Epistaxis and its management: an observational pilot study carried out in 23 hospital centres in France
Volume: 44 - Issue: 2
First page: 151 - Last page: 156
J.M. Klossek - X. Dufour - C. Beauvillain de Montreuil - J.P. Fontanel - R. Peyn?®gre - E. Reyt - M. Rugina - M. Samardzic - E. Serrano - D. Stoll - C. Chevillard
Objective: The purpose of this study is to describe the treatment of epistaxis in hospital emergency departments and to identify the principal risk factors for more severe episodes of bleeding.
Study protocol: Prospective cross-sectional epidemiological study
Material and Methods: This study was carried out in 23 hospital centres in France, most of them teaching hospitals. Every patient presenting non-traumatic epistaxis or else associated with hereditary hemangioma during two consecutive and separate 24-hour periods were included.
Results: Fifty patients were included in the study. Nasal bleeding was stopped within 30 minutes for 47 patients. Fourteen patients were hospitalized. The risk factors for severe epistaxis included either copious bleeding or else bleeding for more than 6 hours or patients aged 65 and over. A history of repeated nasal packing and/or taking medication with a known hemorrhagic risk was associated with the amount and duration of bleeding (p < 0.05).
Conclusion: Risk factors for severe epistaxis should be identified as to improve patient care and avoid treatment failure or useless hospitalization.
Rhinology 44-2: 151-156, 2006
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