Hydrogenology
Hydrogenology editorial study record

Effect of hydrogen/oxygen therapy for ordinary COVID-19 patients: a propensity-score matched case-control study

Zeng Y, Guan W, Wang K, Jie Z, Zou X, Tan X, Li X, Chen X, Ren X, Jiang J, Zheng Z, Shi J, Zhong N. · BMC Infectious Diseases. 2023;23:440.

HumanInhaled H₂Published 2023
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Human

Reported design

Three-centre retrospective propensity-score-matched case-control study

Research topic

Respiratory health

Administration classification

Inhaled H₂

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Adults hospitalized in China with ordinary, non-severe COVID-19 between December 2019 and March 2020.

Sample

180 eligible records before matching: 42 H₂/O₂ and 138 oxygen. The principal 1:2 matched analysis included 33 H₂/O₂ and 55 oxygen patients.

Duration

At least six hours/day for more than seven consecutive days; clinical follow-up through discharge and day-28 discharge-rate analysis.

Intervention

Nasal-mask H₂/O₂ for at least six hours daily on more than seven consecutive days, plus standard care.

Hydrogen form

Brown's gas / oxyhydrogen at an H₂:O₂ volume ratio of 2:1.

H₂ specification

Total mixture flow was 3.0 L/min; direct 2:1 calculation gives H₂ flow 2.0 L/min and O₂ flow 1.0 L/min.

H₂ flow

2,000 mL/min.

O₂ delivered with H₂

1,000 mL/min.

Comparator

Standard care plus low-flow air/oxygen therapy below 3.0 L/min, with duration adjusted clinically.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Hospital length of stay, discharge by days 14, 21 and 28, day-5 SpO₂, vital signs, respiratory symptoms, adverse events and mortality.

Reported result

Matched median stay was 12 versus 13 days and later discharge rates and day-5 SpO₂ favored H₂/O₂. Day-14 discharge did not differ significantly. Gender and time from symptom onset were not associated with stay within the H₂/O₂ subgroup; no significant adverse effects were observed.

Results-extraction completeness

The complete free PMC article and supplementary-analysis descriptions were checked for the unmatched and matched cohorts, gas ratio/flow, schedule, primary and null results, safety, funding and conflicts.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Retrospective nonrandomized study with small matched groups, propensity matching on only age, sex and time to admission, possible unmeasured confounding, incomplete post-treatment laboratory/SpO₂ data and early-pandemic care. Public Chinese grants were reported and authors declared no competing interests.

Applies directly to

Ordinary COVID-19 hospitalized during the original 2019–2020 outbreak; contemporary treatment relevance is uncertain.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 37386364 · DOI: 10.1186/s12879-023-08424-4

Publisher access

Free full article in PubMed Central.

Extraction basis

Complete PMC article, supplementary-analysis descriptions and PubMed metadata; full-text extraction checked 9 August 2026.

Record revision

2026-08-10