Literature DB >> 34767493

Pregnant and Peripartum Women with COVID-19 Have High Survival with Extracorporeal Membrane Oxygenation: An Extracorporeal Life Support Organization Registry Analysis.

Erika R O'Neil1,2, Huiming Lin3, Amir A Shamshirsaz1,2, Emily E Naoum4, Peter R Rycus5, Peta M A Alexander6,7, Jamel P Ortoleva8, Meng Li3, Marc M Anders1,2.   

Abstract

Entities:  

Mesh:

Year:  2022        PMID: 34767493      PMCID: PMC8787244          DOI: 10.1164/rccm.202109-2096LE

Source DB:  PubMed          Journal:  Am J Respir Crit Care Med        ISSN: 1073-449X            Impact factor:   21.405


× No keyword cloud information.
To the Editor: In the United States, 131,512 pregnant and peripartum women have been affected by coronavirus disease (COVID-19), with 200 associated deaths (0.15%) (1). The hormonal, physiological, and immunomodulatory changes during pregnancy increase susceptibility to respiratory infections and may predispose women to more severe presentations of COVID-19 (2). COVID-19 in pregnant or peripartum women is associated with higher risk for preterm birth, preeclampsia, cesarean delivery, and perinatal death and higher rates of ICU admission, mechanical ventilation, and extracorporeal membrane oxygenation (ECMO) when compared with pregnant or peripartum women without COVID-19 or when compared with nonpregnant women with COVID-19 (2–4). Venovenous (VV) ECMO is an invasive strategy to support oxygenation and ventilation for respiratory failure when conventional therapies have failed. We investigated the survival and complications of pregnant and/or peripartum women with COVID-19 supported with VV ECMO reported to the Extracorporeal Life Support Organization (ELSO) Registry. This retrospective cohort study included all adult women (⩾18 yr) supported on VV ECMO with COVID-19 between January 2020 and April 2021 reported to the ELSO Registry, representing 213 international centers in 36 countries. The primary outcome was survival to hospital discharge, and secondary outcomes were ECMO-related complications in the pregnant and/or peripartum cohort. Pregnant state was collected in the ELSO COVID-19 addendum as a comorbidity. Comorbidities and ECMO-related complications were defined according to ELSO data definitions. This study was granted an exemption by the Baylor College of Medicine Institutional Review Board. We compared pregnant and peripartum patients with the nonpregnant female cohort with categorical variables as exact numbers with percentages and continuous variables as median values with interquartile ranges. Categorical data were analyzed with Fisher’s exact or Pearson’s chi-square and continuous variables with the Wilcoxon-Mann-Whitney test. Overlap propensity score weighting was performed to investigate the effects of pregnancy on outcomes while adjusting for bias due to potential confounders. Propensity scores for patients being pregnant were estimated using a multivariable logistic regression model with a priori identified factors (race, age, pre-ECMO cardiac arrest, admission time to ECMO initiation, driving pressure, mean airway pressure, pH, PaO/FiO ratio, asthma, chronic heart disease, diabetes, hypertension, overweight/obesity, disseminated intravascular coagulation, neurological disease, chronic kidney disease, acute kidney injury, acute respiratory distress syndrome, heart failure, myocarditis, pneumonia, pneumothorax, septic shock, nonpulmonary infections, pulmonary vasodilators, buffering agents, and renal replacement therapy). Then, overlap propensity score–weighted logistic regression models were used to compare outcomes between pregnant and nonpregnant patients, in which each patient is weighted by the probability of belonging to the opposite status of her pregnancy (5). Bonferroni correction was used to correct for 10 outcomes in the propensity score analysis, leading to statistical significance if a P value < 0.05/10 = 0.005. There were 1,180 adult female patients supported with VV ECMO for COVID-19, of whom 100 were pregnant or peripartum patients. Univariate analysis showed that pregnant or peripartum patients were younger (32.4 vs. 49.3 yr; P < 0.01) and more commonly Hispanic (27.0% vs. 20.7%; odds ratio [OR], 2.33; 95% confidence interval [CI], 1.30–4.2), Black (19.0% vs. 16.7%; OR, 2.04; 95% CI, 1.08–3.87), or Asian (13.0% vs. 8.4%; OR, 2.77; 95% CI, 1.34–5.69) (Table 1). Nonpregnant patients were more likely to have comorbidities. The majority of patients in both groups were proned before ECMO. There were no differences in pre-ECMO status or ECMO duration (Table 1). Comparing the pregnant and/or peripartum cohort with the propensity score–adjusted comparator cohort, the pregnant or peripartum group were more likely to survive to hospital discharge (84% vs. 51.5%; overlap propensity score–weighted OR, 1.18; 95% CI, 1.10–1.27) and suffered fewer ECMO-related renal complications (overlap propensity score–weighted OR, 0.90; 95% CI, 0.84–0.97) (Figure 1). There were no other ECMO-related complication differences between cohorts.
Table 1.

Demographics, Comorbidities, Pre-ECMO Support, and ECMO Run Variables of Pregnant or Peripartum and Nonpregnant Women Supported on VV ECMO for COVID-19

 All Pregnant or Peripartum Patients (N = 100)All Nonpregnant Female Patients (N = 1,080)P Value
Age, yr32.4 (28.4–36.8)49.3 (40.6–57.6)<0.001
Weight, kg85.0 (71.4–104.5)92.0 (77.7–111.0)0.02
Overweight or obesity53 (53.0)735 (68.1)<0.01
Race/ethnicity   
 White22 (22.0)426 (39.4)Reference
 Hispanic27 (27.0)224 (20.7)0.005
 Black19 (19.0)180 (16.7)0.03
 Asian13 (13.0)91 (8.4)0.01
Comorbidities   
 Asthma15 (15.0)219 (20.3)0.24
 Malignancy027 (2.5)0.11
 Immunocompromised079 (7.3)<0.01
 Chronic heart disease1 (1.0)26 (2.4)0.37
 Hypertension20 (20.0)392 (36.3)<0.01
 Heart failure5 (5.0)35 (3.2)0.35
 Chronic lung disease048 (4.4)0.03
 Diabetes20 (20.0)362 (33.5)<0.01
 Neurological disease11 (11.0)121 (11.2)0.95
 DIC3 (3.0)15 (1.4)0.21
 ARDS80 (80.0)910 (84.3)0.27
 Pneumonia61 (61.0)665 (61.6)0.91
 Pneumothorax14 (14.0)128 (11.9)0.53
 Septic shock24 (24.0)282 (26.1)0.64
 Chronic kidney failure1 (1.0)31 (2.9)0.27
 Acute kidney failure13 (13.0)271 (25.1)<0.01
Pre-ECMO support   
 Invasive ventilation: PEEP, cm H2O14 (12–16) (n = 89)14 (11–16) (n = 927)0.97
 Invasive ventilation: PIP, cm H2O35 (31–38) (n = 70)34 (31–39) (n = 730)0.92
 Invasive ventilation: MAP, cm H2O23 (19–26) (n = 55)22 (19–25) (n = 577)0.76
 Invasive ventilation: driving pressure, cm H2O21 (28–26) (n = 70)21 (17–25) (n = 709)0.55
 PF ratio68 (57–87) (n = 87)70 (57–91) (n = 876)0.55
 Any pulmonary vasodilators33 (33.0)376 (34.8)0.72
 Neuromuscular blockers71 (71.0)823 (76.2)0.25
 Prone positioning58 (58.0)627 (58.1)0.99
 Intubation to ECMO initiation, h97 (25–187) (n = 87)77 (25–149) (n = 933)0.30
 Pre-ECMO cardiac arrest3 (3.0)29 (2.7)0.90
ECMO run   
 Hours ECMO396 (219–735)401 (211–688) (n = 1,080)0.65

Definition of abbreviations: ARDS = acute respiratory distress syndrome; COVID-19 = coronavirus disease; DIC = disseminated intravascular coagulation; ECMO = extracorporeal membrane oxygenation; MAP = mean airway pressure; PEEP = positive end-expiratory pressure; PF = PaO/FiO; PIP = peak inspiratory pressure; VV ECMO = venovenous extracorporeal membrane oxygenation.

Data are shown as median (interquartile range) or n (%).

Figure 1.

Survival and extracorporeal membrane oxygenation (ECMO)-related complications of the propensity score–matched cohorts, comparing the pregnant and peripartum patients with the nonpregnant female patients. Pregnant and peripartum patients had higher survival (overlap propensity score–weighted odds ratio, 1.18; 95% confidence interval, 1.10–1.27) and suffered fewer ECMO-related renal complications (overlap propensity score–weighted odds ratio, 0.90; 95% confidence interval, 0.84–0.97) than the nonpregnant group.

Demographics, Comorbidities, Pre-ECMO Support, and ECMO Run Variables of Pregnant or Peripartum and Nonpregnant Women Supported on VV ECMO for COVID-19 Definition of abbreviations: ARDS = acute respiratory distress syndrome; COVID-19 = coronavirus disease; DIC = disseminated intravascular coagulation; ECMO = extracorporeal membrane oxygenation; MAP = mean airway pressure; PEEP = positive end-expiratory pressure; PF = PaO/FiO; PIP = peak inspiratory pressure; VV ECMO = venovenous extracorporeal membrane oxygenation. Data are shown as median (interquartile range) or n (%). Survival and extracorporeal membrane oxygenation (ECMO)-related complications of the propensity score–matched cohorts, comparing the pregnant and peripartum patients with the nonpregnant female patients. Pregnant and peripartum patients had higher survival (overlap propensity score–weighted odds ratio, 1.18; 95% confidence interval, 1.10–1.27) and suffered fewer ECMO-related renal complications (overlap propensity score–weighted odds ratio, 0.90; 95% confidence interval, 0.84–0.97) than the nonpregnant group. Pregnant and peripartum women with COVID-19 have increased morbidity, ICU admission, mechanical ventilation, need for ECMO support, and mortality when compared with nonpregnant women with COVID-19 (2–4). The Society for Maternal-Fetal Medicine guidelines for the management of severe COVID-19 acute respiratory distress syndrome endorses the use of ECMO for postpartum patients and pregnant women <32 weeks’ gestation with refractory hypoxemia, to facilitate in utero fetal development (6). The Society for Maternal-Fetal Medicine recommends that ECMO should not be withheld from pregnant patients who may potentially benefit (6). Indeed, our study supports the use of VV ECMO in this population, with increased survival for pregnant and peripartum women with severe COVID-19 who received VV ECMO support compared with a propensity-matched cohort of VV ECMO–supported nonpregnant women with COVID-19. We report that pregnant and peripartum women supported on ECMO for COVID-19 were more likely to be Hispanic, Black, or Asian when compared with the nonpregnant cohort. Severe maternal morbidity, or unexpected outcomes of pregnancy that result in short- or long-term health consequences, are more prevalent in non-Hispanic Black women and Hispanic women than in White women in the United States (7). During the pandemic, Black and Hispanic pregnant women were disproportionately affected by COVID-19 (4, 8). These racial and ethnic disparities in severe maternal morbidity and mortality are evident in our study. Pregnant and peripartum women were less likely to sustain renal complications than the women of reproductive age supported on ECMO in our study. Angiotensin II, progesterone, and increased nitric oxide, produced during pregnancy, increase renal plasma flow by decreasing vascular resistance, which may explain the lower rates of renal injury (9). Although previously considered higher-risk ECMO candidates, pregnant and peripartum women did not sustain more ECMO-related complications, consistent with other reports (10). Importantly, no pregnant or peripartum women sustained limb complications, despite the majority experiencing femoral vein cannulations. Lastly, these pregnant and peripartum women with COVID-19 sustained few bleeding complications and no more than their matched nonpregnant cohort, despite anticoagulation and pregnancy-related coagulation changes. Our study has limitations. Retrospective, registry-based studies are at risk of selective reporting by centers. Unidentified confounders may be present, despite incorporating a propensity score analysis with overlap weighting by accounting for 28 variables. The pregnancy indicator in the ELSO COVID-19 addendum does not distinguish if actively pregnant or how many weeks postpartum. In addition, the outcomes of the pregnancy and outcomes beyond hospital discharge are not known. The use of VV ECMO to support pregnant and peripartum women with respiratory failure from COVID-19 was associated with lower in-hospital mortality and ECMO-related renal complications than those in nonpregnant females. This vulnerable population should be considered for VV ECMO support for COVID-19.
  8 in total

1.  Racial and Ethnic Disparities in the Incidence of Severe Maternal Morbidity in the United States, 2012-2015.

Authors:  Lindsay K Admon; Tyler N A Winkelman; Kara Zivin; Mishka Terplan; Jill M Mhyre; Vanessa K Dalton
Journal:  Obstet Gynecol       Date:  2018-11       Impact factor: 7.661

2.  Overlap Weighting: A Propensity Score Method That Mimics Attributes of a Randomized Clinical Trial.

Authors:  Laine E Thomas; Fan Li; Michael J Pencina
Journal:  JAMA       Date:  2020-06-16       Impact factor: 56.272

Review 3.  Renal physiology of pregnancy.

Authors:  Katharine L Cheung; Richard A Lafayette
Journal:  Adv Chronic Kidney Dis       Date:  2013-05       Impact factor: 3.620

4.  Successful Treatment of Pregnant and Postpartum Women With Severe COVID-19 Associated Acute Respiratory Distress Syndrome With Extracorporeal Membrane Oxygenation.

Authors:  Jairo H Barrantes; Jamel Ortoleva; Erika R O'Neil; Erik E Suarez; Sharon Beth Larson; Aniket S Rali; Cara Agerstrand; Lorenzo Grazioli; Subhasis Chatterjee; Marc Anders
Journal:  ASAIO J       Date:  2021-02-01       Impact factor: 2.872

5.  Maternal and Neonatal Morbidity and Mortality Among Pregnant Women With and Without COVID-19 Infection: The INTERCOVID Multinational Cohort Study.

Authors:  José Villar; Shabina Ariff; Robert B Gunier; Ramachandran Thiruvengadam; Stephen Rauch; Alexey Kholin; Paola Roggero; Federico Prefumo; Marynéa Silva do Vale; Jorge Arturo Cardona-Perez; Nerea Maiz; Irene Cetin; Valeria Savasi; Philippe Deruelle; Sarah Rae Easter; Joanna Sichitiu; Constanza P Soto Conti; Ernawati Ernawati; Mohak Mhatre; Jagjit Singh Teji; Becky Liu; Carola Capelli; Manuela Oberto; Laura Salazar; Michael G Gravett; Paolo Ivo Cavoretto; Vincent Bizor Nachinab; Hadiza Galadanci; Daniel Oros; Adejumoke Idowu Ayede; Loïc Sentilhes; Babagana Bako; Mónica Savorani; Hellas Cena; Perla K García-May; Saturday Etuk; Roberto Casale; Sherief Abd-Elsalam; Satoru Ikenoue; Muhammad Baffah Aminu; Carmen Vecciarelli; Eduardo A Duro; Mustapha Ado Usman; Yetunde John-Akinola; Ricardo Nieto; Enrico Ferrazi; Zulfiqar A Bhutta; Ana Langer; Stephen H Kennedy; Aris T Papageorghiou
Journal:  JAMA Pediatr       Date:  2021-08-01       Impact factor: 16.193

Review 6.  Coronavirus disease 2019 (COVID-19) pandemic and pregnancy.

Authors:  Pradip Dashraath; Jing Lin Jeslyn Wong; Mei Xian Karen Lim; Li Min Lim; Sarah Li; Arijit Biswas; Mahesh Choolani; Citra Mattar; Lin Lin Su
Journal:  Am J Obstet Gynecol       Date:  2020-03-23       Impact factor: 8.661

7.  Update: Characteristics of Symptomatic Women of Reproductive Age with Laboratory-Confirmed SARS-CoV-2 Infection by Pregnancy Status - United States, January 22-October 3, 2020.

Authors:  Laura D Zambrano; Sascha Ellington; Penelope Strid; Romeo R Galang; Titilope Oduyebo; Van T Tong; Kate R Woodworth; John F Nahabedian; Eduardo Azziz-Baumgartner; Suzanne M Gilboa; Dana Meaney-Delman
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2020-11-06       Impact factor: 17.586

8.  Coronavirus disease 2019 pregnancy outcomes in a racially and ethnically diverse population.

Authors:  Olga Grechukhina; Victoria Greenberg; Lisbet S Lundsberg; Uma Deshmukh; Jennifer Cate; Heather S Lipkind; Katherine H Campbell; Christian M Pettker; Katherine S Kohari; Uma M Reddy
Journal:  Am J Obstet Gynecol MFM       Date:  2020-10-07
  8 in total
  2 in total

1.  Evolving outcomes of extracorporeal membrane oxygenation during the first 2 years of the COVID-19 pandemic: a systematic review and meta-analysis.

Authors:  Ryan Ruiyang Ling; Kollengode Ramanathan; Kiran Shekar; Daniel Brodie; Jackie Jia Lin Sim; Suei Nee Wong; Ying Chen; Faizan Amin; Shannon M Fernando; Bram Rochwerg; Eddy Fan; Ryan P Barbaro; Graeme MacLaren
Journal:  Crit Care       Date:  2022-05-23       Impact factor: 19.334

2.  Delivery decision in pregnant women rescued by ECMO for severe ARDS: a retrospective multicenter cohort study.

Authors:  Sarah Aissi James; Christophe Guervilly; Mathieu Lesouhaitier; Alexandre Coppens; Clément Haddadi; Guillaume Lebreton; Jacky Nizard; Nicolas Brechot; Benjamin Assouline; Ouriel Saura; David Levy; Lucie Lefèvre; Pétra Barhoum; Juliette Chommeloux; Guillaume Hékimian; Charles-Edouard Luyt; Antoine Kimmoun; Alain Combes; Matthieu Schmidt
Journal:  Crit Care       Date:  2022-10-17       Impact factor: 19.334

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.