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http://www.medscape.com/viewarticle/408298
Infections Behind Bars
Hepatitis
C: A Correctional-Public Health Opportunity
from
Medscape
Infectious Diseases
Anne
S. De Groot, MD, Elizabeth Stubblefield, Joe Bick, MD
For
a variety of reasons, many diseases are present at a higher
prevalence in prisons and jails. Mental illness, HIV,
hepatitis B and C, and drug and alcohol addiction are just a
few of the conditions that are common in prisoners entering
the correctional system. What is often seen as an overwhelming
burden to correctional healthcare systems should more
appropriately be seen as a tremendous public health
opportunity. The stark truth is that most inmates will
eventually be released from prisons and jails. Once released,
many of them either do not have access to healthcare or fail
to avail themselves of it. In focusing healthcare resources on
the incarcerated, society has the opportunity to decrease
crime rates (mental illness, addiction), prevent transmission
(HIV, hepatitis, other sexually transmitted diseases [STDs]),
and lower lifetime costs associated with untreated diseases.
This article will focus on the challenges and opportunities
associated with the treatment of hepatitis C virus (Hepatitis C Virus) in
the incarcerated.
Epidemiology of Hepatitis C Virus in Correctional Settings
Hepatitis
C infection outstrips HIV in correctional settings in terms of
sheer numbers of inmates living with this infection (Table 1).
According to a recent analysis performed by Dr. Ted Hammett (Abt
Associates, Cambridge Massachusetts) and reported to Congress,[1] between 1.0 and 1.25 million individuals harboring chronic Hepatitis C Virus
infection were released from prisons and jails in the United
States in 1996, or approximately 30% (29% to 32%) of the
estimated 4.5 million individuals living with chronic Hepatitis C Virus
infection in the United States. The prevalence of Hepatitis C Virus
infection among US prisoners is at least 10-fold higher than
the estimated prevalence of 2% in the general population.[2] Outside of correctional settings, 79% of current
injection drug users (IDUs) have Hepatitis C Virus infection.[3]
In fact, young IDUs acquire Hepatitis C Virus infection at rates 4 times
higher than the rate of acquisition of HIV; after 5 years of
continuous injection drug use, 90% of IDUs are Hepatitis C Virus infected.
Hepatitis C Virus
prevalence studies in correctional settings are rare; however,
some statistics have been compiled from a number of sources by
HIV and Hepatitis in
Prison Project In the Colorado state prisons, for
example, the prevalence of Hepatitis C Virus among inmates has been reported
to be 30%.[4]
A recent survey of Arizona reported a 31.3% prevalence rate
among inmates (Gerard Chamberlin, personal communication). In Maryland,
the prevalence of Hepatitis C Virus among state inmates has been noted to be
slightly higher, at 38%.[5]
One county jail in semi-rural Massachusetts recently
reported that 20.7% of its jail inmates had Hepatitis C Virus infection
(Hampden County).[6] In Virginia, 30% to 40% of inmates
have been reported to have Hepatitis C Virus infection.[7]
Approximately the same rate has been reported in Washington
state (30% to 40%).[8]
The prevalence of Hepatitis C Virus among state inmates in Pennsylvania is
slightly lower, at 13%.[9]
Reflecting
their higher rate of participation in HIV and Hepatitis C Virus risk
behaviors, incarcerated women exhibit about a third higher Hepatitis C Virus
co-infection rate than incarcerated men.[10]
For example, in a sample of incoming inmates in California,
54% of women inmates, compared with only 40% of men inmates,
have Hepatitis C Virus infection.[11]
In Connecticut, 1 in 3 women (32%) incarcerated at the
only state facility for women inmates has Hepatitis C Virus infection.[12] In Texas, 37% of incarcerated women and 28% of incarcerated
men have Hepatitis C Virus infection.[3]Wisconsin reported Hepatitis C Virus infection rates among women inmates
that are almost 2-fold higher than the rates among men: 21%
for women, 12.4% for men, 13.2% overall.[13]
Hispanics
and non-Hispanic blacks have higher rates of Hepatitis C Virus and HBV
infection and chronic disease than whites; most cases of Hepatitis C Virus
and HBV infections are found among persons who are male,
members of minority populations, and 30 to 49 years of age.[3]
These race- and class-related risk factors for hepatitis
infection probably contribute to the current concentration of
Hepatitis C Virus- and HBV-infected persons in prisons and jails.
Screening for and Treating Hepatitis C Virus in Correctional Facilities
The
CDC lists correctional institutions, HIV counseling and
testing sites, and drug and STD treatment programs as sites
where hepatitis screening and interventions should take place.
(See Table 2 for screening recommendations.) Correctional
facilities that screen for Hepatitis C Virus and educate their inmates about
Hepatitis C Virus are performing a significant public service, since
approximately 50% of persons with hepatitis are unaware of
their hepatitis infection.[1]
Testing for hepatitis infection informs the patient and
physician about the potential for and possible existence of
liver damage, and it should serve as an important prompt for a
discussion about risky behaviors and transmission to others.[1]
Treatment of Hepatitis C Virus
The
current standard of care in community settings is to treat
chronic Hepatitis C Virus patients who meet treatment selection criteria
with a combination of ribavirin/interferon alpha (Table 3).
Most correctional facilities have either developed protocols
for screening and treating Hepatitis C Virus-infected inmates, or are in the
process of developing these protocols. However, the criteria
for Hepatitis C Virus treatment may vary slightly from one correctional
system to another. The CDC is in the process of developing a
set of guidelines for Hepatitis C Virus screening and treatment that may
assist correctional facilities with their decision-making
process. (A draft of the hepatitis recommendations that are
proposed for publication in MMWR [Morbidity and
Mortality Weekly Report] in the fall of this year can be
obtained by contacting Rob
Lyerla or Cindy Wientraub
or by calling 404-371-5460.)
In
general, eligible patients meet the following criteria: (1)
have evidence of persistent Hepatitis C Virus infection and inflammation
based on liver function test (LFT) abnormalities and
detectable virus in the blood stream; (2) have enough time
left in their sentence to allow for completion of treatment
(6-12 months) (3) are committed to a life free from substance
and alcohol abuse; (4) are educated about potential Hepatitis C Virus
treatment side effects and willing to adhere to an arduous
course of treatment.
Standard
therapy is to provide daily treatment with ribavirin (usually
5-6 pills divided into 2 doses) and thrice-weekly
alpha-interferon injections. (See Table 3 for dosing and side
effects of treatment regimens.) Pegylated interferon, a new
form of interferon that permits once-weekly dosing, was
approved by the FDA this year. Monotherapy is currently used
only if the patient cannot take ribavirin due to toxicities or
side effects.
Response Rates
Combination
therapy consistently yields higher rates of sustained response
compared with monotherapy. (A sustained response implies that
Hepatitis C Virus RNA remains undetectable for 6 months or longer after
therapy stops.) With combination therapy, 40% of
treatment-naive patients respond. Patients with genotype-1
have sustained response rates of 25% to 30% (slightly better
response rates are seen with lower baseline Hepatitis C Virus viral loads).
Non-genotype-1 patients achieve response rates of 60% to 65%.[14,15] Other factors that increase the likelihood of a response to
therapy include age younger than 45, female gender, and mild
(rather than advanced) chronic inflammation on liver biopsy.
Histologic improvement occurs in 86% of patients who achieve a
sustained response and 39% of patients who relapse after
initial response to combination therapy.[15]
Cost vs Benefits
As
with many other chronic medical conditions, morbidity and
mortality attributable to Hepatitis C Virus may not manifest themselves
until well after the end of incarceration. Treatment is often
ineffective, poorly tolerated, and prohibitively expensive.
Many correctional systems, still reeling from the impact of
providing HIV treatment, have been slow to embrace wide-scale
treatment of hepatitis C. Additionally, the therapy in most
cases is being given to IDUs who are in forced institutional
abstinence, have not had and will not have drug treatment, and
will therefore probably be promptly reinfected upon release.
Despite
these concerns, some state medical directors have led the way
and adopted clear protocols for the screening and treatment of
Hepatitis C Virus in their facilities. These individuals are mindful that a
year 2001 dollar spent on treatment may reduce the eventual
cost (to society) of caring for patients who may require liver
transplants in 20-30 years.[4,16] Furthermore, combination therapy of Hepatitis C Virus is leading to higher
rates of cure (up to 88% in carefully selected patients);
therefore, the overall cost-effectiveness of Hepatitis C Virus interventions
in corrections is improving.
Cost-benefit
analyses have been performed. For example, medical decision
analyst J. Wong calculated that 6 months of combination
therapy resulted in net savings in the range of $400 to $3500
over the lifetime of each Hepatitis C Virus-infected patient.[17]
Dr. Wong's analysis ranked combination therapy for Hepatitis C Virus in the
same range of cost-effectiveness as stool guaiac testing,
pneumococcal vaccination, coronary bypass surgery, and
mammography.[17]
Liver Biopsy
The
need for confirming the extent of damage to the liver by Hepatitis C Virus
and chronic HBV infection is another area of debate, since
obtaining liver biopsies can be both costly and logistically
complicated in correctional settings. LFTs can be normal in
patients with rather advanced cirrhotic features. Likewise,
LFTs may be consistently elevated in hepatitis C patients with
normal histology. Some state correctional systems do not
routinely perform liver biopsies prior to initiating
treatment, because of cost and logistical difficulties. Other
states (eg, Florida) believe biopsies are the only real way to
measure disease progression over time and therefore have made
arrangements to do them on site at very reduced costs ($200
per biopsy). Depending on the cost of obtaining a liver
biopsy, electing to treat all incarcerated individuals who
meet the criteria for treatment may be more cost-effective for
society as a whole than management by biopsy.[17]
The Lowest-Cost Intervention: Education
The
lowest-cost intervention for the prevention of hepatitis
infection is education. Given the risk of acquiring Hepatitis C Virus (not
to mention HIV), all bloodborne pathogen screening events
should lead to careful discussion of the risks of acquiring
HIV, HBV, and Hepatitis C Virus infection (for those patients who have
negative hepatitis serologies). The risk of transmitting
hepatitis should also be made very clear (see Resources for
information on educational materials).
The
impact of continued drug use should also be made very clear to
patients, especially those who are not yet Hepatitis C Virus infected. For
those inmates who are already Hepatitis C Virus infected, education should
be provided on the impact of alcohol abuse on Hepatitis C Virus progression
(4-fold increase in risk of progression, risk of liver damage
directly correlated with alcohol intake) and the risk of
transmission to uninfected sexual partners. Inmates who have
Hepatitis C Virus infection should, at the very least, be educated about
options for treatment even if they are not eligible for
treatment while incarcerated (see Resources for information on
expanded access programs).
Additional Considerations
Another
low-cost (but not no-cost) intervention is vaccination. For
Hepatitis C Virus-infected patients, vaccination against HBV and HAV is
routinely recommended, as these relatively inexpensive
vaccines may reduce the risk of fulminant liver failure and
the need for liver transplantation for Hepatitis C Virus-infected patients.
A new schedule of HBV vaccination (3 shots at 0, 1, and 4
months) has received approval. The first shot provides up to
50% protection, and the series does have efficacy even if it
is given over several years, so the new CDC guidelines are
expected to encourage initiating HBV vaccination even in jail
settings.
Management of Hepatitis C Virus in Correctional Settings
Since
the incidence of side effects to Hepatitis C Virus combination therapy can
be relatively high and it can be difficult for incarcerated
patients to quickly gain access to their clinician to report
side effects, it is important to:
- Spend time preparing the patient for potential
treatment-related side effects
- Prescribe PRN medications for symptom management
- Consider following the patients in a dedicated
hepatitis clinic
- Consider establishing a support group for
patients under Hepatitis C Virus treatment
- Utilize peer education programs when possible
- Use a nurse or other staff person to regularly
check in with patients who are receiving Hepatitis C Virus treatment so
that side effects can be rapidly addressed
Without
a good support system, a high percentage of patients will fail
to complete therapy. Because of the high cost of treatment,
time spent preparing patients and supporting them while on
treatment is likely to be cost-effective. Table 4 provides
guidelines for monitoring treatment.
HIV and Hepatitis C Virus Coinfection
Analyses
of the effect of Hepatitis C Virus and HIV co-infection on progression of
either disease are often confounded by concurrent risk factors
for progression. However, available data seem to indicate that
HIV infection accelerates Hepatitis C Virus liver disease. Persons who are
co-infected (HIV/Hepatitis C Virus) appear to have a 12- to 300-fold higher
risk of developing hepatocellular carcinoma compared with
noncarriers.[18]
Furthermore, antiretroviral agents can contribute to liver
inflammation, and this may be more frequent in those who have
underlying chronic hepatitis due to Hepatitis C Virus or HBV. Ritonavir and
nevirapine appear to be the antiretroviral therapy medications
that are most commonly associated with liver inflammation in
Hepatitis C Virus/HIV co-infected patients.[19]
The
impact of Hepatitis C Virus infection on HIV infection is less clear. In
some studies, Hepatitis C Virus infection does not appear to have an effect
on the progression of HIV.[20]
Other studies have reported an association between more rapid
progression to AIDS or death in HIV-infected patients,
particularly among those who were co-infected with Hepatitis C Virus
genotypes 1a and 1b.[21,22] However, a report by Sulkowski[23]
at the 8th National Conference on Retroviruses and
Opportunistic Infections (CROI), contraindicated these
findings, suggesting that risk of progression was more closely
linked to lack of access to medical care (for HIV) in his
cohort of African American patients who had HIV and Hepatitis C Virus
co-infection.
Response
to Hepatitis C Virus therapy in individuals who also have HIV infection
appears to be equivalent to that of non-HIV-infected
individuals.[24] A recent study in JAMA by Sulkowski and
associates[19] indicates that 88% of co-infected patients tolerate concurrent Hepatitis C Virus
treatment and highly active antiretroviral therapy (HAART).
Following successful Hepatitis C Virus treatment, co-infected patients are
not more likely to relapse after Hepatitis C Virus treatment than are
patients who do not have concurrent HIV infection.
Currently,
when exclusionary criteria are not present (see Table 2),
treatment of hepatitis C is recommended for patients when CD4
and viral load values reflect good response to antiretroviral
treatment. Although some controversy remains with regard to
the definition of a good response to HAART, a stable CD4+
T-cell count greater than 200 with a stable viral load less
than 400 is generally accepted.[25]
Conclusion
The
cost of Hepatitis C Virus treatment is expected to be a major barrier to
wide implementation of the guidelines in prisons and jails.
There is a concern that treatment could overwhelm some
systems' healthcare budgets. The high prevalence of hepatitis
infections among incarcerated individuals and the availability
of treatments with less than 100% efficacy force difficult
decision making in correctional health facilities.
The
clustering of individuals with hepatitis and other treatable
illnesses in correctional facilities creates not only
challenges but opportunities as well. With an effective public
health-correctional collaboration, the opportunity exists to
make a tremendous impact on the health of society as a whole.
Without such initiatives, many prisoners will eventually
return untreated to the communities from which they came.
Prisons and jails are an ideal site for introducing public
health interventions that will have a positive impact on
hard-to-reach communities; this opportunity to improve public
health should not be overlooked.
It
must be noted, however, that the cost savings that may accrue
from treatment of prisoners are primarily to society as a
whole. While treatment of incarcerated individuals for
hepatitis and HIV is the right thing to do and can
tremendously benefit the public health, it is not realistic to
expect correctional systems to shoulder this financial burden
without assistance. Guidelines and standards for selecting
patients who are to be treated, while providing access to care
for Hepatitis C Virus-infected individuals regardless of incarceration
status, are forthcoming from the CDC. Correctional physicians
eagerly anticipate further guidance from state and federal
health officials on supplemental sources of funding for Hepatitis C Virus
treatment initiatives in correctional settings.
Acknowledgements
This article is modified from an article by Anne S. De Groot
entitled Hepatitis C Virus: The Correctional Conundrum, published in HEPP
News, Vol. 4 (4), April 2001. Available at: http://www.hivcorrections.org/archives/april01/.
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Dr. De Groot is Director, TB/HIV Research Lab and Chief Editor, HIV and
Hepatitis Education/Prison Project, Brown University,
Providence, Rhode Island, and staff, HIV in Prison
Project, Yale University, New Haven, Connecticut. Ms.
Stubblefield is Managing Editor of HIV and
Hepatitis Education Prison Project (HEPP) News at
Brown University. Dr. Bick is Director, HIV
Treatment Unit, California Medical Facility, California
Department of Corrections, Vacaville.
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