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"Coasting" (interrupción de las gonadotrofinas) para la prevención del síndrome de hiperestimulación ovárica

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Resumen

Antecedentes

El síndrome de hiperestimulación ovárica (SHEO), producido por una estimulación ovárica excesiva, es un trastorno iatrogénico que puede ser mortal. La incidencia informada de SHEO moderado a grave varía del 0,6% al 5% de los ciclos de fecundación in vitro (FIV). Los factores que contribuyen al SHEO no se han explicado de una manera completa. La liberación de las sustancias vasoactivas secretadas por los ovarios bajo estimulación de la gonadotrofina coriónica humana (hCG) puede desempeñar una función clave en el desencadenamiento de este síndrome. Esta afección se caracteriza por un cambio masivo del líquido del compartimiento intravascular al tercer espacio, lo que da lugar a una profunda depleción intravascular y a hemoconcentración.

Objetivos

Evaluar el efecto del aplazamiento de las gonadotrofinas ("coasting") en la prevención del síndrome de hiperestimulación ovárica en los ciclos de reproducción asistida.

Métodos de búsqueda

Para la actualización de esta revisión se realizaron búsquedas en el Registro de Ensayos del Grupo Cochrane de Ginecología y Fertilidad, CENTRAL, MEDLINE (PubMed), CINHAL, PsycINFO, Embase, Google y clinicaltrials.gov hasta el 6 de julio de 2016.

Criterios de selección

Solo se incluyeron ensayos controlados aleatorizados (ECA) en los que se utilizó el "coasting" para prevenir el SHEO.

Obtención y análisis de los datos

Dos autores de la revisión de forma independiente seleccionaron los ensayos y extrajeron los datos. Cualquier desacuerdo se resolvió mediante debate. Se estableció contacto con los autores de los estudios para solicitar información adicional o datos faltantes. Las comparaciones de las intervenciones incluyeron "coasting" versus ningún "coasting", "coasting" versus aspiración folicular unilateral temprana (AFUT), "coasting" versus antagonista de la hormona liberadora de gonadotrofina (antagonista), "coasting" versus administración de hormona foliculoestimulante en el momento de la administración del factor desencadenante hCG (codesencadenante de FSH) y "coasting" versus cabergolina. El análisis estadístico se realizó según las guías Cochrane. Los desenlaces primarios fueron el SHEO moderado o grave y los nacidos vivos.

Resultados principales

Se incluyeron ocho ECA (702 mujeres con alto riesgo de desarrollar SHEO). La calidad de la evidencia fue baja o muy baja. Las limitaciones principales fueron el fracaso en el informe de los nacidos vivos, el riesgo de sesgo debido a la falta de información acerca de los métodos de los estudios y la imprecisión debido a las tasas reducidas de eventos y la falta de datos. Cuatro de los estudios solo se publicaron como resúmenes y proporcionaron datos limitados.

"Coasting" versus ningún "coasting"

Las tasas de SHEO fueron menores en el grupo de "coasting" (OR 0,11; IC del 95%: 0,05 a 0,24; I² = 0%, dos ECA; 207 mujeres; evidencia de calidad baja), lo que indica que si el 45% de las mujeres desarrollaron SHEO moderado o grave sin "coasting", entre el 4% y el 17% de las mujeres lo desarrollarían con "coasting". Hubo muy pocos datos para determinar si hubo diferencias entre los grupos en las tasas de nacidos vivos (OR 0,48; IC del 95%: 0,14 a 1,62; un ECA; 68 mujeres; evidencia de calidad muy baja), embarazo clínico (OR 0,82; IC del 95%: 0,46 a 1.44; I² = 0%; dos ECA; 207 mujeres; evidencia de calidad baja), embarazo múltiple (OR 0,31; IC 95% 0,12 a 0,81; un ECA; 139 mujeres; evidencia de calidad baja), o aborto espontáneo (OR 0,85; IC 95% 0,25 a 2,86; I² = 0%; dos ECA; 207 mujeres; evidencia de calidad muy baja).

"Coasting" versus AFUT

Hubo muy pocos datos para determinar si hubo diferencias entre los grupos en las tasas de SHEO (OR 0,98; IC del 95%: 0,34 a 2,85; I² = 0%; dos ECA; 83 mujeres; evidencia de calidad muy baja), o de embarazo clínico (OR 0,67; IC del 95%: 0,25 a 1,79; I² = 0%; dos ECA; 83 mujeres; evidencia de calidad muy baja); ningún estudio informó sobre los nacidos vivos, los embarazos múltiples ni los abortos espontáneos.

"Coasting" versus antagonista

Un ECA (190 mujeres) informó esta comparación y no ocurrieron eventos de SHEO en ninguno de los grupos. Hubo muy pocos datos para determinar si hubo diferencias entre los grupos en las tasas de embarazo clínico (OR 0,74; IC del 95%: 0,42 a 1,31; un ECA; 190 mujeres; evidencia de calidad baja), o en las tasas de embarazo múltiple (OR 1,00; IC del 95%: 0,43 a 2,32; un ECA; 98 mujeres; evidencia de calidad muy baja); el estudio no informó sobre los nacidos vivos o los abortos espontáneos.

"Coasting" versus codesencadenante de FSH

Las tasas de SHEO fueron mayores en el grupo de "coasting" (OR 43,74; IC del 95%: 2,54 a 754,58; un ECA; 102 mujeres; evidencia de calidad muy baja), con 15 eventos en el dicho grupo y ninguno en el grupo de codesencadenante de FSH. Hubo muy pocos datos para determinar si hubo diferencias entre los grupos en las tasas de embarazo clínico (OR 0,92; IC del 95%: 0,43 a 2,10; un ECA; 102 mujeres; evidencia de calidad baja). Este estudio no informó datos apropiados para el análisis sobre los nacidos vivos, los embarazos múltiples ni los abortos espontáneos, aunque declaró que no hubo diferencias significativas entre los grupos.

"Coasting" versus cabergolina

Hubo muy pocos datos para determinar si hubo diferencias entre los grupos en las tasas de SHEO (OR 1,98; IC del 95%: 0,09 a 5,68; p = 0,20; I² = 72%; dos ECA; 120 mujeres; evidencia de calidad muy baja), con 11 eventos en el grupo de "coasting" y seis en el grupo de cabergolina. La evidencia indicó que el "coasting" se asoció con tasas más bajas de embarazo clínico (OR 0,38; IC del 95%: 0,16 a 0,88; p = 0,02; I² =0%; dos ECA; 120 mujeres; evidencia de calidad muy baja), pero solo hubo 33 eventos en total. Estos estudios no informaron datos apropiados para el análisis sobre los nacidos vivos, los embarazos múltiples ni los abortos espontáneos.

Conclusiones de los autores

Hubo evidencia de calidad baja que indica que el aplazamiento de las gonadotrofinas redujo las tasas de SHEO moderado o grave más que no realizar aplazamiento. No hubo evidencia que indique que el aplazamiento de las gonadotrofinas fuera más beneficioso que otras intervenciones, aunque hubo evidencia de calidad muy baja de un único estudio pequeño que indicó que la administración de un codesencadenante de FSH en el momento de la administración de hCG podría ser mejor para reducir el riesgo de SHEO que el aplazamiento. Hubo muy pocos datos para determinar de manera clara si hubo diferencias entre los grupos para otros desenlaces.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Resumen en términos sencillos

"Coasting" (interrupción de las gonadotrofinas) para prevenir el síndrome de hiperestimulación ovárica

Pregunta de la revisión

Evaluar el efecto del aplazamiento de las gonadotrofinas para prevenir el síndrome de hiperestimulación ovárica en los ciclos de reproducción asistida.

Antecedentes

El síndrome de hiperestimulación ovárica (SHEO) es una complicación causada por el uso de hormonas para inducir la ovulación (liberación de los óvulos) en la FIV (fecundación in vitro). En ocasiones las hormonas pueden sobrestimular los ovarios. El SHEO grave es potencialmente mortal. Un método utilizado para tratar y reducir el riesgo de SHEO es el aplazamiento de las gonadotropinas o el aplazamiento prolongado. El mismo incluye la interrupción de una hormona (gonadotrofina) antes de la ovulación.

Fecha de la búsqueda

Se incluyeron estudios hasta el 6 de julio de 2016.

Características de los estudios

Se identificaron ocho ensayos controlados aleatorizados (702 mujeres) que compararon el aplazamiento de las gonadotrofinas con otra intervención para prevenir el síndrome de hiperestimulación ovárica. Las otras intervenciones incluyeron ningún aplazamiento, aspiración folicular unilateral temprana (extracción de los folículos de un ovario diez a 12 horas después de la administración de gonadotrofina coriónica humana [hCG]), antagonista de la hormona liberadora de gonadotrofina (GnRH) (fármacos que bloquean la liberación de las hormonas luteinizante [LH] y foliculoestimulante [FSH]), y codesencadenante de FSH (dosis extra de FSH administrada en el mismo momento que la hCG).

Resultados clave

Hubo evidencia de calidad baja que indica que el aplazamiento de las gonadotrofinas redujo las tasas de SHEO moderado o grave más que no realizar aplazamiento. No hubo evidencia que indique que el aplazamiento de las gonadotrofinas fuera más beneficioso que otras intervenciones, aunque hubo evidencia de calidad muy baja de un único estudio pequeño que indicó que la administración de un codesencadenante de FSH en el momento de la administración de hCG podría ser mejor para reducir el riesgo de SHEO que el aplazamiento. Hubo muy pocos datos para determinar de manera clara si hubo diferencias entre los grupos para otros desenlaces.

Calidad de la evidencia

La calidad de la evidencia fue baja o muy baja. Las limitaciones principales fueron el fracaso en el informe de los nacidos vivos, el riesgo de sesgo debido a la falta de información acerca de los métodos de los estudios y la imprecisión debido a las tasas reducidas de eventos y la falta de datos. Cuatro de los estudios solo se publicaron como resúmenes y proporcionaron datos limitados.

Authors' conclusions

Implications for practice

There was low‐quality evidence to suggest a benefit to using coasting rather than no coasting, to reduce rates of moderate or severe OHSS. Evidence did not suggest that coasting was more beneficial than other interventions such as early unilateral follicular aspiration, gonadotrophin‐releasing hormone antagonist or cabergoline. There was very low‐quality evidence from a single small study to suggest that using FSH co‐trigger at the time of HCG administration may be better at reducing the risk of OHSS than coasting. There were too few data to determine clearly whether there was a difference between the groups for any other outcomes. Therefore, at present, clinicians may wish to employ other strategies for preventing OHSS rather than just coasting, until further evidence has accumulated.

Implications for research

Given the current practice of "freeze all" and the use of antagonist protocols with agonist trigger, further research into coasting may not be relevant.

Summary of findings

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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

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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

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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

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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

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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.

Background

Description of the condition

Ovarian hyperstimulation syndrome (OHSS) is an iatrogenic, potentially life threatening condition resulting from excessive ovarian stimulation. The American Society for Reproductive Medicine (ASRM) noted that the incidence of OHSS is difficult to determine, as there is no consensus definition. Estimates of the incidence of moderate to severe OHSS range from 0.6% to 5% of assisted reproduction cycles (ASRM 2016; Calhaz‐Jorge 2016; Kawwass 2015). Studies of risk factors for OHSS have identified younger age, black race, ovulation, tubal factor, unexplained infertility, younger age, and possibly a lower body mass index (ASRM 2016).

In addition, polycystic ovarian syndrome (PCOS) or an ultrasonographic ovarian appearance of polycystic ovaries (presence of multiple, small follicles at the periphery of the ovary with echogenic stroma); establishment of pregnancy during assisted reproduction treatment (ART); human chorionic gonadotrophin (hCG) supplementation of the luteal phase; and high serum estradiol (E2; higher than 2500 pg/ml) were reported to be associated with OHSS.

Rabau and colleagues originally classified OHSS as mild, moderate or severe (Rabau 1967; Schenker 1978). Golan 1989 subsequently modified it by incorporating ultrasonographic measurement of the stimulated ovaries (Table 1). Navot 1992 introduced further modification by differentiating between the severe and the life threatening form of OHSS (Table 2). There was further classification from Rizk 1999 (Table 3).

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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

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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

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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

The factors leading to this syndrome have not been completely elucidated. It seems likely that the release of vasoactive substances, for example vascular endothelium growth factor (VEGF) secreted by the ovaries under hCG stimulation, play a key role in triggering this syndrome (Goldsman 1995; Tsirigotis 1994). As more follicles are recruited in response to gonadotrophin stimulation, the mass of the granulosa cells increases, while at the same time, the cells gain functional maturation. These two factors, acting synergistically, cause a concomitant increase in serum estradiol levels and vasoactive substances (as yet poorly defined (Agrawal 1999; Al‐Shawaf 2001)). This condition is characterised by a massive shift of fluid from the intra‐vascular compartment to the third space, resulting in profound intra‐vascular depletion and haemoconcentration (Rabau 1967; Schenker 1978).

Alternative strategies (embryo freezing, antagonist cycles, intravenous albumin infusion, agonist trigger, cabergoline) have been proposed for women undergoing ART who are at high risk of OHSS. Each of these strategies may reduce, but not eliminate, the risk.

Description of the intervention

Coasting, or prolonged coasting, may be defined as a process whereby: (1) gonadotrophin therapy is discontinued while administration of gonadotrophin‐releasing hormone agonist (GnRHa) is continued; (2) there is a delay, by a variable number of days, in administering hCG injection to trigger oocyte maturation prior to oocyte retrieval, until safe estradiol levels are attained (Sher 1993). Coasting should not be initiated too early, or too late. The effective duration of coasting is still to be determined. Many authors believe that each IVF centre should identify its own cut‐off limit of serum estradiol, follicle size, or both, at the onset of coasting, and hCG administration (Al‐Shawaf 2001; Waldenstrom 1999; Table 4).

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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

It has also been postulated that follicles of varying size have a different threshold to gonadotrophins, and smaller follicles appear to be more susceptible to gonadotrophin deprivation than larger follicles (Fluker 1999). When coasting is initiated prior to 30% of follicles having attained a mean diameter of 15 mm, an abrupt arrest in follicular development and a rapid decline in plasma estradiol usually compromise the oocyte quality. But the quality of the oocytes is also compromised, and large cystic follicles are commonly encountered, if most of the follicles are larger than 15 mm in mean diameter when coasting is implemented (Sher 1995).

How the intervention might work

It was suggested that this approach prevents severe OHSS by removing the follicle stimulating hormone (FSH) stimulation of granulosa cells, thereby inhibiting their proliferation and reducing the number of granulosa cells available for luteinization (Sher 1995). This would allow continued follicular growth and maturation, while reducing the risk of OHSS (Fluker 1999). Tortoriello 1998 also suggested that the falling FSH concentration induces an increased apoptosis of granulosa cells, which results in a reduction of chemical mediators or precursors that augment fluid extravasation.

Why it is important to do this review

Ovarian hyperstimulation syndrome is a potentially life threatening condition associated with super‐ovulation in ART. Coasting is a widespread practise, for which evidence is currently lacking. Therefore, it is important to establish, from the scientific literature, whether coasting can reduce the incidence of this condition.

Objectives

To assess the effect of withholding gonadotrophins (coasting) in the prevention of ovarian hyperstimulation syndrome (OHSS) in assisted reproduction cycles.

Methods

Criteria for considering studies for this review

Types of studies

We included randomised controlled trials (RCTs), in which coasting was used as a preventive strategy to reduce OHSS. We excluded cross‐over trials, and trials that explored ovulation induction treatment without in vitro fertilisation (IVF) or intra‐cytoplasmic sperm injection (ICSI).

Types of participants

  • Women of reproductive age, undergoing super‐ovulation in IVF or ICSI cycle

Types of interventions

Coasting is the withholding of gonadotrophins. A definition is provided under the Description of the intervention section of this report. Early unilateral follicular aspiration involves the aspiration of every visible follicle from one ovary between 10 to 12 hours after the administration of human chorionic gonadotrophin (hCG). We considered these comparisons:

  • Coasting versus no coasting;

  • Coasting versus early unilateral follicular aspiration;

  • Coasting versus gonadotrophin‐releasing hormone antagonist

  • Coasting versus pure FSH co‐trigger;

  • Coasting versus cabergoline.

Types of outcome measures

Primary outcomes

The primary outcomes of this systematic review were:

  1. incidence of moderate or severe OHSS, as defined in the included studies;

  2. live birth rate.

Secondary outcomes

The secondary outcomes were:

  1. clinical pregnancy rate per woman randomised, as defined in the included studies;

  2. multiple pregnancy rate;

  3. miscarriage rate;

  4. number of oocytes retrieved.

Search methods for identification of studies

Electronic searches

We searched the following electronic databases and trial registers (last searched 6 July 2016):

We combined the MEDLINE search with the Cochrane highly sensitive search strategy for identifying randomised trials, from chapter 6 of the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011). We combined the Embase search with trial filters developed by the Scottish Intercollegiate Guidelines Network (SIGN) (www.sign.ac.uk/methodology/filters.html#random).

Searching other resources

We handsearched the reference list of articles retrieved by the search, and contacted the trial authors if we required additional data. We handsearched relevant journals not included in the Cochrane register.

Data collection and analysis

Selection of studies

Two review authors (NNA and ADA in the original review; ADA and JB in the 2011 update, and ADA and RH in the current (2017) update) scanned the titles and abstracts of the identified studies. They removed studies that were clearly irrelevant. For this update, ADA and RH retrieved the full texts of potentially relevant articles, and independently assessed them for inclusion. Disagreement was resolved by consensus.

Data extraction and management

The review authors (ADA and RH for this update) independently extracted data using forms designed according to Cochrane guidelines. Where studies had multiple publications, the main trial report was used as the reference, and additional details supplemented from the additional papers. We contacted authors of the original papers for additional information, if necessary. Disagreements were resolved by consensus.

Assessment of risk of bias in included studies

The review authors independently assessed the included studies for risk of bias, using the Cochrane 'Risk of bias' assessment tool to assess: sequence generation; allocation concealment; blinding of participants, providers, and outcome assessors; completeness of outcome data, and selective outcome reporting. They resolved disagreements by consensus.

Measures of treatment effect

For dichotomous data, we used the number of events in the control and intervention groups to calculate Mantel Haenszel odds ratios (OR), in a fixed‐effect model. For continuous data, we calculated mean differences (MD) between groups, in a fixed‐effect model. We reported the 95% confidence intervals (CI) with all treatment effects.

Unit of analysis issues

We presented data per woman randomised and not per cycle. We analyzed multiple pregnancy and miscarriage rate per woman (primary analysis) and also per pregnancy. We analyzed multiple pregnancy as one live birth.

Dealing with missing data

Where more than 20% of participants were lost to follow‐up or dropped out, we did not include the data in the meta‐analysis. Where data were missing, we contacted the original authors for further information.

Assessment of heterogeneity

Statistical heterogeneity was assessed using the I² statistic (Higgins 2011). If the I² exceeded 50%, we deemed that there was substantial heterogeneity.

Assessment of reporting biases

If eight or more original papers were identified, we had planned to produce a funnel plot, in an attempt to identify publication bias.

Data synthesis

For dichotomous data, we used the Mantel Haenszel method for the meta‐analysis, with a fixed‐effect model. For continuous data, we used the inverse variance method, with a fixed‐effect model.

We combined data in the following comparisons:

  • Coasting versus no treatment (no coasting)

  • Coasting versus other treatments (e.g. early unilateral follicular aspiration, antagonist, GnRHa, FSH co‐trigger, and cabergoline), each as a separate comparison.

Subgroup analysis and investigation of heterogeneity

We did not do any subgroup analyses. If heterogeneity had exceeded 50%, we would have conducted subgroup or sensitivity analysis, exploring clinical or methodological differences between the studies that might explain the data. When we were unable to satisfactorily explain heterogeneity, we deemed the data unsuitable to include in the meta‐analysis.

Sensitivity analysis

When heterogeneity was high (over 50%), we had planned to conduct sensitivity analysis, based on the quality of the included studies as indicated in the 'Risk of bias' table, and whether the data were from a full paper or conference proceedings. Had there been sufficient studies, we would have conducted sensitivity analyses, even if heterogeneity was not high.

Overall quality of the body of evidence: Summary of findings table

We prepared 'Summary of findings' tables using GRADEpro software and Cochrane methods (GRADEpro GDT 2014; Higgins 2011). These tables summarized the overall quality of the body of evidence for the main review outcomes (OHSS, live birth, clinical pregnancy, adverse effects), using five GRADE criteria (study limitations (i.e. risk of bias), consistency of effect, imprecision, indirectness, and publication bias). For each outcome, we justified, documented, and incorporated into the reporting of the results, our judgements about the quality of the evidence quality (high, moderate, low, or very low).

Results

Description of studies

Results of the search

In the search conducted in 2016, we identified and assessed the full text of six potentially eligible studies. We excluded two studies and included four. The updated review now includes eight studies; 14 studies have been excluded. See the Characteristics of included studies and Characteristics of excluded studies tables and the PRISMA study‐flow chart Figure 1 for details.


Study flow diagram: July 2016 search for 2017 review update

Study flow diagram: July 2016 search for 2017 review update

Included studies

Design

Eight RCTs, with 702 women, met the inclusion criteria (Aboulgar 2007; Aflatoonian 2006; Dalal 2014; Egbase 1999; Egbase 2011; Kamthane 2007; Lukaszuk 2011; Sohrabvand 2009). They were conducted in Egypt, Iran, India, Kuwait, Poland, and the UK. Aboulgar 2007, Egbase 1999, Lukaszuk 2011, and Sohrabvand 2009 were full publications, the other four were only reported in conference abstracts.

Participants

All eight trials included women at high risk of developing OHSS. Egbase 2011 defined this as 15 or more follicles in each ovary, E2 of at least 3500 pg/ml, and two leading follicles with at least an 18 mm diameter. Lukaszuk 2011 defined this as women who had unsuccessfully undergone a previous long protocol and ICSI procedure, complicated by moderate or severe OHSS. Aboulgar 2007 defined it as at least 20 follicles in both ovaries, 90% of which had less than a 14 mm mean diameter, and E2 of at least 3000 pg/ml. Aflatoonian 2006 used the same criteria, although they did not define the mean diameter of follicles. Kamthane 2007 defined women at risk of OHSS as having follicles larger than 10 mm in diameter, or E2 higher than 700 pg/ml on day 7 or day 8. Egbase 1999 defined risk for OHSS as an E2 threshold of 6000 pg/ml. Sohrabvand 2009 included women with at least 20 follicles in both ovaries, the majority of which had diameters less than14 mm, and a serum E2 level of 3000 pg/ml. Dalal 2014 included women with at least 20 follicles of more than 11 mm, E2 levels higher than 300ng/ml on day 9 of stimulation, or both.

Interventions

Kamthane 2007 and Lukaszuk 2011 compared coasting with no coasting; Aflatoonian 2006 and Egbase 1999 compared coasting with early unilateral follicular aspiration; Aboulgar 2007 compared coasting with antagonist administration; and Egbase 2011 compared coasting with FSH administration at the time of hCG trigger (FSH co‐trigger). Sohrabvand 2009 and Dalal 2014 compared coasting with cabergoline.

Outcomes

For our primary outcomes, all the included studies reported OHSS rates, but only one reported data suitable for analysis on live birth (Kamthane 2007). For our secondary outcomes, all trials reported clinical pregnancy, three reported multiple pregnancy (Aboulgar 2007; Egbase 2011; Lukaszuk 2011), three reported miscarriage (Egbase 2011; Kamthane 2007; Lukaszuk 2011), and all reported the number of oocytes retrieved.

Excluded studies

Fourteen studies were excluded. One was randomised but the control was matched retrospectively (Aboulghar 1998) . The other 13 studies were excluded because they were not randomised. Four were prospective observational studies (Al‐Shawaf 2001; Lee 1998; Sher 1995; Waldenstrom 1999). Six were retrospective observational studies (Benadiva 1997; Esinler 2013; Fluker 1999; Herrero 2011; Tortoriello 1998; Tortoriello 1999; Ulug 2002). Two studies were retrospective case‐control studies (Dhont 1998; VanderStraeten 1998).

Risk of bias in included studies

See the 'Characteristics of included studies' table for details, and Figure 2 and Figure 3 for summaries.


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

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.

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

Allocation

Egbase 1999 and Egbase 2011 reported using computer generated random allocation to the intervention groups. Sohrabvand 2009 reported using block randomization. Dalal 2014 reported using a randomization software (www.randomizer.org). There were no details on the method of randomization in the other studies.

Dalal 2014, Aboulgar 2007, and Egbase 1999 provided adequate information on allocation concealment. No details were provided by Aflatoonian 2006, Kamthane 2007, Sohrabvand 2009. or Egbase 2011.

Blinding

None of the included studies reported on blinding. Blinding of investigators and women is not possible in these interventions, which are based on timing. Outcome assessors could have been blinded to allocation of intervention.

Incomplete outcome data

All randomised participants were included in the data analyses reported by Dalal 2014, Egbase 2011, Lukaszuk 2011, Sohrabvand 2009, Aboulgar 2007, and Egbase 1999. There were no details provided by Aflatoonian 2006 or Kamthane 2007.

Selective reporting

Dalal 2014 and Aflatoonian 2006 were reported in conference abstracts, and did not report outcomes a priori. Kamthane 2007 and Egbase 2011 summarized the a priori outcomes in their conference abstracts. There was no evidence in the literature of a full paper publication for these four studies. None of the studies except Kamthane 2007 reported live birth, but they were rated as at unclear risk of selective reporting.

Other potential sources of bias

There were no other sources of bias that were identified.

Effects of interventions

See: 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; 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; Summary of findings 5 Coasting compared to cabergoline for preventing ovarian hyperstimulation syndrome

'Summary of findings' tables for comparisons with usable data can be referred to in summary of findings Table for the main comparison, summary of findings Table 3, summary of findings Table 2, and summary of findings Table 4.

1. Coasting versus no coasting

Two trials compared coasting (N = 102) with no coasting (N = 105 (Kamthane 2007; Lukaszuk 2011)).

Primary outcomes
1.1 Moderate or severe ovarian hyperstimulation syndrome (OHSS)

There were fewer cases of moderate or severe OHSS in the coasting group than in the no coasting group (OR 0.11, 95% CI 0.05 to 0.24; 2 RCTs; 207 women; I2 = 0%; low quality evidence; P < 0.00001; Analysis 1.1). Refer to Figure 4.


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

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

1.2 Live birth

One trial reported on live birth (Kamthane 2007). It was unclear whether there was any difference between coasting and no coasting for this outcome (OR 0.48, 95% CI 0.14 to 1.62; 68 women; very low quality evidence; P = 0.24; Analysis 1.2). Refer to Figure 5.

Secondary outcomes
1.3 Clinical pregnancy

Two trials reported on the rate of clinical pregnancy (Kamthane 2007; Lukaszuk 2011). It was unclear whether there was any difference between the groups (OR 0.82, 95% CI 0.46 to 1.44; 2 RCTs; 207 women; I2 = 0%; low quality evidence; P = 0.49; Analysis 1.3).

1.4 Multiple pregnancy

One trial reported on the rate of multiple pregnancy (Lukaszuk 2011). The evidence suggested fewer multiple pregnancies per woman in the coasting group (OR 0.31, 95% CI 0.12 to 0.81, 139 women, low quality evidence, P = 0.02; Analysis 1.4). This finding persisted when the data were analyzed per pregnancy (OR 0.18, 95% CI 0.06 to 0.58; 56 women).

1.5 Miscarriage

Both trials reported this outcome. It was unclear whether there was any difference between the groups in the rate of miscarriage per woman (OR 0.85, 95% CI 0.25 to 2.86, 2 RCTs, 207 women, very low quality evidence, Analysis 1.5). This finding persisted when the data were analyzed per pregnancy (OR 1.05, 95% CI 0.28 to 3.88.; 2 RCTs; 207 women; I2 = 0%).

1.6 Number of oocytes retrieved

Both trials reported on the number of oocytes retrieved. The evidence suggested that fewer oocytes were retrieved in women undergoing coasting than no coasting (MD ‐3.86, 95% CI ‐4.38 to ‐333; 2 RCTs; 76 women; I2 = 0%; low quality evidence; P < 0.00001; Analysis 1.6).

2. Coasting versus early unilateral follicular aspiration

Two studies compared coasting (N = 42) with early unilateral follicular aspiration (N = 41 (Aflatoonian 2006; Egbase 1999)).

Primary outcomes
2.1 Moderate or severe ovarian hyperstimulation syndrome (OHSS)

It was unclear whether there was any difference between the groups (OR 0.98, 95% CI 0.34 to 2.85; 2 RCTs; 83 women; I2 = 0%; very low quality evidence; P = 0.97; I² = 0%; Analysis 2.1). Refer Figure 5.


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

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

2.2 Live birth

No data suitable for analysis were reported by either trial. The authors of one trial stated that there was no significant difference between the groups (Egbase 2011).

Secondary outcomes
2.3 Clinical pregnancy

It was unclear whether there was any difference between the groups (OR 0.67, 95% CI 0.25 to 1.79; 2 RCTs; 83 women; I2 = 0%; very low quality evidence; P = 0.42; I² = 0%; Analysis 2.2).

2.4 Multiple pregnancy

This outcome was not reported by either trial.

2.5 Miscarriage

This outcome was not reported by either trial.

2.6 Number of oocytes retrieved

Both trials reported this outcome. Heterogeneity was evident (I² = 87%). The heterogeneity may be due to the differences in the cut‐off for oestrogen levels in the definition of high risk for OHSS. Aflatoonian 2006 used a cut‐off level of > 3000 pg/ml E2 and Egbase 1999 used a cut‐off level of > 6000 pg/ml E2.

3. Coasting versus gonadotrophin‐releasing hormone antagonist (antagonist)

One trial compared coasting with antagonist (Aboulgar 2007).

Primary outcomes
3.1 Moderate or severe ovarian hyperstimulation syndrome (OHSS)

There were no instances of OHSS in either group (N = 190).

3.2 Live birth

Live birth was not reported in this trial.

Secondary outcomes
3.3 Clinical pregnancy

It was unclear whether there was any difference between the groups (OR 0.74, 95% CI 0.42 to 1.31; 190 women; low quality evidence; P = 0.31; Analysis 3.2).

3.4 Multiple pregnancy

It was unclear whether there was any difference between the groups in the rate of multiple pregnancy per woman (OR 0.84, 95% CI 0.39 to 1.80; 190 women; very low quality evidence; P = 0.65; Analysis 3.3). This finding persisted when the data were analyzed per pregnancy (OR 1.0; 95% CI 0.43 to 2.32; 98 women).

3.5 Miscarriage

Miscarriage was not reported in this trial.

3.6 Number of oocytes retrieved

The evidence suggested that there were fewer oocytes retrieved in the group receiving coasting (MD ‐2.44, 95% CI 4.30 to ‐0.58; 190 women; P = 0.01; Analysis 2.3).

4. Coasting versus follicle stimulating hormone co‐trigger

One trial compared coasting versus FSH administration at the time of hCG trigger (N = 102; Egbase 2011).

Primary outcomes
4.1 Moderate or severe ovarian hyperstimulation syndrome (OHSS)

Fifteen cases of moderate or severe OHSS occurred, all in the coasting group (OR 43.74, 95% CI 2.54 to 754.58; 102 women; very low quality evidence; P = 0.009; Analysis 4.1).

4.2 Live Birth

The authors reported that there was no evidence of a difference between the groups for this outcome (data not available).

Secondary outcomes
4.3 Clinical Pregnancy

It was unclear whether there was a difference between the groups (OR 0.92, 95% CI 0.43 to 2.01; 102 women; low quality evidence; P = 0.84; Analysis 4.2).

4.4 Multiple Pregnancy

The trial authors reported that there was no evidence of a difference between the groups for this outcome (data not available).

4.5 Miscarriage

The trial authors reported that there was no evidence of a difference between the groups for this outcome (data not available).

4.6 Number of oocytes retrieved

The evidence suggested that fewer oocytes were retrieved in women undergoing coasting than FSH co‐trigger (MD ‐17.80, 95% CI ‐19.05 to ‐16.55; 102 women; P < 0.00001; Analysis 3.4).

5. Coasting versus cabergoline

Two trials compared coasting versus cabergoline (N = 120 (Dalal 2014; Sohrabvand 2009)).

Primary outcomes
5.1 Moderate or severe ovarian hyperstimulation syndrome (OHSS)

There was insufficient evidence to determine whether there was a difference between the two groups (OR 1.98, 95% CI 0.09 to 5.68; 120 women; I² = 72%; very low quality evidence; P=0.20, Analysis 5.1). Refer to Figure 6. Heterogeneity was high (72%) and there is no reason to explain this heterogeneity.


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

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

5.2 Live Birth

Live birth rates were not reported in these trials.

Secondary outcomes
5.3 Clinical Pregnancy

There was evidence of a difference in clinical pregnancy favouring the cabergoline group compared to the coasting group (OR 0.38, 95% CI 0.16 to 0.88; 2 RCTs; 120 women; very low quality evidence; P = 0.02; I² = 0%; Analysis 5.2).

5.4 Multiple Pregnancy

Multiple pregnancy rates were not reported in these trials.

5.5 Miscarriage

Miscarriage rates were not reported in these trials.

5.6 Number of oocytes retrieved

In one trial (Sohrabvand 2009) the evidence suggested that fewer oocytes were retrieved in women undergoing coasting than cabergoline (MD ‐4.3, 95% CI 7.88 to ‐0.72; 60 women; P 0.02; Analysis 5.4). The authors of one trial (Dalal 2014) stated that there was significant difference between the groups but no data were provided.

Other analyses

There were insufficient data to conduct planned sensitivity analyses or to construct a funnel plot.

Discussion

Summary of main results

There was low‐quality evidence to suggest that coasting reduced moderate or severe OHSS more than no coasting. There was very low‐quality evidence suggesting that using FSH co‐trigger prevented moderate and severe OHSS better than coasting, but the evidence was derived from only one small trial. There was no clear evidence of any difference in the rate of moderate or severe OHSS or in the achievement of clinical pregnancy when coasting was compared with early unilateral follicular aspiration (very low‐quality evidence), GnRH antagonist (low or very low quality evidence), or cabergoline (low or very low‐quality evidence). Nor was there evidence to suggest a benefit in live birth from coasting compared with no coasting, although the data were from a single trial only. It was difficult to draw any conclusions about the number of oocytes obtained due to the statistical heterogeneity of the studies. Nor was there any clear evidence of differences between the groups in clinical pregnancy, multiple pregnancies, live births or miscarriage rates.

Overall completeness and applicability of evidence

Only eight randomised trials were identified, and four of these were conference abstracts that never became full publications. The completeness and applicability of the data were substantially limited by this factor. Authors were contacted, but did not respond directly, and some missing data were obtained from another Cochrane review. Only one of the trials reported data suitable for analysis on the outcome of live birth. There may be additional interventions that have not been compared yet with coasting, in a randomised controlled trial.

Quality of the evidence

The overall quality of the evidence was low or very low. The main limitations were failure to report live birth, risk of bias due to lack of information about study methods, and imprecision due to low event rates and lack of data. Four of the studies were published only as abstracts, with limited data and no evidence of full publication (Aflatoonian 2006; Dalal 2014; Egbase 2011; Kamthane 2007). Three to four years is longer than expected to publish a full paper. With the exception of the number of oocytes retrieved, the statistical heterogeneity between studies was acceptable. The inclusion criteria and OHSS classification used varied between the studies.

Potential biases in the review process

The authors attempted to identify all potential studies using a variety of methods. One of the main biases, as mentioned above, is that several of the trials were only published as conference abstracts. There may be other relevant data which were not reported. Therefore, the results of the review must be interpreted with caution.

Agreements and disagreements with other studies or reviews

In some excluded studies, the higher the oestrogen level at the beginning of coasting, the less effective the intervention was at preventing OHSS, regardless of the duration of the coasting period (see Aboulghar 1998; Dhont 1998; Fluker 1999; Lee 1998; Sher 1995; Waldenstrom 1999). The inclusion criterion for this review was oestrogen levels higher than 2500 pg/ml. The four included trials used a cut‐off of 3000 pg/ml, and this may, in part, explain the lack of effect.

Study flow diagram: July 2016 search for 2017 review update
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
Figure 6

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

Comparison 1 Coasting versus no coasting, Outcome 1 OHSS.
Figures and Tables -
Analysis 1.1

Comparison 1 Coasting versus no coasting, Outcome 1 OHSS.

Comparison 1 Coasting versus no coasting, Outcome 2 Live birth.
Figures and Tables -
Analysis 1.2

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

Comparison 1 Coasting versus no coasting, Outcome 3 Clinical pregnancy.
Figures and Tables -
Analysis 1.3

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

Comparison 1 Coasting versus no coasting, Outcome 4 Multiple pregnancy.
Figures and Tables -
Analysis 1.4

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

Comparison 1 Coasting versus no coasting, Outcome 5 Miscarriage.
Figures and Tables -
Analysis 1.5

Comparison 1 Coasting versus no coasting, Outcome 5 Miscarriage.

Comparison 1 Coasting versus no coasting, Outcome 6 Number of oocytes retrieved.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
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.
Figures and Tables -
Analysis 5.1

Comparison 5 Coasting versus cabergoline, Outcome 1 OHSS.

Comparison 5 Coasting versus cabergoline, Outcome 2 Clinical pregnancy rate.
Figures and Tables -
Analysis 5.2

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

Comparison 5 Coasting versus cabergoline, Outcome 3 Number of oocytes retrieved.
Figures and Tables -
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

Figures and Tables -
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

Figures and Tables -
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

Figures and Tables -
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

Figures and Tables -
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.

Figures and Tables -
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

Figures and Tables -
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

Figures and Tables -
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

Figures and Tables -
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

Figures and Tables -
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]

Figures and Tables -
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]

Figures and Tables -
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]

Figures and Tables -
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]

Figures and Tables -
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]

Figures and Tables -
Comparison 5. Coasting versus cabergoline