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Percutaneous endoscopic gastrostomy versus nasogastric tube feeding for adults with swallowing disturbances

机译:成人吞咽障碍的经皮内镜胃造口术与鼻胃管喂养

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摘要

BackgroundA number of conditions compromise the passage of food along the digestive tract. Nasogastric tube (NGT) feeding is a classic, time-proven technique, although its prolonged use can lead to complications such as lesions to the nasal wing, chronic sinusitis, gastro-oesophageal reflux, and aspiration pneumonia. Another method of infusion, percutaneous endoscopy gastrostomy (PEG), is generally used when there is a need for enteral nutrition for a longer time period. There is a high demand for PEG in patients with swallowing disorders, although there is no consistent evidence about its effectiveness and safety as compared to NGT.ObjectivesTo evaluate the effectiveness and safety of PEG compared with NGT for adults with swallowing disturbances.Search methodsWe searched The Cochrane Library, MEDLINE, EMBASE, and LILACS from inception to January 2014, and contacted the main authors in the subject area. There was no language restriction in the search.Selection criteriaWe planned to include randomised controlled trials comparing PEG versus NGT for adults with swallowing disturbances or dysphagia and indications for nutritional support, with any underlying diseases. The primary outcome was intervention failure (e.g. feeding interruption, blocking or leakage of the tube, no adherence to treatment).Data collection and analysisWe used standard methodological procedures expected by The Cochrane Collaboration. For dichotomous and continuous variables, we used risk ratio (RR) and mean difference (MD), respectively with the random-effects statistical model and 95% confidence interval (CI). We assumed statistical heterogeneity when I² > 50%.Main resultsWe included 11 randomised controlled studies with 735 participants which produced 16 meta-analyses of outcome data. Meta-analysis indicated that the primary outcome of intervention failure, occurred in lower proportion of participants with PEG compared to NGT (RR 0.18, 95% CI 0.05 to 0.59, eight studies, 408 participants, low quality evidence) and this difference was statistically significant. For this outcome, we also subgrouped the studies by endoscopic gastrostomy technique into pull, and push and not reported. We observed a significant difference favouring PEG in the pull subgroup (RR 0.07, 95% CI 0.01 to 0.35, three studies, 90 participants). Thepush subgroup contained only one clinical trial and the result favoured PEG (RR 0.05, 95% CI 0.00 to 0.74, one study, 33 participants) techniques. We found no statistically significant difference in cases where the technique was not reported (RR 0.43, 95% CI 0.13 to 1.44, four studies, 285 participants).There was no statistically significant difference between the groups for meta-analyses of the secondary outcomes of mortality (RR 0.86, 95% CI 0.58 to 1.28, 644 participants, nine studies, very low quality evidence), overall reports of any adverse event at any follow-up time point (ITT analysis, RR 0.83, 95% CI 0.51 to 1.34), 597 participants, 6 studies, moderate quality evidence), specific adverse events including pneumonia (aspiration) (RR 0.70, 95% CI 0.46 to 1.06, 645 participants, seven studies, low quality evidence), or for the meta- analyses of the secondary outcome of nutritional status including weight change from baseline, and mid-arm circumference at endpoint, although there was evidence in favour of PEG for meta-analyses of mid-arm circumference change from baseline (MD 1.16, 95% CI 1.01 to 1.31, 115 participants, two studies), and levels of serum albumin were higher in the PEG group (MD 6.03, 95% CI 2.31 to 9.74, 107 participants).For meta-analyses of the secondary outcomes of time on enteral nutrition, there was no statistically significant difference (MD 14.48, 95% CI -2.74 to 31.71; 119 participants, two studies). For meta-analyses of quality of life measures (EuroQol) outcomes in two studies with 133 participants, for inconvenience (RR 0.03, 95% CI 0.00 to 0.29), discomfort (RR 0.03, 95% CI 0.00 to 0.29), altered body image (RR 0.01, 95% CI 0.00 to 0.18; P = 0.001) and social activities (RR 0.01, 95% CI 0.00 to 0.18) the intervention favoured PEG, that is, fewer participants found the intervention of PEG to be inconvenient, uncomfortable or interfered with social activities. However, there were no significant differences between the groups for pain, ease of learning to use, or the secondary outcome of length of hospital stay (two studies, 381 participants).Authors' conclusionsPEG was associated with a lower probability of intervention failure, suggesting the endoscopic procedure may be more effective and safe compared with NGT. There is no significant difference in mortality rates between comparison groups, or in adverse events, including pneumonia related to aspiration. Future studies should include details of participant demographics including underlying disease, age and gender, and the gastrostomy technique.
机译:背景许多条件影响食物沿消化道的通过。鼻胃管(NGT)喂养是一项经过时间验证的经典技术,尽管长期使用会导致并发症,例如鼻翼病变,慢性鼻窦炎,胃食管反流和吸入性肺炎。当需要较长时间的肠内营养时,通常使用另一种输注方法,即经皮内窥镜胃造口术(PEG)。吞咽障碍患者对PEG的需求量很高,尽管与NGT相比其有效性和安全性尚无统一的证据。目的为了评估吞咽障碍成年人与PEG相比NGT的有效性和安全性。从成立到2014年1月,Cochrane图书馆,MEDLINE,EMBASE和LILACS均与该领域的主要作者联系。选择标准我们计划纳入随机对照试验,比较吞咽障碍或吞咽困难和营养支持适应症以及任何潜在疾病的成年人的PEG与NGT。主要结果是干预失败(例如进食中断,管子堵塞或泄漏,不依从治疗)。数据收集和分析我们使用了Cochrane Collaboration期望的标准方法学程序。对于二分变量和连续变量,我们分别使用风险比(RR)和均值差(MD)以及随机效应统计模型和95%置信区间(CI)。当I²> 50%时,我们假设统计上的异质性。主要结果我们纳入了11个随机对照研究,有735名参与者,进行了16项结果数据的荟萃分析。荟萃分析表明,与NGT相比,干预失败的主要结果发生在PEG参与者中的比例较低(RR 0.18,95%CI 0.05至0.59,八项研究,408名参与者,低质量证据),这种差异具有统计学意义。对于这一结果,我们还通过内窥镜胃造口术技术将研究分为拉,推和未报道。我们观察到在拉动亚组中有利于PEG有显着差异(RR 0.07,95%CI 0.01至0.35,三项研究,90名参与者)。推进亚组仅包含一项临床试验,结果支持PEG(RR 0.05,95%CI 0.00至0.74,一项研究,33名参与者)技术。在未报告该技术的情况下(RR 0.43,95%CI 0.13 to 1.44,四项研究,285名参与者),我们没有发现统计学上的显着差异。死亡率(RR 0.86,95%CI 0.58至1.28,644名参与者,九项研究,非常低的质量证据),在任何随访时间点的任何不良事件的总体报告(ITT分析,RR 0.83,95%CI 0.51至1.34 ),597名参与者,6项研究,中等质量的证据),特定的不良事件包括肺炎(吸入)(RR 0.70、95%CI 0.46至1.06、645名参与者,七项研究,低质量的证据),或用于营养状况的次要结果,包括基线的体重变化和终点的中臂围,尽管有证据支持PEG进行中臂围从基线变化的荟萃分析(MD 1.16,95%CI 1.01至1.31 115名参与者,两名研究),并且PEG组的血清白蛋白水平较高(MD 6.03,95%CI 2.31至9.74,107位参与者)。对于肠内营养时间的次要结局的荟萃分析,差异无统计学意义( MD 14.48,95%CI -2.74至31.71; 119名参与者,两项研究)。在两项有133名参与者的研究中对生活质量测量结果(EuroQol)进行荟萃分析,为您带来不便(RR 0.03,95%CI 0.00至0.29),不适(RR 0.03,95%CI 0.00至0.29),身体图像改变(RR 0.01,95%CI 0.00至0.18; P = 0.001)和社交活动(RR 0.01,95%CI 0.00至0.18)干预措施偏向PEG,即较少的参与者发现PEG干预不便,不舒服或干扰社交活动。然而,两组之间在疼痛,学习易用性或住院时间的次要结局方面无显着差异(两项研究,381名参与者)。作者的结论PEG与干预失败的可能性较低相关,表明与NGT相比,内镜手术可能更有效,更安全。比较组之间的死亡率或包括与吸入有关的肺炎在内的不良事件的死亡率没有显着差异。未来的研究应包括参与者人口统计学的详细信息,包括潜在疾病,年龄和性别以及胃造口术。

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