Sindgikar Seema Pavaman, Shenoy Krithika Damodar, Kamath Nutan, Shenoy Rathika
Associate Professor, Department of Paediatrics, K S Hegde Medical Academy, NITTE University, Mangalore, Karnataka, India.
Intern, Department of Paediatrics, Kasturba Medical College, Manipal University, Mangalore, Karnataka, India.
J Clin Diagn Res. 2017 Sep;11(9):SC11-SC14. doi: 10.7860/JCDR/2017/28793.10632. Epub 2017 Sep 1.
Organic Acidurias (OA) accounts between 10% and 40% of confirmed Inborn Errors of Metabolism (IEM) in India. With prompt recognition and management, better survival but adverse neurodevelopmental outcome is reported.
To study the clinical and metabolic presentation, management with immediate and long term outcome of symptomatic children with confirmed OA.
Hospital based study of symptomatic children diagnosed to have OA between 2003 and 2009 and the survivors followed up over next five years. Diagnosis was based on clinical and metabolic presentation and confirmed by spectrometry analyses of urine and blood. Management, immediate outcome, compliance to treatment and recurrence of crises were documented. Neurodevelopmental outcome was assessed in follow up. Mean with Standard Error (Mean ± SE) and frequencies with percentages were calculated.
Of 72 cases suspected to have IEM, 38 (52.8%) were confirmed of (IEM), and out of which 15 (39.5%) had OA. Methyl malonic acidemia, multiple carboxylase deficiency and Propionic Acidemia (PA) constituted the largest proportion. Neurodevelopmental issues (73.3%) and metabolic crisis (53.3%) were common presenting features. Mean ± SE of ammonia was 639.0±424.1 μg/dl and lactate was 33.6±4.9 mg/dl. Mean pH, bicarbonate, and anion gap was 7.27±0.07, 14.1±2.3 and 17.9±2.3 respectively. Management was protocol based. Death was reported in two cases of PA; other morbidities were seen in five. Recurrent crisis (46.7%) complicated the follow up in survivors. Spasticity, extrapyramidal movement disorder, intellectual subnormality, autism spectrum, attention deficit hyperactivity disorder and sensory neural deafness were seen amongst survivors, in spite of compliance to therapy.
OA is part of differential diagnosis in sick children and treatment needs to be prompt and specific. Prognosis is guarded even with long term cofactor supplementation in the symptomatic.
在印度,有机酸血症(OA)占确诊的先天性代谢缺陷(IEM)的10%至40%。据报道,通过及时识别和管理,患者存活率有所提高,但神经发育结局不良。
研究确诊为OA的有症状儿童的临床和代谢表现、即时及长期治疗效果。
对2003年至2009年间诊断为OA的有症状儿童进行基于医院的研究,并对存活者在接下来的五年进行随访。诊断基于临床和代谢表现,并通过尿液和血液的光谱分析得以证实。记录治疗、即时治疗效果、治疗依从性和危机复发情况。随访时评估神经发育结局。计算均值及标准误(Mean ± SE)以及频率和百分比。
在72例疑似患有IEM的病例中,38例(52.8%)确诊为IEM,其中15例(39.5%)患有OA。甲基丙二酸血症、多种羧化酶缺乏症和丙酸血症(PA)占比最大。神经发育问题(73.3%)和代谢危机(53.3%)是常见的表现特征。氨的均值±标准误为639.0±424.1μg/dl,乳酸为33.6±4.9mg/dl。平均pH值、碳酸氢盐和阴离子间隙分别为7.27±0.07、14.1±2.3和17.9±2.3。治疗基于方案进行。PA患者中有2例死亡报告;另外5例出现其他病症。复发危机(46.7%)使存活者的随访复杂化。尽管坚持治疗,但存活者中仍出现痉挛、锥体外系运动障碍、智力发育迟缓、自闭症谱系障碍、注意力缺陷多动障碍和感音神经性耳聋。
OA是患病儿童鉴别诊断的一部分,治疗需要及时且具有针对性。即使对有症状者进行长期辅助因子补充,预后仍不容乐观。