Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multicenter Cohort, 2016-2023

被引:11
作者
Rodriguez, Katherine M. [1 ,2 ,3 ]
Vaught, Jordan [1 ,2 ]
Salz, Lisa [3 ]
Foley, Jennifer [1 ]
Boulil, Zaineb [1 ]
Van Dongen-Trimmer, Heather M. [4 ]
Whalen, Drewann [5 ]
Oluchukwu, Okonkwo [5 ,6 ]
Liu, Kuang Chuen [5 ,6 ]
Burton, Jennifer [5 ,6 ]
Syngal, Prachi [5 ,6 ]
Vargas-Shiraishi, Ofelia [7 ]
Kingsmore, Stephen F. [3 ]
Sanford Kobayashi, Erica [3 ,4 ,7 ]
Coufal, Nicole G. [1 ,2 ,3 ]
机构
[1] Rady Childrens Hosp, San Diego, CA 92123 USA
[2] Univ Calif San Diego, Dept Pediat, San Diego, CA 92093 USA
[3] Rady Childrens Inst Genom Med, San Diego, CA 92123 USA
[4] OSF Childrens Hosp Illinois, Peoria, IL USA
[5] Cedars Sinai Med Ctr, Dept Pediat, Los Angeles, CA USA
[6] Univ Illinois, Coll Med Peoria, Dept Pediat, Peoria, IL USA
[7] Childrens Hosp Orange Cty, Dept Pediat, Orange, CA USA
基金
美国国家卫生研究院;
关键词
child; critical care; intensive care units; pediatric; phenotype; whole-genome sequencing; JOINT CONSENSUS RECOMMENDATION; MEDICAL GENETICS; AMERICAN-COLLEGE; STANDARDS; GUIDELINES; VARIANTS; UTILITY; ACMG;
D O I
10.1097/PCC.0000000000003522
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
OBJECTIVES:Analysis of the clinical utility of rapid whole-genome sequencing (rWGS) outside of the neonatal period is lacking. We describe the use of rWGS in PICU and cardiovascular ICU (CICU) patients across four institutions. DESIGN:Ambidirectional multisite cohort study. SETTING:Four tertiary children's hospitals. PATIENTS:Children 0-18 years old in the PICU or CICU who underwent rWGS analysis, from May 2016 to June 2023. INTERVENTIONS:None. MEASUREMENTS AND MAIN RESULTS:A total of 133 patients underwent clinical, phenotype-driven rWGS analysis, 36 prospectively. A molecular diagnosis was identified in 79 patients (59%). Median (interquartile range [IQR]) age was 6 months (IQR 1.2 mo-4.6 yr). Median time for return of preliminary results was 3 days (IQR 2-4). In 79 patients with a molecular diagnosis, there was a change in ICU management in 19 patients (24%); and some change in clinical management in 63 patients (80%). Nondiagnosis changed management in 5 of 54 patients (9%). The clinical specialty ordering rWGS did not affect diagnostic rate. Factors associated with greater odds ratio (OR [95% CI]; OR [95% CI]) of diagnosis included dysmorphic features (OR 10.9 [95% CI, 1.8-105]) and congenital heart disease (OR 4.2 [95% CI, 1.3-16.8]). Variables associated with greater odds of changes in management included obtaining a genetic diagnosis (OR 16.6 [95% CI, 5.5-62]) and a shorter time to genetic result (OR 0.8 [95% CI, 0.76-0.9]). Surveys of pediatric intensivists indicated that rWGS-enhanced clinical prognostication (p < 0.0001) and contributed to a decision to consult palliative care (p < 0.02). CONCLUSIONS:In this 2016-2023 multiple-PICU/CICU cohort, we have shown that timely genetic diagnosis is feasible across institutions. Application of rWGS had a 59% (95% CI, 51-67%) rate of diagnostic yield and was associated with changes in critical care management and long-term patient management.
引用
收藏
页码:699 / 709
页数:11
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