Contraception
Volume 78, Issue 2 , Pages 136-142 , August 2008

Increasing intrauterine contraception use by reducing barriers to post-abortal and interval insertion

  • Suzan Goodman

      Affiliations

    • University of California, San Francisco, San Francisco, CA 94110, USA
    • Corresponding Author InformationCorresponding author. University of California, San Francisco, CA 94110. Tel.: +1 415 202 4679; fax: +1 415 206 8387.
  • ,
  • Sarah K. Hendlish

      Affiliations

    • Planned Parenthood Golden Gate, San Francisco, CA 94109, USA
  • ,
  • Courtney Benedict

      Affiliations

    • Planned Parenthood Golden Gate, San Francisco, CA 94109, USA
  • ,
  • Matthew F. Reeves

      Affiliations

    • University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA
    • Magee-Women's Research Institute, Pittsburgh, PA 15261, USA
  • ,
  • Madeline Pera-Floyd

      Affiliations

    • Planned Parenthood Golden Gate, San Francisco, CA 94109, USA
  • ,
  • Anne Foster-Rosales

      Affiliations

    • University of California, San Francisco, San Francisco, CA 94110, USA
    • Planned Parenthood Golden Gate, San Francisco, CA 94109, USA

Received 4 August 2007 ,Revised 4 March 2008 ,Accepted 13 March 2008.

References 

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  13. Ogawa OD, Sokoloff A, Reeves MF, Steinauer J, Darney PD, Drey EA. Postabortion insertion of intrauterine contraception in the first and second trimesters. Obstet Gynecol. 2007;109(4 Suppl):61S
  14. Ortayli N, Bulut A, Sahin T, Sivin I. Immediate postabortal contraception with the levonorgestrel intrauterine device, Norplant, and traditional methods. Contraception. 2001;63:309–314
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  19. Stanwood NL, Grimes DA, Schulz KF. Insertion of an intrauterine contraceptive device after induced or spontaneous abortion: a review of the evidence. Br J Obstet Gynaecol. 2001;108:1168–1173
  20. Shea K. 2005. Personal communication regarding PPFA manual of medical standards and guidelines. 15 May, New York.
  21. Grimes DA, Schulz KF. Antibiotic prophylaxis for intrauterine contraceptive device insertion. Cochrane Database Syst Rev. 2001;2:CD001327
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 Financial support for this study was provided by FEI Women's Health (now DuraMed), producers of Paragard® T380A intrauterine copper contraceptive, who sponsored a Staff Training Pilot at Planned Parenthood Golden Gate (part of the intervention study). Ms. Hendlish is concurrently a research consultant for Berlex, Inc (now Bayer Health Care, Inc.), producers of Mirena® levonorgestrel-releasing intrauterine system.

PII: S0010-7824(08)00134-0

doi: 10.1016/j.contraception.2008.03.008

Contraception
Volume 78, Issue 2 , Pages 136-142 , August 2008