Renal Pre-Contrast Screening (CT / MRI)
Screening questionnaire to identify patients at higher risk of renal dysfunction (eGFR <45 mL/min/1.73 m²), a level below which the risk of contrast-induced nephropathy (on CT with iodinated contrast) increases significantly. Also effectively stratifies nephrogenic systemic fibrosis (NSF) risk before gadolinium-enhanced MRI, with potential for cost savings and streamlined care. High sensitivity and moderate-to-good specificity; validated for ambulatory use.

Renal Pre-Contrast Screening (CT / MRI)
Answer the 6 questions below. All are required.
Answer all questions to generate the result.
Evidence
In a study of 1361 ambulatory patients, for detecting eGFR <45 mL/min/1.73 m² the questionnaire showed sensitivity of 92.9%, specificity of 65.3%, PPV of 2.7% and NPV of 99.9%. (Too et al., Eur J Radiol 2015)
The questionnaire also effectively stratifies nephrogenic systemic fibrosis (NSF) risk before gadolinium-enhanced MRI, with potential for cost savings and streamlined care. When the decision to administer gadolinium is based solely on questionnaire responses at the time of order, sensitivity of 71.4% for detecting eGFR <30 mL/min/1.73 m², specificity of 74.2%, PPV of 2.9% and NPV of 99.6% were observed. (Choyke et al., Radiology 2003)
How renal pre-contrast screening (Choyke) works
The Choyke questionnaire identifies ambulatory patients at higher risk of renal dysfunction (eGFR <45 mL/min/1.73 m²), a level below which the risk of iodinated contrast-induced nephropathy increases significantly. It also stratifies nephrogenic systemic fibrosis (NSF) risk before gadolinium-enhanced MRI.
Choyke diagnostic performance in ambulatory patients
Choyke positive
Serum creatinine and eGFR calculation are recommended before IV contrast.
Choyke negative
Very low probability of relevant renal dysfunction. In the standard ambulatory setting, creatinine/eGFR is generally not required before IV contrast.
When NOT to use simplified screening
Do not use simplified screening in hospitalized/unstable patients, with suspected acute kidney injury, or when institutional protocol requires creatinine/eGFR. The questionnaire was validated in ambulatory patients and does not replace clinical judgment in higher-risk scenarios.