Pelvic inflammatory disease

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Pelvic inflammatory disease
Blausen 0732 PID-Sites.png
Drawing showing the usual sites of infection in pelvic inflammatory disease
Classification and external resources
ICD-10 N70 -N77
ICD-9 614-616
DiseasesDB 9748
MedlinePlus 000888
eMedicine emerg/410
Patient UK Pelvic inflammatory disease
MeSH D000292

Pelvic inflammatory disease or pelvic inflammatory disorder (PID) is an infection of the upper part of the female reproductive system namely the uterus, fallopian tubes, or the ovaries.[1] Often there may be no symptoms.[2] Signs and symptoms, when present may include: lower abdominal pain, vaginal discharge, fever, burning with urination, pain with sex, or irregular menstruation.[1][2] Untreated PID can result in long term complications including: infertility, ectopic pregnancy, chronic pelvic pain, and cancer.[1][3][4]

Infections by Neisseria gonorrhoeae or Chlamydia trachomatis are present in 75 to 90 percent of cases. Often multiple different bacteria are involved.[1] Without treatment about 10% of those with a chlamydial infection and 40% of those with a gonorrhea infection will develop PID.[1][5] Risk factors are similar to those of sexually transmitted infections generally and include a high number of sexual partners and drug use. Vaginal douching may also increase the risk. The diagnosis is typically based on the presenting signs and symptoms. It is recommended that the disease be considered in all women of childbearing age who have lower abdominal pain. A definitive diagnosis of PID is made by finding pus involving the fallopian tubes during surgery. Ultrasound may also be useful in diagnosis.[1]

Efforts to prevent the disease include: not having sex or having few sexual partners and using condoms.[6] Screening women at-risk for chlamydial infection followed by treatment decreases the risk of PID.[7] If the diagnosis is suspected, treatment is typically advised.[1] Treating a woman's sexual partners should also occur.[7] In those with mild or moderate symptoms a single injection of the antibiotic ceftriaxone along with 2 weeks of doxycycline and possibly metronidazole by mouth is recommended. For those who do not improve after three days or who have severe disease intravenous antibiotics should be used.[8]

Globally about 106 million cases of chlamydia and 106 million cases of gonorrhea occurred in 2008.[5] The number of cases of PID however, is not clear.[9] It is estimated to affect about 1.5% of young women yearly.[9] In the United States PID is estimated to affect about one million people yearly.[10] A type of intrauterine device (IUD) known as the Dalkon shield led to increased rates of PID in the 1970s. Current IUDs are not associated with this problem after the first month.[1]

Signs and symptoms[edit]

Illustration of pelvic inflammatory disease

Symptoms in PID range from none to severe. If there are symptoms, then fever, cervical motion tenderness, lower abdominal pain, new or different discharge, painful intercourse, uterine tenderness, adnexal tenderness, or irregular menstruation may be noted.[11][12][1][2][13]

Other complications include: endometritis, salpingitis, tubo-ovarian abscess, pelvic peritonitis, periappendicitis, and perihepatitis.

Cause[edit]

Chlamydia trachomatis and Neisseria gonorrhoeae are usually the main cause of PID. Data suggest that PID is often polymicrobial.[14] Isolated anaerobes and facultative microorganisms have been obtained from the upper genital tract. N. gonorrhoeae has been isolated from fallopian tubes, facultative and anaerobic organisms were recovered from endometrial tissues.[15][16]

The anatomical structure of the internal organs and tissues of the female reproductive tract provides a pathway for pathogens to enter the pelvic cavity thorough the infundibulum. The disturbance of the naturally occurring microbiota of the female genital tract increases the risk of PID.[17]

In a large study, N. gonorrhoea was the most common isolate. C. trachomatis was second most common, and least common were infections caused exclusively by anaerobes and facultative organisms. Anaerobes and facultative bacteria were also isolated from 50% of the patients from whom Chlamydia and Neisseria were recovered; thus, anaerobes and facultative bacteria were present in the upper genital tract of nearly two-thirds of the PID patients.[15] PCR and serological tests have associated extremely fastidious organism with endometritis, PID, and tubal factor infertility. Bacterial phylotypes and microbiotas now associated with PID and bacterial vaginosis are listed below.[15]

Microbiota recovered from pelvic infections[edit]

Diagnosis[edit]

Mucopurulent cervical discharge seen on a Q-tip
Micrograph of salpingitis - a component of pelvic inflammatory disease. H&E stain.

Upon examination, mucopurulent cervicitis and or urethritis may be observed. In severe cases more testing may be required such as laproscopy, intra-abdominal bacteria sampling and culturing, or tissue biopsy.[14][18]

Laproscopy can visualize 'violin-string' adhesions, characteristic of Fitz-Hugh-Curtis perihepatitis and other absesses that may be present.[18]

Other imaging methods can aid in diagnosis. These are: ulstrasonography, computed tomography (CT), and magnetic imaging (MRI)[18] Blood tests can also help identify the presence of infection: the erythrocyte sedimentation rate (ESR), the C-reactive protein (CRP) level, and chlamydial and gonococcal DNA probes.[18][14]

Nucleaic acid amplification tests (NAATs), direct fluorescein tests (DFA), and enszyme linked immunosorbent assays (ELISA) are highly sensitive tests that can identify specific pathogens present. Serology testing for antibodies is not as useful since the presence of the microorganisms in healthy people can confound interpreting the antibody titer levels, although aniitbody levels can indicate whether an infection is recent or long term.[14]

Definitive criteria include: histopathologic evidence of endometritis, thickened filled Fallopian tubes, or laparoscopic findings. Gram-stain/smear becomes definitive in the identification of rare, atypical or and possibly more serious organisms.[19] Two thirds of patients with laparoscopic evidence of previous PID were not aware they had PID, however even asymptomatic PID can cause serious harm.

Laparoscopic identification is helpful in diagnosing tubal disease, a 65–90% positive predictive value exists in patients with presumed PID.[20]

Upon gynecologic ultrasound, a potential finding is tubo-ovarian complex, which is edematous and dilated pelvic structures as evidenced by vague margins, but without abscess formation.[21]

Differential diagnosis[edit]

A number of other causes may produce similar to PID symptoms including: appendicitis, ectopic pregnancy, hemorrhagic or ruptured ovarian cysts, twisted ovarian, and endometriosis and gastroenteritis among others.[1][22]

Pelvic inflammatory disease is more likely to reoccur when there is a prior history of the infection, recent sexual contact, recent onset of menses, or an IUD (intrauterine device) in place or if the partner has a sexually transmitted infection.[23]

Acute pelvic inflammatory disease is highly unlikely when recent intercourse has not taken place or an IUD is not being used. A sensitive serum pregnancy test is typically obtained to rule out ectopic pregnancy. Culdocentesis will differentiate hemoperitoneum (ruptured ectopic pregnancy or hemorrhagic cyst) from pelvic sepsis (salpingitis, ruptured pelvic abscess, or ruptured appendix).

Pelvic and vaginal ultrasounds are helpful in the diagnosis of PID. In the early stages of infection, the ultrasound may appear normal. As the disease progresses, nonspecific findings can include free pelvic fluid, endometrial thickening, uterine cavity distension by fluid or gas. In some instances the borders of the uterus and ovaries appear indistinct. Enlarged ovaries accompanied by increased numbers of small cysts correlates with PID.[24]

Laparoscopy is often utilized to diagnose pelvic inflammatory disease, and it is important if the diagnosis is not certain or if the person has not responded to antibiotic therapy after 48 hours.[citation needed]

No single test has adequate sensitivity and specificity to diagnose pelvic inflammatory disease. A large multisite U.S. study found that cervical motion tenderness as a minimum clinical criterion increases the sensitivity of the CDC diagnostic criteria from 83% to 95%. However, even the modified 2002 CDC criteria do not identify women with subclinical disease.[25]

Prevention[edit]

Regular sexually transmitted infections testing is important for prevention. The risk of contracting pelvic inflammatory disease can be reduced by the following:

  • Using barrier methods such as condoms; see human sexual behavior for other listings.
  • Seeking medical attention if you are experiencing symptoms of PID.
  • Seeking medical attention after learning that a current or former sex partner has, or might have had a sexually transmitted infection.
  • Scheduling regular gynecological (pelvic) exams with STI testing to screen for symptom-less PID and to discuss sexual history.[26]
  • Getting a STI history from your current partner and insisting they be tested and treated before intercourse.
  • Diligence in avoiding vaginal activity, particularly intercourse, after the end of a pregnancy (delivery, miscarriage, or abortion) or certain gynecological procedures, to ensure that the cervix closes.
  • Abstinence[27]

Treatment[edit]

Treatment is often started without confirmation of infection because of the serious complications that may result from delayed treatment. Treatment depends on the infectious agent and generally involves the use of antibiotic therapy. If there is no improvement within two to three days, the patient is typically advised to seek further medical attention. Hospitalization sometimes becomes necessary if there are other complications. Treating sexual partners for possible STIs can help in treatment and prevention.[7]

The CDC guidelines state that the site route of antibiotic administration affects the short or long-term major outcome of women with mild or moderate disease.[28]

For women with PID of mild to moderate severity, parenteral and oral therapies appear to be efficacious.[29][30] Clinical experience should guide decisions regarding transition to oral therapy, which usually can be initiated within 24–48 hours of clinical improvement.[31] Typical regimens include cefoxitin or cefotetan plus doxycycline, and clindamycin plus gentamicin.[32] An alternative parenteral regimen is ampicillin/sulbactam plus doxycycline.[32] Another alternative is to use a parenteral regimen with ceftriaxone or cefoxitin plus doxycycline.[32]

Prognosis[edit]

Even when the PID infection is cured, effects of the infection may be permanent. This makes early identification essential. Treatment by medical providers who can prescribe appropriate curative treatment is very important in the prevention of damage to the reproductive system. Since early gonococcal infection may be asymptomatic, regular screening of individuals at risk for common agents (history of multiple partners, history of any unprotected sex, or people with symptoms) or because of certain procedures (post pelvic operation, postpartum, miscarriage orabortion).[medical citation needed]

If the initial infection is mostly in the lower tract, after treatment the person may have few difficulties. If the infection is in the fallopian tubes or ovaries, more serious complications are more likely to occur.[medical citation needed]

Complications[edit]

PID can cause scarring inside the reproductive system, which can later cause serious complications, including chronic pelvic pain, infertility, ectopic pregnancy (the leading cause of pregnancy-related deaths in adult females), and other complications of pregnancy. Occasionally, the infection can spread to in the peritoneum causing inflammation and the formation of scar tissue on the external surface of the liver (Fitz-Hugh-Curtis syndrome).[33]

Fertility may be restored in women affected by PID with tuboplastic surgery. In vitro fertilization (IVF) has been used to bypass tubal problems and is successful resulting in higher delivery rates.[medical citation needed]

Epidemiology[edit]

Globally about 106 million cases of chlamydia and 106 million cases of gonorrhea occurred in 2008.[5] The number of cases of PID; however, is not clear.[9] It is estimated to affect about 1. 5% of young women yearly.[9] In the United States PID is estimated to affects about one million people yearly.[10]

Rate are highest with teenagers and first time mothers. PID causes over 100, 000 women to become infertile in the US each year.[34][35]

See also[edit]

References[edit]

  1. ^ a b c d e f g h i j Mitchell, C; Prabhu, M (December 2013). "Pelvic inflammatory disease: current concepts in pathogenesis, diagnosis and treatment.". Infectious disease clinics of North America 27 (4): 793–809. PMID 24275271. 
  2. ^ a b c "Pelvic Inflammatory Disease (PID) Clinical Manifestations and Sequelae". cdc.gov. October 2014. Retrieved 21 February 2015. 
  3. ^ Chang, A. H.; Parsonnet, J. (2010). "Role of Bacteria in Oncogenesis". Clinical Microbiology Reviews 23 (4): 837–857. doi:10.1128/CMR.00012-10. ISSN 0893-8512. 
  4. ^ Chan, Philip J.; Seraj, Ibrahim M.; Kalugdan, Theresa H.; King, Alan (1996). "Prevalence of Mycoplasma Conserved DNA in Malignant Ovarian Cancer Detected Using Sensitive PCR–ELISA". Gynecologic Oncology 63 (2): 258–260. doi:10.1006/gyno.1996.0316. ISSN 0090-8258. 
  5. ^ a b c World Health Organization (2012). "Global incidence and prevalence of selected curable sexually transmitted infections - 2008" (PDF). who.int. pp. 2, 19. Retrieved 22 February 2015. 
  6. ^ "Pelvic Inflammatory Disease (PID) Patient Counseling and Education". cdc.gov. October 2014. Retrieved 21 February 2015. 
  7. ^ a b c "Pelvic Inflammatory Disease (PID) Partner Management and Public Health Measures". cdc.gov. October 2014. Retrieved 21 February 2015. 
  8. ^ "2010 STD Treatment Guidelines Pelvic Inflammatory Disease". cdc.gov. August 15, 2014. Retrieved 22 February 2015. 
  9. ^ a b c d Eschenbach, D (2008). "Acute Pelvic Inflammatory Disease". Glob. libr. women's med. doi:10.3843/GLOWM.10029. ISSN 1756-2228. 
  10. ^ a b "Self-Study STD Modules for Clinicians - Pelvic Inflammatory Disease (PID) Next Centers for Disease Control and Prevention Your Online Source for Credible Health Information CDC Home Footer Separator Rectangle Epidemiology". cdc.gov. October 2014. Retrieved 21 February 2015. 
  11. ^ "Pelvic inflammatory disease (PID) Symptoms; Diseases and Conditions". Mayo Clinic. Retrieved 2015-03-12. 
  12. ^ Kumar, MD, Ritu; Bronze, MD, Michael Stuart. "Pelvic Inflammatory Disease Empiric Therapy". Medscape. Retrieved 2015-03-30. 
  13. ^ Zakher, Bernadette; Cantor MD, Amy G.; Daeges, Monica; Nelson MD, Heidi (16 December 2014). "Review: Screening for Gonorrhea and Chlamydia: A Systematic Review for the U.S. Prevententive Services Task Force". Annals of Internal Medicine 161 (12): 884–894. doi:10.7326/M14-1022. 
  14. ^ a b c d e f Ljubin-Sternak, Suncanica; Mestrovic, Tomislav (2014). "Review: Clamydia trachonmatis and Genital Mycoplasmias: Pathogens with an Impact on Human Reproductive Health". Journal of Pathogens 2014 (183167). doi:10.1155/204/183167. PMC 4295611. 
  15. ^ a b c d Clark, Natalie; Tal, Reshef; Sharma, Harsha; Segars, James (2014). "Microbiota and Pelvic Inflammatory Disease". Seminars in Reproductive Medicine 32 (01): 043–049. doi:10.1055/s-0033-1361822. ISSN 1526-8004. 
  16. ^ a b Lis, R.; Rowhani-Rahbar, A.; Manhart, L. E. (2015). "Mycoplasma genitalium Infection and Female Reproductive Tract Disease: A Meta-Analysis". Clinical Infectious Diseases. doi:10.1093/cid/civ312. ISSN 1058-4838. PMID 25900174. 
  17. ^ Sharma, Harsha; Reshef, Tal; Clark, Natalie A.; Segars, James H. (January 2014). "Microbiota and Pelvic Inflammatory Disease". Semin. Reprod Med 32 (1). doi:10.1055/s-0033-1361822. 
  18. ^ a b c d Moore MD, Suzanne. Rivlin MD, Michel, ed. "Pelvic Inflammatory Disease". Medscape, Drugs and Diseases, Background. Medscape. Retrieved 31 March 2015. 
  19. ^ Loscalzo, Joseph; Andreoli, Thomas E.; Cecil, Russell L.; Carpenter, Charles A.; Griggs, Robert C. (2001). Cecil essentials of medicine. Philadelphia: W. B. Saunders. ISBN 0-7216-8179-4. OCLC 43051599. 
  20. ^ Lauren Nathan; DeCherney, Alan H.; Pernoll, Martin L. (2003). Current obstetric & gynecologic diagnosis & treatment. New York: Lange Medical Books/McGraw-Hill. ISBN 0-8385-1401-4. OCLC 150148652. 
  21. ^ Tuboovarian complex by Emily C. Wasco and Gillian Lieberman MD. Beth Israel Deaconess Medical Center. October 17, 2003
  22. ^ "Pelvic Pain in Women". Patient.co.uk. Retrieved 2015-03-12. 
  23. ^ "Pelvic Inflammatory Disease". CDC Fact Sheet. Retrieved 2015-03-12. 
  24. ^ Hoffman, Barbara (2012). Williams gynecology, 2nd edition. New York: McGraw-Hill Medical. p. 42. ISBN 0071716726. 
  25. ^ Blenning CE, Muench J, Judkins DZ, Roberts KT (2007). "Clinical inquiries. Which tests are most useful for diagnosing PID?". J Fam Pract 56 (3): 216–20. PMID 17343812. 
  26. ^ Smith KJ, Cook RL, Roberts MS (2007). "Time from sexually transmitted infection acquisition to pelvic inflammatory disease development: influence on the cost-effectiveness of different screening intervals". Value Health 10 (5): 358–66. doi:10.1111/j.1524-4733.2007.00189.x. PMID 17888100. 
  27. ^ "Prevention - STD Information from CDC". Center For Disease Control. Retrieved 2015-02-21. 
  28. ^ Walker CK, Wiesenfeld HC (2007). "Antibiotic therapy for acute pelvic inflammatory disease: the 2006 Centers for Disease Control and Prevention sexually transmitted diseases treatment guidelines". Clin. Infect. Dis. 44 (Suppl 3): S111–22. doi:10.1086/511424. PMID 17342664. 
  29. ^ Ness RB, Hillier SL, Kip KE ea. Bacterial vaginosis and risk of pelvic inflammatory disease. Obstet Gynecol 2004; 44 (Supp 3): S111–22.
  30. ^ Smith KJ, Ness RB, Wiesenfeld HC, et al. Cost-effectiveness of alternative outpatient pelvic inflammatory disease treatment strategies. Sex Transm Dis 2007; 34: 960–6.
  31. ^ "CDC - References - 2010 STD Treatment Guidelines". cdc.gov. 
  32. ^ a b c "CDC - Pelvic Inflammatory Disease - 2010 STD Treatment Guidelines". cdc.gov. 
  33. ^ "Pelvic Inflammatory Disease". MedScape. Retrieved 2015-03-10. 
  34. ^ "STD Facts — Pelvic inflammatory disease (PID)". Retrieved 2015-04-17. 
  35. ^ Sutton MY, Sternberg M, Zaidi A, St Louis ME, Markowitz LE (December 2005). "Trends in pelvic inflammatory disease hospital discharges and ambulatory visits, United States, 1985–2001". Sex Transm Dis 32 (12): 778–84. PMID 16314776. 

External links[edit]