Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School Children's Hospital, Hannover, Germany.
Center for Congenital Kidney Diseases, Center for Rare Diseases, Hannover Medical School, Hannover, Germany.
Nat Rev Nephrol. 2019 Sep;15(9):577-589. doi: 10.1038/s41581-019-0161-4. Epub 2019 Jun 13.
Achieving normal growth is one of the most challenging problems in the management of children with chronic kidney disease (CKD). Treatment with recombinant human growth hormone (GH) promotes longitudinal growth and likely enables children with CKD and short stature to reach normal adult height. Here, members of the European Society for Paediatric Nephrology (ESPN) CKD-Mineral and Bone Disorder (MBD), Dialysis and Transplantation working groups present clinical practice recommendations for the use of GH in children with CKD on dialysis and after renal transplantation. These recommendations have been developed with input from an external advisory group of paediatric endocrinologists, paediatric nephrologists and patient representatives. We recommend that children with stage 3-5 CKD or on dialysis should be candidates for GH therapy if they have persistent growth failure, defined as a height below the third percentile for age and sex and a height velocity below the twenty-fifth percentile, once other potentially treatable risk factors for growth failure have been adequately addressed and provided the child has growth potential. In children who have received a kidney transplant and fulfil the above growth criteria, we recommend initiation of GH therapy 1 year after transplantation if spontaneous catch-up growth does not occur and steroid-free immunosuppression is not a feasible option. GH should be given at dosages of 0.045-0.05 mg/kg per day by daily subcutaneous injections until the patient has reached their final height or until renal transplantation. In addition to providing treatment recommendations, a cost-effectiveness analysis is provided that might help guide decision-making.
实现正常生长是慢性肾脏病(CKD)患儿管理中最具挑战性的问题之一。重组人生长激素(GH)治疗可促进纵向生长,使 CKD 和身材矮小的儿童可能达到正常成人身高。在这里,欧洲儿科学肾脏病学(ESPN)CKD-矿物质和骨代谢紊乱(MBD)、透析和移植工作组的成员提出了在透析和肾移植后接受 GH 治疗的 CKD 儿童的临床实践建议。这些建议是在儿科内分泌学家、儿科肾脏病学家和患者代表的外部咨询小组的投入下制定的。我们建议,如果患有持续生长障碍的 3-5 期 CKD 或正在接受透析的儿童已经充分解决了其他潜在的可治疗生长障碍的危险因素,并且具有生长潜力,那么他们应该是 GH 治疗的候选者。对于符合上述生长标准并已接受肾移植的儿童,如果未发生自发性追赶生长且无法使用无类固醇免疫抑制,则建议在移植后 1 年开始 GH 治疗。GH 应每天通过皮下注射给予 0.045-0.05mg/kg/天的剂量,直到患者达到最终身高或进行肾移植。除了提供治疗建议外,还提供了成本效益分析,可能有助于指导决策。