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Research on the intelligent internet nursing model based on the child respiratory and asthma control test scale for asthma management of preschool children 被引量:1
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作者 Chuan-Feng Pei Li Zhang +2 位作者 Xi-Yan Xu Zhen Qin Hong-Mei Liang 《World Journal of Clinical Cases》 SCIE 2023年第28期6707-6714,共8页
BACKGROUND Childhood asthma is a common respiratory ailment that significantly affects preschool children.Effective asthma management in this population is particularly challenging due to limited communication skills ... BACKGROUND Childhood asthma is a common respiratory ailment that significantly affects preschool children.Effective asthma management in this population is particularly challenging due to limited communication skills in children and the necessity for consistent involvement of a caregiver.With the rise of digital healthcare and the need for innovative interventions,Internet-based models can potentially offer relatively more efficient and patient-tailored care,especially in children.AIM To explore the impact of an intelligent Internet care model based on the child respiratory and asthma control test(TRACK)on asthma management in preschool children.METHODS The study group comprised preschoolers,aged 5 years or younger,that visited the hospital's pediatric outpatient and emergency departments between January 2021 and January 2022.Total of 200 children were evenly and randomly divided into the observation and control groups.The control group received standard treatment in accordance with the 2016 Guidelines for Pediatric Bronchial Asthma and the Global Initiative on Asthma.In addition to above treatment,the observation group was introduced to an intelligent internet nursing model,emphasizing the TRACK scale.Key measures monitored over a six-month period included the frequency of asthma attack,emergency visits,pulmonary function parameters(FEV1,FEV1/FVC,and PEF),monthly TRACK scores,and the SF-12 quality of life assessment.Post-intervention asthma control rates were assessed at six-month follow-up.RESULTS The observation group had fewer asthma attacks and emergency room visits than the control group(P<0.05).After six months of treatment,the children in both groups had higher FEV1,FEV1/FVC,and PEF(P<0.05).Statistically significant differences were observed between the two groups(P<0.05).For six months,children in the observation group had a higher monthly TRACK score than those in the control group(P<0.05).The PCS and MCSSF-12 quality of life scores were relatively higher than those before the nursing period(P<0.05).Furthermore,the groups showed statistically significant differences(P<0.05).The asthma control rate was higher in the observation group than in the control group(P<0.05).CONCLUSION TRACK based Intelligent Internet nursing model may reduce asthma attacks and emergency visits in asthmatic children,improve lung function,quality of life,and the TRACK score and asthma control rate.The effect of nursing was significant,allowing for development of an asthma management model. 展开更多
关键词 Child respiratory and asthma control test scale Intelligent internet nursing model PRESCHOOLERS Childhood asthma Administration Healthcare
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Correlation between the Childhood-Asthma Control Test and the Criterion for Clinical Asthma Control
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作者 Carlos José Ortiz-Lizcano Jürg Niederbacher-Velásquez Luis Alfonso Díaz-Martínez 《Health》 CAS 2016年第7期623-629,共7页
Setting: Three pediatric pneumatologist offices in Bucaramanga, Colombia. Objective: To establish the concordance between medical criteria and the Childhood-Asthma Control Test (cACT). Design: Study of the assessment ... Setting: Three pediatric pneumatologist offices in Bucaramanga, Colombia. Objective: To establish the concordance between medical criteria and the Childhood-Asthma Control Test (cACT). Design: Study of the assessment of diagnostic technology using transverse sampling. 127 asthma patients aged between 4 and 11 years and their parents filled before clinical evaluation made by a pediatric pneumologist. Patients were classified as controlled or not controlled. Criteria validity was established comparing this classification using Cohen’s kappa and performance indicators according to ROC analysis. Results: 78% of the patients were controlled;patients who are not controlled have a higher score in cACT (mean difference: 3.25 points). Concordance among cACT subscales is acceptable (ρ = 0.554). cACT’s sensitivity was 53.6%, specificity 78.8%, positive likelihood ratio (LR+) 2.53, and negative likelihood ratio (LR-) 0.59. The best cut-off point is 15, with 98% sensitivity, a specificity of 14.3%, LR+ in 1.14, and LR- in 0.14. Conclusions: cACT is a valid tool to determine asthma control in children without replacing medical criteria or other clinical tests. In populations with difficult access to high complexity services, it is useful to decide whether urgent referral to the specialist is necessary. 展开更多
关键词 asthma TREATMENT control Evaluation Childhood-asthma control Test
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Evaluation of Asthma Symptoms to Assess Asthma Control Status in a Primary Care Setting: An Exploratory Analysis of Pooled Data from Three Trials
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作者 Soichiro Hozawa Michikazu Terada Maki Hozawa 《Open Journal of Respiratory Diseases》 2018年第2期21-32,共12页
Background: Primary care physicians in Japan see many patients in a given day;consequently, they find it challenging to devote sufficient time for detailed clinical consultation and evaluation of asthma control status... Background: Primary care physicians in Japan see many patients in a given day;consequently, they find it challenging to devote sufficient time for detailed clinical consultation and evaluation of asthma control status. The aim of this study was to investigate asthma symptoms that reveal the presence of inadequately controlled asthma. Methods: A pooled analysis of baseline data from 100 patients with asthma treated with inhaled corticosteroid(s) (ICS) alone or ICS/long-acting beta-agonist who participated in three previous clinical trials was performed. Asthma control status and asthmatic symptoms were determined using a five-item Asthma Control Questionnaire, and whether asthmatic symptoms reflect clinical markers was investigated. Results: Nocturnal awakening owing to asthmatic symptoms was observed only in the uncontrolled asthma group. Patient-reported wheezing was not observed in the group with well-controlled asthma, but was observed in all patients in the uncontrolled asthma group. Virtually all patients, irrespective of asthma control status, reported symptoms in the morning, limitation of normal daily activities, and shortness of breath. Conclusions: The presence of nocturnal awakening due to asthma and wheezing likely reflected uncontrolled asthma. These results will lead to re-recognition that clinical interview, querying nocturnal awakening from asthma and wheezing is a simple and useful approach to assess asthma control status in a primary care setting. 展开更多
关键词 asthma control STATUS asthma control Questionnaire NOCTURNAL AWAKENING WHEEZING Primary Care
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Current asthma control predicts future risk of asthma exacerbation: a 12-month prospective cohort study 被引量:9
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作者 WEI Hua-hua ZHOU Ting +5 位作者 WANG Lan ZHANG Hong-ping FU Juan-juan WANG Lei JI Yu-lin WANG Gang 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第17期2986-2993,共8页
Background The performance of asthma control test (ACT) at baseline for predicting future risk of asthma exacerbation has not been previously demonstrated. This study was designed to explore the ability of the basel... Background The performance of asthma control test (ACT) at baseline for predicting future risk of asthma exacerbation has not been previously demonstrated. This study was designed to explore the ability of the baseline ACT score to predict future risk of asthma exacerbation during a 12-month follow-up. Methods This post hoc analysis included data from a 12-month prospective cohort study in patients with asthma (n=290). The time to the first asthma exacerbation was analyzed and the association between baseline ACT scores and future risk of asthma exacerbation was calculated as adjusted odds ratio (OR) using Logistic regression models. Further, sensitivity and specificity were estimated at each cut-point of ACT scores for predicting asthma exacerbations. Results The subjects were divided into three groups, which were uncontrolled (U, n=128), partly-controlled (PC, n=111), and well controlled (C, n=51) asthma. After adjustment, the decreased ACT scores at baseline in the U and PC groups were associated with an increased probability of asthma exacerbations (OR 3.65 and OR 5.75, respectively), unplanned visits (OR 8.03 and OR 8.21, respectively) and emergency visits (OR 20.00 and OR 22.60, respectively) over a 12-month follow-up period. The time to the first asthma exacerbation was shorter in the groups with U and PC asthma (all P 〈0.05). The baseline ACT of 20 identified as the cut-point for screening the patients at high risk of asthma exacerbations had an increased sensitivity of over 90.0% but a lower specificity of about 30.0%. Conclusion Our findings indicate that the baseline ACT score with a high sensitivity could rule out patients at low risk of asthma exacerbations and predict future risk of asthma exacerbations in clinical practice. 展开更多
关键词 asthma control test future risk asthma exacerbation
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Impact of guideline adherence and race on asthma control in children
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作者 Shahid I.Sheikh Nancy A.Ryan-Wenger +3 位作者 Judy Pitts Rodney Britt Jr Grace Paul Lisa Ulrich 《World Journal of Pediatrics》 SCIE CAS CSCD 2021年第5期500-507,共8页
Background Asthma control in African Americans(AA)is considered more difficult to achieve than in Caucasian Americans(CA).The aim of this study was to compare asthma control over time among AA and CA children w hose a... Background Asthma control in African Americans(AA)is considered more difficult to achieve than in Caucasian Americans(CA).The aim of this study was to compare asthma control over time among AA and CA children w hose asthma is managed per NAEPP(EPR-3)guidelines.Methods This was a one-year prospective study of children referred by their primary care physicians for better asthma care in a specialty asthma clinic.All children received asthma care per NAEPP guidelines.Results were compared between CA and AA children at baseline and then at three-month intervals for one year.Results Of the 345 children,ages 2-17 years(mean=6.2±4),220(63.8%)were CA and 125(36.2%)were AA.There were no significant differences in demographics other than greater pet ownership in CA families.At baseline,AA children had significantly more visits to the Emergency Department for acute asthma symptoms(mean=2.3±3)compared to CA(1.4±23,P=0.003).There were no other significant differences in acute care utilization,asthma symptoms(mean days/month),or mean asthma control test(ACT)scores at base line.Within 3-6 months,in both groups,mean ACT scores,asthma symptoms and acute care utilization significantly improved(P<0.05 for all)and change over time in both groups was comparable except for a significantly greater decrease in ED visits in AA children compared to CA children(P=002).Conclusion Overall,improvement in asthma control during longitudinal assessment was similar between AA and CA children because of consistent use of NAEPP asthma care guidelines. 展开更多
关键词 asthma asthma control CHILDREN Guideline adherence RACE
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Curative effect of heat-sensitive moxibustion on chronic persistent asthma: a multicenter randomized controlled trial 被引量:21
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作者 Rixin Chen Mingren Chen +13 位作者 Jun Xiong Zhenhai Chi B0 Zhang Ning Tian Zhenhua Xu Tangfa Zhang Wanyao Li Wei Zhang Xiaofeng Rong Zhen Wang Gang Sun Baohe Ge Guoxiong Yu Nanchang Song 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2013年第5期584-591,共8页
OBJECTIVE:To compare the curative effects of heat-sensitive moxibustion with conventional drugs on chronic persistent asthma and seek a valuable therapy to replaceWestern Medicine.METHODS:The participants in this mult... OBJECTIVE:To compare the curative effects of heat-sensitive moxibustion with conventional drugs on chronic persistent asthma and seek a valuable therapy to replaceWestern Medicine.METHODS:The participants in this multi-center,randomized,and controlled study were randomly divided into two groups:group A(n=144),treated with heat-sensitive moxibustion(50 sessions)and group B(n=144),treated with Seretide(salmeterol50μg/fluticasone 250μg,twice a day).The scores of asthma control test(ACT),forced expiratory volume in 1 second(FEV1),peak expiratory flow(PEF),and attack frequency were measured after 15,30,60,and 90 days of treatment.Patients followed up3 and 6 months after treatment.RESULTS:There was a significant difference(P=0.0002)in the ACT score and lung function between the two groups after 3 months of treatment and(P=0.000 03)during the follow-up visits.In addition,heat-sensitive moxibustion reduced attack frequency in the period from inclusion to the6-month follow-up visit.CONCLUSION:This study shows that heat-sensitive moxibustion may have a comparable curative effect toSeretide(salmeterol/fluticasone)on asthma. 展开更多
关键词 Moxibustion asthma Randomized controlled trial Heat sensitive Seretide
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Evaluation of asthma control: a questionnaire-based survey in China 被引量:5
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作者 Su Nan Lin Jiangtao +8 位作者 Chen Ping Li Jing Wu Changgui Yin Kaisheng Liu Chuntao Chen Yiqiang Zhou Xin Yuan Yadong Huang Xingang 《Chinese Medical Journal》 SCIE CAS CSCD 2014年第11期2030-2036,共7页
Background Little is known about asthma control and perception of asthma among asthmatic patients in China.This study marked the first survey conducted on a national scale that aimed at obtaining baseline information ... Background Little is known about asthma control and perception of asthma among asthmatic patients in China.This study marked the first survey conducted on a national scale that aimed at obtaining baseline information on asthma control and patients' perception of asthma and providing a point of reference for future studies.Methods This face-to-face,questionnaire-based survey was conducted from April 2007 to March 2008 with 3 069 asthmatic patients from the respiratory outpatient clinics of 36 general hospitals located in 10 geographically dispersed cities.Results Consistent with the Global Initiative for Asthma (GINA) guidelines,28.7% and 45.0% of our patients achieved control and partial control,respectively.Of the patients in the study,only 21.8% had used a peak flow meter (PFM),and 6.6% of these patients used it daily.Inhaled corticosteroids (ICS) plus a long-acting β2 agonist (LABA) and ICS were the two most common medication regimens and were used in 45.6% and 30.4% of patients,respectively.Asthma had a significant effect on the patients' life and work.A considerable number of hospitalizations,emergency department visits,and sick days were observed.Conclusion Despite improvements in asthma control and ICS and PFM compliance compared with past literature,the current level of asthma control countrywide continues to fall short of the goals set in the GINA. 展开更多
关键词 asthma QUESTIONNAIRE control MANAGEMENT
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T-Helper I Cell/T-Helper 2 Cell Balance with Anti Inflammatory Therapy in Partly Controlled Asthmatic Children
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作者 Gamal Abdel Naser Yamamah Hala Hamdy Shaaban +3 位作者 Emad Ezzat Salama Nevine El Helaly Solaf Kamel Elham Mostafa 《Journal of Life Sciences》 2012年第11期1206-1213,共8页
The authors aimed to assess Thl (T-helper cell 1)/Th2 (T-helper cell 2) balance, through evaluation of serum IFN-γ (interferon gamma) and IL-4 (interleukin 4), during asthma exacerbation and study the effect ... The authors aimed to assess Thl (T-helper cell 1)/Th2 (T-helper cell 2) balance, through evaluation of serum IFN-γ (interferon gamma) and IL-4 (interleukin 4), during asthma exacerbation and study the effect of anti inflammatory therapy. A randomized prospective case-control study was designed. The sludy included 30 asthmatic patients, aging 8-14 years. All were diagnosed as partly controlled asthmatics. Twenty, age and sex matched, healthy children were included in the study as control group All participants were subjected to medical history, clinical examination, pulmonary function testing, eosinophilic blood counting, estimation of serum interleukine-4 and interferon gamma. Patients were treated for 6 weeks with 2 different anti inflammatory drugs. All methods were then repeated for follow up. IL-4 serum level was significantly higher in subjects with partly controlled asthma than in control subjects (P = 0.01), and then in asthmatic patients after therapy (P = 0.0000), while IFN-), serum level was significantly lower in subjects with partly controlled asthma than in control subjects (P = 0.01), and than in asthmatic patients after therapy (P = 0.0000). Interferon gamma showed a significant negative correlation with IL-4 among the healthy control group (r = -0.559, P = 0.010). Both LTA (leukotriene antagonist) and ICS (inhaled corticosteroids) therapy lead to significant improvement, but there were no statistically significant differences (P 〉 0.05) between them as regard the pulmonary functions and the laboratory evaluating parameters. Both serum levels of IL-4 and IFN-γ, could be used as a reliable inflammatory biomarker for the evaluation and follow up of asthmatic patients. 展开更多
关键词 THL TH2 IFN-γ IL-4 partly controlled asthma LTA ICS.
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难治性哮喘发作患儿哮喘控制水平及其影响因素的潜在剖面分析
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作者 易享 彭小燕 肖宁 《全科护理》 2026年第5期976-980,共5页
目的:探讨难治性哮喘发作患儿的哮喘控制水平及其潜在影响因素,为临床精准识别个体特征并制定针对性护理干预策略提供理论依据。方法:选取2023年1月—2024年12月在某三级甲等医院儿科就诊的281例难治性哮喘发作患儿为研究对象。通过一... 目的:探讨难治性哮喘发作患儿的哮喘控制水平及其潜在影响因素,为临床精准识别个体特征并制定针对性护理干预策略提供理论依据。方法:选取2023年1月—2024年12月在某三级甲等医院儿科就诊的281例难治性哮喘发作患儿为研究对象。通过一般资料调查表收集患儿一般资料,采用儿童抑郁症和焦虑障碍自评量表(SDS‑C、SAS‑C)评估患儿心理状态,采用哮喘药物依从性报告量表(MARS‑A)评估患儿用药依从性,采用哮喘控制测试(ACT)量表评估哮喘控制水平。使用Mplus 8.3软件进行潜在剖面分析,通过单因素分析和多因素Logistic回归分析筛选和探讨影响因素。结果:潜在剖面分析将患儿分为轻度控制不良组(30.25%)、中度控制不良组(38.79%)和重度控制不良组(30.96%)。多因素Logistic回归分析显示,暴露于二手烟、哮喘病程、规律使用吸入性糖皮质激素情况、用药依从性、抑郁和焦虑是影响患儿哮喘控制水平类别的影响因素(P<0.05)。结论:难治性哮喘发作患儿的哮喘控制水平存在明显的差异,且受多种因素影响。护理人员应针对患儿的个体特征,制定个性化的护理干预措施,以提高哮喘控制水平,改善患儿预后。 展开更多
关键词 难治性哮喘 哮喘控制水平 影响因素 潜在剖面分析
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中药治疗儿童咳嗽变异性哮喘随机对照试验设计的分析与思考
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作者 卢宣君 王继萱 +5 位作者 胡思源 柳平 郜统勋 梁浩东 曾静 栾奕博 《药物评价研究》 北大核心 2026年第1期8-21,共14页
目的 通过分析近10年中药治疗儿童咳嗽变异性哮喘(CVA)的随机对照试验(RCT),思考现存问题并提出解决策略,为儿童CVA中药临床试验设计提供参考。方法 系统检索中国学术期刊全文数据库(CNKI)、万方数据库(Wanfang Data)、中国生物医学文... 目的 通过分析近10年中药治疗儿童咳嗽变异性哮喘(CVA)的随机对照试验(RCT),思考现存问题并提出解决策略,为儿童CVA中药临床试验设计提供参考。方法 系统检索中国学术期刊全文数据库(CNKI)、万方数据库(Wanfang Data)、中国生物医学文献数据库(SinoMed)、维普生物医学数据库(VIP)、PubMed、Web of Science、Embase、Cochrane Library及临床试验注册平台中关于中药治疗儿童CVA的RCT文献,对纳入文献进行质量评价,分析基本特征,思考问题与对策。结果 共纳入82项RCT研究,ROB 2.0偏倚风险评估显示72项“有一定风险”、5项“高风险”、5项“低风险”。纳入研究的样本量为8 772例,随机方法中以简单随机法居多(51项),7项实施了盲法,3项进行了分配隐藏,疗程集中在1个月及以内(54项),干预措施以中药联用化学药为主(66项)。共报告127种结局指标,分为7类,包括症状/体征(18种)、中医病证(5种)、理化检测(79种)、生活质量(7种)、远期预后(8种)、安全性事件(8种)、其他指标(2种)。结论 中药治疗儿童CVA的RCT设计需进一步提升疾病认识、规范研究设计、明确临床定位、精准诊断辨证、重视结局指标,提高方法学质量,进而开展设计严谨的RCT,为中药治疗儿童CVA提供循证依据。 展开更多
关键词 咳嗽变异性哮喘 中药 儿童 随机对照试验 结局指标
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学龄期支气管哮喘发作患儿症状控制现状及其影响因素的潜在剖面分析
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作者 肖宁 易享 彭小燕 《全科护理》 2026年第1期182-186,共5页
目的:对学龄期支气管哮喘发作患儿症状控制现状进行潜在剖面分析,并探讨其影响因素。方法:采用一般资料调查表、哮喘控制测试量表、儿童焦虑性情绪障碍筛查表和儿童抑郁障碍自评量表对182例学龄期支气管哮喘发作患儿进行调查。结果:学... 目的:对学龄期支气管哮喘发作患儿症状控制现状进行潜在剖面分析,并探讨其影响因素。方法:采用一般资料调查表、哮喘控制测试量表、儿童焦虑性情绪障碍筛查表和儿童抑郁障碍自评量表对182例学龄期支气管哮喘发作患儿进行调查。结果:学龄期支气管哮喘发作患儿症状控制类别包括低症状控制组(28.57%)、中等症状控制组(41.76%)和高症状控制组(29.67%)3个类别。Logistic回归分析结果显示,患儿病程、使用吸入性糖皮质激素、用药依从性、居住地空气污染情况、焦虑和抑郁均是支气管哮喘发作患儿症状控制类别的影响因素(P<0.05)。结论:学龄期支气管哮喘发作患儿症状控制类别存在异质性,病程、使用吸入性糖皮质激素、用药依从性、居住地空气污染情况、焦虑和抑郁均是支气管哮喘发作患儿症状控制类别的影响因素。医护人员应根据不同类别的学龄期支气管哮喘发作患儿症状控制水平及其影响因素制订个性化干预方案。 展开更多
关键词 学龄期 支气管哮喘 症状控制 潜在剖面分析
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Asthma Patient Care: The Pharmacist’s Perspective
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作者 Rana Rasheed Farrag Mamdouh Ahmed Zaki +1 位作者 Taher El-Naggar Manal El-Hamamsy 《Pharmacology & Pharmacy》 2014年第6期551-559,共9页
Aim of the Study: To compare effect of asthma care by pharmacist intervention versus routine care on asthma control. Patients and Methods: A 2-month randomised, controlled trial was conducted in outpatient clinics of ... Aim of the Study: To compare effect of asthma care by pharmacist intervention versus routine care on asthma control. Patients and Methods: A 2-month randomised, controlled trial was conducted in outpatient clinics of Ain Shams University Hospitals, Cairo, Egypt. Patients were randomly assigned to receive routine care or a pre-defined pharmacist intervention. This intervention was mainly focused on patient education, improving inhalation technique and medication assessment. Primary outcome was the level of asthma control, as assessed by the Asthma Control Questionnaire (ACQ). Results: By the end of the study, intervention patients who received a written action plan significantly improved their ACQ results than routine care group who did not receive a plan (p < 0.0001). Inhalation technique and adherence to controller medication were significantly better in the intervention group. Conclusion: The present study results provide supportive evidence concerning pharmacists’ favourable effects on asthma patient care and support pharmacists as valuable members of the health care team. 展开更多
关键词 asthma control QUESTIONNAIRE asthma Action PLAN Patient Education ADHERENCE INHALATION Technique
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大剂量布地奈德联合沙丁胺醇治疗支气管哮喘急性发作期的临床效果及对炎性指标的影响 被引量:1
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作者 李穗华 陈智如 +3 位作者 全佳 李娜梅 范翠苗 谭文惠 《临床合理用药》 2025年第15期7-10,共4页
目的观察大剂量(2 mg)布地奈德联合沙丁胺醇治疗支气管哮喘急性发作期患者的临床效果及对超敏C反应蛋白(hs-CRP)、缺氧诱导因子-1α(HIF-1α)等炎性因子水平的影响。方法将2021年2月—2024年2月于广东省第二人民医院就诊的支气管哮喘急... 目的观察大剂量(2 mg)布地奈德联合沙丁胺醇治疗支气管哮喘急性发作期患者的临床效果及对超敏C反应蛋白(hs-CRP)、缺氧诱导因子-1α(HIF-1α)等炎性因子水平的影响。方法将2021年2月—2024年2月于广东省第二人民医院就诊的支气管哮喘急性发作期80例,根据随机数字表法分为试验组和对照组,每组40例。对照组采用小剂量(1 mg)吸入用布地奈德混悬液联合沙丁胺醇气雾剂治疗,试验组采用大剂量(2 mg)吸入用布地奈德混悬液联合沙丁胺醇气雾剂治疗,2组均治疗1周。比较2组临床症状消失时间,治疗前后肺功能指标[呼气流量峰值(PEF)、第1秒用力呼气容积(FEV_(1))、一秒率(FEV_(1)/FVC)]、哮喘控制测试量表(ACT)评分、炎性因子[hs-CRP、肿瘤坏死因子-α(TNF-α)、白介素-6(IL-6)、HIF-1α]。结果试验组气促、咳嗽、喘息、胸闷消失时间均短于对照组(P<0.01)。治疗1周后,2组PEF、FEV_(1)、FEV_(1)/FVC均增高,且试验组高于对照组(P<0.01);2组ACT评分均升高,且试验组高于对照组(P<0.01);2组血清hs-CRP、TNF-α、IL-6、HIF-1α水平均降低,且试验组低于对照组(P<0.01)。结论大剂量布地奈德对支气管哮喘急性发作期患者的治疗效果更加显著,能有效减短症状消失时间,改善肺功能,控制哮喘和炎性反应。 展开更多
关键词 支气管哮喘 布地奈德 沙丁胺醇 哮喘控制测试量表 炎性因子 缺氧诱导因子-1Α
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补充维生素D对支气管哮喘急性发作期患儿肺功能的影响 被引量:1
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作者 王辉 杨波 《临床误诊误治》 2025年第8期68-72,共5页
目的探讨补充维生素D(VD)治疗对支气管哮喘急性发作期患儿肺功能的影响。方法选取2021年1月至2022年6月儿科门诊收治的80例支气管哮喘急性发作期患儿,采用随机数字表法分为观察组和对照组各40例。对照组在常规治疗基础上给予布地奈德气... 目的探讨补充维生素D(VD)治疗对支气管哮喘急性发作期患儿肺功能的影响。方法选取2021年1月至2022年6月儿科门诊收治的80例支气管哮喘急性发作期患儿,采用随机数字表法分为观察组和对照组各40例。对照组在常规治疗基础上给予布地奈德气雾剂雾化吸入治疗,观察组在对照组基础上给予维生素D滴剂治疗,2组均治疗8周。比较2组临床症状、体征消失时间,治疗前后嗜酸粒细胞(EOS)、总免疫球蛋白E(TIgE)、血清25-羟维生素D 3[25-(OH)D 3]水平,治疗前后第1秒用力呼气容积(FEV1)、FEV1占用力肺活量比值(FEV1/FVC)、呼气峰值流速(PEF)、呼气高峰流量(PEFR),治疗前后儿童哮喘控制测试(C-ACT)评分、儿童生命质量量表(PedsQL)哮喘模块评分,以及治疗期间不良反应。结果观察组气喘、咳嗽、呼吸困难、肺哮鸣音消失时间均短于对照组(P<0.01)。治疗后,2组EOS、TIgE均低于治疗前(P<0.05),但组间比较无差异(P>0.05);治疗后,观察组25-(OH)D 3水平高于治疗前,且高于对照组(P<0.05,P<0.01)。治疗后,2组FEV1、FEV1/FVC、PEF、PEFR水平均高于治疗前,且观察组高于对照组(P<0.05,P<0.01)。治疗后,2组C-ACT评分、PedsQL哮喘模块评分均高于治疗前(P<0.05),但组间比较无差异(P>0.05)。治疗期间观察组不良反应发生率为20.00%(8/40),对照组为17.50%(7/40),比较差异无统计学意义(P>0.05)。结论补充VD治疗可明显缩短支气管哮喘急性发作期患儿临床症状体征持续时间,提高肺功能,且安全性较好。 展开更多
关键词 支气管哮喘 急性发作 儿童 维生素D 嗜酸粒细胞 第1秒用力呼气容积 儿童哮喘控制测试 药物毒性
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丹龙口服液治疗支气管哮喘(热哮证)安全性和有效性的临床研究
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作者 李得民 吕天宜 +7 位作者 雷翔 李文军 王新民 查日田 靳端阳 黄燕 疏欣杨 张洪春 《世界中医药》 北大核心 2025年第1期125-129,共5页
目的:评价丹龙口服液在广泛使用条件下治疗支气管哮喘(热哮证)的安全性和有效性。方法:选择符合入组条件的支气管哮喘热哮证受试者2000例,受试者在接受常规治疗的基础上,口服丹龙口服液,1支(10 mL)/次,3次/d,持续7 d。比较干预前后受试... 目的:评价丹龙口服液在广泛使用条件下治疗支气管哮喘(热哮证)的安全性和有效性。方法:选择符合入组条件的支气管哮喘热哮证受试者2000例,受试者在接受常规治疗的基础上,口服丹龙口服液,1支(10 mL)/次,3次/d,持续7 d。比较干预前后受试者中医证候积分、肺功能检查、哮喘控制问卷评分(ACQ)等疗效指标的改善情况及不良事件发生率、血常规、尿常规、血生化及十二导联心电图等安全性指标变化情况。结果:受试者基线期中医证候总积分为(11.49±3.37)分,治疗后中医证候总积分相对基线的变化值为(-6.50±3.68)分,差异有统计学意义(P<0.0001)。受试者基线期肺功能指标第1秒用力呼气容积(FEV_(1))、用力肺活量(FVC)、FEV_(1)/用力肺活量(FVC)、最大呼气中期流量(MMEF)、呼气峰值流量(PEF)值分别为(1.69±0.75)L、(2.59±0.90)L、(77.15±16.33)%、(1.37±0.81)L/s、(3.18±2.24)L/s,治疗后相对于基线的变化值分别为(0.30±0.38)L、(0.29±0.40)L、(6.51±12.16)%、(0.37±0.69)L/s、(0.60±1.51)L/s,差异有统计学意义(P<0.0001)。受试者基线期ACQ平均分为(1.61±0.51)分,治疗后相对基线的变化值为(-0.76±0.42)分,差异有统计学意义(P<0.0001)。相关不良事件发生42例55例次,发生率为2.10%。相关不良事件的严重程度为“1级”35例(1.75%),“2级”8例(0.40%)。结论:丹龙口服液具有缓解热哮证症状、改善肺功能、提高哮喘控制水平的作用,且安全性良好。 展开更多
关键词 丹龙口服液 支气管哮喘 热哮证 广泛人群 中医证候积分 肺功能 哮喘控制水平 安全性
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针刺治疗支气管哮喘急性发作期临床疗效的meta分析 被引量:2
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作者 刘祁祁 刘俊麟 +2 位作者 杨洋 曹文心 李竹英 《海南医科大学学报》 北大核心 2025年第6期443-456,共14页
目的:通过meta分析综合评价针刺对支气管哮喘急性发作期的临床疗效。方法:通过计算机检索8个数据库(PubMed、Embase、Web of Science、The Cochrane Library、中国生物医学文献数据库、维普数据库、中国知网和万方)从建库至2024年10月1... 目的:通过meta分析综合评价针刺对支气管哮喘急性发作期的临床疗效。方法:通过计算机检索8个数据库(PubMed、Embase、Web of Science、The Cochrane Library、中国生物医学文献数据库、维普数据库、中国知网和万方)从建库至2024年10月1日针刺治疗哮喘急性发作期的随机对照试验。2名研究员独立评估纳入文献的质量并提取数据。使用RevMan 5.4对数据进行合并和分析。二分类结果以风险比(RR)报告,连续结果以均数差(SD)/标准化均数差(SMD)报告,均报告95%CI。采用Cochrane工具评估偏倚风险,采用GRADE方法对证据质量进行评级。结果:共纳入19项随机对照试验,涉及2137名患者。meta分析结果显示:针刺治疗后的有效率[RR=2.01,95%CI(1.32,3.06),n=90,I^(2)=0%,P=0.001,低质量]优于假针,针刺治疗后的中医症状体征总积分[MD=−5.99,95%CI(−9.32,−2.66),n=90,I^(2)=93%,P=0.0004,低质量]低于假针。与药物治疗相比,针刺可提高治疗后的的IFN‑γ水平[SMD=0.27,95%CI(0.02,0.53),n=249,P=0.04,I^(2)=3%,低质量],FVC[SMD=0.54,95%CI(0.15,0.94),n=233,I^(2)=52%,P=0.006,极低质量],降低治疗后中医症状体征总积分[MD=−1.04,95%CI(−1.76,−0.32),n=606,I^(2)=76%,P<0.00001,低质量]。但是,针刺对治疗后有效率[RR=1.11,95%CI(0.98,1.26),n=1006,I^(2)=94%,P=0.11,极低质量]、FEV1[SMD=0.10,95%CI(−0.29,0.49),n=1329,I^(2)=90%,P=0.61,极低质量]、FEV1/FVC[MD=1.40,95%CI(−2.45,5.25),n=840,I^(2)=71%,P=0.47,极低质量]、PEF[SMD=0.13,95%CI(−0.23,0.48),n=1239,I^(2)=87%,P=0.49,极低质量]和IL‑4[SMD=−0.43,95%CI(−1.04,0.18),n=249,I^(2)=82%,P=0.17,极低质量]与药物治疗相比几乎没有差异。针刺联合对照可提高治疗的有效率[RR=1.22,95%CI(1.13,1.32),n=418,I^(2)=0%,中质量]、IFN‑γ[MD=4.96,95%CI(3.23,6.68),n=234,I^(2)=43%,P<0.00001,低质量]和治疗后肺功能,包括FVC[SMD=0.57,95%CI(0.31,0.83),n=234,I^(2)=0%,P<0.00001,低质量]、FEV1[SMD=1.03,95%CI(0.31,1.76),n=464,I^(2)=92%,P=0.005,低质量]和PEF[SMD=1.27,95%CI(0.23,2.31),n=288,I^(2)=94%,P=0.02,极低质量]。但与对照组相比联合治疗对治疗后FEV1/FVC[MD=11.54,95%CI(−1.03,24.11),n=230,I^(2)=97%,P=0.07,极低质量]和治疗后IL‑4水平[MD=−8.78,95%CI(−18.31,0.76),n=234,I^(2)=90%,P=0.07,极低质量]几乎没有差异。结论:证据表明针刺在治疗急性哮喘加重期可能比假针灸更有效。联用针刺的综合疗法在提高治疗的有效率、改善肺功能以及促进IFN‑γ表达比单用药物更有效。然而,研究之间的证据强度较低,需要新的高质量研究来提供更明确的证据。 展开更多
关键词 针刺 支气管哮喘 META分析 随机对照试验
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青海省儿童支气管哮喘病情控制情况的影响因素分析 被引量:2
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作者 董玥阳 赵海燕 +2 位作者 任屹东 焦雨 周玲 《安徽医药》 2025年第4期705-709,共5页
目的评估青海省5~14岁儿童支气管哮喘控制情况,并分析影响病情的相关因素,为疾病预防及病情的控制提供理论依据。方法选取2021年10月至2023年6月青海大学附属医院90例患有支气管哮喘的5~14岁儿童,以问卷形式收集病儿及其主要看护人一般... 目的评估青海省5~14岁儿童支气管哮喘控制情况,并分析影响病情的相关因素,为疾病预防及病情的控制提供理论依据。方法选取2021年10月至2023年6月青海大学附属医院90例患有支气管哮喘的5~14岁儿童,以问卷形式收集病儿及其主要看护人一般信息,采用儿童哮喘控制测试(C-ACT)评估哮喘控制水平,分为完全控制组与未完全控制组,采用单、多因素分析对哮喘影响病情控制情况的因素进行分析。结果调查共90例儿童,问卷完成率为100%,完全控制组61例(67.78%),未完全控制组29例(32.22%);经单因素分析显示,过敏史、用药依从性、近1个月反复呼吸道感染史和浮尘或沙尘天气,差异有统计学意义(P<0.05)。采用多因素logistic回归分析显示,过敏史[OR=3.06,95%CI:(1.06,8.82),P<0.05]、用药依从性[OR=4.11,95%CI:(1.42,11.90),P<0.05]、近1月反复呼吸道感染史[OR=3.51,95%CI:(1.21,10.16),P<0.05]、浮尘或沙尘天气[OR=3.18,95%CI:(1.04,9.75),P<0.05]是影响哮喘控制的危险因素。结论青海省儿童支气管哮喘病情控制不佳,过敏史、用药依从性、反复呼吸道感染史和浮尘或沙尘天气等是病情控制不佳的不良因素,应对以上因素进行针对性的预防,从而更有效地控制病情。 展开更多
关键词 哮喘 儿童 病情控制 影响因素 青海省
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自我效能理论指导的肺康复训练在支气管哮喘患者中的应用 被引量:1
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作者 钱海碧 梁桂兴 《中国当代医药》 2025年第22期155-159,共5页
目的探讨自我效能理论指导的肺康复训练在支气管哮喘患者中的应用效果。方法回顾性分析2023年12月至2024年12月广东省中医院呼吸科收治的64例支气管哮喘患者的临床资料,按照不同干预方法分为观察组和对照组,每组32例。对照组实施常规护... 目的探讨自我效能理论指导的肺康复训练在支气管哮喘患者中的应用效果。方法回顾性分析2023年12月至2024年12月广东省中医院呼吸科收治的64例支气管哮喘患者的临床资料,按照不同干预方法分为观察组和对照组,每组32例。对照组实施常规护理,观察组在对照组的基础上实施自我效能理论指导的肺康复训练。比较两组患者的自我效能(GSES)、肺康复训练依从性、肺功能指标及哮喘控制情况。结果干预后,两组患者GSES评分、用力肺活量、第1秒用力呼气容积及呼气流量峰值均高于本组干预前,且观察组指标均高于对照组,差异有统计学意义(P<0.05)。观察组肺康复训练总依从率、哮喘总控制率均高于对照组,差异有统计学意义(P<0.05)。结论自我效能理论指导的肺康复训练可有效提高支气管哮喘患者的自我效能和训练依从性,改善肺功能和哮喘控制效果。 展开更多
关键词 自我效能 肺康复训练 支气管哮喘 依从性 哮喘控制
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慢性鼻窦炎控制评估标准研究进展 被引量:2
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作者 张玥 杨玉成 《中国眼耳鼻喉科杂志》 2025年第1期78-82,84,共6页
慢性鼻窦炎(CRS)是发生于鼻腔鼻窦黏膜的一种高度异质性的慢性炎症性疾病,复发率高,严重影响患者的生活质量。目前仍无根治手段。欧洲鼻窦炎和鼻息肉意见书(EPOS)借鉴哮喘的诊疗经验,提出将CRS作为慢性疾病进行长期管理,引入疾病控制的... 慢性鼻窦炎(CRS)是发生于鼻腔鼻窦黏膜的一种高度异质性的慢性炎症性疾病,复发率高,严重影响患者的生活质量。目前仍无根治手段。欧洲鼻窦炎和鼻息肉意见书(EPOS)借鉴哮喘的诊疗经验,提出将CRS作为慢性疾病进行长期管理,引入疾病控制的概念,从此确立了CRS治疗的新目标;期望通过制订出最佳的CRS控制评估标准,用以评估疾病负担、指导治疗、评估疗效。截至目前,CRS控制评估标准仍处于发展阶段,尚未形成统一的标准,以EPOS提出的控制评级研究最为充分,应用最为广泛。本文对CRS的控制评估发展背景及现状进行介绍并做一综述,为CRS控制评估在中国的应用与发展提供参考。 展开更多
关键词 慢性鼻窦炎 哮喘 疾病控制 疾病管理 疾病严重程度
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标准化病历管理云平台联合互联网医院应用于儿童哮喘管理的效果评价 被引量:1
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作者 刘丹 钟礼立 +3 位作者 杨图宏 吴记梅 覃霞 何艳 《中国医药科学》 2025年第8期89-93,共5页
目的探讨标准化病历管理云平台联合互联网医院应用于儿童哮喘管理的效果评价。方法选取2022年1—12月在湖南省人民医院儿童哮喘标准化门诊诊断为哮喘并加入儿童哮喘标准化病历管理云平台的160例患儿作为研究对象,进行为期1年的管理,对... 目的探讨标准化病历管理云平台联合互联网医院应用于儿童哮喘管理的效果评价。方法选取2022年1—12月在湖南省人民医院儿童哮喘标准化门诊诊断为哮喘并加入儿童哮喘标准化病历管理云平台的160例患儿作为研究对象,进行为期1年的管理,对入组患儿的肺功能指标、儿童哮喘控制测试(C-ACT)、哮喘症状控制水平分级进行随访。比较管理前后哮喘患儿指标的变化。结果与管理前比较,管理后的哮喘患儿肺功能和控制水平整体改善。FEV_(1)/FVC的实测值/预测值在管理6、12个月较管理前升高,差异有统计学意义(P<0.05);PEF、FEF50、FEF75和MMEF在管理3、6和12个月均高于管理前,差异有统计学意义(P<0.05)。C-ACT评分在管理3、6和12个月后较管理前均提高,差异有统计学意义(P<0.01)。良好控制率在管理6、12个月后较管理前均提高,差异有统计学意义(P<0.05)。结论标准化病历管理云平台联合互联网医院应用于儿童哮喘的管理是目前线下管理模式的一种重要补充,能有效提高哮喘儿童的肺功能及哮喘控制水平,值得推广。 展开更多
关键词 儿童哮喘 标准化病历管理云平台 互联网医院 肺功能 控制水平
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