Long-term oxygen therapy in conditions other than chronic obstructive pulmonary disease. 2000

J Zieliński
Institute of Tuberculosis and Lung Diseases, Warsaw, Poland. j.zielinski@igichp.edu.pl

Prescriptions of LTOT in non-COPD diseases vary from 20% to 60% of the total number of patients profiting from this form of treatment. It seems that in countries where the percentage of non-COPD indications is still high, the proportions will change toward higher use of LTOT in COPD patients in the near future. There is a death of controlled studies evaluating the effects of LTOT in non-COPD diseases. There are at least two important factors preventing realization of such studies. First, non-COPD indications for LTOT encompass a large number of diseases. Each of them should be separately studied because of differences in the pathophysiological mechanisms and natural history of the diseases. Small numbers of patients with a specific diagnosis would require multicenter, international studies, which are difficult to perform in a rigorous manner. A more important handicap is ethical reasons. Many years ago LTOT was approved as a routine method of treatment for severe stable hypoxemia. It would be difficult to obtain the approval of any ethics committee for a project proposing a control group of hypoxemic patients to be deprived of oxygen for a long period of time. It would also be difficult to find clinicians eager to participate in such a study. Do we need such studies at all, even in an era of evidence-based medicine? Probably not for diseases presenting with airway obstruction such as CF or bronchopulmonary dysplasia. The effects of LTOT in COPD may also be applied to those diseases. But there remains a group of diseases with restrictive patterns of ventilatory impairment. A typical feature of these diseases is a severe decrease in arterial oxygen tension and saturation during exercise. Oxygen supplementation during exercise has already been found to relieve hypoxemia and to increase exercise capacity. Life is motion. Perhaps we should not bother too much about prolongation of the life of our patients, which would be difficult to prove anyway. We should rather concentrate on assuring them as much mobility and enjoyment of life as possible. In other words we should work on adding life to years rather than adding years to life. For this, ambulatory oxygen is the best option.

UI MeSH Term Description Entries
D007738 Kyphosis Deformities of the SPINE characterized by an exaggerated convexity of the vertebral column. The forward bending of the thoracic region usually is more than 40 degrees. This deformity sometimes is called round back or hunchback. Hyperkyphosis,Hyperkyphoses,Kyphoses
D008134 Long-Term Care Care over an extended period, usually for a chronic condition or disability, requiring periodic, intermittent, or continuous care. Care, Long-Term,Long Term Care
D010102 Oxygen Inhalation Therapy Inhalation of oxygen aimed at restoring toward normal any pathophysiologic alterations of gas exchange in the cardiopulmonary system, as by the use of a respirator, nasal catheter, tent, chamber, or mask. (From Dorland, 27th ed & Stedman, 25th ed) Inhalation Therapy, Oxygen,Therapy, Oxygen Inhalation,Inhalation Therapies, Oxygen,Oxygen Inhalation Therapies,Therapies, Oxygen Inhalation
D011658 Pulmonary Fibrosis A process in which normal lung tissues are progressively replaced by FIBROBLASTS and COLLAGEN causing an irreversible loss of the ability to transfer oxygen into the bloodstream via PULMONARY ALVEOLI. Patients show progressive DYSPNEA finally resulting in death. Alveolitis, Fibrosing,Idiopathic Diffuse Interstitial Pulmonary Fibrosis,Fibroses, Pulmonary,Fibrosis, Pulmonary,Pulmonary Fibroses,Alveolitides, Fibrosing,Fibrosing Alveolitides,Fibrosing Alveolitis
D003550 Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. Mucoviscidosis,Cystic Fibrosis of Pancreas,Fibrocystic Disease of Pancreas,Pancreatic Cystic Fibrosis,Pulmonary Cystic Fibrosis,Cystic Fibrosis, Pancreatic,Cystic Fibrosis, Pulmonary,Fibrosis, Cystic,Pancreas Fibrocystic Disease,Pancreas Fibrocystic Diseases
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000860 Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. Anoxia,Oxygen Deficiency,Anoxemia,Deficiency, Oxygen,Hypoxemia,Deficiencies, Oxygen,Oxygen Deficiencies
D014397 Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. Pulmonary Consumption,Pulmonary Phthisis,Pulmonary Tuberculoses,Pulmonary Tuberculosis,Tuberculoses, Pulmonary,Consumption, Pulmonary,Consumptions, Pulmonary,Phthises, Pulmonary,Phthisis, Pulmonary,Pulmonary Consumptions,Pulmonary Phthises

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