# Factors Associated With Complications in Patients With Hematological Malignancies and Febrile Neutropenia: A Cohort Study

**Authors:** Jose C Alvarez-Payares, Santiago Alvarez-Lopez, Jose E. Agámez-Gomez, Juan C. Hernandez-Rodriguez, Alejandra Ramírez-Roldán, Ángel D. Molina-Prado, Manuela Cardona-Jaramillo, Adriana M. Trejos-Tenorio, Sigifredo Ospina-Ospina, Ioka de la Peña-Lozano, Daniel Barrera-Correa, Daniel A. Ribero-Vargas, Edwin J Ariza-Parra, Amado J. Karduss-Urueta

PMC · DOI: 10.7759/cureus.81750 · 2025-04-05

## TL;DR

This study explores factors linked to complications and mortality in patients with blood cancers and febrile neutropenia, finding that no single factor clearly predicts outcomes.

## Contribution

The study identifies potential risk factors for mortality in febrile neutropenia patients with hematological malignancies in a specific clinical setting.

## Key findings

- Gram-negative bacteria were most commonly isolated in febrile neutropenia cases.
- Conditions like COPD and prolonged neutropenia were associated with higher mortality in bivariate analysis.
- No statistically significant predictors of complications or mortality were found in multivariate analysis.

## Abstract

Introduction

Febrile neutropenia (FN) in patients with hematological malignancy (HM) is associated with multiple hospital complications including mortality. Although different strategies for early detection and prompt treatment have been established, it is a heterogeneous population with risk factors that are difficult to detect. The data available on the prediction of such complications is limited and there lies the importance of characterizing this type of patients in our environment and evaluating the factors related to the adverse outcomes.

Methods

The study is a retrospective cohort study conducted at San Vicente Foundation University Hospital (HUSVF) and Alma Mater Hospital of Antioquia (HAMA) in Medellín, Colombia, between January 2018 and December 2020, including patients diagnosed with FN who presented FN at the time of diagnosis or up to 30 days after receiving chemotherapy. The main objective was to determine the factors related to mortality and severe complications (ICU admission, need for vasopressors, or need for mechanical ventilation), while the secondary objective was the microbiological characterization of this population.

Results

Of the 190 FN episodes, 134 (70.5%) had a clinical focus of infection. A causal agent was identified in 125 episodes (65.8%), with the majority being bacteria in 112 cases (92.6%) of the isolates. The most frequently identified bacteria were Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. Gram-negative bacilli were isolated in 85 (86%) cases, and resistance was present in 38 cases (44.7%), with both extended-spectrum beta-lactamase (ESBL) and Klebsiella pneumoniae Carbapenemase (KPC) detected in nine (10.5%). In 53 (34.4%) episodes, some complications occurred during FN. The 30-day all-cause mortality was 53 (34.4%), with 27 (50.9%) of these cases associated with complications. Of the 45 (86.5%) patients who died from any cause, all did so during their first episode of FN. In the bivariate analysis, the following factors were associated with higher mortality: hypertension (OR 2.58, 95% CI 1.19-5.58; p=0.014), chronic obstructive pulmonary disease (COPD) (OR 10.2, 95% CI 1.11-93.8; p=0.013), chronic kidney disease (OR 4.27, 95% CI 0.975-18.7; p=0.038), prolonged neutropenia (OR 2.34, 95% CI 1.1-4.95; p=0.024), and lactate dehydrogenase (LDH) levels greater than two times the upper normal limit (UNL) (OR 3.24, 95% CI 1.35-7.75; p=0.007). In contrast, normal albumin levels before chemotherapy were associated with lower mortality (OR 0.381, 95% CI 0.15-0.95; p=0.036). In the multivariate analysis, none of the identified factors were statistically significant in predicting complications or mortality.

Conclusion

No factors related to complications or mortality were found in the multivariate analysis. However, the heterogeneity of the population suggests that these outcomes are not determined by a single factor, and a study with a larger sample may be needed to confirm them.

## Linked entities

- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** chronic kidney disease (MESH:D051436), infection (MESH:D007239), FN (MESH:D064147), neutropenia (MESH:D009503), HM (MESH:D019337), died (MESH:D003643), hypertension (MESH:D006973), COPD (MESH:D029424)
- **Chemicals:** KPC (-)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Escherichia coli (E. coli, species) [taxon 562], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Klebsiella pneumoniae (species) [taxon 573]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12051409/full.md

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Source: https://tomesphere.com/paper/PMC12051409