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Antepartum complications
Week
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Obstetrical assessment unit/ triage
Antepartum complications eg. cystitis, abdo pain, injury Antepartum hemorrhage ? PROM Preterm labour Gestational HTN/pre-eclampsia Outpatient inductions
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Antepartum Complications
APH Antepartum Hemorrhage PPROM Pre-labour Rupture of Membranes
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Antepartum Hemorrhage
Definition: - Vaginal bleeding any time from 20 weeks to term - 2% to 5% of all pregnancies affected
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Antepartum Hemorrhage
Causes: Abruptio Placenta 40% Placenta Previa 20% Unclassified 35% Lower Genital Tract Lesion 5%
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Antepartum Hemorrhage
Physiology: - Uterus receives 1% of maternal cardiac output in non gravid state - Rises to 20% in the third trimester - Potential for massive bleeding and significant mortality and morbidity - Previa and Abruption 60% of APH
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Placenta Previa Definition: Localization of the placenta near or over the cervical os -detectable by antenatal ultrasound - Complete, partial or marginal Incidence: - 0.3%-0.5% of all pregnancies
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Placenta Previa Low lying placenta:
Affects appx. 30% of early pregnancies but only 0.5% persist Repeated US advised in second trimester - If placenta is within 2 cm of the os (by transvaginal ultrasound), risk exists for bleeding through effacement and dilatation
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Placenta Previa Predisposing Factors: Prior placenta previa
First pregnancy following any uterine surgery eg. C/S Multiple gestation Uterine malformation Multiparity Advanced maternal age
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Abruptio Placenta Definition: Incidence:
Premature separation from the uterine wall of a normally implanted placenta Incidence: - 1%-2% of all pregnancies - 5%-16% if previous Hx of abruption (identify on antenatal records if possible)
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Abruptio Placenta Classification:
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Abruptio Placenta Maternal hypertension Prior abruption
Predisposing Factors: Maternal hypertension Prior abruption Abdominal trauma Maternal smoking (> 1 ppd) Multiparity Advanced maternal age (> 35 years) Substance abuse (cocaine and alcohol) Uterine malformation
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Abruptio Placenta A short umbilical cord
Predisposing Factors (cont): A short umbilical cord Rapid uterine decompression (multiple gestation, polyhydramnios) Thrombophilia However…Most abruptions are idiopathic
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Antepartum Hemorrhage
Placenta Previa and Abruptio Placenta Diagnosis: Avoid a pelvic exam until Placenta Previa has been ruled out (see antenatal record/OASIS) History and physical may give clues TV ultrasound is definitive for Dx previa Abruption is not a radiologic diagnosis, however
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Abruptio vs. Placenta Previa
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Antepartum Hemorrhage
Previa and Abruptio Management: Remember you have 2 patients Determine hemodynamic stability Prompt Fetal Health Surveillance If unstable ABC’s, large bore IV’s x-match, INR/PTT, fibrinogen O2 (fetus sensitive to hypoxia) continued maternal-fetal surveillance
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Antepartum Hemorrhage
Previa and Abruptio Management (cont): Kleihauer-Betke test may confirm abruption WinRho (Rh immune globulin) when indicated Monitor 4-24 hours for evidence of fetal compromise Consider transfer to high risk centre Consider steroids for <34 weeks Always weigh risk of significant subsequent bleeding vs. fetal maturity
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Pre-labour Rupture of Membranes
ROM before labour PROM >37 weeks PPROM <37 weeks
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PROM Latent period = interval between PROM and onset of labour
90% of term PROM will have spontaneous labour within 24 hours Likelihood decreases with PROM more remote from term 28-32 week PPROM has 50% likelihood of labour by 24 hours, 80% by 1 week
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PROM Incidence: Term PROM 2-10% of pregnancies PPROM
33% of preterm deliveries
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PROM Etiology: Idiopathic Infection – check VSS, esp. temp.
Polyhydramnios - ? Recent US Cervical incompetence Uterine abnormality Following cervical cerclage or amniocentesis Trauma Previous cervical surgery (e.g. conization)
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PROM Etiology (cont.): Past OB history (gestational age at delivery, including PPROM) Black Race Smoker Drugs, lifestyle, stress Nutrition
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PROM Complications - Term PROM Fetal/neonatal infection
Maternal infection Umbilical cord compression / prolapse
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PROM Diagnosis: History
30% of women with Hx of leakage do not have ROM Ddx: vaginitis (infectious vs. physiologic), urine, semen, sweat Routine digital exam is not indicated because of infection risk Speculum exam - for confirmation of ROM, cervical status, and to exclude cord prolapse Determine GBS status
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PROM Speculum Exam (RN assist): Sterile technique
Must visualize cervix Fluid pooling in posterior fornix Free flow of fluid from cervical os – may try coughing or fundal pressure pH testing of fluid Nitrazine test - non specific Causes of false positive: blood, semen, BV Ferning
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PROM Ferning
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PROM Management - all gestations: Confirmation of the diagnosis
Assessment of maternal and fetal well-being Determination of the presence of any associated condition Abdominal exam for presentation Assessment of cervical status Digital examination should be avoided whenever possible (especially when preterm and expectant management is being considered)
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PROM Management - >37 weeks:
Term PROM Trial – Hannah et al, NEJM 1996;334: induction of labor with oxytocin or prostaglandin E2, and expectant management, result in similar rates of neonatal infection and cesarean section induction with oxytocin resulted in a lower risk of maternal infection and women viewed induction of labor more positively than expectant management Don’t induce if not cephalic!
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PROM Management - >34 weeks:
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PROM Management - >34 weeks:
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PROM Management - >34 weeks:
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PROM Management >37 weeks - Bottom Line : Avoid digital exam
Assess for infection - mat and fetal vital signs Do appropriate swabs Recommend GBS chemoprophylaxis at the onset of labour, if GBS + Offer oxytocin
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PROM Management 34-37 weeks - Bottom Line : As for Term PROM but also…
Consider transfer to higher centre/OBS consult Ultrasound for fluid, cervical length, position Individualized mgt. based on risks, patient preference and availability of resources Consider induction more readily if GBS positive Maternal-fetal surveillance if expectant management
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Pre-labour Rupture of Membranes
Management <34 weeks - Bottom Line : Consider transfer to higher centre Ultrasound for fluid, cervical length, position Refer to OB Collect Fluid for fetal lung maturity if possible Steroids Antibiotics (IV x 2 days then PO x 5 days) Try for expectant management (OP if possible)
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Preterm Labour Definition:
Regular uterine contractions accompanied by cervical dilatation/effacement at gestation <37 weeks
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Preterm Labour Incidence 7-10% of pregnancies
1-2% pregnancies before 34 weeks
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Preterm Labour Importance of Accurate Dating
>34 week delivery have survival rate approximately equal to term babies They may need longer hospital stay for feeding or other difficulties
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Preterm Labour Importance of Accurate Dating
Long term neonatal adverse sequelae occur mainly in <30 week In extreme preterm deliveries, 10 days can make a big difference E.g.. Survival can go from 0-30% or from 30-55% in a 10 day period
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Preterm Labour Importance of Accurate Dating
By 20 weeks, women should know the EDD, from accurate menstrual data, or by 18 week or earlier ultrasound
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Preterm Labour
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Preterm Labour Etiology: Idiopathic Antepartum hemorrhage PPROM
Chorioamnionitis Multiple pregnancy Incompetent Cervix Maternal Disease (e.g. HTN) Smoking, stress, drugs, EtOH
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Preterm Labour Etiology: 72% spontaneous labour
28% indicated deliveries GDM IDDM Non reassuring FHR IUGR Abruption Fetal Demise Chorioamnionitis
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Preterm Labour Diagnosis:
Women should be instructed early to watch for Contractions PV fluid PV bleeding Low Back pain/pressure Change in vaginal discharge Diagnosis must be made by physical examination, NOT over the telephone
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Preterm Labour Diagnosis: Newer strategies include Cervical Sonography
Fetal Fibronectin
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Fetal Fibronection (FFN)
Large molecular weight glycoprotein Promotes cellular adhesion Released when the extracellular matrix of the chorionic/decidual interface is disrupted Normally found in cervico-vaginal secretions until 22 weeks gestation but is virtually never found between 24 and 34 weeks gestation unless the cervix has undergone premature effacement and dilatation
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Contraindications to FFN
• Estimated gestational age <24 weeks or >34 completed weeks • Preterm rupture of membranes • Cervix ≥3 cm dilatation • Cervical cerclage • Active vaginal bleeding • Vaginal exam or sexual intercourse in the past 24 hours
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Fibronectin A negative test confers a more than 95% likelihood of the woman remaining undelivered for the 14 days
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Fibronectin False positive tests may be caused by: i. Digital exam prior to the speculum collection of the sample ii. More than a minimal amount of blood in the specimen (fFN is present in plasma) iii. The presence of amniotic fluid in the specimen(amniotic fluid contains high levels of fFN) iv. Intercourse within the previous 24 hours (fFN is present in seminal fluid)
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Preterm Labour Management: Strategies are not particularly effective
Especially when not instituted early
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Preterm Labour Treatment:
No evidence to suggest that bed rest will prolong or arrest preterm labour <40% will be candidate for tocolysis
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Preterm Labour Tocolysis: No evidence for Yes evidence for Fluid
Sedation Mag Sulfate (MgSO4) Yes evidence for CCBs (nifedipine) Oxytocin antagonists (antocin - not approved in Canada/USA) PG synthetase inhibitors (indomethecin)
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Preterm Labour Tocolysis - Contraindication:
Contraindication to specific agent Contraindication to prolonging pregnancy Medical indication e.g. PIH with protein Chorioamnionitis Mature fetus IUFD Imminent delivery
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Preterm Labour Minimizing Neonatal Morbidity/Mortality:
Respiratory Distress Syndrome (RDS) is significant cause of M&M Other conditions such as intraventricular hemorrhage, necrotizing enterocolitis, persistent pulmonary hypertension are more likely in the setting of RDS Prevention with antenatal glucocorticoid therapy is well established
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Preterm Labour When should glucocorticoids be given?:
Lower gestation limit - 24 weeks Upper gestation limit - 34 weeks Prophylactic administration - depends on diagnosis and risk, e.g. preterm previa and bleeding Repeated administration - not recommended
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Preterm Labour Steroid options: Betamethasone 12mg IM q 24h x 2 doses
Dexamethasone 6mg IV/IM q 12h x 4 doses. Don’t use in the presence of chorioamnionitis Always use with tocolytics Often used without tocolytics as well
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Preterm Labour Summary - Preterm Labour: Prompt and accurate diagnosis
Identify and treat underlying cause, if possible Attempt to prolong pregnancy if appropriate Intervene to minimize neonatal morbidity and mortality Antenatal steroid therapy GBS prophylaxis Maternal transport (best place in Level III hospital, worst place is during transport)
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GBS (Group B strep) Incidence of serious neonatal infection 0.32 per 1000 births (NEJM, 2009) Early (0-6 days) vs Late (6-90) 50 % of infants will be colonized, but only 2% will develop symptoms Universal screening at weeks Vaginal-rectal swab Self collections just as good (Hicks 2009)
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GBS Recent study (NEJM, 2009)
74.4% of GBS disease occurred in term infants ( although preterm ones have higher incidence) 61% of term infants with GBS disease were born to GBS negative women
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GBS Role of PCR rapid testing (low sensitivity 30-80%)
Role for vaccine Widespread use of antibiotics contributes to resistance Does positive test mean pregnancy is higher risk?
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Out-patient induction
Reasons must be documented – compelling, convincing and consented Method should match the situation Patient preference must be considered
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Outpatient induction CERVIDIL - most commonly used at TOH-Civic campus
Increasing use of Foley inductions Ensure patient is suitable for OP induction Needs reassuring U/S within hr Bishop Score…
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Outpatient induction Cervidil (10mg dinoprostone) - PGE2
Bishop score <7 Posterior fornix Monitor FHR & uterine activity – 1-2 hours If no labour, may repeat x1 (24 hr later) DOCUMENTATION Show them how to insert cervidil. Look at the explicit instructions that come in the box. ? Is there a video? Don’t hesitate to call staff in for the first one, if uncertain.
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