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Hepatitis C Screening in Isfahan Drop in Centers: An Experience Description



Meshkati M1 ; Ataei B2 ; Nokhaodian Z3 ; Yaran M3 ; Babak A4 ; Zadeh MRA5 ; Farshad M5 ; Adibi P5
Authors
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Authors Affiliations
  1. 1. Isfahan University of Medical Sciences Health Center, Isfahan, Iran
  2. 2. Department of Infectious Diseases, School of Medicine and Infectious and Tropical Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Infectious and Tropical Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Disease Control Unit, Isfahan Province Health Center, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Welfare Organization, Isfahan, Iran

Source: Journal of Isfahan Medical School Published:2011

Abstract

Background: Hepatitis C virus (HCV) is a major public health problem in the world which drug injection is a primary mode of transmission for it. So, this study was conducted to determine seroprevalence of HCV in intravenous drug abusers (IVDA) in Isfahan province Drop in centers (DIC). Methods: This qualitative/quantitave study used triangulation method in data collection and analysis. Five semi-structured focus groups with open-ended questions were disposed to evaluate and discuss on aspects of the study. Intravenous drug abusers in Isfahan province Drop in centers by non-probable purposive sampling method entered into the study voluntarily and blood sample was obtained from them. Serum samples were tested for HCV-Ab using ELISA method. Finding: There were seven govermental Drop in centers including 4 related to Isfahan University of Medical Sciences and 3 related to welfare organization which contained 1581 intravenous drug abusers members. From them, 539 patients (34%) enterd into the study from which, 250 (47.1%) patients were positive for HCV-Ab without significant differences between men and women. The main impressive factors for the project were wage for blood obtaning, occupational insurance, problems in interview and sampling, and time restriction. Conclusion: This was a good experience for other investigators and health directors' strategies to design simillar studies or harm reduction.
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