A novel coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in December 2019 in Wuhan, Hubei Province, China.1 Since then the disease has spread to many countries and was declared a public health emergency of international concern (PHEIC) by the World health organization on 30 January 2020.2 Prior to this time, 6 coronavirus species were known to cause human disease, four of which is known to cause common cold-like infections in immunecompetent humans (229E,OC43,HKU1,NL63), the other two namely, severe acute respiratory syndrome coronavirus(SARS-COV) and the Middle East respiratory syndrome coronavirus (MERS-CoV), are zoonotic in origin and are known to cause severe respiratory disease in humans. A lot is known about the disease whose common symptoms are fever, cough and shortness of breath. Globally, as at 8th September 2020, there have been 27,236,916 confirmed cases of COVID-19, including 891,031 deaths, reported to WHO with increasing numbers everyday.3

In spite of all efforts to contain the pandemic, the number of infections and deaths from COVID-19 keeps increasing. Elderly persons and adults with other background medical conditions have been the worst affected.4 Many documented studies on COVID-19 are mostly on adults and some on older children with few on neonates.

In Italy, Japan, and Thailand, there were community based infections with cases of SARS-CoV-2 associated pneumonia reported in children.4–6 Reported paediatric cases were mainly family cluster cases with epidemiological links to adults.4–6 Peadiatric cases appear to have a milder clinical course than those in adults and rarely deaths have been reported in children.6 These may imply that pediatric cases may play a role in community spread of SARS-CoV-2 since the viral shedding may continue from nasal secretions as well as through fecal matter for several weeks after diagnosis.7 Infections of SARS-CoV-2 in neonates have been said to be mild also.7 The reason behind the less susceptibility and mild infections of SARS-CoV-2 in neonates is largely unclear especially as neonates are not generally protected from respiratory viral infections. Although vertical transmission of COVID-19 is still being debated, maternal COVID19 infections especially when associated with severe hypoxia and fever may result in fetal distress, premature delivery and other risks.

Limited evidence exists however on mode of transmission, prevalence and clinical features of COVID-19 in neonates. It has been shown that mothers may transmit the infections by droplets during breastfeeding or by vertical transmission.8 Common presentations of fever and respiratory signs have been found to occur in neonates with COVID-19 however other existing co- morbidities such as prematurity and chromosomal disorder makes it unclear as to the actual cause of these signs.1,9 Other times, neonates may present with non-specific symptoms such as lethargy and dehydration making diagnosis difficult. Treatment of COVID-19 have been largely symptomatic with no definitive therapy.3,7 Drug trials have been largely done in adult population. A clear understanding of the symptomatology of COVID-19 among neonates, its mode of transmission and diagnosis is needed to improve public health and clinical response. There is some knowledge gap with regards to COVID-19 in neonates despite its epidemiological importance, and therefore, it is our objective to describe the documented modes of transmission, clinical features, treatment, complications and outcome of infections of SARS-CoV-2 in neonates by a systematic review of existing literature.


The Preferred Reporting Items for systematic Reviews and Meta-Analysis (PRISMA) checklist for reporting a systematic review or meta-analysis protocol was used for this review (Online Supplementary Document, Appendix 1).10

Search strategy and selection criteria

A systematic search for literature was conducted on 5th April 2020 and on 4th August 2020. The databases searched include PubMed, Ovid MEDLINE, EMBASE, CINAHL, Web of Science, and Google Scholar. Other COVID-19 data provided freely by various institutions on their websites were also retrieved. The search terms used included keywords, text words and medical subject headings (MeSH) terms and subheadings of the following: COVID-19, SARS-CoV-2, Corona virus, Newborn, Neonate, exposure, vertical transmission, breastfeeding, droplet infection.

Box 1. Selection criteria

Inclusion criteria

  • Primary Studies (Original studies) that used any study design
  • Studies published in English language
  • Studies that reported COVID-19 exposure, transmission, infection, and disease in the newborn

Exclusion criteria

  • Review articles
  • Studies published in other languages

Inclusion and exclusion criteria

We included primary studies that were carried out globally either in hospitals or in the communities such as case reports, case series, cross-sectional studies and other qualitative or quantitative studies and published in English language, between January and August 2020 which reported COVID-19 exposure, transmission, infection, and disease in the newborn.. Review articles and studies in other languages apart from English were excluded.

Study selection

A total 1250 studies were identified from the initial search of databases and institutional sources 1830 from other sources including institutionally provided data. After duplicates were removed, the number of remaining publications was 530 articles, and these were reviewed for inclusion based on information contained in titles and abstracts.

Studies not addressing exposure of transmission to or infection in newborns were excluded to give a total of 109 full text articles. These were assessed further, and 56 full text articles were included for the review (Figure 1).


Data extraction

A data extraction form was developed and reviewed by all authors. Data was extracted for each paper using the standardised form with the following domains: the name of first author and year of publication, study location, study design, clinical features, laboratory and radiological findings, diagnosis of Covid-19, treatment and outcome. Two of the reviewers extracted the data independently and discrepancies were resolved by discussion and consensus. The references were tracked using EndNote reference manager where duplicates were also removed.

Quality assessment of studies

Quality assessment of studies was done using the Newcastle Ottawa Scale for Case Control Studies,11 Quality Assessment Tool for Observational Cohort and Cross-Sectional Studies,12 and the Tool for Evaluating the Methodological Quality of Case Reports and Case Series13 (Online Supplementary Document, Appendix 2). All the case reports and case series included in this review fulfilled the quality criteria (Online Supplementary Document, Appendix 3). For the cross sectional studies, most of the studies had “not applicable” or “cannot determine” as responses to the questions on sample size calculation, measurement of exposure and outcome variables and on statistical analysis, but fulfilled the criteria with regards to questions on study objectives, study population and sampling (Online Supplementary Document, Appendix 4).

Ethics considerations

Ethical approval was not required for this study because it is a systematic review with no direct involvement of human or animal study participants.


Study characteristics

Fifty-six studies were included in this review. Thirty one of the studies were conducted in China while the remaining studies were carried out in Iran (five)1,14–17, South Korea (two)2,18, USA (seven)3,19–24, Italy (four)25–28, Spain (three)29–31, Peru (one)4, France (one)32, Australia (one)33, Belgium (one)34 (Table 1). All the studies were published between January and August 2020 (Table 1). The study designs included in this review were 33 case reports, 13 case series, one expanded case series, one case control study, and eight cross-sectional studies(Table 1). From the included studies, a total of 416 neonates were examined between few hours old and 28 days of age. A total of 38 neonates had PCR-confirmed COVID-19 disease following testing (Table 2). Fourteen (36.8%) out of the 38 neonates that tested positive had no symptoms.14–16,23,25,29,34–39

Table 1: General characteristics of studies included in the review
First Author Year Month Country Region or State Type of Study No of neonates
Alzamora4 2020 April Peru NS Case report 1
Dehan Liu40 2020 March China Wuhan Case series 11
Mi Seon Han2 2020 April South Korea Seoul Case report 1
Peng Z5 2020 April China Chongqing Case report 1
Na Li41 2020 March China Wuhan case control 17
Pu Yang42 2020 April China Wuhan Case Series 7
Siyu Chen9 2020 March China Hubei Case series 5
Wei Liu43 2020 April China Wuhan Cross sectional 19
Xiali Xiong6 2020 April China Beijing Case report 1
Lingkong Zeng44 2020 March China Wuhan Cross sectional 33
Kamali Aghdam1 2020 April Iran Tehran Case report 1
Lingkong Zeng7 2020 April China Wuhan Case report 1
Wang Shaoshuai8 2020 March China Wuhan Case report 1
Chen Yan45 2020 March China Wuhan Case report 4
Munoz3 2020 May USA Houston Case report 1
Zhu46 2020 Feb`` China Wuhan Cross sectional 10
Nan Yu47 2020 March China Wuhan Cross sectional 7
Cuifang Fan48 2020 March China Wuhan Case series 2
Li Yao49 2020 March China Hefei Case report 1
Zhuang Siying50 2020 February China Wuhan Case report 1
Bai Bailiang51 2020 March China Shaanxi Case report 1
Patek Paul21 2020 April USA Royal oak Case report 1
Sinelli MT27 2020 May Italy Monza Case report 1
Hantoushzadeh Sedigheh14 2020 April Iran Tehran Case series 7
Vikramaditya Dumpa22 2020 May USA New York Case Report 1
Xiaolin Hu37 2020 April China Wuhan Case series 7
Alonso Diaz31 2020 April Spain Madrid Case report 1
Iqbal S24 2020 April USA Washington Case report 1
Khan S52 2020 April China Wuhan Case series 17
Belinda Lowe33 2020 April Australia Queensland Case report 1
Ferrazzi E28 2020 April Italy Lombardia Cross sectional 42
Zamaniyan M15 2020 April Iran Sari Case report 1
Lu D53 2020 April China Hefei Case report 1
Wang J54 2020 March China Wuhan Case report 1
Sun M38 2020 May China Zhengzhou Case series 3
Wu Y55 2020 May China Wuhan Case Series 5
Piersigilli34 2020 May Belgium Brussels Case report 1
Chen Huijun39 2020 February China Wuhan Cross sectional 9
Xiaotong Wang56 2020 February China Suzhou Case report 1
Zhi-Jiang Zhang36 /2020 March China Case series 4
Zeng H57 2020 March China Wuhan Case series 6
Dong Lan58 2020 March China Wuhan Case report 1
Buonsenso25 2020 April Italy ? Case series 2
Noelle23 2020 May USA New York Cross sectional 18
Jie Yan59 2020 July China Wuhan Expanded case series 116
Yan Ting wu35 2020 July China Wuhan Cross sectional 30
Eun-Kyung Lee18 2020 July South Korea Daegu Case report 1
Fatemeh Eghbalian16 2020 July Iran Hamadan Case report 1
Gregorio-Hernández29 2020 June Spain ? Case series 2
Serafina Perrone26 2020 May Italy Parma Case report 1
Mahdavi17 2020 June Iran Shahroud Case Report 1
Rishi Lumba19 2020 July USA New York Case report 1
Rocio30 2020 June Spain Barcelona Case report 1
Salik20 2020 May USA New York Case report 1
Ying Xiong60 2020 July China Wuhan Case report 1
Soumeth Abasse32 2020 August France Mayotte Case report 1
Table 2: Clinical, laboratory presentations, and management outcomes of COVID-19 exposed and infected neonates
First Author Clinical features Laboratory findings Radiological findings Diagnosis of COVID-19 Treatment Outcome
Li Yao None Normal ND Negative nasopharyngeal, anal, peripheral blood samples None Alive
Zhuang Siying. Reduced milk intake Elevated Myoglobin and CK-MB Normal Negative urine, pharyngeal, breast milk, peripheral blood sample Supportive Alive
Bai Bailiang. None ND ND Negative amniotic, placental, breast milk and cord blood sample Supportive Alive
Patek Paul Fever, cyanosis, reduced milk intake, fussiness Decreased neutrophil, deranged liver function test bilateral perihilar streaking without focal Positive nasopharyngeal sample Supportive, oxygen, antibiotic, antiviral Alive
Sinelli MT Cyanosis, poor suck, bradypnoea Normal white blood cell parameters, Arterial blood gas analysis demonstrated moderate hypoxia mild bilateral ground-glass opacities Positive nasopharyngeal sample Supportive, oxygen, antibiotic Alive
Hantoushzadeh Sedigheh None (5) Not applicable (5) ND (4) Lymphopenia (1) Not applicable (5) ND (5) Not applicable (3) Negative (2) Positive on day 7 (1) ND (3) Not applicable (5) Supportive (2) None (3) Not applicable (5) Fetal demise (3) Alive (5)
Vikramaditya Dumpa Fever, feed intolerance, tachycardia Normal white blood cell parameters ND Positive nasopharyngeal sample Supportive, antibiotic Alive
Xiaolin Hu None (7) Normal white blood cell parameters (7), normal liver function test (7), normal creatinine kinase (7), normal C-reactive protein (7), normal procalcitonin (7) Normal (7) Positive nasopharyngeal, oropharngeal, amniotic fluid, peripheral blood sample (1) Others (6) negative samples Supportive (1), antibiotic (1), None (6) Alive (7)
Alonso Díaz Fast breathing, dyspnea, cyanosis, Mild acidosis Ground glass opacities mainly in the perihilar area Positive nasopharyngeal sample Supportive, oxygen, antibiotic Alive
Chen S None (5) ND (5) ND (5) Negative nasopharyngeal sample Supportive (5) Antibiotic (5) Antiviral (5) All alive
Iqbal S None Normal white blood cell parameter ND Negative nasopharyngeal, oropharyngeal, rectal sample Supportive Alive
Chen Y None (2) Fast breathing (1) Dyspnea (1) Edema (2) Rash (20 Normal white blood cell parameters (3) Normal LFT (3) ND (1) Normal (3) ND (1) Negative throat sample (4) Supportive (4) Oxygen (1) Alive
Xiong X None Normal immunoglobin ND Negative nasopharyngeal, throat, rectal, amniotic fluid, placental, breast milk Supportive Alive
Khan S Not available ND Normal USS finding Positive throat samples in 2 babies, Negative amniotic, placental, cord blood in 17 babies Supportive Alive
Belinda Lowe None ND ND Negative throat sample Supportive Alive
Ferrazzi E Abdominal distension, fast breathing, dyspnea, cyanosis, feed intolerance, reduced milk intake (1) ND ND Positive nasopharyngeal samples (3) Supportive (42) Oxygen (1) Antibiotic (1) All alive
Zamaniyan M None ND ND Positive nasopharyngel and amniotic fluid samples. Negative throat sample Supportive Alive
Lu D None ND Normal findings Negative nasopharyngeal, oropharyngeal, peripheral blood Supportive Alive
Munoz AC Nasal congestion, fast breathing, dyspnea, reduced milk intake, tachycardia, hypothermia, hypotension Lymphocytosis, increased cytokine levels, acidosis bilateral linear opacities and consolidation in right upper lobe Positive nasopharyngeal sample Supportive, oxygen, antibiotic Alive
Wang J Fever, vomiting, reduced milk intake, diarrhea Thrombocytopenia, positive for occult blood, Normal LFT, CK, immunoglobulin, cytokines Patchy fuzzy shadows Positive anal, throat sample Supportive, interferon Alive
Sun M None (1) Fast breathing (2) Dyspneoa (2) Neutrophilia (1) Normal finding (1), ND (2) Positive (1) Negative (2) Supportive (3) Oxygen (2) Antibiotic (2) All alive
Wu Y None (5) Leucopenia (1) Lymphopenia (1) Positive immunoglobulin (1) ND (1) Negative throat sample (1) Positive breast milk sample (1) Supportive (5) All alive
Wei Liu None Normal white blood cell, CK, LFT, immunoglobulin, cytokine Normal Negative stool, throat, amniotic fluid, breast milk samples Supportive Alive
Kamali Aghdam Fever, fast breathing, dyspnea, lethargy, tachycardia, mottling Normal white blood cell parameters, LFT, CK Normal Positive nasopharyngeal sample Supportive, oxygen, antibiotic, antiviral Alive
Piersigilli None Lymphopenia Bilateral streaky infiltrates Positive nasopharyngeal sample, Negative breast milk sample Supportive, oxygen Alive
Zhu Huaping Fever (), abdominal distension (), fast breathing (6), cyanosis, feeding intolerance, vomiting, reduced milk intake, tachycardia Thrombocytopenia (2), deranged LFT (2), Evidence of Infections, RDS, Pneumothorax, granular and scattered patchy shadows Negative nasopharyngeal sample Supportive, oxygen, Alive (9) Neonatal death (1)
Peng Z Fast breathing, moaning Leucopenia, reduced procalcitonin Reduced lung volume Negative saliva, plasma, urine, anal, throat sample Supportive, oxygen, antibiotics Alive
Wang Shaoshuai Ruddy skin appearance, vomiting Lymphopenia, deranged LFT, increased cytokine Thickened lung texture, High density nodular shadow Positive nasopharyngeal, anal samples. Negative placental, breast milk and cord blood samples Supportive, antibiotic Alive
Cuifang Fan Fever (1), abdominal distension (1) Lymphopenia (2) Diffuse haziness (1) ND (1) Negative nasopharyngeal, amniotic fluid, placental, breast milk, cord blood samples Supportive, antibiotics Alive
Yu Nan None (6) Fast breathing (1) ND (7) Evidence of mild pulmonary infection (1) Positive nasopharyngeal sample (1) Negative nasopharyngeal sample (2) ND (4) Supportive (1) Antibiotic (1) All alive
Zeng Lingkong Fever (2), fast breathing (3), lethargy (1), vomiting (1) Leucocytosis (1), normal LFT (3), increased CK (1) Evidence of pneumonia (3) Positive nasopharyngeal and anal samples (3) Negative amniotic fluid, breast milk and cord blood samples (3) Supportive (3), Oxygen (1) antibiotic (1) All alive
Huijun Chen ND (9) Increased CK (1) ND (9) Positive nasopharyngeal (1), negative nasopharyngeal samples (5), ND (3) Negative amniotic, breast milk and cord blood samples (9) Supportive (9) All alive
Xiaotong Wang None ND ND Negative stool, throat, amniotic fluid, placental and cord blood samples Supportive Alive
Zhi-Jiang Zhang None (1) Fever (2), dyspnea (1), vomiting (1), cough (1) ND (4) ND (1) Increased lung markings Positive nasopharyngeal samples (2) Positive anal samples (2) Supportive (4) All alive
Zeng H None Elevated immunoglobulin (2) ND Negative throat and peripheral blood samples Not available All alive
Dong Lan None Leukocytosis, elevated immunoglobulin and cytokines, Normal Negative nasopharyngeal samples Not available Alive
Zeng Lingkong Ruddy skin appearance, fast breathing, vomiting, sneezing, reduced milk intake Normal white blood cell parameters, LFT, CK, immunoglobulin Opacities Positive anal, pharyngeal samples Supportive Alive
Buonsenso None (2) ND (2) ND (2) Positive nasopharyngeal samples Supportive (1) All alive
Pu Yang. None (6), vomiting (1) Elevated cytokines (5) Evidence of RDS (5) Negative throat, amniotic fluid, cord blood samples Supportive (7) All alive
Alzamora. Dyspnea, cough Normal white blood cell parameters, immunoglobulin Normal Positive nasopharyngeal sample Supportive, oxygen
Noelle None ND ND Negative nasopharyngeal Supportive, oxygen Alive
Jie Yan None ND ND Negative Oxygen (1) Alive (115) Fetal death (1)
Yan Ting wu None (29) Fever (1) Leukocytosis (5) Neutrophil (5) ND (25) Opacities (5) Positive nasopharyngeal samples (2) Supportive (5) Interferon (3) None (25) All alive
Mi Seon Fever, vomiting, cough, jaundice, tachycardia Normal white blood cell parameters, LFT, CK, immunoglobulin Normal Positive nasopharyngeal, oropharyngeal, saliva, stool, plasma, urine Supportive Alive
Na Li ND ND ND Negative throat samples Supportive All alive
Dehan Liu ND ND ND Negative nasopharyngeal samples None All alive
Eun-Kyung Lee None Normal white cell parameters Normal Negative nasopharyngeal, oropharyngeal, stool, urine, amiotic fluid, placenta, peripheral blood and cord blood samples None Alive
Fatemeh Eghbalian None Normal white cell parameters, LFT Normal Positive oropharyngeal, stool, saliva, plasma, urine, anal, throat, rectal, pharyngeal, amniotic fluid, breast milk, peripheral blood, cord blood None Alive
Gregorio-Hernández None ND thin pleural line with conserved lung sliding (1), B-lines, consolidation (1), A pattern, B lines, superficial consolidation (1) Positive nasopharyngeal samples (2) Positive bronchoalveolar aspirate (1) None (2) Supportive (1) Oxygen (1) All alive
Serafina Perrone None ND ND Negative nasopharyngeal and breast milk samples Supportive (1) Oxygen (1) Alive
Mahdavi Fever, dyspnea, lethargy, cyanosis, cough, reduced milk intake, nasal congestion Normal white cell parameters Consolidation with air bronchograms Positive nasopharyngeal sampl Supportive, oxygen, antibiotic, antiviral Alive
Rishi Lumba. None Neutrophilia, normal cytokine, LFT, CK, immunoglobulin Normal Negative nasopharyngeal, oropharyngeal, stool, saliva, plasma, urine, anal, throat, rectal, pharyngeal, amniotic fluid, breast milk, peripheral blood, cord blood Antibiotic Alive
Rocio Fever, nasal discharge, hypertonia Normal white cell parameters and LFT, increased CK Normal Positive nasopharyngeal sample Antibiotic Alive
Salik Fast breathing, cyanosis, lethargy, feed intolerance ND Bilateral pulmonary granular opacities and reduced lung volumes Positive nasopharyngeal sample None Alive
Soumeth Abasse None Normal white cell parameters and LFT, increased CK Ground glass opacities and consolidation Positive nasopharyngeal sample None Alive
Ying Xion. Not available Neutrophilia, lymphopenia, increased cytokines Bronchovascular shadows and ground-glass opacity Positive oropharyngeal sample None Alive

ND: Not documented; LFT: Liver function test; Creatine kinase;

Clinical and laboratory features

The following are clinical and/or laboratory examinations and results that were described by the studies.

Clinical features

  1. Systemic features: Thirteen studies reported neonatal fever after birth to a COVID-19 positive mother with a total of 17 neonates.1,2,17,21,22,30,35,36,38,44,46,48,54 Four studies showed that four neonates had lethargy.1,17,20,44 Swollen superficial lymph nodes was identified in a COVID-19 positive male neonate,7 and hypothermia was reported in one neonate (Table 3).3
Table 3: Summary of neonatal clinical presentations by number of studies
Clinical Features
Number of studies Number of babies (Proportion of exposed and positive babies with symptoms)
Systemic Features Fever1,2,17,21,22,30,35,36,38,44,46,48,54 13 17(4.1%)
Lethargy1,17,20,44 4 4(1.0%)
Lymphadenopathy7 1 1 (0.2%)
Hypothermia3 1 1 (0.2%)
Edema45 1 2(0.5%)
Respiratory Features
Cough2,4,17,36 4 4(1.0%)
nasal discharge, nasal congestion and stuffiness1–3,17,30 6 6(1.4%)
Tachpynoea1,3,5,7,20,28,31,38,44–47 12 21(5.1%)
RDS42,44 2 5(1.2%)
Mild respiratory distress1,4,32 3 3(0.7%)
Moaning/Mild grunting5,42 2 3(0.7%)
Asphyxia38,44,59 3 4 (1.0%)
Sneezing7 1 1(0.2%)
Cardiovascular Features
Tachycardia1–3,22,46 5 5(1.2%)
Dyspnoea1,4,17,28,31,36,38,45 8 9(2.2%)
Cyanosis3,17,20,21,27,28,31,38,44,46 10 12(2.9%)
Hypotension3 1 1(0.2%)
Skin/Dermatological features
Cutaneous mottling1 1 1(0.2%)
Whole body Jaundice2 1 1(0.2%)
Rash45,46 2 3(0.7%)
Ruddy Skin colour7,8 2 2 (0.5%)
Skin Ulceration45 1 1(0.2%)
Gastrointestinal Features
Abdominal Distension28,46,48 3 3(0.7%)
Reduced feeding and feeding intolerance3,7,22,28,44,46 6 8 (1.9%)
Reduced milk intake3,7,17,21,28,46,50,54 8 8(1.9%)
Bloating and gastric bleeding46 1 1(0.2%)
Vomiting2,7,8,30,36,42,44,46,54 9 9(2.2%)
Diarrhoea7,54 2 2(0.5%)
  1. Respiratory features reported include cough (four neonates),2,4,17,36 nasal discharge, congestion and stuffiness (6 neonates),1–3,17,30 tachypnoea (21 neonates),1,3,5,7,28,31,38,44–47 respiratory distress syndrome (5 neonates),42,44 mild respiratory distress (3 neonates),1,4,32 moaning (3 neonates),5,45 asphyxia (4 neonates),38,44,59 and sneezing (1 neonate) (Table 3).7

  2. Cardiovascular features include tachycardia in 5 neonates, cyanosis in 12 neonates, dyspnoea in 9 neonates1,4,17,28,31,36,38,45 and hypotension in one neonate (Table 3).3

  3. Skin/dermatological features reported include cutaneous mottling (one neonate),1 whole body jaundice (one neonate),2 rash (3 neonates),45,46 ruddy skin colour (2 neonates)7,8 and skin ulceration (one neonate) (Table 3).45

  4. Gastrointestinal features: Abdominal distension was reported in 3 neonates,28,46,48 reduced feeding and feeding intolerance in 8 neonates,3,7,22,28,44,46 and reduced milk intake in 8 neonates.3,7,17,21,28,46,50,54 Milk refusal, bloating and gastric bleeding was reported among COVID-19 negative neonates born to positive mothers in one study.46 Nine studies reported vomiting in nine neonate2,7,8,30,36,42,44,46,54 (Table 3) while diarrhoea was reported in two neonates in two studies.7,54

Radiological and laboratory results

  1. SARS-COV-2 testing following childbirth: 38 (9.0%) neonates had PCR confirmed COVID-19 infection. For majority of the babies, nasopharyngeal swab was used for testing.

  2. Radiological features reported include bilateral perihilar streaking (one neonate),21 ground glass opacities (12 neonates,3,7,20,27,31,32,35,60 consolidation (3 neonates),3,17,32 patchy fuzzy shadows (one neonate),54 bilateral streaky infiltrates (one neonate),34 pneumothorax (one neonate),46 reduced lung volume(two neonates),5,20 thickened lung texture (one neonate),8 diffuse haziness (one neonate),48 mild pulmonary infection (two neonates),46,47 pneumonia (4 neonates),44,48 Respiratory distress syndrome (RDS) (4 neonates),38,42,46 Bronchovascular shadows (2 neonates),46,60 increased lung markings (3 neonates) (Table 4).36

Table 4: Laboratory features, Radiological features, and Treatment
Features Number of Studies Number of Neonates (Proportion of exposed and positive babies with symptoms)
Radiological Features
Bilateral perihilar streaking21 1 1(0.2%)
Ground glass opacities3,7,20,27,31,32,35,60 8 12(2.9%)
Consolidation3,17,32 3 3(0.7%)
Patchy fuzzy shadows54 1 1(0.2%)
Bilateral streaky infiltrates34 1 1(0.2%)
Pneumothorax46 1 1(0.2%)
Reduced lung volume5,20 2 2(0.5%)
Thickened lung texture8 1 1(0.2%)
Diffuse haziness48 1 1(0.2%)
Mild pulmonary infection46,47 2 2(0.5%)
Pneumonia44,48 2 4(1.0%)
RDS38,42,46 3 4(1.0%)
Bronchovascular shadows46,60 2 2(0.5%)
Increased Lung markings36 1 3(0.7%)
Laboratory Features
Elevated WBC count35,44,45,58 4 10(2.4%)
Abnormal LFT8,21,46 3 4(1.0%)
Elevated Cytokines3,42,58 3 3(0.7%)
Elevated Creatine Kinase8,30,39,42,44 5 9 (2.2%)
Lymphopenia8,14,34,48,55 5 6(1.4%)
Antiviral1,9,17,21,47 5 9(2.2%)
Interferon35,54 2 4(1.0%)
Antibiotics1,3,5,8,9,17,19,21,22,27,28,30,31,35,37,38,44,48 18 23(5.5%)
Oxygen/ventilation3–5,17,21,23,26–29,31,34,38,42,44,45,59 17 22 (5.3%)

WBC: White blood cell; RDS: Respiratory distress syndrome

  1. Other laboratory findings identified include: Elevated white blood cell (WBC) count (10 noenates),35,44,45,58 Abnormal Liver Function Test (LFT) (four neonates),8,21,46 Elevated cytokines (two neonates), 3,42,58 elevated creatine kinase (nine),8,30,39,42,44 Lymphopenia (6 neonates) (Table 4).8,14,34,48,55


Among the 38 neonates that tested positive, vertical transmission was reported in 11 neonates, while horizontal transmission was reported in 17 babies. The route of transmission was not clear in the remaining babies (Table 5).

Table 5: Modes of neonatal COVID-19 exposures and transmissions in included studies
Mode of transmission Number of Studies Number of babies
Horizontal (Person to Person)1–3,7,14,21,22,25,27,28,31,34,36,38,39,54 16 17
Vertical transmission4,35–37,59 5 11
Uncertain about mode of transmission8,15,29,44,47 3 10

Treatment received

Treatment was supportive for majority of the babies. Few received antiviral (9 neonates),1,9,17,21,47 antibiotics 23 neonates),1,3,5,8,9,17,19,21,22,27,28,30,31,35,37,38,44,48 and oxygen therapy/ventilation (22 neonates) (Table 4).4,5,17,21,23,26–29,31,34,38,42,44,45,59

Outcomes and complications

The complications reported include pneumonia, pneumothorax, refractory shock, and hypoxic respiratory failure. Neonates who tested positive were discharged after they tested negative to the virus. All the COVID-19 positive babies survived (Table 2). Three of the studies reported neonatal death in 5 neonates but these babies were not tested before death.14,46,59


The review examined studies that looked at the exposure to, transmission and infection of neonates as well as clinical manifestation, laboratory findings and outcomes of neonates whose mothers had COVID-19 infection. Few neonates of mothers with COVID-19 infection in this review tested positive to the virus. This finding does not support vertical transmission as a major mode of infection of the newborn. It should be noted however that quite a number of the neonates were delivered through caesarean section and the health care workers may have observed adequate infection prevention and control measures. Some of the neonates who had positive results had close contacts with other family members diagnosed with coronavirus and possibly got the infection from person-to-person transmission.1–3 Wang et al8 reported a positive test of COVID-19 in a 36 hour-old neonate in Wuhan, China. A possibility of nosocomial infection was entertained by the authors because the initial cord blood and placenta test results were negative for severe acute respiratory syndrome corona virus 2 (SARS-CoV-2). However, the finding of positive nasopharyngeal and anal swabs among 3 out of 33 neonates whose mothers had COVID-19 pneumonia by day 2 of life by Zeng et al44 raises the possibility of vertical transmission. Duran et al61 in a systematic review of neonatal cases also did not find any evidence of vertical transmission of corona virus.

Most of the neonates who were positive for SARS-CoV-2 had mild clinical symptoms. Mild symptoms according to World Health Organisation (WHO) interim guideline is when the patient has uncomplicated upper respiratory tract viral infection with non-specific symptoms such as fever, fatigue, cough, malaise and rarely may present with diarrhea, nausea, and vomiting.62 This finding is similar to reports in older children who also presented with mild or moderate clinical symptoms.63,64 The findings of cough, tachypnea, nasal discharge in neonates who tested positive for COVID-19 observed in this review is in keeping with findings in some studies carried out among older children and adults.65–67

Lymphopenia observed among these neonates has also been reported in older paediatric age groups.68 In adults with COVID -19 infection, lymphopenia is associated with poor prognosis and is an indicator of severe disease.68–70 Possible explanations for lymphopenia include direct infection of the lymphocytes, damage to lymphoid organs, disruption of activities of cytokines resulting in apoptosis of lymphocytes.70 Fever was a significant finding in newborns delivered to COVID-19 positive mothers, despite the fact that quite a number of these babies were negative. This could be as a result of maternal cytokines transferred passively to the fetus and evoking immune response in the neonatal period. The implication of this finding is the fact that the presence of fever in a newborn during this period of COVID-19 pandemic may be a good reason to screen mothers for SARS-CoV-2 infection. In adult populations, fever was also a frequent finding alongside fatigue and cough during presentation in the hospital.65,66

Gastrointestinal symptoms appear to be a common finding in neonates who were positive for COVID-19. These have also been reported among other paediatric age groups.71 Symptoms such as reduced feeding, vomiting and diarrhea may be due to the body’s response to acute viral replication in the gastrointestinal tract. Therefore, the presence of gastrointestinal features in a neonate born to a COVID-19 positive mother or who may have been exposed to a COVID -9 positive individual, may raise a suspicion of COVID-19 infection in the neonate. SARS-COV-2 RNA has been demonstrated in stool samples of hospitalized patients with COVID-19 with some still having positive stool test even after respiratory samples have tested negative, thereby posing a risk of feco-oral transmission.72

There is currently no definitive drug treatment for COVID-19 infection. In this review, supportive therapy which includes administration of intravenous fluids, intranasal oxygen were the mainstay of treatment for COVID-19 positive neonates because many of them had mild clinical symptoms. Some of the neonates received intravenous antibiotics as a way of preventing secondary bacterial infection. A few studies documented the use of antiviral drugs like oseltamivir and acyclovir.1,9,14,18 The effect of these drugs in the clinical course of COVID-19 infection is still being evaluated. In this review most of the neonates did not receive antiviral drugs and still had good outcome. The use of oseltamivir has been reported among adults with COVID-19 infection without significant outcome or change in disease progression.65 Chloroquine and hydroxychloroquine have been demonstrated to have in vitro activity against SARS-CoV-2.73 The combination of hydroxychloroquine and azithromycin has been reported to improve clinical outcomes among adult population in France,74 though this was a retrospective study and therefore has its limitations. In a randomized control trial in Spain among adult population with mild COVID-19 infection, no benefit was observed with use of hydroxychloroquine.75 Recently the U.S Food and Drug Administration (FDA) issued emergency use authorization of remdesivir for the treatment of suspected or laboratory confirmed severe cases of COVID-19 in adult and children.76 Therefore, more clinical trials are needed to determine the effective drug treatment for COVID-19 in both adults and children.

Most of the neonates born to COVID- 19 mothers had good outcomes. This finding gives credence to the fact that the infection is mild in neonates. Since there is currently no evidence of transmission of the virus in breast milk and because of the mild illness in this age group, WHO interim guideline recommends that infants born to mothers with suspected, probable or confirmed COVID-19 should be fed according to standard infant feeding guidelines, while applying necessary precautions for infection prevention and control.62

Strengths and limitations

One of the strengths of this study is that it’s a comprehensive global review. Secondly, it included both babies that tested negative though exposed to COVID-19 positive mothers and babies that tested positive. One limitation of this review is that it included mainly case reports and case series, which do not provide high quality evidence; however, these are the major kinds of research available considering the fact that neonatal COVID-19 is a new and evolving disease.


The clinical manifestations of COVID-19 in neonates are mild and outcomes are better than in adult population. There is currently little evidence of vertical transmission in neonates. Given immunological susceptibility of neonates and the fact that COVID-19 is a newly emerged and evolving disease, it is important to continue in-depth research using higher quality study designs and methodologies.


This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Authorship contributions

OBE, CDO: study conceptualization and design. OBE, ICA, INO, CDO, OUA, OWD, EE: data extraction, analysis and interpretation of results, manuscript drafting and approval of the final manuscript for publication.

Competing interests

The authors completed the Unified Competing Interest form at www.icmje.org/coi_disclosure.pdf (available upon request from the corresponding author), and declare no conflicts of interest.