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Epidemiology and partner notification
P41 Women's health study of Mycoplasma genitalium: a feasibility study
  1. S Dave1,
  2. S R Kerry2,
  3. P Oakeshott2,
  4. F McGregor3,
  5. E Cannon3,
  6. J M Stephenson1
  1. 1University College London, London, UK
  2. 2St. George's University of London, London, UK
  3. 3CNWL Camden Provider Services, London, UK

Abstract

Background The role of Mycoplasma genitalium (∼3% prevalence in women) in PID is unclear. An opportunity exists to study its natural history since there are no UK treatment guidelines. We conducted a feasibility study.

Objectives In women attending GUM clinics to determine: (1) recruitment and follow-up rates after 3 and 6 months, (2) feasibility of obtaining NHS numbers, (3) facilitators and barriers to follow-up.

Methods Women aged 16–24 years recruited from two GUM clinics completed a questionnaire and provided two self-taken vaginal samples. One sample was tested for chlamydia. We are testing for M genitalium and conducting 3-month follow-up.

Results Recruitment rate was 67% (199/296). Non-responders were similar in age to responders (20.6 SD 2.5 vs 20.7 SD 2.5 years) but more likely to come from ethnic minority groups: 56% (37/66) vs 36% (71/195), p<0.05. Among responders, mean sexual debut age was 16.3 years (range 12–23 n=198); 59% (116/195) reported ≥2 sexual partners and 17% (31/186) consistently used condoms in the preceding 12 months. 8.2% (16/197) had chlamydia and 0.5% (1/197) gonorrhoea on testing. At recruitment 196 participants consented to NHS numbers being obtained and used to access medical records; 197 participants agreed to 3-month follow-up. We have been able to contact ∼50% of participants for follow-up.

Discussion Most women consented to NHS number and medical record access. This is important for investigating long-term sequelae of STIs. Fewer women took part in follow-up than agreed at recruitment. It is important to understand the reasons for this.

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