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白喉-百日咳-破伤风疫苗:市售产品的反应原性

Diphtheria-pertussis-tetanus vaccine: reactogenicity of commercial products.

作者信息

Barkin R M, Pichichero M E

出版信息

Pediatrics. 1979 Feb;63(2):256-60.

PMID:440817
Abstract

Parents from four practices were surveyed to ascertain reactions of children to diphtheria-pertussis-tetanus (DPT) vaccine in the 48 hours after immunization. Vaccines were administered according to current recommendations. Responses were scored in three categories: temperature, behavioral changes, and local reactions. Questionnaires were returned by 1,232 (84.9%) patients. Only 7.0% reported no reaction, while 336 (27.3%) reported mild, 722 (58.6%) moderate, and 88 (7.1%) severe reactions. Over 50% experienced temperatures of at least 100 F, and 80% noted behavioral changes; 72.2% had local reactions. No encephalitis, seizures, or hospitalizations were reported. Reactogenicity was similar for the five immunizations of the recommended series and the two manufacturers evaluated. Reported reactions in the control group were significantly lower than in the study group. These reaction rates underline the need to reevaluate present DPT vaccines.

摘要

对来自四个医疗机构的家长进行了调查,以确定儿童在接种白喉-百日咳-破伤风(DPT)疫苗后48小时内的反应。疫苗按照当前建议进行接种。反应分为三类进行评分:体温、行为变化和局部反应。1232名(84.9%)患者返回了问卷。只有7.0%的人报告无反应,而336人(27.3%)报告有轻度反应,722人(58.6%)报告有中度反应,88人(7.1%)报告有重度反应。超过50%的人经历了至少100华氏度的体温,80%的人有行为变化;72.2%的人有局部反应。未报告有脑炎、癫痫发作或住院情况。对于推荐系列的五次接种以及评估的两家制造商,反应原性相似。对照组报告的反应明显低于研究组。这些反应率突出了重新评估现有DPT疫苗的必要性。

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