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1.
Dig Dis Sci ; 63(10): 2813-2814, 2018 10.
Article in English | MEDLINE | ID: mdl-30043282

ABSTRACT

The original version of the article unfortunately contained errors in Table 3, Risk Factor column headings "Age > 50 (n = 115)," "Age > 50-64 (n = 154)," and "Age > 65 + (n = 60)."

2.
Dig Dis Sci ; 63(9): 2259-2266, 2018 09.
Article in English | MEDLINE | ID: mdl-29779083

ABSTRACT

BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease. Severe NAFLD with advanced fibrosis results in substantial morbidity and mortality. Associated with metabolic syndrome, NAFLD is often initially clinically silent, yet intensive lifestyle intervention with 7% or greater weight loss can improve or resolve NAFLD. Using a Veterans Health Administration (VHA) liver biopsy cohort, we evaluated simple noninvasive fibrosis scoring systems to identify NAFLD with advanced fibrosis (or severe disease) to assist providers. METHODS: In our retrospective study of a national VHA sample of patients with biopsy-proven NAFLD or normal liver (2005-2015), we segregated patients by fibrosis stage (0-4). Non-NAFLD liver disease was excluded. We evaluated the diagnostic accuracy of the NAFLD fibrosis score (NFS), fibrosis-4 calculator (FIB-4), aspartate aminotransferase-to-alanine aminotransferase ratio (AST/ALT ratio), AST-to-platelet ratio index (APRI), and body mass index, AST/ALT ratio, and diabetes (BARD) score by age groups. RESULTS: We included 329 patients with well-defined liver histology (296 NAFLD and 33 normal controls without fibrosis), in which 92 (28%) had advanced (stage 3-4) fibrosis. Across all age groups, NFS and FIB-4 best predicted advanced fibrosis (NFS with 0.676 threshold: AUROC 0.71-0.76, LR + 2.30-22.05, OR 6.00-39.58; FIB-4 with 2.67 threshold: AUROC of 0.62-0.80, LR + 4.70-27.45, OR 16.34-59.65). CONCLUSIONS: While NFS and FIB-4 scores exhibit good diagnostic accuracy, FIB-4 is optimal in identifying NAFLD advanced fibrosis in the VHA. Easily implemented as a point-of-care clinical test, FIB-4 can be useful in directing patients that are most likely to have advanced fibrosis to GI/hepatology consultation and follow-up.


Subject(s)
Decision Support Techniques , Liver Cirrhosis/diagnosis , Liver/pathology , Non-alcoholic Fatty Liver Disease/diagnosis , United States Department of Veterans Affairs , Veterans Health , Adolescent , Adult , Aged , Alanine Transaminase/blood , Area Under Curve , Aspartate Aminotransferases/blood , Biomarkers/blood , Biopsy , Body Mass Index , Clinical Enzyme Tests , Databases, Factual , Diabetes Mellitus/diagnosis , Diabetes Mellitus/epidemiology , Female , Health Status , Humans , Liver Cirrhosis/blood , Liver Cirrhosis/epidemiology , Liver Cirrhosis/pathology , Male , Middle Aged , Non-alcoholic Fatty Liver Disease/blood , Non-alcoholic Fatty Liver Disease/epidemiology , Non-alcoholic Fatty Liver Disease/pathology , Platelet Count , Point-of-Care Testing , Predictive Value of Tests , Prevalence , Prognosis , ROC Curve , Reproducibility of Results , Retrospective Studies , Risk Factors , Severity of Illness Index , United States/epidemiology , Young Adult
3.
Contemp Clin Trials ; 50: 5-15, 2016 09.
Article in English | MEDLINE | ID: mdl-27417982

ABSTRACT

Despite the availability of efficacious treatments, only half of patients with hypertension achieve adequate blood pressure (BP) control. This paper describes the protocol and baseline subject characteristics of a 2-arm, 18-month randomized clinical trial of titrated disease management (TDM) for patients with pharmaceutically-treated hypertension for whom systolic blood pressure (SBP) is not controlled (≥140mmHg for non-diabetic or ≥130mmHg for diabetic patients). The trial is being conducted among patients of four clinic locations associated with a Veterans Affairs Medical Center. An intervention arm has a TDM strategy in which patients' hypertension control at baseline, 6, and 12months determines the resource intensity of disease management. Intensity levels include: a low-intensity strategy utilizing a licensed practical nurse to provide bi-monthly, non-tailored behavioral support calls to patients whose SBP comes under control; medium-intensity strategy utilizing a registered nurse to provide monthly tailored behavioral support telephone calls plus home BP monitoring; and high-intensity strategy utilizing a pharmacist to provide monthly tailored behavioral support telephone calls, home BP monitoring, and pharmacist-directed medication management. Control arm patients receive the low-intensity strategy regardless of BP control. The primary outcome is SBP. There are 385 randomized (192 intervention; 193 control) veterans that are predominately older (mean age 63.5years) men (92.5%). 61.8% are African American, and the mean baseline SBP for all subjects is 143.6mmHg. This trial will determine if a disease management program that is titrated by matching the intensity of resources to patients' BP control leads to superior outcomes compared to a low-intensity management strategy.


Subject(s)
Antihypertensive Agents/therapeutic use , Disease Management , Hypertension/drug therapy , Research Design , Adolescent , Adult , Black or African American , Age Factors , Aged , Antihypertensive Agents/administration & dosage , Behavior Therapy/methods , Blood Pressure Monitoring, Ambulatory , Exercise , Female , Health Behavior , Humans , Hypertension/therapy , Male , Medication Therapy Management/organization & administration , Middle Aged , Patient Care Team/organization & administration , Sex Factors , United States , United States Department of Veterans Affairs , Young Adult
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