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Ventilation-induced acute kidney injury in acute respiratory failure: Do PEEP levels matter?
Indexado
WoS WOS:001461608900001
Scopus SCOPUS_ID:105000547419
DOI 10.1186/S13054-025-05343-5
Año 2025
Tipo revisión

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Acute Respiratory Distress Syndrome (ARDS) is a leading cause of morbidity and mortality among critically ill patients, and mechanical ventilation (MV) plays a critical role in its management. One of the key parameters of MV is the level of positive end-expiratory pressure (PEEP), which helps to maintain an adequate lung functional volume. However, the optimal level of PEEP remains controversial. The classical approach in clinical trials for identifying the optimal PEEP has been to compare "high" and "low" levels in a dichotomous manner. High PEEP can improve lung compliance and significantly enhance oxygenation but has been inconclusive in hard clinical outcomes such as mortality and duration of MV. This discrepancy could be related to the fact that inappropriately high or low PEEP levels may adversely affect other organs, such as the heart, brain, and kidneys, which could counteract its potential beneficial effects on the lung. Patients with ARDS often develop acute kidney injury, which is an independent marker of mortality. Three primary mechanisms have been proposed to explain lung-kidney crosstalk during MV: gas exchange abnormalities, such as hypoxemia and hypercapnia; remote biotrauma; and hemodynamic changes, including reduced venous return and cardiac output. As PEEP levels increase, lung volume expands to a variable extent depending on mechanical response. This dynamic underlies two potential mechanisms that could impair venous return, potentially leading to splanchnic and renal congestion. First, increasing PEEP may enhance lung aeration, particularly in highly recruitable lungs, where previously collapsed alveoli reopen, increasing lung volume and pleural pressure, leading to vena cava compression, which can contribute to systemic venous congestion and abdominal organ impairment function. Second, in lungs with low recruitability, PEEP elevation may induce minimal changes in lung volume while increasing airway pressure, resulting in alveolar overdistension, vascular compression, and increased pulmonary vascular resistance. Therefore, we propose that high PEEP settings can contribute to renal congestion, potentially impairing renal function. This review underscores the need for further rigorous research to validate these perspectives and explore strategies for optimizing PEEP settings while minimizing adverse renal effects.

Revista



Revista ISSN
Critical Care 1466-609X

Métricas Externas



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Disciplinas de Investigación



WOS
Critical Care Medicine
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Benites, Martin H. Hombre Clínica Las Condes - Chile
Universidad Finis Terrae - Chile
Pontificia Universidad Católica de Chile - Chile
Escuela de Medicina - Chile
2 Suarez-Sipmann, Fernando Hombre Inst Salud Carlos III - España
La Princesa Univ Hosp - España
UPPSALA UNIV - Suecia
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias - España
Hospital Universitario de la Princesa - España
Uppsala Universitet - Suecia
3 Kattan, Eduardo - Pontificia Universidad Católica de Chile - Chile
4 Cruces, Pablo - Universidad Nacional Andrés Bello - Chile
Hosp Carmen Dr Luis Valentin Ferrada - Chile
Facultad de Ciencias de la Vida - Chile
5 Retamal, Jaime - Pontificia Universidad Católica de Chile - Chile

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Financiamiento



Fuente
Fondo Nacional de Desarrollo Científico y Tecnológico
Fondo Nacional de Desarrollo Cientfico y Tecnolgico

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Agradecimientos



Agradecimiento
We thank Claudio Cisterna for his contribution to creating the figures for this review.
Supported by a grant by Fondo Nacional de Desarrollo Cient\u00EDfico y Tecnol\u00F3gico (FONDECYT 1241897).

Muestra la fuente de financiamiento declarada en la publicación.