Paediatrics, All India Institute of Medical Sciences, Patna, Bihar, India.
Neonatology, AIIMS, Patna, Bihar, India.
BMJ Paediatr Open. 2024 Oct 11;8(1):e002902. doi: 10.1136/bmjpo-2024-002902.
Neonatal jaundice is the most common cause of neonatal morbidity and rehospitalisation in the first week of life, affecting approximately 60% of term and 80% of preterm neonates, with 10% requiring phototherapy to prevent bilirubin-induced neurological dysfunction. Enterohepatic circulation contributes 10%-20% of the body's bilirubin load, and oral calcium-phosphate can inhibit this process by binding to unconjugated bilirubin and acting as a bilirubin-trapping agent in the gut. This study aimed to evaluate the efficacy of oral calcium phosphate as an adjunct to phototherapy in reducing phototherapy duration, improving bilirubin decline rate and lowering rebound hyperbilirubinaemia incidence.
This double-blind, placebo-controlled randomised controlled trial with a 1:1 allocation ratio was conducted in the neonatal intensive care unit of a tertiary care hospital in Eastern India. The investigator and the analyst were blinded to the treatment assignments. Eligible neonates with neonatal jaundice requiring phototherapy as per the 'American Academy of Pediatrics or 'National Institute for Health and Care Excellence' guidelines were enrolled and randomly assigned to receive either oral calcium phosphate or placebo.
The total duration of phototherapy was significantly lower in the intervention group compared with placebo (18.8±5.63 hours vs 24.3±4.50 hours; mean difference=-5.55 (95% CI -7.82 to -3.28), p<0.001). The rate of fall of bilirubin (mg/dL/hour) was also significantly higher in the intervention group (0.186±0.0137 vs 0.116±0.0088; mean difference=0.0693 (95% CI 0.0642 to 0.0745), p<0.001). The intervention group showed a trend towards a decrease in the incidence of rebound hyperbilirubinaemia, with a relative risk of 0.30 ((95% CI 0.0891 to 1.01), p=0.066).
The use of oral calcium phosphate results in a statistically significant reduction in phototherapy hours, an improvement in the rate of bilirubin decline and a decrease in rebound hyperbilirubinaemia incidence. This allows for shorter hospital stays and reduces the need for rehospitalisation, resulting in less mother-baby dyad separation, lower hospital resource consumption and reduced financial burden on parents.
Clinical-trials-registry-India, Ref No.CTRI/2022/03/041203, dated 21 March 2022https://ctri.nic.in/Clinicaltrials/showallp.php?mid1=57944&EncHid=&userName=Phototherapy.
新生儿黄疸是新生儿生命的第一周最常见的发病原因和再住院原因,约 60%的足月新生儿和 80%的早产儿会受到影响,其中 10%需要光疗来预防胆红素诱导的神经功能障碍。肠肝循环占身体胆红素负荷的 10%-20%,口服钙-磷可以通过与未结合胆红素结合,并在肠道中充当胆红素捕获剂来抑制这个过程。本研究旨在评估口服钙-磷作为光疗辅助手段,以减少光疗时间、提高胆红素下降率和降低胆红素反弹发生率的疗效。
这是一项在印度东部一家三级保健医院新生儿重症监护病房进行的双盲、安慰剂对照随机对照试验,分配比例为 1:1。研究者和分析者对治疗分配均设盲。符合需要根据“美国儿科学会”或“国家卫生与保健卓越研究所”指南进行光疗的新生儿黄疸标准的新生儿被纳入研究并随机分配接受口服钙-磷或安慰剂。
与安慰剂组相比,干预组的光疗总持续时间显著降低(18.8±5.63 小时 vs 24.3±4.50 小时;平均差值=-5.55(95%CI -7.82 至 -3.28),p<0.001)。干预组的胆红素下降率(mg/dL/小时)也显著更高(0.186±0.0137 与 0.116±0.0088;平均差值=0.0693(95%CI 0.0642 至 0.0745),p<0.001)。干预组显示出降低胆红素反弹发生率的趋势,相对风险为 0.30(95%CI 0.0891 至 1.01),p=0.066)。
口服钙-磷的使用可显著减少光疗时间,提高胆红素下降率,降低胆红素反弹发生率。这可以缩短住院时间,减少再住院的需要,从而减少母婴分离,降低医院资源消耗和减轻父母的经济负担。
印度临床试验注册中心,注册号 CTRI/2022/03/041203,日期 2022 年 3 月 21 日https://ctri.nic.in/Clinicaltrials/showallp.php?mid1=57944&EncHid=&userName=Phototherapy。