Clinical features of infants with SARS-CoV-2 infection: a systematic review and meta-analysis
Introduction
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection leads to coronavirus disease 2019 (COVID-19) (1), which has become a pandemic since it was discovered in December 2019. Multiple variants of SARS-CoV-2 have subsequently emerged, with some variants of concern (such as Alpha, Beta, Delta, and Omicron) varying in their transmissibility and virulence (2-4). The Alpha variant is more transmissible than the wild-type of SARS-CoV-2 among children (5). A recent study found that children may play an important role in transmission of the Delta variant compared with previously circulating SARS-CoV-2 variants (6). A large cohort study found that individuals aged 10–19 years infected with the Omicron variant were less likely to be hospitalized than those infected with the Delta variant (7). Globally, by August 2022, almost 600 million cases of SARS-CoV-2 infection and almost 6.5 million deaths had been reported to the World Health Organization (https://covid19.who.int/).
The clinical severity of SARS-CoV-2 infection varies according to age and the infecting variant, and ranges from asymptomatic infection to critical illness and death (8-10). The most common features of SARS-CoV-2 infection are fever, cough, fatigue, and loss of taste and smell (11-14). Although children with COVID-19 generally have milder symptoms than adults, infants are susceptible to infection (15-18). Raschetti et al. (19) performed a meta-analysis that included 176 neonates with SARS-CoV-2 infection and found that 55% of infected neonates developed clinical features of COVID-19. In addition, Bhuiyan et al. (20) conducted a meta-analysis of clinical features of COVID-19 disease in children aged younger than 5 years and found that 50% of the cases were in infants; however, Bhuiyan et al. (20) did not report the clinical features of COVID-19 in infants. Therefore, the aim of this systematic review and meta-analysis was to summarize the clinical features of SARS-CoV-2 infection in infants. We present the following article in accordance with the PRISMA reporting checklist (available at https://apm.amegroups.com/article/view/10.21037/apm-22-933/rc).
Methods
This systematic review and meta-analysis were registered in the International Prospective Register of Systematic Reviews (CRD42022332861). This study was performed by reviewing previous publications; therefore, ethical approval was not required.
Literature search
Relevant publications were searched in four significant databases (PubMed, Web of Science, Scopus, and Cochrane Library), without language restriction, for articles published before May 1, 2022. The following terms were used for the literature search: (“severe acute respiratory syndrome coronavirus 2” OR “SARS-CoV-2” OR “COVID-19” OR “2019 Novel Coronavirus” OR “2019-nCoV Diseases”) AND (“neonate” OR “newborn” OR “infant”). In addition, the reference lists of the articles identified were searched manually for further relevant publications. Studies that were reported in more than one publication were included only once in the analysis.
Inclusion and exclusion criteria
Two researchers (F Xiao and M Tang) independently reviewed and assessed studies for eligibility. Studies were required to meet following inclusion criteria: (I) infants aged from birth to 1 year; (II) confirmed SARS-CoV-2 infection; and (III) the clinical features of SARS-CoV-2 infection in infants were reported. The exclusion criteria were as follows: (I) case reports, reviews, preprint studies, and conference abstracts; (II) studies with less than ten infants with SARS-CoV-2 infections; and (III) studies for which the full text was not available.
Data collection and quality assessment
Two authors (F Xiao and M Tang) extracted data independently, and the third author (K Yan) resolved disagreements. The following data were extracted: the name of the first author, year of publication, number of infants with SARS-CoV-2 infection, age of the infected infants, the definition of the severity of COVID-19 (table available at: https://cdn.amegroups.cn/static/public/apm-22-933-01.pdf); clinical features (such as fever and cough), and the number of clinical features. The tool for evaluating the methodological quality of case reports and case series was used for the quality assessment in case series studies (21). This tool included four domains: selection, ascertainment, causality, and reporting. The Newcastle-Ottawa scale was used for quality assessment in cohort studies (22).
Statistical analysis
The pooled results were reported as proportions with 95% confidence intervals (CIs). Heterogeneity was evaluated using the I2 statistic (23). Values of I2<25%, 25–50%, and >50% indicated low, moderate, and high heterogeneity, respectively. When I2<50%, a fixed effects model was used; however, when I2>50%, a random effects model was selected. Sensitivity analysis was conducted to explore the source of heterogeneity and evaluate the stability of the pooled results. The funnel plots and Egger’s test evaluated potential publication bias when the number of included studies was not less than ten in the analysis (24). All statistical analyses were conducted by the ‘meta’ (version 5.2-0) and ‘metafor’ (version 3.4-0) packages in the RStudio software (version 1.2.5033, RStudio PBC, Boston, MA, USA).
Results
Study selection and characteristics of included studies
A total of 14,779 potentially relevant studies were obtained in the databases. Finally, based on our inclusion and exclusion criteria, 44 studies with 6,304 infants with SARS-CoV-2 infections were included in this study. Of these studies, 13 studies (25-37), 23 studies (38-60), and 8 studies (61-68) published in 2020, 2021, and 2022, respectively. The detailed process of study selection is shown in Figure 1. The detailed clinical characteristics included are presented in Table 1. Results of quality assessments are demonstrated in Table S1 and Table S2.
Table 1
Author | Total number of patients | Age group* | Number of asymptotic infections | Mild symptoms | Moderate symptoms | Severe symptoms | Respiration symptoms | Nasal symptoms | Fever | Cough | Diarrhea | Vomit | Rash | Feeding difficulty |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Díaz-Corvillón et al. [2020] (25) | 37 | Mixed | 16/37 | 18/21 | – | 3/21 | – | – | – | – | – | – | – | – |
Schwartz et al. [2022] (26) | 22 | Neonate | 2/22 | – | – | – | 15/22 | – | 5/22 | 3/22 | 1/22 | – | – | 1/22 |
Sun et al. [2020] (27) | 36 | Mixed | 1/36 | – | – | – | – | 6/36 | 17/36 | 28/36 | 9/36 | 4/36 | – | – |
Mithal et al. [2020] (28) | 18 | Mixed | 1/18 | – | – | – | 1/18 | 5/18 | 14/18 | 8/18 | 1/18 | 5/18 | ||
Bellino et al. [2020] (29) | 528 | Mixed | 43/528 | 104/528 | – | 21/528 | – | – | – | – | – | – | – | – |
Parri et al. [2020] (36) | 61 | Mixed | 5/39 | 26/61 | 7/39 | 1/39 | – | – | – | – | – | – | – | – |
Maltezou et al. [2020] (30) | 23 | Mixed | 5/23 | 6/23 | 11/23 | 1/23 | – | – | – | – | – | – | – | – |
Gale et al. [2021] (38) | 66 | Neonate | 7/66 | – | – | 28/66 | 24/66 | 26/66 | 35/66 | 11/66 | 4/66 | – | 2/66 | 33/66 |
Biko et al. [2021] (39) | 82 | Mixed | 17/82 | – | – | – | 13/82 | 29/82 | 42/82 | 37/82 | 10/82 | 12/82 | – | 8/82 |
Peng et al. [2021] (40) | 41 | Mixed | 3/41 | – | – | – | – | – | – | – | – | – | – | – |
Soysal et al. [2021] (41) | 27 | Mixed | 3/27 | 8/27 | 1/27 | – | – | – | – | – | – | – | – | – |
Kulkarni et al. [2021] (55) | 12 | Mixed | 4/12 | – | – | – | 5/12 | 3/12 | 7/12 | – | – | 1/12 | – | 2/12 |
Zhang et al. [2021] (42) | 36 | Mixed | 2/36 | – | – | – | – | – | 18/36 | 13/36 | 5/36 | – | – | – |
More et al. [2021] (60) | 143 | Mixed | 102/132 | – | – | – | – | – | – | – | – | – | – | – |
More et al. [2021] (60) | 39 | Mixed | 14/27 | – | – | – | – | – | – | – | 2/39 | – | – | – |
Paret et al. [2021] (54) | 22 | Mixed | 1/22 | – | – | – | 1/22 | 2/22 | 20/22 | 3/22 | – | 1/22 | 2/22 | 2/22 |
Shaiba et al. [2021] (65) | 36 | Mixed | 2/36 | 25/36 | 5/36 | – | – | – | 25/34 | – | – | – | – | – |
Ochoa et al. [2022] (61) | 86 | Mixed | 30/86 | – | – | – | – | – | – | – | – | – | – | – |
Akin et al. [2022] (62) | 176 | Neonate | 19/176 | – | – | – | 33/176 | 14/176 | 113/176 | 38/176 | 14/176 | – | 3/176 | 45/176 |
Iijima et al. [2022] (63) | 13 | Mixed | 1/13 | – | – | – | 9/13 | 8/13 | 7/13 | – | 2/13 | – | 7/13 | |
Funk et al. [2022] (68) | 829 | Mixed | 14/829 | – | – | – | – | – | – | – | – | – | – | |
Albuali et al. [2022] (64) | 115 | Mixed | 74/115 | – | – | – | 13/115 | – | 71/115 | 30/115 | 15/115 | – | – | – |
Shaiba et al. [2022] (65) | 898 | Mixed | 140/898 | – | – | – | 218/898 | 219/898 | 603/898 | 216/898 | 217/898 | 103/898 | 63/898 | 158/898 |
Lu X et al. [2020] (37) | 31 | – | – | 6/31 | 25/31 | 0/31 | – | – | – | – | – | – | – | – |
Kainth et al. [2020] (31) | 19 | – | – | 14/19 | 5/19 | 0/19 | – | – | – | – | – | – | – | – |
Panetta et al. [2020] (32) | 27 | – | – | 24/27 | – | – | – | – | 22/27 | – | – | – | – | – |
Drouin et al. [2021] (58) | 97 | Mixed | – | 25/97 | 17/97 | 10/97 | 14/97 | 22/97 | 44/97 | 17/97 | 12/97 | 15/97 | 6/97 | 21/97 |
Bayesheva et al. [2021] (44) | 156 | – | – | – | 20/156 | 0/156 | – | – | – | – | – | – | – | – |
Zachariah et al. [2020] (34) | 14 | Mixed | – | – | – | – | 1/14 | – | – | – | – | – | – | – |
Kanburoglu et al. [2020] (33) | 37 | Neonate | – | – | – | – | 9/37 | 2/37 | 18/37 | 10/37 | 2/37 | – | 1/37 | 6/37 |
Leung [2021] (50) | 749 | Neonate | – | – | – | – | 187/749 | – | 402/749 | 394/749 | – | – | – | – |
Ouldali et al. [2021] (47) | 193 | Mixed | – | – | – | – | 53/189 | 117/188 | 162/186 | 71/188 | 44/190 | 24/189 | – | 7/176 |
Nanavati et al. [2021] (46) | 21 | Neonate | – | – | – | – | 5/21 | – | – | – | – | 1/21 | – | – |
Shah et al. [2021] (57) | 18 | Neonate | – | – | – | – | 5/18 | – | 3/18 | – | – | – | – | – |
Spoulou et al. [2021] (48) | 14 | Mixed | – | – | – | – | 2/14 | 9/14 | 11/14 | 3/14 | 4/14 | – | – | 3/14 |
Yaman et al. [2022] (49) | 12 | Neonate | – | – | – | – | 5/12 | – | 5/12 | 6/12 | – | – | – | 7/12 |
Yarden Bilavski et al. [2021] (52) | 75 | Mixed | – | – | – | – | 1/75 | 18/75 | – | 12/75 | 6/75 | – | 3/75 | 6/75 |
Munian et al. [2021] (51) | 19 | Neonate | – | – | – | – | 7/19 | – | – | – | 2/19 | 2/19 | – | 3/19 |
Ji et al. [2021] (45) | 40 | Mixed | – | – | – | – | 2/40 | 5/40 | 30/40 | 28/40 | 8/40 | 4/40 | – | – |
Marks et al. [2022] (67) | 1,137 | Mixed | – | – | – | – | 85/252 | 135/252 | – | 119/252 | – | 40/252 | – | 75/252 |
Hassan et al. [2021] (53) | 41 | Neonate | – | – | – | – | – | 16/41 | 36/41 | 12/41 | 6/41 | 3/41 | – | 9/41 |
McLaren et al. [2020] (35) | 20 | Mixed | – | – | – | – | – | – | 7/20 | – | – | – | – | – |
Leibowitz et al. [2021] (56) | 20 | Mixed | – | – | – | – | – | – | 20/20 | – | – | – | – | – |
Andina-Martinez et al. [2022] (66) | 12 | Mixed | – | – | – | – | – | – | 9/12 | – | – | – | – | 1/12 |
Wanga et al. [2021] (59) | 206 | Mixed | – | – | – | – | – | – | – | – | – | – | – | 7/176 |
*, the mixed studies were infants (≤1 year).
Meta-analysis
Proportion of asymptomatic infection
Totally, 22 studies (25-30,36,38-43,54,55,60-65,68) with 23 trials of 3,301 infants with SARS-CoV-2 infections were included for asymptomatic infection analysis. The proportion of asymptomatic infection was 20% (95% CI: 11–28%, I2=97%, P<0.01) in infants with SARS-CoV-2 infection (Table 2 and Figure 2A).
Table 2
Group | Total and subgroup analyses | Subcategories | No. of trials | No. of patients | Model | Proportion | 95% CI | I2 | τ2 | P | Publication bias |
---|---|---|---|---|---|---|---|---|---|---|---|
Asymptomatic infection | Total analysis | 23 | 3,301 | Random | 0.20 | 0.11–0.28 | 97% | 0.0412 | <0.01 | Yes | |
Subgroup by year | 2020 | 7 | 703 | Random | 0.13 | 0.04–0.22 | 77% | 0.0121 | <0.01 | NC | |
2021 | 10 | 481 | Random | 0.22 | 0.07–0.38 | 97% | 0.058 | <0.01 | None | ||
2022 | 6 | 2,117 | Random | 0.22 | 0.04–0.41 | 99% | 0.0529 | <0.01 | NC | ||
Subgroup by number | <100 | 17 | 623 | Random | 0.11 | 0.09–0.13 | 80% | 0.0144 | <0.01 | Yes | |
≥100 | 6 | 2,678 | Random | 0.29 | 0.04–0.55 | 99% | 0.1039 | <0.01 | NC | ||
Subgroup by age | Neonate | 6 | 460 | Random | 0.26 | 0.12–0.55 | 96% | 0.8092 | <0.01 | NC | |
Infants (mixed age) | 17 | 2,841 | Random | 0.15 | 0.07–0.23 | 96% | 0.0233 | <0.01 | Yes | ||
Disease severity | Mild symptoms | – | 10 | 870 | Random | 0.48 | 0.30–0.65 | 96% | 0.0752 | <0.01 | Yes |
Moderate symptoms | – | 8 | 428 | Random | 0.27 | 0.10–0.44 | 93% | 0.0579 | <0.01 | NC | |
Severe symptoms | – | 9 | 980 | Random | 0.08 | 0–0.16 | 90% | 0.0136 | <0.01 | NC | |
Clinical features | Respiration symptoms | – | 22 | 2,948 | Random | 0.23 | 0.18–0.29 | 81% | 0.2304 | <0.01 | Yes |
Subgroup by year | 2020 | 4 | 91 | Random | 0.26 | 0–0.53 | 91% | 0.0749 | <0.01 | NC | |
2021 | 14 | 1,416 | Random | 0.23 | 0.18–0.30 | 66% | 0.1363 | <0.01 | None | ||
2022 | 4 | 1,441 | Random | 0.21 | 0.14–0.32 | 88% | 0.1596 | <0.01 | NC | ||
Subgroup by number | <100 | 16 | 569 | Random | 0.21 | 0.12–0.29 | 88% | 0.0248 | <0.01 | Yes | |
≥100 | 6 | 2,379 | Random | 0.24 | 0.18–0.30 | 80% | 0.0761 | <0.01 | NC | ||
Subgroup by age | Neonate | 9 | 1,120 | Random | 0.32 | 0.23–0.41 | 73% | 0.0136 | <0.01 | NC | |
Infants (mixed age) | 13 | 1,828 | Random | 0.15 | 0.09–0.21 | 95% | 0.0107 | <0.01 | None | ||
Nasal symptoms | 17 | 2,067 | Random | 0.31 | 0.21–0.40 | 95% | 0.0342 | <0.01 | Yes | ||
Subgroup by year | 2020 | 3 | 91 | Random | 0.16 | 0.07–0.35 | 55% | 0.2555 | 0.11 | NC | |
2021 | 10 | 637 | Random | 0.33 | 0.21–0.44 | 92% | 0.0291 | <0.01 | Yes | ||
2022 | 4 | 1,339 | Random | 0.30 | 0.12–0.75 | 98% | 0.8751 | <0.01 | NC | ||
Subgroup by number | <100 | 13 | 553 | Random | 0.28 | 0.19–0.37 | 84% | 0.0244 | <0.01 | Yes | |
≥100 | 4 | 1,514 | Random | 0.29 | 0.12–0.71 | 98% | 0.8236 | <0.01 | NC | ||
Subgroup by age | Neonate | 4 | 320 | Random | 0.22 | 0.04–0.40 | 93% | 0.0325 | <0.01 | NC | |
Infants (mixed age) | 13 | 1,747 | Random | 0.33 | 0.23–0.44 | 94% | 0.0345 | <0.01 | None | ||
Fever | 26 | 2,803 | Random | 0.64 | 0.57–0.71 | 92% | 0.061 | <0.01 | None | ||
Subgroup by year | 2020 | 6 | 160 | Random | 0.52 | 0.34–0.71 | 81% | 0.0434 | <0.01 | NC | |
2021 | 15 | 1,429 | Random | 0.66 | 0.56–0.77 | 95% | 0.071 | <0.01 | None | ||
2022 | 5 | 1,214 | Fixed | 0.67 | 0.64–0.69 | 0% | 0 | 0.7 | NC | ||
Subgroup by number | <100 | 21 | 679 | Random | 0.62 | 0.54–0.72 | 88% | 0.0813 | <0.01 | None | |
≥100 | 5 | 2,124 | Random | 0.67 | 0.55–0.78 | 96% | 0.0191 | <0.01 | NC | ||
Subgroup by age | Neonate | 8 | 1,121 | Random | 0.50 | 0.34–0.66 | 86% | 0.046 | <0.01 | NC | |
Infants (mixed age) | 18 | 1,682 | Random | 0.68 | 0.60–0.77 | 91% | 0.0507 | <0.01 | None | ||
Cough | 21 | 2,989 | Random | 0.34 | 0.26–0.42 | 93% | 0.0308 | <0.01 | None | ||
Subgroup by year | 2020 | 4 | 113 | Random | 0.41 | 0.13–0.69 | 93% | 0.0739 | <0.01 | NC | |
2021 | 12 | 1,422 | Random | 0.33 | 0.23–0.44 | 94% | 0.0279 | <0.01 | None | ||
2022 | 5 | 1,454 | Random | 0.32 | 0.21–0.44 | 93% | 0.0166 | <0.01 | NC | ||
Subgroup by number | <100 | 15 | 611 | Random | 0.35 | 0.24–0.45 | 89% | 0.0385 | <0.01 | None | |
≥100 | 6 | 2,378 | Random | 0.35 | 0.24–0.45 | 97% | 0.0181 | <0.01 | NC | ||
Subgroup by age | Neonate | 7 | 1,103 | Random | 0.29 | 0.18–0.41 | 95% | 0.0199 | <0.01 | NC | |
Infants (mixed age) | 14 | 1,886 | Random | 0.37 | 0.27–0.48 | 91% | 0.0362 | <0.01 | None | ||
Diarrhea | 17 | 1,983 | Random | 0.13 | 0.09–0.16 | 84% | 0.0037 | <0.01 | Yes | ||
Subgroup by year | 2020 | 3 | 95 | Random | 0.11 | 0.01–0.25 | 71% | 0.0184 | 0.03 | NC | |
2021 | 11 | 699 | Random | 0.13 | 0.09–0.17 | 63% | 0.0025 | <0.01 | None | ||
2022 | 3 | 1,189 | Random | 0.15 | 0.06–0.25 | 96% | 0.0068 | <0.01 | NC | ||
Subgroup by number | <100 | 13 | 604 | Fixed | 0.1 | 0.07–0.12 | 34% | 0.0005 | 0.11 | Yes | |
≥100 | 4 | 1,379 | Random | 0.17 | 0.10–0.25 | 91% | 0.0106 | <0.01 | NC | ||
Subgroup by age | Neonate | 7 | 400 | Fixed | 0.07 | 0.05–0.10 | 0% | 0 | 0.78 | NC | |
Infants (mixed age) | 10 | 1,583 | Random | 0.17 | 0.13–0.22 | 73% | 0.0051 | <0.01 | Yes | ||
Vomit | 13 | 1,722 | Fixed | 0.13 | 0.11–0.15 | 0% | 0.006 | 0.76 | None | ||
Subgroup by year | 2021 | 9 | 523 | Fixed | 0.11 | 0.09–0.14 | 0% | 0 | 0.84 | NC | |
2022 | 3 | 1,163 | Fixed | 0.13 | 0.10–0.18 | 45% | 0.032 | 0.16 | NC | ||
Subgroup by number | <100 | 10 | 383 | Fixed | 0.13 | 0.10–0.17 | 0% | 0 | 0.85 | Yes | |
≥100 | 3 | 1,339 | Fixed | 0.13 | 0.10–0.15 | 34% | 0.0002 | 0.22 | NC | ||
Subgroup by age | Neonate | 3 | 81 | Fixed | 0.07 | 0.02–0.14 | 0% | 0 | 0.81 | NC | |
Infants (mixed age) | 10 | 1,641 | Fixed | 0.13 | 0.11–0.14 | 0% | 0.0073 | 0.71 | None | ||
Rash | 8 | 1,389 | Random | 0.04 | 0.02–0.06 | 63% | 0.0004 | <0.01 | NC | ||
Subgroup by year | 2021 | 4 | 260 | Fixed | 0.05 | 0.02–0.08 | 0% | 0 | 0.64 | NC | |
Subgroup by number | <100 | 6 | 315 | Fixed | 0.04 | 0.02–0.07 | 0% | 0 | 0.84 | NC | |
Subgroup by age | Neonate | 3 | 279 | Fixed | 0.02 | 0–0.04 | 0% | 0 | 0.68 | NC | |
Infants (mixed age) | 5 | 1,110 | Fixed | 0.06 | 0.04–0.07 | 0% | 0 | 0.87 | NC | ||
Feeding difficulty | 19 | 2,044 | Random | 0.20 | 0.14–0.26 | 89% | 0.0145 | <0.01 | Yes | ||
Subgroup by year | 2020 | 3 | 77 | Fixed | 0.19 | 0.11–0.31 | 40% | 0.064 | 0.19 | NC | |
2021 | 10 | 440 | Random | 0.22 | 012–0.31 | 83% | 0.0187 | <0.01 | None | ||
2022 | 6 | 1,527 | Random | 0.21 | 0.09–0.32 | 95% | 0.0167 | <0.01 | NC | ||
Subgroup by number | <100 | 15 | 542 | Random | 0.21 | 0.13–0.28 | 80% | 0.0175 | <0.01 | Yes | |
≥100 | 4 | 1,502 | Random | 0.16 | 0.07–0.37 | 93% | 0.6826 | <0.01 | NC | ||
Subgroup by age | Neonate | 7 | 373 | Random | 0.26 | 0.13–0.39 | 87% | 0.0264 | <0.01 | NC | |
Infants (mixed age) | 12 | 1,671 | Random | 0.16 | 0.10–0.23 | 89% | 0.0081 | <0.01 | None |
CI, confidence interval; NC, not conducted.
Proportion of disease severity
Overall, ten studies (25,29-32,36,37,41,43,58) reported mild symptoms, eight studies reported moderate symptoms (30,31,36,37,41,43,44,58), and nine studies (25-27,29,30,36-38,58) reported severe symptoms. The proportion of mild symptoms was 48% (95% CI: 30–65%, I2=96%, P<0.01, Figure 2B), moderate symptoms was 27% (95% CI: 10–44%, I2=93%, P<0.01, Figure 3A), and severe symptoms was 8% (95% CI: 0–16%, I2=90%, P<0.01, Figure 3B, Table 2).
Proportion of clinical symptoms
As shown in Table 2, respiratory symptoms were evaluated in 22 studies (26,28,33,34,38,39,45-52,54,55,57,58,62,64,65,67), and the proportion of these was 23% (95% CI: 18–29%, I2=81%, P<0.01, Figure S1A). Nasal symptoms were evaluated in 17 studies (27,28,33,38,39,45,47,48,52-55,58,62,63,65,67), and the proportion of these was 31% (95% CI: 21–40%, I2=95%, P<0.01, Figure S1B). Fever was evaluated in 26 studies. Of these studies, six studies (26-28,32,33,35) published in 2020, 15 studies (38,39,42,43,45,47-50,53-58) published in 2021, and five studies (62-66) published in 2022. The proportion of this symptom was 64% (95% CI: 57–71%, I2=92%, P<0.01, Figure S1C). Cough was evaluated in 21 studies (26-28,33,38,39,42,45,47-50,52-54,58,62-65,67), and the proportion of this symptom was 34% (95% CI: 26–42%, I2=93%, P<0.01, Figure S1D). Diarrhea were evaluated in 17 studies (26,27,33,38,39,42,45,47,48,51-53,58,60,62,64,65), and the proportion of this symptom was 13% (95% CI: 9–16%, I2=84%, P<0.01, Figure S2A). Vomit was evaluated in 13 studies (27,39,45-47,51,53-55,58,63,65,67), and the proportion of this symptom was 13% (95% CI: 11–14%, I2=0%, P=0.76, Figure S2B). Rashes were evaluated in 8 studies (28,33,38,52,54,58,62,65), and the proportion of this symptom was 4% (95% CI: 2–6%, I2=63%, P<0.01, Figure S2C). Feeding difficulty was evaluated in 19 studies (26,28,33,38,39,48,49,51-55,58,59,62,63,65-67), and the proportion of this symptom was 20% (95% CI: 14–26%, I2=89%, P<0.01, Figure S2D). Results of subgroup analyses were provided in Table 2.
Sensitivity analysis
Sensitivity analysis was performed by excluding individual studies in the overall analysis. Results were as follows: no study showed a proportion of >1% for respiratory symptoms, diarrhea, and vomit (Figure S3A-S3C); no study showed a proportion of >2% for fever, cough, and feeding difficulty (Figure S3D-S3F); no study showed a proportion of >3% for asymptomatic infection and nasal symptoms (Figure S3G,S3H); and no study showed a proportion of >5% for mild symptoms (Figure S3I).
Publication bias
Publication bias was found in the following analyses: asymptomatic infection; mild symptoms; respiratory symptoms; nasal symptoms; diarrhea; and feeding difficulty (Table 2). Fever analysis, cough analysis, and vomit analysis did not show the presence of publication bias (Table 2).
Discussion
To the best of our knowledge, this is the most comprehensive systematic review and meta-analysis that summarizes current data on clinical features of infants with SARS-CoV-2 infection. This study found that the prevalence of asymptomatic infection was 20% in infants with SARS-CoV-2 infection. Disease severity were mild in 48% of infants, moderate in 27% of infants, and severe in 8% of infants with COVID-19. Notably, the most common features of SARS-CoV-2 infection in infants were fever (64%), cough (34%), and nasal symptoms (31%).
Infants infected with the SARS-CoV-2 virus are often asymptomatic and present with no clinical symptoms or significant chest imaging findings; however, these asymptomatic infections are still contagious (69). Infants with asymptomatic infection may be a source of transmission, which poses a challenge for infection control and requires timely diagnosis. Studies reported that the rate of asymptomatic infants ranged from 2% to 77% (60,68). By performing a meta-analysis, this study found that the prevalence of asymptomatic infection was 20% in 3,301 infants with SARS-CoV-2 infection. We conducted further subgroup analyses by year, because most of studies did not provide information on the SARS-CoV-2 variant. The subgroup analysis found that the proportion of asymptomatic infection is 13%, 22%, and 22% in 2020, 2021, and 2022, respectively. The proportion of asymptomatic infection was lower in 2020 than in 2021 and 2022. Early in 2020, Dong et al. (15) reported the asymptomatic rate of infants was 1.9% (7/376) in China. Our study found a higher asymptomatic rate by combining studies published in 2020. This may be attributable to the evolution of virus. On November 30, 2021, the United States designated the Omicron variant as a variant of concern. The variant led to a higher rate of pediatric hospitalizations in children younger than 17 years (70). A recent study reported that 13.5% (14/104) of children (age <3 years) with SARS-CoV-2 infection were asymptomatic cases during the outbreak of Omicron (71). However, the number of published studies of infants infected with the Omicron variant is limited in issued studies. Thus, further investigation into the rate of asymptomatic infections in infants is necessary during the Omicron pandemic.
Our analysis of the combined data found that 48% of infants infected with SARS-CoV-2 had mild disease, 27% had moderate disease, and 8% had severe disease. There are two explanations for the higher incidence of mild/moderate disease in infants. First, children may have a different qualitative response to the SARS-CoV-2 than adults (72). Second, the angiotensin-converting enzyme-2 receptors bind to SARS-CoV-2 spike protein and promote the incorporation of SARS-CoV-2 into human cells (73). Children have less angiotensin-converting enzyme-2 in the nasal epithelium, which may contribute to the protection against SARS-CoV-2 (74). A recent study reported that by measuring hospitalization rates, children with Omicron variant infection have less severe disease than the Delta variant infection (75). Currently, the number of published studies on infants infected with the Omicron variant is still limited; however, close attention should be given to the infants, regardless of the variant type.
A recent meta-analysis (76) included 215 studies with 132,647 COVID-19 patients that found four common features: fever (76.2%), coughing (60.4%), fatigue (33.6%), and dyspnea (26.2%). Similarly, our study found that fever was the most common clinical feature (64%), followed by cough (34%), and nasal symptoms (31%) in infants with COVID-19. Furthermore, our subgroup analyses found that while most of the clinical features (such as fever, nasal symptoms, and respiratory symptoms) were mild in the neonate group, feeding difficulty were severe; this may be in relation to neonates’ vulnerability to feeding difficulties. Moreover, feeding difficulty may be the only present symptom in infants; therefore, the possibility of COVID-19 should not be excluded, particularly when infants have had contact with SARS-CoV-2 infected.
Other features, such as fatigue and myalgia, were not listed in the included studies. This is most likely because infants have underdeveloped language skills and, therefore cannot communicate symptoms. Notably, a longitudinal cohort study (77) investigated 1,127 COVID-19 survivors with 2 years of follow-up and reported several prevalent symptoms, such as sleep difficulties (31%), fatigue or muscle weakness (31%), and joint pain (18%); none of these symptoms could be mentioned in infants. This raises at least three scientific questions that need to be urgently answered: (I) Will these infants develop complications in the distant future after infection, such as those in adults? (II) Will these complications heal on their own? If so, approximately how long will these symptoms persist in infants? (III) Do these complications affect the infant’s brain development, including higher cognitive functioning? These is a need for future longitudinal prospective cohort studies that must respond to these scientific questions, as they are critical to infant development.
Certain limitations should be addressed. First, very few included studies reported the detailed variants of SARS-CoV-2; thus, this study could not conduct subgroup analysis based on variants. Second, there was significant heterogeneity in most of the analyses, and while further subgroup analyses also showed considerable heterogeneity, this may have been due to differences in methods and bias of included studies. However, by sensitivity analysis, we found that no study showed a proportion of more than 5% in the overall analysis, which supports our results’ reliability. Third, only published studies were included for meta-analysis, while preprint studies and unpublished data were excluded; therefore, publication bias may be evitable. Fourth, most of the included studies were retrospective designs; therefore, selection bias exists in this study. Fifth, six of the analyses found evidence of publication bias. This may by caused by factors such as language bias and availability bias; however, further subgroup analyses found the proportions were similar in these six kinds of analyses, which supported the reliable of our results. Considering these limitations, well-designed trials are needed in future studies.
In conclusion, this study found that 20% of infants with SARS-CoV-2 infections were asymptomatic, while most infants with COVID-19 presented with mild symptoms. Additionally, fever and cough were the most common clinical features in these infants. This study explores the clinical features of infants infected with SARS-CoV-2 to aid health policymakers in constituting a more logical policy for the COVID-19 pandemic.
Acknowledgments
Funding: None.
Footnote
Reporting Checklist: The authors have completed the PRISMA reporting checklist. Available at https://apm.amegroups.com/article/view/10.21037/apm-22-933/rc
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://apm.amegroups.com/article/view/10.21037/apm-22-933/coif). The authors have no conflicts of interest to declare.
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