COVID-19 Vaccine Safety Studies among Vulnerable Populations: A Systematic Review and Meta-analysis of 120 Observational Studies and Randomized Clinical Trials

Publication date: Dec 28, 2024

BACKGROUND The COVID-19 vaccines were rapidly developed and tested, but concerns about vaccine-related adverse events remain, especially in vulnerable groups like pregnant women, children, and those with certain health conditions. This review aims to summarize rates of such adverse events in individuals often not included in randomized clinical trials (RCT). METHOD From December 2019 to February 2022, we searched Embase and Medline for observational studies and RCTs on adverse events post-COVID-19 vaccination in vulnerable groups. We examined serious and non-serious events in individuals with specific medical conditions, infants, children, pregnant individuals, and socioeconomically disadvantaged individuals. Cumulative risks for all events were calculated. The Incidence rate (IR) and 95% confidence intervals were reported for those studies that met the follow-up period criteria based on the referenced literature. For events with data on exposed and unexposed groups, we calculated the odds ratio. Pooled incidence rates were calculated per 1000 person-days using a random-effects model. Sub-group analyses were conducted based on vaccine types and doses, with heterogeneity assessed using I2. FINDINGS Of the 4,254 papers, 235 met eligibility criteria, including 120 studies with 171,073 participants (113 observational, eight RCTs. We examined 17 severe and 7 non-severe adverse event categories. Lymphadenopathy (IR: 1.95[1.20;3.19]), autoimmune disease and multiple sclerosis flare-up (1.13 [0.47;2.68]), and cardiac symptoms (0.26[0.00;10.58]) were the most severe events. Allergic reactions were more common among autoimmune (7.03[4.10;12.06]) and cancer (4.87[2.21;10.76]) groups. vaccinees who received the second dose of vaccine had higher proportions of disease flare-ups (39.27 [18.08;85.31] vs 22.13 [10.22; 47.93]); cardiac symptoms (6.11[2.05-18.22] vs 3.78[2.53-5.65]); and cardiac events (5.34[1.69;16.90] vs 5.05[1.40,18.19]) in observational studies. INTERPRETATION This review highlights COVID-19 vaccine safety in vulnerable populations, enhancing vaccination strategies. Further real-world research is needed to validate and extend our findings, especially in addressing safety gaps among vulnerable groups.

PDF

Concepts Keywords
Gastroenterologist Adverse
Korean Al
Leukemia Covid
Vaccination141 Cross
Dose
Events
Medrxiv
Mrna
Pooled
Preprint
Safety
Sectional
Vaccination
Vaccine
Vaccines

Semantics

Type Source Name
disease MESH COVID-19
drug DRUGBANK Methionine
disease MESH Lymphadenopathy
disease MESH autoimmune disease
disease MESH multiple sclerosis
disease MESH Allergic reactions
disease MESH cancer
disease MESH cardiac events
disease MESH complications
disease IDO process
disease MESH death
disease MESH arthralgia
disease MESH syndrome
disease IDO quality
disease IDO country
disease MESH immune disease
disease MESH Dravet syndrome
disease MESH myocardial infarction
disease MESH myocarditis
disease MESH chest pain
disease IDO symptom
disease MESH Recurrence
disease MESH hypertension
disease MESH Paresthesia
disease MESH numbness
disease MESH tremor
disease MESH tinnitus
disease MESH gestational hypertension
disease MESH stillbirth
disease MESH Thromboembolism
disease MESH neonatal deaths
disease IDO susceptibility
disease MESH pericarditis
disease MESH anaphylaxis
disease MESH seizures
disease MESH urticaria
disease IDO immunosuppression
disease MESH immunocompromised patients
disease MESH cardiac arrhythmias
disease MESH Stroke
disease MESH Arthritis
disease MESH Gastrointestinal Disease
disease MESH HIV infection
pathway REACTOME HIV Infection
disease MESH systemic sclerosis
disease MESH myopathies
disease IDO history
disease MESH Emergency
disease MESH systemic lupus erythematosus
pathway KEGG Systemic lupus erythematosus
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH Inflammatory Bowel Disease
pathway KEGG Inflammatory bowel disease
disease MESH rheumatic diseases
disease MESH Epilepsy
disease MESH Colitis
disease MESH Psoriasis
pathway REACTOME Fertilization
disease MESH Pregnancy Outcomes
disease MESH multiple myeloma
disease MESH chronic lymphocytic leukemia

Download Document

(Visited 1 times, 1 visits today)