Pelvic Inflammatory Disease



Pelvic Inflammatory Disease



DIAGNOSTIC SUMMARY




• Dyspareunia.


• Mucopurulent cervical discharge.


• Pelvic pain; bilateral adnexal tenderness.


• Palpable adnexal mass.


• Elevated temperature (>101° F).


• Cervical motion tenderness.


• White blood cell count 20,000/μL, with marked leukocytosis and/or elevated sedimentation rate


• Neisseria gonorrhea and Chlamydia trachomatis most common, followed by Ureaplasma urealyticum, Mycoplasma hominis, Streptococcus spp., Escherichia coli, Haemophilus influenzae, Peptostreptococcus, and Peptococcus.*


• Transvaginal ultrasound showing thickened, fluid-filled tubes or tubo-ovarian mass.


• Acute and chronic endometritis on endometrial biopsy.


• Laparoscopy is the gold standard.


• New Centers for Disease Control and Prevention (CDC) rec-ommendations are that all sexually active adolescents un-dergo routine screening for Chlamydia during annual pelvic examinations.


• CDC also recommends that routine screening of asymptomatic women between ages 20 and 24 years should be considered, particularly if she has a new male sexual partner, has more than one male sexual partner, or does not use barrier contraception.



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GENERAL CONSIDERATIONS


Pelvic inflammatory disease (PID) is a categorical name for a range of pelvic infections and inflammations. The CDC defines PID as abdominal and adnexal tenderness and cervical motion tenderness in the absence of another definable cause of symptoms. Diagnosis does not require elevated white blood cell (WBC) count, erythrocyte sedimentation rate (ESR), or fever. Salpingitis is a particular condition under PID (adnexa always involved by definition); noninfectious states (pelvic adhesions and chronic salpingitis) also are included. PID leads to 2.5 million outpatient visits annually in the United States. Twenty-five percent of patients have serious long-term sequelae with risk of recurrence. Risk of ectopic pregnancy increases sixfold after one episode of PID. PID carries a 13% risk of infertility after one infection and a 70% risk after three.



Etiology


Organisms listed above are implicated in the etiology of PID; Neisseria gonorrhoeae and Chlamydia trachomatis are the most common. Asymptomatic chlamydial infections are a major cause of PID. A higher proportion of PID cases are ascribed to C. trachomatis than to N. gonorrhea.




• N. gonorrhea (GC): a delicate and fastidious species with high infectivity, preferring human columnar and transitional epithelia. In less than 1 hour after intercourse GC can establish itself on the urethral mucosa, resisting the flow of urine. Favored sites in the lower female genital tract are Bartholin’s and Skene’s glands, urethra, and endocervical canal. Spreading occurs from the endocervix across endometrium to tubal mucosa or by migration through subendothelial vascular and lymphatic channels. The most common method of spreading is vector; GC attached to spermatozoa are physically carried to the fallopian tubes. Retrograde menstruation or uterine contractions during intercourse are other modes of dissemination. Acute state: GC and polymorphonuclear leukocytes accumulate in subepithelial connective tissue, causing patchy destruction of overlying mucosa. Consequent mucosal thinning may facilitate GC penetration into deeper tissue; GC survive only a short time in the fallopian tubes. Descent of the microbe beyond surfaces being examined makes it difficult to detect. Concomitant infections occur; the primary role of GC is paving the way for secondary invaders from normal vaginal flora. C. trachomatis and anaerobic bacteria superinfections are possible.


• C. trachomatis (CT): 20%-30% of PID cases are caused by CT; acute chlamydial PID may be subclinical or silent in 66%-75% of cases. Lab diagnosis is difficult. It is frequently asymptomatic.


• Anaerobes: most commonly isolated from fallopian tubes or cul-de-sacs of PID patients. They are probably not the chief causative agents, but opportunists commonly found in immunocompromised hosts. They generally are of endogenous origin; cervixes and vaginas of normal healthy women contain anaerobes and aerobes. Anaerobic infections are more common in older patients and women with a history of prior PID.


• Other organisms: facultative aerobic organisms in tuboperitoneal fluids from women with salpingitis include coliforms, Haemophilus influenzae, streptococci, and Mycoplasma hominis. M. hominis is a common agent of polymicrobial milieu of PID, present in 81% of female patients with GC and 64% of those without.



Complications


Sequelae of PID are abdominal pain, infertility, ectopic pregnancy, dyspareunia. Dyspareunia often is not investigated but is frequently found in the post-PID sufferer.





Risk Factors


These include sexual contact, age, use or history of use of intrauterine device (IUD), previous history of PID, earlier “sexual debut,” especially with multiple sexual partners.





Pathogen Access to Upper Female Tract


Menstruation, sperm, and trichomonads help transport pathogens into the salpinx.




• Infections occurring around menses tend to be GC rather than CT. Menstrual regurgitation may carry sloughed endometrium with attached GC or intracellular CT that proliferate in tubal epithelium or on peritoneal surfaces.


• Human sperm: bacteriospermia is a cause of infertility in men; 66%-75% of men who tested positive for GC were asymptomatic. Sperm are vectors. Cervical mucus is an effective mechanical and immunologic barrier between flora of the vagina and upper tract. Yet organisms attached to sperm can easily traverse mucus column. Sperm migrate through menstrual plasma but not during the luteal phase or through cervical mucus of pregnancy. Sperm is intimately associated with cytomegalovirus, Toxoplasma, Ureoplasma urealyticum, and Chlamydia.


• Motile trichomonads are another transporter, ascending from the vagina to the fallopian tubes, carrying additional invaders. Key observation: trichomonads are never isolated from human beings when heavy bacterial contamination is absent.



DIAGNOSIS


Pelvic or lower abdominal pain is the most dependable symptom of PID, but it is not specific. Rebound tenderness is not reliable; cervical motion tenderness and adnexal tenderness are much more common. Clinical picture is misleading; many patients with PID have atypical signs and symptoms. Some have no signs and symptoms at all.


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Apr 3, 2017 | Posted by in GENERAL & FAMILY MEDICINE | Comments Off on Pelvic Inflammatory Disease

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