Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Hsiao FY
------>authors3_c=
------>paper_class1=2
------>Impact_Factor=None
------>paper_class3=0
------>paper_class2=0
------>vol=
------>confirm_bywho=None
------>insert_bywho=m001089023
------>Jurnal_Rank=None
------>authors4_c=
------>comm_author=
------>patent_EDate=None
------>authors5_c=
------>publish_day=7
------>paper_class2Letter=None
------>page2=
------>medlineContent=
------>unit=G0100
------>insert_date=20081212
------>iam=4
------>update_date=None
------>author=???
------>change_event=1
------>ISSN=
------>authors_c=
------>score=12
------>journal_name=
------>paper_name=A Retrospective Surveillance of Antituberculosis Therapy- Induced Hepatotoxicity.
------>confirm_date=None
------>tch_id=093056
------>pmid=17545706
------>page1=
------>fullAbstract=OBJECTIVE: Hepatotoxicity is a significant complication of antiretroviral therapy (ART). We assessed the incidence of and risk factors for hepatotoxicity among HIV-infected individuals on ART in South Africa. DESIGN: We conducted a retrospective cohort study in a workplace HIV care program in South Africa which uses a first-line regimen of efavirenz, zidovudine, and lamivudine and provides routine clinical and laboratory monitoring. METHODS: We included subjects with baseline and follow-up alanine transaminase and aspartate aminotransferase tests. Severe hepatotoxicity cases were identified during the first 12 months of ART. Potential risk factors, including concomitant medication use, tuberculosis, and hepatitis B and C, were determined from clinical records, database queries, and serological testing. Associations with hepatotoxicity were investigated using Cox proportional hazards modeling. RESULTS: Of the 868 subjects (94% male, median age 41 years), the median nadir CD4 cell count was 136/microl, 25% received concomitant tuberculosis treatment during ART, and 17% of a randomly selected subset were positive for hepatitis B surface antigen (HBsAg). We identified 7.7 episodes of severe hepatotoxicity per 100 person-years. Tuberculosis treatment increased risk 8.5 fold, positive HBsAg 3.0 fold, and nadir CD4 cells count < 100/microl 1.9 fold. Importantly, the fraction of patients with severe hepatotoxicity on ART (4.6%) was similar to the fraction with liver enzyme elevations > 5 times the upper limit of normal before starting ART (4%). CONCLUSIONS: In this African ART cohort, we found a low incidence of and minimal morbidity due to hepatotoxicity. HBsAg and concomitant tuberculosis therapy significantly increased the risk of hepatotoxicity.
------>tmu_sno=None
------>sno=20777
------>authors2=Lee CN
------>authors3=Lee JA
------>authors4=Lin YM
------>authors5=
------>authors6=
------>authors6_c=
------>authors=Hsiao FY
------>delete_flag=0
------>SCI_JNo=None
------>authors2_c=
------>publish_area=1
------>updateTitle=Hepatotoxicity in an African antiretroviral therapy cohort: the effect of tuberculosis and hepatitis B.
------>language=2
------>check_flag=None
------>submit_date=None
------>country=NULL
------>no=
------>patent_SDate=None
------>update_bywho=None
------>publish_year=2004
------>submit_flag=None
------>publish_month=9
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z