6. Erectile Dysfunction
PSYCHOGENIC IMPOTENCE
NORMAL SEXUAL FUNCTION REQUIREMENT
Self-confidence
Absence of anxiety
Presence of arousal
physical stimulations
Ability to focus attention on sexual activity
PSYCHOGENIC DYSFUNCTION PRODUCE
Exaggerated suprasacral inhibition
Excessive sympathetic outflow
7. Erectile Dysfunction
ETIOLOGY
PSYCHOGENIC IMPOTENCE
LUE CLASSIFICATIONS
1. Anxiety and fear of failure
2. Depression (drug or disease induced)
3. Marital conflict strained relationship
4. Ignorance, misinformations , religious beliefs
5. Psychotic and personality disorder
9. Erectile Dysfunction
ETIOLOGY
Psychogenic Impotence
Primary
• Sexually repressed patient from religiously family background
– Sex was not discussed
– sex was sinful and immoral
Secondary
• Poorly understood admixture of variable factors
– Emotional
– Familial
– Cognitive
– Cultural
– Maturational
– Biologic
– Temperamental
21. Erectile Dysfunction
Endocrine And Metabolic Disorders
D.M
• 50% of diabetic patients
• ED not correlelate with the severity of the disease or
the adequacy of control
• Duration of the disease is a greater risk
• Mechanism is complex
– Vascular microangiopthy
– Accelerated atherosclerosis
– Peripheral neuropathy
– Endocrine
22. Erectile Dysfunction
Endocrine And Metabolic Disorders
Hypergonadotrophic Hypogonadism
• Klinefelter
• Chemotherapeutic agents
• Radiation
Hypogonadotrophic Hypogonadism
• Kallmanns (hypogonadism and almost invariably infertility and anosmia)
• Prader-Willi (low muscle tone, short stature, incomplete sexual development, cognitive disabilities, problem
behaviors, and a chronic feeling of hunger that can lead to excessive eating and life-threatening obesity)
• Laurence-Moon-Biedl (obesity, retinitis pigmentosa, polydactyly, hypogonadism, and renal failure)
32. Erectile Dysfunction
HISTORY
Carful History And Physical Examination Are The Most
Important Part Of Overall Evaluation
Specify type of sexual dysfunction
Onset of dysfunction
Duration
Situation
Morning erection
Risk factors
Medications
38. Erectile Dysfunction
Special Studies
Nocturnal Penile Tumescence Test
• Normally occurs at REM sleep
• 3-5 episodes
• Psychogenic ED have positive test
• Negative test does not indicate organic ED
• Test at home or in sleep lab
• Measures tumescence not rigidity
• Not commonly used routinely
39.
40. Erectile Dysfunction
Special Studies
Assessment Of Penile Blood Flow
• Penile-brachial index (PBI)
– Penile systolic bl.P/brachial systolic bl.P
– Normal >0.7
– Vasculogenic arterial ED <0.7
• USE 10mhz Doppler probe
• Abandoned test
– Doppler signal is not specific
– Difficult to specify the exact vessel
– Study in flaccid penis
– Operator dependant
41. Erectile Dysfunction
Special Studies
Assessment Of Penile Blood Flow
Penile Doppler study
• Doppler study pre and after vasoactive ICI
• It is the commonly used test
• Rigid erection after ICI indicate normal arteries
Peak systolic velocity
End-diastolic velocity
Diameter of cavernosal arteries
42.
43. Erectile Dysfunction
Special Studies
Assessment Of Penile Blood Flow
ANGIOGRAPHY
Selective bilateral internal iliac arteries
Selective bilateral internal pudendal arteries
Invasive
Expensive
With significant risk
Prior for revascularization procedures only
44.
45. Erectile Dysfunction
Special Studies
Dynamic Infusion Cavernometry And
Cavernosography
Confirm diagnosis of venogenic ED
Infusion of warmed heparinized saline at a flow rate to achieve
erection
Infusion of contrast for Cavernosography
Record of flow rate required to maintain erction
46. Erectile Dysfunction
Special Studies
Neurologic Testing
Patient with high index of suspicion of Neurogenic ED
1. Pelvic parasympathetic nerves evaluation
Cystometry
2. Somatic pudendal nerve evaluation
Perineal EMG
Bulbocavernosus reflex latency test
3. Suprasacral afferent pathway evaluation
Genitocerebral evoked response
52. Erectile Dysfunction
Nitric Oxide
• Released from noncholinergic nonadrenergic nerves
• Stimulate guanylate cyclase enzyme
• Increase production of cGMP
• Cavernous smooth muscle relaxation
• Tumescence and erection
• Phosphodiesterase convert cGMP into GMP
• Sildenafil inhibits type 5 PDE leading to enhancing NO
relaxant effect
54. Erectile Dysfunction
Nonsurgical
Avanafil
• Is a potent selective phosphodiesterase type 5 (PDE5)
inhibitor newly developed for treating (ED).
• Preclinical and clinical phase I studies showed that
avanafil had :
– Enhanced selectivity
– Faster onset of action
– Favourable side-effect profile relative to currently available PDE5 inhibitors.
• As the result of phase III clinical trial for the efficacy and
safety of avanafil treatment (100 and 200 mg), taken as
needed over a period of 12 weeks, in Korean patients with
ED, avanafil is an effective and well-tolerated therapy for ED
of broad-spectrum aetiology and severity.
55. Erectile Dysfunction
Nonsurgical
Phosphodiesterase 5 Inhibitors
SILDENAFIL CITRATE
• FDA approval in 1998
• Significant advance in medical therapy of ED
• Success rate of 65-80%
• Intact neural input is necessary
• Sexual stimulation is required