Observational studyBMJ open2026
Respiratory syncytial virus infection in COPD exacerbations: the RECODE study protocol.
Observational study in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06735612 (Respiratory Syncytial Virus Infection in Exacerbations of Chronic Obstructive Pulmonary Diasease), which is not on this map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Respiratory Syncytial Virus Infection in Exacerbations of Chronic Obstructive Pulmonary Diasease: the RECODE Study
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionPatients with chronic obstructive pulmonary disease (COPD) often suffer episodes of exacerbation (ECOPD). Respiratory syncytial virus (RSV) is an increasingly recognised cause of illness in adults. Yet the prevalence of RSV during ECOPD and its association with clinically relevant outcomes remain insufficiently defined. The RECODE study sought to determine the prevalence of RSV infection in patients with ECOPD and to assess the association between RSV and hospitalisation, length of stay, acute cardiovascular events and/or death. METHODS AND ANALYSIS: Prospective, multicentre, observational, controlled (RSV-positive cases vs RSV-negative controls), longitudinal study (NCT06735612). Adults ≥50 years with ECOPD will be enrolled at urgent-care presentation (V1), contacted by telephone at day 15 (V2) and seen in the clinic at 3 months (V3). RSV status will be determined by Reverse Transcription (RT-PCR) on nasopharyngeal swabs; additional measures include paired serology, routine clinical data, spirometry at V3 and predefined outcomes. ETHICS AND DISSEMINATION: The leading Ethics Committee was that of Clinic Barcelona (HCB/2024/0771). All participating centres accepted this approval or requested local approval from their respective Institutional Review Boards (Appendix). Results will be disseminated in international publications and meeting presentations as well as in a plain language summary to be distributed among participating patients. TRIAL REGISTRATION NUMBER: NCT06735612.
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Registered trials
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.