# Age–Comorbidity Interactions and Clinical Outcomes in Septic Shock: An Emergency Department-Based Multicenter Cohort Study

**Authors:** Seung Jin Maeng, Jong Eun Park, Gun Tak Lee, Sung Yeon Hwang, Minha Kim, Sejin Heo, Tae Ho Lim, Sung Phil Chung, Sung-Hyuk Choi, Tae Gun Shin

PMC · DOI: 10.3390/healthcare14060722 · Healthcare · 2026-03-12

## TL;DR

Older patients with comorbidities have higher mortality in septic shock, suggesting risk assessments should consider both age and health conditions.

## Contribution

This study identifies a significant interaction between age and comorbidities in predicting mortality in septic shock patients.

## Key findings

- Elderly patients with comorbidities had the highest 28-day mortality rate (27.5%).
- The presence of any comorbidity independently increased mortality odds (aOR 2.67).
- Age-related mortality gradients were modified by comorbidity burden (p for interaction = 0.008).

## Abstract

What are the main findings?
Age and comorbidities are independently associated with mortality in septic shock.There was a significant interaction between age and comorbidity status in mortality.

Age and comorbidities are independently associated with mortality in septic shock.

There was a significant interaction between age and comorbidity status in mortality.

What are the implications of the main findings?
The strong age–comorbidity interaction suggests that risk assessment should move beyond age alone and incorporate comorbidity profiles in patients with sepsis.

The strong age–comorbidity interaction suggests that risk assessment should move beyond age alone and incorporate comorbidity profiles in patients with sepsis.

Background: Sepsis remains a leading cause of mortality worldwide. This study evaluated the independent and combined effects of age and chronic comorbidities on clinical outcomes in patients with septic shock. Methods: We conducted a multicenter retrospective observational study to evaluate the factors associated with 28-day mortality in the Korean Shock Society registry between 2015 and 2023. Adults with suspected infection and refractory hypotension or hypoperfusion within 6 h of emergency department (ED) arrival were included. Patients were grouped by age (<50, 50–74, and ≥75 years) and comorbidity status. Comorbidities encompass major chronic conditions including hypertension, diabetes mellitus, malignancy, history of organ transplant, dementia, nursing home residence, chronic disease of cardiac, lung, liver, and kidney. The primary outcome was 28-day mortality. Multivariable logistic regression analysis was used. Results: Among 8787 patients (median age 70.2 years), the 28-day mortality rate was 22.9% (n = 2018). Elderly patients with comorbidities had the highest mortality (27.5%). Additionally, patients aged over 50 with at least one comorbidity accounted for 18% of the total cohort (n = 1605) but accounted for nearly 80% of all 28-day deaths. Although younger patients without comorbidities represented a small subgroup, their mortality was not negligible (7.3%) and was substantially higher with comorbidities (22.2%). Compared with patients <50 years, adjusted odds ratios (aORs) of 28-day mortality were 1.81 (95% CI, 1.08–3.03) for 50–74 years and 3.21 (95% CI, 1.92–5.37) for ≥75. The presence of any comorbidities was independently associated with higher odds of 28-day mortality compared with no comorbidity (aOR 2.67; 95% CI, 1.57–4.54). A significant interaction between age and comorbidity status (p for interaction = 0.008) suggested that the age-related gradient in mortality differed depending on comorbidity burden. Conclusions: Age and comorbidities were both significantly associated with septic shock mortality, and their significant interaction demonstrates effect modification, indicating that the prognostic impact of comorbidities differs by age group and that age-related mortality gradients are influenced by comorbidity burden.

## Linked entities

- **Diseases:** diabetes mellitus (MONDO:0005015), malignancy (MONDO:0004992), dementia (MONDO:0001627), cardiac disease (MONDO:0005267), lung disease (MONDO:0005275), liver disease (MONDO:0005154), kidney disease (MONDO:0001343)

## Full-text entities

- **Diseases:** diabetes mellitus (MESH:D003920), chronic disease of cardiac, lung, liver, (MESH:D029424), hypertension (MESH:D006973), Sepsis (MESH:D018805), kidney (MESH:D007674), deaths (MESH:D003643), hypotension (MESH:D007022), malignancy (MESH:D009369), Shock (MESH:D012769), Septic Shock (MESH:D012772), infection (MESH:D007239), dementia (MESH:D003704)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026241/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026241/full.md

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Source: https://tomesphere.com/paper/PMC13026241