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Original Research Communication |
1 From the Department of Human Nutrition and Dietetics and the Division of Epidemiology, University of Illinois at Chicago.
2 Address reprint requests to CL Braunschweig, University of Illinois at Chicago, Department of Human Nutrition, 1919 W Taylor Street (M/C 517), Chicago, IL 60612. E-mail: braunsch{at}uic.edu.
| ABSTRACT |
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Objective: We reviewed systematically and aggregated statistically the results of prospective randomized clinical trials (PRCTs) to examine the relations among the nutrition interventions, complications, and mortality rates.
Design: We conducted a MEDLINE search for PRCTs comparing the effects of enteral and parenteral nutrition in adults. Two different people abstracted data for the method and outcomes separately. We used fixed-effects meta-analysis technique to combine the relative risks (RRs) of the outcomes of infection, nutrition support complications, other complications, and mortality.
Results: Twenty-seven studies in 1828 patients met the study criteria. Aggregated results showed a significantly lower RR of infection with tube feeding (0.64; 95% CI: 0.54, 0.76) and standard care (0.77; 95% CI: 0.65, 0.91). A priori hypotheses showed a lower RR of infection with tube feeding than with parenteral nutrition, regardless of nutritional status, presence of cancer, year of study publication, or quality of the study method. In studies in which participants had high rates of protein-energy malnutrition, there was a significantly higher risk of mortality (3.0; 95% CI: 10.9, 8.56) and a trend toward a higher risk of infection with standard care than with parenteral nutrition (1.17; 95% CI: 0.88, 1.56).
Conclusions: Tube feeding and standard care are associated with a lower risk of infection than is parenteral nutrition; however, mortality is higher and the risk of infection tends to be higher with standard care than with parenteral nutrition in malnourished populations.
Key Words: Meta-analysis enteral nutrition parenteral nutrition prospective randomized clinical trials tube feeding oral diets intravenous dextrose MEDLINE
| INTRODUCTION |
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| METHODS |
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Nutritional interventions
Parenteral nutrition is designed to provide nutrition to patients who cannot be nourished adequately by enteral nutrition for a critical period of time. Because of the inherent risk and higher cost of parenteral nutrition, it should not be used as a substitute for enteral nutrition if either standard care or tube feeding is feasible. Also, because of physiologic changes that are caused by gastrointestinal tract dysfunction, outcomes observed in populations with functional gastrointestinal tracts might be different from those observed in populations without adequate gastrointestinal function. The criteria met by populations included in the meta-analysis are listed in Table 1
. Tube feeding was defined as either surgical or nonsurgical placement of a small flexible tube into the gastrointestinal tract to provide required nutrients. Standard care was defined as the gradual reintroduction of an oral diet as tolerated after its interruption was caused by a disease or a surgical procedure that resulted in several days of inadequate nutrient intake and the use of intravenous dextrose or fluids for hydration.
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The method used in each study was evaluated for the quality of these characteristics: concealed randomization, comparability of groups at baseline, endpoints (blinded to staff or not), well-described treatment protocols, well-defined outcomes, and analysis by intent to treat. One point was given for each of these traits and a study-quality score that ranged from 0 to 6 for each investigation was calculated. Studies were categorized into those with low study-quality score (<4 points) and those with a high study-quality score (
4 points), and separate subgroup analyses were performed for each category.
PEM in hospitalized patients has been associated with high rates of morbidity and mortality (46). To address this possible source of heterogeneity, the nutritional status of patients at the time of enrollment was examined. Each investigator's definition of PEM was used when possible. When this was not specifically stated, an unplanned body weight loss of
15% of normal body weight was used as the cutoff for PEM classification. Studies were categorized into 2 groups on the basis of the percentage of participants with PEM (% PEM) those with <50% (low) and those with
50% (high), and the subgroups were analyzed separately.
The skill with which specialized nutrition support is provided has improved since it was first used in patient care. To assess whether time-induced changes led to discrepant results, studies were divided into equal groups of those that were relatively recent (1992 or later) and those that were not recent (earlier than 1992) publications, and separate subgroup analyses were performed for each category.
Finally, because previous investigations reported little or no effect of specialized nutrition support on outcomes in cancer patients (7), we speculated that differences in outcomes might be caused by the presence of cancer in the patients. Therefore, the studies were categorized into 2 groups on the basis of the percentage of participants with cancer: <50% (low) and
50% (high), and the subgroups were analyzed separately.
Analysis
The PRCTs were divided into 2 categories: 1) tube feeding compared with parenteral nutrition and 2) standard care compared with parenteral nutrition. This categorization allowed for the examination of aggregated differences observed in outcomes when the route of aggressive nutrition support varied (tube feeding compared with parenteral nutrition) and when aggressive intravenous nutrition support was compared with little or no nutritional intervention (standard care compared with parenteral nutrition). To avoid the loss of each group's independence, meta-analysis techniques were used to prevent any group from being compared with more than one other group. For example, a parenteral nutrition group could not be compared with a tube-fed group and then with a standard care group because it would then not be an independent comparison. Hence, 5 investigations used a method to randomly assign patients that resulted in some of the groups being eliminated from our analysis. Holter and Fischer (8) and Thompson et al (9) randomly assigned patients to normally nourished standard care control, malnourished parenteral nutrition, and malnourished standard care groups; only the malnourished parenteral nutrition and standard care groups were included in the analysis. Greenberg et al (10) randomly assigned patients to parenteral nutrition, tube-fed, partial parenteral nutrition, and partial standard care groups; only those in the parenteral nutrition and tube-fed groups were included in the analysis. Dunham et al (11) randomly assigned patients to parenteral nutrition, tube-fed, partial parenteral nutrition, and partial enteral nutrition groups; only those randomly assigned to the parenteral nutrition and tube-fed groups were included in the analysis. Von Meyenfeldt et al (12) randomly assigned patients to 4 groups: malnourished parenteral nutrition, malnourished tube- fed, malnourished standard care, and normally nourished standard care groups; only the malnourished parenteral nutrition and tube-fed groups were included.
RRs and 95% CIs were calculated for each investigation and for each outcome variable. A fixed-effects meta-analysis technique modeled after the Mantel-Haenszel method was used to estimate summary RRs and their 95% CIs (13). CIs for the common RR that did not include unity were considered significant. To determine whether the investigations within each group for each outcome had widely discrepant RRs, a test for heterogeneity was done (14). We considered P < 0.05 to be statistically significant.
| RESULTS |
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In studies in populations with high percentages of PEM, standard care was associated with a significantly higher risk of mortality (RR: 3.0; 95% CI: 1.09, 8.56; Figure 7
) and a trend toward a higher risk of infection (RR: 1.17, 95% CI: 0.88, 1.56; Figure 5
) than was parenteral nutrition. The risk of infection was found to be lower for standard care than for parenteral nutrition in the relatively recent studies (RR: 0.62; 95% CI: 0.50, 0.76), studies with low rates of PEM (RR: 0.61; 95% CI: 0.50, 0.76), studies with a high percentage of patients with higher study-quality scores (RR: 0.63; 95% CI: 0.49, 0.80), and studies with a high percentage of patients with cancer (RR: 0.78; 95% CI: 0.65, 0.92; Figure 5
). Subgroup analyses could not be completed for nutrition support complications because of the insufficient number of studies that reported this information. The risk of other complications was lower for standard care than for parenteral nutrition in studies with lower study-quality scores (RR: 0.61; 95% CI: 0.4, 0.91). Additional analysis for other complications could not be completed because of the inadequate numbers in the different categories.
To determine whether the lower risk of infection observed with enteral nutrition was due to the categorization of catheter sepsis as an infection instead of a nutritional support complication, these events were removed. The RRs and 95% CIs were recalculated for studies that reported them, and new aggregated RRs were calculated. There were a total of 36 reported events of catheter sepsis (n = 2 tube feeding compared with n = 23 parenteral nutrition; n = 1 standard care compared with n = 10 parenteral nutrition). The risk of infection remained significantly lower in a comparison of parenteral nutrition for both tube feeding and standard care (RR: 0.70; 95% CI: 0.58, 0.83) and standard care (RR: 0.79; 95% CI: 0.67, 0.94). To determine whether the higher risk of nutrition support complications in tube-fed populations was due to the exclusion of catheter sepsis from this category, this event was categorized as a nutrition support complication. The RRs and 95% CIs were recalculated for studies that reported them, and new aggregated RRs were calculated. The risk of nutrition support complications was reduced from 1.35 to 1.05, and the CI included unity (95% CI: 0.79, 1.4).
| DISCUSSION |
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It was reported in animals that enteral nutrition more so than does parenteral nutrition lowers the risk of infection by preserving the gastrointestinal tract's integrity and enhancing its ability to provide an immunocompetent barrier to endogenous gut bacteria, which prevents the occurrence of bacterial translocation (3739); however, the role that enteral nutrition plays in preventing bacterial translocation in human investigations is still debated (40). We cannot suggest that our findings support the hypothesis of a protective role for aggressive enteral nutrition (tube feeding) in preventing bacterial translocation because there are several aspects of our meta-analysis design that prohibited this. Specifically, none of the studies included in our analysis investigated bacterial translocation as a primary hypothesis, and all types of infection were grouped together within our infection category, which further limited interpretation. Also, we cannot determine from our results whether aggressive enteral nutrition reduced the risk of infection or whether parenteral nutrition led to a higher risk of infection. Our finding of fewer infections associated with both tube feeding and standard care than with parenteral nutrition in normally nourished populations suggests that it is not that enteral nutrition does not result in a lower risk of infection but rather that parenteral nutrition results in a higher risk of infection.
The higher risk of infection associated with parenteral nutrition may be partially explained by the higher number of patients with hyperglycemia in this population. Elevated glucose concentrations reduce neutrophil chemotaxis and phagocytosis and were found to be an independent risk factor for short-term infection in patients undergoing coronary artery surgery (41). Of the 20 trials that compared tube feeding with parenteral nutrition, 16 included data on infection (12, 15, 16, 18, 19, 2127, 3235) and 7 reported data on hyperglycemia (15, 16, 18, HREF="#R20">20, 21, 22, 23), 6 of which reported data on both infection and hyperglycemia (15, 16, 18, 21, 22, 23). In all of these investigations, hyperglycemia occurred more frequently in patients who received parenteral nutrition than in those who were tube fed; however, because of the way the data were presented, it was not possible to discern whether persons with infection were also those with hyperglycemia. To be included in this meta-analysis, feeding protocols for both tube feeding and parenteral nutrition had to provide energy at or above estimated needs; however, tube-fed patients frequently receive less than the amount prescribed because of feeding intolerance and interruptions. To determine whether the hyperglycemia reported was caused by the greater energy infusion received by parenteral nutrition than by tube feeding, the 5 investigations that reported both infection and hyperglycemia were reviewed. Patients randomly assigned to receive parenteral nutrition received less energy than did the tube-fed patients in one investigation (18), approximately equal amounts in 4 investigations (15, 16, 22, 23), and greater amounts in one investigation (21). Thus, the hyperglycemia was not caused by a difference in the amounts of energy that were dispensed. Standard parenteral nutrition solutions contain 6075% of energy as dextrose, whereas standard tube feeding solutions contain 4055% of energy as dextrose. Metabolic alterations that accompany the stress response result in more endogenous glucose production and reduce the capacity to oxidize plasma glucose directly (42). The higher incidence of hyperglycemia caused by excessive glucose loads that are superimposed on the stress response in parenteral nutrition may lead to an impaired immune response that contributes to the observed higher risk of infection.
Overall, a significantly higher risk of nutrition support complications was found to be associated with tube feeding than with parenteral nutrition, although there was significant heterogeneity (P = 0.04). When separated into the a priori categories, these results remained, and heterogeneity was not significant in the relatively recent studies or in those with higher study-quality score. Many of the complications (eg, diarrhea and abdominal distention) associated with tube feeding occur frequently but are considered to be less severe clinically than are those associated with parenteral nutrition. To address this, the less severe complications of tube feeding, such as diarrhea, vomiting, and ileus, were limited to the instances in which they required medication or feedings to be stopped for
24 h. Thus, although 8 of the 20 studies that compared tube feeding with parenteral nutrition reported diarrhea, our definitions restricted its inclusion as a nutrition support complication to just 3 studies, and there were no instances of vomiting or ileus with use of the modified criteria. The technical risks involved with inserting and maintaining feeding tubes can be significant and are often underrated. Six of the 20 trials that compared tube feeding with parenteral nutrition reported problems with feeding tube placement and maintenance and accounted for 14% (9 of 66) of the reported nutrition support complications. As previously discussed, catheter sepsis, a severe complication associated with parenteral nutrition, was categorized as an infection instead of as a nutrition support complication. When catheter sepsis was categorized as a nutrition support complication, the differences in the risk of nutrition support complications between tube feeding and parenteral nutrition were eliminated (RR: 1.05; 95% CI: 0.79, 1.4). Our findings of a substantial risk of these various untoward events caused by both tube feeding and parenteral nutrition were based on definitions that minimized the inclusion of medically insignificant events. They illustrate the need to weigh these risks against the potential benefits before the initiation of either type of nutrition support.
The nutritional status of patients influenced the risk of infection and mortality in trials that compared standard care with parenteral nutrition but not in trials that compared tube feeding with parenteral nutrition. When aggregated, standard care was associated with a higher risk of infection and mortality in the 3 trials of populations that had high percentages of PEM; however, in the 4 trials of normally nourished populations, it was associated with a lower risk of infection. These findings illustrate 2 major points: 1) failure to provide adequate nutrition to populations with PEM is associated with untoward consequences, and 2) parenteral nutrition should not be initiated in normally nourished populations, unless there is a good reason to do so.
The issue of the number of days to wait before initiating enteral or parenteral nutrition in normally nourished populations is complex and frequently discussed. The goal is to prevent a deterioration in nutritional status, which precipitate poorer outcomes; however, it must be determined whether the benefit of the intervention exceeds its risk. Ascertaining the number of days to wait before the initiation of aggressive nutrition support was not one of our selected objectives; however, several of the PRCTs reviewed in this meta-analysis addressed this issue. Sandstrom et al (30) reported that 60% of their patients began eating on their own 89 d after surgery, and those that had not begun eating by 14 d had significantly higher mortality rates than did those randomly assigned to the parenteral nutrition group that did not have complications or to the standard care group that had begun eating before 14 d. Sax et al (17) and Brennan et al (28) found that an average of 12 d was required for parenteral nutrition patients to consume adequate energy orally. Several of the trials that compared tube feeding with parenteral nutrition reported the number of days required for adequate oral intake. McClave et al (16) found that patients who received parenteral nutrition required 7.1 ± 1.1 d and tube-fed patients required 5.6 ± 0.8 d to begin oral intake. Adams et al (32) reported that 87% of parenteral nutrition patients began oral intake 10 ± 6 d after injury, and Sako et al (25) found that a mean of 20 d was required for parenteral nutrition patients to resume an adequate oral intake. Collectively, these results suggest that most normally nourished patients begin to eat 610 d after surgery or a hospital admission for a disease that necessitates bowel rest can achieve an adequate oral intake within 6-20 d. Our findings suggest that 710 d is a reasonable amount of time to wait before initiating parenteral nutrition in normally nourished patients who have not begun eating spontaneously.
The limitations of our study were similar to those for any meta-analysis of PRCTs. For example, each author used different definitions for the outcome variables evaluated. Thus, there was a concern that we were comparing "apples with oranges." A meta-analysis of small trials may overestimate treatment effects (43), and only 5 of the 27 studies reviewed had >50 patients per treatment group. Other concerns were the paucity of PRCTs in populations with PEM and the scarcity of PRCTs that compared standard care with parenteral nutrition and that reported nutritional support complications and other complications. These concerns limited our ability to make generalized practice recommendations.
A goal of this meta-analysis was to provide an interim guide for clinical decision-making until the results of large trials conducted in populations with marginal gastrointestinal function are available. A comprehensive search of the literature was done with the use of clinically relevant criteria for both study selection and assessed outcomes. In a broad spectrum of patients with compromised gastrointestinal function with tube feeding, we found fewer infections in those who were tube-fed than in those who received parenteral nutrition. These findings were similar, although not as strong, in a comparison of standard care with parenteral nutrition in normally nourished patients. We also found a higher risk of nutrition support complications with tube feeding than with parenteral nutrition. Collectively, these results suggest that waiting 710 d to initiate any form of aggressive nutrition intervention may be prudent for normally nourished populations with compromised gastrointestinal function. Studies that compare outcomes of tube feeding with those of standard care in both normally nourished and malnourished populations are needed. Finally, studies comparing the costs associated with of providing either tube feeding or parenteral nutrition with those of standard care are needed to guide clinicians, hospital administrators, and third-party payers in their decision-making.
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