Diagnosis of tetanus immunization status: multicenter assessment of a rapid biological test.

Isabelle Colombet, Colette Saguez, Marie-José Sanson-Le Pors, Benoît Coudert, Gilles Chatellier, Pierre Espinoza
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引用次数: 40

Abstract

Diagnosis of tetanus immunization status by medical interview of patients with wounds is poor. Many protected patients receive unnecessary vaccine or immunoglobulin, and unprotected patients may receive nothing. The aim of this study is to evaluate the feasibility and accuracy of the Tetanos Quick Stick (TQS) rapid finger prick stick test in the emergency department for determining immunization status. We designed a prospective multicenter study for blinded comparison of TQS with an enzyme-linked immunosorbent assay (ELISA). Adults referred for open wounds in 37 French hospital emergency departments had the TQS after receiving standard care (emergency-TQS). TQS was also performed in the hospital laboratory on total blood (blood/lab-TQS) and serum (serum/lab-TQS). ELISA was performed with the same blood sample at a central laboratory. We assessed concordance between emergency-TQS and blood/lab-TQS by the kappa test and the diagnostic accuracy (likelihood ratios) of medical interview, emergency-TQS, and lab-TQS. ELISA was positive in 94.6% of the 988 patients included. Concordance between blood/emergency-TQS and blood/lab-TQS results was moderate (kappa=0.6), with a high proportion of inconclusive blood/emergency-TQS tests (9.8%). Likelihood ratios for immunization were 3.0 (95% confidence interval [CI], 1.8 to 5.1), 36.6 (95% CI, 5.3 to 255.3), 89.1 (95% CI, 5.6 to 1,405.0), and 92.7 (95% CI, 5.9 to 1,462.0) for medical interview, blood/emergency-TQS, blood/lab-TQS, and serum/lab-TQS, respectively. The sensitivity of the blood/emergency-TQS was 76.7%, and the specificity was 98% by reference to the ELISA. TQS use in the emergency room could make tetanus prevention more accurate if its technical feasibility were improved, and our assessment will be supplemented by a cost effectiveness study.

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破伤风免疫状态的诊断:快速生物试验的多中心评估。
创伤患者的医学访谈对破伤风免疫状况的诊断较差。许多受保护的患者接种了不必要的疫苗或免疫球蛋白,而未受保护的患者可能什么也没有接种。本研究的目的是评价破伤风快速针刺试验(TQS)在急诊科用于确定免疫状态的可行性和准确性。我们设计了一项前瞻性多中心研究,将TQS与酶联免疫吸附试验(ELISA)进行盲法比较。37家法国医院急诊科转介的开放性伤口的成年人在接受标准治疗(emergency-TQS)后有TQS。同时在医院化验室进行全血(blood/lab-TQS)和血清(serum/lab-TQS) TQS。ELISA在中心实验室对相同的血液样本进行检测。我们通过卡帕试验评估急诊tqs和血液/实验室tqs之间的一致性,以及医学访谈、急诊tqs和实验室tqs的诊断准确性(似然比)。纳入的988例患者中,94.6%的人ELISA检测呈阳性。血/急诊tqs与血/实验室tqs结果的一致性为中等(kappa=0.6),血/急诊tqs结果不确定的比例较高(9.8%)。医学访谈、血液/紧急tqs、血液/实验室tqs和血清/实验室tqs的免疫似然比分别为3.0(95%置信区间[CI], 1.8至5.1)、36.6 (95% CI, 5.3至255.3)、89.1 (95% CI, 5.6至1,405.0)和92.7 (95% CI, 5.9至1,462.0)。血/急诊tqs与ELISA对照敏感性为76.7%,特异性为98%。如果提高TQS在急诊室的技术可行性,可以使破伤风预防更加准确,我们的评估将辅以成本效益研究。
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