Charoenkwan Kittipat, Matovinovic Elizabeth
Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, 110 Intawaroros Road, Chiang Mai, 50200, Thailand.
Cochrane Database Syst Rev. 2014 Dec 12;2014(12):CD004508. doi: 10.1002/14651858.CD004508.pub4.
This is an updated version of the original Cochrane review published in 2007. Traditionally, after major abdominal gynaecologic surgery postoperative oral intake is withheld until the return of bowel function. There has been concern that early oral intake would result in vomiting and severe paralytic ileus with subsequent aspiration pneumonia, wound dehiscence, and anastomotic leakage. However, evidence-based clinical studies suggest that there may be benefits from early postoperative oral intake.
To assess the effects of early versus delayed (traditional) initiation of oral intake of food and fluids after major abdominal gynaecologic surgery.
We searched the Menstrual Disorders and Subfertility Group's Specialised Register, the Cochrane Central Register of Controlled Trials (CENTRAL), electronic databases (MEDLINE, EMBASE, CINAHL), and the citation lists of relevant publications. The most recent search was conducted 1 April 2014. We also searched a registry for ongoing trials (www.clinicaltrials.gov) on 13 May 2014.
Randomised controlled trials (RCTs) were eligible that compared the effect of early versus delayed initiation of oral intake of food and fluids after major abdominal gynaecologic surgery. Early feeding was defined as oral intake of fluids or food within 24 hours post-surgery regardless of the return of bowel function. Delayed feeding was defined as oral intake after 24 hours post-surgery and only after signs of postoperative ileus resolution.
Two review authors selected studies, assessed study quality and extracted the data. For dichotomous data, we calculated the risk ratio (RR) with a 95% confidence interval (CI). We examined continuous data using the mean difference (MD) and a 95% CI. We tested for heterogeneity between the results of different studies using a forest plot of the meta-analysis, the statistical tests of homogeneity of 2 x 2 tables and the I² value. We assessed the quality of the evidence using GRADE methods.
Rates of developing postoperative ileus were comparable between study groups (RR 0.47, 95% CI 0.17 to 1.29, P = 0.14, 3 RCTs, 279 women, I² = 0%, moderate-quality evidence). When we considered the rates of nausea or vomiting or both, there was no evidence of a difference between the study groups (RR 1.03, 95% CI 0.64 to 1.67, P = 0.90, 4 RCTs, 484 women, I² = 73%, moderate-quality evidence). There was no evidence of a difference between the study groups in abdominal distension (RR 1.07, 95% CI 0.77 to 1.47, 2 RCTs, 301 women, I² = 0%) or a need for postoperative nasogastric tube placement (RR 0.48, 95% CI 0.13 to 1.80, 1 RCT, 195 women).Early feeding was associated with shorter time to the presence of bowel sound (MD -0.32 days, 95% CI -0.61 to -0.03, P = 0.03, 2 RCTs, 338 women, I² = 52%, moderate-quality evidence) and faster onset of flatus (MD -0.21 days, 95% CI -0.40 to -0.01, P = 0.04, 3 RCTs, 444 women, I² = 23%, moderate-quality evidence). In addition, women in the early feeding group resumed a solid diet sooner (MD -1.47 days, 95% CI -2.26 to -0.68, P = 0.0003, 2 RCTs, 301 women, I² = 92%, moderate-quality evidence). There was no evidence of a difference in time to the first passage of stool between the two study groups (MD -0.25 days, 95% CI -0.58 to 0.09, P = 0.15, 2 RCTs, 249 women, I² = 0%, moderate-quality evidence). Hospital stay was shorter in the early feeding group (MD -0.92 days, 95% CI -1.53 to -0.31, P = 0.003, 4 RCTs, 484 women, I² = 68%, moderate-quality evidence). Infectious complications were less common in the early feeding group (RR 0.20, 95% CI 0.05 to 0.73, P = 0.02, 2 RCTs, 183 women, I² = 0%, high-quality evidence). In one study, the satisfaction score was significantly higher in the early feeding group (MD 11.10, 95% CI 6.68 to 15.52, P < 0.00001, 143 women, moderate-quality evidence).
AUTHORS' CONCLUSIONS: Early postoperative feeding after major abdominal gynaecologic surgery for either benign or malignant conditions appeared to be safe without increased gastrointestinal morbidities or other postoperative complications. The benefits of this approach include faster recovery of bowel function, lower rates of infectious complications, shorter hospital stay, and higher satisfaction.
这是2007年发表的原始Cochrane综述的更新版本。传统上,腹部妇科大手术后,在肠道功能恢复之前会禁止经口摄入。人们担心早期经口摄入会导致呕吐和严重的麻痹性肠梗阻,进而引发吸入性肺炎、伤口裂开和吻合口漏。然而,循证临床研究表明,术后早期经口摄入可能有益。
评估腹部妇科大手术后早期与延迟(传统)开始经口摄入食物和液体的效果。
我们检索了月经失调与生育力低下组专业注册库、Cochrane对照试验中心注册库(CENTRAL)、电子数据库(MEDLINE、EMBASE、CINAHL)以及相关出版物的参考文献列表。最近一次检索于2014年4月1日进行。我们还于2014年5月13日检索了正在进行的试验注册库(www.clinicaltrials.gov)。
符合条件的随机对照试验(RCT)为比较腹部妇科大手术后早期与延迟开始经口摄入食物和液体效果的试验。早期喂养定义为术后24小时内经口摄入液体或食物,无论肠道功能是否恢复。延迟喂养定义为术后24小时后且仅在术后肠梗阻症状缓解后经口摄入。
两位综述作者选择研究、评估研究质量并提取数据。对于二分数据,我们计算风险比(RR)及95%置信区间(CI)。我们使用平均差(MD)及95%CI检验连续数据。我们通过Meta分析的森林图、2×2表格同质性的统计检验及I²值检验不同研究结果之间的异质性。我们使用GRADE方法评估证据质量。
各研究组术后肠梗阻发生率相当(RR 0.47,95%CI 0.17至1.29,P = 0.14,3项RCT,279名女性,I² = 0%,中等质量证据)。当我们考虑恶心或呕吐或两者的发生率时,各研究组之间没有差异的证据(RR 1.03,95%CI 0.64至1.67,P = 0.90,4项RCT,484名女性,I² = 73%中等质量证据)。各研究组在腹胀方面没有差异的证据(RR 1.07,95%CI 0.77至1.47,2项RCT,301名女性,I² = 0%)或术后放置鼻胃管的需求方面(RR 0.48,95%CI 0.13至1.80,1项RCT,195名女性)。早期喂养与肠鸣音出现时间缩短相关(MD -0.32天,95%CI -0.61至 -0.03,P = 0.03,2项RCT,338名女性,I² = 52%,中等质量证据)且排气开始更快(MD -0.21天,95%CI -0.40至 -0.01,P = 0.04,3项RCT,444名女性,I² = 23%,中等质量证据)。此外,早期喂养组女性更快恢复固体饮食(MD -1.47天,95%CI -2.26至 -0.68,P = 0.0003,2项RCT,301名女性,I² = 92%,中等质量证据)。两组在首次排便时间上没有差异的证据(MD -0.25天,95%CI -0.58至0.09,P = 0.15,2项RCT,249名女性,I² = 0%,中等质量证据)。早期喂养组住院时间更短(MD -0.92天,95%CI -1.53至 -0.31,P = 0.003,4项RCT,484名女性,I² = 68%,中等质量证据)。早期喂养组感染性并发症较少见(RR 0.20,95%CI 0.05至0.73,P = 0.02,2项RCT,183名女性,I² = 0%,高质量证据)。在一项研究中,早期喂养组的满意度得分显著更高(MD 1️⃣1️⃣1️⃣0️⃣,95%CI 6.68至15.52,P < 0.00001,143名女性,中等质量证据)。
腹部妇科大手术后,无论是良性还是恶性疾病,术后早期喂养似乎是安全的,不会增加胃肠道发病率或其他术后并发症。这种方法的益处包括肠道功能恢复更快、感染性并发症发生率更低、住院时间更短以及满意度更高。