Next Article in Journal
The Broad Host Range Phage vB_CpeS_BG3P Is Able to Inhibit Clostridium perfringens Growth
Next Article in Special Issue
Plasma Total Antioxidant Capacity and Carbonylated Proteins Are Increased in Pregnant Women with Severe COVID-19
Previous Article in Journal
VZV Infection of Primary Human Adrenal Cortical Cells Produces a Proinflammatory Environment without Cell Death
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Communication

Severe COVID-19 in Cardiopath Young Pregnant Patient without Vertical Transmission

by
Ana Paula Figueiredo de Montalvão França
1,2,†,
Danielly do Vale Pereira
3,†,
Elaine Valéria Rodrigues
3,†,
Flávia Nunes Vieira
3,†,
Karine Santos Machado
3,†,
Pedro Aleixo Nogueira
4,†,
Ricardo Roberto de Souza Fonseca
1,2,† and
Luiz Fernando Almeida Machado
1,2,*
1
Biology of Infectious and Parasitic Agents Post-Graduate Program, Federal University of Pará, Belém 66075-110, PA, Brazil
2
Virology Laboratory, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, PA, Brazil
3
Santa Casa de Misericórdia do Pará Foundation, Belém 66075-110, PA, Brazil
4
School of Medicine, University Center of State of Pará, Belém 66060-575, PA, Brazil
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Viruses 2022, 14(4), 675; https://doi.org/10.3390/v14040675
Submission received: 11 January 2022 / Revised: 3 February 2022 / Accepted: 23 February 2022 / Published: 25 March 2022
(This article belongs to the Special Issue Emerging Virus Infections in Adverse Pregnancy Outcomes II)

Abstract

:
The new betacoronavirus, known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the cause of COVID-19, and has spread rapidly around the world, reaching more than 200 countries, around 364 million people and causing more than 5 million deaths according to the World Health Organization, so this paper reports a fatal case of SARS-CoV-2 infection in a young pregnant woman with heart disease, without vertical transmission. A 26 years old patient at 28th week of pregnancy with regular prenatal care, presented dry cough, high fever, and severe respiratory distress. Due to her clinical symptoms, she sought medical care at a cardiology hospital in Northern Brazil. The medical conditions she presented were heart disease, rheumatic fever history and had no recent record of national or international travel. She was hospitalized and after clinical stabilization, she was referred for an emergency cesarean intervention. The young mother and the newborn were transferred to the intensive care unit after surgery, where diagnostic tests for respiratory viral infections, including SARS-CoV-2, were performed. The mother tested positive, while her newborn was negative for SARS-CoV-2 demonstrating no vertical transmission of SARS-CoV-2 in this severe case. This study reveals that despite the mother’s initially mild symptoms, she progressed to severe clinical conditions resulting in death, although no vertical transmission was observed. This report highlights the relevance of comorbidities for the unfavorable clinical course of COVID-19.

1. Introduction

In early December 2019, in Wuhan city, Hubei province, some cases of severe acute respiratory syndrome emerged. This respiratory infection spread rapidly worldwide, leading to great levels of public health concern. The World Health Organization (WHO) named this illness Coronavirus Disease 2019 (COVID-19) and its virus etiological agent SARS-CoV-2 [1,2]. The symptomatic patient presents comprehensive symptoms such as cough, fever, fatigue, loss of smell and taste, and shortness of breath [3].
Epidemiological data identified an increased risk for severe illness of COVID-19, in population groups with cardiovascular diseases, kidney injuries, lung diseases, cancer, diabetes, immunosuppression, hypertension, obesity, or other comorbidities [4,5]. These health risk conditions seem to be involved in the pathogenesis of severe COVID-19 disease, developing severe respiratory symptoms as respiratory distress, severe pneumonia, respiratory failure, and cardiovascular complications that may lead to death [6,7,8].
According to WHO [2], Brazil reported 24,535,884 confirmed cases and 624,413 deaths by SARS-CoV-2 by February 2022. Currently, Brazil is ranked in third place in cumulative deaths by COVID-19 worldwide. Among the obstetric population (pregnant and postpartum patients) who developed severe acute respiratory distress related to infection by SARS-CoV-2, the fatality rate was about 7% in Brazil from February 2020 to January 2022. The main risk factors in this group were obesity, diabetes, and cardiovascular disease [9]. It is due to this fact that the COVID-19 pandemic seriously affects the Brazilian health-care system, especially specialized maternal services, as the availability of structures, medicines and health professionals were directed to the treatment of COVID-19, leaving maternal health services on the sidelines. This report aimed to describe the clinical characteristics of a young pregnant cardiopathic woman who developed a severe case of SARS-CoV-2 infection with death, without vertical transmission of SARS-CoV-2 to the neonate.

2. Materials and Methods

2.1. Study Design

A 26-year-old female at 28 weeks of pregnancy, with a Body Mass Index (BMI) of 26.6 (height = 160, weight = 68), attending regular prenatal care and with a medical history of heart disease due to rheumatic fever is the subject of this study. She looked for medical care in a cardiology hospital in Belém city, Pará, Northern Brazil, with a ventricular tachyarrhythmia without acute or chronic respiratory infection symptoms. At admission (March 2020), she reported no history of recent national or international traveling, and her medical reports indicated a mitral valve replacement in 2011 due to mitral valve stenosis.
Following initial medical care and clinic stabilization, the patient was discharged 16 days after admission with stable clinical conditions, good fetal health, and no respiratory-infection symptoms. After five days of discharge, she returned to the same hospital seeking medical care with the clinical report of dry cough, high fever (above 39 °C), respiratory distress, tachycardia (>145 Beats Per Minute, BPM), high blood pressure (147/95 mmHg), tachypnea (44 Incursions Per Minute, IPM), and a blood oxygen saturation level of 72%. The patient was undergoing endotracheal intubation and Invasive Mechanical Ventilation (IMV). Samples of blood and nasopharyngeal fluid were collected to screen for the laboratory diagnosis of viral respiratory infections such as influenza A and B, parainfluenza, respiratory syncytial virus, rhinovirus, adenovirus, SARS-CoV-2, and other routine tests.
The patient was taken to the surgery room for an emergency cesarean procedure. The mother and the newborn female baby required intensive care and IMV. A post-operative thoracic Computed Tomography (CT) of the mother’s lung showed multiple ground-glass parenchymal opacities, predominantly in the upper lobes, involving more than 60% of both lungs (Figure 1). On the day after admission and surgery, she began therapy with tazocin + oseltamivir, chloroquine + azithromycin, and dobutamine. The patient evolved to septic shock, which reversed within 24 h.

2.2. Clinical Protocol

She presented a rapid clinical improvement on the second day (D2) after surgery. There was a reduction in her major clinical parameters. The temperature was at 37.5 °C, heartbeats 82 BPM, blood pressure 130/80 mmHg, respiratory rate 20 IPM, and oxygen saturation 96%, while the IMV procedure was sustained. The IMV extubation was performed when respiratory stabilization was achieved. On D3, a new blood test was carried out (and performed on a daily routine). The results stated are in Table 1. On D4, the real-time reverse transcriptase-polymerase chain reaction (RT-PCR) assay tested positive for SARS-CoV-2. After the confirmed diagnosis, the patient remained conscious, hemodynamically stable (90 mmHg Invasive Blood Pressure (IBP) and heartbeats 80 bpm), breathing without IMV (oxygen saturation 95%), complaining of persistent dry cough, and mild breath pain. No vasoactive medication was used. The vital signs were at normal ranges despite the oxygen saturation beginning to vary between 93% and 98%. This supplemental oxygen was delivered by a nasal cannula.
On D4 and D5, the patient oscillated between periods of sleepiness and motor agitation. She presented fever episodes, dry cough and periods of ventricular tachyarrhythmia. The ventricular tachyarrhythmia was controlled with amiodarone, administered via a continuous infusion pump. The patient complained of chewing and deglutition difficulties, so she was provided with enteral nutrition. On D6, the medical examination reported moderate somnolence, fatigue, responsiveness to commands, eupneic, 95 mmHg IBP, heartbeats 70 BPM, mitral murmur, O2 administered by nasal catheter, blood oxygen saturation 95%, oliguria, dry cough, and leukocytosis up to 12,000/mm3. On the night of D7, diarrhea and abdominal discomfort started that led to naso-enteral tube closure.
On D7, the patient’s clinical symptoms worsened. The clinical parameters were tachycardia (132 BPM), hypertension (141/110 mmHg), respiratory difficulty returned, requiring endotracheal intubation and IMV. On D9, norepinephrine and dobutamine were administered. She presented PaO2/FIO2 163 mmHg, leukocytosis, and the auscultation of bilateral snoring in the lung bases. On D10 and D11, the patient’s clinical symptoms worsened significantly. She presented ventricular tachycardia, hemodynamic instability (163 BPM), hypotension (83/44 mmHg), PaO2/FIO2 mmHg, and respiratory distress. The patient was kept in the prone position and kept for 12 h, increasing the PaO2/FIO2 ratio to 130 mmHg.
On D12, the respiratory conditions and clinical parameters became even worse. The oxygen saturation dropped to 56%, auscultation showed coarse breath sounds, wheezes and coarse crackles. The medical team performed procedures of hemodynamic stabilization, but there was no improvement. The patient progressed to cardiorespiratory arrest and death, despite all attempts of cardiopulmonary resuscitation. Possible causes of progressive clinical worsening leading to cardiac death might be due to continuous stress, overweight condition, and uncertain COVID-19 treatment at the time of hospitalization.
During the mother’s hospitalization, the newborn was fully assisted by the Newborn Intensive Care Unit (NICU) team. The baby’s nasopharyngeal and oropharyngeal secretions were collected, then tested for the same respiratory viral infections tested in her mother. All results were negative, including SARS-CoV-2. During hospitalization in the NICU, the newborn remained asymptomatic without leukocytosis throughout the period. No other treatment was necessary at the NICU. The baby remained under observation in the NICU for eight days until hospital discharge. His follow-up showed no vertical transmission for SARS-CoV-2.

3. Results

3.1. Specimen Collection and Diagnostic Testing for SARS-CoV-2

The mother’s clinical samples were collected from the nasopharynx and oropharynx, by swabs. The samples from the newborn were collected with mini swabs by the Intensive Care Unit (ICU) professionals and placed in 2 mL of universal viral transport media. Both samples were subjected to RT-PCR assay following the Charité protocol for influenza A and B, parainfluenza, respiratory syncytial virus, rhinovirus, adenovirus, and SARS-CoV-2 as recommended by WHO and by the Brazilian Ministry of Health [8,9]. Testing consisted of extraction of nucleic acid in a QIAamp Diagnostics platform, followed by RT-PCR on Applied Biosystems 7500 Real-Time PCR System [10].

3.2. Patient’s Labor and Personal Protective Equipment (PPE)

The emergency cesarean was performed at an operating room close to the ICU and obstetrics/neonatology departments. It was prepared following the safety protocols. The surgical environment and its surfaces were disinfected using 2% chlorhexidine. All healthcare professionals participating in the surgery and postoperatively wore specific individual protective equipment for the prevention of COVID-19, such as face shield, gloves, N95 masks, cape, disposable surgical cap, and shoe covers up to the knees.
The delivery was supported by a team consisting of an obstetrician, pediatrician, and nurses, evolving without obstetric complications due to the distance and protection measures maintained for the newborn. To prevent COVID-19 dissemination, the umbilical cord was clamped immediately, and there was no maternal contact with the newborn. The baby was born at 31 weeks, weighed 1534 g, and Apgar scored 5 in the first and fifth minutes. Afterward, the female baby was placed in an incubator under IVM due to severe respiratory distress resulting from moderate prematurity and sent to the NICU, where she remained under constant observation.

4. Discussion

Since the spread of the COVID-19 pandemic, many questions have been raised about SARS-CoV-2 transmission. In this paper, we reported a case of premature labor due to severe COVID-19 illness without vertical transmission [11,12]. The mother, a young woman with heart disease and mitral valve replacement, had a confirmed diagnosis of COVID-19 during her 28th week of pregnancy requiring emergency delivery. The mother did not respond to the treatment because of COVID-19 clinical complications, that evolved to death 12 days after delivering. The baby evolved well with no signs of vertical transmission and negative results for SARS-CoV-2. This case report illustrates some aspects of this emerging viral outbreak that are not yet fully understood, especially about mother-to-child transmission [13,14].
According to the patient and her husband, on her initial evaluation at the hospital, she had no recent national and international travelling history or had not been in contact with people from regions affected by SARS-CoV-2. Although the source of her infection is unknown, her case shows that in Brazil, community transmission was already active by February/March 2020 [15,16]. Initially, pregnant women, as well as cardiopathic, elderly, obese, and diabetics patients were classified as at-risk groups for SARS-CoV-2, which could evolve to unfavorable clinical outcomes. Pregnant women with cardiomyopathy are a special risk group, with little scientific information with regard to the chances of vertical transmission [12,16]. Here, is a case of a severe COVID-19 that evolved to death, suggesting a higher viral load of SARS-CoV-2, and higher risk of vertical transmission [17], no viral transmission was observed.
The literature shows that most pregnant women are asymptomatic or show mild symptoms. Only a minority of cases among pregnant women infected by SARS-CoV-2 required ICU admission and IVM. During the analysis of these studies, there were no reports of vertical transmissions. Currently, there is no clearcut information on how immune regulation is related to pregnancy, how it alters the course of COVID-19, neither how the mother’s immune system inhibits transmission of the virus to the fetus [18].
The risk of vertical transmission is still poorly understood. Up to this date, there has been no firm support for this type of transmission [18,19]. An important result is that the nasopharyngeal swab sample was collected within the first 24 h of the newborn’s life, which showed a negative result for SARS-CoV-2 [18]. It is believed that in addition to the maternal immune system, pre- and trans-operative care in cesarean sections, such as wearing masks by the mother, disinfection of surgical environment, and isolation measures implemented immediately after birth, decreases the chances of contagion of the newborn [19].
Among the relevant information in this case, we called attention to the patient’s initial visit to the emergency department due to a condition of ventricular tachyarrhythmia, when she was hospitalized for the first time for 16 days without signs, or symptoms of any acute or chronic respiratory infection. At that time, testing for SARS-CoV-2 was very scarce in Brazil, and only suspected cases were routinely tested [20]. However, just 5 days after her first hospital discharge, she returned with severe dyspnea, and a high fever of 39 °C, rapidly evolving during her medical care for severe respiratory distress. This case reaffirms the difficulty of predicting the prognosis of patients belonging to the risk groups for COVID-19, who are susceptible to developing the severe and unfavorable clinical complications of the disease. Additionally, is worth emphasizing the importance of monitoring the rules of social distancing, and lockdown during the pandemic, by the government and federal authorities, as cases of community transmission is real [12,13,14,15,16,17,18,19,20].
More than a year since the COVID-19 outbreak, there is still no clear evidence about the best and safest way to deliver babies, and how it can increase or decrease the contagious risk of SARS-CoV-2. Furthermore, SARS-CoV-2 transmission occurs mainly through the air by respiratory droplets, body fluids contact (blood, saliva, and urine), sneezes, coughs, phlegm and interpersonal close contact, followed by contact with mouth, nose, and/or the eyes. During vaginal delivery, it is suggested that the contact of the newborn with maternal body fluids can be a possible risk of transmission. However, some studies have demonstrated SARS-CoV-2 negative results in the amniotic fluid, cord blood, and breast milk. This reinforces the idea of a reduced risk of vertical transmission [21,22,23].
This article describes an unusually severe case of COVID-19 in a pregnant young woman with mitral valve replacement who went into emergency labor during the complication of the disease without vertical transmission. The premature baby evolved well, without immediate or later signs of the SARS-CoV-2 infection. Despite the integrated participation of the team composed of physicians (gynecologist, obstetrician, neonatologist, cardiologist and infectious disease specialist) and nurses (obstetrician, neonatologist and cardiologist) to care both mother and newborn, the mother died of COVID-19 complications despite of the treatment recommendations at the time (March 2020) [21,22,23].

5. Conclusions

We assume that the SARS-CoV-2 infection in the young pregnant woman in this study had a fatal development due to her previous clinically extremely vulnerable comorbidities. This includes a combination of pregnancy and cardiomyopathy, which differs from other cases described in the literature that include a healthy women population. It is important to note that, besides the severe and acute COVID-19 course, the baby was delivered by an emergency cesarean and showed no sign of early or late SARS-CoV-2 infection. It corroborates with the lower likelihood of SARS-CoV-2 vertical transmission. More studies are needed to understand how this protection happens.

Author Contributions

All authors contributed to the research development. A.P.F.d.M.F., R.R.d.S.F. and L.F.A.M., were involved in the research conceptualization; A.P.F.d.M.F., D.d.V.P., E.V.R., F.N.V. and K.S.M., conducted the clinical evaluation; P.A.N., R.R.d.S.F. and L.F.A.M., drafted the initial manuscript; L.F.A.M., R.R.d.S.F. and A.P.F.d.M.F., were responsible for data analysis; R.R.d.S.F., were responsible for paper draft; R.R.d.S.F. and L.F.A.M., were involved in review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Institutional Review Board Statement

This study was conducted in accordance with the Declaration of Helsinki, and patient’s family after the study provided the informed and written consent to this case report. Ethic Committee Name: Research Ethics Committee with Human Beings of the Institute of Health Sciences of the Federal University of Pará, Belém, Brazil. Approval Code: CAAE 33470020.0.1001.0018. Approval Date: 9 March 2020.

Informed Consent Statement

All informations regarding patient and her newborn were included in the study after providing informed and written consent.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. World Health Organization (WHO). Pneumonia of Unknown Cause—China. 2020. Available online: https://www.who.int/csr/don/05-january-2020-pneumonia-of-unkown-cause-china/en/ (accessed on 21 March 2020).
  2. World Health Organization (WHO). Novel Coronavirus—China. 2020. Available online: https://www.who.int/csr/don/12-january-2020-novel-coronavirus-china/en/ (accessed on 22 March 2020).
  3. Zhu, N.; Zhang, D.; Wang, W.; Li, X.; Yang, B.; Song, J.; Zhao, X.; Huang, B.; Shi, W.; Lu, R.; et al. A novel Coronavirus from patients with pneumonia in China, 2019. N. Engl. J. Med. 2020, 382, 727–733. [Google Scholar] [CrossRef] [PubMed]
  4. Huang, C.; Wang, Y.; Li, X.; Ren, L.; Zhao, J.; Hu, Y.; Zhang, L.; Fan, G.; Xu, J.; Gu, X.; et al. Clinical Features of Patients Infected with 2019 Novel Coronavirus in Wuhan, China. Lancet 2020, 395, 497–506. [Google Scholar] [CrossRef] [Green Version]
  5. Wang, D.; Hu, B.; Hu, C.; Zhu, F.; Liu, X.; Zhang, J.; Wang, B.; Xiang, H.; Cheng, Z.; Xiong, Y.; et al. Clinical Characteristics of 138 Hospitalized Patients with 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China. JAMA 2020, 323, 1061–1069. [Google Scholar] [CrossRef] [PubMed]
  6. Holshue, M.L.; DeBolt, C.; Lindquist, S.; Lofy, K.H.; Wiesman, J.; Bruce, H.; Spitters, C.; Ericson, K.; Wilkerson, S.; Tural, A.; et al. First Case of 2019 Novel Coronavirus in the United States. N. Engl. J. Med. 2020, 382, 929–936. [Google Scholar] [CrossRef] [PubMed]
  7. Iqbal, S.N.; Overcash, R.; Mokhtari, N.; Saeed, H.; Gold, S.; Auguste, T.; Mirza, M.U.; Ruiz, M.E.; Chahine, J.J.; Waga, M.; et al. An Uncomplicated Delivery in a Patient with COVID-19 in the United States. N. Engl. J. Med. 2020, 382, e34. [Google Scholar] [CrossRef] [PubMed]
  8. Brazilian Ministry of Health (BMH). Coronavirus Epidemiological Bulletin 2021. 2021. Available online: https://covid.saude.gov.br/pt/ (accessed on 21 December 2021).
  9. World Health Organization (WHO). Laboratory Testing of Human Suspected Cases of Novel Coronavirus (nCoV) Infection—Interim Guidance. 2020. Available online: https://www.who.int/health-topics/coronavirus/laboratory-diagnostics-for-novel-coronavirus (accessed on 1 April 2020).
  10. Corman, V.M.; Landt, O.; Kaiser, M.; Molenkamp, R.; Meijer, A.; Chu, D.K.; Bleicker, T.; Brünink, S.; Schneider, J.; Schmidt, M.L.; et al. Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Eurosurveillance 2020, 25, 2000045. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Peng, Z.; Wang, J.; Mo, Y.; Duan, W.; Xiang, G.; Yi, M.; Bao, L.; Shi, Y. Unlikely SARS-CoV-2 vertical transmission from mother to child: A Case Report. J. Infect. Public Health 2020, 13, 818–820. [Google Scholar] [CrossRef] [PubMed]
  12. Yan, J.; Guo, J.; Fan, C.; Juan, J.; Yu, X.; Li, J.; Feng, L.; Li, C.; Chen, H.; Qiao, Y.; et al. Coronavirus Disease 2019 (COVID-19) in Pregnant Women: A Report Based on 116 Cases. Am. J. Obstet. Gynecol. 2020, 223, 111.e1–111.e14. [Google Scholar] [CrossRef] [PubMed]
  13. Yang, Z.; Wang, M.; Zhu, Z.; Liu, Y. Coronavirus disease 2019 (COVID-19) and pregnancy: A systematic review. J. Matern.-Fetal Neonatal Med. 2020, 30, 1–4. [Google Scholar] [CrossRef] [PubMed]
  14. Dashraath, P.; Wong, J.L.J.; Lim, M.X.K.; Lim, L.M.; Li, S.; Biswas, A.; Choolani, M.; Mattar, C.; Su, L.L. Coronavirus disease 2019 (COVID-19) pandemic and pregnancy. Am J Obstet Gynecol. 2020, 222, 521–531. [Google Scholar] [CrossRef] [PubMed]
  15. Qiancheng, X.; Jian, S.; Lingling, P.; Lei, H.; Xiaogan, J.; Weihua, L.; Gang, Y.; Shirong, L.; Zhen, W.; GuoPing, X.; et al. Coronavirus disease 2019 in pregnancy. Int. J. Infect. Dis. 2020, 95, 376–383. [Google Scholar] [CrossRef] [PubMed]
  16. Lima, S.S.; Queiroz, M.A.F.; Machado, L.F.A.; Vallinoto, A.C.R.; Ishak, M.D.O.G.; Ishak, R. Retrospective epidemiology of the SARS-CoV-2 (and COVID-19) epidemic among 27 Brazilian cities. J. Clin. Virol. Plus 2021, 1, 100053. [Google Scholar] [CrossRef]
  17. Alzamora, M.C.; Paredes, T.; Caceres, D.; Webb, C.M.; Valdez, L.M.; La Rosa, M. Severe COVID-19 during Pregnancy and Possible Vertical Transmission. Am. J. Perinatol. 2020, 18, 861–865. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Schwartz, D.A. An Analysis of 38 Pregnant Women With COVID-19, Their Newborn Infants, and Maternal-Fetal Transmission of SARS-CoV-2: Maternal Coronavirus Infections and Pregnancy Outcomes. Arch. Pathol. Lab. Med. 2020, 144, 799–805. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Mehan, A.; Venkatesh, A.; Girish, M. COVID-19 in pregnancy: Risk of adverse neonatal outcomes. J. Med. Virol. 2020, 92, 2295–2297. [Google Scholar] [CrossRef] [PubMed]
  20. Takemoto, M.L.; Menezes, M.D.O.; Andreucci, C.B.; Knobel, R.; Sousa, L.; Katz, L.; Fonseca, E.B.; Nakamura-Pereira, M.; Magalhães, C.G.; Diniz, C.S.; et al. Clinical characteristics and risk factors for mortality in obstetric patients with severe COVID-19 in Brazil: A surveillance database analysis. BJOG 2020, 127, 1618–1626. [Google Scholar] [CrossRef] [PubMed]
  21. Fenizia, C.; Biasin, M.; Cetin, I.; Vergani, P.; Mileto, D.; Spinillo, A.; Gismondo, M.R.; Perotti, F.; Callegari, C.; Mancon, A.; et al. Analysis of SARS-CoV-2 vertical transmission during pregnancy. Nat. Commun. 2020, 11, 5128. [Google Scholar] [CrossRef] [PubMed]
  22. Kotlyar, A.M.; Grechukhina, O.; Chen, A.; Popkhadze, S.; Grimshaw, A.; Tal, O.; Taylor, H.S.; Tal, R. Vertical transmission of coronavirus disease 2019: A systematic review and meta-analysis. Am. J. Obstet. Gynecol. 2021, 224, 35–53.e3. [Google Scholar] [CrossRef] [PubMed]
  23. Goh, X.L.; Low, Y.F.; Ng, C.H.; Amin, Z.; Ng, Y.P.M. Incidence of SARS-CoV-2 vertical transmission: A meta-analysis. Arch. Dis. Child.-Fetal Neonatal Ed. 2021, 106, 112–113. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Thoracic computerized tomography showed multiple ground-glass parenchymal opacities, predominantly in the upper lobes of both lungs. Bilateral pleural effusion with parenchymal consolidations. Bilateral multifocal distribution. The extent of pulmonary involvement estimated was greater than 60%. Such findings are consistent with viral pneumonia and differential diagnosis of COVID-19 (31 March 2020, day 2 of the onset of symptoms).
Figure 1. Thoracic computerized tomography showed multiple ground-glass parenchymal opacities, predominantly in the upper lobes of both lungs. Bilateral pleural effusion with parenchymal consolidations. Bilateral multifocal distribution. The extent of pulmonary involvement estimated was greater than 60%. Such findings are consistent with viral pneumonia and differential diagnosis of COVID-19 (31 March 2020, day 2 of the onset of symptoms).
Viruses 14 00675 g001
Table 1. Daily laboratory results of the pregnant woman with COVID-19 following the cesarean procedure.
Table 1. Daily laboratory results of the pregnant woman with COVID-19 following the cesarean procedure.
TestReferences Days Following Cesarean Procedure
D2D3D4D5D6D7D8D9D10D11
02/0403/0404/0405/0406/0407/0408/0409/0410/0411/04
C reactive protein (mg/dL)<1.00.52.07.424.69.0--15.69.0-
Sodium (mmol/L)137–145146149150147148--147146149
Potassium (mmol/L)3.5–5.1 3.43.23.92.42.7--3.04.14.9
pCO2 (mmhg)35–45 76343632.4100--44.44744
pO2 (mmhg)75–1007616519178.4107--56130139
Urea (mg/dL)15–36 2548452628--2433-
Creatinine (mg/dL)0.52–1.040.30.30.20.20.3--0.20.2-
Calcium (mg/dL)8.4–10.2 7.87.38.07.4---7.26.9-
Hemoglobin (g/dL)12–18 9.18.68.98.68.9--8.57.8-
Hematocrit (%)36–5527.723.62726.228.1--24.125-
Leukocytes (per mm3)4.000–10.0009022677111.57012.03013.40013.550-10.4309985-
Segments (per mm3)5.232473935648.62511.517------
Lymphocyte (per mm3)1.160–4.10030691355133910041221--6271011-
Lactic acid (mmol/L)0.5–2.0 2.30.60.70.90.7--1.01.54.9
Total bilirubin (mg/dL)0.2–1.3 0.320.290.250.200.70-----
Platelets (per mm3)150.000–440.000162.800161.600197.900259.00---233.100206.300-
AST (U/L)14–36713969----8695-
ALT (U/L)<35231916----1516-
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

França, A.P.F.d.M.; Pereira, D.d.V.; Rodrigues, E.V.; Vieira, F.N.; Machado, K.S.; Nogueira, P.A.; Fonseca, R.R.d.S.; Machado, L.F.A. Severe COVID-19 in Cardiopath Young Pregnant Patient without Vertical Transmission. Viruses 2022, 14, 675. https://doi.org/10.3390/v14040675

AMA Style

França APFdM, Pereira DdV, Rodrigues EV, Vieira FN, Machado KS, Nogueira PA, Fonseca RRdS, Machado LFA. Severe COVID-19 in Cardiopath Young Pregnant Patient without Vertical Transmission. Viruses. 2022; 14(4):675. https://doi.org/10.3390/v14040675

Chicago/Turabian Style

França, Ana Paula Figueiredo de Montalvão, Danielly do Vale Pereira, Elaine Valéria Rodrigues, Flávia Nunes Vieira, Karine Santos Machado, Pedro Aleixo Nogueira, Ricardo Roberto de Souza Fonseca, and Luiz Fernando Almeida Machado. 2022. "Severe COVID-19 in Cardiopath Young Pregnant Patient without Vertical Transmission" Viruses 14, no. 4: 675. https://doi.org/10.3390/v14040675

APA Style

França, A. P. F. d. M., Pereira, D. d. V., Rodrigues, E. V., Vieira, F. N., Machado, K. S., Nogueira, P. A., Fonseca, R. R. d. S., & Machado, L. F. A. (2022). Severe COVID-19 in Cardiopath Young Pregnant Patient without Vertical Transmission. Viruses, 14(4), 675. https://doi.org/10.3390/v14040675

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop