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Management of Mid-Trimester Premature Rupture of Membranes: Intention to Treat. By Dr. Alexander E. Omu MBBS, FMCOG, FWAS, FICS, FRCOG Professor. Department.

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Presentation on theme: "Management of Mid-Trimester Premature Rupture of Membranes: Intention to Treat. By Dr. Alexander E. Omu MBBS, FMCOG, FWAS, FICS, FRCOG Professor. Department."— Presentation transcript:

1 Management of Mid-Trimester Premature Rupture of Membranes: Intention to Treat. By Dr. Alexander E. Omu MBBS, FMCOG, FWAS, FICS, FRCOG Professor. Department of Obstetrics and Gynaecology, Faculty of Medicine Kuwait University, Senior Consultant Maternity Hospital. Kuwait Prepared for

2 Objectives of the presentation 1.Definitions 2.Introduction 3.Etiology of PROM 4.Diagnosis 5.Clinical course of PPROM 6.Management of PPROM Use of corticosteroids Antibiotic therapy Tocolysis Amnioinfusion Cervical plugging 7. Adjuncts to Management 8. Special circumstances affecting the Management. Multiple Pregnancy Cervical Cerclage 9. Areas of future research 10. Conclusion

3 Introduction ☺ Dilemma of Management of Midtrimester preterm premature rupture of membranes (PPROM) Lack of consensus on the management. An increased risk of Early Preterm Birth and Extreme prematurity Fetal infectious morbidity, Pulmonary hypoplasia, Skeletal deformities and Potter's facies. ☺ Maternal infections and the sequelae ☺ Significant contribution to perinatal mortality. ☺. The aim of expectant management is to extend latency and to maximize gestational age at delivery. ☺. Advances in obstetric and neonatal care continue to improve outcomes for extremely premature infants with use of surfactant agents, maternal steroids, and advancements in neonatal technologies. RCOG(2006): Preterm Prelabour Rupture of Membranes. Guidelines No. 44 A C OG (2007). Premature rupture of membranes. ACOG Practice Bulletin No. 80. Obstetrics and Gynecology, 109: 1007–19. A C OG (2008). Use of progesterone to reduce preterm birth. ACOG Committee Opinion No Obstetrics and Gynecology, 112: 963–965. Intubated preterm baby in an incubator

4 Definition ☺ Premature rupture of membranes prior to onset of labour regardless of the gestation ☺Preterm premature rupture of membranes (PPROM) rupture of the fetal membranes before the onset of labor at less than 37 weeks gestation. ☺ The accepted limit of viability is 24 weeks of gestation, with scattered reports of survivors at weeks ☺ Midtrimester (Previable) PPROM at 14-<24 weeks ☺ Incidence of PPROM is approximately 1-4 % of all pregnancies and about % of all preterm deliveries. ☺ Midtrimester PPROM is % of PPROM Maxwell GL. Obstet Gynecol Surv 1993;48: Carrol et al. CurrOpin Obstet Gynecol1996;11:441-8

5 Aetiology of PPROM Bryant-Greenwood and Millar.. Biol Reprod 2000; 63: Kumar et al. Placenta 2009; 30: Strohl et al.. Placenta 2010; 31: 18-24

6 Challis et al. Reproductive Sciences.2009; 16:

7 Mechanisms ‘Physiology of PROM ☺ Rupture of the fetal membranes, term or preterm Collagen remodeling, with activation of matrix metalloproteinases (MMPs), Relaxin apoptosis and proinflammatory cytokines: TNF- , IL-1a and IL-8 Moore et al Placenta 2006; 27: 1037: ☺. Vaginally delivered AROM FM contain a weak zone overlying the cervix. El Khwad et al.. J. Soc Gynecol Invest 2006; 13 :191-5 ☺ Separation of the amnion from choriodecidua at delivery is almost universal. Hypothesis that FM layer separation is part of the FM weakening process during normal parturition. Strohl et al. Placenta 2010;31:18-24

8 The sequence of FM rupture Separation of amnion from choriodecidua occurs as part of normal term FM rupture. FMs become significantly weaker as a result of this separation. ☺ FM components stretch together under load; ☺ A mnion separates from choriodecidua; ☺ C horiodecidua ruptures; ☺ A mnion distends further, nonelastically; and ☺ Amnion ruptures. Arikat et al.. Am J. Obstet Gynecol 2006; 194: 211-7

9 Effects of Stage of lung development

10 1. History of Drainage of liquor 2. Sterile speculum examination- visual observation of direct flow from cervix and pooling in posterior fornix. 3. Ferning test 4. Nitrazine test 5. Amnisure 6. Fetal fibronection Biomaker of impeding labour Prolactin  -fetal protein Ultrasound Weekly HVS Weekly CBC NST BPP or Modified BPP Vital signs ***Routine Amniocentesis Not recommended Digital examination be avoided DIAGNOSIS OF PPROM RCOG (2006);Guideline No % positive

11 Management of Midtrimester PPROM: KEY POINTS ☺ Midtrimester PPROM is associated with the same risk factors as PPROM later in gestation ☺ Approximately 75% of these women will deliver within 1 week of presentation. ☺ The frequency of chorioamnionitis is higher early in the latency period and at lower residual amniotic fluid volumes ☺ Abruptio placentae and cord prolapse are more common in pregnancies complicated by PPROM ☺ Neonatal survival is primarily related to gestational age at delivery, and is comparable to that in preterm deliveries matched for gestational age without PPROM. ☺. The neonatal risk of both pulmonary hypoplasia and musculoskeletal deformation decrease with advancing gestational age, shorter latency, and greater residual amniotic fluid volume. ☺. Maternal risks from midtrimester PPROM are lower than fetal/neonatal risks and include infection, need for cesarean delivery, and need for classical hysterotomy. ☺. Absence of amniotic fluid leakage associated with resealing of membranes and reaccumulation of amniotic fluid confers a prognosis comparable to that of pregnancies without PPROM.

12 MANAGEMENT ☺ Prophylactic antibiotics. Erythromycin 250 mg 6 hourly for 10 days Any pennicilin, Clindamycin and gentamycin; Increased latency period. Usefulness proven by 22 RCTs in 6000 women- RCOG Guigeline No 36; Kenyon et al ORACLE 1. Lancet 2001;979: ☺. Antenatal corticosteroids from 24 weeks of gestation Meta-analysis of 15 RCTs in 1400: Reduced risks of RDS, IVH and NEC ☺. Prophylactic tocolysis: In women with uterine activity and require transfer or antenatal corticosteroids. No effect on latency period or reduce neonatal morbidity. ☺.Amnioinfusion. Not supported by Cochrane Review and many other studies. but a recent study of 71 women with PPROM before 26 weeks showed intrauterine survival was higher in treated group than in control group (64.8% vs 32.3 %, P<0.001) De Santis et al. Fetal Diagn Ther 2003;18: ☺. Fibrin glue to improve AFI and reduce Pulmonary hypoplasia. Some success stories. Still needs more research. Sciscione et al.. Am J. Obstet Gynecol 2001; 184: Outpatient monitoring- Rigorous selection process-

13 For children whose mothers had pPROM, the prescription of antibiotics seemed to have little effect on the health and educational attainment of children at 7 years which was surprising since antibiotics might have been expected to improve clinical outcomes in this group as positive amniotic fluid cultures are found in 32% of women at presentation, and in as many as 75% during subsequent labour. The reasons for this are not clear but might be linked to the length of antibiotic exposure which in this group of women was fairly short, since about 60% gave birth within a week. There is also evidence that antibiotics neither eradicate nor prevent intra–amniotic infection.

14 For children whose mothers had spontaneous preterm labour the prescription of erythromycin (with or without co-amoxiclav) was associated with an increase in the proportions of children with any level of functional impairment from 38% to 42% (OR 1.18, 95% CI 1.02–1.37). Similarly proportions of children with cerebral palsy increased from 1.7% to 3.3% (OR 1.93, 95% CI 1.21–3.09) associated with erythromycin and from 1.9% to 3.2% (OR 1.69, 95% CI 1.07–2.67) with co–amoxiclav. There was a suggestion that more children who developed cerebral palsy had been born to mothers who had received both antibiotics.40 It is not clear why receipt of antibiotics increased the risk of functional impairment and cerebral palsy. Rates of subclinical infection in this group are found to be relatively low at 13–22%, and an absence of benefit is therefore not unexpected, but evidence of harm is surprising.

15 Spontaneous labor 29 (50.9) Chorioamnionitis 18 (31.6) Nonreassuring fetal testing 5 (8.8) Intrauterine fetal demise 5 (8.8) Indications for Delivery among Patients with PPROM from 14 to 23 Completed Weeks' Gestation* Falk et al. J. Perinatol 2004; 24: 611–616. The most common complications of neonates include respiratory distress syndrome (RDS), intraventricular hemorrhage (IVH), necrotizing enterocolitis (NEC), and sepsis. The maternal risks include the uterine infection and its sequelae.

16 Fig 2 Perinatal outcome according to gestation at Midtrimester PROM and Delivery

17 Outcome of Expectant Managemennt of Midtrimester PPROM A plea for limits 1 Mean Maternal antenatal Hospital stay 21 days (2-35) 2. Cesarean section rate 33.7% 3. Postpartum infection morbidity 32.4% And Neonatal complications Pulmonary Hypoplasia Respiratory Distress Syndrome Potter”s facies “in very early midtrimeste PPROM, the maternal complication rate outweighs the poor neonatal outcome and expectant management should be reconsidered Grisaru-Granosky et al. J. Perinatol 2003; 23:

18 OUTCOME OF MIDTRIMESTER PPROM 1.In three small studies of PROM managed expectantly, (a) Perinatal survival ranged from 25% to 63%, (b) Normal neurologic and physical development occurred in 55% to 68% of survivors. (c) Chorioamnionitis occurred in 41% to 77% of the patients in these studies. Taylor and Garite. 1984; 64: Major and Kitzmiller. Am J Obstet Gynecol 1990; 163: In 1993, Morales and Talley summarized six studies of expectant management of midtrimester PROM that demonstrated neonatal survival ranging from 22% to 63%, with approximately 60% of survivors having normal development at I year. Morales and Talley Am J Obstet Gynecol 1993; 168: Mercer's analysis of four midtrimester PROM studies using age-specific survival rates revealed a 23% rate of survival for PROM at 22 weeks EGA or earlier, compared with 53.9% at 23 weeks or more. Mercer BM. Obstet Gynecol Clin North Am 1992; 19:

19 A.Mitrimester PPROM in TWINS/Higher order ***Counseling 1.Termination of pregnancy if symptomatic 2. Conservative management: Counselling Consent. Surveillance for chorioamnionitis * Glucocorticoids at and beyond 24 week. * Antibiotic: Ampicillin Amoxacillin Erythromycin Azithromycin. Metronidazole No Tocolysis * Termination at 34 weeks unless indicated earlier. 3 Rescue of Twin 2 after spontaneous expulsion of twin 1. antibiotics, corticosteroids and tocolysis (MgSO4 * Serial ultrasounds until 34 weeks to assess cervical length?  Biophysical profiles (BPP) should begin at 28 weeks.  Delivery plan should be at weeks of gestation 1 de Jong et al. Eur J Obstet Gynecol Reprod Biol. 1995;63: Jazayeri et al. J Reprod Med. 2002;47: Mercer et al. Am J Obstet Gynecol. 1993;168: Preis et al. Ginekol Pol. 2004: Special considerations Others 1.Infertility Male factor Many failures 2. Cervical Cerclage removal 3 Older women 4 Patient’s wish 5 Ethics

20 Other factors affecting neonatal survival rates ☺ Socio-economic status ☺ Neonatal technology ☺ Use of surfactant ☺ Staff Expertise and training ☺ Time and Place: EPICURE, EPIPAGE and EPILLI ☺ (a) Only 16% of those born at 22 weeks admitted to NICU, only 1% survived until discharge. Of those born in the 23rd week, 54% were admitted to the neonatal intensive care unit and only 11% survived. (b) Neurological and developmental disability after extremely preterm birth (22–25 weeks) was observed in 49% of babies evaluated after 30 months. Bodeau-Livinoc et al. Paediatrics: 2008; 122: ☺. Other authors have concluded that expectant management of PPROM offers better perinatal and long-term survival than previously believed. Of ten infants born following successfully managed PPROM occurring weeks, four were alive 5 years later, 3/4 had survived without any major impairment neurological impairment. H Helmer. BJOG 2006; 113: ☺. In Germany, intervention is mandatory if there is even a small chance of survival.

21 Future Research ☺ Role and Genetics of Relaxin, Fibulin and Matrix metalloproteinases Family of Proteins ☺ Possible Drug Development to be used for prophylaxis ☺ Research into resuscitation of extreme low birthweight babies. ☺ Give every baby delivered alive a chance to live

22 Conclusions 1.Early Diagnosis and surveillance 2.Counselling and involvement of couple in decisions. 3.While PPROM at very early gestation is a serious complication and a major management dilemma often associated with poor outcome, the prognosis is not without hope. Albert Einstein Wiston Churchill Charles Darwin Isaac Newton 4. Don’t Abort Destiny. 4. What is common among these men?

23 THANK YOU


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