Barraclough Katherine A, Wiggins Kathryn J, Hawley Carmel M, van Eps Carolyn L, Mudge David W, Johnson David W, Whitby Michael, Carpenter Sally, Playford E Geoffrey
Department of Nephrology, University of Queensland at Princess Alexandra Hospital, Brisbane, Australia.
Am J Kidney Dis. 2009 Jul;54(1):95-103. doi: 10.1053/j.ajkd.2009.03.010. Epub 2009 May 29.
Primary hepatitis B virus (HBV) vaccination through the intramuscular (IM) route is less efficacious in dialysis patients than in the general population. Previous studies suggest improved seroconversion with intradermal (ID) vaccination.
Prospective open-label randomized controlled trial.
SETTING & PARTICIPANTS: Hemodialysis patients nonresponsive to primary HBV vaccination.
Revaccination with either ID (10 microg of vaccine every week for 8 weeks) [DOSAGE ERROR CORRECTED] or IM (40 microg of vaccine at weeks 1 and 8) HBV vaccine .
proportion of patients achieving HBV surface antibody (anti-HBs) titer of 10 IU/L or greater within 2 months of vaccination course.
time to seroconversion, predictors of seroconversion, peak antibody titer, duration of seroprotection, and safety and tolerability of vaccine.
Anti-HBs titer to 24 months.
59 patients were analyzed. Seroconversion rates were 79% ID versus 40% IM (P = 0.002). The unadjusted odds ratio for seroconversion for ID versus IM was 5.5 (95% confidence interval [CI], 1.6 to 18.4) and increased with adjustment for baseline differences. The only factor predictive of seroconversion was the ID vaccination route. The geometric mean peak antibody titer was significantly greater in the ID versus IM group: 239 IU/L (95% CI, 131 to 434) versus 78 IU/L (95% CI, 36 to 168; P < 0.001). There was a trend toward longer duration of seroprotection with ID vaccination. ID vaccine was safe and well tolerated.
Inability to distinguish whether the mechanism of the greater efficacy of ID vaccination was the cumulative effect of multiple injections or route of administration; use of anti-HBs as a surrogate marker of protection; lack of evidence of long-term protection.
Significantly greater seroconversion rates and peak antibody titers can be achieved with ID compared with IM vaccination in hemodialysis patients nonresponsive to primary vaccination. ID vaccination should become the standard of care in this setting.
通过肌内注射(IM)途径进行的原发性乙型肝炎病毒(HBV)疫苗接种在透析患者中的效果不如在普通人群中。先前的研究表明皮内注射(ID)疫苗接种可提高血清转化率。
前瞻性开放标签随机对照试验。
对原发性HBV疫苗接种无反应的血液透析患者。
采用ID(每周10微克疫苗,共8周)[剂量错误已纠正]或IM(第1周和第8周各40微克疫苗)HBV疫苗进行再次接种。
在疫苗接种疗程的2个月内达到HBV表面抗体(抗-HBs)滴度为10 IU/L或更高的患者比例。
血清转化时间、血清转化的预测因素、抗体峰值滴度、血清保护持续时间以及疫苗的安全性和耐受性。
抗-HBs滴度至24个月。
分析了59例患者。ID组血清转化率为79%,而IM组为40%(P = 0.002)。ID组与IM组血清转化的未调整优势比为5.5(95%置信区间[CI],1.6至18.4),并在对基线差异进行调整后增加。唯一可预测血清转化的因素是ID疫苗接种途径。ID组的几何平均抗体峰值滴度显著高于IM组:239 IU/L(95% CI,131至434)对78 IU/L(95% CI,36至168;P < 0.001)。ID疫苗接种有血清保护持续时间更长的趋势。ID疫苗安全且耐受性良好。
无法区分ID疫苗接种效果更好的机制是多次注射的累积效应还是给药途径;使用抗-HBs作为保护的替代标志物;缺乏长期保护的证据。
与IM疫苗接种相比،在对原发性疫苗接种无反应的血液透析患者中،ID疫苗接种可显著提高血清转化率和抗体峰值滴度。在这种情况下,ID疫苗接种应成为标准治疗方法。