Our ability to risk assess is poor and we seem to be driven by fear and hope as much as by rational evidence.
The overall immunogenicity of influenza vaccine across time points and the three influenza strains assessed was poor (Range HAI ≥40 = 31 58%).
The overall quality of reporting of the RCTs assessed was poor to moderate, with only 4 of the 15 items being reported in over 90% of the articles.
Comments: Broselow tape 2007 edition B. Only colour zone accuracy was assessed, which was poor in children > 18 kg.
However, the external validity of assessing change was poor in the PROMIS PF and UE as well as some follow-up time points of the PROMIS PI and qDASH when mean scores were compared in the subsamples with no-change in condition versus meaningful change.
In age adjusted models, there was evidence in the majority of studies that lower childhood SEP (i.e. less affluence), however it had been assessed, was associated with poorer physical capability levels, however this was assessed (Figures 3 6).
Overall, information from the included trials needed to assess risk of bias was poor and therefore the trials were graded as unclear for most domains.
Outcomes assessed were self-reported poor overall health and psychological distress.
The predictive value for bacteraemia was poor for all assessed clinical parameters.
Quality of reporting assessed using CONSORT criteria was poor.
