Diggle Linda, Deeks Jonathan J, Pollard Andrew J
Oxford Vaccine Group, Centre for Clinical Vaccinology and Tropical Medicine, Department of Paediatrics, University of Oxford, Churchill Hospital, Oxford OX3 7LJ.
BMJ. 2006 Sep 16;333(7568):571. doi: 10.1136/bmj.38906.704549.7C. Epub 2006 Aug 4.
To assess the immunogenicity of vaccines for infants and to investigate whether the incidence of reactogenicity is reduced after each immunisation dose using needles of varying lengths and gauges.
Randomised controlled trial.
18 general practices within two UK primary care trusts.
696 healthy infants vaccinated at 2, 3, and 4 months of age, with follow-up to 5 months of age.
Combined diphtheria, tetanus, whole cell pertussis, and Haemophilus influenzae type b vaccine and a serogroup C meningococcal glycoconjugate vaccine administered using either a wide, long needle (23 gauge/0.6 mm diameter, 25 mm), a narrow, short needle (25 gauge/0.5 mm diameter, 16 mm), or a narrow, long needle (25 gauge, 25 mm).
Local and general reactions recorded by parents for three days after each dose; and diphtheria, tetanus, and H influenzae type b antibody concentrations and functional antibody against serogroup C Neisseria meningitidis 28-42 days after the third dose.
Local reactions to diphtheria, tetanus, whole cell pertussis, H influenzae type b vaccinations decreased significantly with wide, long needles compared with narrow, short needles. At all three doses one less infant experienced local reactions at days 1, 2, or 3 for every six to eight vaccinated. Significantly fewer infants vaccinated with the long needle experienced severe local reactions. Non-inferiority of the immune response was shown using a wide, long needle rather than a narrow, short needle for serogroup C meningococcal glycoconjugate vaccine and for diphtheria but not for H influenzae type b or tetanus, although no evidence was found of a decrease. Little difference was found between needles of the same length but different gauges in local reaction or immune response.
Long (25 mm) needles for infant immunisations can significantly reduce vaccine reactogenicity at each dose while achieving comparable immunogenicity to that of short (16 mm) needles. Trial registration Current Controlled Trials ISRCTN62032215 [controlled-trials.com].
评估婴儿疫苗的免疫原性,并调查使用不同长度和规格的针头在每次接种疫苗后反应原性的发生率是否降低。
随机对照试验。
英国两个初级保健信托基金内的18家普通诊所。
696名健康婴儿,分别在2个月、3个月和4个月龄时接种疫苗,并随访至5个月龄。
使用宽而长的针头(23号/直径0.6毫米,25毫米)、窄而短的针头(25号/直径0.5毫米,16毫米)或窄而长的针头(25号,25毫米)接种白喉、破伤风、全细胞百日咳和b型流感嗜血杆菌联合疫苗以及C群脑膜炎球菌糖结合疫苗。
家长记录每次接种后三天内的局部和全身反应;以及第三次接种后28 - 42天白喉、破伤风和b型流感嗜血杆菌抗体浓度以及针对C群脑膜炎奈瑟菌的功能性抗体。
与窄而短的针头相比,宽而长的针头接种白喉、破伤风、全细胞百日咳、b型流感嗜血杆菌疫苗后的局部反应显著减少。在所有三次接种中,每六至八名接种疫苗的婴儿中,在第1、2或3天经历局部反应的婴儿少一名。使用长针头接种疫苗的婴儿出现严重局部反应的明显较少。对于C群脑膜炎球菌糖结合疫苗和白喉疫苗,使用宽而长的针头而非窄而短的针头显示免疫反应无劣效性,但对于b型流感嗜血杆菌或破伤风疫苗则不然,尽管未发现下降的证据。在局部反应或免疫反应方面,相同长度但不同规格的针头之间差异不大。
用于婴儿免疫接种的长(25毫米)针头可在每次接种时显著降低疫苗反应原性,同时实现与短(16毫米)针头相当的免疫原性。试验注册号:Current Controlled Trials ISRCTN62032215 [controlled-trials.com] 。