Journal List > Korean J Gastroenterol > v.63(1) > 1007221

Yoo, Kim, Jang, Choi, Moon, Park, Lee, Kim, Kim, Lee, Lee, Kim, Cho, and Jung: Clinical Features and Risk Factors for Severe Complications among Patients with Acute Hepatitis A Virus Infection in The Jeonbuk Province of Korea

Abstract

Background/Aims

The frequency of symptomatic acute HAV infections in adulthood are increasing in Korea. This study analyzes the clinical severity in patients with acute HAV infection and investigates risk factors associated with three severe complications: prolonged cholestasis, acute kidney injury, and acute liver failure.

Methods

We performed a retrospective analysis of 726 patients diagnosed from January 2006 to December 2010 at three tertiary hospitals in Jeonbuk Province, Republic of Korea with acute HAV infection.

Results

In the group of 726 patients, the mean age was 30.3 years, 426 (58.6%) were male, and 34 (4.7%) were HBsAg positive. Severe complications from acute HAV infection occurred as follows: prolonged cholestasis in 33 (4.6%), acute kidney injury in 17 (2.3%), and acute liver failure in 16 (2.2%). Through multivariate analysis, age ≥40 years (OR 2.63, p=0.024) and peak PT (INR) ≥1.5 (OR 5.81, p=0.035) were found to be significant risk factors for prolonged cholestasis. Age ≥40 years (OR 5.24, p=0.002) and female gender (OR 3.11, p=0.036) were significant risk factors for acute kidney injury. Age ≥40 years (OR 6.91, p=0.002), HBsAg positivity (OR 5.02, p=0.049), and peak total bilirubin (OR 1.11, p=0.001) were significant risk factors for acute liver failure.

Conclusions

Age ≥40 years, female gender, HBsAg positivity, peak PT (INR) ≥1.5, and peak total bilirubin were significant risk factors for severe complications in acute HAV infections.

References

1. Jeong SH, Lee HS. Hepatitis A: clinical manifestations and management. Intervirology. 2010; 53:15–19.
crossref
2. Lee H, Cho HK, Kim JH, Kim KH. Seroepidemiology of hepatitis A in Korea: changes over the past 30 years. J Korean Med Sci. 2011; 26:791–796.
crossref
3. Lee D, Cho YA, Park Y, et al. Hepatitis a in Korea: epidemiological shift and call for vaccine strategy. Intervirology. 2008; 51:70–74.
crossref
4. Lee D, Ki M, Lee A, et al. A nationwide seroprevalence of total antibody to hepatitis A virus from 2005 to 2009: age and area-ad-justed prevalence rates. Korean J Hepatol. 2011; 17:44–50.
crossref
5. Kang HM, Jeong SH, Kim JW, et al. Recent etiology and clinical features of acute viral hepatitis in a single center of Korea. Korean J Hepatol. 2007; 13:495–502.
crossref
6. Lee SS, Byoun YS, Jeong SH, et al. Type and cause of liver disease in Korea: single-center experience, 2005–2010. Clin Mol Hepatol. 2012; 18:309–315.
crossref
7. Lee TH, Kim SM, Lee GS, et al. Clinical features of acute hepatitis A in the Western part of Daejeon and Chungnam province: single center experience. Korean J Gastroenterol. 2006; 47:136–143.
8. Kim JI, Kim YS, Jung YK, et al. Factors influencing the severity of acute viral hepatitis A. Korean J Hepatol. 2010; 16:295–300.
crossref
9. Ajmera V, Xia G, Vaughan G, et al. Acute Liver Failure Study Group. What factors determine the severity of hepatitis A-related acute liver failure? J Viral Hepat. 2011; 18:e167–e174.
crossref
10. Jung YM, Park SJ, Kim JS, et al. Atypical manifestations of hepatitis A infection: a prospective, multicenter study in Korea. J Med Virol. 2010; 82:1318–1326.
crossref
11. Choi HK, Song YG, Han SH, et al. Clinical features and outcomes of acute kidney injury among patients with acute hepatitis A. J Clin Virol. 2011; 52:192–197.
crossref
12. Polson J, Lee WM. American Association for the Study of Liver Disease. AASLD position paper: the management of acute liver failure. Hepatology. 2005; 41:1179–1197.
crossref
13. Park HS, Choi BY, Kwon YD. Rapid increase in the national treatment costs for hepatitis A infections in Korea. Tohoku J Exp Med. 2011; 226:85–93.
crossref
14. Kim DY, Kim IH, Jeong SH, et al. A nationwide seroepidemiology of hepatitis C virus infection in South Korea. Liver Int. 2013; 33:586–594.
crossref
15. Cho HC, Paik SW, Kim YJ, et al. Seroprevalence of anti-HAV among patients with chronic viral liver disease. World J Gastroenterol. 2011; 17:236–241.
crossref
16. Almasio PL, Amoroso P. HAV infection in chronic liver disease: a rationale for vaccination. Vaccine. 2003; 21:2238–2241.
crossref
17. Chu CM, Liaw YF. Increased incidence of fulminant hepatic failure in previously unrecognized HBsAg carriers with acute hepatitis independent of etiology. Infection. 2005; 33:136–139.
crossref
18. Kim KM, Eo SJ, Gwak GY, et al. Comparison of the clinical features of hepatitis A between HBsAg-positive and HBsAg-negative patients. Gut Liver. 2011; 5:500–505.
crossref
19. Vento S, Garofano T, Renzini C, et al. Fulminant hepatitis associated with hepatitis A virus superinfection in patients with chronic hepatitis C. N Engl J Med. 1998; 338:286–290.
crossref
20. Willner IR, Uhl MD, Howard SC, Williams EQ, Riely CA, Waters B. Serious hepatitis A: an analysis of patients hospitalized during an urban epidemic in the United States. Ann Intern Med. 1998; 128:111–114.
crossref
21. Rezende G, Roque-Afonso AM, Samuel D, et al. Viral and clinical factors associated with the fulminant course of hepatitis A infection. Hepatology. 2003; 38:613–618.
crossref
22. Kim JH, Yeon JE, Baik SK, et al. Genotypic shift of the hepatitis A virus and its clinical impact on acute hepatitis A in Korea: a nationwide multicenter study. Scand J Infect Dis. 2013; 45:811–818.
crossref

Table 1.
Comparison of Clinical Characteristics of Acute HAV Infection Patients with the Presence of Prolonged Cholestasis
Variable Prolonged cholestasis (n=33) Non-cholestasis (n=693) p-value
Age (yr) 35.0±12.4 30.1±9.4 0.004
Age ≥40 years 9 (27.3) 83 (12.0) 0.010
Female 20 (60.6) 277 (40.0) 0.441
HBsAg positivity 1 (3.0) 33 (4.8) 0.646
Anti-HCV positivity 0 (0) 1 (0.1) >0.999
Laboratory values at admission      
 White blood cells (/mm3) 5,904±4,061 5,387±2,380 0.473
 Hemoglobin (g/dL) 14.4±1.9 14.4±1.7 0.915
 Platelet (103/mm3) 164.6±88.9 171.1±85.9 0.678
 Prothrombin time (INR) 1.4±0.5 1.2±0.3 0.019
 Prothrombin time (INR) ≥1.5 14 (42.4) 91 (13.1) <0.001
 Total bilirubin (mg/dL) 4.7±3.5 4.7±4.2 0.963
 AST (IU/L) 1,868±2,150 2,070±2,549 0.654
 ALT (IU/L) 2,084±1,993 2,290±1,916 0.548
 Creatinine (mg/dL) 0.7±0.2 0.8±0.3 0.440
Laboratory values at peak time      
 Prothrombin time (INR) 1.8±1.4 1.3±0.5 0.053
 Prothrombin time (INR) ≥1.5 14 (42.4) 123 (17.7) <0.001
 Total bilirubin (mg/dL) 20.3±11.8 6.4±3.6 <0.001
 AST (IU/L) 4,377±5,636 2,357±2,560 0.049
 ALT (IU/L) 3,208±2,772 2,665±1,976 0.275
 Creatinine (mg/dL) 2.0±2.8 1.0±0.9 0.065
Hospitalization time (day) 44.7±18.8 11.1±5.2 <0.001

All results were presented as mean±SD or n (%).

Table 2.
Comparison of Clinical Characteristics of Acute HAV Infection Patients with the Presence of Acute Kidney Injury
Variable Acute kidney injury (n=17) Non-acute kidney injury (n=709) p-value
Age (yr) 37.2±7.3 30.1±9.6 0.003
Age ≥40 years 7 (41.2) 85 (12.0) <0.001
Female 12 (70.6) 285 (40.2) 0.024
HBsAg positivity 1 (5.9) 33 (4.7) 0.562
Anti-HCV positivity 0 (0) 1 (0.1) >0.999
Laboratory values at admission      
 White blood cells (/mm3) 7,786±5,168 5,353±2,355 0.071
 Hemoglobin (g/dL) 14.6±2.7 14.4±1.7 0.767
 Platelet (103/mm3) 118.9±52.7 172.0±86.3 0.012
 Prothrombin time (INR) 1.4±0.4 1.2±0.3 0.046
 Prothrombin time (INR) ≥1.5 6 (35.3) 99 (14.0) 0.026
 Total bilirubin (mg/dL) 4.4±2.5 4.7±4.2 0.795
 AST (IU/L) 1,167±1,440 2,083±2,548 0.140
 ALT (IU/L) 1,858±1,491 2,291±1,927 0.359
 Creatinine (mg/dL) 0.8±0.2 0.8±0.3 0.850
Laboratory values at peak time      
 Prothrombin time (INR) 1.6±0.5 1.3±0.6 0.101
 Prothrombin time (INR) ≥1.5 9 (52.9) 128 (18.1) <0.001
 Total bilirubin (mg/dL) 11.6±9.5 6.9±5.0 0.058
 AST (IU/L) 5,056±7,040 2,386±2,595 0.138
 ALT (IU/L) 3,152±2,700 2,679±2,001 0.483
 Creatinine (mg/dL) 6.7±3.5 0.9±0.2 <0.001
Hospitalization time (day) 20.9±13.8 12.5±9.3 0.023

All results were presented as mean±SD or n (%).

Table 3.
Clinical Characteristics of Acute HAV Infection Patients with the Presence of Acute Liver Failure
Variable Acute liver failure (n=16) Non-acute liver failure (n=710) p-value
Age (yr) 38.6±9.0 30.1±9.5 0.002
Age ≥40 years 7 (43.8) 85 (12.0) <0.001
Female 8 (50.0) 289 (40.7) 0.455
HBsAg positivity 3 (18.8) 31 (4.4) 0.007
Anti-HCV positivity 0 (0) 1 (0.1) 0.881
Laboratory values at admission      
 White blood cells (/mm3) 6,052±5,772 5,395±2,359 0.656
 Hemoglobin (g/dL) 14.9±1.0 14.4±1.7 0.856
 Platelet (103/mm3) 119±33.8 171±86.4 <0.001
 Prothrombin time (INR) 1.8±0.5 1.2±0.3 <0.001
 Prothrombin time (INR) ≥1.5 12 (75.0) 92 (13.0) <0.001
 Total bilirubin (mg/dL) 4.3±3.6 4.7±4.2 0.676
 AST (IU/L) 3,038±4,285 2,039±2,478 0.367
 ALT (IU/L) 2,490±2,566 2,276±1,903 0.659
 Creatinine (mg/dL) 0.8±0.2 0.9±0.9 0.685
Laboratory values at peak time      
 Prothrombin time (INR) 2.5±1.7 1.3±0.5 0.013
 Prothrombin time (INR) ≥1.5 16 (100.0) 105 (14.8) <0.001
 Total bilirubin (mg/dL) 15.0±14.2 6.9±4.7 0.036
 AST (IU/L) 7,391±6,049 2,337±2,583 0.004
 ALT (IU/L) 5,049±1,890 2,636±1,991 0.001
 Creatinine (mg/dL) 2.4±3.1 1.1±1.3 0.111
Hospitalization time (day) 18.1±10.7 12.5±9.5 <0.001

All results were presented as mean±SD or n (%).

Table 4.
Risk Factors Associated with Three Major Complications of Acute HAV Infection (Multivariate Analysis)
Major complicaion OR 95% CI p-value
Prolonged cholestasis      
 Age ≥40 years 2.63 1.136–6.076 0.024
 Peak prothrombin time 5.81 1.132–29.774 0.035
 (INR) ≥1.5      
Acute kidney injury      
 Age ≥40 years 5.24 1.861–14.743 0.002
 Female 3.11 1.079–8.936 0.036
Acute liver failure      
 Age ≥40 years 6.91 2.001–23.849 0.002
 HBsAg positivity 5.02 1.005–25.022 0.049
 Peak total bilirubin 1.11 1.043–1.190 0.001
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