Hepatitis C in state correctional facilities

被引:64
作者
Spaulding, A [1 ]
Greene, C
Davidson, K
Schneidermann, M
Rich, J
机构
[1] Rhode Isl Hosp, Div Infect Dis, Providence, RI 02903 USA
[2] Rhode Isl Dept Correct, Cranston, RI USA
[3] Brown Univ, Sch Med, Providence, RI 02912 USA
[4] Miriam Hosp, Div Infect Dis, Providence, RI 02906 USA
关键词
hepatitis C; prisons; review; cost analysis;
D O I
10.1006/pmed.1998.0418
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: No previous studies have examined the extent to which correctional facilities in the United States screen for and treat hepatitis C (HCV) infection. Methods: Medical directors of state correctional facilities responded to a survey assessing the degree to which prisons screen for and treat hepatitis C, To estimate numbers of inmates eligible for interferon treatment and to examine costs associated with HCV management, we constructed a feasibility model that incorporated screening criteria used in California and Rhode Island. Results: Thirty-six states and Washington, DC, responded, resulting in a survey response rate of 73%, representing 77% of all inmates in state facilities nationwide. Colorado alone reported routine screening. Only California reported conducting a systematic seroprevalence study, which found that 39.4% of male inmates were hepatitis C antibody positive in 1994, Seventy-three percent of the respondents sometimes consider treating with interferon, Four states follow a standard protocol. The feasibility model suggests that treating suitably screened inmates is a reasonable expenditure for correctional systems. Conclusion: Prison may be an appropriate setting for treatment of hepatitis C, If accompanying substance abuse issues are addressed, instituting HCV treatment for certain eligible incarcerated individuals may be a worthy target for public health dollars. (C) 1999 American Health Foundation and Academic Press.
引用
收藏
页码:92 / 100
页数:9
相关论文
共 31 条
[1]   THE NATURAL-HISTORY OF COMMUNITY-ACQUIRED HEPATITIS-C IN THE UNITED-STATES [J].
ALTER, MJ ;
MARGOLIS, HS ;
KRAWCZYNSKI, K ;
JUDSON, FN ;
MARES, A ;
ALEXANDER, WJ ;
HU, PY ;
MILLER, JK ;
GERBER, MA ;
SAMPLINER, RE ;
MEEKS, EL ;
BEACH, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (27) :1899-1905
[2]  
ALTER MJ, 1993, INFECT AGENT DIS, V2, P155
[3]  
ALTER MJ, 1997, NIH CONSENSUS STATE, P67
[4]  
ANNO BJ, 1996, J CORRECT HEALTH CAR, V3, P67
[5]  
[Anonymous], 1997, HEPATOLOGY, V26, pS2
[6]   Modeling therapeutic benefit in the midst of uncertainty - Therapy for hepatitis C [J].
Bennett, WG ;
Pauker, SG ;
Davis, GL ;
Wong, JB .
DIGESTIVE DISEASES AND SCIENCES, 1996, 41 (12) :S56-S62
[7]  
BROWN BS, 1993, HDB RISK AIDS INJECT, P338
[8]   Hepatitis B and C in New South Wales prisons: Prevalence and risk factors [J].
Butler, TG ;
Dolan, KA ;
Ferson, MJ ;
McGuinness, LM ;
Brown, PR ;
Robertson, PW .
MEDICAL JOURNAL OF AUSTRALIA, 1997, 166 (03) :127-130
[9]  
CAMP CG, 1996, CORRECTIONS YB 1996
[10]  
CARITHERS RL, 1997, NIH CONS DEV C MAN H, P83