Center for Advanced Intestinal Rehabilitation, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
J Pediatr Gastroenterol Nutr. 2024 Feb;78(2):217-222. doi: 10.1002/jpn3.12075. Epub 2023 Dec 10.
D-lactic acidosis (DLA) is a serious complication of short bowel syndrome (SBS) in children with intestinal failure (IF). Malabsorbed carbohydrates are metabolized by bacteria in the intestine to D-lactate which can lead to metabolic acidosis and neurologic symptoms.
A retrospective chart review was performed in children ≤18 years old with SBS who had one of the following criteria: unexplained metabolic acidosis, neurologic signs or symptoms, history of antibiotic therapy for small bowel bacterial overgrowth, or high clinical suspicion of DLA. Cases had serum D-lactate concentration >0.25 mmol/L; controls with concentrations ≤0.25 mmol/L.
Of forty-six children, median age was 3.16 (interquartile range (IQR): 1.98, 5.82) years, and median residual bowel length was 40 (IQR: 25, 59) cm. There were 23 cases and 23 controls. Univariate analysis showed that cases had significantly lower median bicarbonate (19 vs. 24 mEq/L, p = 0.001), higher anion gap (17 vs. 14 mEq/L, p < 0.001) and were less likely to be receiving parenteral nutrition, compared with children without DLA. Multivariable analysis identified midgut volvulus, history of intestinal lengthening procedure, and anion gap as significant independent risk factors. Midgut volvulus was the strongest independent factor associated with DLA (adjusted odds ratio = 17.1, 95% CI: 2.21, 133, p = 0.007).
DLA is an important complication of pediatric IF due to SBS. Patients with IF, particularly those with history of midgut volvulus, having undergone intestinal lengthening, or with anion gap acidosis, should be closely monitored for DLA.
D-乳酸酸中毒(DLA)是儿童短肠综合征(SBS)伴肠衰竭(IF)的严重并发症。未被吸收的碳水化合物在肠道内被细菌代谢为 D-乳酸,从而导致代谢性酸中毒和神经系统症状。
对患有 SBS 的≤18 岁儿童进行回顾性图表审查,这些儿童符合以下标准之一:不明原因的代谢性酸中毒、神经症状或体征、小肠细菌过度生长的抗生素治疗史,或 DLA 的高度临床怀疑。病例的血清 D-乳酸浓度>0.25mmol/L;对照组的浓度≤0.25mmol/L。
在 46 名儿童中,中位年龄为 3.16(四分位距(IQR):1.98,5.82)岁,中位残留肠长度为 40(IQR:25,59)cm。有 23 例病例和 23 例对照。单变量分析表明,病例的中位碳酸氢盐明显较低(19 对 24 mEq/L,p=0.001),阴离子间隙较高(17 对 14 mEq/L,p<0.001),且不太可能接受肠外营养。多变量分析确定中肠旋转不良、肠延长术史和阴离子间隙是显著的独立危险因素。中肠旋转不良是与 DLA 相关的最强独立因素(调整后的优势比=17.1,95%可信区间:2.21,133,p=0.007)。
DLA 是儿童 SBS 引起 IF 的一个重要并发症。患有 IF 的儿童,尤其是有中肠旋转不良、肠延长术史或阴离子间隙酸中毒病史的儿童,应密切监测 DLA。