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慢性肾脏病3期患者肌肉注射20毫克与40毫克乙肝疫苗后血清转化的随机对照试验

A Randomized Controlled Trial of Seroconversion After 20 Mg versus 40 mg Intramuscular Hepatitis B Virus Vaccination in Patients with Chronic Kidney Disease Stage 3.

作者信息

Krairittichai Udom, Sethakarun Sethaporn

出版信息

J Med Assoc Thai. 2017 Feb;100 Suppl 1:S1-7.

Abstract

BACKGROUND

There is as yet no guideline for hepatitis B virus (HBV) vaccination in chronic kidney disease (CKD). There is also insufficient evidence to support the theory that the immune response to a double dose (40 μg) of HBV vaccine is greater than that achieved by the standard dose (20 μg).

OBJECTIVE

To compare seroconversion of the four-dose regimen (at 0, 1, 2, 6 months) of intramuscular recombinant DNA HBV vaccination using the standard 20 μg with that of 40 μg in patients with CKD stage 3.

MATERIAL AND METHOD

This study included 39 patients with CKD stage 3 who had neither history of HBV vaccination nor markers of HBV infection, namely hepatitis B surface antigen (HBs Ag), antibody to hepatitis B core antigen (anti-HBc), or antibody to hepatitis B surface antigen (anti-HBs). After randomization, 20 patients were given 20 μg and 19 patients received 40 μg of vaccine in a four-dose regimen of HBV immunization. Immune response was assessed by measuring anti-HBs at the 2nd, 6th, 7th and 12th months. Anti-HBs at levels equal to or more than 10 IU/L were considered to constitute seroconversion.

RESULTS

Rates of seroconversion in the 20 μg versus the 40 μg groups at the 2nd, 6th, 7th, 12th month were 50.0%:52.6% (p = 0.869), 65.0%:100.0% (p = 0.004), 95.0%:100.0% (p = 0.323) and 80.0%:100.0% (p = 0.040) respectively. Six months after completing the vaccination, some patients (20.0%) in the 20 μg group had lost their immune response while all in the 40 μg group still maintained their seroconversion. During the study, there was no significant change in eGFR in the two groups (p>0.05), and minor adverse effects including local pain, malaise, fatigue, and dizziness were not significantly different between the two groups.

CONCLUSION

Seroconversion rates of the two groups were not significantly different after completion of HBV vaccination, but only patients in the group receiving the double dose were able to maintain seroconversion 6 months later. The proper hepatitis B vaccination for patients with CKD stage 3 with negative makers of HBV should be immunization with a four-dose regimen using 40 μg of vaccine.

摘要

背景

目前尚无慢性肾脏病(CKD)患者乙肝病毒(HBV)疫苗接种的指南。也没有足够的证据支持双倍剂量(40μg)HBV疫苗的免疫反应大于标准剂量(20μg)这一理论。

目的

比较慢性肾脏病3期患者使用标准20μg与40μg肌肉注射重组DNA HBV疫苗四剂次方案(0、1、2、6个月)的血清学转换情况。

材料与方法

本研究纳入39例慢性肾脏病3期患者,这些患者既无HBV疫苗接种史,也无HBV感染标志物,即乙肝表面抗原(HBs Ag)、乙肝核心抗体(抗-HBc)或乙肝表面抗体(抗-HBs)。随机分组后,20例患者接受20μg疫苗,19例患者接受40μg疫苗,采用四剂次HBV免疫方案。在第2、6、7和12个月通过检测抗-HBs评估免疫反应。抗-HBs水平等于或高于10 IU/L被认为构成血清学转换。

结果

第2、6、7、12个月时,20μg组与40μg组的血清学转换率分别为50.0%:52.6%(p = 0.869)、65.0%:100.0%(p = 0.004)、95.0%:100.0%(p = 0.323)和80.0%:100.0%(p = 0.040)。完成疫苗接种6个月后,20μg组部分患者(20.0%)失去免疫反应,而40μg组所有患者仍维持血清学转换。研究期间,两组的估算肾小球滤过率(eGFR)无显著变化(p>0.05),两组间包括局部疼痛、不适、疲劳和头晕在内的轻微不良反应无显著差异。

结论

HBV疫苗接种完成后两组的血清学转换率无显著差异,但只有接受双倍剂量的组在6个月后能够维持血清学转换。对于HBV标志物阴性的慢性肾脏病3期患者,合适的乙肝疫苗接种方案应为采用40μg疫苗的四剂次免疫方案。

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