Acyclovir Reduces the Duration of Fever in Patients with Infectious Mononucleosis-like Illness

被引:6
作者
Usami, Osamu [1 ]
Saitoh, Hiroki [1 ]
Ashino, Yugo [2 ]
Hattori, Toshio [3 ]
机构
[1] Tohoku Univ Hosp, Dept Comprehens Infect, Sendai, Miyagi, Japan
[2] Tohoku Univ, Dept Emerging Infect Dis, Sch Med, Sendai, Miyagi 9808574, Japan
[3] Tohoku Univ, Lab Disaster Related Infect Dis, Int Res Inst Disaster Sci IRIDeS, Sendai, Miyagi 9808574, Japan
关键词
acyclovir; Epstein-Barr virus; fever; infectious mononucleosis like illness; lymphadenopathy; HERPES-SIMPLEX-VIRUS; EPSTEIN-BARR-VIRUS; ANTIVIRAL AGENTS; VALACYCLOVIR; MANAGEMENT; EXPRESSION; DIAGNOSIS; HHV-7; EBV;
D O I
10.1620/tjem.229.137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acyclovir is known for its antiviral activity against some pathogenic viruses such as the Epstein-Barr virus (EBV) that causes infectious mononucleosis (IM) and IM-like illness. Therefore, We empirically administered acyclovir to patients with suspected EBV-IM and IM like-illness, upon their admission to our hospital. We admitted 25 patients, who were hospitalized for fever and lymphadenopathy, to the Tohoku University Hospital Infectious Disease Ward. As part of treatment, 8 of these patients were given acyclovir (750 mg/day) with their consent and were assigned to the acyclovir group; the remaining 17 patients were assigned to the control group. The mean age of acyclovir patients (all men) was 42 +/- 5.2 years, and that of control patients (13 men and 4 women) was 31 +/- 3.0 years. The cause of illness was confirmed as EBV-IM in 6 patients (1, acyclovir; 5, control), and remained unknown for the other 19 IM-like illness patients (7, acyclovir; 12, control). A shorter duration of hospitalization and fever was observed in the acyclovir compared to that in the control patients (hospitalization duration: 16 +/- 3.7 vs. 27 +/- 7.7 days, P = 0.36; fever duration: 4.5 +/- 1.8 vs. 18 +/- 6.5 days, P = 0.04). Additionally, serum amyloid A (SAA) levels were lower in acyclovir than that in control patients (98 +/- 37 vs. 505 +/- 204 mu g/mL, P = 0.02). Therefore, we propose that acyclovir is a potential therapeutic agent for both EBV-IM and IM like-illnesses. Future studies should further examine its mechanism of action.
引用
收藏
页码:137 / 142
页数:6
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