is therefore much welcomed. However, we do not feel that it answers the question; more specifically, it does not allow them to draw the conclusion that the use of the prophylaxis described should be extended to all women undergoing elective termination of pregnancy in the first trimester.Women were allocated to the high risk group if they gave any history suggestive of PID or sexually transmitted disease. Whilst these factors attempt to identify a group at increased risk of developing post-abortal PID by way of their risk of having a sexually transmitted disease, we feel it is neither specific enough nor appropriate. Although the authors failed to screen all subjects for sexually transmitted diseases, they did so in more than 50% of patients, who were presumably still subject to the same selection criteria. Their figures show that in the screened population the incidence of chlamydia, a major aetiological agent of post-abortal PID, in the low risk group was twice that in the high risk group. Additionally, there were two cases of gonorrhoea in the former but none in the latter. These figures would suggest that their criteria used to define risk were unsound.It is established that the risk factors for the acquisition of chlamydia include: a short duration of present relationship, a lack of condom use and the age of the woman, with higher risk being linked to the ages of 18 to 25 years (Fish et al.
AUTHORS' REPLY
Sir,The reported incidence of postabortal PID is variable. In comparison with previous reports, the incidence of postabortal PID in our study was low. The overall incidence of PID was 2.8 ? ' a and in women who were not treated with antibiotics, the low risk control group, the incidence was 3.6%. The identification of women who have an increased risk of suffering PID after legal abortion is not a simple matter. In our study the women were allocated to the high risk group if they gave any history of previous PID or sexually transmitted disease, as recommended by Sonne-Holm et al. (1981).By this procedure, however, we did not intend to identify women with an increased risk of having a sexually transmitted disease as indicated by Wilkinson and Hamilton-Fairley. Whilst having a sexually transmitted disease undoubtedly is a risk factor for postabortal PID, our data indicate that it is not the only risk factor. In 32 women, a sexually transmitted microbial agent was found (i.e., Chlamydia trachomatis or Neisseria gonorrhoea but PID was diagnosed in only two of these women (6.3 YO). Twenty women with PID were negative for C. trachomatis and N . gonorrhoea. The incidence of postabortal PID in both our low risk groups was decreased, compared with our high risk groups.More specifically, the incidence of PID in the low risk control group without prophylactic treatment was not elevated compared with the two high risk groups, in both of which the women were treated with prophylactic antibiotics and the incidence in the low risk ceftriaxone group was significantly lower than the incidence in the high risk groups (i.e.,...