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AASLD2020[1025]血小板计数作为补偿的检查工具 [复制链接]

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发表于 2020-11-3 20:56 |只看该作者 |倒序浏览 |打印
1025
PLATELET COUNT AS A SCREENING TOOL FOR COMPENSATED
CIRRHOSIS
Pallavi Surana1, Julian Hercun2, Varun Takyar3, David E.
Kleiner4, Theo Heller5 and Christopher Koh5, (1)Liver Disease
Branch, National Institute of Diabetes and Digestive and Kidney
Diseases, (2)Liver Diseases Branch, National Institutes of
Diabetes and Digestive and Kidney Diseases, (3)University of
California, Los Angeles, (4)Laboratory of Pathology, National
Cancer Institute, (5)Liver Diseases Branch, National Institute
of Diabetes and Digestive and Kidney Diseases
Background: Platelet count has been used as a component of
non-invasive fibrosis scores and alone as a surrogate marker
for the screening of portal hypertension and varices (i e
Baveno VI criteria) Platelet count, solely, has not been used
as a non-invasive marker for the identification of cirrhosis.
With the discovery of effective therapies, management and
treatment of chronic viral hepatitis is often the responsibility of
primary care providers. A simplified means to detect cirrhosis
would therefore be beneficial to ensure optimal care and
potential referral to specialty care for management Objective:
To evaluate the clinical utility of a single routinely monitored
laboratory test in identifying cirrhosis, along with a cut-off
value, in chronic viral hepatitis patients. Methods: Clinical,
biochemical and histologic laboratory data from treatment
naive chronic viral hepatitis B (HBV), C (HCV), and D (HDV)
patients at the NIH Clinical Center were evaluated from 1985-
2019 Data was randomly divided into representative training
and validation cohorts Laboratory markers were tested for
their ability to identify cirrhosis (Ishak ≥5) using receiver
operating characteristic curves and an optimal cut-off by
Youden’s Index was calculated within the training cohort The
final cut-off was tested within the validation cohort. Results:
Overall, 1028 subjects (HCV=701, HBV=240 and HDV=86),
66% male, with mean (standard deviation) age of 45(11)
years were evaluated Within the training cohort (n=715),
platelets performed the best at identifying cirrhosis compared
to other laboratory markers (AUROC = 0 86 (0 82-0 90)) All
other tested markers (alanine aminotransferase, aspartate
aminotransferase, prothrombin time, alkaline phosphatase)
had AUROCs <= 0 77 The optimal platelet cut-off for detecting
cirrhosis in the entire cohort was 143 k/uL This cut-off value
performed equally well in the validation cohort (n=309) (Table
1) Conclusion: In patients with chronic viral hepatitis,
platelet counts can accurately stratify patients with cirrhosis
A platelet count >143 K/uL appears to have the most clinical
utility in ruling out cirrhosis The use of platelet counts should
be considered for ensuring optimal care and management of
patients with chronic viral hepatitis.

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发表于 2020-11-3 20:57 |只看该作者
1025
血小板计数作为补偿的检查工具
治愈
Pallavi Surana1,Julian Hercun2,Varun Takyar3,David E.
Kleiner4,Theo Heller5和Christopher Koh5,(1)肝病
国立糖尿病与消化与肾脏研究所分所
疾病,(2)国立卫生研究院肝病科
糖尿病,消化道和肾脏疾病,(3)
加利福尼亚,洛杉矶,(4)美国国家病理学实验室
癌症研究所,国家研究所(5)肝病科
糖尿病与消化道和肾脏疾病
背景:血小板计数已被用作
非侵入性纤维化评分并单独作为替代指标
用于筛查门脉高压和静脉曲张(i e
Baveno VI标准)仅未使用血小板计数
作为鉴定肝硬化的非侵入性标志物。
随着有效疗法的发现,管理和
慢性病毒性肝炎的治疗通常是
初级保健提供者。一种检测肝硬化的简便方法
因此有利于确保最佳护理和
可能转介到专科治疗以进行管理目标:
评估单个常规监测的临床效用
鉴定肝硬化的实验室检查以及临界值
价值,在慢性病毒性肝炎患者中。方法:临床
治疗的生化和组织学实验室数据
天真的慢性乙型肝炎病毒(HBV),丙型肝炎病毒(HCV)和丁型肝炎病毒(HDV)
从1985年起对NIH临床中心的患者进行了评估
2019年数据随机分为代表性培训
和验证队列对实验室标记物进行了测试
使用接收器识别肝硬化(Ishak≥5)的能力
运行特性曲线和最佳截止点
优登的指数是在
最终临界值在验证队列中进行了测试。结果:
总共有1028名受试者(HCV = 701,HBV = 240和HDV = 86),
66%的男性,平均年龄(标准差)为45(11)
在培训队列中评估了几年(n = 715),
血小板在识别肝硬化方面表现最好
至其他实验室标记(AUROC = 0 86(0 82-0 90))全部
其他测试标记(丙氨酸转氨酶,天冬氨酸
氨基转移酶,凝血酶原时间,碱性磷酸酶)
AUROCs <= 0 77检测的最佳血小板截止值
整个队列的肝硬化为143 k / uL
在验证队列中表现同样出色(n = 309)(表
1)结论:在慢性病毒性肝炎患者中,
血小板计数可以准确地将肝硬化患者分层
血小板计数> 143 K / uL似乎具有最大的临床意义
排除肝硬化的实用程序应使用血小板计数
考虑确保最佳护理和管理
慢性病毒性肝炎患者。
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