# Differences in the Evolution of Clinical, Biochemical, and Hematological Indicators in Hospitalized Patients with COVID-19 According to Their Vaccination Scheme: A Cohort Study in One of the World’s Highest Hospital Mortality Populations

**Authors:** Martha A. Mendoza-Hernandez, Jose Guzman-Esquivel, Marco A. Ramos-Rojas, Vanessa V. Santillan-Luna, Carmen A. Sanchez-Ramirez, Gustavo A. Hernandez-Fuentes, Janet Diaz-Martinez, Valery Melnikov, Fabian Rojas-Larios, Margarita L. Martinez-Fierro, Daniel Tiburcio-Jimenez, Iram P. Rodriguez-Sanchez, Osiris G. Delgado-Enciso, Ariana Cabrera-Licona, Ivan Delgado-Enciso

PMC · DOI: 10.3390/vaccines12010072 · Vaccines · 2024-01-11

## TL;DR

This study found that vaccinated patients with COVID-19 had better outcomes, especially those who received the Pfizer vaccine, in a high-mortality Mexican hospital cohort.

## Contribution

The study provides novel evidence on how different vaccines affect clinical outcomes in hospitalized patients in a high-mortality population.

## Key findings

- Pfizer-vaccinated patients had a 2.4-times lower risk of death compared to unvaccinated individuals.
- AstraZeneca vaccination did not significantly reduce mortality compared to no vaccination.
- Pfizer recipients showed lower levels of inflammatory markers like ferritin and D-dimer.

## Abstract

COVID-19 vaccines primarily prevent severe illnesses or hospitalization, but there is limited data on their impact during hospitalization for seriously ill patients. In a Mexican cohort with high COVID-19 mortality, a study assessed vaccination’s effects. From 2021 to 2022, 462 patients with 4455 hospital days were analyzed. The generalized multivariate linear mixed model (GENLINMIXED) with binary logistic regression link, survival analysis and ROC curves were used to identify risk factors for death. The results showed that the vaccinated individuals were almost half as likely to die (adRR = 0.54, 95% CI = 0.30–0.97, p = 0.041). When stratifying by vaccine, the Pfizer group (BNT162b2) had a 2.4-times lower risk of death (adRR = 0.41, 95% CI = 0.2–0.8, p = 0.008), while the AstraZeneca group (ChAdOx1-S) group did not significantly differ from the non-vaccinated (adRR = 1.04, 95% CI = 0.5–2.3, p = 0.915). The Pfizer group exhibited a higher survival, the unvaccinated showed increasing mortality, and the AstraZeneca group remained intermediate (p = 0.003, multigroup log-rank test). Additionally, BNT162b2-vaccinated individuals had lower values for markers, such as ferritin and D-dimer. Biochemical and hematological indicators suggested a protective effect of both types of vaccines, possibly linked to higher lymphocyte counts and lower platelet-to-lymphocyte ratio (PLR). It is imperative to highlight that these results reinforce the efficacy of COVID-19 vaccines. However, further studies are warranted for a comprehensive understanding of these findings.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, VCP (valosin containing protein) [NCBI Gene 7415] {aka CDC48, FTDALS6, TERA, p97}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}
- **Diseases:** smoker (MESH:C000719328), Systemic arterial hypertension (MESH:D000081029), coronavirus disease (MESH:D018352), hyper (MESH:D007589), hypertension (MESH:D006973), Death (MESH:D003643), AKI (MESH:D058186), PSI (MESH:D045169), lung damage (MESH:D008171), Illness (MESH:D002908), Chronic kidney disease (MESH:D051436), injury to people or property (MESH:C000719191), infections (MESH:D007239), hypoxemia (MESH:D000860), function (MESH:D003291), COVID (MESH:D000086382), Pneumonia (MESH:D011014), neutrophilia (MESH:C563010), hepatic damage (MESH:D056486), diabetes (MESH:D003920), Hospital (MESH:D003428), bacterial co-infection (MESH:D060085), bacterial infection (MESH:D001424), hyper-inflammatory (MESH:D007249), smoking (MESH:D015208), lymphopenia (MESH:D008231), CKD (MESH:D012080)
- **Species:** Adenoviridae (family) [taxon 10508], Gammacoronavirus (genus) [taxon 694013], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** BNT162b2 — Mus musculus (Mouse), Hybridoma (CVCL_J920), ChAdOx1-S — Gallus gallus (Chicken), Chicken bursal lymphoma, Cancer cell line (CVCL_1T28)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10821037/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC10821037/full.md

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Source: https://tomesphere.com/paper/PMC10821037