- Open Access
Therapeutic challenges in hepatitis C-infected injection drug using patients
© Cooper and Mills; licensee BioMed Central Ltd. 2006
Received: 05 August 2006
Accepted: 10 November 2006
Published: 10 November 2006
Hepatitis C Viral (HCV) infection in the injection drug user (IDU) population is a major medical concern. Concurrent substance abuse, co-morbid mental health conditions, poor socioeconomic status and a complex treatment protocol that is often incompatible with the life styles of IDUs combine to account for poor uptake and completion of HCV treatment. This article discusses HCV antiviral treatment issues relevant to IDUs chronically infected with this virus. The effect of non-injected substances of abuse on treatment outcome is considered. Priority issues requiring research are discussed.
Given its high incidence and prevalence, the complications of chronic hepatitis C virus (HCV) infection will impact the morbidity and mortality of at-risk populations in the developed world for the foreseeable future . Those with substance abuse concerns, and particularly injection drug users (IDUs), are at a greater risk of HCV infection . In North America, injection drug use remains the primary risk factor for new and chronic infections. In Canada, injection drug use is estimated to account for over half of all current HCV infections . Approximately 55% of active and 49% of post injection drug users are HCV infected . Although therapy is available for HCV infection, there are multiple obstacles that diminish the likelihood of past and present IDUs receiving combination interferon and ribavirin HCV treatment. In this article, we discuss relevant HCV antiviral treatment issues pertaining to IDUs chronically infected with HCV. We additionally consider the effect of other substances of abuse on treatment and priority issues requiring research.
Influence of substance use on natural history of HCV
Not all individuals with chronic HCV infection will progress to advanced stages of fibrosis and end-stage liver disease. During the initial period of evaluation of a HCV infected patient, the physician formulates an impression regarding the likelihood of poor outcome based on risk factors for rapid progression (e.g. immune suppression, alcohol use), physical examination, laboratory evaluation and liver biopsy. Although the final decision to initiate HCV antiviral therapy is made on a case-by-case basis, treatment is strongly recommended for those having or at least predicted to have more progressive disease.
The practice of drug injection is not known to directly influence the rate of HCV progression despite the potential for multiple repeat exposures to various genotypes and quasi-species. However, there are several factors associated with injection drug use which may contribute to accelerated progression . Chief among these is excess alcohol use which is generally defined as more that 50 grams of alcohol per day (i.e. approximately 3–4 beers per day). Concurrent excess alcohol consumption is found in 40% of active IDUs . In our own clinic, we found that 75% of past injection drug users have a history of excess alcohol use compared to 32% in those who acquired HCV infection through other means (χ2, p < 0.001). In addition to increasing risk behaviors , alcohol is well known to accelerate the rate of hepatic fibrosis and reduce the time to cirrhosis in HCV [7–9]. Clearly, concurrent alcohol use in HCV is a factor predicting increased need for HCV therapy but is also a factor limiting eligibility for access to therapy. Furthermore, HCV antiviral therapy efficacy is diminished in those engaging in excess alcohol use (see below). As a primary measure, support for alcohol reduction and cessation is needed in those with HCV, irrespective of injection drug use.
Although not supported by strong evidence, it is plausible that poor nutrition may play a role in influencing HCV progression. Relative malnutrition and micronutrient deficiency likely compromise the livers ability to control chronic infection, contain inflammation and resorb fibrotic material as it is produced . Nutrition is often substandard in substance users. Deficient food intake, anorexia, nausea, vomiting, poor gastrointestinal absorption, altered metabolism and increased energetic expenditure contribute to a poor nutritional status in alcoholics [11, 12] and injection drug users .
Factors influencing treatment consideration
Psychiatric health is an important variable to consider when determining the initiation of HCV antiviral therapy. Those living with chronic HCV infection and those with current or past injection drug use  have a heavy burden of psychiatric illness [15–18]. In our clinic, depression was identified in 62% of patients at initial evaluation using the Center for Epidemiologic Studies of Depression Scale (CES-D) [18, 19]. To compound this problem, interferon-based HCV therapies are well-known to increase the frequency and severity of depression  and other psychiatric illness . The high frequency of depression among HCV-infected patients is multifactoral. As in other populations with chronic illnesses, such as cancer and diabetes, alcohol intake, smoking, and depression often co-occur and influence mental well-being [21–24]. The inter-relationships between the bio-psycho-social variables within HCV-infected injection drug users are not fully understood and deserve continued study. We and other groups are evaluating the use of prophylactic antidepressants in those initiating interferon-based HCV treatment [25, 26].
There are several concrete obstacles to the successful delivery of HCV antiviral therapy to IDUs. Suitable shelter is not always available and a lack of safe storage facilities for HCV therapies negates successful adherence and treatment success. The absence of refrigeration, which is required for interferon storage between weekly dosing, may compromise patients' ability to receive HCV therapy. Poor attendance for outpatient clinical assessments is partially explained by limited or cost-prohibitive transportation options.
Other obstacles to treatment are less tangible. Mistrust of the medical community may influence patient willingness to be assessed and initiation of HCV antiviral therapy. This is, in part, fostered by multiple sources of inaccurate or misinterpreted information pertaining to HCV disease and treatment that can be found in the lay literature and on the internet. Another contributing factor is the poor treatment that many IDUs have experienced from law enforcement services and medical personnel. The negative view of IDUs among many in the medical community  necessitates that medical personnel consider the complex socioeconomic obstacles that placed the patient in the risk category to begin with. This mistrust represents an additional obstacle to the diagnosis and delivery of health care, including HCV antiviral therapy. Recent guidelines and commentaries have clearly stated that ongoing substance abuse should not preclude consideration for treatment [28, 29]. This attitude has resonated within the community of health care professionals delivering HCV care, which seem more willing to consider treatment in this population, assuming that a reasonable degree of stability in substance use has been achieved by the patient.
A further concern for physicians dealing with HCV IDU patients is the patient's exposure to physical and sexual violence . Populations at risk for physical and sexual violence are at a heightened risk for exposure to HIV and viral hepatitis infections. Although intervening on behalf of patients by physicians is challenging, we should be aware that this population is at an increased risk for violence and that initial intake discussions should specifically target issues of physical and sexual violence.
Influence of injection drug use
For patients no longer using injection drugs, the success of therapy is determined by the same predictors (e.g. adherence, genotype) as those without a history of injection drug use. For those with active use, issues related to adherence, tolerance and effectiveness, psychological health, and risk of re-infection are important considerations.
In general, adherence to antimicrobial therapy is diminished in active drug users [31–33]. However, studies demonstrate that adherence varies widely among IDU patients and can, in some cases, approach that of populations without substance abuse [34–36]. Programs with special expertise in providing care for drug users can increase adherence rates to as high as 80% [37–42].
There is little conclusive data to suggest that HCV antiviral therapy is tolerated less well or is less effective in those with concurrent injection use. In fact, in one study, sustained virological response rates comparable to other HCV-treated populations were achieved despite relapses to drug use in 80% of the patients receiving therapy . This group attributed their success to providing multidisciplinary care that included expertise in liver disease and substance abuse management. Other studies replicate these findings. A 29% sustained virological response rate was achieved in a population of 66 methadone recipients . This cohort had a high level of concurrent psychiatric illness (80%), concurrent alcohol use while on therapy (20%) and one-third relapsed into illicit drugs use. Therapy was effectively and safely delivered by provision of mental health care and appropriate resources to stabilize ongoing substance use.
Re-infection is often cited as justification to withhold HCV antiviral treatment from those with ongoing injection drug use. Although there is a risk and documented examples of have been cited , re-infection is a rare occurrence. HCV is generally acquired early in the career of an IDU as a result of inexperience and lack of knowledge regarding safe injecting techniques. Most patients presenting to clinic for therapy have a long history of injection drug use and are therefore less likely to commit the same errors in safe needle use as their junior counterparts. Of course, education and support for safe injection practices is an important component of care delivery to those treated for HCV infection. Support for safe injection facilities, needle exchange programs and provision of injection equipment have been demonstrated to reduce infection rates [46–49]. It is reasonable to assume that this benefit would extend to those who successfully clear HCV with antiviral therapy.
Influence of alcohol on HCV treatment
Alcohol consumption impairs the efficacy of interferon-based HCV therapy [50, 51]. There are several ways in which alcohol is thought to produce this negative influence on treatment outcomes. Most studies suggest that excess alcohol consumption increases HCV RNA levels [52–57]. In mice, alcohol consumption blunts HCV-specific T-helper and cytotoxic T lymphocytes response as well as cytokine expression [58, 59]. Furthermore, decreased interferon-γ levels, resulting from alcohol-induced dendritic cell dysfunction [59, 60] likely influence HCV RNA levels. Both HCV RNA level and immune status predict sustained virologic response rates to interferon-based HCV treatment.
Although ongoing controlled alcohol (or other substance abuse) should not preclude HCV drug therapy , cessation of alcohol use should be emphasized as a highly beneficial therapeutic intervention. Physicians are in an optimal situation to encourage alcohol reduction strategies and brief discussions with patients may reduce alcohol intake . With successful alcohol reduction, liver inflammation and fibrosis will be reduced, HCV RNA levels will decline, and the probability of response to HCV drug therapy will be increased. This intervention requires sustained patient and physician commitment to alcohol cessation programs and patience.
Other substances of concern
Influence of smoking and marijuana use
High rates of cigarette smoking have been reported among HCV patients in Canada, Europe, and the Far East[18, 62–64]. In our own cohort, the rate of cigarette smoking (63%) reported in HCV infection was much higher than the Canadian national average rate of 24% [18, 65]. Smoking is also common among injection drug users .
Cigarette smoking has many known negative health consequences  and has been consistently associated with reduced health-related quality of life [18, 67, 68]. The negative physical effects of smoking have been found to be more severe in those with chronic medical conditions, including liver disease. In a cross-sectional study of 6095 individuals with HCV, cigarette smoking along with alcohol abuse were both independently associated with elevated ALT levels . Tobacco smoking has also been linked to hepatocellular carcinoma [21, 22] and increased Knodell fibrosis . Among Japanese patients with chronic liver disease (67% were HCV positive), hepatocellular carcinoma was higher for smokers and was independent of alcohol use (Relative Risk 15.4) . Smoking may also increase histological activity in chronic HCV patients irrespective of alcohol use . These findings justify further systematic assessment of the impact of smoking on those living with chronic liver disease.
Cigarette smoking has been associated with clinically relevant decrements in physical and mental health-related quality of life in those chronically infected with HCV [18, 71]. Given that cigarette smoking is a modifiable health behavior, these findings may have important clinical implications. Smoking cessation interventions may help improve health-related quality of life for those with HCV-infection [72, 73]. Further study of the effectiveness of psychological and/or pharmacological treatments for smoking cessation and relapse prevention, and the impact of these interventions on HCV patients' long-term health-related quality of life are justified.
The tar in marijuana contains similar carcinogens to those found in tobacco cigarettes . Furthermore, marijuana smoking has been associated with increased risk of head and neck cancer . To be fair, patient testimony suggests that marijuana many play a valuable role in attenuating the many side effects associated with interferon and ribavirin-based HCV treatment. In fact, treatment outcomes have been reported to be improved in those using marijuana compared to those not . Future research on the influence of marijuana smoking on liver disease progression, HCV health-related quality of life and HCV treatment efficacy should be pursued.
Influence of HIV co-infection on HCV progression and treatment
As a result of common risk factors for exposure, HCV and HIV are often found concurrently. The pace of HCV-induced hepatic fibrosis is accelerated in those with HIV co-infection [7, 75]. As a result, the burden of end stage liver disease and liver-related death is increased [76, 77]. For these reasons, HCV treatment evaluation is essential in those with HIV-HCV co-infection. The likelihood of successfully clearing HCV infection with interferon and ribavirin-based therapy is diminished in those with HIV co-infection, even with well managed HIV disease [78, 79]. Treatment side effects are not inconsequential but, in general, not substantially more plentiful or severe in co-infection [78, 79]. Traditionally, there have been concerns pertaining to interactions between ribavirin and HIV antiretrovirals [80, 81]. As didanosine, stavudine and zidovudine use diminish as safer alternates become available, concerns about nucleoside drug interactions with ribavirin have diminished. It is clear that pegylated interferon use in this immune compromised population does not result in a greater risk of infectious complications or HIV-defining opportunistic infections [78, 82].
Investigation and validation of treatment strategies which will improve adherence to viral hepatitis drug therapy are required to ensure that individuals who use injection drugs or other substances of abuse derive the maximal possible benefits from current viral hepatitis therapies. Given the wide spread use of medicinal marijuana in this population, quantification of the benefits and negative consequences of regular, long term use is mandatory. Rigorous evaluation of the safety, purported benefits and effect on quality of life are required for the many alternative and herbal remedies used by those living with HCV.
Many patients seek alternative sources of health care for a variety of reasons, including cultural relations, belief-systems, the concept of detoxifying their liver, and the potential therapeutic benefits of alternative therapies. Acupuncture, a traditional Asian intervention, often used for addiction and substance cravings, has been evaluated in a number of randomized trials. The evidence, has however, shown consistently that acupuncture is ineffective in addictive drug use [83, 84]. A popular herbal medicine used by patients with liver disorders, including HCV, is Milk Thistle (Silybum marianum). Although the safety of Milk Thistle is now largely established , the therapeutic effectiveness is still uncertain. Some evidence suggests that it has therapeutic effectiveness in hepatitis B/C in reducing liver-related mortality. However, better quality studies indicate this result is uncertain . There are currently large trials enrolling HCV patients to determine Milk Thistle's impact on HCV specific outcomes.
It is plausible that the course and outcome of HCV many differ in those infected by injection drug use. Inoculum size and frequency of exposure may perturb the viral-host immune interaction. The poor nutrition status of injection drug uses may influence HCV pathogenesis and response to therapy. Well-designed analyses of this issue, which control for key confounders including alcohol use and nutritional status would provide clarity.
The need to implement interventions to reduce the infection rate of HCV among IDUs is critical. Although ongoing research is vital to ensure optimal application of techniques to limit the spread of HCV in this high risk group, this should not be used as an excuse to delay introduction of practices which are now well known to be effective) [46–49].
HCV infection in the IDU population is a major medical concern, one that is likely to remain for the foreseeable future. The difficulties of delivering current interferon-based HCV treatment to this population are well known. Co-morbid mental health concerns, concurrent substance use and abuse, poor socioeconomic status, exposure to violence and a treatment protocol that is often not compatible with the schedules of injection drug users combine to account for poor uptake and completion of HCV treatment. Moral and financial support from government for this disenfranchised population would perhaps provide the greatest impetus to allow for successful delivery of HCV treatment to this population. In a more favorable climate, practices demonstrated to reduce harmful behavior and effectively manage the above risk factors and co-morbidities in the IDU population could produce improvement in individual and population health. This, in turn would make HCV drug treatment more accessible to a larger proportion of those requiring therapy.
- Remis RS: The prevalence of hepatitis in Canada. 2003, , Health CanadaGoogle Scholar
- Heintges T, Wands JR: Hepatitis C virus: epidemiology and transmission. Hepatology. 1997, 26: 521-526. 10.1002/hep.510260338.View ArticlePubMedGoogle Scholar
- Remis : Epidemiology of hepatitis C virus infection in Canada, 2002: March 27-31; Vancouver, B.C.. 2004,Google Scholar
- Thomas DL, Astemborski J, Rai RM, Anania FA, Schaeffer M, Galai N, Nolt K, Nelson KE, Strathdee SA, Johnson L, Laeyendecker O, Boitnott J, Wilson LE, Vlahov D: The natural history of hepatitis C virus infection: host, viral, and environmental factors. Jama. 2000, 284: 450-456. 10.1001/jama.284.4.450.View ArticlePubMedGoogle Scholar
- Stein MD, Charuvastra A, Anderson B, Sobota M, Friedmanna PD: Alcohol and HIV risk taking among intravenous drug users. Addict Behav. 2002, 27: 727-736. 10.1016/S0306-4603(01)00205-2.View ArticlePubMedGoogle Scholar
- Anderson BJ, Gogineni A, Charuvastra A, Longabaugh R, Stein MD: Adverse drinking consequences among alcohol abusing intravenous drug users. Alcohol Clin Exp Res. 2001, 25: 41-45. 10.1111/j.1530-0277.2001.tb02125.x.View ArticlePubMedGoogle Scholar
- Benhamou Y, Bochet M, Di Martino V, Charlotte F, Azria F, Coutellier A, Vidaud M, Bricaire F, Opolon P, Katlama C, Poynard T: Liver fibrosis progression in human immunodeficiency virus and hepatitis C virus coinfected patients. The Multivirc Group. Hepatology. 1999, 30: 1054-1058. 10.1002/hep.510300409.View ArticlePubMedGoogle Scholar
- Freeman AJ, Dore GJ, Law MG, Thorpe M, Von Overbeck J, Lloyd AR, Marinos G, Kaldor JM: Estimating progression to cirrhosis in chronic hepatitis C virus infection. Hepatology. 2001, 34: 809-816. 10.1053/jhep.2001.27831.View ArticlePubMedGoogle Scholar
- Tong MJ, el-Farra NS, Reikes AR, Co RL: Clinical outcomes after transfusion-associated hepatitis C. N Engl J Med. 1995, 332: 1463-1466. 10.1056/NEJM199506013322202.View ArticlePubMedGoogle Scholar
- Caly WR, Strauss E, Carrilho FJ, Laudanna AA: Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study. Nutr J. 2003, 2: 10-10.1186/1475-2891-2-10.PubMed CentralView ArticlePubMedGoogle Scholar
- Lieber CS: Alcohol and the liver: 1994 update. Gastroenterology. 1994, 106: 1085-1105.PubMedGoogle Scholar
- Muller MJ: Malnutrition in cirrhosis. J Hepatol. 1995, 23 Suppl 1: 31-35.PubMedGoogle Scholar
- Smit E, Tang A: Nutritional assessment in intravenous drug users with HIV/AIDS. J Acquir Immune Defic Syndr. 2000, 25 Suppl 1: S62-9. 10.1097/00042560-200010001-00010.View ArticlePubMedGoogle Scholar
- Kokkevi A, Stefanis C: Drug abuse and psychiatric comorbidity. Compr Psychiatry. 1995, 36: 329-337. 10.1016/S0010-440X(95)90113-2.View ArticlePubMedGoogle Scholar
- Dwight MM, Kowdley KV, Russo JE, Ciechanowski PS, Larson AM, Katon WJ: Depression, fatigue, and functional disability in patients with chronic hepatitis C. J Psychosom Res. 2000, 49: 311-317. 10.1016/S0022-3999(00)00155-0.View ArticlePubMedGoogle Scholar
- Dieperink E, Willenbring M, Ho SB: Neuropsychiatric symptoms associated with hepatitis C and interferon alpha: A review. Am J Psychiatry. 2000, 157: 867-876. 10.1176/appi.ajp.157.6.867.View ArticlePubMedGoogle Scholar
- Sylvestre DL: Treating hepatitis C in methadone maintenance patients: an interim analysis. Drug Alcohol Depend. 2002, 67: 117-123. 10.1016/S0376-8716(02)00010-8.View ArticlePubMedGoogle Scholar
- Balfour L, Cooper C, Kowal J, Tasca GA, Silverman AL, Kane M, Garber G: Depression and cigarette smoking independently contribute to reduced quality of life among Canadians living with hepatitis C. Can J Gastroenterol In press. 2005Google Scholar
- Radloff LS: The CED-D scale: a self-report depression scale for research in the general population. Applied Psychological Measurements. 1977, 1: 385-401.View ArticleGoogle Scholar
- Bonaccorso S, Puzella A, Marino V, Pasquini M, Biondi M, Artini M, Almerighi C, Levrero M, Egyed B, Bosmans E, Meltzer HY, Maes M: Immunotherapy with interferon-alpha in patients affected by chronic hepatitis C induces an intercorrelated stimulation of the cytokine network and an increase in depressive and anxiety symptoms. Psychiatry Res. 2001, 105: 45-55. 10.1016/S0165-1781(01)00315-8.View ArticlePubMedGoogle Scholar
- Kuper H, Tzonou A, Kaklamani E, Hsieh CC, Lagiou P, Adami HO, Trichopoulos D, Stuver SO: Tobacco smoking, alcohol consumption and their interaction in the causation of hepatocellular carcinoma. Int J Cancer. 2000, 85: 498-502. 10.1002/(SICI)1097-0215(20000215)85:4<498::AID-IJC9>3.0.CO;2-F.View ArticlePubMedGoogle Scholar
- Mukaiya M, Nishi M, Miyake H, Hirata K: Chronic liver diseases for the risk of hepatocellular carcinoma: a case-control study in Japan. Etiologic association of alcohol consumption, cigarette smoking and the development of chronic liver diseases. Hepatogastroenterology. 1998, 45: 2328-2332.PubMedGoogle Scholar
- Duffy SA, Terrell JE, Valenstein M, Ronis DL, Copeland LA, Connors M: Effect of smoking, alcohol, and depression on the quality of life of head and neck cancer patients. Gen Hosp Psychiatry. 2002, 24: 140-147. 10.1016/S0163-8343(02)00180-9.View ArticlePubMedGoogle Scholar
- Haire-Joshu D, Heady S, Thomas L, Schechtman K, Fisher EB: Depressive symptomatology and smoking among persons with diabetes. Res Nurs Health. 1994, 17: 273-282.View ArticlePubMedGoogle Scholar
- Klein M, Cooper C: A randomized, placebo controlled trial of citalopram for the prevention of depression and its consequences in HIV-Hepatitis C co-infected individuals initiating pegylated interferon/ribavirin therapy.Google Scholar
- Schaefer M, Schwaiger M, Garkisch AS, Pich M, Hinzpeter A, Uebelhack R, Heinz A, van Boemmel F, Berg T: Prevention of interferon-alpha associated depression in psychiatric risk patients with chronic hepatitis C. J Hepatol. 2005, 42: 793-798. 10.1016/j.jhep.2005.01.020.View ArticlePubMedGoogle Scholar
- O'Connor PG, Selwyn PA, Schottenfeld RS: Medical care for injection-drug users with human immunodeficiency virus infection. N Engl J Med. 1994, 331: 450-459. 10.1056/NEJM199408183310707.View ArticlePubMedGoogle Scholar
- Seeff LB, Hoofnagle JH: National Institutes of Health Consensus Development Conference: management of hepatitis C: 2002. Hepatology. 2002, 36: S1-2. 10.1002/hep.1840360702.View ArticlePubMedGoogle Scholar
- Edlin BR, Seal KH, Lorvick J, Kral AH, Ciccarone DH, Moore LD, Lo B: Is it justifiable to withhold treatment for hepatitis C from illicit-drug users?. N Engl J Med. 2001, 345: 211-214. 10.1056/NEJM200107193450311.PubMed CentralView ArticlePubMedGoogle Scholar
- Braitstein P, Li K, Tyndall M, Spittal P, O'Shaughnessy MV, Schilder A, Johnston C, Hogg RS, Schechter MT: Sexual violence among a cohort of injection drug users. Soc Sci Med. 2003, 57: 561-569. 10.1016/S0277-9536(02)00403-3.View ArticlePubMedGoogle Scholar
- Pablos-Mendez A, Knirsch CA, Barr RG, Lerner BH, Frieden TR: Non-adherence in tuberculosis treatment: predictors and consequences in New York City. Am J Med. 1997, 102: 164-170. 10.1016/S0002-9343(96)00402-0.View ArticlePubMedGoogle Scholar
- Haubrich RH, Little SJ, Currier JS, Forthal DN, Kemper CA, Beall GN, Johnson D, Dube MP, Hwang JY, McCutchan JA: The value of patient-reported adherence to antiretroviral therapy in predicting virologic and immunologic response. California Collaborative Treatment Group. Aids. 1999, 13: 1099-1107. 10.1097/00002030-199906180-00014.View ArticlePubMedGoogle Scholar
- Lucas GM, Cheever LW, Chaisson RE, Moore RD: Detrimental effects of continued illicit drug use on the treatment of HIV-1 infection. J Acquir Immune Defic Syndr. 2001, 27: 251-259.View ArticlePubMedGoogle Scholar
- Sackett DL, SNow JC: The magnitude of compliance and noncompliance. Compliance in Health Care. Edited by: Haynes RB, Taylor DW and Sackett DL. 1979, Baltimore, Johns Hopkins University Press, 11-22.Google Scholar
- Miller NH: Compliance with treatment regimens in chronic asymptomatic diseases. Am J Med. 1997, 102: 43-49. 10.1016/S0002-9343(97)00467-1.View ArticlePubMedGoogle Scholar
- Cochrane MG, Bala MV, Downs KE, Mauskopf J, Ben-Joseph RH: Inhaled corticosteroids for asthma therapy: patient compliance, devices, and inhalation technique. Chest. 2000, 117: 542-550. 10.1378/chest.117.2.542.View ArticlePubMedGoogle Scholar
- Broers B, Morabia A, Hirschel B: A cohort study of drug users' compliance with zidovudine treatment. Arch Intern Med. 1994, 154: 1121-1127. 10.1001/archinte.154.10.1121.View ArticlePubMedGoogle Scholar
- Samet JH, Libman H, Steger KA, Dhawan RK, Chen J, Shevitz AH, Dewees-Dunk R, Levenson S, Kufe D, Craven DE: Compliance with zidovudine therapy in patients infected with human immunodeficiency virus, type 1: a cross-sectional study in a municipal hospital clinic. Am J Med. 1992, 92: 495-502. 10.1016/0002-9343(92)90746-X.View ArticlePubMedGoogle Scholar
- Mezzelani P, Venturini L, Turrina G, Lugoboni F, Des Jarlais DC: High compliance with a hepatitis B virus vaccination program among intravenous drug users. J Infect Dis. 1991, 163: 923-View ArticlePubMedGoogle Scholar
- Marco A, Cayla JA, Serra M, Pedro R, Sanrama C, Guerrero R, Ribot N: Predictors of adherence to tuberculosis treatment in a supervised therapy programme for prisoners before and after release. Study Group of Adherence to Tuberculosis Treatment of Prisoners. Eur Respir J. 1998, 12: 967-971. 10.1183/09031936.98.12040967.View ArticlePubMedGoogle Scholar
- Lorvick J, Thompson S, Edlin BR, Kral AH, Lifson AR, Watters JK: Incentives and accessibility: a pilot study to promote adherence to TB prophylaxis in a high-risk community. J Urban Health. 1999, 76: 461-467. 10.1007/BF02351503.PubMed CentralView ArticlePubMedGoogle Scholar
- Harrison K, Vlahov D, Jones K, Charron K, Clements ML: Medical eligibility, comprehension of the consent process, and retention of injection drug users recruited for an HIV vaccine trial. J Acquir Immune Defic Syndr Hum Retrovirol. 1995, 10: 386-390.View ArticlePubMedGoogle Scholar
- Backmund M, Meyer K, Von Zielonka M, Eichenlaub D: Treatment of hepatitis C infection in injection drug users. Hepatology. 2001, 34: 188-193. 10.1053/jhep.2001.25882.View ArticlePubMedGoogle Scholar
- Sylvestre DL: Treatment of HCV in the methadone patient.: April 26-28; Chicago, Illinois. 2002, American Association for the Study of Liver Diseases, 103-107.Google Scholar
- Dalgard O, Bjoro K, Hellum K, Myrvang B, Skaug K, Gutigard B, Bell H: Treatment of chronic hepatitis C in injecting drug users: 5 years' follow-up. Eur Addict Res. 2002, 8: 45-49. 10.1159/000049487.View ArticlePubMedGoogle Scholar
- Edlin BR: Prevention and treatment of hepatitis C in injection drug users. Hepatology. 2002, 36: S210-9. 10.1002/hep.1840360727.PubMed CentralView ArticlePubMedGoogle Scholar
- Burris S, Lurie P, Abrahamson D, Rich JD: Physician prescribing of sterile injection equipment to prevent HIV infection: time for action. Ann Intern Med. 2000, 133: 218-226.View ArticlePubMedGoogle Scholar
- Marsch LA: The efficacy of methadone maintenance interventions in reducing illicit opiate use, HIV risk behavior and criminality: a meta-analysis. Addiction. 1998, 93: 515-532. 10.1046/j.1360-0443.1998.9345157.x.View ArticlePubMedGoogle Scholar
- Centres for Disease Control. Fact Sheet: physician prescription of sterile syringes to injection drug users[on-line]. Available: http://www.cdc.gov/idu/facts/physician.htm). Academy of Educational Development.Google Scholar
- Bhattacharya R, Shuhart MC: Hepatitis C and alcohol: interactions, outcomes, and implications. J Clin Gastroenterol. 2003, 36: 242-252. 10.1097/00004836-200303000-00012.View ArticlePubMedGoogle Scholar
- Tabone M, Sidoli L, Laudi C, Pellegrino S, Rocca G, Della Monica P, Fracchia M, Galatola G, Molinaro GC, Arico S, Pera A: Alcohol abstinence does not offset the strong negative effect of lifetime alcohol consumption on the outcome of interferon therapy. J Viral Hepat. 2002, 9: 288-294. 10.1046/j.1365-2893.2002.00360.x.View ArticlePubMedGoogle Scholar
- Ragni MV, Bontempo FA: Increase in hepatitis C virus load in hemophiliacs during treatment with highly active antiretroviral therapy. J Infect Dis. 1999, 180: 2027-2029. 10.1086/315143.View ArticlePubMedGoogle Scholar
- Oshita M, Hayashi N, Kasahara A, Hagiwara H, Mita E, Naito M, Katayama K, Fusamoto H, Kamada T: Increased serum hepatitis C virus RNA levels among alcoholic patients with chronic hepatitis C. Hepatology. 1994, 20: 1115-1120. 10.1016/0270-9139(94)90745-5.View ArticlePubMedGoogle Scholar
- Cromie SL, Jenkins PJ, Bowden DS, Dudley FJ: Chronic hepatitis C: effect of alcohol on hepatitic activity and viral titre. J Hepatol. 1996, 25: 821-826. 10.1016/S0168-8278(96)80284-4.View ArticlePubMedGoogle Scholar
- Cooper C, Cameron DW: Effect of alcohol use on the impact of effective antiretroviral therapy for HIV co-infection on plasma HCV levels. Clin Infect Dis. 2005, 41: S105-109. 10.1086/429506.View ArticlePubMedGoogle Scholar
- Lucas GM, Gebo KA, Chaisson RE, Moore RD: Longitudinal assessment of the effects of drug and alcohol abuse on HIV-1 treatment outcomes in an urban clinic. AIDS. 2002, 16: 767-774. 10.1097/00002030-200203290-00012.View ArticlePubMedGoogle Scholar
- Pessione F, Degos F, Marcellin P, Duchatelle V, Njapoum C, Martinot-Peignoux M, Degott C, Valla D, Erlinger S, Rueff B: Effect of alcohol consumption on serum hepatitis C virus RNA and histological lesions in chronic hepatitis C. Hepatology. 1998, 27: 1717-1722. 10.1002/hep.510270635.View ArticlePubMedGoogle Scholar
- Geissler M, Gesien A, Wands JR: Inhibitory effects of chronic ethanol consumption on cellular immune responses to hepatitis C virus core protein are reversed by genetic immunizations augmented with cytokine-expressing plasmids. J Immunol. 1997, 159: 5107-5113.PubMedGoogle Scholar
- Szabo G, Mandrekar P, Dolganiuc A, Catalano D, Kodys K: Reduced alloreactive T-cell activation after alcohol intake is due to impaired monocyte accessory cell function and correlates with elevated IL-10, IL-13, and decreased IFNgamma levels. Alcohol Clin Exp Res. 2001, 25: 1766-1772. 10.1111/j.1530-0277.2001.tb02188.x.PubMedGoogle Scholar
- Bain C, Fatmi A, Zoulim F, Zarski JP, Trepo C, Inchauspe G: Impaired allostimulatory function of dendritic cells in chronic hepatitis C infection. Gastroenterology. 2001, 120: 512-524. 10.1053/gast.2001.21212.View ArticlePubMedGoogle Scholar
- Emmen MJ, Schippers GM, Bleijenberg G, Wollersheim H: Effectiveness of opportunistic brief interventions for problem drinking in a general hospital setting: systematic review. Bmj. 2004, 328: 318-10.1136/bmj.37956.562130.EE.PubMed CentralView ArticlePubMedGoogle Scholar
- Winfried H, Zimmer C, Schiedermaier P, Grandt D: Biopschosocial predictors of health-related quality of life in patients with chronic hepatitis C. Psychosom Med. 2004, 66: 954-958. 10.1097/01.psy.0000145824.82125.a8.View ArticleGoogle Scholar
- Pessione F, Ramond MJ, Njapoum C, Duchatelle V, Degott C, Erlinger S, Rueff B, Valla DC, Degos F: Cigarette smoking and hepatic lesions in patients with chronic hepatitis C. Hepatology. 2001, 34: 121-125. 10.1053/jhep.2001.25385.View ArticlePubMedGoogle Scholar
- Sladden TJ, Hickey AR, Dunn TM, Beard JR: Hepatitis C virus infection: impacts on behaviour and lifestyle. Aust N Z J Public Health. 1998, 22: 509-511.View ArticlePubMedGoogle Scholar
- Canadian tobacco use monitoring survey (CTUMS): prevalence 2000-2002. Edited by: Canada H. 2000Google Scholar
- Clarke JG, Stein MD, McGarry KA, Gogineni A: Interest in smoking cessation among injection drug users. Am J Addict. 2001, 10: 159-166. 10.1080/105504901750227804.View ArticlePubMedGoogle Scholar
- Vogt MT, Hanscom B, Lauerman WC, Kang JD: Influence of smoking on the health status of spinal patients: the National Spine Network database. Spine. 2002, 27: 313-319. 10.1097/00007632-200202010-00022.View ArticlePubMedGoogle Scholar
- Olufade AO, Shaw JW, Foster SA, Leischow SJ, Hays RD, Coons SJ: Development of the Smoking Cessation Quality of Life questionnaire. Clin Ther. 1999, 21: 2113-2130. 10.1016/S0149-2918(00)87242-2.View ArticlePubMedGoogle Scholar
- Wang CS, Wang ST, Chang TT, Yao WJ, Chou P: Smoking and alanine aminotransfererase levels in hepatitis C virus infection: implications for prevention of hepatitis C virus progression. Arch Intern Med. 2002, 162: 811-815. 10.1001/archinte.162.7.811.View ArticlePubMedGoogle Scholar
- Hezode C, Lonjon I, Roudot-Thoraval F, Mavier JP, Pawlotsky JM, Zafrani ES, Dhumeaux D: Impact of smoking on histological liver lesions in chronic hepatitis C. Gut. 2003, 52: 126-129. 10.1136/gut.52.1.126.PubMed CentralView ArticlePubMedGoogle Scholar
- Chong CA, Gulamhussein A, Heathcote EJ, Lilly L, Sherman M, Naglie G, Krahn M: Health-state utilities and quality of life in hepatitis C patients. Am J Gastroenterol. 2003, 98: 630-638. 10.1111/j.1572-0241.2003.07332.x.View ArticlePubMedGoogle Scholar
- Lancaster T, Stead LF: Individual behavioural counselling for smoking cessation. Cochrane Database Syst Rev. 2005, CD001292-Google Scholar
- Fisher EB, Haire-Joshu D, Morgan GD, Rehberg H, Rost K: Smoking and smoking cessation. Am Rev Respir Dis. 1990, 142: 702-720.View ArticlePubMedGoogle Scholar
- Hashibe M, Ford DE, Zhang ZF: Marijuana smoking and head and neck cancer. J Clin Pharmacol. 2002, 42: 103S-107S.View ArticlePubMedGoogle Scholar
- Lesens O, Deschenes M, Steben M, Belanger G, Tsoukas CM: Hepatitis C virus is related to progressive liver disease in human immunodeficiency virus-positive hemophiliacs and should be treated as an opportunistic infection. J Infect Dis. 1999, 179: 1254-1258. 10.1086/314720.View ArticlePubMedGoogle Scholar
- Qurishi N, Kreuzberg C, Luchters G, Effenberger W, Kupfer B, Sauerbruch T, Rockstroh JK, Spengler U: Effect of antiretroviral therapy on liver-related mortality in patients with HIV and hepatitis C virus coinfection. Lancet. 2003, 362: 1708-1713. 10.1016/S0140-6736(03)14844-1.View ArticlePubMedGoogle Scholar
- Palella FJ, Baker RK, Moorman AC, Chmiel JS, Wood KC, Brooks JT, Holmberg SD: Mortality in the Highly Active Antiretroviral Therapy Era: Changing Causes of Death and Disease in the HIV Outpatient Study. J Acquir Immune Defic Syndr. 2006, 43: 27-34. 10.1097/01.qai.0000233310.90484.16.View ArticlePubMedGoogle Scholar
- Torriani FJ, Rodriguez-Torres M, Rockstroh JK, Lissen E, Gonzalez-Garcia J, Lazzarin A, Carosi G, Sasadeusz J, Katlama C, Montaner J, Sette H, Passe S, De Pamphilis J, Duff F, Schrenk UM, Dieterich DT: Peginterferon Alfa-2a plus ribavirin for chronic hepatitis C virus infection in HIV-infected patients. N Engl J Med. 2004, 351: 438-450. 10.1056/NEJMoa040842.View ArticlePubMedGoogle Scholar
- Carrat F, Bani-Sadr F, Pol S, al. : Pegylated Interferon Alfa-2b vs Standard Interferon Alfa-2b, Plus Ribavirin, for Chronic Hepatitis C in HIV_Infected Patients. Jama. 2004, 292: 2839-2848. 10.1001/jama.292.23.2839.View ArticlePubMedGoogle Scholar
- Lafeuillade A, Hittinger G, Chadapaud S: Increased mitochondrial toxicity with ribavirin in HIV/HCV coinfection. Lancet. 2001, 357: 280-281. 10.1016/S0140-6736(00)03618-7.View ArticlePubMedGoogle Scholar
- Salmon-Ceron D, Chauvelot-Moachon L, Abad S, Silbermann B, Sogni P: Mitochondrial toxic effects and ribavirin. Lancet. 2001, 357: 1803-1804. 10.1016/S0140-6736(00)04921-7.View ArticlePubMedGoogle Scholar
- Cooper CL, Al-Bedwawi S, Lee C, Garber G: Rate of infectious complications during interferon-based therapy for hepatitis C is not related to neutropenia. Clin Infect Dis. 2006, 42: 1674-1678. 10.1086/504386.View ArticlePubMedGoogle Scholar
- Ter Riet G, Kleijnen J, Knipschild P: A meta-analysis of studies into the effect of acupuncture on addiction. Br J Gen Pract. 1990, 40: 379-382.PubMed CentralPubMedGoogle Scholar
- Mills EJ, Wu P, Gagnier J, Ebbert JO: Efficacy of acupuncture for cocaine dependence: a systematic review & meta-analysis. Harm Reduct J. 2005, 2: 4-10.1186/1477-7517-2-4.PubMed CentralView ArticlePubMedGoogle Scholar
- Mills E, Wilson K, Clarke M, Foster B, Walker S, Rachlis B, DeGroot N, Montori VM, Gold W, Phillips E, Myers S, Gallicano K: Milk thistle and indinavir: a randomized controlled pharmacokinetics study and meta-analysis. Eur J Clin Pharmacol. 2005, 61: 1-7. 10.1007/s00228-004-0843-z.View ArticlePubMedGoogle Scholar
- Rambaldi A, Jacobs BP, Iaquinto G, Gluud C: Milk thistle for alcoholic and/or hepatitis B or C virus liver diseases. Cochrane Database Syst Rev. 2005, 2:Google Scholar
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