Table 3. Interventions shown to reduce rates of caesarean birth.
Author, Year* | Intervention and comparator | Caesarean birth (CB); RR/OR (95% CI), number of trials; n = number of participants |
---|---|---|
Alfirevic 2014 | Oral misoprostol for IOL versus placebo/no treatment in pregnant women | RR 0.72 (0.54 to 0.95), 8 trials, n = 1029 |
Alfirevic 2016 | All pharmacological (all routes and doses), mechanical and complementary methods used for IOL versus placebo/no intervention in pregnant women carrying a viable fetus and who are eligible for any method of third-trimester cervical ripening or IOL | 586 trials, n = 96771 - Vaginal PGE2 (gel) OR 0.79 (0.65 to 0.94) - Intracervical PGE2 OR 0.83 (0.69 to 0.98) - Vaginal misoprostol tablet < 50μg OR 0.70 (0.57 to 0.85) - Vaginal misoprostol tablet ≥ 50μg OR 0.73 (0.59 to 0.88) - Oral misoprostol tablet ≥ 50μg OR 0.72 (0.58 to 0.88) - Titrated (low-dose) oral misoprostol solution OR 0.62 (0.47 to 0.80)Foley catheter OR 0.76 (0.61 to 0.95) - Membrane sweeping OR 0.74 (0.53 to 0.99) - Buccal/sublingual misoprostol OR 0.68 (0.51 to 0.89) |
Bohren 2017 | Continuous, one-to-one intrapartum support versus usual care in any birth setting | RR 0.75 (0.64 to 0.88), 24 trials, n = 15347 |
Cluver 2015 |
Interventions to facilitate ECV at term versus placebo/no intervention | Beta stimulants RR 0.77 (0.67 to 0.88), 6 trials, n = 742; Tocolytics in nulliparous RR 0.85 (0.75 to 0.97), 2 trials, n = 170 |
Dodd 2017 |
Progestogen by any route (IV, IM, oral or vaginal) for the prevention of preterm birth versus placebo or no treatment | Vaginal progesterone RR 0.93 (0.88 to 0.98), 6 trials, n = 2143 |
East 2014 |
Use of fetal pulse oximetry (FPO) with or without concurrent use of conventional fetal monitoring versus conventional only (no pulse oximetry) in women in labour where fetal monitoring is clinically indicated | FPO and CTG vs CTG only from 36 weeks; FBS prior to study entry RR 0.44 (0.24 to 0.81), 1 trial, n = 146 |
Gulmezoglu 2012 | Labour induction versus expectant management in pregnant women at or beyond term at low risk for complications | All women RR 0.89 (0.81 to 0.97), 21 trials, n = 8749; 41 weeks RR 0.74 (0.58 to 0.96), 4 trials, n = 998; Cervix unfavourable RR 0.88 (0.80 to 0.98), 8 trials, n = 5051 |
Hapangama 2009 | Mifepristone for third trimester cervical ripening or IOL versus placebo/no treatment in pregnant women due for third trimester IOL carrying a viable fetus | Mifepristone all doses RR 0.74 (0.60 to 0.92), 9 trials, n = 1043 |
Hodnett 2010 | Standardized or individualized programs of additional social support versus usual care for pregnant women believed at high risk for giving birth to babies that are either preterm or weigh less than 2500 gm, or both, at birth | RR 0.87 (0.78 to 0.97), 9 trials, n = 4522 |
Hofmeyr 2012b | Amnioinfusion (AI) versus no AI in women whose babies were considered to be at increased risk of, or had FHR patterns suggestive of, umbilical cord compression in labour | Transcervical AI RR 0.62 (0.46 to 0.83), 13 trials, n = 1493; CS for suspected fetal distress RR 0.46 (0.31to 0.68), 12 trials, n = 1588 |
Hofmeyr 2014 | Amnioinfusion for meconium-stained liquor in labour versus no amnioinfusion in women in labour with moderate or thick meconium staining of the amniotic fluid | RR 0.59 (0.41 to 0.84), 3 trials, n = 1137 (limited peripartum surveillance) |
Hofmeyr 2015 | ECV versus no ECV in pregnant women with babies in the breech presentation at or near term | RR 0.57 (0.40 to 0.82), 8 trials, n = 1305 |
Kavanagh 2006 | Hyaluronidase versus placebo/no treatment for third trimester cervical ripening or IOL in pregnant women due for third trimester induction of labour, carrying a viable fetus | All women RR 0.37 (0.22 to 0.61), 1 trial, n = 168; Primiparae RR 0.43 (0.23 to 0.81), 1 trial, n = 94; Multiparae RR 0.28 (0.12 to 0.67), 1 trial, n = 74; Women with previous caesarean RR 0.35 (0.15 to 0.81), 1 trial, n = 29 |
Lavender 2013 | Labour management using a partogram versus no partogram in women with singleton pregnancies, cephalic in spontaneous labour at term | Low-resource setting RR 0.38 (0.24 to 0.61), 1 trial, n = 434 |
Smith 2006 |
Complementary and alternative therapies used in labour (but not biofeedback) with or without concurrent use of pharmacological or non-pharmacological interventions versus placebo or no treatment in women in spontaneous or induced labour, for pain management in labour | Hypnosis RR 0.46 (0.30 to 0.72), 1 trial, n = 520 |
Smith 2011a | Acupuncture or acupressure versus placebo, no treatment for pain management in labour | Acupressure RR 0.24 (0.11 to 0.54), 1 trial, n = 120 |
Wei 2013 |
Early augmentation with amniotomy and oxytocin versus conservative form of management in pregnant women in spontaneous labour | Prevention studies RR 0.87 (0.77 to 0.99), 11 trials, n = 7753 |
*See S1 File for full references to the reviews