What to know
Note: Overall risk of bias was calculated by dividing the total number of valuable trial characteristics by the total number of possible characteristics and applying these categories:
- ≤ 25% = high risk of bias;
- > 25% to ≤ 50% = moderate risk of bias;
- > 50% = low risk of bias.
Table 8: Evaluation of Risk of Bias in Studies Using C-I Dressings among Patients Aged ≥ 18 Years with Short-term, Non-tunneled Central Venous Catheters
| Author Publication Year |
Arvaniti 20124 |
Roberts 19985 |
Ruschulte 20093 |
Timsit 20092 |
Timsit 20121 |
|---|---|---|---|---|---|
| Described as randomized | ✓ | ✓ | ✓ | ✓ | ✓ |
| Randomization appropriately performed | ✓ | ✓ | ✓ | ✓ | |
| Described as double–blind | |||||
| Outcome assessor blinded | ✓ | ✓ | ✓ | ✓ | |
| Study participant blinded | |||||
| Investigator blinded | |||||
| Attrition described | ✓ | ✓ | ✓ | ✓ | ✓ |
| Attrition smaller than 10–15% of assigned patients | ✓ | n/a | ✓ | ✓ | ✓ |
| Attrition appropriately analyzed | ✓ | n/a | ✓ | ✓ | ✓ |
| Funding source(s) disclosed and no obvious conflict of interest | |||||
| Overall Risk of Bias | Low | Moderate | Low | Low | Low |
Table 9: Evaluation of Risk of Bias in Studies Using C-I Dressings among Patients Aged < 18 Years with Short-term, Non-tunneled Central Venous Catheters
| Author Publication Year |
Garland 20016 |
Levy 20058 |
Duzkaya 20167 |
|---|---|---|---|
| Described as randomized | ✓ | ✓ | ✓ |
| Randomization appropriately performed | ✓ | ✓ | ✓ |
| Described as double–blind | |||
| Outcome assessor blinded | |||
| Study participant blinded | |||
| Investigator blinded | |||
| Attrition described | ✓ | ✓ | ✓ |
| Attrition smaller than 10–15% of assigned patients | ✓ | ||
| Attrition appropriately analyzed | |||
| Funding source(s) disclosed and no obvious conflict of interest | |||
| Overall Risk of Bias | Moderate | Moderate | Moderate |