Analysis of mRNA COVID-19 Vaccine Uptake Among Immunocompromised Individuals in a Large US Health System.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
03 Jan 2023
Historique:
entrez: 20 1 2023
pubmed: 21 1 2023
medline: 25 1 2023
Statut: epublish

Résumé

Immunocompromised individuals are at increased risk for severe outcomes due to SARS-CoV-2 infection. Given the varying and complex nature of COVID-19 vaccination recommendations, it is important to understand COVID-19 vaccine uptake in this vulnerable population. To assess mRNA COVID-19 vaccine uptake and factors associated with uptake among immunocompromised individuals from December 14, 2020, through August 6, 2022. This cohort study was conducted with patients of Kaiser Permanente Southern California (KPSC), an integrated health care system in the US. The study included patients aged 18 years or older who were immunocompromised (individuals with an immunocompromising condition or patients who received immunosuppressive medications in the year prior to December 14, 2020) and still met criteria for being immunocompromised 1 year later. Age, sex, self-identified race and ethnicity, prior positive COVID-19 test result, immunocompromising condition, immunomodulating medication, comorbidities, health care utilization, and neighborhood median income. Outcomes were the number of doses of mRNA COVID-19 vaccine received and the factors associated with receipt of at least 4 doses, estimated by hazard ratios (HRs) and 95% Wald CIs via Cox proportional hazards regression. Statistical analyses were conducted between August 9 and 23, 2022. Overall, 42 697 immunocompromised individuals met the study eligibility criteria. Among these, 18 789 (44.0%) were aged 65 years or older; 20 061 (47.0%) were women and 22 635 (53.0%) were men. With regard to race and ethnicity, 4295 participants (10.1%) identified as Asian or Pacific Islander, 5174 (12.1%) as Black, 14 289 (33.5%) as Hispanic, and 17 902 (41.9%) as White. As of the end of the study period and after accounting for participant censoring due to death or disenrollment from the KPSC health plan, 78.0% of immunocompromised individuals had received a third dose of mRNA COVID-19 vaccine. Only 41.0% had received a fourth dose, which corresponds to a primary series and a monovalent booster dose for immunocompromised individuals. Uptake of a fifth dose was only 0.9% following the US Centers for Disease Control and Prevention (CDC) recommendation to receive a second monovalent booster (ie, fifth dose). Adults aged 65 years or older (HR, 3.95 [95% CI, 3.70-4.22]) were more likely to receive at least 4 doses compared with those aged 18 to 44 years or 45 to 64 years (2.52 [2.36-2.69]). Hispanic and non-Hispanic Black adults (HR, 0.77 [95% CI, 0.74-0.80] and 0.82 [0.78-0.87], respectively, compared with non-Hispanic White adults), individuals with prior documented SARS-CoV-2 infection (0.71 [0.62-0.81] compared with those without), and individuals receiving high-dose corticosteroids (0.88 [0.81-0.95] compared with those who were not) were less likely to receive at least 4 doses. These findings suggest that adherence to CDC mRNA monovalent COVID-19 booster dose recommendations among immunocompromised individuals was low. Given the increased risk for severe COVID-19 in this vulnerable population and the well-established additional protection afforded by booster doses, targeted and tailored efforts to ensure that immunocompromised individuals remain up to date with COVID-19 booster dose recommendations are warranted.

Identifiants

pubmed: 36662525
pii: 2800691
doi: 10.1001/jamanetworkopen.2022.51833
pmc: PMC9860519
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2251833

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Auteurs

Sara Y Tartof (SY)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.
Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California.

Jeff M Slezak (JM)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Laura Puzniak (L)

Pfizer Inc, Collegeville, Pennsylvania.

Vennis Hong (V)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Timothy B Frankland (TB)

Kaiser Permanente Hawaii Center for Integrated Health Care Research, Honolulu.

Fagen Xie (F)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Bradley K Ackerson (BK)

Southern California Permanente Medical Group, Harbor City.

Harpreet Takhar (H)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Oluwaseye A Ogun (OA)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Sarah Simmons (S)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Joann M Zamparo (JM)

Pfizer Inc, Groton, Connecticut.

Hung Fu Tseng (HF)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Luis Jodar (L)

Pfizer Inc, Collegeville, Pennsylvania.

John M McLaughlin (JM)

Pfizer Inc, Collegeville, Pennsylvania.

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Classifications MeSH