Clinical Impact of Multiplex Molecular Diagnostic Testing in Children With Acute Gastroenteritis Presenting to an Emergency Department: A Multicenter Prospective Study

被引:5
作者
Pavia, Andrew T. [1 ,2 ,10 ]
Cohen, Daniel M. [3 ]
Leber, Amy L. [3 ]
Daly, Judy A. [4 ]
Jackson, Jami T. [5 ]
Selvarangan, Rangaraj [5 ]
Kanwar, Neena [5 ]
Bender, Jeffrey M. [6 ]
Bard, Jennifer Dien
Festekjian, Ara [6 ]
Duffy, Susan [7 ]
Larsen, Chari [1 ,2 ]
Holmberg, Kristen M. [8 ]
Bardsley, Tyler [9 ]
Haaland, Benjamin [9 ]
Bourzac, Kevin M. [8 ]
Christopher, Stockmann
Chapin, Kimberle C. [9 ]
Leung, Daniel T. [1 ,2 ,10 ]
机构
[1] Univ Utah, Spencer Fox Eccles Sch Med, Dept Pediat, Salt Lake City, UT USA
[2] Univ Utah, Spencer Fox Eccles Sch Med, Dept Internal Med, Salt Lake City, UT USA
[3] Nationwide Childrens Hosp, Dept Pediat, Columbus, OH USA
[4] Univ Utah, Spencer Fox Eccles Sch Med, Dept Pathol, Salt Lake City, UT USA
[5] Childrens Mercy Hosp, Kansas City, MO USA
[6] Univ Southern Calif, Childrens Hosp Los Angeles, Keck Sch Med, Los Angeles, CA USA
[7] BioMerieux, Salt Lake City, UT USA
[8] Univ Utah, Sch Med, Dept Populat Hlth Sci, Salt Lake City, UT USA
[9] Brown Univ, Rhode Isl Hosp, Warren Alpert Med Sch, Dept Pathol & Lab Med, Providence, RI USA
[10] Univ Utah, Div Pediat Infect Dis, Spencer Fox Eccles Sch Med, 30 Mario Capecchi Dr, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
pediatric gastroenteritis; diarrhea; multiplex polymerase chain reaction; diagnosis; outcomes; INFECTIOUS-DISEASES SOCIETY; GASTROINTESTINAL PATHOGENS; DIARRHEAL DISEASE; GUIDELINES; ETIOLOGY; MANAGEMENT; BURDEN; PANELS; GEMS;
D O I
10.1093/cid/ciad710
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Multiplex molecular diagnostic panels have greatly enhanced detection of gastrointestinal pathogens. However, data on the impact of these tests on clinical and patient-centered outcomes are limited.Methods We conducted a prospective, multicenter, stepped-wedge trial to determine the impact of multiplex molecular testing at 5 academic children's hospitals on children presenting to the emergency department with acute gastroenteritis. Caregivers were interviewed on enrollment and 7-10 days after enrollment to determine symptoms, risk factors, subsequent medical visits, and impact on family members. During the pre-intervention period, diagnostic testing was performed at the clinician's discretion . During the intervention period, multiplex molecular testing was performed on all children, with results available to clinicians. The primary outcome was return visits to a healthcare provider within 10 days of enrollment.Results Potential pathogens were identified by clinician-ordered tests in 19 of 571 (3.3%) in the pre-intervention period compared with 434 of 586 (74%) in the intervention period; clinically relevant pathogens were detected in 2.1% and 15%, respectively. In the multivariate model, the intervention was associated with a 21% reduction in the odds of any return visit (odds ratio, 0.79; 95% confidence interval, .70-.90) after adjusting for potential confounders. Appropriate treatment was prescribed in 11.3% compared with 19.6% during the intervention period (P = .22).Conclusions Routine molecular multiplex testing for all children who presented to the ED with acute gastroenteritis detected more clinically relevant pathogens and led to a 21% decrease in return visits. Additional research is needed to define patients most likely to benefit from testing. Clinical Trials Registration. NCT02248285.Conclusions Routine molecular multiplex testing for all children who presented to the ED with acute gastroenteritis detected more clinically relevant pathogens and led to a 21% decrease in return visits. Additional research is needed to define patients most likely to benefit from testing. Clinical Trials Registration. NCT02248285. Limited data exist on the impact of sensitive multiplex molecular panels for gastroenteritis. In a multicenter trial, implementation of multiplex molecular testing for pediatric emergency department patients with gastroenteritis increased detection of clinically significant pathogens and reduced return visit .
引用
收藏
页码:573 / 581
页数:9
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