【慢性肾脏病患儿蛋白质能量消耗的危险因素分析】。

Y Liang, Y P Jiang, H Wang, N Zhou, Q Fu, Y Shen
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引用次数: 0

摘要

目的:分析慢性肾脏病(CKD)患儿蛋白质能量消耗(PEW)的临床特点及危险因素。方法:对2018年1月至2023年1月在首都医科大学附属北京儿童医院住院的231例慢性肾脏病患儿的临床资料进行回顾性分析,探讨PEW的发生率。根据CKDEW的诊断标准,将其分为CKDEW组和非PEW组。两组间比较采用独立样本t检验和卡方检验,危险因素采用多元Logistic回归分析。结果:231名儿童中,男性138名,女性93名,访视年龄9.9(7.9,16.0)岁;1期6例,2期14例,3期51例,4期36例,5期124例。共有30名儿童(13.0%)在7岁时被诊断为CKD PEW。1(3.8,13.2)年,其中1例为1期,1例为2期,5例为3期、5例为4期,18例为5期。非PEW组共有201例(87.0%),在11.8(8.5,12.2)岁时确诊,其中1期5例,2期13例,3期46例,4期31例,5期106例。卡方检验和t检验显示,CKD PEW组的收缩压、舒张压、出生体重和二氧化碳结合能力低于非PEW组((109±22)vs.(120±20)mmHg(1mmHg=0.133kPa)、(72±19)vs,多因素logistic回归分析显示,二氧化碳结合力和出生体重是儿童CKDPEW的独立保护因素(OR分别为0.81和0.36,95%CI分别为0.73-0.90和0.17-0.77,均为P0.001);CKD儿童PEW的风险在二氧化碳结合能力每增加1mmol/L时降低0.187倍,在出生体重每增加1kg时降低0.638倍。结论:慢性肾脏病患儿蛋白质能量消耗的发生率低于以往研究。PEW可出现在CKD 1-2期,临床应注意CKD早期。低出生体重CKD儿童易患PEW,积极纠正代谢性酸中毒可以降低CKDPEW的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Risk factors analysis of protein energy wasting in children with chronic kidney disease].

Objective: To analyze the clinical characteristics and risk factors of protein energy wasting (PEW) in children with chronic kidney disease (CKD). Methods: Clinical data of 231 children with chronic kidney disease hospitalized in Beijing Children's Hospital affiliated to Capital Medical University from January 2018 to January 2023 were retrospectively analyzed to explore the incidence of PEW. According to the diagnostic criteria of CKDPEW, they were divided into a CKDPEW group and a non PEW group. The comparison between the groups was performed by independent-sample t test and Chi-squared test, and the risk factors were analyzed by multivariate Logistic regression. Results: Among the 231 children, there were 138 males and 93 females, with a visiting age of 9.9 (7.9, 16.0) years; 6 cases were in stage 1, 14 cases in stage 2, 51 cases in stage 3, 36 cases in stage 4, and 124 cases in stage 5. A total of 30 children (13.0%) with CKD PEW were diagnosed at the age of 7. 1 (3.8, 13.2) years, including 1 case in stage 1, 1 case in stage 2, 5 cases in stage 3, 5 cases in stage 4, and 18 cases in stage 5. There were a total of 201 cases (87.0%) in the non PEW group, diagnosed at the age of 11.8 (8.5, 12.2) years, including 5 cases in stage 1, 13 cases in stage 2, 46 cases in stage 3, 31 cases in stage 4, and 106 cases in stage 5. The Chi-squared test and t test showed that the systolic blood pressure, diastolic blood pressure, birth weight and carbon dioxide binding capacity of the CKD PEW group were lower than those of the non PEW group ((109±22) vs. (120±20) mmHg (1 mmHg=0.133 kPa), (72±19) vs. (79±16) mmHg, (2.9±0.5) vs. (3.2±0.6) kg, (17±4) vs. (19±4) mmol/L,t=2.85, 2.14, 0.67, 2.63, all P<0.05). Multivariate logistic regression analysis showed that carbon dioxide binding capacity and birth weight were independent protective factors of CKDPEW in children (OR=0.81 and 0.36, 95%CI=0.73-0.90 and 0.17-0.77, respectively; both P<0.01); the risk of PEW in CKD children decreased by 0.187 times for every 1 mmol/L increment in carbon dioxide binding capacity, and 0.638 times for every 1 kg increment in birth weight. Conclusions: The incidence of protein energy expenditure in children with chronic kidney disease is lower than that in the previous researches. PEW can appear in CKD 1-2 stage, and attention should be paid to it in the early stage of CKD in clinical practice. Low birth weight CKD children are susceptible to PEW, and actively correcting metabolic acidosis can reduce the risk of CKDPEW.

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