Diaphragmatic Paralysis Workup

  • Author: Nader Kamangar, MD, FACP, FCCP, FCCM; Chief Editor: Zab Mosenifar, MD   more...
 
Updated: Jun 3, 2011
 

Laboratory Studies

Arterial blood gas analysis demonstrates hypoxemia in persons with bilateral diaphragmatic paralysis. Hypoxemia develops from atelectasis and ventilation-perfusion mismatching. Progressive hypercapnia also develops with disease progression.

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Imaging Studies

In contrast to bilateral disease, physicians can usually diagnose unilateral paralysis with only radiographic studies.[3]

  • Chest radiography
    • This study reveals elevated hemidiaphragms, small lung volumes, and atelectasis.
    • In unilateral diaphragmatic paralysis, chest radiographic findings strongly suggest the diagnosis (see the image below).
  • Fluoroscopy
    • Because accessory muscle contraction may create the appearance of diaphragmatic movement, this study may mislead the physician when diagnosing bilateral diaphragmatic paralysis (see the image below).
    • Fluoroscopic sniff test (in which paradoxical elevation of the paralyzed diaphragm is observed with inspiration) can confirm chest radiographic findings regarding unilateral diaphragmatic paralysis (see the image below).[4]
  • Computed tomography scanning of the chest: This study may be indicated in certain patients to evaluate for potential causes of diaphragmatic paralysis that are due to mediastinal pathology.
  • Magnetic resonance imaging of the neck: This study may be indicated in certain patients to determine the presence of pathologic conditions involving the spinal column or nerve roots that are causing diaphragmatic paralysis.
  • Ultrasonography
    • M-mode ultrasonography is the latest method to evaluate the paralyzed diaphragm. The paralyzed side shows no active caudal movement of the diaphragm with inspiration and abnormal paradoxical movement (ie, cranial movement on inspiration), particularly with the sniff test.
    • M-mode ultrasonography is a relatively simple and accurate test for diagnosing paralysis of the diaphragm in the adult population, and it can be performed at the bedside and can be easily repeated if paralysis is not thought to be permanent.[5]
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Other Tests

  • Pulmonary function testing and arterial blood gas analysis
    • Measuring the vital capacity in the upright and supine positions is the most important pulmonary function test.
    • Normally, vital capacity in recumbency decreases by 10%. In unilateral paralysis, the vital capacity shows a decrease to 70-80% of the predicted level. The decrement is usually slightly more significant in the supine position.
    • In contrast, patients with bilateral diaphragmatic paralysis show a 50% decrease in vital capacity when they are supine. This decrease is from cephalad displacement of abdominal contents.
  • Electromyography
    • Record diaphragmatic electromyography (EMG) findings with other surface or esophageal electrodes; however, EMG has a limited role in unilateral diaphragmatic paralysis.
    • EMG may reveal a neuropathic or myopathic pattern, depending on etiology. Phrenic nerve stimulation at the neck can differentiate between neuropathy and myopathy.
  • Measurement of transdiaphragmatic pressure
    • This is the criterion standard for diagnosis.
    • This test is performed by placing a thin-walled balloon transnasally at the lower end of the esophagus, allowing reflection of the changes in pleural pressure. Then, a second balloon manometer is placed in the stomach to reflect changes in intra-abdominal pressure.
    • The difference between the 2 readings is the transdiaphragmatic pressure. Consult with an expert to perform the test and interpret the results. This measurement can help differentiate diaphragmatic paralysis from other causes of respiratory failure.
  • Maximal inspiratory pressures: Patients with diaphragmatic dysfunction and paralysis have a decrease in maximal inspiratory pressures (PI max). These patients cannot generate high negative inspiratory pressures. Therefore, the Pl max in these patients is less negative than -60 cm water.
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Contributor Information and Disclosures
Author

Nader Kamangar, MD, FACP, FCCP, FCCM  Associate Professor of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of California, Los Angeles, David Geffen School of Medicine, Olive View-UCLA Medical Center; Associate Program Director, Pulmonary and Critical Care Multi-Campus Fellowship Program, Cedars-Sinai/West Los Angeles Veterans Affairs/Los Angeles Kaiser Permanente/Olive View-UCLA Medical Center; Site Director, Pulmonary/Critical Care Fellowship Program, Olive View-UCLA Medical Center

Nader Kamangar, MD, FACP, FCCP, FCCM is a member of the following medical societies: American Academy of Sleep Medicine, American Association of Bronchology, American College of Chest Physicians, American College of Physicians, American Lung Association, American Medical Association, American Thoracic Society, California Thoracic Society, and Society of Critical Care Medicine

Disclosure: Nothing to disclose.

Coauthor(s)

Shahriar Pirouz, MD  Resident Physician, Department of Internal Medicine, Olive View University of California Los Angeles Medical Center

Disclosure: Nothing to disclose.

Sat Sharma, MD, FRCPC  Professor and Head, Division of Pulmonary Medicine, Department of Internal Medicine, University of Manitoba; Site Director, Respiratory Medicine, St Boniface General Hospital

Sat Sharma, MD, FRCPC is a member of the following medical societies: American Academy of Sleep Medicine, American College of Chest Physicians, American College of Physicians-American Society of Internal Medicine, American Thoracic Society, Canadian Medical Association, Royal College of Physicians and Surgeons of Canada, Royal Society of Medicine, Society of Critical Care Medicine, and World Medical Association

Disclosure: Nothing to disclose.

Specialty Editor Board

Ryland P Byrd Jr, MD  Professor, Department of Internal Medicine, Division of Pulmonary Medicine and Critical Care Medicine, Program Director of Pulmonary Diseases and Critical Care Medicine Fellowship, James H Quillen College of Medicine, East Tennessee State University; Medical Director of Respiratory Therapy, James H Quillen Veterans Affairs Medical Center

Ryland P Byrd Jr, MD is a member of the following medical societies: American College of Chest Physicians and American Thoracic Society

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Daniel R Ouellette, MD, FCCP  Associate Professor of Medicine, Wayne State University School of Medicine; Consulting Staff, Pulmonary Disease and Critical Care Medicine Service, Henry Ford Health System

Daniel R Ouellette, MD, FCCP is a member of the following medical societies: American College of Chest Physicians and American Thoracic Society

Disclosure: Boehringer Ingleheim Honoraria Speaking and teaching; Pfizer Honoraria Speaking and teaching; Astra Zeneca Honoraria Speaking and teaching

Timothy D Rice, MD  Associate Professor, Departments of Internal Medicine and Pediatrics and Adolescent Medicine, St Louis University School of Medicine

Timothy D Rice, MD is a member of the following medical societies: American Academy of Pediatrics and American College of Physicians

Disclosure: Nothing to disclose.

Chief Editor

Zab Mosenifar, MD  Director, Division of Pulmonary and Critical Care Medicine, Director, Women's Guild Pulmonary Disease Institute, Professor and Executive Vice Chair, Department of Medicine, Cedars Sinai Medical Center, University of California, Los Angeles, David Geffen School of Medicine

Zab Mosenifar, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, American Federation for Medical Research, and American Thoracic Society

Disclosure: Nothing to disclose.

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