Fecal Microbiota Transplantation for Clostridioides difficile Infection in Immunocompromised Pediatric Patients

被引:4
|
作者
Conover, Katie R. [1 ]
Absah, Imad [2 ]
Ballal, Sonia [3 ]
Brumbaugh, David [4 ]
Cho, Stanley [5 ]
Cardenas, Maria C. [2 ]
Knackstedt, Elizabeth Doby [6 ]
Goyal, Alka [7 ]
Jensen, M. Kyle [8 ]
Kaplan, Jess L. [9 ]
Kellermayer, Richard
Kociolek, Larry K. [10 ]
Michail, Sonia
Oliva-Hemker, Maria
Reed, Anna W.
Weatherly, Madison [3 ]
Kahn, Stacy A. [3 ]
Nicholson, Maribeth R. [11 ]
机构
[1] Vanderbilt Univ, Dept Gen Pediat, Med Ctr, Nashville, TN USA
[2] Mayo Clin, Div Pediat Gastroenterol Hepatol & Nutr, Childrens Ctr, Rochester, MN USA
[3] Boston Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, Boston, MA USA
[4] Childrens Hosp Colorado, Div Pediat Gastroenterol Hepatol & Nutr, Aurora, CO USA
[5] Texas Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, Houston, TX USA
[6] Univ Utah, Primary Childrens Hosp, Div Pediat Infect Dis, Salt Lake City, UT USA
[7] Lucile Packard Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, Palo Alto, CA USA
[8] Univ Utah, Primary Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, Salt Lake City, UT USA
[9] Mass Gen Hosp Children, Div Pediat Gastroenterol Hepatol & Nutr, Boston, MA USA
[10] Ann & Robert H Lurie Childrens Hosp Chicago, Div Pediat Infect Dis, Chicago, IL USA
[11] Monroe Carell Jr Childrens Hosp Vanderbilt, Div Pediat Gastroenterol Hepatol & Nutr, 2200 Childrens Way, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
children; infection; malignancy; serious adverse events; RISK-FACTORS; RECURRENT; CHILDREN;
D O I
10.1097/MPG.0000000000003714
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: We sought to evaluate the safety and effectiveness of fecal microbiota transplantation (FMT) for recurrent Clostridioides difficile infection (CDI) in pediatric immunocompromised (IC) patients. Methods: This is a multicenter retrospective cohort study of pediatric participants who underwent FMT between March 2013 and April 2020 with Results: Of 59 pediatric patients identified at 9 centers, there were 42 who met inclusion and no exclusion criteria. Included patients had a median age of 6.7 years. Etiology of IC included: solid organ transplantation (18, 43%), malignancy (12, 28%), primary immunodeficiency (10, 24%), or other chronic conditions (2, 5%). Success rate was 79% after first FMT and 86% after 1 or more FMT. There were no statistically significant differences in patient characteristics or procedural components when patients with a failed FMT were compared to those with a successful FMT. There were 15 total serious adverse events (SAEs) in 13 out of 42 (31%) patients that occurred during the follow-up period; 4 (9.5%) of which were likely treatment-related. There were no deaths or infections with multidrug resistant organisms during follow-up and all patients with a SAE fully recovered. Conclusions: The success rate of FMT for recurrent CDI in this pediatric IC cohort is high and mirrors data for IC adults and immunocompetent children. FMT-related SAEs do occur (9.5%) and highlight the need for careful consideration of risk and benefit.
引用
收藏
页码:440 / 446
页数:7
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