Risk of severe herpes simplex virus infection in systemic lupus erythematosus: analysis of epidemiology and risk factors analysis in Taiwan

2019 ◽  
Vol 78 (7) ◽  
pp. 941-946 ◽  
Author(s):  
Tzu-Hao Li ◽  
Chien-Chih Lai ◽  
Wen-Hsiu Wang ◽  
Wei-Sheng Chen ◽  
Yen-Po Tsao ◽  
...  

ObjectivePatients with systemic lupus erythematosus (SLE) are susceptible to herpes simplex virus (HSV) infection, which occasionally leads to severe complications including meningoencephalitis and keratitis. However, few attempts to analyse the associated incidence and risk factors have been made.MethodsWe enrolled patients with SLE recorded between 1997 and 2012 and compared the incidence rate (IR) of severe HSV infection, including meningoencephalitis, septicaemia, ocular and visceral involvement, and other specific complications demanding hospitalisation, with that of a non-SLE cohort. A Cox multivariate proportional hazards model was applied to analyse the risk factors of severe HSV infection in patients with SLE.ResultsA total of 122 520 subjects (24 504 patients with SLE and 98 016 age-matched and sex-matched non-SLE controls) were included, and a higher IR of severe HSV infection was revealed in the SLE group (IR ratio=3.93, p<0.001). In patients with SLE, previous oral and genital infection (HR=2.29, p=0.049), intravenous steroid pulse therapy (HR=5.32, p<0.001) and daily oral dose of over 7.5 mg of prednisolone (HR=1.59, p=0.024) were independent risk factors for severe HSV infection, whereas age of ≤18 (HR=0.45, p=0.029) was a protective factor.ConclusionsPatients with SLE are at higher risk of severe HSV infection, and related risk factors include being older than 18 years, having a history of HSV mucocutaneous infection, recent receipt of steroid pulse therapy and a daily oral dose of steroid over 7.5 mg prednisolone.

2014 ◽  
Vol 20 (1) ◽  
pp. 42-44 ◽  
Author(s):  
Francisca Sabugo ◽  
Ricardo Espinoza-Araya ◽  
Manuel F. Meneses ◽  
Miguel Cuchacovich

2010 ◽  
Vol 20 (1) ◽  
pp. 98-101 ◽  
Author(s):  
Hideki Wakui ◽  
Masaru Togashi ◽  
Ayumi Omokawa ◽  
Shin Okuyama ◽  
Rie Masai ◽  
...  

2002 ◽  
Vol 161 (9) ◽  
pp. 503-504 ◽  
Author(s):  
Yuichi Tabata ◽  
Ichiro Kobayashi ◽  
Nobuaki Kawamura ◽  
Motohiko Okano ◽  
Kunihiko Kobayashi

2011 ◽  
Vol 39 (1) ◽  
pp. 86-93 ◽  
Author(s):  
JI-MIN KIM ◽  
SEUNG-KI KWOK ◽  
JI HYEON JU ◽  
HO-YOUN KIM ◽  
SUNG-HWAN PARK

Objective.To determine the characteristics of hemophagocytic syndrome (HPS) in adult Korean patients with systemic lupus erythematosus (SLE).Methods.We reviewed the medical records of 1033 adult patients with SLE for a recent 14-year period and identified 15 patients who had developed HPS. Forty-two age- and sex-matched patients with SLE admitted for other manifestations were included as disease controls. Features of HPS in these patients were analyzed.Results.Reactive HPS occurred from some distinct causes during the course of SLE. HPS was associated with SLE in 11 patients (4 at onset of SLE and 7 at SLE flare), infection in 3 patients (2 bacterial infection; 1 viral infection), and drug use (azathioprine) in 1 patient. Common clinical features included fever (93.3%), hepatomegaly (60.0%), and splenomegaly (60.0%). Steroid pulse therapy (46.7%), immunosuppressants (46.7%), and intravenous immunoglobulin (46.7%) were frequently used for treatment of HPS. One patient (6.7%) died. Compared with SLE patients without HPS, those with HPS showed a higher SLEDAI score (p = 0.003) and lower levels of plasma leukocytes (p < 0.001), hemoglobin (p = 0.013), and platelets (p < 0.001) as well as a higher serum C-reactive protein level (p = 0.039) and a lower serum albumin level (p = 0.004).Conclusion.HPS was observed in 1.5% of adult Korean patients with SLE. The occurrence of HPS was most frequently associated with the SLE disease activity. Profound pancytopenia, a high SLEDAI score, and notable changes in the level of acute-phase reactants can be the characteristics of SLE patients with HPS.


2019 ◽  
Vol 48 (1) ◽  
pp. 50-53
Author(s):  
Md Abdur Razzaque ◽  
Mohammad Ziaul Haider ◽  
Md Nahduzzamane Sazzad ◽  
Shamim Ahmed ◽  
Md Abu Shahin ◽  
...  

A 65-year old Bangladeshi woman with Systemic Lupus Erythematosus (SLE) developed Parkinson-like movement disorder. Steroid pulse therapy followed by prednisolone was most effective in this case. Psychosis, seizure and meningitis are common central nervous system (CNS) manifestations in SLE patients, and Parkinson-like rigidity or tremors are rare. Bangladesh Med J. 2019 Jan; 48 (1): 50-53


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