Table 2. Qualitative assessment of included studies.
Reference | Randomisation | Allocationconcealment | Blinding | Intentionto TreatAnalysis | Loss tofollow-up |
Rackow et al [23] | Low risk | Unclear riskd | High risk | Low risk | Low risk |
Metildi et al [25] | Low risk | Unclear riskd | High risk | Low risk | Low risk |
Rackow et al [24] | Unclear riska | Unclear riskd | High risk | Low risk | Low risk |
SAFE [13] | Low risk | Low risk | Low risk | Low risk | Low risk |
Veneman et al [29] | Unclear riska | Low risk | High risk | Low risk | Low risk |
Maitland et al [30] | Unclear riska | Low risk | High risk | Low risk | Low risk |
Maitland et al [31] | Unclear riska | Low risk | High risk | Low risk | Low risk |
Akech et al [26] | High riskb | Unclear riskd | High risk | Low risk | Low risk |
Friedman et al [22] | Unclear riska | Low risk | High risk | Low risk | High riskc |
van der et al [27] | Unclear riska | Low risk | High risk | Low risk | Low risk |
Dolecek et al [28] | Low risk | Unclear riskd | High risk | Low risk | Low risk |
FEAST [36] | Low risk | Low risk | High risk | Low risk | Low risk |
EARSS [20] | Unclear riske | Unclear riske | High risk | Unclear riske | Unclear riske |
CRISTAL [37] | Low risk | Low risk | High risk | Low risk | Low risk |
ALBIOS [21] | Low risk | Low risk | High risk | Low risk | Low risk |
Just mention the word of random.
A quasi-randomised design was used, whereby fluid interventions were allocated sequentially in blocks of ten.
4 patients (11%) were excluded because of inadequate data collection.
not reported.
The research has not yet been published.