| Literature DB >> 33708529 |
Jiajun Yuan1,2, Han Qian3, Shiyan Cao4, Bin Dong1, Xiaoyu Yan5, Shuanghong Luo6, Min Zhou1, Sha Zhou7, Botao Ning1,3, Liebin Zhao1,2,8.
Abstract
In order to investigate the clinical features of pregnant women and their neonates with coronavirus disease 2019 (COVID-19) and the evidence of vertical transmission of COVID-19, we retrieved studies included in PubMed, Medline and Chinese databases from January 1, 2000 to October 25, 2020 using relevant terms, such as 'COVID-19', 'vertical transmission' et al. in 'Title/Abstract'. Case reports and case series were included according to the inclusion and exclusion criteria. We conducted literature screening and data extraction, and performed literature bias risk assessment. Total of 13 case series and 16 case reports were collected, including a total of 564 pregnant women with COVID-19 and their 555 neonates, of which 549 neonates received nucleic acid test for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and 18 neonates was diagnosed with COVID-19. The positive rate is 3.28%. Amniotic fluid of one woman was tested positive for SARS-CoV-2. The majority of infected neonates were born under strict infection control and received isolation and artificial feeding. Up till now, there is no sufficient evidence to exclude the possibility of vertical transmission for COVID-19 based on the current available data. 2021 Translational Pediatrics. All rights reserved.Entities:
Keywords: Coronavirus disease 2019 (COVID-19); neonates; pregnant women; severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); vertical transmission
Year: 2021 PMID: 33708529 PMCID: PMC7944168 DOI: 10.21037/tp-20-144
Source DB: PubMed Journal: Transl Pediatr ISSN: 2224-4336
Figure 1Literature screening process
13 case series report bias risk assessment
| Item | Breslin N ( | Liu W ( | Chen Y ( | Chen S ( | Yu N ( | Zeng L ( | Zhu H ( | Prabhu M ( | Salvatore CM ( | Oncel MY ( | Wu YT ( | Yan J ( | Hu XL ( |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1. Is the hypothesis/aim/objective of the study stated clearly in the abstract, introduction, or methods section? | 2 | 1 | 2 | 1 | 1 | 0 | 2 | 1 | 1 | 1 | 1 | 1 | 1 |
| 2. Are the characteristics of the participants included in the study described? | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| 3. Were the cases collected in more than one center? | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 1 | 0 | 1 | 0 |
| 4. Are the eligibility criteria (inclusion and exclusion criteria) for entry into the study explicit and appropriate? | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| 5. Were participants recruited consecutively? | 1 | 1 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | 1 | 2 | 0 |
| 6. Did participants enter the study at a similar point in the disease? | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| 7. Was the intervention clearly described in the study? | 0 | 1 | 2 | 1 | 1 | 2 | 2 | 1 | 2 | 1 | 1 | 1 | 1 |
| 8. Were additional interventions (co-interventions) clearly reported in the study? | 0 | 2 | 1 | 1 | 1 | 2 | 2 | 1 | 2 | 1 | 1 | 1 | 1 |
| 9. Are the outcome measures clearly defined in the introduction or methods section? | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 2 | 1 |
| 10. Were relevant outcomes appropriately measured with objective and/or subjective methods? | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| 11. Were outcomes measured before and after intervention? | 0 | 2 | 2 | 2 | 1 | 1 | 1 | 0 | 1 | 2 | 1 | 1 | 1 |
| 12. Were the statistical tests used to assess the relevant outcomes appropriate? | 1 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 0 |
| 13. Was the length of follow-up reported? | 1 | 0 | 2 | 0 | 1 | 0 | 2 | 1 | 1 | 1 | 1 | 1 | 0 |
| 14. Was the loss to follow-up reported? | 1 | 0 | 2 | 0 | 1 | 0 | 2 | 1 | 1 | 1 | 1 | 1 | 0 |
| 15. Does the study provide estimates of the random variability in the data analysis of relevant outcomes? | 2 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 0 |
| 16. Are adverse events reported? | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| 17. Are the conclusions of the study supported by results? | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| 18. Are both competing interests and sources of support for the study reported? | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| 19. Is the study prospective? | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 2 | 0 | 0 | 0 |
| 20. Are the evaluation staff blinded? | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
1: yes; 0: no; 2: unclear.
Maternal characteristics
| All mothers (N=564) | |
|---|---|
| Country | |
| China | 245 (43.44%) |
| America | 192 (34.04%) |
| Turkey | 125 (22.16%) |
| Japan | 1 (0.02%) |
| Iran | 1 (0.02%) |
| Age, years | 30.21 (20–41) |
| Not reported | 238 (42.2%) |
| Method of diagnosis | |
| Laboratory confirmed (PCR) | 486 (86.17%) |
| Clinically diagnosed | 78 (13.83%) |
| Maternal symptoms | |
| Symptomatic | 318 (56.38%) |
| Asymptomatic | 121 (21.45%) |
| Not reported | 125 (22.16%) |
| Type of maternal symptoms | |
| Fever | 180/318 (56.6%) |
| Cough | 130/318 (40.88%) |
| Shortness of breath | 51/318 (16.04%) |
| Myalgia | 29/318 (9.2%) |
| Gastrointestinal | 17/318 (5.35%) |
| Gestational age at admission or diagnosis | 37.5 (30–41) |
| Not reported | 179 (31.74%) |
| Onset of diagnosis or symptoms to delivery, days | 2.95 (0–38) |
| Not reported | 257 (45.57%) |
| Treatment before delivery | 98 (17.38%) |
| Delivery | |
| Giving birth | 522 (92.55%) |
| Preterm delivery (<37 weeks) | 104/522 (19.92%) |
| Mode of delivery | |
| Caesarean delivery | 328/522 (62.84%) |
| Vaginal delivery | 116/522 (22.22%) |
| Not reported | 78/522 (14.94%) |
| Associated comorbidities | 135 (23.94%) |
| Not reported | 269 (47.7%) |
PCR, polymerase chain reaction.
Neonatal characteristics
| All neonates (N=555) | |
|---|---|
| Gender | |
| Male | 231 (41.62%) |
| Female | 192 (34.59%) |
| NR | 132 (23.78%) |
| Prematurity (<37 weeks) | 105 (18.92%) |
| Birthweight, grams | 2,470.38 (1,830–2,691) |
| NR | 88 (15.86%) |
| Mode of delivery | |
| Cesarean delivery | 372 (67.03%) |
| Vaginal delivery | 182 (32.79%) |
| Apgar score | |
| 1 min | 8.53 (6–10) |
| 5 min | 9.38 (8–10) |
| Tested for SARS-CoV-2 | |
| Yes | 549 (98.92%) |
| No | 6 (1.08%) |
| Mode of testing | |
| Neonatal examination materials | 549 (100%) |
| Maternal examination materials | 134 (24.41%) |
| Results of test | |
| Negative | 536/549 (97.63%) |
| Positive | 18/549 (3.28%) |
NR, not reported. SARS-CoV-2: the severe acute respiratory syndrome coronavirus 2. Neonatal examination materials: nasopharyngeal swabs, anal swabs, sputum sample, peripheral blood, urine, feces, serum antibodies (IgG and IgM for SARS-CoV-2). Maternal examination materials: amniotic fluid, placental tissue, vaginal secretions, breast milk, umbilical cord blood.
Characteristics of neonates with COVID-19
| Case No. | Author | Country | Gender | Premature | Mode of delivery | Birthweight, grams | Apgar at 1 and 5 min | Infection prevention | Separation | Mode of feeding | Maternal treatment | Diagnostic time | SARS-CoV-2 RT-PCR | Serum IgG and IgM | Maternal examination materials | Time of symptoms | Turn negative |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Yu N ( | China | NR | No | CD | 3,250 | 8, 9 | NR | Yes | NR | Yes | 36 h | Unclear (+) | NR | PT and UCB (-) | NR | NR |
| 2 | Zeng L ( | China | Male | No | CD | NR | NR | Stricta | Yes | NR | NR | 2 d | NPS and AS (+) | NR | NR | 2d | 6d |
| 3 | Zeng L ( | China | Male | No | CD | NR | NR | Stricta | Yes | NR | NR | 2 d | NPS and AS (+) | NR | NR | NR | 6d |
| 4 | Zeng L ( | China | Male | Yes (31w, 2d) | CD | NR | 3, 4 | Stricta | Yes | NR | NR | 2 d | NPS and AS (+) | NR | NR | NR | 7d |
| 5 | Li MD ( | China | Male | No | CD | NR | NR | Stricta | Yes | FM | No | 3 d | NPS (+) | NR | NR | NR | NR |
| 6 | Alzamora MC ( | American | Male | Yes (33w) | CD | 2,970 | 6, 8 | Stricta | Yes | FM | Yes | 16 h | NPS (+) | NR | NR | 6d | NR |
| 7 | Zamaniyan M ( | Iran | Female | Yes (32w) | CD | 2,350 | 8, 9 | Stricta | Yes | FM | Yes | 24 h | NPS (+) | NR | VS and UCB (-), AF (+) | NR | NR |
| 8 | Dong L ( | China | Female | No | CD | 3,120 | 9, 10 | NR | Yes | NR | Yes | 2 h | NPS (-) | (+) | VS (-) | NR | NR |
| 9 | Oncel MY ( | Turkey | Male | Yes (26w) | CD | 1,010 | 2, 6 | NR | Yes | FM | Yes | 1 d | DTA (+) | NR | NR | NR | 7d |
| 10 | Oncel MY ( | Turkey | Male | Yes (33w) | VD | 1,950 | 7, 8 | NR | Yes | FM | Yes | 5 d | NPS (+) | NR | NR | NR | 11d |
| 11 | Oncel MY ( | Turkey | Female | No | CD | 2,980 | 8, 9 | NR | Yes | FM | Yes | 5 d | NPS (+) | NR | NR | NR | 7d |
| 12 | Oncel MY ( | Turkey | Male | No | CD | 3,700 | 8, 9 | NR | Yes | FM | Yes | 2 d | NPS (+) | NR | NR | NR | 6d |
| 13 | Wu YT ( | China | Female | No | CD | 3,360 | 9, 10 | Not strict | No | NR | Yes | NR | TS (+) | NR | NR | Asymptomatic | NR |
| 14 | Wu YT ( | China | Female | No | CD | 3,570 | 9, 10 | Not strict | No | NR | No | NR | TS (+) | (-) | NR | 3d | NR |
| 15 | Wu YT ( | China | Female | No | CD | 2,760 | 10, 10 | Not strict | No | NR | Yes | NR | TS (-) | (+) | NR | Asymptomatic | NR |
| 16 | Wu YT ( | China | Female | No | CD | 2,940 | 10, 10 | Not strict | No | NR | Yes | NR | TS (-) | NR | NR | Asymptomatic | NR |
| 17 | Wu YT ( | China | Female | No | CD | 3,120 | 9, 10 | Not strict | No | NR | Yes | NR | TS (-) | (+) | NR | Asymptomatic | NR |
| 18 | Hu X ( | China | Male | No | CD | 3,250 | 8, 10 | Stricta | Yes | FM | No | 24–36 h | TS, feces and urine (+) | NR | AF (-) | Asymptomatic | NR |
COVID-19, coronavirus disease 2019; w, weeks; d, days; h, hours; CD, Cesarean delivery; VD, vaginal delivery; NR, not reported; FM, Formula milk; SARS-CoV-2, the severe acute respiratory syndrome coronavirus 2; RT-PCR, reverse transcriptase-polymerase chain reaction; (+): positive; (-): negative; NPS, nasopharyngeal swab; AS, anal swab; DTA, deep tracheal aspirate; TS, throat swab; Maternal examination materials: amniotic fluid (AF), placental tissue (PT), vaginal secretions (VS), breast milk (BM), umbilical cord blood (UCB). a, Strict measures to prevent infection were done during delivery, which was pointed out in the article.