eMedicine Specialties > Pediatrics: General Medicine > Pulmonology

Aspiration Syndromes: Treatment & Medication

Author: Cecilia P Mikita, MD, MPH, Associate Program Director, Allergy-Immunology Fellowship, Chief, Clinical Services, Allergy-Immunology Clinic, Walter Reed Army Medical Center
Coauthor(s): Charles Callahan, DO, Professor, Deputy Chief of Clinical Services, Walter Reed Army Medical Center
Contributor Information and Disclosures

Updated: Apr 21, 2008

Treatment

Medical Care

  • Conservative therapy is the initial treatment of choice to prevent aspiration syndromes and often results in significant improvement in respiratory symptoms. Position infants in the prone or upright position. Avoid placing infants younger than 6 months in a seated position for approximately 90 minutes after a feed. Do not feed the infant within 90 minutes before bedtime. Elevation of the head of the bed approximately 30° may help, although young infants may slide down the bed during the night. Dietary modifications include thickening feeds for infants; breastfeeding; decreasing volume of feeds (10-20 mL/kg per feeding); and feeding small, frequent meals. Patients with swallowing dysfunction may benefit from certain food consistencies, positioning, and adaptive feeding equipment or utensils.
  • The management of an acute aspiration event consists of conservative management, observation, and possible antibiotic therapy. Initially, the patient's upper airway should be cleared and endotracheal intubation should be considered if the patient is unable to protect his airway. Close monitoring in an inpatient setting is recommended for at least 48 hours. Initially, empiric antibiotic therapy is not recommended, even if fever, clinical, laboratory, or radiographic findings are present. Selection of resistant organisms with the use of empiric, broad-spectrum antibiotic therapy is always a concern, especially in an uncomplicated chemical pneumonitis picture. If the patient fails to improve after 48 hours, the addition of broad-spectrum antibiotics is recommended.
  • A second or third generation cephalosporin is appropriate to cover potential gram-positive flora from the oropharynx and gram-negative organisms from the GI tract. Anaerobic coverage is not routinely required initially. Limited and controversial data on the role of corticosteroids in the management of acute aspiration events are available. Numerous animal studies and clinical trials fail to demonstrate a significant beneficial effect of corticosteroids after acute aspiration events. Based on these data, routine administration of systemic corticosteroids is not recommended.

Surgical Care

  • Surgical management with Nissen fundoplication and/or gastrojejunostomy is generally not first-line therapy for gastroesophageal reflux (GER) lung disease but may be appropriate for some individuals with neurological impairment.14 Surgical treatment of curable anatomic disorders, such as malrotation, is paramount.
  • Patients who are neurologically impaired, have GER, and require a feeding tube are usually initially treated with fundoplication and gastrostomy. However, a percutaneous endoscopic gastrojejunostomy may be an intermediate step before surgical intervention.
  • Several surgical procedures have been tried as an adjunct to fundoplication and gastrostomy to prevent direct aspiration. Total laryngectomy, glottic closure, tracheostomy, and injection of Teflon into the vocal cords have all been tried in patients with persistent direct aspiration.
  • Laryngotracheal separation, with or without end-to-side laryngoesophagectomy, has been tried more recently in children with neurological impairment who have intractable aspiration pneumonia as an adjunct to fundoplication and gastrostomy.15 In this procedure, the larynx and trachea are permanently divided; therefore, aspiration can never occur, but phonation is sacrificed.

Consultations

  • A primary care provider can successfully provide routine medical care for children with aspiration syndromes.
  • Consultation with a speech-language pathologist or occupational therapist is recommended to assess swallowing dysfunction. Oral structure and function, clinical signs of safe swallowing, and positioning should be assessed.
  • Refer patients to a pediatric pulmonologist and/or pediatric gastroenterologist if the patient does not respond to conservative or simple medical therapy or if the ordered studies are equivocal.
  • A pediatric neurologist should thoroughly evaluate patients with possible neuromuscular disorders.

Diet

  • Several dietary modifications can be initiated to decrease the risk of aspiration. Decreasing volume and increasing frequency of feeds, breastfeeding, thickening feeds, and not feeding within 90 minutes of nap or bedtime may decrease GER and aspiration.
  • Special feeding equipment or utensils and positioning may also help patients with swallowing dysfunction or anatomical defect.
  • In certain cases, transpyloric feedings may be necessary to decrease the risk of aspiration.
  • In addition, avoidance of certain foods (eg, caffeine, fatty meals, carbonated beverages, peppermint, citrus) may decrease GER in older children and adults.
  • If the volume of aspiration is greater than 10% of the bolus feed, enteral feeds may not be appropriate.

Activity

  • Simple modifications in activity help decrease incidence of physiologic and pathologic GER.
  • Elevation of the head of the bed approximately 30° and avoidance of seated devices for approximately 90 minutes after feeding may decrease GER and aspiration.
  • Avoidance of prolonged use of seated devices in very young infants may be beneficial.

Medication

Consider medical therapy if conservative therapies have failed. One may consider an upper GI before the administration of medications to rule out an anatomic abnormality.

Prokinetic agents

These agents are used to augment cholinergic activity and to improve motility in the GI tract.


Cisapride (Propulsid)

Increases LES tone, improves esophageal peristalsis, increases gastric contractions, and accelerates gastric emptying. Has been associated with serious, and sometimes fatal, cardiovascular toxicity. In the United States, only available through an investigational limited access program by Janssen Pharmaceutica (1-877-795-4247). May still be commercially available in other countries. Must obtain a 12-lead ECG before initiation of therapy. Do not give if QTc >450 ms.

Adult

10-20 mg PO qid; 15 min before meals and hs

Pediatric

0.1 mg/kg/dose PO tid; 15 min before meals and hs; not to exceed 10 mg qid

Avoid combinations with drugs known to inhibit CYP450 3A4 or prolong the QT interval (eg, erythromycin, clarithromycin, troleandomycin; fluconazole, itraconazole, ketoconazole; astemizole; indinavir, ritonavir; bepridil, terodiline; quinidine, procainamide, sotalol; sertindole; nefazodone, amitriptyline, maprotiline; prochlorperazine, promethazine; sparfloxacin; grapefruit juice)
Cimetidine or ranitidine increase bioavailability; atropine decreases effect; cisapride decreases absorption of digoxin and increases toxicity of warfarin and digoxin

Documented hypersensitivity; CYP450 3A4 inhibitors (eg, erythromycin, ketoconazole, ritonavir) decrease elimination and increase toxicity of cisapride; cardiomyopathy; congestive heart failure; history of ventricular arrhythmias; history of prolonged QTc intervals, ischemic, or valvular heart disease; known family history of congenital QT syndrome; second or third degree AV block; sick sinus syndrome; renal failure; respiratory failure; conditions that result in electrolyte disorders, such as severe dehydration, vomiting, or malnutrition

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

Consult a pediatric gastroenterologist for use of this medication; obtain baseline ECG and serum electrolytes, calcium, magnesium, and phosphate before starting this regimen


Metoclopramide (Reglan, Clopra, Maxolon)

Increases resting esophageal sphincter tone, improves gastric tone and peristalsis, relaxes the pyloric sphincter, and augments duodenal peristalsis with the net effect of increasing GI motility and decreasing reflux potential. Dopamine antagonist that stimulates acetylcholine release in the myenteric plexus. Acts centrally on chemoreceptor triggers in the floor of the fourth ventricle, which provides important antiemetic activity.

Adult

5-10 mg PO qid

Pediatric

0.1 mg/kg/dose PO qid

Anticholinergic agents may antagonize effects of metoclopramide; opiate analgesics may increase metoclopramide toxicity in CNS

Documented hypersensitivity; pheochromocytoma or GI hemorrhage, obstruction or perforation; history of seizure disorders

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Administer 30 min before feeds and hs; adjust dose in renal failure; monitor for extrapyramidal adverse effects to include chorea, dystonia, akinesia, dyskinesias, myoclonus, or ballism; caution in history of mental illness or Parkinson disease


Bethanechol (Urecholine)

Cholinergic agent that increases tone, amplitude of contractions, peristaltic activity, and secretions of the GI tract.

Adult

10-50 mg PO tid/qid

Pediatric

0.1-0.2 mg/kg/dose PO ac and hs; not to exceed 4 doses/d

Concurrent administration with ganglion-blocking compounds may cause drop of blood pressure to critical levels

Documented hypersensitivity; peptic ulcer disease, asthma, obstructive pulmonary disease, bradycardia, vasomotor instability, hypotension, atrioventricular conduction defects, hyperthyroidism, epilepsy, mechanically obstructed GI or GU tract

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

May cause hypotension, nausea, bronchospasm, salivation, flushing, abdominal cramps

Histamine (H2) receptor antagonists

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 and work best in nonerosive esophagitis. Because of the superiority of proton pump inhibitors (PPIs), H2 blockers may be reserved for use in patients unable to tolerate PPIs.


Cimetidine (Tagamet)

Inhibits histamine stimulation of the H2 receptor in gastric parietal cells, which, in turn, reduces gastric acid secretion, gastric volume, and reduced hydrogen concentrations.

Adult

150 mg PO qid; not to exceed 600 mg/d

Pediatric

4-10 mg/kg/dose PO qid

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

May increase levels of many drugs; adjust dose or discontinue treatment if changes in renal function occur


Ranitidine (Zantac)

Inhibits histamine stimulation of the H2 receptor in gastric parietal cells, which, in turn, reduces gastric acid secretion, gastric volume, and reduced hydrogen concentrations.

Adult

150 mg PO bid; not to exceed 600 mg/d

Pediatric

1-2 mg/kg/dose PO bid; not to exceed 6 mg/kg/d

Inhibits CYP450 2D6 and 3A4; may decrease effects of ketoconazole and itraconazole; may alter serum levels of ferrous sulfate, diazepam, nondepolarizing muscle relaxants, and oxaprozin
May increase levels of nifedipine; may decrease levels of ketoconazole, itraconazole, delavirdine

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

Caution in renal or liver impairment; if changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment

Proton pump inhibitors

These agents act by blocking the enzyme system responsible for active transport of protons into the GI lumen (ie, hydrogen/potassium adenosine triphosphatase [H+/K+ ATPase]) of the gastric parietal cell, also known as the proton pump.

Administer with the first meal of the day; children with nasogastric or gastrostomy tubes may have granules mixed with an acidic juice, and then the tubes are flushed to prevent blockage.


Omeprazole (Prilosec)

Inhibits gastric acid secretion. Used for the short-term treatment (4-8 wk) of GER disease.

Adult

20 mg PO qd for 4-8 wk

Pediatric

Not established, limited data available; 0.6-0.7 mg/kg/dose PO qd; may be increased to 0.6-0.7 mg/kg/dose PO bid

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

Administer 30 min ac; do not chew or crush capsule

More on Aspiration Syndromes

Overview: Aspiration Syndromes
Differential Diagnoses & Workup: Aspiration Syndromes
Treatment & Medication: Aspiration Syndromes
Follow-up: Aspiration Syndromes
Multimedia: Aspiration Syndromes
References

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Further Reading

Keywords

aspiration syndromes, aspirate, aspiration into the lungs, gastroesophageal reflux, GER, swallowing dysfunction, neurological disorders, neurologic disorders, structural abnormalities, fluid aspiration, foreign body aspiration, foreign substance aspiration, pneumonia, aspiration pneumonia, deglutition pneumonia, bronchopneumonia, cricopharyngeal dysfunction, cricopharyngeal incoordination of infancy, transient pharyngeal muscle dysfunction, superior laryngeal nerve damage, vocal cord paralysis, cerebral palsy, muscular dystrophy, Riley-Day syndrome, familial dysautonomia

anatomic disorders, cleft palate, esophageal atresia, tracheoesophageal fistula, duodenal obstruction, malrotation, motility disorders, achalasia, microaspiration, asthma, gastroenteritis, eosinophilic esophagitis, pharyngeal dysphagia, nasopharyngeal reflux, sudden infant death syndrome, acute life-threatening episode, ALTE, recurrent wheezing, apnea, chronic cough, recurrent pneumonia, upper respiratory infection, URI, obstructive apnea, bronchorrhea, failure to thrive, stridor, hoarseness, night sweats, purulent sputum, bronchopulmonary dysplasia, pulmonary abscess, pulmonary fibrosis, bronchiectasis, fever, tachypnea, small airway obstruction, pneumonitis 

Contributor Information and Disclosures

Author

Cecilia P Mikita, MD, MPH, Associate Program Director, Allergy-Immunology Fellowship, Chief, Clinical Services, Allergy-Immunology Clinic, Walter Reed Army Medical Center
Cecilia P Mikita, MD, MPH is a member of the following medical societies: American Academy of Allergy Asthma and Immunology, American Academy of Pediatrics, American College of Allergy, Asthma and Immunology, and Clinical Immunology Society
Disclosure: Nothing to disclose.

Coauthor(s)

Charles Callahan, DO, Professor, Deputy Chief of Clinical Services, Walter Reed Army Medical Center
Charles Callahan, DO is a member of the following medical societies: American Academy of Pediatrics, American College of Chest Physicians, American College of Osteopathic Pediatricians, American Thoracic Society, Association of Military Surgeons of the US, and Christian Medical & Dental Society
Disclosure: Nothing to disclose.

Medical Editor

Thomas Scanlin, MD, Chief, Division of Pediatric Pulmonary & Cystic Fibrosis, Assistant Professor, Department of Pediatrics, Robert Wood Johnson University Medical Group
Thomas Scanlin, MD is a member of the following medical societies: American Thoracic Society and Society for Pediatric Research
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc
Disclosure: Pfizer Inc Stock Investment from broker recommendation; Avanir Pharma Stock Investment from broker recommendation

Managing Editor

Heidi Connolly, MD, Associate Professor of Pediatrics and Psychiatry, University of Rochester;Director, Pediatric Sleep Medicine Services, Strong Sleep Disorders Center
Heidi Connolly, MD is a member of the following medical societies: American Academy of Pediatrics, American Thoracic Society, and Society of Critical Care Medicine
Disclosure: Nothing to disclose.

CME Editor

Mary E Cataletto, MD, Associate Director, Division of Pediatric Pulmonology, Winthrop University Hospital; Associate Professor, Department of Clinical Pediatrics, State University of New York at Stony Brook
Mary E Cataletto, MD is a member of the following medical societies: American Academy of Pediatrics, American Heart Association, and American Thoracic Society
Disclosure: Nothing to disclose.

Chief Editor

Michael R Bye, MD, Attending Physician, Pediatric Pulmonary Medicine, Columbia University Medical Center; Professor of Clinical Pediatrics, Division of Pulmonary Medicine, Columbia University College of Physicians and Surgeons
Michael R Bye, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Chest Physicians, and American Thoracic Society
Disclosure: Merck Honoraria Speaking and teaching

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