More than 50% of people with chronic hepatitis C virus (HCV) infection may not be aware of their infection . Because approximately 75% of cases are among persons born between 1945 and 1965 [1-3], age-cohort screening of asymptomatic adults with no recognized risk factors is thought to increase identification and treatment for these patients. In addition to required HCV screening in the specific birth cohort, healthcare providers should screen patients with other risk factors for HCV infection (see the Risk-Based Screening section of this guideline).
As part of HCV screening and diagnosis, a series of serologic and virologic tests are used, including laboratory-based antibody tests, point-of-care rapid HCV antibody tests for initial screening, and laboratory-based HCV RNA tests for HCV diagnosis.
|KEY POINT: REPORTING|
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Hepatitis C Virus Infection Guideline Committee, December 2017
|NEW YORK STATE REQUIREMENT|
In NYS, physicians, physician assistants, and nurse practitioners delivering primary care must provide HCV screening, regardless of setting and without regard to certification. Care providers working in hospitals (inpatient units and outpatient clinics) and other healthcare settings where primary care services are being delivered are also required to offer HCV screening. Emergency departments are not required by law to offer HCV screening, but in NYS, they are encouraged to do so.
If the initial screening is reactive, clinicians must offer follow-up healthcare, including HCV diagnostic testing, or referral to an experienced HCV care provider. By requiring HCV antibody screening for this age cohort in traditional medical settings and supporting screening efforts in community-based locations, NYS is actively seeking to identify people with chronic HCV infection and link them to treatment before irreversible liver damage occurs.
In response to the law, hospitals, clinics, health centers, and other primary care medical facilities have established HCV screening programs. During the first year of implementing the law, there was a 51% increase in specimens submitted for HCV testing. Testing rates among active Medicaid clients increased 52%. Among persons with newly diagnosed HCV infection, linkage to care increased approximately 40% in NYS (excluding New York City) and 11% in New York City .
However, people with HCV infection may face significant barriers to accessing care in clinical settings, including lack of health insurance, physical disability, ongoing substance use, mental health disorders, and housing instability. Locating HCV screening sites in a variety of community-based organizations, such as syringe exchange programs, sexually transmitted disease (STI) clinics, and local health departments, is integral to the effort to provide HCV screening, treatment, and education in diverse settings.
Birth cohort screening is particularly important because patients may not be aware of or remember exposures or may not disclose prior behavioral risks for HCV infection (see the Risk-Based Screening section of this guideline). Patient education is needed to ensure that patients know about risk factors for transmitting or acquiring HCV infection. While birth cohort screening is important, screening for HCV beyond the required birth cohort is needed in areas where HCV prevalence is high.
- See NYSDOH: Hepatitis C Educational Materials
- Flanigan CA, Leung SJ, Rowe KA, et al. Evaluation of the Impact of Mandating Health Care Providers to Offer Hepatitis C Virus Screening to All Persons Born During 1945-1965 – New York, 2014. MMWR Morb Mortal Wkly Rep 2017;66(38):1023-26. [PMID: 28957037]
Hepatitis C Virus Infection Guideline Committee, December 2017
In the United States, an estimated 60% of chronic HCV infections result from use of shared needles, syringes, or other drug-use paraphernalia . Overall, sexual transmission accounts for approximately 5% of HCV infections, although transmission rates differ in select groups, as discussed below. Vertical transmission (transmission from mother to child) accounts for 5% to 6% of infection; receipt of contaminated organs or blood component transfusions before HCV testing of the blood supply began in 1992 accounts for approximately 5% of HCV infections . The average incidence of anti-HCV seroconversion after unintentional needle sticks or sharps exposures from a source with confirmed HCV infection is estimated at 1.8% , and HCV infection has also resulted from unsterile skin piercing activities, such as tattoos in prisons (1%) . There are a few case reports that might suggest transmission during trauma, including biting  and fist fighting , when there is potential for blood-to-blood transmission, but there are insufficient data to limit patients with HCV from participating in sports such as boxing or wrestling at this time.
Injection drug use: Sharing of injection drug use (IDU) equipment is an efficient method of transmitting HCV. In the United States, a reduction in new HCV infections between 1992 and 2009 was attributed to expansions of syringe-access programs, safer injection practices among people who inject drugs (PWID), and increased enrollment in drug treatment programs . However, HCV prevalence among PWID entering substance use treatment in New York City (n = 1,535) was 67% (95% confidence interval: 66% to 70%) during the 2006 to 2013 period and was not significantly different from that observed from 2000 to 2001 .
The demographics of IDU now include many young people living in suburban and rural regions . Adolescents and young adults may advance to IDU after first becoming addicted to prescription oral opioids . Reports from several states (including New York State), underscore the importance of awareness of HCV risk among adolescent and young adult patients and of offering HCV screening to this population [8-13].
|KEY POINTS: HCV SCREENING IN ADOLESCENTS AND YOUNG ADULTS|
Intranasal drug use: In a systematic review of 28 studies on the prevalence of HCV in noninjecting drug users who smoked, sniffed, or snorted such drugs as heroin, powder or crack cocaine, or methamphetamine, investigators found HCV prevalence rates ranging from 2.3% to 35.3% [15,16]. Among noninjecting drug users, sharing of oral and nasal drug use equipment is associated with an increased risk of HCV infection [17-19]. In addition, blood and HCV RNA have been confirmed in the nasal secretions and drug-sniffing paraphernalia of HCV-infected intranasal drug users .
Sexual transmission: Because many with HCV infection have a history of drug use, estimation of sexual transmission is a challenge (as reviewed in ). Sexual transmission of HCV among monogamous heterosexual couples is infrequent. The estimated maximum prevalence of HCV infection among sex partners of individuals with chronic HCV infection was only 1.2%, and the maximum incidence of HCV transmission through sex contact was 0.07% per year or approximately 1 per 190,000 sexual contacts . Sexual transmission risk increases in the setting of multiple partners, STIs, HIV, and exposure to blood . Several reports have demonstrated isolated outbreaks of sexual HCV transmission among MSM with HIV infection who engage in receptive anal intercourse [12,23-25]. In a report from New York City on sexual transmission among HIV-infected MSM with no previous history of injection drug use, new HCV infections were highly correlated with receptive anal intercourse, engaging in sex while using methamphetamine, or participating in group sex .
History of incarceration: Incarcerated populations are a significant but declining portion of the HCV epidemic in the United States [26-28]. A study from 2009 to 2013 at two maximum-security prisons in New York State estimated an HCV prevalence of 10.1%; injection drug use, being the partner of a PWID, and HIV diagnosis were most strongly associated with HCV infection . In 2015, 22.2% of newly reported cases of chronic or acute HCV infection in New York State (excluding New York City) had a reported history of incarceration . In New York City, the rate of newly reported chronic HCV infection in 2015 was 86.3 per 100,000. In the incarcerated population of the city, the rate was 964.3 per 100,000 for the same year .
Exposure to blood in a healthcare setting: The average incidence of anti-HCV seroconversion after unintentional needle sticks or sharps exposures from a source with HCV infection is 1.8% . Healthcare-related transmission of HCV is documented infrequently in the United States [30,31]. In 2014, among reported acute HCV cases that included information on exposure type, 1% was considered to be occupationally acquired .
Hemodialysis: The estimated 8% prevalence of anti-HCV antibodies among chronic hemodialysis patients is significantly higher than the estimated 1.6% prevalence in the general U.S. population . Nationally, 36 cases of acute HCV infection in 19 different hemodialysis clinics in 8 states were reported between 2014 and 2015, with epidemiologic and viral sequencing confirming transmission between patients . The Centers for Disease Control and Prevention (CDC) recommend HCV antibody screening upon admission for chronic hemodialysis patients, followed by screening every 6 months thereafter [33,34]. The National Kidney Foundation stratifies by prevalence and recommends antibody screening upon admission to facilities with a low HCV prevalence and consideration of HCV RNA testing upon admission to facilities with high HCV prevalence .
Receipt of blood transfusion or organ transplant before 1992 or clotting factor concentrates from human plasma before 1987: Donor screening for HCV infection and inactivation procedures for pooled plasma and plasma derivative products have virtually eliminated the risk of HCV transmission through blood products in the United States [1,36].
Vertical transmission: A 2011 meta-analysis estimated that the risk of vertical HCV infection to children of HCV antibody-reactive and HCV RNA detectable women was 5.8% for children of HIV-uninfected women and 10.8% for children of women with HIV infection . From 2011 to 2014, the national rate of HCV infection among women of childbearing age (15-44 years old) increased by 22% (from 139 to 169 per 100,000), and the national rate of infants born to women diagnosed with HCV infection increased by 68% (from 0.19% to 0.32%) . Factors associated with an increased risk of perinatal transmission include HIV coinfection and higher maternal HCV viral loads [37,39]. Neither delivery by cesarean-section nor refraining from breastfeeding has been demonstrated to reduce vertical transmission .
Tattoos, piercings, or acupuncture obtained in nonsterile settings: Tattoos or piercings obtained in nonsterile settings, and especially those obtained during incarceration, have been associated with HCV infection, even after controlling for injection drug use and transfusion before 1992 [40,41]. Low levels of HCV RNA have been detected on acupuncture needles from individuals known to have HCV infection , although acupuncture has not been established as a confirmed route of transmission.
HIV infection: HCV infection is common among persons with HIV infection because the routes of acquisition are similar. For decades, injection drug use has been recognized as the main risk factor for HIV/HCV coinfection, but an increasing number of sexually transmitted HCV infections have been documented in MSM with HIV [43-45]. In a recent study among MSM with HIV in Europe, Australia, and Canada, HCV incidence significantly increased from 1990 to 2014 . Analyses of data from the Multicenter AIDS Cohort Study (MACS) in the United States and from a cohort of HIV-infected MSM in San Diego demonstrated a similar rise in HCV incidence among MSM [46,47]. In this population, sexual acts that may tear mucous membranes, sex while using methamphetamines, and having other STIs have been associated with HCV infection [43,44].
Unexplained liver disease or abnormal transaminase levels: In primary care patients with an alanine transaminase (ALT) level 50 to 100 IU/L, HCV prevalence is 10-fold higher than in the general population, whereas hepatitis B (HBV) prevalence was not increased .
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