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Update on Pharmaceutical and Minimally Invasive Management Strategies for Chronic Obstructive Pulmonary Disease

DOI: 10.1155/2011/257496

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Abstract:

Chronic obstructive pulmonary disease (COPD) is a debilitating pulmonary disorder with systemic effects, and it is the fourth leading cause of death in the United States. COPD patients not only develop respiratory limitations, but can also demonstrate systemic wasting, features of depression, and can succumb to social isolation. Smoking cessation is crucial, and pharmacotherapy with bronchodilators is helpful in symptom management. Inhaled corticosteroids may be beneficial in some patients. In addition, pulmonary rehabilitation and palliative care are important components under the right clinical circumstance. This review highlights current guidelines and management strategies for COPD and emphasizes novel pharmacotherapy and minimally invasive (nonsurgical) lung-volume reduction interventions that may prove to be of significant benefit in the future. 1. Epidemiology Chronic obstructive pulmonary disease (COPD) is a syndrome characterized by chronic and progressive airflow reduction that is scarcely reversible and by inflammation of the small airways. It is the potential functional consequence of two diseases that can often coexist in the same patient, such as panlobular emphysema and fibrosing chronic bronchiolitis with or without significant centrilobular emphysema. It can also include chronic bronchitis (the presence of a chronic productive cough for 3 months or more in each of 2 consecutive years) [1, 2]. Chronic bronchitis per se is a smoking related disease of large airways that often resolves after smoking cessation. Nevertheless, patients with COPD who suffer from chronic bronchitis generally show faster functional decline, more exacerbations, and greater morbidity and mortality. Furthermore, a greater percentage of subjects with chronic cough and phlegm who continue to smoke can have COPD as compared with smokers without symptoms when functionally reassessed after 8 years [3]. However, the majority of patients with chronic bronchitis will not suffer from COPD [2, 3]. Therefore, chronic bronchitis itself can be considered as both a risk factor for COPD, and a worse prognostic factor in the presence of COPD. COPD typically progresses over time and is associated with an increased inflammatory response of the lung to continued environmental exposures which is often tobacco smoke [4]. The natural history of COPD is punctuated by breathlessness especially on exertion with daily activities of normal living, increased production and purulence of sputum, overall health decline, and episodes of exacerbations that require medical attention and

References

[1]  R. Buhl and S. G. Farmer, “Future directions in the pharmacologic therapy of chronic obstructive pulmonary disease,” Proceedings of the American Thoracic Society, vol. 2, no. 1, pp. 83–93, 1995.
[2]  T. E. Albertson, S. Louie, and A. L. Chan, “The diagnosis and treatment of elderly patients with acute exacerbation of chronic obstructive pulmonary disease and chronic bronchitis,” Journal of the American Geriatrics Society, vol. 58, no. 3, pp. 570–579, 2010.
[3]  R. De Marco, S. Accordini, I. Cerveri et al., “Incidence of chronic obstructive pulmonary disease in a cohort of young adults according to the presence of chronic cough and phlegm,” American Journal of Respiratory and Critical Care Medicine, vol. 175, no. 1, pp. 32–39, 2007.
[4]  Global Initiative for Chronic Obstructive Lung Disease, “Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease,” NHLBI/WHO Workshop Report, National Heart, Lung, and Blood Institute, Bethesda, Md, USA, 2001, http://www.goldcopd.com/.
[5]  U.S. Environmental Protection Agency, “Chronic obstructive pulmonary disease prevalence and mortality,” December 2009, http://cfpub.epa.gov/eroe/index.
[6]  A. Jemal, E. Ward, Y. Hao, and M. Thun, “Trends in the leading causes of death in the United States, 1970–2002,” Journal of the American Medical Association, vol. 294, no. 10, pp. 1255–1259, 2005.
[7]  D. M. Mannino, D. M. Homa, L. J. Akinbami, E. S. Ford, and S. C. Redd, “Chronic obstructive pulmonary disease surveillance–United States, 1971-2000,” Morbidity and Mortality Weekly Report, vol. 51, no. 6, pp. 1–16, 2002.
[8]  Centers for Disease Control, “Deaths from chronic obstructive pulmonary disease, United States 2000–2005,” Morbidity and Mortality Weekly Report, vol. 57, no. 45, pp. 1229–1232, 2008.
[9]  N. R. Anthonisen, M. A. Skeans, R. A. Wise, J. Manfreda, R. E. Kanner, and J. E. Connett, “The effects of a smoking cessation intervention on 14.5-year mortality: a randomized clinical trial,” Annals of Internal Medicine, vol. 142, no. 4, pp. 233–239, 2005.
[10]  R. L. Berger, M. M. DeCamp, G. J. Criner, and B. R. Celli, “Lung volume reduction therapies for advanced emphysema: an update,” Chest, vol. 138, no. 2, pp. 407–417, 2010.
[11]  P. M. A. Calverley, J. A. Anderson, B. Celli et al., “Salmeterol and fluticasone propionate and survival in chronic obstructive pulmonary disease,” The New England Journal of Medicine, vol. 356, no. 8, pp. 775–789, 2007.
[12]  D. P. Tashkin, B. Celli, S. Senn et al., “A 4-year trial of tiotropium in chronic obstructive pulmonary disease,” The New England Journal of Medicine, vol. 359, no. 15, pp. 1543–1554, 2008.
[13]  B. Celli, M. Decramer, S. Kesten, D. Liu, S. Mehra, and D. P. Tashkin, “Mortality in the 4-year trial of tiotropium (UPLIFT) in patients with chronic obstructive pulmonary disease,” American Journal of Respiratory and Critical Care Medicine, vol. 180, no. 10, pp. 948–955, 2009.
[14]  C. Vogelmeier, P. Kardos, S. Harari, S. J. M. Gans, S. Stenglein, and J. Thirlwell, “Formoterol mono- and combination therapy with tiotropium in patients with COPD: a 6-month study,” Respiratory Medicine, vol. 102, no. 11, pp. 1511–1520, 2008.
[15]  R. Bone, M. Boyars, S. R. Braun et al., “In chronic obstructive pulmonary disease, a combination of ipratropium and albuterol is more effective than either agent alone: an 85-day multicenter trial. COMBIVENT Inhalation Aerosol Study Group,” Chest, vol. 105, no. 5, pp. 1411–1419, 1994.
[16]  N. Gross, D. Tashkin, R. Miller, J. Oren, W. Coleman, and S. Linberg, “Inhalation by nebulization of albuterol-ipratropium combination (Dey combination) is superior to either agent alone in the treatment of chronic obstructive pulmonary disease,” Respiration, vol. 65, no. 5, pp. 354–362, 1998.
[17]  T. S. Lapperre, J. B. Snoeck-Stroband, M. M. E. Gosman et al., “Effect of fluticasone with and without salmeterol on pulmonary outcomes in chronic obstructive pulmonary disease: a randomized trial,” Annals of Internal Medicine, vol. 151, no. 8, pp. 517–527, 2009.
[18]  E. D. Telenga, H. A. M. Kerstjens, D. S. Postma, N. H. Ten Hacken, and M. van den Berge, “Inhaled corticosteroids in chronic obstructive pulmonary disease: a review,” Expert Opinion on Pharmacotherapy, vol. 11, no. 3, pp. 405–421, 2010.
[19]  A. Kliber, L. D. Lynd, and D. D. Sin, “The effects of long-acting bronchodilators on total mortality in patients with stable chronic obstructive pulmonary disease,” Respiratory Research, vol. 11, article 56, 2010.
[20]  M. B. Drummond, E. C. Dasenbrook, M. W. Pitz, D. J. Murphy, and E. Fan, “Inhaled corticosteroids in patients with stable chronic obstructive pulmonary disease: a systematic review and meta-analysis,” Journal of the American Medical Association, vol. 300, no. 20, pp. 2407–2416, 2008.
[21]  S. Singh, A. V. Amin, and Y. K. Loke, “Long-term use of inhaled corticosteroids and the risk of pneumonia in chronic obstructive pulmonary disease,” Archives of Internal Medicine, vol. 169, no. 3, pp. 219–229, 2009.
[22]  R. ZuWallack, “The nonpharmacologic treatment of chronic obstructive pulmonary disease: advances in our understanding of pulmonary rehabilitation,” Proceedings of the American Thoracic Society, vol. 4, no. 7, pp. 549–553, 2007.
[23]  L. Nici, C. Donner, E. Wouters et al., “American Thoracic Society/European Respiratory Society statement on pulmonary rehabilitation,” American Journal of Respiratory and Critical Care Medicine, vol. 173, no. 12, pp. 1390–1413, 2006.
[24]  K. A. Hardin, F. Meyers, and S. Louie, “Integrating palliative care in severe chronic obstructive lung disease,” COPD: Journal of Chronic Obstructive Pulmonary Disease, vol. 5, no. 4, pp. 207–220, 2008.
[25]  M. T. Claessens, J. Lynn, Z. Zhong et al., “Dying with lung cancer or chronic obstructive pulmonary disease: insights from SUPPORT. Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatments,” Journal of the American Geriatrics Society, vol. 48, supplement 5, pp. S146–S153, 2000.
[26]  P. A. Kvale, W. A. Conway, and E. O. Coates, “Continuous or nocturnal oxygen therapy in hypoxemic chronic obstructive lung disease. A clinical trial,” Annals of Internal Medicine, vol. 93, no. 3, pp. 391–398, 1980.
[27]  C. Stuart-Harris, J. M. Bishop, and T. J. H. Clark, “Long term domiciliary oxygen therapy in chronic hypoxic cor pulmonale complicating chronic bronchitis and emphysema,” The Lancet, vol. 1, no. 8222, pp. 681–686, 1981.
[28]  A. J. Crockett, J. M. Cranston, J. R. Moss, and J. H. Alpers, “Survival on long-term oxygen therapy in chronic airflow limitation: from evidence to outcomes in the routine clinical setting,” Internal Medicine Journal, vol. 31, no. 8, pp. 448–454, 2001.
[29]  J. C. Hogg, F. Chu, S. Utokaparch et al., “The nature of small-airway obstruction in chronic obstructive pulmonary disease,” The New England Journal of Medicine, vol. 350, no. 26, pp. 2645–2653, 2004.
[30]  P. K. Jeffery, “Remodeling and inflammation of bronchi in asthma and chronic obstructive pulmonary disease,” Proceedings of the American Thoracic Society, vol. 1, no. 3, pp. 176–183, 2004.
[31]  K. F. Rabe, E. D. Bateman, D. O'Donnell, S. Witte, D. Bredenbr?ker, and T. D. Bethke, “Roflumilast: an oral anti-inflammatory treatment for chronic obstructive pulmonary disease: a randomised controlled trial,” The Lancet, vol. 366, no. 9485, pp. 563–571, 2005.
[32]  C. H. Compton, J. Gubb, R. Nieman et al., “Cilomilast, a selective phosphodiesterase-4 inhibitor for treatment of patients with chronic obstructive pulmonary disease: a randomised, dose-ranging study,” The Lancet, vol. 358, no. 9278, pp. 265–270, 2001.
[33]  S. I. Rennard, N. Schachter, M. Strek, K. Richard, and O. Amit, “Cilomilast for COPD: results of a 6-month, placebo-controlled study of a potent, selective inhibitor of phosphodiesterase 4,” Chest, vol. 129, no. 1, pp. 56–66, 2006.
[34]  M. A. Giembycz, “An update and appraisal of the cilomilast phase III clinical development programme for chronic obstructive pulmonary disease,” British Journal of Clinical Pharmacology, vol. 62, no. 2, pp. 138–152, 2006.
[35]  R. A. McIvor, “Future options for disease intervention: important advances in phosphodiesterase 4 inhibitors,” European Respiratory Review, vol. 16, no. 105, pp. 105–112, 2007.
[36]  P. M. Calverley, K. F. Rabe, U.-M. Goehring, S. Kristiansen, L. M. Fabbri, and F. J. Martinez, “Roflumilast in symptomatic chronic obstructive pulmonary disease: two randomised clinical trials,” The Lancet, vol. 374, no. 9691, pp. 685–694, 2009.
[37]  L. M. Fabbri, P. M. Calverley, J. L. Izquierdo-Alonso et al., “Roflumilast in moderate-to-severe chronic obstructive pulmonary disease treated with longacting bronchodilators: two randomised clinical trials,” The Lancet, vol. 374, no. 9691, pp. 695–703, 2009.
[38]  The Medical News, “FDA issues complete response letter for roflumilast NDA,” May 2010, http://www.news-medical.net/news/20100518/.
[39]  “Gen: genetic engineering and biotechnology news,” July 2010, http://www.genengnews.com/.
[40]  P. N. Dekhuijzen and W. J. van Beurden, “The role for N-acetylcysteine in the management of COPD,” International Journal of Chronic Obstructive Pulmonary Disease, vol. 1, no. 2, pp. 99–106, 2006.
[41]  M. M. E. Bridgeman, M. Marsden, W. MacNee, D. C. Flenley, and A. P. Ryle, “Cysteine and glutathione concentrations in plasma and bronchoalveolar lavage fluid after treatment with N-acetylcysteine,” Thorax, vol. 46, no. 1, pp. 39–42, 1991.
[42]  M. Linden, E. Wieslander, A. Eklund, K. Larsson, and R. Brattsand, “Effects of oral N-acetylcysteine on cell content and macrophage function in bronchoalveolar lavage from healthy smokers,” European Respiratory Journal, vol. 1, no. 7, pp. 645–650, 1988.
[43]  G. C. Riise, I. Qvarfordt, S. Larsson, V. Eliasson, and B. A. Andersson, “Inhibitory effect of N-acetylcysteine on adherence of Streptococcus pneumoniae and Haemophilus influenzae to human oropharyngeal epithelial cells in vitro,” Respiration, vol. 67, no. 5, pp. 552–558, 2000.
[44]  E. M. Grandjean, P. Berthet, R. Ruffmann, and P. Leuenberger, “Efficacy of oral long-term N-acetylcysteine in chronic bronchopulmonary disease: a meta-analysis of published double-blind, placebo-controlled clinical trials,” Clinical Therapeutics, vol. 22, no. 2, pp. 209–221, 2000.
[45]  C. Stey, J. Steurer, S. Bachmann, T. C. Medici, and M. R. Tramer, “The effect of oral N-acetylcysteine in chronic bronchitis: a quantitative systematic review,” European Respiratory Journal, vol. 16, no. 2, pp. 253–262, 2000.
[46]  M. Decramer, M. Rutten-Van M?lken, P. N. R. Dekhuijzen et al., “Effects of N-acetylcysteine on outcomes in chronic obstructive pulmonary disease (Bronchitis Randomized on NAC Cost-Utility Study, BRONCUS): a randomised placebo-controlled trial,” The Lancet, vol. 365, no. 9470, pp. 1552–1560, 2005.
[47]  R. Zuin, A. Palamidese, R. Negrin, L. Catozzo, A. Scarda, and M. Balbinot, “High-dose N-acetylcysteine in patients with exacerbations of chronic obstructive pulmonary disease,” Clinical Drug Investigation, vol. 25, no. 6, pp. 401–408, 2005.
[48]  V. M. Keatings, P. D. Collins, D. M. Scott, and P. J. Barnes, “Differences in interleukin-8 and tumor necrosis facfor-α in induced sputum from patients with chronic obstructive pulmonary disease or asthma,” American Journal of Respiratory and Critical Care Medicine, vol. 153, no. 2, pp. 530–534, 1996.
[49]  I. De Godoy, M. Donahoe, W. J. Calhoun, J. Mancino, and R. M. Rogers, “Elevated TNF-α production by peripheral blood monocytes of weight-losing COPD patients,” American Journal of Respiratory and Critical Care Medicine, vol. 153, no. 2, pp. 633–637, 1996.
[50]  S. I. Rennard, C. Fogarty, S. Kelsen et al., “The safety and efficacy of infliximab in moderate to severe chronic obstructive pulmonary disease,” American Journal of Respiratory and Critical Care Medicine, vol. 175, no. 9, pp. 926–934, 2007.
[51]  D. A. Mahler, S. Huang, M. Tabrizi, and G. M. Bell, “Efficacy and safety of a monoclonal antibody recognizing lnterleukin-8 in COPD: a pilot study,” Chest, vol. 126, no. 3, pp. 926–934, 2004.
[52]  J. F. Donohue, “COPD management: current therapies and novel treatment approaches,” Journal COPD Management, March 2006.
[53]  S. Gompertz and R. A. Stockley, “A randomized, placebo-controlled trial of a leukotriene synthesis inhibitor in patients with COPD,” Chest, vol. 122, no. 1, pp. 289–294, 2002.
[54]  F. J. Martinez, J. L. Curtis, and R. Albert, “Role of macrolide therapy in chronic obstructive pulmonary disease,” International Journal of Chronic Obstructive Pulmonary Disease, vol. 3, no. 3, pp. 331–350, 2008.
[55]  T. A. R. Seemungal, T. M. A. Wilkinson, J. R. Hurst, W. R. Perera, R. J. Sapsford, and J. A. Wedzicha, “Long-term erythromycin therapy is associated with decreased chronic obstructive pulmonary disease exacerbations,” American Journal of Respiratory and Critical Care Medicine, vol. 178, no. 11, pp. 1139–1147, 2008.
[56]  I. Basyigit, F. Yildiz, S. K. Ozkara, E. Yildirim, H. Boyaci, and A. Ilgazli, “The effect of clarithromycin on inflammatory markers in chronic obstructive pulmonary disease: preliminary data,” Annals of Pharmacotherapy, vol. 38, no. 9, pp. 1400–1405, 2004.
[57]  D. Banerjee, D. Honeybourne, and O. A. Khair, “The effect of oral clarithromycin on bronchial airway inflammation in moderate-to-severe stable COPD: a randomized controlled trial,” Treatments in Respiratory Medicine, vol. 3, no. 1, pp. 59–65, 2004.
[58]  W. Janssens, R. Bouillon, B. Claes et al., “Vitamin D deficiency is highly prevalent in COPD and correlates with variants in the vitamin D-binding gene,” Thorax, vol. 65, no. 3, pp. 215–220, 2010.
[59]  P. N. Black and R. Scragg, “Relationship between serum 25-hydroxyvitamin D and pulmonary function in the third national health and nutrition examination survey,” Chest, vol. 128, no. 6, pp. 3792–3798, 2005.
[60]  L. F?rli, J. Halse, E. Haug et al., “Vitamin D deficiency, bone mineral density and weight in patients with advanced pulmonary disease,” Journal of Internal Medicine, vol. 256, no. 1, pp. 56–62, 2004.
[61]  A. Fishman, F. Martinez, K. Naunheim et al., “A randomized trial comparing lung-volume-reduction surgery with medical therapy for severe emphysema,” The New England Journal of Medicine, vol. 348, no. 21, pp. 2059–2073, 2003.
[62]  G. J. Criner and A. L. Sternberg, “National emphysema treatment trial: the major outcomes of lung volume reduction surgery in severe emphysema,” Proceedings of the American Thoracic Society, vol. 5, no. 4, pp. 393–405, 2008.
[63]  B. J. Make and A. M. Fein, “Is volume reduction surgery appropriate in the treatment of emphysema? No,” American Journal of Respiratory and Critical Care Medicine, vol. 153, no. 4, pp. 1205–1207, 1996.
[64]  S. Sabanathan, J. Richardson, and S. Pieri-Davies, “Bronchoscopic lung volume reduction,” Journal of Cardiovascular Surgery, vol. 44, no. 1, pp. 101–108, 2003.
[65]  A. Ernst and D. Anantham, “Invasive procedures for emphysema,” Americal Colllege of Chest Physicians, PCCSU, vol. 24, no. 12, 2010.
[66]  C. K. Choong, P. T. Macklem, J. A. Pierce et al., “Airway bypass improves the mechanical properties of explanted emphysematous lungs,” American Journal of Respiratory and Critical Care Medicine, vol. 178, no. 9, pp. 902–905, 2008.
[67]  H. F. Lausberg, K. Chino, G. A. Patterson et al., “Bronchial fenestration improves expiratory flow in emphysematous human lungs,” Annals of Thoracic Surgery, vol. 75, no. 2, pp. 393–398, 2003.
[68]  E. A. Rendina, T. De Giacomo, F. Venuta et al., “Feasibility and safety of the airway bypass procedure for patients with emphysema,” Journal of Thoracic and Cardiovascular Surgery, vol. 125, no. 6, pp. 1294–1299, 2003.
[69]  C. K. Choong, L. Phan, P. Massetti et al., “Prolongation of patency of airway bypass stents with use of drug-eluting stents,” Journal of Thoracic and Cardiovascular Surgery, vol. 131, no. 1, pp. 60–64, 2006.
[70]  P. F. G. Cardoso, G. I. Snell, P. Hopkins et al., “Clinical application of airway bypass with paclitaxel-eluting stents: early results,” Journal of Thoracic and Cardiovascular Surgery, vol. 134, no. 4, pp. 974–981, 2007.
[71]  I. Y. P. Wan, T. P. Toma, D. M. Geddes et al., “Bronchoscopic lung volume reduction for end-stage emphysema: report on the first 98 patients,” Chest, vol. 129, no. 3, pp. 518–526, 2006.
[72]  D. E. Wood, R. J. McKenna, R. D. Yusen et al., “A multicenter trial of an intrabronchial valve for treatment of severe emphysema,” Journal of Thoracic and Cardiovascular Surgery, vol. 133, no. 1, pp. 65–e2, 2007.
[73]  Emphasys Medical, Inc., “Executive Summary, P070025, Zephyr Endobronchial Valve System. U.S. P070025,” in Presented at: Anesthesiology and Respiratory Therapy Devices Panel, Gathersburg, Md, USA, December 2008.
[74]  E. P. Walker, “FDA advisers recommend rejection of airway valve for emphysema,” December 2008, http://www.medpagetoday.com/.
[75]  S. C. Springmeyer, C. T. Bolliger, T. K. Waddell, X. Gonzalez, and D. E. Wood, “Treatment of heterogeneous emphysema using the spiration IBV valves,” Thoracic Surgery Clinics, vol. 19, no. 2, pp. 247–253, 2009.
[76]  N. S. Hopkinson, T. P. Toma, D. M. Hansell et al., “Effect of bronchoscopic lung volume reduction on dynamic hyperinflation and exercise in emphysema,” American Journal of Respiratory and Critical Care Medicine, vol. 171, no. 5, pp. 453–460, 2005.
[77]  S. C.S. Chung, M. J. Peters, S. Chen, L. Emmett, and A. J. Ing, “Effect of unilateral endobronchial valve insertion on pulmonary ventilation and perfusion: a pilot study,” Respirology, vol. 15, no. 7, pp. 1079–1083, 2010.
[78]  E. P. Ingenito, J. J. Reilly, S. J. Mentzer et al., “Bronchoscopic volume reduction: a safe and effective alternative to surgical therapy for emphysema,” American Journal of Respiratory and Critical Care Medicine, vol. 164, no. 2, pp. 295–301, 2001.
[79]  J. Reilly, G. Washko, V. Pinto-Plata et al., “Biological lung volume reduction: a new bronchoscopic therapy for advanced emphysema,” Chest, vol. 131, no. 4, pp. 1108–1113, 2007.
[80]  G. J. Criner, V. Pinto-Plata, C. Strange et al., “Biologic lung volume reduction in advanced upper lobe emphysema phase 2 results,” American Journal of Respiratory and Critical Care Medicine, vol. 179, no. 9, pp. 791–798, 2009.

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