Srinivasan Ramesh, Meyer Rosan, Padmanabhan Ramnarayan, Britto Joseph
Paediatric Intensive Care Unit, St. Mary's Hospital, Praed Street, London W2 1NY, United Kingdom.
J Pediatr Gastroenterol Nutr. 2006 Feb;42(2):171-3. doi: 10.1097/01.mpg.0000189335.62397.cf.
Diarrhea is frequently observed among critically ill children (CIC) admitted for intensive care. There is increasing evidence that probiotics decrease the incidence of acute infectious and nosocomial and antibiotic induced diarrhea amongst children hospitalized in nonintensive care settings. Despite theoretic advantages for the use of probiotics in CIC, safety has remained a concern in this vulnerable group. The objective of this study was to establish clinical safety (invasive infection/colonization) of Lactobacillus casei shirota (LCS) used as a probiotic in CIC.
Prospective, descriptive pilot study on children admitted to a pediatric intensive care unit. Data regarding safety were collected on the initial recruits to a randomized controlled trial aimed to study the effects of LCS on stool frequency and consistency in CIC. Safety was assessed by bacteriologic surveillance for LCS in surface swabs and endotracheal aspirates (colonization) as well as blood, urine, and sterile body fluid cultures (invasive infection/bacteremia).
Safety data were available on 28 patients. LCS was cultured from the feces of five of the six study subjects who opened bowels during their stay on the pediatric intensive care unit. There was no evidence of either colonization or bacteremia with LCS in bacteriologic cultures obtained from study subjects. The preparation was well tolerated with no apparent side effects.
Our pilot safety study suggests that the use of LCS as a probiotic in enterally fed CIC is safe.
在入住重症监护病房的危重症儿童(CIC)中,腹泻较为常见。越来越多的证据表明,益生菌可降低非重症监护病房住院儿童急性感染性腹泻、医院获得性腹泻及抗生素相关性腹泻的发生率。尽管在危重症儿童中使用益生菌理论上有诸多益处,但在这一弱势群体中,安全性仍是一个令人担忧的问题。本研究的目的是确定在危重症儿童中用作益生菌的干酪乳杆菌代田株(LCS)的临床安全性(侵袭性感染/定植)。
对入住儿科重症监护病房的儿童进行前瞻性描述性试点研究。在一项旨在研究LCS对危重症儿童大便频率和稠度影响的随机对照试验中,对最初招募的受试者收集安全性数据。通过对表面拭子和气管内吸出物(定植)中的LCS进行细菌学监测以及对血液、尿液和无菌体液培养物(侵袭性感染/菌血症)来评估安全性。
有28例患者的安全性数据。在儿科重症监护病房住院期间排便的6名研究对象中,有5人的粪便中培养出了LCS。在从研究对象获得的细菌学培养物中,没有LCS定植或菌血症的证据。该制剂耐受性良好,无明显副作用。
我们的试点安全性研究表明,在经肠内喂养的危重症儿童中使用LCS作为益生菌是安全的。