Perioperative medicine & outcomes

Impact of a multimodal prehabilitation program on postoperative cognitive dysfunction: a single-center randomized controlled trial

J Clin AnesthPublished Prespecified substudy of a single-centre randomised controlled trial

Primary result · POCDResult — go to the resultOdds ratio 1.37 95% CI 0.54–3.50

Authors' conclusion

In this randomized controlled trial, a 4-6-week multimodal prehabilitation program did not reduce postoperative cognitive dysfunction 3 months after cardiac surgery.

Study context

Population
Patients aged ≥50 years undergoing elective CABG and/or valve surgery116 completed 3-month follow-up
Participants
134 patients
Comparison
4-6 weeks multimodal prehabilitation vs standard preoperative care
  • Prehabilitationn = 53
  • Controln = 63reference
Primary endpoint
POCD (≥1.5 SD below normative values in at least 2 cognitive tests, excluding the Mini-Mental State Examination)
Follow-up
3 months

Primary result

POCD

Odds ratio

1.37

95% CI 0.54–3.50

P = 0.52

Events by treatment group

Prehabilitation vs Control
OR 1.37 (95% CI 0.54–3.50); P = 0.52

As reported in the abstract

Further findings

Factors associated with postoperative cognitive dysfunction (POCD) (multivariable analysis): preoperative cognitive impairment

OR (95% CI)P value
Preoperative cognitive impairmentIndependently associated13.28 (4.06–43.41)P < 0.001
OutcomeOR (95% CI)P value
Factors associated with POCD (multivariable analysis): prehabilitationNot independently associated1.09 (0.35–3.45)P = 0.877

Physical activity levels at 3 months and POCD

OR (95% CI)P value
Higher physical activity levelsAssociated with lower odds of POCD0.97 (0.95–1.00)P = 0.047

Original publication

Impact of a multimodal prehabilitation program on postoperative cognitive dysfunction: a single-center randomized controlled trial. J Clin Anesth. Published 14 August 2026. doi:10.1016/j.jclinane.2026.112300

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