Suppression of follicular rupture with meloxicam, a cyclooxygenase-2 inhibitor: potential for emergency contraception

被引:49
|
作者
Jesam, Cristian [1 ]
Maria Salvatierra, Ana [1 ]
Schwartz, Jill L. [2 ]
Croxatto, Horacio B. [3 ]
机构
[1] ICMER, Santiago, Chile
[2] Eastern Virginia Med Sch, CONRAD, Arlington, VA USA
[3] Univ Santiago, Santiago, Chile
关键词
cyclooxygenase-2; inhibitors; meloxicam; emergency contraception; delayed follicular rupture; dysfunctional ovulation; OVARIAN-FUNCTION; MENSTRUAL-CYCLE; DOUBLE-BLIND; LEVONORGESTREL; OVULATION; MIFEPRISTONE;
D O I
10.1093/humrep/dep392
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
There is evidence that cyclooxygenase-2 (COX-2) inhibitors can prevent or delay follicular rupture. COX-2 inhibitors, such as meloxicam, may offer advantages over emergency contraception with levonorgestrel, such as extending the therapeutic window for up to 24 h. We assessed the effect of meloxicam administered in the late follicular phase upon ovulation in women. This was a single center, double blind, crossover study designed to assess the effects in 27 eligible women (18-40 years old, surgically sterilized with regular menstrual cycles) of meloxicam, 15 or 30 mg/day, administered orally for five consecutive days during the late follicular phase, starting when the leading follicle reached 18 mm diameter. Volunteers underwent two treatment cycles separated by one resting cycle, with randomization to dose sequence. Main outcomes were follicular rupture; serum LH, progesterone and estradiol (E(2)) levels; and incidence of adverse events. Twenty-two volunteers completed the study. There were no differences between meloxicam doses in menstrual cycle length. Dysfunctional ovulation was observed in 11/22 (50%) cycles treated with 15 mg/day and 20/22 (90.9%) cycles with 30 mg/day (P = 0.0068). All women had normal luteal phase progesterone levels; mean maximal values +/- SEM were 42 +/- 4.1 and 46.8 +/- 2.6 nmol/l for 15 and 30 mg/day groups, respectively. There were no serious adverse events, and no changes in LH and E(2) levels or in cycle length. Meloxicam 30 mg given for five consecutive days in the late follicular phase is safe, effective and may be an alternative form of emergency contraception.
引用
收藏
页码:368 / 373
页数:6
相关论文
共 50 条
  • [1] Suppression of Follicular Rupture With Meloxicam, A Cyclooxygenase-2 Inhibitor: Potential for Emergency Contraception EDITORIAL COMMENT
    Jesam, Cristian
    Maria Salvatierra, Ana
    Schwartz, Jill L.
    Croxatto, Horacio B.
    OBSTETRICAL & GYNECOLOGICAL SURVEY, 2010, 65 (05) : 314 - 316
  • [2] Meloxicam - Clinical data on a preferential cyclooxygenase-2 inhibitor
    Distel, M
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 1998, 4 (05) : S32 - S39
  • [3] Oral administration of the cyclooxygenase-2 (COX-2) inhibitor meloxicam blocks ovulation in non-human primates when administered to simulate emergency contraception
    Hester, Kim E.
    Harper, Michael J. K.
    Duffy, Diane M.
    HUMAN REPRODUCTION, 2010, 25 (02) : 360 - 367
  • [4] Tocolytic effect of the cyclooxygenase-2 inhibitor, meloxicam: Studies on uterine contractions in the rat
    Yousif, MH
    Thulesius, O
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 1998, 50 (06) : 681 - 685
  • [5] Inhibition of cyclooxygenase-2 by meloxicam supports hematopoiesis
    Streitova, D.
    Hofer, M.
    Pospisil, M.
    Znojil, V.
    Hola, J.
    Vacek, A.
    EXPERIMENTAL HEMATOLOGY, 2007, 35 (09) : 96 - 97
  • [6] Effects of the selective cyclooxygenase-2 inhibitor meloxicam on renal hemodynamics compared to indomethacin.
    Birck, R
    Knoll, T
    Braun, C
    VanderWoude, FJ
    Rohmeiss, P
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1997, 8 : A1584 - A1584
  • [7] Effect of the specific cyclooxygenase-2 inhibitor meloxicam on tumour growth and cachexia in a murine model
    Hussey, HJ
    Tisdale, MJ
    INTERNATIONAL JOURNAL OF CANCER, 2000, 87 (01) : 95 - 100
  • [8] Premedication with cyclooxygenase-2 inhibitor meloxicam reduced postoperative pain in patients after oral surgery
    Aoki, T.
    Yamaguchi, H.
    Naito, H.
    Shiiki, K.
    Izawa, K.
    Ota, Y.
    Sakamoto, H.
    Kaneko, A.
    INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2006, 35 (07) : 613 - 617
  • [9] Demonstration of Antiallodynic Effects of the Cyclooxygenase-2 Inhibitor Meloxicam on Established Diabetic Neuropathic Pain in Mice
    Kimura, Satoko
    Kontani, Hitoshi
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2009, 110 (02) : 213 - 217
  • [10] Chemoprevention for gastric carcinoma in rat duodenogastric reflux model by a selective cyclooxygenase-2 inhibitor, meloxicam
    Fujimura, Takashi
    Oba, Masaru
    Oyama, Katsunobu
    Miyashita, Tomoharu
    Kinami, Shinichi
    Ninomiya, Itasu
    Fushida, Sachio
    Nishimura, Genichi
    Ohta, Tetsuo
    Miwa, Koichi
    CANCER RESEARCH, 2006, 66 (08)