Read Rosen & Barkin's 5-Minute Emergency Medicine Consult Online

Authors: Jeffrey J. Schaider,Adam Z. Barkin,Roger M. Barkin,Philip Shayne,Richard E. Wolfe,Stephen R. Hayden,Peter Rosen

Tags: #Medical, #Emergency Medicine

Rosen & Barkin's 5-Minute Emergency Medicine Consult (266 page)

BOOK: Rosen & Barkin's 5-Minute Emergency Medicine Consult
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ESSENTIAL WORKUP
  • A well-hydrated, comfortable child with a normal physical exam and recent history of good weight gain may not need any ED workup beyond assuring good follow-up.
  • Children who show evidence of distress, dehydration, discomfort, respiratory distress, or poor weight gain require further evaluation.
DIAGNOSIS TESTS & NTERPRETATION
Lab
  • Initial assessment if child failing to thrive or appears malnourished:
    • CBC, urinalysis, electrolytes, BUN, glucose, erythrocyte sedimentation rate (ESR) and/or CRP, thyroid functions, LFTs, total protein, and albumin
  • Cultures of blood, urine, if concern of infection—CSF analysis and culture if concern for meningitis
  • Serum NH3, urine for organic acids, and blood for inborn errors or metabolism if concern for metabolic disorders
Imaging
  • CXR if suspected cardiopulmonary concerns
  • EKG if cardiac disease suspected
  • Referral or admission for ultrasound and other imaging studies as indicated. Fiberoptic or videofluoroscopic evaluation of swallowing may be needed.
  • MRI if concerns for brainstem, skull base, or spinal problems
Diagnostic Procedures/Surgery
  • May need a multidisciplinary evaluation involving speech pathologist, pediatrician, and potentially an otolaryngologist.
  • Surgical correction of specific pathology
DIFFERENTIAL DIAGNOSIS

Feeding disorder encompasses symptoms observed as a final pathway for many disorders.

Specific clues to the etiology may include:

  • Prolonged feeding, fatigue:
    • Consider cardiac disease.
  • Recurrent pneumonias:
    • Consider chronic aspiration.
  • Stridor with feeds:
    • Consider glottic or subglottic anomalies.
  • Suck–swallow–breathing coordination:
    • Consider nasal congestion, choanal atresia.
  • Vomiting, diarrhea, abdominal pain, colic:
    • Consider allergy or GER.
TREATMENT
PRE HOSPITAL
  • Assess vital signs and hydration; resuscitate as necessary.
  • Assess for and treat hypoglycemia.
INITIAL STABILIZATION/THERAPY
  • Cardiovascular/respiratory/fluid resuscitation as needed
  • Assess for and treat hypoglycemia if suspected.
ALERT
  • Certain inborn errors of metabolism (glycogen storage diseases) can cause profound hypoglycemia if unable to take PO feeds—if known or suspected, IV dextrose should be started immediately
  • Bilious vomiting in a young infant may be a sign of malrotation with volvulus causing intestinal ischemia—this requires emergent surgical consultation.
ED TREATMENT/PROCEDURES
  • Treat dehydration if present:
    • Oral rehydration if practical
    • IV if PO contraindicated, not tolerated, or impractical
  • Ondansetron for acute vomiting
  • Treat respiratory distress if present:
    • Nasal suction to clear secretions prior to feeding may be very helpful in young infants with URI/bronchiolitis symptoms
    • Oxygen and other interventions as needed
  • Treat infection if suspected.
ALERT

Patients with severe malnutrition are at risk for sepsis AND may have blunted physiologic responses—a high index of suspicion for infection is warranted in severely malnourished patients.

MEDICATION

Ondansetron: 0.1 mg/kg IV or PO q8h PRN nausea or vomiting—min. oral dose 2 mg, max. dose 4 mg:

  • Monitor if patient at risk of QT prolongation
  • For short-term use (2–3 doses) in patients >6 mo.
  • Review FDA black box warning re QT prolongation
FOLLOW-UP
DISPOSITION
Admission Criteria
  • Suspected systemic infection
  • Inability to maintain hydration
  • Sustained hypoxia during feeding
  • Significant failure to thrive:
    • Particularly in infants <3 mo
  • Decompensated cardiopulmonary disease
  • Symptomatic anemia or endocrine dysfunction
  • Negligent or overwhelmed caretaker
Discharge Criteria
  • Demonstrated ability to tolerate oral feedings
  • Weight gain if failure to thrive
  • Reliable caretaker and follow-up
Issues for Referral
  • Specific referrals based on source of problem
  • For complex or chronic feeding problems, a multidisciplinary approach is often needed.
  • Chronic disease process may interfere with feeding AND increase caloric needs:
    • Nonoral nutrition such as percutaneous endoscopic gastrostomy (PEG) tubes are often needed to address these issues.
FOLLOW-UP RECOMMENDATIONS
  • When available, a primary provider is the most important resource for follow-up.
  • In the case of complex problems, a multidisciplinary approach is often needed—the primary provider is often in the best position to coordinate this.
PEARLS AND PITFALLS
  • Successful feeding in infants requires coordinated, effective interaction of complex physiologic, developmental, and environmental factors.
  • The factors are interdependent—disruption of 1 often leads to disruption of others:
    • Premature infant gavage fed for immature suck–swallow coordination, misses critical period for developing this reflex—develops aversion to oral stimulus because of recurrent noxious stimuli.
  • Feeding problems of recent, acute onset are likely to have a single identifiable cause:
    • Gastroenteritis, pyloric stenosis, pharyngitis, sepsis
  • In an infant with upper respiratory symptoms the answer may be as simple as vigorously suctioning the nose to effectively clear it immediately before feeding
  • More chronic, long-term problems are more likely to have multifactorial and/or subtle causes:
    • Feeding is an essential part of the parent–child interaction:
      • Dysfunctional interaction may be the cause of or a response to a feeding problem.
  • Chronic feeding issues of medical origin may result in continued behavioral feeding difficulties even after the medical problem is corrected.
  • Swallowing disorders and aspiration are frequently occult.
ADDITIONAL READING
  • Arvedson JC. Assessment of pediatric dysphagia and feeding disorders: Clinical and instrumental approaches.
    Dev Disabil Res Rev
    . 2008;14(2):118–127.
  • Bernard-Bonnin AC. Feeding problems of infants and toddlers.
    Can Fam Physician
    . 2006;52(10):1247–1251.
  • McDevitt, Barbara E. Vomiting, spitting up, and feeding disorders. In: Baren JM, Rothrock SG, Brennan JA, et al, eds.
    Pediatric Emergency Medicine
    . Philadelphia, PA: Saunders-Elsevier; 2008:319–327.
See Also (Topic, Algorithm, Electronic Media Element)
  • Failure to Thrive
  • Feeding Tube Complications
  • Inborn Errors of Metabolism
  • Intussusception
  • Irritable Infant
  • Malrotation
  • Pyloric Stenosis
  • Vomiting, Pediatric
CODES
ICD9
  • 779.31 Feeding problems in newborn
  • 783.0 Anorexia
  • 783.3 Feeding difficulties and mismanagement
ICD10
  • P92.9 Feeding problem of newborn, unspecified
  • R63.0 Anorexia
  • R63.3 Feeding difficulties
FEEDING TUBE COMPLICATIONS
Colleen N. Hickey

Jennifer L. Kolodchak
BASICS
DESCRIPTION
  • Extubation:
    • Accidental or intentional
    • More common with nasoenteric tubes compared with percutaneous endoscopic gastrostomy (PEG) tubes, gastrostomy tubes (G tubes), or jejunostomy tubes (J tubes)
  • Occlusion:
    • Small diameter:
      • Most common with nasoenteric tubes
    • Pill fragments
    • Inadequate flushing
    • Physical incompatibilities between formula and medications:
      • Adherence of formula residue to inner wall
    • Essential to rule out malposition, fracture, and dislodgment
  • Peristomal wound infections:
    • Risk factors:
      • Malnutrition
      • Stomal leak
      • Local irritation
      • Poor wound care
      • Immunosuppression
      • Diabetes mellitus
      • Poor wound healing
      • Obesity
    • Excessive traction on tube:
      • Leads to delayed maturation of gastrocutaneous tract
      • Increases stomal leakage
  • Stoma leak:
    • Problematic with distal obstruction (mechanical or dysmotility); more common with high gastric residual
    • Excessive tube motion
  • Aspiration pneumonia:
    • At risk:
      • Impaired cough/gag reflex
      • Delayed gastric emptying from ileus
      • Obstruction
      • Gastroparesis
      • Gastroesophageal reflux (frequent with large nasoenteric tube)
  • Diarrhea:
    • Medication induced:
      • Antibiotics
      • Promotility agents
    • Overgrowth of
      Clostridium difficile
      , other bacteria, or
      Candida
    • High osmolar formula
  • Feeding intolerance:
    • High residual suggests GI motility dysfunction
    • Delivery is too rapid
    • High osmolarity formula
    • Lactose or fat intolerance
    • Low serum albumin
  • Uncommon complications:
    • Abdominal wall hematoma
    • Fistulas:
      • Hepatogastric
      • Gastrocolic
      • Colocutaneous
    • Perforation (usually with placement)
    • Pressure sores/ulcerations
    • GI bleeding
      • Esophagitis, gastric pressure ulcers, concomitant PUD
    • Gastric outlet obstruction
      • Partial or complete obstruction at the pylorus or duodenum by part of tube or Foley catheter balloon used for temporary replacement
    • Buried bumper syndrome
      • Rare but potentially serious
      • Bumper becomes lodged between the gastric wall and skin due to gastric ulceration from excessive tension
    • Bowel volvulus around PEG tube
BOOK: Rosen & Barkin's 5-Minute Emergency Medicine Consult
7.03Mb size Format: txt, pdf, ePub
ads

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