Impact of withholding early parenteral nutrition in adult critically ill patients on ketogenesis in relation to outcome

Withholding parenteral nutrition until one week after intensive care unit (ICU) admission (late-PN) was previously shown to accelerate recovery and reduce infections in critically ill adults and children, as compared to early supplementing insufficient enteral feeding with parenteral nutrition (early-PN) [1, 2]. In a detailed secondary analysis of the pediatric PEPaNIC randomized controlled trial (RCT), we previously identified enhanced ketogenesis as potential mediator of part of this outcome benefit. Indeed, late-PN increased plasma concentrations of the ketone 3-hydroxybutyrate (3HB) up to sixfold, with a peak effect on day 2 [3]. Increased 3HB independently associated with an accelerated weaning from mechanical ventilation and a shorter time to live ICU discharge. These associations remained significant after adjusting for ketogenic regulators, suggesting a direct mediator role [3].

In this secondary analysis of patients included in the EPaNIC RCT (n = 4640), we studied whether late-PN had a similar impact on ketones in critically ill adults as compared with early-PN, and whether this may have mediated its outcome benefits. To this purpose, we quantified plasma 3HB with an enzymatic assay [3] in the predefined subgroup of patients with a surgical contraindication to enteral nutrition [1]. In this subgroup (509/517 patients with available plasma), there was a larger difference in caloric intake than in the total study population (Fig. 1a), and the outcome benefits of late-PN appeared to be more pronounced [1] (Table1).

We first performed a time course analysis in a propensity-score-matched subset of 110 patients (Table 1), to study whether late-PN enhanced ketogenesis and to identify the day of maximal effect (if any) (Fig. 1b). In the matched subset, late-PN significantly increased plasma 3HB from day 1 until day 7 (all P ≤ 0.0013), with a maximal effect on day 2. Subsequently, we quantified plasma 3HB on this day of maximal effect in all patients with a surgical contraindication to enteral nutrition. In these patients, late-PN significantly (P < 0.0001) increased plasma 3HB. Thereafter, we studied a potential mediator role of this 3HB effect on time to live ICU discharge, live ICU discharge within 8 days, and incidence of new infection through multivariable Cox, respectively logistic regression analysis, adjusted for baseline risk factors (age, BMI, malignancy, APACHEII score, NRS score, diagnostic group). Plasma 3HB did not independently associate with time to live ICU discharge (P = 0.54), live ICU discharge within 8 days (P = 0.23) or incidence of new infection (P = 0.71).

We demonstrated that withholding early parenteral nutrition induced ketogenesis in adult ICU patients with a surgical contraindication to enteral nutrition [3]. However, ketone concentrations were only modestly elevated as compared to the much larger effect in critically ill children, and in contrast to critically ill children, plasma 3HB did not independently associate with enhanced recovery. Also in health, the ketogenic response is known to be more pronounced in children than in adults [4]. Although speculative, this may explain why critically ill children had a more pronounced outcome benefit than adults [1, 2]. Also in critically ill children, however, there was no independent association of 3HB with incidence of infections, which suggests that other mechanisms are involved in outcome protection through late-PN. In this regard, we previously identified increased autophagy as one potential mediator [5]. Of note, especially in early-PN adult patients, a considerable number of 3HB measurements were assigned the detection limit (0.04 mmol/L) due to lower concentrations, which may have obscured detecting a mediating role of ketones on outcome.

In conclusion, withholding early parenteral nutrition enhanced ketogenesis in critically ill adults, but in contrast to children, increased ketones did not explain the improved outcome. This suggests clinical benefits of omitting early-PN were mediated through other mechanisms.