eMedicine Specialties > Pediatrics: General Medicine > Gastroenterology

Gastroesophageal Reflux: Treatment & Medication

Author: Steven M Schwarz, MD, FAAP, FACN, AGAF, Professor of Pediatrics, Children's Hospital at Downstate, SUNY-Downstate Medical Center
Coauthor(s): Andre Hebra, MD, Chief, Division of Pediatric Surgery, Medical University of South Carolina; Professor of Surgery and Pediatrics, Medical University of South Carolina
Contributor Information and Disclosures

Updated: May 13, 2009

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.

      Algorithm for evaluation and "step-up" management...

      Algorithm for evaluation and "step-up" management of gastroesophageal reflux (GER).

      Algorithm for evaluation and "step-up" management...

      Algorithm for evaluation and "step-up" management of gastroesophageal reflux (GER).

    • 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.

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. N...

Diagram illustrating the Nissen fundoplication. Note how the stomach is wrapped around the esophagus (360º wrap).

Diagram illustrating the Nissen fundoplication. N...

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).

    Algorithm for evaluation and "step-up" management...

    Algorithm for evaluation and "step-up" management of gastroesophageal reflux (GER).

    Algorithm for evaluation and "step-up" management...

    Algorithm for evaluation and "step-up" management of gastroesophageal reflux (GER).

  • 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

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

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

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

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

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

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

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

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

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

Contributor Information and Disclosures

Author

Steven M Schwarz, MD, FAAP, FACN, AGAF, Professor of Pediatrics, Children's Hospital at Downstate, SUNY-Downstate Medical Center
Steven M Schwarz, MD, FAAP, FACN, AGAF is a member of the following medical societies: American Academy of Pediatrics, American College of Nutrition, American College of Physician Executives, American Gastroenterological Association, American Pediatric Society, Gastroenterology Research Group, New York Academy of Medicine, North American Society for Pediatric Gastroenterology and Nutrition, and Society for Pediatric Research
Disclosure: TAP Pharmaceuticals Honoraria Speaking and teaching; Curemark, LLC Consulting fee Board membership; Centocor, Inc. Grant/research funds Independent contractor

Coauthor(s)

Andre Hebra, MD, Chief, Division of Pediatric Surgery, Medical University of South Carolina; Professor of Surgery and Pediatrics, Medical University of South Carolina
Andre Hebra, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American College of Surgeons, American Medical Association, American Pediatric Surgical Association, Association for Academic Surgery, Society of Laparoendoscopic Surgeons, South Carolina Medical Association, Southeastern Surgical Congress, and Southern Medical Association
Disclosure: Nothing to disclose.

Medical Editor

Jayant Deodhar, MD, Associate Professor in Pediatrics, BJ Medical College, India; Honorary Consultant, Departments of Pediatrics and Neonatology, King Edward Memorial Hospital, India
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

B U K Li, MD, Professor of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Director, Pediatric Fellowships and Gastroenterology Fellowship, Medical Director, Functional Gastrointestinal Disorders and Cyclic Vomiting Program, Medical College of Wisconsin; Attending Gastroenterologist, Children's Hospital of Wisconsin
B U K Li, MD is a member of the following medical societies: Alpha Omega Alpha, American Gastroenterological Association, and North American Society for Pediatric Gastroenterology and Nutrition
Disclosure: Nothing to disclose.

CME Editor

Steven M Schwarz, MD, FAAP, FACN, AGAF, Professor of Pediatrics, Children's Hospital at Downstate, SUNY-Downstate Medical Center
Steven M Schwarz, MD, FAAP, FACN, AGAF is a member of the following medical societies: American Academy of Pediatrics, American College of Nutrition, American College of Physician Executives, American Gastroenterological Association, American Pediatric Society, Gastroenterology Research Group, New York Academy of Medicine, North American Society for Pediatric Gastroenterology and Nutrition, and Society for Pediatric Research
Disclosure: TAP Pharmaceuticals Honoraria Speaking and teaching; Curemark, LLC Consulting fee Board membership; Centocor, Inc. Grant/research funds Independent contractor

Chief Editor

Carmen Cuffari, MD, Associate Professor, Department of Pediatrics, Division of Gastroenterology/Nutrition, Johns Hopkins University School of Medicine
Carmen Cuffari, MD is a member of the following medical societies: American College of Gastroenterology, American Gastroenterological Association, North American Society for Pediatric Gastroenterology, Hepatology and Nutrition, and Royal College of Physicians and Surgeons of Canada
Disclosure: Nothing to disclose.

 
 
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