Literature reviews  >  Articles for review > Simms et al. Diagnosis of pelvic inflammatory disease...

 

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There is insufficient evidence to support existing diagnostic criteria, based on clinical presentation, for the diagnosis of pelvic inflammatory disease.

Diagnosis of pelvic inflammatory disease: time for a rethink.
Simms I, Warburton F, Westrom L.
Sexually Transmitted Infections 2003;79:491-494.

 

Summary:

Question
What is the accuracy with which signs and symptoms predict the presence of pelvic inflammatory disease (PID) as determined using laparoscopy as the diagnostic gold standard?

Design
This study describes the use of three analytical techniques to compare the accuracy with which clinical presentation predicted the presence of laparoscopically diagnosed PID.

Participants
Data from 623 women who attended the department of Obstetrics and Gynecology, Lund University Hospital, between 1960 and 1969, with first episodes of suspected PID were analyzed.

Description of Tests and Diagnostic Standard
The minimum criteria for a diagnosis of PID based on signs and symptoms were lower quadrant bilateral abdominal or pelvic pain of less than 3 weeks' duration, together with two or more of the following: abnormal vaginal discharge, fever >38oC, vomiting, menstrual irregularity, ongoing bleeding, symptoms of urethritis, rectal temperature >38oC, marked tenderness of pelvic organs on bimanual examination, adnexal mass, and ESR >15 mm in the first hour. Laparoscopy was used to confirm a diagnosis of PID.

Main Outcome Measures
The sensitivity and specificity of each sign or symptom for the diagnosis of PID as determined by laparoscopy were calculated. The likelihood ratio and post-test probability of each sign or symptom were compared with the pretest probability of PID. The combination of signs and symptoms that most effectively predicted the presence of PID were determined.

Main Results
Laparoscopy confirmed PID in 494 (79%) of 623 women. The sensitivity of each sign or symptom for the diagnosis of PID compared to laparoscopy ranged from 10% to 74% except for tenderness of pelvic organs on bimanual examination (99%) and ESR (81%). The specificity of each sign or symptom for the diagnosis of PID compared to laparoscopy ranged from 0.01% to 77% except for proctitis symptoms (92%) and vomiting (88%). The post-test probability of PID was not significantly different from the pretest probability for any sign or symptom. The likelihood ratios ranged from 0.97 to 1.73. Three variables combined significantly influenced the prediction of the presence of PID: ESR, fever, and adnexal tenderness. The combination of these three signs and symptoms compared with laparoscopy for the diagnosis of PID is shown in the table. These variables correctly classified 65% of patients with laparoscopically diagnosed PID.

Authors' Conclusions
The Lund and other available datasets provide insufficient evidence to support existing PID diagnostic guidelines and have limitations for the formulation of new ones. A new evidence base is urgently needed, which will require either a new investigation of the association between clinical presentation and PID based on a laparoscopic gold standard, or the development of new diagnostic tests.

Source of funding: Not given

For correspondence: Ian Simms, HPA Communicable Disease Surveillance Centre, 61 Colindale Avenue, London NW9 5EQ, UK. E-mail address: ian.simms@hpa.org.uk.

   

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