Impacts of Corticosteroid Therapy at Acute Stage of Hospital-Onset Clostridioides difficile Infections

被引:1
|
作者
Lee, Ching -Chi [1 ,2 ]
Lee, Jen-Chieh [2 ]
Chiu, Chun-Wei [3 ]
Tsai, Pei -Jane [4 ,5 ,6 ]
Ko, Wen -Chien [4 ,7 ]
Hung, Yuan -Pin [2 ,3 ,7 ,8 ]
机构
[1] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Clin Med Res Ctr, Tainan 704, Taiwan
[2] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Internal Med, Tainan 704, Taiwan
[3] Tainan Hosp, Dept Internal Med, Minist Hlth & Welf, Tainan 700, Taiwan
[4] Natl Cheng Kung Univ, Coll Med, Dept Med Lab Sci & Biotechnol, Tainan 704, Taiwan
[5] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Pathol, Tainan, Taiwan
[6] Natl Cheng Kung Univ, Ctr Infect Dis & Signaling Res, Tainan, Taiwan
[7] Natl Cheng Kung Univ, Coll Med, Dept Med, Tainan 704, Taiwan
[8] Natl Cheng Kung Univ, Coll Med, Dept Microbiol & Immunol, Tainan, Taiwan
来源
关键词
steroid; prednisolone; Clostridioides difficile; diarrhea; recurrence; intensive care unit; immunosuppression; RISK; EPIDEMIOLOGY; OUTCOMES; DISEASE;
D O I
10.2147/IDR.S377967
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: The influence of corticosteroid therapy before or after the onset of Clostridioides difficile infections (CDIs) on the clinical outcomes of adults with hospital-onset CDIs was investigated. Materials and Methods: A clinical study was conducted on the medical wards of a teaching hospital between January 2013 and April 2020. Adults (aged > 20 years) with hospital-onset CDIs (ie, symptom onset at least 48 hours after hospitalization) were included. "Corticosteroid therapy during acute CDIs" was defined as the receipt of a corticosteroid at the prednisolone equivalent (PE) dose of >10 mg for at least 48 hours within one week after the CDI diagnosis. "Prior corticosteroid exposure" was defined as the receipt of a corticosteroid at the PE dose of >5 mg PE for at least 48 hours within one month before the CDI diagnosis.Results: Of the 243 adults with hospital-onset CDIs, patients (44, 18.1%) who received corticosteroid therapy during acute CDIs were more likely to have prior corticosteroid exposure (86.4% vs 11.9%, P <0.001) and CDI episodes in intensive care units (31.8% vs 10.8%, P =0.001). Of note, a crucial association between corticosteroid therapy during acute CDIs and CDI recurrence was evidenced (13.6% vs 1.5%, P =0.002). Prior corticosteroid exposure was not associated with favorable CDI outcomes in terms of successful treatment (78.3% vs 74.9%, P =0.89), in-hospital crude mortality (17.4% vs 24.0%, P =0.61), or CDI recurrence (4.3% vs 5.3%, P = 1.00). However, for 177 patients without prior corticosteroid exposure, corticosteroid therapy during acute CDIs was linked to a higher proportion of CDI recurrence (33.3% vs 5.3%, P =0.046). Conclusion: Corticosteroid therapy during acute CDIs might impact the recurrence of CDIs, particularly in those with a lack of prior corticosteroid exposure.
引用
收藏
页码:5387 / 5396
页数:10
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