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      Association Between Preoperative Proteinuria and Postoperative Acute Kidney Injury and Readmission

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          Abstract

          <div class="section"> <a class="named-anchor" id="ab-soi180035-1"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e571">Question</h5> <p id="d9130567e573">What is the association between preoperative proteinuria and postoperative acute kidney injury and 30-day unplanned readmission among patients with and without known renal dysfunction at the time of surgery? </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-2"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e576">Findings</h5> <p id="d9130567e578">In this population-based study of 153 767 patients with and without known preoperative renal dysfunction, preoperative proteinuria was an indicator of probable postoperative acute kidney injury and 30-day unplanned readmission independent of preoperative renal dysfunction. </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-3"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e581">Meaning</h5> <p id="d9130567e583">Identification and early intervention of patients at risk for postoperative acute kidney injury through preoperative urinalysis assessments may improve patient outcomes. </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-4"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e588">Importance</h5> <p id="d9130567e590">Proteinuria indicates renal dysfunction and is a risk factor for morbidity among medical patients, but less is understood among surgical populations. There is a paucity of studies investigating how preoperative proteinuria is associated with surgical outcomes, including postoperative acute kidney injury (AKI) and readmission. </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-5"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e593">Objective</h5> <p id="d9130567e595">To assess preoperative urine protein levels as a biomarker for adverse surgical outcomes.</p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-6"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e598">Design, Setting, and Participants</h5> <p id="d9130567e600">A retrospective, population-based study was conducted in a cohort of patients with and without known preoperative renal dysfunction undergoing elective inpatient surgery performed at 119 Veterans Affairs facilities from October 1, 2007, to September 30, 2014. Data analysis was conducted from April 4 to December 1, 2016. Preoperative dialysis, septic, cardiac, ophthalmology, transplantation, and urologic cases were excluded. </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-7"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e603">Exposures</h5> <p id="d9130567e605">Preoperative proteinuria as assessed by urinalysis using the closest value within 6 months of surgery: negative (0 mg/dL), trace (15-29 mg/dL), 1+ (30-100 mg/dL), 2+ (101-300 mg/dL), 3+ (301-1000 mg/dL), and 4+ (&gt;1000 mg/dL). </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-8"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e608">Main Outcomes and Measures</h5> <p id="d9130567e610">Primary outcome was postoperative predischarge AKI and 30-day postdischarge unplanned readmission. Secondary outcomes included any 30-day postoperative outcome. </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-9"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e613">Results</h5> <p id="d9130567e615">Of 346 676 surgeries, 153 767 met inclusion criteria, with the majority including orthopedic (37%), general (29%), and vascular procedures (14%). Evidence of proteinuria was shown in 43.8% of the population (trace: 20.6%, 1+: 16.0%, 2+: 5.5%, 3+: 1.6%) with 20.4%, 14.9%, 4.3%, and 0.9%, respectively, of the patients having a normal preoperative estimated glomerular filtration rate (eGFR). In unadjusted analysis, preoperative proteinuria was significantly associated with postoperative AKI (negative: 8.6%, trace: 12%, 1+: 14.5%, 2+: 21.2%, 3+: 27.6%; <i>P</i> &lt; .001) and readmission (9.3%, 11.3%, 13.3%, 15.8%, 17.5%, respectively, <i>P</i> &lt; .001). After adjustment, preoperative proteinuria was associated with postoperative AKI in a dose-dependent relationship (trace: odds ratio [OR], 1.2; 95% CI, 1.1-1.3, to 3+: OR, 2.0; 95% CI, 1.8-2.2) and 30-day unplanned readmission (trace: OR, 1.0; 95% CI, 1.0-1.1, to 3+: OR, 1.3; 95% CI, 1.1-1.4). Preoperative proteinuria was associated with AKI independent of eGFR. </p> </div><div class="section"> <a class="named-anchor" id="ab-soi180035-10"> <!-- named anchor --> </a> <h5 class="section-title" id="d9130567e624">Conclusions and Relevance</h5> <p id="d9130567e626">Proteinuria was associated with postoperative AKI and 30-day unplanned readmission independent of preoperative eGFR. Simple urine assessment for proteinuria may identify patients at higher risk of AKI and readmission to guide perioperative management. </p> </div><p class="first" id="d9130567e629">This population-based study examines the outcomes of acute kidney injury and readmission in patients with preoperative proteinuria. </p>

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          For the general population, the clinical relevance of an increased urinary albumin excretion rate is still debated. Therefore, we examined the relationship between urinary albumin excretion and all-cause mortality and mortality caused by cardiovascular (CV) disease and non-CV disease in the general population. In the period 1997 to 1998, all inhabitants of the city of Groningen, the Netherlands, aged between 28 and 75 years (n=85 421) were sent a postal questionnaire collecting information about risk factors for CV disease and CV morbidity and a vial to collect an early morning urine sample for measurement of urinary albumin concentration (UAC). The vital status of the cohort was subsequently obtained from the municipal register, and the cause of death was obtained from the Central Bureau of Statistics. Of these 85 421 subjects, 40 856 (47.8%) responded, and 40 548 could be included in the analysis. During a median follow-up period of 961 days (maximum 1139 days), 516 deaths with known cause were recorded. We found a positive dose-response relationship between increasing UAC and mortality. A higher UAC increased the risk of both CV and non-CV death after adjustment for other well-recognized CV risk factors, with the increase being significantly higher for CV mortality than for non-CV mortality (P=0.014). A 2-fold increase in UAC was associated with a relative risk of 1.29 for CV mortality (95% CI 1.18 to 1.40) and 1.12 (95% CI 1.04 to 1.21) for non-CV mortality. Urinary albumin excretion is a predictor of all-cause mortality in the general population. The excess risk was more attributable to death from CV causes, independent of the effects of other CV risk factors, and the relationship was already apparent at levels of albuminuria currently considered to be normal.
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            The previous conventional wisdom that survivors of acute kidney injury (AKI) tend to do well and fully recover renal function appears to be flawed. AKI can cause end-stage renal disease (ESRD) directly, and increase the risk of developing incident chronic kidney disease (CKD) and worsening of underlying CKD. In addition, severity, duration, and frequency of AKI appear to be important predictors of poor patient outcomes. CKD is an important risk factor for the development and ascertainment of AKI. Experimental data support the clinical observations and the bidirectional nature of the relationships between AKI and CKD. Reductions in renal mass and nephron number, vascular insufficiency, cell cycle disruption, and maladaptive repair mechanisms appear to be important modulators of progression in patients with and without coexistent CKD. Distinction between AKI and CKD may be artificial. Consideration should be given to the integrated clinical syndrome of diminished GFR, with acute and chronic stages, where spectrum of disease state and outcome is determined by host factors, including the balance of adaptive and maladaptive repair mechanisms over time. Physicians must provide long-term follow-up to patients with first episodes of AKI, even if they presented with normal renal function.
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              Long-term risk of mortality and acute kidney injury during hospitalization after major surgery.

              To determine the relationship between long-term mortality and acute kidney injury (AKI) during hospitalization after major surgery. AKI is associated with a risk of short-term mortality that is proportional to its severity; however the long-term survival of patients with AKI is poorly studied. This is a retrospective cohort study of 10,518 patients with no history of chronic kidney disease who were discharged after a major surgery between 1992 and 2002. AKI was defined by the RIFLE (Risk, Injury, Failure, Loss, and End-stage Kidney) classification, which requires at least a 50% increase in serum creatinine (sCr) and stratifies patients into 3 severity stages: risk, injury, and failure. Patient survival was determined through the National Social Security Death Index. Long-term survival was analyzed using a risk-adjusted Cox proportional hazards regression model. In the risk-adjusted model, survival was worse among patients with AKI and was proportional to its severity with an adjusted hazard ratio of 1.18 (95% confidence interval [CI], 1.08-1.29) for the RIFLE-Risk class and 1.57 (95% CI, 1.40-1.75) for the RIFLE-Failure class, compared with patients without AKI (P < 0.001). Patients with complete renal recovery after AKI still had an increased adjusted hazard ratio for death of 1.20 (95% CI, 1.10-1.31) compared with patients without AKI (P < 0.001). In a large single-center cohort of patients discharged after major surgery, AKI with even small changes in sCr level during hospitalization was associated with an independent long-term risk of death.
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                Author and article information

                Journal
                JAMA Surgery
                JAMA Surg
                American Medical Association (AMA)
                2168-6254
                September 01 2018
                September 19 2018
                : 153
                : 9
                : e182009
                Affiliations
                [1 ]Birmingham and Tuscaloosa Health Services Research and Development Unit, Birmingham Veterans Affairs Medical Center, Birmingham, Alabama
                [2 ]Department of Surgery, University of Alabama at Birmingham
                [3 ]Center for Healthcare Organization and Implementation Research, Veterans Affairs Boston Healthcare System, Boston, Massachusetts
                [4 ]Department of Surgery, Boston University School of Medicine, Boston, Massachusetts
                [5 ]School of Medicine, Harvard University, Boston, Massachusetts
                [6 ]Veterans Affairs Palo Alto Healthcare System, Palo Alto, California
                [7 ]Department of Surgery, Stanford University, Stanford, California
                [8 ]Milwaukee Veterans Affairs Medical Center, Milwaukee, Wisconsin
                [9 ]Department of Medicine, Medical College of Wisconsin, Milwaukee
                [10 ]Department of Surgery, Medical College of Wisconsin, Milwaukee
                [11 ]Veterans Affairs Central Western Massachusetts Health Care System, Leeds
                [12 ]Center for Applied Health Research, Baylor Scott and White Health, Temple, Texas
                [13 ]Department of Medicine, Texas A&M Health Science Center, Temple
                Article
                10.1001/jamasurg.2018.2009
                6233648
                29971429
                4388a050-7e40-4312-aa61-67ff19856acd
                © 2018
                History

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