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The Proceedings of the American Thoracic Society 5:513-518 (2008)
© 2008 The American Thoracic Society
doi: 10.1513/pats.200708-124ET
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Oxygen Therapy in Chronic Obstructive Pulmonary Disease

Victor Kim1, Joshua O. Benditt2, Robert A. Wise3 and Amir Sharafkhaneh4

1 Division of Pulmonary and Critical Care Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania; 2 University of Washington Medical Center, Pulmonary and Critical Care Medicine, Seattle, Washington; 3 Division of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland; and 4 Department of Pulmonary Medicine, Veterans Administration Medical Center, Houston, Texas

Correspondence and requests for reprints should be addressed to Victor Kim, M.D., Temple University School of Medicine, 785 Parkinson Pavilion, 3401 North Broad Street, Philadelphia, PA 19140. E-mail: victor.kim{at}tuhs.temple.edu

ABSTRACT

Since the introduction of oxygen as a therapeutic agent 70 years ago, much has been learned regarding the detrimental effects of hypoxemia and the beneficial impact of oxygen therapy. It is projected that there are close to 800,000 patients receiving long-term oxygen therapy (LTOT) in the United States, at a cost of approximately $1.8 billion annually. The large numbers of patients receiving supplemental oxygen as treatment and the high costs incurred in providing oxygen therapy necessitate the practitioner to know the indications for LTOT as well its effects on survival, pulmonary hemodynamics, sleep, and exercise capacity. It is now recognized that the basis for LTOT prescription for all patients is founded on data that are over 25 years old and that only involve a very select cohort of patients. It is clear that further studies are required to assess the effects of oxygen on patients with chronic obstructive pulmonary disease with only mild hypoxemia, not only survival but also on neurocognitive function, quality of life, exercise physiology, and sleep quality. In addition, although proven to be safe when prescribed long term to individuals with lung disease, there are some concerns about worsening carbon dioxide retention and increased oxidant injury. The goals of this article are to briefly describe the indications for chronic oxygen administration, the physiologic effects of treatment, and potential toxicities, as well as its effect on morbidity and mortality.

Key Words: chronic obstructive pulmonary disease • oxygen therapy • long-term oxygen therapy • nocturnal oxygen desaturation • hypoxemia

Since the introduction of oxygen as a therapeutic agent 70 years ago, much has been learned regarding the detrimental effects of hypoxemia and the beneficial impact of oxygen therapy. It is projected that there are close to 800,000 patients receiving long-term oxygen therapy (LTOT) in the United States, at a cost of approximately $1.8 billion annually (1). The large numbers of patients receiving supplemental oxygen as treatment and the high costs incurred in providing oxygen therapy necessitate the practitioner to know the indications for LTOT as well its effects on survival, pulmonary hemodynamics, sleep, and exercise capacity. It is now recognized that the basis for LTOT prescription for all patients is founded on very old data (>25 yr) in a very select patient group. It is clear that further studies are required to assess the effects of oxygen on patients with chronic obstructive pulmonary disease (COPD) with only mild hypoxemia on not only survival but also on neurocognitive function, quality of life, exercise physiology, and sleep quality. In addition, although proven to be safe when prescribed long term to individuals with lung disease, there are some concerns about worsening carbon dioxide retention and increased oxidant injury. The goals of this article are to briefly describe the indications for chronic oxygen administration, the physiologic effects of treatment, and potential toxicities, as well as its effect on long-term morbidity and mortality.

EFFECTS OF HYPOXEMIA

Hypoxemia has several physiologic consequences. There is no significant increase in ventilation with decreases in PaO2 that results in levels remaining above 60 mm Hg, but as PaO2 falls below 55 mm Hg, there is a marked rise in minute ventilation (VE), with a subsequent fall in PaCO2. Hypoxemia causes peripheral vascular beds to dilate, which induces a compensatory tachycardia and a subsequent increase in cardiac output to improve oxygen delivery. Regional pulmonary vasoconstriction occurs in response to alveolar hypoxia in an effort to match ventilation and perfusion. Erythropoietin secretion increases causing erythrocytosis, thereby increasing oxygen carrying capacity. These compensatory mechanisms can cause detrimental long-term effects, such as polycythemia, pulmonary hypertension, and right ventricular failure. On a cellular level, mitochondrial function declines, anaerobic glycolysis occurs, and lactate/pyruvate ratio increases. Patients may have impaired judgment at low levels of hypoxemia, with progressive loss of cognitive and motor functions, and eventually loss of consciousness as severe hypoxemia ensues. Other nonspecific symptoms of hypoxemia include headache, breathlessness, palpitations, angina, restlessness, and tremor.

SHORT-TERM EFFECTS OF OXYGEN ADMINISTRATION

In addition to relieving arterial hypoxemia and alleviation of the consequences listed above, supplemental oxygen has several therapeutic benefits. Oxygen improves breathlessness in both normal subjects and in those with COPD during exercise (2–4). Exercise tolerance is improved in those who develop significant hypoxemia as well as in those with only mild to moderate hypoxemia (5). Although this phenomenon has been observed by many investigators, the responsible mechanisms remain a matter of debate. In COPD, the perceived decrease in breathlessness and improvement in exercise capacity may be due to decreased VE (4), a decrease in dynamic hyperinflation (6), alleviation of hypoxic pulmonary vasoconstriction and improved hemodynamics (e.g., decrease in pulmonary vascular resistance and increase in cardiac output) (7), or increased oxygen delivery (8). O'Donnell and colleagues (6) performed cardiopulmonary exercise tests in 11 hypoxic and hypercapnic patients with severe COPD (PaO2, 52 ± 2 mm Hg, and PaCO2, 48 ± 2 mm Hg, respectively) while breathing room air or 60% FIO2 in random order. Oxygen administration resulted in a decrease in dyspnea scores, higher inspiratory capacity, and decreased respiratory rate compared with room air. Dean and coworkers (7) randomized 12 patients with severe COPD to compressed air or 40% inhaled oxygen during exercise. In those treated with oxygen, cycle ergometry endurance time increased by 40%, maximal right ventricular systolic pressures (via Doppler echocardiography) decreased, and the rate of rise of right ventricular systolic pressure was decreased. Morrison and Stovall found that hypoxemic patients with COPD who showed an improvement in exercise capacity with supplemental oxygen had significant increases in both cardiac output and oxygen content during exercise (8).

Alternative proposed mechanisms include an improvement in ventilatory muscle function (9) and altered ventilatory muscle recruitment (10). Oxygen flow may also stimulate upper airway and facial receptors of the trigeminal nerve and reflexively inhibit central ventilatory drive (11). Finally, there also appears to be a direct effect of oxygen administration on the perception of dyspnea independent of any changes in VE (3). On the basis of these studies, it has been recommended by some to use supplemental oxygen for all patients with COPD while undergoing pulmonary rehabilitation. However, the current evidence does not support the routine use of oxygen in normoxemic patients with COPD during exercise (12).

Oxygen administration decreases VE and work of breathing during acute respiratory failure (ARF) in COPD. A study conducted in 20 patients with COPD, both in a chronic stable condition and during ARF, found no difference in VE between patients with chronic, stable COPD and normal control subjects (13). In ARF, however, application of oxygen at 5 L/minute decreased VE by 14%, mostly by a decrease in respiratory rate without a compensatory increase in tidal volume. ARF was also associated with increased work of breathing, as evidenced by a fivefold increase in mouth occlusion pressure. This rise in mouth occlusion pressure decreased by 40% after oxygen administration. These effects of oxygen on ventilation and work of breathing may help prevent respiratory muscle fatigue during ARF, particularly in patients with chronic respiratory insufficiency who have a higher baseline ventilatory demand.

EFFECT OF LTOT ON MORTALITY

Chronic hypoxemia leading to the development of cor pulmonale portends a poor prognosis, with mortality ranging anywhere from 32 to 100% (14, 15). Early noncontrolled studies showed a reduction in mortality in patients with COPD, cor pulmonale, and severe hypoxemia with the use of continuous oxygen therapy for 7 to 41 months (16). Two landmark studies performed in the late 1970s, the Nocturnal Oxygen Therapy Trial (NOTT) (17) and the British Medical Research Council (MRC) Long-Term Domiciliary Oxygen Therapy Trial (18), examined the effects of LTOT on survival and physiologic function in patients with severe chronic bronchitis and emphysema.

The British MRC trial (18) was conducted in the late 1970s and reported in March of 1981. It was performed in three centers in the United Kingdom and enrolled 87 patients, all younger than 70 years, who had chronic bronchitis or emphysema with irreversible airway obstruction (FEV1 range, 0.58–0.75 L), severe hypoxemia (PaO2 range, 49.4–51.8 mm Hg), carbon dioxide retention (PaCO2, 56–60 mm Hg), and a history of cor pulmonale (mean pulmonary artery pressure range, 32.3–35.0 mm Hg). Patients randomized to receive oxygen were given 2 L/minute of oxygen via nasal prongs for at least 15 hours a day. In 5 years of survival follow-up, 19 of the 42 oxygen-treated patients died, compared with 30 of 45 control subjects who did not receive oxygen and died. Mortality appeared to be highest in the subgroup of patients who had the highest elevations in baseline PaCO2 and red cell mass. Although mortality was favorably affected by long-term oxygen use, there were no statistically significant differences in the rate of decrease of FEV1 or PaO2, or increase in PaCO2, red cell mass, or pulmonary artery pressures. However, there appeared to be a trend that LTOT prevented a progressive decrease in PaO2 and in the rate of increase in pulmonary vascular resistance without provoking a further increase in PaCO2.

The NOTT (17), sponsored by the National Heart, Lung, and Blood Institute, reported the effects of continuous versus nocturnal oxygen therapy in hypoxemic patients with COPD. This multicenter study enrolled 203 hypoxemic patients with COPD who were randomly allocated to receive either continuous oxygen therapy or 12 hours of nocturnal oxygen therapy. All subjects were followed for at least 12 months to determine the effects of oxygen therapy on survival, pulmonary vascular pressures, neuropsychological function, and quality of life. Mortality in the 203 patients was followed for an average of 19.3 months. Eighty nocturnal oxygen and 87 continuous oxygen therapy subjects were followed for 12 months, whereas 29 nocturnal oxygen and 37 continuous oxygen therapy patients were followed for 24 months. Overall mortality of the subjects assigned to continuous oxygen therapy and nocturnal oxygen therapy over 3 years of observation is shown in Figure 1. A total of 64 subjects died in the trial, 41 in the nocturnal oxygen therapy group and 23 in the continuous oxygen therapy group. At all six centers, mortality for the nocturnal oxygen therapy group exceeded that for the continuous oxygen therapy group.


Figure 1
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  		Figure 1. Overall mortality in the patients enrolled in the National Oxygen Treatment Trial. Circles (upper curve) represent continuous oxygen therapy group. Squares (lower curve) represent nocturnal oxygen therapy group. Twelve-month mortality in the nocturnal oxygen group was 20.6%, versus 11.9% in the continuous oxygen therapy group. Twenty-four–month mortality in the nocturnal oxygen group was 40.8% versus 22.4% in the continuous oxygen treatment group. Reprinted by permission from Reference 17.

 
When the effect of continuous versus nocturnal therapy was assessed for its impact on physiologic variables, no significant changes were found in arterial blood gas values, lung volumes, FEV1, maximum work attained, mean pulmonary artery pressures, or cardiac index. However, hematocrit values were more reduced in patients on continuous oxygen therapy than those randomized to nocturnal treatment (~7% difference), as was pulmonary vascular resistance (17.6% greater decrease in pulmonary vascular resistance found in the group receiving continuous vs. nocturnal therapy).

It should be recognized that, although both of the above studies showed improved survival, patients were not comparable between studies (Table 1). Patients in the MRC study tended to be more ill and with more evidence of resting hypercapnia and cor pulmonale. Furthermore, patients in the MRC study had a significant number of participants who continued to smoke even after enrollment into the trial (27% in the control group and 44% in the placebo group), whereas no comment was made on the incidence of continued smoking in NOTT patients. Finally, the MRC study found no statistically significant impact of nocturnal oxygen therapy versus no oxygen treatment on physiologic variables, whereas the NOTT study found a statistically significantly greater decrease in pulmonary vascular resistance and absolute hematocrit associated with continuous oxygen therapy. The causal relationship between a reduction in hematocrit and pulmonary vascular resistance on influencing survival, whether using continuous or nocturnal oxygen therapy, was not established, however.


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  		TABLE 1. COMPARSION OF BRITISH MEDICAL RESEARCH COUNCIL AND NOCTURNAL OXYGEN THERAPY TRIAL LONG-TERM OXYGEN TREATMENT TRIALS

 
Despite their differences, these two prospective and controlled trials appear to establish that nocturnal oxygen therapy is better than no oxygen therapy at all, and continuous oxygen therapy is better than nocturnal oxygen therapy in severely hypoxemic patients with elevated hematocrit, pulmonary artery pressure, and respiratory acidosis. In an attempt to extend the above findings to patients who suffer from less severe disease and only moderate hypoxemia, Gorecka and colleagues (19) evaluated 135 patients (PaO2, 56–65 mm Hg at rest) with advanced airflow obstruction (FEV1, 0.83 L) who were randomly allocated to receive no oxygen therapy or LTOT. Patients assigned to either group were followed every 3 months for at least 3 years. The cumulative survival rates for the group at large were 88% at 1 year, 77% at 2 years, and 66% at 3 years. The authors found no significant difference in survival rates between the two patient groups treated with LTOT versus control therapy. Patients who were younger, had better spirometric values, and had higher body mass index showed better survival. This was similar to the findings of other studies, in which no survival benefit was found in patients with COPD given supplemental oxygen when severe hypoxemia or cor pulmonale was not present.

Similarly, no study has shown a survival benefit when oxygen is prescribed for exercise-induced oxygen desaturation. Most recently, the National Emphysema Treatment Trial (NETT) research group performed a retrospective analysis on the normoxemic participants in the medical arm of NETT (unpublished data). They found that the normoxemic patients who reported continuous oxygen use had greater dyspnea, lower quality of life, worse lung function, worse exercise capacity, and more frequent exercise desaturation compared with the normoxemic patients who did not use oxygen therapy. In those who experienced desaturation during exercise, no difference in survival was found based on reported oxygen use. It must be noted, however, that oxygen use was not given in a prospective, randomized fashion, and the available data may help identify a sicker group of patients with a greater risk of death.

OXYGEN THERAPY AND PULMONARY HEMODYNAMICS IN COPD

Substantial evidence suggests that the presence of secondary pulmonary hypertension in COPD increases the risk for hospitalization (20) and is associated with worsened survival (21, 22). Because of the known association of resting hypoxemia with the development of secondary pulmonary hypertension, investigators have focused on supplemental oxygen as treatment for hypoxemic COPD patients with pulmonary hypertension. Data from the NOTT group found that oxygen therapy in hypoxemic patients with COPD is associated with favorable but minimal changes in the magnitude of pulmonary hypertension at rest and during exercise (23). Furthermore, they tend to suggest that favorable changes in pulmonary hemodynamics secondary to oxygen supplementation are enhanced in the group of patients that receives oxygen continuously, compared with those who receive it on an intermittent daily basis (23). It is difficult to attribute the improvements in survival of patients with COPD receiving continuous versus nocturnal oxygen therapy solely to changes in pulmonary hemodynamics on the basis of the available data. In addition, the response to acute administration of oxygen on pulmonary hemodynamics does not appear to predict the long-term effects of oxygen therapy on survival (24). Further studies are required to determine the causal relationship of oxygen supplementation on pulmonary hemodynamics and survival, and to predict which subgroups of patients with pulmonary hypertension and hypoxemic COPD are more likely to benefit from long-term administration.

OXYGENATION AND SLEEP IN COPD

Sleep disturbance is common in patients with COPD. Increased sleep latency, decreased total sleep time, decreased slow-wave sleep, and decreased REM sleep have been noted in many polysomnographic studies of patients with COPD (25–29). Approximately 30 to 70% of patients with COPD complain of insomnia, early morning awakenings, morning tiredness, or daytime sleepiness (29–31). Common reasons include medication side effects, airflow obstruction, and hypercapnia, but perhaps the most important is nocturnal oxygen desaturation (NOD). Approximately 25 years ago, Koo and colleagues (32) studied 15 normoxemic patients with severe COPD (FEV1, 0.96 L) and found a mean decrease in PaO2 of 13.5 mm Hg and a mean increase of PaCO2 of 8.3 mm Hg during REM sleep. Up to 25% of patients with COPD exhibit REM-related hypoventilation and NOD, despite having a daytime PaO2 above 60 mm Hg (33). Determining who will develop NOD is difficult without nocturnal oximetry or polysomnography; assessments of daytime gas exchange or pulmonary function are unable to differentiate those patients who experience desaturation at night and those who do not (33, 34). It has been suggested that oxygen therapy improves sleep continuity and quality in those who experience desaturation (27), although this phenomenon has not been demonstrated in all studies (see Table 2) (27).


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  		TABLE 2. EFFECTS OF OXYGEN ON SLEEP QUALITY IN CHRONIC OBSTRUCTIVE PULMONARY DISEASE WITH NOCTURNAL OXYGEN DESATURATION

 
NOD may lead to the development of pulmonary hypertension and cor pulmonale in patients with COPD. Levi-Valensi and coworkers (34) investigated the relationship between sleep variables and daytime pulmonary hemodynamics in 40 patients with COPD with daytime PaO2 of 60 to 70 mm Hg. Mean pulmonary artery pressure was higher in those who demonstrated significant oxygen desaturation compared with those who did not (19.1 ± 4.7 vs. 16.9 ± 1.9 mm Hg, respectively). Oxygen therapy during sleep may prevent nocturnal hypoxemia and possibly the development of pulmonary hypertension. However, two recent clinical studies examining normoxemic patients with COPD with evidence of nocturnal desaturation found neither an improvement in survival with nocturnal oxygen despite a reduction in pulmonary artery pressures nor a delay in the time to prescription of continuous oxygen therapy (35, 36). Therefore, similar to exercise-induced hypoxemia, it is unclear whether LTOT in this circumstance has long-term benefits. Given the lack of survival advantage, screening for nocturnal desaturation in normoxemic patients with COPD should probably be reserved for those with hypercapnia, erythrocytosis, or evidence of pulmonary hypertension.

OXYGEN AND AIR TRAVEL

Ascent to high altitude via air travel exposes patients to hypobaric conditions, which increases risk of hypoxemia. Pressurizing the aircraft cabin limits the fall in atmospheric pressure to an altitude of 8,000 ft, allowing ascent to much higher altitudes. Oxygen supplementation is indicated if the predicted PaO2 at 8,000 ft is less than 50 mm Hg. Those with an SpO2 greater than 95% or a PaO2 greater than 72 mm Hg while breathing ambient air at sea level will most likely not require oxygen supplementation. For those who do not meet these criteria, an equation has been advocated to predict PaO2 at an 8,000-ft altitude in normocapnic patients with COPD (37):

Formula 1(1)

Determining the liter flow needed to restore normoxemia during flight is slightly more difficult. In one series, the use of 2 L/minute of supplemental oxygen was sufficient for those who did not require oxygen at sea level (38). Predicting the liter flow for those who already require oxygen at sea level can be done with a hypoxic gas inhalation test (39). Using a 35% Venturi mask with nitrogen as the supply gas instead of oxygen, the entrained ambient air will result in a fraction of inspired oxygen of 16%, thereby mimicking the hypoxic conditions at approximately 6,700 ft. The PaO2 can be measured while the patient is breathing in supplemental oxygen through a nasal cannula.

INDICATIONS FOR LTOT

The indications for LTOT are summarized in Table 3. The requirements for medical necessity for Medicare coverage have been based primarily on the entry criteria for the NOTT (17), but have been refined on the basis of five consensus conferences on LTOT (40, 41). These guidelines apply not only to hypoxemic patients with COPD but also to those with hypoxemia secondary to other pulmonary and cardiac diseases (38).


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  		TABLE 3. INDICATIONS FOR LONG-TERM OXYGEN THERAPY

 
LTOT is indicated for those who are hypoxemic at rest (PaO2 < 55 mm Hg or SaO2 < 88%) or who have borderline hypoxemia (PaO2, 56–59 mm Hg, or SaO2 < 89%) with evidence of cor pulmonale or polycythemia. In addition, many of those with resting hypoxemia will have increased oxygen requirements during exertion and sleep, so it is prudent for the clinician caring for these patients to assess their oxygen needs during these situations. In the United States, Medicare also allows oxygen to be prescribed during sleep if PaO2 is less than 55 mm Hg, SaO2 is less than 88%, or if there is a fall in PaO2 of more than 10 mm Hg or a fall in SaO2 of more than 5% with signs or symptoms of hypoxemia. The latter indication is defined by the Center for Medicare and Medicaid Services as "impaired cognitive process, restlessness, or insomnia." Oxygen may also be prescribed during exercise if the PaO2 falls to 55 mm Hg or the SaO2 falls to 88%.

ACCENTUATION OF HYPERCAPNIA

Of concern are worsening carbon dioxide retention and respiratory acidosis when oxygen is administered to patients with chronic hypercapnia. The most commonly believed mechanism for this phenomenon is the blunting of hypoxic ventilatory drive and hypoventilation. Aubier and colleagues (42) administered 100% oxygen noninvasively to patients with COPD and ARF, which resulted in an acute 18% decrease in Formula 1E. After 15 minutes of breathing 100% oxygen, however, Formula 1E returned to 93% of baseline values while breathing room air. Despite the near normalization of ventilation, the PaCO2 increased about 23 mm Hg, and the average PaO2 reached 225 mm Hg. Approximately 5 mm Hg (22%) was attributed to the decrease in Formula 1E; 7 mm Hg (30%) was attributed to a reduction of hemoglobin's affinity to bind and carry CO2, also known as the Haldane effect. Oxyhemoglobin shifts the CO2 hemoglobin dissociation curve to the right, thereby increasing the amount of CO2 dissolved in blood, which determines PaCO2. The largest component of acute hypercapnia (11 mm Hg, 48%) was attributed to increased dead-space ventilation. Therefore, it seems that acute administration of supranormal levels of oxygen to patients with COPD and with ARF can lead to hypercapnia, and the primary mechanism is the release of hypoxic vasoconstriction in underventilated lung causing ventilation–perfusion imbalance, not hypoventilation. However, with controlled administration of oxygen, breathlessness can be alleviated and hypoxemia treated without significant increases in arterial carbon dioxide tension.

CONTROVERSIES AND CONCERNS

Who will benefit from LTOT needs to be refined, with more rigorous collection of outcome data in a variety of patient populations. The data showing survival benefit of LTOT in hypoxemic patients with COPD are more than 25 years, and no study since then has shed any further light on its therapeutic potential. As an example, three studies have found no survival benefit in COPD with only mild hypoxemia in the absence of cor pulmonale or severe desaturation (16, 19, 43). The average use of oxygen in these studies was, however, 13.5 hours/day or less, which may have been an inadequate duration to show a survival advantage. Nevertheless, other benefits of oxygen therapy in this group may include improvement in symptoms of depression and anxiety, neuropsychological function, exercise capacity, and quality of life (44–46). Further studies are necessary to delineate which patients with mild hypoxemia would have a survival benefit, and what other therapeutic benefits may be derived from oxygen therapy.

LTOT has potential consequences as well. In addition to accentuation of hypercapnia, chronic oxygen therapy may also accelerate oxidant injury. Hyperoxia can produce cellular injury through production of reactive oxygen species, which can result in tissue inflammation and cell death (47, 48). Recent studies have shown that supplemental oxygen increases exhaled biomarkers of oxidative stress and airway inflammation (49–52). In contrast, in one study of nine normoxemic, cachectic patients with COPD, short-term oxygen supplementation had no effect on plasma inflammatory biomarkers while at rest and actually decreased evidence of exercise-induced oxidative stress (53). Interestingly, the NETT research group found that oxygen use was an independent risk factor for death compared with those not using oxygen therapy (hazard ratio, 1.36; 95% confidence interval, 1.02–2.10) in those randomized to the medical arm of the NETT (54). Whether oxygen use contributed to earlier mortality or simply was an epimarker of a sicker patient group is difficult to discern on the basis of their data. In light of these findings, the growing body of literature linking oxidant injury to COPD pathogenesis makes the potential toxicity of LTOT difficult to ignore and underscores the importance of identifying the optimal candidate.

CONCLUSIONS

Oxygen therapy offers significant short- and long-term benefits in those with COPD. Immediate benefits include alleviation of hypoxemia and its sequelae, improvement in exercise capacity, reduction of dyspnea, and possibly sleep consolidation. Long-term use has been shown to improve survival in severely hypoxemic patients with COPD and cause a slight reduction in pulmonary artery pressure. On the basis of the above studies, patients with a resting PaO2 of less than 55 mm Hg (SaO2 < 88%), those with a PaO2 of 56–59 mm Hg with signs of tissue hypoxemia (e.g., cor pulmonale, polycythemia, impaired cognition), and those who experience desaturation during sleep or exercise should be considered for LTOT. The benefits of oxygen therapy in those with mild to moderate hypoxemia, although they may not include a reduction in mortality, may include improvements in mood, neurocognitive function, and quality of life. Further randomized controlled studies are needed to confirm or refute prior data in this patient group.

FOOTNOTES

The National Emphysema Treatment Trial (NETT) is supported by contracts with the National Heart, Lung, and Blood Institute (N01HR76101, N01HR76102, N01HR76103, N01HR76104, N01HR76105, N01HR76106, N01HR76107, N01HR76108, N01HR76109, N01HR76110, N01HR76111, N01HR76112, N01HR76113, N01HR76114, N01HR76115, N01HR76116, N01HR76118, and N01HR76119), the Centers for Medicare and Medicaid Services (CMS), and the Agency for Healthcare Research and Quality (AHRQ).

Conflict of Interest Statement: None of the authors has a financial relationship with a commercial entity that has an interest in the subject of this manuscript.

(Received in original form August 14, 2007; accepted in final form November 3, 2007)

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