Oxygen is not for hypoventilation in neuromuscular disease by E.A. Oppenheimer MD, FCCP
Preface by Linda - This isn't an easy topic to digest but it is important to know if a doctor ever wants to put you on oxygen because you are having chronic breathing difficulties. Read carefully and keep with your medical papers.
If progressive respiratory failure occurs in people with neuromuscular disease, an abnormal nocturnal oximetry study is often an early indication that hypoventilation is occurring. There are significant periods of decreased oxygen levels in the blood or hypoxemia during sleep when lying flat, in addition to decreases in vital capacity (VC), maximum inspiratory force (MIF), and maximum expiratory force (MEF). Decreased oxygen saturation (SaO2) combined with increasing carbon dioxide (CO2) retention of hypercapnia are the hallmarks of hypoventilation. This is sometimes called ventilatory pump failure, due to the weakened respiratory muscles.
Patients with neuromuscular diseases who are developing progressive respiratory failure due to respiratory muscle weakness will die unless mechanical ventilation is used. The rate of progression is often hard to predict. Some patients seem suddenly to experience life-threatening hypercapnic respiratory failure. They may not have been aware of gradually increasing symptoms and signs, particularly since they are often not physically active and are often not being regularly monitored with simple pulmonary function tests.
Administering oxygen does not provide assistance to the weakening respiratory muscles, but gives both the patient and the doctor the false impression that appropriate treatment is being provided. While in fact hypoventilation is mistaken for an oxygen transfer problem. Indeed, administering oxygen can mask the problem. Also there is a danger of causing respiratory depression by giving oxygen. Oxygen is not the treatment for hypoventilation. It will improve the SaO2, but not the hypoventilation and may increase the danger of dying of sudden respiratory failure.
In hypercapnic respiratory failure due to hypoventilation, the SaO2 falls due to the rise of the CO2. The alveoli in the lungs (tiny gas exchange units) should clear most of the CO2 out with each breath. Instead, with hypoventilation, CO2 accumulates and thus there is decreased room in the alveoli for oxygen. When mechanical ventilation using room air is provided, it lowers the CO2 in the alveoli, corrects the SaO2, and rests the respiratory muscles. The ventilator should be adjusted to achieve a normal SaO2, on room air. If oxygen is being administered, one cannot use noninvasive oximetry to tell whether enough assisted ventilation is being provided; repeated arterial blood gas specimens (ABGs) would be needed.
When there is respiratory failure in neuromuscular patients (ALS, post-polio, SMA, muscular dystrophy, etc.) who have no additional pulmonary disease that impairs oxygen transfer, the ventilator set-up is adjusted to:
* be comfortable for the patient
* achieve SaO2 of 95% or higher on room air (this can be measured with a finger-sensor oximeter)
* assist the patient to effectively cough and clear secretions
* provide improved oral communication (if vocal communication is possible).
It has been common for people using noninvasive nasal ventilation (NPPV) with a bi-level positive pressure unit to use inadequate settings; frequently, they are not monitored with clinical evaluation and oximetry. The EPAP is often set too high - usually it should not be higher than 3-4 cm H2O; the IPAP is set too low - usually it needs to be 12-16 cm H2O and adjusted to achieve an oxygen saturation of 95% or higher.
Some situations may require administering oxygen, such as pneumonia due to infection or aspiration. If this occurs in patients with respiratory muscle weakness and hypoventilation, then it is important to provide both assisted ventilation and supplemental oxygen, and use ABGs to monitor them.
Address: E.A. Oppenheimer, MD, FCCP, Pulmonary Medicine, Southern California Permanente Medical Group, 4950 Sunset Blvd., Los Angeles, CA 90027-5822
REFERENCES
Bach, J.R. (1999). Guide to the evaluation and management of neuromuscular disease. Philadelphia, PA: Hanley & Belfus.
Gay, P.C., & Edmonds, L.C. (1995). Severe hypercapnia after low-flow oxygen therapy in patients with neuromuscular disease and diaphragmatic dysfunction. Mayo Clinic Proceedings, 70(4), 327-330.
Hsu, A., & Staats, B. (1998). "Postpolio" sequelae and sleep-related disordered breathing. Mayo Clinic Proceedings, 73, 216-224.
Krachman, S., & Criner, G.J. (1998). Hypoventilation syndromes, Clinics in Chest Medicine, 19(1), 139-155.

Additional Observations about Oxygen in Neuromuscular Disease
Anita Simonds, MD, FRCP, Royal Brompton Hospital, London, England (a.simonds@rbh.nthames.nhs.uk)
I agree completely with Dr. Oppenheimer that assisted ventilation is the appropriate therapy for alveolar hypoventilation. Apart from a limited number of situations such as pneumonia or lung fibrosis, oxygen therapy is usually inappropriate and may prove hazardous. Clearly, in an acute pneumonia O2 therapy can be entrained into the ventilator system. Fortunately, in the United Kingdom, this message is getting across to healthcare workers and patients. There is still some inequity in providing noninvasive ventilation, but the situation is improving.
Lisa S. Krivickas, MD, Instructor in PM&R, Harvard Medical School, Director of EMG, Spaulding Rehabilitation Hospital (LKrivickas@compuserve.com)
The analogy that I often use in regard to patients with respiratory failure from neuromuscular disease is that their lungs are like a deflated balloon which they are not strong enough to inflate. To inflate the balloon, mechanical assistance to force air into the balloon is needed. Blowing oxygen across the mouth of the balloon (the equivalent of using supplementary oxygen delivered by nasal cannula) will do nothing to inflate the balloon.
The case series published by the Mayo Clinic (see reference to Gay & Edmonds, 1995) demonstrates the dangers of administering as little as 1 to 2 L/min of nasal cannula oxygen. Patients with a variety of neuromuscular disorders experienced marked CO2 retention; several became obtunded and required intubation or died when placed on 0.5 to 2L of nasal cannula oxygen.
Reprinted from IVUN News, Spring 2000 Vol. 14 No. 9 with permission of Gazette International Networking Institute, 4207 Lindell Blvd., #110, St. Louis, MO 63108-2915.

Dr. Greg Carter comments on the same article:
The articles referenced by Linda, one written by Dr. Edward Oppenheimer and the other by my good friend Dr. Lisa Krivickas, are right on the money in pointing out that oxygen is not necessarily the answer for breathing problems in CMT.
People with CMT have "weak bellows," in other words the muscles that bring air into and out of the lungs are weak. Since breathing out is primarily a passive activity the main problem is bringing air into the lungs and this is the job of the diaphragm, our main breathing muscle. Simply providing supplemental oxygen doesn't solve this problem at all since you still need to get the oxygen into the lungs. Further, too much oxygen can be dangerous and actually suppress the drive to breathe in some cases.
Assistive breathing devices, such as bimodal positive airway pressure (BiPAP) are much more effective and actually try to correct the problem by assisting the weakened diaphragm by providing a positive pressure pushing air into the lungs. BiPAP takes a bit of getting used to but working closely with a skilled respiratory therapist under the supervision of a physician should help. Once the patient is set up with appropriate and comfortable pressure settings and a good fitting mask or other interface, they should begin feeling better quickly.