Contrast-induced acute kidney injury

Changed by Muhammad Naeem, 5 Sep 2014

Updates to Article Attributes

Body was changed:

Contrast nephropathy is the third most common cause of all hospital-acquired acute renal failurefailures and accounts for approximately 10% of all cases. ItThere is usually asymptomatic andstill an ongoing debate regarding its occurrence after the intravenous contrast administration, because most of the cases occur after intraarterial administration of contrast for angiographic procedures. Even though the incidence is more likely in patients with preexisting renal failure, diabetes or dehydration.5% after intravenous contrast administration.6

Definition

So far there are no standards to report the CIN, therefore, definition used in literature are variable. The definition of contrast nephropathy relies on serial plasma creatinine concentrations. A baseline creatinine level should be obtained before the procedure. The peak effect on creatinine occurs at between 48 and 72 hours.  Many centres are also now using estimated glomerular filtration rate (eGFR) as the assessment of renal function prior to intravenous contrast investigations where practicable.  This is calculated from the patient's age,race, sex and serum creatinine level.  Online calculators are also available to assist in easily calculating eGFR.5

  • relative : 25% rise in creatinine over baseline
  • absolute : rise of greater than 44μmol/L

In a review of PCI for coronary artery disease, the incidence of contrast nephropathy was 3.3% overall. 25% of the cases had a baseline serum creatinine of over 177μmol/L.

Contrast-induced acute kidney injury (CI-AKI) has now also been described in which injury or damage to the kidney has taken place, but is sub-clinical in that no measurable reduction in renal filtration is apparent.4

Risk stratification

Risk for most normal individuals with no risk factors is based on baseline renal function.

  • low : Cr < 130μmol/L or CrCl > 60ml/min
  • medium : Cr 130 - 200μmol/L or CrCl 60 - 30ml/min
  • high : Cr > 200μmol/L or CrCl < 30ml/min

For those using eGFR

  • very low risk: > 60 mL/min
  • low risk: 45 - 59 mL/min
  • moderate: 30 - 45 mL/min
  • high risk: < 30mls mL/min
High dose contrast

However, if they are going to have an investigation with more than 300ml of iodinated contrast or two studies less than 72 hours apart, their risk is elevated to the medium group irrespective of their baseline renal function.

Predisposing risk factors

Patients with risk factors are automatically elevated to higher risk groups:

  • diabetes mellitus, multiple myeloma, CHF, cirrhosis, nephrotic syndrome, sepsis
    • low : as above
    • medium : Cr 110 - 130μmol/L or CrCl < 90ml/min
    • high : Cr 130 - 200μmol/L or CrCl <60ml/min
  • renal transplant, dehydration or hypotension
    • low : not possible
    • medium : even if their renal function is normal
    • high : Cr 130 - 200μmol/L or CrCl 60 - 30ml/min

Treatment

The most important factor is adequate prehydration and assessment of renal function. Risk stratification helps to determine what the most appropriate preparation is:

  • low : oral fluids only
  • medium :
    • IV 0.9% N. Saline for 12 hours before and after the procedure
    • @ 48 hours : if the creatinine is 25% above baseline, a further check 5 days post-procedure should be taken
  • high
    • IV 0.9% N. Saline for 12 hours before and after the procedure
    • NAC 600mg orally bd (3 does before the procedure and one afterwards)
    • check Creatinine at baseline, 48 hours, 5 days and 10 days
  • -<p><strong>Contrast nephropathy</strong> is the third most common cause of all hospital-acquired acute renal failure and accounts for approximately 10% of all cases. It is usually asymptomatic and is more likely in patients with preexisting renal failure, diabetes or dehydration.</p><h4>Definition</h4><p>The definition of contrast nephropathy relies on serial plasma creatinine concentrations. A baseline creatinine level should be obtained before the procedure. The peak effect on creatinine occurs at between 48 and 72 hours.  Many centres are also now using estimated glomerular filtration rate (eGFR) as the assessment of renal function prior to intravenous contrast investigations where practicable.  This is calculated from the patient's age,race, sex and serum creatinine level.  Online calculators are also available to assist in easily calculating eGFR.<sup>5</sup></p><ul>
  • -<li>
  • -<strong>relative</strong> : 25% rise in creatinine over baseline</li>
  • -<li>
  • -<strong>absolute</strong> : rise of greater than 44μmol/L</li>
  • -</ul><p>In a review of PCI for coronary artery disease, the incidence of contrast nephropathy was 3.3% overall. 25% of the cases had a baseline serum creatinine of over 177μmol/L.</p><p>Contrast-induced acute kidney injury (CI-AKI) has now also been described in which injury or damage to the kidney has taken place, but is sub-clinical in that no measurable reduction in renal filtration is apparent.<sup>4</sup></p><h4>Risk stratification</h4><p>Risk for most normal individuals with no risk factors is based on baseline renal function.</p><ul style="background-position: 2px 2px; margin: 10px; padding: 0px 5px; border-left-color: rgb(185, 196, 208); border-left-width: 20px; border-left-style: solid; background-repeat: no-repeat no-repeat; background-color: rgb(255, 255, 255);">
  • -<li>
  • -<strong>low</strong> : Cr &lt; 130μmol/L <em>or</em> CrCl &gt; 60ml/min</li>
  • -<li>
  • -<strong>medium </strong>: Cr 130 - 200μmol/L <em>or</em> CrCl 60 - 30ml/min</li>
  • -<li>
  • -<strong>high : </strong>Cr &gt; 200μmol/L or CrCl &lt; 30ml/min</li>
  • +<p><strong>Contrast nephropathy</strong> is the third most common cause of all hospital-acquired acute renal failures and accounts for approximately 10% of all cases. There is still an ongoing debate regarding its occurrence after the intravenous contrast administration, because most of the cases occur after intraarterial administration of contrast for angiographic procedures. Even though the incidence is 5% after intravenous contrast administration.<sup>6</sup>  </p><h4>Definition</h4><p>So far there are no standards to report the CIN, therefore, definition used in literature are variable. The definition of contrast nephropathy relies on serial plasma creatinine concentrations. A baseline creatinine level should be obtained before the procedure. The peak effect on creatinine occurs at between 48 and 72 hours.  Many centres are also now using estimated glomerular filtration rate (eGFR) as the assessment of renal function prior to intravenous contrast investigations where practicable.  This is calculated from the patient's age,race, sex and serum creatinine level.  Online calculators are also available to assist in easily calculating eGFR.<sup>5</sup></p><ul>
  • +<li>
  • +<strong>relative</strong> : 25% rise in creatinine over baseline</li>
  • +<li>
  • +<strong>absolute</strong> : rise of greater than 44μmol/L</li>
  • +</ul><p>In a review of PCI for coronary artery disease, the incidence of contrast nephropathy was 3.3% overall. 25% of the cases had a baseline serum creatinine of over 177μmol/L.</p><p>Contrast-induced acute kidney injury (CI-AKI) has now also been described in which injury or damage to the kidney has taken place, but is sub-clinical in that no measurable reduction in renal filtration is apparent.<sup>4</sup></p><h4>Risk stratification</h4><p>Risk for most normal individuals with no risk factors is based on baseline renal function.</p><ul>
  • +<li>
  • +<strong>low</strong> : Cr &lt; 130μmol/L <em>or</em> CrCl &gt; 60ml/min</li>
  • +<li>
  • +<strong>medium </strong>: Cr 130 - 200μmol/L <em>or</em> CrCl 60 - 30ml/min</li>
  • +<li>
  • +<strong>high : </strong>Cr &gt; 200μmol/L or CrCl &lt; 30ml/min</li>
  • -<li>
  • -<strong>very low risk</strong>: &gt; 60 mL/min</li>
  • -<li>
  • -<strong>low risk</strong>: 45 - 59 mL/min</li>
  • -<li>
  • -<strong>moderate</strong>: 30 - 45 mL/min</li>
  • -<li>
  • -<strong>high ris</strong>k: &lt; 30mls mL/min</li>
  • +<li>
  • +<strong>very low risk</strong>: &gt; 60 mL/min</li>
  • +<li>
  • +<strong>low risk</strong>: 45 - 59 mL/min</li>
  • +<li>
  • +<strong>moderate</strong>: 30 - 45 mL/min</li>
  • +<li>
  • +<strong>high ris</strong>k: &lt; 30mls mL/min</li>
  • -<li>
  • -<a title="diabetes mellitus" href="/articles/diabetes-mellitus">diabetes mellitus</a>, <a title="Multiple Myeloma" href="/articles/multiple-myeloma-1">multiple myeloma</a>, CHF, <a title="Cirrhosis" href="/articles/cirrhosis">cirrhosis</a>, <a title="nephrotic syndrome" href="/articles/nephrotic-syndrome">nephrotic syndrome</a>, sepsis<ul>
  • -<li>
  • -<strong>low</strong> : as above</li>
  • -<li>
  • -<strong>medium</strong> : Cr 110 - 130μmol/L <em>or</em> CrCl &lt; 90ml/min</li>
  • -<li>
  • -<strong>high</strong> : Cr 130 - 200μmol/L <em>or</em> CrCl &lt;60ml/min</li>
  • +<li>
  • +<a href="/articles/diabetes-mellitus">diabetes mellitus</a>, <a href="/articles/multiple-myeloma-1">multiple myeloma</a>, CHF, <a href="/articles/cirrhosis">cirrhosis</a>, <a href="/articles/nephrotic-syndrome">nephrotic syndrome</a>, sepsis<ul>
  • +<li>
  • +<strong>low</strong> : as above</li>
  • +<li>
  • +<strong>medium</strong> : Cr 110 - 130μmol/L <em>or</em> CrCl &lt; 90ml/min</li>
  • +<li>
  • +<strong>high</strong> : Cr 130 - 200μmol/L <em>or</em> CrCl &lt;60ml/min</li>
  • -</li>
  • +</li>
  • -<li>
  • -<strong>low</strong> : not possible</li>
  • -<li>
  • -<strong>medium</strong> : even if their renal function is normal</li>
  • -<li>
  • -<strong>high</strong> : Cr 130 - 200μmol/L <em>or</em> CrCl 60 - 30ml/min</li>
  • +<li>
  • +<strong>low</strong> : not possible</li>
  • +<li>
  • +<strong>medium</strong> : even if their renal function is normal</li>
  • +<li>
  • +<strong>high</strong> : Cr 130 - 200μmol/L <em>or</em> CrCl 60 - 30ml/min</li>
  • -</li>
  • +</li>
  • -<li>
  • -<strong>low</strong> : oral fluids only</li>
  • -<li>
  • +<li>
  • +<strong>low</strong> : oral fluids only</li>
  • +<li>
  • -<li>IV 0.9% N. Saline for 12 hours before and after the procedure</li>
  • -<li>@ 48 hours : if the creatinine is 25% above baseline, a further check 5 days post-procedure should be taken</li>
  • +<li>IV 0.9% N. Saline for 12 hours before and after the procedure</li>
  • +<li>@ 48 hours : if the creatinine is 25% above baseline, a further check 5 days post-procedure should be taken</li>
  • -</li>
  • -<li>
  • +</li>
  • +<li>
  • -<li>IV 0.9% N. Saline for 12 hours before and after the procedure</li>
  • -<li>NAC 600mg orally bd (3 does before the procedure and one afterwards)</li>
  • -<li>check Creatinine at baseline, 48 hours, 5 days and 10 days</li>
  • +<li>IV 0.9% N. Saline for 12 hours before and after the procedure</li>
  • +<li>NAC 600mg orally bd (3 does before the procedure and one afterwards)</li>
  • +<li>check Creatinine at baseline, 48 hours, 5 days and 10 days</li>
  • -</li>
  • +</li>

References changed:

  • 5. Katzberg RW, Lamba R. Contrast-induced nephropathy after intravenous administration: fact or fiction?. (2009) Radiologic clinics of North America. 47 (5): 789-800, v. <a href="https://doi.org/10.1016/j.rcl.2009.06.002">doi:10.1016/j.rcl.2009.06.002</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/19744594">Pubmed</a> <span class="ref_v4"></span>

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