- Brief report
- Open Access
High prevalence of hepatitis C virus infection and low level of awareness among people who recently started injecting drugs in a cross-sectional study in Germany, 2011–2014: missed opportunities for hepatitis C testing
Harm Reduction Journal volume 17, Article number: 7 (2020)
In Germany, risk of hepatitis C virus (HCV) infection is highest among people who inject drugs (PWID). New injectors (NI) are particularly vulnerable for HCV-acquisition, but little is known about health seeking behaviour and opportunities for intervention in this group. We describe characteristics, HCV prevalence, estimated HCV incidence and awareness of HCV-status among NIs and missed opportunities for hepatitis C testing.
People who had injected drugs in the last 12 months were recruited into a cross-sectional serobehavioural study using respondent-driven sampling in 8 German cities, 2011–2014. Data on sociodemographic characteristics, previous HCV testing and access to care were collected through questionnaire-based interviews. Capillary blood was tested for HCV. People injecting drugs < 5 years were considered NI.
Of 2059 participants with available information on duration of injection drug use, 232 (11% were NI. Estimated HCV incidence among NI was 19.6 infections/100 person years at risk (95% CI 16–24). Thirty-six percent of NI were HCV-positive (thereof 76% with detectable RNA) and 41% of those HCV-positive were unaware of their HCV-status. Overall, 27% of NI reported never having been HCV-tested. Of NI with available information, more than 80% had attended low-threshold drug services in the last 30 days, 24% were released from prison in the last 12 months and medical care was most commonly accessed in hospitals, opioid substitution therapy (OST)-practices, practices without OST and prison hospitals.
We found high HCV-positivity and low HCV-status awareness among NI, often with missed opportunities for HCV-testing. To increase early diagnosis and facilitate treatment, HCV-testing should be offered in all facilities, where NI can be reached, especially low-threshold drug services and addiction therapy, but also prisons, hospitals and practices without OST.
Chronic hepatitis C virus (HCV) infection can lead to liver cirrhosis, liver failure and hepatocellular carcinoma. Currently, no effective vaccine exists but infections can be cured with antiviral treatment. The WHO aims at eliminating viral hepatitis as a public health threat by 2030  and Germany has committed to this elimination agenda. A joint strategy for HIV, hepatitis B/C and other sexually transmitted infections was published by the German Ministry of Health in 2016 . Major obstacles to overcome include a high proportion of people who are not aware of their infection and, linkage to care .
Germany is a low prevalence country for HCV infection. In a population-based survey of the general adult population living in Germany conducted in 2008–2011, HCV-antibody prevalence was 0.3% and HCV-RNA prevalence 0.2% . People who inject drugs (PWID) are underrepresented in this survey and account for nearly 80% of newly diagnosed HCV infections notified in Germany with information on the mode of transmission .
Several studies have found HCV incidence to be highest in the first years of injection drug use (IDU) [6, 7], but little is known about the health seeking behaviour and opportunities for intervention in people who recently began injecting drugs, which in the following are referred to as “new injectors” (NI). Therefore, we analysed data from a cross-sectional study among PWID in Germany to describe HCV prevalence, estimated incidence and missed opportunities for HCV-testing and promotion of prevention measures in this group, with a focus on settings that could be used to reach NI in Germany and similar countries.
We analysed data from the DRUCK-study, a cross-sectional study conducted between 2011 and 2014 using respondent-driven sampling to recruit PWID that had injected drugs in the last 12 months in one of eight German cities (Berlin, Essen, Leipzig, Munich, Frankfurt, Hanover, Hamburg, Cologne). Data on sociodemographic characteristics, previous HCV testing and access to care were collected through questionnaire-based face-to-face interviews. Capillary blood was tested for HCV antibodies and RNA. More detailed methods and the full study protocol have been published elsewhere [8, 9]. To capture all participants who had been exposed to HCV, we defined participants with detectable HCV antibody and/or HCV-RNA as HCV-positive for this analysis.
We defined NI as people injecting drugs for less than 5 years and long-term injectors (LI) as people injecting drugs for 5 years or longer.
Stata version 15.1 was used to carry out statistical analyses. X2-tests were performed and odds ratios using univariable logistic regression were calculated to compare groups.
Assuming that all participants were HCV-negative before they began injecting drugs, we estimated HCV incidence among NI as follows: date of study participation, month and year of birth and age when IDU was initiated was collected. Using stochastic simulation and assuming uniform distribution, we simulated the (unknown) month injection drug use was initiated and the (unknown) later time point HCV infection occurred based on 200 realisations in each case. For each realisation, we performed a bootstrap to account for the sampling error and characterised the resulting probability distribution by its mean and the 2.5 and 97.5 percentiles.
Of 2077 participants that provided a blood sample, information on duration of IDU was available for 2059 of whom 232 (11%) were NI (range 8.1% in Cologne (former West Germany) - 19.8% in Leipzig (former East Germany)).
Of NI, 31% were female, 27% were first-generation migrants and 22% reported being homeless (defined as reporting living on the streets or in homeless shelters as main residence in the last 12 months).
Compared to LI, NI were significantly older at the time of initiation of IDU, were significantly less likely to have injected cocaine and significantly more likely to have injected methamphetamines (mainly in Leipzig) in the last 30 days. We did not find any significant differences in unsafe drug injecting behaviour in the last 30 days between LI and NI.
In study cities with syringe vending machines, NI were significantly more likely than LI to have used them to obtain sterile injecting equipment in the last 30 days (53% vs 38%, p = 0.006) and to mention them as their main source of sterile syringes and needles (28% vs 16%, p = 0.004).
For a detailed comparison of NI and LI see Table 1.
HCV-status, history of HCV-testing and awareness of HCV positivity
Of 2077 participating PWID, 66% (n = 1361) were HCV-positive: 22% (n = 457) were anti-HCV-positive and RNA-negative, 41% (n = 857) anti-HCV and RNA-positive, 2.3% (n = 47) anti-HCV-negative and RNA-positive. Prevalence of HCV-antibody and/or RNA positivity was 36% in NI and increased with duration of IDU, reaching 72% in participants injecting drugs for 10 years or longer. NI were less likely to be HCV-positive (36% vs 70%, p < 0.0001), but among HCV-positives, a higher proportion of NI had detectable HCV-RNA (76% vs 66%, p = 0.06); while proportions of NI and LI with chronic infection (anti-HCV-positive, detectable RNA) were comparable (58% vs 63%, p = 0.31), the proportions of recent infections (anti-HCV-negative, detectable RNA) were significantly higher in NI (18.1% vs 2.4%, p < 0.0001).
HCV positivity among NI was lowest in Leipzig and Munich (both 20%) and highest in Hamburg (58%).
Estimated HCV incidence among NI was 19.6 infections/100 person years at risk (95% CI 16–24); if only participants injecting less than 2 years were considered, estimated incidence was 36.4 infections/100 person years at risk (95% CI 21–56).
NI were less likely to ever have been tested for HCV (73% vs 94%, p < 0.0001) and if HCV positive, more likely to be unaware of their HCV status (41% vs 13%, p < 0.0001). Reported testing experience among NI was lowest in Leipzig (38%) and in the other study cities ranged between 67% (Cologne) and 89% (Hamburg).
Uptake of medical care and addiction services: access points used by NI
In order to identify ways to reach NI, this part of the analysis focuses on NI.
Medical care was accessed by 82% of NI (n = 192) within the last 12 months. Most commonly mentioned last access points were practices without addiction services (31%, 58/186), practices offering opioid substitution therapy (OST, 30%, 55/186), hospitals (27%, 50/186) and prison hospitals (6.5%, 12/186).
Release from prison in the last 12 months was reported by 24% (37/152 with information, not asked in 2 study cities).
At the time of study, 75% of NI had already received at least one form of addiction therapy: 62% had ever received inpatient detoxification, 54% OST, thereof 29% currently and 34% had ever received long-term addiction therapy (93% as inpatient).
Information on last visit to low threshold drug services was collected in 5 study cities; in those 83% (105/127) reported attendance in the last 30 days.
Previous HCV testing among NI
Of NI that reported previous HCV-testing, 85% (130/153) provided details on the place where this was performed; the five most commonly mentioned places were practices providing OST (35%, 45/130), hospitals (33%, 43/130), practices without addiction services (14%, 18/130), low threshold drug services (8.5%, 11/130) and prisons (8.5%, 11/130).
Of 56 NI (27%) that reported never having been tested for HCV, 29% (n = 16) were HCV-positive. Previous access to addiction services was reported by 57%: 46% had been in inpatient detoxification, 27% in long-term addiction therapy programs and 27% in outpatient OST, thereof 18% currently (see Table 2). At least 21 NI without self-reported HCV testing experience had attended low-threshold drug services in the last 30 days (75%, 21/28 with information).
In the preceding 12 months, 24% (10/41 with information) were released from prison and 79% had sought medical care; most commonly mentioned points of contact were hospitals (40%) and practices without addiction services (37%).
Reported HCV testing experience was higher in females (78% vs 71%, p = 0.33), first-generation migrants (29% vs 21%, p = 0.25) and NI living in their own accommodation (52% vs 41%, p = 0.16); however, differences were not statistically significant (Table 2).
Significantly lower testing experience was reported from NI younger than 25 years (OR in univariable analysis 2.2, 95% CI 1.2–4.2) and those injecting amphetamines or methamphetamines (OR in univariable analysis 4.3, 95% CI 1.8–10.1).
Although low threshold drug services were the most commonly reported source of sterile needles and syringes, NI that denied previous HCV testing were significantly less likely to report them as source (46% vs 67%, p = 0.01) and were more likely than NI with testing experience to obtain their syringes and needles from syringe vending machines (36% vs 25%, p = 0.3) and pharmacies (26% vs 18%, p = 0.2) (Table 2).
NI without OST experience were less likely to ever have undergone HCV testing (56% vs 87%, p < 0.0001). They had a shorter duration of IDU (median 2 vs 3 years, p = 0.02), a lower HCV prevalence (27% vs 43% with OST, p = 0.014) and most commonly accessed medical care in practices without OST (51%), hospitals (26%) and prisons (10%).
HCV-positive NI that last accessed medical care in hospitals were more likely to be unaware of their HCV infection than those that last accessed care in OST-practices (OR 9.9, 95% CI 2.2–43).
We found high HCV positivity and low awareness of HCV-positive status among participating NI. Among NI-estimated HCV incidence was 19.6/100 person years at risk, comparable to the estimated incidence among NI in New York 2000/2001 and slightly lower than in Catalonia 2010/2011 (18 and 25/100 person years at risk, respectively; both using a similar definition of NI, [10, 11]). Estimated HCV incidence was higher in study participants with IDU below 2 years (36/100 person years at risk), supporting that HCV infection often occurs early after initiation of IDU.
HCV prevalence was more than 100-times higher in NI than in a representative study of the “general adult population in Germany” and more than 220-times in LI . Given that seroprevalence increases with time of IDU, it is especially important to reach NI with prevention measures and early HCV-testing.
Studies suggest that awareness of HCV positivity is associated with sustained protective behavioural changes, for example reducing injection risk behaviour [12, 13]. Awareness is a prerequisite for being linked into care and receiving antiviral treatment. Additionally it provides an opportunity for counselling around safer injection practices and linkage to effective prevention measures like OST, needle exchange and other harm reduction services.
In our study, more than 40% of HCV-positive NI were unaware of their HCV status, often with missed opportunities for HCV testing.
More than 50% of NI that reported never having been tested for HCV had previously been in contact with addiction therapy, many in an inpatient setting or in the form of OST, which involves regular engagement with services. Engagement in addiction therapy is an important opportunity for HCV testing that should not be missed.
As could be shown in other studies, we found that NI engaged in OST were more likely to have been tested for HCV than those not receiving OST . However, focusing on OST facilities, does exclude non-opioid dependent PWID and NI that are not (yet) linked to these services.
NI in our study often accessed medical care in hospitals or primary care without focus on addiction care and OST.
In the context of acute medical presentation in hospitals, HCV screening and discussion of test results are challenging. Although an American pilot study showed that emergency room-based HCV testing focused on PWID could be successfully integrated into clinical practice, finding a high prevalence of HCV, the study also encountered significant challenges linking those found to be HCV-positive to care . Nevertheless, testing in emergency departments could at least help improve the level of awareness of one’s HCV-status, a first step in the cascade of care. Opt-out testing for blood borne viruses including HCV reduces barriers and stigma around testing; in several emergency department-based studies, it was feasible and identified unknown HCV-infections [16, 17]. However, implementing routine screening policies in emergency rooms has rarely been attempted in Germany and will face considerable financial and logistical challenges.
Primary medical care is another setting that provides opportunities for HCV-testing. This should be enhanced for example through increasing awareness among physicians and decreasing barriers e.g. through on-site testing  or opt-out testing .
Low threshold drug services are important needle/syringe exchange sites in Germany. They were frequented by a high proportion of NI making them ideal places for integrated testing. Unfortunately—and in contrast to many other countries—in Germany, it is required that a physician is on-site when HCV-testing is performed and test results are given, which currently greatly limits feasibility for testing in this setting. Training non-physician providers to perform testing could increase feasibility and uptake of HCV-testing and has been successfully employed in other countries e.g. Scotland .
Other alternatives might be targeted distribution of HCV self-test kits in low threshold drug services or through vending machines, which would require legal changes (HIV self-tests are currently freely available, but HCV self-tests are not).
In the UK and in the USA, distribution of HIV self-tests through vending machines at venues frequented by gay men is being explored [21, 22]. To our knowledge, this has never been tested for PWID, but since they are used to vending machines for clean injection equipment, it might be worth studying acceptance and use of providing access to HCV self-test kits through vending machines for PWID.
Pharmacies, as the other important supplier of sterile injection equipment, currently play no role in other aspects of the HCV care cascade in Germany. However, studies from other countries suggest that they can be valuable and successfully offer and enhance HCV-testing, linkage to specialist care and even provide treatment [23,24,25]. Pharmacies could also be a source to access (free or subsidised) HCV self-tests.
In our study, if available, syringe vending machines were an important source for syringes and needles for NI and were more frequently used by NI with shorter duration of IDU.
This finding is in line with a previous study among PWID in Berlin, that users of vending machines often reported a shorter duration of IDU . The authors suggest that in the first time after initiation of IDU, PWID might prefer to obtain their injection equipment anonymously and may not (yet) be willing to visit other drug services . French data showed that vending machines were used by younger PWID, that were hardly reached by other syringe programs . Although they do not facilitate HCV-testing or support NI in other aspects of harm reduction, syringe vending machines are a valuable prevention measure, supplying sterile injection equipment around the clock.
Almost 25% of NI that reported no previous HCV testing had been in prison in the last 12 months. PWID are overrepresented in prison populations worldwide, making prisons suitable settings to deliver HCV prevention (and care) interventions, including HCV-screening [28,29,30]. According to a review and a cross-sectional survey, measures in European prisons are currently inadequate and need to be scaled up [28, 29]. Universal opt-out HCV-screening in prisons was found to be cost-effective and able to reduce HCV transmission in an American study . It has been introduced in California  and has increased screening uptake among prisoners in England .
Homelessness was reported by more than 20% of NI in our study, comparable to the findings of a very similar study of NI in Catalonia . Unstable housing has been found to be a risk factor for HCV infection among PWID in Vancouver , and in Puerto Rico, homeless PWID were significantly more likely to engage in high-risk injection behaviour than other PWID . There is experience e.g. from London on how to reach the homeless population with HCV services [36, 37] .
It is important that HCV-counselling and testing are not restricted to medical addiction care, especially for NI. It should be offered in all facilities or settings where NI can be reached, including hospitals and primary medical care, prisons and needle/syringe exchange sites, especially low-threshold drug services. To reach HCV elimination goals and increase feasibility of HCV-testing in the setting of low-threshold drug services which are frequented by the majority of NI, consideration should be given to allow trained non-physician providers to conduct HCV testing. Feasibility and acceptability of HCV self-testing for PWID should be explored.
The number of NI was small, so results have to be interpreted with caution. HCV-testing experience was self-reported; it is therefore possible that participants have been tested without their knowledge or that recall was incorrect. If participants reported no previous HCV-testing, reasons for this were not explored, so we cannot rule out that a test was offered but not accepted. Most seeds (initial study participants selected as recruiters/who “initiate sampling chains”) were recruited through low-threshold drug services which were also used as study sites; this might have led to overestimation of contact with low-threshold drug services in some of the cities. As this was a cross-sectional study, we cannot draw conclusions on causality. There were regional differences in the size and characteristics of the population and as the population of NI is unknown, our sample might not be representative of all new injectors in Germany. Nevertheless the DRUCK study is the first large bio-behavioural study of current PWID in Germany and provides valuable information about characteristics of this group.
Availability of data and materials
The datasets generated and analysed during the current study are not publicly available to protect research participants’ privacy.
Hepatitis C virus
Injection drug use
Long-term injectors (injecting drugs for 5 years or more)
New injectors (injecting drugs for less than 5 years)
Opioid substitution therapy
People who inject drugs
Global Hepatitis Report 2017. Geneva: World Health Organization; 2017. Licence: CC BY-NC_SA 3.0 IGO.
German Federal Ministry of Health and Federal Ministry for Economic Cooperation and Development. Integrated strategy for HIV, hepatitis B and C and other sexually transmitted infections. Available from https://www.bundesgesundheitsministerium.de/fileadmin/Dateien/5_Publikationen/Praevention/Broschueren/Strategy_HIV_HEP_STI.pdf, Accessed 09 10 2019. 2016.
Webster D, Klenerman P, Dusheiko GM. Hepatitis C. Lancet. 2015;2015(385):1124–35.
Poethko-Muller C, Zimmermann R, Hamouda O, Faber M, Stark K, Ross RS, et al. Epidemiology of hepatitis A, B, and C among adults in Germany: results of the German Health Interview and Examination Survey for Adults (DEGS1). Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013;56(5–6):707–15.
Zimmermann R, Meurs L, Schmidt D, Kollan C, Dudareva S, Bremer V. Zur Situation bei wichtigen Infektionskarankheiten in Deutschland. Hepatitis C im Jahr 2017. Epid Bull 2018;29:271–281. doi 1017886/EpiBull-2018-035. 2018.
Roy E, Boudreau JF, Boivin JF. Hepatitis C virus incidence among young street-involved IDUs in relation to injection experience. Drug Alcohol Depend. 2009;102(1–3):158–61.
Hagan H, Pouget ER, Ces Jarlais DC, Lelutiu-Weinberger C. Meta-regression of Hepatitis C virus infection in relation to time since onset of illicit drug injection: the influence of time and place. Am J Epidemiol. 2008;168(10):1099–109.
Zimmermann R, Marcus U, Schaffer D, Leicht A, Wenz B, Nielsen S, et al. A multicentre sero-behavioural survey for hepatitis B and C, HIV and HTLV among people who inject drugs in Germany using respondent driven sampling. BMC public health. 2014;14:845.
Wenz B, Nielsen S, Gassowski M, Santos-Hovener C, Cai W, Ross RS, et al. High variability of HIV and HCV seroprevalence and risk behaviours among people who inject drugs: results from a cross-sectional study using respondent-driven sampling in eight German cities (2011-14). BMC Public Health. 2016;16:927.
Folch C, Casabona J, Espelt A, Majó X, Merono M, Gonzalez V, et al. High prevalence and incidence of HIV and HCV among new injecting drug users with a large proportion of migrants- is prevention failing? Substance Use & Misuse, doi: 103109/1082608420151092991. 2016.
Des Jarlais DC, Perlis T, Arasteh K, Torian LV, Hagan H, Beatrice S, et al. Reductions in hepatitis C virus and HIV infections among injecting drug users in New York City, 1990–2001. AIDS (London). 2005;19(Suppl 3):S20–5.
Aspinall EJ, Weir A, Sacks-Davis R, Spelman T, Grebely J, Higgs P, et al. Does informing people who inject drugs of their hepatitis C status influence their injecting behaviour? Analysis of the Networks II study. Int J Drug Policy. 2014;25(1):179–82.
Bruneau J, Zang G, Abrahamowicz M, Jutras-Aswad D, Daniel M, Roy E. Sustained drug use changes after hepatitis C screening and counseling among recently infected persons who inject drugs: a longitudinal study. Clin Infect Dis. 2014;58(6):755–61.
Butler K, Day C, Dietze P, Bruno R, Alati R, Burns L. The potential reach of opioid substitution settings to deliver HCV care to people who inject drugs in Australia. J Subst Abus Treat. 2015;58:90–4.
Anderson ES, Pfeil SK, Deering LJ, Todorovic T, Lippert S, White DA. High-impact hepatitis C virus testing for injection drug users in an urban ED. Am J Emerg Med. 2016;34(6):1108–11.
Orkin C, Flanagan S, Wallis E, Ireland G, Dhairyawan R, Fox J, et al. Incorporating HIV/hepatitis B virus/hepatitis C virus combined testing into routine blood tests in nine UK emergency departments: the “going viral” campaign. HIV medicine. 2016;17(3):222–30.
O'Connell S, Lillis D, Cotter A, O'Dea S, Tuite H, Fleming C, et al. Opt-out panel testing for HIV, hepatitis B and hepatitis C in an urban emergency department: a pilot study. PLoS One. 2016;11(3):e0150546.
Bajis S, Dore GJ, Hajarizadeh B, Cunningham EB, Maher L, Grebely J. Interventions to enhance testing, linkage to care and treatment uptake for hepatitis C virus infection among people who inject drugs: a systematic review. Int J Drug Policy. 2017;47:34–46.
O’Kelly M, Byrne D, Naughten E, Bergin C, Williams C. Opt-out testing for blood-borne viruses in primary care: a multicentre, prospective study. Br J Gen Pract. 2016;66(647):e392–6.
Hepatitis C Trust. Eliminating hepatitis C in Scotland: a call to action. Available from: http://www.hcvaction.org.uk/sites/default/files/resources/Eliminating%20Hepatitis%20C%20FINAL.pdf, Accessed 29.01.2019. 2018.
Stafylis C, Natoli LJ, Murkey JA, Gordon KK, Young SD, MR MG, et al. Vending machines in commercial sex venues to increase HIV self-testing among men who have sex with men. mHealth. 2018;4:51.
Martin Fisher Foundation. Digital vending machines, actively promoting and normalising HIV testing in any venue, https://www.themartinfisherfoundation.org/digital-vending-machines/, Accessed 11.03.2019.
Radley A, Tait J, Dillon JF. DOT-C: a cluster randomised feasibility trial evaluating directly observed anti-HCV therapy in a population receiving opioid substitute therapy from community pharmacy. Int J Drug Policy. 2017;47:126–36.
Radley A, Melville K, Tait J, Stephens B, Evans JMM, Dillon JF. A quasi-experimental evaluation of dried blood spot testing through community pharmacies in the Tayside region of Scotland. Front Gastroenterol. 2017;8(3):221–8.
Kugelmas M, Pedicone LD, Lio I, Simon S, Pietrandoni G. Hepatitis C point-of-care screening in retail pharmacies in the United States. Gastroenterol Hepatol. 2017;13(2):98–104.
Stark K, Leicht A, Müller R. Characteristics of users of syringe vending machines in Berlin. Soz Praventivmed. 1994;39(4):209–16.
Obadia Y, Feroni I, Perrin V, Vlahov D, Moatti JP. Syringe vending machines for injection drug users: an experiment in Marseille, France. Am J Public Health. 1999;89(12):1852–4.
Arain A, Robaeys G, Stover H. Hepatitis C in European prisons: a call for an evidence-informed response. BMC Infect Dis. 2014;14(Suppl 6):S17.
Bielen R, Stumo SR, Halford R, Werling K, Reic T, Stover H, et al. Harm reduction and viral hepatitis C in European prisons: a cross-sectional survey of 25 countries. Harm Reduct J. 2018;15(1):25.
Stone J, Fraser H, Lim AG, Walker JG, Ward Z, MacGregor L, et al. Incarceration history and risk of HIV and hepatitis C virus acquisition among people who inject drugs: a systematic review and meta-analysis. Lancet Infect Dis. 2018;18(12):1397–409.
He T, Li K, Roberts MS, Spaulding AC, Ayer T, Grefenstette JJ, et al. Prevention of hepatitis C by screening and treatment in U.S. prisons. Ann Intern Med. 2016;164(2):84–92.
Morris MD, Brown B, Allen SA. Universal opt-out screening for hepatitis C virus (HCV) within correctional facilities is an effective intervention to improve public health. Int J Prison Health. 2017;13(3–4):192–9.
Public Health England. Summary report: national engagement event for blood-borne virus (BBV) opt-out testing in prisons in England, 2017. https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/707591/Event_Report_FINAL.pdf, Accessed 06 08 2018.
Kim C, Kerr T, Li K, Zhang R, Tyndall MW, Montaner JS, et al. Unstable housing and hepatitis C incidence among injection drug users in a Canadian setting. BMC Public Health. 2009;9:270.
Reyes JC, Robles RR, Colon HM, Matos TD, Finlinson HA, Marrero CA, et al. Homelessness and HIV risk behaviors among drug injectors in Puerto Rico. J Urban Health. 2005;82(3):446–55.
Surey J. Mobile community-based liver health assessment in underserved populations: the HepCare Project. Slides presented at INHSU 2018. Available from www.inhsu2018.com. 2018.
Swan D, Cullen W, Macias J, Oprea C, Story A, Surey J, et al. Hepcare Europe - bridging the gap in the treatment of hepatitis C: study protocol. Expert Rev Gastroenterol Hepatol. 2018;12(3):303–14.
We thank all study participants and all staff members of the low-threshold drug services and cooperating partners involved in the planning and conduction of the study. We also acknowledge the RKI-laboratory team for all validation and testing procedures during the main study.
We would like to thank Matthias an der Heiden for his statistical support.
DRUCK Study group:
Claus-Thomas Bock (Robert Koch Institute, Department of Infectious Diseases, Division for Viral Gastroenteritis and Hepatitis Pathogens and Enteroviruses, BockC@rki.de),
Norbert Bannert (Robert Koch Institute, Department for Infectious Diseases, Division for HIV and other Retroviruses, BannertN@rki.de).
Claudia Santos-Hövener (Robert Koch Institute, Department of Epidemiology and Health Monitoring, Unit of Social Determinants, Santos-HoevenerC@rki.de),
Norbert Scherbaum (LVR-Hospital Essen, Department of Addictive Behaviour and Addiction Medicine, Medical Faculty, University of Duisburg-Essen, Germany, firstname.lastname@example.org).
Jürgen Klee (AIDS-Hilfe Frankfurt e.V.; Juergen.Klee@frankfurt.aidshilfe.de).
Andreas Hecht (Sozialdienst Katholischer Männer e.V.; email@example.com).
Dirk Schaeffer (Deutsche Aids-Hilfe e.V., firstname.lastname@example.org).
The study was funded by the Robert Koch Institute (pilot) and the German Federal Ministry of Health. The Federal Ministry of Health was not involved in the study design, in the collection, analysis and interpretation of the data, the writing of the manuscript or the decision to submit the paper for publication.
Ethics approval and consent to participate
Ethical approval was received from the ethics committee at Charité University Hospital, Berlin, Germany, in May 2011 and with an amendment approved on 19 November 2012 (No EA4/036/11). All participants provided a written informed consent. No personal data allowing identification of study participants was collected. The Federal Commissioner for Data Protection and Freedom of Information approved the study protocol on 29 November 2012 (III-401/008#0035).
Consent for publication
Prof. Dr. N. Scherbaum received honoraria for several activities (advisory boards, lectures, manuscripts and educational material) by the factories Abbvie, Hexal, Janssen-Cilag, Lundbeck, MSD, Medice, Mundipharma, Reckitt-Benckiser/Indivior and Sanofi-Aventis. During the last 3 years, he participated in clinical trials financed by the pharmaceutical industry. The other authors declare no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Enkelmann, J., Gassowski, M., Nielsen, S. et al. High prevalence of hepatitis C virus infection and low level of awareness among people who recently started injecting drugs in a cross-sectional study in Germany, 2011–2014: missed opportunities for hepatitis C testing. Harm Reduct J 17, 7 (2020). https://doi.org/10.1186/s12954-019-0338-y
- New injectors
- Hepatitis C testing