Abstract
Background
There is a need to develop specific care route for vulnerable people with hepatitis C virus.
Objective
At a nurse-led clinic, we aimed to: (1) report the prevalence of patients initiating an hepatitis C treatment who (a) achieved sustained virologic response and (b) were adherent to their treatment; and (2) explore factors associated with adherence and sustained virologic response.
Design
A clinical record-based prospective cohort study.
Setting
A community-based nurse-led clinic coordinating outreach services for people with hepatitis C virus in Québec City, Québec, Canada.
Population
All patients initiating an hepatitis C treatment at the nurse-led clinic from January 1, 2012 to December 31, 2017 (end of data collection).
Methods
Patients were followed from the day they initiated their hepatitis C treatment, up to 24 weeks after the end of the treatment. Sustained virologic response was achieved if hepatitis C virus ribonucleic acid (RNA) was undetectable or below the lower limit of quantification at week 12 or later. Patients who reported hepatitis C treatment completion without missing any doses were considered adherent. Factors associated with adherence and sustained virologic response were identified using adjusted prevalence ratios.
Results
A total of 171 patients infected with hepatitis C virus (women: n = 51, 30%; criminal record: n = 102, 60%; substance addiction: n = 99, 58%) initiated an hepatitis C treatment at the nurse-led clinic. Overall, 126/171 (74%) patients were adherent. Patients using illicit drugs were less likely to be adherent (adjusted prevalence ratio 0.77, 95% confidence interval 0.67–0.89). Among 156/171 (91%) patients with an hepatitis C virus RNA test post-treatment, 96% (n = 149) achieved sustained virologic response. Patients who were less likely to achieve sustained virologic response were those who were non-adherent (adjusted prevalence ratio 0.81, 95% confidence interval 0.68–0.98) or who had a criminal record (adjusted prevalence ratio 0.87, 95% confidence interval 0.79–0.97).
Conclusions
A nurse-led clinic could fill an important gap in hepatitis C health services targeted at vulnerable people in a community setting, to drive adherence and achievement of sustained virologic response.
Keywords: Interprofessional relations, Medication adherence, Nurse-led clinic, Street drugs, Substance-related disorders, Sustained virologic response
1. Introduction
Hepatitis C virus triggers a global pandemic, with 71 million people infected worldwide (The Polaris Observatory HCV Collaborators, 2017). About 75–85% of patients infected with hepatitis C virus will progress to chronic infection (Chen and Morgan, 2006). Over the years, chronic hepatitis C virus infection will slowly and progressively damage the liver, placing people at an increased risk of liver cirrhosis, hepatocellular carcinoma, liver failure, and deaths from hepatitis C (Axley et al., 2018; de Oliveria Andrade et al., 2009; Stanaway et al., 2016).
Evidence shows that anti-hepatitis C virus treatment can cure hepatitis C virus infection in a majority of patients in 8–12 weeks (American Association for the Study of Liver Diseases, Infectious Diseases Society of America, 2019; Miller et al., 2014; Shah et al., 2018). Hence, the primary goal of chronic hepatitis C treatment is to eradicate the virus, termed as sustained virologic response, i.e. absence of viremia 12 weeks after the end of treatment (Jacobson et al., 2012). Sustained virologic response is associated with a 75–90% reduced risk of hepatocellular carcinoma, a 80–97% decreased risk of liver-related mortality, and a 70–90% lower risk of overall mortality (Smith-Palmer et al., 2015).
Antiviral therapy should be considered in all patients with chronic hepatitis C (Backus et al., 2018). Given the improved efficacy, tolerability, and safety of interferon-free over interferon-based regimens with ribavirin (Feld et al., 2015, McHutchison et al., 2009, Suwanthawornkul et al., 2015, Zeuzem et al., 2018), interferonfree regimens are now recommended (Shah et al., 2018). Several direct-acting antiviral agent regimens, with or without ribavirin, have been approved in Canada and elsewhere (American Association for the Study of Liver Diseases, Infectious Diseases Society of America, 2019; Miller et al., 2014; Shah et al., 2018). Selection of treatment regimens is dependent on various factors, including: previous hepatitis C treatment, liver disease stage, specific comorbidities (e.g. chronic kidney disease, decompensated cirrhosis, postliver transplantation, hepatitis B coinfection); hepatitis C virus genotype, viral load, and resistance testing (to determine whether adding ribavirin should be considered); and factors accelerating disease progression (Shah et al., 2018). Number of pills per day and duration of treatment should also be considered when selecting treatment regimens (Shah et al., 2018).
In high-income countries, up to 90% of vulnerable people (e.g. those experiencing imprisonment or substance use disorders) are infected with hepatitis C virus (Aldridge et al., 2018). Vulnerable people are commonly excluded from mainstream society as they experience several barriers to treatment engagement and adherence (Luchenski et al., 2018). As a result, they are more likely to experience poor health outcomes (Lewer et al., 2019) and quality of life (Gentil et al., 2019; Lewer et al., 2019). In patients infected with hepatitis C virus, high-drinking and substance addiction have been reported as factors delaying treatment uptake (Socias et al., 2019). Hence, there is a need to develop specific care route to engage the most vulnerable and excluded populations in their hepatitis C care (Luchenski et al., 2018; Popping et al., 2019). Actual interventions, however, have been insufficient to effectively prevent the transmission of HCV among vulnerable people (Larney et al., 2017; Popping et al., 2019).
A nurse-led model of care could facilitate access to evidence-based hepatitis C treatments among those at high risk of sexually transmitted and blood-borne infections, including vulnerable people (Richmond et al., 2020). In a nurse-led approach to care, nurses deliver holistic patient-centered care and consolidate a network of outreach services for vulnerable people, connecting them with gastroenterologists and infectious disease specialists, as well as with other allied healthcare professionals (e.g. pharmacists, nutritionists, outreach workers). Although a nurse-led model of care has been reported to help achieve sustained virologic response among prisoners (Lloyd et al., 2013; Papaluca et al., 2019; Perrett, 2011), it has provided inconclusive results in a community setting (Lewis et al., 2016). Accordingly, we conducted this study with the objective of calculating the prevalence of patients who achieved sustained virologic response after initiating an hepatitis C treatment at a community-based nurse-led clinic (primary objective). Our secondary objectives included: to assess the prevalence of patients who were adherent to their prescribed hepatitis C treatment; and to explore factors associated with treatment adherence and achievement of sustained virologic response.
2. Methods
We herein follow the STROBE and RECORD recommendations for reporting of observational non-experimental studies (Benchimol et al., 2015; Vandenbroucke et al., 2007) (Supplementary Material 1).
2.1. Study design, setting, and population
We conducted a non-experimental prospective cohort study in which we abstracted medical records of all individuals who initiated an hepatitis C treatment at the Clinique de solidarité SABSA, a nurse-led clinic located in Québec City, Québec, Canada, from January 1st, 2012 (date at which hepatitis C treatment started at this nurse-led clinic) to December 31st, 2017 (end of data collection). Co-author IT had full access to the database population used to create the study population. The day of initiation of the hepatitis C treatment at the nurse-led clinic marked patients’ entry into the cohort. Standard follow-up visits at the clinic were scheduled at week 1, 2, and 4 after treatment initiation. Follow-up was completed 24 weeks after the end of treatment. A detailed description of healthcare services provided at the clinic is provided as Supplementary Material 2.
The present study was approved by the CHU de Québec Research Center–Université Laval Institutional Ethics Committee (2017-3618, 2016-2017-26 MP). The Ethics Committee did not require researcher to obtain informed consent from individuals whose data were abstracted for the present study.
2.2. Variables and measurements
An array of variables was abstracted from the patients’ records by co-author IT with help of a research assistant (the full list of variables can be found in Supplementary Material 3). We abstracted the following information recorded prior to treatment initiation: diagnostic date, hepatitis C virus genotype and infection source. We also abstracted various clinical parameters (e.g. alanine aminotransferase; gamma-glutamyl transpeptidase; and liver fibrosis, categorized either as absent/mild, moderate, severe, or advanced) (de Ledinghen et al., 2006) recorded at hepatitis C treatment initiation. We abstracted data on comorbid physical and mental health problems, patients’ sociodemographic characteristics (e.g. sex; highest attained level of education; and monthly income), self-reported alcohol consumption, current smoking status, and history of recent illicit drug use. Finally, we abstracted the prescribed hepatitis C treatment and its duration (e.g. 8, 12, 24 weeks).
From clinical records, we assessed whether patients had missed at least one dose and whether they had taken the prescribed hepatitis C treatment until the last prescribed dose. We considered patients who reported treatment completion without missing any doses as adherent. Patients for whom information on missing doses or treatment completion was lacking were considered as non-adherent.
For the period prior to treatment initiation, the treatment period, and the 12-week period following the end of the treatment, we abstracted data on patients’ health services utilization, including the number of encounters with a nurse, a pharmacist, an outreach worker or a gastroenterologist.
We recorded whether sustained virologic response was achieved 12 weeks after the end of treatment (primary outcome). Sustained virologic response was considered achieved if hepatitis C virus ribonucleic acid (RNA) was undetectable or below the lower limit of quantification at week 12 (Jacobson et al., 2012). Patients for whom no information on sustained virologic response was available at week 12 but who achieved sustained virologic response at week 24 were considered as having achieved sustained virologic response at week 12. Those for whom there was no information on sustained virologic response were deemed not having achieved sustained virologic response.
The clinic's nurse partitioner (co-author IT) was the only research team member to have access to clinical records and, therefore, was also the only one in charge of data abstraction. Once completed, all data abstraction forms were checked for reliability by another researcher. Observed invalid, extreme, missing or out-of-range values were reported to co-author IT in charge of data abstraction for additional check. If needed, errors were corrected.
2.3. Statistical analyses
All statistical analyses were performed using SAS (Cary, NC, USA). Patients' characteristics were described using frequency distributions, as well as means and standard deviations. Among patients initiating an hepatitis C treatment at the nurse-led clinic, we calculated the prevalence of patients who achieved sustained virologic response and the prevalence of patients who were adherent to the prescribed hepatitis C treatment. A statistician performed univariate regression analyses of the association between study outcomes and each of the independent variables. Variables statistically significant at the 20% level were grouped and a reduced multivariate model was obtained by removing one by one variables not statistically significant at the 5% level of significance. The final multivariate model was fitted using a working-Poisson regression, allowing us to present adjusted prevalence ratios, with associated 95% confidence intervals. Similar analyses were conducted to estimate the association between treatment adherence and the independent variables. Additional details regarding our statistical analyses are provided as Supplementary Material 4.
3. Results
3.1. Flow of patients initiating an hepatitis C treatment at the nurse-led clinic
From January 1st, 2012 to December 31st, 2017, 171 patients initiated an hepatitis C treatment at the nurse-led clinic. All were included in our analyses. Two patients died from an overdose during the treatment period and 158/169 (93.5%) met a nurse at the end of their treatment. One patient died from an overdose during the 12 weeks that followed. A total of 136/168 patients (81.0%) attended the visit scheduled at week 12 and 136/168 (81.0%) attended the last visit scheduled at week 24. Detailed reasons for missing appointments are provided in Fig. 1.
Fig. 1.
Flowchart of selected patients throughout the study.
3.2. Characteristics of patients initiating an hepatitis C treatment
Among the 171 patients recruited in this cohort, 120 (70.2%) were male, 120 (70.2%) had less than a college or a university degree, and 95 (55.6%) earned less than US$750 (CA$1,000) per month. About 60% of patients (n = 102) had a criminal record (Table 1).
Table 1.
Sociodemographic characteristics of patients at treatment initiation (N = 171).
| Characteristics | N | (%) |
|---|---|---|
| Sex | ||
| Male | 120 | (70.2%) |
| Female | 51 | (29.8%) |
| Sexual orientation | ||
| Heterosexual | 165 | (96.5%) |
| Other | 6 | (3.5%) |
| Age (years) | ||
| 22 to 45: quantile 1 | 45 | (26.3%) |
| 46 to 52: quantile 2 | 47 | (27.5%) |
| 53 to 59: quantile 3 | 39 | (22.8%) |
| 60 to 75: quantile 4 | 40 | (23.4%) |
| Country of birth | ||
| Canada | 162 | (94.7%) |
| Other | 9 | (5.3%) |
| Marital status | ||
| Single | 109 | (63.7%) |
| In relationship | 62 | (36.3%) |
| Residential status | ||
| Housed | 159 | (93.0%) |
| Homeless (including shelters and transitional housing) | 12 | (7.0%) |
| Place of residence | ||
| Québec City, La Cité-Limoilou district (where SABSA is located) | 91 | (53.2%) |
| Québec City, any other district | 41 | (24.0%) |
| Outside Québec City, but within the Capitale-Nationale administrative region | 13 | (7.6%) |
| Outside the Capitale-Nationale administrative region | 26 | (15.2%) |
| Highest attained level of education | ||
| Elementary school | 61 | (35.7%) |
| High school diploma | 40 | (23.4%) |
| Diploma of vocational studies | 19 | (11.1%) |
| College degree | 24 | (14.0%) |
| ≥Bachelor's degree | 10 | (5.9%) |
| Missing data | 17 | (9.9%) |
| Primary occupation | ||
| Work or study | 59 | (34.5%) |
| Retired | 15 | (8.8%) |
| Unemployed | 97 | (56.7%) |
| Monthly incomea | ||
| From US$375 to US$749 | 95 | (55.6%) |
| ≥US$750 | 75 | (43.9%) |
| Missing data | 1 | (0.5%) |
| Medication insurance coverage | ||
| Public | 139 | (81.3%) |
| Private | 32 | (18.7%) |
| Had a criminal record | ||
| No | 69 | (40.4%) |
| Yes | 102 | (59.6%) |
Data on monthly income were collected in Canadian dollars: As of February 12, 2020, CA$ 1 = US$ 0.753761.
As shown in Table 2, about half of patients were overweight or obese (n = 90, 52.6%). About 80% of individuals had at least one comorbid mental health problem, the most common being substance addiction (n = 99, 57.9%). Illicit injection drug use in the past 30 days was self-reported by 37 patients (21.6%), with 25 and 19 patients reporting having injected cocaine and opioid, respectively (Table 3). About 40% of patients (n = 68) reported recent use of illicit non-injection drugs such as amphetamine (n = 30) and cannabis (n = 46).
Table 2.
Clinical characteristics of patients at treatment initiation (N = 171).
| Clinical characteristics | N | (%) |
|---|---|---|
| Patients | ||
| Body mass index (kg/m2) | ||
| <18.5: underweight | 4 | (2.3%) |
| 18.5 to 24.9: normal weight | 55 | (32.2%) |
| 25 to 29.9: overweight | 58 | (33.9%) |
| >30: obese | 32 | (18.7%) |
| Missing data | 22 | (12.9%) |
| Had any of the following physical health problems: | 115 | (67.3%) |
| Comorbid physical health problem: | ||
| Cancer (other than hepatocellular carcinoma) | 3 | (1.8%) |
| Hepatocellular carcinoma | 2 | (1.2%) |
| Diabetes | 26 | (15.2%) |
| Chronic pain | 35 | (20.5%) |
| Hepatitis B | 9 | (5.3%) |
| Cardiovascular disease | 41 | (24.0%) |
| Chronic inflammatory disease | 16 | (9.4%) |
| Chronic pulmonary disease | 39 | (22.8%) |
| Chronic kidney disease | 10 | (5.9%) |
| Thromboembolic disease | 2 | (1.2%) |
| Human immunodeficiency virus/acquired immune deficiency syndromea | 7 | (4.1%) |
| Had any of the following mental health problems: | 135 | (79.0%) |
| Comorbid mental health problem: | ||
| Anxiety | 52 | (30.4%) |
| Alcoholism | 40 | (23.4%) |
| Bipolarity | 6 | (3.5%) |
| Schizophrenia | 7 | (4.1%) |
| Substance addiction | 99 | (57.9%) |
| Adjustment disorder | 2 | (1.2%) |
| Attention deficit disorder | 20 | (11.7%) |
| Personality trouble | 60 | (35.1%) |
| Active major depressive disorder, first episode | 2 | (1.2%) |
| Recurrent major depressive disorder | 52 | (30.4%) |
| Other mental health problem | 4 | (2.3%) |
| Alanine aminotransferase (U/L) | ||
| ≥0 and ≤50b | 67 | (39.2%) |
| >50 | 85 | (49.7%) |
| Missing data | 19 | (11.1%) |
| Total bilirubin (mmol/L) | ||
| ≥0 et ≤21b | 121 | (70.8%) |
| >21 | 8 | (4.7%) |
| Missing data | 42 | (24.6%) |
| Creatinine (μml/L) | ||
| <55 | 13 | (7.6%) |
| ≥55 et ≤105b | 121 | (70.8%) |
| >105 | 10 | (5.9%) |
| Missing data | 27 | (15.8%) |
| Gamma-glutamyl transpeptidase (U/L) | ||
| <50b | 55 | (32.2%) |
| ≥50 | 67 | (39.2%) |
| Missing data | 49 | (28.7%) |
| Haemoglobin (g/L) | ||
| <140 | 66 | (38.6%) |
| ≥140 et ≤180b | 91 | (53.2%) |
| Missing data | 14 | (8.2%) |
| Platelet count (109/L) | ||
| <150 | 48 | (28.1%) |
| ≥150 et ≤400b | 110 | (64.3%) |
| Missing data | 13 | (7.6%) |
| Thyroid-stimulating hormone (mUI/L) | ||
| <0,25 | 1 | (0.6%) |
| ≥0,25 et ≤5b | 123 | (71.9%) |
| >5 | 5 | (2.9%) |
| Missing data | 42 | (24.6%) |
| Hepatitis C virus | ||
| Hepatitis C virus genotype | ||
| 1a | 93 | (54.4%) |
| 1b | 15 | (8.8%) |
| 2 | 13 | (7.6%) |
| 3 | 43 | (25.1%) |
| 4, 5, 6 and 1+3 | 7 | (4.1%) |
| Hepatitis C virus infection | ||
| Injection drug use | 140 | (81.9%) |
| Other mode of transmissionc | 31 | (18.1%) |
| Liver fibrosis | ||
| Absent, mild or severe fibrosis (F3-F0) | 74 | (43.3%) |
| Advanced fibrosis (F4) or cirrhosis | 77 | (45.0%) |
| Missing data | 20 | (11.7%) |
These seven people who were co-infected with human immunodeficiency virus had an undetectable viral load.
Normal values.
Other modes of transmission include: using intranasal drugs; recipients of blood transfusions; being born to a mother infected with hepatitis C virus; unregulated tattooing and piercing in prisons, etc.
Table 3.
Recent illicit drug, alcohol, and tobacco use by patients before treatment initiation (N = 171).
| Substance used in the past 30 days | N | (%) |
|---|---|---|
| Illicit injection drug | ||
| None used | 134 | (78.4%) |
| Used only one drug | 29 | (17.0%) |
| Used ≥2 drugs | 8 | (4.7%) |
| Injected: | ||
| Amphetamine | 1 | (0.6%) |
| Cocaine | 25 | (14.6%) |
| Opioid | 19 | (11.1%) |
| Another injection drug | 1 | (0.6%) |
| Illicit non-injection drug | ||
| None used | 103 | (60.2%) |
| Used only one drug | 45 | (26.3%) |
| Used ≥2 drugs | 23 | (13.5%) |
| Used: | ||
| Amphetamine | 30 | (17.5%) |
| Cocaine or crack | 13 | (7.6%) |
| Cannabis | 46 | (26.9%) |
| Opioid | 5 | (2.9%) |
| Gamma hydroxybutyrate (GHB) drug | 1 | (0.6%) |
| Another stimulant | 1 | (0.6%) |
| Number of standard alcohol drinks per weeka | ||
| 0 | 103 | (60.2%) |
| 1 to 7 | 24 | (14.0%) |
| 8 to 14 | 8 | (4.7%) |
| 15 to 21 | 9 | (5.3%) |
| >21 | 26 | (15.2%) |
| Drink alcohol, but could not recall how many drinks a week | 1 | (0.6%) |
| High-risk drinking | 37 | (21.6%) |
| Current tobacco smoker | 112 | (65.5%) |
In women, low-risk drinking is defined as no more than 10 standard drinks a week. In men, low-risk drinking is defined as no more than 3 drinks a day or 15 standard drinks a week. One standard drink is equivalent to one regular beer (340 ml/12 oz, 5% alcohol), one glass of wine (140 ml/5oz, 12% alcohol), one glass of fortified wine (85 ml/3oz, 20% alcohol) and one shot of spirits (45 ml/1.5 oz, 40% alcohol).
3.3. Characteristics of hepatitis C treatments
A total of 56 patients (32.7%) have had a prior hepatitis C treatment before entering the cohort. These patients were seeking another treatment either due to prior treatment failure (n = 50, 89.2%) or due to hepatitis C virus re-infection (n = 6, 10.7%). Patients (n = 166, 97.1%) were mostly prescribed the hepatitis C drug treatment by a gastroenterologist. Two-thirds of patients (n = 106, 62.0%) were prescribed a direct-acting antiviral without ribavirin (Supplementary Material 5). While 133 patients (77.8%) were treated for 8 or 12 weeks, 8 patients (4.7%) had a treatment duration of 48 weeks.
3.4. Adherence to the hepatitis C treatment
Due to adverse reactions, physicians prescribed hepatitis C treatment discontinuation for eight patients. A total of 158 patients attended the visit scheduled at the end of the hepatitis C treatment (hence, 6 patients [3.5%] were deemed to be non-adherent due to missing information for this outcome in their record). Among these 158 patients, 93% (n = 147) reported having completed the treatment and 126 (85.7%) also reported having taken all prescribed doses. These 126 patients (73.7% of the cohort) were considered as adherent to their prescribed treatment.
3.5. Characteristics associated with adherence to the hepatitis C treatment
Results of univariate regression analyses of the association between treatment adherence and each of the independent variables are presented as Supplementary Material 6. Multivariate analyses showed that patients reporting a recent use of illicit drugs were less likely to be adherent (recent use vs. non-use of illicit drugs: adjusted prevalence ratio 0.77, 95% confidence interval 0.67–0.89). Patients who were prescribed an hepatitis C treatment length of 48 weeks (vs. 8 or 12 weeks) were also less likely to be adherent to their hepatitis C treatment (adjusted prevalence ratio 0.29, 95% confidence interval 0.09–0.94).
3.6. Health services used during the treatment period
Prior to and during the hepatitis C treatment period, all patients were seen by a nurse (Table 4). Nearly all patients (n = 163, 95.3%) met a gastroenterologist prior to initiating the treatment, while less than half of patients (n = 71, 44.9%) met a gastroenterologist during the treatment period. During the treatment period, about half of patients attended more visits at the clinic than what was scheduled (43.0%).
Table 4.
Health services use by the 171 patients before, during, and after treatment.
| Health services | From the first visit at the nurse-led clinic to treatment initiation (N = 171) |
During the course of the hepatitis C treatment (N = 158) |
During the 12-week period following treatment cessation (N = 136) |
|||
|---|---|---|---|---|---|---|
| N | (%) | N | (%) | N | (%) | |
| Was hospitalized | 10 | (5.9%) | 8 | (5.1%) | 2 | (1.5%) |
| Visited the emergency | 10 | (5.9%) | 13 | (8.2%) | 5 | (3.8%) |
| Consulted a nutritionist | 5 | (2.9%) | 2 | (1.3%) | 0 | (0%) |
| Consulted a pharmacist | 77 | (45.0%) | 2 | (1.3%) | 0 | (0%) |
| Consulted an outreach worker | 87 | (50.9%) | 73 | (46.2%) | 51 | (38.6%) |
| Consulted a nurse | 171 | (100.0%) | 158 | (100.0%) | 131 | (99.2%) |
| Consulted a general practitioner | 33 | (19.3%) | 37 | (23.4%) | 24 | (18.2%) |
| Consulted an infectious disease physician | 6 | (3.5%) | 6 | (3.8%) | 7 | (5.3%) |
| Consulted a gastroenterologist | 163 | (95.3%) | 71 | (44.9%) | 52 | (39.4%) |
| Consulted another specialist doctor | 27 | (15.8%) | 22 | (13.9%) | 14 | (10.6%) |
| Received services from a community organization | 68 | (39.8%) | 67 | (39.2%) | 53 | (39.9%) |
| Mean number (±standard deviation) of visits scheduled at the nurse-led clinic | N/A | N/A | 5.8 | (± 4.2) | 2.9 | (± 0.7) |
| Mean number (±standard deviation) of visits scheduled at the nurse-led clinic that patients attended | N/A | N/A | 6.9 | (± 4.9) | 4.0 | (± 2.4) |
| Difference between the number of visits scheduled and the number of visits that occurred at the nurse-led clinic | ||||||
| Lower number | N/A | N/A | 29 | (18.4%) | 14 | (10.6%) |
| Equal number | N/A | N/A | 61 | (38.6%) | 53 | (40.2%) |
| Higher number | N/A | N/A | 68 | (43.0%) | 65 | (49.2%) |
N/A: Not applicable
3.7. Sustained virologic response
Among the 171 patients who initiated an hepatitis C treatment, 133 (77.8%) had an hepatitis C virus RNA test 12 weeks after the end of treatment. Of these 133 patients, 95.5% (n = 127) achieved sustained virologic response. Twenty-four weeks after the end of treatment, 135 patients had an hepatitis C virus RNA test (including 23 patients who did not have an hepatitis C virus RNA test 12 weeks before). Of these 135 patients, 127 (93.4%) achieved sustained virologic response. Only one person was re-infected with hepatitis C virus due to injection drug use. The remaining 7 patients did not achieve sustained virologic response at week 24 due to treatment failure. A total of 156 patients had an hepatitis C virus RNA test during the study period, of whom 149 (95.5%) achieved sustained virologic response (15 patients were deemed not to have achieved sustained virologic response due to missing data for this outcome in their record). The 149 patients who achieved sustained virologic response correspond to 87.1% of the cohort.
3.8. Characteristics associated with achievement of sustained virologic response
Results of univariate regression analyses of the association between sustained virologic response achievement and each of the independent variables are presented as Online Supplementary Material 7. In multivariate analyses, patients who had a criminal record were less likely to achieve sustained virologic response (patients who had a criminal record vs. not: adjusted prevalence ratio 0.87, 95% confidence interval 0.79–0.97). Patients who were non-adherent to their hepatitis C treatment were also less likely to achieve sustained virologic response (non-adherent vs. adherent adjusted prevalence ratio 0.81, 95% confidence interval 0.68–0.98).
4. Discussion
4.1. Key findings
First, this prospective cohort study shows that a high proportion of vulnerable people initiating an hepatitis C treatment at a community-based nurse-led clinic adhered to their hepatitis C treatment and achieved sustained virologic response. Second, an hepatitis C treatment length of 48 weeks (vs. 8 or 12 weeks) and recent use of illicit drugs (vs. non-use) were identified as key independent factors associated with a lower likelihood of adherence in our study population. Third, patients with a criminal record and those who were non-adherent to the prescribed hepatitis C treatment were less likely to achieve sustained virologic response.
4.2. Explanation of findings
Our results show that more than half of patients initiating an hepatitis C treatment at the nurse-led clinic had a criminal record and were considered as having substance addictions. When provided with nurse-led care in the community, a high proportion of these vulnerable people not only engage in their care by attending all their scheduled follow-up visits, but are also adherent to their treatment and, in turn, achieve sustained virologic response. As such, this study adds to a growing body of evidence from studies conducted in prison settings suggesting that nurse-led clinic can safely and efficiently coordinate interdisciplinary hepatitis C care (Perrett, 2011; Tait et al., 2010), as well as improve treatment uptake (Lloyd et al., 2013) and outcomes in people with hepatitis C (Overton et al., 2019; Papaluca et al., 2019). Our results nevertheless contrast with those of a cluster randomized controlled trial comparing nurse-initiated vs. physician-initiated hepatitis C therapy in a community setting (Lewis et al., 2016). In this trial, where nurses’ role was limited to offering immediate antiviral therapy, uptake and adherence remained poor in vulnerable people and were not different between the two groups (Lewis et al., 2016). By contrast, in the present study, services provided at the nurse-led clinic were both tailored to the specific needs of the vulnerable populations and highly consistent with strategies developed to improve satisfaction with care among vulnerable people (Gentil et al., 2020). For instance, patients could attend all their hepatitis C-related medical appointments in a strategic location, close to where they lived (a key enabler to treatment engagement among vulnerable people) (Wolstenholme et al., 2020). To avoid transport-related problems, outreach workers picked up patients for their appointments and drove them to the clinic. Nurses who acted as case managers ensured continuity of care (Gentil et al., 2020) as well as provision of health and social services that tackled not only the physical and mental illnesses of vulnerable patients, but also their addictions, as others called for (Luchenski et al., 2018). As such, services provided at the community-based nurse-led clinic may have driven its apparent success in terms of uptake, adherence, and sustained virologic response.
Our findings suggest that recent illicit drug use (vs. non-use) and hepatitis C treatment duration (48 weeks vs. 8 or 12 weeks) are key factors associated with a reduced likelihood of treatment adherence. Treatment non-adherence and having a criminal record were identified as independent factors associated with a lower likelihood of sustained virologic response achievement. These findings are consistent with those from a previous meta-analysis that showed that recent illicit drug use was associated with non-adherence (Hajarizadeh et al., 2018). Treatment adherence has also been reported in the past to be the strongest predictor for sustained virologic response (Vo et al., 2015).
4.3. Future directions
Effective treatments are widely available and concerted efforts to eliminate hepatitis C virus as a public health threat have been called for by the World Health Organization (World Health Organization, 2016). In this context, our findings are noteworthy, not only because hepatitis C treatment uptake by vulnerable people is crucial to meet the 2030 hepatitis C virus elimination target (World Health Organization, 2016), but also because studies have shown that people with substance addictions and those with low monthly income are less likely to undertake an hepatitis C treatment than others (Nitulescu et al., 2019; Saeed et al., 2020). Our results suggest that a nurse-led clinic can successfully reach vulnerable populations in a community setting, in order to assist them in being cured from hepatitis C virus. There is now a need to assess the comparative impact of this nurse-led model of care for vulnerable people, compared to usual physician-led care, on adherence, sustained virologic response, but also healthcare costs.
4.4. Strengths and limitations
This study has several strengths. All individuals initiating an hepatitis C treatment at the nurse-led clinic during the study period were included. We were able to comprehensively describe patients, hepatitis C virus infections, and hepatitis C treatments received. We were also able to study an array of sociodemographic, clinical, and behavioural characteristics potentially associated with treatment adherence and sustained virologic response achievement.
This study has also limitations. First, data used in this study were originally collected for clinical purpose. Data misclassification may therefore have occurred (with patients potentially underreporting illicit drug use). Second, patients for whom we found in their clinical record no information on treatment completion (3.5% of patients) and on sustained virologic response (8.8% of patients) were considered as non-adherent and as not having achieved virologic response, respectively. Therefore, the proportion of patients who were found to be adherent to their treatment and the proportion of those who achieved sustained virologic response may have been underestimated. Finally, in the absence of a comparison group, we were not able to assess the effectiveness of this nurse-led model of care compared to standard physician-led care. The results of this present study send a potential efficacy signal.
5. Conclusions
Our results suggest that a nurse-led clinic offering outreach services for people infected with hepatitis C virus could fill an important gap in hepatitis C health services delivered in a community setting. We believe these results can be generalized to patients who initiate an hepatitis C treatment in clinics that serve vulnerable patient populations similar to those enrolled in this cohort.
Tweetable abstract
High adherence and sustained virologic response in vulnerable people initiating an #Hepc treatment at a community-based #NPsLead clinic.
Contribution of the paper
What is already known about the topic
Hepatitis C virus triggers a global pandemic. Effective treatments, including direct-acting antivirals, are available and can cure hepatitis C virus infection in most patients.
In high-income countries, up to 90% of vulnerable people are infected with hepatitis C virus. Adherence to hepatitis C treatment is suboptimal in this population.
There is a need to develop specific care route to engage the most vulnerable populations in their hepatitis C care. Actual interventions, however, have been insufficient to effectively prevent the transmission of hepatitis C virus among vulnerable people in a community setting.
What this paper adds
This prospective cohort study shows that a community-based nurse-led clinic engages vulnerable people in their care. Patients attend their follow-up visits, adhere to their hepatitis C treatment, and achieve sustained virologic response.
This study identifies hepatitis C treatment length of 48 weeks (vs. 8 or 12 weeks) and recent use of illicit drugs (vs. non-use) as independent factors associated with a lower likelihood of adherence.
This study suggests that patients with a criminal record and those who are non-adherent to the prescribed hepatitis C treatment might be less likely to achieve sustained virologic response.
List of abbreviations
RNA: Ribonucleic acid
Authors' contributions
All authors contributed to the study design. MG wrote the initial draft and [IT, JPG, JM revised it for important intellectual content. All authors have given final approval of the version to be published and agree to be accountable for all aspects of the work.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgments
Acknowledgements
We are grateful to the Clinique de solidarité SABSA Board of Directors who agreed to give us access to patients' records. We also thank Annabelle Moisan-De Serres, M.Sc. for assistance in collecting the data, Myrto Mondor, M.Sc. for conducting statistical analyses, and Dr. Marie-Louise Vachon, M.D. for commenting on a previous version of this manuscript.
Funding sources
This study was made possible through financial support from Merck Canada Inc. to the CHU de Québec-Université Laval Foundation. This study received additional financial support from the CHU de Québec-Université Laval Foundation. The funding sources had no role in the design of this study and had no role during its execution, analyses, interpretation of the data, or decision to submit the results. MG is a postdoctoral fellow supported by the Canadian Institutes of Health Research and the Fonds de recherche du Québec – Santé.
Footnotes
Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.ijnsa.2021.100029.
Contributor Information
Myriam Gagné, Email: Myriam.Gagne@unityhealth.to.
Isabelle Têtu, Email: Isabelle.tetu.1@ulaval.ca.
Jean-Pierre Grégoire, Email: Jean-Pierre.Gregoire@pha.ulaval.ca.
Jocelyne Moisan, Email: Jocelyne.Moisan@pha.ulaval.ca.
Appendix. Supplementary materials
References
- Aldridge R.W., Story A., Hwang S.W., Nordentoft M., Luchenski S.A., Hartwell G., Tweed E.J., Lewer D., Vittal Katikireddi S., Hayward A.C. Morbidity and mortality in homeless individuals, prisoners, sex workers, and individuals with substance use disorders in high-income countries: a systematic review and meta-analysis. Lancet. 2018;391:241–250. doi: 10.1016/S0140-6736(17)31869-X. (10117) [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zeuzem S., Foster G.R., Wang S., Asatryan A., Gane E., Feld J.J., Asselah T., Bourliere M., Ruane P.J., Wedemeyer H., Pol S., Flisiak R., Poordad F., Chuang W.L., Stedman C.A., Flamm S., Kwo P., Dore G.J., Sepulveda-Arzola G., Roberts S.K., Soto-Malave R., Kaita K., Puoti M., Vierling J., Tam E., Vargas H.E., Bruck R., Fuster F., Paik S.W., Felizarta F., Kort J., Fu B., Liu R., Ng T.I., Pilot-Matias T., Lin C.W., Trinh R., Mensa F.J. Glecaprevir-pibrentasvir for 8 or 12 weeks in HCV genotype 1 or 3 infection. N. Engl. J. Med. 2018;378(4):354–369. doi: 10.1056/NEJMoa1702417. [DOI] [PubMed] [Google Scholar]
- Axley P., Ahmed Z., Ravi S., Singal A.K. Hepatitis C virus and hepatocellular carcinoma: a narrative review. J. Clin. Transl. Hepatol. 2018;6(1):79–84. doi: 10.14218/JCTH.2017.00067. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Backus L.I., Belperio P.S., Shahoumian T.A., Mole L.A. Direct-acting antiviral sustained virologic response: impact on mortality in patients without advanced liver disease. Hepatology. 2018;68(3):827–838. doi: 10.1002/hep.29811. [DOI] [PubMed] [Google Scholar]
- Benchimol E.I., Smeeth L., Guttmann A., Harron K., Moher D., Petersen I., Sorensen H.T., von Elm E., Langan S.M., Record Working Committee The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) statement. PLoS Med. 2015;12(10) doi: 10.1371/journal.pmed.1001885. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen S.L., Morgan T.R. The natural history of hepatitis C virus (HCV) infection. Int. J. Med. Sci. 2006;3(2):47–52. doi: 10.7150/ijms.3.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Ledinghen V., Douvin C., Kettaneh A., Ziol M., Roulot D., Marcellin P., Dhumeaux D., Beaugrand M. Diagnosis of hepatic fibrosis and cirrhosis by transient elastography in HIV/hepatitis C virus-coinfected patients. J. Acquir. Immune Defic. Syndr. 2006;41(2):175–179. doi: 10.1097/01.qai.0000194238.15831.c7. [DOI] [PubMed] [Google Scholar]
- de Oliveria Andrade L.J., D’Oliveira A., Melo R.C., De Souza E.C., Costa Silva C.A., Parana R. Association between hepatitis C and hepatocellular carcinoma. J. Glob. Infect. Dis. 2009;1(1):33–37. doi: 10.4103/0974-777X.52979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feld J.J., Jacobson I.M., Hezode C., Asselah T., Ruane P.J., Gruener N., Abergel A., Mangia A., Lai C.L., Chan H.L., Mazzotta F., Moreno C., Yoshida E., Shafran S.D., Towner W.J., Tran T.T., McNally J., Osinusi A., Svarovskaia E., Zhu Y., Brainard D.M., McHutchison J.G., Agarwal K., Zeuzem S., Astral-Investigators Sofosbuvir and velpatasvir for HCV genotype 1, 2, 4, 5, and 6 infection. N. Engl. J. Med. 2015;373(27):2599–2607. doi: 10.1056/NEJMoa1512610. [DOI] [PubMed] [Google Scholar]
- Gentil L., Grenier G., Bamvita J.M., Dorvil H., Fleury M.J. Profiles of quality of life in a homeless population. Front. Psychiatry. 2019;10:10. doi: 10.3389/fpsyt.2019.00010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gentil L., Grenier G., Bamvita J.M., Fleury M.J. Satisfaction with health and community services among homeless and formerly homeless individuals in Quebec, Canada. Health Soc. Care Community. 2020;28(1):22–33. doi: 10.1111/hsc.12834. [DOI] [PubMed] [Google Scholar]
- Hajarizadeh B., Cunningham E.B., Reid H., Law M., Dore G.J., Grebely J. Direct-acting antiviral treatment for hepatitis C among people who use or inject drugs: a systematic review and meta-analysis. Lancet Gastroenterol. Hepatol. 2018;3(11):754–767. doi: 10.1016/S2468-1253(18)30304-2. [DOI] [PubMed] [Google Scholar]
- Jacobson I.M., Poordad F., Brown R.S., Jr., Kwo P.Y., Reddy K.R., Schiff E. Standardization of terminology of virological response in the treatment of chronic hepatitis C: panel recommendations. J. Viral Hepat. 2012;19(4):236–243. doi: 10.1111/j.1365-2893.2011.01552.x. [DOI] [PubMed] [Google Scholar]
- Larney S., Peacock A., Leung J., Colledge S., Hickman M., Vickerman P., Grebely J., Dumchev K.V., Griffiths P., Hines L., Cunningham E.B., Mattick R.P., Lynskey M., Marsden J., Strang J., Degenhardt L. Global, regional, and country-level coverage of interventions to prevent and manage HIV and hepatitis C among people who inject drugs: a systematic review. Lancet Glob. Health. 2017;5(12) doi: 10.1016/S2214-109X(17)30373-X. e1208-e1220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lewer D., Aldridge R.W., Menezes D., Sawyer C., Zaninotto P., Dedicoat M., Ahmed I., Luchenski S., Hayward A., Story A. Health-related quality of life and prevalence of six chronic diseases in homeless and housed people: a cross-sectional study in London and Birmingham, England. BMJ Open. 2019;9(4) doi: 10.1136/bmjopen-2018-025192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lewis H., Kunkel J., Axten D., Dalton J., Gardner H., Tippett A., Wynne S., Wilkinson M., Foster G.R. Community nurse-led initiation of antiviral therapy for chronic hepatitis C in people who inject drugs does not increase uptake of or adherence to treatment. Eur. J. Gastroenterol. Hepatol. 2016;28(11):1258–1263. doi: 10.1097/MEG.0000000000000711. [DOI] [PubMed] [Google Scholar]
- Lloyd A.R., Clegg J., Lange J., Stevenson A., Post J.J., Lloyd D., Rudge G., Boonwaat L., Forrest G., Douglas J., Monkley D. Safety and effectiveness of a nurse-led outreach program for assessment and treatment of chronic hepatitis C in the custodial setting. Clin. Infect. Dis. 2013;56(8):1078–1084. doi: 10.1093/cid/cis1202. [DOI] [PubMed] [Google Scholar]
- Luchenski S., Maguire N., Aldridge R.W., Hayward A., Story A., Perri P., Withers J., Clint S., Fitzpatrick S., Hewett N. What works in inclusion health: overview of effective interventions for marginalised and excluded populations. Lancet. 2018;391(10117):266–280. doi: 10.1016/S0140-6736(17)31959-1. (10117) [DOI] [PubMed] [Google Scholar]
- McHutchison J.G., Lawitz E.J., Shiffman M.L., Muir A.J., Galler G.W., McCone J., Nyberg L.M., Lee W.M., Ghalib R.H., Schiff E.R., Galati J.S., Bacon B.R., Davis M.N., Mukhopadhyay P., Koury K., Noviello S., Pedicone L.D., Brass C.A., Albrecht J.K., Sulkowski M.S., Ideal Study Team Peginterferon alfa-2b or alfa-2a with ribavirin for treatment of hepatitis C infection. N. Engl. J. Med. 2009;361(6):580–593. doi: 10.1056/NEJMoa0808010. [DOI] [PubMed] [Google Scholar]
- Miller M.H., Agarwal K., Austin A., Brown A., Barclay S.T., Dundas P., Dusheiko G.M., Foster G.R., Fox R., Hayes P.C., Leen C., Millson C., Ryder S.D., Tait J., Ustianowski A., Dillon J.F. British viral hepatitis group, British society of gastroenterology liver committee, British association for the study of liver, Scottish society of gastroenterology, Scottish viral hepatitis group, Scottish viral hepatitis nurses group. Aliment Pharmacol. Ther. 2014;39(12):1363–1375. doi: 10.1111/apt.12764. Review article: 2014 UK consensus guidelines - hepatitis C management and direct-acting anti-viral therapy. [DOI] [PubMed] [Google Scholar]
- Nitulescu R., Young J., Saeed S., Cooper C., Cox J., Martel-Laferriere V., Hull M., Walmsley S., Tyndall M., Wong A., Klein M.B. Variation in hepatitis C virus treatment uptake between Canadian centres in the era of direct-acting antivirals. Int. J. Drug Policy. 2019;65:41–49. doi: 10.1016/j.drugpo.2018.08.012. [DOI] [PubMed] [Google Scholar]
- Overton K., Clegg J., Pekin F., Wood J., McGrath C., Lloyd A., Post J.J. Outcomes of a nurse-led model of care for hepatitis C assessment and treatment with direct-acting antivirals in the custodial setting. Int. J. Drug Policy. 2019;72:123–128. doi: 10.1016/j.drugpo.2019.02.013. [DOI] [PubMed] [Google Scholar]
- Papaluca T., McDonald L., Craigie A., Gibson A., Desmond P., Wong D., Winter R., Scott N., Howell J., Doyle J., Pedrana A., Lloyd A., Stoove M., Hellard M., Iser D., Thompson A. Outcomes of treatment for hepatitis C in prisoners using a nurse-led, statewide model of care. J. Hepatol. 2019;70(5):839–846. doi: 10.1016/j.jhep.2019.01.012. [DOI] [PubMed] [Google Scholar]
- Perrett S.E. Prisoner health: assessing a nurse-led hepatitis C testing clinic. Br. J. Nurs. 2011;20(10):611–614. doi: 10.12968/bjon.2011.20.10.611. [DOI] [PubMed] [Google Scholar]
- Popping S., Bade D., Boucher C., van der Valk M., El-Sayed M., Sigurour O., Sypsa V., Morgan T., Gamkrelidze A., Mukabatsinda C., Deuffic-Burban S., Ninburg M., Feld J., Hellard M., Ward J. The global campaign to eliminate HBV and HCV infection: international Viral Hepatitis Elimination Meeting and core indicators for development towards the 2030 elimination goals. J. Virus Erad. 2019;5(1):60–66. doi: 10.1016/S2055-6640(20)30281-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richmond J.A., Gallagher L., McDonald L., O’Sullivan M., Fitzsimmons C., Pedrana A. Achieving hepatitis C elimination by using person-centered, nurse-led models of care: a discussion of four international case studies. Gastroenterol. Nurs. 2020;43(4):303–309. doi: 10.1097/SGA.0000000000000458. [DOI] [PubMed] [Google Scholar]
- Saeed S., Strumpf E., Moodie E.E.M., Wong L., Cox J., Walmsley S., Tyndall M., Cooper C., Conway B., Hull M., Martel-Laferriere V., Gill J., Wong A., Vachon M.L., Klein M.B., Canadian Co-Infection Cohort Study Investigators Eliminating structural barriers: the impact of unrestricted access on hepatitis C treatment uptake among people living with HIV. Clin. Infect. Dis. 2020;71(2):363–371. doi: 10.1093/cid/ciz833. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shah H., Bilodeau M., Burak K.W., Cooper C., Klein M., Ramji A., Smyth D., Feld J.J., Canadian Association for the Study of the Liver The management of chronic hepatitis C: 2018 guideline update from the Canadian Association for the Study of the Liver. CMAJ. 2018;190(22) doi: 10.1503/cmaj.170453. E677-E687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith-Palmer J., Cerri K., Valentine W. Achieving sustained virologic response in hepatitis C: a systematic review of the clinical, economic and quality of life benefits. BMC Infect. Dis. 2015;15(1):19. doi: 10.1186/s12879-015-0748-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Socias M.E., Ti L., Wood E., Nosova E., Hull M., Hayashi K., Debeck K., Milloy M.J. Disparities in uptake of direct-acting antiviral therapy for hepatitis C among people who inject drugs in a Canadian setting. Liver Int. 2019;39(8):1400–1407. doi: 10.1111/liv.14043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stanaway J.D., Flaxman A.D., Naghavi M., Fitzmaurice C., Vos T., Abubakar I., Abu-Raddad L.J., Assadi R., Bhala N., Cowie B., Forouzanfour M.H., Groeger J., Hanafiah K.M., Jacobsen K.H., James S.L., MacLachlan J., Malekzadeh R., Martin N.K., Mokdad A.A., Mokdad A.H., Murray C.J.L., Plass D., Rana S., Rein D.B., Richardus J.H., Sanabria J., Saylan M., Shahraz S., So S., Vlassov V.V., Weiderpass E., Wiersma S.T., Younis M., Yu C., El Sayed Zaki M., Cooke G.S. The global burden of viral hepatitis from 1990 to 2013: findings from the Global Burden of Disease Study 2013. Lancet. 2016;388(10049):1081–1088. doi: 10.1016/S0140-6736(16)30579-7. (10049) [DOI] [PMC free article] [PubMed] [Google Scholar]
- Suwanthawornkul T., Anothaisintawee T., Sobhonslidsuk A., Thakkinstian A., Teerawattananon Y. Efficacy of second generation direct-acting antiviral agents for treatment naive hepatitis C genotype 1: a systematic review and network meta-analysis. Plos One. 2015;10(12):e0145953. doi: 10.1371/journal.pone.0145953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tait J.M., McIntyre P.G., McLeod S., Nathwani D., Dillon J.F. The impact of a managed care network on attendance, follow-up and treatment at a hepatitis C specialist centre. J Viral Hepat. 2010;17(10):698–704. doi: 10.1111/j.1365-2893.2009.01227.x. [DOI] [PubMed] [Google Scholar]
- The Polaris Observatory HCV Collaborators Global prevalence and genotype distribution of hepatitis C virus infection in 2015: a modelling study. Lancet Gastroenterol. Hepatol. 2017;2(3):161–176. doi: 10.1016/S2468-1253(16)30181-9. [DOI] [PubMed] [Google Scholar]
- Vandenbroucke J.P., von E.E., Altman D.G., Gotzsche P.C., Mulrow C.D., Pocock S.J., Poole C., Schlesselman J.J., Egger M. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration. PLoS Med. 2007;4(10):e297. doi: 10.1371/journal.pmed.0040297. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vo K.P., Vutien P., Akiyama M.J., Vu V.D., Ha N.B., Piotrowski J.I., Wantuck J., Roytman M.M., Tsai N., Cheung R., Li J., Nguyen M.H. Poor sustained virological response in a multicenter real-life cohort of chronic hepatitis C patients treated with pegylated interferon and ribavirin plus telaprevir or boceprevir. Dig. Dis. Sci. 2015;60(4):1045–1051. doi: 10.1007/s10620-015-3621-0. [DOI] [PubMed] [Google Scholar]
- Wolstenholme D., Poll R., Tod A. Innovating access to the nurse-led hepatitis C clinic using co-production. J. Res. Nurs. 2020;25(3):211–224. doi: 10.1177/1744987120914353. [DOI] [PMC free article] [PubMed] [Google Scholar]
- World Health Organization . World Health Organization; Geneva, Switzerland: 2016. Combating Hepatitis B and C to Reach Elimination by 2030. [Google Scholar]
- American Association for the Study of Liver Diseases, Infectious Diseases Society of America, 2019. HCV guidance: recommendations for testing, managing, and treating hepatitis C. Available at: www.hcvguidelines.org. [DOI] [PMC free article] [PubMed]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.

