Next Article in Journal
Nasal CPAP in the Pediatric Ward to Reduce PICU Admissions for Severe Bronchiolitis?
Previous Article in Journal
Rate of Total Hip Replacement after Legg Calve Perthes Disease in a Canadian Province
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Case Report

Early Outcome of Multisystem Inflammatory Syndrome in Neonates Diagnosed following Prenatal Maternal COVID-19 Infection: A Three-Case Series

1
Children’s Clinical Hospital, 500002 Brasov, Romania
2
Faculty of Medicine, Transilvania University, 500002 Brasov, Romania
3
Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel
*
Author to whom correspondence should be addressed.
Pediatr. Rep. 2023, 15(4), 591-598; https://doi.org/10.3390/pediatric15040054
Submission received: 15 July 2023 / Revised: 25 September 2023 / Accepted: 27 September 2023 / Published: 10 October 2023

Abstract

:
Background: The aim of this case series report is to evaluate the characteristics of multisystem inflammatory syndrome (MIS) in neonates following prenatal maternal COVID-19 infection. Methods: We present a case series of three newborns (≤28 days of age) diagnosed with MIS due to the vertical transmission of SARS-CoV2 infection and admitted from 1 January 2021 to 1 June 2023. The inclusion criteria were negative RT-PCR-SARS-CoV-2 test in infants, initial negative IgM-SARS-CoV-2 in infants followed by the emergence of positive IgG-SARS-CoV-2 antibodies in infants and maternal COVID-19 infection in the third trimester of pregnancy. Patients enrolled in this case series were admitted due to acute febrile illnesses. Results: All three cases occurred in patients born at a mean gestational age of 39 weeks and who were appropriate for gestational age. The mean age at admission was 18.3 days. Fibrinogen (>400 mg/dL) and ferritin (>120 mg/dL) were elevated above the upper normal limit. Elevated levels of myocardial biomarkers (D-dimers, N-terminal pro b-type natriuretic peptide troponin T and creatine phosphokinase myocardial band) were recorded, with normal heart function evaluated using echocardiography. All three patients were treated with antibiotics; one received intravenous immunoglobulin. A 4-week follow-up was completed in two patients when their myocardial biomarkers and ferritin were still elevated but lower compared with previous examinations. D-dimers levels were normalized in 2/3 patients. Conclusions: Subclinical myocarditis was diagnosed as an early outcome in infants with MIS diagnosed postnatally due to the vertical transmission of SARS-CoV2 infection and may represent a new challenge for pediatricians in the pandemic era.

1. Introduction

The era of the COVID-19 pandemic has brought a multitude of changes in everyone’s lives and represented a great challenge for healthcare professionals all over the world.
The SARS-CoV-2 virus spreads extremely fast and affects patients of all ages. Even though most children with SARS-CoV-2 infection had asymptomatic or mild forms of the disease, pediatric specialists observed, diagnosed and treated some complications that were gathered under the title of multi-systemic inflammatory syndrome of the child (MIS-C), and this became an exclusion diagnosis in neonatal pathology [1]. It is important to mention that the SARS-CoV-2 virus is linked to release of a cytokine storm, leading to higher risks of thrombosis and increased D-dimers levels [2].
A few case reports implied that MIS in neonates (MIS-N) develops secondary to maternal SARS-CoV-2 infection, unlike MIS-C where SARS-CoV-2 infection and multisystem inflammation occur in the same patient [3]. Infants born to mothers with COVID-19 contracted during pregnancy were shown to develop an early neonatal inflammatory condition [4].
Pregnant women are considered to be a population category that is more vulnerable to COVID-19 infection; therefore, newborns coming from SARS-CoV-2-positive mothers could be more susceptible to SARS-CoV-2 infection by vertical or horizontal transmission [5].
The aim of this case series’ presentation was to describe the clinical and laboratory characteristics of MIS-N in three newborns who were hospitalized at our medical center with this condition and to review the medical literature (at the level of case reports and case series) published in respect to this topic.

2. Patients and Methods

Patients enrolled in this case series were admitted at the Children Hospital of Brasov from 1 January 2021 to 1 June 2023 for acute common febrile illnesses. MIS-N was an additional diagnosis, following various laboratory investigations and according to their family history.
The inclusion criteria for MIS-N diagnosis were as follows:
-
Negative RT-PCR-SARS-CoV-2 test in infants;
-
Negative IgM-SARS-CoV-2 antibodies in infants;
-
Positive IgG-SARS-CoV-2 antibodies in infants;
-
Maternal COVID-19 infection diagnosed in the third trimester of pregnancy.
None of the mothers was vaccinated against SARS-CoV-2.
The parents of the patients provided their written informed consent for the processing of personal data.
In order to complete this literature review, we used PubMed and Google Scholar as search engines. The keywords used were MISC-N, neonates and COVID-19; newborns; and MIS-C. A total of 17 case reports or case series (57 newborns were included) were retrieved (Supplementary Table S1) [6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22]. The number of patients included in the case series ranged from 2 to 20 newborns.

3. Results

Patient no. 1 was a 5-day-old male newborn who presented in the emergency room (ER) with a fever (38.9 °C), drowsiness and apathy that started 24 h before admission (Table 1). He was born through vaginal delivery, at term (39 weeks gestational age), with a normal birth weight and no obstetrical events to mention; he was breastfed.
The mother had a mild form of COVID-19 infection during her last trimester of pregnancy (diagnosed by a positive RT-PCR SARS-CoV-2 test).
Blood tests upon admission showed elevated levels of ferritin and fibrinogen as inflammatory markers, with negative blood, urine, stool, nasal and throat swab cultures. He had positive IgG antibodies for the SARS-CoV-2 virus, while the RT-PCR SARS-CoV-2 test and IgM antibodies for the same virus were negative. The complete blood count showed normal leukocytes and platelets values. Myocardial biomarkers were high as well (Figure 1).
Abdominal and transfontanellar ultrasounds showed no mentionable defects. Echocardiography revealed a small patent foramen ovale.
The treatment administered consisted of ampicillin (30 mg/kg four times a day) during his 14 days of hospitalization. He also received corticosteroids and intravenous immunoglobulins. Methylprednisolone was administered at 0.93 mg/kg every 6 h for 2 days, followed by hydrocortisone hemisuccinate 2.5 mg/kg/four times a day for the following 7 days. Intravenous immunoglobulins were administered in the first dose of 0.75 g/kg/day, starting on the ninth day of hospitalization, and a second dose of 0.5 g/kg/day was given on day 11 of admission.
The evolution was favorable; the patient was discharged with no known sequelae, and the follow-up examination (4 weeks later) revealed decreased levels of cardiac biomarkers, except for D-dimer levels, which remained elevated.
The second patient was a 25-day-old female newborn who presented in the ER with bloody diarrheic stools (maximum 13 stools/24 h) starting 7 days before admission, accompanied by a high fever (>39 °C) starting 2 days before presentation.
She was delivered naturally at 39 weeks gestational age, with a normal birth weight and APGAR score. She was fed breast milk and formula.
The mother had a mild form of COVID-19 infection during her last trimester of pregnancy, with diagnosis based on a positive RT-PCR SARS-CoV-2 test.
Blood tests upon admission revealed high levels of ferritin, with negative blood, urine and stool cultures (Table 1). She had negative tests for rotavirus, adenovirus and campylobacter infections. She had positive IgG antibodies for the SARS-CoV-2 virus; the RT-PCR SARS-CoV-2 test and IgM antibodies for the same virus were negative.
The complete blood count of the neonate showed no mentionable modifications. Myocardial biomarkers were elevated (Figure 1).
Abdominal and transfontanellar ultrasounds showed no mentionable defects. Echocardiography revealed a small atrial septal defect.
She received 7 days of intravenous ampicillin—50 mg/kg/day/three times per day. Her clinical evolution was good, and she was discharged after 7 days. Four weeks later, her check-up blood tests showed lower levels of cardiac biomarkers.
The third patient was a 25-day-old female who presented in the ER with cough, rhinorrhea and mild respiratory distress starting 4 days before (Table 1). She was febrile (around 39.5 °C) from 48 h before admission. She was born by caesarian section, at term (39 weeks gestational age), with a normal birth weight (3620 g) and without any obstetrical events, and she was fed formula.
Her mother had a severe form of COVID-19 shortly before antepartum and died 6 days after giving birth.
Blood tests upon admission revealed a slightly elevated C-reactive protein and high levels of ESR and ferritin, with negative blood, urine, stool, nasal and throat swab cultures. The RT-PCR SARS-CoV-2 test and IgM antibodies for the same virus were negative, with positive IgG antibodies.
The complete blood count was normal. She had abnormal levels of NT-pro-BNP, troponin T and CK-MB.
The abdominal ultrasound revealed moderate hydronephrosis.
She received intravenous ampicillin—37.5 mg/kg/four times daily and gentamicin 5 mg/kg once a day for 6 days—and was discharged in good general condition after 7 days of hospitalization.
She did not present for her 4-week follow-up check-up.
Figure 1 presents the graphical display of the elevated values of the myocardial biomarkers (D-dimers—Figure 1A; NT-pro-BNP—Figure 1B; Troponin T—Figure 1C; CK-MB—Figure 1D) found during the hospitalization of the three patients included in this case series presentation compared to values considered normal by the laboratory.

4. Discussion

When analyzing the English-language medical literature available on MIS-N, we retrieved 17 case reports or case series describing 57 newborns; of the 17 reports, 13 were from India, while the United States, Saudi Arabia, Brazil and Thailand contributed to the series with 1 case each. In preparing the analysis of these reports, we realized the unexpected predominance of MIS-N cases in India and some other restricted geographic areas, and we were aware that this may be a limitation of our present study.
Of the 57 patients analyzed in this literature search, 6 had a fatal outcome [4,12,13] and 1 underwent limb amputation [9]. Cardiac involvement (left ventricular dysfunction mentioned in six patients), cardiogenic shock, pericardial effusion and pulmonary hemorrhage were present in 12, 2, 2 and 1 reports, respectively. The mortality rates in MIS-N are not known, but the literature reports mortality rates of 1.7–20% for children diagnosed with MIS-C in India, South Africa and Pakistan [20,21,22,23].
When comparing the cases from the literature with our three cases, the similarities in the age group (all of them were <30 days old) were evident. As for the condition at discharge, the majority of them (50/57) were discharged without any known sequelae, similarly to the neonates presented in our study.
Differences may be found in the analyzed relevant literature in respect to the presence of cardiac shock [4,6,10,15], aortic and intra-cardiac thrombosis [9,12], pericardial effusion [11] and coronary artery dilations [4,7]. None of our cases had clinical manifestations of cardiac involvement, and no ultrasound modifications raised the possibility of MISC-N-related myocarditis.
As a matter of fact, the prognosis of children born from COVID-19-infected mothers is considered good, with little chance of long-term consequences [24]. All patients included in our case series had favorable evolution during admission and were discharged in a good general state.
The follow-up examination at 4 weeks after discharge was completed by two of the patients. The newborns were in good general condition, with an upward weight curve. Their myocardial biomarkers and ferritin were still elevated but lower than in previous examinations (Table 1).
Apart from the cardiac involvement, two cases of newborns with erythematous rash were reported in the literature [6,17], while none of our cases presented cutaneous pathologies.
Finally, as seen above, a great number of similarities between the cases were reported, and they only cover a small part of the clinical diversity this syndrome presents, highlighting the need to conduct more studies on this subject and emphasizing the need to screen newborns for MIS-N, although it is considered that the vertical transmission rate of SARS-CoV-2 virus is rather low [25] and that the course of infection for healthy newborns is asymptomatic or characterized by mild clinical manifestations only [26].

5. Conclusions

Subclinical myocarditis is one of the early outcomes of multisystem inflammatory syndrome in infants related to prenatal maternal COVID-19 infection, representing a new challenge for pediatricians of the pandemic era.
Further research on this topic is needed, as well as a follow-up of patients in evolution, in order to find out if the COVID-19 infection in pregnant women will have real long-term consequences [27] on children’s health, particularly related to the occurrence of cardiovascular or neurodevelopmental conditions [28].

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/pediatric15040054/s1. Table S1. MIS-N in newborns: review of literature.

Author Contributions

All authors contributed to the study conception and design. Patients involved in this case series were diagnosed and treated by O.G.F.-P. as the attending physician. The cardiological and echocardiographic examinations were performed by B.P. The laboratory investigations were processed by A.I. Material preparation, data collection and the first draft of the manuscript were performed and written by M.T., I.L. and E.P. The literature review was carried out by I.L. The first version of the manuscript was reviewed, corrected and completed by O.G.F.-P. and E.L. English spelling was revised by E.L. and O.G.F.-P., and the second version of the manuscript was corrected by E.L., O.G.F.-P. and M.M. All authors have read and agreed to the published version of the manuscript.

Funding

The authors declare that no funds, grants or other support were received during the preparation of this manuscript.

Institutional Review Board Statement

The Ethics Committee of Children’s Clinical Hospital Brasov approved this prospective observational study presenting a case series of three infants.

Informed Consent Statement

Freely given written informed consent to participate in this study and to be published in the results of the research, based on the patients’ medical recordings, was obtained from the parents of all three patients included. The identity of the patients was respected.

Data Availability Statement

Data is available on request due to privacy and ethical restrictions. The data presented in this study are available on request from the corresponding author. The data are not publicly available due to the confidential nature of personal patients’ information.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

CK-MBcreatine phosphokinase myocardial band
COVID-19coronavirus disease 2019
CRPC reactive protein
ERemergency room
ESRerythrocyte sedimentation rate
Ig Gimmunoglobulin G
Ig Mimmunoglobulin M
MISmultisystem inflammatory syndrome
MIS-Cmultisystem inflammatory syndrome in children
MIS-Nmultisystem Inflammatory syndrome in neonates
NT-pro-BNPN-terminal pro b-type natriuretic peptide
RT-PCRreverse transcription polymerase chain reaction
SARS-CoV-2severe acute respiratory syndrome coronavirus 2

References

  1. Molloy, E.J.; Nakra, N.; Gale, C.; Dimitriades, V.R.; Lakshminrusimha, S. Multisystem inflammatory syndrome in children (MIS-C) and neonates (MIS-N) associated with COVID-19: Optimizing definition and management. Pediatr. Res. 2022, 93, 1499–1508. [Google Scholar] [CrossRef]
  2. Słomka, A.; Kowalewski, M.; Żekanowska, E. Coronavirus Disease 2019 (COVID–19): A Short Review on Hematological Manifestations. Pathogens 2020, 9, 493. [Google Scholar] [CrossRef]
  3. Zhu, F.; Zozaya, C.; Zhou, Q.; De Castro, C.; Shah, P.S. SARS-CoV-2 genome and antibodies in breastmilk: A systematic review and meta-analysis. Arch. Dis. Child. Fetal. Neonatal. Ed. 2021, 106, 514–521. [Google Scholar] [CrossRef]
  4. Pawar, R.; Gavade, V.; Patil, N.; Mali, V.; Girwalkar, A.; Tarkasband, V.; Loya, S.; Chavan, A.; Nanivadekar, N.; Shinde, R.; et al. Neonatal multisystem inflammatory syndrome (MIS-N) associated with prenatal maternal SARS-CoV-2: A case series. Children 2021, 8, 572. [Google Scholar] [CrossRef]
  5. Matyas, M.; Valeanu, M.; Hasmasanu, M.; Voina, B.; Tutu, A.; Zaharie, G.C. The Effect of Maternal SARS-CoV-2 Infection on Neonatal Outcome. Children 2023, 10, 771. [Google Scholar] [CrossRef]
  6. Saha, S.; Pal, P.; Mukherjee, D. Neonatal MIS-C: Managing the cytokine storm. Pediatrics 2021, 148, e2020042093. [Google Scholar] [CrossRef] [PubMed]
  7. Divekar, A.A.; Patamasucon, P.; Benjamin, J.S. Presumptive neonatal multisystem inflammatory syndrome in children associated with Coronavirus disease 2019. Am. J. Perinatol. 2021, 38, 632–636. [Google Scholar] [CrossRef] [PubMed]
  8. Shaiba, L.A.; Hadid, A.; Altirkawi, K.A.; Bakheet, H.M.; Alherz, A.M.; Hussain, S.A.; Sobaih, B.H.; Alnemri, A.M.; Almaghrabi, R.; Ahmed, M.; et al. Case Report: Neonatal multi-System inflammatory syndrome associated with SARS-CoV-2 exposure in two cases from Saudi Arabia. Front. Pediatr. 2021, 9, 652857. [Google Scholar] [CrossRef] [PubMed]
  9. Amonkar, P.S.; Gavhane, J.B.; Kharche, S.N.; Kadam, S.S.; Bhusare, D.B. Aortic thrombosis in a neonate with COVID-19-related fetal inflammatory response syndrome requiring amputation of the leg: A case report. Paediatr. Int. Child. Health 2021, 41, 211–216. [Google Scholar] [CrossRef]
  10. Kappanayil, M.; Balan, S.; Alawani, S.; Mohanty, S.; Leeladharan, S.P.; Gangadharan, S.; Jayashankar, J.P.; Jagadeesan, S.; Kumar, A.; Gupta, A.; et al. Multisystem inflammatory syndrome in a neonate, temporally associated with prenatal exposure to SARS-CoV-2: A case report. Lancet Child. Adolesc. Health 2021, 5, 304–308. [Google Scholar] [CrossRef]
  11. Lima, A.R.; Cardoso, C.C.; Bentim, P.R.; Voloch, C.M.; Rossi, Á.D.; da Costa, R.M.M.; da Paz, J.A.S.; Agostinho, R.F.; Figueiredo, V.R.; Júnior, J.S.; et al. Maternal SARS-CoV-2 infection associated to systemic inflammatory response and pericardial effusion in the Newborn: A case report. J. Pediatric. Infect. Dis. Soc. 2021, 10, 536–539. [Google Scholar] [CrossRef]
  12. Gupta, P.; Tamatam, P.R.; Dhulipudi, B.; Vardhelli, V.; Deshabhotla, S.; Oleti, T.P. Neonatal multisystem inflammatory syndrome (MIS-N) associated with maternal SARS-CoV-2 exposure. Indian J. Pediatr. 2022, 89, 827–828. [Google Scholar] [CrossRef]
  13. More, K.; Aiyer, S.; Goti, A.; Parikh, M.; Sheikh, S.; Patel, G.; Kallem, V.; Soni, R.; Kumar, P. Multisystem inflammatory syndrome in neonates (MIS-N) associated with SARS-CoV2 infection: A case series. Eur. J. Pediatr. 2022, 181, 1883–1898. [Google Scholar] [CrossRef]
  14. Chakravarty, S.; Gupta, V.; Gupta, A.; Nishu Sain, K.; Valjiyani, S. Neonatal Multisystem Inflammatory Syndrome (MIS-N). J. Biomed. Res. Environ. Sci. 2022, 3, 174–176. [Google Scholar]
  15. Shinde, M.D.; Khamkar, A.M.; Pote, P.D.; Suryawanshi, P.B. Fetal inflammatory response syndrome associated with SARS-CoV-2 exposure in utero. Pediatr. Oncall J. 2021, 19. [Google Scholar] [CrossRef]
  16. Amulya, G.A.-O.; Kaur, A.; Sharma, M. Multisystem Inflammatory Syndrome in a neonate with prenatal exposure to COVID-19. Indian J. Pediatr. 2022, 89, 314. [Google Scholar] [CrossRef]
  17. Nitya, U.S.; Devassy, B.M.; Joseph, S.; Anila, A.P.; George, R.; Sreenivasan, V.K. Intrauterine onset of multisystem inflammatory syndrome in a neonate temporally associated with maternal COVID-19. Indian J. Rheumatol. 2022, 17, 289–293. [Google Scholar]
  18. Harish, J.; Tambekar Satish, D.; Ashtekar Shishir, P. Mirgunde, Swati Khot, Shrikant Mane, Neonatal multisystem inflammatory syndrome associated with prenatal maternal SARS-CoV-2 exposure: A case series. Medip Acad. Int. J. Contemp. Pediatr. 2022, 9, 381–386. [Google Scholar]
  19. Sojisirikul, N.; Lapphra, K.; Ngerncham, S.; Charuvanij, S.; Durongpisitkul, K.; Curlin, M.E.; Chokephaibulkit, K. Neonatal Multisystem Inflammatory Syndrome (MIS-N): The first case report in Thailand. COVID 2022, 2, 1265–1269. [Google Scholar] [CrossRef]
  20. Kaushik, A.; Gupta, S.; Sood, M.; Sharma, S.; Verma, S. A systematic review of multisystem inflammatory syndrome in children associated with SARS-Cov-2 infection. Pediatr. Infect. Dis. J. 2020, 39, e340–e346. [Google Scholar] [CrossRef] [PubMed]
  21. Chinniah, K.; Bhimma, R.; Naidoo, K.L.; Archary, M.; Jeena, P.; Hoosen, E.; Singh, S.; Lawler, M.; Naby, F.; Masekela, R. Multisystem inflammatory syndrome in children associated with SARS-CoV-2 infection in Kwazulu-Natal, South Africa. Pediatr. Infect. Dis. J. 2023, 42, e9–e14. [Google Scholar] [CrossRef] [PubMed]
  22. Mohsin, S.S.; Abbas, Q.; Chowdhary, D.; Khalid, F.; Sheikh, A.S.; Ali Khan, Z.G.; Aslam, N.; Bhatti, O.A.; Inam, M.; Saleem, A.F.; et al. Multisystem inflammatory syndrome (MIS-C) in Pakistani children: A description of the phenotypes and comparison with historical cohorts of children with Kawasaki disease and myocarditis. PLoS ONE 2021, 16, e0253625. [Google Scholar] [CrossRef]
  23. Nayak, S.; Panda, P.C.; Biswal, B.; Agarwalla, S.K.; Satapathy, A.K.; Jena, P.K.; Gulla, K.M.; Rath, D.; Mahapatra, A.; Mishra, P.; et al. Eastern India collaboration on Multisystem inflammatory syndrome in children (EICOMISC): A multicenter observational study of 134 cases. Front. Pediatr. 2022, 10, 834039. [Google Scholar] [CrossRef] [PubMed]
  24. Wróblewska-Seniuk, K.; Basiukajć, A.; Wojciechowska, D.; Telge, M.; Miechowicz, I.; Mazela, J. Clinical Characteristics of Newborns Born to Mothers with COVID-19. J. Clin. Med. 2021, 10, 4383. [Google Scholar] [CrossRef]
  25. Moza, A.; Duica, F.; Antoniadis, P.; Bernad, E.S.; Lungeanu, D.; Craina, M.; Bernad, B.C.; Paul, C.; Muresan, C.; Nitu, R.; et al. Outcome of Newborns with Confirmed or Possible SARS-CoV-2 Vertical Infection—A Scoping Review. Diagnostics 2023, 13, 245. [Google Scholar] [CrossRef]
  26. Pawłowska, M.; Pokorska-Śpiewak, M.; Talarek, E.; Mania, A.; Hasiec, B.; Żwirek-Pytka, E.; Stankiewicz, M.; Stani, M.; Frańczak-Chmura, P.; Szenborn, L.; et al. Clinical Course and Severity of COVID-19 in 940 Infants with and without Comorbidities Hospitalized in 2020 and 2021: The Results of the National Multicenter Database SARSTer-PED. J. Clin. Med. 2023, 12, 2479. [Google Scholar] [CrossRef]
  27. McCarthy, J.; Liu, D.; Kaskel, F. The Need for Life-Course Study of Children Born to Mothers with Prior COVID-19 Infection. JAMA Pediatr. 2021, 175, 1097–1098. [Google Scholar] [CrossRef]
  28. Edlow, A.G.; Castro, V.M.; Shook, L.L.; Kaimal, A.J.; Perlis, R.H. Neurodevelopmental outcomes at 1 year in infants of mothers who tested positive for SARS-CoV-2 during pregnancy. JAMA Netw. Open 2002, 5, e2215787. [Google Scholar] [CrossRef] [PubMed]
Figure 1. (AD). The elevated levels of myocardial biomarkers for each of the three patients.
Figure 1. (AD). The elevated levels of myocardial biomarkers for each of the three patients.
Pediatrrep 15 00054 g001
Table 1. Summary of the 3 cases.
Table 1. Summary of the 3 cases.
Case Number123
AdmissionApril 2022June 2021December 2021
Age at admission (days)52525
BirthnaturalnaturalC-section
Gestational age (weeks)393939
Birth weight (g)340031003620
APGAR score9910
Maternal COVID-19 infection disease severitymildmildSevere (fatal)
Feedingbreastfeedingmixed feedingformula
Symptoms onset before admission (days)174
Signs and symptoms
Fever<3 days<3 days<3 days
otherDrowsiness, apathybloody diarrheic stools Cough, rhinorrhea, mild respiratory distress
Inflammation biomarkers
CRP (mg/dL)0.480.262.1
ESR (mm/h)--50
Fibrinogen (mg/dL)590506-
Ferritin (µg/L)460246174.5
D-dimers (mg/L)5034.941.46
Myocardial biomarkers
NT-pro-BNP (pg/dL)17631299841
Troponin T (pg/dL) 3540.5927.38
CK-MB (U/L)657447
Cultures
Bloodnegativenegativenegative
Urinenegativenegativenegative
Stoolnegativenegativenegative
Nasal swabnegativenot performednegative
Throat swabnegativenot performednegative
Ultrasound
Abdominal normalnormalhydronephrosis
Echocardiographypatent foramen ovaleatrial septal defect -
Transfontanellar ultrasoundnormalnormalnormal
Treatment
Intravenous Immunoglobulins yesnono
Antibioticsampicillinampicillinampicillin + gentamicin
Corticosteroidsmethylprednisolone; hydrocortisone hemi succinatenono
Hospitalization days1477
Follow-up
D-dimers (mg/L)500.71not done
NT-pro-BNP (pg/dL)322352not done
Troponin T (pg/dL) 3537.25not done
CK-MB(U/L)49not donenot done
CRP (mg/dL)0.40.45not done
Ferritin (mg/dL)Not performed162not done
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Terciu, M.; Luca, I.; Panait, E.; Leibovitz, E.; Mitrica, M.; Popovici, B.; Ilea, A.; Falup-Pecurariu, O.G. Early Outcome of Multisystem Inflammatory Syndrome in Neonates Diagnosed following Prenatal Maternal COVID-19 Infection: A Three-Case Series. Pediatr. Rep. 2023, 15, 591-598. https://doi.org/10.3390/pediatric15040054

AMA Style

Terciu M, Luca I, Panait E, Leibovitz E, Mitrica M, Popovici B, Ilea A, Falup-Pecurariu OG. Early Outcome of Multisystem Inflammatory Syndrome in Neonates Diagnosed following Prenatal Maternal COVID-19 Infection: A Three-Case Series. Pediatric Reports. 2023; 15(4):591-598. https://doi.org/10.3390/pediatric15040054

Chicago/Turabian Style

Terciu, Maria, Ioana Luca, Emilia Panait, Eugene Leibovitz, Maria Mitrica, Bianca Popovici, Anca Ilea, and Oana Gabriela Falup-Pecurariu. 2023. "Early Outcome of Multisystem Inflammatory Syndrome in Neonates Diagnosed following Prenatal Maternal COVID-19 Infection: A Three-Case Series" Pediatric Reports 15, no. 4: 591-598. https://doi.org/10.3390/pediatric15040054

APA Style

Terciu, M., Luca, I., Panait, E., Leibovitz, E., Mitrica, M., Popovici, B., Ilea, A., & Falup-Pecurariu, O. G. (2023). Early Outcome of Multisystem Inflammatory Syndrome in Neonates Diagnosed following Prenatal Maternal COVID-19 Infection: A Three-Case Series. Pediatric Reports, 15(4), 591-598. https://doi.org/10.3390/pediatric15040054

Article Metrics

Back to TopTop