Engler Renata J M, Nelson Michael R, Collins Limone C, Spooner Christina, Hemann Brian A, Gibbs Barnett T, Atwood J Edwin, Howard Robin S, Chang Audrey S, Cruser Daniel L, Gates Daniel G, Vernalis Marina N, Lengkeek Marguerite S, McClenathan Bruce M, Jaffe Allan S, Cooper Leslie T, Black Steve, Carlson Christopher, Wilson Christopher, Davis Robert L
Military Vaccine Agency-Vaccine Healthcare Centers Network (currently Defense Health Agency, Immunization Healthcare Branch), Walter Reed National Military Medical Center, Bethesda, Maryland, United States of America; Department of Medicine and Pediatrics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Department of Medicine and Pediatrics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America; Allergy-Immunology-Immunizations, Walter Reed National Military Medical Center, Bethesda, Maryland, United States of America.
PLoS One. 2015 Mar 20;10(3):e0118283. doi: 10.1371/journal.pone.0118283. eCollection 2015.
Although myocarditis/pericarditis (MP) has been identified as an adverse event following smallpox vaccine (SPX), the prospective incidence of this reaction and new onset cardiac symptoms, including possible subclinical injury, has not been prospectively defined.
The study's primary objective was to determine the prospective incidence of new onset cardiac symptoms, clinical and possible subclinical MP in temporal association with immunization.
New onset cardiac symptoms, clinical MP and cardiac specific troponin T (cTnT) elevations following SPX (above individual baseline values) were measured in a multi-center prospective, active surveillance cohort study of healthy subjects receiving either smallpox vaccine or trivalent influenza vaccine (TIV).
New onset chest pain, dyspnea, and/or palpitations occurred in 10.6% of SPX-vaccinees and 2.6% of TIV-vaccinees within 30 days of immunization (relative risk (RR) 4.0, 95% CI: 1.7-9.3). Among the 1081 SPX-vaccinees with complete follow-up, 4 Caucasian males were diagnosed with probable myocarditis and 1 female with suspected pericarditis. This indicates a post-SPX incidence rate more than 200-times higher than the pre-SPX background population surveillance rate of myocarditis/pericarditis (RR 214, 95% CI 65-558). Additionally, 31 SPX-vaccinees without specific cardiac symptoms were found to have over 2-fold increases in cTnT (>99th percentile) from baseline (pre-SPX) during the window of risk for clinical myocarditis/pericarditis and meeting a proposed case definition for possible subclinical myocarditis. This rate is 60-times higher than the incidence rate of overt clinical cases. No clinical or possible subclinical myocarditis cases were identified in the TIV-vaccinated group.
Passive surveillance significantly underestimates the true incidence of myocarditis/pericarditis after smallpox immunization. Evidence of subclinical transient cardiac muscle injury post-vaccinia immunization is a finding that requires further study to include long-term outcomes surveillance. Active safety surveillance is needed to identify adverse events that are not well understood or previously recognized.
虽然心肌炎/心包炎(MP)已被确认为天花疫苗(SPX)接种后的不良事件,但这种反应以及新发心脏症状(包括可能的亚临床损伤)的前瞻性发病率尚未得到前瞻性定义。
本研究的主要目的是确定与免疫接种存在时间关联的新发心脏症状、临床及可能的亚临床MP的前瞻性发病率。
在一项多中心前瞻性主动监测队列研究中,对接种天花疫苗或三价流感疫苗(TIV)的健康受试者,测量接种SPX后(高于个体基线值)的新发心脏症状、临床MP以及心脏特异性肌钙蛋白T(cTnT)升高情况。
接种疫苗后30天内,10.6%的SPX接种者和2.6%的TIV接种者出现新发胸痛、呼吸困难和/或心悸(相对风险(RR)4.0,95%置信区间:1.7 - 9.3)。在1081名接受完整随访的SPX接种者中,4名白人男性被诊断为可能的心肌炎,1名女性被诊断为疑似心包炎。这表明接种SPX后的发病率比接种前心肌炎/心包炎背景人群监测率高出200多倍(RR 214,95%置信区间65 - 558)。此外,在临床心肌炎/心包炎风险窗口期,31名无特定心脏症状的SPX接种者的cTnT较基线(接种SPX前)升高超过2倍(>第99百分位数),符合可能的亚临床心肌炎的拟议病例定义。该发生率比明显临床病例的发病率高60倍。在TIV接种组中未发现临床或可能的亚临床心肌炎病例。
被动监测显著低估了天花免疫后心肌炎/心包炎的真实发病率。牛痘免疫后亚临床短暂心肌损伤的证据是一个需要进一步研究以纳入长期结局监测的发现。需要进行主动安全监测以识别尚未完全了解或先前未被认识的不良事件。