Literature DB >> 32996648

Pregnancies recovered from SARS-CoV-2 infection in second or third trimester: obstetric evolution.

P Vigil-De Gracia1, L C Caballero2, J Sánchez3, J Espinosa3, S Campana4, A Quintero5, C Luo4, J Ng4.   

Abstract

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Year:  2020        PMID: 32996648      PMCID: PMC7537281          DOI: 10.1002/uog.23134

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   8.678


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Since December 2019, the world has been impacted by COVID‐19, caused by the virus SARS‐CoV‐2. This disease can affect the entire population, with the oldest and those with comorbidities being the most severely affected. During the first 7 months of the COVID‐19 outbreak, findings have been reported in thousands of affected pregnant women, which has allowed us to gain an understanding of the effects of SARS‐CoV‐2 infection in pregnancy , . We have learned that the risk of complication, hospitalization, admission to the intensive care unit and need for ventilation is greater in pregnant women with COVID‐19 than in non‐pregnant affected adults. Increased rates of Cesarean section, premature birth, prelabor rupture of the membranes (PROM) and other obstetric complications have been found to be associated with COVID‐19 , . However, the maternal and perinatal outcomes of continuing pregnancies that have recovered from maternal SARS‐CoV‐2 infection are as yet unknown. We analyzed data from pregnant women with symptoms of COVID‐19 and positive reverse transcription polymerase chain reaction (RT‐PCR) for SARS‐CoV‐2 between 8 March and 15 August 2020, who later recovered, as determined by negative clinical assessment or RT‐PCR at least 35 days after the onset of symptoms, delivered at one of four hospitals in the Republic of Panama (Complejo Metropolitano de la Caja de Seguro Social, Hospital Santo Tomás, Hospital Luis “Chicho” Fabrega and Hospital José Domingo De Obaldía). All women provided signed consent. The study was approved by the national bioethics committee (protocol reference: EC‐CNBI‐2020‐04‐45). Table 1 shows the findings of the 15 participating patients, including one twin pregnancy. In 10 (66.7%) pregnancies, the diagnosis was made during the second trimester, and in five (33.3%) it was made in the third trimester. There were three severe cases and two required mechanical ventilation for more than 1 week, but these pregnancies continued for more than 10 weeks after diagnosis. Three pregnancies were complicated by PROM, occurring very preterm in two cases. Only four pregnancies reached 39 weeks; the others did not due to obstetric complication or spontaneous onset of labor. Five neonates were admitted to the neonatal intensive care unit. There were three perinatal deaths, of which one occurred intrauterine without an apparent cause and two occurred postnatally due to prematurity.
Table 1

Summary of maternal characteristics, symptoms and delivery details in 15 pregnancies that recovered from second‐ or third‐trimester maternal SARS‐CoV‐2 infection

CaseAge (years)SymptomsSeverityGA at diagnosis (weeks)GA at delivery (weeks)Symptom onset‐to‐delivery interval (days)Maternal comorbidityMode of deliveryBirth weight (g)NICU admissionObservations
1* 20Cough, SoBMild20 + 628 + 050PROMCS855, 955Yes (both)Premature delivery 26 days after PROM, both twins died at 3 weeks
224Fever, coughMild23 + 434 + 376ObesityVaginal2840NoSOL
322Headache, runny noseMild28 + 637 + 158Obesity, PROMCS3110NoSOL
422Fever, cough

Severe†

26 + 437 + 679ObesityVaginal2605NoFGR, mother admitted to ICU for 10 days
526Fever, coughMild26 + 434 + 052PROMVaginal2439YesPremature delivery 50 days after PROM
635AnosmiaMild33 + 039 + 547CH, obesityCS3336No
729Fever, SoBSevere†27 + 337 + 673ObesityCS3720NoMother admitted to ICU for 10 days, SOL
836Fever, coughMild25 + 237 + 385PEVaginal3190No
923Fever, headache, runny noseMild34 + 240 + 242ObesityCS3434No
1022FeverMild31 + 136 + 135ObesityVaginal2749NoSOL
1133Headache, runny nose, anosmiaMild22 + 328 + 140CS 960NoDied in‐utero with no apparent cause
1235Fever, headache, SoBSevere18 + 230 + 587OverweightCS1150YesPremature
1323Fever, cough, headacheMild34 + 040 + 547ObesityVaginal3511No
1423Fever, headache, runny noseMild22 + 528 + 542PECS1311YesPremature
1528Runny nose, sore throatMild25 + 040 + 0105 OverweightVaginal3120No

Twin pregnancy. †Admitted to intensive care unit (ICU).

CH, chronic hypertension; CS, Cesarean section; FGR, fetal growth restriction; GA, gestational age; NICU, neonatal intensive care unit; PE, pre‐eclampsia; PROM, prelabor rupture of membranes; SoB, shortness of breath; SOL, spontaneous onset of labor.

Summary of maternal characteristics, symptoms and delivery details in 15 pregnancies that recovered from second‐ or third‐trimester maternal SARS‐CoV‐2 infection Severe† Twin pregnancy. †Admitted to intensive care unit (ICU). CH, chronic hypertension; CS, Cesarean section; FGR, fetal growth restriction; GA, gestational age; NICU, neonatal intensive care unit; PE, pre‐eclampsia; PROM, prelabor rupture of membranes; SoB, shortness of breath; SOL, spontaneous onset of labor. This first report of pregnant women infected with SARS‐CoV‐2 with subsequent recovery demonstrates that these patients continue to be at high obstetric risk, especially due to PROM and labor before 39 weeks. These pregnancies should be monitored closely until delivery. Eleven of the 15 (73.3%) patients in this series presented with PROM, spontaneous labor or maternal complication before 39 weeks of gestation, and only one out of 10 (10.0%) women diagnosed in the second trimester reached 39 weeks of gestation. These findings are of concern as they suggest the possibility of chronic inflammation with alteration at the placental or membrane level, triggering the culmination of pregnancy. A study of 16 placentas from COVID‐19 patients reported an increase in the rates of maternal and fetal vascular malperfusion features, as compared with controls. Two cases delivered more than 30 days after the onset of symptoms and these placentas showed fetal vascular malperfusion (clustered avascular villi, hypercoiled umbilical cord and chorangiosis) . The possible inflammatory effect at the uterine or placental level in patients with COVID‐19 has also been suggested as an explanation for excessive uterine activity reported in the cardiotocographic trace and for intrauterine death . More research is needed in pregnant patients recovered from COVID‐19, and such studies should include analysis of placentas according to the recovery time, in order to obtain more information to guide follow‐up and counseling of these patients. In our opinion, in pregnant patients recovered from SARS‐CoV‐2 infection, there is a ‘placental inflammatory syndrome’ characterized by spontaneous onset of labor, premature birth, PROM, alteration in the cardiotocographic trace, fetal distress, perinatal death and placental changes. Undoubtedly, alteration of the mother's state of health during pregnancy caused by SARS‐CoV‐2 infection can have long‐term effects on the health of offspring, which seem to originate from the placenta. It is interesting to note that most of the patients had some comorbidity. At this stage, we cannot be sure if this is characteristic of the majority of pregnant women infected with SARS‐CoV‐2 in Panama. However, the included pregnancies represent, at the time of writing, all those that had recovered and continued pregnancy for at least 5 weeks after initial symptoms. In conclusion, the findings from this series of cases show that pregnant women who have recovered from COVID‐19 remain at high obstetric risk, especially due to prematurity. Gestational age at the time of diagnosis of the disease will largely determine the prognosis, and a possible placental inflammatory syndrome is responsible for the perinatal side effects.
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