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1.
N Engl J Med ; 319(13): 813-7, 1988 Sep 29.
Article in English | MEDLINE | ID: mdl-3166108

ABSTRACT

Progesterone is essential to sustain pregnancy in the first eight weeks. Its synthesis requires the enzyme 3 beta-hydroxysteroid dehydrogenase (3-HSD). We tested the efficacy of an orally administered 3-HSD inhibitor, epostane, in terminating unwanted early pregnancy. Fifty women in the fifth through eight weeks of pregnancy took epostane (200 mg orally every six hours) for seven days. By day 14, pregnancy had been terminated in 42 of the 50 patients (84 percent). Eight women (16 percent) did not abort and underwent dilation and curettage. Vaginal blood loss occurred on average on the third day of epostane treatment, and abortion on the fifth day. Two patients had incomplete abortions; one required a transfusion because of blood loss. Nausea was frequent (in 86 percent), but 76 percent of the participants concluded that epostane was preferable to dilation and curettage. The mean (+/- SD) pretreatment progesterone level (76 +/- 16 nmol per liter) decreased by day 7 (to 16 +/- 11 nmol per liter) and day 14 (to 10 +/- 9 nmol per liter) in those who aborted; levels of human chorionic gonadotropin also decreased from the mean at base line (73 +/- 72 kIU per liter) to 18 +/- 7 kIU per liter on day 7 and 9 +/- 5 kIU per liter on day 14. In those who did not abort after epostane treatment, progesterone levels decreased only slightly by day 7 (to 52 +/- 21 nmol per liter) and rose again (to 81 +/- 18 nmol per liter) by day 14. Among women who responded to epostane, normal menstrual periods had resumed by day 42 after the beginning of treatment in 72 percent. We conclude that epostane taken orally is an effective and safe method for the noninvasive termination of undesired early pregnancy.


PIP: The efficacy of the 3 beta-hydroxysteroid dehydrogenase inhibitor epostane in terminating early pregnancy was investigated in 50 women who were in the 5th-8th weeks of pregnancy. In previous studies, epostane has been shown to reduce progesterone levels significantly in pregnant and nonpregnant women without disruption of subsequent menstrual cycles or adverse effects on adrenal steroidogenesis or hepatic function. The study subjects received 200 mg of epostane orally every 6 hours for 7 days. In 42 women (84%), the pregnancy was terminated by the 14th day after epostane treatment was initiated. There were more responders among primigravidas (90%) than among multigravidas (76%), although the difference was not statistically significant. On average, vaginal blood loss occurred on the 3rd day of treatment and abortion on the 5th day. The mean pretreatment progesterone level (76 + or - 16 nmol/liter) decreased by day 7 to 16 + or - 11 nmol/liter and by day 14 to 10 + or - 9 nmol/liter in women who aborted, while levels of human chorionic gonadotropin decreased from a baseline mean of 73 + or - kIU/liter to 18 + or - 7 kIU/liter on day 7 and 9 + or - 5 kIU/liter on day 14. In women who did not abort, progesterone levels decreased only slightly 7 days after epostane treatment (to 52 + or - 21 nmol/liter) and rose again to 81 + or - 18 nmol/liter by day 14. 86% of study subjects reported treatment-related nausea; however, in 64%, the nausea was no worse than pretreatment nausea. 76% indicated epostane was preferable to dilation and curettage. Normal menstrual periods were resumed by day 42 after the initiation of treatment in 72% of the women who responded to epostane. Overall, these findings suggest that epostane is an effective alternative method for the termination of unwanted pregnancy in the 1st 8 weeks of gestation and should be given serious consideration as a noninvasive alternative to dilation and curettage.


Subject(s)
3-Hydroxysteroid Dehydrogenases/antagonists & inhibitors , Abortifacient Agents, Steroidal , Abortifacient Agents , Androstenols/pharmacology , Abortifacient Agents/administration & dosage , Abortifacient Agents/adverse effects , Abortifacient Agents, Steroidal/administration & dosage , Abortifacient Agents, Steroidal/adverse effects , Administration, Oral , Adult , Androstenols/administration & dosage , Androstenols/adverse effects , Dilatation and Curettage , Female , Humans , Menstruation/drug effects , Pregnancy , Pregnancy Trimester, First , Progesterone/blood , Tablets
2.
Ned Tijdschr Geneeskd ; 131(5): 204-8, 1987 Jan 31.
Article in Dutch | MEDLINE | ID: mdl-3822009

ABSTRACT

PIP: Vacuum curettage is the most efficient way of terminating unwanted pregnancies for amenorrhea periods not exceeding 12 weeks. Although fairly safe, the method can cause complications such as infections, bleeding, perforations and incomplete evacuations, and the long term effects are uncertain. The use of medicinal drugs has several advantages, e.g., damage to the cervix can be eliminated. Epostane, a steroid still in clinical trial phase, inhibits progesterone genesis and synthesis in the corpus luteum and placenta, which may lead to abortion. 50 informed and consenting women, above 18 and pregnant less than 8 weeks, determined echographically, were tested with the drug in order to check for efficiency and possible side effects. A dose of 200 mg was given orally during 7 days. Progesterone levels in serum were determined by radioimmunoassay, on day 0, 7 and 14. the results was evaluated on the 14th day. Of the 50, a group of 8 were still pregnant. The progesterone levels in the luteal phase, and the rate of decrease of progesterone concentrations, although on an average higher in the non-respondent group, showed some individual inconsistencies pointing to other hormonal agents responsible for protecting pregnancy. The results also indicated clear but insignificant responsive differences between primi- and multiparous women (90% vs. 76%), which were only minimally reflected in progesterone concentrations. When progesterone production, after 5-6 weeks of amenorrhea, is shifted from the corpus luteum to the placenta, in the corpo-luteal phase, chances of blocking progesterone synthesis are considered theoretically to be the highest. The number of responses during that time period confirmed this. Of importance for dispensation on an out-patient basis is to establish how much blood loss occurs. The tests showed clinically accepted norms.^ieng


Subject(s)
Abortifacient Agents, Steroidal , Abortifacient Agents , Abortion, Induced , Androstenols , Adult , Androstenols/adverse effects , Female , Humans , Pregnancy , Progesterone/blood
5.
Br J Obstet Gynaecol ; 89(11): 931-4, 1982 Nov.
Article in English | MEDLINE | ID: mdl-7171502

ABSTRACT

Ultrasonographic measurements of the yolk sac were made during first trimester in 100 pregnancies. The results were related to the crown-rump length of the embryos and showed an increase in size from 7 to 11 weeks menstrual age. A possible relation between anomalies in yolk sac development and embryonic development was studied in six patients by means of serial weekly ultrasonographic examinations. In one case with absence of the yolk sac embryonic death occurred at 10 weeks menstrual age; the embryo had spina bifida.


Subject(s)
Ultrasonography , Yolk Sac/anatomy & histology , Anthropometry , Embryo, Mammalian/anatomy & histology , Female , Gestational Age , Humans , Pregnancy , Prospective Studies , Yolk Sac/physiology
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