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1.
Pediatr Blood Cancer ; 70(3): e30193, 2023 03.
Article in English | MEDLINE | ID: covidwho-20233114

ABSTRACT

Vulnerable patient populations have seen decreased rates of vaccination against SARS-CoV2-19 (COVID-19) due to hesitancies and distrust, magnified by a paucity of data for certain populations. The rate of COVID-19 vaccination in children with sickle cell disease (SCD) remains low despite the risk for severe complications, resulting in continued infections and hospitalizations from COVID-19. We sought to describe vaccine reactions, including vaso-occlusive crises, emergency department visits, and hospitalizations, in children with SCD. Our findings will start to provide the necessary vaccine side effect data to inform patients, caregivers, and clinicians considering the COVID-19 primary vaccination series.


Subject(s)
Anemia, Sickle Cell , COVID-19 Vaccines , COVID-19 , Drug-Related Side Effects and Adverse Reactions , Child , Humans , Anemia, Sickle Cell/therapy , Anemia, Sickle Cell/drug therapy , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19/complications , COVID-19 Vaccines/adverse effects , RNA, Viral/therapeutic use , SARS-CoV-2
2.
J Pediatr Hematol Oncol ; 45(2): 88-90, 2023 03 01.
Article in English | MEDLINE | ID: covidwho-2222905

ABSTRACT

The Coronavirus Disease 2019 (COVID-19) pandemic led to the swift development of multiple vaccinations. Vaccine side effects were well-documented in the healthy adult cohort and included fever and lymphadenopathy, however, side effects in the pediatric immunocompromised population have not been reported. This retrospective study investigated vaccine-eligible children and adolescent young adult oncology patients 12 to 35 years old. We found uncommon, mild, and self-limiting side effects among pediatric cancer patients and survivors. This data will help guide pediatric and AYA oncologists in providing anticipatory guidance and serve as a guide to managing lymphadenopathy as a potential confounder of malignancy.


Subject(s)
COVID-19 , Drug-Related Side Effects and Adverse Reactions , Lymphadenopathy , Neoplasms , Adolescent , Young Adult , Humans , Child , Adult , COVID-19 Vaccines , Retrospective Studies , Neoplasms/epidemiology , Vaccination
4.
J Infect ; 82(3): 329-338, 2021 03.
Article in English | MEDLINE | ID: covidwho-1062466

ABSTRACT

BACKGROUND: The clinical impact of severe coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), in immunocompromised patients has not been systematically evaluated. METHODS: We reviewed current literature reporting on COVID-19 in cancer (CA), hematopoietic cell (HCT), and solid organ transplant (SOT) patients and compared their clinical data and outcomes to the general population. For adult CA, HCT and SOT patients, an extensive search strategy retrieved all articles published until July 20, 2020 by combining the terms coronavirus, coronavirus infection, COVID-19, and SARS-CoV-2 in PubMed, Cochrane, and Web of Science, and following the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines. For the pediatric CA cohort, a global COVID-19 registry was used. For the general population cohort, a large meta-analysis was used to compare pooled prevalence estimates, and two large meta-analyses were utilized to serve as pooled comparators for hospitalized COVID-19 patients. FINDINGS: Compared to the general population, adult CA and SOT patients with COVID-19 had higher comorbidities, greater levels of inflammatory markers at diagnosis, and higher rates of intensive care and hospital mortality. Pediatric CA patients and HCT patients with COVID-19 tended to have clinical presentations and outcomes similar to the general population. INTERPRETATION: To our knowledge, this is the first systematic review evaluating COVID-19 phenotype and outcomes in immunocompromised patients and comparing them to the general population, which shows that hospital outcomes appear to be worse in adult CA and SOT patients, potentially due to their higher co-morbidity burden. FUNDING: None.


Subject(s)
COVID-19 , Hematopoietic Stem Cell Transplantation , Neoplasms , Organ Transplantation , Adult , Child , Humans , Immunocompromised Host , Organ Transplantation/adverse effects , SARS-CoV-2
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