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结核病与结核菌素质量:初衷虽好,结果却具误导性。

Tuberculosis and tuberculin quality: best intentions, misleading results.

作者信息

Rangel-Frausto M S, Ponce-De-León-Rosales S, Martinez-Abaroa C, Hasløv K

机构信息

Division of Hospital Epidemiology, National Institute of Medical Sciences and Nutrition Tlalpan, México, DF.

出版信息

Infect Control Hosp Epidemiol. 2001 Aug;22(8):481-4. doi: 10.1086/501937.

Abstract

OBJECTIVE

To compare the performance of three purified protein derivative (PPD) formulations: Tubersol (Connaught); RT23, Statens Serum Institut (SSI); and RT23, Mexico, tested in Mexican populations at low and high risk for tuberculosis (TB).

DESIGN

A double-blinded clinical trial.

SETTING

A university hospital in Mexico City.

PARTICIPANTS

The low-risk population was first or second-year medical students with no patient contact; the high-risk population was healthcare workers at a university hospital.

METHODS

Each of the study subjects received the three different PPD preparations. Risk factors for TB, including age, gender, occupation, bacille Calmette-Guérin (BCG) status, and TB exposure, were recorded. A 0.1-mL aliquot of each preparation was injected in the left and right forearms of volunteers using the Mantoux technique. Blind readings were done 48 to 72 hours later. Sensitivity and specificity were calculated at 10 mm of induration using Tubersol as the reference standard. The SSI tested the potency of the different PPD preparations in previously sensitized guinea pigs.

RESULTS

The low-risk population had a prevalence of positive PPD of 26%. In the low-risk population, RT23 prepared in Mexico, compared to the 5 TU of Tubersol, had a sensitivity of 51%, a specificity of 100%, a positive predictive value of 100%, and a negative predictive value of 86%. The RT23 prepared at the SSI had a sensitivity of 69%, a specificity of 99%, a positive predictive value of 95%, and a negative predictive value of 90%. In the high-risk population, the prevalence of positive PPD was 57%. The RT23 prepared in Mexico had a sensitivity of 33%, a specificity of 100%, and a positive predictive value of 53%; the RT23 prepared at the SSI had a sensitivity of 91%, a specificity of 98%, a positive predictive value of 98%, and a negative predictive value of 89%. RT23 used in Mexico had a potency of only 23% of that of the control. There was no statistical association among those with a positive PPD, irrespective of previous BCG vaccination (relative risk, 0.97; 95% confidence interval, 0.76-1.3;P=.78).

CONCLUSIONS

Healthcare workers had twice the prevalence of positive PPD compared to medical students. RT23 prepared in Mexico had a low sensitivity in both populations compared to 5 TU of Tubersol and RT23 prepared at the SSI. Previous BCG vaccination did not correlate with a positive PPD. Low potency of the RT23 preparation in Mexico was confirmed in guinea pigs. Best intentions in a TB program are not enough if they are not followed by high-quality control.

摘要

目的

比较三种纯化蛋白衍生物(PPD)制剂的性能:结核菌素纯蛋白衍化物(Connaught公司生产);RT23,丹麦国家血清研究所(SSI)生产;以及在墨西哥生产的RT23,在墨西哥结核病(TB)低风险和高风险人群中进行测试。

设计

一项双盲临床试验。

地点

墨西哥城的一家大学医院。

参与者

低风险人群为没有接触过患者的大一或大二医学生;高风险人群为一家大学医院的医护人员。

方法

每位研究对象接受三种不同的PPD制剂。记录结核病的风险因素,包括年龄、性别、职业、卡介苗(BCG)接种情况和结核病接触史。使用曼托试验技术将每种制剂的0.1 mL等分试样注射到志愿者的左右前臂。48至72小时后进行盲法读数。以结核菌素纯蛋白衍化物为参考标准,在硬结为10 mm时计算敏感性和特异性。SSI在先前致敏的豚鼠中测试了不同PPD制剂的效力。

结果

低风险人群中PPD阳性率为26%。在低风险人群中,与5 TU结核菌素纯蛋白衍化物相比,墨西哥生产的RT23的敏感性为51%,特异性为100%,阳性预测值为100%,阴性预测值为86%。SSI生产的RT23的敏感性为69%,特异性为99%,阳性预测值为95%,阴性预测值为90%。在高风险人群中,PPD阳性率为57%。墨西哥生产的RT23的敏感性为33%,特异性为100%,阳性预测值为53%;SSI生产的RT23的敏感性为91%,特异性为98%,阳性预测值为98%,阴性预测值为89%。墨西哥使用的RT23的效力仅为对照的23%。PPD阳性者之间无统计学关联,无论之前是否接种过卡介苗(相对风险,0.97;95%置信区间,0.76 - 1.3;P = 0.78)。

结论

医护人员的PPD阳性率是医学生的两倍。与5 TU结核菌素纯蛋白衍化物和SSI生产的RT23相比,墨西哥生产的RT23在这两个人群中的敏感性都较低。先前接种卡介苗与PPD阳性无关。在豚鼠中证实了墨西哥生产的RT23制剂效力较低。结核病项目中仅有良好意愿是不够的,还需要高质量的控制。

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