Systematic reviews including this primary study

loading
5 articles (5 References) loading Revert Studify

Systematic review

Unclassified

期刊 The Cochrane database of systematic reviews
Year 2019
Loading references information
BACKGROUND: People with febrile neutropaenia are usually treated in a hospital setting. Recently, treatment with oral antibiotics has been proven to be as effective as intravenous therapy. However, the efficacy and safety of outpatient treatment have not been fully evaluated. OBJECTIVES: To compare the efficacy (treatment failure and mortality) and safety (adverse events of antimicrobials) of outpatient treatment compared with inpatient treatment in people with cancer who have low-risk febrile neutropaenia. SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 11) in the Cochrane Library, MEDLINE via Ovid (from 1948 to November week 4, 2018), Embase via Ovid (from 1980 to 2018, week 48) and trial registries (National Cancer Institute, MetaRegister of Controlled Trials, Medical Research Council Clinical Trial Directory). We handsearched all references of included studies and major reviews. SELECTION CRITERIA: Randomised controlled trials (RCTs) comparing outpatient with inpatient treatment for people with cancer who develop febrile neutropaenia. The outpatient group included those who started treatment as an inpatient and completed the antibiotic course at home (sequential) as well as those who started treatment at home. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed trial eligibility, methodological quality, and extracted data. Primary outcome measures were: treatment failure and mortality; secondary outcome measures considered were: duration of fever, adverse drug reactions to antimicrobial treatment, duration of neutropaenia, duration of hospitalisation, duration of antimicrobial treatment, and quality of life (QoL). We estimated risk ratios (RRs) with 95% confidence intervals (CIs) for dichotomous data; we calculated weighted mean differences for continuous data. Random-effects meta-analyses and sensitivity analyses were conducted. MAIN RESULTS: We included ten RCTs, six in adults (628 participants) and four in children (366 participants). We found no clear evidence of a difference in treatment failure between the outpatient and inpatient groups, either in adults (RR 1.23, 95% CI 0.82 to 1.85, I2 0%; six studies; moderate-certainty evidence) or children (RR 1.04, 95% CI 0.55 to 1.99, I2 0%; four studies; moderate-certainty evidence). For mortality, we also found no clear evidence of a difference either in studies in adults (RR 1.04, 95% CI 0.29 to 3.71; six studies; 628 participants; moderate-certainty evidence) or in children (RR 0.63, 95% CI 0.15 to 2.70; three studies; 329 participants; moderate-certainty evidence).According to the type of intervention (early discharge or exclusively outpatient), meta-analysis of treatment failure in four RCTs in adults with early discharge (RR 1.48, 95% CI 0.74 to 2.95; P = 0.26, I2 0%; 364 participants; moderate-certainty evidence) was similar to the results of the exclusively outpatient meta-analysis (RR 1.15, 95% CI 0.62 to 2.13; P = 0.65, I2 19%; two studies; 264 participants; moderate-certainty evidence).Regarding the secondary outcome measures, we found no clear evidence of a difference between outpatient and inpatient groups in duration of fever (adults: mean difference (MD) 0.2, 95% CI -0.36 to 0.76, 1 study, 169 participants; low-certainty evidence) (children: MD -0.6, 95% CI -0.84 to 0.71, 3 studies, 305 participants; low-certainty evidence) and in duration of neutropaenia (adults: MD 0.1, 95% CI -0.59 to 0.79, 1 study, 169 participants; low-certainty evidence) (children: MD -0.65, 95% CI -0.1.86 to 0.55, 2 studies, 268 participants; moderate-certainty evidence). With regard to adverse drug reactions, although there was greater frequency in the outpatient group, we found no clear evidence of a difference when compared to the inpatient group, either in adult participants (RR 8.39, 95% CI 0.38 to 187.15; three studies; 375 participants; low-certainty evidence) or children (RR 1.90, 95% CI 0.61 to 5.98; two studies; 156 participants; low-certainty evidence).Four studies compared the hospitalisation time and found that the mean number of days of hospital stay was lower in the outpatient treated group by 1.64 days in adults (MD -1.64, 95% CI -2.22 to -1.06; 3 studies, 251 participants; low-certainty evidence) and by 3.9 days in children (MD -3.90, 95% CI -5.37 to -2.43; 1 study, 119 participants; low-certainty evidence). In the 3 RCTs of children in which days of antimicrobial treatment were analysed, we found no difference between outpatient and inpatient groups (MD -0.07, 95% CI -1.26 to 1.12; 305 participants; low-certainty evidence).We identified two studies that measured QoL: one in adults and one in children. QoL was slightly better in the outpatient group than in the inpatient group in both studies, but there was no consistency in the domains included. AUTHORS' CONCLUSIONS: Outpatient treatment for low-risk febrile neutropaenia in people with cancer probably makes little or no difference to treatment failure and mortality compared with the standard hospital (inpatient) treatment and may reduce time that patients need to be treated in hospital.

Systematic review

Unclassified

期刊 Journal of Clinical Oncology
Year 2016
Loading references information

Systematic review

Unclassified

期刊 Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Year 2016
Loading references information
背景技术在负压伤口治疗(NPWT)中,用气密敷料覆盖伤口,施加负压。这被认为是促进愈合。我们对文献进行了更新,系统的综述评估了NPWT。方法:我们系统地搜索PubMed和Cochrane图书馆数据库,用于治疗急性或慢性伤口的NPWT的随机对照试验(RCT)。主要结果是完全伤口闭合。结果:除了早期IQWiG对本主题的评论之外,我们还发现了9项RCT的报告。 9项新试验中有5项涉及不在市场上的NPWT系统。在9份新报告中只有5项说明完全伤口关闭的频率。仅有两项试验发现有利于NPWT的统计学显着效果.9项新试验中的8项研究结果难以解释,因为明显偏倚,并且因为多种类型的伤口得到治疗。结论:虽然NPWT可能有积极作用,但我们没有发现明显的证据表明,NPWT伤口愈合愈合比常规治疗好。仍然需要良好的RCT来评估NPWT。

Systematic review

Unclassified

期刊 Cochrane Database of Systematic Reviews
Year 2016
Loading references information
背景:儿茶酚-O-甲基转移酶(COMT)酶在多巴胺降解中起关键作用,而COMT Val158Met多态性(rs4680)与前额叶皮层的酶活性和多巴胺浓度的显着差异相关。多项研究分析了与抗精神病反应有关的COMT Val158Met变体。在这里,我们进行了荟萃分析,检查了COMT Val158Met与抗精神病反应之间的关系。方法:使用PubMed,Web of Science和PsycInfo数据库(03/01/2015)进行的搜索得到了23项研究,调查了精神分裂症和分裂症情绪障碍中COMT Val158Met变异和抗精神病反应。使用每项研究的原始标准来确定应答者/无应答者。如果没有使用二进制反应定义,则要求作者根据至少30%的阳性和阴性综合征量表评分减少(或其他量表中的等效物)来定义反应。分析是在固定效应模型下进行的。结果:10项研究符合荟萃分析的纳入标准。分析了另外5种抗精神病药物治疗样品的Val158Met和应答,并纳入荟萃分析(ntotal = 1416)。 Met / Met个体比Val-载体更有可能发生反应(P = 0.039,ORMet / Met = 1.37,95%CI:1.02-1.85)。 Met / Met患者相对于Val-载体的阳性症状也有明显改善(P = 0.030,SMD = 0.24,95%CI:0.024-0.46)。对非典型抗精神病药物(n = 1207)治疗的患者的posthoc分析显示Met / Met患者相对于Val-载体显着更有可能作出反应(P = .0098,ORMet / Met = 1.54,95%CI:1.11-2.14) ,而典型的抗精神病药物治疗患者(n = 155)没有差异(P = .65)。结论:我们的研究结果表明,COMT Val158Met多态性与精神分裂症和分裂症情感障碍患者抗精神病药物的反应有关。对于非典型抗精神病药物,这种作用可能更为显着。 (PsycINFO数据库记录(c)2016 APA,保留所有权利)

Systematic review

Unclassified

期刊 Annals of oncology : official journal of the European Society for Medical Oncology / ESMO
Year 2011
Loading references information
目的:系统地回顾关于统计过程控制(以控制图为核心工具)如何应用于医疗质量改进的文献,并检查与此类应用相关的益处,限制,障碍和便利因素。数据来源:涵盖1966年至2004年6月期间的有关数据库的原始文章,包括Web of Science and Medline。研究选择:从1990年至2004年间发表的311篇文章,57篇实证研究中,符合纳入标准。方法:采用标准化数据抽象形式提取与审查问题相关的数据,并对数据进行主题分析。结果:统计过程控制应用于广泛的环境和专业,在不同的组织水平和直接由患者使用97个不同的变量。审查结果揭示了12类福利,6类限制,10类障碍和23种因素,促进其应用,并在本报告中全面引用。统计过程控制帮助不同的行为者管理变化并改善医疗流程。它还使得患有例如哮喘或糖尿病的患者能够管理自己的健康,并且因此具有治疗特性。其功能取决于正确和智能的应用,这不一定是一个微不足道的任务。本综述对11种智能应用的方法进行了目录,包括风险调整和数据分层。结论:统计过程控制是一个多功能的工具,可以帮助不同的利益相关者管理医疗改革和改善患者的健康。