dr. anmar nassir, frcs(c) canadian board in general urology fellowship in andrology (u of ottawa)...
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Dr. Anmar Nassir, FRCS(C)
Canadian board in General UrologyFellowship in Andrology (U of Ottawa)Fellowship in EndoUrology and Laparoscopy (McMaster Univ)
Assisstent Prof Umm Al-QuraConsultant Urology King Faisal Specialist Hospital
NONSURGICAL MANAGEMENT OF ERECTILE DYSFUNCTION
Lifestyle Change Medication Change Herbal Supplements Pelvic Floor Muscle Exercises Psychosexual Therapy Hormonal Therapy Pharmacologic Therapy
SildenafilSildenafil VardenafilVardenafil TadalafilTadalafilCmax (ng/mL)Cmax (ng/mL) 450450 20.920.9 378378
Tmax (hr)Tmax (hr) 0.80.8 0.7-0.90.7-0.9 22
Onset of actionOnset of action 15 min to 1 hr15 min to 1 hr 15 min to 1 hr15 min to 1 hr 15 min to 2 hr15 min to 2 hr
Half-lifeHalf-life 3-5 hr3-5 hr 4-5 hr4-5 hr 17.5 hr17.5 hr
BioavailabilityBioavailability 40%40% 15%15% Not testedNot tested
Fatty foodFatty food Reduced absorptionReduced absorption Reduced absorptionReduced absorption No effectNo effect
Recommended Recommended dosagedosage
25, 50, 100 mg25, 50, 100 mg 5, 10, 20 mg5, 10, 20 mg 5, 10, 20 mg5, 10, 20 mg
SildenafilSildenafil VardenafilVardenafil TadalafilTadalafilSide effectsSide effects
Headache, dyspepsia, Headache, dyspepsia, facial flushingfacial flushing
YesYes YesYes YesYes
Backache, myalgiaBackache, myalgia RareRare RareRare YesYes
Blurred/blue visionBlurred/blue vision YesYes RareRare RareRare
Precaution with Precaution with antiarrhythmicsantiarrhythmics
NoNo YesYes NoNo
Contraindication with nitratesContraindication with nitrates YesYes YesYes YesYes
Adverse events: PDE5 inhibitors
Adverse eventAdverse eventSildenafil Sildenafil (flexible dose)(flexible dose)
Tadalafil Tadalafil (20 mg)(20 mg)
Vardenafil Vardenafil (flexible dose)(flexible dose)
HeadacheHeadache 1616 1515 1515
FlushingFlushing 1010 33 1111
Nasopharyngitis/Nasopharyngitis/rhinitis/nasal congestionrhinitis/nasal congestion
44 33 99
DyspepsiaDyspepsia 77 88 44
Abnormal visionAbnormal vision 33
SinusitisSinusitis 33
Flu syndromeFlu syndrome 33
DiarrheaDiarrhea 33
MyalgiaMyalgia 33
NAION
Nonarteritic Anterior Ischemic Optic Neuropathy
Reported in men using sildenafil, vardenafil, and tadalafil n= 38, 1, and 4, respectively / total of 30 million users of PDE-5
Many of those affected had risk factors such as: hypertension, diabetes, or hyperlipidemia,
Some men showed causal relationship with recurrence of NAION after rechallenge with PDE-5 inhibitors.
WARNINGS
All three PDE-5 inhibitors warn against the use in patients with:
Myocardial infarction within the previous 90 days Unstable angina or angina occurring during sexual
intercourse New York Heart Association class II or greater heart failure
in the previous 6 months Uncontrolled arrhythmias, Hypotension (>90/50 mm Hg) Uncontrolled hypertension (>170/100 mm Hg) Stroke within the previous 6 months hereditary degenerative retinal disorders, retinitis pigmentosa Tendency to develop priapism (e.g., sickle cell anemia,
leukemia)
Common Intracavernous Agents
Drug Dose range Advantages Side Effects
Papaverine 7.5-60 mg Low cost; Stable at room temp
Fibrosis, priapism; Elevation of liver enzymes
Alprostadil 1-60 μg Metabolized in penis; Priapism rare
Painful erection; Requires refrigeration; Relatively expensive
Papaverine + phentolamine + alprostadil
0.1-1.0 mL Most potent Requires refrigeration
Combination of papaverine and phentolaminePapaverine (30 mg) and phentolamine (0.5 mg) An erection sufficient for sexual intercourse was
achieved in 115 (72%) as follows: vasculogenic (48%), psychogenic (93%), neurogenic (92%), diabetic (68%), idiopathic (63%), traumatic (60%), alcohol-related (80%), drug-related (75%).
After a mean follow-up period of 14.1 months, 55 (48%) were still successfully using intracavernous
therapy. A total of 22 episodes of priapism occurred in 16 patients One patient developed corporeal fibrosis.
Trimix
Three mixture containing: 2.5 mL papaverine (30 mg/mL), 0.5 mL phentolamine (5 mg/mL), 0.05 mL alprostadil (500 μg/mL)
74% of patients were maintained at a dose of less than 0.25 mL per injection ,averaging 3.1 uses per month.
65% were continuing injection therapy and of these,
89% were satisfied with the drug combination. 5.6% prolonged erections of more than 3 hours. No patient developed fibrosis or nodules.