Depot versus daily administration of gonadotrophin releasing hormone agonist protocols for pituitary desensitization in assisted reproduction cycles

被引:12
作者
Albuquerque, LE [1 ]
Saconato, H [1 ]
Maciel, MC [1 ]
机构
[1] Assoc Estudo Fertilidade, Sao Paulo, Brazil
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2005年 / 01期
关键词
D O I
10.1002/14651858.CD002808.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Gonadotrophin-releasing hormone agonist (GnRHa) has been widely used in cycles of in vitro fertilization (IVF). Among the various types of GnRHa ovarian stimulation protocols, the long protocol presents the best clinical pregnancy rates per cycle initiated ( GnRHa administration until the suppression of ovarian activity is evident, within approximately 14 days). There are two types of GnRHa administration that can be used to lead to hypophysis desensitization in the IVF cycle in the long protocol: one consisting of daily GnRHa low doses, and another with the administration of analogues in higher long-acting doses (depot). There are controversies in the data as far as the number of ampoules to be used in the cycles with the depot GnRHa treatment, as well as regarding the number of follicles made available, the number of oocytes, fertilization, implantation and pregnancy rates. Objectives The objective of this study is to compare the use of a single long-acting depot dose to that of daily GnRHa doses in in vitro fertilization cycles. Search strategy We searched the Cochrane Menstrual Disorders and SubfertilityGroup's specialised register of trials (searched 15 April 2004), Cochrane Central Register of Controlled Trials (Issue 2, 2004), MEDLINE ( 1984 to April 2004), EMBASE (1984 to June 2003), LILACS (1984 to April 2004) and reference lists of articles. Selection criteria Types of studies: RCTs comparing depot and daily administration of GnRHa for long protocols in IVF treatment cycles. Types of participants: Couples with any cause of infertility. Types of interventions: Ovarian stimulation with human follicle stimulating hormone (hFSH) and/or human menopausal gonadotropin (hMG) and/or recombinant follicle stimulating hormone (rFSH) in IVF treatment cycles. Types of outcome measures: Clinical pregnancy rates per woman, per oocyte retrieval procedure, per embryo transfer, number of oocytes retrieved, oocyte fertilization rates, ongoing/delivered pregnancy rates per cycle started, abortion rates, multiple pregnancy rates, number of ampoules of gonadotropin employed, ovarian hyperstimulation syndrome (OHSS) incidence rates, cost analysis and patient convenience. Data collection and analysis The reviewers evaluated allocation concealment, classified as adequate, uncertain or inadequate. Two reviewers extracted the data independently. All analyses were performed according to the intention-to-treat method. Main results Six studies, with a total of 552 women, were included and analysed. The studies do not indicate that there is statistically significant difference between the use of depot GnRHa or daily GnRHa in the primary outcome, clinical pregnancy rates per woman (OR 0.94, 95% CI 0.65 to 1.37). However, there was sufficient evidence that the use of depot GnRHa for pituitary desensitization in IVF cycles increased the number of gonadotrophins ampoules (WMD 3.30, 95% CI 1.27 to 5.34) and the duration of the ovarian stimulation (WMD 0.56, 95% CI 0.31 to 0.81), as compared with daily GnRHa. Authors' conclusions Although we recognise that the clinical pregnancy rates per woman are not the ideal primary outcome, we found no evidence of differences between the long protocol using depot or daily GnRHa for IVF cycles. However, the use of depot GnRHa is associated with increased requirements for gonadotrophins and a longer time required for ovarian stimulation. If these differences could be shown to translate into economic benefit, depot GnRHa should increase the overall costs of IVF treatment.
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共 48 条
[1]   MODULATION OF THE STEROIDOGENESIS OF CULTURED HUMAN GRANULOSA-LUTEIN CELLS BY GONADOTROPIN-RELEASING-HORMONE ANALOGS [J].
BUSSENOT, I ;
AZOULAYBARJONET, C ;
PARINAUD, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 76 (05) :1376-1379
[2]   A comparison of three gonadotrophin-releasing hormone analogues in an in-vitro fertilization programme: a prospective randomized study [J].
Dada, T ;
Salha, O ;
Baillie, HS ;
Sharma, V .
HUMAN REPRODUCTION, 1999, 14 (02) :288-293
[3]  
Dal Prato L, 2001, HUM REPROD, V16, P1409
[4]  
DAYA S, 1999, COCHRANE LIB, V3
[5]   METHODS FOR COMBINING RANDOMIZED CLINICAL-TRIALS - STRENGTHS AND LIMITATIONS [J].
DEMETS, DL .
STATISTICS IN MEDICINE, 1987, 6 (03) :341-350
[6]   The long-acting gonadotropin-releasing hormone analogues impaired the implantation rate [J].
Devreker, F ;
Govaerts, I ;
Bertrand, E ;
VandenBergh, M ;
Gervy, C ;
Englert, Y .
FERTILITY AND STERILITY, 1996, 65 (01) :122-126
[7]   CLINICAL OUTCOME OF A PILOT EFFICACY STUDY ON RECOMBINANT HUMAN FOLLICLE-STIMULATING-HORMONE (ORG-32489) COMBINED WITH VARIOUS GONADOTROPIN-RELEASING-HORMONE AGONIST REGIMENS [J].
DEVROEY, P ;
MANNAERTS, B ;
SMITZ, J ;
BENNINK, HC ;
VANSTEIRTEGHEM, A .
HUMAN REPRODUCTION, 1994, 9 (06) :1064-1069
[8]   COMBINATION OF LONG AND SHORT-TERM GNRH ANALOG PROTOCOLS - A NEW THERAPEUTIC APPROACH TO PERSISTENT HIGH PROGESTERONE LEVELS IN IVF CYCLES [J].
DICKER, D ;
GOLDMAN, GA ;
ASHKENAZI, J ;
FELDBERG, D ;
SHELEF, M ;
GOLDMAN, JA .
HUMAN REPRODUCTION, 1991, 6 (02) :203-205
[9]   Effects of gonadotrophin-releasing hormone agonists on human ovarian steroid secretion in vivo and in vitro -: results of a prospective, randomized in-vitro fertilization study [J].
Dor, J ;
Bider, D ;
Shulman, A ;
Levron, J ;
Shine, S ;
Mashiach, S ;
Rabinovici, J .
HUMAN REPRODUCTION, 2000, 15 (06) :1225-1230
[10]   Long-term down-regulation does not improve pregnancy rates in an in vitro fertilization program [J].
Fábregues, F ;
Balasch, J ;
Creus, M ;
Cívico, S ;
Carmona, F ;
Puerto, B ;
Vanrell, JA .
FERTILITY AND STERILITY, 1998, 70 (01) :46-51