Abstract
Neutrophils play an important role in immunological function. Neutropenic patients are vulnerable to infection, and except fever is present, inflammatory reactions are scarce in many cases. Additionally, because infections can worsen rapidly, early evaluation and treatments are especially important in febrile neutropenic patients. In cases in which febrile neutropenia is anticipated due to anticancer chemotherapy, antibiotic prophylaxis can be used, based on the risk of infection. Antifungal prophylaxis may also be considered if long-term neutropenia or mucosal damage is expected. When fever is observed in patients suspected to have neutropenia, an adequate physical examination and blood and sputum cultures should be performed. Initial antibiotics should be chosen by considering the risk of complications following the infection; if the risk is low, oral antibiotics can be used. For initial intravenous antibiotics, monotherapy with a broadspectrum antibiotic or combination therapy with two antibiotics is recommended. At 3 5 days after beginning the initial antibiotic therapy, the condition of the patient is assessed again to determine whether the fever has subsided or symptoms have worsened. If the patient's condition has improved, intravenous antibiotics can be replaced with oral antibiotics; if the condition has deteriorated, a change of antibiotics or addition of antifungal agents should be considered. If the causative microorganism is identified, initial antimicrobial or antifungal agents should be changed accordingly. When the cause is not detected, the initial agents should continue to be used until the neutrophil count recovers.
Original language | English |
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Pages (from-to) | 285-321 |
Number of pages | 37 |
Journal | Infection and Chemotherapy |
Volume | 43 |
Issue number | 4 |
DOIs | |
State | Published - Aug 2011 |
Bibliographical note
Funding Information:We warmly thank the participants of the SAFHS and SAFDGS for their contribution, enthusiasm, and cooperation. This study is part of the Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi- Ethnic Samples (T2D-GENES) Consortium, funded by the European Commission (HEALTH-F4-2007-201413), Wellcome Trust (090367, 090532, 098381), Medical Research Council (G0601261), and NIH/NIDDK (RC2-DK08839, DK105535, DK085524, DK085545, DK085584, DK085501, DK098032, DK078616, DK085526). The whole-genome sequencing was done commercially by Complete Genomics, Inc. Additional genetic and phenotypic data were provided by the San Antonio Family Heart Study and San Antonio Family Diabetes/Gallbladder Study, which are supported by NIH Grants R01 HL0113323, P01 HL045222, R01 DK047482, and R01 DK053889. SAFHS gene expression data were generated through a donation from the Azar and Shepperd families. J.G.W. was supported by U54GM115428 from the National Institute of General Medical Sciences. S.C., S.L., J.K., J. Lee, and T.P. were supported by the Bio-Synergy Research Project (2013M3A9C4078158) of the Ministry of Science, ICT and Future Planning through the National Research Foundation of Korea, and Korea Health Technology R&D Project through the Korea Health Industry Development Institute, funded by the Ministry of Health and Welfare (HI15C2165, HI16C2037). A.K.M. was supported by American Diabetes Association Mentor-Based Postdoctoral Fellowship #7-12-MN-02. M.I.M. is a Wellcome Trust Senior Investigator. The research was supported by the National Institute for Health Research (NIHR), Oxford Biomedical Research Centre. The views expressed are those of the authors and not necessarily those of the National Health Service, NIHR, or Department of Health, United Kingdom.
Funding Information:
and R01 DK053889. SAFHS gene expression data were generated through a donation from the Azar and Shepperd families. J.G.W. was supported by U54GM115428 from the National Institute of General Medical Sciences. S.C., S.L., J.K., J. Lee, and T.P. were supported by the Bio-Synergy Research Project (2013M3A9C4078158) of the Ministry of Science, ICT and Future Planning through the National Research Foundation of Korea, and Korea Health Technology R&D Project through the Korea Health Industry Development Institute, funded by the Ministry of Health and Welfare (HI15C2165, HI16C2037). A.K.M. was supported by American Diabetes Association Mentor-Based Postdoctoral Fellowship #7-12-MN-02. M.I.M. is a Wellcome Trust Senior Investigator. The research was supported by the National Institute for Health Research (NIHR), Oxford Biomedical Research Centre. The views expressed are those of the authors and not necessarily those of the National Health Service, NIHR, or Department of Health, United Kingdom.
Funding Information:
ACKNOWLEDGMENTS. We warmly thank the participants of the SAFHS and SAFDGS for their contribution, enthusiasm, and cooperation. This study is part of the Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES) Consortium, funded by the European Commission (HEALTH-F4-2007-201413), Wellcome Trust (090367, 090532, 098381), Medical Research Council (G0601261), and NIH/NIDDK (RC2-DK08839, DK105535, DK085524, DK085545, DK085584, DK085501, DK098032, DK078616, DK085526). The whole-genome sequencing was done commercially by Complete Genomics, Inc. Additional genetic and phenotypic data were provided by the San Antonio Family Heart Study and San Antonio Family Diabetes/Gallbladder Study, which are supported by NIH Grants R01 HL0113323, P01 HL045222, R01 DK047482,
Keywords
- Fever
- Korea
- Neutropenia
- Practice guideline