Liver disease pregnancy Flashcards
(34 cards)
Risk of chronic carriage of Hep B if infected at delivery?
90%
subsequent cirrhosis and hepatocellular carcinoma
Risk of Hep B vertical transmission related to antigen status.
HBsAg +, HbeAg+ = 95%
HBsAg +, HBeAg- = 2-15%
Measurement of HBV DNA has replaced HBeAG as most sensitive test of viral activity.
Risk of HBV transplacental transmission?
5%
List significance of following ab/ag presence:
- HBsAb
- HBsAg
- HBcAb
- HBeAg
- vaccination or previous infection
- infected
- natural infection previously
- active viral replication
Risk of chronic infection after HBV exposure in adults?
10%. 25% of those develop chronic liver disease.
When is tenofovir indicated antenatally?
third trimester
HBV DNA >200,000IU/mL or 10^6 log copies/mL
What is the effect of antenatal tenofovir on infant infection?
RR 0.15 SS
Neonatal HBV immunisation consists of:
- HBIG <12 hrs after delivery
- DTAP <12 hours after delivery
- DTAP 6w, 3m, 5m
Reduces risk of infection RR0.08
Less effective if LBW or preterm.
Risk factors for hepatitis C?
80% of IVDU or blood product dependent patients
<5% sexually transmitted.
Course of hepatitis C infection in adults?
15-30% of untreated patients develop cirrhosis within 20 years
27% of those will develop hepatocellular carcinoma in 10 years.
Determinate of Hepatitis C vertical transmission ?
HCV viral load
1% RNA negative mothers
5% RNA positive mothers
Management of HCV in pregnancy
direct acting antivirals pre conceptually + treatment
DAA contraindicated antenatally
NIPT/MSS1 (no invasive tests if possible)
Avoid FSE/FBS
Bfing. Start DAA after finished + contraception.
No vaccines for HCV prevention.
No increase risk of congenital abnormalities, miscarriage or prematurity. Detection of infant infection reliable 3mo PP.
Prevalence of obstetric cholestasis?
0.7%
Risk factors for obstetric cholestasis?
family (autosomal dominant inheritance)
hep C carriage
gallstones
multiple pregnancy
Genetic pathology of obstetric cholestasis
MDR3 gene- hepatocellular transport system
lower oestriol circulates
bile salts accumulate—> vasoconstriction
dyslipidaemia
hyperbilirubinaemia
liver autoantibody screen?
anti-mitochondrial, anti-smooth muscle antibodies
Perinatal mortality/morbidity associated with obstetric cholestasis?
mortality = 1.1-3.5% (used to be 11%) stillbirth= 1.5% intrapartum fetal distress = 2-22% fetal arrhythmia preterm birth 25% meconium 44% vitamin K deficiency (intracranial haemorrhage)
Maternal intrapartum risks of obstetric cholestasis
LSCS fetal distress
PTB
PPH 2-22%
When would UCDA be prescribed for cholestasis?
non significant improvement in maternal itch scores. does not seem to effect any other perinatal/maternal outcomes.
Evidence for timing of delivery with peak BS <100
no difference in stillbirth rate compared with background population risk before 39 weeks gestation.
BS >100 individualise timing. HR 30.50 stillbirth. May be reasonable to consider timing ~36 weeks.
Delivery considerations of cholestasis?
What was the peak BS level LFTs BP monitoring CTG in induction/labour active management 3rd stage coagulation profile at start (vitamin K if PTT prolonged) IVL Neonatal vitamin K Avoid oestrogen OC's Repeat LFT >10/7.
Risk of AFLP in pregnancy?
1/7000-20,000
Risk factors AFLP
male fetus (3:1)
primigravida
multiple preganncy
homozygous genetic defect in child (LCHAD deficiency)
LCHAD function
catalyses step in beta oxidation of mitochondrial fatty acid
instead unmetabolised long-chain fatty acids spill into maternal circulation
leads to hepatotoxicity
LCHAD def also impairs placental vasopressinase enzyme degradation. Increases ADH= polydipsia, polyuria.