1,078
Views
41
CrossRef citations to date
0
Altmetric
Reviews

Current treatment of atypical mycobacteriosis

&
Pages 2787-2799 | Published online: 25 Nov 2009

Bibliography

  • Wolinsky E. Nontuberculous mycobacteria and associated diseases. Am Rev Respir Dis 1979;119(1):107-59
  • Griffith DE, Aksamit T, Brown-Elliot BA, An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med 2007;175:367-416
  • Martin-Casabona N, Bahrmand AR, Bennedsen J, Nontuberculous mycobacteria: patterns of isolation. A multi-country retrospective survey. Int J Tuberc Lung Dis 2004;8(10):1186-93
  • McIlleron H, Wash P, Burger A, Determinants of rifampin, isoniazid, pyrazinamide, and ethambutol pharmacokinetics in a cohors of tuberculosis patients. Antimicrob Agents Chemother 2006;50(4):1170-7
  • Almeida D, Nuermberger E, Tasneen R, Paradoxical effect of isoniazid on the activity of rifampin-pyrazinamide combination in a mouse model of tuberculosis. Antimicrob Agents Chemother 2009;53(10):4178-84
  • Dooley K, Flexner C, Hackman J, Repeated administration of high-dose intermittent rifapentine reduces rifapentine and moxifloxacin plasma concentrations. Antimicrob Agents Chemother 2008;52(11):4037-42
  • Nijland HM, Ruslami R, Suroto AJ, Rifampicin reduces plasma concentrations of moxifloxacin in patients with tuberculosis. Clin Infect Dis 2007;45(8):1001-7
  • Taki H, Ogawa K, Nakagawa T, Clinical analysis of drug interaction between rifampicin and clarithromycin which are used for treating pulmonary Mycobacterium avium complex infection. Kekkaku 2007;82(8):641-6
  • Wallace RJ, Brown BA, Griffith DE, Reduced serum levels of clarithromycin in patients treated with multidrug regimens including rifampin or rifabutin for Mycobacterium avium-M. intracellulare infection. J Infect Dis 1995;171(3):747-50
  • Yamamoto F, Harada S, Mitsuyama T, Concentration of clarithromycin and 14-R-hydroxy-clarithromycin in plasma of patients with Mycobacterium avium complex infection, before and after the addition of rifampicin. Jpn J Antibiot 2004;57(1):124-33
  • Ruslami R, Nijland HM, Alisjahbana B, Pharmacokinetics and tolerability of a higher rifampin dose versus the standard dose in pulmonary tuberculosis patients. Antimicrob Agents Chemother 2007;51(7):2456-1
  • Martin-Casabona N, Bahrmand AR, Bennedsen J, Nontuberculous mycobacteria: patterns of isolation. A multi-country retrospective survey. Int J Tuberc Lung Dis 2004;8(10):1186-93
  • Ben Salah I, Cayrou C, Raoult D, Drancourt M. Mycobacterium marseillense sp. nov., Mycobacterium timonense sp. nov. and Mycobacterium bouchedurhonense sp. nov., novel species in the Mycobacterium avium complex. Int J Syst Evol Microbiol 2009. [Epub ahead of print]
  • van Ingen J, Boeree MJ, Kösters K, Proposal to elevate Mycobacterium avium complex ITS sequevar MAC-Q to Mycobacterium vulneris sp. nov. Int J Syst Evol Microbiol 2009. [Epub ahead of print]
  • Tortoli E, Rindi L, Garcia MJ, Proposal to elevate the genetic variant MAC-A, included in the Mycobacterium avium complex, to species rank as Mycobacterium chimaera sp. nov. Int J Syst Evol Microbiol 2004;54(Pt 4):1277-85
  • Kim RD, Greenberg DE, Ehrmantraut ME, Pulmonary nontuberculous mycobacterial disease. Prospective study of a distinct preexisting syndrome. Am J Respir Crit Care Med 2008;178:1066-74
  • Dailloux M, Abalain ML, Laurain C, Respiratory infections associated with nontuberculous mycobacteria in non-HIV patients. Eur Respir J 2006;28(6):1211-5
  • Kim RD, Greenberg DE, Ehrmantraut ME, Pulmonary nontuberculous mycobacterial disease: prospective study of a distinct preexisting syndrome. Am J Respir Crit Care Med 2008;178(10):1066-74
  • Brettle RP. Mycobacterium avium intracellulare infection in patients with HIV or AIDS. J Antimicrob Chemother 1997;40:156-60
  • Wolinsky E. Mycobacterial diseases other than tuberculosis. Clin Infect Dis 1992;15(1):1-10
  • Hocqueloux L, Lesprit P, Herrmann JL, Pulmonary Mycobacterium avium complex disease without dissemination in HIV-infected patients. Chest 1998;113(2):542-8
  • Escalonilla P, Esteban J, Soriano ML, Cutaneous manifestations of infection by nontuberculous mycobacteria. Clin Exp Dermatol 1998;23:214-21
  • van Ingen J, Bendien SA, de Lange WC, Clinical relevance of non-tuberculous mycobacteria isolated in the Nijmegen-Arnhem region, The Netherlands. Thorax 2009;64(6):502-6
  • The Research Committee of the British Thoracic Society. First randomised trial of treatments for pulmonary disease caused by M. avium intracellulare, M. malmoense, and M. xenopi in HIV negative patients: rifampicin, ethambutol and isoniazid versus rifampicin and ethambutol. Thorax 2001;56:167-72
  • Griffith DE. Therapy of nontuberculous mycobacterial disease. Curr Opin Infect Dis 2007;20(2):198-203
  • Heginbothom ML. The relationship between the in vitro drug susceptibility of opportunist mycobacteria and their in vivo response to treatment. Int J Tuberc Lung Dis 2001;5(6):539-45
  • NCCLS. Susceptibility testing of mycobacteria, nocardiae and other aerobic actinomycetes; approved standard. NCCLS document M24-A. 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898, USA: NCCLS; 2003
  • Pierce M, Crampton S, Henry D, A randomized trial of clarithromycin as prophylaxis against disseminated Mycobacterium avium complex infection in patients with advanced acquired immunodeficiency syndrome. N Engl J Med 1996;335(6):384-91
  • Havlir DV, Dubé MP, Sattler FR, Prophylaxis against disseminated Mycobacterium avium complex with weekly azithromycin, daily rifabutin, or both. California Collaborative Treatment Group. N Engl J Med 1996;335(6):392-8
  • Sendi PP, Craig BA, Meier G, Cost-effectiveness of azithromycin for preventing Mycobacterium avium complex infection in HIV-positive patients in the era of highly active antiretroviral therapy. The Swiss HIV Cohort Study. J Antimicrob Chemother 1999;44(6):811-7
  • Phillips P, Chan K, Hogg R, Azithromycin prophylaxis for Mycobacterium avium complex during the era of highly active antiretroviral therapy: evaluation of a provincial program. Clin Infect Dis 2002;34(3):371-8
  • Aberg JA, Wong MK, Flamm R, Presence of macrolide resistance in respiratory flora of HIV-Infected patients receiving either clarithromycin or azithromycin for Mycobacterium avium complex prophylaxis. HIV Clinical Trials 2001;2(6):453-9
  • Rossi M, Flepp M, Telenti A, Disseminated M. avium complex infection in the Swiss HIV Cohort Study: declining incidence, improved prognosis and discontinuation of maintenance therapy. Swiss Med Wkly 2001;131(31-32):471-7
  • El-Sadr WM, Burman WJ, Grant LB, Discontinuation of prophylaxis for Mycobacterium avium complex disease in HIV-infected patients who have a response to antiretroviral therapy. Terry Beirn Community Programs for Clinical Research on AIDS. N Engl J Med 2000;342(15):1085-92
  • Shafran SD, Mashinter LD, Phillips P, Successful discontinuation of therapy for disseminated Mycobacterium avium complex infection after effective antiretroviral therapy. Ann Intern Med 2002;137(9):734-7
  • McGrath EE, McCabe J, Anderson PB, Guidelines on the diagnosis and treatment of pulmonary non-tuberculous mycobacteria infection. Int J Clin Pract 2008;62(12):1947-55
  • Jenkins PA, Campbell IA, Banks J, Clarithromycin vs ciprofloxacin as adjuncts to rifampicin and ethambutol in treating opportunist mycobacterial lung diseases and an assessment of Mycobacterium vaccae immunotherapy. Thorax 2008;63:627-34
  • Lam PK, Griffith DE, Aksamit TR, Factors related to response to intermittent treatment of Mycobacterium avium complex lung disease. Am J Respir Crit Care Med 2006;173(11):1283-9
  • Griffith DE, Brown-Elliott BA, Langsjoen B, Clinical and molecular analysis of macrolide resistance in Mycobacterium avium complex lung disease. Am J Respir Crit Care Med 2006;174(8):928-34
  • Kohno Y, Ohno H, Miyazaki Y, In vitro and in vivo activities of novel fluoroquinolones alone and in combination with clarithromycin against clinically isolated Mycobacterium avium complex strains in Japan. Antimicrob Agents Chemother 2007;51(11):4071-6
  • Bermudez LE, Inderlied CB, Kolonoski P, Activity of moxifloxacin by itself and in combination with ethambutol, rifabutin, and azithromycin in vitro and in vivo against Mycobacterium avium. Antimicrob Agents Chemother 2001;45(1):217-22
  • Koh WJ, Kim YH, Kwon OJ, Surgical treatment of pulmonary diseases due to nontuberculous mycobacteria. J Korean Med Sci 2008;23(3):397-401
  • García-García A, Gálvez J, de Julián-Ortiz JV, New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method. J Antimicrob Chemother 2004;53(1):65-73
  • Huitric E, Verhasselt P, Andries K, Hoffner SE. In vitro antimycobacterial spectrum of a diarylquinoline ATP synthase inhibitor. Antimicrob Agents Chemother 2007;51(11):4202-4
  • Taillard C, Greub G, Weber R, Clinical implications of Mycobacterium kansasii species heterogeneity: Swiss National Survey. J Clin Microbiol 2003;41(3):1240-4
  • Cattamanchi A, Nahid P, Marras TK, Detailed analysis of the radiographic presentation of Mycobacterium kansasii lung disease in patients with HIV infection. Chest 2008;133(4):875-80
  • Tompkins JC, Witzig RS. Mycobacterium kansasii in HIV patients: clarithromycin and antiretroviral effects. Int J Tuberc Lung Dis 2007;11(3):331-7
  • Nakamura T, Yamamura Y, Tsuruta T, Mycobacterium kansasii arthritis of the foot in a patient with systemic lupus erythematosus. Intern Med 2001;40(10):1045-9
  • Bernard L, Vincent V, Lortholary O, Mycobacterium kansasii septic arthritis: French retrospective study of 5 years and review. Clin Infect Dis 1999;29(6):1455-60
  • Neuberger A, Sprecher H, Oren I. Septic arthritis caused by Mycobacterium kansasii in a prosthetic knee joint. J Clin Microbiol 2006;44(7):2648-9
  • Alcaide F, Calatayud L, Santín M, Martín R. Comparative in vitro activities of linezolid, telithromycin, clarithromycin, levofloxacin, moxifloxacin, and four conventional antimycobacterial drugs against Mycobacterium kansasii. Antimicrob Agents Chemother 2004;48(12):4562-5
  • da Silva Telles MA, Chimara E, Ferrazoli L, Riley LW. Mycobacterium kansasii: antibiotic susceptibility and PCR-restriction analysis of clinical isolates. J Med Microbiol 2005;54(Pt 10):975-9
  • Klein JL, Brown TJ, French GL. Rifampin resistance in Mycobacterium kansasii is associated with rpoB mutations. Antimicrob Agents Chemother 2001;45(11):3056-8
  • Shitrit D, Baum GL, Priess R, Pulmonary Mycobacterium kansasii infection in Israel, 1999-2004: clinical features, drug susceptibility, and outcome. Chest 2006;129(3):771-6
  • Cynamon MH, Elliott SA, DeStefano MS, Yeo AE. Activity of clarithromycin alone and in combination in a murine model of Mycobacterium kansasii infection. The J Antimicrob Chemother 2003;52(2):306-7
  • Guna R, Muñoz C, Domínguez V, In vitro activity of linezolid, clarithromycin and moxifloxacin against clinical isolates of Mycobacterium kansasii. J Antimicrob Chemother 2005;55(6):950-3
  • Brown-Elliott BA, Crist CJ, Mann LB, In vitro activity of linezolid against slowly growing nontuberculous Mycobacteria. Antimicrob Agents Chemother 2003;47(5):1736-8
  • Jiva TM, Jacoby HM, Weymouth LA, Mycobacterium xenopi: innocent bystander or emerging pathogen? Clin Infect Dis 1997;24:226-32
  • van Ingen J, Boeree MJ, de Lange WC, Mycobacterium xenopi clinical relevance and determinants, the Netherlands. Emerg Infect Dis 2008;14(3):385-9
  • Esteban J, Molleja A, Górgolas M, Fernández-Roblas R. Clinical significance of the isolation of Mycobacterium xenopi. Med Clín (Barc) 1999;113(1):38-9
  • Katoch VM. Infections due to non-tuberculous mycobacteria (NTM). Indian J Med Res 2004;120:290-304
  • Manfredi R, Nanetti A, Morelli S, A decade surveillance study of Mycobacterium xenopi disease and antimicrobial susceptibility levels in a reference teaching hospital of northern Italy: HIV-associated versus non-HIV-associated infection. HIV Clin Trials 2004;5(4):206-15
  • Juffermans NP, Verbon A, Danner SA, Mycobacterium xenopi in HIV-infected patients: an emerging pathogen. AIDS 1998;12:1661-6
  • Lounis N, Truffot-Pernot C, Bentoucha A, Efficacies of clarithromycin regimens against Mycobacterium xenopi in mice. Antimicrob Agents Chemother 2001;45(11):3229-30
  • Butler WR, O'Connor SP, Yakrus MA, Mycobacterium celatum sp. nov. Int J Syst Bacteriol 1993;43:539-48
  • Christiansen DC, Roberts GD, Patel R. Mycobacterium celatum, an emerging pathogen and cause of false positive amplified Mycobacterium tuberculosis direct test. Diagn Microbiol Infect Dis 2004;49:19-24
  • Tortoli E, Piersimoni C, Bacosi D, Isolation of the newly described species Mycobacterium celatum from AIDS patients. J Clin Microbiol 1995;3(1):37-140
  • Zurawski CA, Cage GD, Rimland D, Blumberg HM. Pneumonia and bacteremia due to Mycobacterium celatum masquerading as Mycobacterium xenopi in patients with AIDS: an underdiagnosed problem? Clin Infect Dis 1997;24:140-3
  • Asiedu K, Scherpbier R, Raviglione M. Buruli ulcer. Mycobacterium ulcerans infection. Geneva: World Health Organization; 2000
  • World Health Organization. Provisional guidance on the role of specific antibiotics in the management of Mycobacterium ulcerans disease (Buruli ulcer). World Health Organization, editor. Geneva: World Health Organization; 2004
  • O'Brien DP, Athan E, Hughes A, Johnson PD. Successful treatment of Mycobacterium ulcerans osteomyelitis with minor surgical debridement and prolonged rifampicin and ciprofloxacin therapy: a case report. J Med Case Rep 2008;27(2):123
  • Dega H, Bentoucha A, Robert J, Bactericidal activity of rifampin-amikacin against Mycobacterium ulcerans in mice. Antimicrob Agents Chemother 2002;46(10):3193-6
  • Lefrançois S, Robert J, Chauffour A, Curing Mycobacterium ulcerans infection in mice with a combination of rifampin-streptomycin or rifampin-amikacin. Antimicrob Agents Chemother 2007;51(2):645-50
  • Marsollier L, Honoré N, Legras P, Isolation of three Mycobacterium ulcerans strains resistant to rifampin after experimental chemotherapy of micee. Antimicrob Agents Chemother 2003;47(4):1228-32
  • Chauty A, Ardant MF, Adeye A, Promising clinical efficacy of streptomycin-rifampin combination for treatment of buruli ulcer (Mycobacterium ulcerans disease). Antimicrob Agents Chemother 2007;51(11):4029-35
  • Etuaful S, Carbonnelle B, Grosset J, Efficacy of the combination rifampin-streptomycin in preventing growth of Mycobacterium ulcerans in early lesions of Buruli ulcer in humans. Antimicrob Agents Chemother 2005;49(8):3182-6
  • Ji B, Chauffour A, Robert J, Jarlier V. Bactericidal and sterilizing activities of several orally administered combined regimens against Mycobacterium ulcerans in mice. Antimicrob Agents Chemother 2008;52(6):1912-6
  • Ji B, Chauffour A, Robert J, Orally administered combined regimens for treatment of Mycobacterium ulcerans infection in mice. Antimicrob Agents Chemother 2007;51(10):3737-9
  • Ji B, Lefrançois S, Robert J, In vitro and in vivo activities of rifampin, streptomycin, amikacin, moxifloxacin, R207910, linezolid, and PA-824 against Mycobacterium ulcerans. Antimicrob Agents Chemother 2006;50(6):1921-6
  • Johnson PD, Hayman JA, Quek TY, Consensus recommendations for the diagnosis, treatment and control of Mycobacterium ulcerans infection (Bairnsdale or Buruli ulcer) in Victoria, Australia. Med J Aust 2007;186(2):64-8
  • De Groote MA, Huitt G. Infections due to rapidly growing mycobacteria. Clin Infect Dis 2006;42(12):1756-63
  • Brown-Elliott BA, Wallace RJ Jr. Clinical and taxonomic status of pathogenic nonpigmented or late-pigmenting rapidly growing mycobacteria. Clin Microbiol Rev 2002;15(4):716-46
  • Esteban J, Martín-de-Hijas NZ, Fernández AI, Epidemiology of infections due to non-pigmented rapidly growing Mycobacteria diagnosed in an urban area. Eur J Clin Microbiol Infect Dis 2008;27(10):951-7
  • Martín-de-Hijas NZ, García-Almeida D, Ayala G, Biofilm development by clinical strains of non-pigmented rapidly growing mycobacteria. Clin Microbiol Infect 2009;15:931-6
  • Fernandez-Roblas R, Esteban J, Cabria F, In vitro susceptibilities of rapidly growing mycobacteria to telithromycin (HMR 3647) and seven other antimicrobials. Antimicrob Agents Chemother 2000;44(1):181-2
  • Fernández-Roblas R, Martín-de-Hijas NZ, Fernández-Martínez AI, In vitro activity of tigecycline and 10 other antimicrobials against non-pigmented rapidly growing mycobacteria. Antimicrob Agents Chemother 2008;52(11):4184-6
  • Wallace RJ Jr, Brown-Elliott BA, Ward SC, Activities of linezolid against rapidly growing mycobacteria. Antimicrob Agents Chemother 2001;45(3):764-7
  • Vera-Cabrera L, Brown-Elliott BA, Wallace RJ, In vitro activities of the novel oxazolidinones DA-7867 and DA-7157 against rapidly and slowly growing mycobacteria. Antimicrob Agents Chemother 2006;50(12):4027-9
  • Yang SC, Hsueh PR, Lai HC, High prevalence of antimicrobial resistance in rapidly growing mycobacteria in Taiwan. Antimicrob Agents Chemother 2003;47(6):1958-62
  • Esteban J, Gadea I, Torres MV, A comparison between disk diffusion and microdilution for susceptibility testing of Mycobacterium fortuitum complex. J Chemother 2002;14(6):547-53
  • Woods GL, Bergmann JS, Witebsky FG, Multisite reproducibility of Etest for susceptibility testing of Mycobacterium abscessus, Mycobacterium chelonae, and Mycobacterium fortuitum. J Clin Microbiol 2000;38(2):656-61
  • Wallace RJ Jr, Meier A, Brown BA, Genetic basis for clarithromycin resistance among isolates of Mycobacterium chelonae and Mycobacterium abscessus. Antimicrob Agents Chemother 1996;40(7):1676-81
  • Esteban J, Martin-de-Hijas NZ, Garcia-Almeida D, Prevalence of erm methylase genes in clinical isolates of non-pigmented, rapidly growing mycobacteria. Clin Microbiol Infect 2009;15:919-23
  • Esteban J, Martin-de-Hijas NZ, Ortiz-Perez A, Detection of lfrA and tap efflux pump genes among clinical iso-lates of non-pigmented rapidly growing mycobacteria. Int J Antimicrob Agents 2009;34:454-6
  • Nash KA, Andini N, Zhang Y, Intrinsic macrolide resistance in rapidly growing mycobacteria. Antimicrob Agents Chemother 2006;50(10):3476-8
  • Driscoll MS, Tyring SK. Development of resistance to clarithromycin after treatment of cutaneous Mycobacterium chelonae infection. J Am Acad Dermatol 1997;36(3 Pt 1):495-6
  • Rodriguez Diaz JC, Lopez M, Ruiz M, Royo G. In vitro activity of new fluoroquinolones and linezolid against non-tuberculous mycobacteria. Int J Antimicrob Agents 2003;21(6):585-8
  • Wallace RJ, Brown-Elliot BA, Crist CJ, Comparison of the in vitro activity of the glycylcycline tigecycline (formerly GAR-936) with those of tetracycline, minocycline, and doxycycline against isolates of nontuberculous mycobacteria. Antimicrob Agents Chemother 2002;46(10):3164-7
  • Peres E, Khaled Y, Krijanovski OI, Mycobacterium chelonae necrotizing pneumonia after allogeneic hematopoietic stem cell transplant: report of clinical response to treatment with tigecycline. Transpl Infect Dis 2009;11(1):57-63
  • Tam WO, Yew WW, Yam WC, Pacemaker infections due to rapidly growing mycobacteria: further experience. Int J Tuberc Lung Dis 2007;11(1):118
  • Aubry A, Chosidow O, Caumes E, Sixty-three cases of Mycobacterium marinum infection: clinical features, treatment, and antibiotic susceptibility of causative isolates. Arch Intern Med 2002;162(15):1746-52
  • Streit M, Böhlen LM, Hunziker T, Disseminated Mycobacterium marinum infection with extensive cutaneous eruption and bacteremia in an immunocompromised patient. Eur J Dermatol 2006;16(1):79-83
  • Aubry A, Jarlier V, Escolano S, Antibiotic susceptibility pattern of Mycobacterium marinum. Antimicrob Agents Chemother 2000;44(11):3133-6
  • Flynn CM, Kelley CM, Barrett MS, Jones RN. Application of the Etest to the antimicrobial susceptibility testing of Mycobacterium marinum clinical isolates. J Clin Microbiol 1997;35(8):2083-6
  • Springer B, Wu WK, Bodmer T, Isolation and characterization of a unique group of slowly growing mycobacteria: description of Mycobacterium lentiflavum sp. nov. J Clin Microbiol 1996;34(5):1100-7
  • Niobe SN, Bebear CM, Clerc M, Disseminated Mycobacterium lentiflavum infection in a human immunodeficiency virus-infected patient. J Clin Microbiol 2001;39(5):2030-2
  • Tortoli E, Bartoloni A, Erba ML, Human infections due to Mycobacterium lentiflavum. J Clin Microbiol 2002;40(2):728-9
  • Molteni C, Gazzola L, Cesari M, Mycobacterium lentiflavum infection in immunocompetent patient. Emerg Infect Dis 2005;11(1):119-22
  • Cabria F, Torres MV, García-Cía JI, Cervical lymphadenitis caused by Mycobacterium lentiflavum. Pediatric Infect Dis J 2002;21(6):574-5
  • Hoefsloot W, Boeree MJ, van Ingen J, The rising incidence and clinical relevance of Mycobacterium malmoense: a review of the literature. Int J Tuberc Lung Dis 2008 12(9):987-93
  • The_Research_Committee_of_the_British_Thoracic_Society. Pulmonary disease caused by M. malmoense in HIV negative patients: 5-yr follow-up of patients receiving standardised treatment. Eur Respir J 2003;21:478-82
  • Wayne LG, Sramek HA. Agents of newly recognized or infrequently encountered mycobacterial diseases. Clin Microbiol Rev 1992;5(1):1-25
  • Hoffner SE, Hjelm U, Kallenium G. Susceptibility of Mycobacterium malmoense to antibacterial drugs and drug combinations. Antimicrob Agents Chemother 1993;37(6):1285-8
  • Elsayed S, Read R. Mycobacterium haemophilum osteomyelitis: case report and review of the literature. BMC Infect Dis 2006;10(6):70
  • Jarzembowski JA. Nontuberculous mycobacterial infections. Arch Pathol Lab Med 2008;132:1333-41

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.