Diagnostic Implications of Long-Term Polymerase Chain Reaction Data for Human Metapneumovirus.

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
Jeong Su Han, Jae-Sik Jeon, Jae Kyung Kim
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引用次数: 0

Abstract

Background: The aim of this study was to systematically examine the annual, seasonal, age-specific, and gender-specific epidemiological trends of human metapneumovirus (hMPV) infections, utilizing extensive real-world data collected over 18 years through a consistent testing methodology and analytical protocol.

Methods: Real-time reverse transcription polymerase chain reaction assay results of patients admitted to Dankook University Hospital (2007 - 2024) were retrospectively analyzed. Descriptive statistics were used to assess annual, age-specific, and seasonal trends in hMPV positivity rates. We further evaluated the feasibility of using these data to establish robust epidemiological surveillance systems and standardized monitoring metrics.

Results: Among 23,284 specimens, 991 (4.2%) were positive for hMPV. The highest annual positivity rates were recorded in 2007 (7.7%) and 2011 (8.1%). Children aged 2 - 11 years exhibited the highest positivity rate (6.0%), with positivity rates declining with increasing age, except for a slight increase in individuals aged ≥ 65 years. Seasonally, infections peaked in spring (11.1%), followed by summer (2.8%), winter (1.4%), and autumn (0.8%). Since the onset of the coronavirus disease 2019 (COVID-19) pandemic (2020 - 2024), the overall positivity rate dropped to 1.6% from 4.7% before the pandemic, accompanied by notable changes in seasonal patterns.

Conclusions: This study revealed significant shifts in hMPV epidemiology following the COVID-19 pandemic, including reduced overall circulation, disrupted spring seasonality, and persistent impacts on high-risk pediatric populations. These findings provide evidence to optimize diagnostic testing for hMPV while providing actionable evidence to adjust optimal diagnostic testing windows, enhance infection prevention strategies, and implement focused monitoring of high-risk populations. Specifically, hMPV testing should be prioritized for pediatric patients during the typical peak months (March - May) and expanded to include atypical winter peaks (December - February) in the post-pandemic era. For older adults (≥ 65 years), targeted testing during winter months may enhance diagnostic yield and support timely clinical management.

人偏肺病毒长期聚合酶链反应数据的诊断意义
背景:本研究的目的是系统地检查人类偏肺病毒(hMPV)感染的年度、季节性、年龄特异性和性别特异性流行病学趋势,利用18年来通过一致的测试方法和分析方案收集的大量真实世界数据。方法:回顾性分析檀国大学附属医院2007 - 2024年住院患者实时逆转录聚合酶链反应检测结果。描述性统计用于评估hMPV阳性率的年度、特定年龄和季节性趋势。我们进一步评估了利用这些数据建立强有力的流行病学监测系统和标准化监测指标的可行性。结果:23284例标本中hMPV阳性991例(4.2%)。年阳性率最高的年份是2007年(7.7%)和2011年(8.1%)。2 ~ 11岁儿童阳性率最高(6.0%),阳性率随年龄增长而下降,65岁以上略有上升。从季节上看,感染高峰在春季(11.1%),其次是夏季(2.8%)、冬季(1.4%)和秋季(0.8%)。自2019冠状病毒病(2019 -19)大流行(2020 - 2024年)爆发以来,总体阳性率从大流行前的4.7%降至1.6%,并伴有明显的季节性变化。结论:本研究揭示了2019冠状病毒病大流行后hMPV流行病学的显著变化,包括整体循环减少、春季季节性中断以及对高危儿科人群的持续影响。这些发现为优化hMPV诊断检测提供了证据,同时为调整最佳诊断检测窗口、加强感染预防策略和实施高危人群重点监测提供了可操作的证据。具体而言,hMPV检测应在典型高峰月份(3月至5月)优先针对儿科患者,并在大流行后时代扩大到包括非典型冬季高峰(12月至2月)。对于老年人(≥65岁),在冬季进行有针对性的检测可以提高诊断率并支持及时的临床管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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