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The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive()
OBJECTIVE: To examine the rate of ovulatory disruption when intramuscular depot medroxyprogesterone acetate (DMPA) is administered across graded stages of dominant follicle development. STUDY DESIGN: We assigned enrolled participants to one of three preassigned dominant follicle size groups: 12-14 m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749364/ https://www.ncbi.nlm.nih.gov/pubmed/33367229 http://dx.doi.org/10.1016/j.conx.2020.100050 |
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author | Schickler, Robyn Crabtree-Sokol, Diana Patel, Jasmine Bender, Nicole Nelson, Anita L. Nguyen, Brian T. |
author_facet | Schickler, Robyn Crabtree-Sokol, Diana Patel, Jasmine Bender, Nicole Nelson, Anita L. Nguyen, Brian T. |
author_sort | Schickler, Robyn |
collection | PubMed |
description | OBJECTIVE: To examine the rate of ovulatory disruption when intramuscular depot medroxyprogesterone acetate (DMPA) is administered across graded stages of dominant follicle development. STUDY DESIGN: We assigned enrolled participants to one of three preassigned dominant follicle size groups: 12-14 mm, 15–17 mm and ≥ 18 mm. We followed dominant follicles via serial transvaginal ultrasound (TVUS) until the follicles reached their assigned size, at which time we administered DMPA. For 5 consecutive days thereafter, we followed the follicles via TVUS to observe follicle rupture and obtained serum luteinizing hormone (LH), estradiol, and progesterone concentrations. In the following 2 weeks, we collected serum progesterone concentrations twice weekly to detect possible ovulatory delay or dysfunction. We also collected serum medroxyprogesterone acetate (MPA) concentrations at 1 and 24 h after DMPA administration to examine against ovulatory outcomes. RESULTS: Twenty-six of 29 enrolled women completed the study. DMPA suppressed ovulation in 17/26 (65%) and caused ovulatory dysfunction in 1/26 (4%) participants. Larger follicles were more likely to rupture despite DMPA (12–14 mm: 0/10 (0%); 15–17 mm: 3/10 (30%); ≥ 18 mm: 6/6 (100%); p < .01). Pre-DMPA LH concentrations ranged from 13.8 to 93.7 IU/L (mean 49.0 IU/L) in cases of follicle rupture. We observed no cases of follicle rupture when DMPA was administered through cycle day 12. All 24-h MPA concentrations exceeded those needed for ovulation suppression. CONCLUSION: DMPA suppressed and additionally disrupted ovulation in 65% and 4% of observed cycles, respectively. DMPA may provide effective emergency contraception as well as ongoing contraception if administered prior to an expected ovulation and specifically before the LH surge. IMPLICATIONS: DMPA may be an alternative form of emergency contraception that can also self-bridge to ongoing contraception. As ovulation was not observed among any follicles when DMPA was given through cycle day 12, women who initiate DMPA up through cycle day 12 may not require backup contraception. |
format | Online Article Text |
id | pubmed-7749364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77493642020-12-22 The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() Schickler, Robyn Crabtree-Sokol, Diana Patel, Jasmine Bender, Nicole Nelson, Anita L. Nguyen, Brian T. Contracept X Article OBJECTIVE: To examine the rate of ovulatory disruption when intramuscular depot medroxyprogesterone acetate (DMPA) is administered across graded stages of dominant follicle development. STUDY DESIGN: We assigned enrolled participants to one of three preassigned dominant follicle size groups: 12-14 mm, 15–17 mm and ≥ 18 mm. We followed dominant follicles via serial transvaginal ultrasound (TVUS) until the follicles reached their assigned size, at which time we administered DMPA. For 5 consecutive days thereafter, we followed the follicles via TVUS to observe follicle rupture and obtained serum luteinizing hormone (LH), estradiol, and progesterone concentrations. In the following 2 weeks, we collected serum progesterone concentrations twice weekly to detect possible ovulatory delay or dysfunction. We also collected serum medroxyprogesterone acetate (MPA) concentrations at 1 and 24 h after DMPA administration to examine against ovulatory outcomes. RESULTS: Twenty-six of 29 enrolled women completed the study. DMPA suppressed ovulation in 17/26 (65%) and caused ovulatory dysfunction in 1/26 (4%) participants. Larger follicles were more likely to rupture despite DMPA (12–14 mm: 0/10 (0%); 15–17 mm: 3/10 (30%); ≥ 18 mm: 6/6 (100%); p < .01). Pre-DMPA LH concentrations ranged from 13.8 to 93.7 IU/L (mean 49.0 IU/L) in cases of follicle rupture. We observed no cases of follicle rupture when DMPA was administered through cycle day 12. All 24-h MPA concentrations exceeded those needed for ovulation suppression. CONCLUSION: DMPA suppressed and additionally disrupted ovulation in 65% and 4% of observed cycles, respectively. DMPA may provide effective emergency contraception as well as ongoing contraception if administered prior to an expected ovulation and specifically before the LH surge. IMPLICATIONS: DMPA may be an alternative form of emergency contraception that can also self-bridge to ongoing contraception. As ovulation was not observed among any follicles when DMPA was given through cycle day 12, women who initiate DMPA up through cycle day 12 may not require backup contraception. Elsevier 2020-12-03 /pmc/articles/PMC7749364/ /pubmed/33367229 http://dx.doi.org/10.1016/j.conx.2020.100050 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Schickler, Robyn Crabtree-Sokol, Diana Patel, Jasmine Bender, Nicole Nelson, Anita L. Nguyen, Brian T. The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
title | The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
title_full | The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
title_fullStr | The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
title_full_unstemmed | The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
title_short | The potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
title_sort | potential for intramuscular depot medroxyprogesterone acetate as a self-bridging emergency contraceptive() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749364/ https://www.ncbi.nlm.nih.gov/pubmed/33367229 http://dx.doi.org/10.1016/j.conx.2020.100050 |
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