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Research Article| Volume 117, P195-200, April 2022

Characteristics and Outcomes of COVID-19 in Reproductive-Aged Pregnant and Nonpregnant Women in Osaka, Japan

Open AccessPublished:January 29, 2022DOI:https://doi.org/10.1016/j.ijid.2022.01.054

      Highlights

      • There were 4,156 COVID-19 notifications in females aged 10–49 years.
      • Of the 4,156 notifications, 29 (0.7%) were pregnant women.
      • All pregnant women had mild or asymptomatic disease.
      • Among women with COVID-19, pregnant women were more likely to be hospitalized.
      • There were no intensive care unit admissions and no deaths due to COVID-19 in pregnant women.

      Abstract

      Objective

      To describe the clinical characteristics and outcomes of reproductive-aged female patients with coronavirus disease 2019 (COVID-19).

      Methods

      We conducted a retrospective study of female patients aged 10–49 years, diagnosed with COVID-19 in Osaka, Japan, between January and November 2020. We assessed their epidemiological and clinical characteristics according to their pregnancy status.

      Results

      A total of 4,156 patients were enrolled, of whom 29 (0.7%) were pregnant. Most patients exhibited mild symptoms, and 10.8% of the cases were asymptomatic. No moderate or severe cases were observed in pregnant women, whereas only 0.1% of the nonpregnant women had severe disease at diagnosis. No clusters were observed in the pregnant patients; however, most acquired the infection from a family member. Of the 29 pregnant women, 22 (75.9%) were hospitalized; whereas among the nonpregnant women, 579 (14.0%) were hospitalized (p < 0.001). No patients were admitted to the intensive care unit, and there were no deaths among women aged 10–49 years.

      Conclusions

      Pregnant women accounted for 0.7% of the total cases of COVID-19 among women aged 10–49 years. Pregnant women were more likely to be hospitalized but generally had mild disease.

      Keywords

      Abbreviations:

      COVID-19 (coronavirus disease 2019), ICU (intensive care unit), SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2)

      Introduction

      Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first reported in Wuhan, China (
      • Li Q
      • Guan X
      • Wu P
      • Wang X
      • Zhou L
      • Tong Y
      • et al.
      Early transmission dynamics in Wuhan, China, of novel coronavirus–infected pneumonia.
      ,
      • Zhou F
      • Yu T
      • Du R
      • Fan G
      • Liu Y
      • Liu Z
      • et al.
      Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study.
      ), and rapidly spread worldwide, imposing a major burden on healthcare systems globally. Pregnant women are considered to be at a higher risk of severe morbidity and mortality from other respiratory infections, such as influenza or SARS (
      • Allotey J
      • Stallings E
      • Bonet M
      • Yap M
      • Chatterjee S
      • Kew T
      • et al.
      Clinical manifestations, risk factors, and maternal and perinatal outcomes of coronavirus disease 2019 in pregnancy: living systematic review and meta-analysis.
      ,
      • Blitz MJ
      • Grünebaum A
      • Tekbali A
      • Bornstein E
      • Rochelson B
      • Nimaroff M
      • et al.
      Intensive care unit admissions for pregnant and nonpregnant women with coronavirus disease 2019.
      ,
      • Vintzileos WS
      • Muscat J
      • Hoffmann E
      • John NS
      • Vertichio R
      • Vintzileos AM
      • et al.
      Screening all pregnant women admitted to labor and delivery for the virus responsible for coronavirus disease 2019.
      ,
      • Xu S
      • Shao F
      • Bao B
      • Ma X
      • Xu Z
      • You J
      • et al.
      Clinical manifestation and neonatal outcomes of pregnant patients with coronavirus disease 2019 pneumonia in Wuhan, China. Open forum infectious diseases.
      ), than nonpregnant women. COVID-19 has caused serious concerns about its potential to cause adverse events and poor outcomes in pregnant women. A high incidence of obstetric complications has been reported in pregnant women infected with COVID-19 (
      • Sahin D
      • Tanacan A
      • Erol SA
      • Yucel Yetiskin FD
      • Besimoglu B
      • Ozden Tokalioglu E
      • et al.
      Management of pregnant women with COVID-19: A tertiary pandemic center experience on 1416 cases.
      ). Preterm delivery is the most common obstetric complication, followed by miscarriage. While the effect of COVID-19 on miscarriage has not been confirmed, the majority of previous studies have reported an increased rate of preterm delivery (
      • Chmielewska B
      • Barratt I
      • Townsend R
      • Kalafat E
      • van der Meulen J
      • Gurol-Urganci I
      • et al.
      Effects of the COVID-19 pandemic on maternal and perinatal outcomes: a systematic review and meta-analysis.
      ,
      • Dey M
      • Singh S
      • Tiwari R
      • Nair VG
      • Arora D
      • Tiwari S.
      Pregnancy outcome in first 50 Sars-Cov-2 positive patients at our center.
      ,
      • Sahin D
      • Tanacan A
      • Erol SA
      • Yucel Yetiskin FD
      • Besimoglu B
      • Ozden Tokalioglu E
      • et al.
      Management of pregnant women with COVID-19: A tertiary pandemic center experience on 1416 cases.
      ).
      Concerning the immunology of SARS-CoV-2 infection in pregnant women, investigations have shown an increase in anti-SARS-CoV-2 IgM and IgG antibodies in infected pregnant women. The elevation in IgM and IgG antibodies in pregnant SARS-CoV-2-infected patients may be owing to an aggressive immunological response, including cytokine storm (
      • Chaubey I
      • Vignesh R
      • Babu H
      • Wagoner I
      • Govindaraj S
      • Velu V.
      SARS-CoV-2 in Pregnant Women: Consequences of Vertical Transmission.
      ,
      • Dong L
      • Tian J
      • He S
      • Zhu C
      • Wang J
      • Liu C
      • et al.
      Possible vertical transmission of SARS-CoV-2 from an infected mother to her newborn.
      ,
      • Iyer AS
      • Jones FK
      • Nodoushani A
      • Kelly M
      • Becker M
      • Slater D
      • et al.
      Persistence and decay of human antibody responses to the receptor binding domain of SARS-CoV-2 spike protein in COVID-19 patients.
      ). The cytokine storm is a burst of inflammatory cytokine molecules that causes the human body to attack its own cells and tissues, leading to a variety of adverse health problems (
      • Dhama K
      • Patel SK
      • Pathak M
      • Yatoo MI
      • Tiwari R
      • Malik YS
      • et al.
      An update on SARS-CoV-2/COVID-19 with particular reference to its clinical pathology, pathogenesis, immunopathology and mitigation strategies.
      ,
      • Fenizia C
      • Biasin M
      • Cetin I
      • Vergani P
      • Mileto D
      • Spinillo A
      • et al.
      Analysis of SARS-CoV-2 vertical transmission during pregnancy.
      ,
      • Narang K
      • Enninga EAL
      • Gunaratne MD
      • Ibirogba ER
      • Trad ATA
      • Elrefaei A
      • et al.
      SARS-CoV-2 infection and COVID-19 during pregnancy: a multidisciplinary review.
      ,
      • Soy M
      • Keser G
      • Atagündüz P
      • Tabak F
      • Atagündüz I
      • Kayhan S.
      Cytokine storm in COVID-19: pathogenesis and overview of anti-inflammatory agents used in treatment.
      ). SARS-CoV-2 infection led to an increase in COVID-19 disease severity from mild to severe in pregnant women and intermittent death, depending on the extent of cellular and tissue damage caused by the cytokine storm (
      • Chaubey I
      • Vignesh R
      • Babu H
      • Wagoner I
      • Govindaraj S
      • Velu V.
      SARS-CoV-2 in Pregnant Women: Consequences of Vertical Transmission.
      ). Considering the particulars of immune status and physiological features in pregnant women, there is a need to investigate the differences in the clinical characteristics and severity of COVID-19 between pregnant and nonpregnant women and the potential impact of SARS-CoV-2 infection on the clinical outcomes of the fetus and neonate.
      SARS-CoV-2 infection has been reported to be more severe in pregnant women than in nonpregnant women (
      • Villar J
      • Ariff S
      • Gunier RB
      • Thiruvengadam R
      • Rauch S
      • Kholin A
      • et al.
      Maternal and neonatal morbidity and mortality among pregnant women with and without COVID-19 infection: the INTERCOVID multinational cohort study.
      ). Studies conducted in the United States and France have shown that pregnancy is a risk factor for severe disease and that COVID-19 during pregnancy may increase the risk of preterm birth, but the mortality rate among pregnant women is similar to that of nonpregnant women of the same age (
      • Ellington S
      • Strid P
      • Tong VT
      • Woodworth K
      • Galang RR
      • Zambrano LD
      • et al.
      Characteristics of women of reproductive age with laboratory-confirmed SARS-CoV-2 infection by pregnancy status—United States, January 22–June 7, 2020.
      ,
      • Kayem G
      • Lecarpentier E
      • Deruelle P
      • Bretelle F
      • Azria E
      • Blanc J
      • et al.
      A snapshot of the Covid-19 pandemic among pregnant women in France.
      ). In contrast, some studies from China showed that the clinical manifestations and characteristics of COVID-19 in pregnant women were similar to those of nonpregnant women (
      • Cheng B
      • Jiang T
      • Zhang L
      • Hu R
      • Tian J
      • Jiang Y
      • et al.
      Clinical characteristics of pregnant women with coronavirus disease 2019 in Wuhan, China. Open Forum Infectious Diseases.
      ,

      Wei L, Gao X, Chen S, Zeng W, Wu J, Lin X, et al. Clinical characteristics and outcomes between pregnant and non-pregnant women with Coronavirus disease 2019: a retrospective cohort study. 2020.

      ,
      • Xu S
      • Shao F
      • Bao B
      • Ma X
      • Xu Z
      • You J
      • et al.
      Clinical manifestation and neonatal outcomes of pregnant patients with coronavirus disease 2019 pneumonia in Wuhan, China. Open forum infectious diseases.
      ,
      • Yu N
      • Li W
      • Kang Q
      • Xiong Z
      • Wang S
      • Lin X
      • et al.
      Clinical features and obstetric and neonatal outcomes of pregnant patients with COVID-19 in Wuhan, China: a retrospective, single-centre, descriptive study.
      ). In spite of the growing number of studies on pregnant women with COVID-19 worldwide, it is still unclear whether the disease severity and death rate in reproductive-aged women with SARS-CoV-2 infection vary according to pregnancy status (
      • Godoi APN
      • Bernardes GCS
      • Nogueira LS
      • Alpoim PN
      • MdB Pinheiro
      Clinical Features and Maternal-fetal Results of Pregnant Women in COVID-19 Times.
      ).
      In Japan, the first laboratory-confirmed COVID-19 case was detected on January 16, 2020. Subsequently, the first laboratory-confirmed COVID-19 case in Osaka Prefecture was detected on January 29, 2020. As of September 30, 2021, a total of 1,696,936 patients with laboratory-confirmed COVID-19 were identified nationwide and a total of 199,553 patients were identified in Osaka Prefecture (
      Ministry of Health LaWoJ
      Cumulative number of confirmed COVID-19 cases by prefecture.
      ). However, few studies have described how the COVID-19 pandemic affected reproductive-aged women in Japan, specifically comparing pregnant and nonpregnant women (
      • Katayama Y
      • Zha L
      • Kitamura T
      • Hirayama A
      • Takeuchi T
      • Tanaka K
      • et al.
      Characteristics and Outcomes of Pediatric COVID-19 Patients in Osaka, Japan.
      ,
      • Tanaka K
      • Zha L
      • Kitamura T
      • Katayama Y
      • Takeuchi T
      • Komukai S
      • et al.
      Characteristics and outcomes of older patients with coronavirus disease 2019 in Japan.
      ,
      • Zha L
      • Sobue T
      • Takeuchi T
      • Tanaka K
      • Katayama Y
      • Komukai S
      • et al.
      Characteristics and Survival of Intensive Care Unit Patients with Coronavirus Disease in Osaka, Japan: A Retrospective Observational Study.
      ). To address this knowledge gap, we conducted a retrospective observational study of reproductive-aged pregnant and nonpregnant women with COVID-19 in Osaka, Japan.

      Methods

      Study design and setting

      We conducted a retrospective observational study on COVID-19 among reproductive-aged women in the Osaka Prefecture, Japan, between January 2020 and November 2020. The details of the data collection are described elsewhere (
      • Hirayama A
      • Masui J
      • Murayama A
      • Fujita S
      • Okamoto J
      • Tanaka J
      • et al.
      The characteristics and clinical course of patients with COVID-19 who received invasive mechanical ventilation in Osaka, Japan.
      ,
      • Zha L
      • Sobue T
      • Takeuchi T
      • Tanaka K
      • Katayama Y
      • Komukai S
      • et al.
      Characteristics and Survival of Intensive Care Unit Patients with Coronavirus Disease in Osaka, Japan: A Retrospective Observational Study.
      ). In accordance with the Infectious Diseases Control Law, the Osaka Prefecture Government conducted an active epidemiological investigation to collect epidemiological data on patients with COVID-19 using a uniform data-collection system (
      Government OP
      The press release on providing COVID-19 patients data for academic research institutes.
      ,
      Ministry of Health LaWoJ
      Treatment guidelines Version 4.2 of COVID-19 Infection.
      ). Among patients with COVID-19 who were registered in the system by the end of November 2020 and whose follow-up was completed, we focused on women of reproductive age who were pregnant or not. Therefore, not all the cases in November 2020 were included.
      Information on patients with COVID-19 was collected, including sex, age group, city of residence, presence of comorbidities, disease severity at diagnosis, date of symptom onset, surge, cluster, close contacts, hospital admission, date of hospital admission, date of discharge, status at discharge (alive or death), date of death, and treatment (including oxygen therapy, mechanical ventilation, renal replacement therapy, intensive care unit [ICU] admission, and extracorporeal membrane oxygenation). Age was classified in 10-year intervals as the Osaka Prefecture Government withheld precise age information in order to protect the privacy of patients with COVID-19. Accordingly, we designated reproductive-aged women as those aged 10–49 years old in this study. The period until June 13, 2020 was considered to be the first surge, followed by the second surge between June 14 and October 9, 2020, and the third surge thereafter (
      Government OP
      Osaka Prefecture New Coronavirus Countermeasures Headquarters Meeting.
      ). A cluster was defined as a group of five or more individuals who tested positive for SARS-CoV-2 and had an epidemiological relationship to the index patient (
      Diseases NIoI
      Guidelines for Conducting Active Epidemiological Surveillance of Patients with Novel Coronavirus Infections.
      ). The local public health centers defined close contacts as those who examined, nursed, or cared for the patient without protective equipment; lived with or had prolonged contact with the patient; had contact with the patient without protection for longer than 15 minutes at a distance of less than 1 meter; or was directly exposed to contaminated materials (
      Diseases NIoI
      Guidelines for Conducting Active Epidemiological Surveillance of Patients with Novel Coronavirus Infections.
      ). Disease severity at diagnosis were categorized as mild, moderate, or severe (
      Ministry of Health LaWoJ
      Treatment guidelines Version 4.2 of COVID-19 Infection.
      ). The date of symptom onset was defined as the date on which the first symptoms were reported (
      • Takeuchi T
      • Imanaka T
      • Katayama Y
      • Kitamura T
      • Sobue T
      • Shimazu T.
      Profile of patients with novel coronavirus disease 2019 (COVID-19) in Osaka Prefecture, Japan: a population-based descriptive study.
      ,
      • Takeuchi T
      • Kitamura T
      • Hirayama A
      • Katayama Y
      • Shimazu T
      • Sobue T.
      Characteristics of patients with novel coronavirus disease (COVID-19) during the first surge versus the second surge of infections in Osaka Prefecture, Japan.
      ). In cases where the date of symptom onset was unknown, we used the date of medical treatment, hospital admission, or any change in symptoms, whichever occurred first.
      This study was approved by the Osaka University Hospital Ethical Review Committee (reference no. 20397). The informed consent requirement was waived.

      Statistical analysis

      Categorical variables were reported as frequencies and proportions, and continuous variables were reported as the median and interquartile range (IQR). Pearson chi-square test was used to compare categorical variables, and the Wilcoxon rank-sum test was used to compare continuous variables between pregnant and nonpregnant women. All tests were two-tailed, and statistical significance was defined as a P value of < 0.05. Statistical analyses were performed using Stata version 16 (StataCorp. 2015, College Station, TX, USA).

      Results

      Eligible patients

      Of the 14,864 patients with COVID-19, 4156 (28.0%) were reproductive-aged female patients, of whom 29 (0.7%) were pregnant and 4127 (99.3%) were nonpregnant (Figure 1).
      Figure 1
      Figure 1Patient flowchart
      Legend: Of the 14,864 patients with COVID-19, 4156 (28.0%) were reproductive-aged female patients, of whom 29 (0.7%) were pregnant and 4127 (99.3%) were nonpregnant.

      Patient epidemiological characteristics

      Table 1 shows the baseline epidemiological characteristics of the reproductive-aged female patients with COVID-19. Approximately half of the nonpregnant women (47.7%) and pregnant women (48.3%) were aged 20–29 years old. The age distribution differed significantly according to pregnancy status (p = 0.035). The prevalence of comorbidities was similar among pregnant and nonpregnant women (6.9% and 8.7%, respectively). The most common disease severity at the time of diagnosis was mild (3564 cases, 85.8%), followed by asymptomatic (448 cases, 10.8%). No moderate or severe cases were observed in the pregnant women, whereas 0.1% of nonpregnant patients had severe disease at the time of diagnosis. No clusters were seen among pregnant women, while 4.2% of nonpregnant women were part of a cluster. More than half of the pregnant women were considered close contacts (17 cases, 58.6%), compared with approximately one-third in the nonpregnant group (1344 cases, 32.6%; p = 0.003). Of the 29 pregnant women, 22 (75.9%) were hospitalized; whereas among the nonpregnant women, 579 (14.0%) were hospitalized (p < 0.001).
      Table 1Epidemiological characteristics of reproductive-aged pregnant and nonpregnant women in Osaka Prefecture, Japan
      FactorTotalPregnantNot pregnantP-value
      Groups compared using Pearson chi-square test.
      N(%)N(%)N(%)
      No. of patients4,156(100.0)29(100.0)4,127(100.0)
      Age0.035
       10–19 years old399(9.6)1(3.4)398(9.6)
       20–29 years old1,982(47.7)14(48.3)1968(47.7)
       30–39 years old923(22.2)12(41.4)911(22.1)
       40–49 years old852(20.5)2(6.9)850(20.6)
      Geographic area0.061
       Osaka City2,375(57.1)10(34.5)2365(57.3)
       Other areas in Osaka Prefecture1,709(41.1)19(65.5)1690(40.9)
       Outside Osaka Prefecture65(1.6)0(0.0)65(1.6)
       Unknown7(0.2)0(0.0)7(0.2)
      Comorbidities0.738
       No3,797(91.4)27(93.1)3770(91.3)
       Yes359(8.6)2(6.9)357(8.7)
      Disease severity at diagnosis0.899
       Asymptomatic448(10.8)3(10.3)445(10.8)
       Mild3,564(85.8)26(89.7)3538(85.7)
       Moderate3(0.1)0(0.0)3(0.1)
       Severe3(0.1)0(0.0)3(0.1)
       Unknown138(3.3)0(0.0)138(3.3)
      Surge0.001
       First (∼ Jun. 13)465(11.2)9(31.0)456(11.0)
       Second (Jun. 14 ∼ Oct. 9)2,629(63.3)18(62.1)2611(63.3)
       Third (Oct. 10 ∼)1,062(25.6)2(6.9)1060(25.7)
      Cluster0.938
       No3,983(95.8)29(100.0)3954(95.8)
       Medical institution77(1.9)0(0.0)77(1.9)
       University9(0.2)0(0.0)9(0.2)
       School7(0.2)0(0.0)7(0.2)
       Child facility10(0.2)0(0.0)10(0.2)
       Other clusters70(1.7)0(0.0)70(1.7)
      Close contact0.003
       No2,795(67.3)12(41.4)2783(67.4)
       Yes1,361(32.7)17(58.6)1344(32.6)
      Hospitalization<0.001
       No3,497(84.1)7(24.1)3490(84.6)
       Yes601(14.5)22(75.9)579(14.0)
       Unknown58(1.4)0(0.0)58(1.4)
      low asterisk Groups compared using Pearson chi-square test.
      Figure 2 shows the distribution of gestational weeks among pregnant women with COVID-19. The number of pregnant patients were evenly distributed in the first, second, and third trimesters of gestation. The median gestation was 19 weeks among those with a known gestation.
      Figure 2
      Figure 2Distribution of gestational weeks among pregnant women with COVID-19
      Legend: shows the distribution of gestational weeks among pregnant women with COVID-19. The number of pregnant patients were evenly distributed in the first, second, and third trimesters of gestation. The median gestation was 19 weeks among those with a known gestation.

      Clinical features

      Table 2 shows the clinical characteristics of the hospitalized reproductive-aged female patients. The median number of days from onset to hospitalization was 6 days (IQR: 4–9 days) in total. The median length of hospital stay was 9 days (IQR: 7–14 days) in total. The time from onset to hospitalization and the length of hospital stay did not differ significantly according to pregnancy status. One patient received oxygen therapy, but none received mechanical ventilation, renal replacement therapy, or extracorporeal membrane oxygenation, and there were no ICU admissions or deaths in pregnant women. No severe diseases or deaths were observed despite pregnancy status.
      Table 2Clinical characteristics of hospitalized reproductive-aged pregnant and nonpregnant women in Osaka Prefecture, Japan
      FactorTotalPregnantNot pregnantP-value
      No. of hospitalized patients60122579
      Days to hospitalization, median (IQR)
      Number of individuals with missing data on the following variables: days to hospitalization n = 3; length of hospital stay n = 13.
      6(4, 9)5(3, 8)6(4, 9)0.130
      Groups compared using Wilcoxon rank-sum test.
      Length of hospital stay, median (IQR)
      Number of individuals with missing data on the following variables: days to hospitalization n = 3; length of hospital stay n = 13.
      9(7, 14)9(7, 13)9(7, 14)0.845
      Groups compared using Wilcoxon rank-sum test.
      Oxygen therapy, n (%)23(3.8)1(4.6)22(3.8)0.858
      Groups compared using Pearson chi-square test.
      Mechanical ventilator, n (%)
      Mechanical ventilator including noninvasive positive pressure ventilation.
      3(0.5)0(0.0)3(0.5)NA
      Intensive care unit, n (%)3(0.5)0(0.0)3(0.5)NA
      Renal replacement therapy, n (%)0(0.0)0(0.0)0(0.0)NA
      Extracorporeal membrane oxygenation, n (%)0(0.0)0(0.0)0(0.0)NA
      Death, n (%)0(0.0)0(0.0)0(0.0)NA
      Abbreviations: IQR, interquartile range; NA, not available.
      low asterisk Groups compared using Wilcoxon rank-sum test.
      Groups compared using Pearson chi-square test.
      Number of individuals with missing data on the following variables: days to hospitalization n = 3; length of hospital stay n = 13.
      § Mechanical ventilator including noninvasive positive pressure ventilation.

      Discussion

      This is a population-based retrospective study to report the characteristics and outcomes of COVID-19 among reproductive-aged female patients in Osaka Prefecture, Japan. The proportion of pregnant women with COVID-19 was < 1%. Most reproductive-aged female patients exhibited mild symptoms, and the proportion of asymptomatic patients was approximately one-tenth of the total patients. No moderate or severe cases were observed in pregnant women, while only 0.1% of severe cases were seen in nonpregnant women at diagnosis. No clusters were observed in pregnant patients; however, most of them acquired infection from a family member. Although approximately three-quarters of the pregnant women were hospitalized, only a few of the patients were hospitalized in the nonpregnant group. Moreover, no ICU admissions or deaths were observed in reproductive-aged female patients. This study provides information on the actual situation of SARS-CoV-2 infection among reproductive-aged female patients. This information could be used to help prevent its transmission.
      The majority of pregnant women in this study were 30–39 years old, which is reflective of the average age of pregnant women in Japan (over 30 years old) (
      Statistics Bureau MoIAaC
      Statistical Handbook of Japan 2019: Statistics Bureau, Ministry of Internal Affairs and Communications, Japan.
      ). Regarding the transmission route, there were no clusters among pregnant women with COVID-19. This may be because pregnant women generally follow the government recommendations to stay alert and safe and avoid going out unnecessarily during the COVID-19 pandemic in Japan. Conversely, the proportion of pregnant patients who acquired the infection from a close contact was approximately 1.5 times higher than that in nonpregnant women. As pregnant women are more likely to stay at home, the most likely source of infection among pregnant women is a family member. Therefore, to protect pregnant women from infection, in addition to self-prevention, measures should also be taken to prevent infection in their families.
      The high proportion of hospitalization in pregnant patients indicates that, considering the specific situation in pregnant women, most pregnant patients were admitted to the hospital for observation in Osaka, Japan. In this study, none of pregnant women with COVID-19 required intensive care admission or ventilatory support. Previous studies on hospitalized pregnant women with COVID-19 have shown that the proportion of cases requiring mechanical ventilator or ICU care was 1.5% to 7.6% (
      • Elshafeey F
      • Magdi R
      • Hindi N
      • Elshebiny M
      • Farrag N
      • Mahdy S
      • et al.
      A systematic scoping review of COVID-19 during pregnancy and childbirth.
      ,
      • Salem D
      • Katranji F
      • Bakdash T.
      COVID-19 infection in pregnant women: Review of maternal and fetal outcomes.
      ). Furthermore, no deaths were observed among the reproductive-aged female patients in this study. This result is similar to that in studies from China, which reported death rates of 0–1.5% in pregnant women with COVID-19 (
      • Cheng B
      • Jiang T
      • Zhang L
      • Hu R
      • Tian J
      • Jiang Y
      • et al.
      Clinical characteristics of pregnant women with coronavirus disease 2019 in Wuhan, China. Open Forum Infectious Diseases.
      ,

      Wei L, Gao X, Chen S, Zeng W, Wu J, Lin X, et al. Clinical characteristics and outcomes between pregnant and non-pregnant women with Coronavirus disease 2019: a retrospective cohort study. 2020.

      ,
      • Xu S
      • Shao F
      • Bao B
      • Ma X
      • Xu Z
      • You J
      • et al.
      Clinical manifestation and neonatal outcomes of pregnant patients with coronavirus disease 2019 pneumonia in Wuhan, China. Open forum infectious diseases.
      ,
      • Yu N
      • Li W
      • Kang Q
      • Xiong Z
      • Wang S
      • Lin X
      • et al.
      Clinical features and obstetric and neonatal outcomes of pregnant patients with COVID-19 in Wuhan, China: a retrospective, single-centre, descriptive study.
      ). Further observational studies are required to determine whether there are regional differences in the severity of COVID-19 and mortality rates among pregnant women with COVID-19. Understanding of the effect of SARS-CoV-2 infection, particularly its effect on pregnant women and neonates, is still insufficient. Further research is required to provide an evidence-based foundation for the medical management of pregnant patients with COVID-19.
      Currently, the COVID-19 vaccination is being administered globally. As research institutes and pharmaceutical companies around the world are still conducting clinical trials on drugs that are expected to treat the SARS-CoV-2 infection, vaccination is a proven method of controlling the COVID-19 pandemic. Pregnant women were initially excluded from active vaccination because the safety of the vaccine had not been established. However, many pregnant women have been vaccinated in other countries, and the severity and frequency of adverse reactions are comparable with those seen by nonpregnant women, with no fatal adverse events reported in either the fetus or mother (
      • Goncu Ayhan S
      • Oluklu D
      • Atalay A
      • Menekse Beser D
      • Tanacan A
      Moraloglu Tekin O, et al. COVID-19 vaccine acceptance in pregnant women.
      ,
      • Sukarno A
      • Kurniawan MH
      • Awaluddin AI.
      EFFICACY, IMMUNOGENICITY AND SIDE EFFECT OF COVID-19 VACCINE ON PREGNANT AND LACTATING WOMEN: A SYSTEMATIC REVIEW.
      ). In Japan, the three societies, including the Japan Society of Obstetrics and Gynecology, Japan Association of Obstetricians and Gynecologists, and Japan Society for Infectious Diseases in Obstetrics and Gynecology, issued a “Notice on COVID-19 Vaccination” for pregnant and nursing women, declaring that pregnant women are encouraged to have the vaccine, as are their husbands or partners (
      Gynecology JSoOaGJAoOaGJSfIDiOa
      Notice on COVID-19 Vaccination.
      ). In the United States, the American College of Obstetricians and Gynecologists (ACOG) and the Society for Maternal-Fetal Medicine (SMFM) have issued comments strongly recommending that all pregnant women be vaccinated against COVID-19, both at term and after delivery, to avoid the risk of infection, severe illness, and death (S
      SMFM Aa
      ACOG and SMFM Recommend COVID-19 Vaccination for Pregnant Individuals.
      ). Given the scarcity of available drugs for pregnant women infected with COVID-19, strict and active infection prevention, including vaccination, is essential.
      This study has some limitations. First, the dataset does not include information on delivery and fetal outcomes in pregnant women with COVID-19. Second, because this study analyzed epidemiological data collected by public health centers in accordance with the Infectious Diseases Control Law, specific information on comorbidities and medications was not available. Third, the data provided by Osaka Prefecture did not include all cases. In this context, the number of cases, treatment, and other information available on the Osaka Prefecture website are different from ours. Despite these limitations, this study provides important basic epidemiological information on COVID-19 among women of reproductive age in Osaka Prefecture.

      Conclusions

      We reveal the characteristics and outcomes of reproductive-aged female patients with COVID-19 using a comprehensive registry encompassing the whole Osaka Prefecture in Japan. Pregnant women accounted for 0.7% of the total cases of COVID-19 among women of reproductive age, and there were no deaths observed in pregnant or nonpregnant women. This study provides a baseline for long-term monitoring of COVID-19 among women of reproductive age in Osaka Prefecture.

      Conflict of Interest

      All authors declare no conflict of interest.

      Funding

      None.

      Acknowledgments

      We thank all the staff members of the Osaka Prefectural Government and public health centers in Osaka for their efforts in collecting the data used in the study and all the medical staff who treated patients with COVID-19. We also thank our colleagues from the Osaka University Center of Medical Data Science and Advanced Clinical Epidemiology Investigator's Research Project for providing their insights and expert advice to help improve our research.

      Author contributions

      LZ and TK conceived the study design. LZ and KT drafted the manuscript. LZ performed statistical analyses. TSo, AH, TT, TK, YK, SK, and TSh input their clinical expertise and critically revised the manuscript. All authors approved the version for publication. TK supervised the whole manuscript.

      Ethical Approval

      This study has been approved by the Research Ethics Committee of Osaka University (Approval No. 20397).

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