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Open Access Research article

Outcomes of hepatitis C screening programs targeted at risk groups hidden in the general population: a systematic review

Freke R Zuure1*, Anouk T Urbanus12, Miranda W Langendam3, Charles W Helsper4, Charlotte HSB van den Berg12, Udi Davidovich1 and Maria Prins12

Author Affiliations

1 Public Health Service of Amsterdam, the Netherlands, Infectious Diseases Cluster, P.O. Box 2200, Amsterdam 1000 CE, The Netherlands

2 Center for Infection and Immunology Amsterdam (CINIMA), Academic Medical Center (University of Amsterdam), P.O. Box 22660, Amsterdam 1100 DD, The Netherlands

3 Dutch Cochrane Centre, Academic Medical Center, P.O. Box 22660, Amsterdam 1100 DD, The Netherlands

4 Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, P.O. Box 85500, Utrecht 3508 GA, The Netherlands

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BMC Public Health 2014, 14:66  doi:10.1186/1471-2458-14-66


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/14/66


Received:2 September 2013
Accepted:10 January 2014
Published:22 January 2014

© 2014 Zuure et al.; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Effective screening programs are urgently needed to provide undiagnosed hepatitis C virus (HCV)-infected individuals with therapy. This systematic review of characteristics and outcomes of screening programs for HCV focuses on strategies to identify HCV risk groups hidden in the general population.

Methods

We conducted a comprehensive search of MEDLINE and EMBASE databases for articles published between 1991–2010, including studies that screened the general population using either a newly developed (nonintegrated) screening program or one integrated in existing health care facilities. Look-back studies, prevalence studies, and programs targeting high-risk groups in care (e.g., current drug users) were excluded.

Results

After reviewing 7052 studies, we identified 67 screening programs: 24 nonintegrated; 41 programs integrated in a variety of health care facilities (e.g., general practitioner); and 2 programs with both integrated and nonintegrated strategies. Together, these programs identified approximately 25,700 HCV-infected individuals. In general, higher HCV prevalence was found in programs in countries with intermediate to high HCV prevalence, in psychiatric clinics, and in programs that used a prescreening selection based on HCV risk factors. Only 6 programs used a comparison group for evaluation purposes, and 1 program used theory about effective promotion for screening. Comparison of the programs and their effectiveness was hampered by lack of reported data on program characteristics, clinical follow-up, and type of diagnostic test.

Conclusions

A prescreening selection based on risk factors can increase the efficiency of screening in low-prevalence populations, and we need programs with comparison groups to evaluate effectiveness. Also, program characteristics such as type of diagnostic test, screening uptake, and clinical outcomes should be reported systematically.

Keywords:
HCV; Testing; Case finding; Case detection; Reporting guidelines

Background

Hepatitis C virus (HCV) infection, primarily a blood-borne virus and first identified in 1989, is a major public health problem. Worldwide an estimated 130–170 million individuals are HCV-antibody positive [1], of whom approximately 75% are chronically infected and at risk for the development of cirrhosis, which can lead to liver cancer and death [2,3]. In chronically infected patients, the onset of HCV infection and the development of cirrhosis are usually asymptomatic [2,4]; many infections remain undetected or are diagnosed at a late stage. In the United States of America (USA), an estimated 43% to 72% of HCV infections are undiagnosed [5-7]. In 2001, successful combination therapy for HCV became widely accessible [8,9] and more effective therapeutic options are becoming available [10,11]. Effective screening programs are urgently needed to provide undiagnosed HCV-infected individuals with therapy and to spread information about preventive measures that each person should take, thus decreasing future morbidity and mortality.

There are several types of screening strategies such as mass population screening, selective screening, or case finding (i.e., opportunistic screening [12]). Selective screening of risk groups for HCV (see below) has been recommended [13,14]. Some of the high risk groups for HCV are relatively easy to reach and have been targeted by screening programs as part of specialized medical care (e.g., current drug users (DUs) on methadone treatment who have injected drugs in the past [15], hemophiliacs [16], and HIV-infected individuals receiving clinical care [17]). However, other risk groups are more difficult to target for screening. For example, persons at risk for HCV infection through occasional injecting drug use (IDU) in the remote past will not attend programs targeted at active injecting drug users and might not identify themselves as being at risk for HCV infection. The same holds true for individuals who received a blood transfusion before 1992. These groups can be considered as ‘hidden risk groups’ among the general population. The size of this hidden population may be substantial. A recent study estimated that of the total population of HCV-infected individuals in a high-income country, only 34% are in relatively easy to reach high-risk groups such as hemophiliac patients, HIV-infected patients, and persons with a history of IDU; 41% are first-generation migrants and 25% belong to other risk groups [18].

Risk groups for HCV infection[13,14]

• Individuals with a history of injecting drug use (IDU), including those who injected only a limited number of times many years ago and do not consider themselves to be drug users

• Individuals who received clotting factor concentrates produced before 1987 or a blood transfusion or an organ transplant before 1992 including hemophiliac patients (systematic screening of blood donors for HCV antibodies was introduced in 1991) [19]

• Individuals with occupational exposure to infected blood

• People living with HIV

• Chronic hemodialysis patients

• Children born to HCV-infected mothers

• Individuals exposed to HCV-infected blood through invasive procedures or blood product transfusions due to absence of precautionary measures to prevent transmission, mostly in low-resource settings. This group includes first-generation migrants.

Finding an effective strategy to identify the hidden population of undiagnosed HCV-infected individuals is challenging. An overview of HCV screening programs provides insight into strategies that have been used so far and their outcomes, and can provide insight into the best way forward. In our review, we systematically evaluate characteristics and outcomes of HCV screening programs targeted at risk groups hidden in the general population. We focused in particular on the promotion of the screening program, whether or not prescreening selection criteria were used, and the use of psychosocial theory or knowledge about determinants facilitating participation in screening programs, since health promotion programs that are based on theory are more likely to be effective than those that are not [20]. We discuss the implications of these findings for future HCV screening strategies.

Methods

Search strategy

We searched in the MEDLINE (PubMed) and EMBASE databases for articles published in any language before July 27, 2010. A comprehensive strategy was used to include all possible studies in which individuals were screened for HCV. Search terms included hepatitis C (Medical Subject Headings [MeSH] for PubMed and Explosion search [Exp] for Embase) or HCV or “hepatitis C” in title or abstract combined with search terms in title or abstract that reflect screening (i.e., mass screening [MeSH/Exp], screen*, “case finding*”, “case identification*”, “case detection*”, “hepatitis C testing”, “HCV testing”) or search terms in title or abstract and/or MeSH/Exp that reflect campaigns or evaluation of health programs (i.e., campaign*, health promotion, health service*”, feasibility, pilot*, “program* evaluation*”, “program* effect*”, “*health care quality”). The search was limited to articles published after 1990 since a more sensitive second-generation HCV antibody test was introduced in 1991 [21]. The complete search strategy including truncation characters is available from the authors. In addition, we screened the reference lists of the articles that were included in the selection.

Study selection

Studies were included if they reported screening of individuals in the general population, including screening in primary care facilities that are not related to specific HCV risk groups. Screening is defined as testing for HCV antibodies. Exclusion criteria included ‘look-back’ studies, in which recipients of HCV-infected donor blood are notified and offered screening and studies conducted in specific, identifiable risk groups for HCV that are in specialized care: injecting drug users, HIV-infected individuals, incarcerated individuals, hemodialysis patients, or multitransfused patients such as hemophiliac patients. In addition, studies were excluded if 1) the study was designed to assess the prevalence in a given population, and/or 2) if the study was undertaken to investigate transmission rates and determinants or the association between HCV infection and another medical condition, and/or 3) nothing was reported about notification, referral, or medical follow-up of participants (these studies were considered prevalence studies, not aiming to identify HCV infections). The latter criterion did not apply to studies describing HCV screening at the general practitioner (GP) clinic, since notification of results in this setting is considered to take place. Articles in languages other than English, Dutch, French, German, or Spanish were excluded if there was no English abstract of if the English abstract did not yield enough data.

The first selection round was based on title and abstract (if available) only and was done by four authors (FZ, AU, CH, and CvdB). The database including the titles and abstracts obtained through the search was split in four. The reviewers independently screened two of the subdatabases each so that each title/abstract was screened in duplicate. Studies were included in the second screening round if selected by at least one reviewer. The second selection round comprised screening of the full-text articles. Two authors (FZ and AU) independently screened all articles for eligibility using the aforementioned criteria. Any discrepancies were resolved by discussion until consensus was reached, and unresolved discrepancies were arbitrated by a third reviewer (MP).

Data extraction and validity checking

Data regarding program characteristics and program outcomes (see Parameters of screening programs) were extracted and cross-checked by two reviewers (FZ and AU). If the study reported HCV prevalence, but without specifying whether it concerned HCV-antibody or HCV-RNA prevalence, and if information about the test that was used was lacking, we assumed it to be HCV-antibody prevalence. Since the studies were performed in different periods of time, different types of tests were used over the years. Therefore the prevalences were qualified depending on the test used. Anti-HCV and HCV-RNA prevalence rates of studies were considered suboptimal 1) if data was collected prior to 1994 when sensitivity and specificity of tests were not optimal [19,22] or 2) if studies did not confirm reactive HCV antibody test results by immunoblot or PCR to eliminate false positives. Tests were considered valid if performed after 1993 and if 1) second- or higher- generation immunoblot assays from Ortho, Chiron, Novartis (RIBA), Innogenetics (LiaTek), Pasteur (DECISCAN HCV), Genelabs Diagnostics (HCV BLOT), or Mikrogen (recomBlot HCV IgG 2.0) were used to confirm HCV antibody reactive results or 2) PCR was used to confirm HCV- antibody reactive results. The validity of outcomes of studies that did not indicate which test was used, and studies that used dried blood spot (DBS), oral fluid screening, or immunoblot assays different from those indicated above, was considered undecided.

We distinguished two types of settings and presented the screening programs according to these: integrated and nonintegrated screening. Integrated screening refers to programs that are integrated within already existing health care facilities, whereas in nonintegrated screening, the program is exclusively set up for the screening. In addition, since screening strategies may differ according to the HCV prevalence in a specific country, data are presented not only by the type of setting, but also separately for low HCV prevalence (≤2%) ) and intermediate to high HCV-prevalence countries (>2%; country-specific prevalence estimates were obtained from reference [23]).

Parameters of screening programs

Program characteristics

• Country (and region, if applicable) of the study

• Estimated HCV antibody prevalence in the country

• Calendar year(s) of data collection

• Duration of enrolment/screening period

• Setting (i.e., whether HCV screening was integrated within already existing health care facilities or whether the program was exclusively set up for the screening [i.e., nonintegrated screening])

• Use of psychosocial theory or previous research findings as a basis for communicating the screening and for stimulating screening uptake

• Size of the targeted population

• Use of media activities and/or personal invitations to promote screening

• Use of screening criteria based on HCV risk factors

• Incentive or participant’s costs for screening

• Anonymous or nonanonymous participation

• Type of HCV test(s) that was used for screening

• Screening for other diseases performed

• Use of a comparison group for evaluation purposes

Program outcomes

• Response rate (i.e., proportion of the target population that was screened)

• Number of participants (i.e., number of individuals that were screened)

• Number of HCV cases identified

• Number of HCV cases already known

• HCV-antibody prevalence

• Risk profile of identified cases

• Proportion of HCV-antibody positives with detectable HCV RNA

• Number of referrals to specialist

• Start and outcomes of treatment

Results

The search strategy identified 5,263 records from the MEDLINE database and 6,300 from the EMBASE database. After duplicates were eliminated, 7,052 of 11,563 records remained. Of those, 737 were selected as potentially relevant to the review, and full-text articles were retrieved and reviewed independently in duplicate. We excluded 677 articles; 652 articles because they did not meet the inclusion criteria (the majority because they were prevalence studies, or studies that only reported statements about HCV screening guidelines and policy, not including any screening results), and 3 Japanese articles and 1 Italian because they did not provide an English abstract. In addition, 20 articles (two Chinese [24,25], eight Japanese [26-33], one Icelandic [34], four Russian [35-38], two Turkish [39,40], one Czech [41], and two Taiwanese [42,43]) seemed relevant on the basis of the English abstracts, but were excluded as the abstracts alone did not yield enough information for review. One article was excluded because the same data were reported in two papers [44,45]. Of the 60 studies remaining, references lists were screened yielding an additional 106 potentially relevant records. The full-text articles were retrieved and screened independently in duplicate, and 7 of the 106 studies were selected for inclusion. In total, 67 studies remained in the final selection.

The 67 studies identified were done in the USA (n = 27), Europe (n = 27; mostly France and the United Kingdom [UK]), Asia (n = 4), Australia (n = 4), South America (n = 3), Egypt (n = 1) and Saudi Arabia (n = 1). We identified 24 nonintegrated and 41 integrated studies, plus two studies that used both strategies (the latter are shown in the paragraph below for the results of the nonintegrated part of their program, and in the subsequent paragraphs for the results of the integrated part of their program) [46,47]. A total of 85% (22/26) of the non-integrated programs and all of the integrated programs were from low HCV-prevalence countries.

Nonintegrated HCV screening programs in low HCV-prevalence countries (n = 22)

Program characteristics

Additional file 1: Table S1 presents the 20 nonintegrated HCV screening programs and the 2 programs that combined an integrated and non-integrated screening approach that were performed in low HCV prevalence countries. In total, 12 of the 22 programs were carried out in the USA. The table is sorted by population type; seven studies were aimed at screening the general population; the other 15 studies targeted specific groups in which a higher HCV prevalence might have been expected (e.g., migrants, homeless individuals, firefighters, surgeons). Five of the 22 programs reported the use of personal screening invitations either face to face or by mail, and 12 reported the use of media activities to attract individuals for screening. Eight studies reported the possibility for individuals to participate anonymously. Only nine of 22 studies reported the costs for participants to be screened; in all of them, screening was offered free of cost, and one study offered a t-shirt as an incentive for screening [48].

Additional file 1: Table S1. Nonintegrated screening programs in low HCV-prevalence countries (≤2%) [23,46-54,111-123].

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This file can be viewed with: Microsoft Word ViewerOpen Data

With respect to screening procedures, except for two, all programs used venipuncture to collect serum. A program targeted at firefighters [49] used home specimen collection kits for serum collection. A program targeted at migrants [46] initially used oral fluid HCV antibody tests followed by a blood test for those who tested positive (no further details reported). In the majority (16/22) of the programs, participants were also screened for other infections (mostly HIV and hepatitis B virus [HBV]) or elevated liver enzymes (alanine aminotransferase [ALT], aspartate aminotransferase [AST]).

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 19 to 8,650. The screening uptake was reported in 13/22 studies, and varied from >20% in a screening program at a local health fair in the USA [50] to 100% in a program that used household visits to identify transfusion recipients and invite them for screening in Cuba [51]. The HCV prevalence varied from 0% to 28.3%. The latter was found in a community-based screening program in New York City targeted at migrants from the former Sovjet Union. HCV risk-profile data were available for only a subset of the HCV-infected individuals in that study and included intramuscular injections and blood transfusions. Some of the programs among a so-called ‘general population’ (see Additional file 1: Table S1, row 1–7) that found relatively high HCV prevalences (e.g., 10.5% in a walk-in clinic [52]), did not collect risk profile data of their participants, limiting the interpretability of their findings. Two of 22 studies used a prescreening risk assessment in order to limit screening to those with established HCV risk factors: one did not report the prevalence nor screening uptake [53]; the study in Cuba reported the highest screening uptake (100%) and found relatively high HCV prevalence (8.6%), but absolute numbers were small.

Four of the 22 programs screened primarily people from Asia, either through screening programs in Asia (Japan), or programs in Western countries targeting Asian migrants. In all but one of these programs, relatively high HCV prevalences were found, varying from 5.2% to 19.7%. In contrast, the programs targeting those with occupational risk for HCV (n = 7) found relatively low HCV prevalences (all <1.1%, except for 3.6% among firefighters and 5.3% among health care workers involved with liver transplantations).

We did not notice clear differences in screening uptake or HCV prevalence related to the use of personal invitations for screening, the use of media to attract individuals for screening, and whether or not individuals were screened for other infections as well. In general, a lower HCV prevalence was found in the studies (n = 8) that provided anonymous screening for HCV; however, most of these studies (6/8) targeted those with occupational risk for HCV, explaining the lower prevalence.

Only one study compared the results of their outreach screening program with data collected in the same period at a screening clinic that is visited by individuals on their own initiative [54]. A higher prevalence of HCV was found during outreach screening (4.9% versus 1.6%, respectively). However, the number of individuals that returned to obtain their test results was much lower for the outreach approach (65.8% versus 91.8%, respectively). Only one study reported the proportion of identified HCV-infected individuals that started treatment (37%) [53], but did not report how many of those reached a sustained virological response (SVR).

Nonintegrated HCV screening programs in intermediate to high HCV-prevalence countries (n = 4)

Program characteristics

Table 1 presents the four nonintegrated HCV screening programs that were performed in intermediate to high HCV-prevalence countries (Taiwan [n = 2], Pakistan [n = 1] and Egypt [n = 1]). All studies targeted the general population; one targeted children less than 16 years of age. A study from Egypt reported household visits to personally invite individuals for screening [55]; the study among children reported personal invitations (method not specified) [56]. All except the study among children reported the use of media activities to attract individuals for screening. A risk-based screening selection was used in the program in Egypt, where screening was limited to those with symptoms and ALT levels ≥ 2 times the upper limit of normal. None of the studies reported the possibility for individuals to participate anonymously. Two studies reported about the costs for participants to be screened; one of them offered screening free of cost, whereas the other program [57] offered screening at 20% of the market value. None of the studies used a comparison group for evaluation purposes. With respect to screening procedures, all four studies used venipuncture for specimen collection. A study from Pakistan [57] used a rapid HCV antibody test. In most (3/4) studies, participants were also screened for other infections (mostly HBV) but not for HIV.

Table 1. Nonintegrated screening programs in intermediate to high HCV-prevalence countries (>2%)

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 47 to 157,720. The screening uptake was reported in two studies; it was very low (<1%) in a city screening program in Pakistan [57], and very high (93.6%) in a screening program in kindergartens and schools in Taiwan [56]. Although the screening uptake in the latter was high, the prevalence was low (0.9%). The HCV prevalences in the other programs varied from 4.4% in a community-based screening program in Taiwan [58] up to 78.8% in a program in Egypt that limited screening to those with symptoms and increased ALT levels [55]. None of the studies reported the proportion of HCV-infected patients that started treatment and/or reached SVR.

Integrated HCV screening programs

We identified 41 HCV screening programs in the following clinics that offer care not related to liver disease: sexually transmittable diseases (STD) clinics (n = 11); GP clinics (n = 10, including two programs that also used a nonintegrated approach); Veterans Affairs (VA) clinics (n = 5); antenatal/obstetric/fertility clinics (n = 5); clinics for psychiatric patients (n = 3); and other clinics or services (n = 7). Tables 2, 3, 4, 5, 6 and 7 present the programs separately for each type of setting. All programs were carried out in low HCV-prevalence countries.

Table 2. Integrated screening programs at clinics for sexually transmitted diseases (STD)

Table 3. Integrated screening programs at general practitioner (GP) clinics

Table 4. Integrated screening programs at VA clinics

Table 5. Integrated screening programs in antenatal/obstetric/fertility clinics

Table 6. Integrated screening programs in psychiatric clinics

Table 7. Integrated screening programs integrated in other clinics or services

Clinics for sexually transmitted diseases (n = 11)

Program characteristics

The majority (7/11) of the HCV screening programs in STD clinics were carried out in the USA (see Table 2). None of the studies reported the use of personal invitations or media to promote HCV screening. In five of the 11 programs, screening was limited to high-risk groups for HCV, varying from single groups (e.g., people with a history of IDU [64], or MSM [60]) to individuals from multiple risk groups, such as those who have had body piercing or tattooing in unsanitary conditions, transfusion recipients before 1987, or those who have had a needlestick injury [59]. None of the studies reported whether or not individuals were charged for screening, or whether anonymous participation in the screening program was possible. None of the programs used a comparison group for evaluation purposes. All programs used venipuncture for specimen collection.

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 618 to 90,424. Six of the 11 programs reported the screening uptake, which varied from 14.0% to 95.8%. The HCV prevalence varied from 0.1% to 28.0%. Of the five studies that limited HCV screening to HCV risk groups, four reported a high prevalence (>15%). In contrast, the prevalences in the six studies without a risk selection varied from 0.1% to 4.9%. In all programs at the STD clinics, a history of IDU was found in the risk profile of the identified HCV-infected individuals, or was found associated with HCV infection. None of the studies reported the proportion of HCV-infected patients that started treatment and/or reached SVR.

General practitioners’ clinics (n = 12)

Program characteristics

The majority (8/12) of the HCV-screening programs in GP clinics were carried out in France (see Table 3). In most programs (9/12), screening was limited to HCV risk groups within the GP-patient population (specific migrant groups [46,47]; risk groups such as those with a history of IDU and recipients of blood transfusions before 1991 [70,72,73,75-78]). One program was carried out in a health care center that attracted people with poor access to health care, mostly migrants [44], and one was carried out in an area of low socioeconomic status [71]. In two of the 12 programs, individuals who were in the GP’s waiting room were approached and invited for screening [44,46], and five programs used media activities to attract individuals for screening. Of the 12 studies, four reported that screening was free of cost [70,73,78,99], whereas the others did not report participants’ costs for screening. Only the screening program among people with poor access to health care offered the possibility of anonymous screening [44].

In reference to screening procedures, all but two studies used venipuncture for specimen collection. Two screening programs used oral fluid HCV antibody tests, followed by blood tests for those who tested positive. The majority (9/12) of the programs focused solely on HCV screening. The three programs that screened predominantly migrants also included HBV screening [44,46,47].

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 117 to 15,952. Six of the 12 programs reported the screening uptake, which varied from 27.8% to 82.5%. The HCV prevalence varied from 0% to 30.8%. Of the 12 programs, three primarily screened migrants (prevalences 0%, 1.2% and 5.8%), seven used risk factors other than being a migrant as criteria for screening (prevalences 1.4% to 30.8%), and one was performed in an area of low socioeconomic status (prevalence 12.8%). In contrast, one program that did not use risk factors as screening criteria, and was not performed in an area of low socioeconomic status, found a relatively low prevalence of 0.4% [74]. We did not notice clear differences in screening uptake or HCV prevalence related to the use of media to attract individuals for screening. Further, we could not assess whether personally inviting individuals for screening or screening for more than just HCV could have influenced the screening uptake, since these studies did not report the screening uptake.

Four studies checked the results of their screening program against data collected in the same period in comparison clinics or data collected prior to the screening program. A study from the Netherlands concluded that the addition of primary care practice support leads to considerable improvements in medical awareness regarding HCV infection in primary care, which is likely to have a positive effect on case finding (that effect, however, could not be indisputably demonstrated) [76]. A study from France concluded that information and training that is adapted to GPs’ medical practice can lead to more active involvement of GPs in screening for HCV infection [77]. During the intervention the number of GPs that prescribed HCV screening increased, and more HCV-infected patients were detected compared with the year before. Another study from France compared two interventions in the GP clinic; GPs in intervention 1 prescribed HCV screening if HCV risk factors were identified during questioning of patients, whereas GPs in intervention 2 placed posters and leaflets on HCV risk factors in their waiting rooms to motivate patients at risk to discuss screening [78]. The numbers of tests prescribed by GPs was relatively low in both interventions, and outcomes of the two interventions with regard to the number of tests and the HCV prevalence were comparable. In a study from Scotland, HCV screening was offered to all GP visitors aged 30–54 years and 117 individuals were screened (prevalence: 12.8%, 15/117), whereas in a comparison clinic, where no intervention for HCV screening was introduced, no individuals were screened for HCV [71]. Two of these programs reported the proportion who started treatment (18% and 38%), but only one of these two programs reported the proportion of treated individuals (n = 2) who reached SVR (50%, n = 1) [71].

Veterans affairs clinics (n = 5)

Program characteristics

Table 4 presents the five HCV screening programs in VA clinics in the USA. No personal invitations or media activities were reported. All screening programs limited the screening to risk groups within the veteran population. In one program, screening was limited to veterans who were admitted for an alcohol and noninjecting drug rehabilitation program [82], while other programs used an extensive list of risk factors, including history of drug use, blood transfusion prior to 1992, and Vietnam veteran. None of the programs reported whether or not individuals could participate anonymously, participants’ costs for screening, or a comparison group for evaluation purposes. All programs used venipuncture for specimen collection and screened solely for HCV.

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 338 to 12,485. The screening uptake was described in three of the five programs, varying from 41.9% to 99.4%. The HCV prevalence in most programs was around 5%, but the program among veterans who were admitted to an alcohol and noninjecting drug rehabilitation program was substantially higher (23.1%). The proportion of patients that started treatment was described in three studies and varied from 15% to 38%. Four studies reported the SVR rate among those who started treatment, ranging from 33% to 47%.

Antenatal/obstetric/fertility clinics (n = 5)

Program characteristics

Of the five programs, three were carried out in the UK, one in the USA and one in Brazil (see Table 5). The programs targeted pregnant women, except for a British study in a fertility clinic that was targeted at couples. Media activities to promote the screening programs were described in only one of the five studies; this study used information leaflets to inform women about the screening program, and a personal invitation for participation by the midwife [87]. None of the programs used a risk assessment strategy to limit screening to those at risk. The programs did not report the possibility to screen anonymously, or a comparison group for evaluation purposes. The one program reporting screening costs was free of cost to participants [88].

With respect to screening procedures, all but one study used venipuncture for specimen collection. One study used DBS for anti-HCV screening and a second generation ELISA followed by HCV RNA testing using venous blood for confirmation [88]. In all but one program, participants were also screened for other infections (mainly HIV and HBV) or elevated liver enzymes (ALT/AST).

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 1,658 to 31,081. In the two studies reporting screening uptake, rates were very high (≥98%). In all but one program, the HCV prevalences were low, varying from 0.2% to 0.8%. In women at risk for perinatal complications, HCV prevalence was 4.6% [86]. In one of the five programs, results of the clinical follow-up and treatment were reported, showing that 67.9% of those identified with chronic HCV started treatment after delivery, and 80% of those who completed treatment achieved SVR [84].

Psychiatric clinics (n = 3)

Program characteristics

Of the three HCV screening programs in psychiatric clinics, two were carried out in Australia, and one in the USA (see Table 6). One program aimed to evaluate whether screening by risk factors would be effective, and limited the HCV screening program in one unit to those with a history of IDU and those exposed to contaminated blood products, whereas in the other unit all patients were screened [90]. In the other two programs, no risk selection was used for participation in the screening program. One program promoted screening by using media [91]. The programs did not offer the possibility to screen anonymously, and did not report about participants’ costs for screening. Concerning screening procedures, all studies used venipuncture for specimen collection, and all studies exclusively screened for HCV.

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 36 to 98. All programs reported the screening uptake, varying from 20.5% to 100%. The HCV prevalences varied from 3.2% in the unit without pre-screening risk selection [90], to 41.7% in the unit where screening was limited to those who reported a history of IDU or exposure to contaminated blood products. Noninjecting drug use and history of IDU were reported as the main risk factors among the identified cases. All three programs referred the HCV-infected individuals to a specialist. Of interest, in two programs [90,91], post-test counseling addressing various topics (e.g., education about the illness, risk behavior, safe injection practices, secondary prevention) was also offered to those who reported risk factors but tested HCV negative.

One of the three studies reported that their program was based on psychosocial theory or knowledge about determinants facilitating participation in HCV screening programs. This program promoted screening by using leaflets outlining HCV, its risk factors, and the importance of screening, and used individually tailored pre- and post-test counseling that was adapted to individual knowledge and cultural understandings where appropriate [91]. Although the uptake of screening in that study was relatively low (20.5%), the prevalence was relatively high (19.7%), especially considering the fact that no prescreening risk selection was used.

Other clinics (n = 7)

Program characteristics

In total, seven HCV screening programs were integrated in other clinics or services (see Table 7). These programs varied widely, from screening patients at an emergency health unit in France [92] to screening couples that wish to get married in Saudi Arabia [93]. Two programs targeted MSM; one in an outreach service for HIV point-of-care testing in the UK [95], and another in a community care facility in the USA [96].

The study in the USA reported the use of media activities to attract participants, wherein MSM were recruited through advertisements as well as by referral of medical staff [96]. Two of the seven studies used a prescreening selection; a program at an emergency health unit only screened those with a reported risk factor [92], and in France, only those with elevated ALT levels as determined during routine medical check-up were screened for HCV [94]. None of the programs reported about the possibility of anonymous screening, or a comparison group for evaluation purposes. The one study reporting about participants’ costs for screening mentioned that it was free [96]. With respect to screening procedures, all studies used venipuncture for specimen collection. Four of the seven programs also screened for other diseases (mainly HBV).

Program outcomes

The number of individuals screened for HCV antibodies per program ranged from 55 to 74,662. The screening uptake was reported in three out of seven programs, varying from 66.2% to 77.6%. The HCV prevalence varied from 0.3% in a mandatory premarital screening program in Saudi Arabia [93] to 11.5% in a program for MSM [96]. Only one study reported the number of patients that started treatment, which was zero [92].

Discussion

This systematic review describes characteristics and outcomes of HCV screening programs in the general population, and includes 67 programs. In total, 24 of them were exclusively set up for the purpose of HCV screening, whereas 41 were integrated in already existing health care facilities (not aimed at HCV risk groups), and two programs used both an integrated and nonintegrated approach. Altogether, the programs that were published identified approximately 25,700 HCV-infected individuals. Clearly, large-scale, and long-term screening and referral programs are needed to address the HCV-related burden of disease in an era of potent therapy for HCV.

The programs were highly heterogenic in their organization, recruitment, and screening procedure, and the vast majority did not use a comparison group to assess the effectiveness of their screening program. Hence, we cannot draw firm conclusions as to which screening program strategy, or which program characteristic (e.g., free-of-cost vs. low-cost screening, anonymous vs. nonanonymous screening, use of particular media to promote screening) is more effective than another in attracting or motivating individuals for screening or in attracting those at higher risk for HCV. Screening programs that compare different recruitment and screening strategies are needed to gain insight into effectiveness of strategies and program characteristics.

In addition, many studies did not report program characteristics (e.g., the laboratory tests that were used). The same was true for screening uptake and follow-up data regarding HCV-related care, and even if reported, there was not much consistency (e.g., some reported the SVR rate among those who completed treatment, whereas others reported that treatment was ‘rather successful’). The underreporting and the lack of uniformity of data reporting greatly hinder the comparison of screening programs. Data reporting standards (see Parameters of screening programs) are needed to be able to compare screening program characteristics and outcomes in order to find out which factors are effective. If demonstration projects for HCV screening are not able to demonstrate direct effects in terms of number of individuals who tested positive for HCV that are linked to care, secondary evaluation measures could be used. For instance by monitoring rates of HCV screening and positivity in the hospital or referral laboratory and by comparing these data with data from previous years or from hospitals or laboratories that were not involved in the demonstration project.

In general, we noticed relatively high HCV prevalences in programs that used a prescreening selection based on HCV risk factors (especially in programs that used elevated ALT or a history of IDU as indications for HCV screening) or migrant status, in programs that were carried out in intermediate to high HCV-prevalence countries or regions, and in programs in psychiatric clinics. Also, relatively high HCV prevalences were found in nonintegrated programs in low HCV-prevalence countries that targeted the general population (see Additional file 1: Table S1, row 1–7), even without a prescreening risk assessment. These programs might have screened a self-referred population, and may have attracted those at risk of HCV in the general population, and therefore observed prevalences are higher than those in the general population. For the study by Hayashi etal (see Additional file 1: Table S1), screening was performed in a specific region in Japan with a presumably high HCV prevalence, explaining the very high prevalence that was found. In most studies, a history of IDU was the main risk factor among the identified HCV-infected individuals. In general, low HCV prevalences were found in programs that targeted health care workers, and in programs that were carried out in antenatal clinics. Programs in STD and GP clinics that did not use a prescreening risk selection also found relatively low HCV prevalences.

Only one study reported that the promotion of the screening program was based on theoretical insights or knowledge about determinants facilitating participation in screening programs. None of the studies reported the use of simple tools that may increase the screening uptake, such as reminder messages [100], or support with planning of when and how to get screened (i.e., creating implementation intentions [101]). In many studies, and especially those describing nonintegrated programs, the uptake of screening was not reported.

We found that integrated screening programs in general screened a larger number of individuals than did nonintegrated screening programs in low HCV-prevalence countries. Integrated screening programs have three advantages in that they do not have to attract their target population for screening, and they can use a facility that is familiar to the public. In addition, they can facilitate continuous screening and follow-up of individuals at relatively low cost, whereas nonintegrated programs offer screening usually for a limited period. On the other hand, integrated screening programs only reach those who have a reason to visit such facilities (unless media campaigns have been used to attract more people), whereas nonintegrated programs may attract a different risk population that otherwise would not be screened and do not perceive themselves at risk for HCV (i.e., the hidden population). We believe that both approaches are useful and complementary. In addition, since nonintegrated screening in general is more complex to organize, it may be efficient to screen for other diseases simultaneously, when risk groups overlap.

We identified several studies that did not confirm HCV antibody test results. Many of the identified programs targeted asymptomatic individuals in the general population with a relatively low HCV prevalence. In such populations, unconfirmed HCV antibody test results may include 35% (range: 15%–60%) false-positive test results [102]. Hence, the program outcomes that are reported may include a substantial degree of uncertainty, and should be interpreted with care. We like to emphasize that HCV screening programs should use validated screening methods, and describe the tests that were used when publishing the results of their screening programs.

As for study limitations, the majority of the screening programs that were evaluated in this review occurred in just a few countries (USA, UK, and France), most likely since this review was limited to studies published in English, French, German, Spanish, and Dutch. Therefore, the results may not be generalizable to other (non-Western) countries or countries with a higher HCV prevalence. With respect to publication bias, this review only includes screening programs that were published and programs that were successful in identifying HCV-infected individuals may have been more likely to be published. However, we did identify several programs in which no individuals were diagnosed. Furthermore, as identification of HCV-infected individuals serves a clinical goal and not necessarily a scientific goal, not all screening efforts have been evaluated or published. Our search identified several announcements of HCV screening activities [103,104] or cost-effectiveness evaluations of screening activities [105] that did not provide any further information about the screening program and/or outcomes. Further, our review describes several screening programs, but it cannot determine the efficiency and effectiveness of these screening programs in preventing future HCV-related morbidity and mortality. Measuring these effects of HCV screening programs is a challenge because randomized, controlled trials or comparison groups and decades of follow-up time are required. As an alternative method, mathematical modelling studies can be useful to estimate long-term effects of screening programs (e.g., [106,107]), especially when certain program outcomes (e.g., participation rate, prevalence) are used as parameters in the model. The efficiency and effectiveness of screening also depends on the uptake and outcomes of therapy and other preventive measures that may follow from diagnosis. Efficiency relates to the number needed to be screened to identify a treatable case of HCV. Surprisingly, most studies did not report such data, and merely mentioned that HCV-infected individuals were notified of their test result and referred for clinical care. Following Wilson and Jungners third screening principle [108], facilities for diagnosis and treatment should be available. This means that the screening program itself is as important as the efforts that are undertaken to bring identified patients into care and have them benefit from preventive measures and/or treatment. Hence, evaluation reports of screening programs should include clinical follow-up and systematically report outcomes.

A recent systematic review by Jones etal on the effectiveness and cost-effectiveness of interventions aimed at raising awareness of and/or increasing engagement in case finding and screening with high-risk groups for HCV and HBV and practitioners included only programs with a comparison group (e.g., randomized controlled trials, pre- and postintervention data, repeated cross-sectional studies) [109]. About half of the studies (12/25) included in that review were aimed at high-risk groups for HCV that are relatively easy to target, such as current IDU and incarcerated individuals, whereas our review includes studies that aimed to identify the hidden population of HCV-infected individuals. Jones etal identified drug services and primary care as settings in which interventions could effectively increase screening uptake. They also found that DBS screening in addition to venipuncture might increase HCV screening uptake in drugs services or prisons. In our review, a few studies reported the use of home collection tests, DBS, or oral fluid tests, but these studies did not demonstrate high screening uptake. Further insight into the effect of alternative noninvasive screening procedures on screening uptake is needed. As in our review, Jones etal concluded that improvement of health outcomes following diagnosis for those identified with chronic HCV deserves careful attention.

In the United States it has recently been recommended that all people born between 1945 and 1965 should be offered a one-time screening without prior risk assessment [110], since HCV prevalence in this group is four times greater than adults aged 20 years or older who were born outside of the birth cohort, and identifying this group through a high risk profile has been unsuccessful so far. More importantly, this screening strategy is estimated to be cost-effective assuming an uptake of 15% [106]. Although a relatively low uptake of 15% was assumed in the cost-effectiveness model in the USA, those who participate may not be representative for the total population of baby boomers. It may be that those at lower risk for HCV (i.e., the worried-well) could be more likely to respond. Thus, although it may be promising, the effectiveness of such an intervention needs to be demonstrated in practice. Nevertheless, it should be examined whether it is feasible and cost-effective to implement such a birth cohort screening in countries with a lower HCV prevalence.

Conclusions

HCV infection has serious health implications and, at the start of the era of potent therapy for HCV, screening programs are not yet reaching all potentially infected individuals worldwide. Therefore more effective programs are urgently needed. This review identified 67 screening programs that targeted HCV risk groups that are hidden in the general population. Relatively high HCV prevalences were found in programs that used a prescreening selection based on a HCV risk profile or migrant status, in programs that were carried out in intermediate to high HCV-prevalence countries or regions, and in programs in psychiatric clinics. In general, low HCV prevalences were found in programs that targeted health care workers and pregnant women. The reported use of motivational communication based on theory and/or determinants facilitating screening, and tools to increase HCV screening uptake were virtually absent. Comparison of the screening programs was strongly hindered by the lack of reported data on screening uptake, program characteristics, the type of diagnostic tests used, and clinical outcomes. In addition, only a few programs used a comparison group to evaluate program effectiveness.

We suggest that for low HCV-prevalence populations, the use of prescreening selection criteria should be considered to increase efficiency. In addition, to be able to assess screening program effectiveness, programs using a comparison group are needed. To improve comparability of screening programs and outcomes, it is necessary for all programs to systematically report program characteristics, screening uptake, the type of diagnostic tests that were used, as well as clinical outcomes.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

FRZ and ATU designed and performed the literature review, collected data from individual studies, participated in data interpretation, and drafted the manuscript. CWH and CHSBB participated in the study selection process, UD contributed to the study design and drafting of the manuscript. MWL supervised the study, and led the writing. MP conceived and supervised the study, participated in the study selection process, and led the writing. All authors read and approved the final manuscript.

Acknowledgements

This study was conducted within the Sarphati Initiative: the Academic Collaborative Center on Public Health of Noord Holland and Flevoland, the Netherlands. The study was funded by the Netherlands Organization for Health Research and Development (ZonMw; grant numbers 505040598104, 71150001, and 61200016). The authors would like to thank Heleen Dysterinck and Arnold Leenders of the Medical Library of the Academic Medical Center, Amsterdam, for their help with defining the search strategy and the use of Reference Manager; Jan Vlierhuis and his colleagues of the library of the Public Health Service of Amsterdam for their help with retrieving the articles; Nienke Alberts of the Public Health Service of Amsterdam for screening the Spanish language articles; Roel Coutinho of the National Center for Public Health and the Environment, Bilthoven, the Netherlands, and Gerjo Kok of Maastricht University, the Netherlands for their contribution to the manuscript; Theo Cuypers of Sanquin Blood Supply, Amsterdam, the Netherlands, for advice on the reliability of HCV diagnostic tests; and Susan T. Landry for editing of the manuscript.

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Pre-publication history

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