快速床边基因分型以避免新生儿重症监护中氨基糖苷类药物引起的耳毒性。
Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care.
机构信息
Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
School of Biological Sciences, Division of Evolution, Infection and Genomics, University of Manchester, Manchester, United Kingdom.
出版信息
JAMA Pediatr. 2022 May 1;176(5):486-492. doi: 10.1001/jamapediatrics.2022.0187.
IMPORTANCE
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.
OBJECTIVE
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.
DESIGN, SETTING, AND PARTICIPANTS: 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.
INTERVENTIONS
Neonates were tested for the m.1555A>G variant via the rapid POCT on admission to the neonatal intensive care unit.
MAIN OUTCOMES AND MEASURES
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.
RESULTS
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.
CONCLUSIONS AND RELEVANCE
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.
重要性
氨基糖苷类药物通常被开处方用于治疗新生儿败血症。MT-RNR1 m.1555A>G 变异体易发生严重的氨基糖苷类药物诱导的耳毒性 (AIO)。目前的基因分型方法需要数天时间,在急性情况下不可行。
目的
在将这项技术应用于急性新生儿环境之前,开发一种用于 m.1555A>G 变异体的快速床边检测 (POCT),以指导抗生素的开具并避免 AIO。
设计、地点和参与者:这项实用的前瞻性实施试验招募了 2020 年 1 月 6 日至 2020 年 11 月 30 日期间在英国的 2 家大型新生儿重症监护病房住院的新生儿。
干预措施
新生儿在入住新生儿重症监护病房时通过快速 POCT 检测 m.1555A>G 变异体。
主要结果和措施
主要结局评估所有接受抗生素治疗的婴儿中成功检测到变异体的新生儿比例。次要结局衡量实施是否与常规临床实践呈负相关以及系统的性能。该研究在统计学上有足够的能力来检测在实施 MT-RNR1 POCT 前后抗生素给药时间的显著差异。
结果
共招募了 751 名新生儿,中位(范围)年龄为 2.5(0-198)天。MT-RNR1 POCT 能够在 26 分钟内对 m.1555A>G 变异体进行基因分型。临床前验证显示 100%的灵敏度(95%CI,93.9%-100.0%)和特异性(95%CI,98.5%-100.0%)。确定了 3 名携带 m.1555A>G 变异体的参与者,他们均避免了氨基糖苷类抗生素。总的来说,424 名(80.6%)接受抗生素治疗的婴儿成功检测到该变异体,抗生素的平均使用时间与以往相同。
结论和相关性
MT-RNR1 POCT 在不干扰正常临床实践的情况下得到整合,并且基于基因型指导抗生素的开具和避免 AIO。这种方法在改变实践的时间范围内确定了 m.1555A>G 变异体,广泛采用可能会显著降低 AIO 的负担。