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PubHealth.info®
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PakMed) presents scientific information mainly
based on abstracts of articles published on a variety of public health issues/topics,
particularly encompassing
population planning, disease prevention, maternal and child health,
and communicable and
non-communicable diseases (like HIV AIDS, malaria, etc) that are
affecting a significant portion of population in developing and
developed
countries. Here you can find abstracts of articles published on a variety of public health
topics under category "Contraception
(Birth Control) and Family Planning".
Contraception (birth control)
is a regimen of one or more actions, devices, or medications followed in
order to deliberately prevent or reduce the likelihood of a woman
becoming pregnant or giving birth. Therefore contraception is the
utilization of various and sundry surgical procedures, devices,
practices, agents, or drugs with the intention of preventing conception
or impregnation (pregnancy). Methods and intentions typically termed
birth control may be considered a pivotal ingredient to family
planning. Birth control is a controversial political and ethical
issue in many cultures and religions, and although it is generally less
controversial than abortion specifically. |
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| CATEGORY: |
Contraception (Birth Control) and Family Planning |
| Bioavailability of the Yuzpe and levonorgestrel regimens of emergency |
| contraception: vaginal vs. oral administration. |
| Kives S; Hahn PM; White E; Stanczyk FZ; Reid RL |
| Contraception. 2005;71:197-201. |
| Separate crossover studies compared the bioavailability or oral vs. vaginal routes of administration for the Yuzpe |
| (n=5) and levonorgestrel regimens (n=4) of emergency contraception. Twice the standard dose of the Yuzpe regimen |
| (200 µg of ethinyl estradiol, 1000 µg of levonorgestrel) or the levonorgestrel regimen (1500 µg of levonorgestrel) was |
| self-administered vaginally. One week later, each subject received orally the standard dose of the assigned |
| medication. Serial blood samples were collected over 24 h and assayed for levonorgestrel and ethinyl estradiol (for |
| the Yuzpe regimen only). Paired t tests were used to compared oral vs. vaginal administration for maximum |
| concentration (C(-max)), time to maximum concentration (T(-max)) and area under the curve over 24 h (AUC(-0-24)). |
| Relative bioavailability (vaginal/oral) was derived from AUC(-0-24). Vaginal administration of double the standard |
| dose of the Yuzpe regimen resulted in a lower C(-max) (vaginal=5.4 vs. oral=14.6 ng/mL, p=.038) and a later T(max) |
| (5.9 vs 2.0 h, p=.066) for levonorgestrel, compared to oral administration. Corresponding ethinyl estradiol |
| concentrations were higher 786 vs. 391 pg/mL, p=.039) and peaked later 4.0 vs. 1.9 hr, p=.154) with vaginal |
| administration. Relative bioavailabilities for the levonorgestrel and ethinyl estradiol were 58% and 175%, respectively. |
| Similarly, vaginal administration of the levonorgestrel regimen resulted in a lower C(-max) (vaginal=5.4 vs. oral=15.2 |
| ng/mL, p=.006) and a later T(-max) (7.4 vs. 1.3 h, p=.037) for levonorgestrel, compared to oral administration. The |
| relative bioavailability was 62%. Our preliminary data suggest that vaginal administration of these emergency |
| contraception regimens appears to require at least three times the standard oral dose to achieve equivalent systemic |
| levonorgestrel concentrations. (PubHealth.info Document ID: CONT1T 72-06) |
| PubHealth.info NOTE: The author(s) of this article titled, "Bioavailability of the Yuzpe and levonorgestrel regimens of |
| emergency contraception: vaginal vs. oral administration.", is(are) Kives S; Hahn PM; White E; Stanczyk FZ; Reid |
| RL. The source of this article is "Contraception. 2005;71:197-201.". This article was published in 2005 in English |
| language(s). (PubHealth.info® Document ID: CONT1T 72-06. All rights reserved with PubHealth.info) PIN: 72 |
| This article is peer-reviewed. |
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