Hall Samuel A L, Shaikh Abdul, Teh Kailin, Tantiongco Mahsa, Coghlan Douglas, Karapetis Chris S, Chinnaratha Mohammad A, Woodman Richard, Muller Kate R, Wigg Alan J
Hepatology and Liver Transplant Medicine Unit, Flinders Medical Centre, Adelaide, South Australia, Australia.
Department of Medicine, The Queen Elizabeth Hospital, Adelaide, South Australia, Australia.
Intern Med J. 2018 Aug;48(8):936-943. doi: 10.1111/imj.13740.
International guidelines recommend screening for hepatitis B virus (HBV) infection prior to administration of rituximab, due to high risk of HBV reactivation in at-risk patients.
To determine: (i) adherence to the South Australian (SA) protocol for HBV screening; (ii) HBV prevalence in patients receiving rituximab; and (iii) outcomes of patients at risk of HBV reactivation.
All patients commenced on rituximab at the six major SA public hospitals during a 12-month period were included in the study. Adherence was assessed by documentation of both hepatitis B surface antigen (HBsAg) and hepatitis B core antibody (HBcAb) prior to initiation of rituximab. Patients were observed for a minimum of 6 months following rituximab initiation.
Four hundred and thirty eight patients were included in the study. The main indication for rituximab therapy was haematological malignancy (76.0%). Two hundred and nine (47.7%) failed to receive appropriate HBV screening, 86 (19.6%) had neither HBsAg nor HBcAb performed, and 119 (27.2%) had only HBsAg performed. The identified prevalence of at-risk cases (either HBsAg- or HBcAb-positive) within the study population was 4.6% (20/438 cases). One case of HBV reactivation was identified, but none led to acute liver failure, transplantation or death.
Poor adherence to HBV screening protocols suggests the need for targeted clinician education and system redesign. While the rate of reactivation was low, the prevalence of at-risk patients in this population was high and justifies further initiatives to increase adherence rates to HBV screening pre-rituximab.
国际指南建议,由于高危患者中乙肝病毒(HBV)再激活风险较高,在使用利妥昔单抗之前应进行HBV感染筛查。
确定:(i)南澳大利亚州(SA)HBV筛查方案的依从性;(ii)接受利妥昔单抗治疗患者的HBV患病率;(iii)有HBV再激活风险患者的转归。
纳入在12个月期间于SA的6家主要公立医院开始使用利妥昔单抗的所有患者。通过在开始使用利妥昔单抗之前记录乙肝表面抗原(HBsAg)和乙肝核心抗体(HBcAb)来评估依从性。在开始使用利妥昔单抗后对患者进行至少6个月的观察。
438例患者纳入研究。利妥昔单抗治疗的主要指征是血液系统恶性肿瘤(76.0%)。209例(47.7%)未接受适当的HBV筛查,86例(19.6%)既未检测HBsAg也未检测HBcAb,119例(27.2%)仅检测了HBsAg。在研究人群中确定的高危病例(HBsAg阳性或HBcAb阳性)患病率为4.6%(20/438例)。确定了1例HBV再激活,但均未导致急性肝衰竭、移植或死亡。
对HBV筛查方案的依从性较差表明需要有针对性的临床医生教育和系统重新设计。虽然再激活率较低,但该人群中高危患者的患病率较高,这证明有必要采取进一步措施提高利妥昔单抗治疗前HBV筛查的依从率。