Skip to main content
Harm Reduction Journal logoLink to Harm Reduction Journal
. 2020 Jan 10;17:7. doi: 10.1186/s12954-019-0338-y

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

Julia Enkelmann 1,2,3,, Martyna Gassowski 4, Stine Nielsen 4,5, Benjamin Wenz 4, Stefan Roß 6, Ulrich Marcus 4, Viviane Bremer 4, Ruth Zimmermann 4; DRUCK Study group
PMCID: PMC6954578  PMID: 31924208

Abstract

Background

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.

Methods

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.

Results

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.

Conclusion

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.

Keywords: HCV, PWID, New injectors, Hepatitis C testing, Germany

Background

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 [1] 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 [2]. Major obstacles to overcome include a high proportion of people who are not aware of their infection and, linkage to care [3].

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% [4]. 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 [5].

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.

Methods

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.

Results

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.

Table 1.

Sociodemographic characteristics, drug injection behaviour and HCV-status, awareness and testing experience of PWID participating in the German DRUCK-study 2011–2014 by duration of injection drug use

Injecting drugs < 5 years (N = 232) Injecting drugs ≥ 5 years (N = 1827) p
n Proportionk (%) n Proportionk (%)
Sociodemographic characteristics
 Female 73 31.5 403 22.1 0.001**
 Age ≤ 25 years 71 30.6 62 3.4 < 0.001***
 2nd-generation migranta 26 11.2 273 14.9 0.128
 1st-generation migrantb 63 27.2 393 21.5 0.051
 Did not graduate from school 46 19.8 250 13.7 0.012*
 A-level 23 9.9 182 10.0 0.982
Main place of residence in the last 12 months (max 2 entries)
 Own flat 111 48.1 1040 57.5 0.006**
 With family or friends 57 24.7 297 16.4 0.002**
 Homeless, staying in shelters 50 21.7 258 14.3 0.003**
 Ever homelessc 132 57.1 1226 67.3 0.002**
 Ever in prison 143 61.9 1518 83.3 < 0.001***
 Released from prison in the last 12 monthsd 37 24.3 332 24.2 0.965
Sources of income in the last 12 months
 Job (including unemployment benefit I) 61 26.4 384 21.2 0.069
 State benefits 171 74.0 1548 85.3 < 0.001***
 Selling newspapers, begging, dealing 110 47.6 673 37.1 0.002**
 Sex work 17 7.4 60 3.3 0.002**
Injection behavior
 Age at first injection < 18 years 19 8.2 623 34.1 < 0.001***
 Injecting daily in the last 30 days 63 34.2 452 30.1 0.244
Substance injected in the last 30 daysf
 Heroin 130 56.0 1109 60.8 0.165
 Cocaine 73 31.5 752 41.2 0.004**
 Crack 10 4.3 98 5.4 0.504
 Speed (amphetamines) 11 4.7 60 3.3 0.254
 Crystal (metamphetamines) g 17 7.4 64 3.5 0.005**
Substance consumed in the last 30 days
 Heroin 180 77.6 1355 74.3 0.217
 Cocaine 95 41.0 908 49.8 0.011*
 Crack 54 23.4 461 25.3 0.534
 Speed (amphetamines) 49 21.1 234 12.8 0.001**
 Crystal (metamphetamines)g 23 10.0 97 5.3 0.005**
Most common setting of drug injection in the last 30 daysh
 Alone at homee 76 42.2 678 45.4 0.425
 In consumption roome,i 24 27.6 195 31.9 0421
 With good acquaintancese 75 41.2 484 32.4 0.017*
 With steady partnere 24 13.3 241 16.1 0.317
 With hardly known or unknown peoplee 15 8.3 125 8.4 0.984
Unsafe use in the last 30 dayh
 Used used needles or syringes 19 10.4 133 8.8 0.482
 Used water from a shared container 45 24.7 316 21.4 0.302
 Used used spoons or filters 40 22.1 280 18.7 0.268
Source for sterile needles and syringes in the last 30 daysh
 Low threshold services 115 62.2 1069 70.2 0.025*
 Syringe vending machinej 48 52.8 290 37.9 0.006**
 Pharmacy (bought) 67 38.2 656 44.1 0.142
Access to addiction therapy
 Ever in detoxification 143 61.6 1517 83.2 < 0.001***
 Ever in weaning/rehabilitation program 80 34.5 1004 55.1 < 0.001***
 Ever in outpatient substitution therapy 126 54.3 1532 84.0 < 0.001***
 Currently in outpatient substitution therapy 68 29.3 945 51.8 < 0.001***
HCV status, awareness and testing experience
 HCV positive 83 35.8 1270 69.5 < 0.001***
 Detectable HCV-RNA 63 27.2 836 45.8 < 0.001***
 Of HCV positive: Unaware of HCV positive status 33 40.7 157 12.6 < 0.001***
 Ever tested for HCV 153 73.2 1653 93.6 < 0.001***
 Report negative HCV test, last test > 12 months ago 32 36.8 135 38.8 0.730

aBorn in Germany, mother and/or father born abroad

bBorn outside of Germany

cDefined as reporting living on the streets or in homeless shelters as main residence in the last 12 months

dNot asked in Berlin, Essen

eLast 30 days

fSubstance consumed in last 30 days and most common mode of consumption injection

gMethamphethamine use was concentrated in Leipzig (East Germany) and to a lower extent in Munich (South Germany), while it played almost no role in other study cities

hOnly answered if participants injected drugs in the last 30 days

iInformation available for Essen, Berlin, Hamburg; reported use of drug consumption rooms varied widely between cities: highest use in Hamburg (> 60% reported by NI and LI), lowest use in Berlin (< 10% reported by NI and LI)

jExist in Berlin, Essen, Cologne, Munich

kof responding participants

*p < 0.05

**p < 0.01

***p < 0.001

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).

Table 2.

HCV-status, awareness, injection behaviour and access to addiction and medical care of new injectors by self-reported HCV-testing experience prior to study

Reported previous HCV-test (N = 153) Reported no previous HCV-test (N= 56) p
n %i n %i
Sociodemographic characteristic
 Female 49 32.0 14 25.0 0.327
 Age 25 years 39 25.5 24 42.9 0.015*
 1st-generation migranta 45 29.4 12 21.4 0.251
 2nd-generation migrantb 13 8.5 6 10.7 0.621
 Mainly homeless, staying in sheltersc 31 20.4 17 30.4 0.130
 Ever in prison 94 61.8 36 64.3 0.747
 Released from prison in the last 12 monthsd 22 23.2 10 24.4 0.876
HCV status
 HCV-positive 64 41.8 16 28.6 0.081
 Detectable HCV-RNA 47 30.7 14 25.0 0.421
 Of HCV-positive: unaware of HCV-positive status 14 22.6 16 100.0 < 0.001***
Access to addiction therapy
 Drug addiction ever treated 128 83.7 32 57.1 < 0.001***
 Ever in detoxification 105 68.6 26 46.4 0.008**
 Ever in weaning/rehabilitation program 60 39.2 15 26.8 0.097
 Ever in outpatient substitution 101 66.0 15 26.8 < 0.001***
 Currently in outpatient substitution 52 34.0 10 17.9 0.024*
 Sought medical care within the last 12 months 127 83.0 44 78.6 0.462
If accessed medical care within 12 months: last access point
 Hospital 25 20.2 17 39.5 0.012*
 Practice without addiction services 37 29.8 16 37.2 0.371
 Practice with OST 44 35.5 6 14.0 0.008**
 Detention facilities (prison hospital) 11 8.9 1 2.3 0.152
 Low threshold drug services 4 3.2 1 2.3 0.765
 Rehabilitation 2 1.6 1 2.3 0.762
 Local public health office 1 0.8 1 2.3 0.430
Main source for sterile needles and syringes in the last 30 days
 Low threshold services 80 67 21 46 0.011*
 Bought in pharmacies 21 18 12 26 0.224
 Syringe vending machinee 16 25 8 36 0.325
 Visited low threshold drug services in the last 30 daysf 77 88 21 75 0.112
Drug injection behaviour in the last 30 daysg
 Injected drugs 126 82.4 47 83.9 0.789
 Daily injection 46 36.8 13 27.7 0.260
 Injection of heroin 93 60.8 26 46.4 0.063
 Injection of cocaine 55 36.0 13 23.1 0.082
 Injection of crack 8 5.3 2 3.6 0.613
 Injection of amphetamines 7 4.6 4 7.1 0.462
 Injection of methamphetaminesh 5 3.3 11 19.6 < 0.001

aBorn in Germany, mother and/or father born abroad

bBorn outside of Germany

cDefined as reporting living on the streets or in homeless shelters as main residence in the last 12 months

dNot asked in Berlin, Essen

eSubstance consumed in the last 30 days and most common mode of consumption injection

eExist in Berlin, Essen, Cologne, Munich

fNot asked in Berlin, Essen, Leipzig

gSubstance consumed in the last 30 days and most common mode of consumption injection

hConsumption of methamphethamine was concentrated in Leipzig (East Germany) and to a lower extent in Munich (South Germany), while it played almost no role in other study cities

iof responding participants

*p < 0.05

**p < 0.01

***p < 0.001

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).

Discussion

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 [4]. 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 [14]. 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 [15]. 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 [18] or opt-out testing [19].

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 [20].

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 [2325]. 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 [26]. 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 [26]. French data showed that vending machines were used by younger PWID, that were hardly reached by other syringe programs [27]. 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 [2830]. 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 [31]. It has been introduced in California [32] and has increased screening uptake among prisoners in England [33].

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 [10]. Unstable housing has been found to be a risk factor for HCV infection among PWID in Vancouver [34], and in Puerto Rico, homeless PWID were significantly more likely to engage in high-risk injection behaviour than other PWID [35]. There is experience e.g. from London on how to reach the homeless population with HCV services [36, 37] .

Conclusion

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.

Limitations

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.

Acknowledgements

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, norbert.scherbaum@uni-due.de).

Jürgen Klee (AIDS-Hilfe Frankfurt e.V.; Juergen.Klee@frankfurt.aidshilfe.de).

Andreas Hecht (Sozialdienst Katholischer Männer e.V.; andreas.hecht@skm-koeln.de).

Dirk Schaeffer (Deutsche Aids-Hilfe e.V., dirk.schaeffer@dah.aidshilfe.de).

Abbreviations

HCV

Hepatitis C virus

IDU

Injection drug use

LI

Long-term injectors (injecting drugs for 5 years or more)

NI

New injectors (injecting drugs for less than 5 years)

OST

Opioid substitution therapy

PWID

People who inject drugs

Authors’ contributions

JE performed the analysis and drafted the manuscripts, supported by RZ, SN and MG. RZ and UM designed the study. BW, SN and MG were scientific coordinators of the study. VB provided expertise and support throughout the study. SR and team validated and tested samples from dried blood spots during the pilot study. All authors critically reviewed the manuscript. All authors read and approved the final manuscript.

Funding

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.

Availability of data and materials

The datasets generated and analysed during the current study are not publicly available to protect research participants’ privacy.

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

Not applicable.

Competing interests

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.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Julia Enkelmann, Email: enkelmannj@rki.de.

Martyna Gassowski, Email: gassowskim@rki.de.

Stine Nielsen, Email: stine.nielsen12@gmail.com.

Benjamin Wenz, Email: wenz.benjamin@gmail.com.

Stefan Roß, Email: stefan.ross@uni-due.de.

Ulrich Marcus, Email: marcusu@rki.de.

Viviane Bremer, Email: bremerv@rki.de.

Ruth Zimmermann, Email: zimmermannr@rki.de.

DRUCK Study group:

Claus-Thomas Bock, Norbert Bannert, Claudia Santos-Hövener, Norbert Scherbaum, Jürgen Klee, Andreas Hecht, and Dirk Schaeffer

References

  • 1.Global Hepatitis Report 2017. Geneva: World Health Organization; 2017. Licence: CC BY-NC_SA 3.0 IGO.
  • 2.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.
  • 3.Webster D, Klenerman P, Dusheiko GM. Hepatitis C. Lancet. 2015;2015(385):1124–1135. doi: 10.1016/S0140-6736(14)62401-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.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):707–715. doi: 10.1007/s00103-013-1673-x. [DOI] [PubMed] [Google Scholar]
  • 5.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.
  • 6.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):158–161. doi: 10.1016/j.drugalcdep.2009.01.006. [DOI] [PubMed] [Google Scholar]
  • 7.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):1099–1109. doi: 10.1093/aje/kwn237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.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. doi: 10.1186/1471-2458-14-845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.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. doi: 10.1186/s12889-016-3545-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.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. [DOI] [PubMed]
  • 11.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–S25. doi: 10.1097/01.aids.0000192066.86410.8c. [DOI] [PubMed] [Google Scholar]
  • 12.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):179–182. doi: 10.1016/j.drugpo.2013.08.005. [DOI] [PubMed] [Google Scholar]
  • 13.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):755–761. doi: 10.1093/cid/cit938. [DOI] [PubMed] [Google Scholar]
  • 14.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;58:90–94. doi: 10.1016/j.jsat.2015.06.008. [DOI] [PubMed] [Google Scholar]
  • 15.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):1108–1111. doi: 10.1016/j.ajem.2016.03.004. [DOI] [PubMed] [Google Scholar]
  • 16.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):222–230. doi: 10.1111/hiv.12364. [DOI] [PubMed] [Google Scholar]
  • 17.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. doi: 10.1371/journal.pone.0150546. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.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. doi: 10.1016/j.drugpo.2017.07.002. [DOI] [PubMed] [Google Scholar]
  • 19.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–e396. doi: 10.3399/bjgp16X685225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.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.
  • 21.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. doi: 10.21037/mhealth.2018.10.03. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.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.
  • 23.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;47:126–136. doi: 10.1016/j.drugpo.2017.05.042. [DOI] [PubMed] [Google Scholar]
  • 24.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):221–228. doi: 10.1136/flgastro-2016-100776. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.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. [PMC free article] [PubMed] [Google Scholar]
  • 26.Stark K, Leicht A, Müller R. Characteristics of users of syringe vending machines in Berlin. Soz Praventivmed. 1994;39(4):209–216. doi: 10.1007/BF01309220. [DOI] [PubMed] [Google Scholar]
  • 27.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):1852–1854. doi: 10.2105/AJPH.89.12.1852. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.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. doi: 10.1186/1471-2334-14-S6-S17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.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. doi: 10.1186/s12954-018-0230-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.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):1397–1409. doi: 10.1016/S1473-3099(18)30469-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.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. doi: 10.7326/M15-0617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.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):192–199. doi: 10.1108/IJPH-07-2016-0028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Public Health England . Summary report: national engagement event for blood-borne virus (BBV) opt-out testing in prisons in England. 2017. [Google Scholar]
  • 34.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. doi: 10.1186/1471-2458-9-270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.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):446–455. doi: 10.1093/jurban/jti073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.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.
  • 37.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):303–314. doi: 10.1080/17474124.2018.1424541. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets generated and analysed during the current study are not publicly available to protect research participants’ privacy.


Articles from Harm Reduction Journal are provided here courtesy of BMC

RESOURCES