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Coasting疗法(抑制促性腺激素)预防卵巢过度刺激综合征

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Referencias

References to studies included in this review

Aboulgar 2007 {published data only}

Aboulghar M, Mansour R, Amin Y, Al‐Inany H, Aboulghar M, Serour G. A prospective randomized study comparing coasting with GnRH antagonist administration in patients at risk for severe OHSS. Reproductive Biomedicine Online 2007;15(3):271‐9. CENTRAL

Aflatoonian 2006 {published data only}

Aflatoonian A, Mahani I, Tabibnejad N, Aflatoonian B, Aflatoonian R. Comparison of coasting with aspiration half of follicles before hCG injection for prevention of OHSS in ART cycles. Human Reproduction 2006;21(Suppl 1):i37. CENTRAL

Dalal 2014 {published and unpublished data}

Dalal R, Mishra A. Comparison of coasting with cabergoline administration for prevention of early severe OHSS in ART cycles. BJOG Eposter2014:78. CENTRAL

Egbase 1999 {published data only}

Egbase PE, Al Sharhan M, Grudzinskas JG. Early unilateral follicular aspiration compared with coasting for the prevention of severe ovarian hyperstimulation syndrome: a prospective randomized study. Human Reproduction 1999;14(6):1421‐5. CENTRAL

Egbase 2011 {published data only}

Egbase P, Al Sharhan M, Masangcay M, Egbase E. Follicle stimulating hormone (FSH) administer with trigger dose human chorionic gonadotropin (hCG) completely prevents ovarian hyperstimulation syndrome (OHSS). Randomised controlled trial. Fertility and Sterility 2011;96(3):S20. CENTRAL

Kamthane 2007 {published data only}

Kamthane V, Goswami S, Ghosh S, Chattopadhay R, Chakravarty B. Does coasting prevent OHSS without compromising pregnancy outcome?. Human Reproduction 2004;19 Suppl(6):i121. CENTRAL

Lukaszuk 2011 {published data only}

Lukaszuk K, Liss J, Jakiel G. 'Internal Coasting' for prevention of ovarian hyperstimulation syndrome (OHSS) in IVF/ICSI. Ginekol Pol 2011;82:812‐6. CENTRAL

Sohrabvand 2009 {published data only}

Sohrabvand F, Ansaripour MD, Bagheri M, Shariat M, Jafarabadi M. Cabergoline versus coasting in the prevention of ovarian hyperstimulation syndrome and assisted reproductive outcome in high risk patients. International Journal of Fertility and Sterility 2009;3(1):35‐40. CENTRAL

References to studies excluded from this review

Aboulghar 1998 {published data only}

Aboulghar MA, Mansour RT, Serour GI, Sattar M, Ranzy AM, Amin Y. Successful prevention of ovarian hyperstimulation syndrome by reduction of human menopausal gonadotrophin dose following by delayed HCG injection. Human Reproduction 1998;13:243‐4. CENTRAL

Al‐Shawaf 2001 {published data only}

Al‐Shawaf T, Zosmer A, Hussain S, Tozer A, Panay N, Wilson C, et al. Prevention of severe ovarian hyperstimulation syndrome in IVF with or without ICSI and embryo transfer: a modified 'coasting' strategy based on ultrasound identification of high‐risk patients. Human Reproduction 2001;1(16):24‐30. CENTRAL

Benadiva 1997 {published data only}

Benadiva CA, Davis O, Kligman I, Moomjy M, Hung‐Ching L, Rosenwaks Z. Withholding gonadotropin administration is an effective alternative for the prevention of ovarian hyperstimulation syndrome. Fertility and Sterility 1997;67(4):724‐7. CENTRAL

Dhont 1998 {published data only}

Dhont M, Van der Straeten F, De Sutter P. Prevention of severe ovarian hyperstimulation by coasting. Fertility and Sterility 1998;70(9):847‐50. CENTRAL

Esinler 2013 {published data only}

Esinler I, Bozdag G. Preventing ovarian hyperstimulation syndrome: cabergoline versus coasting. Archives of Gynecology and Obstetrics 2013;288:1159‐63. CENTRAL

Fluker 1999 {published data only}

Fluker MR, Hooper WM, Yuzpe A. Withholding gonadotropins ('coasting') to minimize the risk of ovarian hyperstimulation during superovulation and in vitro fertilization‐embryo transfer cycles. Fertility and Sterility 1999;71(2):294‐301. CENTRAL

Herrero 2011 {published data only}

Herrero L, Pareja S, Losada C, Cobo AC, Pellicer A, Garcia‐Velasco. Avoiding the use of human chorionic gonadotrophin combined with oocyte vitrification and GnRH agonist versus coasting: a new strategy to avoid ovarian hyperstimulation syndrome.. Fertility and Sterility 2011;95(3):1137‐40. CENTRAL

Lee 1998 {published data only}

Lee C, Tummon I, Martin J, Nisker J, Power S, Tekpetey F. Does withholding gonadotropin administration prevent severe ovarian hyperstimulation syndrome?. Human Reproduction 1998;13(5):1157‐8. CENTRAL

Sher 1995 {published data only}

Sher G, Zouves C, Feinman M, Maassarani G. 'Prolonged coasting': an effective method for preventing severe ovarian hyperstimulation syndrome in patients undergoing in vitro fertilization. Human Reproduction 1995;10(12):3107‐9. CENTRAL

Tortoriello 1998 {published data only}

Tortoriello DV, McGovern P, Colon JM, Skurnick JH, Lipetz K, Santoro N. 'Coasting' does not adversely affect cycle outcome in a subset of highly responsive in vitro fertilization patients. Fertility and Sterility 1998;69(3):454‐60. CENTRAL

Tortoriello 1999 {published data only}

Tortoriello DV. Exogenous gonadotropin withdrawal for the prevention of severe ovarian hyperstimulation syndrome: a critical review. Assisted Reproduction 1999;9(1):17‐22. CENTRAL

Ulug 2002 {published data only}

Ulug U, Bahceci M, Erden HF, Shalev E, Ben‐Shlomo I. The significance of coasting duration during ovarian stimulation for conception in assisted fertilization cycles. Human Reproduction 2002;17(2):310‐3. CENTRAL

VanderStraeten 1998 {published data only}

Van der Straeten F, De Sutter P, Dhont M. Prevention of threatening ovarian hyperstimulation by coasting. Assisted Reproduction 1998;21(4):200‐4. CENTRAL

Waldenstrom 1999 {published data only}

Waldenstrom U, Kahn J, Marsk L, Nilsson S. High pregnancy rates and successful prevention of severe ovarian hyperstimulation syndrome by 'prolonged coasting' of very hyperstimulated patients: a multicentre study. Human Reproduction 1999;14(2):294‐7. CENTRAL

Agrawal 1999

Agrawal R, Tan SL, Wild S, Sladkevicius P, Engnrann L, Payne N, et al. Serum vascular endothelium growth factor concentrations in in vitro fertilization cycles predict the risk of ovarian hyperstimulation syndrome. Fertility and Sterility 1999;71:287‐93.

ASRM 2016

Practice Committee of the American Society for Reproductive Medicine. Prevention and treatment of moderate and severe ovarian hyperstimulation syndrome: a guideline. Fertility and Sterility 2016;106:1634‐47.

Calhaz‐Jorge 2016

Calhaz‐Jorge C, De Geyter C, Kupka MS, de Mouzon, Erb K, Mocanu E, et al. Assisted reproductive technology in Europe, 2012: results generated from European registers by ESHRE. Human Reproduction 2016;31(8):1638‐52.

Golan 1989

Golan A, Ron‐El R, Herman A, Soffer Y, Wainraub Z, Caspi E. Ovarian hyperstimulation syndrome: an update review. Obstetrical and Gynaecological Survey 1989;44:430‐40.

Goldsman 1995

Goldsman MP, Pedram A, Dominiguez CE, Ciuffardi I, Levin E, Asch RH. Increased capillary permeability induced by human follicular fluid: a hypothesis for an ovarian origin of the hyperstimulation syndrome. Fertility and Sterility 1995;63:268‐72.

GRADEpro GDT 2014 [Computer program]

GRADE Working Group, McMaster University. GRADEpro GDT. Version accessed prior to November 2016. Hamilton (ON): GRADE Working Group, McMaster University, 2014.

Higgins 2011

Higgins JPT, Green S, editors. Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 (updated March 2011). The Cochrane Collaboration, 2011. Available from www.handbook.cochrane.org.

Kawwass 2015

Kawwass JF, Kissin DM, Kulkarni AD, Creanga AA, Session DR, Callaghan WM, et al. Safety of assisted reproductive technology in the United States, 2000‐2011. JAMA 2015;313(1):88.

Navot 1992

Navot D, Bergh PA, Laufer N. Ovarian hyperstimulation syndrome in novel reproductive technologies: prevention and treatment. Fertility and Sterility 1992;58:249‐61.

Rabau 1967

Rabau E, Serr DM, David A, Mashiach S, Lunenfield B. Human menopausal gonadotrophins for anovulation and sterility. American Journal of Obstetrics and Gynaecology 1967;98:92‐8.

Rizk 1999

Rizk B, Aboulghar MA. Classification, pathophysiology and management of ovarian hyperstimulation syndrome. In: Brinsden P editor(s). A Textbook of In Vitro Fertilization and Assisted Reproduction. 2nd Edition. London: Parthenon Publishing, 1999:131‐55.

Schenker 1978

Schenker JG, Weinstein D. Ovarian hyperstimulation syndrome: a current survey. Fertility and Sterility 1978;30:255‐68.

Sher 1993

Sher G, Salem R, Feinman M, Dodge S, Zouves C, Knutzen V. Eliminating the risk of life‐endangering complications following overstimulation with menotropin fertility agents: a report on women undergoing in vitro fertilization and embryo transfer. Obstetrics and Gynaecology 1993;81(6):1009‐11.

Tsirigotis 1994

Tsirigotis M, Craft I. Ovarian hyperstimulation syndrome (OHSS): how much do we really know about it?. European Journal of Obstetrics and Gynecology 1994;55(3):151‐5.

References to other published versions of this review

D'Angelo 2000

D'Angelo A, Amso N. "Coasting" (withholding gonadotropins) for the treatment of Ovarian Hyperstimulation Syndrome. Cochrane Database of Systematic Reviews 2000, Issue 4. [DOI: 10.1002/14651858.CD002811]

D'Angelo 2002

D'Angelo A, Amso N. "Coasting" (withholding gonadotrophins) for preventing ovarian hyperstimulation syndrome. Cochrane Database of Systematic Reviews 2002, Issue 3. [DOI: 10.1002/14651858.CD002811]

D'Angelo 2011

D'Angelo A, Brown J, Amso NN. Coasting (withholding gonadotrophins) for preventing ovarian hyperstimulation syndrome. Cochrane Database of Systematic Reviews 2011, Issue 1. [DOI: 10.1002/14651858.CD002811]

D'Angelo 2011b

D'Angelo A, Brown J, Amso NN. Coasting (withholding gonadotrophins) for preventing ovarian hyperstimulation syndrome. Cochrane Database of Systematic Reviews 2011, Issue 6. [DOI: 10.1002/14651858.CD002811]

Characteristics of studies

Characteristics of included studies [ordered by study ID]

Aboulgar 2007

Methods

Randomised controlled trial, single centre.

Participants

Eygpt.

IVF centre. Of 1536 women undergoing IVF/ICSI, 190 were eligible and randomised.

Inclusion: undergoing first IVF trial, at actual risk of developing severe OHSS with large number of follicles (≥ 20) on both ovaries, with 90% of the follicles being small (< 14 mm in mean diameter), and estradiol concentration ≥ 3000 pg/ml.

Age in the coasting group was 30 ± 4.9 years, and in the antagonist group was 29.6 ± 4.6 years

Interventions

Ovarian stimulation using long GnRH agonist down‐regulation protocol.

Coasting group (N = 96) hMG injections stopped and GnRH agonist continued. HmCG given when E2 ≤ 3000 pg/ml. Oocyte retrieval performed 36 hours after HCG administration.

GnRHa group (N = 94) treated with subcutaneous GnRH antagonist (ganirelix acetate 250 µg) daily until day of HCG administration. GnRH agonist was discontinued with the start of antagonist and hMG injections continued daily until E2 ≤ 3000 pg/ml, then 10,000 IU of hCG given. Oocyte retrieval performed 36 hours after HCG administration.

Embryo transfer on day 2 or day 3 with two to three embryos transferred.

Outcomes

The primary outcomes were number of high quality embryos. Secondary outcomes were days of intervention, number of oocytes, pregnancy rate, multiple pregnancy, number of cryopreserved embryos and incidence of severe OHSS

Notes

Sample size calculation estimated N = 182

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Unclear risk

'randomised' ‐ no other details

Allocation concealment (selection bias)

Low risk

'dark, sealed envelopes .... created by a third party not involved in the allocation process.' 'sequentially numbered'

Blinding (performance bias and detection bias)
All outcomes

High risk

'The patient was informed about the allocated arm'

Incomplete outcome data (attrition bias)
All outcomes

Low risk

All those randomised were analyzed, no loss to follow‐up reported

Selective reporting (reporting bias)

Unclear risk

Did not report live birth

Aflatoonian 2006

Methods

Randomised controlled trial

Participants

Iran and UK study

52 women undergoing IVF treatment cycles at high risk for developing OHSS (> 20 follicles in both ovaries, serum estradiol = E2 > 3000 pg/ml).

Interventions

Induction of ovulation with long protocol beginning with pituitary desensitisation with subcutaneous buserelin and followed by hMG 3 amp from day 2.

On day 9 randomised to:

Coasting group (N = 27) IVF/ICSI defined as presence of > 10 follicles per ovary with a leading follicle > 17 mm and E2 > 3000 pg/ml (maximum 3 days). Then 10000 units hCG administered and oocyte retrieval 34 to 36 hours later.

Aspiration follicle group (N = 26) had > 15 follicles 15 to 16mm in each ovary and E2 > 3000 pg/ml. Unilateral aspiration follicular aspiration performed before hCG administration. Oocyte retrieval performed 34 to 36 hours later in the other ovary.

Embryo transfer was done 2 days later in both groups.

Outcomes

Number of follicles, number of oocytes, pregnancy rate, OHSS.

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Unclear risk

'randomized controlled trial'

Allocation concealment (selection bias)

Unclear risk

No details

Blinding (performance bias and detection bias)
All outcomes

High risk

No blinding

Incomplete outcome data (attrition bias)
All outcomes

Unclear risk

No details

Selective reporting (reporting bias)

Unclear risk

Outcomes not mentioned in methods ‐ this was a conference abstract. Did not report live birth.

Dalal 2014

Methods

Randomised control trial

Participants

India study

60 women undergoing IVF considered at risk of OHSS (> 20 follicles of more than 11 mm, serum E2 > 3000 pg/ml on day 9 of stimulation, or both).

Interventions

Coasting group (30 patients), exogenous gonadotropins were withheld to allow E2 to decrease while GnRH‐a was maintained. Then 10,000 units hCG was administrated and oocyte retrieval was performed 36 hours later

Cabergoline group (30 patients) were administered with 0.5 mg cabergoline tablet on day of hCG injection, continued for 8 days.

Outcomes

Number of mature oocytes, number of embryos, clinical pregnancy rate, OHSS

Notes

Source of funding not stated and no correspondence details for author. Obtained missing data from another review

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

Computer generated randomization

Allocation concealment (selection bias)

High risk

No allocation concealment

Blinding (performance bias and detection bias)
All outcomes

High risk

No blinding

Incomplete outcome data (attrition bias)
All outcomes

Low risk

All participants analyzed

Selective reporting (reporting bias)

Unclear risk

Outcomes not mentioned in methods. Did not report live birth

Egbase 1999

Methods

Randomised controlled trial; parallel prospective design; single centre; power calculation included; randomization based on serially numbered sealed envelopes.

Participants

Kuwait study

37 women recruited:

30 infertile women (consented and randomised) < 39 years, considered at risk of OHSS (15 coasting/15 EUFA);
E2 (major risk factor for OHSS) was > 6000 pg/ml;
Mean (± SD) age (coasting) 33.5 ± 2.8, (EUFA) 34.6 ± 3.2;
Duration of infertility: not stated;
Causes of infertility: unexplained (2 versus 2); anovulation (2 versus 2); tubal factor (1 versus 3); tubal + anovulation (2 versus 2); male factor (5 versus 4); male factor + anovulation (5 versus 4); BMI > 30 (13 versus 10) and > 40 (6 versus 5).

Interventions

Treatment group: coasting (hMG injections were withheld until E2 < 3000 pg/ml and GnRh‐a continued until day of hCG; duration 3 to 7 days).
Control group: early unilateral follicular flushing (left ovarian follicular aspiration 10 to 12 hours after hCG administration).

Outcomes

Method of diagnosing different grades of OHSS: Schenker and Weinstein (1978) and Navot criteria (1992).
Moderate and severe OHSS
Clinical pregnancy rate/woman
Number of oocytes retrieved
Fertilization rate
Number of embryos transferred

Notes

Source of funding: not stated. Authors contacted on two occasions ‐ extra data obtained

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

Computer generated random numbers

Allocation concealment (selection bias)

Low risk

"serially numbered sealed envelopes"

Blinding (performance bias and detection bias)
All outcomes

High risk

No blinding

Incomplete outcome data (attrition bias)
All outcomes

Low risk

All patients analyzed

Selective reporting (reporting bias)

Unclear risk

Outcomes not mentioned in methods. Did not report live birth

Egbase 2011

Methods

Randomised controlled trial, single centre, randomization based on serially numbered sealed envelopes.

Participants

Kuwait study, 102 women recruited undergoing IVF cycles at risk of OHS with serum E2 ≥ 3500 pg/ml, > 15 follicles in each ovary and two leading follicles of ≥18mm in size.

Interventions

Coasting group (N = 51): long protocol starting dose 225 iu hMG, hMG was withheld until E2 levels fell < 1500 pg/ml, when trigger dose HCG was administered.

FSH co‐trigger group (N = 51): Long protocol, pure FSH was administered with the trigger dose of hCG, regardless of the E2 levels ≥ 3500 pg/ml.

Three cleaved D3 or two D5 blastocyst embryos transferred.

Outcomes

Golan 2009 classification of OHSS used

Moderate or severe OHSS

Clinical pregnancy rate (48.6% versus 51.8%)

Number of oocytes retrieved (8.6 ± 2.9 versus 26.4 ± 3.5)

Multiple pregnancy rate, live birth rate, miscarriage rate (reported as no significant difference)

Notes

Source of funding not stated, author contacted twice, responded once with partial data.

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

Computer generated random numbers

Allocation concealment (selection bias)

Low risk

"serially numbered sealed envelopes"

Blinding (performance bias and detection bias)
All outcomes

High risk

No blinding

Incomplete outcome data (attrition bias)
All outcomes

Low risk

All participants analyzed

Selective reporting (reporting bias)

Unclear risk

Outcomes not mentioned in methods. Did not report data suitable for analysis on live birth

Kamthane 2007

Methods

Randomised study

Participants

68 patients at risk of developing OHSS, aged 25 to 38 years undergoing controlled ovarian hyperstimulation in IVF/ICSI.

Inclusion: intermediate follicles (11 to 14mm) > 10, E2 > 700 pg/ml on day 7 or day 8 of controlled ovarian hyperstimulation, or both

Interventions

Group A (N = 16) early coasting from day 8 onwards on basis of high E2 (> 700 pg/ml).

Group B (N = 18) late coasting when one of the follicles reached 15 mm; E2 < 700 pg/ml on day 8 but number of intermediate follicles were more than 10.

Group C (N = 34) no coasting, E2 level of 3000 pg/ml to < 4000 pg/ml hCG day. These women had neither E2 > 700 pg/ml, nor intermediate follicles > 10mm.

Outcomes

OHSS severity, terminal E2 mean number of oocytes retrieved, endometrial thickness, clinical pregnancy, miscarriage, live birth.

Notes

Women with E2 > 4000 pg/ml on hCG day had transvaginal ovum retrieval, and following fertilisation, the embryos were frozen and not transferred in that cycle. These women received prophylactic IV albumin and were excluded from the study.

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

'randomised'

Allocation concealment (selection bias)

Unclear risk

No details

Blinding (performance bias and detection bias)
All outcomes

Unclear risk

No details

Incomplete outcome data (attrition bias)
All outcomes

Unclear risk

Women who were excluded due to high E2 levels were not detailed

Selective reporting (reporting bias)

Low risk

All a priori outcomes reported

Lukaszuk 2011

Methods

Randomised controlled trial, single centre, randomization based on generated table of random numbers

Participants

139 women recruited, who had unsuccessfully undergone standard long protocol ICSI procedure complicated by moderate or severe OHSS. For the next cycle, women randomised to standard long protocol or 'internal' coasting.

Interventions

Coasting group (N = 68): long protocol, received 2 days 225 iu hMG, then 2 days without hMG and 150 hMG for remainder of the stimulation period.

Control group (N = 71): received standard dose hMG as in the first cycle.

All patient underwent ICSI (routine practice in the centre) and maximum two embryos transferred on D3 for women < 36 and three embryos for older women.

Outcomes

Rizk and Aboulgar OHSS classification used

Moderate or severe OHSS

Clinical pregnancy rate

Number of oocytes retrieved

Multiple pregnancy rate

Notes

Source of funding not stated; author contacted twice ‐ no response.

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

'randomised'.

Allocation concealment (selection bias)

Low risk

only known to administrative staff

Blinding (performance bias and detection bias)
All outcomes

High risk

No blinding

Incomplete outcome data (attrition bias)
All outcomes

Low risk

All participants analyzed

Selective reporting (reporting bias)

Low risk

Includes expected outcomes

Sohrabvand 2009

Methods

Randomised controlled trial

Participants

60 participants undergoing IVF at risk of developing OHSS (20 follicles in both ovaries, majority < 15 mm in diameter and serum E2 level 3000 pg/ml)

Interventions

All participants underwent long protocol with a starting dose of 75 to150 iu r‐FSH, and dose adjusted on individual response.

In Cabergoline Group A (30 patients), when the number of follicles exceeded 20, with at least two leading follicles 18 mm, 10,000 hCG was administered and 0.5 mg oral cabergoline was started immediately for seven days after hCG administration

In Coasting Group B (30 patients), when the number of follicles was 20 or more and mean leading follicle was 16 mm, gonadotrophin was ceased until E2 levels dropped below 3000 pg/ml.

All participants underwent ICSI procedure and 2 to 3 embryos transferred, depending on patient's age and quality of embryos.

Outcomes

Number of oocytes, clinical pregnancy rate, OHSS

Notes

Source of funding not stated. Attempts made to contact authors but there was no response

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

block randomization

Allocation concealment (selection bias)

Unclear risk

not stated

Blinding (performance bias and detection bias)
All outcomes

High risk

No blinding

Incomplete outcome data (attrition bias)
All outcomes

Low risk

All participants data analyzed

Selective reporting (reporting bias)

Low risk

Main outcome measure reported

OHSS: ovarian hyperstimulation syndrome

EUFA: early unilateral follicular aspiration

E2: estradiol

BMI: body mass index

hMG: human menopausal gonadotrophin

GnRh‐a: gonadotrophin‐releasing hormone analogue

hCG: human chorionic gonadotrophin

FSH: Follicle stimulating hormone

Characteristics of excluded studies [ordered by study ID]

Study

Reason for exclusion

Aboulghar 1998

Prospective randomised trial with historical control

Al‐Shawaf 2001

Prospective observational study

Benadiva 1997

Retrospective observational study

Dhont 1998

Retrospective case‐control study

Esinler 2013

Retrospective cohort study

Fluker 1999

Retrospective observational study

Herrero 2011

Retrospective observational study

Lee 1998

Prospective observational study

Sher 1995

Prospective observational study

Tortoriello 1998

Retrospective observational study

Tortoriello 1999

Retrospective observational study

Ulug 2002

Retrospective observational study

VanderStraeten 1998

Retrospective case‐control study

Waldenstrom 1999

Prospective observational study

Data and analyses

Open in table viewer
Comparison 1. Coasting versus no coasting

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

2

207

Odds Ratio (M‐H, Fixed, 95% CI)

0.11 [0.05, 0.24]

Analysis 1.1

Comparison 1 Coasting versus no coasting, Outcome 1 OHSS.

Comparison 1 Coasting versus no coasting, Outcome 1 OHSS.

2 Live birth Show forest plot

1

68

Odds Ratio (M‐H, Fixed, 95% CI)

0.48 [0.14, 1.62]

Analysis 1.2

Comparison 1 Coasting versus no coasting, Outcome 2 Live birth.

Comparison 1 Coasting versus no coasting, Outcome 2 Live birth.

3 Clinical pregnancy Show forest plot

2

207

Odds Ratio (M‐H, Fixed, 95% CI)

0.82 [0.46, 1.44]

Analysis 1.3

Comparison 1 Coasting versus no coasting, Outcome 3 Clinical pregnancy.

Comparison 1 Coasting versus no coasting, Outcome 3 Clinical pregnancy.

4 Multiple pregnancy Show forest plot

1

139

Odds Ratio (M‐H, Fixed, 95% CI)

0.31 [0.12, 0.81]

Analysis 1.4

Comparison 1 Coasting versus no coasting, Outcome 4 Multiple pregnancy.

Comparison 1 Coasting versus no coasting, Outcome 4 Multiple pregnancy.

5 Miscarriage Show forest plot

2

207

Odds Ratio (M‐H, Fixed, 95% CI)

0.85 [0.25, 2.86]

Analysis 1.5

Comparison 1 Coasting versus no coasting, Outcome 5 Miscarriage.

Comparison 1 Coasting versus no coasting, Outcome 5 Miscarriage.

6 Number of oocytes retrieved Show forest plot

2

207

Mean Difference (IV, Fixed, 95% CI)

‐3.86 [‐4.38, ‐3.33]

Analysis 1.6

Comparison 1 Coasting versus no coasting, Outcome 6 Number of oocytes retrieved.

Comparison 1 Coasting versus no coasting, Outcome 6 Number of oocytes retrieved.

Open in table viewer
Comparison 2. Coasting versus early unilateral follicular aspiration (EUFA)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

2

83

Odds Ratio (M‐H, Fixed, 95% CI)

0.98 [0.34, 2.85]

Analysis 2.1

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 1 OHSS.

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 1 OHSS.

2 Clinical Pregnancy Show forest plot

2

83

Odds Ratio (M‐H, Fixed, 95% CI)

0.67 [0.25, 1.79]

Analysis 2.2

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 2 Clinical Pregnancy.

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 2 Clinical Pregnancy.

3 Number of oocytes retrieved Show forest plot

2

83

Mean Difference (IV, Fixed, 95% CI)

‐4.42 [‐6.08, ‐2.75]

Analysis 2.3

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 3 Number of oocytes retrieved.

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 3 Number of oocytes retrieved.

Open in table viewer
Comparison 3. Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

1

190

Odds Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Analysis 3.1

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 1 OHSS.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 1 OHSS.

2 Clinical Pregnancy Show forest plot

1

190

Odds Ratio (M‐H, Fixed, 95% CI)

0.74 [0.42, 1.31]

Analysis 3.2

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 2 Clinical Pregnancy.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 2 Clinical Pregnancy.

3 Multiple pregnancy Show forest plot

1

190

Odds Ratio (M‐H, Fixed, 95% CI)

0.84 [0.39, 1.80]

Analysis 3.3

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 3 Multiple pregnancy.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 3 Multiple pregnancy.

4 Number of oocytes retrieved Show forest plot

1

190

Mean Difference (IV, Fixed, 95% CI)

‐2.44 [‐4.30, ‐0.58]

Analysis 3.4

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 4 Number of oocytes retrieved.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 4 Number of oocytes retrieved.

Open in table viewer
Comparison 4. Coasting versus FSH co‐trigger with hCG administration

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

1

102

Odds Ratio (M‐H, Fixed, 95% CI)

43.74 [2.54, 754.58]

Analysis 4.1

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 1 OHSS.

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 1 OHSS.

2 Clinical pregnancy Show forest plot

1

102

Odds Ratio (M‐H, Fixed, 95% CI)

0.92 [0.43, 2.01]

Analysis 4.2

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 2 Clinical pregnancy.

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 2 Clinical pregnancy.

3 Number of oocytes retrieved Show forest plot

1

102

Mean Difference (IV, Fixed, 95% CI)

‐17.80 [‐19.05, ‐16.55]

Analysis 4.3

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 3 Number of oocytes retrieved.

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 3 Number of oocytes retrieved.

Open in table viewer
Comparison 5. Coasting versus cabergoline

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

2

120

Odds Ratio (M‐H, Fixed, 95% CI)

1.98 [0.69, 5.68]

Analysis 5.1

Comparison 5 Coasting versus cabergoline, Outcome 1 OHSS.

Comparison 5 Coasting versus cabergoline, Outcome 1 OHSS.

2 Clinical pregnancy rate Show forest plot

2

120

Odds Ratio (M‐H, Fixed, 95% CI)

0.38 [0.16, 0.88]

Analysis 5.2

Comparison 5 Coasting versus cabergoline, Outcome 2 Clinical pregnancy rate.

Comparison 5 Coasting versus cabergoline, Outcome 2 Clinical pregnancy rate.

3 Number of oocytes retrieved Show forest plot

1

60

Mean Difference (IV, Fixed, 95% CI)

‐4.30 [‐7.88, ‐0.72]

Analysis 5.3

Comparison 5 Coasting versus cabergoline, Outcome 3 Number of oocytes retrieved.

Comparison 5 Coasting versus cabergoline, Outcome 3 Number of oocytes retrieved.

Study flow diagram: July 2016 search for 2017 review update
Figuras y tablas -
Figure 1

Study flow diagram: July 2016 search for 2017 review update

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 2

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 3

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Forest plot of comparison: 3 Coasting versus no coasting, outcome: 3.1 OHSS.
Figuras y tablas -
Figure 4

Forest plot of comparison: 3 Coasting versus no coasting, outcome: 3.1 OHSS.

Forest plot of comparison: 1 Coasting versus EUFA, outcome: 1.1 OHSS.
Figuras y tablas -
Figure 5

Forest plot of comparison: 1 Coasting versus EUFA, outcome: 1.1 OHSS.

Forest plot of comparison: 5 Coasting versus cabergoline, outcome: 5.1 OHSS.
Figuras y tablas -
Figure 6

Forest plot of comparison: 5 Coasting versus cabergoline, outcome: 5.1 OHSS.

Comparison 1 Coasting versus no coasting, Outcome 1 OHSS.
Figuras y tablas -
Analysis 1.1

Comparison 1 Coasting versus no coasting, Outcome 1 OHSS.

Comparison 1 Coasting versus no coasting, Outcome 2 Live birth.
Figuras y tablas -
Analysis 1.2

Comparison 1 Coasting versus no coasting, Outcome 2 Live birth.

Comparison 1 Coasting versus no coasting, Outcome 3 Clinical pregnancy.
Figuras y tablas -
Analysis 1.3

Comparison 1 Coasting versus no coasting, Outcome 3 Clinical pregnancy.

Comparison 1 Coasting versus no coasting, Outcome 4 Multiple pregnancy.
Figuras y tablas -
Analysis 1.4

Comparison 1 Coasting versus no coasting, Outcome 4 Multiple pregnancy.

Comparison 1 Coasting versus no coasting, Outcome 5 Miscarriage.
Figuras y tablas -
Analysis 1.5

Comparison 1 Coasting versus no coasting, Outcome 5 Miscarriage.

Comparison 1 Coasting versus no coasting, Outcome 6 Number of oocytes retrieved.
Figuras y tablas -
Analysis 1.6

Comparison 1 Coasting versus no coasting, Outcome 6 Number of oocytes retrieved.

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 1 OHSS.
Figuras y tablas -
Analysis 2.1

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 1 OHSS.

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 2 Clinical Pregnancy.
Figuras y tablas -
Analysis 2.2

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 2 Clinical Pregnancy.

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 3 Number of oocytes retrieved.
Figuras y tablas -
Analysis 2.3

Comparison 2 Coasting versus early unilateral follicular aspiration (EUFA), Outcome 3 Number of oocytes retrieved.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 1 OHSS.
Figuras y tablas -
Analysis 3.1

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 1 OHSS.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 2 Clinical Pregnancy.
Figuras y tablas -
Analysis 3.2

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 2 Clinical Pregnancy.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 3 Multiple pregnancy.
Figuras y tablas -
Analysis 3.3

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 3 Multiple pregnancy.

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 4 Number of oocytes retrieved.
Figuras y tablas -
Analysis 3.4

Comparison 3 Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist), Outcome 4 Number of oocytes retrieved.

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 1 OHSS.
Figuras y tablas -
Analysis 4.1

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 1 OHSS.

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 2 Clinical pregnancy.
Figuras y tablas -
Analysis 4.2

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 2 Clinical pregnancy.

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 3 Number of oocytes retrieved.
Figuras y tablas -
Analysis 4.3

Comparison 4 Coasting versus FSH co‐trigger with hCG administration, Outcome 3 Number of oocytes retrieved.

Comparison 5 Coasting versus cabergoline, Outcome 1 OHSS.
Figuras y tablas -
Analysis 5.1

Comparison 5 Coasting versus cabergoline, Outcome 1 OHSS.

Comparison 5 Coasting versus cabergoline, Outcome 2 Clinical pregnancy rate.
Figuras y tablas -
Analysis 5.2

Comparison 5 Coasting versus cabergoline, Outcome 2 Clinical pregnancy rate.

Comparison 5 Coasting versus cabergoline, Outcome 3 Number of oocytes retrieved.
Figuras y tablas -
Analysis 5.3

Comparison 5 Coasting versus cabergoline, Outcome 3 Number of oocytes retrieved.

Summary of findings for the main comparison. Coasting versus no coasting for prevention of ovarian hyperstimulation syndrome

Coasting versus no coasting for prevention of ovarian hyperstimulation syndrome (OHSS)

Population: Women undergoing assisted reproduction
Setting: Assisted reproduction clinics
Intervention: Coasting
Comparison: No coasting

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with no coasting

Risk with coasting

OHSS

457 per 1000

85 per 1000
(40 to 168)

OR 0.11
(0.05 to 0.24)

207
(2 RCTs)

⊕⊕⊝⊝
LOW1,2

Live birth

265 per 1000

147 per 1000
(48 to 368)

OR 0.48
(0.14 to 1.62)

68
(1 RCT)

⊕⊝⊝⊝
VERY LOW1,3

Clinical pregnancy

390 per 1000

344 per 1000
(228 to 480)

OR 0.82
(0.46 to 1.44)

207
(2 RCTs)

⊕⊕⊝⊝
LOW1,2

Multiple pregnancy

268 per 1000

102 per 1000
(42 to 228)

OR 0.31
(0.12 to 0.81)

139
(1 RCT)

⊕⊝⊝⊝
LOW1,2

Miscarriage

57 per 1,000

49 per 1,000

(15 to 148)

OR 0.85

(0.25 to 2.86)

207
(2 studies)

⊕⊕⊝⊝
VERY LOW1,3

*The risk in the intervention group (and its 95% confidence interval) is based on the mean risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; OR: Odds ratio;

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded one level for serious risk of bias: one study did not clearly describe the methods used, studies not blinded

2 Downgraded one level for serious imprecision: few events, wide confidence intervals, or both

3 Downgraded two levels for very serious imprecision: very few events, very wide confidence intervals, or both

Figuras y tablas -
Summary of findings for the main comparison. Coasting versus no coasting for prevention of ovarian hyperstimulation syndrome
Summary of findings 2. Coasting versus early unilateral follicular aspiration for preventing ovarian hyperstimulation syndrome

Coasting versus early unilateral follicular aspiration for preventing ovarian hyperstimulation syndrome (OHSS)

Population: Women undergoing assisted reproduction
Setting: Assisted reproduction clinics
Intervention: Coasting
Comparison: Early unilateral follicular aspiration (EUFA)

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with early unilateral follicular aspiration (EUFA)

Risk with coasting

OHSS

244 per 1000

240 per 1000
(99 to 479)

OR 0.98
(0.34 to 2.85)

83
(2 RCTs)

⊕⊝⊝⊝
VERY LOW1,2

Live birth

No data available

Clinical Pregnancy

317 per 1000

237 per 1000
(104 to 454)

OR 0.67
(0.25 to 1.79)

83
(2 RCTs)

⊕⊝⊝⊝
VERY LOW1,2

Multiple pregnancy

No data available

Miscarriage

No data available

*The risk in the intervention group (and its 95% confidence interval) is based on the mean risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; OR: Odds ratio

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded one level for serious risk of bias: one study did not clearly describe methods, lack of blinding

2 Downgraded two levels for very serious imprecision: very few events and very wide confidence intervals

Figuras y tablas -
Summary of findings 2. Coasting versus early unilateral follicular aspiration for preventing ovarian hyperstimulation syndrome
Summary of findings 3. Coasting versus gonadotrophin‐releasing hormone antagonist for preventing ovarian hyperstimulation syndrome

Coasting versus gonadotrophin‐releasing hormone antagonist for preventing ovarian hyperstimulation syndrome (OHSS)

Population: Women undergoing assisted reproduction
Setting: Assisted reproduction clinics
Intervention: Coasting
Comparison: Gonadotrophin‐releasing hormone antagonist

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with gonadotrophin‐releasing hormone antagonist

Risk with coasting

OHSS

Not estimable

Not estimable

not estimable

190
(1 RCT)

⊕⊕⊝⊝
VERY LOW1,2

Live birth

No data available

Clinical Pregnancy

553 per 1000

478 per 1000
(342 to 619)

OR 0.74
(0.42 to 1.31)

190
(1 RCT)

⊕⊕⊝⊝
LOW1,3

Multiple pregnancy

181 per 1000

156 per 1000
(79 to 284)

OR 0.84
(0.39 to 1.80)

98
(1 RCT)

⊕⊕⊝⊝
VERY LOW1,2

Miscarriage

No data available

*The risk in the intervention group (and its 95% confidence interval) is based on the mean risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio; OR: Odds ratio

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded one level due to serious risk of bias: method of sequence generation not reported, lack of blinding

2 Downgraded two levels due to very serious imprecision: no OHSS occurred in either group. Few events for multiple pregnancy.

3 Downgraded one level due to serious imprecision. Wide confidence intervals, few events

Figuras y tablas -
Summary of findings 3. Coasting versus gonadotrophin‐releasing hormone antagonist for preventing ovarian hyperstimulation syndrome
Summary of findings 4. Coasting versus follicle stimulating hormone administration at time of hCG for preventing ovarian hyperstimulation syndrome

Coasting versus follicle stimulating hormone (FSH) administration at time of hCG trigger in preventing ovarian hyperstimulation syndrome (OHSS)

Population: Women undergoing assisted reproduction
Setting: Assisted reproduction clinics
Intervention: Coasting
Comparison: FSH co‐trigger with hCG administration

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with FSH co‐trigger with hCG administration

Risk with Coasting

OHSS

Not estimable

Not estimable

OR 43.74
(2.54 to 754.58)

102
(1 RCT)

⊕⊝⊝⊝
VERY LOW1,2

Live birth

No data available

Clinical Pregnancy

510 per 1000

489 per 1000
(309 to 676)

OR 0.92
(0.43 to 2.01)

102
(1 RCT)

⊕⊕⊝⊝1,3
LOW

Multiple pregnancy

No data available

Miscarriage

No data available

*The risk in the intervention group (and its 95% confidence interval) is based on the mean risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; OR: Odds ratio; hCG: human chorionic gonadotrophin

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded one level due to serious risk of bias: method of sequence generation not reported, lack of blinding

2 Downgraded two levels due to very serious imprecision: only 15 events, all in one arm.

3 Downgraded one level due to serious imprecision: very wide confidence intervals

Figuras y tablas -
Summary of findings 4. Coasting versus follicle stimulating hormone administration at time of hCG for preventing ovarian hyperstimulation syndrome
Summary of findings 5. Coasting compared to cabergoline for preventing ovarian hyperstimulation syndrome

Coasting compared to cabergoline for preventing ovarian hyperstimulation syndrome (OHSS)

Population: Women undergoing assisted reproduction
Setting: Assisted reproduction clinics
Intervention: Coasting
Comparison: Cabergoline

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with cabergoline

Risk with Coasting

OHSS

100 per 1000

180 per 1000
(71 to 387)

OR 1.98
(0.69 to 5.68)

120
(2 RCTs)

⊕⊝⊝⊝1,2
VERY LOW

Live birth

Not reported

Clinical pregnancy rate

367 per 1000

180 per 1000
(85 to 338)

OR 0.38

(0.16 to 0.88)

120
(2 RCTs)

⊕⊕⊝⊝1
VERY LOW

Multiple pregnancy

Not reported

Miscarriage

Not reported

*The risk in the intervention group (and its 95% confidence interval) is based on the mean risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio; OR: Odds ratio

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded two levels due to very serious risk of bias: one study did not clearly define method, method of sequence generation not reported, lack of blinding

2 Downgraded one level due to serious imprecision: very few events and/or wide confidence interval.

Figuras y tablas -
Summary of findings 5. Coasting compared to cabergoline for preventing ovarian hyperstimulation syndrome
Table 1. Golan classification of ovarian hyperstimulation syndrome

Classification

Size of ovaries

Grade

Symptoms

Mild

5 to 10 cm

grade 1

abdominal tension and discomfort

grade 2

grade 1 signs plus nausea, vomiting, diarrhoea, or a combination

Moderate

> 10 cm

grade 3

grade 2 signs plus ultrasound evidence of ascites

Severe

> 12 cm

grade 4

grade 3 signs plus clinical evidence of ascites, pleural effusion and dyspnoea, or a combination

grade 5

grade 4 signs plus haemoconcentration increased blood viscosity, hypovolaemia, decreased renal perfusion, oliguria

Figuras y tablas -
Table 1. Golan classification of ovarian hyperstimulation syndrome
Table 2. Navot classification of severe ovarian hyperstimulation syndrome

Severe

Critical

Variably enlarged ovary

Variably enlarged ovary

Massive ascites ± hydrothorax

Tense ascites ± hydrothorax

Hct > 45% (> 30% increment over baseline value)

Hct > 55%

WBC > 15,000

WBC > 35,000

Oliguria

Creatinine 1.0 to 1.5

Creatinine > 1.6

Creatinine clearance > 50 ml/min

Creatinine clearance < 50ml/min

Liver dysfunction

Renal failure

Anasarca

Thromboembolic phenomena

Adult respiratory distress syndrome (ARDS)

Navot 1992

Hct: haematocrit

WBC: white blood cells

Figuras y tablas -
Table 2. Navot classification of severe ovarian hyperstimulation syndrome
Table 3. Aboulghar and Rizk classification of ovarian hyperstimulation syndrome (1999)

Moderate

Severe Grade A

Severe Grade B

Severe Grade C

Discomfort, pain, nausea, distension, ultrasonic evidence of ascites and enlarged ovaries, normal haematological and biological profile

Dyspnoea, oliguria, nausea, vomiting, diarrhoea, abdominal pain, clinical evidence of ascites, marked distension of abdomen or hydro‐thorax, US showing large ovaries and marked ascites, normal biochemical profile

Grade A plus massive tension ascites, markedly enlarged ovaries, severe dyspnoea and marked oliguria, increased haematocrit, elevated serum creatinine and liver dysfunction

Complications such as respiratory distress syndrome, renal shut‐down, or venous thrombosis

Figuras y tablas -
Table 3. Aboulghar and Rizk classification of ovarian hyperstimulation syndrome (1999)
Table 4. Different coasting regimens

Authors

E2 at coasting

E2 at hCG

Number and follicle size

Coasting time

Sher 1995

> 3000 pg/mL or > 11,000 pmol/L*

< 3000 pg/mL or < 11,000 pmol/L*

> 29 follicles at least 30% > 15 mm

3 to 11 days (mean 6.1)

Benadiva 1997

≥ 3000 pg/ml or ≥ 11,000 pmol/l*

< 3000 pg/ml or < 11,000 pmol/l*

at least 3 follicles of 15.6 ± 1.4 mm

1.9 ± 0.9 days

Tortoriello 1998

> 3000 pg/ml or > 11,000 pmol/l*

< 3000 pg/mL or < 11,000 pmol/L*

5 follicles at least 16 mm, two of which are at least 19 mm

1 to 5 days

Dhont 1998

> 2500 pg/ml or > 9000 pmol/l*

< 2500 pg/ml or < 9000 pmol/l*

≥ 20 follicles > 15 mm

1 to 6 days (mean 1.94)

Lee 1998

> 2700 pg/ml or > 10,000 pmol/l*

no values given

many immature follicles < 3 at 18 mm

3 days

VanderStraeten 1998

> 2500 pg/ml or > 9000 pmol/l*

< 2500 pg/ml or < 9000 pmol/l*

≥ 20 follicles > 14 mm

1 to 6 days (mean 1.94)

Egbase 1999

> 6000 pg/ml or > 22,000 pmol/l*

< 3000 pg/ml or 11,000 pmol/l*

> 15 follicles, each of > 18 mm in each ovary

4.9 ± 1.6 days

Waldenstrom 1999

> 2700 pg/ml or > 10,000 pmol/l*

< 2700 pg/ml or < 10,000 pmol/l*

> 25 follicles, at least 3 follicles > 17 mm

3 to 6 days (mean 4.3)

Fluker 1999

> 3000 pg/ml or > 11,000 pmol/l*

25% decline < 2250 pg/ml or 8250 pmol/l*

> 3 follicles of > 18 mm

3 to 5 days (mean 3.4 ± 0.1)

Al‐Shawaf 2001

> 3600 pg/ml or > 13,000 pmol/l*

< 2700 pg/ml or < 10,000 pmol/l*

at least 25% of the follicles > 15 mm

2 to 9 days (mean 3.4 ± 1.6)

Aboulghar 1998

> 3000 pg/ml or > 11,000 pmol/l*

< 5500 pg/ml or < 20,000 pmol/l*

> 20 follicles at least 15 mm

2.8 days

Ulug 2002

> 4000 pg/ml or > 14,684 pmol/l*

< 4000 pg/ml or < 14,684 pmol/l*

> 20 follicles, at least 30% of them >15 mm

2.9 ± 0.33 days

* conversion factor to SI unit, 3.671

Figuras y tablas -
Table 4. Different coasting regimens
Comparison 1. Coasting versus no coasting

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

2

207

Odds Ratio (M‐H, Fixed, 95% CI)

0.11 [0.05, 0.24]

2 Live birth Show forest plot

1

68

Odds Ratio (M‐H, Fixed, 95% CI)

0.48 [0.14, 1.62]

3 Clinical pregnancy Show forest plot

2

207

Odds Ratio (M‐H, Fixed, 95% CI)

0.82 [0.46, 1.44]

4 Multiple pregnancy Show forest plot

1

139

Odds Ratio (M‐H, Fixed, 95% CI)

0.31 [0.12, 0.81]

5 Miscarriage Show forest plot

2

207

Odds Ratio (M‐H, Fixed, 95% CI)

0.85 [0.25, 2.86]

6 Number of oocytes retrieved Show forest plot

2

207

Mean Difference (IV, Fixed, 95% CI)

‐3.86 [‐4.38, ‐3.33]

Figuras y tablas -
Comparison 1. Coasting versus no coasting
Comparison 2. Coasting versus early unilateral follicular aspiration (EUFA)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

2

83

Odds Ratio (M‐H, Fixed, 95% CI)

0.98 [0.34, 2.85]

2 Clinical Pregnancy Show forest plot

2

83

Odds Ratio (M‐H, Fixed, 95% CI)

0.67 [0.25, 1.79]

3 Number of oocytes retrieved Show forest plot

2

83

Mean Difference (IV, Fixed, 95% CI)

‐4.42 [‐6.08, ‐2.75]

Figuras y tablas -
Comparison 2. Coasting versus early unilateral follicular aspiration (EUFA)
Comparison 3. Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

1

190

Odds Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Clinical Pregnancy Show forest plot

1

190

Odds Ratio (M‐H, Fixed, 95% CI)

0.74 [0.42, 1.31]

3 Multiple pregnancy Show forest plot

1

190

Odds Ratio (M‐H, Fixed, 95% CI)

0.84 [0.39, 1.80]

4 Number of oocytes retrieved Show forest plot

1

190

Mean Difference (IV, Fixed, 95% CI)

‐2.44 [‐4.30, ‐0.58]

Figuras y tablas -
Comparison 3. Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist)
Comparison 4. Coasting versus FSH co‐trigger with hCG administration

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

1

102

Odds Ratio (M‐H, Fixed, 95% CI)

43.74 [2.54, 754.58]

2 Clinical pregnancy Show forest plot

1

102

Odds Ratio (M‐H, Fixed, 95% CI)

0.92 [0.43, 2.01]

3 Number of oocytes retrieved Show forest plot

1

102

Mean Difference (IV, Fixed, 95% CI)

‐17.80 [‐19.05, ‐16.55]

Figuras y tablas -
Comparison 4. Coasting versus FSH co‐trigger with hCG administration
Comparison 5. Coasting versus cabergoline

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 OHSS Show forest plot

2

120

Odds Ratio (M‐H, Fixed, 95% CI)

1.98 [0.69, 5.68]

2 Clinical pregnancy rate Show forest plot

2

120

Odds Ratio (M‐H, Fixed, 95% CI)

0.38 [0.16, 0.88]

3 Number of oocytes retrieved Show forest plot

1

60

Mean Difference (IV, Fixed, 95% CI)

‐4.30 [‐7.88, ‐0.72]

Figuras y tablas -
Comparison 5. Coasting versus cabergoline