Interventions for treatment of COVID-19: a protocol for a living systematic review with network meta-analysis including individual patient data (The LIVING Project)

被引:27
作者
Juul, Sophie [1 ]
Nielsen, Niklas [2 ]
Bentzer, Peter [2 ]
Veroniki, Areti Angeliki [3 ,4 ]
Thabane, Lehana [5 ]
Linder, Adam [2 ]
Klingenberg, Sarah [1 ]
Gluud, Christian [1 ]
Jakobsen, Janus Christian [1 ,6 ]
机构
[1] Copenhagen Univ Hosp, Rigshosp, Ctr Clin Intervent Res, Copenhagen Trial Unit, Blegdamsvej 9, DK-2100 Copenhagen O, Denmark
[2] Lund Univ, Helsingborg Hosp, Anesthesia & Intens Care, Dept Clin Sci Lund, Lund, Sweden
[3] Univ Ioannina, Sch Educ, Dept Primary Educ, Ioannina, Greece
[4] St Michaels Hosp, Li Ka Shing Knowledge Inst, Knowledge Translat Program, Toronto, ON, Canada
[5] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
[6] Univ Southern Denmark, Fac Hlth Sci, Odense, Denmark
关键词
TRIAL SEQUENTIAL-ANALYSIS;
D O I
10.1186/s13643-020-01371-0
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background COVID-19 is a rapidly spreading virus infection that has quickly caused extensive burden to individual, families, countries, and the globe. No intervention has yet been proven effective for the treatment of COVID-19. Some randomized clinical trials assessing the effects of different drugs have been published, and more are currently underway. There is an urgent need for a living, dynamic systematic review that continuously evaluates the beneficial and harmful effects of all available interventions for COVID-19. Methods/design We will conduct a living systematic review based on searches of major medical databases (e.g., MEDLINE, EMBASE, CENTRAL) and clinical trial registries from their inception onwards to identify relevant randomized clinical trials. We will update the literature search once a week to continuously assess if new evidence is available. Two review authors will independently extract data and perform risk of bias assessment. We will include randomized clinical trials comparing any intervention for the treatment of COVID-19 (e.g., pharmacological interventions, fluid therapy, invasive or noninvasive ventilation, or similar interventions) with any comparator (e.g., an "active" comparator, standard care, placebo, no intervention, or "active placebo") for participants in all age groups with a diagnosis of COVID-19. Primary outcomes will be all-cause mortality and serious adverse events. Secondary outcomes will be admission to intensive care, mechanical ventilation, renal replacement therapy, quality of life, and non-serious adverse events. The living systematic review will include aggregate data meta-analyses, Trial Sequential Analyses, network meta-analysis, and individual patient data meta-analyses. Risk of bias will be assessed with domains, an eight-step procedure will be used to assess if the thresholds for clinical significance are crossed, and the certainty of the evidence will be assessed by Grading of Recommendations, Assessment, Development and Evaluations (GRADE). Discussion COVID-19 has become a pandemic with substantial mortality. A living systematic review evaluating the beneficial and harmful effects of pharmacological and other interventions is urgently needed. This review will continuously inform best practice in treatment and clinical research of this highly prevalent disease. Systematic review registration PROSPERO CRD42020178787
引用
收藏
页数:12
相关论文
共 50 条
[1]
[Anonymous], EFFECTIVENESS SAFETY
[2]
[Anonymous], 2020, N ENGL J MED
[3]
[Anonymous], Stata Statistical Software
[4]
[Anonymous], BMJ EVID BASED MED
[5]
[Anonymous], N ENG J MED
[6]
[Anonymous], 2020, N ENGL J MED
[7]
[Anonymous], 2015, INT C HARM TECHN REQ
[8]
[Anonymous], 2015, BMJ-BRIT MED J, DOI DOI 10.1136/BMJ.G7647
[9]
OPERATING CHARACTERISTICS OF A BANK CORRELATION TEST FOR PUBLICATION BIAS [J].
BEGG, CB ;
MAZUMDAR, M .
BIOMETRICS, 1994, 50 (04) :1088-1101
[10]
Apparently conclusive meta-analyses may be inconclusive-Trial sequential analysis adjustment of random error risk due to repetitive testing of accumulating data in apparently conclusive neonatal meta-analyses [J].
Brok, Jesper ;
Thorlund, Kristian ;
Wetterslev, Jorn ;
Gluud, Christian .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2009, 38 (01) :287-298