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. 2018 Jun 25;10(7):820. doi: 10.3390/nu10070820

Table 3.

Summary of studies included within review.

Study Design and Sample Size Patient, Population. or Problem Intervention, Prognostic
Factor or Exposure
Comparison or Intervention Outcomes Main Findings
Dreyer et al., 2013 [20] RCT n = 28 TKR patients 20 g of essential amino acids (EAA) twice daily between meals for 1 week before and 2 weeks after TKR. Placebo supplementation (20 g (100% alanine) Muscle atrophy, muscle strength, and functional mobility. The placebo group exhibited greater quadriceps muscle atrophy (−14.3 ± 3.6% change) from baseline to 2 weeks post-surgery. EAAs also attenuated atrophy in the non-operated quadriceps and in the hamstring and adductor muscles of both extremities. The EAA group demonstrated better functional mobility at 2 and 6 weeks post-operatively (all p < 0.05).
Nishizaki et al., 2015 [21] RCT n = 23 TKR patients Beta-hydroxy beta-methylbutyrate (HMB; 2400 mg), l-arginine (Arg; 14,000 mg) and l-glutamine (Gln; 14,000 mg) (HMB/Arg/Gln) (158 kcal of energy) for 5 days before the surgery and for 28 days after the surgery. Patients fasted on the day of surgery. Control food (orange juice, 226 kcal of energy and 280 mg of protein) Body weight, bilateral knee extension strength, rectus femoris cross-sectional area. Maximal quadriceps strength was 1.1 ± 0.62 Nm/kg pre-surgery and 0.7 ± 0.9 Nm/kg 14 days post-surgery in the control group (p = 0.02). In the HMB/Arg/Gln group, maximum quadriceps strength was 1.1 ± 0.3 Nm/kg before surgery and 0.9 ± 0.4 Nm/kg 14 days after surgery. The muscle loss was significant in the control group, but not in the intervention group.
Alito and de Aguilar-Nascimento 2016 [22] Pilot RCT n = 32 THR patients 6 h pre-operative fasting for solids, an oral drink (200 mL of 12.5% maltodextrin) up to 2 h before induction of anesthesia, restricted intravenous fluids (only 1000 mL of cystalloid fluid after surgery), and pre-operative immune nutrition (600 mL/day of Impact—Nestle, Brazil) for 5 days prior to surgery. Control group (traditional care, 6–8 h of pre-operative fasting, intravenous hydration until the 1st post-operative day and no pre-operative immune supplementation) Length of stay, C-reactive protein. Median length of stay (LOS) was 3 (2–5) days in the intervention group and 6 (3–8) days in controls (p < 0.01). Post-operative C-reactive protein was higher in the control group (p < 0.001).
Aronsson et al., 2008 [23] Pilot RCT n = 29 THR patients Carbohydrate-rich drink (an iso-osmolar carbohydrate-rich solution: 12.5 g carbohydrate/100 mL, pH 5.0) pre-operatively. Placebo drink (flavored water) IGF-1 and IGFBP-1 were determined in serum by RIA. Body composition was determined by dual energy X-ray absorptiometry (performed the day before surgery and at 6–8 weeks after surgery) Compared to placebo, the authors found a relative increase in IGF-1 bioavailability post-operatively after a carbohydrate-rich drink given shortly before surgery. There were no significant differences in the changes in fat or lean body mass between groups (p = 0.08).
Hartsen et al., 2012 [24] RCT n = 60 ASA physical status I–III patients scheduled for THR 400 mL of an oral 12.5% carbohydrate solution Placebo drink (flavored water) Visual analog scales were used to score six discomfort parameters. Immediately after surgery, carbohydrate-treated patients were less hungry (median scores 9.5 vs. 22 mm) and experienced less nausea (0 vs. 1.5 mm) (p < 0.05).
Ljunggren and Hahn 2012 [25] RCT n = 57 THR patients Tap Water: 800 mL by mouth, 2 h before entering the operating room OR
Nutrition: an iso-osmolar carbohydrate drink (50 kcal/100 mL) 800 mL in the evening before the surgery (day 0), and 400 mL 2 h before entering the operating room (day 1).
Fasting (no food or water from midnight before the surgery) Intravenous glucose tolerance, physical stress, muscle catabolism, body fluid volumes, complications, wellbeing, and insulin sensitivity. Pre-operative ingestion of tap water or a nutritional drink had no statistically significant effect on glucose clearance, insulin sensitivity, post-operative complications, or wellbeing in patients undergoing THR.
Nygren et al., 1999 [26] RCT n = 16 THR patients Pre-operative oral iso-osmolar carbohydrate administration (800 mL 12.5% carbohydrates), the evening before the operation. Another 400 mL of the same beverage was allowed 2 h after midnight, taken no later than 2 h before the initiation of anesthesia. Placebo drink Insulin sensitivity Patients given a carbohydrate drink shortly before elective surgery displayed less reduced insulin sensitivity (−16% (not significant)) after surgery compared to patients undergoing surgery after an overnight fast (37% p < 0.05 vs. pre-operatively). Insulin sensitivity and whole-body glucose disposal were reduced in both groups.
Soop et al., 2001 [27] RCT n = 15 THR patients Carbohydrate-rich drink (12.5 g/100 mL carbohydrate, 12% monosaccharides, 12% disaccharides, 76% polysaacharides, 285 mosmol/kg), 800 mL between 7 p.m. and 12:00 a.m. on the evening before surgery and 400 mL on the morning of surgery. Placebo drink (acesulfame-K, 0.64 g/100 mL citrate, 107 mosmol/kg) Glucose, lactate and insulin concentrations, glycerol, NEFA, glucoregulatory hormone concentrations, glucose kinetics, and substrate utilization. Whole-body insulin sensitivity decreased by 18% in the intervention group vs. 43% in the placebo group. This was attributable to a less reduced glucose disposal in peripheral tissues and increased glucose oxidation rates.
Soop et al., 2004 [28] RCT n = 14 THR patients Carbohydrate rich drink (12.5 g /100 mL carbohydrate, 12% monosaccharides, 12% disaccharides, 76% polysaacharides, 285 mosm/kg, 800 mL between 7 p.m. and 12:00 a.m. on the evening before surgery and 400 mL on the morning of surgery. Placebo drink Glucose kinetics, substrate utilization, nitrogen balance, ambulation time, food consumption, and LOS. Whole-body glucose disposal and nitrogen balance were similar between groups. Pre-operative carbohydrate treatment significantly attenuated post-operative endogenous glucose release (0.69 (0.07) vs. 1.21 (0.13) mg kg−1, (p < 0.01), compared to the placebo group. Whole-body glucose disposal and nitrogen balance were similar between groups.

RCT = Randomized Clinical Trial; IGF = Insulin like growth factor; IGFBP = Insulin like growth factor binding protein; RIA = Radioimmunoassay; ASA = American Society of Anesthesiologists; NEFA = nonesterified free fatty acid.