Capnography for assessing nocturnal hypoventilation and predicting compliance with subsequent noninvasive ventilation in patients with ALS

Sung-Min Kim, Kyung Seok Park, Hyunwoo Nam, Suk-Won Ahn, Suhyun Kim, Jung-Joon Sung, Kwang-Woo Lee, Sung-Min Kim, Kyung Seok Park, Hyunwoo Nam, Suk-Won Ahn, Suhyun Kim, Jung-Joon Sung, Kwang-Woo Lee

Abstract

Background: Patients with amyotrophic lateral sclerosis (ALS) suffer from hypoventilation, which can easily worsen during sleep. This study evaluated the efficacy of capnography monitoring in patients with ALS for assessing nocturnal hypoventilation and predicting good compliance with subsequent noninvasive ventilation (NIV) treatment.

Methods: Nocturnal monitoring and brief wake screening by capnography/pulse oximetry, functional scores, and other respiratory signs were assessed in 26 patients with ALS. Twenty-one of these patients were treated with NIV and had their treatment compliance evaluated.

Results: Nocturnal capnography values were reliable and strongly correlated with the patients' respiratory symptoms (R(2) = 0.211-0.305, p = 0.004-0.021). The duration of nocturnal hypercapnea obtained by capnography exhibited a significant predictive power for good compliance with subsequent NIV treatment, with an area-under-the-curve value of 0.846 (p = 0.018). In contrast, no significant predictive values for nocturnal pulse oximetry or functional scores for nocturnal hypoventilation were found. Brief waking supine capnography was also useful as a screening tool before routine nocturnal capnography monitoring.

Conclusion: Capnography is an efficient tool for assessing nocturnal hypoventilation and predicting good compliance with subsequent NIV treatment of ALS patients, and may prove useful as an adjunctive tool for assessing the need for NIV treatment in these patients.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. The average level of end-tidal…
Figure 1. The average level of end-tidal carbon dioxide (ETCO2) measured by waking supine capnography correlated significantly with arterial partial pressure of carbon dioxide (PaCO2) level, as measured by arterial blood gas analysis (p<0.001).
Figure 2. Correlations between nocturnal respiratory symptoms…
Figure 2. Correlations between nocturnal respiratory symptoms (orthopnea) with respiratory monitoring results.
Scores from orthopnea questionnaire were strongly correlated with the average level of ETCO2 (R2 = 0.305, p = 0.004) (A) and the duration of hypercapnea measured by nocturnal capnography (R2 = 0.211, p = 0.021) (B).
Figure 3. Receiver operating characteristic (ROC) curve…
Figure 3. Receiver operating characteristic (ROC) curve for the duration of nocturnal hypercapnea relative to the total sleep time (ETCO2>47%) and the average nocturnal ETCO2 level (avr ETCO2) as predictors of good compliance with subsequent noninvasive ventilation (NIV) treatment.
The areas under the curve (AUCs) were 0.846 (95% confidence interval, CI: 0.628–1.000) and 0.856 (95% CI: 0.00–1.000), respectively.
Figure 4. The average ETCO 2 level…
Figure 4. The average ETCO2 level obtained with brief wake capnography screening (wake avr ETCO2) correlated significantly with symptoms of patients for nocturnal hypoventilation (orthopnea; p = 0.021) (A) and duration of nocturnal hypercapnea relative to the total sleep time (nocturnal ETCO2>47%; p<0.001) (B).
Figure 5. ROC curves for average ETCO…
Figure 5. ROC curves for average ETCO2 measured by wake capnography screening and average SaO2 measured by wake pulse oximetry screening as predictors of good compliance with subsequent NIV treatment.
The AUC values were 0.840 (95% CI: 0.628–1.000) and 0.192 (95% CI: 0.000–0.389), respectively.

References

    1. Schiffman PL, Belsh JM. Pulmonary function at diagnosis of amyotrophic lateral sclerosis. Rate of deterioration. Chest. 1993;103:508–513.
    1. Atalaia A, De Carvalho M, Evangelista T, Pinto A. Sleep characteristics of amyotrophic lateral sclerosis in patients with preserved diaphragmatic function. Amyotroph Lateral Scler. 2007;8:101–105.
    1. Bourke SC, Tomlinson M, Williams TL, Bullock RE, Shaw PJ, et al. Effects of non-invasive ventilation on survival and quality of life in patients with amyotrophic lateral sclerosis: a randomised controlled trial. Lancet Neurol. 2006;5:140–147.
    1. Kim SM, Lee KM, Hong YH, Park KS, Yang JH, et al. Relation between cognitive dysfunction and reduced vital capacity in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 2007;78:1387–1389.
    1. Newsom-Davis IC, Lyall RA, Leigh PN, Moxham J, Goldstein LH. The effect of non-invasive positive pressure ventilation (NIPPV) on cognitive function in amyotrophic lateral sclerosis (ALS): a prospective study. J Neurol Neurosurg Psychiatry. 2001;71:482–487.
    1. Andersen PM, Borasio GD, Dengler R, Hardiman O, Kollewe K, et al. Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group. Amyotroph Lateral Scler. 2007;8:195–213.
    1. Bach JR, Bianchi C, Aufiero E. Oximetry and indications for tracheotomy for amyotrophic lateral sclerosis. Chest. 2004;126:1502–1507.
    1. Bourke SC, Bullock RE, Williams TL, Shaw PJ, Gibson GJ. Noninvasive ventilation in ALS: indications and effect on quality of life. Neurology. 2003;61:171–177.
    1. Radunovic A, Mitsumoto H, Leigh PN. Clinical care of patients with amyotrophic lateral sclerosis. Lancet Neurol. 2007;6:913–925.
    1. Bach JR. Management of patients with neuromuscular disease. Philadelphia, PA: Hanley & Belfus; 2004. p. xvi, 414 p.
    1. Magnan A, Philip-Joet F, Rey M, Reynaud M, Porri F, et al. End-tidal CO2 analysis in sleep apnea syndrome. Conditions for use. Chest. 1993;103:129–131.
    1. Sanders MH, Kern NB, Costantino JP, Stiller RA, Strollo PJ, Jr, et al. Accuracy of end-tidal and transcutaneous PCO2 monitoring during sleep. Chest. 1994;106:472–483.
    1. Kirk VG, Batuyong ED, Bohn SG. Transcutaneous carbon dioxide monitoring and capnography during pediatric polysomnography. Sleep. 2006;29:1601–1608.
    1. Brooks BR, Miller RG, Swash M, Munsat TL. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1:293–299.
    1. Braunwald E, Harrison TR. Harrison's principles of internal medicine. New York ; London: McGraw-Hill, Medical Pub. Division; 2001. p. 2 v. (xxxii, 2629, [2170] p., [2632] p. of plates).
    1. Leigh PN, Abrahams S, Al-Chalabi A, Ampong MA, Goldstein LH, et al. The management of motor neurone disease. J Neurol Neurosurg Psychiatry. 2003;74(Suppl 4):iv32–iv47.
    1. Buhre W, Rossaint R. Perioperative management and monitoring in anaesthesia. Lancet. 2003;362:1839–1846.
    1. Liu SY, Lee TS, Bongard F. Accuracy of capnography in nonintubated surgical patients. Chest. 1992;102:1512–1515.
    1. Kotterba S, Patzold T, Malin JP, Orth M, Rasche K. Respiratory monitoring in neuromuscular disease - capnography as an additional tool? Clin Neurol Neurosurg. 2001;103:87–91.
    1. Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, et al. The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci. 1999;169:13–21.
    1. Leger P, Bedicam JM, Cornette A, Reybet-Degat O, Langevin B, et al. Nasal intermittent positive pressure ventilation. Long-term follow-up in patients with severe chronic respiratory insufficiency. Chest. 1994;105:100–105.
    1. Kribbs NB, Pack AI, Kline LR, Smith PL, Schwartz AR, et al. Objective measurement of patterns of nasal CPAP use by patients with obstructive sleep apnea. Am Rev Respir Dis. 1993;147:887–895.
    1. Lo Coco D, Marchese S, Pesco MC, La Bella V, Piccoli F, et al. Noninvasive positive-pressure ventilation in ALS: predictors of tolerance and survival. Neurology. 2006;67:761–765.
    1. Miller RG, Rosenberg JA, Gelinas DF, Mitsumoto H, Newman D, et al. Practice parameter: The care of the patient with amyotrophic lateral sclerosis (An evidence-based review). Muscle Nerve. 1999;22:1104–1118.
    1. Whitesell R, Asiddao C, Gollman D, Jablonski J. Relationship between arterial and peak expired carbon dioxide pressure during anesthesia and factors influencing the difference. Anesth Analg. 1981;60:508–512.
    1. Mitsumoto H, Chad DA, Pioro EP. Amyotrophic lateral sclerosis. Philadelphia: F.A. Davis.; 1998. p. xxv, 480 p.
    1. Lechtzin N, Wiener CM, Shade DM, Clawson L, Diette GB. Spirometry in the supine position improves the detection of diaphragmatic weakness in patients with amyotrophic lateral sclerosis. Chest. 2002;121:436–442.
    1. Bach JR. Bilevel pressure vs volume ventilators for amyotrophic lateral sclerosis patients. Chest. 2006;130:1949; author reply 1949–1950.
    1. Tuggey JM, Elliott MW. Randomised crossover study of pressure and volume non-invasive ventilation in chest wall deformity. Thorax. 2005;60:859–864.

Source: PubMed

3
Abonnere