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Management of Late-Preterm Premature Rupture of Membranes : The PPROMEXIL-2 Trial

Management of Late-Preterm Premature Rupture of Membranes : The PPROMEXIL-2 Trial. Journal Club October 2012 Supervised by Prof.Abdulrahim Rouzi Presented by Dr.Ayman Bukhari. The evidence for the management of near term prelabor rupture of membranes is poor .

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Management of Late-Preterm Premature Rupture of Membranes : The PPROMEXIL-2 Trial

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  1. Management ofLate-Preterm Premature Ruptureof Membranes: The PPROMEXIL-2 Trial Journal Club October 2012 Supervised by Prof.AbdulrahimRouzi Presented by Dr.AymanBukhari

  2. The evidence for the management of near term prelaborrupture of membranes is poor. • (PPROM) is associated with neonatal morbidity and mortality as well as maternal morbidity. • In international guidelines, no clear recommendation is given on the management of PPROM between 34 and 37 weeks.

  3. Am J ObstetGynecol 2012;207:276.e1-10.

  4. www.AJOG.org The first trial (PPROMEXIL) from 2007 -2009 showed that in women with (PPROM), the incidence of neonatal sepsis was low, and (IoL) did not reduce this risk.

  5. www.AJOG.org Because the first trial was underpowered and because of a lower-than-expected incidence of neonatal sepsis , a second trial (PPROMEXIL-2), aiming to randomize 200 patients to improve the evidence in near-term PPROMwas done

  6. MATERIALS AND METHODS • In a nationwide multicenter study, nonlaboring women with PPROM between 34 and 37 w were eligible for inclusion. Patients were randomized to IoL or expectant management. The Primary Outcome Measure was Neonatal Sepsis.

  7. www.AJOG.org • Women with a singleton or twin pregnancy not in labor 24 hours after PPROM between 34-37 w were eligible • PPROM had to be diagnosed after 26 weeks. • Randomizationwas performed for (IoL) v.s expectant management (EM). • Women with Monochorionicmultiple pregnancy NonreassuringCTG MSL Major fetal anomalies where not eligible HELLP Severe PET Signs of intrauterine infections

  8. www.AJOG.org • If women were allocated to IoL, labor was induced within 24 hours after randomization. • If a cesarean section was indicated, this was done as soon as feasible after randomization. • Women allocated to EM were monitored according to a standard local protocol, until delivery started spontaneously.

  9. www.AJOG.org • If a participant reached 37 w, labor was induced. • Labor was induced prior to 37 w when there were any other indication. • Antibiotics were administered according to local protocols.

  10. www.AJOG.org • In pregnancies with PPROM prior to 34 weeks, corticosteroids were given. • Administration of tocolyticswas dependent on the local protocols.

  11. www.AJOG.org • When the local investigator classified a case as sepsis , the case was judged by an independent panel of pediatricians who were not aware of the allocation of randomization.

  12. Secondary neonatal outcome measures • RDS • Asphyxia • Hypoglycemia • Hyperbilirubinemia, • Total length of hospital stay • Admission and length of stay on the (NICU) • Perinatal death.

  13. Secondary maternal outcome measures • APH • Chorioamnionitis • Total length of hospital stay • Admission to (ICU) • Mode of delivery and need for anesthesia.

  14. Statistical analysis and metaanalysis • Within a well-organized nationwide Dutch research consortium, it seemed feasible to recruit 200 patients within approximately 1year.

  15. Statistical analysis and metaanalysis • These 200 patientscombined with the previous trials would provide the power calculation as calculated by the investigators for the total of (1812 women).

  16. Statistical analysis and metaanalysis • Therefore , no separate power calculation was donefor this trial. • The RRs, absolute risk reduction, mean difference (MD), and 95% CIs were calculated for the relevant outcome measures. • P .05 was considered to indicate statistical significance.

  17. www.AJOG.org From December 2009 until January 2011, a total of 241 women were asked to participate in the trial,

  18. RESULTS 100 women were randomized to IoL and 95 to EM. • Neonatal sepsis was seen in 3 neonates (3.0%) in the IoL-group versus 4 neonates (4.1%) in the EM group • (RR, 0.74; 95% CI, 0.17–3.2).

  19. RESULTS • One of the sepsis cases in the IoL group resulted in neonatal death because of asphyxia. • There were no significant differences in secondary outcomes.

  20. Baseline characteristics • The median gestational age at randomization was 251 days= 35w+6d • (17%) had PPROM prior to 34 w. • Women in the IoL group delivered on average 3.5 days earlier (95% CI, 1.8–5.2 days) than women in the EM group. • Women in the EM group stayed on average 4.4 days longer in the hospital (95% CI, 2.2– 6.7 days).

  21. www.AJOG.org • The different modes of delivery was not statistically significant. • Fewer cesarean sections in the IoLgroup (13 [13%] vs 22 [22%]; RR, 0.58; 95% CI, 0.31–1.08; P .081).

  22. www.AJOG.org • Antibiotics during admission and during labor were administered equally. • There were no differences in the rates of epidural and/or spinal analgesia.

  23. Neonatal sepsis • Neonatal sepsis was seen in (3.0%) in the IoLgroup (4.1%) in the EM group (RR, 0.74; 95%CI, 0.17–3.2).

  24. Metaanalysis • From 9 different studies. • A total of 1428 neonates were analyzed. The risk ratio of all outcome were not statistically different.

  25. COMMENT • In this PPROMEXIL-2 trial, It was foundthat induction of labor did not reduce the incidence of neonatal sepsis, nor did it influence the rates of cesarean section and RDS.

  26. www.AJOG.org • IoL did reduce the risk of clinical chorioamnionitis, but without a significant difference in histological chorioamnionitis.

  27. www.AJOG.org • As shown in the metaanalysis based on more than 1400 neonates, expectant management seems to be a safe strategy with respect to NNS, RDS, and C/S rates.

  28. Limitations of the study • The results as presented in the current trial should be interpreted with some cautionbecause of the fact that no proper power calculation was done.

  29. Limitations of the study • The overrepresentation of women with gestational age longer than 35 weeks can be caused by the fact that women between 34 and 35 weeks of gestation more often refused to participate.

  30. Limitations of the study • The hesitation of clinicians to induce labor before 35 weeks may also have influenced this outcome.

  31. Limitations of the study • The number needed to treat with the combined result of the first and second trials is 71 for 1 case of neonatal sepsis.

  32. The Study Conclusion • This current trial expanded the amount of evidence on the management of near-term PPROM with an additional 195 women. • Still, the incidence of neonatal sepsis is low after these pregnancies, and this rate is not reduced by induction of labor. • Induction of labor does not increase the risk of any other adverse neonatal or maternal outcomes.

  33. Shall we change our practice?

  34. Epidemiological facts say that metaanalysis does not substitute a properly done RCT. • They said , they did this because the first study was not enough,,,

  35. Nevertheless, they did not calculate the power & the number of patients needed to answer the research question, and they did the metaanalysis only

  36. So this study, epidemiologically does not answer the question and this is the true limitation of the study

  37. This study shows that you need to know about epidemiology & statistics. • The fact that this study was published in a prestigious international journal which is among best 10 journals in Ob/Gyn does not mean that we take it as a fact & change our practice accordingly!

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