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Clinical Trial
. 2018 Aug;72(8):1159-1166.
doi: 10.1038/s41430-018-0256-1. Epub 2018 Jul 13.

Safety and efficacy of n-3 fatty acid-based parenteral nutrition in patients with obstructive jaundice: a propensity-matched study

Affiliations
Clinical Trial

Safety and efficacy of n-3 fatty acid-based parenteral nutrition in patients with obstructive jaundice: a propensity-matched study

Qiong Gong et al. Eur J Clin Nutr. 2018 Aug.

Abstract

Background: It is reported that lipid emulsion enriched in n-3 fatty acids (FAs) helps us to improve postoperative recovery for surgical patients with biliary tract disease. Its role for postoperative patients with obstructive jaundice is as yet unclear. The object of this study was to evaluate the safety and efficacy of n-3 fatty acid-based parenteral nutrition (PN) for patients with obstructive jaundice following surgical procedures.

Methods: Data were collected from patients with obstructive jaundice who received PN, including n-3 PUFA-enriched lipid emulsions and standard non-enriched lipid emulsions (e.g., soybean oil). We then calculated a propensity score, the probability of receiving different PN, by the propensity score matched (PSM) method. After matching, we compared isonitrogenous total PN with 20% Structolipid and 10% n-3 fatty acid (Omegaven, Fresenius-Kabi, Germany) (treatment group) to Structolipid alone (control group) for 5 days postoperatively, in the absence of enteral nutrition.

Results: Before the propensity score matching, there were 226 patients enrolled. After propensity score stratification, 108 cases remained, and all covariates were balanced. Among matched patients with PN, patients in the control group were at a higher risk for long-term jaundice recovery (12.9 ± 8.5 VS 16.4 ± 7.9 P = 0.029), lower velocity of reduction in jaundice (P = 0.045), and lower pre-albumin (P = 0.002). No significant difference as found in terms of comorbidities, white blood cell (WBC), albumin and other aspects.

Conclusion: PN with n-3 PUFA-enriched lipid emulsions was safe and effective in accelerating jaundice recovery for patients after surgical procedures. This trial was registered at clinicaltrials.gov as NCT03376945.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Flow chart of cohort (It shows the process of screening the patients treated or untreated with n-3 FA in the initial and final propensity score matched sample. We screened a total of 827 patients with obstructive jaundice in Tongji Hospital between May 2014 and June 2017. Finally, 108 cases were enrolled into the PSM cohort for the last statistical calculation)
Fig. 2
Fig. 2
The differences of inflammatory reaction between two groups after operation. There were no differences in WBC or GRAN between two groups (P = 0.943, P = 0.410), respectively
Fig. 3
Fig. 3
During the postoperative period, patients in the n-3 group had rapid jaundice recovery (a) (P = 0.045), shorter duration of the jaundice recovery (b) (P = 0.029), lower cholesterol (c) (P = 0.045) and higher pre-albumin (d) (P= 0.002),

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