eMedicine Specialties > Pediatrics: General Medicine > Gastroenterology
Gastroesophageal Reflux: Treatment & Medication
Updated: May 13, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
- Because most cases are functional gastroesophageal reflux (GER), reassurance is the only treatment needed.
- Conservative measures may include upright positioning after feeding, elevating the head of the bed, prone positioning (infants >6 mo), and providing small, frequent feeds thickened with cereal.5
- Older children benefit from a diet that avoids tomato and citrus products, fruit juices, peppermint, chocolate, and caffeine-containing beverages. Smaller, more frequent feeds are recommended, as is a relatively lower fat diet because lipid retards gastric emptying. Proper eating habits are encouraged and weight loss and avoidance of alcohol and tobacco are recommended when applicable.
- Prone positioning may be recommended, at least for the first postprandial hour. However, the association of prone positioning with sudden infant death syndrome (SIDS) has brought its use into debate. Observations suggest that SIDS in the prone position is related to either suffocation or rebreathing carbon dioxide and is associated with puffy bedding material. Clearly, the use of the prone position during infancy must be based on a careful risk-to-benefit analysis. When it is advised, only very firm bedding material (no pillows) must be used. Bed elevations offer no added advantage to the prone position, and seated positions are not recommended.
- Thickening of formula provides a therapeutic advantage, particularly when excessive vomiting is associated with suboptimal weight gain. Even for infants with normal weight gain, thickened and reduced volume feedings may reduce the frequency and amount of vomiting episodes, ameliorating the concerns of an anxious caregiver. For formula-fed infants younger than 3 months, thickening is typically achieved by the addition of 1 tablespoon of rice cereal per 2 oz of formula. A recent meta-analysis examined the effect of thickened-feed interventions in gastroesophageal reflux.6
- Younger formula-fed infants may benefit from a prethickened, proprietary formula (Enfamil-AR; Mead-Johnson Nutritionals Inc, Evansville, IN). For breast-fed infants, aside from increasing feeding frequency, expressed breast milk may be thickened as described. Also, early introduction of rice cereal feedings (at age 3 mo) may be attempted. Recent work suggests that formula thickening is superior to positioning in promoting weight gain and reducing clinical symptoms in infants with gastroesophageal reflux.5
- Results of medical therapy are generally met with a better long-term response, leading to elimination of antisecretory medications (when prescribed) during infancy. This is primarily because normal development of GI motility includes resolution of physiologic gastroesophageal reflux by age 1 year (in most cases by age 6 mo). In mild, uncomplicated cases, more frequent thickened feeds and, in some cases, postprandial prone positioning may yield an excellent therapeutic response. In more severe cases, in addition to dietary management, pharmacologic intervention is directed at reducing gastric acid secretion. As pharmacotherapy has improved, the need for surgical therapy (fundoplication) has markedly decreased. Nevertheless, antireflux surgery remains one of the most common surgical procedures performed during infancy and early childhood.
- Current guidelines from the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) involve the use of "step-up" and "step-down" therapy, which should be instituted under the guidance of a pediatric gastroenterologist.7,8
- Media file 2 is a diagnostic and therapeutic algorithm to aid in the evaluation and management of gastroesophageal reflux. The diagram outlines the major points addressed in this article.
- In the case of pharmacologic intervention, "step-up" therapy involves progression from diet and lifestyle changes to H2 receptor blockade medications (eg, ranitidine, nizatidine) to proton pump inhibitors (eg, omeprazole, lansoprazole).9 Both classes of acid antisecretory have proven safe and effective for both infants and children in reducing gastric acid output.
- In combination with diet and lifestyle changes, this management guideline should obviate the need for surgery in the vast majority of cases. One important exception, however, may be children with moderate-to-severe neurodevelopmental disabilities who typically manifest both dysphagia and gastroesophageal reflux and are at high risk for aspiration. In these patients, conservative therapy alone may not be sufficient in preventing reflux-associated complications. However, careful monitoring under optimal nonsurgical therapy should be conducted before considering operative intervention.
- Media file 2 is a diagnostic and therapeutic algorithm to aid in the evaluation and management of gastroesophageal reflux. The diagram outlines the major points addressed in this article.
Surgical Care
The goal of surgery for gastroesophageal reflux disease (GERD) is to reestablish the antireflux barrier, without creating obstruction to the food bolus. In general, the Nissen fundoplication, which is a complete 360° wrap, best controls the symptoms of gastroesophageal reflux;10 however, it may lead to more episodes of dysphagia (difficulty and discomfort with swallowing) and gas bloat than a partial wrap (see Media file 3).
Diagram illustrating the Nissen fundoplication. Note how the stomach is wrapped around the esophagus (360º wrap).
Before operative intervention, patients should be evaluated with a thorough history and physical examination, and results of medical treatment (nonoperative therapy) should be well documented. In infants and young children, performing upper GI series (upper GI contrast study) prior to performance of fundoplication is advisable in order to rule out other possible pathologies that may be causing emesis.
- The goals of medical therapy in gastroesophageal reflux are to decrease acid secretion and, in many cases, to reduce gastric emptying time. The "step-up" approach described herein is directed at decreasing acid content of the refluxate. However, other components of the refluxate (eg, bile, pepsin, trypsin) may also lead to esophageal mucosal injury, and these gastric fluid components may exert damaging effects even under conditions of gastric alkalinization. Thus, some patients under antisecretory treatment may have normal pH probe studies yet continue to have the symptoms of gastroesophageal reflux.11,12 In these cases, the development of EEI as a diagnostic tool may prove invaluable.
- When rigorous "step-up" therapy has failed, or when complications of gastroesophageal reflux pose a short or long-term survival risk, the goal of surgical antireflux procedures is to "tighten" the region of the lower esophageal sphincter (LES) and, if possible, reduce hiatal herniation of the stomach (occasionally seen in patients with GERD).
- Surgical treatment of gastroesophageal reflux should be considered for the following patients:
- Infants and children who have failed "step-up" therapy for gastroesophageal reflux (typically over 12 wk) and those who cannot be weaned off of acid-reducing medications should be considered for surgical treatment.
- Those with an atypical presentation, especially respiratory, whose symptoms are clearly associated with gastroesophageal reflux (eg, obstructive apnea temporally associated with reflux during pH monitoring) should be considered for surgical treatment. However, a period of medical therapy (including acid blockade) under close monitoring conditions should be attempted in many cases prior to recommending a surgical approach
- Patients with complications of gastroesophageal reflux, such as aspiration, stricture of the esophagus, or Barrett esophagus should be considered for surgical treatment. Patients with neurologic impairment that requires feeding gastrostomy who are found to have pathologic reflux and remain medication dependent should also be considered for surgery.
- Patients with chronic reflux and recurrence of anastomotic stricture after repair of esophageal atresia should be considered for surgical treatment.
- Observations related to the possible need for gastrostomy include the following:
- Small gastric volumes, decreased compliance in infants, and slow gastric emptying rate following the fundoplication procedure may necessitate a gastrostomy procedure to accompany a fundoplication.
- Patients who are neurologically impaired or who have an inability to tolerate feeds also need an accompanying gastrostomy.
- For those who fail medical therapy, continuous intragastric administration of feeds alone (via nasogastric tube) is another option.13 This method is often used in preterm infants who have a significantly greater surgical risk. In these cases, adequate nutritional management, in conjunction with appropriate medical therapy, may permit the infant to "outgrow" reflux while optimizing weight gain.
Consultations
- In addition to pediatric gastroenterological referral, pulmonary consultation may be required to comanage respiratory complications (see Media file 2).
- Surgical consultation may be required if medical treatment is not successful.
Diet
A change in diet is part of the lifestyle modifications in an infant or child who has been diagnosed with gastroesophageal reflux.- In infants, small, frequent feeds are recommended. Also, parents should thicken formula with rice cereal. One tablespoon of dry rice cereal added to 2 oz of milk formula increases the caloric intake to 24 calories per ounce instead of 20 calories per ounce. Feeding volumes should be reduced, in association with increased feeding frequency. For breast-fed infants, early introduction of rice cereal by spoon (at 3-4 mo) may provide a similar thickening effect (expressed breast milk may also be thickened as above). Constipation may be a troublesome consequence of cereal supplementation; however, specific therapy for this problem is not usually required.
- In children, small, frequent meals are also recommended. Greasy and spicy foods, which increase postprandial reflux by increasing gastric distention and slowing gastric emptying, should be avoided. Chocolate, peppermint, tomato products, citrus, and caffeine, which lowers LES pressure, should also be avoided.
Activity
Several lifestyle changes have been shown to decrease the frequency of gastroesophageal reflux.- Appropriate weight management of overweight or obese children is important. Obesity has been cited as a risk factor in the development of gastroesophageal reflux.
- Infants and children diagnosed with gastroesophageal reflux should avoid the seated or the supine position shortly after meals. In addition, sleeping in the prone position has been demonstrated to decrease the frequency of gastroesophageal reflux; however, that same position has been shown to have an association with SIDS.
- Studies that monitored esophageal acid exposure after elevation of the head of the bed showed a decrease in reflux activity in adults. Placing blocks under the head of the bed or placing a foam wedge under the patient's mattress can accomplish this.
Medication
Therapeutic response for gastroesophageal reflux may take up to 2 weeks. If treatment is successful, weight increases and vomiting episodes decrease. Recurrent aspiration pneumonia or apnea is cause for decreased length of medical therapy. Note that the so-called "prokinetic agents" have been omitted from the following drug list. No currently available prokinetic drug (eg, metoclopramide) has been demonstrated to exert a significant influence in the number or frequency of reflux episodes.
Antacids
These agents are used as diagnostic tools to provide symptomatic relief in infants. Associated benefits include symptomatic alleviation of constipation (aluminium antacids) or loose stools (magnesium antacids).
Aluminum hydroxide (ALternaGEL, Amphojel)
Increases gastric pH >4 and inhibits proteolytic activity of pepsin, reducing acid indigestion. Antacids can initially be used in mild cases. No effect on frequency of reflux but decreases its acidity.
Adult
5-15 mL/dose PO qd/qid
Pediatric
2.5-5 mL/dose PO qd/qid
Decreases effects of tetracyclines, ranitidine, ketoconazole, benzodiazepines, penicillamine, phenothiazines, digoxin, indomethacin, isoniazid; corticosteroids decrease effects of aluminum in hyperphosphatemia
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Caution in recent massive upper GI hemorrhage and infants; renal failure may cause aluminum toxicity; can cause constipation
Magnesium hydroxide (Phillips Milk of Magnesia)
Used as antacid to relieve indigestion. Also causes osmotic retention of fluid, which distends colon and increases peristaltic activity that provides laxative effect. Forms magnesium chloride in vivo after reacting with stomach hydrochloric acid.
Adult
5-15 mL PO qid ac and hs
Pediatric
2.5-5 mL prn; not to exceed 4 doses per d
Decreases effects of tetracyclines, digoxin, indomethacin, and iron salts
Documented hypersensitivity; colostomy, ileostomy, renal failure, fecal impaction, and appendicitis
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Caution in severe renal impairment and infants; can cause diarrhea
H2 Receptor Antagonists
Like antacids, these agents do not reduce the frequency of reflux but decrease the amount of acid in the refluxate by inhibiting acid production. All are equipotent when used in equivalent doses. They are most effective in patients with nonerosive esophagitis and are considered the drug of choice in children because of well-established pediatric doses and liquid forms.
Nizatidine (Axid)
Competitively inhibits histamine at the H 2 receptor of the gastric parietal cells, resulting in reduced gastric acid secretion, gastric volume, and reduced hydrogen concentrations.
Adult
300 mg PO hs or 150 mg bid
Pediatric
<12 years: Not established; limited data suggest the following:
Neonates: 2-4 mg/kg PO q8-12h or 2 mg/kg IV q6-8h
Infants: 2-3 mg/kg/dose PO q8-12h
Children: 2-3 mg/kg/dose PO q6-8h
>12 years: Administer as in adults
Absorption slightly decreased (10%) when coadministered with antacids containing aluminum and magnesium hydroxides; coadministration with high dose aspirin (ie, 3900 mg/d) increases serum salicylate level
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Caution in renal or liver impairment; if changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment; may increase risk of necrotizing enterocolitis in premature infants
Cimetidine (Tagamet)
Inhibits histamine at H2 receptors of gastric parietal cells, resulting in reduced amounts of gastric acid secretion, gastric volume, and hydrogen ion concentrations.
Adult
10-15 mg/kg/dose PO/IV/IM qid ac and hs; alternatively, 800 mg PO bid or 400 mg PO qid
Pediatric
Neonates: 5-20 mg/kg/d PO/IV/IM divided q6-12h
Infants: 10 mg/kg/d PO/IV/IM divided q6-12h; not to exceed 300 mg/dose
Children: 20-40 mg/kg/d PO/IV/IM divided q6h
Can increase blood levels of theophylline, warfarin, tricyclic antidepressants, triamterene, phenytoin, quinidine, propranolol, metronidazole, procainamide, and lidocaine
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Elderly patients may experience confusional states; may cause impotence and gynecomastia in young males; may increase levels of many drugs; adjust dose or discontinue treatment if changes in renal function occur; adverse effects include headache and pancytopenia
Ranitidine (Zantac)
Inhibits histamine stimulation of the H2 receptor in gastric parietal cells, which reduces gastric acid secretion, gastric volume, and hydrogen ion concentrations.
Adult
3.5 mg/kg/dose PO bid/tid ac and hs; alternatively, 150 mg PO bid or 75 mg PO bid
Pediatric
Neonates: 2-4 mg/kg PO q8-12h or 2 mg/kg IV q6-8h
Infants: 2-3 mg/kg/dose PO q8-12h
Children: 2-3 mg/kg/dose PO q6-8h
May decrease effects of ketoconazole and itraconazole; may alter serum levels of ferrous sulfate, diazepam, nondepolarizing muscle relaxants, and oxaprozin
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Caution in renal or liver impairment; if changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment; adverse effects include headache and malaise
Famotidine (Pepcid)
Competitively inhibits histamine at H2 receptor of gastric parietal cells, resulting in reduced gastric acid secretion, gastric volume, and hydrogen ion concentrations.
Adult
10 mg PO bid
Pediatric
1-1.2 mg/kg/d PO divided q8-12h; not to exceed 80 mg/d
0.6-0.8 mg/kg/d IV divided q8-12h
May decrease effects of ketoconazole and itraconazole; levels may increase with hydrochlorothiazide; fluconazole levels may decrease with long-term coadministration of rifampin; may increase concentrations of theophylline, phenytoin, tolbutamide, cyclosporine, glyburide, and glipizide; effects of anticoagulants may increase with fluconazole coadministration
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
If changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment
Proton pump inhibitors
These agents are indicated in patients who require complete acid suppression (eg, infants with chronic respiratory disease or neurologic disabilities). Administer with the first meal of the day. Children with nasogastric or gastrostomy tubes may have granules mixed with an acidic juice or suspensions; tubes must then be flushed to prevent blockage.
Lansoprazole (Prevacid)
Suppresses gastric acid secretion by specific inhibition of the (H+, K+)-ATPase enzyme system (ie, proton pump) at the secretory surface of the gastric parietal cell. Blocks the final step of acid production. The effect is dose-related and inhibits both basal and stimulated gastric acid secretion, thus increasing gastric pH. Easy to administer to children because available as cap, PO disintegrating tab, and granules for PO susp.
Adult
30 mg PO qd
Pediatric
<1 year: Not established; 1-2 mg/kg/d PO suggested as "step-up" therapy
1-11 years:
<30 kg: 15-30 mg PO qd or 1-2 mg/kg/d; not to exceed 30 mg qd; administer for up to 12 wk
>30 kg: 30 mg PO qd; administer for up to 12 wk
>11 years: Administer as in adults
Take before meals; do not chew or crush capsules
Cytochrome P450 isoenzyme CYP2C19 and CYP3A3/4 substrate; increases theophylline clearance mildly (∼10%); may increase warfarin effects; may interfere with the absorption of ketoconazole, ampicillin, iron salts, and digoxin; sucralfate delays and decreases lansoprazole absorption by 30%; cranberry juice significantly reduces gastric pH and may reduce proton pump inhibitors effectiveness
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Consider adjusting dose in liver impairment; Prevacid SoluTabs contain aspartame, which is metabolized to phenylalanine and must be used with caution in patients with phenylketonuria
Omeprazole (Prilosec)
Decreases gastric acid secretion by inhibiting the parietal cell H+/K+ ATPase pump. Used for the short-term and long-term treatment (4-8 wk to 12 mo) of GERD.
Adult
GERD: 20 mg PO qd
Pediatric
Wide dosage range of 0.7-3.3 mg/kg/d PO has been reported in the pediatric literature
May decrease effects of itraconazole and ketoconazole; may increase toxicity of warfarin, digoxin, and phenytoin
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Bioavailability may increase in elderly patients; adverse effects include headache, rash, diarrhea, hypergastrinemia, and polyps
Esomeprazole (Nexium)
S-isomer of omeprazole. Inhibits gastric acid secretion by inhibiting H+/K+ -ATPase enzyme system at secretory surface of gastric parietal cells.
Used in severe cases of and patients not responding to H2 antagonist therapy.
Used for up to 4 wk to treat and relieve symptoms of active duodenal ulcers; may be used up to 8 wk to treat all grades of erosive esophagitis.
Adult
20 mg PO qd for 4 wk
Pediatric
<1 year: Not established
1-11 years: 10-20 mg PO qd for up to 8 wk
12-17 years: 20-40 mg PO qd for up to 8 wk
Extensively metabolized by CYP2C19 and CYP3A4, also inhibits CYP2C19; coadministration with CYP2C19 and CYP3A4 inhibitors (eg, voriconazole) may increase esomeprazole levels, but dosage adjustment is not normally required; may decrease atazanavir plasma levels; decreases diazepam clearance by 45%; postmarketing surveillance found coadministration with warfarin may increase INR and prothrombin time; amoxicillin or clarithromycin may increase plasma levels of esomeprazole when used concurrently; may reduce absorption of dapsone; may increase levels of diazepam and GI absorption of digoxin; may decrease absorption of iron, ketoconazole and itraconazole
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Symptomatic relief with proton pump inhibitors may mask symptoms of gastric malignancy; frequently occurring (>1%) adverse effects include headache, diarrhea, nausea, flatulence, abdominal pain, constipation, and xerostomia
More on Gastroesophageal Reflux |
| Overview: Gastroesophageal Reflux |
| Differential Diagnoses & Workup: Gastroesophageal Reflux |
Treatment & Medication: Gastroesophageal Reflux |
| Follow-up: Gastroesophageal Reflux |
| Multimedia: Gastroesophageal Reflux |
| References |
| « Previous Page | Next Page » |
References
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Further Reading
Keywords
GER, gastroesophageal reflux disease, GERD, motility, heartburn, physiologic GER, lower esophageal sphincter, LES, esophagus, transient LES relaxation, tLESR, failure to thrive, erosive esophagitis, esophageal stricture formation, chronic respiratory disease, Barrett esophagus, esophageal mucosal dysplasia, asthma, gastric outlet obstruction, reactive airway disease, laryngeal inflammatory disease, otitis media, otalgia, chronic sinusitis, heartburn, apnea, bradycardia, pneumonitis, waterbrash, Sandifer syndrome, opisthotonus, torticollis, laryngitis, halitosis, pharyngitis, hiatal hernia, gastroparesis, pyloric stenosis, apparent life-threatening event, ALTE, treatment, diagnosis




Treatment & Medication: Gastroesophageal Reflux