Bladder Flashcards

1
Q

Bladder first

A

tier: exercise, lifestyle, and complementary therapies

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2
Q

Bladder second

A

tier: pharmacotherapies
Anti-muscarinic agents
Beta-adrenergic therapy
Initial agent depends on side effect profile and insurance coverage

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3
Q

Anti-muscarinics most

A

Most commonly prescribed

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4
Q

Anti-muscarinics act primarly

A

Act primarily by increasing bladder capacity and decreasing urgency through blockade of muscarinic receptor stimulation by acetylcholine during bladder storage

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5
Q

Anti-muscarinics start

A

Start lowest dose and titrate up (if needed) after 2 weeks

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6
Q

Anti-muscarinics f/u

A

Start lowest dose and titrate up (if needed) after 2 weeks

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7
Q

Anti-muscarinics CI

A

CI: uncontrolled tachyarrhythmias, myasthenia gravis, gastric retention and narrow angle-closure glaucoma

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8
Q

Anti-muscarinics AE

A

AE: urinary retention, dry mouth, constipation, blurred vision for near objects, tachycardia, drowsiness, and decreased cognitive function

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9
Q

Beta3-adrenoceptor agonist (mirabegron

A

Promotes selective beta receptor stimulation of the detrusor muscle to enhance smooth muscle relaxation.

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10
Q

Mirabegron - Initial medication and as different choice for patients who do not tolerate or respond to antimuscarinic medications

A

Are at risk for central nervous system side effects (eg, dementia), orr have a contraindication to antimuscarinic medication.

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11
Q

Mirabegron maybe useful

A

for patients already taking a cholinesterase inhibitor for whom it is preferable to avoid adding antimuscarinic agents.

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12
Q

Mirabegron has similar efficacy to

A

antimuscarinics but may be somewhat better tolerated.

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13
Q

Mirabegron - Close monitoring

A

Close monitoring – monitor for new-onset urinary retention by measuring at f/u in 4 to 6 weeks or has any new symptoms

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14
Q

Mirabegron adverse effects

A

– CI in severe or uncontrolled HTN
HTN – monitor BP
Dry mouth, constipation
Urinary retention

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15
Q

Can use anti-muscarinic and

A

beta 3 agonist medications together

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16
Q

BPH increases as men

A

age and can contribute to urinary symptoms that may benefit from medical or surgical treatment.

17
Q

treatements for BPH

A

Lifestyle modifications
Alpha-adrenergic receptor blockers
Phosphodiesterase type 5 inhibitors
5-alpha reductase inhibitors to prevent progression

18
Q

Alpha-adrenergic receptor blockers initial

A

therapy in most patients with LUTS/BPH

19
Q

Alpha-adrenergic receptor blockers bladdder outlet

A

outlet obstruction (BOO) is primarily mediated by alpha-1 adrenergic receptors located on prostatic smooth muscle, which are upregulated in the stromal glandular hyperplasia seen in BPH.

20
Q

Alpha-adrenergic receptor blockers blcoking

A

signaling through the alpha-adrenergic receptorsleads to relaxation of the smooth muscle of the bladder neck and the prostatic urethra.

21
Q

Alpha-adrenergic blockers - SE

A

SE: dizziness and rhinitis; hypotension

22
Q

Alpha-adrenergic blockers - Agents with greater

A

Agents with greater selectivity have fewer systemic SE but are associated with a higher frequency of retrograde or anejaculation (8 to 28 percent).

23
Q

Alpha-adrenergic blockers patietns

A

prescribed alpha-1adrenergicblockers should be counseled about the possibility of intraoperative floppy iris syndrome (IFIS).

24
Q

Phosphodiesterase type 5 inhibitors - used in men with

A

Used in men with BPH-related symptoms and ED

25
Q

Phosphodiesterase type 5 inhibitors reproted adverse

A

Reported adverse effects with PDE5 inhibitors are relatively rare, with the more commonly reported effects consisting of headache, flushing, dyspepsia, nasal congestion, back pain, myalgias, and sinusitis.

26
Q

Phosphodiesterase type 5 inhibitors there is an increased risk of

A

hypotension in patients also using certain alpha-adrenergic blockers

27
Q

In men with low post-void residual urine volumes

A

and irritative symptoms, anticholinergics or beta-3 agonists are a reasonable alternative to alpha-1 adrenergic antagonists for initial medical therapy

28
Q

In men with demonstrated benign prostatic enlargement (BPE), treatment with

A

In men with demonstrated benign prostatic enlargement (BPE), treatment with

29
Q

For patients with low post-void residual urine

A

volumes and irritative symptoms (eg, frequency, urgency) that persist during monotherapy with an alpha-1 adrenergic antagonist or anticholinergic agents, we use combination treatment with alpha-1 adrenergic antagonists and anticholinergic agents or beta-3 agonists