Transcript Slide 1
3rd June, 2011 The virus/es Epidemiology/Statistics HBV disease complications and Transmission Risk groups Prevention, Vaccination HAV HBV Hepatitis A and B are inflammatory diseases of the liver1 Caused by different viruses with different modes of transmission1,2 Both HAV and HBV provoke liver damage1,3 Both diseases have similar signs and symptoms1,3 A chronic carrier state may develop 1. WHO, Hepatitis A, only after hepatitis B2 WHO/CDS/CSR/EDC/2000.7 2. CDC, Hepatitis B, Pink book, 2007 3. WHO, WHO/CS/CSR/LYO/2002.2: Despite the differences in their modes of transmission and clinical outcome, the geographical distribution of HAV and HBV are similar Anti-hepatitis A virus prevalence High Intermediate Low 1.5 million cases per yr CDC, Travelers’ health: yellow book, 2007 Hepatitis B surface antigen (HBsAg) prevalence High Intermediate Low Mast, et al. MMWR Recomm Rep 2006; 55 (RR16): 1–25 Prevalence in General Population – 7-10% Prevalence in Pregnant Women – 9.3% (2001 KPA study) and HBeAg - 8.8% HBV Markers of Kenyans by early teens – 70%-90% Prevalence in Blood Donors 5 – 7% HBeAg in child bearing age women +ve for HBsAg –8 - 23.6% HBeAg higher in children – 60% Wankya et al EAMJ 1979 Okoth et al 1990 EAMJ Sept. 2006 KPA study Acute infection with jaundice Acute infection, (can last for long) asymptomatic or subclinical Chronic infection - Chronic Liver Disease - Liver cirrhosis - HCC Symptoms Antibody titre HBeAg anti-HBe Total anti-HBc IgM anti-HBc anti-HBs HBsAg 0 4 8 12 16 20 24 28 32 36 Weeks after exposure 52 100 CDC, Hepatitis B slide set, 2007 Acute (6 months) Chronic (years) anti-HBe HBeAg HBsAg Antibody titre Total anti-HBc IgM anti-HBc 0 4 8 12 16 20 24 28 32 36 52 Weeks after exposure CDC, Hepatitis B slide set, 2007 100 80 80 60 Chronic infection 60 40 40 20 20 Symptomatic infection (%) Chronic infection (%) 100 Symptomatic infection 0 Birth 1–6 months 7–12 months 1–4 years 0 Older children and adults Age at infection CDC, Hepatitis B slide set, 2007 High Blood Serum Wound exudate s Moderate Semen Vaginal fluid Saliva Low / not detectable Urine Faeces Sweat Tears Breast milk CDC, Hepatitis B slide set, 2007 100-times more infectious than the human immunodeficiency virus (HIV) Transmitted by exposure to infected body fluids (e.g. blood, semen, vaginal secretions): WHO, WHO/CS/CSR/LYO/2002.2: Hepatitis B Horizontal - Most important than vertical - Intrafamilial spread important, (between siblings and btw spouses) - Intrafamilial more important than school spread - high infection rate in infants & children with highest prevalence reached by age ten (may be due to higher HBeAg rate) Greenfield1986 & Wankya 1979) (Okoth et al 1983 &1990) (Bowry 1983) ( If mother positive for HBsAg and HBeAg 70%-90% of infants infected 90% of infected infants become chronically infected If positive for HBsAg only 5%-20% of infants infected 90% of infected infants become chronically infected In Asia the rate of HBeAg is highest at 40% hence high PT PT is present in Kenya but less common than horizontal Sexual transmission exists but no studies yet Parenteral transmission less Hepatitis A Isolation of Pathogen FDA vaccine Licensure Efficacy Hepatitis B 1973 1965 1995 1981 94-100% 80-100% NO SPECIFIC ANTIVIRAL TREATMENT AVAILABLE FOR BOTH Improved Sanitation and Hygiene Safe Sex Screening of pregnant mothers Vaccination for all, newborns, children, travellers Two types of HBV immunization: - HBV specific immunoglobulin injection - Short term protection - Cab be used at birth to reduce perinatal transmission in HBsAg + mothers Active Immunization: - Current HBV vaccines are based on synthetically Recombinant HBsA - Contain sections of HBV protein to stimulate a natural immune response - available locally: Euvax B and Engerix B Babies born to infected mothers1 Persons living in countries where hepatitis B is endemic1 Family members and sexual contacts of a person infected with hepatitis B1 Healthcare workers (e.g. surgeons, dentists)1 Institutionalised people (developmentally disabled)2 Public safety workers (e.g. police force, fire service, prison service)3 Travellers1 People who have multiple sex partners and men who have sex with men3 Patients on haemodialysis3 Injecting drug users1 1. WHO, WHO/CS/CSR/LYO/2002.2: Hepatitis B 2. Mast, et al. MMWR Recomm Rep 2006; 55 (RR16): 1–25 Patients with chronic liver disease3.4 CDC, Viral hepatitis B fact sheet, 2007 4. Oldfield & Keefe, Rev Gastroenterol Disord 2007; 7: 1–21 Travellers to areas endemic for both hepatitis A and B People at occupational risk Institutionalised individuals Sexually active homosexual men Patients with chronic liver disease Van Damme & Van Herck, Expert Rev Vaccines 2004; 3: 249–67 Hepatitis B is the most important Vaccinepreventable communicable disease Vaccine: One of the most widely used vaccine in the world Safe, used for >25 yrs 95% effective in preventing children and adults from developing chronic infection Reports of success in reducing carrier rates in children generally from 8-15% to <1% Effective 70-90% in preventing PT given alone within 12 hrs of birth or with Immunoglobulins Co administration with other vaccines together or separately Vaccines: targeting 2000, 2nd WSIPD Advances in Vaccinology, (1)2007 Taiwan: seroprevalence decreased from 9.8% in 1984 to 0.7% in 1999 and incidence decreased from 0.7:100,000 in 1981/1986 to 0.36:100,000 in 1990-1994 in children. Chan CY. Et al. Legend of hepatitis B vaccination: Taiwan experience. J. Gastroenterol. Hepatol. 2004; 19;: 121-126. 1992 WHO recommendation for universal Hep B vaccination in all highly endemic (HBsAg carriage rate>8%)countries by 1995 and all other countries by 1997 Min age of vaccination - birth (monovalent) Schedules – 0,1, 6-12 months - 0,1,2 months for rapid schedule No need for a booster dose in routine vaccination SAGE Recommendation: - In all regions of the world, Perinatal transmission is responsible for a sizable proportion of CHB infections. Hence all infants should receive the first dose of Hep B vaccine as soon as possible after birth. World Health Organization:1 consider in areas of intermediate endemicity supplements health education and improved sanitation persons at increased risk of hepatitis A virus infection should also be vaccinated Schedule: First dose: 12–23 months: a booster 6- 12m later 1. WHO, Wkly Epidemiol Rec 2000; 5: 38–44 2. Fiore, et al. MMWR Recomm Rep 2006; 55 (RR07: 1–23 Mass vaccination has dramatically reduced the incidence of Hib infections in children under the age of 5 Vaccine in now used in routine immunization schedule in more than 100 countries worldwide Vaccines available in Combination with DPT Pentavalent, Pentaxim, and with HepB Titanrix www.paho.org/English/HVP/hvp_hib_text.htm Options: I. Birth, 6 wks, 6m II. Birth, 6wks, 6-9m III. 6wks, 10w, 6-9m IV. 6wks, 10wk, 14wk For HBsAg mothers use the Birth, 6wk, 6mo schedule (birth dose given within 4-12hrs) Birth 6 Wks 1O Wks 14 Wks 9 Months BCG, OPV OPV, DPT/Hib/HepB OPV/DPT/Hib/HepB OPV/DPT/Hib/HepB Measles, Yellow Fever Mother & Child Health Booklet MOH 216 Maragua study, high risk group Plasma derived HB vaccine – 90.2% Recombinant HB vaccine – 99.1% Difference significant Presently vaccine in u se is Recombinant Okoth et al 1990 Senegal - 93% - 95% seroconversion, - no effect on age, maternal Ab, pregnancy, SA, Good seroconversion in babies- 93% Im administration not sc Booster doses at 5-10 yrs Mass hepatitis B Vaccination programmes: Kenya, Gambia, Cameroon CKiire Gutt 1996; 38: S5-S12 The serological response to hepatitis B vaccines is lower for HIV-infected children and adults than for uninfected persons of similar age. Serological response rates have varied, but most studies have reported that only 25–50% of HIV-infected children have developed protective antibodies. 126M – Hep B 20M- Hib 17m – Yellow fever 1.2 B single use syringes distributed for safe vaccination http://www.gavialliance.org Hepatitis B is a serious disease with serious complications and Chronicity Its a major contributing factor to HCC Has a variable prevalence with high endemicity in the developing world It is effectively preventable by the use of Vaccination