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Author: Manish K Singh, MD, Assistant Professor, Pain Management, Department of Neurology, Drexel College of Medicine, Hahnemann University Hospital

Manish K Singh is a member of the following medical societies: American Academy of Neurology, American Academy of Pain Medicine, American Association of Physicians of Indian Origin, American Headache Society, American Medical Association, and American Society of Regional Anesthesia and Pain Medicine

Coauthor(s): Elizabeth E Puscheck, MD, Associate Professor, Department of Obstetrics and Gynecology, Wayne State University School of Medicine; In Vitro Fertilization Director, Medical Director, Gynecologic Ultrasound Director, Clinical Endocrine Laboratory Consultant, Department of Obstetrics and Gynecology, University Women's Care; Jashvant Patel, MD, Medical Director, Department of Pain Medicine and Comprehensive Rehabilitation, Medical College of Pennsylvania Hahnemann University

Editors: Suzanne R Trupin, MD, Clinical Professor of Obstetrics and Gynecology, University of Illinois College of Medicine-Champaign; CEO and Owner, Women's Health Practice; CEO and Owner, Hada Cosmetic Medicine and Midwest Surgical Center; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; A David Barnes, MD, PhD, MPH, FACOG, Consulting Staff, Department of Obstetrics and Gynecology, Mammoth Hospital, Mammoth Lakes, California, Pioneer Valley Hospital, Salt Lake City, Utah, Warren General Hospital, Warren, Pennsylvania and Mountain West Hospital, Tooele, Utah; Frederick B Gaupp, MD, Consulting Staff, Department of Family Practice, Assumption Community Hospital; Michel E Rivlin, MD, Associate Professor, Coordinator, Quality Assurance/Quality Improvement, Department of Obstetrics and Gynecology, University of Mississippi School of Medicine

Author and Editor Disclosure

Synonyms and related keywords: chronic pelvic pain, CPP, bladder dysfunction, bowel dysfunction, sexual dysfunction, depression, anxiety disorder, drug addiction, drug abuse, prostatitis, chronic orchalgia, prostatodynia, pelviccongestion syndrome, endometriosis, uterine leiomyomas, adenomyosis, pelvic inflammatory disease, PID, cervical stenosis, deflecting sigmoid adhesion, pelvic floor relaxation disorder, pudendal neuralgia, somatization, physical abuse, sexual abuse, sexually transmitted disease, STD, nonmenstrual pain, vulvodynia, dyspareunia, Betty maneuver, piriformis syndrome, obturator sign, psoas sign, Patrick test, faber test, adnexal cysts, chronic urinary tract infection, abdominal wall myofascial pain, carcinoma of the colon, chronic intermittent bowel obstruction, cutaneous nerveentrapment, shingles, sleep disorders, chronic ectopic pregnancy, chlamydial endometritis, chlamydial salpingitis, endosalpingiosis, ovarian retention syndrome, residual ovary syndrome, ovarian remnant syndrome, ovarian dystrophy, ovulatory pain, postoperative peritoneal cysts, residual accessory ovary, subacute salpingo-oophoritis, tuberculous salpingitis,atypical dysmenorrhea, endometrial polyps, cervical polyps, leiomyomata, genital prolapse, intrauterine contraceptive device, bladder neoplasm, interstitial cystitis, radiation cystitis, recurrent cystitis, recurrent urethritis, urolithiasis,detrusor-sphincterdyssynergia, urethral diverticulum, chronic urethral syndrome, urethral caruncle, compression fracture of lumbar vertebrae, fibromyalgia, faulty posture, mechanical low back pain, chronic coccygeal pain, muscular strains and sprains, pelvic floor myalgia, levator ani spasm, rectus tendon strain, femoral hernia, perineal hernia, umbilical hernia, spigelian hernia, sciatic hernia, obturator hernia, colitis, chronic constipation, diverticular disease, inflammatory bowel disease, irritable bowel syndrome, herpes zoster infection, degenerative joint disease, disk herniation, spondylosis, abdominalepilepsy, abdominal migraine, neoplasia of spinal cord

Background

Chronic pelvic pain (CPP) is a common problem and presents a major challenge to health care providers because of its unclear etiology, complex natural history, and poor response to therapy.

CPP is poorly understood and, consequently, poorly managed. This condition is best managed using a multidisciplinary approach. Management requires good integration and knowledge of all pelvic organ systems and other systems including musculoskeletal, neurologic, and psychiatric systems.

A significant number of these patients may have various associated problems, including bladder or bowel dysfunction, sexual dysfunction, and other systemic or constitutional symptoms. Other associated problems, such as depression, anxiety, and drug addiction, also may coexist.

In the United States, estimated direct medical costs for outpatient visits for CPP (women aged 18-50 y) is approximately $881.5 million per year (Mathias, 1996).

Pathophysiology

The pathophysiology of CPP is complex and multifactorial. It remains unclear.

Frequency

United States

CPP is a common problem. It affects approximately 1 in 7 women (Mathias, 1996). In one study of reproductive-aged women in primary care practices, the reported prevalence rate of pelvic pain was 39% (Jamieson, 1996). Of all referrals to gynecologists, 10% are for pelvic pain (Reiter, 1990).

International

A similar prevalence of CPP has been described in other countries (Zondervan, 1999).

Mortality/Morbidity

As with other chronic pain, CPP may lead to prolonged suffering, marital and family problems, loss of employment or disability, and various adverse medical reactions from lifelong therapy.

Race

In one study, being African American was found to be a risk factor for pelvic pain (Jamieson, 1996).

Sex

CPP is most common among reproductive-aged women. Common causes of CPP in men include chronic (nonbacterial) prostatitis, chronic orchalgia, and prostatodynia.

Age

CPP is most common among reproductive-aged women, especially those aged 26-30 years (Jamieson, 1996).



History

The proposed definition of chronic pelvic pain (CPP) is nonmenstrual pain of 3 months duration or longer that localizes to the anatomic pelvis and is severe enough to cause functional disability and require medical or surgical treatment. Most authorities agree that patients should be diagnosed with CPP if they have pain primarily located in the pelvis for more than 3 or 6 months duration.

Patient history is important in cases of CPP. Because of the complex etiology and, often, the presence of associated disorders, a general approach with a thorough history that directs further evaluation and appropriate consultations is needed. Perform a detailed review of systems, including reproductive, gastrointestinal, musculoskeletal, urologic, and neuro-psychiatric. As needed, ask specific questions, especially if the patient has an associated disorder. A thorough past history also is important to avoid repeating invasive and expensive procedures.

  • Focus history on characterizing the patient's pain, which can lead to appropriate diagnostic and therapeutic plans.
    • Location of pain: The location of pain is an important part of the history. Ask the patient to describe the pain location and type on a pain diagram (anteroposterior and lateral view of human picture).
    • Precipitating factors: Ask questions about factors that provoke or intensify pain. This may provide clues for possible etiologies or associated disorders. For example, in pelvic congestion syndrome, pain is related to posture and is worse at the end of day. In endometriosis, pain commonly is reported during or after intercourse.
    • Alleviating factors: Alleviating factors may exist. For example, rest may decrease pain of musculoskeletal or adnexal origin.
    • Quality of pain: Various terms can be used to describe the quality of pain. Such terms include throbbing, pounding, shooting, pricking, boring, stabbing, lancinating, sharp cutting, lacerating, pressing, cramping, crushing, pulling, pinching, stinging, burning, splitting, penetrating, piercing, squeezing, and dull aching.
    • Pain distribution: Spreading or radiation of pain also is important in the evaluation of neuropathic pain.
    • Severity or intensity of pain: Use some type of rating system to evaluate pain severity or intensity with a degree of objectivity and reproducibility. Different types of pain scales may be used. Numerical scales are more useful and reliable. The visual analog scale is one of the commonly used numerical scales.
  • Obtain a history specific to different systems and disorders.
    • Gynecologic and obstetric: For example, excessive bleeding with menses suggests uterine leiomyomas or adenomyosis. History of previous surgery may suggest intra-abdominal or pelvic adhesions. Patients with cervical stenosis usually have a history of chronic cervical infection or treatment with cryosurgery/laser surgery/loop excision or endometrial resection. Having multiple sexual partners is a risk factor for pelvic inflammatory disease.
    • Urologic: A detailed history to evaluate the urological system is important. For example, as compared to patients with pelvic pain, patients with interstitial cystitis report urgency and increased frequency of urination as the most distressing features.
    • Gastrointestinal: For example, deflecting sigmoid adhesions are common in women with CPP and frequently are associated with gastrointestinal symptoms.
    • Musculoskeletal: History of vaginal delivery with prolonged second-stage episiotomies or tears may suggest pelvic floor relaxation disorder.
    • Neurologic: Constant burning pain is a common complaint in patients with pudendal neuralgia. Patients may report dysesthesia and vulvodynia but usually not dyspareunia.
    • Psychologic: A good psychosocial or psychosexual history is needed when organic diseases are excluded, or coexisting psychiatric disorders are suggested. Obtain sufficient history to evaluate depression, anxiety disorder, somatization, physical or sexual abuse, drug abuse or dependence, and family problems, marital problems, or sexual problems. Sexual abuse occurring before age 15 years is associated with later development of CPP (Lampe, 2000). Somatization is a common associated psychologic disorder in women with CPP. Somatization scales can be used for evaluation.

Physical

Good rapport, tolerance, and an open-minded approach are important in the evaluation of any patient with chronic pain. A thorough systematic examination usually suggests an appropriate diagnosis and therapy.

  • Obstetric-gynecologic and other system examinations could be long and stressful. Detailed examination of obstetric-gynecologic and other systems can be performed in different positions. Usually, this includes standing, sitting, supine, and lithotomy positions.
  • Lithotomy examination usually includes the following:
    • Visual inspection of the external genitalia
    • Basic sensory testing and evaluation for trigger points
      • A cotton-tipped swab can be used for precise sensory and tender-point evaluation of the vestibule, vaginal cuff, cervical os, paracervical region, and cervical region.
      • Single-digit examinations of the vulva, pubic arch, levator ani coccyx, introitus, urethral, trigonal, cervix, paracervical areas, vaginal fornices, uterus, and adnexa are indicated.
    • Colposcopic evaluation of the vulva and vestibule
    • Sims retractor or single-blade speculum examination of the vagina and pelvic muscles
    • Bimanual pelvic examination
    • Rectovaginal examination
  • Perform detailed examinations for other systems (eg, gastrointestinal, urologic, neurologic, musculoskeletal) as required. For example, gait and posture evaluation, spine examination, and sensory and motor examination often are useful.
    • Betty maneuver (for piriformis syndrome): When abduction of the thigh against resistance is requested, the patient will report pain.
    • Obturator sign (dysfunction of the obturator muscles or fascia)
    • Straight-leg raising test (possible herniated disc, radiculopathy)
    • Psoas sign: If pain is elicited during flexion of hip against resistance, this may suggest dysfunction of the psoas muscles or fascia.
    • Patrick or faber (flexion in abduction and external rotation) test for hip evaluation

Causes

Various reproductive, gastrointestinal, urologic, and neuromuscular disorders may cause or contribute to CPP. Sometimes, multiple contributing factors may exist in a single patient.

  • Extrauterine reproductive disorders
    • Endometriosis
    • Adhesions
    • Adnexal cysts
    • Chronic ectopic pregnancy
    • Chlamydial endometritis or salpingitis
    • Endosalpingiosis
    • Ovarian retention syndrome (residual ovary syndrome)
    • Ovarian remnant syndrome
    • Ovarian dystrophy or ovulatory pain
    • Pelvic congestion syndrome
    • Postoperative peritoneal cysts
    • Residual accessory ovary
    • Subacute salpingo-oophoritis
    • Tuberculous salpingitis
  • Uterine reproductive disorders
    • Adenomyosis
    • Chronic endometritis
    • Atypical dysmenorrhea or ovulatory pain
    • Cervical stenosis
    • Endometrial or cervical polyps
    • Leiomyomata
    • Symptomatic pelvic relaxation (genital prolapse)
    • Intrauterine contraceptive device
  • Urologic disorders
    • Bladder neoplasm
    • Chronic urinary tract infection
    • Interstitial cystitis
    • Radiation cystitis
    • Recurrent cystitis
    • Recurrent urethritis
    • Urolithiasis
    • Uninhibited bladder contractions (detrusor-sphincter dyssynergia)
    • Urethral diverticulum
    • Chronic urethral syndrome
    • Urethral caruncle
  • Musculoskeletal disorders
    • Abdominal wall myofascial pain (trigger points)
    • Compression fracture of lumbar vertebrae
    • Faulty or poor posture
    • Fibromyalgia
    • Mechanical low back pain
    • Chronic coccygeal pain
    • Muscular strains and sprains
    • Pelvic floor myalgia (levator ani spasm)
    • Piriformis syndrome
    • Rectus tendon strain
    • Hernias (eg, obturator, sciatic, inguinal, femoral, spigelian, perineal, umbilical)
  • Gastrointestinal disorders
    • Carcinoma of the colon
    • Chronic intermittent bowel obstruction
    • Colitis
    • Chronic constipation
    • Diverticular disease
    • Inflammatory bowel disease
    • Irritable bowel syndrome
  • Neurologic disorders
    • Neuralgia/cutaneous nerve entrapment (surgical scar in the lower part of the abdomen; usually iliohypogastric, ilioinguinal, genitofemoral, and lateral femoral cutaneous nerves)
    • Shingles (herpes zoster infection)
    • Degenerative joint disease
    • Disk herniation
    • Spondylosis
    • Abdominal epilepsy
    • Abdominal migraine
    • Neoplasia of spinal cord or sacral nerve
  • Psychologic and other disorders
    • Personality disorders
    • Depression
    • Sleep disorders
    • Sexual and/or physical abuse
  • Common causes of CPP in men
    • Chronic (nonbacterial) prostatitis
    • Chronic orchalgia
    • Prostatodynia



Abdominal Hernias
Acute Bacterial Prostatitis and Prostatic Abscess
Adjustment Disorders
Adnexal Tumors
ALA Dehydratase Deficiency Porphyria
Benign Lesions of the Ovaries
Benign Vulvar Lesions
Bipolar Affective Disorder
Bladder Cancer
Carcinoma In Situ of the Urinary Bladder
Cervicitis
Chronic Bacterial Prostatitis
Chronic Fatigue Syndrome
Chronic Pelvic Pain Syndrome and Prostatodynia
Colon Cancer, Adenocarcinoma
Colonic Obstruction
Constipation
Cystitis, Nonbacterial
Depression
Diverticulitis
Dysmenorrhea
Endometrial Carcinoma
Endometriosis
Endometritis
Fibromyalgia
Gonococcal Infections
Gynecologic Pain
Hemorrhagic Cystitis: Noninfectious
Herpes Zoster
Inflammatory Bowel Disease
Infrainguinal Occlusive Disease
Interstitial Cystitis
Intestinal Motility Disorders
Irritable Bowel Syndrome
Lumbar Disc Disease
Lumbar Spondylosis
Malignant Neoplasms of the Small Intestine
Mediterranean Fever, Familial
Mixed Connective-Tissue Disease
Neurogenic Bladder
Nonbacterial Prostatitis
Ovarian Cancer
Pelvic Inflammatory Disease
Perianal Abscess
Perianal Cysts
Porphyria, Acute Intermittent
Pyelonephritis, Chronic
Radiation Cystitis
Rectal Cancer
Reflex Sympathetic Dystrophy
Salpingitis
Sleep Disorders
Somatoform Disorders
Ulcerative Colitis
Urethral Cancer
Urethral Diverticula
Urethral Diverticulum
Urethral Strictures
Urethral Syndrome
Urinary Tract Infection, Females
Urinary Tract Infection, Males
Uterine Cancer
Uterine Prolapse
Vaginitis
Vesicovaginal and Ureterovaginal Fistula
Vulvovaginitis

Other Problems to be Considered

Reproductive system
Adenomyosis
Adhesions
Adnexal tumors
Cervical stenosis
Dyspareunia
Endocervical and endometrial polyps
Endometriosis and endosalpingiosis
Uterine leiomyomas
Ovarian retention syndrome
Ovarian remnant syndrome
Pelvic varicosities and pelvic congestion syndrome
Vulvodynia
Pelvic floor relaxation disorders
Accessory and supernumerary ovaries

Urinary system
Chronic and recurrent urinary tract infections
Urolithiasis
Pelvic floor dysfunction
Urethral diverticula
Chronic urethral syndrome

Gastrointestinal system
Chronic intermittent bowel obstruction
Colitis
Chronic constipation
Diverticular disease
Inflammatory bowel disease
Irritable bowel syndrome
Peritoneal abscess

Other diseases
Hernias (eg, obturator, sciatic, inguinal, femoral, perineal, spigelian, umbilical)
Neoplasia of the spinal cord or sacral nerves
Mononeuropathy and nerve entrapment
Abdominal epilepsy
Abdominal migraines
Pelvic floor pain syndrome
Rectus abdominis pain
Faulty posture
Bipolar affective disorder and depression
Chronic visceral pain syndrome
Chronic fatigue syndrome
Substance abuse
Spinal malformation
Spinal tumors



Lab Studies

  • The decision to perform laboratory or imaging evaluations is based on the need for confirmation of the diagnosis and to help rule out other potentially life-threatening illnesses. Certain investigations sometimes are needed to provide appropriate and safe medical or surgical treatment.
  • Complete blood cell count and sedimentation rate: These tests provide nonspecific findings, but the results can be sensitive indicators of inflammation or infection and, occasionally, malignancy.
  • Serum drug screen: Perform this if any suggestion of prescription or street drug abuse is present.
  • Urine test
    • Urinalysis and urine culture are relatively inexpensive and noninvasive and should be performed when necessary.
    • If hematuria is present, carefully evaluate the condition with a history, physical examination, urine culture, urine cytology, cystourethroscopy, and intravenous pyelography or CT scan.
    • If malignancy is suggested, perform urine cytology in addition to urinalysis and culture, especially if the patient smokes.
  • Sexually transmitted disease testing
    • Testing for sexually transmitted diseases in women with chronic pelvic pain (CPP) includes cervical cultures or smears, syphilis serology (rapid plasma reagent, microhemagglutination-Treponema pallidum), hepatitis B screening, chlamydial polymerase chain reaction, and HIV testing.
    • Other tests used to help rule out specific infections may include vaginal cultures, vaginal wet preparations, vaginal pH, and urine analysis and culture.
  • Hormone assays: Follicle-stimulating hormone level, estradiol level, and gonadotropin-releasing hormone agonist stimulation testing can be helpful in cases of ovarian remnant syndrome.
  • Thyroid-stimulating hormone testing
    • This is used for evaluation of hypothyroidism, especially in a patient with depression.
    • Perform stool guaiac testing in patients with gastrointestinal symptoms and in patients older than 50 years. Testing stool specimens for ova and parasites also may be helpful in selected cases.

Imaging Studies

  • Magnetic resonance imaging
    • MRI is a noninvasive tool that can provide excellent structural information without any radiation harm.
    • Intravenous contrast can be used when inflammation, infection, or malignancy is suggested.
  • CT scan: This is useful in patients with pelvic masses and sometimes is helpful in differentiating an ovarian mass from a uterine mass, but it is more expensive than sonography.
  • Ultrasonography
    • This is a noninvasive diagnostic tool and could be helpful in many patients with CPP.
    • It commonly is used to help identify pelvic masses or cysts and their origin, pelvic varicosities, and hernias (spigelian hernias).
  • Plain film radiography
    • Obtaining chest and spine radiographs may be useful in fractures, infections, tumors, and other structural abnormalities.
    • Flat and upright abdominal radiographs may be obtained to help rule out intestinal obstruction and pelvic infection (eg, tuberculosis).
  • Herniography (perineal hernia herniography)
  • Bone scan
  • Hysterosalpingography
    • Hysterosalpingography (HSG) is not a first-choice diagnostic tool for endometriosis; however, it may be useful in patients with infiltrative endometriosis of the uterosacral ligaments. Adolescents with endometriosis also can be evaluated for obstructive anomalies.
    • HSG may be useful in cases suggestive of endometrial polyps, Asherman syndrome, and adenomyosis.
  • Barium enema radiography, colonoscopy, sigmoidoscopy, upper gastrointestinal series, and anorectal manometry
    • These can be used to evaluate a gastrointestinal etiology of chronic pain.
    • Anorectal balloon manometry can be used to assess colonic transit time.
  • Vaginal sonography
    • This is useful in patients with possible pelvic congestion syndrome.
    • Transuterine venography commonly is recommended.
  • Voiding cystourethrography: When interstitial cystitis is suggested, consider cystoscopy with hydrodistention.
  • Double-balloon cystourethrography: This is a more sensitive diagnostic test than voiding cystourethrography for diagnosing urethral diverticula in women (Jacoby, 1999).

Other Tests

  • Endoscopic procedures used commonly in the evaluation and treatment of patients with CPP include laparoscopy, cystourethroscopy, hysteroscopy, sigmoidoscopy, and colonoscopy.
  • Laparoscopy can be used as a diagnostic tool in patients with CPP, as follows:
    • More than 40% of laparoscopies are performed for the diagnosis of CPP.
    • More then 60% of women with CPP have at least one condition detectable by laparoscopy.
    • Most commonly, diagnoses made via laparoscopy include endometriosis, pelvic adhesions, and chronic pelvic inflammatory disease. Other diagnoses include ovarian cysts, hernias, pelvic congestion syndrome, ovarian remnant syndrome, ovarian retention syndrome, postoperative peritoneal cysts, and endosalpingiosis.
  • Urodynamic testing can be performed if chronic urethral syndrome or interstitial cystitis is suggested in a patient with CPP.
  • Nerve-conducting velocities and needle-electromyographic studies are used to help evaluate compression or entrapment neuropathy and pelvic floor function.
  • Cancer antigen 125 (CA125), used as a diagnostic test, has low sensitivity and specificity.
    • CA125 may be elevated with diseases associated with pelvic pain, such as endometriosis or leiomyomata.
    • CA125 levels also are elevated with malignancy (eg, ovarian, endometrial, colon, or breast cancer), pelvic inflammatory disease, pregnancy, and menses (Howard and Perry, 2000).
    • Perform electroencephalography if the rare disorder of abdominal epilepsy is suggested.



Medical Care

Treatment of pelvic pain is complex in patients with multiple problems. It usually requires specific treatment and simultaneous psychological and physical therapy. A good relationship should be established between the physician and the patient. Treatment of chronic pelvic pain (CPP) must be tailored for the individual patient.

The goals of treatment must be realistic. They should be focused toward restoration of normal function (minimal disability), better quality of life, and prevention of relapse of chronic symptoms.

  • Pharmacotherapy
    • Pharmacotherapy consists of symptomatic abortive therapy to stop or reduce the severity of the acute exacerbations and long-term therapy for chronic pain.
    • Initially, pain may respond to simple over-the-counter (OTC) analgesics such as paracetamol, ibuprofen, aspirin, or naproxen. If treatment results are unsatisfactory, the addition of other modalities or the use of prescription drugs is recommended.
    • If possible, avoid use of barbiturate or opiate agonists. Also discourage long-term use and overuse of all symptomatic analgesics because of the risk of dependence and abuse.
    • Tizanidine may improve the inhibitory function in the central nervous system and can provide pain relief. Therapy with tizanidine is not considered the standard of care
    • Amitriptyline (Elavil) and nortriptyline (Pamelor) are the tricyclic antidepressants (TCAs) used most frequently for chronic pain.
    • The selective serotonin reuptake inhibitors (SSRIs) fluoxetine (Prozac), paroxetine (Paxil), and sertraline (Zoloft) also are prescribed commonly by many physicians. Other antidepressants such as doxepin, desipramine protriptyline, and buspirone also can be used.
  • Physical therapy
    • Physical therapy techniques include hot or cold applications, positioning, stretching exercises, traction, massage, ultrasound therapy, transcutaneous electrical nerve stimulation (TENS), and manipulations. Heat, massage, and stretching can be used to alleviate excess muscle contraction and pain.
    • Pelvic floor training also may be recommended.
  • Psychophysiological therapy
    • Psychophysiological therapy includes reassurance, counseling, relaxation therapy, a stress management program, and biofeedback techniques. With these modalities of treatment, both frequency and severity of chronic pain may be reduced.
    • Biofeedback may be helpful in some patients when combined with medications.

Surgical Care

  • Various minimally invasive techniques may provide pain relief. These techniques include the following:
    • Trigger point injections: These injections are used mostly for localized trigger points (myofascial pain or neuroma).
    • Peripheral nerve blocks: Specific peripheral nerve block with local anesthetic and steroids may be helpful in selected cases.
  • Neuroablation of selected nerves can be performed by using different techniques, including thermocoagulation (radiofrequency ablation), cryoablation, or injection of chemical agents (alcohol, hypertonic saline, phenol).
    • An intrathecal morphine pump may be used, but careful selection for appropriate patients is very important.
    • Sacral nerve stimulation may be effective in the treatment of therapy-resistant pelvic pain syndromes linked to pelvic floor dysfunction (Everaert, 2001).
  • Various surgical procedures may be considered to treat CPP. Surgical procedures include presacral neurectomy (superior hypogastric plexus excision), paracervical denervation (laparoscopic uterine nerve ablation), and uterovaginal ganglion excision (inferior hypogastric plexus excision).

Consultations

Consultation with a psychologist, urologist, neurologist, and gastrointestinal specialist or other appropriate specialists is very important, especially before considering invasive or aggressive management.



Pharmacotherapy consists of symptomatic abortive therapy to stop or reduce the severity of acute exacerbation of pain and long-term therapy for chronic pain.

Drug Category: Analgesics

Generally used in mild to moderate pain; however, also may be effective for severe pain.

Drug NameAcetaminophen (Tylenol)
DescriptionFirst choice for pain, especially during pregnancy and breastfeeding.
Adult Dose650-1000 mg PO q6h prn
Pediatric Dose<3 years: Not established
3-6 years: 10 mg/kg/dose PO; not to exceed 720 mg/d
6-12 years: 10 mg/kg/dose PO; not to exceed 2.6 g/d
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity; known G-6-P deficiency
InteractionsRifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, sulfinpyrazone, hydantoins, ethanol, and isoniazid may increase hepatotoxicity
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsHepatotoxicity possible in patients with chronic alcoholism following various dose levels; severe or recurrent pain or high or continued fever may indicate a serious illness; APAP is contained in many OTC products, and combined use with these products may result in cumulative APAP doses exceeding recommended maximum dose

Drug NameIbuprofen (Advil, Motrin)
DescriptionInhibits inflammatory reactions and pain by decreasing activity of cyclooxygenase, which is responsible for prostaglandin synthesis.
Adult Dose400-800 mg PO q8h while symptoms persist; not to exceed 3.2 g/d
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding
InteractionsCoadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsCategory D in third trimester of pregnancy; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy

Drug NameNaproxen (Aleve, Naprosyn, Naprelan)
DescriptionFor relief of mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing activity of cyclooxygenase, which results in a decrease of prostaglandin synthesis.
Adult Dose275 mg PO tid or 550 mg PO bid
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency
InteractionsCoadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; NSAIDs may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCategory D in third trimester of pregnancy; acute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia, and renal papillary necrosis may occur; patients with preexisting renal disease or compromised renal perfusion risk acute renal failure; leukopenia occurs rarely, is transient, and usually returns to normal during therapy; persistent leukopenia, granulocytopenia, or thrombocytopenia warrants further evaluation and may require discontinuation of drug

Drug Category: Opioids

Commonly used for many pain syndromes.

Drug NameFentanyl (Duragesic patch)
DescriptionPotent narcotic analgesic with much shorter half-life than morphine sulfate. DOC for conscious sedation analgesia. Ideal for analgesic action of short duration during anesthesia and immediate postoperative period. Excellent choice for pain management and sedation; short duration (30-60 min) and easy to titrate.
Easily and quickly reversed by naloxone. When using transdermal dosage form, most patients are controlled with 72-h dosing intervals.
However, some patients require dosing intervals of 48 h.
Available in 12, 25, 50, 75, and 100 mcg doses.
Adult DoseApply 25-100 mcg/h system q48-72h
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; hypotension or potentially compromised airway when it would be difficult to establish rapid airway control
InteractionsPhenothiazines may antagonize analgesic effects of opiate agonists; TCAs may potentiate adverse effects of fentanyl when both drugs are used concurrently
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in hypotension, respiratory depression, constipation, nausea, emesis, and urinary retention; idiosyncratic reaction, known as chest wall rigidity syndrome, may require neuromuscular blockade in order to increase ventilation

Drug Category: Anticonvulsants

Certain antiepileptic drugs (eg, the GABA analogue gabapentin) have proven helpful in some cases of neuropathic pain. Other anticonvulsant agents (eg, pregabalin, clonazepam, topiramate, lamotrigine, zonisamide, tiagabine) have been tried in CPP.

Drug NameGabapentin (Neurontin)
DescriptionHas anticonvulsant properties and antineuralgic effects; however, exact mechanism of action is unknown.
Structurally related to GABA but does not interact with GABA receptors.
Adult Dose100 mg PO hs to 1200 mg PO tid
Pediatric Dose<12 years: Not recommended
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsAntacids may significantly reduce bioavailability (administer at least 2 h following antacids); may significantly increase norethindrone levels
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in severe renal disease; abrupt withdrawal may precipitate seizures

Drug Category: Tricyclic antidepressants

Increase synaptic concentration of serotonin and/or norepinephrine in the CNS by inhibiting reuptake by the presynaptic neuronal membrane. Newer agents include Cymbalta.

Drug NameNortriptyline (Pamelor)
DescriptionDemonstrated effectiveness in the treatment of chronic pain.
Adult Dose25-100 mg PO hs; not to exceed 200 mg/d
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; narrow-angle glaucoma; do not administer to patients who have taken MAOIs in past 14 d
InteractionsCimetidine may increase levels when used concurrently; may increase PT time in patients stabilized with warfarin
PregnancyD - Unsafe in pregnancy
PrecautionsCaution in cardiac conduction disturbances and history of hyperthyroidism, renal impairment, or hepatic impairment; because of pronounced effects in cardiovascular system, best to avoid in patients who are elderly

Drug NameAmitriptyline (Elavil)
DescriptionAnalgesic for certain chronic and neuropathic pain.
Adult Dose25-100 mg PO hs; not to exceed 150 mg/d
Pediatric DoseChildren: 0.1 mg/kg PO hs; increase as tolerated over 2-3 wk to 0.5-2 mg/d PO hs
Adolescents: 25-50 mg/d PO initially; increase gradually to 100 mg/d in divided doses
ContraindicationsDocumented hypersensitivity; patient has taken MAOIs in past 14 d; history of seizures, cardiac arrhythmias, glaucoma, and urinary retention
InteractionsPhenobarbital may decrease effects; coadministration with CYP2D6 enzyme system inhibitors (eg, cimetidine, quinidine) may increase levels; inhibits hypotensive effects of guanethidine; may interact with thyroid medications, alcohol, CNS depressants, barbiturates, and disulfiram
PregnancyD - Unsafe in pregnancy
PrecautionsCaution in cardiac conduction disturbances and history of hyperthyroidism, renal impairment, or hepatic impairment; avoid using in patients who are elderly

Drug Category: Selective serotonin reuptake inhibitors

Selectively inhibit presynaptic serotonin reuptake with minimal or no effect in the reuptake of norepinephrine or dopamine. SSRIs can be used in second-line or third-line treatment of painful diabetic neuropathy. Good for patients who already are depressed.

Drug NameFluoxetine (Prozac)
DescriptionConsidered an alternative to TCAs, with fewer adverse anticholinergic and cardiovascular effects.
Adult Dose10 mg PO in am; increase q2wk up to 60 mg/d
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; concurrently taking MAOIs or took them in the last 2 wk
InteractionsIncreases toxicity of diazepam and trazodone by decreasing clearance; also increases toxicity of MAOIs and highly protein-bound drugs
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsCaution in hepatic impairment and history of seizures; discontinue MAOIs at least 14 d before initiating fluoxetine therapy; anxiety, insomnia, drowsiness, tremor, anorexia, and anorgasmia and other sexual dysfunctions have been reported; nausea, flulike symptoms, and agitation also are noted but resolve within a few weeks

Drug NameSertraline (Zoloft)
DescriptionConsidered an alternative to TCAs, with fewer adverse anticholinergic and cardiovascular effects.
Adult Dose50 mg/d PO in am with 50-mg/d increments q2-3d to 100 mg/d, if tolerated; not to exceed 200 mg/d
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity
InteractionsIncreases toxicity of MAOIs, diazepam, tolbutamide, and warfarin
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in preexisting seizure disorders and in those who have experienced a recent MI, have unstable heart disease, or have hepatic or renal impairment; anxiety, insomnia, drowsiness, tremor, anorexia, and anorgasmia and other sexual dysfunctions have been reported; nausea, flulike symptoms, and agitation also are noted but resolve within a few weeks

Drug NameParoxetine (Paxil)
DescriptionConsidered an alternative to TCAs, with fewer adverse anticholinergic and cardiovascular effects.
Adult Dose10 mg/d PO and titrate up to 50 mg/d
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; concurrent administration with MAOIs or administering within 14 d of discontinuing an MAOIs
InteractionsPhenobarbital and phenytoin decrease effects; alcohol, cimetidine, sertraline, phenothiazines, and warfarin increase toxicity
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsCaution in history of seizures, mania, renal disease, and cardiac disease; anxiety, insomnia, drowsiness, tremor, anorexia, and anorgasmia and other sexual dysfunctions have been reported; nausea, flulike symptoms, and agitation also are noted but resolve within a few weeks



Further Inpatient Care

  • Hospitalization usually is not required for patients with chronic pelvic pain (CPP); however, the need for hospitalization depends on the invasiveness of the treatment choice for pain control and on the severity of the case.

Further Outpatient Care

  • Patients with CPP generally are treated in an outpatient setting and require a variety of health care professionals to optimally manage their condition.

Complications

  • Like other chronic pain, CPP may lead to prolonged suffering, marital or family problems, loss of employment, disability, and various adverse medical reactions from lifelong therapy.

Patient Education



Medical/Legal Pitfalls

  • Good rapport, tolerance, and an open-minded approach are important in the evaluation of any patient with chronic pain.
  • Patients with chronic pelvic pain (CPP) may exhibit exaggerated pain behavior or sensations that seem to be hysterical or appear nonanatomic or nonphysiologic; however, these patients always must be taken seriously and appropriate conservative steps should be taken.
  • Obtaining a thorough past history is important to avoid repeating invasive and expensive procedures.
  • Consultation with a psychologist, urologist, neurologist, and gastrointestinal specialist or other appropriate specialists is very important, especially before considering invasive or aggressive management.

Special Concerns

  • Appropriate caution must be taken during treatment of patients with the following characteristics:
    • Poor response to prior appropriate treatment
    • Unusual unexpected response to prior specific treatment
    • Avoidance of school, work, or other social responsibilities
    • Severe depression
    • Severe anxiety disorder
    • Excessive pain behavior
    • Frequent physician changes
    • Noncompliance with past treatment
    • Drug abuse or dependence
    • Family, marital, or sexual problems
    • History of physical or sexual abuse
  • Pregnancy
    • The use of medication during pregnancy is not contraindicated, but it should be limited and carefully justified.
    • Initially, pain should be managed with nonpharmacologic measures such as reassurance, rest, hot or cold applications, positioning, stretching exercises, massage, ultrasound therapy, TENS, relaxation therapy, and biofeedback. If pain does not respond to a nonpharmacologic approach, symptomatic drugs may be used carefully.
    • Acetaminophen and codeine (alone or in combination) can be used during pregnancy.
    • Nonsteroidal anti-inflammatory drugs such as ibuprofen and aspirin may be considered during the first trimester of pregnancy, but they should be avoided especially during the last trimester. They may constrict or close the fetal ductus arteriosus and may cause maternal and fetal bleeding.
    • Limit benzodiazepine and barbiturate use. Do not use ergotamine, dihydroergotamine, and sumatriptan.
  • CPP in men: Chronic (nonbacterial) prostatitis, chronic orchalgia, and prostatodynia are common causes of CPP in men of any age.



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