hepatitis Flashcards

(33 cards)

1
Q

what is viral hepatitis?

A

Systemic disease caused by viral agents whose primary tissue tropism is the liver

5 well recognized HEPATOTROPIC VIRUSES:

A,b,c,d,e

can happen with other viruses includin :

CMV, Epstein barr virus , Yellow fever virus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

describe hepatitis viruses ?

A

5 types : A,B,C,D,E

Target organ for these viruses is the LIVER ( Tropism )

Basic hepatitis symptoms are similar

Viruses Differ greatly in structure, mode of Replication , mode of transmission, duration of ILLNESS and disease outcome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

which hepatitis virus is transmitted enterically ?

A

A –> mildest and most common

E

FECA/ORAL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

which hepatitis viruses are Parentally transmitted ?

A

B–> serious and live threating

C—> chronicity

D

Either by sex or blood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

describe HAV?

A

Causes about 25-50% of acute hepatitis worldwide –> Cause infectious hepatitis/ epidemic hepatitis

RNA virus

NON-ENVELOPED

Only one stable serotype of HAV –> Difficult to grow in cell culture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how is HAV transmitted?

A

Fecal-oral route

Contaminated food or water ( INFECTED FOOD HANDLERS - RAAW SHELLFISH )

Close personal contact ( Household contact, childday care centers

Inactivated by BOILING FOR 1 MINUTE

Survive prolonged storage at 4 C or below ( survive cold temp )

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

describe pathogenesis of HAV?

A

Incubation period 2-6 weeks = mean 1 month

Replicate in the alimentary tract and spread to the LIVER where it multiplies HEPATOCYTRES

Viraemia is transient = ( virus in blood )

ASYMPTOMATIC INFECTIONS ( very common in children )

Severe disease in adults ( pregnant women )

NO CHRONIC FORM ( ONLY ACUTE )

Complications –> Fulminant hepatitis ( RARE 0.1 )

AGGRESSIVE IN IMMUNODEFICIENT PATIENTS

SELF LIMITING

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe prodromal/ pre icteric phase of HAV?

A

symptoms include :

Fatigue, joint, abdominal pain, malaise , vomitting, lack of appetite, hepatomegaly

its in the initial viral replication stage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

describe icteric phase of HAV?

A

Jaundice–> SKIN , sclera, mucous membrane

Caused by elevated biliruib lvl, bilirubinuria , dark urine, pale stool

Classical presentation of HAV is scleral icterus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Diagnosis of HAV?

A

Signs and Symptoms of acute hepatitis

Elevated LIVER enzymes ( LFTS )

AntiHAV igM antibodies –> APPEAR EARLY AND REMAIN DETECTABLE FOR 4-16 WEEKS

About 1/3 of asymptomatic population may also have anti HAV igG

DIAGNOSIS OF HAV BY IGM IS VERY SPECIFIC TO HEP A

igM then become igG which protect you throughout life

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

HAV prevention ?

A

Killed vaccine

From children from age 2 years

Susceptible adults for high risk of infection

Travelers to endemic areas

Close personal contacts

Food handlers

We dont have treatment only supportive one but we use vaccines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

clues about HEP A?

A

no chronicity ( cuz its only acute and mild )

RNA VIRUS ( non enveloped )

Food handlers

Daycare

Acute onset

OUT BREAK

Asymptomatic management

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

describe HBV?

A

mainly in serum hepatitis/post transfusional hepatitis ( blood or sex )

Small enveloped DNA virus ( hav was rna and non enveloped )

Hepandvirus group

Circular partially DOUBLE stranded DNA viruses ( the DNA strand is not complete )

Has reverse transcriptase ( To complete the DNA strand )

HAS NOT YET BEEN POSSIBLE TO PROPAGATE THE VIRUS IN THE CELL CULTURE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

HBV structure and Antigens ?

A

HbsAG = surface coat protein –> attachment–> virulence factor

HBcAg= Inner core protein

HbeAg= Secreted protein; Function unkown

HBsAg = comes out a lot to distract immune system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How is HBV transmitted?

A

Virus present in blood , SEMEN, saliva , vaginal fluid

HIGHLY infectious- Remain on environmental surface for at least 7 days -> Sex workers, mother to son during birth when blood spills , IV drug abusers, Health workers

Urine, feces, vomitus, nasopharyngeal washing, sputum, sweat, , are not efficient vehicles of transmission unless they CONTAIN BLOOD

HBsAg –> found in breast milk –> unlikely to lead transmission - not a contraindication to breastfeeding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Clinical features of HBV?

A

from asympotmatic infection to FULMINANT HEPATITIS

Average incubation period is 60 days ( 40-90 ) during this time its asymptomatic

Infant, children aged less than 5 years and immunosuppressed adults with newly acquired HBV infection typically are ASYMPTOMATIC

Symptomatic illness is noted in 30-50% of older children, adolscents and adults

When present –> Nausea, vomiting, abdominal pain, fever, dark urine, changes in stool color, hepatomegaly , splenomegaly, jaundice ( when jaundice occur this is icteric phase )

Fullminant HBV infection is uncommon less than 1% but often results in death or liver failure, necessiltating liver transplant

Extrahepatic manifestation –> Skin rash, arthrraglias, arthritis

Fatality rate among persons with reported cases of acute HBV infections is less than 1.5% with highest rates in adults aged older than 55 years

CASUALLY ASSOCIATED WITH HEPATOCELLULARLY CARCINOMA ( PHC )

17
Q

diagnosis of HBV?

A

Signs and Symptoms

Elevated LFT

CONFIRMED BY SEROLOGY :

HBsAg –> surface antigen
HBsAb/antiHBs –> antibody to surface antigen
HBcAb/anti HBc–> antibody to core antigen
HBeAg—> E antigen
HBeAb/anti HBe—> antibody to E antigen

CAN SEE C ANTIGEN CUZ ITS CORE

PCR to detect infectious virion nad estimate viral load

18
Q

Describe HBV serology?

A

HBsAg –> general marker for infection

HBsAb(body)- document recovery and or immunity to HBV

Anti-HBc IgM —> Acute infection

anti-HBc igG —-> Past or chronic infection

HBeAg —> indicates active replication of virus

AntiHBe–> virus no longer replicating but PERSISTING

19
Q

panel of someone immune du to natural infection?

A

Negative surface antigen

Positive antibody for core antigen ( igG)

Positive antibody for surface antigen

20
Q

panel of someone whos immune to vaccination ?

A

Negative surface antigen

Negative antibody for core antigen ( cuz never encountered the virus )

Positive antibody for surface antigen

when you have antibody for surface urs immune

20
Q

panel of someone acutely infected?

A

Positive surface antigen

Positive/negative igG for core antigen

Positive igM for core antigen

Negative antibody for surface antigen

21
Q

panel for chronic infectionn?

A

Positive surface antigen

Positive igG for core antigen

Negative for igM for core antigen ( cuz it goes down )

Negative antibody for surface antigen

22
Q

describe HBV acute infection?

A

Detection of both surface antigen and igM for core antigen and antigen E in blood

indicates ongoing infection

23
Q

describe chronic hepatitis ?

A

Marked by presence of surface antigen for 6 month or more and antibody for CORE antigen

24
describe chronic infection ?
80-90% of persons infected during infancy 30% persons infected before 5 years less than 1%-12% of person infected as older child or adult
25
Treatment of HBV? chronic
interferons nucleoside/nucleotide analogues
26
prevention of HBV?
vaccine --> pre-exposure or active immunity Education HBIG--> post exposure, passive immunity
27
describe HBV vaccines?
first vaccines consisted of Plasma derived surface antigen Recombinant HBV vaccines containing YEAST derived surface antigen 3 dose series ( day 0, day 30, 6 monnth ) If dose is missed continue where with the next scheduled dose if someone has titer antibody more than 10 = immune if its less u need booster the vaccines give u more than 10 antibody titer
28
Post exposure prophylaxis ?
Would and skin sites that have been contact with blood or body fluits should be washed with soap or water For people who are vaccinated as has more than 10 titer no need for post exposure prophylaxis IF person has the less than 10 titer and the source of the surface antigen is UNKNOWN = passive immunity = give antibodies and revaccinate later ( 2 doses 1 month apart )
29
describe hepatitis C?
Positive strand RNA enveloped virus Endemic world-wide -- high incidence in japan, italy, spain, classified into a total of six geno types 1-6 Genotype 1 and 4 has poorer prognosis and response to interferone therapy Transmission similar to hepatitis B Usually ASYMPTOAMTIC or MILD DISEASE Chronic infection is very common 70% ( C for chronicity ) Complications : Chronic liver disease , Hepatocellular carcinoma
30
how is hepatitis C diagnosed ?
HCV antibody --> at least 4 weeks after infection b4 antibody appears HCV RNA --> PCR and branched DNA used to diagnose HCV infection in acute phase HCV antigen --> EIA for HCV antigen is available
31
treatment of HCV?
Ribavirin + IFN alpha Ribavirin is guanosine analong/inhibit nucleoside synthesis/inhibit RNA synthesis INF alpha or pegylated interferon enhance its biologic lifetime NEWER DRUGS --> Sovaldi, Harvoni Genotyping --> 1 and 4 have wors prognosis and poor to treatment
32
Prevention of HCV?
Screening of blood, organ , tissue bonors Blood and body fluid precautions Education risk factors from good to worse BLOOD > SEX > PERINATAL ( same as hep B) NO VACCINES AVAILABLE