# Beyond Respiratory Support: Clinical Profiles and Factors Associated with Mortality in Heart Failure Patients Admitted to the ICU

**Authors:** Duygu Kayar Calili, Suleyman Kalayci, Iffet Tiftikci, Elif Unal Kaya, Demet Bolukbasi, Seval Izdes

PMC · DOI: 10.3390/jcm15041334 · Journal of Clinical Medicine · 2026-02-08

## TL;DR

This study examines heart failure patients in the ICU and finds that those needing invasive ventilation have worse outcomes due to higher disease severity.

## Contribution

The study identifies specific clinical factors linked to mortality in heart failure patients receiving different respiratory therapies in the ICU.

## Key findings

- Patients on invasive mechanical ventilation had higher mortality and worse clinical indicators like elevated lactate and NT-proBNP.
- APACHE II scores, vasopressor use, and NT-proBNP levels were independently associated with mortality.
- Invasive ventilation was linked to longer ICU stays and more severe disease burden.

## Abstract

Background: Patients with heart failure (HF) admitted to the intensive care unit (ICU) often require respiratory support, yet comparative data on different respiratory modalities in this population remain limited. The aim of our study was to analyze clinical characteristics and outcomes of HF patients in the ICU receiving various respiratory therapies, while also identifying factors associated with mortality. Methods: This retrospective observational study categorized patients (n = 692) based on their respiratory treatments into four groups: no treatment (T-NR; n = 280); oxygen therapy (T-O2; n = 220); non-invasive mechanical ventilation (T-NIMV; n = 99); and invasive mechanical ventilation (T-IMV; n = 93). The groups were compared in terms of clinical characteristics, laboratory values at ICU admission and discharge, length of stay, and outcomes. Results: The T-IMV group had significantly higher Acute Physiology and Chronic Health Evaluation II (APACHE II) and updated Charlson Comorbidity Index scores, alongside lower ejection fractions and higher rates of vasopressor/inotrope use (p < 0.05). This group also exhibited higher mortality, longer ICU stays, and more adverse laboratory profiles (elevated lactate, creatinine, N-terminal pro-B-type natriuretic peptide-NT-proBNP, bilirubin; lower albumin). Multivariable analysis confirmed that the APACHE II score, vasopressor/inotrope requirement, and lactate and NT-proBNP levels (at admission) were independently associated with mortality (p < 0.05). Conclusions: Patients requiring IMV demonstrated greater severity of illness, as reflected by higher APACHE II scores, elevated NT-proBNP and lactate levels at admission, as well s increased requirement for vasopressor/inotrope therapy. These variables were associated with mortality, suggesting that the poorer prognosis observed in the IMV group was due to their underlying disease burden.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, LCT (lactase) [NCBI Gene 3938] {aka LAC, LPH, LPH1}
- **Diseases:** APACHE (MESH:D000071069), H (MESH:D000848), hypotension (MESH:D007022), respiratory distress (MESH:D012128), hypoxia (MESH:D000860), pulmonary hypertension (MESH:D006976), diastolic dysfunction (MESH:D018487), ICD (MESH:D057873), acute respiratory failure (MESH:D012131), tricuspid regurgitation (MESH:D014262), impaired renal function (MESH:D007674), arrhythmia (MESH:D001145), organ dysfunction (MESH:D009102), Heart Failure (MESH:D006333), interstitial lung disease (MESH:D017563), peripheral and pulmonary oedema (MESH:D010523), COPD (MESH:D029424), cardiomyopathy (MESH:D009202), cardiac pathology (MESH:D006331), pneumonia (MESH:D011014), liver dysfunction (MESH:D017093), hypercapnia (MESH:D006935), Hypoalbuminemia (MESH:D034141), stroke (MESH:D020521), congestion (MESH:D002311), cardiogenic shock (MESH:D012770), RV failure (MESH:D051437), multiple (MESH:D009104), malignancies (MESH:D009369), DM (MESH:D003920), cardiac output (MESH:D002303), atrial fibrillation (MESH:D001281), ischemic (MESH:D002545), PD (MESH:D008171), CVD (MESH:D002561), pulmonary edema (MESH:D011654), metabolic acidosis (MESH:D000138), obstructive/restrictive lung diseases (MESH:D008173), CKD (MESH:D051436), asthma (MESH:D001249), hepatic dysfunction (MESH:D008107), inflammation (MESH:D007249), cardiac collapse (MESH:D001261), shock (MESH:D012769), injury to (MESH:D014947), Comorbidity (MESH:D004194), critically ill (MESH:D016638), cardiogenic (MESH:D013575), volume overload (MESH:D019190), PAP (OMIM:102200), Mortality (MESH:D003643), HT (MESH:D006973), arterial stiffness (MESH:C566112), bronchiectasis (MESH:D001987)
- **Chemicals:** creatinine (MESH:D003404), PAP (MESH:D010724), bilirubin (MESH:D001663), lactate (MESH:D019344), Cre (-), T (MESH:D014316), O2 (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941283/full.md

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Source: https://tomesphere.com/paper/PMC12941283