SUMMARY
People who inject drugs (PWID) are vulnerable to infections and injuries at injection sites. The factors associated with reporting symptoms of these, seeking related advice, and hospital admission are examined. PWID were recruited in Birmingham, Bristol and Leeds using respondent-driven sampling (N = 855). During the preceding year, 48% reported having redness, swelling and tenderness (RST), 19% an abscess, and 10% an open wound at an injection site. Overall, 54% reported ⩾1 symptoms, with 45% of these seeking medical advice (main sources emergency departments and General Practitioners). Advice was often sought ⩾5 days after the symptom first appeared (44% of those seeking advice about an abscess, 45% about an open wound, and 35% for RST); the majority received antibiotics. Overall, 9·5% reported hospital admission during the preceding year. Ever being diagnosed with septicaemia and endocarditis were reported by 8·8% and 2·9%, respectively. Interventions are needed to reduce morbidity, healthcare burden and delays in accessing treatment.
Key words: Epidemiology, healthcare, people who inject drugs, skin infections, soft tissue infections
INTRODUCTION
People who inject drugs (PWID) are vulnerable to a wide range of bacterial infections, and also to tissue damage, at their injection sites [1, 2]. Infections will arise due to the difficulties in maintaining hygienic injection practices when injecting illicit substances. Poor injection technique, frequent injection, and the reuse of injection equipment, particularly needles, may result in tissue damage at an injection site which can also be become infected [3]. These localized injection site injuries and skin and soft tissue infections can produce a range of symptoms; including abscesses, open wounds, and areas of redness, swelling and tenderness (cellulitis) [1, 2]. Injection-related bacterial infections can also cause systemic illness, such as endocarditis [1, 2], and rarely they may be due to the toxin-producing bacteria that cause anthrax, botulism and tetanus [4]. These infections and injuries can place substantial burdens on healthcare systems [5–9] and can be fatal [1, 2].
The prevalence of the symptoms of recent or current injection-related skin and soft tissue infections and injuries in PWID has been reported to be as high as one in three in studies in North America [10–12] and the UK [13, 14], although lower levels have been reported by studies in Vancouver and Sydney [15, 16]. In the UK there has been concern over the last decade about the extent of injection-related bacterial infections in PWID and the burden that these may be placing on health services [17–20]. A study in 2004 estimated the annual healthcare costs due to injection site infections and injuries in PWID in the UK to be between £15·5 and £47 million [13], but they could be substantially higher [9].
Previous studies of symptoms of injection site infections and injuries in the UK have used simple accessibility approaches to recruit PWID and have only collected limited information on their responses to specific symptoms. This study recruited PWID using respondent-driven sampling (RDS), a form of structured chain referral sampling, which aims to adjust for selection biases that may arise from simple purposive surveys [21, 22]. It also collected more detailed information on PWID responses to individual symptoms than previous UK studies. This paper examines the factors associated with: (a) reporting symptoms of an injection site infection or injury; (b) seeking advice about these symptoms; and (c) being admitted to hospital with these symptoms.
METHODS
PWID were recruited into an unlinked anonymous survey in three major urban areas of England: Bristol (2006), Leeds (2008) and Birmingham (2009), using the same RDS methodology [23]. RDS methods are explained more fully elsewhere [21, 22, 24, 25]. Briefly, RDS recruits subjects through their own social networks. The initial recruits, or ‘seeds’, needed to commence RDS were selected in relation to location within each city and gender through key informant referrals and street outreach. To be eligible participants had to live within the survey area, and be aged >15 years, and have injected drugs during the preceding 4 weeks. Participants underwent a computer-assisted interview, provided a dried blood spot sample (DBS) sample [tested for antibodies to the hepatitis B core antigen (anti-HBc), and hepatitis C (anti-HCV)], and were offered an acknowledgement. Participants were asked to act as recruiters and those who agreed were given three uniquely numbered date-limited coupons. They were instructed to give these coupons only to eligible individuals whom they knew. All participants were screened for eligibility, and for attempted repeat participations, by a single fieldwork coordinator. In chain referral surveys there is a tendency for participants to recruit people like themselves, and a higher probability that people with large networks will be recruited. Therefore, information on the size of participants' networks and the characteristics of who they recruited were used to test for evidence of selection bias and to generate sample weights (RDSAT version 5.4.0. Ithaca, New York: E. Volz & D. D. Heckathorn, 2005). The study received ethical approval (London REC).
Participants were asked if during the preceding year they had any of these symptoms at an injection site: redness, swelling and tenderness (RST); an abscess; or a sore/open wound. For each of the symptoms the participants reported they were asked if, during the preceding year, they had: sought medical advice (i.e. from a doctor or nurse) about that symptom; where they had sought the advice about that symptom; and if they had then been admitted to hospital as a result of that symptom. They were also asked, in relation to the last occasion that they had each symptom, how long after they first noticed that symptom they had sought advice and if they had been prescribed antibiotics on that occasion.
Weighted data from those who fully completed the questionnaire were included in the analyses, which were performed with SPSS v. 19 (SPSS Inc., USA). Bivariate associations between the reporting of symptoms and demographic and environmental characteristics, the drugs used, injecting practice, and recruitment site were examined using χ2 test. Those characteristics found to be associated in the bivariate analysis were then entered using the forward stepwise procedure in SPSS into a logistic regression model with inclusion assessed using the likelihood ratio (with the stepwise probability for inclusion of 0·05 and exclusion of 0·1). For those who reported each symptom, the same approach was then used to assess the factors associated with seeking healthcare advice and with admission to hospital. Each of the three symptoms was examined separately as there are differences in their aetiologies, severity and frequency of occurrence, and also because PWID healthcare-seeking behaviours may vary by symptom.
RESULTS
A total of 855 individuals fully completed the survey questionnaire across the three urban areas (273 in Bristol, 291 in Leeds, 291 in Birmingham). The weighted sample had 217 (25%) women, and there were 113 (13%) participants aged <25 years, with 293 (34%) aged >34 years (mean age 32 years, median age 31 years). One-fifth (181, 21%) had first injected <5 years ago, with 217 (25%) having first injected >14 years ago (mean time since first injection was 10·6 years, median 10 years). During the preceding year, 819 (96%) had injected heroin, 524 (61%) crack-cocaine, 123 (14%) cocaine powder, and 158 (18%) amphetamines. Overall, 56% (479) reported never having experienced an overdose. For 31% (267) their main source of income was illicit (i.e. not employment or benefits); with 6% (54) reporting they had received either money or goods in exchange for sex during the past year. During the preceding year, 574 (67%) had been arrested, 284 (33%) imprisoned, and 430 (50%) homeless. A fifth (19%, 167) had anti-HBc and half (50%, 431) anti-HCV.
During the preceding year almost half (48%, 414) reported having RST, around one-fifth (19%, 160) reported an abscess, and a tenth (10%, 85) reported a sore/open wound at an injection site. Overall, 54% (464) reported having at least one of the three symptoms (i.e. RST, an abscess, or sore/open wound) at an injection site during the preceding year. A quarter (24%, 202) of participants reported having either an abscess or a sore/open wound at an injection site during the preceding year.
The demographic, environmental and drug use characteristics associated with reporting each of the three symptoms in the both the bivariate and multivariate analyses are given in Table 1. In the multivariate analysis reporting an abscess at an injection site was more common in those: who reported an overdose in the preceding year; who injected cocaine; who reported sharing needles or syringes during the preceding year; and who were anti-HCV positive. Those who had sex in the preceding year, but who had not done so in exchange for money or goods were less likely to report an abscess. Reporting a sore/open wound at an injection site was more frequent in those: aged >34 years; who had ever been homeless; who reported their main source of income as being illicit; and who reported ever injecting with a cleaned needle or syringe. RST at an injection site was found to be more common in those: who had ever been homeless; who reported an overdose in the preceding year; who reported sharing needles or syringes during the preceding year; and who reported ever injecting with a cleaned needle or syringe.
Table 1.
Characteristics | Yes | n | Total, N | P | aOR | (95% CI) |
---|---|---|---|---|---|---|
Abscess | ||||||
Age (years) | ||||||
<25 | 7% | 8 | 113 | |||
25–29 | 17% | 46 | 263 | |||
30–34 | 20% | 37 | 186 | |||
⩾35 | 23% | 68 | 293 | 0·002 | † | |
Years since first injected | ||||||
<5 | 9% | 17 | 181 | |||
5–9 | 18% | 43 | 246 | |||
10–14 | 23% | 48 | 212 | |||
⩾15 | 24% | 52 | 217 | 0·001 | † | |
Injected cocaine preceding year | ||||||
No | 17% | 123 | 732 | 1·00 | ||
Yes | 30% | 37 | 123 | <0·001 | 1·78 | (1·14–2·78) |
Injected crack preceding year | ||||||
No | 13% | 43 | 331 | |||
Yes | 22% | 117 | 524 | 0·001 | † | |
Shared N/S preceding year | ||||||
No | 17% | 122 | 730 | 1·00 | ||
Yes | 30% | 38 | 125 | <0·001 | 1·67 | (1·07–2·61) |
Arrested | ||||||
Not in preceding year | 15% | 42 | 281 | |||
In preceding year | 21% | 118 | 574 | 0·048 | † | |
Main source of income | ||||||
Licit | 16% | 92 | 588 | |||
Illicit | 25% | 68 | 267 | 0·001 | † | |
Migration, years lived in current area | ||||||
⩽1 | 11% | 11 | 101 | |||
2–10 | 25% | 50 | 198 | |||
11–20 | 19% | 19 | 99 | |||
⩾21 | 17% | 80 | 457 | 0·019 | † | |
Overdose | ||||||
Never | 14% | 68 | 479 | 1·00 | ||
Yes, not preceding year | 23% | 47 | 200 | 1·50 | (0·97–2·31) | |
Yes, preceding year | 26% | 45 | 175 | 0·001 | 1·69 | (1·09–2·63) |
Sex preceding year | ||||||
No | 26% | 45 | 175 | 1·00 | ||
Yes, but not paid | 16% | 100 | 626 | 0·59 | (0·39–0·90) | |
Yes, but paid | 28% | 15 | 54 | 0·003 | 1·08 | (0·53–2·20) |
Recruitment site | ||||||
Bristol | 24% | 65 | 273 | |||
Leeds | 17% | 50 | 291 | |||
Birmingham | 15% | 45 | 291 | 0·028 | † | |
Anti-HBc test result | ||||||
Positive | 26% | 44 | 167 | |||
Negative | 17% | 116 | 688 | 0·004 | † | |
Anti-HCV test result | ||||||
Positive | 25% | 107 | 431 | 1·00 | ||
Negative | 12% | 53 | 424 | <0·001 | 0·53 | (0·36–0·78) |
Sore or open wound | ||||||
Age (years) | ||||||
<25 | 4% | 5 | 113 | 1·00 | ||
25–29 | 8% | 20 | 263 | 1·81 | (0·66–4·95) | |
30–34 | 11% | 21 | 186 | 2·82 | (1·03–7·72) | |
⩾35 | 13% | 39 | 293 | 0·022 | 3·52 | (1·35–9·19) |
Injected crack preceding year | ||||||
No | 8% | 25 | 331 | |||
Yes | 11% | 60 | 524 | 0·064 | † | |
Ever injected with cleaned N/S | ||||||
No | 7% | 30 | 413 | 1·00 | ||
Yes | 12% | 55 | 442 | 0·011 | 1·79 | (1·11–2·88) |
Homelessness | ||||||
Never | 4% | 4 | 106 | 1·00 | ||
Yes, not preceding year | 12% | 39 | 319 | 3·29 | (1·16–9·30) | |
Yes, preceding year | 10% | 42 | 430 | 0·041 | 2·28 | (0·81–6·42) |
Arrested | ||||||
Not in preceding year | 7% | 20 | 281 | |||
In preceding year | 11% | 65 | 574 | 0·053 | † | |
Main source of income | ||||||
Licit | 8% | 45 | 588 | 1·00 | ||
Illicit | 15% | 41 | 267 | 0·001 | 2·14 | (1·34–3·41) |
Overdose | ||||||
Never | 9% | 41 | 479 | |||
Yes, not preceding year | 9% | 18 | 200 | |||
Yes, preceding year | 15% | 27 | 175 | 0·029 | † | |
Anti-HCV test result | ||||||
Positive | 13% | 54 | 431 | |||
Negative | 7% | 31 | 424 | 0·011 | † | |
Redness, swelling and tenderness | ||||||
Injected cocaine preceding year | ||||||
No | 47% | 343 | 732 | |||
Yes | 57% | 70 | 123 | 0·040 | † | |
Shared N/S preceding year | ||||||
No | 46% | 334 | 730 | 1·00 | ||
Yes | 64% | 80 | 125 | <0·001 | 1·55 | (1·02–2·34) |
Ever injected with cleaned N/S | ||||||
No | 40% | 165 | 413 | 1·00 | ||
Yes | 56% | 249 | 442 | <0·001 | 1·73 | (1·30–2·31) |
Homelessness | ||||||
Never | 31% | 33 | 106 | 1·00 | ||
Yes, not preceding year | 49% | 156 | 319 | 2·01 | (1·24–3·23) | |
Yes, preceding year | 52% | 224 | 430 | 0·001 | 2·16 | (1·36–3·45) |
Main source of income | ||||||
Licit | 46% | 272 | 588 | |||
Illicit | 53% | 142 | 267 | 0·068 | † | |
Overdose | ||||||
Never | 41% | 198 | 479 | 1·00 | ||
Yes, not preceding year | 52% | 105 | 200 | 1·37 | (0·98–1·93) | |
Yes, preceding year | 63% | 110 | 175 | <0·001 | 2·00 | (1·39–2·89) |
Sex preceding year | ||||||
No | 41% | 72 | 175 | |||
Yes, but not paid | 50% | 311 | 626 | |||
Yes, but paid | 58% | 31 | 54 | 0·054 | † | |
Recruitment site | ||||||
Bristol | 55% | 150 | 273 | |||
Leeds | 42% | 121 | 291 | |||
Birmingham | 49% | 143 | 291 | 0·007 | † |
aOR, Adjusted odds ratio; CI, confidence interval; N/S, needle or syringe.
Reporting an abscess not associated with: gender, injecting amphetamine preceding year, injecting heroin preceding year, ever injected with cleaned N/S, homelessness, and imprisonment.
Reporting a sore or open wound not associated with gender, number of years since first injected, injecting amphetamine preceding year, injecting cocaine preceding year, injecting heroin preceding year, shared N/S preceding year, imprisonment, number of years lived in current area, sex preceding year, recruitment site, and anti-HBc test result.
Reporting a redness, swelling and tenderness not associated with: gender, age, number of years since first injected, injecting amphetamine preceding year, injecting crack preceding year, injecting heroin preceding year, being arrested, imprisonment, main source of income, number of years lived in current area, anti-HBc test result, and anti-HCV test result.
Not included in the final model.
Those who reported a symptom were asked if they had sought medical advice about that symptom: 70% (112) of those reporting an abscess, 45% (39) reporting a sore/open wound, and 38% (159) of those reporting RST had all done so. Overall, 209 (24%) of those surveyed had sought advice about one or more of these symptoms during the preceding year (45% of those reporting one or more of the symptoms). The factors associated in the bivariate and multivariate analyses with having sought advice about each symptom in the preceding year are given in Table 2. In the multivariate analysis seeking advice about an abscess at an injection site was more common in women and those anti-HCV positive. Reporting seeking advice about a sore/open wound at an injection site was more frequent in those anti-HCV positive. Seeking advice for RST at an injection site was found to be more common in women, those injecting cocaine, in those recruited in Leeds, and those anti-HCV positive. The two most commonly used sources of advice about these symptoms were accident and emergency departments (most frequently reported for an abscess or sore/open wound) or General Practitioners (most frequently reported for RST); although a range of services had been used (Table 3).
Table 2.
Characteristics | Yes | n | Total, N | P | aOR | (95% CI) |
---|---|---|---|---|---|---|
Abscess | ||||||
Gender | ||||||
Male | 65% | 79 | 121 | 1·00 | ||
Female | 85% | 33 | 39 | 0·022 | 3·04 | (1·14–8·13) |
Recruitment site | ||||||
Bristol | 62% | 40 | 65 | |||
Leeds | 80% | 40 | 50 | |||
Birmingham | 71% | 32 | 45 | 0·099 | † | |
Anti-HCV test result | ||||||
Positive | 76% | 81 | 107 | 1·00 | ||
Negative | 58% | 31 | 53 | 0·025 | 0·46 | (0·22–0·93) |
Sore or open wound | ||||||
Homelessness | ||||||
Never | 25% | 1 | 4 | |||
Yes, not preceding year | 33% | 13 | 39 | |||
Yes, preceding year | 57% | 24 | 42 | 0·071 | † | |
Migration, years lived in current area | ||||||
⩽1 | 75% | 6 | 8 | |||
2–10 | 48% | 11 | 23 | |||
11–20 | 64% | 9 | 14 | |||
⩾21 | 30% | 12 | 40 | 0·033 | † | |
Anti-HBc test result | ||||||
Positive | 63% | 12 | 19 | |||
Negative | 40% | 27 | 67 | 0·077 | † | |
Anti-HCV test result | ||||||
Positive | 56% | 31 | 55 | 1·00 | ||
Negative | 26% | 8 | 31 | 0·006 | 0·25 | (0·09–0·66) |
Redness, swelling and tenderness | ||||||
Gender | ||||||
Male | 34% | 105 | 306 | |||
Female | 50% | 54 | 109 | 0·005 | 2·41 | (1·49–3·91) |
Years since first injected | ||||||
<5 | 23% | 20 | 86 | |||
5–9 | 39% | 45 | 116 | |||
10–14 | 47% | 53 | 113 | |||
⩾15 | 41% | 41 | 100 | 0·007 | † | |
Injected cocaine preceding year | ||||||
No | 35% | 119 | 344 | 1·00 | ||
Yes | 56% | 40 | 71 | <0·001 | 2·37 | (1·36–4·14) |
Injected crack preceding year | ||||||
No | 30% | 45 | 149 | |||
Yes | 43% | 113 | 265 | 0·012 | † | |
Imprisonment | ||||||
Never | 38% | 31 | 81 | |||
Yes, not preceding year | 44% | 88 | 202 | |||
Yes, preceding year | 30% | 39 | 131 | 0·041 | † | |
Main source of income | ||||||
Licit | 35% | 95 | 272 | |||
Illicit | 45% | 63 | 141 | 0·053 | † | |
Sex preceding year | ||||||
No | 40% | 29 | 72 | |||
Yes, but not paid | 36% | 111 | 311 | |||
Yes, but paid | 60% | 18 | 30 | 0·030 | † | |
Recruitment site | ||||||
Bristol | 39% | 59 | 150 | 1·66 | (0·98–2·82) | |
Leeds | 52% | 63 | 121 | 2·53 | (1·45–4·41) | |
Birmingham | 25% | 36 | 143 | <0·001 | 1·00 | |
Anti-HBc test result | ||||||
Positive | 54% | 46 | 85 | |||
Negative | 34% | 112 | 328 | <0·001† | ||
Anti-HCV test result | ||||||
Positive | 49% | 101 | 206 | 1·00 | ||
Negative | 28% | 58 | 208 | <0·001 | 0·50 | (0·32–0·77) |
aOR, Adjusted odds ratio; CI, confidence interval.
Not included in the final model.
Table 3.
Abscess | Sore or open wound | Redness, swelling and tenderness | ||||
---|---|---|---|---|---|---|
n | (%) | n | (%) | n | (%) | |
Where was advice sought from for the symptom during the preceding year? | ||||||
Accident and emergency | 17 | (45) | 55 | (49) | 59 | (38) |
General Practitioner or family doctor | 16 | (42) | 53 | (47) | 86 | (54) |
Needle exchange | 3 | (8·0) | 8 | (7·3) | 10 | (6·4) |
Other drug service | 2 | (5·7) | 5 | (4·2) | 9 | (5·4) |
Pharmacy | 1 | (2·9) | 2 | (2·1) | 4 | (2·8) |
Hostel or homeless service | 1 | (3·4) | 2 | (2·2) | 4 | (2·4) |
Other | 2 | (4·7) | 3 | (2·3) | 4 | (2·8) |
Total | 39 | 112 | 158 | |||
How long after the last occasion the symptom appeared was advice sought? | ||||||
Same or next day | 9 | (23) | 21 | (19) | 38 | (24) |
2–4 days later | 13 | (33) | 41 | (36) | 64 | (41) |
⩾5 days later | 17 | (44) | 50 | (45) | 55 | (35) |
Total | 39 | 112 | 156 | |||
Were participants given antibiotics on the last occasion they had symptoms? | ||||||
Yes | 36 | (93) | 102 | (91) | 129 | (81) |
Total | 39 | 112 | 158 |
Those who sought medical advice about a symptom were asked if they had been admitted to hospital because of that symptom: 45% (51) of those reporting an abscess, 43% (16) of those reporting a sore/open wound, and 30% (47) of those reporting RST had been admitted to hospital. Overall, 81 (9·5%) of the survey participants reported that they had been admitted to hospital during the preceding year when they had one or more of these symptoms (17% of those who had reported one or more of the symptoms, and 39% of those who had sought advice about a symptom). The associations between demographic, environmental and drug use characteristics and reporting admission to hospital for either RST or an abscess in the preceding year are given in Table 4. Only 16 were admitted due to a sore/open wound and so due to small numbers were not considered further. In the multivariate analysis, reporting admission for an abscess at an injection site was more common in those: who had first injected >14 years ago; who had injected crack-cocaine; and who reported sharing needles or syringes during the preceding year. Reporting admission for RST at an injection site was found to be more common in those anti-HCV positive.
Table 4.
Characteristics | Yes | n | Total, N | P | aOR | (95% CI) |
---|---|---|---|---|---|---|
Abscess | ||||||
Gender | ||||||
Male | 52% | 41 | 79 | |||
Female | 30% | 10 | 33 | 0·036 | † | |
Age (years) | ||||||
<25 | 0% | 0 | 5 | |||
25–29 | 30% | 9 | 30 | |||
30–34 | 48% | 15 | 31 | |||
⩾35 | 57% | 27 | 47 | 0·019 | † | |
Years since first injected | ||||||
<5 | 17% | 2 | 12 | 1·00 | ||
5–9 | 43% | 13 | 30 | 7·15 | (1·04–48·9) | |
10–14 | 39% | 13 | 33 | 5·01 | (0·75–33·4) | |
⩾15 | 59% | 23 | 39 | 0·059 | 25·9 | (3·54–189) |
Injected crack preceding year | ||||||
No | 21% | 7 | 33 | 1·00 | ||
Yes | 55% | 44 | 80 | 0·001 | 7·49 | (2·50–22·5) |
Shared N/S preceding year | ||||||
No | 40% | 34 | 85 | 1·00 | ||
Yes | 63% | 17 | 27 | <0·001 | 3·57 | (1·25–10·2) |
Anti-HBc test result | ||||||
Positive | 61% | 19 | 31 | |||
Negative | 39% | 31 | 80 | 0·032 | † | |
Anti-HCV test result | ||||||
Positive | 52% | 42 | 81 | |||
Negative | 29% | 9 | 31 | 0·030 | † | |
Redness, swelling and tenderness | ||||||
Gender | ||||||
Male | 34% | 36 | 105 | |||
Female | 21% | 11 | 53 | 0·079 | † | |
Age (years) | ||||||
<25 | 6·3% | 1 | 16 | |||
25–29 | 37% | 18 | 49 | |||
30–34 | 24% | 10 | 42 | |||
⩾35 | 35% | 18 | 51 | 0·077 | † | |
Injected crack preceding year | ||||||
No | 20% | 9 | 45 | |||
Yes | 34% | 39 | 114 | 0·079 | † | |
Imprisonment | ||||||
Never | 13% | 4 | 31 | |||
Yes, not preceding year | 33% | 29 | 89 | |||
Yes, preceding year | 38% | 15 | 39 | 0·052 | † | |
Anti-HBc test result | ||||||
Positive | 43% | 20 | 47 | |||
Negative | 24% | 27 | 112 | 0·020 | † | |
Anti-HCV test result | ||||||
Positive | 37% | 37 | 101 | 1·00 | ||
Negative | 18% | 10 | 57 | 0·012 | 0·38 | (0·17–0·83) |
aOR, Adjusted odds ratio; CI, confidence interval; N/S, needles or syringe.
Not included in the final model.
In relation to the last occasion they had sought advice about each symptom, participants were asked how long after they first noticed the symptom they had done so (Table 3). Medical advice was sought ⩾5 days after the symptom first appeared by 44% (17) of those reporting an abscess, 45% (50) reporting a sore/open wound, and 35% (55) of those reporting RST. Participants were also asked if they had been given antibiotics on this last occasion: 93% (36) of those reporting an abscess, 91% (102) reporting a sore/open wound, and 81% (129) of those reporting RST had received antibiotics (Table 3).
Participants were also asked if they had ever been diagnosed by a doctor as having either septicaemia or endocarditis (n = 848): 75 (8·8%) and 25 (2·9%), respectively, reported that they had been.
DISCUSSION
Symptoms of injection-related bacterial infections and injuries were common in PWID in the three urban areas. Overall, almost half (48%) reported having RST at an injection site during the preceding year; one-fifth (19%) reported an abscess and a tenth (10%) a sore/open wound. Furthermore, one in 11 and one in 34 reported ever being diagnosed as having septicaemia and endocarditis, respectively.
It is important to consider the limitations and generalizability of these findings. Self-reported symptoms were used in this study, although the accuracy of self-reports can be questioned, studies have shown good concordance between self-reported symptoms and clinical diagnosis [8]. The marginalized and illegal nature of injecting drug use, as well as its comparative rarity, impedes the recruitment of a representative sample of PWID. This study aimed to minimize sampling biases and maximize representativeness by recruiting participants using RDS [21, 22]. RDS aims to reduce recruitment bias when sampling from hidden populations, such as PWID; however, it is not possible to test how successful it has been in achieving this. Even so, RDS is currently regarded as the most appropriate method for recruiting community-based samples of PWID. Finally, since this study recruited at only three urban locations in England, and the levels of two of the symptoms varied by location, these findings should be generalized with caution.
Previous studies of PWID in the UK found that around one-third reported having an abscess, sore, or open wound at an injection site during the preceding year [13, 14], which is higher than the level found in the present study (24%). However, while previous studies have had wider geographical coverage, they have recruited either through health services provided to people who use drugs or from community settings using simple accessibility sampling approaches [13, 14]. The use of these approaches could have resulted in the over-sampling of higher-risk individuals. Similar levels of symptoms to those reported here have been found in studies from other countries [12, 26].
Overall a quarter of the PWID participating in this study had sought advice from a doctor or nurse about one of the three symptoms enquired about in the study. While the majority of those reporting an abscess had sought advice; less than half of those reporting either a sore/open wound or RST had done so. This might reflect the latter symptoms being a more common occurrence, and so more familiar, than abscesses, or these being perceived as being less serious. However, of those who sought advice about their last episode of RST two-thirds had done so within 4 days of it appearing compared to just over half of those reporting the other two symptoms. This could suggest that seeking advice about RST may be related to more severe episodes. The majority of those who sought advice about a symptom reported receiving antibiotics on the last occasion. A number of factors were found to be associated with healthcare utilization in response to the symptoms considered here, including having antibodies to hepatitis C and the use of certain drugs. While these associations need further examination, these factors might be related to having more severe episodes.
Overall, almost one in 10 of the study participants had been admitted to hospital when they had one or more of the symptoms in the preceding year. At one London hospital it was estimated that the average cost of an inpatient admission for a skin and soft tissue infection in PWID is £4180 (with mean length of stay of 12 days) [9]. Considering that there are an estimated 130 000–200 000 PWID in England [27, 28], these findings indicate that injection site infections and injuries in PWID are placing a considerable burden on the healthcare system; with annual inpatient costs alone possibly being between £54 and £84 million.
The healthcare burden associated with injection site infections and injuries is, in part, likely to be due to delays in seeking healthcare. Studies suggest that PWID tend not to seek timely medical care for their injection-related health problems, often resulting in costly emergency treatment [5, 7, 13, 29, 30]. This is supported by the findings presented here, where many of those with symptoms waited at least 5 days before seeking advice, and the most common source of advice for abscesses and sores/open wounds were accident and emergency departments. The delays in PWID seeking treatment probably reflects a number of issues, such as barriers to accessing care, poor compliance with medication and follow-up care, and competing priorities, for example, obtaining money and acquiring and using drugs [5, 7, 30, 31]. It has been suggested that these issues could be addressed through the provision of targeted services in low-threshold agencies, such as, needles and syringe programmes (NSPs). Such interventions have been shown to reduce accident and emergency department attendances, the need for surgery, and the length of in-patient stays [32, 33].
The symptoms examined here were associated with a range of factors with these varying to some extent between each of the three symptoms. This probably reflects differences in their possible aetiologies. An abscess will be due to an infection, and a sore/open wound will most probably be infected, although it might have initially been caused by injecting an acidic drug solution as a result of using excessive acid to dissolve the drug (the brown heroin found in the UK and crack-cocaine both need to be dissolved in an acidic solution prior to injection). RST often reflects an infection; however, it could also be due to an injury caused by poor injection technique, reuse of needles, or injecting an acidic drug solution. The factors found to be associated with one or more of the three symptoms examined here are similar to those associated with injection site infections and injuries in other studies. These include demographic factors (such as age [3, 13, 34] and gender [12–16, 34]), environmental and social factors (such as homelessness [3, 14–16] and source of income [16, 26]), the type drug used [9, 13, 14, 16, 35, 36], injection practice and hygiene [3, 5, 11–14, 34, 35, 37], having overdosed [16], and general health [12, 13, 34, 36].
Together these findings indicate that preventive interventions to reduce injection site infections and injuries need to focus on further reducing the reuse of injecting equipment and improving injection hygiene, and should target those using stimulants, the homeless and those who have recently overdosed. The UK, like many countries, has adopted a range of interventions to reduce the harms associated with injecting drug use, including NSPs and opiate substitution therapy. Recent activities to support reduction of drug-related harm in England have included the National Institute for Health and Clinical Excellence issuing guidance on optimizing NSP provision [38] and a national awareness and information campaign [39]. However, these activities have principally focused on preventing bloodborne viral infections and reducing overdoses. Our findings indicate a need for the evaluation of interventions, and the development of guidance, on preventing, identifying and managing injection site infections and injuries. Development of community-based interventions, such as targeted wound clinics may be an effective approach [32, 33]. As both specialist and pharmacy-based NSPs are widely provided in UK, these could be used to deliver such interventions.
Taken together these findings confirm that injection site infections and injuries are a common experience in PWID in the three cities (and probably in most other urban locations in England), and that the resultant healthcare burden is likely to be substantial. Interventions therefore need to be developed and piloted to reduce the level of injection site infections and injuries in PWID and to support prompt healthcare seeking in those affected.
ACKNOWLEDGEMENTS
We are grateful to all the people who participated in the surveys and to the fieldworkers who performed the data collection. We also thank those who conducted the bloodborne virus testing on the dried blood spot samples, and those who assisted with the running surveys, particularly Steve Jones for coordinating the fieldwork, and Merrington Omakalwala for administrative support.
DECLARATION OF INTEREST
None.
REFERENCES
- 1.Cherubin C, Sapira J. The medical complications of drug addiction and the medical assessment of the intravenous drug user. Annals of Internal Medicine 1993; 119: 1017–1028. [DOI] [PubMed] [Google Scholar]
- 2.Del Guidice P. Cutaneous complication of intravenous drug abuse. British Journal of Dermatology 2004; 150: 1–10. [DOI] [PubMed] [Google Scholar]
- 3.Dwyer R, et al. Prevalences and correlates of non-viral injecting-related injuries and diseases in a convenience sample of Australian injecting drug users. Drug and Alcohol Dependence 2009; 100: 9–16. [DOI] [PubMed] [Google Scholar]
- 4.Hope VD, et al. A decade of spore-forming bacterial infections among European injecting drug users: pronounced regional variation. American Journal of Public Health 2012; 102: 122–125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Darke S, Ross J, Kaye S. Physical injecting sites among injecting drug users in Sydney, Australia. Drug and Alcohol Dependence 2001; 62: 77–82. [DOI] [PubMed] [Google Scholar]
- 6.Kerr T, et al. High rates of primary care and emergency department use among injection drug users in Vancouver. Journal of Public Health (Oxford) 2005; 27: 62–66. [DOI] [PubMed] [Google Scholar]
- 7.Palepu A, et al. Hospital utilization and costs in a cohort of injection drug users. Canadian Medical Association Journal 2001; 165: 415–420. [PMC free article] [PubMed] [Google Scholar]
- 8.Morrison A, Elliott L, Gruer L. Injecting-related harm and treatment seeking behaviour among injecting drug users. Addiction 1997; 92: 1349–1352. [PubMed] [Google Scholar]
- 9.Marks M, et al. Needles and the damage done: reasons for admission and financial costs associated with injecting drug use in a Central London Teaching Hospital. Journal of Infection 2013; 66: 95–102. [DOI] [PubMed] [Google Scholar]
- 10.Takahasi T, et al. Type and location of injection drug use-related soft tissue infections predict hospitalization. Journal of Urban Health 2003; 80: 127–136. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Biswanger I, et al. High prevalence of abscesses and cellulitis among community-recruited injection drug users in San Fransisco. Clinical Infectious Diseases 2000; 30: 579–581. [DOI] [PubMed] [Google Scholar]
- 12.Lloyd-Smith E, et al. Prevalence and correlates of abscesses among a cohort of injection drug users. Harm Reduction Journal 2005; 2: 24. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hope VD, et al. Frequency, factors and costs associated with injection site infections: findings from a national multi-site survey of injecting drug users in England. BMC Infectious Diseases 2008; 8: 120. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Hope VD, et al. The extent of injection site infection in injecting drug users: findings from a national surveillance study. Epidemiology & Infection 2010; 138: 1510–1518. [DOI] [PubMed] [Google Scholar]
- 15.Lloyd-Smith E, et al. Risk factors for developing a cutaneous injection-related infection among injection drug users: a cohort study. BMC Public Health 2008; 8: 405. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Salmon AM, et al. Injecting-related injury and disease among clients of a supervised injecting facility. Drug and Alcohol Dependence 2009; 101: 132–136. [DOI] [PubMed] [Google Scholar]
- 17.Health Protection Agency, Health Protection Scotland, Public Health Wales, and Public Health Agency Northern Ireland. Shooting up: infections among people who inject drugs in the United Kingdom 2010. London: Health Protection Agency, November 2011. [Google Scholar]
- 18.Lamagni TL, et al. Severe Streptococcus pyogenes infections, United Kingdom, 2003–2004. Emerging Infectious Diseases 2008; 14: 202–209. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Irish C, et al. Skin and soft tissue infections and vascular disease among drug users, England [Letter]. Emerging Infectious Diseases 2007; 13: 1510–1511. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Kearns AM, et al. An unusual clone of MRSA causing infection in injecting drug users. Journal of Infection 2004; 49: 49–50. [Google Scholar]
- 21.Abdul-Quader AS, et al. Effectiveness of respondent-driven sampling for recruiting drug users in New York city: findings from a pilot study. Journal of Urban Health 2006; 83: 459–476. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Heckathorn DD. Respondent-driven sampling: a new approach to the study of hidden populations. Social Problems 1997; 44: 174–199. [Google Scholar]
- 23.Turner KM, et al. The impact of needle and syringe provision and opiate substitution therapy on the incidence of hepatitis C virus in injecting drug users: pooling of UK evidence. Addiction 2011; 106: 1978–1988. [DOI] [PubMed] [Google Scholar]
- 24.Heckathorn DD. Respondent-driven sampling II: deriving valid population estimates from chain-referral samples of hidden populations. Social Problems 2002; 49: 11–34. [Google Scholar]
- 25.Salganik MJ, Heckathorn DD. Sampling and estimation in hidden populations using respondent-driven sampling. Sociological Methodology 2004; 34: 193–239. [Google Scholar]
- 26.Pollini RA, et al. High prevalence of abscesses and self-treatment among injection drug users in Tijuana, Mexico. International Journal of Infectious Diseases 2010; 14 (Suppl. 3): e117–122. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Hay G, et al. Capture–recapture and anchored prevalence estimation of injecting drug users in England: national and regional estimates. Statistical Methods in Medical Research 2009; 18: 323–339. [DOI] [PubMed] [Google Scholar]
- 28.Harris RJ, et al. Hepatitis C prevalence in England remains low and varies by ethnicity: an updated evidence synthesis. European Journal of Public Health 2012; 22: 187–192. [DOI] [PubMed] [Google Scholar]
- 29.Ciccarone D, et al. Soft tissue infections among injection drug users – San Francisco, California, 1996–2000. Morbidity and Mortality Weekly Reports. CDC Surveillance Summaries 2001; 50: 381–384. [PubMed] [Google Scholar]
- 30.French M, et al. Chronic illicit drug use, health services utilisation and the cost of medical care. Social Science & Medicine 2000; 50: 1703–1713. [DOI] [PubMed] [Google Scholar]
- 31.van Beek I, Dwyer R, Malcom A. Cocaine injecting: the sharp end of drug related harm! Drug and Alcohol Review 2001; 20 (Harm Reduction Digest 14): 333–342. [Google Scholar]
- 32.Harris H, Young D. Care of injection drug users with soft tissue infections in San Fransisco, California. Archives of Surgery 2002; 137: 1217–1222. [DOI] [PubMed] [Google Scholar]
- 33.Grau L, et al. Expanding harm reduction services through a wound and abscess clinic. American Journal of Public Health 2002; 92: 1915–1917. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Topp L, et al. Prevalence and predictors of injecting-related injury and disease among clients of Australia's needle and syringe programs. Australian and New Zealand Journal of Public Health 2008; 32: 34–37. [DOI] [PubMed] [Google Scholar]
- 35.Murphy E, et al. Risk factors for skin and soft-tissue abscesses among Injection drug users: a case-control study. Clinical Infectious Diseases 2001; 33: 35–40. [DOI] [PubMed] [Google Scholar]
- 36.Spijkerman I, van Ameijden EJ, Mientjes G. Human immunodeficiency virus and other risk factors for skin abscesses and endocarditis among injection drug users. Journal of Clinical Epidemiology 1996; 49: 1149–1154. [DOI] [PubMed] [Google Scholar]
- 37.Vlahov D, et al. Bacterial infections and skin cleaning prior to infection among intreavenous drug users. Public Health Reports 1992; 107: 595–598. [PMC free article] [PubMed] [Google Scholar]
- 38.NICE. Needle and syringe programmes: providing people who inject drugs with injecting equipment. National Institute for Health and Clinical Excellence, Public Health Guidance, PH18, February 2009 (http://guidance.nice.org.uk/PH18).
- 39.Harm Reduction Works. National Treatment Agency for Substance Use and Exchange Supplies (www.harmreductionworks.org.uk/). Accessed 15 August 2013.