Id |
Subject |
Object |
Predicate |
Lexical cue |
T115 |
0-106 |
Sentence |
denotes |
Pharmacological intervention Sample size and criteria Treatment protocol Key findings Conclusion Reference |
T116 |
107-203 |
Sentence |
denotes |
• Tocilizumab for IL-6 cytokine release syndrome • Multicenter Randomized controlled trial (RCT) |
T117 |
204-232 |
Sentence |
denotes |
• Severe COVID-19 infections |
T118 |
233-253 |
Sentence |
denotes |
• 18–85 years of age |
T119 |
254-275 |
Sentence |
denotes |
• Elevated serum IL-6 |
T120 |
276-316 |
Sentence |
denotes |
• N = 94 standard therapy + tocilizumab |
T121 |
317-377 |
Sentence |
denotes |
• N = 94 standard therapy • 4–8 mg/kg tocilizumab i.v. once |
T122 |
378-509 |
Sentence |
denotes |
• Additional dose if fever persists in 24 h after first dose • First phase showed normalization of fever within 24 h of tocilizumab |
T123 |
510-615 |
Sentence |
denotes |
• Improved respiratory function, oxygenation, and pulmonary lesions • Phase 4 study completed in May 2020 |
T124 |
616-633 |
Sentence |
denotes |
• Results pending |
T125 |
634-783 |
Sentence |
denotes |
• Tocilizumab may be a promising investigative therapy to reduce cytokine release syndrome and associated multi-organ damage (ChiCTR2000029765, 2020) |
T126 |
784-882 |
Sentence |
denotes |
• Tocilizumab to mitigate cytokine storm and associated complications • Retrospective cohort study |
T127 |
883-901 |
Sentence |
denotes |
• >18 years of age |
T128 |
902-954 |
Sentence |
denotes |
• Intensive care unit (ICU) COVID-19 hospitalization |
T129 |
955-1003 |
Sentence |
denotes |
• Primary endpoint of hospital-related mortality |
T130 |
1004-1042 |
Sentence |
denotes |
• N = 210 standard care + tocilizumab |
T131 |
1043-1111 |
Sentence |
denotes |
• N = 420 standard care • 400 mg single dose or 8 mg/kg tocilizumab |
T132 |
1112-1266 |
Sentence |
denotes |
• 88% required 1 infusion, 12% received a second infusion • Hazard ratio (HR) 0.71 for hospital related mortality (95% confidence interval (CI) 0.56–0.89) |
T133 |
1267-1349 |
Sentence |
denotes |
• Treatment was more effective in patients with C-reactive protein (CRP) >15 mg/dL |
T134 |
1350-1560 |
Sentence |
denotes |
• HR 0.48 (95% CI 0.30–0.77) than those with CRP <15 mg/dL HR 0.92 (95% CI 0.57–1.48) • Tocilizumab treatment is associated with a lower rate of mortality, particularly in those with enhanced inflammatory state |
T135 |
1561-1652 |
Sentence |
denotes |
• Double blind RCT recently completed with results pending NCT04320615 (Biran et al., 2020) |
T136 |
1653-1727 |
Sentence |
denotes |
• Tocilizumab to mitigate cytokine storm • Prospective observational study |
T137 |
1728-1767 |
Sentence |
denotes |
• Severe or critical COVID-19 infection |
T138 |
1768-1791 |
Sentence |
denotes |
• 25 to 88 years of age |
T139 |
1792-1832 |
Sentence |
denotes |
• N = 21 tocilizumab + standard therapy |
T140 |
1833-1892 |
Sentence |
denotes |
• 42.9% had CVD • 4–8 mg/kg or 400 mg tocilizumab i.v. once |
T141 |
1893-2021 |
Sentence |
denotes |
• 85.7% received single dose of tocilizumab, 14.3% required second dose within 12 h of first dose • Fever normalized within 24 h |
T142 |
2022-2055 |
Sentence |
denotes |
• Reduced O2 therapy requirements |
T143 |
2056-2092 |
Sentence |
denotes |
• Minimal improvement in IL-6 levels |
T144 |
2093-2121 |
Sentence |
denotes |
• CT lung lesion improvement |
T145 |
2122-2190 |
Sentence |
denotes |
• All patients discharged • Limited sample size and no control group |
T146 |
2191-2314 |
Sentence |
denotes |
• Tocilizumab treatment in severe COVID-19 cases may improve clinical symptoms in hyperinflammatory state (Xu et al., 2020) |
T147 |
2315-2436 |
Sentence |
denotes |
• Intensive methylprednisolone regimen +/− tocilizumab for management of cytokine storm • Prospective observational study |
T148 |
2437-2492 |
Sentence |
denotes |
• O2 sat ≤ 94% OR tachypnea, elevated CRP, high D-dimer |
T149 |
2493-2556 |
Sentence |
denotes |
• Primary outcome of hospital discharge or clinical improvement |
T150 |
2557-2601 |
Sentence |
denotes |
• N = 86 methylprednisolone +/− tocilizumab |
T151 |
2602-2635 |
Sentence |
denotes |
• N = 86 standard care • Stage 1: |
T152 |
2636-2709 |
Sentence |
denotes |
Immediate methylprednisolone 250 mg i.v. on day 1, then 80 mg on days 2–5 |
T153 |
2710-2783 |
Sentence |
denotes |
• Stage 2 (lack of clinical improvement or worsening respiratory status): |
T154 |
2784-2897 |
Sentence |
denotes |
Add tocilizumab 8 mg/kg i.v. once between days 2–5 • Improvement in respiratory status HR 1.79 (95% CI 1.20–2.67) |
T155 |
2898-2949 |
Sentence |
denotes |
• Improvement reached in a shorter time vs. control |
T156 |
2950-3178 |
Sentence |
denotes |
• Reduced hospital mortality and need for mechanical ventilation • Short duration of intensive immunosuppressive therapy is associated with improved clinical outcomes in patients with hyperinflammaory state (Ramiro et al., 2020) |
T157 |
3179-3275 |
Sentence |
denotes |
• Ruxolitinib treatment for elevated cytokine levels and inflammatory response • Prospective RCT |
T158 |
3276-3321 |
Sentence |
denotes |
• 18 to 75 years of age with severe infection |
T159 |
3322-3371 |
Sentence |
denotes |
• Primary outcome of time to clinical improvement |
T160 |
3372-3409 |
Sentence |
denotes |
• N = 20 ruxolitinib + standard care |
T161 |
3410-3474 |
Sentence |
denotes |
• N = 21 placebo + standard care • Ruxolitinib 5 mg twice daily |
T162 |
3475-3579 |
Sentence |
denotes |
• Placebo vitamin C 100 mg twice daily • No difference in primary endpoint HR 1.669 (95% CI 0.836–3.335) |
T163 |
3580-3636 |
Sentence |
denotes |
• Improvement in lung computerized tomography (CT) scans |
T164 |
3637-3806 |
Sentence |
denotes |
• Significantly reduced cytokine levels and CRP by day 3 • Ruxolitinib may hasten time of chest CT scan improvement and mitigate systemic inflammation (Cao et al., 2020) |
T165 |
3807-3912 |
Sentence |
denotes |
• Anakinra for targeting the cytokine inflammatory cascade through IL-1 blockade • Open label case series |
T166 |
3913-3933 |
Sentence |
denotes |
• Elevated CRP N = 9 |
T167 |
3934-3981 |
Sentence |
denotes |
• 6/9 with CVD risk factors (diabetes, obesity) |
T168 |
3982-4051 |
Sentence |
denotes |
• 3/9 with hypertension • Anakinra 100 mg every 12 h s.c. on days 1–3 |
T169 |
4052-4124 |
Sentence |
denotes |
• Anakinra 100 mg once daily s.c. on days 4–10 • Fever subsided by day 3 |
T170 |
4125-4165 |
Sentence |
denotes |
• CRP normalized in 5 patients by day 11 |
T171 |
4166-4205 |
Sentence |
denotes |
• Halted progression of CT lung lesions |
T172 |
4206-4276 |
Sentence |
denotes |
• 100% survival • Small case series, potential for confounding factors |
T173 |
4277-4327 |
Sentence |
denotes |
• Potential therapy to target inflammatory cascade |
T174 |
4328-4424 |
Sentence |
denotes |
• Positive results in patients with hypertension and other CVD risk factors (Aouba et al., 2020) |
T175 |
4425-4442 |
Sentence |
denotes |
• Ana-COVID study |
T176 |
4443-4531 |
Sentence |
denotes |
• Anakinra for COVID-19 hyperinflammatory state • Prospective/retrospective cohort study |
T177 |
4532-4581 |
Sentence |
denotes |
• Hospitalized adults with critical lung function |
T178 |
4582-4635 |
Sentence |
denotes |
• Cohort with CVD (hypertension, stroke, cardiopathy) |
T179 |
4636-4707 |
Sentence |
denotes |
• Primary outcome of ICU admission with mechanical ventilation or death |
T180 |
4708-4742 |
Sentence |
denotes |
• N = 52 anakinra + standard care |
T181 |
4743-4812 |
Sentence |
denotes |
• N = 44 standard care • Anakinra 100 mg s.c. twice daily for 3 days |
T182 |
4813-5105 |
Sentence |
denotes |
• Then anakinra 100 mg s.c. once daily for 7 days • Significantly reduced need for mechanical ventilation or death HR 0.22 (0.11–0.41) • Anakinra may be associated with improved outcomes in patients with severe COVID-19 infection, including those with CVD and history of cardiovascular events |
T183 |
5106-5176 |
Sentence |
denotes |
• May be due to mitigation of inflammatory cascade (Huet et al., 2020) |