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Enregistrement W4399565899 · doi:10.1097/cld.0000000000000200

A framework for approaching hepatitis C reinfection in people who use drugs

2024· article· en· W4399565899 sur OpenAlexaboutno aff
Rebecca G. Kim, Jennifer C. Price

Notice bibliographique

RevueClinical Liver Disease · 2024
Typearticle
Langueen
DomaineMedicine
ThématiqueHepatitis C virus research
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésHepatitis CVirologyMedicine

Résumé

récupéré en direct d'OpenAlex

Despite tremendous advances in the management of HCV, including the availability of a curative treatment, an estimated 57 million people worldwide are living with chronic HCV.1 People who inject drugs (PWIDs) are a key at-risk population for both prevalent and incident HCV, and thus are a critical focus for HCV elimination efforts.2,3 Direct-acting antiviral (DAA) therapy is both safe and effective in PWID.4–6 Moreover, in the absence of an effective vaccine for HCV, modeling studies support scaling up DAA access in PWID in a “treatment-as-prevention” strategy.7 However, HCV reinfection after successful DAA treatment remains a concern and could hinder elimination efforts. This review will summarize HCV reinfection incidence and outcomes among PWIDs and will describe a multifaceted approach to addressing HCV reinfection among PWIDs. INCIDENCE OF HCV REINFECTION IN PWIDs In the pre-DAA era, 2 systematic reviews evaluated the incidence of HCV reinfection among PWID who had achieved sustained virologic response (SVR) after HCV treatment. Although over 50 studies were included, they were relatively small with heterogenous populations.8,9 Since the development of DAAs, HCV treatment has become more widely available and effective, and over time, DAA uptake among PWID has increased. In this context, a recent large meta-analysis with over 3790 PWIDs found an overall HCV reinfection rate of 6.2/100 person years (PY) (95% CI: 4.3–8.9) among people reporting recent injection drug use (IDU) and 3.8/100 PY (95% CI: 2.5–5.8) among those receiving opioid agonist therapy (OAT).10 Several additional studies have since been published, with reinfection rates ranging from 1.8/100 PY (95% CI: 0.6–5.6) in a UK cohort treated at an addiction center to 28.7/100 PY (95% CI: 16.3–50.6) among persons in an Australian prison who reported recent IDU and sharing of needles/syringes (Table 1).11–20 In addition to IDU, factors associated with higher rates of reinfection include younger age, experiencing unstable housing or homelessness, receipt of HCV treatment while in prison, and recent needle or syringe sharing.11,13,15,19 Notably, much of this research has been conducted outside of the United States. Given the highly regional nature of drug use epidemics, more data on reinfection rates and risk factors in the United States are needed. TABLE 1 - Incidence of HCV reinfection after sustained virologic response among persons who use drugs References Location Population Study design No. subjects No. reinfections Reinfection rate, per 100 PY (95% CI) Hajarizadeh et al10 International Recent drug use or receiving OAT Meta-analysis 3790 (36 studies) NRa Recent drug use: 5.9 (4.1, 8.5)Recent IDU: 6.2 (4.3, 8.9)Receiving OAT: 3.8 (2.5, 5.8) Cunningham et al11 International People with recent IDU and receiving OAT Clinical Trial 177 8 Overall: 3.1 (1.6–6.3)Sharing needles/syringes: 17.9 (5.8–55.6) Lens et al20 Spain Harm Reduction Center Prospective 168 42 Overall: 31/100 Hosseini-Hooshyar et al12 International HIV/HCV Meta-analysis 9024 (41 studies) 435 Overall: 3.8 (2.8–5.1)MSM: 6.1 (4.5–8.0)IDU: 3.3 (2.0–5.4) Carson et al13 Australia Prison Prospective 161 18 Overall: 12.5 (7.9–19.8)Sharing needle/syringe: 28.7 (16.3–50.6) Beiser et al19 United States Homeless Retrospective 535 74 Overall: 12.0 (9.5–15.1) Young et al14 Canada HIV/HCV Prospective 814 62 Interferon era overall: 2.6 (1.2–4.1)Interferon era IDU: 4.7 (1.4–.79)DAA era overall: 3.4 (2.5–4.4)DAA era IDU: 7.6 (5.3–10) Lindqvist et al15 Sweden Needle and Syringe Program Prospective 339 43 Overall: 9.3 (7.0–12.3) O’Sullivan et al16 UK Addiction Center Prospective 146 19 2013–2017: 1.7 (0.9–3.4)2017–2021: 1.8 (0.6–5.6) Martinello et al17 International Recently acquired HCV Clinical Trial 196 28 Overall: 14.2 (9.8–20.5) Sacks-Davis et al18 International HIV/HCV Pooled data from 6 contributing cohorts 6144 643b Interferon era: 4.6 (4.1–5.1)Early DAA era: 3.4 (2.9–3.9)Broad DAA era: 3.1 (2.6–3.6) aNot reported for all studies.bFirst reinfections.Abbreviations: DAA, direct-acting antiviral; IDU, injection drug use; MSM, men who have sex with men; NR, xxx; OAT, opioid agonist therapy; PY, person years. OUTCOMES OF HCV REINFECTION IN PWID Existing studies suggest that SVR rates are high among patients retreated with DAAs for reinfection, although multiple reinfections can occur.18,20,21 Importantly, high rates of HCV reinfection may be an indicator of high overall mortality. In one study of 94 individuals who underwent HCV treatment at a community needle and syringe program in the United Kingdom, HCV reinfection rate among those who achieved SVR was 21.5/100 PY (95% CI: 13.0–35.7).21 The mortality rate was also high at 5.6/100 PY (95% CI: 2.8–11.1) and was predominantly due to drug overdose or other complications of drug use. In another UK study of 270 PWID who received HCV treatment at an addiction center observed 41 deaths (15%) during the 8-year study period; drug overdose was the most common cause of death among those whose cause of death could be ascertained.16 In a third Canadian study of people living with HIV in clinical care, mortality was three times higher in individuals who experienced HCV reinfection after initial SVR.14 These data underscore the importance of addressing non-liver outcomes and the syndemic of opioid use and viral infections in patients at high risk of HCV reinfection. APPROACH TO HCV REINFECTION IN PWID A framework for approaching reinfection in PWID can be found in Figure 1. First and foremost, treating clinicians should anticipate reinfection to occur in some patients. As more people with HCV are treated and cured, we can expect HCV infections to be concentrated in those at highest risk for exposure. Thus, rather than viewing reinfection as a failure, it should be seen as a positive sign that the population at greatest risk of HCV is being treated.22 Indeed, a recent analysis of pooled data from 6 contributing cohorts of people living with HIV demonstrated that while the overall incidence of HCV declined in people living with HIV from 2015 to 2019, reinfection represented an increasing proportion of incident HCV cases.18 In other words, new HCV infections are occurring in a shrinking population of people at risk, including those with prior successful HCV treatment. Reassuringly, the overall decline in incident cases in the study reinforced the concept of “treatment-as-prevention” and suggested that reinfections did not substantively impact HCV elimination efforts. Thus, providers should not withhold treatment out of fear of reinfection. Instead, providers should be mindful to counsel on reinfection risks early and often and monitor for reinfection with HCV RNA at least annually after SVR. Modeling studies also suggest that simultaneously treating HCV in injecting partners and social networks may reduce reinfection risk.23FIGURE 1: Multifaceted approach to addressing HCV reinfection among people who inject drugs. Abbreviation: SVR, sustained virologic response.Patients who experience reinfection report strong negative emotional responses, especially shame.24 Therefore, it is critical that clinicians are mindful to destigmatize reinfection. Conversations about reinfection should be normalized, and HCV RNA screening after SVR should be standard of practice among individuals with active IDU. Stigmatizing language around HCV “cure,” drug use, and sexual practices should be avoided. Lastly, retreatment should be offered when reinfection occurs. Studies demonstrate a lower risk of reinfection in people receiving OAT; therefore, drug use treatment in addition to DAAs should be offered to all patients with active drug use.10 However, this should not be a requirement prior to DAA treatment. Studies show that reducing payor restrictions (eg, substance use abstinence) leads to increased DAA uptake, particularly among patients with a history of drug use.25 Access to syringe services and safer injection practices is also critical, as sharing needles and syringes is associated with the highest risk of reinfection.11,26 Harm reduction is essential not only for preventing reinfection but also for providing comprehensive whole-person care. PWIDs who experience reinfection have a significantly higher risk of overdose-related death than liver-related death. Thus, optimizing overdose prevention strategies and providing mental health resources is necessary. Finally, homelessness is prevalent among PWIDs.27 People experiencing homelessness have lower rates of SVR with initial treatment and higher rates of reinfection.6,15,19 This may be attributed to their unique challenges with medication retention, including frequent relocation and high rates of property theft, as well as the association of homelessness and injection risk behaviors.17,28 Efforts should be made to link people with unstable housing to social services and to design tailored interventions to improve their access to HCV and drug use treatment. CONCLUSIONS In summary, HCV reinfection should be anticipated, screened for, and treated, particularly among high-risk populations such as PWIDs. HCV retreatment should not be restricted by payers, and persons at higher risk of reinfection should be counseled on harm reduction strategies while also screened for reinfection. Normalization of this approach and destigmatization of reinfection are critical. Nationally, HCV elimination among PWID is a priority, and the Centers for Disease Control and Prevention has numerous approaches to achieve this. Specifically, the Centers for Disease Control and Prevention commits to increase the utilization of HCV prevention services among PWID, to establish comprehensive national viral hepatitis surveillance for public health action, including additional data collection on reinfection rates in the United States, and to reduce barriers to HCV treatment by eliminating eligibility restrictions and expand treatment sites to include substance use treatment centers and correctional facilities.29 The Centers for Disease Control and Prevention’s 2025 Strategic Plan to address viral hepatitis emphasizes the need to support clean needle exchange programs and local policies like the Harm Reduction Community Linkage Projects in Illinois.30 At the systems level, health care systems can support the use of telehealth to improve health care access throughout the HCV care continuum, including evidence-based practices like project Extension for Community Healthcare Outcomes and community-based facilitated telemedicine programs.31,32 Safe medication storage devices to improve medication adherence and achieve SVR with initial treatment and after reinfection should be considered, particularly among people experiencing homelessness.33 HCV point of care testing, when available, can be used to shorten the time to HCV diagnosis and initiation of treatment and to monitor for reinfection.34 Lastly, funding for HCV elimination efforts, innovative treatment approaches like shorter-duration treatment options and long-acting injectables, and research into effective HCV vaccines must be prioritized.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,001
score de la tête « metaresearch » (Gemma)0,007
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: Observationnel
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,091
Score d'incertitude au seuil0,852

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0010,007
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0000,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0000,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,106
Tête enseignante GPT0,430
Écart entre enseignants0,325 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

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Citations1
Publié2024
Routes d'admission1
Résumé présentoui

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