subject:ptl dr shakeri. preterm labor important cause of perinatal mortality & morbidity 50 % of all...

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Subject:PTL Dr shakeri

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  • Slide 1
  • Subject:PTL Dr shakeri
  • Slide 2
  • Preterm labor Important cause of perinatal mortality & morbidity 50 % of all major neurologic handicaps
  • Slide 3
  • Increased in survival Use of C.S Regionalization prenatal care Improved method of mechanical ventilation Use of surfactant Improved nutritional therapy
  • Slide 4
  • Mechanism of labor onset Hormonal (progestron withdrawal) Oxytocin Prostaglandins Cytokines IL.1-IL.6-TNF ( stimulate the amnion and decidua to produce PG) B-TGF ( inhibit PG production) Other factors endothelin nitric oxide (NOS)
  • Slide 5
  • Infection as a cause of preterm labor Linked with symtomatic nongenital infection Subclinical Infection an important cause of PTL a- Histologic chorioamnionitis increased b- recognized infections in mother and neonates c- sepsis and meningitis are increased 3 to 10 fold d- positive culture of amniotic fluid/membrane/decidua 3-24% (
  • Fetal fibronectin presence 20-34 w strongly associated with PTL Sensitivity is low Specificity is high Used to women with intact membrane, cervical dilation less than 3 cm,GA 24-34 w results should be available within 24h False positive (recent intercourse-vaginal examination presence of B.V -vaginal bleeding) >50 ng positive test
  • Slide 20
  • All of these tests fail to meet the goals of an ideal screening test
  • Slide 21
  • Preterm labor defined uterin contractions >4 contractions per 20 minutes Cervical dilation 2cm or more in N..P 3cm or more in M.P Cervical effacement > 80% Uterin contraction and cervical change
  • Slide 22
  • treatment Hormonal treatment Alcohol treatment Bmimetics Mgso4 Antiprostaglandin agents Oxytocin analogs Ca channel blockers
  • Slide 23
  • Absolute CI of tocolytic theraphy Severe preeclampsia Severe abruptio Severe bleeding Frank chorioamnionitis Fetal death Fetal anomaly incompatible with live Severe FGR Mature lung Maternal cardiac arrythmia
  • Slide 24
  • Relative CI to tocolytic therapy Mild chronic hypertension Mild abruptio Stable previa Maternal cardiac disease Hyper thyroidism Uncontrolled diabetes Fetal distress Fetal anomaly Mild IUGR Cervix dilatation greater than 4 cm
  • Slide 25
  • B - adrenergic agonists The most wildly prescribed Ritodrined and terbutaline (SC-IV) Disadvantage - side effect(none of them are completely B2 selective ( Negative B2 effect Maternal hypotension Decreased u.o.p increased glucose secretion Hypokalemia Pulmonary edema
  • Slide 26
  • Negative B1 effect Tachycardia Palpitation Constipation Decreased gastric emptying Hypokalemia Agitation jilleriness
  • Slide 27
  • Severe maternal adverse effect Cardiac arrhythmia Myocardial infraction Pulmonary edema Postpartum cardiomyopathy death
  • Slide 28
  • Fetal effect Tachycardia Increased C.O.P Redistribution of blood flow Increased thickness of inter ventricular septum Neonatal supra ventricular tachycardia Myocardial ischemia and necrosis hydrops Hypoglycemia Intra ventricular hemorrhage
  • Slide 29
  • Are B-mimetics efficacious?
  • Slide 30
  • Magnesium sulfate In recent years, tocolytic of choice in many delivery units Protocol of administration The blood levels of 6-8mg/dl are optimal for tocolysis
  • Slide 31
  • Maternal side effect Common (flushing-sense of warmth-headache nystagmus-nausea-dizziness-lethargy) Serious (pulmonary edema-neuromuscular blockage- osteopenia-respiratory depression-cardiac arrest)
  • Slide 32
  • Neonatal side effect Respiratory depession Decreased beat to beat variability Decreased muscle tone Drowsiness Depression Poor respiratory effort Low apgar score
  • Slide 33
  • Is mgso4 ?efficacious
  • Slide 34
  • Ca channel blocker Mechanism Protocol of Ad Maternal side effect Decrease in mean arterial pressure Symptomatic hypotension Nausea-headache-facial flushing
  • Slide 35
  • Neonatal side effect Well tolerated by the fetus Neonatal heart block Growth restriction, acidosis, stillbirth No protocol established the safety of using these medication together
  • Slide 36
  • Prostaglandin synthesis inhibitors Mechanism Protocol of Ad Fetal CI Growth restriction Renal anomaly Oligohydramnios Chorioamnionitis Ductal dependant cardiac lesion Twin to twin transfusion syndrom
  • Slide 37
  • Maternal CI Renal and hepatic D Active peptic ulcer Poorly control H.T Asthma in aspirin-sensitive patients Coagulation disorder Maternal side effect GI upset and hemorrhage Alteration in coagulation Thrombocytopenia Asthma in aspirin-sensitive patients Renal injury(prolonged treatment)
  • Slide 38
  • Neonatal side effect Constriction of ductus arteriosus Neonatal PHT 5-10% Oligohydraminous increased ADH direct effect on renal blood flow Necrotizing enterocolitis Intraventricular hemorrhage
  • Slide 39
  • Effective agent that is well tolerated by mother and fetus Indomethacin to be comparable to ritodrine and MgSo4 Exposure should be limited to 48 hrs and G.A less than 32 weeks
  • Slide 40
  • Other tocolytic agents Atosiban (analog oxytocin) Nitroglycerin Cyclo-oxygenase inhibitor Progestin Nitroxide inhibitor
  • Slide 41
  • Maintenance tocolysis following arrest of PTL Oral tocolysis with B-mimetic Continous subcutaneous administration of terbutalin Oral MgSO4 Oral nifedipine Long-term tocolysis with prostaglandin synthetases inhibitors is contraindicated
  • Slide 42
  • Maintenance tocolytic agent .
  • Slide 43
  • Ancillary therapy for women in PTL Antibiotic therapy Antibiotic therapy in PTL with intact membrane is not indicated GBS prophylaxis should be administered Hydration therapy Bed rest C.S (all women at risk for PTL prior to 34 weeks receive C.S
  • Slide 44
  • Key points 1. The rate of PTL is increasing in the united states. 2. fFN and vaginal ultrasound of cervix and promising technologies to identify women at risk for preterm delivery. 3. Screening for B.V and T.Vaginal is not indicated. 4. Management of women with asymptomatic shortening of the cervix controversial 5. Tocolytic therapy has not been associated with improvements in neonatal outcome. 6. Weekly courses of antenatal C.S should not be routinely prescribed. 7. Antenatal progesteron therapy may reduce the risk of preterm birth (PTB) and low birth weight (LBW) in women with previous PTB
  • Slide 45