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Article
February 2002

A Systematic Review of Nonpharmacological and Nonsurgical Therapies for Gastroesophageal Reflux in Infants

Author Affiliations

From the Robert Wood Johnson Clinical Scholars Program (Dr Carroll), the Department of Pediatrics (Drs Carroll and Christakis), and the Child Health Institute (Ms Garrison and Dr Christakis), University of Washington, Seattle.

Arch Pediatr Adolesc Med. 2002;156(2):109-113. doi:10.1001/archpedi.156.2.109
Abstract

Background  Nonpharmacological and nonsurgical measures are often recommended for gastroesophageal reflux disease (GERD) in infants, despite ambiguous supporting evidence.

Objective  To conduct a systematic review of rigorously evaluated nonpharmacological and nonsurgical therapies for GERD in infants.

Design/Methods  We searched online bibliographic databases, including MEDLINE, EMBASE, the Cochrane Collaboration and Clinical Trials Database, and alternative medicine databases for the terms gastroesophageal reflux and infants. We selected randomized controlled trials of nonpharmacological and nonsurgical GERD therapies in otherwise healthy infants. Data were extracted from the selected articles regarding reflux, emetic episodes and intraesophageal pH.

Results  We identified 43 relevant studies, of which 10 met the selection criteria. These studies examined positioning, pacifier use, and feeding changes. Positioning at a 60° elevation in an infant seat was found to increase reflux compared with the prone position. No significant difference was shown between the flat and head-elevated prone positions. The impact of pacifier use on reflux frequency was equivocal and dependent on infant position. The protein content of formula was not found to affect reflux. Although no study demonstrated a significant reflux-reducing benefit of thickened infant foods compared with placebo, 1 study detected a significant benefit of formula thickened with carob bean gum compared with rice flour (pH<4 for 5% vs 8% of time). Another study showed that if supplementing with dextrose 5% water or dextrose 10% water, the lower-osmolality fluid was associated with less reflux.

Conclusions  Many conservative measures commonly used to treat GERD in infants have no proven efficacy. Although thickened formulas do not appear to reduce measurable reflux, they may reduce vomiting. Further studies with clinical outcomes are needed to answer questions about efficacy definitively.

GASTROESOPHAGEAL reflux disease (GERD) is a common disease of infancy, with a prevalence of as high as 18% in healthy children, and a frequent reason for visits to primary health care providers.1 Approximately 50% of all healthy infants will vomit more than twice per day.2

A variety of approaches have been used in the treatment of GERD, including pharmacological and nonpharmacological therapies. As many of the pharmacological therapies for reflux, eg, metoclopramide hydrochloride (Reglan) and cisapride (Propulsid), are falling into disfavor or are withdrawn from use, practitioners may rely more on conservative measures as first-line therapy for GERD. These nonpharmacological and nonsurgical therapies include positioning changes, formula changes, and thickening of infant food.

Although these interventions are commonly recommended,3 evidence in support of them is sparse. We therefore undertook a systematic review to summarize the current state of the evidence. To maximize clarity and clinical usefulness, we present the results of that review as distinct evidence summaries detailing the potential benefits and harms of each intervention.

Methods

We searched several bibliographic databases, including MEDLINE (January 1, 1966, through November 30, 2000), the Cochrane Collaboration and Clinical Trials Database (as of November 2000), EMBASE (as of November 2000), and multiple alternative medicine databases. We used the search terms gastroesophageal reflux disease and infants as medical subject headings and keywords. We restricted the results to studies that were conducted in human infants and published in the English language. We reviewed the titles of all returned articles and the bibliographies of all relevant review articles and selected articles to determine whether the studies examined nonpharmacological and nonsurgical therapies for infants with GERD. Articles were immediately excluded if they included drug or surgical therapies or were obviously not clinical trials.

We analyzed studies for adequate inclusion criteria, randomization, and allocation concealment. Although considerable disagreement exists regarding how pathologic GERD should be defined, we accepted any study that defined GERD as reflux into the esophagus with a pH of less than 4.0 for at least 5% of the time, as diagnosed by means of pH probe study findings. Although this cutoff is frequently used as a diagnostic criterion in research and clinical practice, it may or may not adequately correlate with symptomatic reflux in infants.

To meet selection criteria, a study had to randomize otherwise healthy, full-term infants with GERD to treatment and control groups. Crossover trials were accepted if infants were exposed in random order to both treatment and control protocols. Allocation concealment was only considered a requirement for inclusion when all reviewers agreed that it would be feasible to blind such a study, and that the absence of effective blinding could bias the outcome. For example, although blinding may not be feasible in a study of infant positioning, the results of a pH probe are unlikely to be affected by parent or provider knowledge of allocation. All disagreements were resolved via consensus.

Unless otherwise indicated, data are given as mean ± SEM.

Results

Literature search

The systematic literature search identified more than 2500 articles. After excluding articles that did not describe clinical trials or that examined drug or surgical therapy, 35 articles remained and were assessed by all 3 reviewers (A.E.C., M.M.G., and D.A.C.). Articles were most commonly excluded at this stage because they did not describe trials,4-9 or the trials did not specifically study therapies for GERD,10-13 infants with compound medical problems14-17 or premature infants were included,18-21 and a control group or proper randomization was missing.1,22-25 Other studies were eliminated because they included therapies judged to be pharmacological in nature.26,27 Ten randomized controlled trials (RCTs) met selection criteria. Of these, 2 RCTs studied positioning28,29; 3 studied thickened infant food30-32; 4 studied formula changes33-36; and 1 studied nonnutritive sucking.37 Characterisics of these studies are summarized in Table 1.

Characteristics of Included Studies
Characteristics of Included Studies

Positioning

Two of the trials investigated the effect of positioning. One studied the placement of the infant upright in a seat vs lying prone; the other examined the effect of elevation of the head of the bed.

Does placement upright in an infant seat reduce the amount of reflux?

There is no evidence to support this intervention. One RCT29 found that placement in an infant seat (inclined at 60°) was detrimental with respect to GERD. Infants were randomized and studied in paired 2-hour trials using the pH probe to measure reflux. Infants in the seat spent a greater proportion of time in a state of reflux (28.2% ± 6.4%) than did those in the prone position (12.8% ± 3.7%) and had significantly more episodes of reflux (16.0 ± 2.4 vs 10.1 ± 2.3). Although the infant seat has been considered a treatment for GERD, evidence suggests that it actually exacerbates reflux.

Does elevating the head of the bed reduce the amount of reflux?

There is no evidence to support this intervention. One RCT28 found no difference in any measure of reflux between infants in the prone position and those in the prone position with the head of the bed inclined at 30°. Infants were randomized and underwent pH probe studies for 3-hour sessions in a crossover trial that measured the amount of reflux, number of episodes, average length of episodes, number of long episodes, and length of the longest episode. Among the 90 infants with GERD, no difference was seen between the positions for any of these measures.

Nonnutritive sucking

Does pacifier use reduce reflux?

There is no evidence to support this intervention. Orenstein37 studied 48 infants randomized to a prone or seated position. In each position, infants underwent pH probe examination with and without pacifiers in random order for 3 hours. In the prone position, pacifier use increased the number of episodes of reflux in 2 hours (7.2 ± 1.1 to 12.8 ± 2.3 [P = .04]). In the seated position, pacifier use decreased the number of reflux episodes in 2 hours (21.1 ± 3.1 to 14.8 ± 2.6 [P = .03]), but not enough to compensate for the negative effects of the seated position. Total reflux time and reflux clearance were not significantly affected by pacifier use in either position.

Thickened infant food

Four RCTs studied the effect of thickened food on GERD. Two studies compared formula thickened with rice flour with placebo, 1 studied carob bean gum–thickened formula vs placebo, and 1 compared the 2 thickening agents.

Does thickening food with rice flour reduce the amount of reflux?

There is no evidence to support this intervention. Bailey et al31 randomized infants to receive plain apple juice or apple juice thickened with rice flour. Infants received at least 3 feedings of both juice types during 20 to 24 hours in the following 4 positions: prone, prone and elevated 30°, supine, or unrestricted. Reflux was measured by means of a pH probe for 2 hours postprandially. There was no difference between the 2 types of juice in any position, except in the 30° elevated prone position, in which reflux time was increased with thickened juice. Orenstein et al32 assessed reflux by means of technetium Tc 99m sulfur colloid 500-µCi scintigraphy in 20 infants undergoing paired feeding consisting of infant formula alone or formula thickened with rice cereal. The feedings were given 48 to 72 hours apart, and the infants underwent 90-minute postprandial studies. The type of formula had no statistically significant impact on the amount of reflux. However, a significant decrease was found in the number of episodes of frank emesis (1.2 ± 0.7 vs 3.9 ± 0.9 per 90 postprandial minutes).

Does thickening food with carob bean gum preparation reduce the amount of reflux?

There is no evidence to support this intervention. In one RCT,34 20 infants were randomized to receive the control formula (80% casein and 20% whey) or the thickened formula. Both groups also received positional treatment and parental reassurance. Parents kept a regurgitation diary for 1 week, and a 24-hour pH study was performed before and after treatment. Both groups noted improvements compared with baseline, but no significant difference was found in pH monitoring results between the control and treatment groups. There were some intragroup improvements, which led the authors to conclude that thickened formulas reduced the reflux index. However, no significant differences were found between the groups before and after the trial. Parental diaries recorded improvement in the number of regurgitations in both groups, with no significant difference between them.

Is thickening food with carob bean gum more successful than rice flour in reducing reflux?

Yes. In 1 crossover RCT,30 24 infants received a traditional formula thickened with rice flour or a formula thickened with carob bean gum, and formulas were alternated in a nonrandom alteration study. All infants underwent 24-hour pH probe studies. The infants were then randomized to receive 1 of the 2 formulas for the next 2 weeks, with parents scoring their reflux symptoms on diary cards. Parental diaries showed reduction over time in the symptomatic scores for both formulas. The mean (± SD) reductions were significantly greater, however, with the carob bean gum–thickened formula (symptomatic score reduction, 70.4% ± 6.0% vs 48.7% ± 6.2% [P<.01]; reduction in episodes of emesis, 58.1% ± 5.6% vs 34.1% ± 8.8% [P<.05]).

Formula changes

Two RCTs investigated the effect of formula composition on GERD, with equivocal results.

Does the composition of formula have any effect on reflux?

There is no evidence to support this intervention. Tolia et al35 randomized 28 infants to receive casein-predominant, soy-based, and whey-predominant formulas in random order. The infants were given 1 serving of each formula on 3 consecutive days and then underwent measuring for gastric emptying time and reflux by means of scintigraphy. No difference was seen in spitting and vomiting between the formulas. The differences in volume of reflux for each formula were not statistically significant. Another small study33 monitored reflux in 3 infants with GERD by means of a 24-hour pH probe for casein- and whey-based formulas. All 3 infants showed improvement in emesis while receiving the whey-based formulas (1.3 ± 0.6 vs 4.3 ± 0.6 [P<.01]), although the difference between the formulas, based on the results of the pH probe testing, was not statistically significant.

Caloric density and osmolality

Does the caloric density or osmolality of feedings affect reflux?

Possibly. Sutphen and Dillard36 studied the effect of dextrose 5% water (D5W), dextrose 10% water (D10W), and a glucose polymer solution (Polycose; Ross Laboratories, Columbus, Ohio) when rehydrating children with carbohydrate solutions. Nineteen infants underwent pH probe monitoring as they received each solution 1 time in a random order while undergoing the pH probe study. The total minutes of esophageal reflux were significantly lower while receiving the D5W and glucose polymer solutions than while receiving the D10W solution (mean ± 1 SD, 12.0 ± 11.3 and 12.6 ± 8.0, respectively, vs 28.6 ± 28.4 [P<.05]). No significant difference was found in the results in the first postprandial hour, but results became significant when observed for 2 hours postprandially.

Comment

Although often used, these nonpharmacological, nonsurgical approaches to the management of infant GERD lack a sound evidence base. None of the interventions discussed in this review significantly improved reflux. Thickening infant formulas, however, reduced the frequency of frank emesis. Medical textbooks are often used as a proxy for the prevailing opinions of experts.38 In the case of GERD, many textbooks continue to recommend the use of conservative measures, including thickening of juice and formula and upright positioning, despite their lack of proven efficacy.39-45

Many pediatricians and pediatric gasroenterologists prescribe these therapies despite their lack of evidence, often as a means of including parents in the treatment plan when reassurance seems insufficient. Although no evidence suggests that these nonpharmacological therapies are unsafe, they often carry hidden burdens. Wedges (devices that keep infants sleeping at an incline) can be expensive and cumbersome to use, and reliance on them may lead to undue anxiety on occasions when parents fail to use them. Thickening infant foods necessitates bottle feeding, thereby requiring that breastfeeding mothers express breast milk rather than nurse directly. This may be inconvenient and may have an impact on mother-child bonding.

The limitations of this study are that we included only articles and textbooks written in the English language. The number of well-designed clinical trials of nonpharmacological and nonsurgical therapies for reflux is small. Therefore, a potential effect of some of these therapies may have been missed because of the small sample size. This review does not prove that these therapies do not work; it illustrates that no conclusive evidence exists to prove that they do work. Certainly, more studies are needed to answer questions about efficacy definitively.

This systematic review, like others before,46 identified significant gaps in what we know about treating GERD in infants. No quality RCTs have examined changes in feeding volume or frequency. Another area for potential improvement in future research is in the outcome measures used. Thus far, most of the studies have used pH probes to diagnose and monitor GERD. Although pH probes are an objective measure, and thus not subject to bias, they may not reflect clinical symptoms, which constitute the outcome of greatest interest to parents. One potential scoring system might be the 25-point Infant Gastroesophageal Reflux Questionnaire GERD score based on 11 items, including frequency and amount of vomiting, feeding, weight gain, comfort, crying, hiccups, arching, and apnea.47 This test was shown to have a 100% positive predictive value and 94% to 98% negative predictive value in a clinical study of its validity.47 Despite potential problems with bias and comparability between studies, clinical scores may be a more clinically relevant outcome measure in the study of infant GERD.

Accepted for publication September 28, 2001.

What This Study Adds

Nonpharmacological and nonsurgical measures are often recommended for infant gastroesophageal reflux disease, although the evidence in support of them is ambiguous. This review systematically evaluated rigorous studies of these therapies to document their efficacy. Through this review, we hope to make it clear to practitioners that many of these therapies have no proven efficacy. More studies of nonpharmacological and nonsurgical measures are necessary in the future.

Corresponding author: Aaron E. Carroll, MD, Robert Wood Johnson Clinical Scholars Program, H-220 Health Sciences Center, Box 357183, Seattle, WA 98195-7183 (e-mail: acarro@u.washington.edu).

References
1.
Bagucka  BDe Schepper  JPeelman  MVan de Maele  KVandenplas  Y Acid gastro-esophageal reflux in the 10 degrees-reversed-Trendelenburg-position in supine sleeping infants.  Acta Paediatr Taiwan. 1999;40298- 301Google Scholar
2.
Orenstein  SRIzadnia  FKhan  S Gastroesophageal reflux disease in children.  Gastroenterol Clin North Am. 1999;28947- 969Google ScholarCrossref
3.
Tsou  VMBishop  PR Gastroesophageal reflux in children.  Otolaryngol Clin North Am. 1998;31419- 434Google ScholarCrossref
4.
Lynn  MR Use of infant seats for gastroesophageal reflux.  J Pediatr Nurs. 1986;1127- 129Google Scholar
5.
Blecker  UVan Hauthem  HLanciers  SPeeters  SVandenplas  Y The effect of different feeds on the incidence of postcibal gastro-oesophageal reflux in infants as measured by oesophageal pH monitoring.  Eur J Gastroenterol Hepatol. 1992;547- 50Google Scholar
6.
Cucchiara  SDe Vizia  BMinella  R  et al.  Intragastric volume and osmolality affect mechanisms of gastroesophageal reflux (GOR) in children with GOR disease [abstract].  J Pediatr Gastroenterol Nutr. 1995;20468Google ScholarCrossref
7.
Sajwaj  TLibet  JAgras  S Lemon-juice therapy: the control of life-threatening rumination in a six-month-old infant.  J Appl Behav Anal. 1974;7557- 563Google ScholarCrossref
8.
Heacock  HJJeffery  HEBaker  JLPage  M Influence of breast versus formula milk on physiological gastroesophageal reflux in healthy, newborn infants.  J Pediatr Gastroenterol Nutr. 1992;1441- 46Google ScholarCrossref
9.
Kravitz  H Comparison of newborn infants in raised and horizontal cribs.  IMJ Ill Med J. 1975;147389- 390Google Scholar
10.
Tolia  VKauffman  RE Comparison of evaluation of gastroesophageal reflux in infants using different feedings during intraesophageal pH monitoring.  J Pediatr Gastroenterol Nutr. 1990;10426- 429Google ScholarCrossref
11.
Orenstein  SR Effects on behavior state of prone versus seated positioning for infants with gastroesophageal reflux.  Pediatrics. 1990;85765- 767Google Scholar
12.
Billeaud  CGuillet  JSandler  B Gastric emptying in infants with or without gastro-oesophageal reflux according to the type of milk.  Eur J Clin Nutr. 1990;44577- 583Google Scholar
13.
Fabiani  EBolli  VPieroni  G  et al.  Effect of a water-soluble fiber (galactomannans)–enriched formula on gastric emptying time of regurgitating infants evaluated using an ultrasound technique.  J Pediatr Gastroenterol Nutr. 2000;31248- 250Google ScholarCrossref
14.
Meyers  WFHerbst  JJ Effectiveness of positioning therapy for gastroesophageal reflux.  Pediatrics. 1982;69768- 772Google Scholar
15.
Carre  I Postural treatment of children with a partial thoracic stomach ("hiatus hernia").  Arch Dis Child. 1960;35569- 580Google ScholarCrossref
16.
Khoshoo  VZembo  MKing  ADhar  MReifen  RPencharz  P Incidence of gastroesophageal reflux with whey- and casein-based formulas in infants and in children with severe neurological impairment.  J Pediatr Gastroenterol Nutr. 1996;2248- 55Google ScholarCrossref
17.
Kelly  KJLazenby  AJRowe  PCYardley  JHPerman  JASampson  HA Eosinophilic esophagitis attributed to gastroesophageal reflux: improvement with an amino acid–based formula.  Gastroenterology. 1995;1091503- 1512Google ScholarCrossref
18.
Vandenplas  YSacre  LLoeb  H Effects of formula feeding on gastric acidity time and oesophageal pH monitoring data.  Eur J Pediatr. 1988;148152- 154Google ScholarCrossref
19.
Sutphen  JLDillard  VL Medium chain triglyceride in the therapy of gastroesophageal reflux.  J Pediatr Gastroenterol Nutr. 1992;1438- 40Google ScholarCrossref
20.
Sutphen  JLDillard  VL Effect of feeding volume on early postcibal gastroesophageal reflux in infants.  J Pediatr Gastroenterol Nutr. 1988;7185- 188Google ScholarCrossref
21.
Blumenthal  ILealman  GT Effect of posture on gastro-oesophageal reflux in the newborn.  Arch Dis Child. 1982;57555- 556Google ScholarCrossref
22.
Vandenplas  YSacre-Smits  L Gastro-oesophageal reflux in infants: evaluation of treatment by pH monitoring.  Eur J Pediatr. 1987;146504- 507Google ScholarCrossref
23.
Vandenplas  YSacre  L Milk-thickening agents as a treatment for gastroesophageal reflux.  Clin Pediatr (Phila). 1987;2666- 68Google ScholarCrossref
24.
Tobin  JMMcCloud  PCameron  DJ Posture and gastro-oesophageal reflux: a case for left lateral positioning.  Arch Dis Child. 1997;76254- 258Google ScholarCrossref
25.
Orenstein  SRWhitington  PF Positioning for prevention of infant gastroesophageal reflux.  J Pediatr. 1983;103534- 537Google ScholarCrossref
26.
Sutphen  JLDillard  VLPipan  ME Antacid and formula effects on gastric acidity in infants with gastroesophageal reflux.  Pediatrics. 1986;7855- 57Google Scholar
27.
Gouyon  JBBoggio  VFantino  MGillot  ISchatz  BVallin  A Smectite reduces gastroesophageal reflux in newborn infants.  Dev Pharmacol Ther. 1989;1346- 50Google Scholar
28.
Orenstein  SR Prone positioning in infant gastroesophageal reflux: is elevation of the head worth the trouble?  J Pediatr. 1990;117 ((pt 1)) 184- 187Google ScholarCrossref
29.
Orenstein  SRWhitington  PFOrenstein  DM The infant seat as treatment for gastroesophageal reflux.  N Engl J Med. 1983;309760- 763Google ScholarCrossref
30.
Borrelli  OSalvia  GCampanozzi  A  et al.  Use of a new thickened formula for treatment of symptomatic gastrooesophageal reflux in infants.  Ital J Gastroenterol Hepatol. 1997;29237- 242Google Scholar
31.
Bailey  DJAndres  JMDanek  GDPineiro-Carrero  VM Lack of efficacy of thickened feeding as treatment for gastroesophageal reflux.  J Pediatr. 1987;110187- 189Google ScholarCrossref
32.
Orenstein  SRMagill  HLBrooks  P Thickening of infant feedings for therapy of gastroesophageal reflux.  J Pediatr. 1987;110181- 186Google ScholarCrossref
33.
Khoshoo  VFried  MPencharz  P Incidence of gastroesophageal reflux with casein and whey-based formulas.  J Pediatr Gastroenterol Nutr. 1993;17116- 117Google ScholarCrossref
34.
Vandenplas  YHachimi-Idrissi  SCasteels  AMahler  TLoeb  H A clinical trial with an "anti-regurgitation" formula.  Eur J Pediatr. 1994;153419- 423Google Scholar
35.
Tolia  VLin  CHKuhns  LR Gastric emptying using three different formulas in infants with gastroesophageal reflux.  J Pediatr Gastroenterol Nutr. 1992;15297- 301Google ScholarCrossref
36.
Sutphen  JLDillard  VL Dietary caloric density and osmolality influence gastroesophageal reflux in infants.  Gastroenterology. 1989;97601- 604Google Scholar
37.
Orenstein  SR Effect of nonnutritive sucking on infant gastroesophageal reflux.  Pediatr Res. 1988;2438- 40Google ScholarCrossref
38.
Antman  EMLau  JKupelnick  BMosteller  FChalmers  TC A comparison of results of meta-analyses of randomized control trials and recommendations of clinical experts: treatments for myocardial infarction.  JAMA. 1992;268240- 248Google ScholarCrossref
39.
Werlin  S Dysphagia. Hoekelman  Red Primary Pediatric Care. 4th ed. St Louis, Mo Mosby– Year Book Inc2001;1039- 1043Google Scholar
40.
Rudolph  C Gastroenterology and nutrition. Rudolph  Aed Rudolph's Pediatrics. 20th ed. East Norwalk, Conn Appleton & Lange1996;993- 1122Google Scholar
41.
Roy  CCSilverman  AAlagille  DRoy  CCedSilverman  AedAlagille  Ded Gastroesophageal reflux: sucking and swallowing disorders and diseases of the esophagus.  Pediatric Clinical Gastroenterology. 4th ed. St Louis, Mo Mosby– Year Book Inc1995;163- 170Google Scholar
42.
Shaffer  SLiacouras  Ced Gastroesophageal reflux.  Clinical Pediatric Gastroenterology. New York, NY Churchill Livingstone Inc1998;181- 186Google Scholar
43.
Gold  DPettei  MFinberg  Led Gastroesophageal reflux.  Saunders Manual of Pediatric Practice. Philadelphia, Pa WB Saunders Co1998;494- 496Google Scholar
44.
Wasserman  DSchwartz  Med Gastroesophageal reflux.  The 5 Minute Pediatric Consult. 2nd ed. Philadelphia, Pa Lippincott William & Wilkins2000;378- 379Google Scholar
45.
McEvoy  CMcMillan  Jed Sucking and swallowing disorders and gastroenterology.  Oski's Pediatrics: Principles and Practice. 3rd ed. Philadelphia, Pa Lippincott William & Wilkins1999;319- 320Google Scholar
46.
Berg  A Clinical practice guideline panels: personal experience.  J Am Board Fam Pract. 1996;9366- 370Google Scholar
47.
Orenstein  SRShalaby  TMCohn  JF Reflux symptoms in 100 normal infants: diagnostic validity of the Infant Gastroesophageal Reflux Questionnaire.  Clin Pediatr (Phila). 1996;35607- 614Google ScholarCrossref
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