Corda Heike, Kummer Sebastian, Welters Alena, Teig Norbert, Klee Dirk, Mayatepek Ertan, Meissner Thomas
Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital Duesseldorf, Moorenstrasse 5, 40225, Duesseldorf, Germany.
University Children's Hospital, Katholisches Klinikum, Ruhr-Universität Bochum, Bochum, Germany.
Orphanet J Rare Dis. 2017 Jun 2;12(1):108. doi: 10.1186/s13023-017-0653-x.
Treatment of severe diffuse congenital hyperinsulinism (CHI) without sufficient response to diazoxide is complicated by the lack of approved drugs. Therefore, patients are often hospitalized long-term or have to undergo pancreatic surgery if episodes of severe hypoglycaemia cannot be prevented. A long-acting somatostatin analogue, octreotide, has been reported to be an effective treatment option that prevents severe hypoglycaemia in children with CHI, and its off-label use is common in CHI. However, octreotide requires continuous i.v. or s.c. infusion or multiple daily injections. Here, we report our experiences with the use of a monthly application of a long-acting somatostatin analogue, lanreotide autogel® (LAN-ATG), in early infancy.
The mean blood glucose concentration within 7 days before the first LAN-ATG administration were compared to 7 days after the first LAN-ATG administration and increased by 0.75 mmol/L (range 0.39-1.19 mmol/L). In the following weeks intravenous glucose infusions, octreotide, and glucagon treatment could be successfully stopped in all patients 3-20 days after the first LAN-ATG injection without substantial worsening of the hypoglycaemia rate. Increased carbohydrate requirements could be normalized with an average reduction in the carbohydrate-intake of 7 g/kg body weight/d (range 1.75-12.8 g/kg body weight/d). Over a total of 52 treatment months, no serious adverse effects occurred.
Long-term LAN-ATG treatment improved blood glucose concentrations, lowered the frequency of hypoglycaemia or allowed for normalization of oral carbohydrate intake in infants with CHI younger than 6 months of age. No severe side effects were observed. LAN-ATG might be an alternative treatment option in infants with severe CHI who lack risk factors for necrotizing enterocolitis and are not responding to current treatment regimens as an alternative to surgery after careful individual evaluation.
对于严重弥漫性先天性高胰岛素血症(CHI),在对二氮嗪治疗反应不足时,由于缺乏获批药物,治疗变得复杂。因此,如果无法预防严重低血糖发作,患者通常需要长期住院,或者不得不接受胰腺手术。据报道,长效生长抑素类似物奥曲肽是预防CHI患儿严重低血糖的有效治疗选择,其在CHI中的超说明书使用很常见。然而,奥曲肽需要持续静脉内或皮下输注,或每日多次注射。在此,我们报告了在婴儿早期每月应用长效生长抑素类似物兰瑞肽凝胶(LAN-ATG)的经验。
比较首次LAN-ATG给药前7天与首次LAN-ATG给药后7天的平均血糖浓度,血糖浓度升高了0.75 mmol/L(范围为0.39 - 1.19 mmol/L)。在接下来的几周内,所有患者在首次LAN-ATG注射后3 - 20天成功停用了静脉葡萄糖输注、奥曲肽和胰高血糖素治疗,且低血糖发生率没有显著恶化。碳水化合物需求增加的情况得以正常化,碳水化合物摄入量平均减少7 g/kg体重/天(范围为1.75 - 12.8 g/kg体重/天)。在总共52个治疗月中,未发生严重不良反应。
长期LAN-ATG治疗改善了血糖浓度,降低了低血糖频率,或使6个月以下CHI婴儿的口服碳水化合物摄入量正常化。未观察到严重副作用。对于缺乏坏死性小肠结肠炎风险因素且对当前治疗方案无反应的严重CHI婴儿,在经过仔细的个体评估后,LAN-ATG可能是手术之外的另一种治疗选择。