Table 2.
GRADE summary of quality of evidence for primary outcomes: tranexamic acid vs. control treatment in aneurysmal subarachnoid hemorrhage.
| Quality assessment | No of patients | Effect | Quality | Importance | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| No of studies | Design | Risk of bias |
In consis tency |
In direct ness |
Impre cision |
Other conside rations |
TXA | Control | Relative (95% CI) | Absolute | ||
| All-cause mortality | ||||||||||||
| 12 | RCTs | Seriousb | not serious | not serious | Seriousc | none | 417/1702 (24.5%) | 426/1679 (25.4%) | RR 0.97 (0.86 to 1.08) | 8 fewer per 1,000 (from 36 fewer to 20 more) | ⊕⊕○○ LOW | CRITICAL |
| Poor outcome | ||||||||||||
| 5 | RCTs | seriousb | not serious | not serious | Seriousc | none | 503/1249 (40.3%) | 481/1242 (38.7%) | RR 1.04 (0.95 to 1.15) | 15 more per 1,000 (from 19 fewer to 58 more) | ⊕⊕○○ LOW | CRITICAL |
| Rebleeding | ||||||||||||
| 11 | RCTs | serious | Seriousa | not serious | not serious | none | 162/1423 (11.4%) | 284/1416 (20.1%) | RR 0.59 (0.43 to 0.82) | 82 fewer per 1,000 (from 36 fewer to 114 fewer) | ⊕⊕○○ LOW | CRITICAL |
| Cerebral ischemia | ||||||||||||
| 8 | RCTs | Seriousb | Seriousa | not serious | Seriousc | none | 384/1328 (28.9%) | 340/1318 (25.8%) | RR 1.17 (0.95 to 1.46) | 44 more per 1,000 (from 13 fewer to 119 more) | ⊕○○○ VERY LOW | IMPORTANT |
| Hydrocephalus | ||||||||||||
| 7 | RCTs | Seriousb | not serious | not serious | Seriousc | none | 436/1091 (40%) | 399/1089 (36.6%) | RR 1.09 (0.99 to 1.2) | 33 more per 1,000 (from 4 fewer to 73 more) | ⊕⊕○○ LOW | IMPORTANT |
| VTE | ||||||||||||
| 7 | RCTs | Seriousb | not serious | not serious | Seriousc | none | 40/1078 (3.7%) | 34/1073 (3.2%) | RR 1.16 (0.75 to 1.8) | 5 more per 1000 (from 8 fewer to 25 more) | ⊕⊕○○ LOW | IMPORTANT |
Serious imprecision due to high I2 (>50%) and non-overlapping confidence intervals.
Serious risk of bias due to lack of blinding of participants and personnel in some studies.
Serious imprecision due to confidence interval including benefit and harm or low number of events below optimal information size.