Yasuhito Tanaka, Daisuke Nakamoto, Yi Piao, Hajime Mizutani, Ryozo Wakabayashi, Yoshiyuki Saito, Kyung Min Kwon, Harriet Dickinson
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Patients with HBV infections of HbsAg who received ISTs or patients who had resolved HBV infections who received ISTs were identified from the database and evaluated for appropriate management to prevent HBV reactivation.</p><p><strong>Results: </strong>In total, 6242 eligible patients were identified. The proportions of patients with appropriate HBV reactivation management, stratified by the HBV reactivation risk level of IST, was 43.1% (276/641) for high-risk, 40.2% (223/555) for intermediate-risk and 14.9% (741/4965) for low-risk patients. When the evaluation period for the outcome calculation was shortened from 360 to 180 days, the proportion for high risk increased to 52.7%. The odds ratios of large hospitals for receiving appropriate management were 2.16 (95% CI 1.12-4.44) in the high-risk, 4.63 (95% CI 2.34-10.25) in the intermediate-risk and 3.60 (95% CI 3.07-4.24) in the low-risk patients.</p><p><strong>Conclusion: </strong>HBV reactivation management was tailored according to the reactivation risk associated with IST. However, adherence to HBV reactivation management guidelines was sub-optimal, even among high-risk patients. 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引用次数: 0
摘要
导言:尽管 HBV 患者在接受免疫抑制治疗(IST)后有再次感染的风险,但在日本,其风险管理的状况尚不明确。本研究旨在描述在 IST 期间接受 HBsAg 或 HBV 感染缓解的慢性 HBV 感染者中 HBV 再激活预防管理的患者比例:方法:2011 年 4 月至 2021 年 6 月期间,我们利用 JMDC 日本索赔数据库开展了一项回顾性队列研究。从数据库中识别出接受 IST 的 HbsAg 型 HBV 感染患者或接受 IST 的 HBV 感染缓解患者,并对其进行评估,以采取适当的管理措施预防 HBV 再激活:结果:总共确定了 6242 名符合条件的患者。根据 IST 的 HBV 再激活风险水平进行分层,高风险患者接受适当 HBV 再激活管理的比例为 43.1%(276/641),中风险患者为 40.2%(223/555),低风险患者为 14.9%(741/4965)。当计算结果的评估期从 360 天缩短至 180 天时,高风险比例上升至 52.7%。大型医院接受适当管理的几率比分别为:高危患者 2.16(95% CI 1.12-4.44),中危患者 4.63(95% CI 2.34-10.25),低危患者 3.60(95% CI 3.07-4.24):结论:HBV再激活管理是根据与IST相关的再激活风险量身定制的。然而,即使在高危患者中,对 HBV 再激活管理指南的遵守情况也不尽如人意。对于规模较小的医疗机构而言,情况尤其如此,因此有必要开展进一步的教育活动。
Implementation of Guideline-Based HBV Reactivation Management in Patients with Chronic HBV Infections of HBsAg or Resolved HBV Infection Undergoing Immunosuppressive Therapy.
Introduction: Although patients with HBV have a risk of reactivation after immunosuppressive therapy (IST), the status of their risk management is unclear in Japan. This study aims to describe the proportion of patients who received preventive management of HBV reactivation during ISTs in patients with chronic HBV infection of HBsAg or resolved HBV infection.
Method: A retrospective cohort study was conducted using the JMDC Japanese claims database from April 2011 to June 2021. Patients with HBV infections of HbsAg who received ISTs or patients who had resolved HBV infections who received ISTs were identified from the database and evaluated for appropriate management to prevent HBV reactivation.
Results: In total, 6242 eligible patients were identified. The proportions of patients with appropriate HBV reactivation management, stratified by the HBV reactivation risk level of IST, was 43.1% (276/641) for high-risk, 40.2% (223/555) for intermediate-risk and 14.9% (741/4965) for low-risk patients. When the evaluation period for the outcome calculation was shortened from 360 to 180 days, the proportion for high risk increased to 52.7%. The odds ratios of large hospitals for receiving appropriate management were 2.16 (95% CI 1.12-4.44) in the high-risk, 4.63 (95% CI 2.34-10.25) in the intermediate-risk and 3.60 (95% CI 3.07-4.24) in the low-risk patients.
Conclusion: HBV reactivation management was tailored according to the reactivation risk associated with IST. However, adherence to HBV reactivation management guidelines was sub-optimal, even among high-risk patients. This is especially the case for ensuring smaller-sized medical institutions, highlighting the need for further educational activities.
期刊介绍:
Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged.
Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.