Showing posts with label Treatment Response. Show all posts
Showing posts with label Treatment Response. Show all posts

March 26, 2014

New genetic targets IDed for HCV treatment

Provided by Clinical Advisor

March 20, 2014

DNA changes on the IFNL3 gene have been associated with better treatment responses and natural ability to clear infection among patients with hepatitis C infection.

genetics_0513blog_380766

Two single-letter DNA changes on the IFNL3 gene on chromosome 19 have been associated with better treatment responses and natural ability to clear infection among patients with hepatitis C infection, and may offer novel targets for therapy, according to researchers.

“[The IFNL3 gene], has received considerable attention in the field of HCV, as many independent genome-wide association studies have identified a strong association between polymorphisms near IFNL3 and clearance of HCV,” Ram Savan, PhD, assistant professor of immunology at the University of Washington in Seattle and colleagues reported in Nature Immunology. “However, the mechanism underlying this association has remained elusive.”

Previous study findings have shown that patients of Asian descent with HCV respond better to treatment when compared with those of African descent. So researchers pooled data from entire human genomes in hopes of identifying gene clusters associated with a response to therapy for HCV.

Two single-letter genetic variations on the IFNL3 gene located near an area that encodes for interleukin-28B, a cytokine known to play a role in the body's immune defense against viruses, may play a role in the body's ability to control HCV infection.

Individuals who carry the T (for thymidine) variant have an unfavorable outcome in fighting HCV, while those who carry the G (for guanosine) variant have a favorable outcome, the researchers found.

Their data showed that HCV could induce liver cells to target the activities of the IFNL3 gene with two microRNAs. MicroRNAs are silencers: They stop the messengers who transmit information to produce a protein from a gene, in this case the production of the antiviral interferon lambda-3.

These two particular microRNAs are generally turned off in liver cells, until HCV coerces them to act on its behalf. Normally, these so called myomiRs are associated with myosin-encoding genes in skeletal and heart muscle.

"This is a previously unknown strategy by which HCV evades the immune system and suggests that these microRNAs could be therapeutic targets for restoring the host antiviral response," the researchers wrote.

Adding support to this suggestion is the researchers' observation that the bad-acting microRNAs in question could not land on and repress interferon lambda-3, if the host carried the favorable "G" variant. In those cases, the host is able to escape adverse regulation by HCV, the researchers observed.

“Our data reveal a previously unknown mechanism by which HCV attenuates the antiviral response and indicate new potential therapeutic targets for HCV treatment,” the researchers concluded.

References

  1. McFarland AP et al. Nature Immun. 2014;15:72-81.

Disclosure: See study for full list of disclosures.

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March 22, 2014

Metabolic syndrome is associated with poor treatment response to antiviral therapy in chronic hepatitis C genotype 3 patients

Eur J Gastroenterol Hepatol. 2014 Mar 17. [Epub ahead of print]

Aziz H1, Gill U, Raza A, Gill ML.

Abstract

INTRODUCTION: Hepatitis C viral (HCV) infection is caused by an RNA virus. HCV infection is considered to induce systemic disease that causes steatosis, alters lipid metabolism, and results in metabolic syndrome. This study aimed to investigate the therapeutic outcome in HCV genotype 3 patients with metabolic syndrome.

MATERIALS AND METHODS: A total of 621 HCV-positive patients who visited the hospital for treatment were screened. Among these, 441 patients were enrolled for antiviral therapy. These enrolled patients were assessed for metabolic syndrome according to the International Diabetes Federation criteria. Group A included patients with metabolic syndrome and group B included patients without metabolic syndrome. All patients received peginterferon-α2a (180 μg/week) and ribavirin (10 mg/kg/day) for 6 months.

RESULTS: The prevalence of metabolic syndrome in chronic HCV patients was 37.9%. We observed that metabolic syndrome was more common among female compared with male participants (43.9 vs. 28.8%, P=0.005). It was found that sustained virologic response (SVR) rates were significantly higher in the patients in group B (without metabolic syndrome) compared with the patients in group A who had metabolic syndrome (72.2 vs. 43.7%, P<0.05). Older patients were at a higher risk for metabolic syndrome and a correlation of metabolic syndrome with nonresponse to antiviral therapy was observed. An interesting correlation among metabolic syndrome, age, and SVR was found: with age, SVR decreases, while metabolic syndrome increases.

CONCLUSION: Metabolic syndrome has an influence on therapeutic outcomes in terms of SVR. Moreover, this information can identify patients who might have a low chance of attaining an SVR and a timely decision may protect the patients from the adverse effects of therapy.

PMID: 24642690 [PubMed - as supplied by publisher]

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December 13, 2013

Impact of ribavirin priming on viral kinetics and treatment response in chronic hepatitis C genotype 1 infection

Journal of Viral Hepatitis

Volume 21, Issue 1, pages 42–52, January 2014

Original Article

U. Mihm1,†, M.-W. Welker1,†, G. Teuber2,  H. Wedemeyer3, T. Berg4, C. Sarrazin1,  S. Böhm4, U. Alshuth5, E. Herrmann6, S. Zeuzem1,*

Article first published online: 21 JUN 2013

DOI: 10.1111/jvh.12124

© 2013 John Wiley & Sons Ltd

Abstract

Keywords: IL28B genotype;  ribavirin monotherapy;  ribavirin priming;  viral kinetics

Summary

Ribavirin amplifies the interferon-alpha (IFN) signalling cascade. As ribavirin needs 4 weeks to reach steady state, ribavirin priming may optimize hepatic IFN sensitivity before starting a pegylated (PEG)-IFN/ribavirin combination therapy. This study investigated potential benefits of ribavirin priming prior to PEG-IFN2a/ribavirin combination therapy on viral kinetics, on-treatment and sustained virological response (SVR) in chronic hepatitis C virus (HCV) genotype 1 infection. Sixty-eight treatment naive patients were randomized 2:2:1 to ribavirin (ribavirin arm) or placebo (placebo arm) or PEG-IFN2a (PEG-IFN2a arm) for 6 weeks prior to 12 weeks of PEG-IFN2a/ribavirin combination therapy within a double-blind, placebo-controlled trial. Then, standard PEG-IFN2a/ribavirin combination therapy according to the German guidelines was continued under the responsibility of the investigators. Ribavirin was given according to body weight and PEG-IFN2a at a dose of 180 μg subcutaneously once/week. During ribavirin priming, HCV RNA showed a decline of −0.58 log10 IU/mL (P < 0.001) that was unrelated to the IL28B rs12979860 genotype (CC vs CT/TT, P = 0.244). Ribavirin priming did neither increase the PEG-IFN2a-induced first- or second-phase viral decline (P values >0.100) nor on-treatment response or SVR (HCV RNA undetectable at week 12 of combination therapy: ribavirin arm 56%, placebo arm 38%, PEG-IFN2a arm 50%; SVR: ribavirin arm 41%, placebo arm 54%, PEG-IFN2a arm 50%; P values >0.300). In conclusion, ribavirin monotherapy showed a significant antiviral activity that was not influenced by the IL28B genotype. Ribavirin priming prior to PEG-IFN2a/ribavirin combination therapy did neither increase the first- or second-phase viral decline nor on-treatment response or SVR.

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November 10, 2013

Using surveillance data to determine treatment rates and outcomes for patients with chronic hepatitis C virus infection

Hepatology

Accepted Article (Accepted, unedited articles published online and citable. The final edited and typeset version of record will appear in future.)

Liver Injury and Regeneration

Sam Lattimore1,*,Will Irving2,Sarah Collins1,Celia Penman1,Mary Ramsay1, On behalf of the collaboration for the sentinel surveillance of blood-borne virus testing

DOI: 10.1002/hep.26926

Copyright © 2013 American Association for the Study of Liver Diseases

Accepted manuscript online: 9 NOV 2013 04:08AM EST
Manuscript Accepted: 5 NOV 2013
Manuscript Revised: 21 OCT 2013
Manuscript Received: 31 JUL 2013

Keywords: Hepatitis C; epidemiology; surveillance; treatment; England

ABSTRACT

Background & Aims: To develop and validate an algorithm to monitor rates of, and response to, treatment of patients infected with hepatitis C virus (HCV) across England using routine laboratory HCV RNA testing data.

Methods: Hepatitis C testing activity between January 2002 and December011 was extracted from the local laboratory information systems of a sentinel network of 23 laboratories across England. An algorithm based on frequency of HCV RNA testing within a defined time period was designed to identify treated patients. Validation of the algorithm was undertaken for one centre by comparison with treatment data recorded in a clinical database managed by the Trent HCV study group.

Results: In total, 267,887 HCV-RNA test results from 100,640 individuals were extracted. Of these, 78.9% (79,360) tested positive for viral RNA, indicating an active infection, 20.8% (16,538) of whom had a repeat pattern of HCV-RNA testing suggestive of treatment-monitoring. Annual numbers of individuals treated increased rapidly from 468 in 2002, to 3,295 in 2009, but decreased to 3,110 in 2010. Approximately two thirds (63.3; 10,468) of those treated had results consistent with a sustained virological response, including 55.3% and 67.1% of those with a genotype-one and non-one virus, respectively. Validation against the Trent clinical database demonstrated that the algorithm was 95% sensitive and 93% specific in detecting treatment, and 100% sensitive and 93% specific for detecting treatment outcome.

Conclusions: Laboratory testing activity, collected through a sentinel surveillance programme has enabled the first country-wide analysis of treatment and response among HCV-infected individuals. Our approach provides a sensitive, robust, and sustainable method for monitoring service provision across England. (Hepatology 2013;)

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September 22, 2013

Worse Response to PegIFN/RBV for HCV After Transplant in HIV/HCV+ vs HCV+

Provided by NATAP

53rd ICAAC Interscience Conference on
Antimicrobial Agents and Chemotherapy
September 10-13, 2013, Denver CO

53rd ICAAC, September 10-13, 2013, Denver

Mark Mascolini

People coinfected with HIV and HCV had a lower chance of responding to pegylated interferon plus ribavirin (PegIFN/RBV) for recurrent HCV after liver transplantation than did people infected only with HCV [1]. Five-year survival was high in both groups among the minority who achieved sustained virologic response (SVR) to PegIFN/RBV.

Recurrent HCV infection after liver transplantation poses a high risk of liver graft loss and death in HIV/HCV-coinfected people. But aside from data from a few small case series, few findings have emerged on response to PegIFN/RBV among coinfected people with recurrent HCV after transplantation. In part to address that lack, Spanish investigators are conducting the prospective multicenter observational FIPSE study comparing coinfected and monoinfected posttransplant patients [1,2].

The overall cohort includes 149 consecutive HIV/HCV-coinfected patients who had liver transplants between 2002 and 2009 throughout Spain and follow-up until July 2012. FIPSE investigators matched them to 447 HCV-monoinfected people who had liver transplants at the same sites. The researchers also matched HIV/HCV cases and HCV-only controls by calendar year, age, gender, HBV coinfection, and hepatocellular carcinoma status.

The population for the PegIFN/RBV study included 78 coinfected people and 176 monoinfected people who started those drugs for HCV recurrence. Study participants had pretransplant CD4 counts above 100 (or above 200 if they had a previous opportunistic infection) and an HIV load below 50 copies or predicted to be below 50 copies. The analysis excluded people who used heroin or cocaine in the past 2 years and people who abused alcohol in the past 6 months. Treatment for recurrence consisted of PegIFN alpha2a or alpha2b plus 400 to 1000 mg of ribavirin daily.

The 78 coinfected people were significantly younger than monoinfected controls (43 versus 47, P < 0.0001). Coinfected people began PegIFN/RBV significantly sooner after transplantation than did controls (10 versus 15 months, P = 0.024), and a significantly lower proportion of coinfected people had HCV genotype 1 (54% versus 84%, P < 0.0001). A higher proportion of coinfected people had histologically severe HCV reinfection (30% versus 16%, P = 0.0375), though median alanine aminotransferase was significantly lower in the coinfected group (116 versus 175 IU/mL, P = 0.0075). Donor age was marginally older in the coinfected group (53 versus 50, P = 0.147). The groups did not differ significantly in proportion of men (76% and 77%), proportion with pretransplant HCV therapy (38% and 27%), proportion with hepatocellular carcinoma (18% and 16%), MELD score (assessing liver disease toxicity) when listed for transplant (15 in both groups), or type of PegIFN used.

Among the 78 HIV/HCV-coinfected people, 34 (44%) finished 48 weeks of PegIFN/RBV. Of the 44 who discontinued treatment, 17 stopped because of toxicity, 20 for lack of efficacy, and 2 for other reasons; 5 people died before week 48. Among the 176 HCV-monoinfected people, 107 (61%) finished 48 weeks of treatment. Among the 69 who did not, 19 stopped because of toxicity, 37 for lack of efficacy, and 9 for other or unknown reasons; 4 people died before week 48. A significantly higher proportion of coinfected people stopped PegIFN/RBV early (56% versus 39%, P = 0.016), and a significantly higher proportion of the coinfected group stopped because of toxicity (22% versus 11%, P = 0.034).

People with HIV/HCV coinfection had significantly lower rates of early virologic response, end-of-treatment response, or sustained virologic response (P < 0.05 for all comparisons):

PegIFN response rates after transplantation in patients with HIV/HCV vs HCV only:
Early virologic response: 42% versus 53%
End-of-treatment response: 29% versus 44%
Sustained virologic response: 21% versus 36%

A lower proportion of coinfected than monoinfected people with HCV genotype 1 attained SVR (10% versus 33%, P = 0.0079), as did a lower proportion with genotype 2 or 3 (59% versus 80%, not significant). Biochemical response, defined as reaching normal aminotransferase levels at the end of treatment, proved significantly less frequent in coinfected people (27% versus 60%, P < 0.001). Thirty-one people in the HIV/HCV group versus 37 in the HCV-only group died during follow-up (40% versus 21%, P = 0.003).

Among people with HIV, median CD4 count fell from 315 when PegIFN/RBV began to 180 after 6 months of treatment then rebounded to 226 after 12 months and to 310 after 18 months. Proportions of people with a detectable HIV load remained high throughout PegIFN/RBV therapy.

Multivariate analysis determined that not have HIV infection doubled chances of attaining SVR. Three other variables also independently predicted SVR in the total study population:

Chances of SVR with PegIFN/RBV after liver transplantation: HIV no versus yes: hazard ratio [HR] 2.22, 95% confidence interval [CI] 1.18 to 4.17, P = 0.0133 Donor age under 60 versus 60 or older: HR 3.91, 95% CI 1.97 to 7.74, P = 0.0001 Pretreatment HCV load low versus high: HR 2.52, 95% CI 1.42 to 4.47, P = 0.0016 HCV genotype 2/3 versus 1/4: HR 6.31, 95% CI 2.81 to 14.18, P = 0.0001

Patient age, gender, pretransplant anti-HCV therapy, and histologically severe HCV recurrence did not affect SVR chances in this analysis. Among people with HIV, genotype 2 or 3 versus 1 or 4 boosted SVR chances more than 14 times (HR 14.57, 95% CI 3.84 to 55, P < 0.001), while donor age younger than 60 at transplantation was marginally associated with SVR (HR 3.85, 95% CI 0.80 to 18.5, P = 0.0925). Having an AIDS diagnosis or a CD4 nadir below versus above 100 did not affect chances of SVR in this analysis.

Kaplan-Meier estimates of survival from the start of PegIFN/RBV determined that achieving SVR significantly improved 5-year survival probability in HIV/HCV-coinfected people (79% versus 43%, P = 0.0219) and in the HCV-only group (92% versus 60%, P = 0.001).

FIPSE investigators concluded that PegIFN/RBV after HCV recurrence in transplant recipients had lower efficacy (especially with genotypes 1 and 4) and caused more toxicity in HIV/HCV-coinfected people than in comparable HCV-monoinfected people. But survival in responders is satisfactory in both groups.

References

1. Castells L, Rimola A, Manzardo C, et al. Treatment with pegylated interferon plus ribavirin of HIV-infected patients with recurrent hepatitis C virus infection after liver transplantation: a prospective cohort study. 53rd ICAAC. September 10-13, 2013. Denver. Abstract H-1532b.

2. Gastaca M, Aguero F, Rimola A, et al. Liver retransplantation in HIV-infected patients: a prospective cohort study. Am J Transplant. 2012;12:2465-2476. http://onlinelibrary.wiley.com/doi/10.1111/j.1600-6143.2012.04142.x/abstract

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September 10, 2013

Clinical Presentation, Outcome, and Response to Therapy Among Patients With Acute Exacerbation of Chronic Hepatitis C

Clinical Gastroenterology and Hepatology
Volume 11, Issue 9 , Pages 1174-1180.e11, September 2013

Evangelista Sagnelli, Mariantonietta Pisaturo, Maria Stanzione, Vincenzo Messina, Loredana Alessio, Caterina Sagnelli, Mario Starace, Giuseppe Pasquale, Nicola Coppola

published online 15 April 2013.

Abstract

Background & Aims

The slow asymptomatic progression of chronic hepatitis C (CHC) can be interrupted by an acute exacerbation, characterized by increased serum levels of alanine aminotransferase (ALT) and bilirubin and other symptoms of acute hepatitis. We aimed to provide more information about the clinical presentation of acute exacerbation of CHC.

Methods

We identified 82 consecutive patients, from 2 locations in Italy, who had an acute exacerbation of CHC from January 2005 through June 2010; we followed them up for a median period of 36 months. These cases were hepatitis C virus (HCV) RNA positive, hepatitis B surface antigen-negative, and had not received anti-HCV therapy. They were matched with 82 subjects with hepatitis C without reactivation for age, sex, and HCV genotype (controls). Sixty-nine cases and 73 controls were followed up for at least 2 years. Liver biopsy specimens had been taken from 23 cases and 31 controls—once before enrollment in the study and once during the follow-up period.

Results

HCV genotype 2 was detected in 46.4% of cases, and HCV genotype 1 was detected in 43.9%. Among cases, the mean ALT level was 1063 ± 1038 IU/dL, and the mean total bilirubin level was 15.87 ± 7.15 mg/dL. A higher percentage of cases carried the interleukin-28B CC genotype than controls (40.2% vs 24.4%; P < .05). Among cases, 43.5% had a steady increase in ALT level (>2-fold baseline value); for 56.5% of these patients, ALT levels returned to baseline values before the acute exacerbation of chronic hepatitis. Based on comparisons of biopsy specimens, 18 cases (78.3%) and 11 controls (35.5%) had increasing fibrosis, with Ishak scores increasing by more than 2 (P < .005); 14 cases (60.9%) and 3 controls (9.6%) had increases in necroinflammation of more than 2 points (P < .005). Thirty-two cases (46.4%) and 38 controls (52%) received treatment with pegylated interferon and ribavirin; a sustained virologic response was achieved in 26 cases (81.2%) and 23 controls (60.5%).

Conclusions

Although an acute exacerbation of chronic hepatitis is a serious medical condition, most patients achieve a sustained virologic response after treatment with pegylated interferon and ribavirin.

Keywords: Hepatic Flare , Cirrhosis , Response to Therapy , Complication

Abbreviations used in this paper: ALT, alanine aminotransferase, AST, aspartate aminotransferase, CHC, chronic hepatitis C, HAI, Histologic Activity Index, HAV, hepatitis A virus, HBsAg, hepatitis B surface antigen, HCC, hepatocellular carcinoma, HCV, hepatitis C virus, HDV, hepatitis D virus, HEV, hepatitis E virus, IL, interleukin, LB, liver biopsy, peg-IFN, pegylated interferon, SVR, sustained virologic response

Conflicts of interest The authors disclose no conflicts.

Funding This study was supported by a grant from Progetti di Ricerca di Interesse Nazionale (PRIN) 2008, Ministero dell'Istruzione e dell'Università e della Ricerca Scientifica, Rome, Italy “Ottimizzazione Della Diagnosi Eziologica dell'epatite Acuta C E Studio dei Fattori Viro-Immunologici di Guarigione, di Cronicizzazione E di Risposta Alla Terapia Con Interferone,” and in part by a grant from Regione Campania “Progetti per il miglioramento della qualità dell'assistenza, diagnosi e terapia del paziente affetto da AIDS nei settori: immunologia, coinfezioni, informazione e prevenzione,” 2008.

PII: S1542-3565(13)00466-7

doi:10.1016/j.cgh.2013.03.025

© 2013 AGA Institute. Published by Elsevier Inc. All rights reserved.

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September 7, 2013

Formal Hepatitis C Education Enhances HCV Care Coordination, Expedites HCV Treatment and Improves Antiviral Response

Liver International

Samali Lubega, Uchenna Agbim, Miranda Surjadi, Megan Mahoney, Mandana Khalili

Liver International. 2013;33(7):999-1007. 

Abstract and Introduction

Abstract

Background & Aims Formal Hepatitis C virus (HCV) education improves HCV knowledge but the impact on treatment uptake and outcome is not well described. We aimed to evaluate the impact of formal HCV patient education on primary provider-specialist HCV comanagement and treatment.

Methods Primary care providers within the San Francisco safety-net health care system were surveyed and the records of HCV-infected patients before and after institution of a formal HCV education class by liver specialty (2006–2011) were reviewed retrospectively.

Results Characteristics of 118 patients who received anti-HCV therapy were: mean age 51, 73% males and ~50% White and uninsured. The time to initiation of HCV treatment was shorter among those who received formal education (median 136 vs 284 days, P < 0.0001). When controlling for age, gender, race and HCV viral load, non-1 genotype (OR 6.17, 95% CI 2.3–12.7, P = 0.0003) and receipt of HCV education (OR 3.0, 95% CI 1.1–7.9, P = 0.03) were associated with sustained virologic treatment response. Among 94 provider respondents (response rate = 38%), mean age was 42, 62% were White, and 63% female. Most providers agreed that the HCV education class increased patients' HCV knowledge (70%), interest in HCV treatment (52%), and provider-patient communication (56%). A positive provider attitude (Coef 1.5, 95% CI 0.1–2.9 percent, P = 0.039) was independently associated with referral rate to education class.

Conclusions Formal HCV education expedites HCV therapy and improves virologic response rates. As primary care provider attitude plays a significant role in referral to HCV education class, improving provider knowledge will likely enhance access to HCV specialty services in the vulnerable population.

Introduction

Hepatitis C virus (HCV) is the most common chronic blood-borne disease and the leading cause of liver transplantation in the US, affecting an estimated 3.2 million Americans.[1, 2] Recent advancement in antiviral treatment options has significantly increased the response rates to anti-HCV therapy even among the difficult to treat populations.[3, 4] Despite this, it is estimated that only 34–48% of chronic carriers are referred for liver specialist assessment,[5–7] and less than 37% of patients receive treatment for hepatitis C.[6–8] Therefore, instituting models of care that have the potential to overcome barriers and improve access to care represents a critical goal in addressing the HCV epidemic.[9] The Institute of Medicine recently released a report identifying 'missed opportunities' in the prevention and control of HCV, and specifically recommended the development, coordination and evaluation of education programs targeting at-risk populations, as well as improved coordination of hepatitis care delivery services in its national strategy to improve hepatitis care services.[10] In addition, the American Association for the Study of Liver Diseases (AASLD) and Centers for Disease Control and Prevention (CDC) joint conference proceedings on viral hepatitis emphasized the importance of a multidisciplinary approach to HCV care and HCV care coordination, including linkage of infected persons with care and treatment services to improve prevention of viral hepatitis and the effectiveness of treatment.[8]

Patients within the safety-net healthcare systems that predominantly serve the uninsured and underinsured populations are especially at risk for experiencing health disparities, have limited access to care, and represent a growing vulnerable patient population.[11] HCV patient education is associated with positive outcomes in various models of HCV care, including increased disease-specific knowledge,[12, 13] interest in treatment,[14] willingness to accept treatment,[5, 15] and increase liver specialty care clinic attendance.[12, 13] In a prior study within the San Francisco safety-net healthcare system, formal HCV education by liver specialists not only resulted in a significant improvement in HCV knowledge among patients but also appeared to create efficiencies in this healthcare system to allow better access to specialty care for these individuals.[13] Therefore, this patient-centred approach has the potential to impact HCV management, interest in receipt of HCV treatment and treatment outcome. However, the impact of formal HCV education by specialists on facilitating HCV treatment initiation, adherence to treatment and treatment outcome is not clearly understood. Furthermore, although primary care providers have a pivotal role in identifying patients with HCV, referring patients to specialty consultants for treatment, and collaborating with specialty care providers;[16] whether formal patient education by a specialist has a positive impact on HCV co-management between primary and specialty care providers has not been previously studied.

Considering the increasing emphasis on systemic improvements to our healthcare delivery system and enhanced coordination of health services, this study was conducted to evaluate the impact of the institution of a mandatory formal HCV education class by liver specialty providers on HCV treatment initiation and outcomes and to evaluate provider attitudes towards the impact of formal patient education on HCV management.

Materials and Methods

This study consists of 1) a retrospective review of electronic medical records of HCV-infected patients before and after the institution of a mandatory HCV education class prior to initiation of treatment, and 2) a cross-sectional survey of primary care providers within the San Francisco safety-net healthcare system. This healthcare system provides services to over 150,000 patients annually including most of the county's uninsured and underinsured population.[17] This system consists of the San Francisco Community Clinic Consortium, which has ten nonprofit primary care community health centers, and the San Francisco Department of Public Health's Community Health Network, which includes eleven community-based primary care clinics and one acute care hospital with primary care and specialty clinics on-site.[17] This study was approved by the Committee on Human Research of the University of California San Francisco.

Patient Population

Electronic medical records of HCV-infected viremic patients with elevated HCV viral loads, who underwent pegylated interferon (PEG-IFN) and ribavirin combination antiviral therapy in the liver specialty clinic at San Francisco General Hospital (SFGH) from January 2006 to June 2011 were reviewed. This study period includes the period before and after initiation of a mandatory formal HCV education class (November 2007) by the liver specialty clinic. There were no changes in the liver specialty clinic scheduling procedures or the number of providers within the liver clinics during the entire study period. Data included patient demographics, medical and psychiatric co-morbidities, time to initiation of HCV therapy from first liver specialty clinic visit, adherence to HCV treatment (which included measurement of adherence to clinic visits, medications and recommended laboratory testing and procedures) and viral response to anti-HCV therapy. Adherence to anti-HCV medications was defined as use of ≥80% of pegylated interferon and ≥80% of ribavirin for more than 80% of the expected treatment duration.[18] Response to anti-HCV therapy was defined as: early virologic response, EVR (>2-log10 decline in HCV RNA viral load by week 12), end of therapy response, ETR (undetectable HCV RNA viral load at end of therapy) and sustained virologic response, SVR (undetectable HCV RNA viral load at 24 weeks following discontinuation of treatment).

Provider Survey Design and Methods

The provider survey instrument was developed by the study investigators with input from hepatologists, survey design experts and previously published surveys. Content domains included provider and practice characteristics, HCV management practices, provider attitudes regarding HCV education, and provider perception of the impact of HCV education on improvement of HCV management, patient-provider communication, patient HCV knowledge, interest in receipt of therapy, patient adherence to HCV management plan, and access to specialty care. The survey was pilot-tested with 20 physicians and revised based on their feedback. The survey was sent to the 248 primary care providers of the San Francisco safety net healthcare system by mail or electronic mail between electronic email between October 15 and December 15, 2011. A second and third mailing to non-respondents was conducted at 4-week intervals.

HCV Education Class

In November 2007, the liver specialty clinic at San Francisco General Hospital instituted a mandatory formal HCV education class accessible to all HCV-infected patients within San Francisco's safety net healthcare system. Providers who wish to refer patients to liver specialty clinic initially schedule patients in the formal HCV education class offered by this specialty service prior to being evaluated in the liver specialty clinic. The patients are directly scheduled for the formal education class by the primary providers (direct access) based on patient's availability and the classes are offered every 2 weeks. The HCV education class consists of a 2-hour standardized in-person PowerPoint presentation delivered by a liver clinic nurse practitioner. Each class has approximately 25–30 participants and is offered in English and any other languages by using certified interpreters as needed. The class provides information on HCV transmission, diagnosis, symptoms, natural history, severity of liver disease, appropriate candidacy for treatment, response rates of antiviral therapy and side effects of treatment.

Statistical Analysis

Patient data analysis. Patient characteristics were summarized using mean ± SD, median (range) and frequencies. To evaluate patient factors associated with the outcomes SVR and time to initiation of HCV therapy, univariate analysis was performed using Chi-square test (Fisher's exact test when appropriate) for categorical variables and Mann-Whitney test for continuous variable. Multivariable regression modelling evaluating factors associated with SVR and time to initiation of therapy included predictors from an a priori compiled list as well as those with a p value <0.05 as determined by the univariate analysis.

Provider survey data definition and analysis. Provider and practice characteristics were summarized using mean ± SD, median (range) and frequencies. The provider attitude score towards impact of formal HCV education class on HCV management was determined by summing the numerical codes assigned to responses to eleven questions assessing provider attitudes as follows: 4 to an 'strongly agree' response, 3 to an 'agree' response, 2 as 'neither agree or disagree', 1 as 'disagree' and 0 as 'strongly disagree.' Univariate regression analysis was performed to evaluate provider and practice characteristics associated with formal HCV education class. Multivariable regression modelling evaluating factors associated referral to HCV education class included predictors from an a priori compiled list as well as those with a p value <0.05 as determined by the univariate analysis.

For all analysis, statistical significance was assessed at the p-value of <0.05 level (2-sided) in all models. All analysis was performed using SAS version 9.2 (SAS Institute, Inc., 2007, Cary, NC, USA).

Results

Patient Characteristics

During the study period, of the 551 HCV-infected patients who attended the liver specialty clinic, 118 treatment eligible patients underwent antiviral therapy. The overall treatment rates (24% vs 19%, p = 0.1) were similar before and after HCV education class initiation. Patient characteristics of treated and untreated groups were similar with respect to age (50 vs 50, p = 0.43), male gender (62% vs 65%, p = 0.52) and White race (48% vs 39%, p = 0.058). Mode of HCV transmission was predominantly injection drug use in both groups (59% vs 69%, p = 0.25).

Table 1 summarizes the overall patient characteristics of those who underwent antiviral therapy and characteristics by receipt of formal HCV education class. Overall, the majority of patients were middle-aged and approximately half of patients were minorities. Injection drug use (IDU) was the most common HCV risk factor in both groups (59%), and nearly all patients were treatment naïve (94%). Although there was a lower proportion of men among those who received HCV education (50% vs 74%, p = 0.008), other patient and viral characteristics were similar amongst those who did and did not receive formal HCV education.

Table 1.  Characteristics of patients who did or did not undergo formal hepatitis C virus (HCV) education

Patient characteristic Overall (N = 118) Patients who did not receive HCV education (n = 58) Patients who received HCV education (n = 60) P- value*
Age (years), median (quartiles) 51 (42–58) 50 (41–57) 51 (44–58) 0.69
Males (%) 73 (62) 43 (74) 30 (50) 0.008
Race/ethnicity (%)
White 57 (48) 26 (45) 31 (52) 0.90
African American 11 (9) 6 (10) 5 (8)
Latino 22 (19) 11 (19) 11 (18)
Asian/Pacific Islander 28 (24) 15 (26) 13 (22)
English as primary language (%) 84 (71) 39 (67) 45 (75) 0.42
Uninsured (%) 57 (48) 25 (43) 32 (53) 0.28
Income < $15 000 per year (%) 83 (75) 38 (68) 45 (82) 0.13
Concurrent substance abuse treatment (methadone, buprenorphine) (%) 8 (7) 5 (9) 3 (5) 0.49
Duration of HCV infection (years), median (range) 20 (2–52) 21 (2–47) 19 (2–52) 0.75
Prior history of IDU (%) 56 (59) 27 (54) 29 (64) 0.40
HIV coinfection (%) 15 (13) 10 (17) 5 (8) 0.17
HBV coinfection (%) 5 (4) 4 (7) 1 (2) 0.20
Psychiatric comorbidities 47 (40) 24 (41) 23 (38) 0.85
Serum ALT (Units/mL), median (range) 68 (18–586) 72.5 (18–257) 63.5 (18–586) 0.34
Log10 HCV viral load (IU/mL), median (range) 5.9 (3.9–7.1) 5.9 (3.9–6.7) 6.0 (4.3–7.1) 0.43
HCV genotype (%)
1 66 (56) 34 (59) 32 (53) 0.51
2 22 (19) 12 (21) 10 (17)
3 25 (21) 9 (16) 16 (27)
Other 5 (4) 3 (5) 2 (3)
Inflammation grade on histology**(%)
<2 15 (19) 8 (17) 7 (22) 0.77
≥2 63 (81) 38 (83) 25 (78)
Fibrosis stage on histology**(%)
<2 21 (27) 14 (30) 7 (22) 0.45
≥2 57 (73) 32 (70) 25 (78)
Steatosis on histology**(%) 32 (41) 17 (37) 15 (47) 0.48
Treatment naïve (%) 111 (94) 53 (91) 58 (97) 0.27
Early virologic response (%) 93 (88) 42 (82) 51 (93) 0.14
End of treatment response (%) 90 (83) 43 (80) 47 (87) 0.44
Sustained virologic response (%) 61 (59) 27 (50) 34 (68) 0.07
Early discontinuation of therapy because of side effects† (%) 9 (8) 7 (12) 2 (3) 0.09
Adherence to clinic visit (%) 100 (87) 51 (88) 49 (86) 0.79
Adherence to medications (%) 102 (88) 51 (88) 51 (86) 1.0
Adherence to procedures (%) 103 (90) 52 (90) 51 (90) 1.0
Time to initiation of therapy (days), median (quartiles) 184 (102–316) 284 (147–431) 136 (88–212) <0.0001

*P-value refers to the comparison of patients who did and did not receive formal HCV education; statistical significant was designated at P < 0.05 (2-sided).

**Liver biopsy was performed in 78 patients.

†A total of 30 patients discontinued therapy early.

IDU, Injection drug use; HIV, Human Immunodeficiency Virus; HBV, Hepatitis B Virus; ALT, alanine aminotransferase.

With respect to HCV antiviral therapy, although overall adherence to HCV therapy and clinic visits was high (>85%) in those who underwent therapy, there were higher rates of SVR among those who received formal HCV education (68% vs 50%), lower rates of discontinuation of HCV antiviral therapy because of side effects (3% vs 12%), and lower virologic relapse rates following discontinuation of therapy (16% vs 28%), but these did not reach statistical significance. The overall higher rates of SVR observed in this safetynet system is related to the lower proportion of genotype 1 patients (56%) than that reported for the general US population.

Host and Viral Factors Associated With Treatment Initiation and Treatment Outcomes

On univariable analysis, the time to initiation of HCV treatment from initial liver clinic visit date was significantly shorter among those who received formal HCV education compared to those who did not (median 136 vs 284 days, p < 0.0001) (Table 1). On multivariable analysis time to initiation of therapy was negatively associated with receipt of formal HCV education, when controlling for patient age, gender, race and HCV genotype (coef -182, 95%CI -272 to -92 days, p < 0.0001), and also when accounting for severity of liver disease (fibrosis stage >2) on liver biopsy (coef -123, 95%CI -233 to -14 days, p = 0.028).

With respect to treatment outcome, factors associated with achieving SVR on univariate analysis included non-1 genotype HCV (OR 5.4, 95%CI 2.1–15.0 p = 0.0002) and higher grades of inflammation on histology among patients who had a liver biopsy (OR 4.5, 95%CI, 1.3–16.2, p = 0.022). On multivariable analysis (Table 2), when controlling for age, gender, race and baseline HCV viral load, non-1 genotype HCV and receipt of formal HCV education were independently associated with SVR. In addition, accounting for adherence to antiviral therapy did not significantly alter these odds ratios. In the subset of patients who had undergone a liver biopsy prior to HCV therapy, higher grade of liver inflammation (OR 5.9 95%CI 1.3–26.6 p = 0.02) and lower stage of fibrosis (OR 0.23, 95%CI 0.05–0.95, p = 0.043) in addition to non-1 HCV genotype (OR 6.0, 95%CI, 1.6–22.6 p = 0.008) were significantly associated with achieving SVR when controlling for age, gender, race and baseline HCV viral load. Once again, adherence to antiviral therapy did not significantly alter these odds ratios.

Table 2.  Multivariate analysis of factors associated with sustained virologic response to hepatitis C virus (HCV) antiviral therapy

Variables Odds Ratio 95% CI* P value**
Age per decade 0.7 0.4–1.1 0.12
Female gender 0.6 0.2–1.8 0.36
Race (vs White)
African-American 0.8 0.2–4.2 0.80
Latino 0.4 0.1–1.4 0.14
Asian/Pacific Islander 1.5 0.5–4.7 0.51
HCV non-1 genotype (vs genotype 1) 6.2 2.3–16.7 0.0003
Log10 HCV viral load (IU/mL) 0.8 0.3–2.1 0.72
Receipt of formal HCV education 3.0 1.1–7.9 0.031

*95% confidence interval.

**Statistical significance was designated at P < 0.05.

Provider and Practice Characteristics

Out of 248 providers, 94 (38%) responded to the survey. Provider characteristics are summarized in Table 3. The mean age of providers was 42, and the majority was White and female. Most providers held an MD degree and ~40% were in practice for more than 10 years. The median proportion of White patients in practices was 25%, the median proportion of patients with limited English proficiency was 50%, and the median proportion of uninsured patients in practices was reported at 50%.

Table 3.  Provider and practice characteristics in the San Francisco safety net healthcare system (n = 94)

Provider and practice characteristic
Age (mean ± SD) (years) 42 ± 11
Male (%) 25 (27)
Race/ethnicity (%)
White 58 (62)
African American 3 (3)
Latino 5 (5)
Asian American/Pacific Islander 24 (26)
Other 3 (3)
Post-graduate degree (%)
MD 68 (72)
Nurse practitioner 24 (26)
Physician's assistant 2 (2)
Specialty (%)
Internal medicine 48 (51)
Family practice 31 (33)
Infectious disease 1 (1)
HIV 8 (9)
Other 6 (6)
Years in practice
0–10 55 (58.5)
11–20 24 (25.5)
>20 15 (16)
Number of patients seen per week (%)
0–20 35 (37)
21–40 28 (30)
>40 31 (33)
Median proportion of patients by race
White 25
African-American 20
Latino 25
Asian/Pacific Islander 20
Other 2
Median proportion of patients with limited English proficiency 50
Median proportion of patients in practice with
Private or public insurance 50
Uninsured 50

HCV HCV Management Practices

Provider HCV management practices are summarized in . Nearly one quarter of providers reported that HCV patients comprised more than 25% of their practice population. Among HCV patients, the reported mode of transmission for HCV was IDU in more than 80% of patients and ~20% of providers reported current alcohol or illicit drug abuse in over half of their HCV patients. A rate of greater than 10% co-infection with human immunodeficiency virus (HIV) or hepatitis B virus (HBV) among HCV patients was reported by 30% and 17% of providers respectively. Over 75% of providers reported that at least half of their HCV patients have been vaccinated against hepatitis A and hepatitis B, and only 17% reported that more than 25% of the HCV patients had received HCV antiviral therapy.

Table 4.  Hepatitis C virus (HCV) management practices among the San Francisco safety net providers

IDU, Injection drug use; HAV, Hepatitis A Virus; HBV, Hepatitis B Virus; HIV, Human Immunodeficiency Virus.
Practice with more than 25% HCV patients 24
Proportion of HCV patients with history of IDU in practice 85
Proportion of HCV patients in practice who have been vaccinated against HAV
≤25% 13
26–50% 12
51–74% 10
≥75% 65
Proportion of HCV patients in practice who have been vaccinated against HBV
≤25% 9
26–50% 10
51–74% 13
≥75% 68
Proportion of HCV patients in practice who are coinfected with HIV
≤25% 79
26–50% 7
51–74% 1
≥75% 13
Proportion of HCV patients in practice coinfected with HBV
≤25% 98
>25% 2
Proportion of HCV patients in practice currently abusing alcohol or illicit drugs
≤25% 45
26–50% 32
51–74% 9
≥75% 14
Proportion of HCV patients in practice currently undergoing outpatient substance abuse therapy
≤25% 80
26–50% 15
51–74% 0
≥75% 5
Proportion of HCV patients in practice who have received HCV antiviral therapy
≤25% 83
26–50% 9
51–74% 1
≥75% 7

Provider Attitudes Towards Formal HCV Education Class

Nearly all providers (90%) reported being aware of the presence of a formal HCV education class by the liver specialty clinic, and 40% of providers had referred at least half of their HCV patients to the HCV education class. The most common reasons for patient referral to class were to receive general education about HCV disease (62%) and to receive HCV therapy (57%). The most common reasons for not referring patients to the education class were patients' lack of interest in HCV therapy (54%), followed by coexisting psychiatric contraindication to HCV therapy (47%), and ongoing alcohol and/or drug abuse (46%).

Provider attitudes towards the impact of the formal HCV education class on HCV management within their practices are summarized in . On average, a majority of primary care providers agreed that the formal HCV education class increased their patients' HCV knowledge and interest in receipt of HCV treatment. Over half of providers also agreed that the class improved patient communication regarding HCV disease and patient understanding of HCV-related resources. In addition, over half of providers reported that formal HCV education resulted in overall improved management of HCV patients and has helped them address patient concerns about their disease. Moreover, more than 40% of providers agreed that formal HCV education has improved primary care-specialist HCV co-management and increased access to liver specialty care.

Table 5.  Impact of formal hepatitis C virus (HCV) education class on provider practices

Impact of education class Agree (%) Neutral (%) Disagree (%)
Improved my patients' knowledge of HCV disease 70 26 4
Increased patients' interest in being treated for HCV 52 39 9
Increased adherence to HCV-related medical testing such as blood tests, imaging, liver biopsy, clinic visits 30 64 6
Improved patients' understanding of available resources for HCV care within the San Francisco safety net system 55 35 10
Increased my patients' level of interest in substance abuse (illicit drugs, alcohol) therapy 21 65 14
Improved my patient's adherence to my management plan recommendations for other medical conditions (such as hypertension, diabetes, etc.) 23 62 15
Resulted in improved patient communication with me regarding HCV 56 35 8
Helped me better address patient's concerns regarding HCV disease and its management 53 41 6
Overall improved the management of my patients with HCV in my practice 54 39 7
Made it easier for me to co-manage my patients with liver specialty care providers 44 45 11
Increased the access to liver specialty care in our safety net system 41 46 13

Provider and Practice Factors Associated With Referral Rates to Formal HCV Education Class

On univariable analysis, the proportion of patients with HCV in practice (coef -21.2, 95%CI -37.5 to -4.9 percent, p = 0.012), the proportion of uninsured patients in practice (coef 0.65, 95%CI 0.15–1.2 percent, p = 0.012), a positive provider attitude towards the impact of HCV class in practice (coef 1.2, 95%CI -0.13 to 2.6 percent, p = 0.075), and not possessing an MD degree (coef -6.2, 95%CI -12.3 to -0.19 percent, p = 0.044), were associated with referral of patients to the formal HCV education class. On multivariable analysis (), when controlling for provider age, gender and degree, only a positive provider attitude towards the impact of the HCV class was independently associated with higher rates of referral to formal HCV education class.

Table 6.  Multivariate analysis of provider and practice factors associated with referral to formal hepatitis C virus (HCV) education class

Variables Coefficient 95% CI P value
Provider age 0.5 −0.4–1.3 0.29
Provider female gender 11.9 −9.0–32.8 0.26
Provider degree
Non-MD (vs MD) 4.3 −3.4–12.0 0.27
Proportion of HCV patients in practice −15.9 −36.1–4.2 0.12
Proportion of uninsured patients in practice 0.6 −0.1–1.3 0.071
Provider attitude towards impact of formal HCV education class 1.5 0.1–2.9 0.039

Discussion

This is the first study to evaluate the impact of formal HCV patient education on receipt of HCV therapy, treatment outcomes and primary provider HCV management practices in a safety-net healthcare system. We have shown that formal HCV education expedites receipt of HCV antiviral therapy and is associated with higher rates of virologic response to HCV treatment. In addition, a majority of providers reported that the formal HCV education class improved their patient's knowledge, communication, interest in therapy, understanding of resources for HCV management and improved the overall management of the HCV-infected patients in their practice. Furthermore, a positive provider attitude towards the impact of formal HCV education was associated with higher rates of patient referral to the HCV education class.

The vulnerable patient population within the safety-net healthcare system is disproportionally affected by HCV and adverse disease outcomes[11]. A prior study in this healthcare setting has shown that formal HCV education class results in improvement of patient's HCV knowledge across all ages, racial groups, education backgrounds and socioeconomic status.[13] Prior studies have also shown that HCV patients consider HCV education an important healthcare need that results in a marked increase in willingness to accept treatment.[15, 19] In this study, the majority of primary providers also perceived that their patients' HCV knowledge had increased as a result of participation in the class. In addition, over half of providers reported that HCV education class increased their patient's interest in HCV treatment. Moreover, the HCV class appeared to improve patient's understanding of available resources for HCV care within the healthcare system, improved patient-provider communication, assisted providers in addressing patients' concerns regarding HCV disease, and improved overall HCV management within the primary care practice by provider report. These findings are important in that while primary care providers often feel confident in their ability to screen for HCV and provide initial HCV disease evaluation, and believe they should be involved in HCV co-management with specialists, they feel less confident about HCV monitoring and treatment [20–22]. Therefore, in addition to their patient's direct benefit in receipt of education, they too may benefit from additional resources and support in these areas.[20, 21] Indeed, approximately 40% of providers also reported that HCV education class facilitated HCV co-management within their practices and increased access to liver specialty care services.

Interestingly, in this study primary providers did not report a significant increase in patient adherence to HCV management plans or interest in substance abuse therapy within their practices. In the practices surveyed in this study approximately 25% of providers indicated that over 25% of patients within their practice were infected with HCV. In contrast, in a national survey of primary providers, 73% of respondents had reported caring for 5 or less HCV-infected patient within the past year.[23] Given the high prevalence of HCV infection within practices in the San Francisco safety-net healthcare setting, it is possible that our providers had previously implemented their own mechanisms within practices to effectively address substance abuse therapy and adherence to HCV monitoring.

Whether the observed improvement in patient's knowledge and the positive impact on provider practices following formal HCV education actually influences HCV treatment initiation and treatment outcomes has not been previously studied. We have found that the time to initiation of HCV therapy was reduced by half in those patients who underwent formal HCV education compared to those who did not receive disease-specific education. This patient-centred approach to HCV education may have resulted in faster uptake of treatment by helping motivated patients to self-identify, more actively participate in their medical decision-making,[24, 25] and overcome treatment-related fears that impede or delay antiviral therapy.[26] This also suggests that the education class has resulted in efficiencies within this resource-limited healthcare system that allow better utilization of specialty care services in this population.

HCV education appears to improve adherence to HCV therapy.[27, 28] However, there are only limited studies evaluating the role of patient education on HCV treatment outcome. In a study by Cacoub et al., there was a 7% increase in the rate of SVR and 6% decrease in rates of virologic relapse among those received support documents and educational material during individual sessions compared to those who did not receive disease specific education, but these findings did not reach statistical significance.[27] Larrey et al. assessed the impact of ongoing patient education during HCV therapy. In that study, the odds of achieving SVR were 2.5 times higher among patients who received systematic consultation by a nurse regarding patient adherence and the efficacy of therapy compared to those who did not receive the education.[29] Similarly, we have shown that a formal HCV education class prior to HCV treatment resulted in an 18% increase in rates of SVR, and patients who received education were three times more likely to achieve SVR, independent of medication adherence and patient or viral factors. It is known that adherence to anti-HCV medications impacts rates of response to therapy. We did not observe a significant difference in patient adherence to medications in those who did and did not receive patient education. The overall rates of adherence to medication by self-report was high at 88% in this study, similar to that reported in other HCV populations ranging from 76–89%.[30] However, our study did show that patients who attended formal HCV education were less likely to discontinue treatment because of side effects (3% vs 12%), one of the most common reasons for early discontinuation of treatment in several prior studies [9, 31, 32]. Higher rates of early discontinuation of therapy and delay in initiation of treatment in those who did not undergo HCV education, can potentially contribute to lower rates of SVR observed in this population.

The recent single topic conference cosponsored by the AASLD and CDC has emphasized the value of 'systemic changes in our healthcare delivery system and enhanced coordination of prevention and care services through education of the public and healthcare providers, and linkage of infected persons with care and treatment services to successfully prevent viral hepatitis and increase treatment efficacy'[8]. Primary care providers play a significant role in linkage of HCV-infected persons to available HCV care and treatment services. Limited data, predominantly in the HIV-HCV co-infection setting, suggest that provider attitudes affect rates of both provider HCV treatment recommendation and patient uptake of HCV treatment.[33, 34] A national survey of family physicians has also shown that having a positive attitude regarding HCV care in the primary care setting was associated with more provision of HCV care services.[21] Moreover, patients interpret a lack of referral to HCV specialty care or discussion of treatment by primary care providers as an indicator that pursuit of HCV treatment should not be considered a priority.[35] We have shown that a positive provider attitude towards the impact of HCV education is independently associated with higher rates of referral to formal HCV education class. Therefore, increasing provider understanding of the impact of patient education on HCV care and treatment outcomes will be essential to improving patient access to HCV care services and success of antiviral therapy.

The main limitation of this study is the retrospective patient data collection, while the primary strengths include long-term patient follow-up and prospective assessment of provider attitudes and practices. Because the formal HCV education class was instituted as a mandatory component of referral of HCV patients to the liver specialty clinic, the study was limited by a lack of randomization of patients to education vs no education class when evaluating treatment outcomes. However, we were able to utilize a historical control of HCV patients prior to the initiation of education class to compare HCV treatment outcomes. Both the formal HCV education patient cohort and the historical controls likely represent individuals who are motivated to receive HCV therapy and management. Therefore, selection bias is unlikely to play a role in our finding that HCV education significantly impacts time to initiation of HCV therapy and HCV antiviral response. In addition, as the anti-viral therapy regimen (pegylated interferon in combination with ribavirin), the treating providers, and the liver specialty clinic scheduling procedures did not change before and after institution of formal HCV education, it is unlikely that differences in antiviral therapy management practices or scheduling practices overtime would impact the findings. Generalization to other non-safety-net practice settings may also be limited; nevertheless, our results present a potentially effective intervention to improve linkages to HCV specialty care, HCV treatment uptake and treatment outcome.

In summary, formal HCV education by liver specialists creates efficiencies in resource-limited healthcare systems, which not only allows better access to specialty care and treatment services but also improves HCV antiviral effectiveness. Provider attitudes towards the impact of HCV patient education play a significant role in referral to these services. Along with improvements in the healthcare delivery system, interventions directed at increasing provider knowledge of HCV disease and the important role of patient education in improving HCV management will likely enhance HCV care coordination and ultimately amplify the success of antiviral therapy, particularly in vulnerable populations.

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