Médecine Intensive Réanimation, CHU de Nantes, Nantes, France; Université de Nantes, Nantes, France.
EA 7293, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Faculté de Médecine, Université de Strasbourg, Strasbourg, France; Medical Intensive Care Unit, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Lancet. 2018 Jan 13;391(10116):133-143. doi: 10.1016/S0140-6736(17)32146-3. Epub 2017 Nov 8.
BACKGROUND: Whether the route of early feeding affects outcomes of patients with severe critical illnesses is controversial. We hypothesised that outcomes were better with early first-line enteral nutrition than with early first-line parenteral nutrition. METHODS: In this randomised, controlled, multicentre, open-label, parallel-group study (NUTRIREA-2 trial) done at 44 French intensive-care units (ICUs), adults (18 years or older) receiving invasive mechanical ventilation and vasopressor support for shock were randomly assigned (1:1) to either parenteral nutrition or enteral nutrition, both targeting normocaloric goals (20-25 kcal/kg per day), within 24 h after intubation. Randomisation was stratified by centre using permutation blocks of variable sizes. Given that route of nutrition cannot be masked, blinding of the physicians and nurses was not feasible. Patients receiving parenteral nutrition could be switched to enteral nutrition after at least 72 h in the event of shock resolution (no vasopressor support for 24 consecutive hours and arterial lactate <2 mmol/L). The primary endpoint was mortality on day 28 after randomisation in the intention-to-treat-population. This study is registered with ClinicalTrials.gov, number NCT01802099. FINDINGS: After the second interim analysis, the independent Data Safety and Monitoring Board deemed that completing patient enrolment was unlikely to significantly change the results of the trial and recommended stopping patient recruitment. Between March 22, 2013, and June 30, 2015, 2410 patients were enrolled and randomly assigned; 1202 to the enteral group and 1208 to the parenteral group. By day 28, 443 (37%) of 1202 patients in the enteral group and 422 (35%) of 1208 patients in the parenteral group had died (absolute difference estimate 2·0%; [95% CI -1·9 to 5·8]; p=0·33). Cumulative incidence of patients with ICU-acquired infections did not differ between the enteral group (173 [14%]) and the parenteral group (194 [16%]; hazard ratio [HR] 0·89 [95% CI 0·72-1·09]; p=0·25). Compared with the parenteral group, the enteral group had higher cumulative incidences of patients with vomiting (406 [34%] vs 246 [20%]; HR 1·89 [1·62-2·20]; p<0·0001), diarrhoea (432 [36%] vs 393 [33%]; 1·20 [1·05-1·37]; p=0·009), bowel ischaemia (19 [2%] vs five [<1%]; 3·84 [1·43-10·3]; p=0·007), and acute colonic pseudo-obstruction (11 [1%] vs three [<1%]; 3·7 [1·03-13·2; p=0·04). INTERPRETATION: In critically ill adults with shock, early isocaloric enteral nutrition did not reduce mortality or the risk of secondary infections but was associated with a greater risk of digestive complications compared with early isocaloric parenteral nutrition. FUNDING: La Roche-sur-Yon Departmental Hospital and French Ministry of Health.
背景:早期喂养途径是否会影响重症危重病患者的结局仍存在争议。我们假设早期一线肠内营养的结局优于早期一线肠外营养。
方法:在这项在法国 44 家重症监护病房(ICU)进行的随机、对照、多中心、开放标签、平行组研究(NUTRIREA-2 试验)中,接受有创机械通气和升压支持以治疗休克的成年患者(18 岁或以上)在插管后 24 小时内被随机分配(1:1)接受肠外营养或肠内营养,两者均以 20-25 kcal/kg 为目标热量(20-25 kcal/kg 每天)。随机分组采用大小可变的排列块进行分层。由于营养途径无法掩盖,因此无法对医生和护士进行盲法。如果休克得到缓解(连续 24 小时无升压支持且动脉血乳酸 <2 mmol/L),则可以在 72 小时后将接受肠外营养的患者转换为肠内营养。主要终点是意向治疗人群在随机分组后第 28 天的死亡率。本研究在 ClinicalTrials.gov 注册,编号为 NCT01802099。
发现:在第二次中期分析后,独立的数据安全和监测委员会认为完成患者入组不太可能显著改变试验结果,并建议停止患者入组。2013 年 3 月 22 日至 2015 年 6 月 30 日期间,共纳入 2410 例患者并进行随机分组;1202 例患者进入肠内营养组,1208 例患者进入肠外营养组。在第 28 天,肠内营养组有 443(37%)例患者和肠外营养组有 422(35%)例患者死亡(绝对差值估计为 2.0%[95%CI-1.9 至 5.8];p=0.33)。肠内营养组(173[14%]例)和肠外营养组(194[16%]例)的 ICU 获得性感染患者累积发生率无差异(风险比[HR]0.89[95%CI0.72-1.09];p=0.25)。与肠外营养组相比,肠内营养组呕吐的累积发生率更高(406[34%]比 246[20%];HR1.89[1.62-2.20];p<0.0001)、腹泻(432[36%]比 393[33%];1.20[1.05-1.37];p=0.009)、肠缺血(19[2%]比 5[<1%];3.84[1.43-10.3];p=0.007)和急性结肠假性梗阻(11[1%]比 3[<1%];3.7[1.03-13.2];p=0.04)的发生率更高。
解释:在伴有休克的重症成年患者中,早期等热量肠内营养并未降低死亡率或继发感染的风险,但与早期等热量肠外营养相比,与消化并发症的风险增加相关。
经费:La Roche-sur-Yon 地区医院和法国卫生部。
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