确定血液恶性肿瘤患者感染性腹泻的风险因素。

IF 2.8 Q2 INFECTIOUS DISEASES Infection and Chemotherapy Pub Date : 2024-06-01 Epub Date: 2024-01-18 DOI:10.3947/ic.2023.0102
Şükran Şahinkaya, Zeynep Ture, Ali Unal, Gamze Kalın Ünüvar, Ayşegül Ulu Kılıç
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引用次数: 0

摘要

背景:该研究旨在确定因血液恶性肿瘤接受化疗或造血干细胞移植的患者感染性腹泻的风险因素:本研究旨在确定因血液恶性肿瘤接受化疗或造血干细胞移植的患者感染性腹泻的风险因素:本研究为前瞻性观察研究。经实验室检查确定为感染性病原体的患者被定义为感染性腹泻。将腹泻患者分为感染性腹泻和不明原因腹泻,并就人口统计学数据、治疗方法、风险因素、实验室检查结果和预后进行比较:研究中,共有 838 名住院患者,其中 105 人(12.5%)符合定义标准。患者分为两组:67 例(63.8%)不明原因腹泻和 38 例(36.2%)感染性腹泻。这两组患者在年龄、性别、血液恶性肿瘤类型和是否存在合并症方面没有差异。分离微生物中比例最高的是艰难梭菌(12.4%)。感染性腹泻组使用皮质类固醇的比例(39.5%)高于不明原因腹泻组(7.5%)(P vs. 42.1%,P = 0.022)。感染性腹泻组的中位腹泻持续时间为 9(4 - 10)天,而不明原因腹泻组为 5(3 - 8)天(P = 0.012)。根据多变量逻辑回归模型,皮质类固醇治疗增加了感染性腹泻的风险,几率比[OR] = 4.75(置信区间[CI]:1.32 - 17.02)倍。结论:腹泻持续时间可能导致感染性腹泻的风险增加 1.15 倍(CI:1.02 - 1.31),而 GCSF 治疗的 OR = 2.84 倍(CI:0.12 - 0.96)可降低感染性腹泻的风险:结论:血液恶性肿瘤患者感染性腹泻持续时间较长。结论:血液恶性肿瘤患者感染性腹泻持续时间较长,使用皮质类固醇是感染性腹泻的风险因素,而使用 GCSF 则具有保护作用。
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Determination of Risk Factors for Infectious Diarrhea in Patients with Hematological Malignancy.

Background: This study aimed to determine the risk factors of infectious diarrhea in patients undergoing chemotherapy or hematopoietic stem cell transplantation for hematological malignancies.

Materials and methods: This was a prospective, observational study. Patients in whom the infectious agent was determined by laboratory examination were considered to have infectious diarrhea. Patients with diarrhea were categorized as infectious or unidentified and compared in terms of demographic data, treatments, risk factors, laboratory findings, and prognosis.

Results: A total of 838 patients were hospitalized, among which 105 patients who met the inclusion criteria were included (12.5%). The patients were divided into two groups: 67 (63.8%) with unidentified diarrhea and 38 (36.2%) with infectious diarrhea. There were no differences between these groups in terms of age, sex, types of hematological malignancies, and presence of comorbidities. The most commonly isolated microorganism was Clostridioides difficile (12.4%). The rate of corticosteroid use was higher in the group with infectious diarrhea (39.5%) than in the group with unidentified diarrhea (7.5%) (P <0.001). The rate of granulocyte colony-stimulating factor (GCSF) use was higher in patients with unidentified diarrhea than in patients with infectious diarrhea (67.2% vs. 42.1%, P=0.022). The median duration of diarrhea was 9 (4-10) days in the group with infectious diarrhea and 5 (3-8) days in the group with unidentified diarrhea (P=0.012). According to the multivariate logistic regression model, corticosteroid treatment increased the risk of infectious diarrhea by a 4.75-fold (95% confidence interval [CI], 1.32-17.02) times. Moreover, the duration of diarrhea may result in a 1.15 (95% CI, 1.02-1.31) fold increase in the risk of infectious diarrhea, while GCSF treatment had a 2.84 (1/0.35) (95% CI, 0.12-0.96) fold risk-reducing effect against infectious diarrhea.

Conclusion: Infectious diarrhea lasts longer than unidentified diarrhea in patients with hematological malignancies. Although corticosteroid use is a risk factor for developing infectious diarrhea, GCSF use has a protective effect.

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来源期刊
Infection and Chemotherapy
Infection and Chemotherapy INFECTIOUS DISEASES-
CiteScore
6.60
自引率
11.90%
发文量
71
审稿时长
22 weeks
期刊最新文献
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