Epidemiology, Modes of Transmission, and Risk Factors for Hepatitis C Virus (HCV)
July 9-14, 2000
"My opinion is that we just can't tell for sure about some of this because we are bad at measuring human behavior." -- Davis Thomas, e-mail correspondence
BackgroundDuring the 1970s and 1980s, no one knew what was causing hepatitis in certain individuals who had received blood transfusions. Screening tests for hepatitis A (HAV) and hepatitis B (HBV) in the mid-1970s revealed that about 25% of these cases of transfusion-associated hepatitis (TAH) were linked to hepatitis B but not hepatitis A. The remaining 75% of TAH cases, by default, were termed non-A-non-B hepatitis (NANBH) (H. Alter 1999). Ten to twenty percent of individuals who had received multiple blood transfusions (or used plasma products) developed NANBH, with a relative risk of 0.45% per unit transfused (Donahue 1992).
Because primary infection was usually asymptomatic or, at worst, mild, clinicians did not initially consider NANBH to be a very serious disease. It was soon recognized, however, that the seemingly benign NANBH could develop into a chronic hepatitis with markedly elevated liver enzymes. Sometimes the hepatitis resulted in cirrhosis.
According to the National Institutes of Health's (NIH) Harvey Alter, attitudes to NANBH changed in the late 1980s:
The NANBH agent remained a virologic enigma . . . until researchers at the Chiron Corporation used an ambitious molecular approach on large volumes of high-titer infectious chimpanzee plasma from the Centers for Disease Control and Prevention (CDC). They extracted RNA, cloned it into an expression vector, and screened the expressed product with presumed immune sera. A single positive clone was found in the millions screened, and, within a year, the entire genome was sequenced and the agent was identified as a novel flavivirus the hepatitis C virus (HCV). (HJ Alter 1999).
In 1988 Choo and colleagues characterized the hepatitis C virus (HCV), and shortly thereafter, an antibody test was developed to detect infection (Choo 1989; Kuo 1989). When NIH researchers performed HCV assays on archived blood samples, it was determined that 70% to 90% of NANBH cases were actually HCV infections.
Prevalence of HCV Infection in the United States (U.S.)HCV is considered the most common blood-borne infection and is one of the leading causes for liver transplantation among adults in the U.S. After the HCV antibody test became available, epidemiology studies were performed to ascertain the incidence of the infection. The original studies, however, were considered flawed because they were conducted with first-time blood donors, individuals who had already been screened for risk factors such as infectious diseases.
A recently published study by Miriam Alter and colleagues from the Centers for Disease Control and Prevention (CDC) reported that an estimated four million persons nationwide are HCV-antibody-positive (ab+), indicating exposure to the virus. Roughly three-quarters of these have detectable HCV RNA, indicating chronic infection (MJ Alter 1999b). These data hail from the CDC's third National Health and Nutrition Examination Study (NHANES III), conducted between 1988 and 1994, and involving a sample of almost 40,000 persons between the ages of 2 and 89 years.
Out of this group, 21,241 individuals agreed to be both interviewed and tested for antibodies to HCV; of these, 1.8% were found to be HCV-antibody-positive. For the entire U.S., this corresponds to approximately 3.9 million residents infected with HCV. Below is a breakdown of the prevalence of HCV-antibody-positivity classified by race or ethnic group and gender.
Prevalence of Antibody to HCV (Anti-HCV) According to Race or Ethnic Group & Gender in NHANES III
* P<0.05 for comparison with non-Hispanic whites (MJ Alter 1999b)
HCV Prevalence in Blood Donors in Southern EuropeSeveral large HCV epidemiology studies have been published in Italy, France, and Spain. Below is a breakdown of anti-HCV prevalence in selected studies that have been conducted since the early 1990s.
HCV Incidence Rates in Six Large Southern European Cohorts
HCV Prevalence in EgyptWith an estimated HCV infection rate of 25%, Egypt has a higher incidence of HCV infection than any other country in the world (Arthur 1997). The Nile Valley area has higher rates of infection compared to cities and desert areas. The Egyptian HCV epidemic is a result of a widespread treatment campaign against schistosomiasis, an ancient parasitic disease. From the 1920s to the 1980s, the government administered parenteral antischistosomal therapy (usually 6-12 injections) with reusable syringes (Frank 2000). With course of injections taking two to four weeks, an individual infected early in treatment could then spread HCV on a subsequent injection to others who used the same syringe.
Modes of Transmission and Risk GroupsNumerous epidemiology studies have documented that individuals from high-risk groups, including recipients of blood transfusions before 1991, hemophiliacs, intravenous drug users (IDUs), homosexuals, and alcohol abusers have an exceedingly high prevalence of HCV antibodies.
Blood Transfusion Recipients and Hemophiliacs before 1992In the mid-1960s, the rate of post-transfusion hepatitis was greater than 20% (HJ Alter 1972). When donor blood in the U.S. began to be screened and excluded for antibodies to HAV, HBV, and HIV between 1985-1990, the rate of new HCV infections declined by more than 50%, lowering the risk of HCV seroconversion to 1.54% per transfusion patient or to 0.19% per unit transfused (Donahue 1992). In May 1990, a first-generation enzyme immunoassay EIA-1 was introduced to screen U.S. blood donors. It was soon replaced by the much more sensitive multiantigen test (EIA-2) in July 1992. The EIA-2 has dramatically reduced the risk of HCV infection, lowering rates to 0.001% per unit transfused (Schreiber 1996). According to Harvey Alter:
The impact of HCV blood donor screening has been enormous. The single-antigen first-generation enzyme immunoassay (EIA-1) prevented 40,000 HCV infections within the first year, and the second-generation assay (EIA-2) has actually reduced new transfusion-related HCV infections to almost zero. (HJ Alter 1999)
Before 1985, the rate of HCV infection in hemophiliacs who received clotting factor concentrates prepared from plasma pools was at least 90% (CDC 1998). Factor VIII and Factor IX, which inactivated blood-borne viruses such as HCV, were introduced in 1985 and 1987, respectively.
Injection Drug UsersThe rate of HCV infection among IDUs who share contaminated needles, syringes, or drug preparation equipment continues to remain high. In numerous studies conducted around the world, the incidence of HCV among IDUs ranges from 70% to 92% (Esteban 1989; van den Hoek 1990; Donahue 1991; Zeldis 1992; Garfein 1996; Broers 1998; Hershow 1998; van Beek 1998).
With regard to non-injectable drug use, intranasal cocaine use was reportedly associated with HCV infection in a study conducted by Conry-Cantilena from Harvey Alter's group at the NIH (Conry-Cantilena 1996). Finding a highly significant correlation in a multivariate analysis, the author theorized that if the device shared for snorting cocaine (a straw) was contaminated with blood, it could convey virus to denuded nasal mucosa, allowing HCV to enter the bloodstream. This possible mode of transmission-referred to by some as the "bloody straw" theory -- was highly debated, and in 1998, the CDC listed intranasal cocaine users in the category of "Persons for whom routine hepatitis C (HCV) testing is of uncertain need" (CDC 1998).
It appears that this finding by Corny-Cantilena and colleagues may have been a fluke, or merely that intranasal cocaine use is a surrogate for other behavior which could foster HCV transmission. More recently Murphy and colleagues, of the NHLBI Retrovirus Epidemiology Donor Study (REDS), published a study reporting that, in a multivariate logistic regression model, intranasal cocaine use (or use of any other powered drug) was not a risk factor for HCV (Murphy 2000).
Occupational (Needlestick) ExposureThe prevalence of HCV infection in health care workers, including orthopedic, general, and oral surgeons averages 1-2% (Thomas 1993, 1996). The serocoversion rate after an unintentional needlestick injury from an HCV-positive source is ~1.8% (MJ Alter 1994; Puro 1995). It appears that the seroconversion rate with solid needles is lower compared to needlesticks with hollow cannula devices (Puro 1995).
Percutaneous Exposure in Other SettingsWhile apparently rare, HCV transmission has been associated with commercial barbering, tattooing, ear piercing, and religious scarification (Tumminelli 1995; Abildgaard 1991; Thompson 1996; Conry-Cantilena 1996; Murphy 2000). Tumminelli and colleagues found that 38% of Sicilian barbers studied had antibodies to hepatitis C and suggested that shaving was a potential route of transmission. In the REDS study, Murphy and colleagues determined that religious scarification, sharing toothbrush and/or razor, having been tattooed, and having been pierced (body or ear) were all risk factors for HCV seropositivity after controlling for IVDU (OR = 3.8; 1.6; 3.9; and 2.7, respectively).
Perinatal TransmissionMost U.S. and international studies have reported the incidence of anti-HCV positivity in pregnant women to be between 0.7% and 4.4% (Marcellin 1993; Marranconi 1994; Leikin 1994; Hillemanns 1998; Resti 1998; Conte 2000). One recent perinatal transmission study from the metropolitan New York City area documented an ominous 41% anti-HCV incidence rate in a cohort of pregnant women -- 79% of whom were past or present IDUs (Granovsky 1998). The rate of HCV RNA detectability in several international cohorts of anti-HCV-positive women ranges from 65% to 72% (Resti 1998; Granovsky 1998; Conte 2000).
Reported rates of mother-to-infant HCV transmission have ranged from 0% to 36% in numerous studies, with higher rates occurring when mothers are HIV-positive (Ohto 1994; Zanetti 1995; Sabatino 1996; Tovo 1997; Granovsky 1998; Resti 1998; Thomas 1998b; Conte 2000). When these data are analyzed together, the average rate of vertical HCV transmission appears to be approximately 5%. Studies have demonstrated that rates of vertical transmission are dependent upon five factors: 1) presence or absence of HCV RNA in the mother; 2) high or low HCV viral load; 3) HIV status of the mother; 4) vaginal vs. caesarean delivery; and 5) breast vs. bottle feeding.
The only consistent factor found in studies is that vertical transmission does not occur if the mother is HCV RNA-negative at time of birth. In 20 perinatal HCV transmission studies analyzed by Dore and colleagues, none of the 735 aggregate HCVab+ but HCV RNA-negative women gave birth to an HCV-infected infant (Dore 1997). Some studies have documented a decreased incidence of vertical transmission from mothers with low HCV viral load (HCV RNA levels differ among studies). Other studies, however, have not found this correlation to be significant.
Mother's HCV RNA Level and its Correlation with Transmission of HCV to her Newborn: Conflicting Results
Another Italian study of 245 infants found the incidence of HCV vertical transmission higher in coinfected mothers. Overall, 28 (11.4%) of the 245 infants acquired HCV: 3 of 80 (3.7%) whose mothers had HCV infection alone vs. 25 of 165 (15.1%) whose mothers were coinfected (P<0.01) (Tovo 1997).
In a study of solely coinfected mothers, Thomas and colleagues found that the risk of HCV infection was 3.2-fold greater if the infant also acquired HIV compared to HIV-uninfected infants (17.1% of 41 vs. 5.4% of 112, P=0.04). All HCV transmissions were from mothers with HCV RNA viral loads over 2,000,000 copies/mL (Thomas 1998b).
A mother's co-infection was found not to be a significant risk factor for transmitting HCV in a New York multicenter study conducted by Granovsky and colleagues (Granovsky 1998). Five of 73 (7%) coinfected mothers transmitted HCV to their infants compared to 2 of 49 HCV+/HIV- mothers (P=0.7). There was also no significant difference in HCV viral load levels between transmitting and non-transmitting mothers. Lastly, an interesting finding about HIV and its possible enhancement of HCV transmission comes from the largest HCV vertical transmission study yet conducted. In a cohort of 370 anti-HCV-positive women, 15 (4.0%) were coinfected with HIV but did not transmit HCV to their infants. All of the coinfected women were receiving HIV antiretroviral therapy during their pregnancy, and investigators believe that reducing HIV-related immunosuppression may have affected HCV titers and the consequent likelihood of HCV transmission (Conte 2000).
A handful of studies have documented modest increases in the rate of HCV vertical transmission to infants delivered vaginally rather than by caesarean section (Tovo 1997; Granovsky 1998). However, larger studies with more patients have not observed any differences due to mode of delivery (Resti 1998; Mast 1999; Conte 2000). HCV transmission through breast feeding has not been considered a route likely source of infection for infants (Kumar 1998). In the vast majority of studies that evaluated breast feeding in infants born to HCV-positive women, no difference has been observed between bottle and breast feeding (Resti 1998; Tovo 1997; Mast 1999; Conte 2000). In fact, the CDC and the American Academy of Pediatrics do not feel that there is a risk from either breast feeding or vaginal delivery and have chosen not to recommend caesarean section or bottle feeding to HCV-infected mothers without HIV (CDC 1998).
Finally, no diagnostic screening criteria for perinatal HCV infection currently exist. Many studies have theorized about the optimal time to determine the infection status of an infant because various patterns have been observed in both infected and uninfected infants of HCV-positive mothers. For example, Conte and colleagues documented that the rate of HCV-positivity at birth for 366 newborns was 100%, but decreased to 90%, 63%, 16%, and 9% after 4, 8, 12, and 18 months respectively (Conte 2000). HCV RNA was detectable in 18 (4.9%) infants at birth, but 16 became negative by month four, and 6 infants who tested negative at birth became positive at month four. With similar findings from a recent CDC-sponsored study, Mast and colleagues concluded that "anti-HCV testing may not be a reliable marker of perinatal HCV infection until the infant is 2 years of age" (Mast 1999).
There appear to be as many knowns as unknowns with regard to HCV vertical transmission and the exact prognostic factors which lead to infection. According to Johns Hopkins' David Thomas:
Without a randomized clinical trial, perinatal transmission cofactors will be difficult to evaluate conclusively. Even multiple consistent results from observational studies could be misleading. . . . The most conclusive randomized trial would have to include more than 800 mother-infant pairs to detect a twofold increase in transmission with 80% power. (Thomas 1998a)
Sexual TransmissionIs HCV sexually transmissable? For the past 11 years, this question has been widely studied and heavily debated among researchers from Atlanta to Australia. Miriam Alter and colleagues in a 1989 JAMA paper reported the first study to suggest that heterosexual transmission may play an important role in the spread of NANB hepatitis (Alter 1989). In this study, of 140 patients with HCV, 64 patients (46%) had no commonly recognized percutaneous risk factors; 7 (11%) had had multiple sexual partners and were believed to have contracted HCV through sex. Since then, there have been at least 50 articles published (not to mention scads of letters to the editors) in major hepatology, virology, and HIV-related peer-reviewed medical journals which have looked at HCV sexual transmission among the general population, hemophiliacs, heterosexuals, homosexuals, people with HIV and STDs, and sex workers.
Heterosexuals in Long-term Monogamous RelationshipsSexual transmission of HCV between heterosexual couples in long-term monogamous relationships who have no identifiable percutaneous risk factors (or after stratifying for such factors) appears to be quite infrequent. Gordon and colleagues reported that 2 of 42 (4.8%) heterosexual adults who were in stable sexual relationships with an HCV-infected partner developed HCV (Gordon 1992). Since one of the individuals had a risk factor for HCV, only 1 of 42 individuals (2.4%: 95% CI, 0.6-12.9%) was thought to have been infected through sex. Osmond and colleagues found the incidence of HCV to be high in their cohort of 170 men and 170 women in sexual partnerships: 31 (18%) of the women and 56 (33%) of the 170 men tested anti-HCV-positive (Osmond 1993b). Sexual transmission was not demonstrated because IV drug use, a history of a blood transfusion, or hemophilia treatment was associated with all but 2 of 87 HCV infections. No HCV transmissions were documented in a study of 94 husbands whose spouses all contracted HCV from contaminated anti-D immunoglobulin (Meisel 1995) nor in an Australian study which tested 50 heterosexual partners of HCV viremic individuals (Brester 1993). In Asian countries, however, higher rates of sexual transmission in married heterosexual couples have been reported, ranging from 8.8 to 28% (Chang 1994; Nakashima 1995; Chayama 1995).
Two large studies looking at the sexual transmission among female sex partners of HCV-infected hemophiliac males documented a low transmission rate. Eyster and colleagues and Brettler and colleagues found a sexual transmission rate of 2.6% and 2.7%, respectively (Eyster 1991; Brettler 1992).
In an elegant, high-tech study, Zylberberg and colleagues conducted genotypic, sequence, and phylogenetic analyses on 24 anti-HCV-positive couples to ascertain if they harbored the same strain of virus (Zylberberg 1999). The mean duration of the partnership was 12 years (range 1 to 36). Serum HCV RNA was detected in both partners in 18 (75%) of the couples and in only one partner in the other 6 (25%) couples. In the 18 couples who had detectable HCV RNA in both spouses, 11 of 18 (61%) had the same genotype while 7 of 18 (39%) did not. Phylogenetic analysis was conducted in 7 of the 12 genetically concordant couples. In three couples, HCV strains differed by 1 to 3 nucleotides with a sequence similarity of 98% (evolutionary distance 0.065) suggesting that these spouses were infected by a common source. The other four couples differed by 4 to 15 nucleotides (evolutionary distance 0.0129) and thus their strains were considered unrelated. Sexual transmission of HCV was, however, ruled out in the three matched couples because all six spouses had at least one identifiable parental risk factor.
Sex WorkersA small number of studies, mostly outside the U.S., have been conducted among sex workers to ascertain if they are at higher risk for HCV transmission. Wu and colleagues studied 622 sex workers in Taiwan for anti-HCV antibodies and risk factors of transmission (Wu 1993). Seventy- four (12%) of the women were anti-HCV-positive and 60 (~10%) were HCV RNA-positive. In a multivariate analysis, history of paid sex for longer than six months and blood transfusion were positively associated with anti-HCV (P<0.001). Less than 20% of the HCV-infected sex workers had undergone a blood transfusion. Lissen and colleagues tested 310 Spanish female sex workers and 88 of their clients for anti-HCV (Lissen 1993). All denied prior transfusion or intravenous drug use. The prevalence of anti-HCV by ELISA, confirmed by a RIBA-2, was 6.4% among the sex workers and 6.8% among the clients. In contrast to these two studies, a very low rate of HCV positivity was reported in a study of Peruvian sex workers (Hymans 1993). Of 966 sex workers tested, only 7 (0.7%) had antibodies to HCV.
Homosexuals, People with HIV and STDs, and Sex Partners of IDUsThe prevalence of HCV appears to be substantially higher in homosexuals (men who have sex with men [MSM]), and people with HIV and STDs, than in the general population. Below is an analysis of 16 studies, most in high-risk populations, which document either sexual transmission or an infectious disease as a risk factor for HCV.
Both make statements that are far too general and more important do not acknowledge that sex is not a defined act; it means different things to different people, and sexual practices can and do differ widely from household to household. These limitations (i.e., lack of detailing sexual acts or high-risk behavior) are common in a majority of studies reviewed. While some studies document that sleeping with an HIV-positive or HBV-positive individual is a risk factor for transmission, we don't know what was done in bed (if it was in a bed) that created the extra risk. Too often, "high-risk sexual behavior" and "sexual promiscuity" are not defined, nor are we privy to whether condoms were used. Thus, it is the particular sexual act (e.g., insertive vaginal or anal intercourse, oral sex, anal fisting, etc.) that needs to be explored for its risk of HCV transmission. Murphy's belief that sexual transmission is "inefficient at best" is surprising since it contradicts his 1996 JAMA and 2000 Hepatology papers on risk factors for HCV transmission in the REDS cohort, which document that HIV and HBV, and sex with an IDU, respectively, are risk factors in multivariate analyses (Murphy 1996, 2000).
Murphy's argument against sexual transmission -- even in homosexuals -- is weakly supported by a single review article, which fails to note that most studies rejecting the risk of sexual transmission were too small and underpowered to detect such risks (MacDonald 1996). According to Donahue and colleagues, who documented a 1.6% incidence rate of HCV in a cohort of 926 homosexuals, "the small number of HCV-seropositive subjects may have limited the power to identify risk factors for infection" (Donahue 1991). Likewise, Buchbinder aknowledged that the small sample size of her 1994 study (Buchbinder 1994) may have limited its power to find sexual transmission as a risk factor in the multivariate analysis, even though numerous sex acts were identified in the univariate analysis (Susan Buchbinder, personal communication, 2000).
It is not surprising that the risk of HCV sexual transmission appears greater for homosexuals than for heterosexuals. From HIV studies, we have excellent data documenting that the risk of transmitting HIV is greater for homosexuals than heterosexuals, for women from men than for men from women, and for anal than vaginal intercourse (Padian 1991; Kingsley 1990). Moreover, specific sex acts as well as the physical condition of an individual play major roles in establishing risk. For example, Moss and colleagues in 1987 documented that douching before anal sex (vs. not douching) was independently associated with HIV seropositivity (OR, 2.2-2.8) (Moss 1987). Chmiel and colleagues from the Multicenter AIDS Cohort Study (MACS) examined numerous types of sexual behavior between homosexual men and found that, aside from unprotected receptive anal intercourse, "the factor most strongly associated with prevalent HIV infection according to a multiple logistic regression model was rectal trauma, a composite variable which included receptive anal fisting, enemas before sex, reporting of blood around the rectum, and the observation of scarring, fissures or fistulas on rectal examination (OR, 7.7)." (Chmiel 1987)
While such behaviors are physical symptoms and are not universal among all homosexual men, if one partner with HCV has penile sores or ulcers and the other partner has blood around the rectum, fistulas, or fissures, it is plausible that there will be blood-to-blood contact and possible HCV transmission. Documentation of specific risk factors like these is necessary in order to 1) elucidate various ways the virus might enter the body; and 2) define specific "high-risk behavior" so that individuals can be counseled about which sexual practices lower the risk -- no matter how small it might be -- of contracting HCV.
The CDC states that "data indicate overall that sexual transmission of HCV appears to occur, but that the virus is inefficiently spread through this manner." It does, however, call for further research into this controversial area:
More data are needed to determine the risk for, and factors related to, transmission of HCV between long-term steady partners as well among persons with high-risk sexual practices, including whether other STDs promote transmission of HCV by influencing viral load or modifying mucosal barriers. (CDC 1998)
After this call for more data, it is interesting to see that the CDC in its Recommendations for Prevention and Control of Hepatitis C Virus (HCV) Infection places both "long-term steady partners of HIV-positive persons" and "persons with a history of multiple sex partners or sexually transmitted diseases" in the same category as "persons for whom routine HCV testing is of uncertain need [emphasis added]" (CDC 1998).
The CDC and the Infectious Disease Society of America took a more proactive stance in 1999, calling for HIV-infected individuals to be screened for HCV in its revised USPHS/IDSA Guidelines for the Prevention of Opportunistic Infections in People with Human Immunodeficiency Virus (CDC 1999). Acknowledging that many HIV-infected individuals are coinfected with HCV, the guidelines give a nod to the safer-sex practice of condom use:
Although the efficiency of sexual transmission of HCV remains controversial, safer-sexual practices should be encouraged, and barrier precautions (e.g., latex condoms) are recommended to reduce the exposure of sexually transmitted diseases. (CDC 1999)
Why did it take until 1999 for the CDC to issue such a recommendation? In 1993, University of California-San Francisco (UCSF) epidemiologist Dennis Osmond sounded a calm but serious warning, which appeared to fall on deaf ears:
Despite the infrequency of HCV sexual transmission, sexual behavior may still be an important mode of spread if the pool of asymptomatic but infectious carriers is large. Because HCV infection becomes chronic in a high proportion of cases and subclinical hepatitis may be common, there is reason to believe that this carrier pool could be large, and even a low level of sexual transmission may result in a substantial attributable risk. (Osmond 1993a)
A Warning for VeteransA fascinating study was recently presented which infers that the rate of HCV infection in U.S. veterans is 10 times higher than in the general population, and that combat blood exposure is a highly significant risk factor for HCV transmission. Briggs and colleagues from Teresa Wright's group at the San Francisco Veterans Affairs Medical Center (SFVAMC) conducted a study with 791 veterans undergoing routine outpatient phlebotomy at the SFVAMC (Briggs 1999). Participants had their blood screened for anti-HCV positivity by EIA II, which was confirmed by Chiron bDNA. All were asked to answer a detailed questionnaire regarding sociodemographic characteristics and potential HCV risk factors. Of the 791 participants (95% male), 150 (19%) and 110 (13.9%) were anti-HCV-positive and HCV RNA-positive, respectively. The multivariate analysis below documents four significant risk factors, including the surprising finding that those exposed to blood during combat were 2.5 times more likely to develop HCV.
Risk Factors for HCV Infection in San Francisco Veterans: Multivariate Analysis
ConclusionThe discovery of the HCV virus by molecular techniques and the development of an antibody assay in 1989 were the first steps in understanding and identifying the cause of liver disease in blood transfusion recipients. Since then, the sensitivity and specificity of the EIA has markedly improved, and the screening of blood donors has made the blood supply significantly safer (risk of 0.001% per unit transfused). In the U.S., approximately 2% of the population (four million people) are infected with HCV, and HCV appears to more common in Blacks and Hispanics. Internationally, the prevalence ranges from 0.1% to 5%, but in Egypt, it is estimated to be 25%. It is almost certain that blood-to-blood contact is the only way to transmit HCV. Intravenous drug use (IVDU) remains the main mode of transmission, with rates of infection ranging from 75% to 92% in various cohorts. Those engaging in IVDU should be tested for HCV and refrain from sharing syringes, cotton, and cooking equipment. The rate of perinatal transmission of HCV is approximately 5%, and the CDC does not feel that there is a risk from either breast feeding or vaginal delivery. The risk of transmitting HCV sexually is a controversial subject. In monogamous heterosexual couples, there appears to be little if no risk, yet in certain populations, including homosexuals and people with HIV or STDs, the risk appears to be 5-15%. Larger studies are needed to determine which sexual practices place individuals at increased risk of contracting HCV. Until then, individuals with "multiple sexual partners" engaging in "high-risk" sexual behavior should always use condoms.
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This article was provided by Treatment Action Group. It is a part of the publication The Hepatitis Report.