Title: Clinical Course
1Clinical Course
- 10/09/2000 admission at FEMH
- 48y/o male, presented with
- General malaise, poor appetite and abd.
discomfort for 2 wks - Icteric sclera, tea-color urine, BWL (84?79Kgw in
2 wks) - Past history
- Operation, transfusion or systemic disease nil
- Alcoholism for 20 years (??, ½ BPD quitted 3
months ago for fear of BWG) - HBV infection, noted since 10 years ago
deterioration of LFT in recent 4 years - Herb drug 6 days ago for the C.C. and reducing
body weight (?, 1?/?, 3 days) - Family history
- Father (87y/o) HCC
2- Lab.
- GOT 1040, GPT 1405, PT 43.7(11.9), Bil. (T/D)
19.3/11.1, ammonia 111 ?M/L, AFP 207 ng/ml - HBsAg(), HBeAg(-), Anti-HBe(), anti-HCV(-)
- Sonography CLPD, no ascites
- Supportive care, including Lamivudine 100mg/day
(starting on 10/11) - Clear consciousness but deteriorated lab.
- For impending hepatic failure, pt was
transferred to NTUH on 10/13/2000
3- 10/13/2000 admission at NTUH
- Lab.
- HBV DNA 1.47 pg/ml(??PCR, lt0.5 pg/ml),
anti-Delta (-), anti-HAV IgM(-), CMV IgM(-),
EBV-VCA IM(-), HSV (-) - ANA(-), Ceruloplasmin 22.7 mg/dl (-)
- Clinical condition
- Deterioration with ongoing drowsy consciousness,
hyperbilirubinemia, and prolonged PT - Complicated with UGI bleeding
4- 10/19/2000 transfer to SICU
- Dialysis with Biological DT system for 5 times
- Renal shut down, presented with progressive
decreased urine amount, since 10/21 - B/C grew Candida albican S/C grew MRSA,
Neisseria and Yeast-like organisms then,
strongest antibiotics (Imepinem and Amphotericin
B) were used on 10/25 but sepsis seemed
intractable - Continuous venous-venous hemodialysis was started
on 10/27 for renal failure - Bradycardia and hypotension developed on 11/1 and
then recurred even using high dose of
vasopressors and inotropes - Expire was declared on the same day (11/1)
5Serial lab. after transfer to SICU
648y/o male Alcoholism for 20 years HBV carrier
for 10 years
2wks
General malaise, poor appetite and abd.
discomfort
6 days
Herbs, 3 days use for weight reduction and above
symptoms
Icteric sclera, tea-color urine, BWL (5Kgw in 2
weeks)
At FEMH GOT/GPT, Bil(T), PT, NH3, AFP HBsAg(),
HBeAg(-), Anti-HBe(), Anti-HCV(-) Start
Lamivudine 100mg/day on 10/11 Deterioration of
clinical condition
10/9
10/13
At NTUH, GOT/GPT, Bil(T), PT, AFP HBV DNA 1.47
pg/ml HAV, HDV, CMV, EBV, HSV, ANA,
Wilsons(-) Deterioration with ongoing drowsy
consciousness, ?Bil.,?PT
10/19
At SICU Dialysis with Biological DT system,
5X ARF(CVVH), Sepsis (Fungemia Bacteremia)
Expire
11/1
7Acute exacerbation
Supportive care Lamivudine
AHF
Herbs
Biological DT system
MOF
ARF Sepsis
Antibiotics CVVH
Death
8Acute hepatic failureFulminant hepatitis,
fulminant hepatic failure
- Definition by IASL(1996)
- Interval between onset of jaundice and
encephalopathy lt 4 wks - 2 most important complications cerebral edema
and sepsis - Prognostic markers age gt 40 yrs, bilirubin gt 15
mg/dl, PT prolongation gt 25s, cerebral edema (3
or 4 factors, MR gt 90)
9Liver transplantation
- Urgent LT is now the standard Tx for AHF
- One year survival rate 46-89
- Main problems lack of donor livers and few
qualified centers
10Alternatives to LT
- Bridge to LT
- Hepatocyte transplantation, liver-directed gene
therapy, xenotransplantation, extracorporeal
liver support, tissue-engineered organs - Using biological DT system, 4/20 survived
(including 2 FHB, 1 flare-up of HBV) - WJ Ko (ISFA, 2001)
11Acute exacerbation
Supportive care Lamivudine
AHF
Herbs
Biological DT system
MOF
ARF Sepsis
Antibiotics CVVH
Death
12Alcoholic liver disease
- Fatty liver ? Alcoholic hepatitis ? Cirrhosis ?
Hepatoma - Dose and duration dependent (80g/day for 10 yrs
?) - Risk factors female, viral hepatitis, gene,
nutrition - ??(45) 150 cc/day (YF Liaw TJ Chen, 1992)
-
(Small 55, 300cc)
13Alcoholic hepatitis
- GOT/GPT gt 2
- GOT lt 300 IU/dl
- ? Alk-p and ?-GT(15X)
14ALD and HBV
- Alcohol consumption intensifies the liver disease
caused by HBV - Nomura (AJE, 1988)
- Asymptomatic HBV carriers were at risk of hepatic
abnormalities when drinking more than 80g/day - Villa (Lancet, 1982)
15More severe Chronic liver injury
Limited illness
Rapid downhill course
Acute Flare-up
HBeAg Clearance
Mutant HBV
Hepatoma
Chronic hepatitis B
Spontaneous reactivation
Hepatitis A
Hepatitis E ?
Drug reaction
Hepatitis C
Corticosteroid Immuosuppressant C/T
Hepatitis D
16Viral superinfection in chronic HBV carrier
17Superinfection of hepatitis C
18Rapid downhill course
Acute Flare-up
HBeAg Clearance
Mutant HBV
Chronic hepatitis B
Drug reaction
19Natural course of chronic hepatitis B
20Natural course of chronic hepatitis B
- Indicators of HBV replication
- HBeAg HBV DNA in serum
21SeroconversionHBeAg(-), Anti-HBe()
- 17 per year male gt female
- Liaw (1983,1984)
- Cessation of HBV replication and clinical
biochemical resolution - Realdi (1980), Hoofnagle(1981), Sanchez(1984)
22Decompensation in seroconversionIS Sheen
(Gastroenterology, 1985)
- 376 HBeAg(), 7 years
- 165 HBeAg clearance (seroconversion)
- 4 hepatic decompensation (2.42) and one died
23Window period of seroconversionYF Liaw
(Hepatology, 1984)
- Anti-HBe appeared in days to years after
disappearance of HBeAg - 79 in one year
- 41 in one month
- Shortest is 9 days
- Longest is 3 years
- Shorter in patient with AE
Patient Profile HBeAg(-) Anti-HBe()
24AFP in hepatitis B with AEYF Liaw (Liver, 1984)
Patient Profile AFP 207
25Rapid downhill course
Acute Flare-up
HBeAg Clearance
Mutant HBV
Chronic hepatitis B
Drug reaction
26AE in Anti-HBe() HBV DNA()
- AE in Anti-HBe() vs. HBeAg()
- Incidence/year 10.3 vs. 26.8 (plt0.001)
- Bilirubin and AFP slightly higher in Anti-HBe()
- No significance in S/S, GPT and histology
- 62.5 with HBV DNA () reactivation of HBV
infection - YF Liaw (Hepatology, 1987)
- 16 non-cirrhotic Anti-HBe() with AE
- 88 (14/16) with HBV-DNA() reactivation of HBV
infection - MY Lai (Hepato-gastroenterology, 1988)
27Detection of HBV DNA
- Real-time Quantitative PCR
- HBV DNA 1.47 pg/ml ( lt 0.5 0.05 pg/ml)
- 30 X of the minimal detectable titer
?????
28HBV DNA in relation to GPTYF Liaw (Liver, 1988)
29Role of HBV DNA
- An absence or low levels of circulating HBV DNA
(PCR) in the serum on HBV replication - Hepatocellular injury is a likely sequela of the
host immune response to HBV Ag and is not due to
a direct cytopathic effect of the virus
HBV-DNA pg/ml
0
9
0-250
78
67
251-500
CAHCLH
501-1000
20
8
CM CHU (Hepatology,1985)
gt1000
30Pre-Core mutants of HBV
- Carman (Lancet, 1989)
- 7 of 8 anti-HBe() HBV DNA() (mostly CAH)
- TGG?TAG (stop codon) (G-to-A substitution at
nucleotide 1896) resulting in failure to produce
HBeAg - Low prevalence in fulminant hepatitis B in France
and North America(lt10) but high in Israel and
Japan (80-100)
31Pre-Core mutant in TaiwanCM Chu (J Clin
Microbiol, 1996)
Immune tolerance phase Wild type HBV
predominant Immnue clearance phase Precore
mutant emerging Immune integrated phase Precore
mutant prevailing
32Pre-Core mutants after seroconversionRN Chien
(Spring convention, 2000)
- After spontaneous seroconversion
- 67 remain stable
- 33 have AE
- 70 precore mutant (23 of all)
- 21 re-appearance of HBeAg (5 of all)
33AFP in hepatitis B with AEYF Liaw (Liver, 1986)
Patient Profile AFP 207
34Benefit of Lamivudine in AERN Chien (Spring
convention, 2000)
- Hepatitis B with AE (? Bil. PT)
- Lamivudine 150mg/d for 8 weeks
35Rapid downhill course
Acute Flare-up
HBeAg Clearance
Mutant HBV
Chronic hepatitis B
Drug reaction
36????????
- ?????
- ??,??,??,??,??,???,???,???,??,??
- ?????
- ??,??,???,??,??,???,??,???,??,??
- ????
- ??,??,??,??,??,??,??
37?? Scutellariae Radix
- ????
- Liver injuries induced by herbal medicine,
syo-saiko-to (xiao-chai-hu-tang). - Itoh S. (DDS, 1995)
38??? Moutan Radicis Cortex
- ?????
- Hepatitis induced by traditional Chinese herbs
Possible toxic components. - Kane JA. (Gut, 1995)
39?? Gentianae Radix
- ?????
- Hepatitis induced by traditional Chinese herbs
Possible toxic components. - Kane JA. (Gut, 1995)
40Herbal drugs related hepatotoxicity
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43Acute exacerbation
Supportive care Lamivudine
AHF
Herbs
Biological DT system
MOF
ARF Sepsis
Antibiotics CVVH
Death
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