andrew booker - sydney adventist hospital education conferences... · increase in risk of cp with...
TRANSCRIPT
Global problem
15 million babies every year
Leading cause of death children <5 1 million children a year
Estimated 75% could be saved
Stark inequality btw high and low income countries 50% mortality under 32/40 due to lack of basic care
In high income countries most survive
60% Preterm delivery occurs in Africa and Asia
In Australia – 8.6% <37 weeks (of approx 300,000 births)
Most Stillbirths are preterm 84%
Perinatal death rate 20-27 weeks – 708 per 1000 births
37-41 weeks – 2/1000
Indigenous Australians do WORSE 1.7x more likely (approx 14% of births)
Less ANC, high rate of smoking, more chronic illness
Extreme preterm 20-27 weeks Account for 0.8% births
Very Preterm 28-31 weeks Account for 0.8% births
Moderate to Late Preterm 32-36 week Accounting for 7% births
Past history of preterm delivery
Maternal age - <20 and >40
Cervical incompetence
HT/PET/HELLP
Multiples/TTTS
Placenta previa and abruption
Placental insufficiency/IUGR
PROM
Medical – diabetes, HT, renal, rhesus, UTI, Uterus
Substance abuse
Cerebral Palsy
Neurodevelopmental delay
Learning difficulties
Blindness
Deafness
Chronic Respiratory Problems
Social impacts
Economic impacts
Palpable painful contractions without cx change
Hard to establish incidence
60% deliver at term
How do we triage? History
Examination
Cervical assessment with TV ultrasound
Fetal fibronectin
Extracellular glycoprotein
Produced by the chorion “biological glue” Binds the blastocyst to the endometrium
Present up to 22 weeks when the chorion fuses
Simple ward test collected from the posterior fornix
Helpful to determine need for costly transfer
Contraindications include RM, Cx>3cm, Cerclage, bleeding, SI, BV, recent PV
Role in prediction and prevention Checked at routine morph scan
Useful in TPL
Role in those with past history Preterm delivery
Cervical incompetence
Leave to Dr Ramsay to discuss
2003 NEJM, 17 –OH Prog reduced recurrent preterm birth
2011 Ultrasound Obstet gynaecol showed vaginal progesterone reduced risk of preterm birth in those with foreshortened cx
2007 NEJM no benefit of progesterone with twins
Some controversy IM vs PV progesterone
Role of Cerclage clear if PHx preterm birth AND a short cx
2014 Int, J of Gynae and Obstets.Slight prolongation if TPL halted 33 vs 23 days
Preventative Screening normal population 20/40 with swab for BV,
trichomonas, candida
Reduction Birth <37weeks RR 0.55
Reduction in Preterm del & <2500 RR 0.48
Reduction in Preterm del & <1500 RR 0.34
Vienna
Cochrane reviewed - moderate reliability
Threatened Preterm Labour with intact membranes Cochrane review: 14 studies: 7837 women
Dominated by ORACLE 2 with followup to 7 yrs
No sig difference in perinatal or infant mortality
No reduction in preterm birth
Increase in NND RR 1.57
Slight increase risk of functional impairment
Increase in risk of CP with macrolides and beta lactams
Maternal infection reduced RR 0.74
PPROM
Cochrane 22 trials; 6872 women Reduction in Chorio RR 0.66
Decreased babies born at <48hrs and upto 7 days
Decrease Neonatal infeciton RR 0.67
Decrease use of surfactant, O2 therapy and abnormal head scan
Increased risk of NEC with Augmentin
Oracle Childrens Study Little effect on childrens health at 7 years
Cochrane: 12 trials: 3617 women
Expectant Vs Active management
No difference in Neonatal sepsis
Increased risk of ; RDS and ventilation and NICU admission
Neonatal mortality
IOL and LSCS
Endometritis
Decreased risk of chorioamnionitis
Aim - Prevent contractions and allow prolongation of pregnancy
Various agents used Ca channel blockers – Nidepine
Nitric Oxide donors – GTN
MgSO4
B – adrenergic agonists – salbutamol, terbutaline
Cyclooxygenase inhibitors – indomethacin
Oxytocin Receptor antagonist - Atosiban
Mostly used to allow for corticosteroids and transfer
Primary mechanism ?increase surfactant production
Dexamethasone or Betamethasone (24mg/24hrs)
>24hrs through to 7 days
Fetal Benefits Reduction NND 33%
Reduction RDS 44%
Reduction IVH 46%
Fetal Concerns 1 Cochrane review possible increase in CP with multiple
doses
Offered between 24 and 34+6 weeks (??23+)
Benefit after 1st dose
Strongest Data between 26 and 34+6
Safe for mothers No evidence of Puerperal sepsis
No evidence of chorioamnionitis
No maternal deaths