Evidence map›Paper›PMID 39535625›Full record

ArticleInflammopharmacology2025

Role of intravenous vitamin C on outcomes in hospitalized patients with moderate or severe COVID-19: a real life data of Turkish patients.

Burak Uz, Özgür İnce, Can Gümüş, Feyzi Gökosmanoğlu, Emrah Gökay Özgür, Gülnaz Nural Bekiroğlu

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Article in Inflammopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Burak UzDepartment of Hematology, Medicana International Samsun Hospital, Samsun, Türkiye. burakuz78@gmail.com.ORCID http://orcid.org/0000-0001-9326-4301
Özgür İnceDepartment of Chest Diseases, Medicana International Samsun Hospital, Samsun, Türkiye.
Can GümüşDepartment of Clinical Pharmacy, Medicana International Samsun Hospital, Samsun, Türkiye.
Feyzi GökosmanoğluDepartment of Endocrinology, Medicana International Samsun Hospital, Samsun, Türkiye.
Emrah Gökay ÖzgürDepartment of Biostatistics, Marmara University School of Medicine, İstanbul, Türkiye.
Gülnaz Nural BekiroğluDepartment of Biostatistics, Marmara University School of Medicine, İstanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to examine the efficacy of intravenous vitamin C (IV-VC) in the treatment of hospitalized patients with moderate or severe COVID-19.

methodWe conducted a single-center and retrospective study including patients with COVID-19 diagnosis who were hospitalized. Patients were categorized into three groups as those who received low-dose (LDVC group, 2 g/day, n = 183) or high-dose IV-VC (HDVC group, 25 g/day, n = 41) and who did not receive IV-VC (control group, n = 46).

results270 patients aged 19-97 years were enrolled. The median length of stay (LOS) was significantly high (9 days) in patients treated with high-dose VC when compared to patients treated with low-dose VC and control patients (6 vs 5 days, respectively). Need for intensive care unit (ICU) transfer was found to be significantly low in patients treated with low-dose VC (25.7%); contrarily, control patients had significantly higher rates of ICU transfer (67.4%), when compared to patients treated with high-dose VC (39%). Mortality of the LDVC group was significantly lower than that of the HDVC group (11.5 vs 29.3%). However, mortality rates were similar between the control and HDVC groups (21.7 vs 29.3%). According to the multivariate stepwise logistic regression mortality analysis, percent of change (∆%)-BUN was the most significant variable (p < 0.001), the second significant variable was ∆%-AST (p = 0.002), the third significant variable was respiratory distress (p = 0.002), and the fourth significant variable was the IV-VC groups (p = 0.017). The mortality risk of those in the LDVC group was 10.2 times low compared to the control group. Similarly, the risk of mortality in the HDVC group was 6.5 times lower than that of the control group.

conclusionEspecially low and continious doses of IV-VC suggest fewer days of in-hospital LOS and survival benefit in hospitalized patients with moderate and severe COVID-19. Logistic regression analysis revealed that high-dose VC supplementation also had a mortality-reducing effect.

Indexed as

Ascorbic AcidCOVID-19 Drug TreatmentAdministration, IntravenousAdultAgedAged, 80 and overCOVID-19FemaleHospitalizationHospital MortalityHumansIntensive Care UnitsLength of StayMaleMiddle AgedRetrospective StudiesAscorbic AcidCOVID-19Intensive care unitIntravenous vitamin CLength of stayMortality

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.