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. 2020 Apr;46(4):654-672.
doi: 10.1007/s00134-019-05869-7. Epub 2019 Dec 9.

Lung-kidney interactions in critically ill patients: consensus report of the Acute Disease Quality Initiative (ADQI) 21 Workgroup

Affiliations

Lung-kidney interactions in critically ill patients: consensus report of the Acute Disease Quality Initiative (ADQI) 21 Workgroup

Michael Joannidis et al. Intensive Care Med. 2020 Apr.

Abstract

Background: Multi-organ dysfunction in critical illness is common and frequently involves the lungs and kidneys, often requiring organ support such as invasive mechanical ventilation (IMV), renal replacement therapy (RRT) and/or extracorporeal membrane oxygenation (ECMO).

Methods: A consensus conference on the spectrum of lung-kidney interactions in critical illness was held under the auspices of the Acute Disease Quality Initiative (ADQI) in Innsbruck, Austria, in June 2018. Through review and critical appraisal of the available evidence, the current state of research, and both clinical and research recommendations were described on the following topics: epidemiology, pathophysiology and strategies to mitigate pulmonary dysfunction among patients with acute kidney injury and/or kidney dysfunction among patients with acute respiratory failure/acute respiratory distress syndrome. Furthermore, emphasis was put on patients receiving organ support (RRT, IMV and/or ECMO) and its impact on lung and kidney function.

Conclusion: The ADQI 21 conference found significant knowledge gaps about organ crosstalk between lung and kidney and its relevance for critically ill patients. Lung protective ventilation, conservative fluid management and early recognition and treatment of pulmonary infections were the only clinical recommendations with higher quality of evidence. Recommendations for research were formulated, targeting lung-kidney interactions to improve care processes and outcomes in critical illness.

Keywords: Acute kidney injury; Acute respiratory distress syndrome; Extracorporeal membrane oxygenation; Renal replacement therapy; Water-electrolyte balance.

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Conflict of interest statement

MJ has received honoraria and research support from Baxter Healthcare Corp, AM-Pharma, CLS Behring, Fresenius, and Astute Medical. LGF has received honoraria and research support from Astute Medical, La Jolla Pharmaceuticals, Medibeacon, Baxter, and Fresenius. PMH has received honoraria and research support from Baxter and CytoSorbent. MO has received honoraria from Fresenius Medical and Baxter and has an advisory role to Biomerieux and Nxstage. JP has received speaker’s honoraria from Fresenius Medical, Baxter and Nikkiso, research support from Biomerieux and Abbott, and has consulted for Nikkiso, Baxter, Medibeacon and Quark Pharma. SMB has consulted and received research support from Baxter Health Care. MD has received research support from MSD and from ASTUTE medical, speaker fees from MSD, Astellas and Bristol-Myers-Squibb, support to organize educational meetings from MSD, Astellas, and Jazz Pharma and has participated in an advisory board from SANOFI-AVENTIS. VF has received honoraria from HepaWash. EH has received speaker’s fee and travel fee from Alexion, AM Pharma, Sopachem, and Bellco. M. Maggiorini has a MAB membership from Baxter and has received an unrestricted research grant from Baxter. M. Meersch has received lecture fees from Astute Medical, Fresenius Medical and Baxter. PTM has advisory board memberships with FAST Biomedical, AM-Pharma, Sphingotec. TS has an advisory board membership with Xenios and has received speaker fees from Getinge, Xenios, Zoll, Orion Pharma, and Fresenius. JAK has received consulting fees and research support from Astute Medical, Baxter and Fresenius. None of the other authors have any conflicts of interest to declare with regard to this manuscript.

Figures

Fig. 1
Fig. 1
GRADE system for grading recommendations according to strength of recommendation (strong vs. weak) and quality of evidence (high to very low) Modified from Guyatt et al. [8]
Fig. 2
Fig. 2
Possible effects of kidney injury and extracorporeal devices on pulmonary function. Depending on the stage of kidney injury, different processes take place in the injured kidney (e.g. inflammation, necrosis, apoptosis, fibrosis) having different impacts on and possibly injuring the lung trough fluid overload, humoral and cellular mechanisms. Extracorporeal devices for renal and respiratory support may interfere with these processes having possible protective but also detrimental effects on organ function. Renal and pulmonary failure may require combined application of RRT and ECMO (reprinted with permission from http://www.ADQI.org)
Fig. 3
Fig. 3
Possible effects of acute respiratory failure and invasive/non-invasive ventilation on renal function. Both pneumonia and acute exacerbated COPD (AE-COPD) may trigger renal injury by various pathways. These include inflammation/immuno-mediated injury, hypoxaemia, hypercapnia and nephrotoxins. In AE-COPD, air trapping with increased thoracic pressures and right heart failure is frequently contributing to venous congestion. If invasive mechanical ventilation is necessary (e.g. ARDS) biotrauma, barotrauma, release of inflammatory mediators (e.g. IL-6, PAI-1, TNFR-1/2) and haemodynamic compromise may occur. These mechanisms may further contribute to kidney injury eventually leading to impaired GFR up to renal failure. Consequently, renal recovery may occur if the insulting factors are eliminated depending on the degree of injury whether partial or full recovery occurs (reprinted with permission from http://www.ADQI.org)
Fig. 4
Fig. 4
Different possible methods to combine ECMO and CRRT circuits. a The inlet and the outlet of the CRRT device are connected before the centrifugal blood pump in the negative/low-pressure part of the ECMO circuit. High risk of air aspiration. b The inlet of the CRRT device is connected after the centrifugal blood pump in the high-pressure part of the ECMO circuit, while the CRRT outlet is connected before the centrifugal blood pump in the low-pressure part. Another possibility would be the connection of the inlet in the low-pressure part and the outlet in the high-pressure part. Every connection at the low-pressure part has a high risk of air aspiration. c Both the inlet and the outlet of the CRRT device are connected in the high-pressure part after the centrifugal blood pump. d The inlet of the CRRT device is connected directly after the membrane oxygenator, while the outlet is connected directly before the oxygenator. The minimal re-circulation is outweighed by increased safety as the gas exchange membrane is used as a clot and air trap. e The inlet of the CRRT device is connected to the additional port of the backflow cannula, while the outlet is connected directly to the membrane oxygenator. This approach keeps the connectors pre and post oxygenator available for pressure and gas exchange monitoring of the oxygenator. f A haemofilter is integrated into the ECMO circuit in-line, therefore relying on blood flow and pressure provided by the ECMO device alone. Replacement fluid is directly supplied into the ECMO circuit. The inlet of the haemofilter is connected after the centrifugal blood pump into the high-pressure part, while the outlet is connected before the centrifugal blood pump to create a sufficient pressure gradient. g The CRRT device is connected to the patient through a separate catheter and, therefore, being independent of the ECMO circuit (reprinted with permission from http://www.ADQI.org)

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