Pelvic inflammatory disease (PID) is a common cause of acute pelvic pain, and the incidence is increasing. It is an upper genital tract infection and can include one or more of the following: endometritis, salpingitis, tubo-ovarian abscess, and pelvic peritonitis. Prompt treatment and effective contact tracing are important as long-term sequelae include CPP, subfertility, and ectopic pregnancy. Although infection usually ascends from the cervix, cervical swabs can be negative even when pathogenic organisms are isolated from the fallopian tubes. The pain is thought to be due to inflammation, tissue destruction, irritation of peritoneal surfaces, and distortion of anatomy. Right upper quadrant pain and perihepatic adhesions occur in the Fitz-Hugh-Curtis syndrome, which is seen in 10% to 20% of women with PID.
6,7 Clinical features of PID lack sensitivity and specificity but include lower abdominal pain and tenderness, deep dyspareunia, abnormal vaginal/cervical discharge, cervical excitation and adnexal tenderness, and fever.
8 Evidence of acute infection will not always be seen on diagnostic laparoscopy, and therefore, this investigation should be reserved for cases where alternative pathology needs to be excluded or if a pelvic mass is seen on ultrasound (US).
9 Where there is a high index of suspicion, it is recommended that empirical antibiotic treatment should be commenced once swabs have been taken without waiting for culture results or performing further investigations.
9 This is particularly important if other features of sepsis are present, in which instance admission and adherence to local sepsis guidelines is recommended. A number of different organisms are associated with PID, including
Chlamydia trachomatis,
Neisseria gonorrhoea,
Mycoplasma genitalium, and anaerobes.
8 The most commonly implicated organisms vary geographically, and therefore, local guidelines for appropriate antibiotic treatment regimens should always be consulted. There are now high rates of quinolone-resistant gonorrhoea in the Unites States, and, since April 2007, fluoroquinolone antibiotics have no longer been recommended for the treatment of PID in the United States
10; this is increasingly also the case in the United Kingdom. Antibiotic treatment is usually continued for 14 days (with intravenous doses converted to oral once apyrexial), and therefore, patient compliance can be an issue. The presence of an intrauterine contraceptive device (IUCD) only increases the risk of developing PID in the first few weeks after insertion. Leaving the device in situ while mild PID is being treated does not appear to affect the outcome. In severe cases, however, it is recommended that the IUCD be removed.
When there is definite evidence of a pelvic abscess or severe disease, surgery is recommended (either laparoscopy or laparotomy), to drain the abscess and divide pelvic adhesions, there is no good evidence to recommend division of perihepatic adhesions, however.
9 Depending on location, it may also be possible to drain pelvic collections under US guidance. This has been shown to be effective with fewer complications than surgery.
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To prevent reinfection, contact tracing and treatment of all sexual partners from 6 months prior to presentation is recommended.
9 This may be best done through a local genitourinary medicine (GUM) clinic, which will have experience of contact tracing and counseling about the long-term consequences of sexually transmitted infections. If admission is not required and appropriate facilities exist, it may be more effective to refer the woman to a GUM clinic immediately, to be seen the same day, before treatment is started. Sexual intercourse should be avoided until both the patient and her partner have completed a full course of treatment.