Symptom score

症状评分
  • 文章类型: Journal Article
    目的:前列腺癌是老年男性最常见的恶性肿瘤之一,根治性前列腺切除术是局部疾病的既定治疗方法。接受这种手术的患者在围手术期经常会经历负面情绪和症状的增加。可能是由于对疾病及其治疗的担忧。本研究旨在研究涉及全过程可视化和协作护理讨论的新型教育方法对前列腺癌根治术患者围手术期症状和情绪健康的影响。
    方法:前瞻性收集了2021年6月至2023年12月期间入院的310例患者的数据,所有这些患者均计划接受根治性前列腺切除术。这些患者被随机分为干预组(接受新模式教育)或对照组(接受常规教育),每组155名患者。这项研究比较了基本的人口统计信息,焦虑和抑郁评分,对疾病进展分数的恐惧,生活质量分数,主要症状评分,两组围手术期生命体征的变化。
    结果:两组在年龄方面无统计学差异,合并症,保险类型,教育水平,收入,肿瘤病史(P>0.05)。同样,焦虑和抑郁评分没有显著差异,焦虑和抑郁患者的比例,生命体征,在时间1阶段,两组患者对疾病进展的恐惧评分(P>0.05)。在时间2和时间3阶段,干预组表现出更低的焦虑和抑郁评分,焦虑和抑郁患者的比例较低,血压和心率波动明显低于对照组(P<0.05)。根治性前列腺切除术后,患者的主要症状,如疼痛,恶心,和疲劳,在手术后第1-3天使用MADIS症状评估量表进行评估。干预组3种症状评分明显低于对照组(P<0.05);在第4阶段,与对照组相比,干预组患者的生活质量评分也有显著改善(P<0.05).此外,患者的血压和心率在时间4阶段恢复到基线水平,两组间无显著性差异(P>0.05)。然而,干预组在时间4阶段的焦虑和抑郁评分仍显著低于对照组(P<0.05)。此外,两组患者对疾病进展的恐惧评分均低于时间1阶段,与对照组相比,干预组的改善更为明显(P<0.05)。
    结论:被诊断为恶性肿瘤的患者通常会对疾病的进展和即将进行的手术感到恐惧和焦虑。以及围绕他们的治疗和预后的不确定性。在围手术期,这种情绪困扰加剧可能会导致更大的症状负担。利用全过程可视化和协作护理讨论方法,与传统的沟通方式相比,已经被证明可以减轻病人的恐惧,减少焦虑和抑郁,并最终减轻围手术期的症状负担。最终,这种方法可以提高恶性肿瘤患者的整体生活质量。
    OBJECTIVE: Prostate cancer is one of the most common malignant neoplasms in elderly males, with radical prostatectomy being the established therapeutic approach for localized disease. Patients undergoing this surgical procedure frequently experience increased negative emotions and symptomatology during the perioperative period, likely due to concerns about the illness and its treatment. The present study aims to investigate the effects of a novel educational approach involving a whole-process visualization and collaborative nursing discussions on perioperative symptoms and emotional well-being in radical prostatectomy patients.
    METHODS: Data were prospectively collected from 310 patients admitted to the hospital between June 2021 and December 2023, all of whom were scheduled to undergo radical prostatectomy. These patients were randomly assigned to either the intervention group (receiving new model education) or the control group (receiving conventional education), with 155 patients in each group. The study compared basic demographic information, anxiety and depression scores, fear of disease progression scores, quality-of-life scores, main symptom scores, and changes in perioperative vital signs between the two groups.
    RESULTS: No statistically significant differences were observed between the two groups in terms of age, comorbidities, insurance type, education level, income, and tumor history (P > 0.05). Similarly, there were no significant differences in anxiety and depression scores, proportion of patients with anxiety and depression, vital signs, and fear of disease progression scores between the two groups at Time 1 stage (P > 0.05). During stages Time 2 and Time 3, the intervention group exhibited lower anxiety and depression scores, a lower proportion of anxious and depressed patients, as well as significantly reduced blood pressure and heart rate fluctuations compared to the control group (P < 0.05). Following radical prostatectomy, the main symptoms of patients, such as pain, nausea, and fatigue, were assessed using the MADIS Symptom Assessment Scale on days 1-3 post-surgery. The intervention group exhibited significantly lower scores for three symptoms compared to the control group (P < 0.05); at Time 4 stage, the patients in the intervention group also demonstrated significantly improved quality-of-life scores compared to the control group (P < 0.05). Additionally, blood pressure and heart rate of patients returned to baseline levels at Time 4 stage, with no significant difference between the two groups (P > 0.05). Nevertheless, the anxiety and depression scores in the intervention group at the Time 4 stage remained significantly lower than those in the control group (P < 0.05). Additionally, the fear of disease progression scores in both groups were lower than those at the Time 1 stage, with a more pronounced improvement observed in the intervention group compared to the control group (P < 0.05).
    CONCLUSIONS: Patients diagnosed with malignant tumors often experience fear and anxiety regarding the progression of their disease and upcoming surgery, as well as uncertainty surrounding their treatment and prognosis. This heightened emotional distress can contribute to a greater symptom burden during the perioperative period. Utilizing a whole-process visualization and collaborative nursing discussion approach, as compared to traditional communication methods, has been shown to alleviate patients\' fears, reduce anxiety and depression, and ultimately lessen the symptom burden experienced during the perioperative phase. Ultimately, this approach can enhance the overall quality of life for patients facing malignant tumors.
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  • 文章类型: Journal Article
    背景:自闭症谱系障碍(ASD)是一种多因素,无处不在,神经发育障碍,其中肠道症状是最常见的合并症之一。
    方法:在本研究中,来自中国13个城市的1,222名ASD儿童和1,206名2-7岁的典型发展(TD)儿童。对ASD和TD儿童进行身体测量和基本信息问卷。儿童自闭症评定量表(CARS),社会反应量表(SRS),和孤独症行为清单(ABC)用于评估ASD儿童的临床症状。采用6项胃肠道严重程度指数(6-GSI)评价两组患者的肠道症状发生率。
    结果:便秘的检出率,大便气味,ASD儿童的总肠道症状明显高于TD儿童(40.098%vs.25.62%,17.021%与9.287%,和53.601%与41.294%,分别)。表现为肠道合并症的自闭症儿童在ABC上的得分明显更高,SRS,汽车,与没有肠道症状的自闭症儿童相比,提示肠道共病可能加剧ASD儿童的核心症状。
    结论:孤独症患儿的肠功能障碍明显多于TD患儿。这种功能障碍可能会加重ASD儿童的核心症状。
    BACKGROUND: Autism spectrum disorder (ASD) is a multifactorial, pervasive, neurodevelopmental disorder, of which intestinal symptoms collectively represent one of the most common comorbidities.
    METHODS: In this study, 1,222 children with ASD and 1,206 typically developing (TD) children aged 2-7 years were enrolled from 13 cities in China. Physical measurement and basic information questionnaires were conducted in ASD and TD children. The Childhood Autism Rating Scale (CARS), Social Responsiveness Scale (SRS), and Autism Behavior Checklist (ABC) were used to evaluate the clinical symptoms of children with ASD. The six-item Gastrointestinal Severity Index (6-GSI) was used to evaluate the prevalence of intestinal symptoms in two groups.
    RESULTS: The detection rates of constipation, stool odor, and total intestinal symptoms in ASD children were significantly higher than those in TD children (40.098% vs. 25.622%, 17.021% vs. 9.287%, and 53.601% vs. 41.294%, respectively). Autistic children presenting with intestinal comorbidity had significantly higher scores on the ABC, SRS, CARS, and multiple subscales than autistic children without intestinal symptoms, suggesting that intestinal comorbidity may exacerbates the core symptoms of ASD children.
    CONCLUSIONS: Intestinal dysfunction was significantly more common in autistic than in TD children. This dysfunction may aggravate the core symptoms of children with ASD.
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  • 文章类型: Journal Article
    背景:重症肌无力(MG)是一种神经肌肉传递障碍,可将轻度眼部无力带到严重的全身肌无力和残疾。常规治疗有长期副作用,和中草药(CHM)对MG患者显示出可能的疗效和安全性,但是现有的证据不够有力,结果已经过时。
    方法:在7个数据库和临床试验注册中心进行随机对照试验(RCT)的搜索,直到2021年7月。ROB2工具用于评估研究质量,GRADE用于评估整体证据的质量。进行荟萃分析,结果以风险比(RR)或平均差异(MD)和95%置信区间(CI)表示。
    结果:纳入了19个RCT(1283名参与者),对13种CHM进行了充分的随机化,纳入了6个研究复方黄芪的RCT。除了常规治疗外,9名CHM降低了MG的症状评分。与常规治疗相比,复方黄芪加常规治疗(溴吡啶斯的明或泼尼松或两者)可降低症状评分(MD=-3.56,95CI-4.86至-2.26)。CHM组发生的不良事件较少(CHM组的3/247,52/245在对照组中,RR=0.13,95CI0.06至0.30,9项RCT,总共492名参与者)。对生活质量的影响不一致。
    结论:9种CHM可能对改善MG症状有益。证据支持复方黄芪加用常规治疗可能对改善MG症状有额外益处。添加CHM可能比仅给予常规治疗更安全。
    背景:该协议已在PROSPERO(ID:32718)中注册。
    BACKGROUND: Myasthenia Gravis (MG) is a disorder of neuromuscular transmission bringing mild ocular weakness to severe generalized muscle weakness and disability. The conventional treatments have long-term side effects, and Chinese herbal medicines (CHM) have shown possible effect and safety for MG patients, but the existing evidence was not robust enough and the results were out of date.
    METHODS: Searching for randomized controlled trials (RCTs) was conducted in 7 databases and clinical trial registries until July 2021. The ROB 2 tool was used to assess the study quality and GRADE was used to assess the quality of whole evidence. Meta-analyses were conducted and the results were presented as risk ratio (RR) or mean difference (MD) with 95% confidence interval (CI).
    RESULTS: Nineteen RCTs (1283 participants) testing 13 kinds of CHM with adequate randomization were included and six RCTs investigating Compound Huangqi were included in the meta-analyses. In addition to conventional treatment, nine CHMs reduced symptom scores of MG. Compound Huangqi plus conventional treatment (pyridostigmine bromide or prednisone or both) reduced the symptom scores compared with conventional treatment (MD = -3.56, 95%CI -4.86 to -2.26). Less adverse events happened in the CHM groups (3/247 in the CHM groups, 52/245 in the control groups, RR = 0.13, 95%CI 0.06 to 0.30, 9 RCTs, a total of 492 participants). The effect on quality of life was inconsistent.
    CONCLUSIONS: Nine CHMs could probably bring benefit for MG symptom improvement. Moderate to low certainty of evidence supported Compound Huangqi added-on conventional treatment probably bring extra benefit of improving MG symptoms. Adding CHMs could be safer than giving only conventional treatment.
    BACKGROUND: The protocol was registered in PROSPERO (ID: 32718).
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    文章类型: Journal Article
    OBJECTIVE: To observe clinical effects of Tiaoqi Jiangni Decoction combined with mosapride citrate tablets in the treatment of functional dyspepsia and its impact on quality of life.
    METHODS: Seventy-six patients with functional dyspepsia were admitted to Cangzhou Central Hospital of Hebei Province from September 2019 to June 2020. They were selected and randomized into a treatment group and a control group (38 cases in each group). Both groups received mosapride citrate tablets (5 mg/time, 3 times/d). The treatment group was additionally given Tiaoqi Jiangni Decoction.
    RESULTS: The total effective rate of the treatment group was higher than that of the control group (P < 0.05). After treatment, the sub-scores of each symptom and the overall score of traditional Chinese medicine (TCM) syndrome in the treatment group were significantly lower than those in the control group (all P < 0.05). The overall and sub-item scores of the Functional Digestive Disorders Quality of Life Questionnaire (FDDQL) of both groups saw an increase after treatment (all P < 0.05). There was no significant disparity in sleep and stress between the two groups. The treatment group presented a better performance in other aspects than the control group (all P < 0.05). Before treatment, the two groups showed no significant disparity in the gastric emptying rate of barium bar and mental and psychological state. The two indexes were observed with a rise after treatment, with superior results in the treatment group to those in the control group (P < 0.05). No adverse reactions were observed in the two groups. One month after treatment, the treatment group obtained a lower recurrence rate as compared to the control group (P < 0.05).
    CONCLUSIONS: Tiaoqi Jiangni Decoction in combination with mosapride citrate tablets in the treatment of FD yields a significant clinical effect by substantially alleviating patients\' clinical symptoms and improving their quality of life, with no adverse reactions, high safety, and low recurrence rate, which merits further clinical application.
    BACKGROUND: The name of the registry: Chinese Registry of Clinical Trials.
    BACKGROUND: ChiCTR2100063542. Trial URL: http://www.chictr.org.cn/showproj.aspx?proj=6354283.
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  • DOI:
    文章类型: Journal Article
    OBJECTIVE: To study the effect and mechanism of acupoint catgut embedding on patients of postmenopausal osteoporosis (PMOP).
    METHODS: In this prospective study, 90 patients with PMOP who received treatment in our hospital were randomly divided into the drug treatment group (n=45) and drug treatment + catgut embedding group (n=45) according to SPSS random table method. The drug treatment group was given conventional western medicine treatment, and the drug treatment + catgut embedding group was given point embedding therapy. Bone mineral density (BMD), calcium (Ca2+), osteoprotegerin (OPG), estrogen (E2), receptor activator of nuclear factor-kB ligand (RANKL), liver and kidney function and blood lipids were detected before treatment in the two groups, and visual analogue score (VAS) and PMOP symptom score were evaluated. The above-mentioned indexes were detected again 3 months and 6 months after treatment.
    RESULTS: At 3 and 6 months after treatment, the BMD and the levels of Ca2+ and E2 in the two groups were increased, while the levels of OPG and RANKL were decreased, and the improvement in the drug treatment + catgut embedding group was significantly better than that in the drug treatment group (P<0.05). The symptom scores of VAS and PMOP in the drug treatment + catgut embedding group were significantly lower than those in the drug treatment group (all P<0.001). There was no significant difference in the levels of alanine aminotransferase (ALT), total bilirubin (TBil), albumin (ALB), blood urea nitrogen (BUN), serum creatinine (SCr) and serum uric acid (SUA) between the two groups, but the levels of total cholesterol (TC) and triglyceride (TG) in the drug treatment + catgut embedding group were significantly lower than those in the drug treatment group (all P<0.001).
    CONCLUSIONS: Acupoint catgut embedding has a good effect on PMOP, and it can increase BMO and improve the clinical symptoms of patients, which is worthy of clinical promotion.
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  • 文章类型: Journal Article
    建立直立不耐受症状评分系统,以评估直立不耐受,然后比较不同抬头倾斜测试反应之间的症状评分。
    有直立不耐受症状的272名受试者(5-18岁)完成了问卷调查和抬头倾斜测试。根据抬头倾斜试验的血流动力学反应,将受试者分为抬头倾斜试验阴性,血管迷走性晕厥,和体位性心动过速综合征组。
    我们根据头晕的频率建立了症状评分,头痛,视力模糊,心悸,胸部不适,胃肠道症状,大量的汗水,和晕厥。体位性心动过速综合征受试者的中位数得分最高。2.5分预测血管迷走性晕厥的敏感性为75.0%,特异性为50.3%,5.5分预测体位性心动过速综合征的敏感性为69.7%,特异性为72.0%.此外,体位性心动过速综合征患者的中位评分明显高于抬头倾斜试验阴性患者,心率增量为30~39次/min(P<0.01)。
    这表明症状评分在抬头倾斜测试结果中具有一定的预测价值,可以作为初步评估工具。
    To develop an orthostatic intolerance symptom scoring system to assess orthostatic intolerance and then to compare the symptom score among different head-up tilt test responses.
    272 subjects (5-18 years) presenting with orthostatic intolerance symptoms finished questionnaire and head-up tilt test. According to head-up tilt test hemodynamic responses, the subjects were divided into head-up tilt test negative, vasovagal syncope, and postural tachycardia syndrome groups.
    We built up a symptom score according to the frequency of dizziness, headache, blurred vision, palpitations, chest discomfort, gastrointestinal symptoms, profuse perspiration, and syncope. The median score in postural tachycardia syndrome subjects was highest. A score of 2.5 for predicting vasovagal syncope yielded a sensitivity of 75.0% and specificity of 50.3%, a score of 5.5 for predicting postural tachycardia syndrome yielded a sensitivity of 69.7% and specificity of 72.0%. Furthermore, the median score in postural tachycardia syndrome subjects was significantly higher than that in head-up tilt test negative subjects with heart rate increment of 30-39 beats/min (P < .01).
    This suggests that the symptom score has some predictive value in head-up tilt test results, which can be served as a preliminary assessment instrument.
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  • 文章类型: Journal Article
    Barley yellow dwarf (BYD) is a major virus disease which dramatically reduces wheat yield. Introducing BYD resistance genes into commercial varieties has been proven to be effective in reducing damage caused by barley yellow dwarf virus (BYDV). However, only one major resistance gene is readily deployable for breeding; Bdv2 derived from Thinopyrum intermedium is deployed as a chromosomal translocation. In this study, a double haploid (DH) population was developed from a cross between XuBYDV (introduced from China showing very good resistance to BYD) and H-120 (a BYD-sensitive Chinese accession), and was used to identify QTL for BYD resistance. The population was genotyped using an Infinium iSelect bead chip array targeting 90K gene-based SNPs. The disease resistance of DH lines inoculated with BYDV was assessed at the heading stage. The infections were assessed by tissue blot immunoassay (TBIA). Three new QTL were identified on chromosomes 5A, 6A, and 7A for both symptom and TBIA, with all three resistance alleles being inherited from XuBYDV. Some DH lines with the resistance alleles from all three QTL showed high level resistance to BYD. These new QTL will be useful in breeding programs for pyramiding BYD resistance genes.
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  • 文章类型: Journal Article
    OBJECTIVE: To systematically evaluate the clinical efficacy of acupuncture for dysarthria, and to explore the rules of acupoints selection for dysarthria.
    METHODS: The clinical randomized control trial literature regarding acupuncture for dysarthria published before January of 2018 were searched in databases, including CNKI, Wanfang, VIP, CBM, PubMed, Ebsco, Science Direct and Cochrane Library. The information of included studies was extract and the quality was assessed. The Meta analysis was performed by using RevMan 5.3 software. The frequency of acupoints was calculated by using Excel software to analyzed the rules of acupoints selection.
    RESULTS: Totally 21 papers were included, involving 1651 patients. The pooled effects of clinical efficacy: heterogeneity test P =0.74, I 2=0%, OR =6.36, 95% CI: 4.55, 8.88, Z =10.84 (P<0.01), indicating the efficacy in the treatment group was significantly higher than that in the control group. The pooled effects of the symptom score in Frenchay scale: heterogeneity test P =0.56, I 2=0%, WMD =3.20, 95% CI: 1.38, 5.02, Z =3.45 (P<0.01), indicating the efficacy in the treatment group was significantly higher than that in the control group. The acupoints with frequency of more than 5 times were Fengchi (GB 20), Yuye (EX-HN 13), Jinjin (EX-HN 12), Lianquan (CV 23), Baihui (GV 20), tongue-three needles and Yamen (GV15). The meridians with frequency of more than 5 times were the extra channels, governor vessel, gallbladder channel, conception vessel and stomach channel.
    CONCLUSIONS: The clinical efficacy of acupuncture combined with speech training/regular treatment is significantly superior to that of control group (speech training, medication, regular treatment); acupuncture is safe and effective for dysarthria; the majority of selected acupoint is local acupoints around tongue, throat and neck, as well as extra points and empirical points. However, high-quality randomized controlled trials with large sample sizes are still needed to provide further evidence.
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  • 文章类型: Clinical Trial Protocol
    婴儿期牛奶蛋白过敏(CMPA)的症状可能是非特异性的,这可能会延迟正确的诊断并导致不良的临床结果。非IgE介导的CMPA的诊断特别复杂,因为它涉及2至4周的消除饮食,然后口服食物激发(OFC)。奶牛牛奶相关症状评分(CoMiSS)是初级医疗保健提供者的临床资源,旨在提高对CMPA症状的认识,以促进早期诊断。本研究的目的是评估CoMiSS是否可以用作疑似CMPA婴儿的潜在诊断工具。
    本前瞻性将包括0-6个月出现CMPA症状的纯配方喂养婴儿,将在中国10个中心进行的多中心试验。所有婴儿将开始为期2周的基于氨基酸的配方(AAF)试验,同时从饮食中消除所有牛奶蛋白。AAF治疗期后,婴儿将在医院接受标准牛奶配方的开放式OFC,接下来是另外两周的公开家庭挑战。临床症状将记录在标准化症状记分卡上。CoMiSS将在研究进入时确定(CoMiSS1,在AAF开始之前),2周后(CoMiSS2,OFC之前)和再过2周后或提示CMPA症状再次出现时(CoMiSS3)。每次访问时将测量体重和长度。CoMiSS1和2之间的差异作为OFC结果的预测因子也将被评估。将计算基线CoMiSS的诊断准确性。
    这项研究获得了湖南省儿童医院医学伦理委员会的批准,湖南,中国。这项试验的结果将提交给同行评审的儿科营养学或胃肠病学杂志发表。摘要将提交给相关的国家和国际会议。
    NCT03004729;预结果。
    The symptoms of cow\'s milk protein allergy (CMPA) in infancy can be non-specific which may delay a correct diagnosis and cause adverse clinical outcomes. The diagnosis of non-IgE-mediated CMPA is particularly complex as it involves a 2 to 4 week elimination diet followed by oral food challenge (OFC). The Cow\'s Milk-related Symptom Score (CoMiSS) is a clinical resource for primary healthcare providers which aims to increase awareness of CMPA symptoms to facilitate an earlier diagnosis. The aim of the present study is to assess if the CoMiSS can be used as a potential diagnostic tool in infants with suspected CMPA.
    Exclusively formula-fed infants aged 0-6 months presenting with symptoms suggestive of CMPA will be included in this prospective, multicentre trial which will be conducted in 10 centres in China. All infants will commence a 2-week trial of an amino acid-based formula (AAF) while eliminating all cow milk protein from their diets. After the AAF treatment period, infants will undergo an open OFC in hospital with standard cow\'s milk formula, followed by an open home challenge for another 2 weeks. Clinical symptoms will be documented on standardised symptom scorecards. The CoMiSS will be determined at study entry (CoMiSS 1, before the start of the AAF), after 2 weeks (CoMiSS 2, before the OFC) and after a further period of 2 weeks or when symptoms suggestive of CMPA reappear (CoMiSS 3). Weight and length will be measured at each visit. The difference between CoMiSS 1 and 2 as a predictor of the OFC outcome will also be assessed. The diagnostic accuracy of the baseline CoMiSS will be calculated.
    The study was approved by the Hunan Children\'s Hospital Medical Ethics Committee, Hunan, China. The findings of this trial will be submitted for publication in a peer-reviewed journal in paediatric nutrition or gastroenterology. Abstracts will be submitted to the relevant national and international conferences.
    NCT03004729; Pre-results.
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  • 文章类型: Journal Article
    Overactive bladder (OAB) is a common disease. The diagnosis of OAB is based on its symptoms without physiological markers of disease activity. Frequently used assessment methods for OAB include frequency volume chart; urodynamic studies; patient-reported outcomes questionnaires, such as the Overactive Bladder Questionnaire, King\'s Health Questionnaire, patient perception of bladder conditions; and OAB symptom score. The severity of OAB and degree of improvement after treatment can be obtained by comprehensive evaluation. However, a consensus of which evaluations should be used to define the severity of OAB is still lacking. We expect a proper OAB assessment with universal acceptance in the future.
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