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      Association of Statin Use with Risk and Outcome of Acute Kidney Injury in Community-Acquired Pneumonia

      , , , , , , on behalf of the Genetic and Inflammatory Markers of Sepsis (GenIMS) Investigators
      Clinical Journal of the American Society of Nephrology
      American Society of Nephrology (ASN)

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          Abstract

          <div class="section"> <a class="named-anchor" id="d3057757e160"> <!-- named anchor --> </a> <h5 class="section-title" id="d3057757e161">Background and objectives</h5> <p id="d3057757e163">Sepsis is a leading cause of AKI. Animal studies suggest that the pleiotropic effect of statins attenuates the risk for AKI and decreases mortality. This study examined whether statin use was associated with a lower risk for pneumonia-induced AKI and 1-year and cause-specific mortality in patients with AKI. </p> </div><div class="section"> <a class="named-anchor" id="d3057757e165"> <!-- named anchor --> </a> <h5 class="section-title" id="d3057757e166">Design, setting, participants, &amp; measurements</h5> <p id="d3057757e168">Multicenter, prospective cohort study of 1836 patients hospitalized with community-acquired pneumonia. </p> </div><div class="section"> <a class="named-anchor" id="d3057757e170"> <!-- named anchor --> </a> <h5 class="section-title" id="d3057757e171">Results</h5> <p id="d3057757e173">Baseline characteristics differed among statin users and nonusers. Of the 413 patients (22.5%) who received a statin before hospitalization, statin treatment, when adjusted for differences in age, severity of pneumonia, admission from nursing home, health insurance, and propensity for statin use, did not reduce the risk for AKI (odds ratio [OR], 1.32 [95% confidence interval (CI), 1.02–1.69]; <i>P</i>=0.05). Of patients with AKI ( <i>n</i>=631), statin use was associated with a lower risk for death at 1 year (27.8% versus 38.8%; <i>P</i>=0.01), which was not significant when adjusted for differences in age, severity of pneumonia and AKI, use of mechanical ventilation, and propensity score (OR, 0.72 [95% CI, 0.50–1.06]; <i>P</i>=0.09). Among patients with AKI, cardiovascular disease accounted for one third of all deaths. </p> </div><div class="section"> <a class="named-anchor" id="d3057757e187"> <!-- named anchor --> </a> <h5 class="section-title" id="d3057757e188">Conclusions</h5> <p id="d3057757e190">In a large cohort of patients hospitalized with pneumonia, statins did not reduce the risk for AKI. Among patients with AKI, statin use was not associated with lower risk for death at 1 year. The higher risk for AKI observed among statin users may be due to indication bias. </p> </div>

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          Most cited references16

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          Septic acute kidney injury in critically ill patients: clinical characteristics and outcomes.

          Sepsis is the most common cause of acute kidney injury (AKI) in critical illness, but there is limited information on septic AKI. A prospective, observational study of critically ill patients with septic and nonseptic AKI was performed from September 2000 to December 2001 at 54 hospitals in 23 countries. A total of 1753 patients were enrolled. Sepsis was considered the cause in 833 (47.5%); the predominant sources of sepsis were chest and abdominal (54.3%). Septic AKI was associated with greater aberrations in hemodynamics and laboratory parameters, greater severity of illness, and higher need for mechanical ventilation and vasoactive therapy. There was no difference in enrollment kidney function or in the proportion who received renal replacement therapy (RRT; 72 versus 71%; P = 0.83). Oliguria was more common in septic AKI (67 versus 57%; P < 0.001). Septic AKI had a higher in-hospital case-fatality rate compared with nonseptic AKI (70.2 versus 51.8%; P < 0.001). After adjustment for covariates, septic AKI remained associated with higher odds for death (1.48; 95% confidence interval 1.17 to 1.89; P = 0.001). Median (IQR) duration of hospital stay for survivors (37 [19 to 59] versus 21 [12 to 42] d; P < 0.0001) was longer for septic AKI. There was a trend to lower serum creatinine (106 [73 to 158] versus 121 [88 to 184] mumol/L; P = 0.01) and RRT dependence (9 versus 14%; P = 0.052) at hospital discharge for septic AKI. Patients with septic AKI were sicker and had a higher burden of illness and greater abnormalities in acute physiology. Patients with septic AKI had an increased risk for death and longer duration of hospitalization yet showed trends toward greater renal recovery and independence from RRT.
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            The APACHE III Prognostic System

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              Test of the National Death Index and Equifax Nationwide Death Search.

              The authors compared the ability of the National Death Index and the Equifax Nationwide Death Search to ascertain deaths of participants in the Nurses' Health Study. Each service was sent information on 197 participants aged 60-68 years in 1989 whose deaths were reported by kin or postal authorities and 1,997 participants of the same age who were known to be alive. Neither service was aware of the authors' information regarding participants' vital status. The sensitivity of the National Death Index was 98 percent and that of Equifax was 79 percent. Sensitivity was similar for women aged 65-68 years; however, for women aged 61-64 years, the sensitivity of the National Death Index was 97.7 percent compared with 60.2 percent for Equifax. The specificity of both services was approximately 100 percent. The contrast between the sources of these databases and the matching algorithms they employ has implications for researchers and for those planning health data systems.
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                Author and article information

                Journal
                Clinical Journal of the American Society of Nephrology
                CJASN
                American Society of Nephrology (ASN)
                1555-9041
                1555-905X
                June 07 2012
                June 2012
                June 2012
                March 29 2012
                : 7
                : 6
                : 895-905
                Article
                10.2215/CJN.07100711
                3362308
                22461537
                e9c25abc-7395-4265-97f1-5ef84b771075
                © 2012
                History

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