NSG 533 Module 3 Flashcards
Before initiating treatment for ED, a physical examination and thorough medical, social, and medication histories with emphasis on cardiac disease must be taken to assess for ability to safely perform sexual activity and to assess for possible drug interactions.
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o Non-pharmacological interventions for ED
Reduce fat and cholesterol in diet
Decrease or limit alcohol consumption
Eliminate tobacco use and substance abuse
Weight loss if appropriate
Regular exercise
(Regarding ED treatment)
If a medication is removed, consider that it probably will have to be replaced with a reasonable alternative.
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SS____ (psych drug class) are a potential cause of ED. A reasonable replacement or addition (to offset the ED) might be bup_______ (psych med) (assuming no contraindications)
SSRIs
bupropion
du__________ (med for BPH) is a common cause of ED. tar_________ (med) as a replacement for or in combination with a 5-alpha reductase might be reasonable (assuming no contraindications).
Dutasteride
Tardenafil
Note: There are occasions where an offending medication can NOT be discontinued because of a compelling indication and / or lack of a reasonable alternative (eg Beta-blockers in heart failure or SIHD).
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One must consider if the patient is healthy enough for sexual activity (table 51-3) and if so, possible alternatives such as vacuum erection devices or medications
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PD_______ (drug class) - Often considered drug of choice for ED when pharmacotherapy is necessary. There is no convincing evidence that one agent in this class is superior to another. Choice may be based on patient preference, cost, and
PDE5Is
PDE5Is:
Phosphodiesterase type 5 inhibitors
Phosphodiesterase type 5 inhibitors
PDE5Is
Regarding PD________ (ED drug class):
If one agent does not work it may be reasonable to try another from the same class. It is also imperative that patient is properly educated regarding onset and duration of effect, impact of high fat meals, the need for sexual stimulation and an explanation that a single trial is inadequate.
PDE5Is
Regarding ___________ (ED drug class):
There is no drug effect without some type of sexual stimulation because these drugs do not cause penile erections; they only provide the ability of the penis to respond to sexual stimulation.
PDE5Is
Regarding ___________ (ED drug class):
Headache and flushing most common ADRs. Serious cardiac events possible.
PDE5Is
Regarding ___________ (ED drug class):
Significant DIs exist
(+) nitrates - severe hypotension
In an emergent situation, a patient who has taken sildenafil may be given a nitrate after 24 hours; for tadalafil, after 48 hours. Vardenafil does not have a suggested time interval, but blood pressure and heart rate did not change when the drug was taken 24 hours before nitrate administration. These suggested intervals are a direct correlation to half-life and duration of action
PDE5Is
Regarding PD___s (ED drug class):
Prolonging of QT interval (especially vardenafil)
PDE5Is
Regarding ___________ (ED drug class):
Serious cardiovascular events have been associated with these drugs; therefore, they should not be used in patients in whom sexual intercourse is inadvisable because of poor cardiac status.
PDE5Is
Testosterone replacement regimens should ______ be administered to men with normal serum testosterone levels, or in patients with isolated erectile dysfunction as the only sign of hypogonadism.
never
Before initiating any testosterone replacement regimen in patients ____ years and older, patients should be screened for breast cancer, benign prostatic hyperplasia, and prostate cancer. All are testosterone-dependent conditions and theoretically could be worsened by exogenous administration of testosterone
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Regarding testosterone replacement:
Several medications may contribute to decreased testosterone: _________________________________.
(cimetidine, spironolactone, ketoconazole, etc).
Absolute contraindications in testosterone replacement:
- documented history of prostate cancer
- hx of breast cancer
- hct 55% or more
- sensitivity to ingredients in T formulations
______ - PgE1 analog administered by intracavernosal injection & intraurethral inserts
Alprostadil
OTC / Herbals (____________, etc) - limited evidence. Not recommended
Yohimbine
_____ increases urethral resistance, resulting in compensatory changes in bladder function. Obstruction-induced changes in detrusor function, including smooth muscle hypertrophy, compounded by age-related changes in the functioning of the bladder, lead to urinary frequency, urgency, and nocturia, the most bothersome _____-related complaints.
BPH
Diagnosis of BPH includes components such as ________________________.
symptom assessment (AUA score), PE and PSA
_____ is present in small quantities in the serum of men with healthy prostates, but is often elevated in the presence of prostate cancer or other prostate disorders. _____ is not uniquely an indicator of prostate cancer, but may also detect prostatitis or BPH. _____ correlates with prostate size and can be used as a prognostic marker
PSA
Regarding ____ treatment:
Watchful waiting is the most conservative approach for patients with mild symptoms or those with moderate symptoms without bother
◦Appropriate option for patients with mild symptoms (AUA-SI score ≤ 7), and for many with moderate to severe symptoms (AUA-SI ≥ 8) if they are not bothered
◦Behavior modification includes restricting fluids close to bedtime, minimizing caffeine, sweetened drinks and alcohol intake, frequent emptying of the bladder during waking hours (to avoid overflow incontinence and urgency), and avoiding drugs that could exacerbate voiding symptoms (e.g. antihistamines, decongestants).
◦At each visit, assess the patient’s risk of developing acute urinary retention by evaluating the patient’s prostate size or using PSA as a surrogate marker of prostate enlargement
BPH
Regarding _____ the level of symptom distress that individual men are able to tolerate is variable.
BPH
__________ (ED/cardiac drug class) - fairly rapid onset (2-4 weeks) with relatively rapid symptom resolution , durable effect (years) with AUA symptom index (AUASI) improving 30-45%. No effect on prostate size (PSA) or disease progression.
o Relax smooth muscle in bladder neck, urethra & prostate
Alpha-blockers
Regarding BPH, new second generation (a________) (med) and third generation (t___________ and s____________) (med) agents are preferred because of uroselectivity, no need for dose titration and limited orthostasis
alfuzosin
tamsulosin and silodosin
_____________________
Management of moderate to severe BPH in patients with enlarged prostate glands.
Management of patients who desire medical therapy but cannot tolerate alpha-1-adrenergic antagonists and do not have predominately irritant symptoms or concomitant erectile dysfunction (Symptoms are non-bothersome, so the delay in onset would not interfere with Qol)
5 alpha reductase inhibitors (5ARIs)
finasteride/dutasteride
Regarding BPH, this drug class:
Reduce prostate size (and PSA) and thus outlet obstruction
5A__s (BPH med)
5 alpha reductase inhibitors (5ARIs)
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finasteride/dutasteride
Regarding BPH, this drug class, 5A_____:
- Reverses/Slows disease progression
- Decreases the risk of disease complications
Note: although dutasteride blocks both the Type I and Type II iso-enzymes of 5-alpha reductase while finasteride only blocks Type II, there is not a clinically significant difference in outcomes when either is used
5 alpha reductase inhibitors (5ARIs)
finasteride/dutasteride
ADRs – (androgen insufficiency) decreased libido, impotence & ejaculatory disorder, breast tenderness & enlargement
_______ (BP/BPH drug class, -sterides)
5 alpha reductase inhibitors (5ARIs)
finasteride/dutasteride
Peak effect 6-12 months, effect is only durable as long as drug is continued (prostate will return to pre-treatment size (or larger) when / if 5ARIs are stopped
Finasteride & Dutasteride reduces, but does not stop the prostate from producing PSA
If PSA fails to decline by 50% after 6-12 months or an increase of 0.3 ng/L or more above the baseline nadir level, patient should be evaluated for prostate cancer. May also indicate worsening condition or non-compliance with 5 a-reductase inhibitors
5 alpha reductase inhibitors (5ARIs)
finasteride/dutasteride
o Treatment of the signs and symptoms of benign prostatic hyperplasia +/- ED
Relaxes smooth muscle of urethra, prostate and bladder neck
PDE5Is (tadalafil) -
tad______________ may be prescribed alone, or along with an α1-adrenergic antagonist and/or 5α-reductase inhibitor. Although other phosphodiesterase type 5 inhibitors share the same mechanism of action as tadalafil and can improve the AUA Symptom Score, tadalafil (which is the only PDE5I approved by the FDA for this indication) is preferred because of its longer plasma half-life, which is theoretically beneficial in the management of BPH, a chronic disease.
Tadalafil
Comparable efficacy to alpha-blockers for LUTS, but does not increase flow rate or reduce PVR
Peak onset 1-4 weeks
Which med?
t__________ (PDE5I, -fil)
Tadalafil
Adverse reactions
◦Use with alpha-blockers, antihypertensives or substantial amounts of alcohol may lead to hypotension
◦headache, dizziness, flushing, back pain, myalgia, and cyanopsia
Tadalafil
Precautions regarding this med, t____________ (ED drug class).
◦Unstable angina, uncontrolled or high-risk arrhythmias, persistent hypotension, poorly controlled hypertension, or New York Heart Association Classification IV congestive heart failure
Tadalafil
Contraindication
◦Current use of nitrates
Tadalafil
Alpha-blockers offer immediate relief of BPH; 5 alpha-RIs reduce prostate enlargement over time.
Alpha-blockers are the “zosins.” Doxazosin, prazosin, terazosin. α1-adrenergic antagonists are alpha-blockers.
5 alpha-RIs are the “sterides.” Finasteride, dutasteride.
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Regarding ___________ _________ for BPH:
Alpha-blocker offer immediate relief; 5 alpha-RIs reduce prostate enlargement over time
◦In patients with an enlarged prostate gland and an elevated PSA ≥1.4 ng/mL, combination drug therapy with an α1-adrenergic antagonist and a 5α-reductase inhibitor is more beneficial than single drug therapy.
◦Rationale
a-blocker offer immediate relief
5a-RIs reduce prostate enlargement
◦Works better for those with obstructive symptoms
◦May consider stopping a-blocker after 6-12 months, but should continue in those patients with severe symptoms as long as they are responding
Combination therapy
◦-blocker and ______________
(combination therapy BPH)
For men with low post-void residual urine volumes and irritative symptoms (e.g., frequency, urgency) that persist during treatment with an alpha-adrenergic antagonist, combination treatment with an ______________ agent can be tried.
Improved storage voiding parameters and frequency compared with alpha-1-adrenergic antagonist therapy alone
anticholinergic (or β3 agonist)
Regarding combination therapy for BPH using an alpha-blocker and an anticholinergic:
For patients who poorly tolerate anticholinergic adverse effects, an alternative is m________________ (med).
Mirabegron
Combination therapy for BPH utilizing alpha-blocker and an anticholinergic.
The risk of side effects, increased post-void residual urine volume, decreased maximal urinary flow rate, or acute urinary retention is low.
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alpha-blocker and PDE-5Is:
(Comination therapy for BPH and ED)
For men with moderate symptoms of BPH and erectile dysfunction, treatment with daily tadalafil (5 mg/day) alone or in combination with tamsulosin (0.4 mg/day) can be considered
Addition of PDE-5Is to alpha blockers may improve lower urinary tract symptoms
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PDE-5i and 5a-RIs
Addition of PDE-5i to 5a-RIs can offset erectile dysfunction commonly seen with 5a-RIs
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Herbals: No dietary supplement, combination phytotherapeutic agent or other nonconventional therapy is recommended for the management of LUTS (lower urinary tract symptoms) secondary to BPH.
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Commonly used / teratogenic
o __________, Phenytoin, __________________, Carbamazepine, Lithium, ___________________, Thalidomide, _____________, statins
o Warfarin, Phenytoin, Valproic Acid, Carbamazepine, Lithium, ACE inhibitors/ARBs, Thalidomide, Ethanol, statins