CURRENT TREATMENT OPTIONS FOR INVASIVE ASPERGILLOSIS
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | BATISTA, M. V. | |
dc.contributor.author | COSTA, S. F. | |
dc.contributor.author | SHIKANAI-YASUDA, M. A. | |
dc.contributor.author | MOSS, R. B. | |
dc.date.accessioned | 2013-09-23T16:39:42Z | |
dc.date.available | 2013-09-23T16:39:42Z | |
dc.date.issued | 2013 | |
dc.description.abstract | Invasive pulmonary aspergillosis is a major cause of morbidity and mortality in immunocom promised patients, particularly those with hematological malignancies in the setting of profound neutropenia and/or hematopoietic stem cell transplant recipients. The optimal therapy for invasive aspergillosis relies on the restoration of leukocyte counts and effective antifungal treatment initiated at the earliest stage of infection. Several alternative antifungal compounds are currently available. A rational approach should take into account not only the degree of certainty of infection (as codified by the EORTC/MSG classification), but also previous exposure to other antifungals, the pharmacokinetic and pharmacodynamic characteristics of the antifungals employed and the clinical characteristics of the patient. | |
dc.description.index | MEDLINE | |
dc.description.sponsorship | Pfizer | |
dc.description.sponsorship | Merck Sharp Dohme | |
dc.description.sponsorship | Novartis | |
dc.description.sponsorship | United Medical | |
dc.identifier.citation | DRUGS OF TODAY, v.49, n.3, p.213-226, 2013 | |
dc.identifier.doi | 10.1358/dot.2013.49.3.1921234 | |
dc.identifier.issn | 1699-3993 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/1967 | |
dc.language.iso | eng | |
dc.publisher | PROUS SCIENCE, SAU-THOMSON REUTERS | |
dc.relation.ispartof | Drugs of Today | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright PROUS SCIENCE, SAU-THOMSON REUTERS | |
dc.subject | Invasive aspergillosis | |
dc.subject | Antifungal therapy | |
dc.subject | Antifungal drugs | |
dc.subject | Voriconazole | |
dc.subject | Caspofungin | |
dc.subject | Amphotericin B | |
dc.subject | Immunocompromised hosts | |
dc.subject | Polyene antibiotics | |
dc.subject | Azoles | |
dc.subject | Echinocandins | |
dc.subject | Invasive fungal infection | |
dc.subject.other | liposomal amphotericin-b | |
dc.subject.other | empirical antifungal therapy | |
dc.subject.other | hematopoietic-cell transplantation | |
dc.subject.other | fungal-infections | |
dc.subject.other | immunocompromised patients | |
dc.subject.other | colloidal dispersion | |
dc.subject.other | neutropenic patients | |
dc.subject.other | persistent fever | |
dc.subject.other | double-blind | |
dc.subject.other | hematologic malignancies | |
dc.subject.wos | Pharmacology & Pharmacy | |
dc.title | CURRENT TREATMENT OPTIONS FOR INVASIVE ASPERGILLOSIS | |
dc.type | article | |
dc.type.category | review | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Estados Unidos | |
hcfmusp.affiliation.countryiso | us | |
hcfmusp.author.external | MOSS, R. B.:Stanford Univ, Med Ctr, Ctr Excellence Pulm Biol, Dept Pediat, Palo Alto, CA 94304 USA | |
hcfmusp.citation.scopus | 6 | |
hcfmusp.contributor.author-fmusphc | MARJORIE VIEIRA BATISTA | |
hcfmusp.contributor.author-fmusphc | SILVIA FIGUEIREDO COSTA | |
hcfmusp.contributor.author-fmusphc | MARIA APARECIDA SHIKANAI YASUDA | |
hcfmusp.description.beginpage | 213 | |
hcfmusp.description.endpage | 226 | |
hcfmusp.description.issue | 3 | |
hcfmusp.description.volume | 49 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 23527325 | |
hcfmusp.origem.scopus | 2-s2.0-84875756916 | |
hcfmusp.origem.wos | WOS:000316918900006 | |
hcfmusp.publisher.city | BARCELONA | |
hcfmusp.publisher.country | SPAIN | |
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hcfmusp.remissive.sponsorship | Merck | |
hcfmusp.remissive.sponsorship | Novartis | |
hcfmusp.remissive.sponsorship | Pfizer | |
hcfmusp.scopus.lastupdate | 2024-05-17 | |
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