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本文引用的文献

1
Serum lactate dehydrogenase isoenzymes 4 plus 5 is a better biomarker than total lactate dehydrogenase for refractory Mycoplasma pneumoniae pneumonia in children.血清乳酸脱氢酶同工酶 4 加 5 比总乳酸脱氢酶更能作为儿童难治性肺炎支原体肺炎的生物标志物。
Pediatr Neonatol. 2018 Oct;59(5):501-506. doi: 10.1016/j.pedneo.2017.12.008. Epub 2017 Dec 26.
2
Mechanism of resistance acquisition and treatment of macrolide-resistant pneumonia in children.儿童大环内酯类耐药肺炎的耐药获得机制及治疗
Korean J Pediatr. 2017 Jun;60(6):167-174. doi: 10.3345/kjp.2017.60.6.167. Epub 2017 Jun 22.
3
Lactate Dehydrogenase as a Biomarker for Prediction of Refractory Mycoplasma pneumoniae Pneumonia in Children.乳酸脱氢酶作为预测儿童难治性支原体肺炎的生物标志物
Respir Care. 2015 Oct;60(10):1469-75. doi: 10.4187/respcare.03920. Epub 2015 Jun 9.
4
Decision curve analysis.决策曲线分析
JAMA. 2015 Jan 27;313(4):409-10. doi: 10.1001/jama.2015.37.
5
Treatment of mycoplasma pneumonia: a systematic review.支原体肺炎的治疗:系统评价。
Pediatrics. 2014 Jun;133(6):1081-90. doi: 10.1542/peds.2013-3729.
6
Genetic point-of-care diagnosis of Mycoplasma pneumoniae infection using LAMP assay.使用环介导等温扩增法对肺炎支原体感染进行基因即时诊断。
Pediatr Int. 2014 Aug;56(4):547-52. doi: 10.1111/ped.12327. Epub 2014 May 30.
7
Management of refractory Mycoplasma pneumoniae pneumonia: utility of measuring serum lactate dehydrogenase level.难治性肺炎支原体肺炎的管理:血清乳酸脱氢酶水平测量的效用
J Infect Chemother. 2014 Apr;20(4):270-3. doi: 10.1016/j.jiac.2014.01.001. Epub 2014 Jan 31.
8
Clinical features, risk factors and treatment of fulminant Mycoplasma pneumoniae pneumonia: a review of the Japanese literature.猛发性肺炎支原体肺炎的临床特征、危险因素和治疗:日本文献综述。
J Infect Chemother. 2014 Mar;20(3):181-5. doi: 10.1016/j.jiac.2013.09.009. Epub 2013 Dec 11.
9
Methylprednisolone pulse therapy for refractory Mycoplasma pneumoniae pneumonia in children.甲泼尼龙冲击疗法治疗儿童难治性支原体肺炎
J Infect. 2008 Sep;57(3):223-8. doi: 10.1016/j.jinf.2008.06.012. Epub 2008 Jul 25.

乳酸脱氢酶在预测儿童难治性支原体肺炎中的价值:基于决策曲线分析和剂量反应分析的评估

[Value of lactate dehydrogenase in predicting refractory Mycoplasma pneumoniae pneumonia in children: an evaluation based on decision curve analysis and dose-response analysis].

作者信息

Zheng Xue-Xiang, Lin Ji-Lei, Dai Ji-Hong

机构信息

Department of Respiratory Medicine, Children's Hospital of Chongqing Medical University/Ministry of Education Key Laboratory of Child Development and Disorders/National Clinical Research Center for Child Health and Disorders/China International Science and Technology Cooperation Base of Child Development and Critical Disorders/Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2020 Feb;22(2):112-117. doi: 10.7499/j.issn.1008-8830.2020.02.006.

DOI:10.7499/j.issn.1008-8830.2020.02.006
PMID:32051076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7390016/
Abstract

OBJECTIVE

To study the value of lactate dehydrogenase (LDH) in predicting refractory Mycoplasma pneumoniae pneumonia (RMPP) in children.

METHODS

Propensity score matching was used to select 73 children with RMPP (refractory group) and 146 children with non-refractory Mycoplasma pneumoniae pneumonia (common group). The logistic regression analysis, restricted cubic spline model, and decision curve analysis were used to analyze the clinical value of LDH in predicting RMPP.

RESULTS

There were significant differences in the incidence of high fever, white blood cell count, platelet count, percentage of neutrophils, and serum levels of C-reactive protein, procalcitonin, hemoglobin, albumin, glutamic-pyruvic transaminase, aspartate aminotransferase and LDH (P<0.05). There were also significant differences between the two groups in the Mycoplasma pneumoniae-DNA load in nasopharyngeal aspirates and the incidences of pleural effusion, pulmonary consolidation, atelectasis, shortness of breath and skin lesions (P<0.05). The multivariate logistic regression analysis showed that high fever, hemoglobin level, LDH level, and pulmonary consolidation were independent predictive factors for RMPP (OR=10.097, 0.956, 1.006, and 3.756; P<0.05). The results of the restricted cubic spline analysis showed a non-linear dose-response relationship between the continuous changes of LDH and the development of RMPP (P<0.01). The decision curve analysis showed that LDH had an important clinical value in predicting RMPP.

CONCLUSIONS

LDH is an independent predictive factor for the development of RMPP and its intensity of association with the development of RMPP exhibits a non-linear dose-response relationship.

摘要

目的

探讨乳酸脱氢酶(LDH)在预测儿童难治性支原体肺炎(RMPP)中的价值。

方法

采用倾向得分匹配法选取73例RMPP患儿(难治组)和146例非难治性支原体肺炎患儿(普通组)。采用逻辑回归分析、限制性立方样条模型和决策曲线分析来分析LDH在预测RMPP中的临床价值。

结果

两组患儿在高热发生率、白细胞计数、血小板计数、中性粒细胞百分比以及血清C反应蛋白、降钙素原、血红蛋白、白蛋白、谷丙转氨酶、谷草转氨酶和LDH水平方面存在显著差异(P<0.05)。两组患儿在鼻咽抽吸物中肺炎支原体DNA载量以及胸腔积液、肺实变、肺不张、呼吸急促和皮肤病变的发生率方面也存在显著差异(P<0.05)。多因素逻辑回归分析显示,高热、血红蛋白水平、LDH水平和肺实变是RMPP的独立预测因素(OR=10.097、0.956、1.006和3.756;P<0.05)。限制性立方样条分析结果显示,LDH的连续变化与RMPP的发生之间存在非线性剂量反应关系(P<0.01)。决策曲线分析表明,LDH在预测RMPP方面具有重要的临床价值。

结论

LDH是RMPP发生的独立预测因素,其与RMPP发生的关联强度呈现非线性剂量反应关系。