Besunder J B, Anderson R L, Super D M
Department of Pediatrics, MetroHealth Medical Center, Cleveland, OH 44109, USA.
Pediatrics. 1995 Oct;96(4 Pt 1):683-7.
To determine the short-term efficacy of meso-2,3-dimercaptosuccinic acid (DMSA) in mild to moderately lead poisoned children.
Medical records of all pediatric patients receiving 19 days of DMSA between June 1991 and May 1993 were reviewed retrospectively. Patients were included if their pretreatment blood lead concentration (BPb) was 1.21 to 2.36 mumol/L (25 to 49 micrograms/dL) and excluded if they: received DMSA through participation in a pharmaceutical company-sponsored drug study; underwent chelation therapy in the previous 28 days; or received another chelating agent concomitantly with DMSA; or if noncompliance was documented. Homes were inspected and abated of major hazards before chelation therapy. BPb and blood zinc protoporphyrin concentration (ZnP) were obtained at baseline. DMSA was administered in a dose approximating 10 mg/kg per dose every 8 hours for 5 days, followed by 10 mg/kg per dose every 12 hours for 14 days. Baseline laboratory studies were repeated weekly while the patients were receiving therapy and for 2 weeks after therapy, then monthly unless chelated again.
Of the 46 children who were treated with DMSA, 18 were excluded from the analysis. In the remaining 28 children, the mean +/- SD pretreatment BPb and ZnP were 1.79 +/- 0.33 mumol/L (37 +/- 6.9 micrograms/dL) and 1.26 +/- 0.64 mumol/L (71 +/- 36.1 micrograms/dL), respectively. The percent reduction (mean +/- SD) in BPb compared with baseline was -43% +/- 20.8%, -26% +/- 16.9%, and -31% +/- 20.2% on mean days 18, 30, and 80, respectively, whereas the changes in ZnP were -12% +/- 21.7%, -20% +/- 18.1%, and -31% +/- 21.9%, respectively. Eighty percent of patients had 20% or more reduction in their pretreatment BPb and/or ZnP after completion of DMSA therapy (95% confidence interval, 61, 92%). No significant adverse effects were observed except for neutropenia (absolute neutrophil count of 0.752 x 10(9)/L) in one patient.
Our findings support the short-term efficacy of DMSA in children with BPb of 2.36 mumol/L (49 micrograms/dL) or less.
确定中-2,3-二巯基丁二酸(DMSA)对轻度至中度铅中毒儿童的短期疗效。
回顾性分析1991年6月至1993年5月期间接受19天DMSA治疗的所有儿科患者的病历。纳入标准为治疗前血铅浓度(BPb)为1.21至2.36μmol/L(25至49μg/dL),排除标准为:通过参与制药公司赞助的药物研究接受DMSA治疗;在过去28天内接受过螯合治疗;或与DMSA同时接受另一种螯合剂治疗;或有记录显示不依从。在螯合治疗前对家庭进行检查并消除主要危害。在基线时获取BPb和血锌原卟啉浓度(ZnP)。DMSA的给药剂量约为每剂10mg/kg,每8小时一次,共5天,然后每12小时一次,每剂10mg/kg,共14天。在患者接受治疗期间每周重复进行基线实验室检查,治疗后2周也进行检查,然后每月检查一次,除非再次进行螯合治疗。
46例接受DMSA治疗的儿童中,18例被排除在分析之外。在其余28例儿童中,治疗前BPb和ZnP的平均值±标准差分别为1.79±0.33μmol/L(37±6.9μg/dL)和1.26±0.64μmol/L(71±36.1μg/dL)。与基线相比,BPb的平均降低百分比(平均值±标准差)在第18、30和80天分别为-43%±20.8%、-26%±16.9%和-31%±20.2%,而ZnP的变化分别为-12%±21.7%、-20%±18.1%和-31%±21.9%。80%的患者在完成DMSA治疗后,其治疗前BPb和/或ZnP降低了20%或更多(95%置信区间,61,92%)。除1例患者出现中性粒细胞减少(绝对中性粒细胞计数为0.752×10⁹/L)外,未观察到明显不良反应。
我们的研究结果支持DMSA对BPb为2.36μmol/L(49μg/dL)或更低的儿童具有短期疗效。