首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Oral protein-energy supplements in peritoneal dialysis: a multicenter study.
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Oral protein-energy supplements in peritoneal dialysis: a multicenter study.

机译:腹膜透析中口服蛋白质能量补充剂:一项多中心研究。

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BACKGROUND: Protein-energy malnutrition is prevalent in peritoneal dialysis (PD) patients and is associated with increased morbidity and mortality. OBJECTIVE: To evaluate the impact of prophylactic treatment with an oral protein-energy supplement (Protenplus; Fresenius AG, Bad Homburg, Germany) on nutritional parameters in patients starting PD. DESIGN: Prospective, multicenter, randomized study of group A patients (Protenplus, n = 35) and group B (controls, n = 30), with evaluations at baseline and at 6 and 12 months. Statistical Methods: Efficacy of factors by linear mixed model analysis for repeated measurements, chi-square, t-test, and Mann-Whitney test. OUTCOME PARAMETERS: Patient compliance, serum albumin, and other nutritional parameters. RESULTS: No significant differences were found at baseline evaluation. During follow-up, a significant number of group A patients abandoned intake of the supplement due to non-compliance (n = 7) or side effects (n = 8) (chi2 p < 0.01). Patients with lower residual renal function were less likely to comply. The mixed model in the "intention to treat" analysis showed a significant increase related to supplement intake only in total lymphocyte count in group A. The "as treated" analysis of the 29 patients who fulfilled the study (9 in group A, 20 in group B) disclosed that belonging to group A constituted an independent factor for increased lymphocyte count (p < 0.001), body weight (p < 0.03), tricipital skinfold thickness (p < 0.01), middle-arm muscle circumference (p < 0.025), lean body mass (LBM) (p < 0.002), creatinine LBM related to body surface area (p < 0.001), and creatinine generation rate (p < 0.002). However, these data may have been biased by the high rate of noncompliance in group A. CONCLUSIONS: Protenplus proved to be unsuitable as a long term, oral protein-energy supplement in PD patients due to a high rate of noncompliance and intolerance, primarily among patients with lower residual renal function. The question of whether other products, better-tolerated as nutritional supplements, could compensate for daily protein peritoneal losses in long-term PD remains open.
机译:背景:蛋白质能量营养不良在腹膜透析(PD)患者中普遍存在,并与发病率和死亡率增加相关。目的:评估口服蛋白质能量补充剂(Protenplus;费森尤斯公司,德国巴特洪堡,德国)的预防性治疗对开始PD的患者营养参数的影响。设计:对A组患者(Protenplus,n = 35)和B组(对照组,n = 30)进行前瞻性,多中心,随机研究,并在基线,第6和第12个月进行评估。统计方法:通过线性混合模型分析对因子进行重复测量,卡方检验,t检验和曼惠特尼检验的功效。结果参数:患者依从性,血清白蛋白和其他营养参数。结果:基线评估未发现明显差异。在随访期间,由于不依从(n = 7)或副作用(n = 8)(chi2 p <0.01),大量A组患者放弃了补充剂的摄入。残余肾功能较低的患者较少遵从。 “意图治疗”分析中的混合模型显示,仅在A组中,仅在总淋巴细胞计数上与补品摄入量有关的显着增加。完成研究的29名患者的“治疗中”分析(A组9例,A组20例) B组)揭示了A组是淋巴细胞计数(p <0.001),体重(p <0.03),三头肌皮褶厚度(p <0.01),中臂肌肉周长(p <0.025)的独立因素,瘦体重(LBM)(p <0.002),与身体表面积相关的肌酐LBM(p <0.001)和肌酐生成率(p <0.002)。但是,这些数据可能因A组的高违规率而产生了偏差。结论:由于高违规率和不耐受率较高,Protenplus被证明不适合作为PD患者的长期口服蛋白质能量补充剂残余肾功能较低的患者。是否可以更好地耐受其他产品作为营养补品,以弥补长期腹膜透析中每日蛋白质腹膜的损失,这一问题仍然存在。

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