hepatitis c and pregnancy. belopolskaya maria
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Hepatitis C and pregnancy. Belopolskaya Maria. Botkin Infectious Diseases Hospital St Petersburg Russia 2012. Prevalence of chronic hepatitis C infection in the world. http://wwwnc.cdc.gov/travel/yellowbook/2012/chapter-3-infectious-diseases-related-to-travel/hepatitis-c.htm. - PowerPoint PPT PresentationTRANSCRIPT
Hepatitis C and pregnancy.
Belopolskaya Maria
Botkin Infectious Diseases Hospital St Petersburg
Russia2012
Prevalence of chronic hepatitis C infection in the world
http://wwwnc.cdc.gov/travel/yellowbook/2012/chapter-3-infectious-diseases-related-to-travel/hepatitis-c.htm
21,116,5
4,1 2,8
89,2
57,2
4,54,85,3
3,62,2 2,1
7,2
22,115,2 15,1 12,9
7,5 5,5 3,74,29,7
0
10
20
30
40
50
60
70
80
90
100
2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010
Russia SPb
Incidence HCV per 100 000 population
Prevalence of HCV-antibody
Pregnant women have a prevalence of HCV-antibody similar to that at population.
In the world the prevalence of antibody to HCV (anti-HCV) in pregnant women is 0.1% to 2.4%.
In Russia 2.8% of pregnant women have HCV-infection.*
*Ershova O.N. et al., 2005
Mother-to-infant transmission
The rate of mother-to-infant transmission is 4% to 7% per pregnancy when HCV viremia is presented.
43,0%
25,0%
0,2%
1,0%
3,0%
1,0%
14,0%
ChHBV ChHCV mixt ChHAIH NIH Vilson diseaseanother
Hepatic disease in childhood Research Institute of Children's Infections
Screening for chronic HCV infection
In Russia we have routine screening of pregnant women for chronic HCV infection twice during pregnancy: at 1st and 3rd trimesters. Due to this screening we can detect acute forms of HCV-infection during pregnancy.
Benefits of total screening
Observation for women with HCV-infection during pregnancy and after delivery.
Observation for children born from mothers with HCV-infection.
HCV diagnosis of pregnant women
beforepregnancy at time of
pregnancy
0
1020
30
40
50
60
70
80
%
1 pregnancy
2 and more
Possible modes of transmission HCV in a cohort of pregnant women in SPb (n=169)
15%
6%
72%
7%
Intravenous drug use
Sexual transmission
no identifiable riskfactor
iatrogenic risk factors
Clinical course
In the many cases pregnancy does not worsen the course of the chronic HCV-infection. Women with high ALT level in 1st trimester usually have normal level at the 3rd. But after delivery we often see high value of ALT, even higher than before pregnancy (if HCV-RNA+).
ALT level in RNA HCV-positive women
0
20
40
60
80
100
120
1st 2nd 3rd after delivery
Level
AL
T (
IU\m
l)
Routes of HCV transmission
Transplacental transmission in uterus (antenatal transmission)
Transmission during delivery Postnatal transmission – through breast-
feeding or during child-care
Risk factors of vertical HCV transmission (viral factors)
Co-infection HIV increases vertical transmission risk 2–3-times, although this risk can be decreased with administration HAART during pregnancy
Levels of HCV viral load: non-viraemic women have very low risk; high viral load increases vertical transmission risk
HCV-RNA in peripheral blood mononuclear cells increases risk of vertical transmission
According to our data in 2011
N=112
HCV-RNA+ 75 (67%)
viral load 10(5) - 10(6) IU/ml
HCV-RNA- 37 (33%)
ALT> 80U/l after delivery 27 (24%)
Risk factors of HCV vertical transmission (obstetric factors)
Mode of delivery: There is no protective effect of cesarean delivery on HCV vertical transmission compared with vaginal delivery
Obstetric procedures: prolonged rupture of membranes may increase risk, amniocentesis unlikely to increase risk
Prematurity: No evidence of effect Gender: doubles the risk for girls compared with
boys
Breast feeding
No evidence of increased risk through breastfeeding
According to our data HCV RNA can be detected in breast milk from women with high viral load (7% when HCV RNA>10(6)IU/ml)
Frequency of vertical HCV transmission Research Institute of Children's Infections, SPb
7,28,2
10,3 10,4
6,7
0
2
4
6
8
10
12
%
2005 2007 2008 2009 2011
Effect of chronic HCV-infectionon the course and outcomes of pregnancy
•HCV-infection does not affect the reproductive function, the frequency of spontaneous abortions•No effect on the incidence of congenital anomalies •An effect on the course ofpregnancy (frequency of fetal malnutrition, premature birth) depends on the liver disease severity •There exists a risk of vertical transmission
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