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临床试验/NCT04121026
NCT04121026已完成不适用

Validation of a Tuberculosis Treatment Decision Algorithm in HIV-infected Children

Institut National de la Santé Et de la Recherche Médicale, France9 个研究点 分布在 5 个国家目标入组 278 人开始时间: 2019年10月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
278
试验地点
9
主要终点
Proportion of missed TB cases

研究概览

简要总结

TB-Speed HIV is a prospective multicentre management study evaluating the safety and feasibility of the recently proposed PAANTHER TB treatment decision algorithm for HIV-infected children with presumptive TB. It will be conducted in four countries with high and very high TB (Tuberculosis) incidence (Côte d'Ivoire, Uganda, Mozambique, and Zambia) which have not participated in the study that developed the PAANTHER algorithm.

详细描述

The ANRS 12229 PAANTHER 01 (Pediatric Asian African Network for Tuberculosis and HIV Research) study, which enrolled 438 HIV-infected children of median age 7.3 (IQR: 3.3 - 9.7) years with presumptive TB in four countries (Burkina Faso, Cameroon, Cambodia, Vietnam) from 2011 to 2014, aimed at developing a diagnostic prediction score and algorithm for TB treatment decision in HIV-infected children. This was the first study developing a TB diagnostic score exclusively in HIV-infected children, using methods recommended for diagnostic prediction models. Based on microbiological, clinical and radiological features, the best scoring system obtained had a sensitivity of 88.6% and specificity of 61.2% when Xpert MTB/RIF was included in the algorithm. The investigators showed previously that mortality is high in children with both confirmed and unconfirmed TB and that initiation of anti-TB treatment, that occurred at a median time of 7 (IQR: 5 - 11) days in the study, led to delayed ART initiation, which is associated to significantly increased mortality. The score, based on easily collected clinical features, chest radiographic features, Xpert MTB/RIF results, and abdominal ultrasonography, could enable same-day TB treatment decision. Abdominal ultrasonography has shown promise for the diagnosis of TB in both HIV-infected adults and children. In the PAANTHER study, it detected abdominal lymphadenopathy in 50% of culture confirmed TB cases and 35% of all confirmed and unconfirmed cases, with a specificity of 85%.

Developed in tertiary research-experienced health facilities, the PAANTHER score could enable standardized treatment decision in HIV-infected children with presumptive TB, and could be recommended for extensive use in secondary and primary healthcare settings where most of these children are seeking care. However, external validation studies are now needed to assess the predictive performance of the PAANTHER diagnostic score on independent datasets.

The PAANTHER TB treatment decision algorithm will be used for a TB treatment decision by site clinicians in all children enrolled in the study. Validation of the algorithm will be performed by evaluating the safety of withholding TB treatment in children not initiated on treatment as per the PAANTHER TB treatment decision algorithm. The safety of this strategy will be carefully assessed through review of safety reports every 4 to 6 months during study conduct by the safety sub-committee of the SAB.

Occurrence of algorithm failures in terms of missed TB cases (TB cases subsequently detected among untreated cases, i.e. false negatives) and cases with unlikely TB among those initiated on TB treatment as per the algorithm (cases not secondarily validated as confirmed or unconfirmed TB cases by the expert committee, i.e. false positives) will enable to estimate the negative and positive predictive values of the algorithm.

A centralized international Expert Committee will clinically review and validate TB diagnosis in children. This will enable assessment of the added value of new markers (MLR and CRP) and, if need be, to propose a new version of the score based on an optimised predicted probability.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
1 Month 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged 1 month to 14 years
  • Documented HIV-infection (i.e., confirmed before entry into the study)
  • Presumptive TB based on at least one criteria among the following:
  • Persistent cough for more than 2 weeks
  • Persistent fever for more than 2 weeks
  • Recent failure to thrive (documented clear deviation from a previous growth trajectory in the last 3 months or Z score weight/age < 2)
  • Failure of broad spectrum antibiotics for treatment of pneumonia
  • Suggestive CXR features
  • History of contact with a TB case and any of the symptoms listed under point 3 with a shorter duration (< 2 weeks)
  • Informed consent signed by parent/guardian

排除标准

  • Ongoing TB treatment or history of intake of anti-TB drugs in the last 3 months (isoniazid alone or rifampin/isoniazid for preventive therapy is not an exclusion criteria)

结局指标

主要结局

Proportion of missed TB cases

时间窗: 6 months

Proportion of missed TB cases (false negative cases) in children not initiated on treatment as per the PAANTHER TB treatment decision algorithm

次要结局

  • Feasibility of the PAANTHER TB treatment decision algorithm (a): Proportion of children with presumptive TB having completed the algorithm.(6 months)
  • Feasibility of the PAANTHER TB treatment decision algorithm (b): Time to final TB treatment decision(6 months)
  • Proportion of HIV-infected children with unlikely TB among those initiated on treatment as per the PAANTHER TB treatment decision algorithm(6 months)
  • Incidence of morbidity(6 months)
  • Incidence of mortality(6 months)
  • Time to ART initiation in ART-naïve children(6 months)
  • CD4 (absolute count and %) gain(6 months)
  • TB treatment outcomes (a): Weight gain at 6 months (absolute value and percentage of body weight)(6 months)
  • TB treatment outcomes (b): TB symptoms resolution in children on TB treatment(6 months)
  • Feasibility of IPT initiation (a): Time to IPT initiation(6 months)
  • Feasibility of IPT initiation (b): Proportion of children initiated on IPT(6 months)
  • Performance of the Monocyte-to-Lymphocyte Ratio and the C-reactive protein and their potential added value in the PAANTHER score and algorithm to detect TB(6 months)
  • Proportion of NPAs (or sputum) and stool samples with mycobacterium tuberculosis (MTB) detected using Ultra(6 months)
  • Proportion of children with NPA and stool samples collected as per study protocol(6 months)
  • Proportion of NPA-related adverse events (AEs)(6 months)
  • Discomfort/pain/distress experienced by the child during NPA as assessed by the child(Within 3 days of inclusion)
  • Discomfort/pain/distress experienced by the child during NPA as assessed by the parents(Within 3 days of inclusion)
  • Discomfort/pain/distress experienced by the child during NPA as assessed by the nurse(Within 3 days of inclusion)
  • Sensitivity(6 months)
  • Positivity(6 months)

研究者

发起方
Institut National de la Santé Et de la Recherche Médicale, France
申办方类型
Other Gov
责任方
Sponsor

研究点 (9)

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