Literature DB >> 35698478

Effectiveness of Preoperative Symptom Screening in Identifying Pediatric SARS-CoV-2 Infections: A Retrospective Cohort Analysis.

Catherine T McNamara1, Laura C Nuzzi1, Ava G White1, Gabrielle G Massey1, Stephanie D Miller1, Amir H Taghinia1, Brian I Labow1.   

Abstract

Evidence-based protocols identifying COVID-19 cases in pediatric preoperative settings are lacking. With COVID-19 positioned to remain a threat to children, this study examines effectiveness of preoperative COVID-19 symptom screening in pediatric patients.
Methods: This retrospective cohort study included hospital billing/medical record queries of (1) procedures performed under conscious sedation/general anesthesia and (2) laboratory-confirmed COVID-19 (+) cases from April 6, 2020, to June 15, 2020. Descriptive analyses were performed for demographic, procedural, symptom, and COVID-19 test result data obtained from medical records. Bivariate analyses examined associations between SARS-CoV-2 test results and symptom, demographic, and procedural data.
Results: Among 2900 surgical cases, median (interquartile range) age was 8.1 (12.8) years. The majority were male (n = 1609, 55.5%), white (n = 1614, 55.7%), and not Hispanic/Latino (n = 1658, 57.2%). Additionally, 85.4% (n = 2412) of cases were non-emergent. Fifteen COVID-19 (+) cases were identified, for a 0.5% positivity rate. COVID-19 positivity was not associated with sex, American Society of Anesthesiologists physical status, or preoperative symptom status. Notably, 92.9% (n = 13) of COVID-19 (+) cases were asymptomatic. COVID-19 (+) patients were significantly older (15.6 years) than COVID-19 (-) patients (8.0 years). Patients who were not white, were Hispanic/Latino, or had a relatively lower economic status, were more likely to test positive. Conclusions: Preoperative symptom screenings insufficiently identified COVID-19 (+) patients. During outbreaks, testing protocols should be implemented to identify COVID-19 (+) patients. Future research should examine if observations are similar for other variants, and how health disparities associate with COVID-19.
Copyright © 2022 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons.

Entities:  

Year:  2022        PMID: 35698478      PMCID: PMC9186400          DOI: 10.1097/GOX.0000000000004402

Source DB:  PubMed          Journal:  Plast Reconstr Surg Glob Open        ISSN: 2169-7574


Takeaways

Question: Do preoperative symptom screenings accurately identify incidental COVID-19 cases among pediatric patients undergoing surgery? Findings: COVID-19 positivity was 0.5% among the 2900 total procedures included in our retrospective cohort series. The presence of any COVID-19 symptom was not significantly associated with a positive SARS-CoV-2 test result, and approximately 93% of COVID-19 (+) cases were asymptomatic. Meaning: Preoperative screening based on symptoms was insufficient in identifying COVID-19 (+) cases in our sample, highlighting the importance of preoperative SARS-CoV-2 testing in pediatric surgical patients.

INTRODUCTION

The COVID-19 pandemic has become one of the defining moments in healthcare. SARS-CoV-2 infected over 50 million Americans between January 2020 and mid-December 2021, and has disproportionately impacted marginalized communities.[1-7] Throughout the majority of the pandemic, adults have experienced the brunt of infections. However, recent data indicate that SARS-CoV-2 infections are starting to trend younger.[8] As of late September 2021, children have contributed to 16.2% of all positive cases in the United States, compared to just 2.7% in April 2020.[9] Based on current data, this is due in part to vaccination availability, reintroduction of in-person learning, and a variety of other social factors.[10-15] Although children can present with similar symptoms of COVID-19 as adults (fever, cough, shortness of breath, fatigue, diarrhea, and rhinorrhea), pediatric patients are frequently asymptomatic and experience milder disease courses.[3,13,16-25] In rare cases, children have developed multiorgan inflammatory syndrome (MIS-C) or thrombotic microangiopathy (TMA) as a result of SARS-CoV-2 infection; however, the pathogenesis is currently unclear.[26,27] During the initial 2020 shutdowns, elective health services, including surgery, were largely suspended.[28,29] A study including 26 pediatric hospitals reported a 77% drop in surgeries during this time compared to 2019, with an estimated $276.3 million lost from inpatient and outpatient services.[28] Given the health-related downsides and economic costs, a shutdown of this magnitude is unlikely to be repeated. It is critical that we become educated on how to exist with COVID-19 in healthcare, and determine the most effective ways of screening for the virus in children. To date, there have been few studies examining this smaller segment of the COVID-19 population. One recent letter reported that COVID-19 (+) pediatric surgical patients were largely older, and symptomatic, but that those who tested positive did not vary by race, or Hispanic ethnicity.[30] However, this study was limited to a small sample size and short time period. The present study aims to evaluate the effectiveness of preoperative COVID-19 symptom screening relative to SARS-CoV-2 testing in pediatric patients, using a larger sample size and broader time period than the earlier report. Using these data, we aim to propose an evidence-based approach to preoperative COVID-19 screening for children. Our secondary goal is to explore patient characteristics and demographics which may associate with positivity rates within the preoperative pediatric population.

METHODS

After receiving institutional review board approval with a waiver of informed consent, we performed a retrospective review examining COVID-19 symptoms and SARS-CoV-2 test results in preoperative patients at a single pediatric tertiary care medical center. Demographics, clinical presentation, operative procedures, and SARS-CoV-2 test results were all obtained from the medical record. All data were stored and managed in password protected documents within our institution’s security firewall. Nearly all SARS-CoV-2 testing was performed using polymerase chain reaction (PCR) methodology at our institutional core laboratory, and only a small number of tests were performed at an outside institution before patient transfer to our hospital.

Patient Eligibility and Case Selection

Two distinct hospital billing and medical record queries were performed to identify eligible patients (Fig. 1). During the study period, preoperative SARS-CoV-2 testing and COVID-19 symptom screening were both required by our institution for all non-emergent procedures performed under general anesthesia or conscious sedation. The first query identified all patients undergoing procedures under general anesthesia or conscious sedation at our institution from April 6, 2020, through June 15, 2020. This list was then screened to identify laboratory confirmed COVID-19 (+) cases and COVID-19 (−) cases. Patients whose results were unavailable were excluded from all analyses. Upon report of a preoperative positive SARS-CoV-2 test, non-emergent procedures were rescheduled. As the above query only captured completed procedures, rescheduling a procedure due to a positive SARS-CoV-2 test result would exclude it from query results. Thus, to avoid selection bias towards COVID-19 (−) cases, and to ensure all COVID-19 (+) cases reported during preoperative screening were captured, a second query was performed.
Fig. 1.

Schematic of hospital billing and medical record queries. aGeneral anesthesia. bAdditional cases that did not overlap with procedure query.

Schematic of hospital billing and medical record queries. aGeneral anesthesia. bAdditional cases that did not overlap with procedure query. In the second query, laboratory-confirmed COVID-19 (+) cases at our institution were identified using the associated International Classification of Diseases, Tenth Revision (ICD-10), code U07.1 during the same time period. This list was screened for patients who were COVID-19 (+) as a result of preoperative testing, and who did not overlap with the previous procedure query. Patients who tested positive during a clinical or emergency department visit unrelated to an upcoming surgical procedure were excluded from our final sample of COVID-19 (+) cases. To achieve our final cohort, the total number of COVID-19 (+) cases included a combination of both queries, whereas the total number of COVID-19 (−) cases were identified during the initial procedure query.

Statistical Analyses

Analyses were performed using IBM SPSS Version 27 (IBM Corp., Armonk, N.Y.). Frequency distributions were reported for demographics; COVID-19 clinical presentation; procedural data; and test source, type, and results. Unless otherwise stated, variables were dichotomized as follows: race (white versus non-white), ethnicity (Hispanic or Latino versus not Hispanic or Latino) and COVID-19 symptom status (at least one COVID-19 symptom versus asymptomatic). The Mann–Whitney U test was used to compare the difference in median age between COVID-19 (+) and COVID-19 (−) groups. The Fisher exact and Pearson chi-squared tests were used to assess associations of sex, race, ethnicity, American Society of Anesthesiologists (ASA) physical status, and COVID-19 symptom status with SARS-CoV-2 test results, as appropriate. An independent samples t-test was used to evaluate differences in median household income by the SARS-CoV-2 test result. Median household income data were obtained from the US Census Bureau using patient zipcode.[31] Cases with missing data were excluded from analyses. A P value less than 0.05 was considered statistically significant. (See appendix, Supplemental Digital Content 1, which displays the STROBE statement, http://links.lww.com/PRSGO/C76.)

RESULTS

Cohort Demographics

A total of 2900 cases were obtained from both queries. The procedure query resulted in 2953 cases, of which 2885 were COVID-19 (−), 13 were COVID-19 (+), and 55 were excluded due to absent testing data. The COVID-19 (+) case query resulted in 197 cases, of which two additional cases were identified during preoperative screening, and did not overlap with the original query. In total, these queries yielded 15 COVID-19 (+) cases and 2885 COVID-19 (−) cases, with a resulting positivity rate of 0.5% (Table 1). Of note, 99.4% (n = 2882) of test results were obtained using PCR testing, all performed at our institution. All remaining test results (n = 18) were obtained from outside medical records following patient transfer to our institution.
Table 1.

Demographic and Clinical Data

n = 2900 Cases
Median (IQR) age at preoperative screening, y8.1 (12.8)
COVID-19 positivity rate, n (%)15 (0.5)
Sex, n (%)
 Male1609 (55.5)
 Female1291(44.5)
Race, n (%)
 Asian71 (2.4)
 Black or African American148 (5.1)
 Other334 (11.5)
 Unknown733 (25.3)
 White1614 (55.7)
Ethnicity, n (%)
 Hispanic or Latino270 (9.3)
 Not Hispanic or Latino1658 (57.2)
 Unknown972 (33.5)
ASA class, n (%)
 1698 (24.7)
 21203 (42.6)
 3725 (25.7)
 4188 (6.7)
 510 (0.4)
ASA physical status, n (%)
 Non-emergent2412 (85.4)
 Emergent413 (14.6)
Surgical service, n (%)
 Orthopedics522 (18.0)
 Otolaryngology509 (17.6)
 General495 (17.1)
 Gastrointestinal274 (9.4)
 Genitourinary201 (6.9)
 Cardiology174 (6.0)
 Plastic and oral163 (5.6)
 Neurology162 (5.6)
 Eye117 (4.0)
 Oncology111 (3.8)
 Dental50 (1.7)
 Pain50 (1.7)
 Gynecology36 (1.2)
 Medical14 (0.5)
 Pulmonary13 (0.4)
 Dermatology9 (0.3)
Demographic and Clinical Data The median age of the entire cohort was 8.1 years [minimum: <1.2 months; maximum: 59.8 years; interquartile range (IQR): 12.8 years; 5th percentile: 3.5 months, 95th percentile: 21.2 years], and the majority of the sample was male (n = 1609, 55.5%), white (n = 1614, 55.7%), and not Hispanic or Latino (n = 1658, 57.2%). Approximately 85% of all cases were non-emergent (n = 2412), with the greatest number of cases (n = 1203, 42.6%) classified as ASA 2. Orthopedics was the most common surgical service (n = 522, 18.0%).

Symptoms and Cohort Demographics

There was no significant difference in presence of symptoms between COVID-19 (+) and COVID-19 (−) cases (P > 0.99; Table 2). Roughly 93% (n = 13; symptom data unavailable for one case) of COVID-19 (+) cases were asymptomatic. The only presenting symptom in COVID-19 (+) cases was dermatologic (cellulitis), occurring in one case (7.1%), while fever was the most common presenting symptom in COVID-19 (−) cases (n = 72, 2.5%). Additionally, sex and ASA physical status distribution did not significantly vary between COVID-19 (+) and COVID-19 (−) cases (P > 0.05, both; Table 3).
Table 2.

COVID-19-related Symptoms Stratified by SARS-CoV-2 Test Result

Reported COVID-19 Symptoms, n (%)Negative SARS-CoV-2 Test Result, n = 2885 Cases*Positive SARS-CoV-2 Test Result, n = 15 Cases* P
Cough22 (0.8)0 (0.0)
Fever72 (2.5)0 (0.0)
Diarrhea61 (2.1)0 (0.0)
Rhinorrhea17 (0.6)0 (0.0)
Conjunctivitis1 (<0.1)0 (0.0)
Skin symptoms11 (0.4)1 (7.1)
Muscle aches2 (0.1)0 (0.0)
Fatigue27 (0.9)0 (0.0)
Loss of taste and/or smell0 (0.0)0 (0.0)
Shortness of breath59 (2.1)0 (0.0)
Other§1 (<0.1)0 (0.0)
Any symptom220 (7.6)1 (7.1)>0.99

*Symptom percentages do not total 100% as cases could present with multiple symptoms.

†Inclusive of rash or red pigmentation to skin.

‡Analyses not conducted.

§Lung congestion.

Table 3.

Demographic and Clinical Data Stratified by SARS-CoV-2 Test Result

Negative SARS-CoV-2 Test Result, n = 2885 CasesPositive SARS-CoV-2 Test Result, n = 15 Cases P
Median (IQR) age at preoperative screening, y8.0 (12.8)15.6 (7.0) 0.04
Sex, n (%)
 Male1603 (55.6)6 (40.0)0.23
 Female1282 (44.4)9 (60.0)
Race, n (%)
 Non-white*544 (25.3)9 (69.2) 0.001
 White1610 (74.7)4 (30.8)
Ethnicity, n (%)
 Hispanic or Latino265 (13.8)5 (41.7) 0.006
 Not Hispanic or Latino1651 (86.2)7 (58.3)
ASA class, n (%)
 1698 (24.8)0 (0.0)
 21197 (42.6)6 (46.2)
 3719 (25.6)6 (46.2)
 4187 (6.7)1 (7.7)
 510 (0.4)0 (0.0)
ASA physical status, n (%)
 Non-emergent2400 (85.4)12 (85.7)>0.99
 Emergent411 (14.6)2 (14.3)
Surgical service, n (%)
 Orthopedics521 (18.1)1 (6.7)
 Otolaryngology507 (17.6)2 (13.3)
 General489 (16.9)6 (40.0)
 Gastrointestinal274 (9.5)0 (0.0)
 Genitourinary201 (7.0)0 (0.0)
 Cardiology173 (6.0)1 (6.7)
 Plastic and oral163 (5.6)0 (0.0)
 Neurology161 (5.6)1 (6.7)
 Eye117 (4.1)0 (0.0)
 Oncology108 (3.7)3 (20.0)
 Dental50 (1.7)0 (0.0)
 Pain50 (1.7)0 (0.0)
 Gynecology35 (1.2)1 (6.7)
 Medical14 (0.5)0 (0.0)
 Pulmonary13 (0.5)0 (0.0)
 Dermatology9 (0.3)0 (0.0)

*Includes Asian, American Indian or Alaska Native, Black or African American and other. Cases with undisclosed race were excluded from analysis.

†Cases with undisclosed ethnicities were excluded from this analysis.

‡Analysis not conducted.

COVID-19-related Symptoms Stratified by SARS-CoV-2 Test Result *Symptom percentages do not total 100% as cases could present with multiple symptoms. †Inclusive of rash or red pigmentation to skin. ‡Analyses not conducted. §Lung congestion. Demographic and Clinical Data Stratified by SARS-CoV-2 Test Result *Includes Asian, American Indian or Alaska Native, Black or African American and other. Cases with undisclosed race were excluded from analysis. †Cases with undisclosed ethnicities were excluded from this analysis. ‡Analysis not conducted. COVID-19 (+) patients were significantly older (median age: 15.6 years, minimum: 6 months, maximum: 25.4 years, IQR: 7.0 years) than COVID-19 (−) patients (median age: 8.0 years, minimum: <1.2 months, maximum: 59.8 years, IQR: 12.8 years) (P = 0.04). Furthermore, patients who were non-white had 6.7 times the odds of testing positive for SARS-CoV-2 compared to white patients [OR: 6.66, 95% confidence interval (CI): 2.04–21.71, P = 0.001]. Additionally, patients who were Hispanic or Latino had 4.5 times the odds of testing positive for SARS-CoV-2 compared to non-Hispanic or Latino patients (OR: 4.45, 95% CI: 1.40–14.12, P =0.006). Last, COVID-19 (+) patients lived in regions with significantly lower median household incomes (mean income = $73,761.07 ± $32,388.63) compared to COVID-19 (−) patients (mean income = $93,781.18 ± $36,540.20; P = 0.03). Of note, median household income data were unavailable for 43 patients. Additional review of COVID-19 (+) cases showed that one patient tested positive for SARS-CoV-2 before two separate surgical procedures, contributing two COVID-19 (+) cases. As a result, six patients (n = 7/15 cases, 46.7%) had comorbidities before surgery, the most common being obesity (n = 4/7 cases, 57.1%). Postoperative complications data were available for 40.0% (n = 6/15) of COVID-19 (+) patients, with none experiencing surgical complications. There were no unexpected readmissions or reoperations. One patient with COVID-19 died on postoperative day zero; however, the cause of death was attributed to sepsis, pneumonia, and intestinal obstruction within the setting of chronic lung disease and COVID-19.

DISCUSSION

The COVID-19 pandemic has presented one of the greatest healthcare challenges in modern history. A lack of knowledge in the early stages resulted in a catastrophic loss of life, suspension of elective surgical and medical care, and questions regarding the long-term impact on healthcare. Thus, it is essential that we continue to expand our knowledge based on the past two years of experience to facilitate decision-making going forward. In our study, we explored the effectiveness of preoperative COVID-19 screening protocols (routine testing and symptom screening) to provide supportive data for an evidence-based approach for preoperative COVID-19 screening in the pediatric population. We also investigated how patient demographics associated with preoperative COVID-19 status. Although our study sample was not limited to plastic surgery cases alone, plastic surgeons often perform surgeries in conjunction with other specialties. Thus, a diverse sample of surgical specialties provides added relevance and generalizability to our study. The COVID-19 positivity rate in our cohort was 0.5%, similar to other pediatric studies.[3,30,32-35] It has been suggested that lower positivity rates in children are in part a result of less frequent testing, as a consequence of asymptomatic presentation.[22] However, in the present study, all non-emergent cases (approximately 85% of the entire cohort) were tested preoperatively for SARS-CoV-2, regardless of symptom status. This suggests additional causes for lower positivity rates among children, such as inherent or behavioral protection against infection. From a biological standpoint, differential ACE2 receptor expression, fewer risk factors, and differences in innate and adaptive immunity have been postulated as potential justifications for low pediatric infection rates.[13,36,37] On the social-behavioral level, others have suggested lack of travel, school closures, and fewer activities outside the home as possible explanations.[11,13] Of note, the majority of data from this study, similar to other pediatric surgical studies, were collected in the latter part of the 2019–2020 academic year and into the early summer (March–July). In the regions where data were collected for the present (Massachusetts) and previous studies (Texas, Pennsylvania, and Washington), state mandated school closures were instituted during these periods, preventing in-person learning and after-school activities.[3,30,38] Lower morbidity and mortality figures have contributed to the misconception that children are not significantly impacted by COVID-19, especially early in the pandemic.[7,16] Review of COVID-19 (+) surgical cases in our study similarly revealed only one death, and no postoperative complications, or unexpected readmissions or reoperations, analogous to another pediatric study.[39] More recently, however, there was a 10-fold increase in weekly hospitalizations due to COVID-19 from June 2021 to August 2021 in children 0–4 years of age, which coincided with emergence of the Delta variant.[40] These data emphasize the previously overlooked vulnerability of children to this virus, and highlight an immediate need to establish COVID-19 testing protocols for children in the operative setting. In an effort to control COVID-19 transmission in the operative setting, including patient to patient, and patient to provider, it is of primary importance to identify COVID-19 (+) patients. Standard screening questions for COVID-19-related symptoms have become ubiquitous. However, the effectiveness of this symptom-based approach remains unclear in the pediatric preoperative setting. Our study found no significant difference in the presence of symptoms by SARS-CoV-2 test status. These data contrast a previous letter which showed that preoperative COVID-19 (+) pediatric patients were more likely to be symptomatic.[30] The difference may reflect a larger sample size or longer study period relative to the mentioned study. In addition, approximately 93% of COVID-19 (+) cases in our cohort were asymptomatic, considerably higher than several other pediatric studies in which testing was conducted primarily due to exposure and/or presence of symptoms (asymptomatic range: 14.2%–28%), rather than routine screening.[18,22-24] This difference may be due to the underlying reason for testing in associating symptoms to positivity rates. Our data suggest that rigorous preoperative testing rather than screening questions is essential to identify COVID-19 positive children preoperatively. In emergent instances when patients cannot be tested preoperatively, we suggest they be treated as COVID-19 (+) (even when asymptomatic), and established precautions should be exercised. We also found that patients in our study who tested positive for SARS-CoV-2 were significantly older than those who tested negative (median 15.6 versus 8.0 years), mirroring a prior study.[30] The behavioral independence and increased social interaction in older children may account for this finding. However, with the lifting of school closure mandates for the 2021–2022 academic year, schools have largely returned to in-person learning and after-school activities despite transmission of the Delta variant, and appearance of the Omicron variant.[41,42] As a result, the above age difference is likely to be diminished with this return over time. With the opening of schools, emergence of the Omicron variant, and younger students only now becoming eligible for vaccination, a reliance on behavioral protections (masking, handwashing, and social distancing), is still critical to preventing infection.[14,15] However, even in parts of the country with school mask mandates, there have still been outbreaks among children.[12] Given the published effectiveness of masks when donned correctly, these outbreaks suggest that difficulty in managing protective behavioral habits (such as consistent masking) is, and will likely continue to be, a strong contributor to rising infections in children.[43] Although it is important to acknowledge that interactions at school and during school-related activities are not necessarily the only sources of pediatric transmission, a recent study showed that there were significantly greater increases in pediatric SARS-CoV-2 infections in areas of the United States without school mask mandates, relative to those with them.[10] This further supports the importance of masking and other behavioral mitigation strategies. Racial, socioeconomic, and other demographic disparities have been well-documented throughout the pandemic.[2,3,6,44,45] We found that children from racially marginalized families had 570% increased odds of testing positive for SARS-CoV-2 relative to white patients. A similar trend was seen for children who were Hispanic or Latino (350% increase), compared to those who were not. These findings align with those of previous adult and pediatric series, but contrast a recent letter.[3,6,30,44,46] Although a comprehensive analysis of the determinants underlying these trends is beyond the scope of this study, there are several potential contributing factors to be noted. Those who are racially/ethnically marginalized often live in multigenerational homes and crowded areas that do not lend to efficient social distancing, propagating viral spread.[5] Additionally, inequities related to access to healthcare predispose racially/ethnically marginalized families to underlying conditions (asthma, diabetes, etc.), which are all risk factors for severe COVID-19.[47-50] Median household income analyses produced equally interesting results. Analogous to other pediatric and adult data publications, we found that patients testing positive for SARS-CoV-2 resided in areas with significantly lower median household incomes relative to patients testing negative.[44,45] Similar to trends seen for racially/ethnically marginalized individuals, barriers such as the ability to access insurance, quality education and healthcare, and adequate diets for low-income families may result in increased risks for underlying conditions and COVID-19.[47,50-53] These data, in combination with the observed racial/ethnic disparities, further highlight the need to address underlying social determinants of health both within and outside of the context of COVID-19. Limitations of our study should be acknowledged. This study was performed at a single, tertiary pediatric care facility in the Northeastern United States, and thus results may not be generalizable to other institutions. Additionally, conclusions could change based on the circulating variant. The study was conducted over a relatively short period, with a small COVID-19 (+) sample on which to base conclusions. Furthermore, approximately 25% and 33% of patients did not report their race and ethnicity, respectively. Thus, analyses using these data may be over- or underestimated. The hospital query used to identify COVID-19 (+) cases relied on the correct ICD-10 coding. COVID-19 (+) cases incorrectly defined by a code other than U07.1 would not have been captured in our query. Similarly, symptoms were determined based on documentation in the medical record. Incomplete documentation of symptoms could also have underestimated overall COVID-19 symptoms in our pediatric cohort. Moreover, it is important to acknowledge that our institution’s preoperative SARS-CoV-2 testing requirement, irrespective of symptom status, may have biased this study toward asymptomatic patients. It is possible that symptomatic patients scheduled for non-emergent procedures may have elected to cancel their surgery without undergoing testing. As a result, the relative percentage of asymptomatic to symptomatic patients may be overestimated.

CONCLUSIONS AND RECOMMENDATIONS

Accurate and universal preoperative testing is essential to identify pediatric patients infected with SARS-CoV-2 before surgery. Furthermore, screening practices reliant on symptoms alone are ineffective. In light of only newly expanded vaccination eligibility by age, and continued prevalence and emergence of the Delta and Omicron variants respectively, we strongly recommend that all nonemergent patients undergo preoperative SARS-CoV-2 testing, regardless of symptom status. When COVID-19 reaches an endemic stage, we would suggest testing only during local/regional surges. However, as we continue to navigate emerging variants/surges at present, preoperative testing of all non-emergent pediatric patients is recommended.[54] In our sample, patients from racially/ethnically marginalized communities, and those of lower relative economic status were more likely to test positive for SARS-CoV-2. Additional investigation is necessary to address the underlying health determinants responsible for these inequities.
  43 in total

1.  SARS-CoV-2 Positivity Rates Among Children of Racial and Ethnic Minority Groups in Mississippi.

Authors:  Kengo Inagaki; Padma Garg; Charlotte V Hobbs
Journal:  Pediatrics       Date:  2020-10-28       Impact factor: 7.124

2.  Absence of Apparent Transmission of SARS-CoV-2 from Two Stylists After Exposure at a Hair Salon with a Universal Face Covering Policy - Springfield, Missouri, May 2020.

Authors:  M Joshua Hendrix; Charles Walde; Kendra Findley; Robin Trotman
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2020-07-17       Impact factor: 17.586

3.  Coronavirus Disease 2019 in Children - United States, February 12-April 2, 2020.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2020-04-10       Impact factor: 17.586

4.  Disproportionate Impact of COVID-19 Pandemic on Racial and Ethnic Minorities.

Authors:  Brad Boserup; Mark McKenney; Adel Elkbuli
Journal:  Am Surg       Date:  2020-11-24       Impact factor: 0.688

Review 5.  SARS-CoV-2 in children: spectrum of disease, transmission and immunopathological underpinnings.

Authors:  Phoebe C M Williams; Annaleise R Howard-Jones; Peter Hsu; Pamela Palasanthiran; Paul E Gray; Brendan J McMullan; Philip N Britton; Adam W Bartlett
Journal:  Pathology       Date:  2020-08-19       Impact factor: 5.306

6.  Favorable postoperative outcomes for children with COVID-19 infection undergoing surgical intervention: Experience at a free-standing children's hospital.

Authors:  Steven C Mehl; Jackquelin M Loera; Sohail R Shah; Adam M Vogel; Sara C Fallon; Chris D Glover; Laura A Monson; Joyce A Enochs; Larry H Hollier; Monica E Lopez
Journal:  J Pediatr Surg       Date:  2021-01-27       Impact factor: 2.545

7.  Characteristics of patients with coronavirus disease (COVID-19) confirmed using an IgM-IgG antibody test.

Authors:  Jiajia Xie; Chengchao Ding; Jing Li; Yulan Wang; Hui Guo; Zhaohui Lu; Jinquan Wang; Changcheng Zheng; Tengchuan Jin; Yong Gao; Hongliang He
Journal:  J Med Virol       Date:  2020-05-07       Impact factor: 2.327

8.  Systematic review of COVID-19 in children shows milder cases and a better prognosis than adults.

Authors:  Jonas F Ludvigsson
Journal:  Acta Paediatr       Date:  2020-04-14       Impact factor: 4.056

9.  A systematic review and meta-analysis of children with coronavirus disease 2019 (COVID-19).

Authors:  Xiaojian Cui; Zhihu Zhao; Tongqiang Zhang; Wei Guo; Wenwei Guo; Jiafeng Zheng; Jiayi Zhang; Cuicui Dong; Ren Na; Lisheng Zheng; Wenliang Li; Zihui Liu; Jia Ma; Jinhu Wang; Sijia He; Yongsheng Xu; Ping Si; Yongming Shen; Chunquan Cai
Journal:  J Med Virol       Date:  2020-09-28       Impact factor: 20.693

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