Şahinkaya Şükran, Ture Zeynep, Unal Ali, Ünüvar Gamze Kalın, Kılıç Ayşegül Ulu
Department of Infection Control Committee, Erciyes University, Kayseri, Turkey.
Department of Infectious Diseases, Faculty of Medicine, Erciyes University, Kayseri, Turkey.
Infect Chemother. 2024 Jun;56(2):239-246. doi: 10.3947/ic.2023.0102. Epub 2024 Jan 18.
This study aimed to determine the risk factors of infectious diarrhea in patients undergoing chemotherapy or hematopoietic stem cell transplantation for hematological malignancies.
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.
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 (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%) ( <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% 42.1%, =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 (=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.
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.
本研究旨在确定接受化疗或造血干细胞移植治疗血液系统恶性肿瘤患者发生感染性腹泻的危险因素。
这是一项前瞻性观察性研究。通过实验室检查确定感染病原体的患者被视为患有感染性腹泻。腹泻患者被分为感染性或不明原因性,并在人口统计学数据、治疗方法、危险因素、实验室检查结果和预后方面进行比较。
共838例患者住院,其中105例符合纳入标准(12.5%)。患者分为两组:67例(63.8%)为不明原因性腹泻,38例(36.2%)为感染性腹泻。两组在年龄、性别、血液系统恶性肿瘤类型和合并症方面无差异。最常分离出的微生物是(12.4%)。感染性腹泻组皮质类固醇的使用率(39.5%)高于不明原因性腹泻组(7.5%)(<0.001)。不明原因性腹泻患者粒细胞集落刺激因子(GCSF)的使用率高于感染性腹泻患者(67.2%对42.1%,=0.022)。感染性腹泻组腹泻的中位持续时间为9(4 - 10)天,不明原因性腹泻组为5(3 - 8)天(=0.012)。根据多因素逻辑回归模型,皮质类固醇治疗使感染性腹泻的风险增加4.75倍(95%置信区间[CI],1.32 - 17.02)。此外,腹泻持续时间可能使感染性腹泻的风险增加1.15(95%CI,1.02 - 1.31)倍,而GCSF治疗对感染性腹泻有2.84(1/0.35)(95%CI,0.12 - 0.96)倍的风险降低作用。
血液系统恶性肿瘤患者感染性腹泻的持续时间比不明原因性腹泻长。虽然使用皮质类固醇是发生感染性腹泻的危险因素,但使用GCSF有保护作用。