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    J Postgrad Med. 2007 Oct-Dec;53(4):221-7.

    A prospective randomized comparative study of the effects of intranasal and transdermal 17 beta-estradiol on postmenopausal symptoms and vaginal cytology.

    Source

    Adnan Menderes University Faculty of Medicine, Department of Obstetrics and Gynecology, 09100 Aydin, Turkey. arodabasi@gmail.com

    Abstract

    CONTEXT:

    Investigating the adverse effects of oral hormone replacement therapy (HRT), the clinical effectiveness of alternative combinations and route of administrations.

    AIM:

    To compare the effects of intranasal and transdermal 17 beta-estradiol combined with vaginal progesterone on vasomotor symptoms and vaginal cytology.

    SETTINGS AND DESIGN:

    A 12-week, prospective, randomized comparative study was conducted between July 2005 and September 2006.

    MATERIALS AND METHODS:

    Eighty postmenopausal women aged between 42-57 years, who had scores of > or =1.7 on the menopause rating scale-I (MRS-I) items "1-6", were randomly assigned to receive intranasal (300 microg/day, n =40) or transdermal (50 microg/day, n =40) 17 beta-estradiol continuously. All patients also received a vaginal progesterone gel twice weekly. Vasomotor symptoms were evaluated at weeks 0, 4, 8 and 12. Vaginal maturation index (VMI) was evaluated at weeks 0 and 12 of the study.

    STATISTICAL ANALYSES:

    The Mann-Whitney U and the Wilcoxon tests were used. P < 0.05 was regarded as significant.

    RESULTS:

    Thirty-two women in the intranasal and 29 women in the transdermal group completed the study. The total score of the MRS, the sum-scores of Factor 1 "HOT FLUSHES" and Factor 2 "PSYCHE" significantly decreased in both groups at week 4. Factor 3 "ATROPHY" scores significantly decreased only in the transdermal group at week 12. The VMI showed no changes within and between the two groups at the end of the study.

    CONCLUSION:

    Intranasal and transdermal 17beta-estradiol combined with vaginal progesterone gel as a continuous HRT caused a similar decrease in vasomotor symptoms but did not have any significant effect on VMI after 12 weeks of treatment in this study population.

    PMID:
    18097108
    [PubMed - indexed for MEDLINE]
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