Value of early diagnosis of sepsis complicated with acute kidney injury by renal contrast-enhanced ultrasound

BACKGROUND The incidence of acute kidney injury (AKI) in patients with sepsis is high, and the prognosis of patients with septic AKI is poor. The early diagnosis and treatment of septic AKI is of great significance in improving the prognosis of patients with sepsis. AIM To explore the value of contrast-enhanced ultrasound (CEUS), serum creatinine (Scr), and other indicators in the early diagnosis of septic AKI. METHODS Ninety patients with sepsis during hospitalization at Tongji Hospital of Tongji University were recruited as subjects. Each patient was recorded with relevant basic data, clinical indicators, and CEUS results. The patients were divided into AKI group and non-AKI group according to the results of renal function diagnosis after 48 h. On the 7th day, the renal function of the non-AKI group was re-evaluated and the patients were further divided into AKI subgroup and non-AKI subgroup. The differences of the indicators in different groups were compared, and the diagnostic value of each indicator and their combination for septic AKI was analyzed. RESULTS Systemic inflammatory response score (2.58 ± 0.75), blood lactic acid (3.01 ± 1.33 mmol/L), Scr (141.82 ± 27.19 μmol/L), blood urea nitrogen (4.41 ± 0.81mmol/L), and rise time (10.23 ± 2.63 s) in the AKI group were higher than those in the non-AKI group. Peak intensity (PI) (10.78 ± 3.98 dB) and wash in slope (WIS) (1.07 ± 0.53 dB/s) were lower than those in the non-AKI group. The differences were statistically significant (P < 0.05). The PI (12.83 ± 3.77 dB) and WIS (1.22 ± 0.68 dB/s) in the AKI subgroup were lower than those in the non-AKI subgroup, and the differences were statistically significant (P < 0.05). The area under curve (AUC) of Scr for the diagnosis of septic AKI was 0.825 with a sensitivity of 56.76% and a specificity of 100%. The AUCs of WIS and PI (0.928 and 0.912) were higher than those of Scr. Their sensitivities were 100%, but the specificities were 71.70% and 75.47%. The AUC of the combination of three indicators for the diagnosis of septic AKI was 0.943, which was significantly higher than the AUC diagnosed by each single indicator. The sensitivity was 94.59%, and the specificity was 81.13%. CONCLUSION The combination of Scr, PI, and WIS can improve the diagnostic accuracy of septic AKI. PI and WIS are expected to predict the occurrence of early septic AKI.

[1]  Zhe Wang,et al.  Hotspot Analysis of Sepsis Literature , 2018, Medical science monitor : international medical journal of experimental and clinical research.

[2]  T. Horino,et al.  Evaluation of the accuracy of estimated baseline serum creatinine for acute kidney injury diagnosis , 2018, Clinical and Experimental Nephrology.

[3]  L. Duchateau,et al.  Contrast‐Enhanced Ultrasound Examination for the Assessment of Renal Perfusion in Cats with Chronic Kidney Disease , 2017, Journal of veterinary internal medicine.

[4]  J. Prowle Sepsis-Associated AKI. , 2017, Clinical journal of the American Society of Nephrology : CJASN.

[5]  G. Montrucchio,et al.  Platelets and Multi-Organ Failure in Sepsis , 2017, International journal of molecular sciences.

[6]  J. Rizzo,et al.  Correction: Does NGAL reduce costs? A cost analysis of urine NGAL (uNGAL) & serum creatinine (sCr) for acute kidney injury (AKI) diagnosis , 2017, PloS one.

[7]  Borislav D Dimitrov,et al.  Systematic review of prognostic prediction models for acute kidney injury (AKI) in general hospital populations , 2017, BMJ Open.

[8]  I. Castro,et al.  Risk factors for the progression of chronic kidney disease after acute kidney injury. , 2017, Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia.

[9]  C. Ronco,et al.  Biomarkers of acute kidney injury: the pathway from discovery to clinical adoption , 2017, Clinical chemistry and laboratory medicine.

[10]  Y. Liu,et al.  Incidence and diagnosis of Acute kidney injury in hospitalized adult patients: a retrospective observational study in a tertiary teaching Hospital in Southeast China , 2017, BMC Nephrology.

[11]  N. Caplan,et al.  The prevalence and significance of renal perfusion defects in early kidney transplants quantified using 3D contrast enhanced ultrasound (CEUS) , 2017, European Radiology.

[12]  J. Carcillo,et al.  Three Hypothetical Inflammation Pathobiology Phenotypes and Pediatric Sepsis-Induced Multiple Organ Failure Outcome* , 2017, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

[13]  K. Chung Sepsis and Multi-Organ Failure. , 2017, Journal of burn care & research : official publication of the American Burn Association.

[14]  方伯梁,et al.  Three hypothetical inflammation pathobiology phenotypes and pediatric sepsis-induced multiple organ failure outcome , 2017 .

[15]  Sangeeta Mehta,et al.  Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016 , 2017, Intensive Care Medicine.

[16]  J. Kellum,et al.  Sepsis-induced acute kidney injury , 2016, Current opinion in critical care.

[17]  H. Heinze,et al.  Beatmung als Trigger für Organdysfunktion und Sepsis , 2016, Medizinische Klinik - Intensivmedizin und Notfallmedizin.

[18]  Yan Wang,et al.  Acute kidney injury in China: a cross-sectional survey , 2015, The Lancet.

[19]  R. Bellomo,et al.  Sepsis-Induced Acute Kidney Injury. , 2015, Critical care clinics.

[20]  F M Drudi,et al.  Growing indications for CEUS: The kidney, testis, lymph nodes, thyroid, prostate, and small bowel. , 2015, European journal of radiology.

[21]  J. Bakker,et al.  Early lactate clearance-guided therapy in patients with sepsis: a meta-analysis with trial sequential analysis of randomized controlled trials , 2015, Intensive Care Medicine.

[22]  N. Bogavac-Stanojević,et al.  Cost-effectiveness analysis of acute kidney injury biomarkers in pediatric cardiac surgery , 2015, Biochemia medica.

[23]  J. Kellum,et al.  Acute kidney injury in severe sepsis: pathophysiology, diagnosis, and treatment recommendations. , 2015, Journal of veterinary emergency and critical care.

[24]  Michael Bailey,et al.  Goal-directed resuscitation for patients with early septic shock. , 2014, The New England journal of medicine.

[25]  M. Singer The role of mitochondrial dysfunction in sepsis-induced multi-organ failure , 2013, Virulence.

[26]  Huan-huan Tian,et al.  [Risk factors and early diagnosis of acute kidney injury in patients with sepsis]. , 2013, Zhonghua wei zhong bing ji jiu yi xue.

[27]  Michael T. Eadon,et al.  TNF-mediated damage to glomerular endothelium is an important determinant of acute kidney injury in sepsis , 2013, Kidney international.

[28]  A. Khwaja KDIGO Clinical Practice Guidelines for Acute Kidney Injury , 2012, Nephron Clinical Practice.

[29]  T. Ikizler,et al.  Sepsis as a cause and consequence of acute kidney injury: Program to Improve Care in Acute Renal Disease , 2010, Intensive Care Medicine.

[30]  S. Bagshaw,et al.  Fluid balance as a biomarker: impact of fluid overload on outcome in critically ill patients with acute kidney injury , 2008, Critical care.

[31]  H. Spapen Liver Perfusion in Sepsis, Septic Shock, and Multiorgan Failure , 2008, Anatomical record.

[32]  P. Tandon,et al.  Bacterial infections, sepsis, and multiorgan failure in cirrhosis. , 2008, Seminars in liver disease.

[33]  D. Benhamou,et al.  Renal arterial resistance in septic shock: effects of increasing mean arterial pressure with norepinephrine on the renal resistive index assessed with Doppler ultrasonography , 2007, Intensive Care Medicine.

[34]  R. Quigg,et al.  Acute Renal Failure in Endotoxemia Is Caused by TNF Acting Directly on TNF Receptor-1 in Kidney1 , 2002, The Journal of Immunology.

[35]  E. Ivers,et al.  Early Goal-Directed Therapy in the Treatment of Severe Sepsis and Septic Shock , 2001 .

[36]  V. Briner,et al.  Tumor necrosis factor-alpha and lipopolysaccharide induce apoptotic cell death in bovine glomerular endothelial cells. , 1999, Kidney international.

[37]  A. S. Appel,et al.  Acute Renal Failure , 1960, Advances in Experimental Medicine and Biology.