Pharmacy-based interventions for initiating effective contraception following the use of emergency contraception: a pilot study

被引:29
|
作者
Michie, L. [1 ,2 ]
Cameron, S. T. [1 ,2 ]
Glasier, A. [1 ,3 ]
Larke, N. [3 ]
Muir, A. [4 ]
Lorimer, A. [5 ]
机构
[1] Univ Edinburgh, Dept Reprod & Dev Sci, Edinburgh EH16 5SU, Midlothian, Scotland
[2] Chalmers Sexual Hlth Ctr, Edinburgh EH3 9ES, Midlothian, Scotland
[3] London Sch Hyg & Trop Med, London WC1E 7HT, England
[4] NHS Lothian, Dept Hlth & Hlth Policy, Edinburgh EH1 3EG, Midlothian, Scotland
[5] Royal Edinburgh & Associated Hosp, Dept Pharm, Edinburgh EH10 5HF, Midlothian, Scotland
关键词
Morning-after pill; Levonelle; Quick-start; LARC; POP; CHLAMYDIA; HISTORY; WORTH;
D O I
10.1016/j.contraception.2014.05.004
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: In Scotland most women get emergency contraception (EC) from pharmacies. Pharmacists currently cannot provide effective ongoing contraception after EC. In this pilot study, we aimed to determine the feasibility of a larger study designed to ascertain if pharmacy-based interventions can increase the uptake of effective contraception after EC. Study design: This is a pilot study of women presenting for levonorgestrel EC to community pharmacies in Edinburgh, UK, in 2012. Pharmacies were cluster randomized to provide either standard care or one of two interventions: (a) one packet of progestogen-only pills (POPs), giving women 1 month to arrange ongoing contraception; (b) invitation to present the empty EC packet to a family planning clinic (FPC) for contraceptive advice (rapid access). Results: One hundred sixty-eight women were recruited from 11 pharmacies to POP (n=56), rapid access (n=58) and standard care (N=54) groups, respectively. Telephone follow-up was conducted successfully in 102 women (61%) 6-8 weeks later to determine current contraceptive use. In the POP arm, 35/39 (90%) women used the pills provided, and 9/28 women (32%) in the rapid access arm attended the FPC. The proportion of women using effective contraception at follow-up was significantly greater in both POP [56% (22/39), p=<0.001] and rapid access [52% (13/25), p=0.006] groups compared to standard care [16% (5/31)]. The relative probability of a woman using an effective method of contraception versus barrier/no method, after use of EC, was 3.13 [95% confidence interval (CI), 1.90-5.13] in the POP group and 2.57 (95% CI, 1.55-4.27) in the rapid access group. Conclusions: This promising pilot study suggests that simple pharmacy-based interventions may increase the uptake of effective contraception after EC. A larger study is required to provide further validation of these findings. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:447 / 453
页数:7
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