Retrospective case-control study

  • 文章类型: Journal Article
    本研究旨在评估宽带吸收(WBA)在大前庭水管综合征(LVAS)儿童中的临床意义,这可能是儿童LVAS的诊断和预测标志物。
    这是一项单中心回顾性病例对照研究。进行了听力学测量和宽带声抗(WAI)。倾向评分匹配(PSM)被认为是治疗组失衡。采用受试者工作特征(ROC)曲线和ROC曲线下面积(AUC)评价WBA的敏感性和特异性。
    参与者包括2019年至2021年从临床听力学机构招募的42名LVAS儿童和163名6个月至11岁的正常儿童。
    在1259-2000Hz时,LVAS组的鼓室峰值压力(WBATPP)和环境压力(WBAA)下的WBA显着低于对照组,但在4000-6349Hz时升高(p<0.05,功率>0.8)。WBAA(1587Hz)AUC值为0.805,确定分数≤0.565指示LVAS风险。
    WBA有望将LVAS与正常状态区分开,并值得进一步探索作为检查内耳压力对中耳声能传输影响的工具。
    UNASSIGNED: This study aimed to assess the clinical significance of Wideband Absorbance (WBA) in children with Large Vestibular Aqueduct Syndrome (LVAS), which could potentially serve as diagnostic and predictive markers for LVAS in children.
    UNASSIGNED: This was a single-center retrospective case-control study. Audiological measurements and Wideband Acoustic Immittance (WAI) were performed. Propensity score matching (PSM) was considered to treat group imbalance. The Receiver Operating Characteristic (ROC) curves and area under the ROC curve (AUC) were used to evaluate the sensitivity and specificity of WBA.
    UNASSIGNED: Participants included 42 children with LVAS and 163 normal children aged 6 months -11 years recruited from clinical audiology settings between 2019 and 2021.
    UNASSIGNED: The WBA at Tympanometric Peak Pressure (WBATPP) and Ambient Pressure (WBAA) in the LVAS group were significantly lower than those of the control group at 1259-2000 Hz but higher at 4000-6349 Hz (p < 0.05, power >0.8). The WBAA (1587 Hz) AUC value was 0.805, identifying a score ≤0.565 as indicative of a LVAS risk.
    UNASSIGNED: WBA holds promise in distinguishing LVAS from the normal condition and warrants further exploration as a tool to examine the influence of inner ear pressure on acoustic energy transmission in the middle ear.
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  • 文章类型: Journal Article
    目的:急性生理学和慢性健康评估II(APACHEII)基于重症监护病房(ICU)患者的数据,通常与疾病严重程度和预后相关。然而,根据脑肿瘤患者的ICU入院数据,不存在预后预测因子,并且没有研究报告APACHEII与脑肿瘤患者的预后之间存在关联。日本重症监护患者数据库(JIPAD)的建立是为了提高日本重症监护医学的护理质量。我们使用JIPAD根据ICU收治的脑肿瘤术后患者的可用数据来检查与院内死亡率相关的因素。
    方法:2015年4月至2018年3月,在脑肿瘤手术切除或脑肿瘤活检后,年龄≥16岁的患者纳入JIPAD。我们根据血液检查和ICU入住期间的医疗程序检查了与出院时结果相关的因素,肿瘤类型,和APACHEII得分。
    结果:在研究中的1454名患者中(男性:女性比例:1:1.1,平均年龄:62岁),32人(2.2%)在住院期间死亡。在多变量分析中,男性(优势比[OR]2.70,[95%置信区间,CI1.22-6.00]),恶性肿瘤(OR2.51[95%CI1.13-5.55]),APACHEII评分≥15(OR2.51[95%CI3.08-14.3])与住院死亡率显著相关.
    结论:通过在早期发现院内死亡风险较高的病例,改善治疗方法和对患者家属的支持是可能的。
    OBJECTIVE: Acute Physiology and Chronic Health Evaluation II (APACHE II) is based on the data of intensive care unit (ICU) patients and often correlates with disease severity and prognosis. However, no prognostic predictors exist based on ICU admission data for patients with brain tumors, and no studies have reported an association between APACHE II and prognosis in patients with brain tumors. The Japanese Intensive Care Patients Database (JIPAD) was established to improve the quality of care delivered in intensive care medicine in Japan. We used JIPAD to examine factors associated with in-hospital mortality based on available data of postoperative patients with brain tumors admitted to the ICU.
    METHODS: Patients aged ≥16 years enrolled in JIPAD between April 2015 and March 2018 after surgical brain tumor resection or biopsy of brain tumors. We examined factors related to outcomes at discharge based on blood tests and medical procedures performed during ICU admission, tumor type, and APACHE II score.
    RESULTS: Among the 1454 patients (male:female ratio: 1:1.1, mean age: 62 years) in the study, 32 (2.2 %) died during hospital stay. In multivariate analysis, male sex (odds ratio [OR] 2.70, [95 % confidence interval, CI 1.22-6.00]), malignant tumor (OR 2.51 [95 % CI 1.13-5.55]), and APACHE II score ≥15 (OR 2.51 [95 % CI 3.08-14.3]) were significantly associated with in-hospital mortality.
    CONCLUSIONS: By picking up cases with a high risk of in-hospital death at an early stage, it is possible to improve methods of treatment and support for the patient\'s family.
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  • 文章类型: Journal Article
    目的:认识到相关危险因素可能对降低异位妊娠(EP)的发生率具有积极影响。近年来,研究中提到了体重指数(BMI)。然而,关于EP和BMI之间关系的研究很少,并且存在争议。
    方法:以2017~2021年武汉市中心医院收治的EP产妇为病例组,以分娩产妇为对照组进行回顾性研究。对与异位妊娠相关的变量进行χ2检验以发现差异。进行单因素和多因素二元logistic回归分析,奇偶校验,人工流产史,异位妊娠史,自然流产史,阑尾切除术史和BMI(<18.5kg/m2,18.5〜24.9kg/m2,25kg/m2〜29.9kg/m2,≥30kg/m2)合并EP。
    结果:分别为659例EP和1460例。年龄的变量,奇偶校验,人工流产史,宫外孕病史和BMI差异有统计学意义(P<0.05)。多变量分析表明,年龄>35岁[(OR(赔率比),5.415;95CI(置信区间),4.006~7.320,P<0.001],异位妊娠史(OR,3.944;95CI,2.405~6.467;P<0.001),人工流产史(OR,3.365;95CI,2.724~4.158,P<0.001)和低BMI(<18.5kg/m2)(OR,1.929;95CI,1.416~2.628,P<0.001])增加EP的风险。
    结论:异位妊娠史,人工流产史和年龄>35岁是EP的危险因素。除了这些传统因素,我们发现低BMI(<18.5kg/m2)的女性可能会增加EP的风险.
    OBJECTIVE: Acknowledging the associated risk factors may have a positive impact on reducing the incidence of ectopic pregnancy (EP). In recent years, body mass index (BMI) has been mentioned in research. However, few studies are available and controversial on the relationship between EP and BMI.
    METHODS: We retrospectively studied the EP women as a case group and the deliveries as a control group in the central hospital of Wuhan during 2017 ~ 2021. χ2 test of variables associated with ectopic pregnancy was performed to find differences. Univariate and multivariate binary logistic regression analysis was conducted to analyze the association of the variables of age, parity, history of induced abortion, history of ectopic pregnancy, history of spontaneous abortion, history of appendectomy surgery and BMI (< 18.5 kg/m2, 18.5 ~ 24.9 kg/m2, 25 kg/m2 ~ 29.9 kg/m2, ≥ 30 kg /m2) with EP.
    RESULTS: They were 659 EP and 1460 deliveries. The variables of age, parity, history of induced abortion, history of ectopic pregnancy and BMI were different significantly(P < 0.05). Multivariate analysis showed that the variables of age > 35 years old [(OR (Odds Ratio), 5.415; 95%CI (Confidence Interval), 4.006 ~ 7.320, P < 0.001], history of ectopic pregnancy (OR, 3.944; 95%CI, 2.405 ~ 6.467; P < 0.001), history of induced abortion(OR, 3.365; 95%CI, 2.724 ~ 4.158, P < 0.001) and low BMI (< 18.5 kg/m2) (OR, 1.929; 95%CI, 1.416 ~ 2.628, P < 0.001])increased the risk of EP.
    CONCLUSIONS: The history of ectopic pregnancy, history of induced abortion and age > 35 years old were the risk factors with EP. In addition to these traditional factors, we found low BMI (< 18.5 kg/m2) with women may increase the risk to EP.
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  • 文章类型: Journal Article
    背景:如果定期且准确地监测,患者的生命体征是健康的量度。资源匮乏的地区医院人员短缺往往导致病人监测不足,将患者置于未被发现的恶化风险中。
    目的:本研究旨在探讨在资源贫乏的地区/农村医院中,生命体征监测的模式和完整性以及每种生命体征在预测临床恶化事件中的贡献。
    方法:采用回顾性病例对照研究设计,我们比较了来自两家资源不足的地区医院的恶化和未恶化患者的24小时生命体征数据。描述性统计,t检验,和方差分析用于比较患者监测频率和完整性。使用接收器操作员特征曲线下面积和二元逻辑回归分析确定每个生命体征在预测患者恶化中的贡献。
    结果:在24小时内,恶化患者的监测频率(9.58[7.02]倍)高于未恶化患者(4.93[2.66]倍)。然而,未恶化患者的生命体征记录完整性(85.2%)高于恶化患者(57.7%).体温是最常被忽略的生命体征。患者恶化与异常生命体征的频率和每组异常生命体征的数量呈正相关(接收器操作员特征曲线下面积:分别为0.872和0.867)。没有一个生命体征能强烈预测患者的预后。然而,补充氧值>3L/min和心率>139次/min是患者病情恶化的最佳预测因子.
    结论:鉴于小型地区医院资源贫乏且往往地理偏远,谨慎的做法是,护理人员要了解最能表明其护理队列患者病情恶化的生命体征。补充氧气的心动过速患者恶化的风险很高。
    BACKGROUND: Patient vital signs are a measure of wellness if monitored regularly and accurately. Staff shortages in poorly resourced regional hospitals often result in inadequate patient monitoring, putting patients at risk of undetected deterioration.
    OBJECTIVE: This study aims to explore the pattern and completeness of vital sign monitoring and the contribution of each vital sign in predicting clinical deterioration events in resource-poor regional/rural hospitals.
    METHODS: Using a retrospective case-control study design, we compared 24 h of vital sign data from deteriorating and nondeteriorating patients from two poorly-resourced regional hospitals. Descriptive statistics, t-tests, and analysis of variance are used to compare patient-monitoring frequency and completeness. The contribution of each vital sign in predicting patient deterioration was determined using the Area Under the Receiver Operator Characteristic curve and binary logistical regression analysis.
    RESULTS: Deteriorating patients were monitored more frequently (9.58 [7.02] times) in the 24-h period than nondeteriorating patients (4.93 [2.66] times). However, the completeness of vital sign documentation was higher in nondeteriorating (85.2%) than in deteriorating patients (57.7%). Body temperature was the most frequently omitted vital sign. Patient deterioration was positively linked to the frequency of abnormal vital signs and the number of abnormal vital signs per set (Area Under the Receiver Operator Characteristic curve: 0.872 and 0.867, respectively). No single vital sign strongly predicts patient outcomes. However, a supplementary oxygen value of >3 L/min and a heart rate of >139 beats/min were the best predictors of patient deterioration.
    CONCLUSIONS: Given the poor resourcing and often geographical remoteness of small regional hospitals, it is prudent that the nursing staff are made aware of the vital signs that best indicate deterioration for the cohort of patients in their care. Tachycardic patients on supplementary oxygen are at high risk of deterioration.
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  • 文章类型: Journal Article
    背景:阿比特龙和联合雄激素剥夺疗法(ADT)用于治疗转移性去势抵抗性前列腺癌患者。最近,有人认为,单独使用阿比特龙(不含ADT)的疗效可能与持续ADT的阿比特龙相当.这里,我们试图评估ADT停止对开始治疗去势抵抗性前列腺癌的阿比特龙患者的影响.
    方法:我们确定了在2011年至2022年之间在我们机构中单独接受阿比特龙(停用ADT)的39名患者。然后,我们采购了一组相当的39名患者(按年龄匹配,格里森得分,和前列腺特异性抗原[PSA]水平)在同一时期接受阿比特龙并进行ADT。我们评估并比较了两组的临床结果(单独使用阿比特龙与阿比特龙-ADT)关于PSA反应率,无PSA进展生存期,和总体生存率。使用Cox比例风险多变量模型调整结果。
    结果:治疗开始前,阿比特龙组的PSA中位数为12.7(范围:0.2-199)ng/mL,阿比特龙-ADT组为15.5(范围:0.6-212)ng/mL。单独使用阿比特龙可以充分抑制35/37(94.6%)患者的睾丸激素水平。单独接受阿比特龙的患者PSA中位数降低80.2%,而接受阿比特龙加ADT的患者为79.5%。单独接受阿比特龙的患者的PSA无进展生存期中位数为27.4个月,而接受阿比特龙加ADT的患者为25.8个月(风险比[HR]1.10;95%置信区间[CI]0.65-1.71;p=0.82)。此外,在接受阿比特龙联合ADT的患者中,单独使用阿比特龙与3.6年和3.1年的总生存期相关(HR0.90;95%CI0.50-1.62;p=0.72).进行Cox多变量回归分析后,组间PFS或OS无差异。
    结论:与接受阿比特龙联合ADT的患者相比,单独使用阿比特龙的临床结局具有可比性。需要进一步的前瞻性研究来评估阿比特龙单独对治疗结果和成本节约的影响。
    Abiraterone and concurrent androgen deprivation therapy (ADT) are used in the treatment of patients with metastatic castration-resistant prostate cancer. Recently, it has been suggested that the use of abiraterone alone (without ADT) may have comparable efficacy to abiraterone with ongoing ADT. Here, we sought to assess the impact of ADT cessation in patients beginning abiraterone for castration-resistant prostate cancer.
    We identified 39 patients at our institution who received abiraterone alone (with discontinuation of ADT) between 2011 and 2022. We then procured a comparable group of 39 patients (matched by age, Gleason score, and prostate-specific antigen [PSA] level) who received abiraterone with ongoing ADT during the same period. We assessed and compared clinical outcomes in the two groups (abiraterone-alone vs. abiraterone-ADT) with respect to PSA response rates, PSA progression-free survival, and overall survival. Results were adjusted using Cox proportional-hazards multivariable models.
    The median PSA before treatment initiation was 12.7 (range: 0.2-199) ng/mL in the abiraterone-alone group and 15.5 (range: 0.6-212) ng/mL in the abiraterone-ADT group. Use of abiraterone alone adequately suppressed testosterone levels in 35/37 (94.6%) patients. Patients receiving abiraterone alone had a median PSA reduction of 80.2% versus 79.5% in patients receiving abiraterone plus ADT. The median PSA progression-free survival in patients receiving abiraterone alone was 27.4 versus 25.8 months in patients receiving abiraterone plus ADT (hazard ratio [HR] 1.10; 95% confidence interval [CI] 0.65-1.71; p = 0.82). In addition, abiraterone alone was associated with an overall survival of 3.6 versus 3.1 years in patients receiving abiraterone plus ADT (HR 0.90; 95% CI 0.50-1.62; p = 0.72). There were no differences in PFS or OS between groups after performing Cox multivariable regression analyses.
    Use of abiraterone alone was associated with comparable clinical outcomes to patients who received abiraterone together with ADT. Further prospective studies are warranted to evaluate the impact of abiraterone alone on treatment outcomes and cost savings.
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  • 文章类型: Journal Article
    目的:探讨无创正压通气患者面部压力性损伤的特点及危险因素。
    方法:选择2016年1月至2021年12月在台湾某教学医院接受无创正压通气导致面部压力损伤的患者,导致我们病例组共有108名患者。对照组按年龄和性别与三名使用无创通气但未发生面部压力损伤的急性住院患者相匹配,导致对照组324例患者。
    方法:本研究为回顾性病例对照研究。比较病例组不同阶段发生压力性损伤患者的特点,然后确定无创通气相关面部压力性损伤的危险因素。
    结果:无创通气使用时间延长,住院时间较长,较低的布雷登量表得分,前一组白蛋白水平较低。涉及无创通气使用持续时间的二元逻辑回归的多变量分析结果表明,使用该设备4-9天和16天的患者比使用该设备3天的患者发生面部压力损伤的风险更大;就Braden量表评分而言,较高的Braden量表评分与较高的面部压力损伤风险相关.此外,白蛋白水平低于正常范围与较高的面部压力损伤风险相关.
    结论:压力性损伤在较高阶段的患者使用无创通气的持续时间较长,住院时间较长,较低的布雷登量表分数,和较低的白蛋白水平。因此,使用非侵入性通气的持续时间较长,较低的布雷登量表分数,低白蛋白水平也是无创通气相关面部压力损伤的危险因素.
    结论:我们的结果为医院提供了有用的参考,为他们的医疗团队制定预防和治疗面部压力损伤的培训计划,以及起草评估风险的指南,以防止由无创通气引起的面部压力损伤。设备使用的持续时间,布雷登量表得分,尤其是白蛋白水平应认真监测,以减少无创通气治疗的急性住院患者面部压力损伤的发生。
    OBJECTIVE: To explore the characteristics and risk factors of facial pressure injuries in patients using noninvasive positive pressure ventilation.
    METHODS: Patients who developed facial pressure injuries due to non-invasive positive pressure ventilation at a teaching hospital in Taiwan from January 2016 to December 2021 were selected, resulting in a total of 108 patients in our case group. A control group was formed by matching each case by age and gender to three acute inpatients who had used non-invasive ventilation but had not developed facial pressure injuries, resulting in 324 patients in the control group.
    METHODS: This study was a retrospective case-control study. The characteristics of the patients who developed pressure injuries at different stages in the case group were compared, and the risk factors of non-invasive ventilation-related facial pressure injuries were then determined.
    RESULTS: Higher duration of non-invasive ventilation usage, higher length of hospital stay, lower Braden scale score, and lower albumin levels in the former group. The results of multivariate analysis from binary logistic regression involving the duration of non-invasive ventilation usage demonstrated that the patients who used this device for 4-9 days and 16 days were at greater risk of facial pressure injuries than those who used it for 3 days; in terms of the Braden scale score, higher Braden scale scores were correlated with a higher risk of facial pressure injuries. In addition, albumin levels lower than the normal range were correlated with a higher risk of facial pressure injuries.
    CONCLUSIONS: Patients with pressure injuries at higher stages had a higher duration of non-invasive ventilation usage, higher length of hospital stay, lower Braden scale scores, and lower albumin levels. Thus, a longer duration of non-invasive ventilation use, lower Braden scale scores, and lower albumin levels were also risk factors for non-invasive ventilation-related facial pressure injuries.
    CONCLUSIONS: Our results serve as a useful reference for hospitals, both in creating training programs for their medical teams to prevent and treat facial pressure injuries and in drafting guidelines for assessing risk in order to prevent facial pressure injuries caused by non-invasive ventilation. The duration of device usage, Braden scale scores, and albumin levels in particular should be seriously monitored to reduce the occurrence of facial pressure injuries in acute inpatients treated with non-invasive ventilation.
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  • 文章类型: Journal Article
    未经授权:探讨川崎病合并巨噬细胞活化综合征(KD-MAS)的早期预测因素。
    UNASSIGNED:我们于2017年8月至2022年8月对KD儿童进行了回顾性病例对照研究,涉及28例KD-MAS和112例未发展为KD-MAS。基于单变量分析,二元逻辑回归用于确定KD-MAS发展的早期预测因素,并对受试者工作特性曲线(ROC)进行分析,得出最佳截断值。
    未经评估:两个预测因素与KD-MAS的发展有关,PLT(OR=1.013,95CI,1.001-1.026),和血清铁蛋白(OR=0.991,95CI,0.982-0.999)。PLT的截止值为110×109/L,血清铁蛋白的临界值为548.4ng/ml。
    未经批准:患有KD的儿童,其PLT数低于110×109/L,血清铁蛋白水平超过548.4ng/ml更有可能发生KD-MAS。
    UNASSIGNED: To investigate the early predictive factors for Kawasaki disease complicated with macrophage activation syndrome (KD-MAS).
    UNASSIGNED: We performed a retrospective case-control study in children with KD from August 2017 to August 2022, involving 28 cases with KD-MAS and 112 cases not developing KD-MAS. Based on the univariate analysis, binary logistic regression was used to identify the early predictive factors for KD-MAS development, and the receiver operating characteristic curve (ROC) analysis was carried out to obtain the optimal cut-off value.
    UNASSIGNED: Two predictive factors were associated with the development of KD-MAS, which were PLT (OR = 1.013, 95%CI, 1.001-1.026), and serum ferritin (OR = 0.991, 95%CI, 0.982-0.999). The cut-off value of PLT was 110 × 109/L, and the cut-off value of serum ferritin was 548.4 ng/ml.
    UNASSIGNED: Children with KD who had a PLT count under 110 × 109/L, and a serum ferritin level over 548.4 ng/ml are more likely to develop KD-MAS.
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  • 文章类型: Journal Article
    未经授权:围手术期,经验性抗生素升级治疗并不少见,导致术后住院时间更长,医疗费用更高。然而,很少有系统的研究来研究这个问题。在这项病例对照研究中,我们探讨了影响住院期间微创肺手术后经验性抗生素升级治疗的因素,目的是促进术后恢复和合理使用抗生素。
    UNASSIGNED:从医院信息系统(HIS)收集了2019年1月至2020年12月在我们中心接受微创肺手术的患者的数据。根据纳入和排除标准共确定了1,360例。这些患者被分为两组:A组(n=825),其中患者在手术后未接受抗生素升级治疗;B组(n=535),其中患者在手术后接受经验性抗生素升级治疗。采用logistic回归模型分析术后抗菌药物经验性治疗升级的影响因素。
    UNASSIGNED:与A组相比,B组术后住院时间明显延长(5.05±2.78vs.4.49±2.24天,P<0.001),平均总住院费用略高(74,080.85±23,796.51vs.71,798.09±21,307.26元,P=0.067)。多因素分析显示,有统计学意义的因素包括二次肺手术史[比值比(OR):3.267;95%置信区间(CI):1.305-8.178;P=0.011]。术前血红蛋白A1c(HbA1c)≥6.5%(OR:1.603;95%CI:1.143-2.249;P=0.006),术后不明原因发热[体温(T)>38℃;OR:2.494;95%CI:1.321-4.708;P=0.005],术后低蛋白血症(静脉白蛋白给药≥2天;OR:14.125;95%CI:1.777-112.282;P=0.012).
    UNASSIGNED:多因素分析显示,二次肺手术史,术前HbA1c≥6.5%,术后不明原因发热(T>38℃),术后低蛋白血症(<35g/L和静脉白蛋白给药≥2天)是微创肺手术后经验性抗生素升级治疗的独立危险因素.对于术前风险因素,应开展进一步的队列研究,以探索更好的干预指标或措施.对于术后危险因素,围术期动态监测降钙素原,可指导抗菌药物的合理使用,降低耐药风险和住院费用。
    UNASSIGNED: During the perioperative period, empiric antibiotic escalation therapy is not uncommon, leading to longer postoperative hospital stay and higher medical expenses. However, few systematic studies have investigated this issue. In this case-control study, we explored the factors affecting empiric antibiotic escalation therapy after minimally invasive lung surgery during hospitalization, with the aim to enhance recovery after surgery and rational use of antibiotics.
    UNASSIGNED: The data of patients who underwent minimally invasive lung surgery at our center from January 2019 to December 2020 were collected from the hospital information system (HIS). A total of 1,360 cases were identified based on the inclusion and exclusion criteria. These patients were divided into 2 groups: group A (n=825), in which patients did not receive antibiotic escalation therapy after surgery; and group B (n=535), in which patients received empiric antibiotic escalation therapy after surgery. A logistic regression model was used to analyze the influencing factors of empiric antibiotherapy escalation during postoperative hospitalization.
    UNASSIGNED: Compared with group A, group B had significantly longer postoperative hospital stay (5.05±2.78 vs. 4.49±2.24 days, P<0.001) and slightly higher average total hospitalization costs (74,080.85±23,796.51 vs. 71,798.09±21,307.26 yuan, P=0.067). Multivariate analysis showed that the statistically significant factors included history of secondary lung surgery [odds ratio (OR): 3.267; 95% confidence interval (CI): 1.305-8.178; P=0.011], preoperative hemoglobin A1c (HbA1c) ≥6.5% (OR: 1.603; 95% CI: 1.143-2.249; P=0.006), postoperative fever of unknown origin [temperature (T) >38 ℃; OR: 2.494; 95% CI: 1.321-4.708; P=0.005], postoperative hypoalbuminemia (intravenous albumin administration for ≥2 days; OR: 14.125; 95% CI: 1.777-112.282; P=0.012).
    UNASSIGNED: Multivariate analysis showed that history of secondary lung surgery, preoperative HbA1c ≥6.5%, postoperative fever of unknown origin (T >38 ℃), and postoperative hypoalbuminemia (<35 g/L and intravenous albumin administration ≥2 days) were the independent risk factors for empiric antibiotic escalation therapy after minimally invasive lung surgery. For preoperative risk factors, further cohort studies should be conducted to explore better intervention indicators or measures. For postoperative risk factors, perioperative dynamic monitoring of procalcitonin can guide the rational use of antibiotics, reduce the risk of drug resistance and hospitalization cost.
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  • 文章类型: Journal Article
    目的:本研究旨在探讨重症监护病房(ICU)住院期间接受无创正压通气(NIPPV)的患者面部压力损伤(FPI)的相关因素,并确定FPI的预测因素。
    背景:无创正压通气是一种治疗急性和慢性呼吸衰竭患者的方法。然而,FPI可能由于不合适的鼻-口NIPPV面罩和与皮肤表面接触的不适而发生。
    方法:回顾性病例对照研究。
    方法:2018年1月至2020年10月,共纳入397名台湾国立医院收治的患者。患者在住院期间接受NIPPV并常规使用面罩下预防性敷料。患者分为非FPI组(n=357)和FPI组(n=40)。人口统计,临床特征,急性生理学和慢性健康评估II评分,并从医疗记录中收集Braden量表评分。进行Logistic回归分析,以检查各因素对FPI的贡献,报告了比值比。在这项回顾性病例对照研究中使用了STROBE检查表。
    结果:各组在年龄上有显著差异,血清白蛋白,C反应蛋白,体重指数(BMI),疾病严重程度,Braden量表得分,逗留时间,机械通气的持续时间和皮质类固醇的使用。Logistic回归分析显示FPI的危险因素为Braden量表评分[OR=1.630(1.176-2.260)]。BMI[OR=0.396(0.210-1.784)]和皮质类固醇[OR=0.394(0.159-1.811)],这些是NIPPV患者FPI的预测因子。
    结论:在NIPPV面罩下常规使用预防性敷料的患者仍可能发生面部压力损伤。本研究为FPI的继续教育培训提供信息,以便更准确地识别高风险,及时采取预防措施,降低FPI。
    结论:在使用NIPPV面罩的患者中,解决FPI相关因素以防止面部皮肤损伤并减少合并症。
    OBJECTIVE: This study aimed to investigate factors associated with facial pressure injury (FPI) in patients receiving non-invasive positive pressure ventilation (NIPPV) during hospitalisation in the intensive care unit (ICU) and to identify predictors of FPI.
    BACKGROUND: Non-invasive positive pressure ventilation is a method of treating patients with acute and chronic respiratory failure. However, FPI may occur due to unsuitable nasal-oral NIPPV masks and discomfort in contact with the skin surface.
    METHODS: A retrospective case-control study.
    METHODS: From January 2018 to October 2020, a total of 397 patients admitted to a national hospital in Taiwan were enrolled. Patients received NIPPV and routinely used under-mask prophylactic dressings during hospitalisation. Patients were divided into the non-FPI group (n = 357) and the FPI group (n = 40). Demographic, clinical characteristics, acute physiology and chronic health evaluation II scores, and Braden Scale scores were collected from medical records. Logistic regression analysis was performed to examine the contribution of each factor to the FPI, and odds ratios were reported. The STROBE checklist was used in this retrospective case-control study.
    RESULTS: There were significant differences between the groups in age, serum albumin, C-reactive protein, body mass index (BMI), disease severity, Braden Scale score, length of stay, duration of mechanical ventilation and use of corticosteroids. Logistic regression analysis revealed that the risk factor for FPI was the Braden Scale score [OR = 1.630 (1.176-2.260)], BMI [OR = 0.396 (0.210-1.784)] and corticosteroids [OR = 0.394 (0.159-1.811)], which were predictors of FPI in patients with NIPPV.
    CONCLUSIONS: Facial pressure injury may still occur in patients who routinely use prophylactic dressings under NIPPV masks. This study provides information on continuing education training for FPI to more accurately identify high-risk and timely preventive measures to reduce FPI.
    CONCLUSIONS: Addressing FPI-related factors to prevent facial skin damage and reduce comorbidities in patients using NIPPV masks.
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  • 文章类型: Journal Article
    UNASSIGNED: Previous evidence has shown that psychological stress can trigger the onset of autoimmune disease. This study aimed to investigate the prevalence of stressful life events preceding the onset of symptoms in female primary Sjogren\'s syndrome (pSS) in China compared to controls and the possible associations of stressful life events with disease activity.
    UNASSIGNED: This was a hospital-based retrospective case-control study. Sixty-seven consecutive female pSS patients and an equal number of age-matched (± 3 years) healthy controls were recruited for assessment using the related Stressful Life Events Scale. The pSS disease activity was measured by the EULAR Sjogren\'s syndrome disease activity index. Data were analyzed by SPSS, version 23, using chi-square, univariate logistic regression, multiple logistic regression, and partial correlation.
    UNASSIGNED: A higher number of negative stressful life events before disease onset in pSS patients compared with healthy controls suggest that these play a role in increasing the risk of disease occurrence (OR = 2.59, 95% CI: 1.87-3.58, p < 0.05). The number of positive life events did not differ between the two groups. Both the number and severity of the negative stressful life events were also significantly correlated with disease activity.
    UNASSIGNED: Patients with pSS experienced more negative stressful life events in the year preceding the onset of symptoms than controls. Negative stressful life events before symptom onset may be risk factors for pSS and may affect pSS disease activity.
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