Adverse events following HPV vaccination: 11 years of surveillance in Australia

被引:25
作者
Phillips, Anastasia [1 ,2 ,3 ]
Hickie, Megan [4 ]
Totterdell, James [3 ]
Brotherton, Julia [5 ,6 ]
Dey, Aditi [2 ,7 ]
Hill, Richard [4 ]
Snelling, Tom [3 ,8 ,9 ,10 ,11 ]
Macartney, Kristine [2 ,7 ]
机构
[1] Univ Sydney, Sch Publ Hlth, Sydney, NSW 2006, Australia
[2] Natl Ctr Immunisat Res & Surveillance, Westmead, NSW 2145, Australia
[3] Telethon Kids Inst, Wesfarmers Ctr Vaccines & Infect Dis, Nedlands, WA 6009, Australia
[4] Therapeut Goods Adm, Dept Hlth, Woden, ACT 2606, Australia
[5] Victorian Cytol Serv Fdn, Carlton, Vic 3053, Australia
[6] Univ Melbourne, Parkville, Vic 3010, Australia
[7] Univ Sydney, Discipline Child & Adolescent Hlth, Sydney, NSW 2006, Australia
[8] Perth Childrens Hosp, Nedlands, WA 6009, Australia
[9] Curtin Univ, Sch Publ Hlth, Bentley, WA 6102, Australia
[10] Menzies Sch Hlth Res, Darwin, NT, Australia
[11] Charles Darwin Univ, Darwin, NT, Australia
关键词
Human papillomavirus vaccine; Vaccination; Immunization; Vaccine safety; Adverse event; Syncope; HUMAN-PAPILLOMAVIRUS VACCINE; GUILLAIN-BARRE-SYNDROME; VENOUS THROMBOEMBOLISM; TACHYCARDIA SYNDROME; AUTOIMMUNE-DISEASES; REPORTING SYSTEM; SAFETY; RISK; IMMUNIZATION; ANAPHYLAXIS;
D O I
10.1016/j.vaccine.2020.06.039
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Australia was the first country to implement a fully funded vaccination program with quadrivalent human papillomavirus vaccine (4vHPV) in 2007, including males from 2013. We examined adverse events (AE) following vaccination with 4vHPV from 11 years of post-marketing data, focusing on a period of enhanced surveillance and adverse events of special interest (AESI). Methods: AE following 4vHPV doses administered between April 2007 and December 2017 reported to Australia's national regulator, the Therapeutic Goods Administration, were examined; reports collected during enhanced surveillance in 2013 and 2014 were analyzed separately. Age and sex-specific rates, using denominator data from the national HPV vaccination register, were determined. Pre-specified AESI were identified using Medical Dictionary for Regulatory Activities (MedDRA (R)) Preferred Terms and examined in detail. Findings: Following nine million doses of 4vHPV vaccine administered in Australia, 4551 AE reports were identified. The crude reporting rate was 39.8 per 100 000 doses in the funded cohorts, excluding the enhanced surveillance period. The reported rate of syncope in 12 to 13-year-old males and females was 29.6 per 100 000 doses during enhanced surveillance and 7.1 per 100 000 doses during the remaining study period; rates of syncope were higher in younger compared to older adolescents. The rate of anaphylaxis (0.32 per 100 000 doses) was consistent with published rates. Other AESI including autoimmune disease, postural orthostatic tachycardia syndrome, primary ovarian insufficiency, Guillain-Barre syndrome, complex regional pain syndrome and venous thromboembolism, were reported at low rates and analysis did not reveal unexpected patterns that would suggest causal association. Interpretation: AESI, apart from syncope, were reported rarely. The higher rate of syncope among younger adolescents highlights the need for management protocols to prevent syncope-related injury. Analysis of this large, longitudinal dataset in a country with high vaccine uptake, including a period of enhanced surveillance, affirms the safety profile of 4vHPV. (C) 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-NDlicense (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:6038 / 6046
页数:9
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