1.Predictors of Refractory Ascites Development in Patients with Hepatitis B Virus-Related Cirrhosis Hospitalized to Control Ascitic Decompensation.
Ju Hee SEO ; Seung Up KIM ; Jun Yong PARK ; Do Young KIM ; Kwang Hyub HAN ; Chae Yoon CHON ; Sang Hoon AHN
Yonsei Medical Journal 2013;54(1):145-153
PURPOSE: Refractory ascites (RA) is closely related to a high morbidity and mortality. In this study, we investigated predictors of RA development in patients with hepatitis B virus (HBV)-related cirrhosis who were hospitalized to control ascitic decompensation, and determined predictors for survival in patients who experienced RA. MATERIALS AND METHODS: We analyzed 199 consecutive patients with HBV-related cirrhosis who were hospitalized to control ascitic decompensation between January 1996 and December 2008. RESULTS: Multivariate analyses showed that only serum potassium at admission predicted RA development independently [p=0.013; hazard ratio (HR), 2.800; 95% confidence interval (CI), 1.166-6.722]. During the follow-up period, 16 (8.0%) patients experienced RA within 4.2 (range, 1.0-39.2) months after admission for controlling ascitic decompensation, and they survived a median of 8.7 (range, 3.9-51.3) months. Child-Pugh class and RA type were identified as independent prognostic factors affecting the survival in patients with RA (p=0.045; HR, 8.079; 95% CI, 1.231-67.984 and p=0.013; HR, 14.510; 95% CI, 1.771-118.874, respectively). CONCLUSION: Serum potassium was an independent predictor of RA development in patients with HBV-related cirrhosis who were hospitalized to control ascitic decompensation. After RA development, Child-Pugh class and RA type were independent predictors for survival.
Adult
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Aged
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Ascites/complications/*diagnosis/mortality
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Female
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Hepatitis B, Chronic/complications/mortality/*therapy
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Hospitalization
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Humans
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Liver Cirrhosis/complications/mortality/*therapy
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Liver Transplantation
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Male
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Middle Aged
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Multivariate Analysis
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Potassium/blood
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Prognosis
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Retrospective Studies
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Treatment Outcome
2.Bleeding complications in critically ill patients with liver cirrhosis.
Jaeyoung CHO ; Sun Mi CHOI ; Su Jong YU ; Young Sik PARK ; Chang Hoon LEE ; Sang Min LEE ; Jae Joon YIM ; Chul Gyu YOO ; Young Whan KIM ; Sung Koo HAN ; Jinwoo LEE
The Korean Journal of Internal Medicine 2016;31(2):288-295
BACKGROUND/AIMS: Patients with liver cirrhosis (LC) are at risk for critical events leading to Intensive Care Unit (ICU) admission. Coagulopathy in cirrhotic patients is complex and can lead to bleeding as well as thrombosis. The aim of this study was to investigate bleeding complications in critically ill patients with LC admitted to a medical ICU (MICU). METHODS: All adult patients admitted to our MICU with a diagnosis of LC from January 2006 to December 2012 were retrospectively assessed. Patients with major bleeding at the time of MICU admission were excluded from the analysis. RESULTS: A total of 205 patients were included in the analysis. The median patient age was 62 years, and 69.3% of the patients were male. The most common reason for MICU admission was acute respiratory failure (45.4%), followed by sepsis (27.3%). Major bleeding occurred in 25 patients (12.2%). The gastrointestinal tract was the most common site of bleeding (64%), followed by the respiratory tract (20%). In a multivariate analysis, a low platelet count at MICU admission (odds ratio [OR], 0.98; 95% confidence interval [CI], 0.97 to 0.99) and sepsis (OR, 8.35; 95% CI, 1.04 to 67.05) were independent risk factors for major bleeding. The ICU fatality rate was significantly greater among patients with major bleeding (84.0% vs. 58.9%, respectively; p = 0.015). CONCLUSIONS: Major bleeding occurred in 12.2% of critically ill cirrhotic patients admitted to the MICU. A low platelet count at MICU admission and sepsis were associated with an increased risk of major bleeding during the MICU stay. Further study is needed to better understand hemostasis in critically ill patients with LC.
Aged
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Blood Platelets
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Critical Illness
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Female
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Gastrointestinal Hemorrhage/blood/diagnosis/*etiology/mortality
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Hospital Mortality
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Humans
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Intensive Care Units
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Liver Cirrhosis/blood/*complications/diagnosis/mortality
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Male
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Middle Aged
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Multivariate Analysis
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Odds Ratio
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Platelet Count
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Prognosis
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Republic of Korea
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Respiratory Tract Diseases/blood/diagnosis/*etiology/mortality
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Retrospective Studies
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Risk Factors
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Sepsis/blood/complications
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Time Factors
3.Diagnostic value of cystatin C for predicting acute kidney injury in patients with liver cirrhosis.
Mi Yeon CHUNG ; Dae Won JUN ; Su Ah SUNG
The Korean Journal of Hepatology 2010;16(3):301-307
BACKGROUND/AIMS: The present study aimed to determine the role of cystatin C as a prognostic factor for acute kidney injury and survival in cirrhotic patients. METHODS: The study investigated 53 liver cirrhosis patients. The renal function was evaluated by serum creatinine, serum and urine cystatin C, and 24-hour creatinine clearance on admission. Acute kidney injury was defined as a serum creatinine level exceeding the normal range (>1.2 mg/dl) and an increase of at least 50% from the baseline value. Multivariate analysis, receiver operating characteristic curve, and survival analysis were used to investigate prognostic factors for acute kidney injury and survival. RESULTS: Nine of the 53 cirrhotic patients (17.0%) developed acute kidney injury within 3 months. Both serum creatinine and cystatin C were predictive factors for acute kidney injury in univariate analysis, with a diagnostic accuracy of 0.735 (95% confidence interval (CI), 0.525-0.945; p=0.028) for serum cystatin C and 0.698 (95% CI, 0.495-0.901, p=0.063) for creatinine. In multivariate analysis, only serum cystatin C was an independent risk factor for acute kidney injury. The sensitivity and specificity of a serum cystatin C level of >1.23 mg/L to acute kidney injury were 66% and 86%, respectively. Serum cystatin C was positively correlated with the Model for End-Stage Liver Disease (MELD) and MELD-Na scores (r=0.346 and p=0.011, and r=0.427 and p=0.001, respectively). Comparison of the survival rates over the observation period revealed that a serum cystatin C level of >1.23 mg/L was a useful marker for short-term mortality (p<0.001). CONCLUSIONS: The accuracy in predicting acute kidney injury and short-term mortality was higher for a serum cystatin C level of >1.23 mg/L than for the serum creatinine concentration in patients with cirrhosis.
Acute Kidney Injury/complications/*diagnosis/mortality
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Adult
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Aged
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Creatinine/blood
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Cystatin C/*analysis/blood/urine
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Female
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Humans
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Liver Cirrhosis/blood/*complications
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Male
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Middle Aged
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Multivariate Analysis
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Predictive Value of Tests
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ROC Curve
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Risk Factors
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Severity of Illness Index
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Survival Rate
4.Predictive factors that influence the survival rates in liver cirrhosis patients with spontaneous bacterial peritonitis.
Pei Chuan TSUNG ; Soo Hyung RYU ; In Hye CHA ; Hee Won CHO ; Jin Nam KIM ; You Sun KIM ; Jeong Seop MOON
Clinical and Molecular Hepatology 2013;19(2):131-139
BACKGROUND/AIMS: Spontaneous bacterial peritonitis (SBP) has been known to greatly influence the survival rate of patients with liver cirrhosis. However, the factors that affect the survival rate in patients with SBP need to be clarified. METHODS: This study enrolled 95 liver cirrhosis patients diagnosed with SBP. The laboratory findings of their serum and ascitic fluid were examined and the characteristics of the isolated microorganisms in their peritoneal fluid were analyzed. RESULTS: The proportion of patients with culture-positive SBP was 41.1%, and 47 microorganisms were isolated from the ascitic fluid. The proportions of cultured bacteria that were Gram negative and Gram positive were 57.4% and 40.4%, respectively. The proportions of Escherichia coli, Klebsiella species, and Streptococcus species were 25.5%, 19.1%, and 19.1%, respectively. Enterococcus species represented 12.8% of the microorganisms cultured. The overall survival rates at 6, 12, and 24 months were 44.5%, 37.4%, and 32.2%, respectively. There was no relationship between the bacterial factors and the survival rate in SBP. Multivariate analysis revealed that the presence of hepatocellular carcinoma (HCC; P=0.001), higher serum bilirubin levels (> or =3 mg/dL, P=0.002), a prolonged serum prothrombin time (i.e., international normalized ratio >2.3, P<0.001), renal dysfunction (creatinine >1.3 mg/dL, P<0.001), and lower glucose levels in the ascitic fluid (<50 mg/dL, P<0.001) were independent predictive factors of overall survival rate. CONCLUSIONS: HCC, higher serum bilirubin levels, a prolonged serum prothrombin time, renal dysfunction, and lower ascitic glucose levels are associated with higher mortality rates in cirrhotic patients with SBP.
Adult
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Aged
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Anti-Bacterial Agents/therapeutic use
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Ascitic Fluid/metabolism/microbiology
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Bilirubin/blood
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Carcinoma, Hepatocellular/complications/diagnosis
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Creatinine/blood
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Female
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Glucose/analysis
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Gram-Negative Bacteria/isolation & purification
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Gram-Positive Bacteria/isolation & purification
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Humans
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Liver Cirrhosis/complications/*mortality
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Liver Neoplasms/complications/diagnosis
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Male
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Middle Aged
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Multivariate Analysis
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Odds Ratio
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Peritonitis/complications/*diagnosis/drug therapy
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Prognosis
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Prothrombin Time
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Survival Rate
5.Hepatic Venous Pressure Gradient Predicts Long-Term Mortality in Patients with Decompensated Cirrhosis.
Tae Yeob KIM ; Jae Gon LEE ; Joo Hyun SOHN ; Ji Yeoun KIM ; Sun Min KIM ; Jinoo KIM ; Woo Kyoung JEONG
Yonsei Medical Journal 2016;57(1):138-145
PURPOSE: The present study aimed to investigate the role of hepatic venous pressure gradient (HVPG) for prediction of long-term mortality in patients with decompensated cirrhosis. MATERIALS AND METHODS: Clinical data from 97 non-critically-ill cirrhotic patients with HVPG measurements were retrospectively and consecutively collected between 2009 and 2012. Patients were classified according to clinical stages and presence of ascites. The prognostic accuracy of HVPG for death, survival curves, and hazard ratios were analyzed. RESULTS: During a median follow-up of 24 (interquartile range, 13-36) months, 22 patients (22.7%) died. The area under the receiver operating characteristics curves of HVPG for predicting 1-year, 2-year, and overall mortality were 0.801, 0.737, and 0.687, respectively (all p<0.01). The best cut-off value of HVPG for predicting long-term overall mortality in all patients was 17 mm Hg. The mortality rates at 1 and 2 years were 8.9% and 19.2%, respectively: 1.9% and 11.9% with HVPG < or =17 mm Hg and 16.2% and 29.4% with HVPG >17 mm Hg, respectively (p=0.015). In the ascites group, the mortality rates at 1 and 2 years were 3.9% and 17.6% with HVPG < or =17 mm Hg and 17.5% and 35.2% with HVPG >17 mm Hg, respectively (p=0.044). Regarding the risk factors for mortality, both HVPG and model for end-stage liver disease were positively related with long-term mortality in all patients. Particularly, for the patients with ascites, both prothrombin time and HVPG were independent risk factors for predicting poor outcomes. CONCLUSION: HVPG is useful for predicting the long-term mortality in patients with decompensated cirrhosis, especially in the presence of ascites.
Adult
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Aged
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Ascites/mortality
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Female
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Hepatic Veins/*physiopathology
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Humans
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Kaplan-Meier Estimate
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Liver Cirrhosis/blood/complications/diagnosis/*mortality/*physiopathology
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Liver Failure/diagnosis/*mortality/physiopathology
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Male
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Middle Aged
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Predictive Value of Tests
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Prognosis
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Proportional Hazards Models
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ROC Curve
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Retrospective Studies
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Risk Factors
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Severity of Illness Index
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Venous Pressure
6.Five-Year Review of HIV-Hepatitis B Virus (HBV) Co-Infected Patients in a New York City AIDS Center.
Jong Hun KIM ; George PSEVDOS ; Victoria SHARP
Journal of Korean Medical Science 2012;27(7):830-833
A retrospective review of 4,721 human immunodeficiency virus (HIV)-infected patients, followed at St. Luke's Roosevelt Hospital Center, New York City, was conducted from January 1, 2005 to December 31, 2009. HIV-Hepatitis B virus (HBV) co-infection rate was 218/4,721, 4.6%. Among co-infected patients, 19 patients (19/218, 8.7%) died; 13 patients (13/19, 68.4%) died from non-acquired immune deficiency syndrome (AIDS) defining including 2 patients with liver failure. More non-survivors (5 patients, 5/19, 26.3%) had liver cirrhosis than those who survived (8 patients, 8/199, 4.0%; P = 0.002). There were more patients with positive HBV e antigen (HBeAg) among non-survivors, (12 patients, 12/19, 63.2%) than among survivors (74 patients, 74/199, 37.2%; P = 0.047). HIV-HBV co-infection is associated with increased overall mortality. Therefore, use of dual active antiretrovirals, particularly, tenofovir (TDF) based regimen for optimal suppression of HIV-HBV and immune restoration with prevention of high risk behaviors may contribute to improved outcomes.
Adenine/analogs & derivatives/therapeutic use
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Adult
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Anti-HIV Agents/therapeutic use
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Coinfection/drug therapy/mortality
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Female
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HIV Infections/complications/*diagnosis/drug therapy
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Hepatitis B/complications/*diagnosis/drug therapy
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Hepatitis B e Antigens/blood
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Humans
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Liver Cirrhosis/etiology
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Male
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Middle Aged
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New York City
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Organophosphonates/therapeutic use
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Retrospective Studies
7.Rescue therapy with adefovir in decompensated liver cirrhosis patients with lamivudine-resistant hepatitis B virus.
Hyun Young WOO ; Jong Young CHOI ; Seung Kew YOON ; Dong Jin SUH ; Seung Woon PAIK ; Kwang Hyub HAN ; Soon Ho UM ; Byung Ik KIM ; Heon Ju LEE ; Mong CHO ; Chun Kyon LEE ; Dong Joon KIM ; Jae Seok HWANG
Clinical and Molecular Hepatology 2014;20(2):168-176
BACKGROUND/AIMS: Adefovir dipivoxil (ADV) is a nucleotide analogue that is effective against lamivudine-resistant hepatitis B virus (HBV). The aim of this study was to determine the long-term clinical outcomes after ADV rescue therapy in decompensated patients infected with lamivudine-resistant HBV. METHODS: In total, 128 patients with a decompensated state and lamivudine-resistant HBV were treated with ADV at a dosage of 10 mg/day for a median of 33 months in this multicenter cohort study. RESULTS: Following ADV treatment, 86 (72.3%) of 119 patients experienced a decrease in Child-Pugh score of at least 2 points, and the overall end-stage liver disease score decreased from 16+/-5 to 14+/-10 (mean +/- SD, P<0.001) during the follow-up period. With ADV treatment, 67 patients (56.3%) had undetectable serum HBV DNA (detection limit, 0.5 pg/mL). Virologic breakthrough occurred in 38 patients (36.1%) and 9 patients had a suboptimal ADV response. The overall survival rate was 89.9% (107/119), and a suboptimal response to ADV treatment was associated with both no improvement in Child-Pugh score (> or =2 points; P=0.001) and high mortality following ADV rescue therapy (P=0.012). CONCLUSIONS: Three years of ADV treatment was effective and safe in decompensated patients with lamivudine-resistant HBV.
Adenine/*analogs & derivatives/therapeutic use
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Adult
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Aged
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Antiviral Agents/*therapeutic use
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Cohort Studies
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DNA, Viral/blood
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Drug Resistance, Viral
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Female
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Hepatitis B/complications/*drug therapy
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Hepatitis B e Antigens/blood
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Hepatitis B virus/genetics
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Humans
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Lamivudine/*therapeutic use
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Liver Cirrhosis/*diagnosis/etiology/mortality
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Male
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Middle Aged
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Odds Ratio
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Organophosphonates/*therapeutic use
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Retrospective Studies
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Severity of Illness Index
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Survival Rate