Module 3.2.2 (Management of ED) Flashcards

1
Q

Treatment aim for ED?

A

Achieve erection adequate for sexual intercourse

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2
Q

Non-pharmacological considerations for ED?

A
  • Diet, exercise, associated weight loss (metabolic)
  • Smoking cessation
  • Counsellingm, lifestyle changes (psychogenic)
  • Modifying drug therapy causing ED
  • Addressing substance abuse
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3
Q

What 1st to 4th line for ED treatment options after establishing cardiac fitness for sexual activity

A

1st line = PDE5 inhibitors

2nd line = Intracavernosal alprostadil and vacuum erection device

3rd line = Intracavernosal combinations (alprostadil, papaverine, phentolamine (SAS))

4th line = Penile implant

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4
Q

Why are PDE 5 inhibitors (sildenafil, tadalafil, vardenafil, avanafil) first line drugs? What are their A/Es? Max dose per day?

A
  • Drugs of choice: convenience (oral administration), effectiveness, onset of effect: 30-60 minutes

A/Es: headache (>10%), flushing, dizziness, dyspepsia, nasal congestion/rhinitis

  • Avanafil perhaps better tolerated (but less effective)
  • Visual effects (sildenafil), back pain (tadalafil), QT prolongation (vardenafil)

NO more than ONE dose per day

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5
Q

Why are PDE5 inhibitors contraindicated with nitrates? How to use if required for nitrates?

A

Risk of profound hypotension or MI.

  • If nitrate needed, allow at least 24 hours (12 hours with avanafil, 48 hours with tadalafil) after a dose of PDE5 inhibitor. Longer if PDE5 inhibitor elimination delayed.
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6
Q

How long to separate dose of PDE5I and alpha blockers (specifically prazosin) by?

A

4 hours (6 hours with vardenafil)

> because of hypotension

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7
Q

When are PDE-5 inhibitors CI?

A
  • CI in men in whom sexual intercourse not recommended due to CV risk
  • CI with in non-arteritic anterior ischaemic optic neuropathy (NAION) –> avoid when vision loss in one eye = increased risk
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8
Q

What to do if no response to PDE-5 inhibitors?

> lower dose may be needed if got side effects

A
  • Trial max dose on 6 different days 2 hours after meal (avanafil, sildenafil, vardenafil)
  • Trial alternative PDE5 inhibitor
  • Exclude hypogonadism
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9
Q

What are some considerations for alprostadil (prostaglandin E1)? Can be combined with PDE-5? AE? CI?

A

Intracarvesonal injection

2nd line when PDE5 inhibitors ineffective C/I (monotherapy)

  • Max 1 injection in 24 hours (upto 3/week)
  • Dose titration and training in self injection

Combination with PDE 5 = high risk of AE

A/Es: local pain, bruising, haematoma, priapism, cavernosal fibrosis

C/I: genitourinary (e.g. penile implant) when sexual intercourse inadvisable

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10
Q

Papaverine considerations? What is it used with?

A
  • Used alone or in combo with alprostadil
  • Intracavernosal injection
  • Genitourinary and CV CI/s
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11
Q

What is phentolamine only used with?

A

Only used with papaverine and or alprostadil injection (SAS)

> higher chances of priapism

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12
Q

Considerations for

A) vacuum erection devices

B) penile implants

C) testosterone therapy

A

A)

  • require dexterity
  • generally safe, one-off cost

B)

  • last line of treatment
  • high success rate
  • expensive, requires surgery, implant foreign materials and destroy the cavernosal tissue

C)

  • if deficiency diagnosed
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13
Q

What is priapism? Which ED treatment may it occur in and why?

A

Abnormally prolonged erection

  • persistent and painful
  • not caused by sexual desire/stimulation

MEDICAL EMERGENCYYY

> result in permamanent damage to cavernosal tissue

  • 5-10% of those using alprostadil will experience this during dose titration
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14
Q

What medications cause priapism?

A

Intracavernosal therapy for ED (most common), PDE5 inhibitors (infrequent with vardenafil), chlorpromazine, corticosteroids, some antihypertensives (prazosin)

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15
Q

What are some physical causes for priapism?

A

spine/pelvis tumour, sickle cell diseas, leukaemia, blood clots, prostatitis, urethritis, cystitis

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16
Q

treatment for priapism if

A) if present for 2 hours

B) if not subsided in 4 hours

C) >6 hours

A

A)

  • Hot shower and pseudoephedrine 120mg orally (single dose)

> pseudoephedrine = Alpha receptor-mediated vasoconstriction within the corpora cavernosa. Pseudoephedrine is an alpha1-selective adrenergic agonist with no indirect neurotransmitter-releasing action.

B)

  • Repeat above, contact doctor or afrter hours/ED

C)

  • Aspiration of blood from corpora cavernosa
17
Q

Treatemnt for premature ejaculation?

A
  • treat underlying cause first e.g. ED
  • behavioural therapy (stop and start technique)

> difficult to maintain

  • counselling on issues to address anxiety or psychogenic cause

topical

  • lignocaine 2.5% + prilocaine 2.5% cream
  • apply thinly 10-20min prior to intercourse
  • residual cream should be washed off before contact with partner

SSRI

  • prn dosing –> less AE such as anorexia, reduced libido or anejuclation, but risk of withdrawal

> dapoxetine 1-3 hours before intercourse (1 dose/ 24 hours)

> sertraline 3-5 hours before intercourse

> paroxetine 3-5 hours before intercourse

  • daily dosing = preferred

> paroxetine and sertraline

18
Q

What CAM possibly effective for ED?

A

Panax ginseng

1400-2700mg daily has improved sexual function in men with ED

19
Q

What CAM possibly effective for PE?

A

Multi-ingredient cream containing Panax ginseng (SS Cream) –> applied to the glans penis 1 hour prior to, and washed off immediately before intercourse