Volume 33 Issue 12
Dec.  2020
Turn off MathJax
Article Contents

WANG Fang, LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming, WANG Xian Feng, TANG Qi Yuan, ZHOU Xuan, XIAN Wen Jie, CHEN Rui Kun, LI Xuan, LI Zhi Yu, LIAO Li Qun, HE Qing, LIU Lei. Comparison of Clinical Characteristics and Outcomes of Pediatric and Adult Patients with Coronavirus Disease 2019 in Shenzhen, China[J]. Biomedical and Environmental Sciences, 2020, 33(12): 906-915. doi: 10.3967/bes2020.124
Citation: WANG Fang, LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming, WANG Xian Feng, TANG Qi Yuan, ZHOU Xuan, XIAN Wen Jie, CHEN Rui Kun, LI Xuan, LI Zhi Yu, LIAO Li Qun, HE Qing, LIU Lei. Comparison of Clinical Characteristics and Outcomes of Pediatric and Adult Patients with Coronavirus Disease 2019 in Shenzhen, China[J]. Biomedical and Environmental Sciences, 2020, 33(12): 906-915. doi: 10.3967/bes2020.124

Comparison of Clinical Characteristics and Outcomes of Pediatric and Adult Patients with Coronavirus Disease 2019 in Shenzhen, China

doi: 10.3967/bes2020.124
Funds:  This study was supported by the National Clinical Research Center for Infectious Diseases, Funds for the Construction of Key Medical Disciplines in Shenzhen and the Sanming Project of Medicine in Shenzhen [SZSM201612014]
More Information
  • Author Bio:

    WANG Fang, female, born in 1970, MD, and majoring in infectious diseases

    LAI Chang Xiang, male, born in 1990, MS, majoring in infectious diseases

    HUANG Peng Yu, male, born in 1990, MD, majoring in cancer stem cell and reproductive medicine

    LIU Jia Ming, male, born in 1993, MS, majoring in the clinical and basic research of hepatobiliary pancreatic tumor and breast tumor as the research neighborhood

  • Corresponding author: LIU Lei, Tel: 86-755-61222333, E-mail: liuleiszsdsrmyy@163.com; HE Qing, Tel: 86-755-61223251, E-mail: a549719965@163.com
  • §These authors contributed equally to this work and are the co-first authors.
  • Received Date: 2020-04-25
  • Accepted Date: 2020-07-24
  •   Objective  Here we aimed to investigate the difference in clinical characteristics and outcomes between pediatric and adult patients with COVID-19.  Methods  A total of 333 consecutive patients with laboratory-confirmed SARS-CoV-2 infection treated in the departments of Internal medicine of Shenzhen Third People's Hospital from January 11th to February 10th, 2020 were included. The data were obtained from electronic medical records. The epidemiological data, clinical characteristics, length of hospital stays, and outcomes of pediatric and adult patients were compared.  Results  Compared with adult patients, pediatric patients had a shorter time of symptom onset to hospitalization than adults [median time, 1 (IQR, 1.0–1.0) d vs. 3 (IQR, 2.0–6.0) d, P < 0.001], milder or fewer symptoms, less severe chest CT findings. The clinical severity classification of children was less severe than adults. Up to 15th March, the end of the follow-up, 33 (100%) children and 292 (97.3%) adult patients had been discharged from hospital. Only 2 (0.7%) adult patients died, with an overall case mortality of 0.6%. The median length of hospital stay of pediatric patients was shorter than that of adult patients [19 (95% CI: 16.6–21.4) d vs. 21 (95% CI: 19.9–22.1) d, P = 0.024].  Conclusion  Pediatric patients with COVID-19 had milder or less clinical symptoms, less evident pulmonary imaging changes, better prognosis, and shorter length of hospital stay.
  • §These authors contributed equally to this work and are the co-first authors.
  • 加载中
  • [1] Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. The Lancet, 2020; 395, 497−506. doi:  10.1016/S0140-6736(20)30183-5
    [2] World Health Organization. Coronavirus disease (COVID-2019) situation reports. Retrieved from https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports/. [2020-07-01].
    [3] Zhu N, Zhang D, Wang W, et al. A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med, 2020; 382, 727−33. doi:  10.1056/NEJMoa2001017
    [4] Zhou P, Yang X, Wang X, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature, 2020; 579, 270−3. doi:  10.1038/s41586-020-2012-7
    [5] Liu P, Chen W, Chen J. Viral metagenomics revealed sendai virus and coronavirus infection of Malayan Pangolins (Manis javanica). Viruses, 2019; 11, 979. doi:  10.3390/v11110979
    [6] Chan JF, Yuan S, Kok K, et al. A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. The Lancet, 2020; 395, 514−23. doi:  10.1016/S0140-6736(20)30154-9
    [7] Phan LT, Nguyen TV, Luong QC, et al. Importation and human-to-human transmission of a novel coronavirus in Vietnam. N Engl J Med, 2020; 382, 872−4. doi:  10.1056/NEJMc2001272
    [8] Rothe C, Schunk M, Sothmann P, et al. Transmission of 2019-nCoV infection from an asymptomatic contact in Germany. N Engl J Med, 2020; 382, 970−1. doi:  10.1056/NEJMc2001468
    [9] Wu JT, Leung K, Leung GM. Nowcasting and forecasting the potential domestic and international spread of the 2019-nCoV outbreak originating in Wuhan, China: a modelling study. The Lancet, 2020; 395, 689−97. doi:  10.1016/S0140-6736(20)30260-9
    [10] Li Q, Guan X, Wu P, et al. Early transmission dynamics in Wuhan, China, of novel coronavirus-infected pneumonia. N Engl J Med, 2020; 382, 1199−207. doi:  10.1056/NEJMoa2001316
    [11] Guan W, Ni Z, Hu Y, et al. Clinical characteristics of 2019 novel coronavirus infection in China. N Engl J Med, 2020; 382, 1708−20.
    [12] Wei M, Yuan J, Liu Y, et al. Novel coronavirus infection in hospitalized infants under 1 year of age in China. JAMA, 2020; 323, 1313−4. doi:  10.1001/jama.2020.2131
    [13] Peiris J, Chu CM, Cheng V, et al. Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study. The Lancet, 2003; 361, 1767−72. doi:  10.1016/S0140-6736(03)13412-5
    [14] Thabet F, Chehab M, Bafaqih H, et al. Middle East respiratory syndrome coronavirus in children. Saudi Med J, 2015; 36, 484−6. doi:  10.15537/smj.2015.4.10243
    [15] General Office of National Health Committee. Office of State Administration of Traditional Chinese Medicine. Notice on the issuance of a programme for the diagnosis and treatment of novel coronavirus (2019-nCoV) infected pneumonia (trial fifth edition). http://bgs.satcm.gov.cn/zhengcewenjian/2020-02-06/12847.html. [2020-02-06].
    [16] Laboratory diagnostics for novel coronavirus. WHO 2020 (https://www.who.int/health-topics/coronavirus/laboratory-diagnostics-for-novel-coronavirus). [2020-02-06].
    [17] Thompson BT, Chambers RC, Liu KD. Acute respiratory distress syndrome. JAMA, 2012; 377, 562−72.
    [18] Kidney disease Improving global outcomes (KDIGO) acute kidney injury work group. KDIGO clinical practice guideline for acute kidney injury. Kidney Int Suppl, 2012; 2, 1. doi:  10.1038/kisup.2012.1
    [19] Chalasani NP, Hayashi PH, Bonkovsky HL, et al. ACG clinical guideline: the diagnosis and management of idiosyncratic drug-induced liver injury. Am J Gastroenterol, 2014; 109, 950−66. doi:  10.1038/ajg.2014.131
    [20] Gao C, Wang Y, Gu X, et al. Association between cardiac injury andortality in hospitalized patients infected with avian influenza a (H7N9) virus. Crit Care Med, 2020; 48, 451−8.
    [21] Peiris J, Lai ST, Poon L, et al. Coronavirus as a possible cause of severe acute respiratory syndrome. The Lancet, 2003; 361, 1319−25. doi:  10.1016/S0140-6736(03)13077-2
    [22] Wang D, Hu B, Hu C, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus–infected pneumonia in Wuhan, China. JAMA, 2020; 323, 1061−9. doi:  10.1001/jama.2020.1585
  • 加载中
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Figures(2)  / Tables(3)

Article Metrics

Article views(500) PDF downloads(44) Cited by()

Proportional views
Related

Comparison of Clinical Characteristics and Outcomes of Pediatric and Adult Patients with Coronavirus Disease 2019 in Shenzhen, China

doi: 10.3967/bes2020.124
Funds:  This study was supported by the National Clinical Research Center for Infectious Diseases, Funds for the Construction of Key Medical Disciplines in Shenzhen and the Sanming Project of Medicine in Shenzhen [SZSM201612014]
  • Author Bio:

  • Corresponding author: LIU Lei, Tel: 86-755-61222333, E-mail: liuleiszsdsrmyy@163.com HE Qing, Tel: 86-755-61223251, E-mail: a549719965@163.com
  • §These authors contributed equally to this work and are the co-first authors.

Abstract:   Objective  Here we aimed to investigate the difference in clinical characteristics and outcomes between pediatric and adult patients with COVID-19.  Methods  A total of 333 consecutive patients with laboratory-confirmed SARS-CoV-2 infection treated in the departments of Internal medicine of Shenzhen Third People's Hospital from January 11th to February 10th, 2020 were included. The data were obtained from electronic medical records. The epidemiological data, clinical characteristics, length of hospital stays, and outcomes of pediatric and adult patients were compared.  Results  Compared with adult patients, pediatric patients had a shorter time of symptom onset to hospitalization than adults [median time, 1 (IQR, 1.0–1.0) d vs. 3 (IQR, 2.0–6.0) d, P < 0.001], milder or fewer symptoms, less severe chest CT findings. The clinical severity classification of children was less severe than adults. Up to 15th March, the end of the follow-up, 33 (100%) children and 292 (97.3%) adult patients had been discharged from hospital. Only 2 (0.7%) adult patients died, with an overall case mortality of 0.6%. The median length of hospital stay of pediatric patients was shorter than that of adult patients [19 (95% CI: 16.6–21.4) d vs. 21 (95% CI: 19.9–22.1) d, P = 0.024].  Conclusion  Pediatric patients with COVID-19 had milder or less clinical symptoms, less evident pulmonary imaging changes, better prognosis, and shorter length of hospital stay.

§These authors contributed equally to this work and are the co-first authors.
WANG Fang, LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming, WANG Xian Feng, TANG Qi Yuan, ZHOU Xuan, XIAN Wen Jie, CHEN Rui Kun, LI Xuan, LI Zhi Yu, LIAO Li Qun, HE Qing, LIU Lei. Comparison of Clinical Characteristics and Outcomes of Pediatric and Adult Patients with Coronavirus Disease 2019 in Shenzhen, China[J]. Biomedical and Environmental Sciences, 2020, 33(12): 906-915. doi: 10.3967/bes2020.124
Citation: WANG Fang, LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming, WANG Xian Feng, TANG Qi Yuan, ZHOU Xuan, XIAN Wen Jie, CHEN Rui Kun, LI Xuan, LI Zhi Yu, LIAO Li Qun, HE Qing, LIU Lei. Comparison of Clinical Characteristics and Outcomes of Pediatric and Adult Patients with Coronavirus Disease 2019 in Shenzhen, China[J]. Biomedical and Environmental Sciences, 2020, 33(12): 906-915. doi: 10.3967/bes2020.124
    • An outbreak of a novel coronavirus disease emerged in Wuhan, China, in December 2019[1]. The disease rapidly spread to many countries and regions and was later named as Coronavirus Disease 2019 (COVID-19) by WHO. As of July 1st , over 850,000 confirmed cases of COVID-19 and 4,600 deaths had been reported by the National Health Commission of China and a total of global 10,357,662 cases of COVID-19 had been reported by WHO[2]. Full-genome sequencing analysis has uncovered a novel coronavirus that is now named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by the International Committee on Taxonomy of Viruses. SARS-CoV-2 is related to Middle East respiratory syndrome coronavirus (MERS-CoV) and severe acute respiratory syndrome coronavirus (SARS-CoV)[3]. The SARS-CoV-2 is close to bat coronaviruses and bats are currently suggested to be the primary transmission source of SARS-CoV-2 and pangolins are the potential intermediate hosts[4, 5]. Meanwhile, human-to-human transmission and family-aggregated characteristics of the COVID-19 have been reported[6-10].

      So far, there are no specific therapies or vaccines for the COVID-19. The current treatment is symptomatic and supportive treatment. Early diagnosis, early isolation and early treatment are effective strategies for COVID-19 management. At present, the majority of patients with COVID-19 in China are adult patients. In adults, common symptoms of COVID-19 include fever, dyspnea, dry cough, and fatigue, followed by headache and sore throat[11]. Laboratory tests for COVID-19 patients showed that they have normal or low leukocyte counts; and computed tomography scans of chest showed ground-glass opacity. Complication may develop with disease progression and underlying diseases are risk factors for death[1]. Chen reported that COVID-19 was more likely to affect older men with comorbidities, and could result in acute respiratory distress syndrome (ARDS)[2]. On January 20th, 2020, Shenzhen reported a confirmed pediatric case of COVID-19 in China, suggesting children is a susceptible group of COVID-19[6]. The immunity and development in children are unique in comparison to adults. Although the reported pediatric infection rate of COVID-19 is not high, the number of pediatric patients is increasing with the remaining rapid increase in global infected cases. However, data on the clinical characteristics and outcomes between children and adults with COVID-19 are limited[6, 12]. As for SARS and MERS, the clinical symptoms of pediatric patients were relatively mild and the prognosis is relatively good[13, 14]. In this study, we retrospectively compared the clinical characteristics of pediatric and adult patients with COVID-19, in perspectives of route of transmission, symptoms, laboratory and radiographic findings, treatment, and outcome.

    • Patients who were admitted to the departments of internal medicine of Shenzhen Third People’s Hospital from 11th January to 10th February 2020, and with a positive results of nucleic acid test for SARS-CoV-2 were included in this retrospective study. The study protocol was approved by the institutional ethics board of Shenzhen Third People’s Hospital. The ethics committee waived written consents because of the emergency of outbreak, and oral consents were acquired from patients at the time of admission. Shenzhen Third People’s Hospital is one of the major tertiary teaching hospitals of Guangdong province and is the government designated treatment center to treat all patients with COVID-19 in Shenzhen regions. All COVID-19 patients enrolled in this study were diagnosed according to World Health Organization interim guidance[15]. The clinical outcomes (Discharges, fatality, length of hospital stay) were monitored up to 15th March 2020, the final date of follow-up.

    • Patients who presented to the medical center with symptoms or contact history concerning for SARS-CoV-2 infection were triaged and subsequently subjected to nucleic acid test. Confirmed patients received treatment in accordance with the Chinese Programme for the Diagnosis and Treatment of Novel Coronavirus Infected Pneumonia under isolation[15]. All patients received antiviral therapy, including ribavirin, interferon, lopina veletonavir, favipiravir, abidal or choroquine. The symptoms, sign, leukocyte level, c-reactive protein (CRP) level, procalcitonin (PCT) level, and imaging performance of patients were fully taken into account to start antibiotic therapy. Patients were cared for by trained medical staff who recorded clinical data into the electronic medical records. All included patients were followed up until 15th March 2020.

    • Laboratory confirmation of the COVID-19 was made by the Shenzhen Center for Disease Control and Prevention (CDC). COVID-19 was confirmed by quantitative real-time polymerase chain reaction (qRT-PCR) using the same protocol established by the World Health Organization[16]. qRT-PCR detection reagents were provided by the Chinese CDC. Laboratory confirmation was defined as a positive result to next-generation sequencing analysis or reverse-transcriptase polymerase-chain-reaction (qRT-PCR) assay for blood, nasal and pharyngeal swab specimens.

    • Throughout hospitalization, patients were cared for by medical staffs and physicians, who rounded at least daily and recorded epidemiological data, vital signs, clinical data, laboratory results, radiological features, treatment and outcomes into the electronic medical records. At analysis, we retrieved the demographic data, medical history, exposure history, underlying comorbidities, symptoms, signs, laboratory findings, chest computed tomographic (CT) scans, and treatment measures (including antiviral therapy, antibiotics therapy, corticosteroid therapy, respiratory support, kidney replacement therapy). According to the Chinese Programme for the Diagnosis and Treatment of Novel Coronavirus Infected Pneumonia, the severity of patients were classified into mild, moderate, severe and critical[15]. The discharge criteria were: 1. Temperature returned to normal for more than 3 d; 2. Respiratory symptoms improved significantly; 3. Imaging of the lungs showed a marked improvement in acute exudative lesions; 4. Nucleic acid tests were negative for two consecutive respiratory specimens (sampling time interval at least 1 d)[15]. ARDS was defined in accordance with the Berlin definition[17] . Acute kidney injury and acute liver injury were defined according to the kidney disease: Improving Global Outcomes definition and ACG Clinical Guideline[18, 19]. Cardiac injury was defined according to the recognized standard[20]. Children are defined as under the age of 18 and adults are defined as 18 and above. Length of hospital stay was defined as the interval from the date of admission to the date of discharge, death or the last follow-up.

    • Continuous variables were presented as median and interquar tile range (IQR), and were compared using the Mann-Whitney test. Categorical variables were presented as frequ ency and percentage, and were compared using a chi-square test or Fisher’s exact test when appropriate. Bonferroni correction was used for multiple comparison of the same group. The Kaplan-Meier method was used to estimate the length of hospital stay, and then the differences between groups were assessed by a log-rank test using GraphPad Prism version 7.01 (GraphPad, Inc., LaJolla, CA, USA). Other data analyses were performed using SPSS (Social Science Statistics Package) version 23.0. All statistical tests were two-sided, and P < 0.05 was considered statistically significant.

    • As shown in Table 1, of 333 included patients with COVID-19, pediatric patients accounted for 9.9% (33/333) and adult patients accounted for 90.1% (300/333). The median age of adult patients was 47.0 (IQR, 33.0–66.0) years and of pediatric patients was 6 (IQR, 2.5–9.5) years. There were 51.5% female patients in total. No difference in sex was found between pediatric and adult patients (P = 0.451). One hundred and fifty (45.0%) patients had contacted with patients from Hubei province, 22 (6.6%) patients had contacted with patients from other provinces, 13 (3.9%) patients were residents of Shenzhen with no clear contact history, 122 (36.6%) patients were residents of Hubei province, and 26 (7.8%) patients had unknown contact history. There was difference in pandemic exposure (P = 0.025) between pediatric and adult patients. No cross-infection, medical staff infection or nosocomial infection occured in our center.

      Clinical characteristicsCount (%)P value*
      All patients (n = 333)Pediatric patients (n = 33)Adult patients (n = 300)
      Sex0.451
       Female171 (51.4)19 (57.6)152 (50.7)
       Male162 (48.6)14 (42.4)148 (49.3)
      Age, median (IQR)47 (33.0–60.0)6 (2.5–9.5)50 (36.0–61.0)< 0.001
      Epidemiological history0.025
       Contact with patients of Hubei province150 (45.0)23 (69.7)127 (42.3)
       Contact with patients of other provinces22 (6.6)2 (6.1)20 (6.7)
       Residents of Shenzhen with no clear contact history13 (3.9)0 (0.0)13 (4.3)
       Residents of Hubei province122 (36.6)7 (21.2)115 (38.3)
       Others26 (7.8)1 (3.0)25 (8.3)
      Co-infection of other respiratory viruses (n = 323)0.014
       No317 (98.1)29 (90.6)288 (99.0)
       Yes6 (1.9)3 (9.4)3 (1.0)
      Symptom onset to hospitalization, d (IQR)3 (1.0–5.0)1(1.0–1.0)3 (2.0–6.0)< 0.001
      Symptoms and signs
       Fever257 (77.2)11 (33.3)246 (82.0)< 0.001
       Cough168 (50.5)7 (21.2)161 (53.7)< 0.001
       Sputum81 (24.3)2 (6.1)79 (26.3)0.010
       Dyspnea15 (4.5)1 (3.0)14 (4.7)1.000
      Temperature, °C0.078
       < 37.3215 (64.6)28 (84.8)187 (62.3)
       37.3–38.086 (25.8)4 (12.1)82 (27.3)
        38.1–39.031 (9.3)1 (3.0)30 (10.0)
       > 39.01 (0.3)0 (0.0)1 (0.3)
      Heart rate, median (IQR)87 (80–96)98 (88–114)86 (79–95)< 0.001
      Breathing rate, median (IQR)20 (19–20)22 (20–24)20 (19–20)< 0.001
      Systolic pressure, median (IQR), mmHg125 (115.0–136.0)103 (95.5–115.5)126 (116.3–137.8)< 0.001
      Severity< 0.001
       Mild33 (9.9)13 (39.4)20 (6.7)
       Moderate271 (81.4)20 (60.6)251 (83.7)
       Severe and critical29 (8.7)0 (0.0)29 (9.7)
      Underlying diseases78 (23.4)0 (0.0)78 (26.0)0.001
       Hypertension39 (11.7)0 (0.0)39 (13.0)0.055
       Diabetes18 (5.4)0 (0.0)18 (6.0)0.298
       Heart disease15 (4.5)0 (0.0)15 (5.0)0.383
       Chronic lung disease11 (3.3)0 (0.0)11 (3.7)0.545
       Chronic liver disease8 (2.4)0 (0.0)8 (2.7)1.000
       Malignant tumors3 (0.9)0 (0.0)3 (1.0)1.000
       Cerebrovascular disease2 (0.6)0 (0.0)2 (0.7)1.000
       Others7 (2.1)0 (0.0)7 (2.3)1.000
        Note. Data are presented as n (%) and median (interquartile ranges, IQR).
      *P values indicate differences between pediatric and adult patients. P < 0.05 was considered statistically significant.
      Number of patients for whom data were available.

      Table 1.  Baseline clinical characteristics of COVID-19 patients

    • Pediatric patients had higher rate of co-infection of other respiratory viruses (including: respiratory syncytial virus and influenza B virus) compared to adult patients (9.4% vs. 1.0%, P = 0.014). They also had a shorter time of symptom onset to hospitalization than adults [median time, 1 (IQR, 1.0–1.0) d vs. 3 (IQR, 2.0–6.0) d, P < 0.001]. Some symptoms such as fever (33.3% vs. 82.0%, P < 0.001), cough (21.2% vs. 53.7%, P < 0.001), and sputum (6.1% vs. 26.3%, P = 0.010), are rarer in children than in adults. There was a significant difference in clinical severity classification that children had lower grades than adults (children: 39.4% mild, 60.6% moderate, 0.0% severe and critical vs. adults: 6.7% mild, 83.7% moderate, 9.7% severe and critical, P < 0.001). Underlying diseases were reported only by adults, including 39 (13.0%) cases of hypertension, 18 (6%) cases of diabetes, 15 (5%) cases of heart disease, 11 (3.7%) cases of chronic lung disease, 8 (2.7%) cases of chronic liver disease, 3 (1%) cases of malignant tumors, 2 (0.7%) cases of cerebrovascular disease, and 7 (2.3%) cases of other underlying diseases.

    • COVID-19 related laboratory examination data on admission were retrieved and summarized in Table 2. Compared with adult patients, pediatric patients had higher levels of white blood cell counts (P < 0.001), lymphocyte counts (P < 0.001), platelet counts (P < 0.001), aspartate aminotransferase (AST) (P = 0.001), alkaline phosphatase (ALP) (P < 0.001), lactic acid dehydrogenase (LDH) (P = 0.003), creatine kinase-MB (CK-MB) (P < 0.001), PaO2 (P < 0.001), PaO2/FiO2 (P < 0.001), T lymphocyte count (P < 0.001), CD4+ T lymphocytes counts (P < 0.001) and CD8+ T lymphocyte counts (P < 0.001). Compared with adult patients, pediatric patients had lower levels of hemoglobin (Hb) content (P = 0.001), total bilirubin (TBIL) (P = 0.001), alanine aminotransferase (ALT) (P = 0.017), gamma-glutamyltransferase (GGT) (P < 0.001), creatinin (Cr) (P < 0.001), C-reactive protein (CRP) (P < 0.001), interleukin 6 (IL-6) (P < 0.001), erythrocyte sedimentation rate (ESR) (P < 0.001), and arterial blood PH (P = 0.009). Chest CT imaging examination showed a significant difference between children and adults (Figure 1). In children, there were 13 (39.4%) cases with no obvious changes, 9 (27.3%) cases of unilateral lung lesions, and 11 (33.3%) cases of bilateral lung lesions; in adult patients, there were 20 (6.7%) cases with no obvious changes, 26 (8.7%) cases of unilateral lung lesions, and 254 (84.7%) cases of bilateral lung lesions. The results suggested that pediatric patients had milder or hidden lung lesions in the imaging findings (P < 0.001).

      Figure 1.  Chest computed tomographic iimages of pediatric patients and adult patients with coronavirus disease 2019 (COVID-19). (A) Chest CT showing unilateral lung lesions in children. (B) Chest CT showing bilateral lung lesions in children. (C) Chest CT showing unilateral lung lesions in adult. (D) Chest CT showing bilateral lung lesions in adult

        ItemsValue (IQR)P value*
      All patients (n = 333)Pediatric patients (n = 33)Adult patients (n = 300)
      White blood cell count, × 109/L4.6 (3.6−5.7)5.6 (4.5−8.9)4.5 (3.5−5.6)< 0.001
      Neutrophil count, × 109/L2.6 (1.9−3.5)2.2 (1.4−3.8)2.6 (1.9−3.5)0.126
      Lymphocyte count, × 109/L1.3 (1.0−1.7)2.5 (2.0−4.1)1.2 (0.9−1.6)< 0.001
      Hemoglobin, g/L136 (126−146)128 (123−138)137 (127−147)0.001
      Platelet count, × 109/L180 (143−224)253 (214−322)174 (141−209)< 0.001
      Ferritin, pmol/L (n = 62)647.0 (258.9−883.7)212.3 (155.5−835.3) (n = 5)658.7 (287.6−884.4) (n = 57)0.250
      Total bilirubin, μmol/L9.8 (7.6−14.6)8.6 (5.3−11.0)10.1 (7.8−15.2)0.001
      Alanine aminotransferase, U/L20.0 (15.0−31.0)16.0 (11.5−24.1)21.0 (15.0−31.7)0.017
      Aspartate aminotransferase, U/L27.0 (21.0−36.4)38.0 (24.0−48.8)26.0 (20.9−35.0)0.001
      Gamma-glutamyltransferase, U/L24.0 (15.1−39.0)12.8 (11.0−17.5)26.0 (17.0−41.0)< 0.001
      Alkaline phosphatase, U/L (n = 251)50.0 (50.0−78.0)186.5 (154.0−222.8) (n = 24)59.0 (49.0−72.0) (n = 227)< 0.001
      Urea nitrogen, mmol/L4.0 (3.2−4.9)3.8 (3.1−4.8)4.0 (3.2−5.0)0.913
      Creatinin, μmol/L62.0 (49.9−75.2)31.0 (26.0−38.4)65.0 (53.0−78.0)< 0.001
      C-Reactive protein, mg/L (n = 325)10.3 (3.9−27.4)4.3 (0.5−5.5) (n = 31)12.4 (4.8−29.37) (n = 294)< 0.001
      Procalcitonin, ng/mL (n = 274) 3.3 (0.1−5.3)3.0 (0.1−5.7) (n = 27)3.3 (0.1−5.3) (n = 247)0.818
      Interleukin 6, pg/mL (n = 231)10.7 (4.2−19.6)3.3 (2.0−4.5) (n = 21)12.0 (5.0−21.4) (n = 210)< 0.001
      Erythrocyte sedimentation rate, mm/h
      (n = 280)
      30.0 (15.0−48.8)10.0 (5.0−18.5) (n = 25)30.0 (15.0−50.0) (n = 255)< 0.001
      Lactic acid dehydrogenase (n = 296)223.0 (175.0−400.0)278.0 (222.5−561.3) (n = 30)215.0 (170.0−387.3) (n = 266)0.003
      cTnI, μg/L (n = 284)0.012 (0.012−6.000)0.012 (0.012−6.000) (n = 30)0.012 (0.012−6.000) (n = 254)0.266
      Creatine kinase-MB, ng/mL (n = 308)0.54 (0.22−1.07)1.17 (0.40−2.85) (n = 32)0.52 (0.22−1.00) (n = 276)< 0.001
      Prothrombin time, s (n = 314)11.9 (11.3−12.5)12.1 (11.6−11.7) (n = 31)11.8 (11.2−12.5) (n = 283)0.072
      Activated partial thromboplastin time,
      s (n = 316)
      35.5 (32.5−38.7)34.8 (33.0−38.9) (n = 31)35.6 (32.5−38.7) (n = 285)0.772
      D-dimer, μg/mL (n = 313)0.37 (0.26−0.56)0.31 (0.24−0.55) (n = 30)038 (0.26−0.56) (n = 283)0.261
      pH (n = 316)7.42 (7.40−7.44)7.39 (7.37−7.44) (n = 28)7.42 (7.40−7.44) (n = 288)0.009
      PaCO2, mmHg (n = 317)39.0 (35.7−41.4)38.8 (34.4−41.5) (n = 28)39.0 (36.0−41.4) (n = 289)0.340
      PaO2, mmHg (n = 317)92.2 (79.1−106.0)108.0 (103.3−124.0) (n = 28)90.5 (78.0−103.0) (n = 289)< 0.001
      PaO2 /FiO2, mmHg (n = 317)413 (355.0−476.5)514 (491.3−585.3) (n = 28)401 (349.0−462.5) (n = 289)< 0.001
      T lymphocyte count,μL (n = 207)973 (627.0−1314.0)1784.5 (1489.5−2857.8) (n = 22)894 (589.5−1191.0) (n = 185)< 0.001
      CD4 count, μL (n = 207)5,190 (344.0−714.0)852 (740.8−1428.3) (n = 22)499 (335.5−652.5) (n = 185)< 0.001
      CD8 count, μL (n = 207)348 (207.0−515.0)684 (593.8−1050.8) (n = 22)326 (194.5−439.5) (n = 185)< 0.001
      Lung lesions by CT< 0.001
       None, n (%)33 (9.9)13 (39.4)20 (6.7)
       Unilateral, n (%)35 (10.5)9 (27.3)26 (8.7)
       Bilateral, n (%)265 (79.6)11 (33.3)254 (84.7)
        Note. Data are presented as median (interquartile ranges, IQR) and n (%)
      *P values indicate differences between pediatric and adult patients. P < 0.05 was considered statistically significant;
      Number of patients for whom data were available.

      Table 2.  Summary on laboratory and radiographic data of COVID-19 patients

    • All children and adult patients were treated under isolation and in accordance with the Chinese Programme for the Diagnosis and Treatment of Novel Coronavirus Infected Pneumonia[15]. Treatments for patients were summarize in Table 3. All patients received antiviral therapy (ribavirin, interferon, lopina veletonavir, favipiravir, abidal, or chloroquine), and 99 (29.7%) patients received antibiotics (cephalosporins, quinolones, and carbapenems), including 9.1% (3/33) of the pediatric patients and 32.0% (96/300) of the adult patients. Hormonal therapy was received by 30.0% (90/300) of the adult patients and gamma globulin therapy was received by 27.0% (81/300) of the adult patients. No pediatric patients received hormonal or gamma globulin therapy. A total of 18.2% (6/33) pediatric patients and 77.7% (233/300) adult patients received oxygen therapy (P < 0.001). Of pediatricpatients, 5 (15.2%) received nasal cannula and 1 (3.0%) received mask oxygen; of adult patients, 177 (59.0%) received nasal cannula, 6 (2.0%) received mask oxygen, 10 (3.3%) received high-flow oxygen, 24 (8.0%) received noninvasive ventilation, 14 (4.7%) received invasive ventilation, and 2 (0.7%) received extracorporeal membrane oxygenation (ECMO). Of all patients, only 3 (1.0%) adult patients received continuous renal replacement therapy because of acute renal injury. Complications occurred only in adults, and no complications occurred in children; 13 complications in adults included 2 case of acute heart injury (0.6%), 3 cases of acute kidney injury (0.9%), 1 case of acute liver injury (0.3%), and 13 cases (3.9%) of ARDS, including 3 patients with multiple complications.

        ItemsCount (%)P value*
      All patients (n = 333)Pediatric patients (n = 33)Adults patients (n = 300)
      Treatment
       Antiviral333 (100)33 (100)300 (100)NA
       Antibiotics99 (29.7)3 (9.1)96 (32.0)0.006
       Hormonal therapy90 (27.0)0 (0.0)90 (30.0)< 0.001
       Gamma globulin therapy81 (24.3)0 (0.0)81 (27.0)0.001
       Renal replacement therapy3 (0.9)0 (0.0)3 (1.0)1.000
      Oxygen therapy< 0.001
       None94 (28.2)27 (81.8)67 (22.3)
       Nasal cannula182 (54.7)5 (15.2)177 (59.0)
       Face mask7 (2.1)1 (3.0)6 (2.0)
       High flow10 (3.0)0 (0.0)10 (3.3)
       Non-invasive ventilation24 (7.2)0 (0.0)24 (8.0)
       Invasive ventilation14 (4.2)0 (0.0)14 (4.7)
       Invasive + ECMO2 (0.6)0 (0.0)2 (0.7)
      Complication13 (3.9)0 (0.0)13 (4.3)0.455
       Acute heart injury2 (0.6)0 (0.0)2 (0.7)1.000
       Acute kidney injury3 (0.9)0 (0.0)3 (1.0)1.000
       Acute liver injury1 (0.3)0 (0.0)1 (0.3)1.000
       Acute respiratory distress syndrome13 (3.9)0 (0.0)13 (4.3)0.455
        Note. Data are presented as n (%);
      *P values indicate differences between pediatric and adult patients. P < 0.05 was considered statistically significant.

      Table 3.  Treatment and complications in pediatric and adult patients

    • As of the last follow-up time of 15th March 2020, 324 patients had recovered and been discharged, including 33 (100%) of pediatric patients and 292 (97.3%) of adult patients. Only 2 (0.7%) adult patients died, with an overall case fatality rate of 0.6%. Only 7 adult patients are still in hospital. The median length of hospital stay of 333 patients was 21 d (95% CI: 19.8–22.2) (Figure 2A). Pediatric patients had a median hospital stay of 19 (95% CI: 16.6–21.4) d and adult patients had a median length of hospital stay of 21 (95% CI: 19.9–22.1) d. Pediatric patients had a shorter length of hospital stay than adult patients (P = 0.024) (Figure 2B).

      Figure 2.  Analyses of length of hospital stay using Kaplan-Meier method. (A) Length of hospital stay in all the patients. (B) Comparison of length of hospital stay between children and adult.

    • The rapid spread of COVID-19 outbreak has attracted wide attention from society and academia. However, due to the limitation of clinical samples, data on COVID-19 in children are still rarely reported. As a southern province with a population of 11.346 million, Guangdong had confirmed a total of 1,361 cases (as of March 15th) of patients during the COVID-19 outbreak and became the province with the highest number of reported cases of COVID-19 outside Hubei province. Shenzhen, the second largest city in Guangdong province, had reported over 400 patients reported as of 15th March 2020, ranking the first among all cities in Guangdong province. Shenzhen Third People's Hospital is the designated hospital to treat all confirmed COVID-19 patients in Shenzhen. We therefore included a total of 333 cases of COVID-19 patients who were admitted to Shenzhen Third People's Hospital from January 11th to February 10th, 2020 in this report, and they were followed up until March 15th, 2020.

      The data showed that pediatric patients accounted 9.9% of all infected patients, and the rate was much higher than the previous reported 0.9% by Guan et al.[11]. This difference is possibly because of that risk of viral exposure in children was lower at the early outbreak. Another reason may be that pediatric patients are prone to be missed in diagnosis at the early breakout when the pandemic control was not strengthened, because as shown by our data, children had milder or less clinical symptoms, and many confirmed pediatric patients were asymptomatic, they were screened or visited hospital because they had close contact with infected patient. The actual prevalence of SARS-CoV-2 infection in children requires further investigation. SARS-CoV-2 is the seventh coronavirus found to infect humans, and it belongs to the same family as MERS-CoV and SARS-CoV[3]. During SARS and MERS outbreaks, the number of pediatric patients were far less than the number of adult patients, and the clinical manifestations and symptoms of children were also milder than those of adults[14, 21]. Based on the epidemiological characteristics of SARS and MERS in the past and the current pandemic situation in China, it was speculated that the number of children infected will be less than that of adults. We did not find sex difference in the pediatric and adult subgroups (P = 0.451). Female patients were slightly more than male patients [171 (51.4%) vs. 162 (48.6%)], which was inconsistent with the results of previous studies reporting that COVID-19 patients were male-dominated[2, 22]. This can be explained by biased sampling because our sample size is relatively small. Our results agreed that COVID-19 has a clustered onset characteristic, rapid short-term transmission, and the population is generally susceptible[11].

      Compared with adult patients, pediatric patients showed different laboratory results, milder clinical symptoms, less severe lung radiographic changes, lower grade in clinical severity classification, and better clinical outcome. The difference in laboratory tests and vital signs between the two groups may not completely come from SARS-CoV-2 infection, because these indicators and vital signs under physiological conditions are inherently different between children and adults. The overall case fatality rate in our study was 0.6%, and it was significantly lower than that in previous report[11]. No death occurred in pediatric patients. The length of hospital stay was shorter in children than in adults [19 (95% CI: 16.6–21.4) d vs. 21 (95% CI: 19.9–22.1) d, P = 0.024]. The evidence suggested that compared with adult patients, pediatric patients had better treatment outcomes. On the other hand, this milder clinical manifestations in children makes them easily missed out in diagnosis, bringing difficulties to the pandemic control.

      This study had the following limitations. Firstly, this study was a single-center retrospective study, and the number of pediatric patients was relatively small. A limited sample size (only 33 pediatric patients), which would introduce selective bias to the results. It also made our exploration of the characteristics of COVID-19 disease in children limited. Secondly, although we described the clinical characteristics and outcomes of patients with COVID-19, effective treatment strategies remains to be further explored. Thirdly, viral load may be an important indicator of the severity of the disease, but this study failed to explore the difference between viral load in pediatric and adult patients. Fully understanding of the epidemiology, clinical characteristics, and disease prognosis of COVID-19 in children requires more in-depth studies.

    • Pediatric patients with COVID-19 had shorter hospital stays and better prognosis than adult patients. Pediatric patients showed milder or occult clinical symptoms and milder lung lesions at early infection, making pediatric patients prone to be missed in clinical diagnosis. The clinical management of pediatric patients with mild and asymptomatic infection should not be ignored to reduce sources of transmission. Therefore, it is necessary to conduct extensive nucleic acid screening for children who had a contact or exposure history.

    • LIU Lei and HE Qing had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. WANG Fang, LAI Chang Xiang, HUANG Peng Yu, and LIU Jia Ming contributed equally and share first authorship. LIU Lei and HE Qing contributed equally to this article. Data acquisition: WANG Fang and LIU Lei had full access to and took the responsibility for the integrity of all data in the study. Concept and design: LIU Lei, HE Qing, WANG Fang, LAI Chang Xiang, Data analyses and interpretation: LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming, WANG Xian Feng, TANG Qi Yuan, ZHOU Xuan, XIAN Wen Jie, CHEN Rui Kun, LI Xuan, LI Zhi Yu, LIAO Li Qun. Manuscript drafting: WANG Fang, LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming.

      Critical revision of the manuscript for important intellectual content: WANG Fang, LAI Chang Xiang, HUANG Peng Yu, LIU Jia Ming, LIU Lei, HE Qing.

      Administrative, technical, or material support: WANG Fang, LAI Chang Xiang. Supervision: LIU Lei, HE Qing, WANG Fang.

    • The authors declare no competing interests.

Reference (22)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return