Dear Editor,
The Wuhan Coronavirus (recently named SARS-CoV-2) has been making headline news around the world as there are over 60,000 confirmed cases and a total of over 1300 deaths in China alone since the start of the outbreak [1]. The World Health Organization has declared a global emergency as they are trying to control this outbreak. Over 28 countries and territories around the world has been affected but mainly in Asia.
The 21st century has brought us three novel coronavirus causing fatality on a large scale – SARS (severe acute respiratory syndrome) in 2003, MERS (Middle East respiratory syndrome) in 2012, and now the novel coronavirus from Wuhan [2]. As to date, there are only limited data on the consequences of this coronavirus on pregnancy. However, SARS and MERS are responsible for severe complications during pregnancy [3,4].
In a review of previous coronavirus infections in pregnancy, there were 13 cases of SARS-CoV and 11 cases of MERS-CoV reported in the literature [3,4]. Maternal outcome of the 13 cases: 4 cases had miscarriage, 2 opted for termination of pregnancy, 2 succumbed to SARS, 2 required mechanical ventilation, and 3 were treated conservatively. No neonatal adverse effect was noted except for 2 cases born prematurely – one at 28 weeks and the other at 26 weeks (Table 1 ). Maternal outcome of the 11 MERS-CoV cases: 2 were asymptomatic, 3 succumbed to MERS, 2 required mechanical ventilation, 3 were treated conservatively, and 1 refused treatment. No neonatal adverse effects were noted except for 2 intrauterine fetal demise (IUFD) (one at 38 weeks and the other at 20 weeks) and 1 fetal death due to prematurity at 24 weeks gestation (Table 2 ). The most important contributing factor for method of delivery in patients with SARS and MERS seems to be dependent on disease progression resulting in maternal hypoxia leading to fetal distress and prematurity. Neonatal infection due to possible vertical transmission was not detected in any of the SARS or MERS infection except for 1 SARS case in the United States where cord blood and breast milk were positive for the SARS-CoV antibody.
Table 1.
SARS infection and maternal–fetal outcome.
Country | Case | Maternal |
Newborn |
|||
---|---|---|---|---|---|---|
Complication | SARS-CoV Antibody | Delivery | Complication | SARS-CoV antibody | ||
United States | 1 | Progressive Lung Infiltration s/p Mechanical Ventilation | Serum (+) | 38 weeks Cesarean Placenta previa |
No adverse effect | Cord blood (+) Placenta (−) Breast milk (+) Stool (−) |
2 | Lung infiltration s/p antibiotics | Serum (+) | 36 weeks Cesarean Fetal Distress |
No adverse effect | Cord blood (−) Placenta (−) Breast milk (−) Stool (−) |
|
Hong Kong | 1 | SARS fatality with MRSA pneumonia | Nasopharyngeal (+) | 28 weeks Cesarean Fetal Distress |
Necrotizing Enterocolitis with ileal perforation s/p laparotomy | Cord blood (−) Placenta (−) Stool (−) Peritoneal fluid (−) |
2 | Lung infiltration s/p antibiotics | Stool (+) CSF (+) Peritoneal fluid (+) |
26 weeks Cesarean Fetal Distress |
Jejunal perforation s/p laparotomy | Cord blood (−) Placenta (−) Stool (−) Peritoneal fluid (−) |
|
3 | SARS fatality | Stool (+) | 32 weeks Cesarean Maternal Hypoxia |
No adverse effect | Cord blood (−) Placenta (−) Stool (−) |
|
4 | Lung infiltration s/p antibiotics | Nasopharyngeal (+) | 33 weeks X Preterm labor |
No adverse effect | Cord blood (−) Placenta (−) Stool (−) |
|
5 | Progressive Lung Infiltration s/p Mechanical Ventilation | Stool (+) | 37 weeks NSD |
No adverse effect | Cord blood (−) Placenta (−) Stool (−) |
|
Others | 4 miscarriage 2 termination |
Table 2.
MERS infection and maternal–fetal outcome.
Country | Cases | Maternal |
Newborn |
|||
---|---|---|---|---|---|---|
Complication | MERS-CoV antibody | Delivery | Complication | MERS-CoV antibody | ||
Saudi Arabia | 1 | Asymptomatic | Nasopharyngeal (+) | Term NSD |
No Adverse Effects | X |
2 | Asymptomatic | Nasopharyngeal (+) | Term NSD |
No Adverse Effects | X | |
3 | Lung infiltration s/p antibiotics | Nasopharyngeal (+) | 34 weeks Induction |
IUFD | X | |
4 | MERS Fatality | Nasopharyngeal (+) | 38 weeks NSD |
No Adverse Effects | X | |
5 | MERS Fatality | Nasopharyngeal (+) | 24 weeks Cesarean Maternal Hypoxia |
Preterm Expire | X | |
6 | Lung infiltration s/p antibiotics | Nasopharyngeal (+) | Term NSD |
No Adverse Effect | X | |
7 | Progressive Lung Infiltration s/p Mechanical Ventilation | Nasopharyngeal (+) | Term NSD |
No Adverse Effect | X | |
8 | Progressive Lung Infiltration s/p Mechanical Ventilation | Nasopharyngeal (+) | 32 weeks Cesarean Maternal Hypoxia |
No Adverse Effect | X | |
Jordan | 1 | Refuse treatment | EIA (+) | 20 weeks Induction |
IUFD | X |
United Arab Emirates |
1 | MERS Fatality | Nasopharyngeal (−) RT-PCR (+) |
32 weeks Cesarean Maternal Hypoxia |
No Adverse Effects | X |
South Korea | 1 | Lung infiltration s/p antibiotics | RT-PCR (+) | 37 + 5 weeks Cesarean Placenta abruption |
No Adverse Effects | Cord blood (−) Placenta (−) |
As human-to-human transmission exponentially increases, the number of pregnant cases will eventually surface. In light of the new coronavirus (SARS-CoV-2) having similar pathogenic characteristics as SARS-CoV and MERS-CoV, pregnant women who become infected are at risk for adverse maternal and fetal complications [3,4]. Taking this into account, systemic screening of any suspected case is recommended and prompt referral to medical centers capable of handling and treating these cases is imperative.
Declaration of Competing Interest
The author declares no conflict of interest.
References
- 1.https://www.worldometers.info/coronavirus/
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