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Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care

医学 抗生素 耳毒性 基因分型 新生儿重症监护室 检测点注意事项 儿科 重症监护 新生儿败血症 心理干预 重症监护室 败血症 重症监护医学 内科学 基因型 化疗 免疫学 精神科 化学 基因 微生物学 生物 顺铂 生物化学
作者
John McDermott,Ajit Mahaveer,Rachel James,Nicola Booth,M. Turner,Karen Harvey,Gino Miele,Glenda M. Beaman,Duncan Stoddard,Karen Tricker,Rachel Corry,Julia Garlick,Shaun Ainsworth,Thomas Beevers,Iain Bruce,Richard Body,Fiona Ulph,Rhona MacLeod,Peter Roberts,Paul Wilson
出处
期刊:JAMA Pediatrics [American Medical Association]
卷期号:176 (5): 486-486 被引量:59
标识
DOI:10.1001/jamapediatrics.2022.0187
摘要

Aminoglycosides are commonly prescribed antibiotics used for the treatment of neonatal sepsis. The MT-RNR1 m.1555A>G variant predisposes to profound aminoglycoside-induced ototoxicity (AIO). Current genotyping approaches take several days, which is unfeasible in acute settings. To develop a rapid point-of-care test (POCT) for the m.1555A>G variant before implementation of this technology in the acute neonatal setting to guide antibiotic prescribing and avoid AIO. This pragmatic prospective implementation trial recruited neonates admitted to 2 large neonatal intensive care units between January 6, 2020, and November 30, 2020, in the UK. Neonates were tested for the m.1555A>G variant via the rapid POCT on admission to the neonatal intensive care unit. The primary outcome assessed the proportion of neonates successfully tested for the variant of all infants prescribed antibiotics. Secondary outcomes measured whether implementation was negatively associated with routine clinical practice and the performance of the system. The study was statistically powered to detect a significant difference between time to antibiotic administration before and after implementation of the MT-RNR1 POCT. A total of 751 neonates were recruited and had a median (range) age of 2.5 (0-198) days. The MT-RNR1 POCT was able to genotype the m.1555A>G variant in 26 minutes. Preclinical validation demonstrated a 100% sensitivity (95% CI, 93.9%-100.0%) and specificity (95% CI, 98.5%-100.0%). Three participants with the m.1555A>G variant were identified, all of whom avoided aminoglycoside antibiotics. Overall, 424 infants (80.6%) receiving antibiotics were successfully tested for the variant, and the mean time to antibiotics was equivalent to previous practice. The MT-RNR1 POCT was integrated without disrupting normal clinical practice, and genotype was used to guide antibiotic prescription and avoid AIO. This approach identified the m.1555A>G variant in a practice-changing time frame, and wide adoption could significantly reduce the burden of AIO.
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