In recent decades, the induced labor rate has substantially increased, has not always been considered duly justified and accounts for 20% - 30% of all births   .
When cervical conditions are unfavorable, the most frequent form of inducing labor in our country is to administer intravaginal or intracervical prostaglandins  . Until recently, prostaglandin E2, or dinoprostone, has been the most widely used agent in our setting. However, it is an unstable product at room temperature, expensive and exclusively administered vaginally. Misoprostol, or prostaglandin E1, was originally registered to treat peptic ulcers, and has been explored as an agent to induce labor at different doses and posologies. Misoprostol is inexpensive, stable at room temperature and can be taken orally, vaginally or under the tongue. High drug doses and short intervals can trigger maternal-fetal complications, among which uterine hyperstimulation, both with and without altered fetal cardiotocographic registers, stand out which, at times, has led to is limited use. Over the years, different regimes have been explored to find the optimum dose  .
Given the pharmacological change taking place in the clinical practice, the present study considers a comparative analysis between misoprostol and dinoprostone administered vaginally at the aforementioned doses to provide information about their effectiveness and safety for induced deliveries.
2. Material and Methods
A prospective cohort study was conducted during the period between 1 March 2013 and 24 May 2015 that compared the use of misoprostol and dinoprostone in pregnant women who had been induced at the Rey Juan Carlos Hospital in Móstoles (Madrid), Spain. This study included 401 at-term pregnant women who had been medically and obstetrically referred for induced delivery with unfavorable cervical conditions when induction commenced. Of the 401 patients, 241 were induced with misoprostol and 160 with dinoprostone. The inclusion criteria were: singleton pregnancies with live fetus, cephalic presentation at gestational age ≥ 37 weeks, a Bishop score of ≤6 at the start of induction, and no contraindications for vaginal birth or use of prostaglandins. The amniotic sac could be complete or ruptured, but with no sign of regular uterine dynamics. The exclusion criteria were background of cesarean section or other previous uterine surgery, gestational age < 37 weeks, multiple pregnancies, intrauterine fetal death, women infected with human immunodeficiency virus (HIV), and pre-delivery evidence for compromised fetus as intrauterine growth restriction or nor reassuring fetal heart rate monitoring.
Patients were recruited by non-probabilistic sampling of consecutive cases as the inductions in the Obstetrics Block during the study period were indicated.
Following the protocol approved in our center, a check list was used prior to induction to evaluate maternal-fetal conditions and suitability of induction. The pregnant women with a Bishop score below or equal to 6 required a cervical maturity method. As both drugs are considered first-line drugs in this patient group that met the inclusion criteria, the research group offered the patient the chance to participate in the study and she received informed consent. After accepting and signing it, the obstetrician chose the cervical maturity method and followed our center’s Induced Labor Protocol.
Low-dose misoprostol was used in this protocol (25 mg/4h) for a maximum of 24 h (or six doses). Twenty-four hours after cervical maturity commenced, the patient was transferred to the Obstetrics Block if there was no sign of labor dynamics in order to be administered oxytocin intravenously 4 h after being administered the last drug.
When specialists opted for dinoprostone, it was used in its vaginal-insert slow- releasing form with 10 mg, maintained for a maximum 24-hour period, which was when patients were transferred to the Obstetrics Block. Thirty minutes after removing the device, oxytocin was intravenously administered in those patients who did not present regular uterine dynamics.
Any progress made in dilation and delivery, and any decisions about different interventions, e.g., amniotomy, use of analgesia, etc., were monitored according to the hospital’s protocol.
In both cases, socio-demographic variables, pregnancy characteristics, data about induction, birth route and its temporal evolution were collected, along with data about puerperium, neonate characteristics and any maternal-fetal complications.
The study was approved by the Rey Juan Carlos Hospital Research Commission on 21 October 2016.
Sample size estimation was calculated with the result of a pilot study done with the first 50 patients, which evidenced a lower cesarean section rate, from 22% to 12%, for induction with misoprostol. A statistical power of 80%, a 95% confidence interval and a 5% percentage of losses were applied. The required sample size was 154 patients per treatment arm.
In the statistical analysis, the qualitative variables were presented in percentages, while the quantitative ones were presented as means and standard deviations (SD).
A chi-square test was used to evaluate the association between the qualitative variables. A student’s t-test was used to compare the cervical maturity method with the quantitative variables.
The effect measure employed was relative risk (RR), and the difference of the means with their 95%CI.
Explanatory logistic regression modeling was used for the adjustments for all the possible confounder or interaction variables. The initial maximum model included all the variables that were statistically significant or clinically relevant in the univariate analysis.
A 0.05 level of significance was used to compare all the hypotheses. The statistical package employed was SPSS Windows 15.0.
The two study groups, these being 160 pregnant women induced with dinoprostone (40%) and 241 pregnant women induced with misoprostol (60%), were homogeneous for maternal age, personal background and pregnancy characteristics, like gestational age, obstetric pathology throughout pregnancy and parity, and for cervical conditions when induction commenced (Table 1).
The reasons for induction in both study groups were premature membrane rupturing (37.9%), chronologically prolonged pregnancy (19%), gestational diabetes (13.4%) and pregnancy-related hypertension (7%). Some of the more
Table 1. Characteristics of the sample.
*Data are presented as (SD); **GD (gestational diabetes).
frequent reasons, like a ruptured sac and pregnancy-related hypertension, and other less frequent ones, like oligoamnios (4.7%) and induction for small fetus for gestational age (4.2%), were distributed differently between the study groups and were the object of the multivariable analysis (Table 1).
In the group in which cervical maturity was performed by vaginal misoprostol, two doses were necessary in 34% of the cases, and three doses in 25.7%. The mean misoprostol dose was 2.2 tablets (Table 1).
Regarding evolution of cervical conditions after cervical maturity, a mean Bishop score of 6.6 was obtained for misoprostol, and one of 6.1 for dinoprostone, with a difference on the statistical significance limit (p = 0.051) (Table 1).
Oxytocin requirements, needing meconium fluid throughout induction and use of analgesia were similar for the treatment groups.
The cesarean section rate in the misoprostol-induced group was 14%, and 19% in the dinoprostone group [RR = 1.38 (95%CI: 0.89 - 2.13), p = 0.145]. Explanatory logistic regression modeling applied for the adjustments for the possible confounder variables and birth route did not differ according to the cervical maturity method used (Table 2). No differences were found in instrumental deliveries, position during the expulsive, episiotomies or tears according to the cervical maturity method employed, nor for the mean number of days hospitalized. There were more placental retention in the phase when the placenta was expelled in the vaginal deliveries in the dinoprostone-induced group (10.5%) than in the misoprostol-induced group (4.3%), p = 0.02.
Among the reasons for practicing a cesarean section, a lower percentage was found for failed induction in the misoprostol-induced group than for the dinoprostone-induced group (p = 0.028) (Table 2). No differences were found in the cesarean sections for delivery not progressing or for those practiced for risk of losing fetal well-being between both study groups.
The percentage of vaginal birth in less than 24 h from starting induction was 53% in the dinoprostone group and 44% for the misoprostol group. No significant differences were observed between the study groups after adjusting the confounder variables [RR = 1.08 (0.90 - 1.29), p = 0.401] (Table 2).
There were no differences in either the vaginal birth rate in less than 12 h from starting induction (Table 2) or the percentage of failure to reach 3 cm dilation (9.1% in the misoprostol group and 13.8% in the dinoprostone group, p = 0.147).
The time from starting induction to vaginal birth was shorter for the dinoprostone-induced group (median of 20 h) than for the vaginally misoprostol- induced group (median of 23.4 h) (p = 0.018) (Table 2).
Parity is an important predictor factor for induced delivery, and also in its temporal evolution; 96.5% of the multipara and 80.2% of the nulliparous women had a vaginal birth; 38.7% of the nulliparous women and 79.5% of the multiparous had a vaginal birth in less than 24 h from starting induction (p < 0.0001). For the nulliparous women, the time from starting induction to vaginal birth was also shorter for the vaginally dinoprostone-induced group (median of 21 h)
Table 2. Delivery outcomes.
*Adjusted in an explanatory logistic regression model.
Table 3. Maternal and fetal outcomes.
*Data are presented as (SD), mean differences.
than the vaginally misoprostol-induced one (median of 26.7 h) (p = 0.004). No differences were found in the multipara group.
No differences were reported in maternal complications according to the cervical maturity method employed (Table 3).
No differences appeared in the pH value at birth, the Apgar score at 1 minute and 5 minutes, in having to be hospitalized in the Neonatology Unit, nor in the reasons for this hospitalization. However, the mean birth weight was 3133 g in the dinoprostone-induced group and 3283 g in the misoprostol-induced group. This difference was statistically significant (p = 0.002) did not seem clinically relevant to us, but it was included for its adjustment in all the applied logistic regression models (Table 3).
The need for resuscitation types III and IV was greater for the neonates of the vaginally dinoprostone-induced group (9.4%) than for those in the misoprostol- induced one (4.1%), p = 0.034. When we analyzed this difference, we found that the neonates who required neonatal resuscitation had a higher at-risk delivery, which was the reason for induction. The origin of the differences in neonatal resuscitation requirements lay in the reason for induction (pregnancy-related hypertension and meconium-stained amniotic fluid), which did not depend on the cervical maturity method employed (Table 3).
As a result of the Spanish Agency of Medicines’ approval in 2008 of misoprostol being vaginally administered in 25 mcg tablets to induce at-term delivery, we began to opt for the low-dose misoprostol protocol and to substitute the gold standard which, in our setting and in many centres, still involves vaginally administering dinoprostone in its 10 mg slow-releasing form. This change was the reason why we collected the data for the present work. However, the comparison made of these two methods, and with the present dose, has been poorly studied      .
We carefully analyzed the 2010 Cochrane Database of Systematic Reviews (4). Only six of them compared misoprostol, at different doses, with 10 mg dinoprostone in its slow-releasing form. Of these six, only the study by Wing (1997) compared dinoprostone and misoprostol at the 25 mcg/4h dose; i.e., only one of the 121 included studies evaluated the exact dose employed in the present work   , which constitutes the “pharmacological change” taking place in Spanish delivery rooms.
The meta-analyses of Wang, Liu and Austin included 30 articles    . Only Wing, Bolnik and Harms used the same doses as we do for both drugs    . Of these three studies, that by Bolnik simultaneously employed misoprostol and dinoprostone, and intravenous oxytocin perfusion in different protocols. Thus, it is not comparable to the majority of studies, nor to our study, in which oxytocin was used after cervical maturity, and not concomitantly. Harms’ publication used our exact dose, but not exactly the same protocol for dinoprostone (maintained only for 12 h). It is noteworthy that the data reported by Harms, presented in the Obstet Gynecol supplement, are limited by their poster condition in the ACOG’s 50th Anniversary Meeting, held in 2001  . The only publication with a similar dose and protocol to ours was that by Wing, which dates back to 1997, whose characteristics are like those presented herein.
After making the logistic regression model adjustments, we found no differences in birth routes according to the cervical maturity method employed. The cesarean section rate was analyzed in all the studies and meta-analyses. The results reported by the various authors coincided with our results, although they obtained a higher cesarean section rate than we did      .
We obtained a lower cesarean section rate due to failed induction in the misoprostol group, although these data in all the works published to date are contradictory. Works like those of Chitrakar or Belfrage also obtained a lower failed induction percentage for the misoprostol group. However, they identified higher misoprostol doses than the dose we used   . In others, like Wing’s series, at our dose they found no inter-group differences for the reason for performing cesarean section  . We should point out that the time to consider an induction failed is currently a matter of debate. Therefore, the results may not measure exactly the same variable, which maybe the true reason for the difference  .
We observed a difference in the statistical significance limit for the mean Bishop score obtained at the end of cervical maturity, with more favorable necks of the womb in the misoprostol-induced group. This coincides with the few data published on this matter (Chitrakar and Saxena), but are not comparable, however, to our data given the different protocols and doses employed   . The work by Wing does not offer this information  .
Former works have associated induction with misoprostol with higher meconium fluid rates and greater oxytocin requirements     . Both variables were homogeneously distributed between our two study groups. Wing, who used our same dose, published comparable results to ours  . It is quite likely that this discrepancy lies in the different doses used for both drugs.
We obtained no differences in the percentage of “vaginal birth in less than 24 h” and “in less than 12 h” from the start of induction between our groups. Previously studies have either found no differences for this variable or, if they did, they conferred a temporal advantage to misoprostol     . Nevertheless, we thought it was worth analyzing these data in detail. Liu, who reported a higher vaginal birth percentage in <24 h for the misoprostol group, did not include any work that used our same dose for both drugs  . It is worth highlighting that Austin informed about a significant heterogeneity for the variables “accomplishing vaginal birth in less than 24 h” and “in less than 12 h”, justified given the differences in design, the Bishop score at the start of induction, duration of dinoprostone exposure, misoprostol dose and the oxytocin administration protocol  . After running a random effects model, no differences were found when ruling out some works included in the meta-analysis, with two exceptions: when ignoring the studies of Wing and Bolnik, the rate of “accomplishing vaginal birth in less than 12 h” rose for the misoprostol group   ; removing both these studies in this meta-analysis meant eliminating all the works in which misoprostol was used at the 25 mcg/4h dose as opposed to 10 mg dinoprostone administered vaginally; i.e., when the works that reported using high misoprostol doses were left in the meta-analysis (≥50 mg/4-6h), the efficacy of this drug increased. So, although some former analyses confer a temporal advantage to misoprostol, it might be a dose-dependent and not a drug-dependent result.
The time between induction starting and vaginal birth was shorter for the dinoprostone group. Wing, who used the same doses as we did, found no differences in this variable. Other works have conferred a temporal advantage to misoprostol   . Once again, the employed dose was not comparable to ours, so we thought that dose could be behind this discrepancy. Nonetheless, our results are limited and further studies to allow us to draw definite conclusions are needed.
Regarding safety, our work thoroughly analyzed maternal-fetal complications, but found no differences due to the cervical maturity method employed.
Of all the births included, puerperium was normal in 94.5% and presented some pathology in 5.5% (fever, uterine atony, headache, need for blood transfusion or curettage), with no differences according to the cervical maturity method employed. The present series included no uterine rupture.
Data on puerperal complications in the literature are extremely scarce. Most series inform in detail about neonatal data and the sporadic presence of some serious, but infrequent complication, such as uterine rupture. However, all the meta- analyses concluded that the studies were not large enough to evaluate such infrequent and serious maternal-fetal complications     . We think it is necessary to insist on the importance of reporting possible associated complications in detail.
Our main limitation was to not report data on abnormal uterine activity and its consequences on fetal cardiotocographic records. We cannot ignore its importance when evaluating the safety profile of the prostaglandins employed. Wing reported low tachysystole rates (defined as six contractions or more in 10 minutes on at least a 20-minute monitoring window) for the group induced with misoprostol, and no differences for uterine hyperstimulation  . Harms indicated no differences  . Thus, more works are necessary to evaluate the frequency of alterations in uterine contractions at the doses employed under study.
After the analysis, we found discrepancies between the neonatal resuscitation requirements in our work behind the reason for induction, which did not depend on the cervical maturity method used. Other former works that have indicated this information found no differences    .
Our main limitation is the non-randomized study design. Notwithstanding, after applying the logistic regression models needed to adjust the confounder and interaction variables, we believe that the present study shows that our study groups are comparable and homogeneous, and our results are sound.
We found no discrepancy in our series as to the cesarean section rate between labor induction with misoprostol administered vaginally in its low-dose protocol (25 mcg/4-6h, for 24 h at the most) with vaginal dinoprostone induction using 10 mg in its slow-releasing form (for 24 h at the most).
No differences were found in the percentage of pregnant women who underwent vaginal birth in less than 24 h and less than 12 h since induction began, nor in the maternal-neonatal results according to the cervical maturity method used after adjusting for the confounder variables.
Given the pharmacological change taking place in Spanish delivery rooms and the few studies that compare the exact dose and posology used herein, we believe that it is necessary to perform clinical assays to compare misoprostol and dinoprostone at the doses employed herein, and to include the results that relate to induced pregnant women’s satisfaction.
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