Presentation 2

20
BAGIAN NEUROLO GI JOURNAL READIN FEBRUARI 201 OVERACTIVE BLADDER (Barkin J. Overactive Bladder. The Canadian Journal of Urology; 18 (Supplement 1). 2011; 8-113) Disusun oleh : Jasmine F. Hatane NIM. 2008-83-046 Pembimbing : dr. Parningotan Yosi Silalahi, Sp.S

description

Neurologi

Transcript of Presentation 2

Page 1: Presentation 2

BAGIAN NEUROLO GI JOURNAL READING FEBRUARI 2015

OVERACTIVE BLADDER (Barkin J. Overactive Bladder. The Canadian Journal of Urology; 18 (Supplement 1).

2011; 8-113)

Disusun oleh :Jasmine F. Hatane NIM. 2008-83-046

Pembimbing :dr. Parningotan Yosi Silalahi, Sp.S

Page 2: Presentation 2

BACKGROUND

OABurgency with or without urge incontinence, generally accompanied by frequency & nocturia

OAB may be claassified as “wet” or “dry”

Incidence & prevalence of OAB increases with increasing age

Prevalence OAB men = women, men are less likely to have accompanying urge incontinence

Page 3: Presentation 2

A large national United States telephone

survey that was part of the NOBLE program

16.9% of women had OAB (9.3% with urge

incontinence & 7.6% without urge incontinence

16% of men had OAB (2.4 with urge incontinence & 3.6

without urge incontinence

In Canada estimated that OAB affects 12-18%

of populations, & of these individual, one-third have wet OAB &

two-thirds have dry OAB

Page 4: Presentation 2

Symptoms of OAB = LUTS

BPH (in men), Urethral stricture, bladder stone,

atrophic vaginitis or vaginal prolapse (in women)

Neuropathic process, interstitial cystitis, painful bladder syndrome,

diabetes, genitourinary malignancy, UTI

Page 5: Presentation 2

DISCUSSION

Page 6: Presentation 2

Impact of untreated OAB

• Can have a profound negative impact on patient’s psychological well-being, quality of life, & physical health

• Despite the negative impact of OAB symptoms in quality of lifepatients often don’t mention to physicians a normal part of aging or embarrassed to speak about them

Page 7: Presentation 2

DIAGNOSING OAB

patient’s historypresence of LUTS or (DM, CHF, neurological disease, constipation), medication (diuretics,& antidepressants) dietary habit (excessive fluid/caffeine intake)

Physical examinationdistended bladder, vaginal prolapse/atrophy, enlarged prostate (determined by DRE) signs of neurological diseases, phimosis, or meatal stenosis

Patients with incontinence urgency , stress, mixed incontinence

Page 8: Presentation 2

Urinalisis (hematuria/signs

of UTI

Ultrasound postvoid residual

(PVR)

Cytoscopy

• RBCs, WBCs, nitrites, & glucose

• DM• Neurologic conditions• A large prostate• Frailness in elderlypoor

bladder emptying• Hematuria• Pain• Recurrent UTIs• Risk factor bladder cancer (older age,

male, smoker, family history)• Not responding therapy

Page 9: Presentation 2
Page 10: Presentation 2
Page 11: Presentation 2

MANAGING

OAB

Page 12: Presentation 2

Behavioral Therapy

Physiotherapy

Bladder retraining

Fluid management

Page 13: Presentation 2

Antimuscarinic agents

• Mainstays pharmacotheraphy for OAB• Muscarinic receptor in bladderreduce amplitude

of normal & involuntary bladder contractions• Improves the functional capacity of bladder

bladder’s storage volume at the first involuntary contraction

• In bladder M3 muscarinic receptorstimulating detrusor muscular contraction (salivary gland & gut) dry mouth & constipation

Page 14: Presentation 2

• M1 muscarinic receptor (brain)side effect: confusion

• M5 muscarinic receptor (cardiac muscle)side effect : prolonged QT intervalaritmia

• Side effects antimuscarinics : pupillary dilatation, paralysis of lens accomodation, tachycardia, changes in mental status, sweating , dry mouth & respiratory tract, inhibition of GI motility

• Higher dose/all long acting antimuscarinicganglion blockadeorthostatic hypotension, impotence, & muscle weakness

Page 15: Presentation 2
Page 16: Presentation 2

• IR Oxybutynincomparator drug during clinical trials

• Patients showedimproved compliance, improve efficacy ( frequency, urgency, & episode of incontinence) & fewer side effects

• Various authors reportedantimuscarinic treated in elderly patientpotential CNS impairmentmemory deficits, sleep disruption, confusion / hallucinations

• When choosing antimuscarinic drugASTEP “Availability, Safety, Tolerability, Efficacy, & Preference”

Page 17: Presentation 2

Nonmuscarinic agents

May be used alone/in combination with antimuscarinic

Desmopressin acetate (synhthetic form of ADH vasopressin

Desmopressinas a “melt” (60mcg/12omcg), tablet (0.1

mg/0,2mg), or nasal spray

Other nonmuscarinic drugstrcyclic antidepressant imipramine

(tofranil) & amitrityline (Elavil)

Page 18: Presentation 2

• Not respond behavioral therapy

• Can’t tolerate/respond conventional polypharmacologic agents

Severe OAB

• Botulinum toxin A (BOTOX) injections

• neuromodulator (nerve stimulator) implants

• augmentation cystoplasty

Highly specialized, expensive therapies

Page 19: Presentation 2

CONCLUSION

In most cases, patient with OAB can be initially managed at the primary

care level

Prevalence of OAB significantly with age

Behavioral modification & compliance with effective medical therapymost patient enjoy very

satisfactory improvement their OAB symptoms

Researchersstill searching most effective drug with the fewest/least

bothersome /insignificant side effects

Page 20: Presentation 2

Thank you