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Urinary Obstruction

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Urinary Obstruction & Benign Prostatic Hyperplasia (BPH) Xiao Huang, MD; PhD Department of Urology,1st Affiliated Hospital of Zhejiang University, School of Medicine – PowerPoint PPT presentation

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Title: Urinary Obstruction


1
Urinary Obstruction Benign Prostatic
Hyperplasia (BPH)
  • Xiao Huang, MD PhD
  • Department of Urology,1st Affiliated Hospital of
    Zhejiang University, School of Medicine

2
Urinary Obstruction
  • Urinary Tract Anatomy
  • Urinary Obstruction
  • Reason of Urinary Obstruction
  • Hydronephrosis

3
Urinary Tract Anatomy
4
Urinary Obstruction
5
Reason of Urinary Obstruction
6
Obstruction Reason Classification
  • Dynamic and structural
  • Congenital and aquired
  • Populations
  • Child congenital
  • Adults stone, injury, tumor ,TB
  • Women pelvic disease
  • Old men BPH
  • Locations
  • Kidney calculus, tumor, infection, TB, UPJ
    stricture, congenital deformity
  • Ureter stone, tumor, iatrogenic injury,
    ureteritis,TB , Metastatic carcinoma
  • Bladder BPH, bladder neck contracture, tumor,
    calculus, Neurogenic bladder
  • Urethral urethral stricture, Phimosis
    ,Congenital Posterior urethral valve ,stone.

7
Hydronephrosis
  • What is hydronephrosis?
  • Hydronephrosis is a "stretching" or dilation of
    the inside, or collecting part, of the kidney.
  • It often results from a blockage in the ureter
    where it joins the kidney that prevents urine
    from draining into the bladder.
  • Urine is trapped in the kidney and causes it to
    stretch.
  • Hydronephrosis may also be due to abnormal
    backwash or "reflux" of urine into the bladder.

8
Degrees of Hydronephrosis
Kidney function Minimally affected
compensation damage
9
Benign Prostatic Hyperplasia (BPH)
10
Objectives
  • What is a BPH
  • How to approach a patient with LUTS (lower
    urinary tract symptoms)
  • Treatment of BPH

11
Outline
  • 1. Definition of BPH
  • 2. Anatomy and Physiology
  • 3. Microscopic Appearance
  • 4. Prevalence of BPH
  • 5. Etiology
  • 6. Natural History of BPH
  • 7. LUTS
  • 8. Approach to a patient with BPH
  • 9. IPSS
  • 10. Differential Diagnosis
  • 11. Management of BPH
  • 12. Treatment of BPH

12
1.Definition
  • BPH is a nonmalignant enlargement of the prostate
    gland caused by cellular hyperplasia of both
    glandular and stromal elements that leads to
    troublesome lower urinary tract symptoms (LUTS)
    in some men
  • It is the most common benign tumor in men and is
    not a precancerous condition

13
2.Anatomy and physiology
  • The prostate is a compound tubuloalveolar
    exocrine gland of the male mammalian reproductive
    system
  • Function is to store and secrete a clear,
    slightly alkaline fluid that constitutes 10-30
    of the volume of the seminal fluid that along
    with the spermatozoa, constitutes semen
  • Secret is composed of simple sugars and proteins
    (proteolytic enzymes, acid phosphatase,
    prostate-specific antigen)zinc and citric acid

14
Lower urinary tract
15
2. Anatomy and physiology
  • A healthy human prostate is slightly larger than
    a walnut (4cm by 3cm). It surrounds the urethra
    just below the urinary bladder and can be felt
    during a rectal exam. It has anterior, median,
    posterior and two lateral lobes
  • Relations Posterior rectal ampulla
    (Denonvilliers fascia)Superior bladder neck
    Anteriorpubic symphysis (retropubic space of
    Retzius) Inferior urogenital diaphragm
  • Its work is regulated by androgens which are
    responsible for male sex characteristics

16
2.Anatomy and physiology
  • Glandular cells produce milky fluid that
    liquefies semen
  • Smooth muscle cells, which contract during sex
    and squeeze the fluid from the glandular cells
    into the urethra, where it mixes with sperm and
    other fluids to make semen. The muscle cells are
    stimulated by alpha adrenergic receptors
  • Stromal cells (which form the structure of the
    prostate)
  • The prostate gland also contains an enzyme - 5
    alpha-reductase that converts testosterone to
    dihydrotestosterone

17
2.1. Zonal Anatomy(McNeal-1972)
  • Peripheral Zone 70 of the young adult (60-70 of
    CaP)
  • Central Zone 25 (5-10 CaP)
  • Transition Zone 5 ( 10-20 CaP) BPH

18
Zonal Anatomy
19
3.Microscopic Appearance
  • Prostate consists of a thin fibrous capsule under
    which are circulary oriented smooth muscle fibres
    and collagenous tissue. Prostatic stroma lies
    deep to this layer and is composed of connective
    and ellastic tissue and smooth muscle where
    epithelial cells are embeded
  • As a male ages, there are more likely to be small
    concretions within the glandular lumina, called
    corpora amylacea, that represent laminated
    concretions of prostatic secretions. The glands
    are normally separated by stroma
  • The thin layer of connective tissue that
    surrounds the prostate merges with surrounding
    soft tissues, including nerves

20
4.Prevalence of BPH
  • In men 20 to 30 years of age, the prostate weighs
    about 20 g
  • however, the mean prostatic weight increases
    after the age of 50.

21
4.Prevalence of BPH
  • 20 of men age 41-50
  • 50 of men age 51-60
  • 65 of men age 61-70
  • 80 of men age 71-80
  • 90 of men age 81-90
  • lower urinary tract symptoms associated with
    BPH increase with age.

22
Pathophysiology of Clinical BPH Predictive Risk
Factors
  • Increasing age
  • Prostatic enlargement
  • Lower-urinary-tract symptoms (LUTS)
  • Decreased urinary flow rate
  • Elevated prostate-specific antigen (PSA)

Slide I.4
23
5.Etiology of BPH
  • Androgens
  • Estrogens
  • Lifestyle
  • Hereditary(genetic)/Race

24
5.1 Androgens
  • Testosterone and related hormones play a
    permissive role in BPH
  • Androgens have to be present for BPH to occur
  • Administering exogenous testosterone is not
    associated with a significant increase in the
    risk of BPH symptoms
  • Didhydrotestosterone (DHT), a metabolite of
    testosterone is a critical mediator of prostatic
    growth. DHT is synthesized in the prostate from
    circulating testosterone by the action of the
    enzyme 5a-reductase, type 2. This enzyme is
    localized principally in the stromal cells
    hence, these cells are the main site for the
    synthesis of DHT
  • DHT can act in an autocrine fashion on the
    stromal cells or in paracrine fashion by
    diffusing into nearby epithelial cells. In both
    of these cell types, DHT binds to nuclear
    androgen receptors and signals the transcription
    of growth factors that are mitogenic to the
    epithelial and stromal cells. DHT is 10 times
    more potent than testosterone because it
    dissociates from the androgen receptor more
    slowly
  • the active androgen, DHT, is important in
    promoting growth of prostate that would
    eventually lead to symptomatic BPH.

25
Regulation of Prostate Growth Intrinsic and
Extrinsic Factors
Extrinsic factors
Testicular Androgens Estrogens
Nonandrogenic
Intrinsic factors(prostate)
Epithelium Luminal Basal
Neuroendocrine
Stroma Fibroblast Smooth muscle
Extracellular matrix
Nontesticular Endocrine organs
Neurotransmitters Immunologic
Genetic Homeobox genes
Hereditary diseases
Urethra Urine Testis-epididymal
fluid
Environmental Dietary Micro-organisms (
immune response)
Extrinsic factors
Adapted from Lee C et al. In Benign Prostatic
Hyperplasia. Plymouth, United Kingdom Health
Publication, 200179-106.
Slide III.1
26
Regulation of Prostate GrowthRole of
Androgens
  • DHT is the principal androgen responsible for
    prostatic growth and BPH
  • 5?-reductase mediates the conversion of
    testosterone to DHT

OH
OH
5?-reductase
O
O
H
Testosterone
Dihydrotestosterone
Adapted from Bartsch G et al Eur Urol
200037(4)367-380.
Slide III.2
27
5.2 Estrogen
  • BPH occurs when men generally have elevated
    estrogen levels and relatively reduced free
    testosterone levels
  • Prostate tissue becomes more sensitive to
    estrogens and less responsive to DHT
  • Cells taken from the prostates of men who have
    BPH have been shown to grow in response to high
    estradiol levels with low androgens present
  • Estrogens may render cells more susceptible to
    the action of DHT
  • Androgen/estrogen ratio change

28
5.3 Lifestyle
  • On a microscopic level, BPH can be seen in the
    vast majority of men over the age of 70 years,
    around the world
  • Men who lead a western lifestyle have a much
    higher incidence of symptomatic BPH than men who
    lead a traditional or rural lifestyle

29
6.Natural History of BPH
  • Pathological or first phase of BPH -asymptomatic
    and involves a progression from microscopic to
    macroscopic BPH
  • Clinical or second phase of BPH - progression
    from pathological to clinical BPH development
    of LUTS
  • Mechanical and dynamic components are responsible
    for the progression from pathological to clinical
    BPH
  • In clinical BPH, the ratio of stroma to
    epithelium is 5 1
  • Asymptomatic hyperplasia the ratio is 2.71

30
Pathophysiology of Clinical BPH Overlapping but
Independent Features
Adapted from Nordling J et al. In Benign
Prostatic Hyperplasia. Plymouth, United Kingdom
Health Publication, 2001107-166.
Slide I.2
31
7. Lower Urinary Tract Symtoms-LUTS
  • 7.1.Voiding/Obstructive symptoms
  • Hesitancy
  • Intermittency
  • Incomplete voiding
  • Weak urinary stream
  • Straining to pass urine
  • Prolonged micturition
  • Terminal dribbling
  • 7.2.Storage/Irritative symptoms
  • Frequency of urination
  • Nocturia
  • Urgency (compelling need to void that can not be
    deferred)
  • Urge incontinence

32
7. Obstructive and irritative symptoms origin
  • Obstructive symptoms-mechanical obstruction due
    to glandular enlargement as well as dynamic
    obstruction secondary to contraction of the
    smooth muscle of the prostate, urethra and
    bladder neck. This dynamic obstruction is a
    result of sympathetic nervous system mediated
    stimulation of alpha-1adrenoceptors
  • Irritative symptoms - detrusor instability
    related to detrusor muscle changes in response to
    obstruction, such as bladder wall hypertrophy and
    collagen deposition in the bladder
  • Adrenoceptors may be further sub-divided into
    alpha1A and alpha1D subtypes, with alpha1A
    predominant in the prostate and alpha 1D in the
    bladder. Thus blockade of alpha1A may be
    necessary for reduction of obstruction whereas
    the blockade of alpha1D may be required to
    relieve storage symptoms

33
8. Differential Diagnosis
  • 10.2. Prostatic
  • Prostatitis
  • Prostate Cancer
  • 10.1. Pre-prostatic
  • Urethral stricture
  • Bladder neck contracture
  • Bladder tumors
  • Neurogenic bladder
  • Bladder calculi
  • Urinary tract infections

34
9. Approach to a patient with BPH
  • History (LUTS, previous surgery in the GU tract,
    STD and Hx of urethral stricture, prescription
    meds and over the counter meds). Use IPSS
  • Physical Examination digital rectal exam ( R/O
    Canodules, asymmetry, hardened ridges,
    induration R/O prostatitis tenderness,
    bogginess R/O anal malignancy and detect
    undiagnosed neurologic conditions by evaluating
    the sphincter tone and perianal
    sensationAbdomianl exam-distended bladder)
  • Urinalysis- by dipstick and routine microscopy,
    urine culture and sensitivity to R/O infections
    and hematuria
  • Serum PSA-optional to R/O Prostate Cancer

35
9. Approach to a patient with BPH (contd)
  • Upper tract imaging (IVP,CT, U/S) only in
    presence of concomitant urinary tract disease or
    complications-hematuria, UTI, renal
    insufficiency, Hx of stone disease
  • Cystoscopy- only for patients who dont respond
    to medical Trx to determine the need for surgical
    approach
  • Cystometrograms and urodynamic profile -for
    patients with suspected neurologic disease or
    those who failed prostate surgery
  • Flow rate, post-void residual urine determination
    and pressure flow- optional

36
10. IPSS
  • Mild (score 0-7)
  • Moderate (score 8-19)
  • Severe (score 20-35)

37
11. Management of BPH
  • Goal- rapid and sustained relief of symptoms
  • Decrease bladder outlet obstruction
  • Improve bladder emptying
  • Lower detrusor instability
  • Reverse renal insufficiency
  • Prevent future episodes of gross hematuria, UTI
    and urinary retention
  • Quality of life and sexuality
  • Management depends on severity

38
12. Treatment of BPH
  • Lifestyle modification
  • Watchful Waiting
  • Medical Therapy
  • Phytotherapy (alternative)
  • Surgical Treatment Conventional Surgical or
    Minimally Invasive Treatment

39
12. Treatment Algorithm
40
12.1. Lifestyle Changes
  • Enriched diet with ample amounts of fresh fish,
    fruits and vegetables
  • Reduce stress
  • Exercise on a regular basis
  • Weight within normal limits
  • Limit fluid intake, decrease bladder
    irritants-caffeine, alcohol avoid
    anticholinergic drugs, narcotics and skeletal
    muscle relaxants
  • See your doctor if you develop nocturia
  • Be aware of interaction of botanical and medical
    treatment

41
12.2. Watchful Waiting
  • The risk of progression or complications is
    uncertain
  • In men with symptomatic BPH, progression is not
    inevitable and some men undergo spontaneous
    improvement or resolution of their symptoms
  • Retrospective studies on the natural history of
    BPH are inherently subject to bias, related to
    patient selection and the type and extent of
    follow-up. Very few prospective studies
    addressing the natural history of BPH have been
    reported. A large randomized study compared
    finasteride with placebo in men with moderately
    to severely symptomatic BPH and enlarged
    prostates on DRE (McConnell et al, 1998).
    Patients in the placebo arm of the study had a 7
    risk of developing urinary retention over 4 years
  • Appropriate management of men with mild symptom
    scores (0-7)
  • Men with moderate or severe symptoms can also be
    managed in this fashion if they so choose
  • Neither the optimal interval for follow-up nor
    specific endpoints for intervention have been
    defined

42
12.3. Medical Treatment
  • Alpha blockers
  • 5a-Reductase inhibitors
  • Combination Therapy

43
12.3. Medical Treatment
Alpha blockers
  • Initially used for treatment of high blood
    pressure
  • The human prostate and bladder base contain
    alpha-1-adrenoreceptors and the prostate
    contracts to corresponding agonists. The
    contractile properties of the prostate and
    bladder neck are mediated primarily by the
    subtype a1a receptors
  • Alpha blockade improves both objective and
    subjective symptoms and signs of BPH in some
    patients
  • Alpha blockers can be classified according to
    their receptor selectivity as well as their
    half-life
  • Alpha Blockers Oral Dosage
  • Alpha-1 short-acting
  • Prazosin 2mg
    BID
  • Alpha-1, long-acting
  • Terazosin 5 or 10 OD
  • Doxazosin 4 or 8 OD
  • Alpha-1a selective
  • Tamsulosin 0.4 or 0.8 OD


44
12.3. Medical Treatment, Alpha
blockers (contd)
  • Short Acting Prazosin
  • Long-acting Alfuzosin, Doxazosin mesylate,
    Tamsulosin, Terazosin
  • Side Effects dizziness, postural hypotension,
    fatigue, retrograde ejaculation, rhinitis, and
    headaches. May potentiate other antihypertensive
    medications
  • Studies have shown that all of them have
    comparable effectiveness and the future research
    is focussed on improving convenience and
    tolerability
  • Terazosin and doxazosin may decrease the total
    cholesterol as well as LDL fraction. Both may
    cause first-dose syncope so titration is required
  • Alfuzosin and tamsulosin -have alpha 1A
    selectivity and dose titration is not required

45
12.3. Medical Treatment, Alpha
blockers (contd)
  • A study performed at the University of Maryland,
    Baltimore, USA, published in Jan. 2007, TitleA
    review of the clinical efficacy and safety of
    5alpha-reductase inhibitors for the enlarged
    prostate
  • Conclusion alpha-blockers in men with enlarged
    prostate have reported improvements in total
    symptom scores of 10 to 20 compared with
    placebo
  • Do not reduce the risk of long-term complications
    nor disease progression

46
12.3. Medical Treatment 5a-Reductase
inhibitors
  • Finasteride is a 5a-reductase inhibitor that
    blocks the conversion of testosterone to
    dihydrotestosterone. It affects the epithelial
    component of the prostate, resulting in a
    reduction in the size of the gland and
    improvement in symptoms
  • Six months of therapy are required to see the
    maximum effects on prostate size (20 reduction)
    and symptomatic improvement
  • Several randomized, double-blind,
    placebo-controlled trials have compared
    finasteride with placebo. Efficacy, safety, and
    durability are well established
  • Symptomatic improvement is seen only in men with
    enlarged prostates (gt 40 mL)
  • Side effects include decreased libido, decreased
    ejaculate volume, and impotence. Serum PSA is
    reduced by approximately 50 in patients being
    treated with finasteride, but individual values
    may vary, thus complicating cancer detection
  • Cost 73 for 30 day supp.

47
12.3. Medical Treatment 5a-Reductase
inhibitors (contd)
  • Dutasteride not enough data! In 3 double-blind
    trials it reduced acute urinary retention (1.8
    versus 4.2- placebo) and need for surgery (2.2
    vs 4.1) but increased impotence ( 7.3 vs 4.0),
    ejaculation disorder, and gynecomastia and
    lowered libido
  • Cost 84 for 30 day supp.

48
12.3. Medical Treatment 5a-Reductase
inhibitors (contd)
  • Summary
  • Significantly reduced the relative risk for acute
    urinary retention(AUR) and enlarged
    prostate-related surgery, slowed the disease
    progression, and showed greater relief of
    symptoms compared to placebo
  • Dutasteride, improved symptom scores greater
    after 4 years of therapy compared with 2 years
    (-6.4 vs -4.3 points, respectively) and flow
    rates were better (2.6 vs 2.3 mL/sec).
  • Finasteride showed maintenance of the decreased
    risk for AUR and enlarged prostate-related
    surgery over 4 year period
  • Generally well tolerated, with sexual dysfunction
    the most frequently reported adverse effect
    (1-8)

49
12.3. Medical Treatment Combination
therapy
  • Short term
  • Veterans Affairs Cooperative Study, 1229 men with
    BPH randomly assigned to placebo, finasteride,
    terazosin or both for one year. Results as
    follow
  • Terazosin lowered the symptom score and increased
    the peak urinary flow rate when compared with
    placebo
  • Finasteride alone was no better than placebo
  • The combination of finasteride and terazosin was
    no better than terazosin alone

50
12.3. Medical Treatment Combination
therapy (contd)
  • Short term
  • PREDICT trial in which 1095 men were randomly
    assigned to doxazosin, finasterid or both for one
    year. Resluts as follow
  • Doxazosin more effective than finasteride or
    placebo for urinary symptoms and flow rate
  • Combination no more effective than doxazosine
    alone
  • Conclusion Combination treatment with an
    alpha-blocker and a 5ARI is beneficial for
    immediate relief of symptoms ( with
    discontinuation of the alpha-blocker after
    several months of therapy)

51
12.3. Medical Treatment Combination
therapy (contd)
  • Long term
  • Medical Therapy of Prostatic Symptoms (MTOPS)
    trial-3047 men with BPH randomly assign. to
    doxazosin, finasteride, combination therapy or
    placebo were evaluated for symptomatic
    improvement and overall clinical progression of
    the BPH. Follow up 4.5 years. Results as follow
  • Risk of overall progression- reduced to a similar
    degree by doxazosin and finasteride (39 and 34
    when compared to placebo)
  • Combination therapy reduced the risk of clinical
    progression by 66
  • Symptom scores improved with all therapies, but
    to a greater degree with combined therapy

52
Combination Therapy for BPH ( MTOPS Study )
53
12.3. Medical Treatment Combination
therapy(contd)
  • Combination therapy or finasteride alone (but not
    doxazosin alone), reduced the risk of acute
    urinary retention and the need for invasive
    therapy
  • NNT( needed to treat) to prevent one instance of
    overall clinical progression was 8.4 for
    combination therapy, 13.7 for doxazosin, and 15.0
    for finasteride
  • AE -similar with combination therapy and
    monotherapy, with the exception of abnormal
    ejaculation, peripheral edema, and dyspnea, which
    were more common with combination therapy
  • Conclusion long-term combination therapy lowered
    the risk of overall clinical progression of BPH
    significantly more than treatment with either
    drug alone. In addition, combination therapy or
    finasteride alone (but not doxazosin alone),
    reduced the risk of acute urinary retention and
    the need for invasive therapy

54
12.4. Phytotherapy
  • Saw Palmetto Extracts
  • Beta-sitosterol plant extract
  • Rye Grass Pollen Extract
  • Pygeum Africanum

55
12.5. Surgical Treatment Conventional
Surgical Treatment
  • For patient who do not experience response to
    medical treatment in 12-24 months for those
    whose symptoms progress
  • TURP (transurethral resection of the prostate)-
    Gold standard
  • A resectoscope loaded with diathermy loop is
    introduced to the bladder and strips of prostatic
    adenoma are resected and dropped into the
    bladder. The prostate chips are extracted from
    the bladder and hemostasis is achieved with
    electrocautery
  • Under general anesthesia or with a regional
    block 60-90 min. Procedure.Requires 24-48 hours
    observation in hospital

56
12.5. Surgical Treatment Conventional
Surgical Treatment
57
12.5. Surgical Treatment Conventional
Surgical Treatment
  • Efficacy- decrease in symptom scores and increase
    in maximal urinary flow rates
  • Complications bleeding, urethral
    stricture/bladder neck contracture,
    hyper/hypovolemia, retrograde ejaculation (75),
    nausea, vomiting, confusion, hypertension,
    bradycardia, and visual disturbances
  • Treatment of complications diuresis and
    hypertonic saline administration for severe cases

58
12.5. Surgical Treatment Conventional
Surgical Treatment
  • TUIP (Transurethral incision of the prostate)
  • For moderate to severe symptoms and small
    prostate
  • Patients had posterior commisure hyperplasia or
    an elevated bladder neck a muscle resection is
    performed
  • Short-term improvement in BPH symptoms is about
    the same for TUIP as for TURP
  • Lower rate of retrograde ejaculation (25)

59
12.5. Surgical Treatment Conventional
Surgical Treatment
  • Open Prostatectomy
  • Not done routinely
  • When prostate too large for TURP
    (gt100mL)
  • Concomitant conditions - bladder diverticulum or
    bladder stone present,recurrent or persistent
    urinary tract infections,acute urinary
    distention,bladder outlet obstructions,recurrent
    gross hematuria of prostate origin,pathological
    changes in the bladder, ureters, or kidneys due
    to prostate obstruction

60
12.5. Minimally Invasive Surgical
treatment
  • TUMT-transurethral microwave therapy
  • TUNA- transurethral needle ablation
  • Urinary Stents
  • Laser Prostatectomy

61
12.5. Minimally Invasive Surgical
treatment
  • TUMT(transurethral microwave therapy)
  • Performed as a single outpatient visit under
    local anesthesia and an oral analgesic. Improves
    symptom scores and urinary flow rates
  • (TUMT) uses a special catheter with a tip
    containing an antenna to deliver microwave energy
    to the prostate, thus causing high temperatures
    within the prostate without affecting adjacent
    structures. The heat will kill prostate cells, so
    the prostate will effectively become smaller and
    less obstructing to urine flow. Sensors on the
    catheter and on a tube in the rectum enable
    monitoring of the temperatures throughout the
    procedure, and a cooling system circulates water
    within the catheter to protect the urethra
  • Disadvantages the prostate may swell up right
    after therapy due to the heat and a catheter is
    placed for a week. The damaged prostate cells
    will be broken by the body and its molecules
    re-used for several months
  • Symptoms may start decreasing after 3 weeks

62
12.5. Minimally Invasive Surgical
treatment
  • TUNA (transurethral needle ablation)
  • An office procedure performed under local
    anesthesia- improves symptom scores and urinary
    flow rates
  • It uses specially designed catheter through which
    interstitial radio-frequency needles are
    deployed from the tip of it. They will heat the
    tissue resulting in coagulative necrosis
  • The entire procedure lasts 30-60 minutes
  • A catheter is left for 1-4 days after the
    procedure

63
12.5. Minimally Invasive Surgical
treatment
  • Intraurethral Stent
  • Limited long term experience
  • Increases urine flow rates but causes secondary
    obstruction by exuberant granulation tissue
    growth through and around the stent
  • Difficult to remove it formation of bladder
    calculi in 50 of patients
  • Usually for patients with limited life expectancy
    that are not good surgical or anesthetic
    candidates
  • Abandoned by most urologists

64
12.5. Minimally Invasive Surgical
treatment
  • Laser Therapy- The wave of the future
  • Neodymium yttrium-aluminium-garnet (NdYAG)
    -Visual Laser ablation of the Prostate
  • The final result is coagulative necrosis of the
    prostatic urethra and adjacent inner prostatic
    tissue. The obstructive tissue starts to slough
    4-8 weeks post-op leading to an open prostatic
    urethra
    ?
  • Green light laser -Laser Vaporization of
    Prostate- causes rapid vaporization of the
    superficial tissue, with a minimal rim (2 mm) of
    coagulation
  • Advantage immediate TUR-like efect of the
    prostatic urethra, resulting in shorter duration
    of Foley catheterization in the initial post-op
    period ?
  • Holmium-YAG- Laser resection- prostatic lobes are
    resected into multiple small prostate chips that
    fall into the bladder, similar to standard
    electrocautery TURP
  • Advantageimmediate anatomical patency of the
    prostatic urethra, resulting in shorter duration
    of Foley catheterization and higher peak flow
    rates in the initial post-op period
    ?

65
12.5. Minimally Invasive Surgical
treatment
  • Transurethral balloon dilation of the prostate
  • Performed with specially designed catheters
  • Most effective in small prostate (lt40mL)
  • Does not produce retrograde ejaculation
  • May be of value in younger patients wishing to
    avoid or delay TURP, but is unlikely to achieve
    wider application because of the transient
    effects
  • Very rarely used today

66
In Summary
  • BPH (Benign prostatic hyperplasia) becomes
    increasingly common as men age
  • Many men with BPH are asymptomatic or have only
    mild symptoms, and may not require therapy
  • Men who develop upper or lower tract injury will
    require surgery
  • Alpha-adrenergic antagonists provide immediate
    therapeutic benefits and are first line treatment
    for smaller prostates lt40mL and mild symptoms
  • 5-alpha-reductase inhibitors require long-term
    treatment for efficacy and are beneficial for
    larger prostates gt40 mL mild to moderate symptoms

67
In Summary
  • Combined alpha adrenergic antagonist and
    5-alpha-reductase inhibitor therapy appears to be
    superior to either agent alone for long-term Trx
  • The choice of medical treatment may be made on
    the basis of cost and side-effect profile of the
    drug
  • TURP is the GOLD STANDARD for men who require an
    invasive procedure and are in good health
  • Men that are poor candidates for surgery and
    require an invasive surgical procedure should be
    advised on TUNA
  • Other surgical therapies (TUMT, Laser) may be
    reasonable options based on local expertise

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