Hettenbaugh Jacob, Mullane Ryan, Gillispie Gayle, Shostrom Valerie, Flores Linda, Fillaus Jennifer A, Florescu Marius C, Murcek Denise, Tendulkar Ketki K
Department of Internal Medicine, Division of Nephrology, University of Nebraska Medical Center, Omaha, NE 68138, USA.
VA Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.
Infect Dis Rep. 2021 Dec 6;13(4):1036-1042. doi: 10.3390/idr13040094.
Hepatitis B vaccination is recommended in all patients with end-stage kidney disease (ESKD). However, only 50-60% of these patients achieve protective antibody levels if immunized after starting dialysis. Strategies to overcome this low seroconversion rate include a 6-month vaccination schedule starting earlier [chronic kidney disease (CKD) stage 4 and 5] to ensure immunity when patients progress to ESKD. We conducted a quality improvement program to immunize pre-dialysis patients. Patients who were found to have a negative baseline serology with a negative hepatitis B surface antibody level (HBsAb) were offered vaccination on a 6-month schedule (0, 1 and 6 months) with one of two available vaccines within the VA system (Recombivax™ or Engerix™). HBsAb titers were checked 3-4 months later, and titers ≥ 12 mIU/mL were indicative of immunity at VA. Patients who did not seroconvert were offered a repeat schedule of three more doses. We screened 198 patients (187 males and 11 females) with CKD 4 and 5 [glomerular filtration rate (GFR) < 29 mL/min/1.73 m]. The median age of this cohort was 72 years (range 38-92 years). During the study period of 5 years (2015-2020), 10 patients were excluded since their GFR had improved to more than 30 mL/min/1.73 m, 24 others had baseline immunity and 2 refused vaccination. The hepatitis B vaccination series was not started on 106 patients. Of the remaining 56, 12 patients progressed to ESKD and started dialysis before completion of the vaccination schedule, 6 expired and 1 did not come to clinic in 2020 due to the pandemic. Of the 37 patients who completed the vaccination schedule, 16 achieved seroconversion with adequate HBsAb titers, 10 did not develop immunity despite a second hepatitis B vaccination series, while 11 did not get a second series. Given the low seroconversion rate, albeit in a small cohort, vaccination should be considered in patients with earlier stages of CKD. Other options include studies on FDA approved vaccines of shorter duration. We plan to increase awareness among nephrologists, patients and nursing staff about the importance of achieving immunity against hepatitis B.
建议所有终末期肾病(ESKD)患者接种乙肝疫苗。然而,如果在开始透析后进行免疫接种,这些患者中只有50% - 60%能达到保护性抗体水平。克服这种低血清转化率的策略包括更早开始(慢性肾脏病(CKD)4期和5期)为期6个月的疫苗接种计划,以确保患者进展到ESKD时具有免疫力。我们开展了一项质量改进计划,为透析前患者进行免疫接种。对于基线血清学检查为阴性且乙肝表面抗体水平(HBsAb)为阴性的患者,按照6个月的接种计划(0、1和6个月),使用退伍军人事务部(VA)系统内两种可用疫苗之一(重组酵母乙肝疫苗™或乙肝重组疫苗™)进行接种。3 - 4个月后检查HBsAb滴度,滴度≥12 mIU/mL表明在VA系统内具有免疫力。未发生血清转化的患者可再次接种三剂。我们筛查了198例CKD 4期和5期(肾小球滤过率(GFR)< 29 mL/min/1.73 m²)患者(187例男性和11例女性)。该队列的中位年龄为72岁(范围38 - 92岁)。在5年(2015 - 2020年)的研究期间,10例患者因GFR提高到超过30 mL/min/1.73 m²而被排除,24例有基线免疫力,2例拒绝接种。106例患者未开始乙肝疫苗接种系列。在其余56例中,12例进展到ESKD并在完成疫苗接种计划前开始透析,6例死亡,1例因疫情在2020年未到诊所就诊。在完成疫苗接种计划的37例患者中,16例实现了血清转化且HBsAb滴度足够,10例尽管进行了第二轮乙肝疫苗接种仍未产生免疫力,11例未进行第二轮接种。鉴于血清转化率较低,尽管队列较小,但应考虑在CKD早期阶段的患者中进行疫苗接种。其他选择包括对FDA批准的接种时间较短的疫苗进行研究。我们计划提高肾病学家、患者和护理人员对获得乙肝免疫力重要性的认识。