# Weekend admissions and outcomes in patients with pneumonia: a systematic review and meta-analysis

**Authors:** Jiayao Lu, Jing Yang, Xiaofei Cai

PMC · DOI: 10.3389/fpubh.2023.1248952 · 2024-01-17

## TL;DR

This study examines if pneumonia patients admitted on weekends have worse outcomes than those admitted on weekdays.

## Contribution

The study provides a meta-analysis of weekend admissions and outcomes in pneumonia patients, challenging the 'weekend effect' hypothesis.

## Key findings

- Weekend admissions were associated with a marginally higher but non-significant in-hospital mortality risk.
- No significant differences were found in 30-day mortality, ICU admission, or readmission rates between weekend and weekday admissions.

## Abstract

To document pooled evidence on the association between weekend hospital admissions and the potential risks of mortality, intensive care requirements, and readmission among patients with pneumonia.

We performed a systematic search across the PubMed, EMBASE, and Scopus databases. We collected observational studies exploring the association between weekend admissions and outcomes of interest in patients with pneumonia. To analyze the data, we used a random effects model and expressed the effect sizes as pooled odds ratios (ORs) accompanied by their respective 95% confidence intervals (CIs).

The analysis comprised data from 13 retrospective studies. Compared to patients admitted on weekdays, those admitted during the weekend had a non-statistically significant marginally higher risk of in-hospital mortality (OR, 1.02; 95% CI, 1.00, 1.04) but similar 30-day mortality after admission (OR, 1.03; 95% CI, 0.97, 1.10), and similar risks of admission to intensive care unit (OR, 1.04; 95% CI, 0.98, 1.11) and re-admission (OR, 0.85; 95% CI, 0.65–1.12).

Our findings do not support the presence of a “weekend effect” in patients with pneumonia.

PROSPERO, identifier CRD42023425802, https://www.crd.york.ac.uk/prospero/.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** death (MESH:D003643), intestinal obstruction (MESH:D007415), lung infection (MESH:D012141), cardiac arrest (MESH:D006323), trauma (MESH:D014947), aortic aneurysm (MESH:D001014), pulmonary embolism (MESH:D011655), COVID-19 (MESH:D000086382), Pneumonia (MESH:D011014), acute bacterial pneumonia (MESH:D018410), breast cancer (MESH:D001943), community-acquired pneumonia (MESH:D003147), hip fracture (MESH:D006620), arrhythmia (MESH:D001145)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10832039/full.md

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Source: https://tomesphere.com/paper/PMC10832039