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6.
Am J Gastroenterol ; 116(8): 1585, 2021 Aug 01.
Article in English | MEDLINE | ID: mdl-37461860

ABSTRACT

Article Title: A microsimulation model to determine the cost-effectiveness of treat to target strategies for Crohn's disease.

7.
Am J Gastroenterol ; 114(9): 1417, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31490225

ABSTRACT

Article Title: Inflammatory Bowel Disease: A Practical Path to Transitioning from Pediatric to Adult Care.

8.
Am J Gastroenterol ; 114(4): 552, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30950858

ABSTRACT

To receive CME/MOC credit for this activity, please go to: http://acgjournalcme.gi.org/Article Title: Diagnosis and Treatment of Rumination Syndrome: A Critical Review.

9.
Am J Gastroenterol ; 113(10): 1430, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30356159
10.
Dig Dis Sci ; 63(6): 1551-1557, 2018 06.
Article in English | MEDLINE | ID: mdl-29663266

ABSTRACT

BACKGROUND: Practice guidelines recommend screening for hepatitis B virus (HBV) infection prior to initiating treatment of inflammatory bowel disease (IBD) with anti-tumor necrosis factor (anti-TNF) therapy. However, the adherence to these screening guidelines and the clinical outcomes of HBV reactivation following anti-TNF use are not well known. METHODS: This is a retrospective cohort study using the Veterans Health Administration datasets for IBD patients with filled prescriptions for anti-TNFs from 2003 to 2011. Laboratory testing was used to define HBV screening status in the 12 months preceding anti-TNF initiation. Logistic regression models were used to identify predictors of HBV screening. Cases of potential HBV reactivation were identified using ICD-9 codes for HBV infection or acute liver failure or by medications used for HBV infection treatment, and manually reviewed for verification. RESULTS: We identified 3357 IBD patients with filled prescriptions for anti-TNF medications. The HBV testing prior to anti-TNF initiation was 8.1% in 2003 and increased to 43.2% by 2011, with an overall rate of 23.7%. In multivariate analysis, African-American race, facilities with a higher volume of IBD patients, and facilities with an academic affiliation were associated with a higher probability of HBV screening. We did not identify a single case of confirmed clinically relevant HBV reactivation after anti-TNF initiation during 7210 patient-years of medication use. CONCLUSIONS: HBV screening rates prior to anti-TNF initiation are low among IBD patients, but have increased over time. Despite low rates of screening, clinically significant HBV reactivation after anti-TNF initiation in this US cohort was nonexistent.


Subject(s)
Anti-Inflammatory Agents/adverse effects , Hepatitis B virus/pathogenicity , Hepatitis B/virology , Immunocompromised Host , Inflammatory Bowel Diseases/drug therapy , Tumor Necrosis Factor-alpha/antagonists & inhibitors , United States Department of Veterans Affairs , Virus Activation , Adult , Aged , Databases, Factual , Female , Hepatitis B/diagnosis , Hepatitis B/immunology , Hepatitis B virus/immunology , Host-Pathogen Interactions , Humans , Inflammatory Bowel Diseases/diagnosis , Inflammatory Bowel Diseases/immunology , Logistic Models , Male , Middle Aged , Multivariate Analysis , Odds Ratio , Predictive Value of Tests , Retrospective Studies , Risk Factors , Time Factors , Tumor Necrosis Factor-alpha/immunology , United States
15.
Am J Gastroenterol ; 111(4): 492, 2016 04.
Article in English | MEDLINE | ID: mdl-27125712
16.
Hepatol Int ; 9(2): 224-30, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25788197

ABSTRACT

BACKGROUND: This proof-of-concept study compared lamivudine (LAM) with a newer antiviral agent, adefovir dipivoxil (ADF), in preventing hepatitis B virus (HBV) reactivation in chronic HBV patients undergoing chemotherapy. METHODS: Hepatitis B surface antigen (HBsAg) positive patients intended to undergo chemotherapy were randomized to receive either LAM 100 mg daily or ADF 10 mg daily. Anti-viral therapy was started 1 week prior to chemotherapy and until 6 months after completing chemotherapy. The primary outcome was HBV reactivation rate. All patients with viral breakthrough were screened for resistance mutations by direct sequencing. RESULTS: Seventy treatment-naïve patients were consecutively randomized 1:1 to LAM or ADF. The median baseline HBV DNA levels were similar (LAM 3.36 vs. ADF 3.17 log10 copies/mL, p = 0.860). The median duration was 8.3 months on LAM and 10.6 months on ADF (p = 0.220). HBV reactivation was observed in 13/35 (37.1%) on LAM compared with 10/35 (28.6%) on ADF (p = 0.611). The median time to HBV reactivation was 4.6 and 8.1 months, on LAM and ADF respectively. Among these 13 patients, 8/13 (61.5%) on LAM had developed drug resistance mutations but none on ADF had developed drug resistance mutations to ADF (p = 0.003). Both drugs were well tolerated and no severe drug-related toxicities were reported. CONCLUSION: In this randomized clinical study, adefovir and lamivudine demonstrated similar efficacy in preventing hepatitis B reactivation in HBsAg-positive patients undergoing chemotherapy. In patients whose hepatitis B reactivated, adefovir was associated with a lower resistance profile.


Subject(s)
Adenine/analogs & derivatives , Antiviral Agents/therapeutic use , Hepatitis B virus/physiology , Hepatitis B, Chronic/prevention & control , Lamivudine/therapeutic use , Organophosphonates/therapeutic use , Virus Activation/drug effects , Adenine/therapeutic use , Adult , Aged , Aged, 80 and over , Antiviral Agents/adverse effects , DNA, Viral/blood , Drug Resistance, Viral/genetics , Female , Hepatitis B Surface Antigens/blood , Hepatitis B e Antigens/blood , Hepatitis B virus/drug effects , Hepatitis B virus/genetics , Hepatitis B, Chronic/blood , Humans , Lamivudine/adverse effects , Male , Middle Aged , Mutation , Neoplasms/drug therapy , Young Adult
17.
Curr Treat Options Gastroenterol ; 13(1): 130-42, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25619458

ABSTRACT

OPINION STATEMENT: The treatment paradigms and therapeutic options for ulcerative colitis (UC) have rapidly evolved during the past decade. Traditionally, the treatment target has focused on achieving successful induction and maintenance of steroid-free clinical remission. This has been shown to provide a better quality of life and a reduction in complications, hospitalizations, and surgery. Recent studies, however, suggest that achieving "mucosal healing" or endoscopic remission may be the optimal treatment endpoint. In this review, we will examine the treatment goals for UC and the efficacy of each therapy to reach these targets. We will also review the therapeutic options available for UC: mesalamines, steroids, immunomodulators, and biologics, including the first anti-integrin inhibitor, approved in May 2014, for the treatment of UC. Therapeutic drug monitoring, which measures serum drug level and anti-drug antibody concentrations, is emerging as an important clinical decision tool in patients on tumor necrosis factor (TNF)-antagonists. These evolving treatment strategies allow gastroenterologists to optimize control of the disease and offer patients a better quality of life.

18.
F1000Res ; 3: 88, 2014.
Article in English | MEDLINE | ID: mdl-25254098

ABSTRACT

One well recognized and potentially serious complication of chronic immunosuppression in organ transplant recipients is post-transplantation lymphoproliferative disorders (PTLD). This accounts for 20% of all malignancies in transplant recipients, which is four times higher than the general population (1,2). The diagnosis of PTLD is often difficult, due to various manifestations resulting in late diagnosis. We report an unusual presentation of PTLD in a pediatric patient where the diagnosis was achieved only after extensive investigation.

19.
F1000Res ; 3: 35, 2014.
Article in English | MEDLINE | ID: mdl-24715978

ABSTRACT

Severe vitamin deficiency disease is rarely seen in developed countries. We present an atypical case of a young man with scurvy, pellagra, and hypovitaminosis A, caused by longstanding functional abdominal pain that severely limited his ability to eat.

20.
HPB (Oxford) ; 16(8): 758-67, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24467780

ABSTRACT

BACKGROUND: Despite the increasing annual incidence of hepatocellular carcinoma (HCC) in the USA, now estimated at 2.7 cases per 100 000 population, only a small proportion of patients receive treatment and 5-year survival rates range from 9% to 17%. OBJECTIVES: The present study examines the effects of multimodal treatment on survival in a mixed-stage HCC cohort, focusing on the impact of radical therapy in patients with Barcelona Clinic Liver Cancer (BCLC) stage B disease. METHODS: A retrospective review of the medical records of 254 patients considered for HCC treatment between 2003 and 2011 at a large tertiary referral centre was conducted. RESULTS: A total of 195 (76.8%) patients were treated with a median of two liver-directed interventions. Median survival time was 16 months. In proportional hazards analysis, radiofrequency ablation (RFA) and resection were associated with significantly improved 1- and 5-year survival among patients with BCLC stage 0-A disease. In patients with BCLC stage B disease, RFA conferred a survival benefit at 1 year and resection was associated with significantly improved survival at 5 years. CONCLUSIONS: As one of few studies to track the complete course of sequential HCC therapies, the findings of the present study suggest that HCC patients with intermediate-stage (BCLC stage B) disease may benefit from aggressive interventions not currently included in societal guidelines.


Subject(s)
Antineoplastic Agents/therapeutic use , Carcinoma, Hepatocellular/therapy , Catheter Ablation , Hepatectomy , Liver Neoplasms/therapy , Liver Transplantation , Aged , Antineoplastic Agents/adverse effects , Carcinoma, Hepatocellular/mortality , Carcinoma, Hepatocellular/pathology , Catheter Ablation/adverse effects , Catheter Ablation/mortality , Chemotherapy, Adjuvant , Hepatectomy/adverse effects , Hepatectomy/mortality , Humans , Kaplan-Meier Estimate , Liver Neoplasms/mortality , Liver Neoplasms/pathology , Liver Transplantation/adverse effects , Liver Transplantation/mortality , Male , Middle Aged , Neoplasm Staging , Proportional Hazards Models , Retrospective Studies , Risk Factors , San Francisco , Tertiary Care Centers , Time Factors , Treatment Outcome
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