2001
DOI: 10.1016/s0749-0704(05)70198-6
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Infectious Morbidity in Critically Ill Patients With Cancer

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Cited by 142 publications
(102 citation statements)
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References 274 publications
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“…Candidal infections are a major problem in the world, especially among the cancer patients [10][11].…”
Section: Discussionmentioning
confidence: 99%
“…Candidal infections are a major problem in the world, especially among the cancer patients [10][11].…”
Section: Discussionmentioning
confidence: 99%
“…3 Recipients of allogeneic marrow and solid organ transplantation are at additional risk of disease due to opportunistic, facultative intracellular pathogens such as L. monocytogenes, Nocardia asteroids, Legionella pneumophila and Salmonella spp. 2,[16][17][18][19] Most of these opportunistic bacterial infections are observed during the early marrow engraftment period (30 to 180 days). 16,19 In patients undergoing antimicrobial prophylaxis and myelosuppressive treatment for acute (patient 4) or acute exacerbation of chronic GVHD (patient 1) these opportunistic infections may be delayed (Ͼ360 days post BMT).…”
Section: Discussionmentioning
confidence: 99%
“…1,2 In allogeneic transplant recipients with severe CD4 + T cell defects, systemic Listeria monocytogenes infection is seldom seen. [2][3][4] Reactivation of human cytomegalovirus (HCMV), on the other hand, is not uncommon in patients undergoing allogeneic blood, marrow or organ transplants and is associated with a marked increase in short-term morbidity and mortality. 5,6 Reactivation of HCMV is associated with impairment of T lymphocyte recovery due to virus-related marrow aplasia, and graft failure.…”
mentioning
confidence: 99%
“…5,6 Of the various fungal organisms, the non-Aspergillus filamentous molds, such as Alternaria, Cladosporium, Curvularia, Fusarium, Paecilomyces lilacinus, Pseudallescheria boydii, Scedosporium apiospermum, and Scedosporium prolificans, often are not susceptible to commonly prescribed antifungals, including amphotericin B. [5][6][7][8][9][10] Therefore, in patients with fungal infections that most likely will not respond well to amphotericin B, preemptive or empiric therapy with the new, broad-spectrum, triazole-based antifungals; the pneumocandin-echinocandin analogues; or both would be appropriate if clinical identifiers were available to distinguish "clinically significant" fungemia from pseudofungemia. Unfortunately, the current diagnostic guidelines are difficult to implement, because the required histologic analysis of the infected tissue seldom is available in these high-risk transplantation recipients because of the underlying severe thrombocytopenia.…”
mentioning
confidence: 99%