背景:胰腺酶替代疗法(PERT)是胰腺外分泌功能不全(EPI)的标准治疗方法。然而,许多人受到了不适当的对待,在临床剂量方面存在差距,指导方针,和工具来帮助个人滴定。
方法:系统评价确定了不同条件下PERT给药建议的研究和指南,系统地审查和综合PERT总摄入量,膳食/小吃指南,以及随时间的变化,以提供最新的研究和指南中使用的最常见剂量。
结果:这篇对257篇文章的综述发现,PERT给药指南在不同条件下和不同条件下存在很大差异。许多EPI患者服药不足,指南在全球范围内和疾病类型不同,和临床医生开处方也可能发挥作用。最常见的给药指南集中在40,000-50,000单位的脂肪酶/餐的起始剂量,在追求添加剂疗法之前增加高达该数量的2至3倍。指南和研究通常只关注脂肪消化,和每日总剂量的比较显示剂量不足是常见的。大多数PERT研究是关于安全性和有效性,而不是最佳滴定。
结论:当前EPI中PERT的指南显示,给药建议存在很大差异,在疾病类型内和跨疾病类型。这种变化突出了需要进一步研究以优化PERT给药并改善患者预后。医疗保健提供者应考虑根据营养状况和对治疗的反应个性化PERT剂量。考虑到大多数指南都以初始剂量而不是上限为框架,确保定期对患者进行剂量滴定随访。
BACKGROUND: Pancreatic enzyme replacement therapy (PERT) is the standard treatment for exocrine pancreatic insufficiency (EPI). However, many individuals are inadequately treated, with gaps in clinical dosing,
guidelines, and tools to aid individual titration.
METHODS: A systematic review identified research and
guidelines on PERT dosing recommendations across conditions, systematically reviewing and synthesizing total PERT intake, meal/snack
guidelines, and changes over time to provide an up-to-date look at the most common doses used in studies and guidelines.
RESULTS: This review of 257 articles found wide variability in PERT dosing
guidelines within and across conditions. Many patients with EPI are underdosed, with guidelines differing globally and by disease type, and clinician prescribing may also play a role. The most common dosing
guidelines focus on starting doses at 40,000-50,000 units of lipase/meal with increases of up to two to three times this amount before pursuing additive therapies. Guidelines and studies typically focus only on fat digestion, and comparison by total daily dose shows underdosing is common. Most PERT studies are on safety and efficacy rather than optimal titration.
CONCLUSIONS: The current guidelines for PERT in EPI demonstrate substantial variability in dosing recommendations, both within and across disease types. This variation highlights the need for further research to optimize PERT dosing and improve patient outcomes. Healthcare providers should consider individualizing PERT dosing based on nutritional status and response to therapy, ensuring regular follow-up with patients for dose titrations with consideration that most guidelines are framed as initial doses rather than upper limits.