Timing and route of enteral tube-feeding did not reduce death or poor outcome in stroke and dysphagiaPDF
ACP J Club. 2005 Sep-Oct;143:37. doi:10.7326/ACPJC-2005-143-2-037
Related Content in this Issue
• Companion Abstract and Commentary: Protein–energy supplementation of normal hospital diet did not improve outcomes after recent stroke
Clinical Impact Ratings
Phys Med & Rehab:
The FOOD Trial Collaboration. Effect of timing and method of enteral tube feeding for dysphagic stroke patients (FOOD): a multicentre randomised controlled trial. Lancet. 2005;365:764-72. [PubMed ID: 15733717]
In patients with recent stroke and dysphagia, does early initiation of enteral tube-feeding (ETF) (vs no tube-feeding for ≥ 7 d) improve outcomes (study 1)? Does ETF via percutaneous endoscopic gastrostomy (PEG) (vs nasogastric [NG] tube) improve outcomes (study 2)?
Design: 2 randomized controlled trials with similar design (Feed Or Ordinary Diet [FOOD] trials).
Follow-up period: 6 months.
Setting: 83 hospitals in 15 countries (study 1) and 47 hospitals in 11 countries (study 2).
Patients: Patients admitted to hospital with recent stroke (within 7 d before admission) who had dysphagia were enrolled in study 1 (n = 859, mean age 76 y, 46% men, 9% undernourished) if the clinician was uncertain when to start tube-feeding; or study 2 (n = 321, mean age 76 y, 45% men, 22% undernourished) if the clinician chose to start tube-feeding but was uncertain whether to use PEG or NG tube. Patients with subarachnoid hemorrhage were excluded.
Intervention: In study 1, ETF as soon as possible (“early initiation”) via the clinician's preferred method (n = 429) or no tube-feeding (only parenteral fluids were given) for ≥ 7 days (n = 430). In study 2, ETF via PEG (n = 162) or NG tube (n = 159) within 3 days of enrollment.
Outcomes: Death and a composite endpoint of death or poor outcome. Poor outcome was defined as modified Rankin scale (MRS) scores 3 to 5, with the MRS scores ranging from 0 (no symptoms) to 5 (requiring constant attention day and night).
Patient follow-up: 100% (intention-to-treat analysis).
In study 1, early initiation of ETF did not reduce death or the composite endpoint of death or poor outcome more than no tube-feeding for ≥ 7 days (Table). In study 2, ETF via PEG did not reduce death or the composite endpoint of death or poor outcome more than ETF via NG tube (Table).
In patients with recent stroke and dysphagia, early initiation of enteral tube-feeding did not reduce death or poor outcome more than no tube-feeding for ≥ 7 days and enteral tube-feeding via percutaneous endoscopic gastrostomy did not reduce death or poor outcome more than nasogastric tube-feeding.
Sources of funding: National Health Service Research and Development in UK; Stroke Association; Chief Scientist Office of the Scottish Executive; Chest, Heart and Stroke Scotland; Royal Australian College of Physicians.
For correspondence: Professor M. Dennis, Western General Hospital, Edinburgh, Scotland, UK. E-mail firstname.lastname@example.org.
Table. Timing and method of enteral tube-feeding (ETF) in stroke and dysphagia†
|Study||Comparisons||Outcomes at 6 mo||Event rates||RRR (95% CI)||NNT|
|1||Early initiation of ETF vs no ETF for ≥7 d||Death||42% vs 48%||12% (−2 to 24)||Not significant|
|Death or poor outcome||79% vs 80%||1% (−5 to 8)||Not significant|
|2||ETF via PEG vs ETF via NG tube||Death||49% vs 48%||2% (−19 to 28)||Not significant|
|Death or poor outcome||89% vs 81%||10% (−0.06 to 21)||Not significant|
†PEG = percutaneous endoscopic gastrostomy; NG = nasogastric; poor outcome = modified Rankin scale scores 3 to 5 (range 0 to 5). Other abbreviations defined in Glossary; RRR, RRI, NNT, NNH, and CI calculated from data in article.
The 3 FOOD trials by The Food Trial Collaboration add to the evidence base of how best to feed patients with stroke. The protein supplementation study is relatively straightforward. In patients with stroke who are able to take oral nutrition (undernourished or not), additional nutritional supplements beyond a normal hospital diet are probably not necessary. However, the other 2 trials trials require more thought.
The early ETF vs no ETF trial reassures me that no compelling urgency exists to start artificial nutrition in patients with dysphagic stroke. If I need a few additional days to discuss with patients or families the risks and benefits of artificial versus natural nutrition, I have them, keeping in mind that some form of nutrition should be started within the first week. Although I am reassured that NG feedings were not associated with a higher rate of aspiration pneumonia, I am constantly reminded of them being a nuisance every time I use them. In addition, the higher occurrence of gastrointestinal hemorrhages associated with their use (22 in the early ETF vs 11 in the no ETF group, P = 0.04), as found in the study, gives me further pause in ordering them.
The NG vs PEG trial shows that PEG tubes should not be used immediately, but only after an initial 2- to 3-week time-limited trial of NG feeding, allowing the necessary time for patients to resume natural nutrition. Indeed, of the 159 patients originally randomized to NG feeding, only 44 (28%) later received a PEG tube. If artificial nutrition is required beyond 2 to 3 weeks, then PEG feeding is the preferred approach. Previous clinical trials have shown that for patients with persistent dysphagia lasting ≥ 2 weeks, PEG tubes were not only safer (1, 2) but potentially associated with better survival at 6 weeks compared with NG feeding (88% in the PEG group vs 43% in the NG group) (2). Although the previous trials have methodologic shortcomings typical of unblinded trials with small sample sizes, they complement the data from the FOOD trials given that they ask different questions about the timing of PEG tube placement.
The FOOD trials do not, however, address the most challenging aspect of artificial nutrition in patients with stroke: not what or when—but if—artificial nutrition and PEG tubes should be used, because many patients have strong preferences regarding their use (3). The symbolic association of feeding tubes with disability and dependence is borne out by these studies, because 40% to 50% of patients did not survive to 6 months and of those who did, 65% had severe disability (MRS score 4 to 5), 20% had moderate disability (MRS score 3), and only 15% had no or slight disability (MRS score 0 to 2). Eliciting patient preferences regarding the use of feeding tubes and negotiating alternatives, such as hand-feeding (the true risks and benefits are unknown in this population), require intense discussions with concepts and words that most find uncomfortable but are critical for establishing the proper goals of care.
The FOOD trials provide us with a solid foundation of evidence. The marker of good care, however, will be that the treatment patients with dysphagic stroke receive is consistent with the underlying values of what makes their lives worth living.
Robert Holloway, MD, MPH
University of Rochester Medical Center
Rochester, New York, USA
1. Park RH, Allison MC, Lang J, et al. Randomized comparison of percutaneous endoscopic gastrostomy and nasogastric tube feeding in patients with persistent neurological dysphagia. BMJ. 1992;304;1406-9. [PubMed ID: 1628013]
2. Norton B, Homer-Ward M, Donnelly MT, Long RG, Holmes GK. A randomized prospective comparison of percutaneous endoscopic gastrostomy and nasogastric tube feeding after acute dysphagic stroke. BMJ. 1996;312:13-6. [PubMed ID: 8555849]