Department of Clinical Nutrition, OIRM-S, Anna Hospital, Città della Salute e della Scienza, 10126 Turin, Italy.
Ospedale Bambin Gesù, 00165 Rome, Italy.
Nutrients. 2022 Apr 30;14(9):1889. doi: 10.3390/nu14091889.
Background: The European Society for Clinical Nutrition and Metabolism database for chronic intestinal failure (CIF) was analyzed to investigate factors associated with nutritional status and the intravenous supplementation (IVS) dependency in children. Methods: Data collected: demographics, CIF mechanism, home parenteral nutrition program, z-scores of weight-for-age (WFA), length or height-for-age (LFA/HFA), and body mass index-for-age (BMI-FA). IVS dependency was calculated as the ratio of daily total IVS energy over estimated resting energy expenditure (%IVSE/REE). Results: Five hundred and fifty-eight patients were included, 57.2% of whom were male. CIF mechanisms at age 1−4 and 14−18 years, respectively: SBS 63.3%, 37.9%; dysmotility or mucosal disease: 36.7%, 62.1%. One-third had WFA and/or LFA/HFA z-scores < −2. One-third had %IVSE/REE > 125%. Multivariate analysis showed that mechanism of CIF was associated with WFA and/or LFA/HFA z-scores (negatively with mucosal disease) and %IVSE/REE (higher for dysmotility and lower in SBS with colon in continuity), while z-scores were negatively associated with %IVSE/REE. Conclusions: The main mechanism of CIF at young age was short bowel syndrome (SBS), whereas most patients facing adulthood had intestinal dysmotility or mucosal disease. One-third were underweight or stunted and had high IVS dependency. Considering that IVS dependency was associated with both CIF mechanisms and nutritional status, IVS dependency is suggested as a potential marker for CIF severity in children.
分析欧洲临床营养与代谢学会慢性肠衰竭(CIF)数据库,以调查与儿童营养状况和静脉补充(IVS)依赖相关的因素。
收集数据:人口统计学、CIF 机制、家庭肠外营养计划、体重与年龄(WFA)、长度或身高与年龄(LFA/HFA)和体重指数与年龄(BMI-FA)的 z 分数。IVS 依赖程度计算为每日总 IVS 能量与估计静息能量消耗的比值(%IVSE/REE)。
纳入 558 例患者,其中 57.2%为男性。1-4 岁和 14-18 岁时 CIF 机制分别为:SBS 63.3%,37.9%;运动障碍或黏膜疾病:36.7%,62.1%。三分之一的患者 WFA 和/或 LFA/HFA z 分数<−2。三分之一的患者%IVSE/REE>125%。多变量分析显示,CIF 机制与 WFA 和/或 LFA/HFA z 分数相关(黏膜疾病呈负相关)和%IVSE/REE(运动障碍较高,SBS 中结肠连续时较低),而 z 分数与%IVSE/REE 呈负相关。
CIF 在幼年的主要机制是短肠综合征(SBS),而大多数面临成年的患者则存在肠运动障碍或黏膜疾病。三分之一的患者体重不足或发育迟缓,且 IVS 依赖程度较高。考虑到 IVS 依赖与 CIF 机制和营养状况均相关,建议将 IVS 依赖作为儿童 CIF 严重程度的潜在标志物。