Number | Inclusion criteria |
1 | Original prospective cohort studies or randomized controlled trials (RCTs) published in full text and those for which we had full access to all original data and protocols. |
2 | The studies evaluated the differences of the effect of propofol and sevoflurane on postoperative cognitive functions. |
3 | Regarding the intervening measures between different groups, the only difference is that the two groups received propofol or sevoflurane, respectively. Other conditions should be the same. |
4 | Human studies. |
5 | Predefined outcomes: incidence of postoperative MMSE scores and the plasma protein S100β at various time points. |
6 | No minimal sample size or dosing regimen was required for inclusion. |
Number | Exclusion criteria |
1 | The study did not have a control group of patients without propofol use or sevoflurane use. |
2 | They were case studies or case series. |
3 | The report focused exclusively on other topics or outcomes. |
4 | No human data were included. |
5 | Except for the difference of anaesthetic administration, there were other differences between the experimental groups and the control groups. |
6 | Reviews and duplicated publications. |