Risk Factors Associated With Hospitalization and Death in COVID-19 Breakthrough Infections

Author:

Suleyman Geehan12,Fadel Raef3,Brar Indira12ORCID,Kassab Rita3,Khansa Rafa3,Sturla Nicholas3,Alsaadi Ayman3,Latack Katie4,Miller Joseph5ORCID,Tibbetts Robert6,Samuel Linoj6,Alangaden George12,Ramesh Mayur1ORCID

Affiliation:

1. Division of Infectious Disease, Henry Ford Health System , Detroit, Michigan , USA

2. Wayne State University , Detroit , Michigan , USA

3. Department of Internal Medicine, Henry Ford Hospital , Detroit , Michigan , USA

4. Department of Public Health Sciences, Henry Ford Health System , Detroit , Michigan , USA

5. Department of Emergency Medicine, Henry Ford Hospital , Detroit , Michigan , USA

6. Clinical Microbiology, Henry Ford Health System , Detroit , Michigan , USA

Abstract

Abstract Background Characterizations of coronavirus disease 2019 (COVID-19) vaccine breakthrough infections are limited. We aim to characterize breakthrough infections and identify risk factors associated with outcomes. Methods This was a retrospective case series of consecutive fully vaccinated patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a multicenter academic center in Southeast Michigan, between December 30, 2020, and September 15, 2021. Results A total of 982 patients were identified; the mean age was 57.9 years, 565 (59%) were female, 774 (79%) were White, and 255 (26%) were health care workers (HCWs). The median number of comorbidities was 2; 225 (23%) were immunocompromised. BNT162b2 was administered to 737 (75%) individuals. The mean time to SARS-CoV-2 detection was 135 days. The majority were asymptomatic or exhibited mild to moderate disease, 154 (16%) required hospitalization, 127 (13%) had severe–critical illness, and 19 (2%) died. Age (odds ratio [OR], 1.14; 95% CI, 1.04–1.07; P < .001), cardiovascular disease (OR, 3.02; 95% CI, 1.55–5.89; P = .001), and immunocompromised status (OR, 2.57; 95% CI, 1.70–3.90; P < .001) were independent risk factors for hospitalization. Additionally, age (OR, 1.06; 95% CI, 1.02–1.11; P = .006) was significantly associated with mortality. HCWs (OR, 0.15; 95% CI, 0.05–0.50; P = .002) were less likely to be hospitalized, and prior receipt of BNT162b2 was associated with lower odds of hospitalization (OR, 0.436; 95% CI, 0.303–0.626; P < .001) and/or death (OR, 0.360; 95% CI, 0.145–0.898; P = .029). Conclusions COVID-19 vaccines remain effective at attenuating disease severity. However, patients with breakthrough infections necessitating hospitalization may benefit from early treatment modalities and COVID-19-mitigating strategies, especially in areas with substantial or high transmission rates.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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