Certainty assessment | Number of patients | Effect | Certainty | Importance | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
No. of studies | Study design | Bias risk | Inconsistency | Indirectness | Inaccuracy | Other | Intra-venous | Intra-peritoneal | Relative [95% CI] | Absolute (95% CI) | ||
PD withdrawal (Primary treatment failure) | ||||||||||||
2 | RCT | Serious a | Not serious | Not serious | Serious b | None | 13/46 (28.3%) | 4/49 (8.2%) | Cannot estimate | 130 patients decreased per 1000 patients (430 patients decreased to 170 patients increased) (calculated using risk differences) | ⨁⨁◯◯ Low | Critical |
Complications (drug adverse events/safety) | ||||||||||||
2 | RCT | Serious a | Not serious | Not serious | Serious b | None | 4/47 (8.5%) | 0/49 (0.0%) | RR 5.13 [0.63–41.59] | No change per 1000 patients | ⨁⨁◯◯ Low | Critical |
Complications (Infusion pain, vascular leakage of vancomycin) (see Note e) | ||||||||||||
1 | RCT | Serious a | Not serious | Very serious c | Very serious d | None | 1/10 (10.0%) | 0/10 (0.0%) | RR 3.00 [0.14–65.90] | No change per 1000 patients | ||
Peritonitis successfully treated—not reported | ||||||||||||
- | - | - | - | - | - | - | - | - | - | - | - | Critical |
Time till peritonitis successfully treated—not reported | ||||||||||||
- | - | - | - | - | - | - | - | - | - | - | - | Critical |
Reoccurrence of peritonitis—not reported | ||||||||||||
- | - | - | - | - | - | - | - | - | - | - | - | Critical |