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实时聚合酶链反应和定量培养在儿童初步诊断和出院时咽拭子负荷。

Real-Time PCR and Quantitative Culture for Load in Pharyngeal Swabs from Children at Preliminary Diagnosis and Discharge.

机构信息

National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, State Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Beijing 102206, China.

Affiliated Hospital of Beihua University, Jilin 132011, China.

出版信息

Biomed Res Int. 2020 Jan 3;2020:9814916. doi: 10.1155/2020/9814916. eCollection 2020.

Abstract

BACKGROUND

Extensive studies have focused on the diagnosis and treatment of infection; however, rare studies investigated the posttreatment conditions. We analyzed the carrying status of in the respiratory tract of children before and after treatment.

METHODS

Ninety-two children with pneumonia were included in this study. Clinical data were obtained from each patient, and pharyngeal swab sampling was performed at preliminary diagnosis and discharge. Real-time PCR and dilution quantitative culture were utilized to determine the DNA quantification and number of viable from samples collected upon preliminary diagnosis and discharge.

RESULTS

All the 92 cases showed DNA positivity upon preliminary diagnosis, serum IgM antibody was detected in 80 patients, and positivity of culture was observed in 82 cases. Upon discharge, the nucleotide and culture positivity were detected in 87 and 49 cases, respectively. The content of viable was 10-10 CCU/mL and 10-10 CCU/mL in the preliminary diagnosis samples and discharge samples, respectively.

CONCLUSIONS

Real-time PCR was rapid and effective for the qualitative diagnosis of at the early stage, but it cannot be used to evaluate the prognosis of patients with infection. Quantitative analysis for DNA could not directly reflex the viable strain content.

摘要

背景

大量研究集中在感染的诊断和治疗上;然而,很少有研究调查治疗后的情况。我们分析了治疗前后儿童呼吸道中 的携带状态。

方法

本研究纳入 92 例肺炎患儿。从每位患者获取临床数据,并在初步诊断和出院时进行咽拭子采样。利用实时 PCR 和稀释定量培养来确定初步诊断和出院时采集的样本中 的 DNA 定量和活 的数量。

结果

92 例均在初步诊断时显示 DNA 阳性,80 例患者血清 IgM 抗体检测阳性,82 例培养阳性。出院时,87 例检测到核苷酸阳性,49 例检测到培养阳性。初步诊断样本和出院样本中活 的含量分别为 10-10 CCU/mL 和 10-10 CCU/mL。

结论

实时 PCR 可快速有效地定性诊断早期的 感染,但不能用于评估 感染患者的预后。 DNA 的定量分析不能直接反映活菌株的含量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918a/6970502/09aeef130bd8/BMRI2020-9814916.001.jpg

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