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Influenza virus infections in patients with malignancies -- characteristics and outcome of the season 2014/15. A survey conducted by the Infectious Diseases Working Party (AGIHO) of the German Society of Haematology and Medical Oncology (DGHO).

Identifieur interne : 000068 ( Main/Corpus ); précédent : 000067; suivant : 000069

Influenza virus infections in patients with malignancies -- characteristics and outcome of the season 2014/15. A survey conducted by the Infectious Diseases Working Party (AGIHO) of the German Society of Haematology and Medical Oncology (DGHO).

Auteurs : B. Hermann ; N. Lehners ; M. Brodhun ; K. Boden ; A. Hochhaus ; M. Kochanek ; K. Meckel ; K. Mayer ; T. Rachow ; C. Rieger ; E. Schalk ; T. Weber ; A. Schmeier-Jürchott ; P. Schlattmann ; D. Teschner ; M. Von Lilienfeld-Toal

Source :

RBID : pubmed:27838792

English descriptors

Abstract

Influenza virus infections (IVI) may pose a vital threat to immunocompromised patients such as those suffering from malignancies, but specific data on epidemiology and outcome in these patients are scarce. In this study, we collected data on patients with active cancer or with a history of cancer, presenting with documented IVI in eight centres in Germany. Two hundred and three patients were identified, suffering from haematological malignancies or solid tumours; 109 (54 %) patients had active malignant disease. Influenza A was detected in 155 (77 %) and Influenza B in 46 (23 %) of patients (genera not determined in two patients). Clinical symptoms were consistent with upper respiratory tract infection in 55/203 (27 %), influenza-like illness in 82/203 (40 %), and pneumonia in 67/203 (33 %). Anti-viral treatment with oseltamivir was received by 116/195 (59 %). Superinfections occurred in 37/203 (18 %), and admission on an intensive care unit was required in 26/203 (13 %). Seventeen patients (9 %) died. Independent risk factors for death were delayed diagnosis of IVI and bacterial or fungal superinfection, but not underlying malignancy or ongoing immunosuppression. In conclusion, patients with IVI show high rates of pneumonia and mortality. Early and rapid diagnosis is essential. The high rate of pneumonia and superinfections should be taken into account when managing IVI in these patients.

DOI: 10.1007/s10096-016-2833-3
PubMed: 27838792

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pubmed:27838792

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<div type="abstract" xml:lang="en">Influenza virus infections (IVI) may pose a vital threat to immunocompromised patients such as those suffering from malignancies, but specific data on epidemiology and outcome in these patients are scarce. In this study, we collected data on patients with active cancer or with a history of cancer, presenting with documented IVI in eight centres in Germany. Two hundred and three patients were identified, suffering from haematological malignancies or solid tumours; 109 (54 %) patients had active malignant disease. Influenza A was detected in 155 (77 %) and Influenza B in 46 (23 %) of patients (genera not determined in two patients). Clinical symptoms were consistent with upper respiratory tract infection in 55/203 (27 %), influenza-like illness in 82/203 (40 %), and pneumonia in 67/203 (33 %). Anti-viral treatment with oseltamivir was received by 116/195 (59 %). Superinfections occurred in 37/203 (18 %), and admission on an intensive care unit was required in 26/203 (13 %). Seventeen patients (9 %) died. Independent risk factors for death were delayed diagnosis of IVI and bacterial or fungal superinfection, but not underlying malignancy or ongoing immunosuppression. In conclusion, patients with IVI show high rates of pneumonia and mortality. Early and rapid diagnosis is essential. The high rate of pneumonia and superinfections should be taken into account when managing IVI in these patients.</div>
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<CoiStatement>Compliance with ethical standardsFundingPartially funded by Infectognostics Forschungscampus, grant number BMBF 13GW0096D.Conflicts of interestMarie von Lilienfeld-Toal: honoraria, travel grant, and research grant from MSD and Celgene. Honoraria and travel grant from Gilead, Janssen Cilag, and Astellas. Consultant of advisory board for MSD.Daniel Teschner: honoraria and travel grant from Gilead and MSD. Travel grant from Astellas and Jazz. Consultant of advisory board for MSD and Pfizer.Andreas Hochhaus: research support from Novartis, BMS, Pfizer, AriadBeate Hermann: noneNicola Lehners: noneMaria Brodhun, Katharina Boden, Matthias Kochanek, Katharina Meckel, Karin Mayer, Tobias Rachow, Christina Rieger, Enrico Schalk, Thomas Weber, Anna Schmeier-Jürchott, Peter Schlattmann: noneEthical approvalThe study was approved by the ethics committee of Jena University Hospital (3785-05/13).Informed consentNo informed consent was required since this was a retrospective study.</CoiStatement>
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