Psychogenic Factors ED![]()
The most commonly seen emotional problems associated with ED are anxiety
and depression. Anxiety has many causes: performance anxiety (fear of
failure); stressors, such as job and financial worries; and family problems
(aging parents or adolescent problems in children). Although anxiety may be
related to fear of failure, separate relationship problems may be at issue.
Partner disinterest may be present, especially prevalent at the time of
menopause where many bodily changes are occurring. Depression can certainly
cause or aggravate ED and is a leading cause of decreased libido.
The sex therapist should be an integral part of the management team in a sexual function clinic. Very commonly, the therapist deals with performance anxiety and relationship problems. Sometimes, even though physicians have provided a successful treatment, the couple will need some help combating the avoidance that often accompanies ED. The therapist sometimes needs to rule out a more serious anxiety or depression disorder, which may need to be addressed by a psychiatrist.
On the other hand, there is evidence that medically treating the ED has an ameliorative effect on relationships and primary emotional disorders. It can also reverse adverse sexual side effects from the medications themselves. Nurnberg et al (2003) found that sildenafil improved erectile function, arousal, ejaculation, orgasm, and overall satisfaction in men who had dysfunction related to selective serotonin reuptake inhibitor antidepressants. Even in men who have organic or mixed ED, Paige et al (2001) reported that sildenafil not only improved overall sexual satisfaction and increased intercourse satisfaction, but also improved the quality of life in 38% of the men and improved partner relationship in 29% of the men.
ED Is Vascular![]()
It has become apparent that the most common cause of ED is vascular. The
majority of medical conditions that we commonly see as causes of ED affect the
endothelial cell, which is a key component of the corpora cavernosum in
causing vasodilatation and increased blood flow. These conditions are thought
to cause an imbalance between penile vasoconstrictors and vasodilators
(Taub et al, 1993; Seftel, 2002). Also, an
imbalance between trabecular smooth muscle and connective tissue is thought to
be important, especially if one is to factor in aging changes in the penis
(Moreland, 2000).
Even early on, the NIH consensus conference noted that ED occurred more commonly with diabetes mellitus, hypertension, vascular disease, hypogonadism, and elevated cholesterol (NIH Consensus Development Panel on Impotence, 1993). The ongoing Massachusetts Male Aging Study has been following men over time, and apart from the known increase in ED with age, a correlation was found with diabetes mellitus, coronary artery disease, and hypertension (Feldman et al, 1994). In addition to coronary artery disease, smoking and even passive smoke exposure was correlated with ED (Feldman et al, 2000).
The Penile Stress Test![]()
Dr Pritzker, a cardiologist from Minneapolis, Min, brought notice to the
relationship of ED and cardiovascular disease when he studied 50 men who had
ED but no history or symptoms of heart disease
(Pritzker, 1999). Forty of the
50 men had multiple risk factors for heart disease. Cardiac stress tests were
done. None of the men had symptoms, but 28 of the 50 (56%) had a positive
test, consistent with silent ischemia. Twenty of these 28 men submitted to
coronary angiography, and all had significant 1-,2-, or 3-vessel disease. Dr
Prtizker believed that ED might be an early warning sign of impending
symptomatic coronary disease. The rationale proposed is that symptoms occur
first in the penis because the arteries are smaller.
Similar Risks in ED and Cardiovascular Disease![]()
In clinical practice, the results are the same. In 62 general medical
practices, Chew et al (2000)
found that a predominance of conditions that affect the vascular system are
correlated with ED. These included hypertension, ischemic heart disease,
peripheral vascular disease, and diabetes mellitus. In our previous study
evaluating the causes of ED in 990 consecutive consultations, we found
hypertension in 35.8%, diabetes mellitus in 23.1%, atherosclerotic
cardiovascular disease in 19.9%, tobacco abuse in 14.1%, and peripheral
vascular disease in 5.6% (Guay et al,
1999). In a more recent and more focused study of 154
consultations, we found hypertension in 44%, abnormal glucose metabolism
(diabetes mellitus and glucose intolerance) in 34%, tobacco abuse in 16%, and
coronary artery disease in 9% (Walczak et
al, 2002). The surprising findings were that 74% of the men had
elevated low-density lipoprotein (LDL) cholesterol (defined as LDL > 120
mg/dL) and that 79% were overweight (defined as body mass index >26).
Obesity has recently been proven to be a specific and separate primary risk
factor for coronary artery disease
(Suwaidi et al, 2001).
All the above conditions affect the intracorporeal biochemistry, and most will cause endothelial dysfunction with a resultant decrease in nitric oxide metabolism. Other mechanisms at work are the accumulation in the penis of angiotensin II, a powerful vasoconstrictor in hypertension, and decreased neuronal nitric oxide production in diabetes mellitus caused by clinical or subclinical neuropathy. Even the HbA1C molecule itself will affect the endothelial cell in diabetes.
Risk-Factor Modification![]()
Sildenafil has been successful because it will increase the nitric oxide
activity of the penis by retarding the breakdown of its product, cyclic
guanosine menophosphate. In conditions where the neuronal production of nitric
oxide is curtailed, the results with sildenafil have been decreased, such as
nerve damage from radical prostatectomy or neuropathy in persons with
diabetes.
Modification of the medical conditions that affect endothelial function and
nitric oxide production will lead to enhanced treatment success, either as the
sole treatment or as an adjunct to other treatments. Our group found a greater
success (82%) with sildenafil than what was found in the literature when
risk-factor management was undertaken
(Guay et al, 2001). We also
showed that control of diabetes made a difference in the response to
sildenafil, such that men with diabetes with an HbA1C less than 9.0% had a 63%
success rate with sildenafil, whereas those with an HbA1C greater than 9.0%
had a decreased success rate of 44%. We also showed that as the testosterone
level fell, the response to sildenafil decreased and eventually became
ineffective. Derby et al (2000)
warn, however, that modification works better at an earlier age because older
men may not be able to reverse the effects of smoking, obesity, and alcohol
abuse. Increasing age adds another burden to whatever medical factors are
present.
|
An interesting report in 9 men showed objectively that lowering cholesterol increased penile erectile activity after atovastatin therapy (Guay and Jacobson, 2002). These men, after careful evaluation, had only elevated cholesterol as a risk factor for organic ED, proven by abnormal baseline nocturnal testing with the RigiScan portable home monitor. Improved erections and sexual activity occurred after only several months of therapy, as reflected by improvement in the Sex Health Inventory for Men (SHIM) scores and in nocturnal erection parameters. Several of the men who were using sildenafil no longer needed it.
Optimization of Treatment of ED: General![]()
Thus, the first order of business should be to modify the risk factors
whenever possible. This would include bringing blood sugar or blood pressure
under control. It might involve changing offensive medications whenever
possible. Substance abuse should be stopped and hypogonadism, when present,
should be treated. Obesity should be corrected and more aggressive therapy for
hyperlipidemia is necessary.
Optimization of Treatment of ED: Sildenafil![]()
Because sildenafil is the recognized first-line therapy for ED, it is
important to consider what steps should be taken to ensure its maximum
effectiveness. As previously mentioned, we obtained an 82% success rate in 521
men by modifying the medical risk factors
(Guay et al, 2001).
Most prescriptions for sildenafil, however, are not written by specialists in the field but by primary care physicians. More education of primary care physicians is needed. Fawzy (2000) has shown that fewer than half of these physicians routinely questioned their patients about ED symptoms. Time is very limited in a primary care physician's office, and means have to be found to effectively but practically evaluate this situation. Perhaps the abridged form of the International Index of Erectile Function questionnaire could be filled out by the patient in the waiting room (Rosen et al, 1999); its 5 questions are easy to answer and score, which makes it an adequate screening tool. Primary care physicians also have to be trained in sexual dysfunction, as this subject is just starting to be discussed in more depth in medical school.
A frequent scenario is the patient returning to the office claiming failure with sildenafil. Barada (2001) has shown that over half of these men may be salvaged with reeducation. There are identifiable common mistakes. The first is that the patient did not titrate his dose to the maximum of 100 mg. Another common mistake is that men often do not try to use the drug enough times. McCullough et al (2002) have shown that the cumulative probability of success increases with the number of attempts. Men should try each dose 5 or 6 times, up to 8 in some cases, before claiming failure. Another common error is the ingestion of sildenafil too soon after eating, especially a fatty meal. It should be taken several hours after a meal, followed by the 30 to 60 minutes required for activity. Most men are aware that foreplay is needed for sildenafil to have an effect. Many men have to be reminded that maximum effectiveness will be blunted by tobacco usage, excess alcohol, or fatigue.
Treatment satisfaction by both patient and partner is quite important for long-term success of therapy with sildenafil. The need for follow-up is very important, and having the partner present with the patient at some point is equally important in bringing up issues that may have been missed. The Erectile Dysfunction Inventory of Treatment Satisfaction (EDITS) questionnaire was developed specifically to evaluate satisfaction of treatment (Althof et al, 1999), but the IIEF-5 abbreviated questionnaire, also called the SHIM, is also accurate for follow-up evaluation. Satisfaction, both for men previously treated with other methods of ED correction and for those using sildenafil as their first treatment, was shown to be equally positive (above 80%) (Althof, 1999). Partner satisfaction was shown to be quite positive as well (Lewis et al, 2001).
Summary of Important Points![]()
The Table highlights some of the important factors in the evaluation and
treatment of men with ED. Better education of both patients and physicians
caring for them is the common denominator. Initiatives for medical school
education of sexual function and dysfunction have begun and are gaining
momentum. Until these effects are felt in the practice community, educating
physicians in this field will remain a priority.
| References |
|---|
|
|
|---|
Althof SE, Corty EW, Levine SB, et al. EDITS: development of questionnaires for evaluating satisfaction with treatments for erectile dysfunction. Urology. 1999; 53:793-799.[Medline]
Barada J. Successful salvage of sildenafil (Viagra) failures: benefits of patient education and rechallenge with sildenafil. Int J Impot Res. 2001;13(suppl 4):S49.
Carrier S, Zvara P, Lue TF. Erectile dysfunction. Endocrinol Metab Clin North Am. 1994; 23:773-782.[Medline]
Chew KK, Earle CM, Stuckey BGA, et al. Erectile dysfunction in general medical practice: prevalence and clinical correlates. Int J Impot Res. 2000; 12:41-45.[Medline]
Derby CA, Mohr BA, Goldstein I, et al. Modifiable risk factors and erectile dysfunction: can lifestyle changes modify risk? Urology. 2000; 56:302-306.[Medline]
Fawzy A. Practice patterns of primary care physicians in management of erectile dysfunction. Int J Impot Res. 2000; 12(suppl 3):B10.
Feldman HA, Goldstein I, Hatzichristou DG, et al. Impotence and its medical and psychological correlates: results of the Massachusetts Male Aging study. J Urol. 1994; 151:54-61.[Medline]
Feldman HA, Johannes CB, Derby CA. Erectile dysfunction and coronary risk factors: prospective results from the Massachusetts Male Aging Study. Prev Med. 2000; 30:328-338.[Medline]
Guay AT, Jacobson J. Improvement in erectile dysfunction by correction of elevated cholesterol levels [abstract]. Int J Impot Res. 2002;14(suppl 3):S105-S106.
Guay AT, Perez JB, Jacobson J, Newton RA. Efficacy and safety of sildenafil citrate for treatment of erectile dysfunction in a population with associated organic risk factors. J Androl. 2001; 22:793-797.[Abstract]
Guay AT, Velasquez E, Perez JB. Characterization of patients in a medical endocrine-based center for male sexual dysfunction. Endocr Pract. 1999; 5:314-321.
Lewis RB, Bennett CJ, Borkon WD, et al. Patient and partner satisfaction with Viagra (sildenafil citrate) treatment as determined by the erectile dysfunction inventory of treatment satisfaction questionnaire. Urology. 2001; 57:960-965.[Medline]
Lue TF, Donatucci CF. Dysfunction of the venoocclusive mechanism. In: Bennett AH, ed. Impotence: Diagnosis and Management of Erectile Dysfunction. Philadelphia, Pa: WB Saunders; 1994 :197-204.
McCullough AR, Barada JH, Fawzy A, et al. Achieving treatment optimization with sildenafil citrate (Viagra) in patients with erectile dysfunction. Urology. 2002; 60(suppl 2B):28-38.
Moreland RB. Pathophysiology of erectile dysfunction: the contributions of trabecular structure to function and the role of functional antagonism. Int J Impot Res. 2000; 12(suppl 4):S39-S46.
NIH Consensus Development Panel on Impotence. NIH Consensus Conference. Impotence. JAMA. 1993; 270:83-90.[Medline]
Nurnberg HG, Hensley PL, Geleberg AJ, et al. Treatment of
antidepressant-associated sexual dysfunction with sildenafil.
JAMA. 2003; 289:56-64.
Paige NM, Hays RD, Litwin MS, et al. Improvement in emotional well-being and relationships of users of sildenafil. J Urol. 2001; 166:1774-1778.[Medline]
Pickard RS, Powell PH, Zar MA. Nitric oxide and cyclic GMP formation following relaxant nerve stimulation in isolated human corpus cavernosum. Br J Urol. 1995; 75:516-522.[Medline]
Pritzker MR. The penile stress test: a window to the hearts of man? [abstract]. Circulation. 1999; 100(suppl 1):3751.
Rajfer J, Aronson WJ, Bush PA, et al. Nitric oxide as a mediator of relaxation of the corpus cavernosum in response to nonadrenergic, noncholinergic neurotransmission. N Engl J Med. 1992; 326:90-94.[Abstract]
Rosen RC, Cappelleri JC, Smith MD, et al. Development and evaluation of an abridged, 5-item version of the International Index of Erectile Function (IIEF-5) as a diagnostic tool for erectile dysfunction. Int J Impot Res. 1999; 11:319-326.[Medline]
Seftel AD. Challenges in oral therapy for erectile dysfunction.
J Androl. 2002; 23:729-736.
Sharlip ID. Vasculogenic impotence secondary to atherosclerosis/dysplasia. In: Bennett AH, ed. Impotence: Diagnosis and Management of Erectile Dysfunction. Philadelphia, Pa: WB Saunders; 1994:205-212.
Slag MF, Morley JE, Elson MK, et al. Impotence in medical clinic out-patients. JAMA. 1983; 249:1736-1740.[Abstract]
Spark RF, White RA, Connolly PB. Impotence is not always psychogenic: newer insights into hypothalamic-pituitary-gonadal dysfunction.JAMA. 1980; 243:750-755.[Abstract]
Spark RF, Wills CA, Royal H. Hypogonadism, hyperprolactinemia, and temporal lobe epilepsy in hyposexual men. Lancet. 1984; 1:413-417.[Medline]
Suwaidi JA, Higano ST, Holmes DR, et al. Obesity is independently
associated with coronary endothelial dysfunction in patients with normal or
mildly diseased coronary arteries. J Am Coll Cardiol. 2001; 37:1523-1528.
Taub HC, Lerner SE, Melman A, Christ GJ. Relationship between contraction and relaxation in human and rabbit corpus cavernosum. Urology. 1993; 42:698-704.[Medline]
Walczak MK, Lokhandwala N, Hodge MB, Guay AT. Prevalence of cardiovascular risk factors in erectile dysfunction. J Gend Specif Med. 2002; 5:19-24.[Medline]
This article has been cited by other articles:
![]() |
A. J Bank, A. S Kelly, D. R Kaiser, W. W Crawford, B. Waxman, D. A Schow, and K. L Billups The effects of quinapril and atorvastatin on the responsiveness to sildenafil in men with erectile dysfunction Vascular Medicine, November 1, 2006; 11(4): 251 - 257. [Abstract] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |