TABLE 1.
Summary of the Recruitment Process and Visit Plan
Enrolment | Study period | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
preoperative (V0) | intraoperative (V1) | Postoperative (V2.1, V2.2, etc.) | 3-mo follow-up (V3) | 1-yr follow-up (V4) | ||||||
Time point | −7d±7 | 0 | 1d | 2d | 3d | 4d | etc. | 90d±14 | 360d±14 | |
Eligibility screen | X | — | — | — | — | — | — | — | — | — |
Informed consent | X | — | — | — | — | — | — | — | — | — |
Demographic data | — | X | — | — | — | — | — | — | — | — |
Medical history | — | X | — | — | — | — | — | — | X | X |
Cognitive testing | — | X | — | — | — | — | — | — | X | X |
Activities of daily living | X | — | — | — | — | — | — | X | — | |
Frailty | — | X | — | — | — | — | — | — | — | — |
Quality of life | — | X | — | — | — | — | — | — | X | — |
Vital parameters | — | — | X | — | — | — | — | — | — | — |
Delirium screening | — | X | — | X | X | X | X* | X* | — | — |
Medication | — | X | X | X | X | X | X* | X* | X | X |
Pain | — | X | — | X | X | X | X* | X* | — | — |
Mobilization | — | — | — | X | X | X | X* | X* | — | — |
Study visits V0-V4 had to be completed by all participants. V2 included compulsory examinations for the first three days, which were discontinued if the patients did not develop POD.17
Examinations were otherwise continued until POD ended or the patient was discharged.