Inbaraj Leeberk Raja, Shewade Hemant Deepak, Daniel Jefferson, Srinivasalu Vignes Anand, Paul Jabez, Satish S, Kirubakaran Richard, Padmapriyadarsini Chandrasekaran
Department of Clinical Research, Indian Council of Medical Research-National Institute for Research in Tuberculosis, Chennai, India.
Division of Health System Research, Indian Council of Medical Research - National Institute of Epidemiology, Chennai, India.
Front Med (Lausanne). 2023 Jun 20;10:1085010. doi: 10.3389/fmed.2023.1085010. eCollection 2023.
We aimed to determine the effectiveness and safety of the Levofloxacin-containing regimen that the World Health Organization is currently recommending for the treatment of Isoniazid mono-resistant pulmonary Tuberculosis.
Our eligible criteria for the studies to be included were; randomized controlled trials or cohort studies that focused on adults with Isoniazid mono-resistant tuberculosis (HrTB) and treated with a Levofloxacin-containing regimen along with first-line anti-tubercular drugs; they should have had a control group treated with first-line without Levofloxacin; should have reported treatment success rate, mortality, recurrence, progression to multidrug-resistant Tuberculosis. We performed the search in MEDLINE, EMBASE, Epistemonikos, Google Scholar, and Clinical trials registry. Two authors independently screened the titles/abstracts and full texts that were retained after the initial screening, and a third author resolved disagreements.
Our search found 4,813 records after excluding duplicates. We excluded 4,768 records after screening the titles and abstracts, retaining 44 records. Subsequently, 36 articles were excluded after the full-text screening, and eight appeared to have partially fulfilled the inclusion criteria. We contacted the respective authors, and none responded positively. Hence, no articles were included in the meta-analysis.
We found no "quality" evidence currently on the effectiveness and safety of Levofloxacin in treating HrTB.
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022290333, identifier: CRD42022290333.
我们旨在确定世界卫生组织目前推荐的含左氧氟沙星方案治疗异烟肼单耐药肺结核的有效性和安全性。
纳入研究的合格标准为:针对异烟肼单耐药肺结核(HrTB)成人患者的随机对照试验或队列研究,采用含左氧氟沙星方案联合一线抗结核药物治疗;应有一组接受不含左氧氟沙星的一线治疗作为对照组;应报告治疗成功率、死亡率、复发率、进展为耐多药结核病的情况。我们在MEDLINE、EMBASE、Epistemonikos、谷歌学术和临床试验注册库中进行了检索。两位作者独立筛选初筛后保留的标题/摘要和全文,第三位作者解决分歧。
排除重复记录后,我们的检索共找到4813条记录。筛选标题和摘要后排除4768条记录,保留44条。随后,全文筛选后排除36篇文章,8篇似乎部分符合纳入标准。我们联系了各自的作者,但均未得到肯定答复。因此,没有文章纳入荟萃分析。
我们目前未发现关于左氧氟沙星治疗HrTB有效性和安全性的“高质量”证据。
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022290333,标识符:CRD42022290333 。