Kaguelidou Florentia, Alberti Corinne, Biran Valerie, Bourdon Olivier, Farnoux Caroline, Zohar Sarah, Jacqz-Aigrain Evelyne
Assistance Publique - Hôpitaux de Paris, Department of Pediatric Pharmacology and Pharmacogenetics and INSERM CIC1426, Hôpital Robert Debré, Paris, France.
Univ Paris 7-Diderot, Sorbonne Paris Cité, ED 563-EA7323, Paris, France.
PLoS One. 2016 Dec 21;11(12):e0166207. doi: 10.1371/journal.pone.0166207. eCollection 2016.
Proton pump inhibitors are frequently administered on clinical symptoms in neonates but benefit remains controversial. Clinical trials validating omeprazole dosage in neonates are limited. The objective of this trial was to determine the minimum effective dose (MED) of omeprazole to treat pathological acid reflux in neonates using reflux index as surrogate marker.
Double blind dose-finding trial with continual reassessment method of individual dose administration using a Bayesian approach, aiming to select drug dose as close as possible to the predefined target level of efficacy (with a credibility interval of 95%).
Neonatal Intensive Care unit of the Robert Debré University Hospital in Paris, France.
Neonates with a postmenstrual age ≥ 35 weeks and a pathologic 24-hour intra-esophageal pH monitoring defined by a reflux index ≥ 5% over 24 hours were considered for participation. Recruitment was stratified to 3 groups according to gestational age at birth.
Five preselected doses of oral omeprazole from 1 to 3 mg/kg/day.
Primary outcome, measured at 35 weeks postmenstrual age or more, was a reflux index <5% during the 24-h pH monitoring registered 72±24 hours after omeprazole initiation.
Fifty-four neonates with a reflux index ranging from 5.06 to 27.7% were included. Median age was 37.5 days and median postmenstrual age was 36 weeks. In neonates born at less than 32 weeks of GA (n = 30), the MED was 2.5mg/kg/day with an estimated mean posterior probability of success of 97.7% (95% credibility interval: 90.3-99.7%). The MED was 1mg/kg/day for neonates born at more than 32 GA (n = 24).
Omeprazole is extensively prescribed on clinical symptoms but efficacy is not demonstrated while safety concerns do exist. When treatment is required, the daily dose needs to be validated in preterm and term neonates. Optimal doses of omeprazole to increase gastric pH and decrease reflux index below 5% over 24 hours, determined using an adaptive Bayesian design differ among neonates. Both gestational and postnatal ages account for these differences but their differential impact on omeprazole doses remains to be determined.
质子泵抑制剂常用于根据新生儿临床症状给药,但疗效仍存在争议。验证新生儿奥美拉唑剂量的临床试验有限。本试验的目的是使用反流指数作为替代指标,确定治疗新生儿病理性酸反流的奥美拉唑最低有效剂量(MED)。
采用贝叶斯方法的连续重新评估个体剂量给药的双盲剂量探索试验,旨在选择尽可能接近预定义疗效目标水平(可信度区间为95%)的药物剂量。
法国巴黎罗伯特·德布雷大学医院新生儿重症监护病房。
纳入月经龄≥35周且24小时食管内pH监测病理性(定义为24小时内反流指数≥5%)的新生儿。根据出生时的胎龄将招募对象分为3组。
口服奥美拉唑的5个预选剂量,范围为1至3mg/kg/天。
主要结局在月经龄35周及以上时测量,为奥美拉唑开始给药72±24小时后24小时pH监测期间反流指数<5%。
纳入54例反流指数在5.06%至27.7%之间的新生儿。中位年龄为37.5天,中位月经龄为36周。在孕龄小于32周出生的新生儿(n = 30)中,MED为2.5mg/kg/天,估计成功的平均后验概率为97.7%(95%可信度区间:90.3 - 99.7%)。孕龄大于32周出生的新生儿(n = 24)的MED为1mg/kg/天。
奥美拉唑广泛根据临床症状处方,但疗效未得到证实,同时确实存在安全问题。需要治疗时,每日剂量需要在早产和足月新生儿中进行验证。使用适应性贝叶斯设计确定的使胃pH值升高并使24小时内反流指数降至5%以下的奥美拉唑最佳剂量在新生儿中有所不同。胎龄和出生后年龄均导致了这些差异,但它们对奥美拉唑剂量的不同影响仍有待确定。