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Psychiatric Times. Vol. 21 No. 2
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Treating Co-Occurring Substance Use Disorders and Hepatitis C

By Mark L. Willenbring, M.D.
| February 1, 2004
Dr. Willenbring is co-director of the Minneapolis Veterans Affairs Medical Center Hepatitis C Resource Center and professor of psychiatry at the University of Minnesota School of Medicine.

SUD in Hepatitis C Treatment

Screening for SUDs must be routine and thorough, incorporating evidence-based screening methods. Screening for alcohol(Drug information on alcohol)ic beverage drinking should include measures of quantity-frequency, as well as screens for alcohol abuse or dependence. The Alcohol Use Disorders Identification Test (AUDIT) is a well-validated instrument that screens for both nondependent heavy drinking and for alcohol abuse and dependence (Bohn et al., 1995). It is brief (10 items), self-administered and easy to score. The AUDIT-C, composed of the first three items of the AUDIT, appears to accomplish much the same thing in an even shorter format (Bush et al., 1998). Most other screening tests (e.g., the CAGE) only identify patients with possible abuse or dependence and will miss nondependent heavy drinking. If such screens are used, questions about quantity and frequency of drinking need to be added. Screening for other drug use is more effective if questions specifically address each class of drugs. Any drug used more than five times in a lifetime deserve further exploration. Screening should also include urine toxicology screening (with the patient's consent). Clinicians should know which drugs their laboratory will routinely test for and which ones need to be specifically ordered. The synthetic opioids are not routinely assessed in many screening procedures. If a drug screen is positive, but the patient denies drug use, the laboratory should be asked to conduct a confirmatory test using gas chromatography/massspectroscopy.

When patients have a positive screen for an SUD, further evaluation is required to determine whether substance abuse or dependence is present. This can be done in the hepatitis clinic or through referral to an addiction treatment specialist. Patients who are using heroin or other opioids should be specifically referred for opioid agonist therapy such as methadone(Drug information on methadone) (Methadose, Dolophine) or buprenorphine(Drug information on buprenorphine) (Buprenex, Subutex) maintenance. Opioid agonist therapy is the most effective treatment for opioid dependence; most addicted people relapse even when extended detoxification and enhanced psychosocial services are provided (Sees et al., 2000). The best procedure to follow when a patient with a positive screen refuses such a referral is unclear. Patients may be more open to an assessment if the addiction specialist can see patients in the hepatitis clinic. If SUD treatment is recommended, then hepatitis and addiction treatment personnel need to work closely together to support completion of both treatments.

Current guidelines call for abstinence from IDU for at least six months prior to initiating interferon-based treatment for HCV, but available evidence suggests that recent or ongoing IDU does not adversely affect outcomes. In a five-year follow-up of 27 Norwegians who were successfully treated for HCV while injecting drugs, only one case of re-infection was found, even though 33% returned to IDU (Dalgard et al., 2002). Backmund et al. (2001) inducted 50 individuals who were undergoingdetoxification for injected drugs into hepatitis C treatment. The patients demonstrated excellent sustained virologic response rates (36%), and 39 patients did not miss one interferon injection, despite an overall relapse to IDU of 80%. One-half of those who returned to injecting heroin demonstrated sustained virologic response.

Former patients who were heroin-addicted who are currently receiving opioid agonist therapy with methadone or buprenorphine should not be excluded from treatment for HCV, and withdrawal from opioid agonist therapy is contraindicated, since relapse to IDU typically follows. There are no published studies addressing cannabis use in the context of hepatitis C treatment. There is also no evidence that cannabis use interferes with response to hepatitis treatment. Frequent cannabis users or those with symptoms of dependence should be offered referral to an addiction specialist, but if they are otherwise good candidates for hepatitis treatment, there is no reason at this time to deny them that opportunity.

Role of Psychiatrists

Psychiatrists can play an important role in identification, education and referral for chronic HCV infection. Mental disorders, as well as SUDs, place patients at higher risk for contracting HCV infection (Alter et al., 1999; Dieperink et al., 2000), and many HCV infections are not symptomatic. All patients with mental and addictive disorders need to be screened for their risk of HCV infection, and there should be a low threshold for testing, especially among patients with SUDs. All patients with a history of IDU or significant intranasal drug use should be tested.

Prevention plays an important role for patients with chronic hepatitis C infection. All patients should be educated about decreasing the risk for transmission to others. This includes not sharing razors, using condoms and avoiding sharing drug paraphernalia, including needles, cookers, filters (cotton) and nasal tubes. Most studies have found a low risk for long-time sexual partners and other household members. Alcohol use should be avoided or at least minimized. Caution must be used in prescribed medications with potential liver toxicity, although there is no evidence at this time that usual doses of medications such as acetaminophen, divalproex (Depakote) or naltrexone(Drug information on naltrexone) (ReVia) are more likely to be harmful in patients with HCV infection who are not in liver failure. More frequent monitoring of serum transaminases is indicated. In patients with HCV infection and those at high risk (e.g., IDU, intranasal cocaine use, unsafe sexual practices), consideration should be given to vaccination for hepatitis A and B virus infections if immunity is not present already.

Psychiatrists need to provide consultation, support and treatment for patients undergoing antiviral treatment for HCV infection. Antiviral treatment is associated with a high rate of depression and other neuropsychiatric symptoms, and pre-existing psychiatric symptoms are likely to get worse during antiviral treatment (Dieperink et al., 2003). Although no controlled trials are available examining efficacy for treating depression related to interferon treatment, case reports and clinical experience suggest that selective serotonin reuptake inhibitors are safe and effective. Citalopram(Drug information on citalopram) (Celexa) and sertraline(Drug information on sertraline) (Zoloft) may be the best first-line agents, as they have few drug-drug interactions and tend to be well-tolerated. Irritability in the absence of a full depressive syndrome may be quite troublesome, and antidepressants may be of significant benefit in this instance as well. One study identified the Beck Depression Inventory (BDI), given at two to four week intervals, as helpful in early identification of depression (Dieperink et al., 2003). Suicide is an issue as well, especially among patients whose liver disease does not respond to antiviral treatment and who may become hopeless. Suicidal ideation of some kind is endorsed by 20% to 30% of patients during interferon treatment (Dieperink et al., unpublished data), and needs to be further explored so that appropriate treatment can be offered.

A common complaint among gastroenterologists treating HCV infection is that they are unable to receive the support they need from psychiatrists. Psychiatrists can improve access to antiviral therapy for patients by educating ourselves about HCV infection and treatment, and by providing support to patients and to hepatitis providers.

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References
1. Alter MJ (1997), Epidemiology of hepatitis C. Hepatology 26(3 suppl 1):62S-65S.
2. Alter MJ, Kruszon-Moran D, Nainan OV et al. (1999), The prevalence of hepatitis C virus in the United States, 1988 through 1994. N Engl J Med 341(8):556-562.
3. Backmund M, Meyer K, Von Zielonka M, Eichenlaub D (2001), Treatment of hepatitis C infection in injection drug users. Hepatology 34(1):188-193.
4. Bhattacharya R, Shuhart MC (2003), Hepatitis C and alcohol: interactions, outcomes, and implications. J Clin Gastroenterol 36(3):242-252.
5. Bohn MJ, Babor TF, Kranzler HR (1995), The Alcohol Use Disorders Identification Test (AUDIT): validation of a screening instrument for use in medical settings. J Stud Alcohol 56(4):423-432.
6. Bush K, Kivlahan DR, McDonell MB (1998), The AUDIT alcohol consumption questions (AUDIT-C): an effective brief screening test for problem drinking. Ambulatory Care Quality Improvement Project (ACQUIP). Alcohol Use Disorders Identification Test. Arch Intern Med 158(16):1789-1795.
7. Cook PA, McVeigh J, Syed Q (2001), Predictors of hepatitis B and C infection in injecting drug users both in and out of drug treatment. Addiction 96(12):1787-1797.
8. Corrao G, Arico S (1998), Independent and combined action of hepatitis C virus infection and alcohol consumption on the risk of symptomatic liver cirrhosis. Hepatology 27(4):914-919.
9. Dalgard O, Bjoro K, Hellum K et al. (2002), Treatment of chronic hepatitis C in injecting drug users: 5 years' follow-up. Eur Addict Res 8(1):45-49.
10. Diaz T, Des Jarlais DC, Vlahov D et al. (2001), Factors associated with prevalent hepatitis C: differences among young adult injection drug users in lower and upper Manhattan, New York City. Am J Public Health 91(1):23-30.
11. Dieperink E, Ho SB, Thuras P, Willenbring ML (2003), A prospective study of neuropsychiatric symptoms associated with interferon-alpha-2b and ribavirin therapy for patients with chronic hepatitis C. Psychosomatics 44(2):104-112.
12. Dieperink E, Willenbring M, Ho SB (2000), Neuropsychiatric symptoms associated with hepatitis C and interferon alpha: a review. Am J Psychiatry 157(6):867-876.
13. Donato F, Tagger A, Gelatti U et al. (2002), Alcohol and hepatocellular carcinoma: the effect of lifetime intake and hepatitis virus infections in men and women. Am J Epidemiol 155(4):323-331.
14. Estrada AL (2002), Epidemiology of HIV/AIDS, hepatitis B, hepatitis C, and tuberculosis among minority injection drug users. Public Health Rep 117(suppl 1):S126-S134.
15. Hernandez-Aguado I, Ramos-Rincon JM, Avinio MJ et al. (2001), Measures to reduce HIV infection have not been successful to reduce the prevalence of HCV in intravenous drug users. Eur J Epidemiol 17(6):539-554.
16. Maier I, Wu GY (2002), Hepatitis C and HIV co-infection: a review. World J Gastroenterol 8(4):577-579.
17. Okazaki T, Yoshihara H, Suzuki K et al. (1994), Efficacy of interferon therapy in patients with chronic hepatitis C. Comparison between non-drinkers and drinkers. Scand J Gastroenterol 29(11):1039-1043.
18. Saracco G, Olivero A, Ciancio A et al. (2003), Therapy of chronic hepatitis C: a critical review. Curr Drug Targets Infect Disord 3(1):25-32.
19. Sees KL, Delucchi KL, Masson C et al. (2000), Methadone maintenance vs 180-day psychosocially enriched detoxification for treatment of opioid dependence: a randomized controlled trial. JAMA 283(10):1303-1310 [see comments].
20. Thomas DL (2001), Hepatitis C. Epidemiologic quandaries. Clin Liver Dis 5(4):955-968.


 
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