fan therapy

  • 文章类型: Journal Article
    介绍Fan疗法作为缓解接受姑息治疗的患者和患有慢性进行性疾病的患者的呼吸困难的非药物治疗方法而受到关注。然而,风扇治疗对重症监护病房(ICU)危重患者呼吸困难的有效性尚不清楚.本研究旨在探讨风扇疗法对ICU肺移植患者的疗效和安全性。方法对ICU住院期间呼吸困难的肺移植受者(年龄>18岁)进行风扇治疗。使用台式便携式风扇在患者的脸上吹气五分钟,提供风扇治疗。确定风扇治疗前后呼吸困难的强度,使用配对t检验进行统计学分析以评估变化。结果2023年5月至2024年2月,筛选了16例肺移植后入住ICU的患者,八名病人接受风扇治疗。在术后第12天的中位数进行风扇治疗。7例患者(87.5%)通过气管切开术接受了机械通气。风扇治疗前后呼吸困难的平均(±标准偏差)数字评定量表(NRS)分别为5.6±2.3和4.4±1.5(p=0.08)。风扇治疗前后的平均(±标准差)呼吸窘迫观察量表(RDOS)分别为4.8±2.0和3.8±1.7(p=0.03)。未观察到严重不良事件,呼吸频率没有明显变化,氧饱和度,脉搏率,或血压。结论风扇疗法可以安全地缓解肺移植受者在ICU住院期间的呼吸困难。需要在更大的试验中进一步评估以确认本研究的结果。
    Introduction Fan therapy has gained attention as a non-pharmacological treatment for alleviating dyspnea in patients receiving palliative care and in those with chronic progressive diseases. However, the effectiveness of fan therapy for dyspnea in critically ill patients in intensive care units (ICUs) remains unclear. This study aimed to investigate the efficacy and safety of fan therapy for lung transplant patients in the ICU. Methods Fan therapy was performed on lung transplant recipients (age >18 years) who experienced dyspnea during their ICU stay. A tabletop portable fan was used to blow air on the patient\'s face for five minutes providing fan therapy. The intensity of dyspnea before and after the fan therapy was determined, and a statistical analysis was conducted using a paired t-test to evaluate the changes. Results Between May 2023 and February 2024, 16 patients who were admitted to the ICU following lung transplantation were screened, and eight patients received fan therapy. Fan therapy was performed at a median of postoperative day 12. Seven patients (87.5%) received mechanical ventilation via tracheostomy. The mean (±standard deviation) numerical rating scale (NRS) for dyspnea before and after fan therapy was 5.6±2.3 and 4.4±1.5, respectively (p = 0.08). The mean (±standard deviation) respiratory distress observation scale (RDOS) before and after fan therapy was 4.8 ± 2.0 and 3.8 ± 1.7, respectively (p = 0.03). No serious adverse events were observed, and no significant alterations were observed in the respiratory rate, oxygen saturation levels, pulse rate, or blood pressure. Conclusion The findings suggest that fan therapy can be safely used to relieve dyspnea in lung transplant recipients during their ICU stay. Further evaluations in larger trials are required to confirm the results of this study.
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  • 文章类型: Journal Article
    风扇疗法是一种非药物方法,适用于绝症患者,通过引导风扇在患者面部一侧吹气来缓解呼吸困难。迄今为止,尚未对重症监护病房危重患者的风扇治疗进行系统评价.这项范围审查旨在提供迄今为止发表的风扇治疗研究的全面概述,阐明风扇疗法的治疗干预方法,根据现有文献评估其安全性,并探讨其在危重患者中的潜在用途。使用乔安娜·布里格斯研究所的方法进行了范围审查。此范围审查遵循范围审查声明的系统审查和荟萃分析的首选报告项目扩展。所有已发表的研究都是针对接受粉丝治疗的患者进行的,无论年龄大小,疾病,设置,阶段,国家,或随访时间包括在内。数据来源包括在线医学文献分析和检索系统,Embase,Cochrane中央控制试验登记册,护理和相关文献数据库的累积索引。在获得的685项研究中,包括15个,包括晚期癌症和慢性肺病患者。最常见的干预是在休息时对呼吸困难进行一次五分钟的干预。对接受氧疗的患者的研究没有报告不良事件或血压恶化,脉搏率,呼吸频率,或SpO2水平。然而,文献中没有关于危重患者使用风扇疗法的研究.然而,以前的研究表明,风扇治疗是安全的。
    Fan therapy is a non-pharmacological approach useful in terminally ill patients that relieves dyspnea by directing a fan to blow air on one side of the patient\'s face. To date, there has been no systematic review of fan therapy for critically ill patients in the intensive care unit. This scoping review aimed to provide a comprehensive overview of fan therapy studies published to date, clarify the therapeutic intervention methods of fan therapy, evaluate its safety according to existing literature, and explore its potential use in critically ill patients. A scoping review was conducted using the Joanna Briggs Institute methodology. This scoping review follows the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension of the scoping reviews statement. All published studies conducted on patients who received fan therapy regardless of age, disease, setting, phase, country, or follow-up duration were included. The data sources included Medical Literature Analysis and Retrieval System Online, Embase, Cochrane Central Register of Controlled Trials, and Cumulative Index to Nursing and Allied Literature databases. Of the 685 studies obtained, 15 were included, comprising patients with terminal cancer and chronic lung diseases. The most common intervention was a single five-minute intervention for dyspnea at rest. The studies on patients receiving oxygen therapy did not report adverse events or worsening of blood pressure, pulse rate, respiratory rate, or SpO2 levels. However, there are no studies in the literature on the use of fan therapy for critically ill patients. Nevertheless, previous studies suggest that fan therapy is safe.
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  • 文章类型: Journal Article
    BACKGROUND: The application of a handheld fan may reduce patients\' shortness of breath and increase their activity tolerance by enabling cooling and air flow into the second and third branches of the trigeminal nerve.
    OBJECTIVE: The aim of the study was to assess the effects of directing a handheld fan toward the face in the management of lung cancer-related dyspnea.
    METHODS: Using a randomized controlled experimental design, 96 inpatients with lung cancer were evaluated, with the experimental group (n = 49) using a handheld fan to manage dyspnea for 14 days. Dyspnea, respiration rate, oxygen saturation, heart rate, and quality of life were assessed for both groups.
    RESULTS: A statistically significant difference was found in dyspnea scores between groups on the first, seventh, and fourteenth days of fan application, and statistically significant differences were found between groups in dyspnea scores, respiration rates, oxygen saturation, heart rate, and quality of life on the fourteenth day of application.
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  • 文章类型: Journal Article
    BACKGROUND: Dyspnea is a common distressing symptom in patients with malignant and nonmalignant diseases. Fan therapy, which uses a fan to blow air toward the patient\'s face, can alleviate dyspnea; however, its efficacy remains unclear.
    OBJECTIVE: To examine the immediate efficacy of fan therapy for alleviation of dyspnea at rest.
    METHODS: Meta-analysis.
    METHODS: We searched the Cochrane Central Register of Controlled Trials in the Cochrane Library, MEDLINE EBSCO, CINAHL EBSCO, and Scopus from January 1, 1987, to August 21, 2018 (PROSPERO-CRD42018108610). In addition, we hand-searched studies and used the similar articles feature on PubMed to search for articles. Randomized controlled trials comparing the effects of fan therapy with placebo or other interventions to alleviate dyspnea at rest, in which patients were aged ≥18 years, were eligible for inclusion in the review. We excluded articles on long-term intervention involving fan therapy and complex intervention (including fan therapy). The risk of bias assessment was conducted using the Cochrane tool, and the meta-analysis was performed using RevMan version 5.3.
    RESULTS: We identified a total of 218 studies; 2 met our criteria for inclusion in the meta-analysis. Fan therapy significantly improved dyspnea at rest in terminally ill patients with cancer compared to control groups (mean difference: -1.31, 95% confidence interval: -1.79 to -0.83, P < .001). There were no studies that met the inclusion criteria regarding fan therapy for patients with nonmalignant disease.
    CONCLUSIONS: This meta-analysis demonstrated that fan therapy may be an effective intervention for dyspnea at rest in patients with terminal cancer.
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  • 文章类型: Journal Article
    Background: Dyspnea is one of the most common symptoms in patients with advanced disease and terminal illness, associated with poorer quality of life. The efficacy of fan therapy to palliate dyspnea is inconsistent and unclear. Objective: The aim of this meta-analysis was to evaluate the efficacy of fan therapy for the relief of dyspnea in adults with advanced disease and terminal illness. Design: The CENTRAL, MEDLINE, EMBASE, CINAHL, and PsycINFO were searched to retrieve all randomized controlled trials examining the benefits of fan therapy for the relief of dyspnea in patients at the advanced stages of illness. Risk of bias was assessed according to the Cochrane Collaboration standard scheme. Results: Five studies involving 198 adults were identified. Fan therapy was associated with a significant relief of breathlessness intensity immediately after intervention (mean differences [MDs], -1.01; 95% confidence interval [CI], -1.57 to -0.45; p < 0.001) and 10 minutes after intervention (MDs, -0.90; 95% CI, -1.53 to -0.27; p = 0.005). Long-term application of fan therapy for at least one month was not related to changes of dyspnea severity (MDs, 0.10; 95% CI, -1.14 to 1.35; p = 0.870). However, significant heterogeneity and low quality of the included trials limit applicability of the results in general practice. No difference was found in activity performance, respiratory rate and SpO2, changes in other symptom intensities, and adverse events. Conclusion: Current trials provided low-quality evidence for a significant short-term effect after fan therapy in the relief of dyspnea and no beneficial effect in the long-term application in adults with advanced disease and terminal illness.
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  • 文章类型: Clinical Trial
    OBJECTIVE: To clarify the duration required for dyspnea to return to baseline severity after fan therapy, to evaluate whether fan-to-legs therapy or no fan therapy would be a suitable control therapy, and to investigate changes in patients\' face surface temperature after fan therapy.
    METHODS: In this pilot study, all participants received 3 interventions in the following order: no fan, fan to legs, and fan to face. Participants used a fan for 5 minutes, and they scored their dyspnea at 10-minute intervals for 60 minutes or until the score had returned to its baseline value, whichever occurred first. Nine patients with advanced cancer admitted to a palliative care unit were included; they had dyspnea at rest and rated its severity as at least 3 points on a 0- to 10-point numerical rating scale. Descriptive statistics and the Wilcoxon signed rank test were used to analyze the data.
    RESULTS: All patients completed the study. Of the 9 participants, 6 experienced a clinical benefit from using a fan to their faces. Of these patients, only 2 participants\' (2 of 6) dyspnea scores returned to baseline by the end of the 60-minute assessment period after exposure to fan-to-face therapy. In fan-to-legs and no fan settings, there was no change in the dyspnea scores. There were significant differences between the baseline face surface temperature and that after fan-to-face and fan-to-legs settings.
    CONCLUSIONS: When using a crossover design to investigate the effect of fan therapy on dyspnea, 1 hour is an insufficient washout period.
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  • 文章类型: Clinical Trial, Phase II
    BACKGROUND: Fan therapy is often suggested for relieving the symptom of dyspnea in patients with advanced cancer, but relevant literature among Asians is limited.
    OBJECTIVE: Phase 2 clinical trial to assess the clinical feasibility and outcome of using an electric fan to alleviate the symptom of dyspnea in Chinese patients with advanced cancer.
    METHODS: Thirty patients with advanced cancer having unresolved breathlessness were recruited from Hospice and Palliative Care Centre of Kiang Wu Hospital in Macau. Participants were randomly and equally allocated to the experimental group and the control group, respectively.
    METHODS: Verbal numerical rating scale (NRS) of breathlessness, respiratory rate (RR), and saturation of peripheral oxygen (SpO2) was collected before and after the intervention.
    RESULTS: T test was used to analyze the data collected. There was a significant difference in the NRS scores of the experimental group ( P < .01), indicating a significant reduction in the patients\' sensation of breathlessness after fan therapy, whereas no significant difference was found in the objective statistic results of RR and SpO2. No significant difference ( P > .05) was found in the control group for all the 3 variables before and after routine treatment.
    CONCLUSIONS: The results of the study suggested that fan therapy could be effective in alleviating dyspnea in Chinese patients with advanced cancer. It should be considered as one of the nonpharmacological treatment option. Future large-scale phase 3 clinical trials are warranted.
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