Objective. Since December 2019, the coronavirus disease 2019 (COVID-19) has been spread rapidly all over the world, infecting all age groups with this novel virus. In this manuscript, we report characteristics of children with COVID-19 in Mazandaran province, northern Iran. Method. From 12 February to 28 July 2020, medical records of 100 children diagnosed with COVID-19 admitted to the hospitals of Mazandaran province were collected. Patients’ age, gender, clinical symptoms, and signs, in addition to therapeutic management and outcomes, were reported. Results. 57 (57%) boys and 43 girls with the mean age of months were evaluated. 20 patients (20%) were transferred to the PICU (pediatric intensive care unit), and 13 children experienced a severe form of the disease, pediatric inflammatory multisystem syndrome (PIMS). The mean duration of hospitalization was days. Fever (81%), respiratory (79%), gastrointestinal (47%), and neurologic complaints (29%) were experienced by the patients in addition to skin rash (14%). Sixty-two patients needed supplemental oxygen, and 6 of them underwent endotracheal intubation. Leukopenia was reported in 7, anemia in 24, and thrombocytopenia in 12 patients. 4 patients with underlying diseases including chronic renal failure, Down syndrome with cerebral palsy, and morbid obesity died. Conclusion. COVID-19 can cause symptoms in children in two stages. In the first week, upper and lower respiratory symptoms can occur which has lower severity and prevalence compared to adults. But after 2-3 weeks following infection, symptoms of MIS-C or multisystem involvement can occur and COVID-19 should be considered. The most common indication for admission is fever, rash, and respiratory problems.

1. Introduction

Since December 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been spread rapidly around the world and also all age groups were infected with this novel virus [1]. In the first reports of coronavirus disease 2019 (COVID-19), the frequency of disease in children was lower than adults. In a study in China, until January 29, 2020, less than 1% of all patients were younger than 14 years [2]. Later on, when the disease spread to other countries and become well known in Korea, till 19 July 2020, 1.7% of total cases were under 9 years and 5.5% aged between 10 and 19 years [3]. The mortality rate in this age group was very low in both reports [2, 3].

Clinical manifestations of COVID-19 are rare or absent in children and adolescents [4]. The COVID-19 symptoms seem to be less severe in children than in adults [5]. The clinical presentation of pediatric patients may differ from those of the adults and can range from asymptomatic to acute upper respiratory tract infection, gastrointestinal symptoms with shock, or coagulation dysfunction in severe cases [6]. The most common complaint of children is usually nonspecific symptoms of upper respiratory tract infection, such as mild to moderate fever and cough [5]. Fever, rash, and shock with concomitant COVID-19 infection in children were called pediatric inflammatory multisystem syndrome (PIMS) associated with SARS-CoV-2 by the Royal College of Pediatrics and Child Health [7]. Similar to adults, children with comorbidities including chronic kidney and lung diseases, malignancies, diabetes, obesity, anemia, immune disorders, heart disease, and congenital malformations are more likely to develop severe conditions from COVID-19 [8]. In the study by Önal et al. [9] from Turkey, cough, fever, and weakness were reported as the most common complaints, and the majority of patients had mild to moderate signs of illness.

There is a lot of ambiguity in COVID-19 differences between adults and children regarding clinical symptoms, complications, and management. The regional or time variability in virus behavior is also unknown. Hence, early clinical detection of COVID-19 is essential to prevent further spreading [4]. This study is aimed at describing the characteristics and clinical manifestations of children with COVID-19 admitted to hospitals of Mazandaran province, north of Iran, as one of the first provinces involved during the first wave of the pandemic, and investigating prevalence of clinical symptoms, laboratory and radiological findings, and clinical outcomes. We also aimed to identify factors associated with pediatric COVID-19 infection. As the disease is novel and experiences about this virus are low, further understanding and reports of symptoms, clinical findings, and laboratory abnormalities in children may share valuable information with other practitioners and can better inform the ongoing efforts to control this global pandemic.

2. Methodology

2.1. Study Design and Interventions

We identified pediatric patients 1 day to 18 years of age with confirmed or suspected SARS-CoV-2 infection from 12 February 2020 to 28 July 2020 (5 months) admitted to 21 hospitals of Mazandaran province, northern Iran.

A COVID-19 case was defined as SARS-CoV-2 infection by a positive reverse transcription-polymerase chain reaction (RT-PCR) test of a specimen using a nasopharyngeal swab or positive serology (confirmed case), presence of clinical signs or symptoms and a COVID-19 compatible chest CT (computed tomography) scan (probable case), and clinical symptoms and history of known sick contact (suspected case).

Data from each patients’ medical record were obtained through a research form. Demographic data including age, gender, and clinical signs and symptoms including fever, chills, cough, dyspnea, rash, nausea, vomiting, and diarrhea with no other reason were recorded [10, 11]. Chest CT involvement compatible with COVID-19 included patchy infiltration, ground-glass opacity, halo sign, reverse halo sign, and pleural effusion [12].

Clinical data including symptoms and signs in addition to laboratory data and radiologic results, therapeutic management, outcome, and mortality were also reported. Data were extracted from hospital records, hospital information system (HIS) software, and in some instances, telephone contact with parents of the children.

2.2. Outcomes

Outcomes reported included the need for invasive mechanical ventilation, hospital length of stay, and mortality during admission.

2.3. Statistical Analyses

Demographic and clinical characteristics were summarized as frequencies and percentages for categorical variables. Data were analyzed by using SPSS software, version 20.0. Written informed consent was obtained from parents of all patients.

3. Results

3.1. Demographic Characteristics

From a total of 130 COVID-19 hospital records referred for evaluation, 30 cases were excluded due to duplicate admission, inadequate data, or misdiagnosis with COVID-19, and finally, 100 children with the mean age of months (range: 1 day to 18 years) were studied. Of them, 57 were male and 70 children lived in the urban region. Table 1 shows the demographic characteristics of the patients in detail. COVID-19 RT-PCR was performed for 54 patients, and 17 cases were positive (confirmed cases). So, the remaining 83 patients were probable or suspected cases. Twenty children were transferred to the PICU (pediatric intensive care unit) during hospitalization, and 13 of them experienced a severe form of the disease: PIMS. The mean duration of hospitalization in this study was (range: 1-37) days.

3.2. Clinical Symptoms

Fever (77%), cough (62%), and dyspnea (47%) were the most common chief complaints, and 14% of the patients had comorbid diseases.

During the disease course, 81 patients were febrile, and respiratory, gastrointestinal, and neurologic complications occurred in 79%, 47%, and 29%, respectively. Also, 14 children suffered from skin rash. The median duration of symptoms prior to admission was days. Table 1 shows the clinical complaints of the patients in detail.

3.3. Patients’ Medication

All of the patients received antibiotics; ceftriaxone (44%), vancomycin (33%), meropenem (25%), and azithromycin (19%) were the most commonly prescribed antibiotics. Eleven children received intravenous immunoglobulin (IVIG), 13 children received packed cell, and 9 children received albumin. Other treatment modalities like hydroxychloroquine and Kaletra were used for 44 and 19 patients, respectively (Table 2).

3.4. Lab Tests

Leukopenia was reported in 7, anemia in 24, and thrombocytopenia in 12 patients (Table 2). Laboratory data and symptoms of the children with COVID-19 infection are shown in Tables 3 and 4.

3.5. Underlying Diseases

Among 4 died patients, 2 children had chronic renal failure, another one was a Down syndrome with cerebral palsy, and the last one suffered from morbid obesity (16 years, weight 95 kg), and all of them underwent mechanical ventilation. Notably, all of these mortalities occurred in the first 6 weeks of the study period.

3.6. Ventilator Support

Sixty-two patients needed oxygen supplementary performed with noninvasive (mask, nasal cannula, and oxyhood) or invasive devices, of which 6 of them underwent endotracheal intubation, and just one of them survived.

4. Discussion

Fewer children than adults have been affected by the COVID-19 pandemic, and children have different clinical manifestations compared to adults [13]. The prognosis for COVID-19 pneumonia is good in children with no underlying diseases [14]. In this study, during 5 months, A total of 13983 patients were admitted to the hospitals of the Mazandaran province, of which there were 100 cases aged under 18 years (0.7%). Similar to us, in the United States, 5% of total infected patients were children but less than 1% of admitted cases were children [15]. In a study in China, 5.44% of the patients were younger than 16 years [16]. This difference in results may be due to different admission and outpatient policies in other countries.

Although the disease is rare in the neonatal period [1, 10, 11], 3% of admitted children in our study were newborns and 34% of the patients were under 5 years. In the study of Dong et al., 40% of children were aged under 5 years [17]. Qiu et al. and Shekerdemian et al. reported 28% and 30% of the children to be younger than 5 years, respectively [16, 18].

Like other studies [10, 12, 14, 19, 20], the most common presentations of our patients were fever and respiratory complaints including cough and tachypnea and all patients improved with an excellent prognosis. Gastrointestinal complaints like nausea and vomiting, abdominal pain, and diarrhea were also reported in some studies [12, 19, 20]. Neurologic complaints involved a significant number of children in this study, in a spectrum of drowsiness, confusion, headache, and convulsion. Neurologic complications were reported in pediatric COVID-19 [10, 12]. Fever, cough, and dyspnea were the most common presenting symptoms in Derespina et al.’s study [21]. Chao et al. reported cough and fever as the most common symptoms at admission [22]. In Dong et al.’s study, 731 cases of COVID-19 were confirmed in children, of whom more than 90% were asymptomatic or with mild to moderate symptoms [17].

In this study, the median duration of symptoms prior to admission was days. In Chao et al.’s study, patients reported a median duration of symptoms of 3 days before admission [22]. The median duration of symptoms prior to hospitalization was 5 days, and a known sick contact was reported in 50.8% of patients in Derespina et al.’s study [21]. The difference in duration of symptoms may be attributed to different hospitalization policies.

In our report, skin rash presented in 14% of the children. There are reports of dermatologic manifestation in COVID-19, and fever and rash were the first presentation of COVID-19 [12, 23, 24]. In some cases, the rash was associated with PIMS [25, 26].

Elevated acute phase reactants (ESR, CRP) were common in this study; although leukopenia, anemia, and thrombocytopenia were seen in a considerable number of the patients, these abnormalities were also reported in other studies [12, 14, 20, 26].

All of the patients in this study received antibiotics, mostly broad spectrum ones. As the SARS-coV2 is an invasive and novel virus, and there are many coinfection with other organisms, antibiotic prescription is very difficult because there is a concern about the rational usage of antibiotics and drug resistance [10]. Oseltamivir, hydroxychloroquine, and Kaletra were used as antivirals in this study. Although other researchers treated COVID-19 patients with antibiotics [12, 14, 20], there is no strong data about the effectiveness of such drugs in the management of COVID-19.

In the present study, 20% of the patients were transferred to PICU. The exact PICU admission rate in children with COVID-19 remains unknown. Götzinger et al. reported an 8% PICU admission rate in their study in Europe [8]. In Spain, only 16% of confirmed cases were admitted to the PICU [27]. In another study in New York City, the rate of PICU admission was 28% in 46 hospitals [22]. Although some of these studies show a higher rate of critical illness than previously reported, detailed clinical characteristics and multicenter longitudinal outcomes were not reported. The difference in results may be attributed to different PICU admission policies. Also, since we are a referral hospital, all critically ill children needing PICU admission are referred and this increases the number and duration of PICU admission and hospitalization.

In this study, IVIG and packed cells were prescribed for 11 and 13 children with PIMS, respectively. High-dose IVIG (2 g/kg) is considered a treatment modality for COVID-19 patients with PIMS and may decrease the risk of coronary artery disease [28]. In Derespina et al.’s study, none of the patients received IVIG or convalescent plasma [21]. Chen et al. analyzed the treatment of 99 Wuhan patients with COVID-19 and found that 27% of these patients had received IVIG [29]. Riollano-Cruz et al. used IVIG in 80% of their cases with PIMS [30]. Its practical application value in the treatment of COVID-19 needs confirmation in future studies. We prescribed IVIG for patients with coronary artery or cardiac involvement before distinguishing between Kawasaki disease or COVID-19-associated PIMS which improved their outcome.

PIMS presented in 13% of our patients, and all of the mortalities occurred after this event. Different studies were alarmed about the severe form of COVID-19 in children which contributed to inflammatory storm and multiorgan failure [6, 24, 3034].

In this study, 14% of the patients had comorbid diseases and the mortality rate was 4%. The mortality of COVID-19 in children was low in previous studies [12, 17]. The presence of comorbidities is a risk factor for the development of critical illness. In Derespina et al.’s study, 74.3% of the patients admitted to the PICU had at least one comorbidity and 2.9% of the children died [21]. Chao et al. reported one mortality out of 67 patients (1.49%) in their study [22]. Three of our deaths in this study occurred in the first month of the COVID-19 pandemic in other centers, and patients who died had underlying diseases in addition to thrombocytopenia and pulmonary hemorrhage.

This study has the limitations of incomplete medical records and lack of access to chest CT-scan and RT-PCR in some hospitals. Since children with history of contact with confirmed COVID-19 cases and CT findings compatible with COVID-19 were considered a COVID-19 patient, we performed RT-PCR in only 54 cases in which 17 cases were positive. Further studies are needed to better understand underlying pathophysiologies and potential spectrum versus distinctive clinical conditions of the COVID-19 in children.

5. Conclusion

The prevalence of COVID-19 in children is lower than adults, and the most severe form of the disease is PIMS. Mortality is low in this age group and usually occurs in patients with underlying disease or morbid obesity. COVID-19 can cause symptoms in children in two stages. In the first week, upper and lower respiratory symptoms can occur which has lower severity and prevalence compared to adults. But after 2-3 weeks following infection, symptoms of MIS-C or multisystem involvement can occur and COVID-19 should be considered. The most common indication for admission is fever, rash, and respiratory problems.


COVID-19:Coronavirus disease 2019
CT:Computed tomography
HIS:Hospital information system
IVIG:Intravenous immunoglobulin
PIMS:Pediatric inflammatory multisystem syndrome
RT-PCR:Reverse transcription-polymerase chain reaction
SARS-CoV-2:Severe acute respiratory syndrome coronavirus 2.

Data Availability

The trial data used to support the findings of this study are available from the corresponding author upon request.

Ethical Approval

The ethics committee of Mazandaran University of Medical Sciences approved the study protocol (No. IR.MAZUMS.REC.1398.7277).

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

MSR and LSh contributed to the study conception and design. HR, MSR, MRN, and LSh contributed to data collection and patient sampling. FH and MRN contributed to drafting and editing the manuscript. FSM performed the statistical analysis. MSR, LSh, and FH revised the manuscript. MSR and LSh provided study supervision. All authors read and approved the submitted manuscript.


We thank all patients and parents involved in the COVID-19 management and treatment. The deputy of Research and technology of Mazandaran University of Medical Sciences provided the financial support of the study.