Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-r6qrq Total loading time: 0 Render date: 2024-04-27T03:29:48.511Z Has data issue: false hasContentIssue false

39 - Disseminated Mycobacterium avium complex infection

from Part V - Infectious problems in pediatric HIV disease

Published online by Cambridge University Press:  03 February 2010

Robert N. Husson
Affiliation:
Children's Hospital, Boston, MA
Steven L. Zeichner
Affiliation:
National Cancer Institute, Bethesda, Maryland
Jennifer S. Read
Affiliation:
National Cancer Institute, Bethesda, Maryland
Get access

Summary

Non-tuberculous mycobacteria are major opportunistic pathogens of HIV-infected children and adults who have severe immunosuppression. Mycobacterium avium is the predominant pathogen, typically causing systemic infection (referred to as disseminated M. avium complex infection or DMAC). With the advent of highly active antiretroviral therapy (HAART) and the resulting improved preservation of immune competence, DMAC infection has become less common [1]. Among HIV-infected children with advanced disease, however, DMAC infection remains an important cause of morbidity and mortality, so that prevention and management of non-tuberculous mycobacterial infection are important aspects of the care of children with AIDS. With increasing resistance to all classes of antiretroviral drugs over time, and intolerance or poor adherence to therapy, the potential for increased incidence of DMAC infection in HIV-infected children remains a threat.

Epidemiology

Mycobacterium avium and many of the other non-tuberculous mycobacteria are widely distributed in the environment. They are found in water and soil in nature and have been identified in food and in institutional water systems [2, 3]. These organisms are uncommon causes of infection in normal hosts, and thus are opportunistic pathogens in patients with depressed cell-mediated immunity, including those with HIV infection.

While DMAC infection is a major opportunistic infection in North America and Western Europe, it is uncommonly identified in persons with AIDS in Africa or other less-developed areas of the world. It is not known whether this difference reflects differences in distribution of pathogenic strains of MAC in the environment.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Palella, F. J. Jr., Delaney, K. M., Moorman, A. C.. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. Human Immunodeficiency Virus Outpatient Study Investigators. New Engl. J. Med. 338: 13 (1998), 853–60CrossRefGoogle ScholarPubMed
Reyn, C. F., Waddell, R. D., Eaton, T.. Isolation of Mycobacterium avium complex from water in the United States, Finland, Zaire, and Kenya. J. Clin. Microbiol. 31: 12 (1993), 3227–30Google Scholar
Reyn, C., Maslow, J., Barber, T., Falkinham, J. III & Arbeit, R.Persistent colonisation of potable water as a source of Mycobacterium avium infection in Acquired Immune Deficiency Syndrome. Lancet 343 (1994), 1137–41CrossRefGoogle Scholar
Pettipher, C. A., Karstaedt, A. S. & Hopley, M.Prevalence and clinical manifestations of disseminated Mycobacterium avium complex infection in South Africans with acquired immunodeficiency syndrome. Clin. Infect. Dis. 33: 12 (2001), 2068–71CrossRefGoogle ScholarPubMed
Inderlied, C., Kemper, C. & Bermudez, L.The Mycobacterium avium complex. Clin. Microbiol. Rev. 6 (1993), 266–310CrossRefGoogle ScholarPubMed
Guthertz, L., Damsker, B., Bottone, E., Ford, E., Midura, T. & Janda, J.Mycobacterium avium and Mycobacterium intracellulare infections in patients with and without Acquired Immune Deficiency Syndrome. J. Infect. Dis. 160 (1989), 1037–41CrossRefGoogle Scholar
Hazra, R., Lee, S. H., Maslow, J. N. & Husson, R. N.Related strains of Mycobacterium avium cause disease in children with Acquired Immune Deficiency Syndrome and in children with lymphadenitis. J. Infect. Dis. 181: 4 (2000), 1298–303CrossRefGoogle Scholar
Woods, G. L.Susceptibility testing for mycobacteria. Clin. Infect. Dis. 31: 5 (2000), 1209–15Google ScholarPubMed
Dankner, W. M., Lindsey, J. C. & Levin, M. J.Correlates of opportunistic infections in children infected with the human immunodeficiency virus managed before highly active antiretroviral therapy. Pediatr. Infect. Dis. J. 20: 1 (2001), 40–8CrossRefGoogle ScholarPubMed
United States Public Health Service/IDSA Prevention of Opportunistic Infections Working Group. 2001 United States Public Health Service/IDSA Guidelines for the Prevention of Opportunistic Infections in Persons Infected with Human Immunodeficiency Virus (2001), pp. 1–65
Chin, D. P., Hopewell, P. C., Yajko, D. M.. Mycobacterium avium complex in the respiratory or gastrointestinal tract and the risk of M. avium complex bacteremia in patients with human immunodeficiency virus infection. J. Infect. Dis. 169: 2 (1994), 289–95CrossRefGoogle ScholarPubMed
Hoyt, L., Oleske, J., Holland, B. & Connor, E.Nontuberculous mycobacteria in children with acquired immunodeficiency syndrome. Pediatr. Infect. Dis. J. 11 (1992), 354–60CrossRefGoogle ScholarPubMed
Lewis, L., Butler, K., Husson, R.. Defining the population of human immunodeficiency virus-infected children at risk for Mycobacterium avium-intracellulare. J. Pediatr. 121 (1992), 677–83CrossRefGoogle ScholarPubMed
Gleason-Morgan, D., Church, J. A. & Ross, L. A.A comparative study of transfusion-acquired human immunodeficiency virus-infected children with and without disseminated Mycobacterium avium complex. Pediatr. Infect. Dis. J. 13: 6 (1994), 484–8Google ScholarPubMed
Gordin, F., Cohn, D., Sullam, P., Schoenfelder, J., Wynne, P. & Horsburgh, C. J.Early manifestations of disseminated Mycobacterium avium complex disease: A prospective evaluation. J. Infect. Dis. 176 (1997), 126–32CrossRefGoogle ScholarPubMed
Race, E. M., Adelson-Mitty, J., Kriegel, G. R.. Focal mycobacterial lymphadenitis following initiation of protease-inhibitor therapy in patients with advanced Human Immunodeficiency Virus-1 disease. Lancet 351: 9098 (1998), 252–5CrossRefGoogle Scholar
Cinti, S. K., Kaul, D. R., Sax, P. E., Crane, L. R. & Kazanjian, P. H.Recurrence of Mycobacterium avium infection in patients receiving highly active antiretroviral therapy and antimycobacterial agents. Clin. Infect. Dis. 30: 3 (2000), 511–14CrossRefGoogle ScholarPubMed
Havlir, D. V., Schrier, R. D., Torriani, F. J., Chervenak, K., Hwang, J. Y. & Boom, W. H.Effect of potent antiretroviral therapy on immune responses to Mycobacterium avium in human immunodeficiency virus-infected subjects. J. Infect. Dis. 182: 6 (2000), 1658–63CrossRefGoogle ScholarPubMed
Hafner, R., Inderlied, C. B., Peterson, D. M.. Correlation of quantitative bone marrow and blood cultures in Acquired Immune Deficiency Syndrome patients with disseminated Mycobacterium avium complex infection. J. Infect. Dis. 180: 2 (1999), 438–47CrossRefGoogle Scholar
Bogner, J. R., Rusch-Gerdes, S., Mertenskotter, T.. Patterns of Mycobacterium avium culture and Polymerase Chain Reaction positivity in immunodeficient Human Immunodeficiency Virus-infected patients: progression from localized to systematic disease, German Acquired Immune Deficiency Syndrome Study Group (GASG/IDKF). Scand. J. Infect. Dis. 29: 6 (1997), 579–84CrossRefGoogle Scholar
Kalayjian, R. C., Toossi, Z., Tomashefski, J. F. Jr.. Pulmonary disease due to infection by Mycobacterium avium complex in patients with Acquired Immune Deficiency Syndrome. Clin. Infect. Dis. 20: 5 (1995), 1186–94CrossRefGoogle Scholar
Pursner, M., Haller, J. O. & Berdon, W. E.Imaging features of Mycobacterium avium-intracellulare complex (Mycobacterium Avium Complex also Mid-Arm Circumference) in children with Acquired Immune Deficiency Syndrome. Pediatr. Radiol. 30: 6 (2000), 426–9CrossRefGoogle Scholar
Chung, C. J., Sivit, C. J., Rakusan, T. A. & Ellaurie, M.Abdominal lymphadenopathy in children with Acquired Immune Deficiency Syndrome. Pediatr. Acquired Immune Deficiency Syndrome Human Immunodeficiency Virus Infect. 5: 5 (1994), 305–8Google Scholar
Saikia, U. N., Dey, P., Jindal, B. & Saikia, B.Fine needle aspiration cytology in lymphadenopathy of Human Immunodeficiency Virus-positive cases. Acta Cytol. 45: 4 (2001), 589–92CrossRefGoogle Scholar
Jeena, P. M., Coovadia, H. M., Hadley, L. G., Wiersma, R., Grant, H. & Chrystal, V.Lymph node biopsies in Human Immunodeficiency Virus-infected and non-infected children with persistent lung disease. Int. J. Tuberc. Lung Dis. 4: 2 (2000), 139–46Google Scholar
Kaplan, J. E., Hanson, D., Dworkin, M. S.. Epidemiology of human immunodeficiency virus-associated opportunistic infections in the United States in the era of highly active antiretroviral therapy. Clin. Infect. Dis. 30: Suppl. 1 (2000) S5–14CrossRefGoogle ScholarPubMed
Kaplan, J. E., Hanson, D. L., Jones, J. L. & Dworkin, M. S.Viral load as an independent risk factor for opportunistic infections in Human Immunodeficiency Virus-infected adults and adolescents. Acquired Immune Deficiency Syndrome 15: 14 (2001), 1831–6Google Scholar
Currier, J. S., Williams, P. L., Koletar, S. L.. Discontinuation of Mycobacterium avium complex prophylaxis in patients with antiretroviral therapy-induced increases in Cluster of Differentiation4+ cell count. A randomized, double-blind, placebo-controlled trial. Acquired Immune Deficiency Syndrome Clinical Trials Group 362 Study Team. Ann. Intern. Med. 133: 7 (2000), 493–503CrossRefGoogle Scholar
Dworkin, M. S., Hanson, D. L., Kaplan, J. E., Jones, J. L. & Ward, J. W.Risk for preventable opportunistic infections in persons with Acquired Immune Deficiency Syndrome after antiretroviral therapy increases Cluster of Differentiation4+ T lymphocyte counts above prophylaxis thresholds. J. Infect. Dis. 182: 2 (2000), 611–15CrossRefGoogle Scholar
El-Sadr, W. M., Burman, W. J., Grant, L. B.. Discontinuation of prophylaxis for Mycobacterium avium complex disease in Human Immunodeficiency Virus-infected patients who have a response to antiretroviral therapy. Terry Beirn Community Programs for Clinical Research on Acquired Immune Deficiency Syndrome. New Engl. J. Med. 342: 15 (2000), 1085–92CrossRefGoogle Scholar
Aberg, J. A., Yajko, D. M. & Jacobson, M. A.Eradication of Acquired Immune Deficiency Syndrome-related disseminated Mycobacterium avium complex infection after 12 months of antimycobacterial therapy combined with highly active antiretroviral therapy. J. Infect. Dis. 178: 5 (1998), 1446–9CrossRefGoogle Scholar
Soriano, V., Dona, C., Rodriguez-Rosado, R., Barreiro, P. & Gonzalez-Lahoz, J.Discontinuation of secondary prophylaxis for opportunistic infections in Human Immunodeficiency Virus-infected patients receiving highly active antiretroviral therapy. Acquired Immune Deficiency Syndrome 14: 4 (2000), 383–6Google Scholar
Zeller, V., Truffot, C., Agher, R.. Discontinuation of secondary prophylaxis against disseminated Mycobacterium avium complex infection and toxoplasmic encephalitis. Clin. Infect. Dis. 34: 5 (2002), 662–7CrossRefGoogle ScholarPubMed
Horsburgh, C. Jr., Havlik, J., Ellis, D.. Survival of patients with acquired immune deficiency syndrome and disseminated Mycobacterium avium complex infection with and without antimycobacterial chemotherapy. Am. Rev. Respir. Dis. 144 (1991), 557–9CrossRefGoogle ScholarPubMed
Husson, R., Ross, L. A., Sandelli, S.. Orally administered clarithromycin for the treatment of systemic Mycobacterium avium complex infection in children with acquired immunodeficiency syndrome. J. Pediatr. 124 (1994), 807– 14CrossRefGoogle ScholarPubMed
Shafran, S. D., Singer, J., Zarowny, D. P.. A comparison of two regimens for the treatment of Mycobacterium avium complex bacteremia in Acquired Immune Deficiency Syndrome: rifabutin, ethambutol, and clarithromycin versus rifampin, ethambutol, clofazamine and ciprofloxacin. New Engl. J. Med. 335 (1996), 377–83CrossRefGoogle Scholar
Horsburgh, C. R. Jr, Gettings, J., Alexander, L. N. & Lennox, J. L.Disseminated Mycobacterium avium complex disease among patients infected with human immunodeficiency virus, 1985–2000. Clin. Infect. Dis. 33: 11 (2001), 1938–43CrossRefGoogle ScholarPubMed
Havlir, D., Dube, M., Sattler, F.. Prophylaxis against disseminated Mycobacterium avium complex with weekly azithromycin, daily rifabutin, or both. New Engl. J. Med. 335 (1996), 392–8CrossRefGoogle ScholarPubMed
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. New Engl. J. Med. 335 (1996), 384–91CrossRefGoogle ScholarPubMed
Benson, C. A., Williams, P. L., Cohn, D. L.. Clarithromycin or rifabutin alone or in combination for primary prophylaxis of Mycobacterium avium complex disease in patients with Acquired Immune Deficiency Syndrome: A randomized, double-blind, placebo-controlled trial. The Acquired Immune Deficiency Syndrome Clinical Trials Group 196/Terry Beirn Community Programs for Clinical Research on Acquired Immune Deficiency Syndrome 009 Protocol Team. J. Infect. Dis. 181: 4 (2000), 1289–97CrossRefGoogle ScholarPubMed
Craft, J. C., Notario, G. F., Grosset, J. H. & Heifets, L. B.Clarithromycin resistance and susceptibility patterns of Mycobacterium avium strains isolated during prophylaxis for disseminated infection in patients with Acquired Immune Deficiency Syndrome. Clin. Infect. Dis. 27: 4 (1998), 807–12CrossRefGoogle Scholar
Dube, M., Sattler, F., Torriani, F.. A randomized evaluation of ethambutol for prevention of relapse and drug resistance during treatment of Mycobacterium avium complex bacteremia with clarithromycin-based combination therapy. J. Infect. Dis. 176 (1997), 1225–32CrossRefGoogle ScholarPubMed
Ward, T. T., Rimland, D., Kauffman, C., Huycke, M., Evans, T. G. & Heifets, L.Randomized, open-label trial of azithromycin plus ethambutol vs. clarithromycin plus ethambutol as therapy for Mycobacterium avium complex bacteremia in patients with human immunodeficiency virus infection. Veterans Affairs Human Immunodeficiency Virus Research Consortium. Clin. Infect. Dis. 27: 5 (1998), 1278–85CrossRefGoogle Scholar
Dunne, M., Fessel, J., Kumar, P.. A randomized, double-blind trial comparing azithromycin and clarithromycin in the treatment of disseminated Mycobacterium avium infection in patients with human immunodeficiency virus. Clin. Infect. Dis. 31: 5 (2000), 1245–52CrossRefGoogle ScholarPubMed
Gordin, F. M., Sullam, P. M., Shafran, S. D.. A randomized, placebo-controlled study of rifabutin added to a regimen of clarithromycin and ethambutol for treatment of disseminated infection with Mycobacterium avium complex. Clin. Infect. Dis. 28: 5 (1999), 1080–5CrossRefGoogle ScholarPubMed
Chaisson, R. E., Keiser, P., Pierce, M.. Clarithromycin and ethambutol with or without clofazimine for the treatment of bacteremic Mycobacterium avium complex disease in patients with Human Immunodeficiency Virus infection. Acquired Immune Deficiency Syndrome 11: 3 (1997), 311–7Google ScholarPubMed
Hoy, J., Mijch, A., Sandland, M., Grayson, L., Lucas, R. & Dwyer, B.Quadruple-drug therapy for Mycobacterium avium-intracellulare bacteremia in Acquired Immune Deficiency Syndrome patients. J. Infect. Dis. 161 (1990), 801–5CrossRefGoogle Scholar
Kemper, C., Meng, T.-C., Nussbaum, J.. Treatment of Mycobacterium avium complex bacteremia in Acquired Immune Deficiency Syndrome with a four-drug regimen. Ann. Int. Med. 116 (1992), 466–72CrossRefGoogle Scholar
Dube, M. P., Torriani, F. J.See, D.. Successful short-term suppression of clarithromycin-resistant Mycobacterium avium complex bacteremia in Acquired Immune Deficiency Syndrome. California Collaborative Treatment Group. Clin. Infect. Dis. 28: 1 (1999), 136–8CrossRefGoogle Scholar
Piscitelli, S., Flexner, C., Minor, J., Polis, M. & Masur, H.Drug interactions in patients infected with human immunodeficiency virus. Clin. Infect. Dis. 23 (1996), 685–91CrossRefGoogle ScholarPubMed
Tseng, A. & Foisy, M.Management of drug interactions in patients with Human Immunodeficiency Virus. Ann. Pharmacother. 31 (1997), 1040–58CrossRefGoogle Scholar
DeSimone, J. A., Pomerantz, R. J. & Babinchak, T. J.Inflammatory reactions in Human Immunodeficiency Virus-1-infected persons after initiation of highly active antiretroviral therapy. Ann. Intern. Med. 133: 6 (2000), 447–54CrossRefGoogle Scholar
Witzig, R. S., Fazal, B. A., Mera, R. M.. Clinical manifestations and implications of coinfection with Mycobacterium kansasii and human immunodeficiency virus type 1. Clin. Infect. Dis. 21: 1 (1995), 77–85CrossRefGoogle ScholarPubMed
Corbett, E. L., Blumberg, L., Churchyard, G. J.. Nontuberculous mycobacteria: defining disease in a prospective cohort of South African miners. Am. J. Respir. Crit. Care Med. 160: 1 (1999), 15–21CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×