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Original Articles

A novel method for creatinine adjustment makes the revised Lund–Malmö GFR estimating equation applicable in children

, , , , , , & show all
Pages 456-463 | Received 16 Mar 2020, Accepted 21 May 2020, Published online: 06 Jul 2020

Figures & data

Table 1. Patient characteristics.

Figure 1. Plasma/serum creatinine values in 83,157 patients from the reference cohort as a function of age in (A) females (n = 57 > 180 μmol/L) and (B) males (n = 130 > 180 μmol/L). The double line represents the creatinine growth curve based on linear regression with fractional polynomials of age as independent variable (see text).

Figure 1. Plasma/serum creatinine values in 83,157 patients from the reference cohort as a function of age in (A) females (n = 57 > 180 μmol/L) and (B) males (n = 130 > 180 μmol/L). The double line represents the creatinine growth curve based on linear regression with fractional polynomials of age as independent variable (see text).

Figure 2. Individual creatinine growth projections for two hypothetical example pairs of children: (1) age 6 years and normal creatinine levels (boy 34 and girl 35 µmol/L), (2) age 12 years with elevated creatinine levels (boy 121 and girl 108 µmol/L) indicating chronic kidney disease (CKD). Adjusted creatinine for the Lund–Malmö revised equation (LMR18) is obtained by following the corresponding growth curve until age 18 years (marked with crosses).

Figure 2. Individual creatinine growth projections for two hypothetical example pairs of children: (1) age 6 years and normal creatinine levels (boy 34 and girl 35 µmol/L), (2) age 12 years with elevated creatinine levels (boy 121 and girl 108 µmol/L) indicating chronic kidney disease (CKD). Adjusted creatinine for the Lund–Malmö revised equation (LMR18) is obtained by following the corresponding growth curve until age 18 years (marked with crosses).

Table 2. Bias, precision, accuracy (95% confidence intervals) of GFR estimating equations in children 2.0–17.9 years stratified for measured GFR <75 (n = 932) and ≥75 mL/min/1.73 m2 (n = 3 073).

Figure 3. Associations in the validation cohort between age groups and median bias (estimated GFR – measured GFR) of the Lund–Malmö revised equation, both in the original formulation (LMR) and with creatinine adjusted to age 18 years (LMR18). Results stratified by (A) females with mGFR <75 (n = 385) and ≥75 mL/min/1.73 m2 (n = 1309) and (B) males with measured GFR (mGFR) <75 (n = 547) and ≥75 mL/min/1.73 m2 (n = 1764).

Figure 3. Associations in the validation cohort between age groups and median bias (estimated GFR – measured GFR) of the Lund–Malmö revised equation, both in the original formulation (LMR) and with creatinine adjusted to age 18 years (LMR18). Results stratified by (A) females with mGFR <75 (n = 385) and ≥75 mL/min/1.73 m2 (n = 1309) and (B) males with measured GFR (mGFR) <75 (n = 547) and ≥75 mL/min/1.73 m2 (n = 1764).

Table 3. Bias and accuracy (P30) of GFR estimating equations in children 2.0–17.9 years old stratified by sex and measured GFR <75 and ≥75 mL/min/1.73 m2.

Supplemental material

Supplemental Material

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Data availability statement

The EKFC dataset used in the present study is hosted by the Lund University Population Research Platform (LUPOP). Legal and ethical restrictions prevent public sharing of the dataset. Data can be made available for collaborations upon request to interested researchers but would generally require a new ethical permission and the permission of each of the data-owners. You can find contact information for the data host at https://www.lupop.lu.se/