Key result
Postoperative atrial fibrillation occurred in 24.36% of patients undergoing CABG in an interim blinded analysis of an ongoing trial evaluating prophylactic Tocovid, with treatment comparisons pending.
Why the study?
Post-operative atrial fibrillation is linked to poorer outcomes and driven by inflammation and oxidative stress, leading to the hypothesis that antioxidant tocotrienol could prevent it.
Does prophylactic Tocovid (tocotrienol) reduce the occurrence of postoperative atrial fibrillation in patients undergoing elective on-pump CABG or CABG and valve surgery?
RCT (n=202)
Double-blind
Computer-generated randomisation list
No
Does prophylactic Tocovid (tocotrienol) reduce the occurrence of postoperative atrial fibrillation in patients undergoing elective on-pump CABG or CABG and valve surgery?
This interim blinded analysis of an ongoing RCT reports a 24.36% incidence of postoperative atrial fibrillation following CABG, with final unblinded results pending to determine the efficacy of prophylactic tocotrienol.
INTRODUCTION: Post-operative atrial fibrillation (POAF) is associated with poorer outcomes, increased resource utilisation, morbidity and mortality. Its pathogenesis is initiated by systemic inflammation and oxidative stress. It is hypothesised that a potent antioxidant and anti-inflammatory agent such as tocotrienol, an isomer of Vitamin E, could reduce or prevent POAF. AIMS: The aim of this study is to determine whether a potent antioxidative and anti-inflammatory agent, Tocovid, a tocotrienol-rich capsule, could reduce the incidence of POAF and affect the mortality and morbidity as well as the duration of ICU, HDU and hospital stay. METHODS: This study was planned as a prospective, randomised, controlled trial with parallel groups. The control group received placebo containing palm superolein while the treatment group received Tocovid capsules. We investigated the incidence of POAF, the length of hospital stay after surgery and the health-related quality of life. RESULTS: Recruitment commenced in January 2019 but the preliminary results were unblinded as the study is still ongoing. Two-hundred and two patients have been recruited out of a target sample size of 250 as of January 2021. About 75% have completed the study and 6.4% were either lost during follow-up or withdrew; 4% of participants died. The mean age group was 61.44 ± 7.30 years with no statistical difference between the groups, with males having a preponderance for AF. The incidence of POAF was 24.36% and the mean time for developing POAF was 55.38 ± 29.9 h post-CABG. Obesity was not a predictive factor. No statistically significant difference was observed when comparing left atrial size, NYHA class, ejection fraction and the premorbid history. The mean cross-clamp time was 71 ± 34 min and the mean bypass time was 95 ± 46 min, with no difference between groups. There was a threefold increase in death among patients with POAF (p = 0.008) and an increase in the duration of ICU stay (p = 0.01), the total duration of hospital stay (p = 0.04) and reintubation (p = 0.045). CONCLUSION: A relatively low incidence rate of POAF was noted although the study is still ongoing. It remains to be seen if our prophylactic intervention using Tocovid would effectively reduce the incidence of POAF. Clinical Registration Number: US National Library of Medicine. Clinical Trials - NCT03807037. Registered on 16th January 2019. Link: https://clinicaltrials.gov/ct2/show/NCT03807037.
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Musa et al. (2021) conducted an RCT in Postoperative atrial fibrillation (POAF) (n=202). Tocovid (tocotrienol-rich capsule) vs. Placebo (palm superolein) was evaluated on Occurrence of postoperative atrial fibrillation (POAF) of at least 30-s duration. Postoperative atrial fibrillation occurred in 24.36% of patients undergoing CABG in an interim blinded analysis of an ongoing trial evaluating prophylactic Tocovid, with treatment comparisons pending.
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