Pediatric Respiratory Failure Workup

  • Author: Shelley C Springer, MD, MBA, MSc, JD, FAAP; Chief Editor: Timothy E Corden, MD   more...
 
Updated: Jan 27, 2012
 

Approach Considerations

Arterial blood gas (ABG) measurement can be used to define acute respiratory failure. Arbitrary definitions include a partial pressure of CO2 (PaCO2) greater than 50 mm Hg, a partial pressure of oxygen (PaO2) less than 60 mm Hg, or arterial oxygen saturation less than 90%. An elevated serum bicarbonate level suggests metabolic compensation for chronic hypercapnia.

A complete blood count (CBC) may be helpful. Polycythemia suggests chronic hypoxemia.

Electrolyte abnormalities can contribute to weakness; hypokalemia, hypocalcemia, and hypophosphatemia can impair muscle contraction.

Calculate the alveolar-arterial oxygen difference ([A-a]DO2), which is the difference between the alveolar PAO2 and the arterial PaO2. This value is an index of the efficiency of gas exchange by the lungs.

The alveolar gas equation is used to calculate the PAO2 on the basis of the relationship between the pressure of oxygen in inspired gas (PiO2), the PaCO2, and the respiratory quotient (RQ), as follows: PAO2 = FiO2 (Pb - PH 2O) - (PaCO2/RQ).

PiO2 is a function of the fractional concentration of inspired oxygen (FiO2), the barometric pressure (Pb), and the partial pressure of water vapor (PH 2O) in humidified air.

RQ is the ratio of the volume of carbon dioxide expired to the volume of oxygen consumed by an organism. The body normally produces approximately 200 mL of carbon dioxide per minute and consumes approximately 250 mL of oxygen per minute; therefore, RQ is 0.8. Different fuel sources produce different RQ values: the RQ for carbohydrates is 1; protein is 0.8; and fat is 0.7.

In children, (A-a)DO2 is normally 5-10 and reflects venous admixture from anatomic right-to-left shunts, which include the bronchial circulation, thebesian veins, and small arteriovenous anastomoses in the lung.

The PaO2/FiO2 ratio is a commonly used indicator of gas exchange. A PaO2/FiO2 less than 200 is correlated with a shunt fraction greater than 20%. For ventilated patients, a similar calculation is called the oxygen index, calculated by (PaO2 x FiO2/mean airway pressure) x 100. These numbers are used to quickly communicate the severity of respiratory failure and can provide some diagnostic and therapeutic guidance (eg, when to start inhaled nitric oxide).

Imaging studies may include plain radiography or computed tomography (CT), or magnetic resonance imaging (MRI) scans. Fluoroscopy is valuable to evaluate the movement of the diaphragms and dynamic obstructive lesions of both the extrathoracic and intrathoracic airway. Ventilation/perfusion (V/Q) scanning can predict a probability of V/Q mismatch secondary to a pulmonary embolism.

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Imaging Studies

Radiography

Lateral and anteroposterior (AP) radiographs of the neck can reveal a radiopaque foreign body or soft-tissue structures encroaching on the lumen of the airway, such as in acute epiglottitis.

Chest radiographs may yield helpful findings (see examples in the images below).

Bilateral airspace infiltrates on chest radiographBilateral airspace infiltrates on chest radiograph film secondary to acute respiratory distress syndrome that resulted in respiratory failure. Extensive left-lung pneumonia caused respiratory fExtensive left-lung pneumonia caused respiratory failure; the mechanism of hypoxia is intrapulmonary shunting.

Evaluate for abnormalities that require immediate intervention (eg, malpositioned endotracheal tube, pneumothorax).

Common findings associated with respiratory failure include the following:

  • Focal or diffuse pulmonary disease (eg, pneumonia, ARDS)
  • Bilateral hyperinflation (eg, asthma)
  • Asymmetric lung expansion suggesting a bronchial obstruction
  • Pleural effusion
  • Cardiomegaly

If hypoxemia is present but the chest radiograph is clear, this finding could suggest cyanotic congenital heart disease, pulmonary hypertension, or pulmonary emboli.

CT and MRI

Chest CT scanning can be performed when sophisticated diagnostic images are needed. It can further define radiopacities due to vascular, pleural, interstitial, or airway lesions.

Airway CT scanning, MRI, and/or angiography can be used to differentiate deep-tissue structures, bone lesions, and vascular abnormalities.

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Other Pulmonary Function Tests

Useful information may be provided by determination of dead-space volume to tidal gas volume (VD/VT) and determination of the intrapulmonary shunt fraction (Qs/Qt).

Determination of dead-space volume to tidal gas volume

VD/VT is based on the difference between PaCO2 and the CO2 in exhaled gas (PeCO2). PeCO2 is measured by collecting expired gas in a large collection bag and using an infrared CO2 analyzer to measure the PCO2 in a sample of gas.

In a normal lung, the capillary blood equilibrates fully with alveolar gas; therefore, the PeCO2 approximates the PaCO2. As VD/VT increases, the PeCO2 falls below PaCO2.

Reference range VD/VT is approximately 0.30.

VD/VT = (PaCO2 - PeCO2)/PaCO2

Determination of the intrapulmonary shunt fraction

Qs/Qt is the ratio of shunted flow (Qs) to the total flow or cardiac output (Qt). It is derived by the relationship between the oxygen content in arterial blood (CaO2), mixed venous blood (CvO2), and pulmonary capillary blood (CcO2) while breathing FiO2 that equals 1.

Arterial oxygen content (in mL O2/dL) = [1.34 mL O2/g hemoglobin × hemoglobin (in g/dL) × SpO2] + [PaO2 (in mm Hg) × 0.003 mL O2/dL/mm Hg].

Directly measuring pulmonary capillary blood (CcO2) is difficult; therefore, CcO2 is assumed to be 100% when FiO2 equals 1.

The normal intrapulmonary shunt is less than 10%.

Qs/Qt = (CcO2 - CaO2)/(CcO2 - CvO2)

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Bronchoalveolar Lavage and Lung Biopsy

Bronchoalveolar lavage (BAL) is performed to identify a specific infectious pulmonary pathogen; bacterial, viral, and acid-fast bacillus (AFB) cultures and silver stains can be performed. BAL can also be performed to isolate lipid-laden macrophages (suggestive of recurrent aspiration) or pulmonary hemorrhage.

In an intubated patient, samples can be obtained blindly or bronchoscopically.

BAL is indicated in critically ill children to guide antimicrobial therapy and in children whose conditions have deteriorated during therapy.

Lung biopsy may be indicated if BAL does not reveal a pathogen, especially in immunocompromised hosts; it can identify Aspergillus species or Pneumocystis jiroveci. Lung biopsy is also helpful in the diagnosis of sarcoidosis and other granulomatous conditions.

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Other Tests

Electromyography (EMG) or nerve conduction testing can help determine the etiology for neuromuscular weakness leading to respiratory pump failure.

Fiberoptic and rigid bronchoscopy can be performed to assess large and small airways for anatomic abnormalities or foreign bodies.

Nasal airflow tracings coupled with chest-movement recordings (pneumograms) have a specific role in identifying sleep-associated extrathoracic airway obstruction and respiratory control abnormalities.

Thoracentesis is used in patients with pleural effusions, to check the cell count and protein level to determine whether pleural fluid is an exudate or transudate. Other pleural fluid studies include measurement of triglycerides, to determine whether the effusion is chylous, and bacterial and acid-fast bacterial (AFB) cultures. Cytology is used to evaluate for malignant effusions.

Test of respiratory mechanics and lung-volume measurements are most beneficial in following the progression of disease and the effects of treatment over time. Many infants and children cannot cooperate with traditional pulmonary function measurements. Many contemporary pediatric ventilators incorporate sophisticated sensors and software that measure inhaled and exhaled breaths and can display pulmonary flow loops and other pulmonary parametrics. This provides valuable information regarding real-time, as well as trended, pulmonary dynamics.

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Contributor Information and Disclosures
Author

Shelley C Springer, MD, MBA, MSc, JD, FAAP  Clinical Instructor, Department of Pediatrics, University of Vermont College of Medicine; Clinical Instructor, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health; Neonatologist, Pediatrix Medical Group; Assistant Clinical Professor, Department of Pediatrics, University of North Texas Science Center; Assistant Clinical Professor, Department of Pediatrics, Texas A&M Health Science Center College of Medicine

Shelley C Springer, MD, MBA, MSc, JD, FAAP is a member of the following medical societies: American Academy of Pediatrics

Disclosure: Nothing to disclose.

Coauthor(s)

Margaret A Priestley, MD  Assistant Professor of Clinical Anesthesiology and Critical Care, University of Pennsylvania School of Medicine; Clinical Director, Pediatric Intensive Care Unit, The Children's Hospital of Philadelphia

Margaret A Priestley, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, and Society of Critical Care Medicine

Disclosure: Nothing to disclose.

Jimmy W Huh, MD  Associate Professor of Anesthesiology, Critical Care and Pediatrics, Department of Anesthesiology and Critical Care Medicine, Hospital of the University of Pennsylvania and the Children's Hospital of Philadelphia

Jimmy W Huh, MD is a member of the following medical societies: American Academy of Pediatrics and Society of Critical Care Medicine

Disclosure: Nothing to disclose.

Chief Editor

Timothy E Corden, MD  Associate Professor of Pediatrics, Co-Director, Policy Core, Injury Research Center, Medical College of Wisconsin; Associate Director, PICU, Children's Hospital of Wisconsin

Timothy E Corden, MD is a member of the following medical societies: American Academy of Pediatrics, Phi Beta Kappa, Society of Critical Care Medicine, and Wisconsin Medical Society

Disclosure: Nothing to disclose.

References
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  4. Spence KL, Murphy D, Kilian C, McGonigle R, Kilani RA. High-flow nasal cannula as a device to provide continuous positive airway pressure in infants. J Perinatol. Dec 2007;27(12):772-5. [Medline].

  5. Campbell DM, Shah PS, Shah V, Kelly EN. Nasal continuous positive airway pressure from high flow cannula versus Infant Flow for Preterm infants. J Perinatol. Sep 2006;26(9):546-9. [Medline].

  6. Esteban A, Frutos-Vivar F, Ferguson ND, et al. Noninvasive positive-pressure ventilation for respiratory failure after extubation. N Engl J Med. Jun 10 2004;350(24):2452-60. [Medline].

  7. Habashi NM. Other approaches to open-lung ventilation: airway pressure release ventilation. Crit Care Med. Mar 2005;33(3 Suppl):S228-40. [Medline].

  8. Curley MA, Hibberd PL, Fineman LD, et al. Effect of prone positioning on clinical outcomes in children with acute lung injury: a randomized controlled trial. JAMA. Jul 13 2005;294(2):229-37. [Medline].

  9. Willson DF, Thomas NJ, Markovitz BP, et al. Effect of exogenous surfactant (calfactant) in pediatric acute lung injury: a randomized controlled trial. JAMA. Jan 26 2005;293(4):470-6. [Medline]. [Full Text].

  10. Conrad SA, Rycus PT, Dalton H. Extracorporeal Life Support Registry Report 2004. ASAIO J. Jan-Feb 2005;51(1):4-10. [Medline].

  11. Children's Healthcare of Atlanta. Available at http://www.lchoa.org/childrens-hospital-services/critical-care/ECMO-center/Volumes-and-Outcomes. Accessed 14 January, 2012.

  12. Haines NM, Rycus PT, Zwischenberger JB, Bartlett RH, Undar A. Extracorporeal Life Support Registry Report 2008: neonatal and pediatric cardiac cases. ASAIO J. Jan-Feb 2009;55(1):111-6. [Medline].

  13. Extracorporeal Life Support Organization. H1N1 ECLS Registry, Statistics from the H1N1 Registry (as of May 28, 2010). Available at http://www.elso.med.umich.edu/H1N1Registry.html.

  14. Gadek JE, DeMichele SJ, Karlstad MD, Pacht ER, Donahoe M, Albertson TE, et al. Effect of enteral feeding with eicosapentaenoic acid, gamma-linolenic acid, and antioxidants in patients with acute respiratory distress syndrome. Enteral Nutrition in ARDS Study Group. Crit Care Med. Aug 1999;27(8):1409-20. [Medline].

  15. Singer P, Shapiro H. Enteral omega-3 in acute respiratory distress syndrome. Curr Opin Clin Nutr Metab Care. Mar 2009;12(2):123-8. [Medline].

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Bilateral airspace infiltrates on chest radiograph film secondary to acute respiratory distress syndrome that resulted in respiratory failure.
Extensive left-lung pneumonia caused respiratory failure; the mechanism of hypoxia is intrapulmonary shunting.
A Bilevel positive airway pressure support machine is shown here. This could be used in spontaneous mode or timed mode (backup rate could be set).
Table 1. Survival Statistics from CHA, 2005-2009[11]
YearCHA (US)International
200558%54%
200647%53%
200771%56%
200857%54%
200975%55%
Table 2. 2009 Top 5 Diagnoses for ECMO and Survival Rates[11]
DiagnosisCHA (US)International
Bacterial pneumonia74%57%
Viral pneumonia78%63%
Aspiration pneumonia92%66%
Non-ARDS acute respiratory failure62%51%
Other65%52%
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