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303

Prostatitis and MalE cHronic PElVic Pain syndroME

Analgesics, muscle relaxants and neuromodulators

become frustrated by the lack of efficacy seen in

Analgesics can alleviate some of the pain, but

well designed randomized placebo controlled

trials in CP/CPPS despite solid theoretical con­

narcotics should be avoided except for short

siderations, strong anecdotal evidence from

term control of

serious

pain

exacerbations.

clinical practice, and evidence from numerous

Skeletal muscle

relaxants

such

as diazepam,

small usually single center clinical trials. We

baclofen and cyclobenzaprine are utilized in

have come to the realization that it is the very

men with spastic or dysfunctional pelvic floors

restrictive nature of these randomized trials, in

with some anecdotal success. Amitriptyline is

which we routinely exclude over 90% of the

an important adjunct

to neuropathic pain

patients we see in our clinics on a daily basis, in

management, has proven efficacious in inter­

order to enroll very homogenous and compara­

stitial cystitis, and should be considered for

tive populations. The patients in our clinical tri­

the neuropathic

type

pain experienced by

als may not truly represent patients we see in

many men with CP/CPPS. Similarly, the gabap­

our clinical practice. In fact, each patient diag­

entinoids are indicated for neuropathic pain

nosed with CP/CPPS has a unique clinical phe­

control and the results from a recently com­

notype based on etiology, age, duration since

pleted NIH sponsored

randomized

placebo

diagnosis, concurrent disease, associated condi­

controlled trial is available soon. Based on the

tions, symptom trajectory, and coping behav­

results from other similar pain syndromes, we

iors. Based on this new understanding, a clinical

would expect this drug to prove efficacious in

phenotyping classification system was devel­

some patients.

 

 

 

 

 

 

 

 

 

 

oped to describe the characteristics of individ­

 

 

 

 

 

 

 

 

 

 

 

 

 

 

ual patients. The UPOINT system56 describes

Surgery

 

 

 

 

 

 

the following phenotypes; Urinary, Psycho­

 

 

 

 

 

 

social, Organ specific, Neurogenic/systemic and

A number of minimally invasive surgical app­

Tenderness (of muscles). UPOINT is outlined in

roaches

(transurethral

microwave

thermo­

more detail in Table 22.4. The number of

therapy, transurethral radiofrequency needle

UPOINT domains a patient is classified in is

ablation etc.) have been advocated for CP/CPPS,

associated with severity of both general CP/

however no real concrete evidence is available

CPPS symptoms and CP/CPPS related pain.57

to support any suggestion of efficacy.23 Radical

The domains are not correlated with age, but

transurethral and open prostatectomy has sim­

with duration since diagnosis. Each domain is

ilarly been suggested as a last resort and it is

associated with a slightly different impact on

evident from anecdotal experience that this

symptoms and pain. By employing this clinical

may create more harm than benefit for patients

phenotyping system, UPOINT, the physician

with CP/CPPS. Surgery should be restricted to

can categorize patients into one or more

discrete indications, usually those causing

domains using standardized workup (perhaps

lower urinary tract obstruction (urethral

asking a few questions about depression and/or

meatal stenosis, urethral stricture, bladder neck

coping) and then use this information to direct

stenosis).40

 

 

 

 

 

specific and usually multi­modal therapies.

 

 

 

 

 

 

 

Table 22.4 describes how therapies can be tai­

A Practical Management Plan

lored for individual UPOINT domains experi­

enced by the patient. As we learn more about

Table 22.3 describes the various medical thera­

the etiology and pathogenesis of CP/CPPS

(which has so far eluded us), discoveries, includ­

pies that we employ to treat the prostatitis

ing important biomarkers, can be incorporated

syndromes and the evidence (or lack of it) to

into the UPOINT system, allowing for stratifica­

support therapeutic recommendations and sug­

tion of the six domains. The future for patients

gestions. One can quickly determine, that except

diagnosed with a prostatitis syndrome is look­

for the bacterial prostatitis syndromes (Cat I

ing brighter as we can now rationalize our

and II), therapy for the much more prevalent

clinical approach for this difficult medical

CP/CPPS

is poor. Clinical researchers have

condition.

304

Practical Urology: EssEntial PrinciPlEs and PracticE

Table 22.3. Medical therapy for the prostatitis syndromes

 

 

Class

Medication

Indication

Evidence

antibiotics

ciprofloxacin

category i

strong

 

levofloxacin

category ii

strong

 

ofloxacin

category iii

contradictory

 

norfloxacin

cat iii uropath

Moderate

 

doxycline

cat iii no uropath

Weak

 

azithromycin

Early naïve cat iii no uropath

Moderate

 

clarithromycin

late cat iii no uropath

not recommended

 

 

anti-inflammatories

ibuprofen

cat iii monotherapy

Weak/not

 

diclofenac

 

recommended

 

 

 

 

indomethocin

cat iii adjuvant therapy

Weak/moderate

 

celecoxib

 

 

alpha-blockers

terazosin

cat iii

contradictory

 

doxazosin

late cat iii

not recommended

 

tamsulosin

Early naïve cat iii

contradictory

 

 

 

 

alfuzosin

Early naïve cat iii voiding symptoms

suggestive

glycosaminoglycan

Pentosan

cat iii

Weak

 

polysulfate

cat iii suprapubic pain voiding

Weak/suggestive

 

 

symptoms

 

5-alpha reductase

Finasteride

cat iii

not recommended

inhibitors

dutasteride

cat iii large prostate over 40 years old

suggestive

 

tricyclic antidepressants

amitriptyline

cat iii

suggestivea

 

nortriptyline

 

 

gabapentinoids

gabapentin

cat iii

suggestive

 

Pregabalin

 

 

Muscle relaxants

diazepam

cat iii

suggestive

 

Baclofen

 

 

 

cyclobenzaprine

 

 

Phytotherapies

Quercetin

cat iii

Weak/moderate

 

Pollen extract

 

 

 

saw palmetto

 

 

narcotics

demerol

cat i

recommended

 

Morphine

cat ii

recommended

 

 

 

 

 

cat iii

not recommended

Minimally invasive surgery

tUna

cat i, ii and iii

not recommended

 

tUMt

 

 

 

laser therapy

 

 

305

Prostatitis and MalE cHronic PElVic Pain syndroME

Table 22.3. (continued)

 

 

 

Class

Medication

Indication

Evidence

invasive surgery

tUrP

cat i, ii and iii

not recommended

 

radical

 

(unless clear

 

 

surgical indication

 

prostatectomy

 

 

 

– see text)

 

 

 

conservative therapy

diet modification

cat iii

suggestive

 

lifestyle change

 

(anecdotal

 

 

evidence)

 

 

 

 

Physiotherapy

 

 

 

Prostate massage

 

 

 

acupuncture

 

 

 

other alternative

 

 

 

therapies

 

 

aPublication of recently completed niH trial evaluating pregabalin in cPPs may change this recommendation.

Table 22.4. the UPoint clinical phenotyping classification system

 

Upoint domain

Phenotype presentation

Directed therapies

Urinary

obstructive voiding symptoms

alpha blockers

 

 

anticholinergics

 

irritative voiding symptoms

5-alpha reductase inhibitors

 

 

Pyridium

Psychosocial

depression

antidepressants

 

Poor coping behaviors

Psychologist intervention

 

Poor social support

counseling

organ specific

inflammation

anti-inflammatories

 

Pain localized to prostate

Phytotherapies

infection

Bacteria localized to prostate specific specimens

antibiotics

 

History of cat i or ii

 

neurogenic/associated

neuropathic pain

tricyclic antidepressants

conditions

neurogenic abnormalities

gabapentinoids

 

 

associated systemic

specific therapy directed to

 

syndromes

associated condition

 

 

tenderness

Pelvic/perineal muscle spasm

Muscle relaxants

Pelvic floor or side wall

Physiotherapy

 

pain or trigger points

 

suprapubic/abdominal

 

muscle pain

 

306

Practical Urology: EssEntial PrinciPlEs and PracticE

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