Renal function
Renal function, in nephrology, is an indication of the state of the kidney and its role in renal physiology. Glomerular filtration rate (GFR) describes the flow rate of filtered fluid through the kidney. Creatinine clearance rate (C_{Cr} or CrCl) is the volume of blood plasma that is cleared of creatinine per unit time and is a useful measure for approximating the GFR. Creatinine clearance exceeds GFR due to creatinine secretion, which can be blocked by cimetidine. In alternative fashion, overestimation by older serum creatinine methods resulted in an underestimation of creatinine clearance, which provided a less biased estimate of GFR.^{[1]} Both GFR and C_{Cr} may be accurately calculated by comparative measurements of substances in the blood and urine, or estimated by formulas using just a blood test result (eGFR and eC_{Cr}).
The results of these tests are used to assess the excretory function of the kidneys. Staging of chronic kidney disease is based on categories of GFR as well as albuminuria and cause of kidney disease.^{[2]}
Dosage of drugs that are excreted primarily via urine may need to be modified based on either GFR or creatinine clearance.
Contents
 Indirect markers 1

Glomerular filtration rate 2
 Measurement using inulin 2.1

Pressure definition 2.2
 Kf 2.2.1
 PG 2.2.2
 PB 2.2.3
 ∏G 2.2.4
 ∏B 2.2.5

Creatininebased approximations of GFR 3
 Creatinine Clearance CCr 3.1

Estimated values 4
 Estimated creatinine clearance rate (eCCr) using CockcroftGault formula 4.1
 Estimated GFR (eGFR) using Modification of Diet in Renal Disease (MDRD) formula 4.2
 Estimated GFR (eGFR) using the CKDEPI formula 4.3
 Estimated GFR (eGFR) using the Mayo Quadratic formula 4.4
 Estimated GFR for children using Schwartz formula 4.5
 Importance of calibration of the serum creatinine level and the IDMS standardization effort 4.6
 Cystatin C 4.7

Normal ranges 5
 Chronic kidney disease stages 5.1
 See also 6
 References 7

External links 8
 Online calculators 8.1
 Reference links 8.2
Indirect markers
Most doctors use the plasma concentrations of the waste substances of creatinine and urea (U), as well as electrolytes (E), to determine renal function. These measures are adequate to determine whether a patient is suffering from kidney disease.
However, blood urea nitrogen (BUN) and creatinine will not be raised above the normal range until 60% of total kidney function is lost. Hence, the more accurate Glomerular filtration rate or its approximation of the creatinine clearance is measured whenever renal disease is suspected or careful dosing of nephrotoxic drugs is required.
Elevated protein levels in urine mark some kidney disease. The most sensitive marker of proteinuria is elevated urine albumin. Persistent presence of more than 30 mg albumin per gram creatinine in the urine is diagnostic of chronic kidney disease (microalbuminuria is a level of 30–299 mg/L urine or 30299 mg/24 hrs; a concentration of albumin in the urine that is not detected by usual urine dipstick methods).
Glomerular filtration rate
Glomerular filtration rate (GFR) is the volume of fluid filtered from the renal (kidney) glomerular capillaries into the Bowman's capsule per unit time.^{[3]} Central to the physiologic maintenance of GFR is the differential basal tone of the afferent and efferent arterioles (see diagram). In other words, the filtration rate is dependent on the difference between the higher blood pressure created by vasoconstriction of the input or afferent arteriole versus the lower blood pressure created lesser vasoconstriction of the output or efferent arteriole.
Glomerular filtration rate (GFR) is equal to the Clearance Rate when any solute is freely filtered and is neither reabsorbed nor secreted by the kidneys. The rate therefore measured is the quantity of the substance in the urine that originated from a calculable volume of blood. Relating this principle to the below equation  for the substance used, the product of urine concentration and urine flow equals the mass of substance excreted during the time that urine has been collected. This mass equals the mass filtered at the glomerulus as nothing is added or removed in the nephron. Dividing this mass by the plasma concentration gives the volume of plasma which the mass must have originally come from, and thus the volume of plasma fluid that has entered Bowman's capsule within the aforementioned period of time. The GFR is typically recorded in units of volume per time, e.g., milliliters per minute mL/min. Compare to filtration fraction.
 GFR = \frac { \mbox{Urine Concentration} \times \mbox{Urine Flow} }{ \mbox{Plasma Concentration} }
There are several different techniques used to calculate or estimate the glomerular filtration rate (GFR or eGFR). The above formula only applies for GFR calculation when it is equal to the Clearance Rate.
Measurement using inulin
The GFR can be determined by injecting inulin or the inulinanalog sinistrin into the plasma. Since both inulin and sinsitrin are neither reabsorbed nor secreted by the kidney after glomerular filtration, their rate of excretion is directly proportional to the rate of filtration of water and solutes across the glomerular filter. Compared to the MDRD formula, the inulin clearance slightly overestimates the glomerular function. In early stage renal disease, the inulin clearance may remain normal due to hyperfiltration in the remaining nephrons.^{[4]} Incomplete urine collection is an important source of error in inulin clearance measurement.
Pressure definition
More precisely, GFR is the fluid flow rate between the glomerular capillaries and the Bowman's capsule:
{\operatorname{d}Q\over\operatorname{d}t} = K_f \times (P_G  P_B  \Pi_G + \Pi_B)^{[5]}^{[6]}
Where:
 {\operatorname{d}Q\over\operatorname{d}t} is the GFR.
 K_f is called the filtration constant and is defined as the product of the hydraulic conductivity and the surface area of the glomerular capillaries.
 P_G is the hydrostatic pressure within the glomerular capillaries.
 P_B is the hydrostatic pressure within the Bowman's capsule.
 \Pi_G is the colloid osmotic pressure within the glomerular capillaries.
 and \Pi_B is the colloid osmotic pressure within the Bowman's capsule.
K_{f}
Because this constant is a measurement of hydraulic conductivity multiplied by the capillary surface area, it is almost impossible to measure physically. However, it can be determined experimentally. Methods of determining the GFR are listed in the above and below sections and it is clear from our equation that K_f can be found by dividing the experimental GFR by the net filtration pressure:^{[5]}
K_f = \frac{\textrm{GFR}}{\textrm{Net\ Filt.\ Pressure}}=\frac{\textrm{GFR}}{(P_G  P_B  \Pi_G + \Pi_B)}
P_{G}
The hydrostatic pressure within the glomerular capillaries is determined by the pressure difference between the fluid entering immediately from the afferent arteriole and leaving through the efferent arteriole. The pressure difference is approximated by the product of the total resistance of the respective arteriole and the flux of blood through it:^{[6]}
P_a  P_G = R_a \times Q_a
P_G  P_e = R_e \times Q_e
Where:
 P_a is the afferent arteriole pressure.
 P_e is the efferent arteriole pressure.
 R_a is the afferent arteriole resistance.
 R_e is the efferent arteriole resistance.
 Q_a is the afferent arteriole flux.
 And, Q_e is the efferent arteriole flux.
P_{B}
The pressure in the Bowman's capsule and proximal tubule can be determined by the difference between the pressure in the Bowman's capsule and the descending tubule:^{[6]}
P_B  P_d = R_d \times (Q_a  Q_e)
Where:
 P_d is the pressure in the descending tubule.
 And, R_d is the resistance of the descending tubule.
∏_{G}
Blood plasma has a good many proteins in it and they exert an inward directed force called the colloid osmotic pressure on the water in hypotonic solutions across a membrane, i.e., in the Bowman's capsule. Because plasma proteins are virtually incapable of escaping the glomerular capillaries, this oncotic pressure is defined, simply, by the ideal gas law:^{[5]}^{[6]}
\Pi_G = RTc
Where:
 R is the universal gas constant
 T is the temperature.
 And, c is concentration in mol/L of plasma proteins (remember the solutes can freely diffuse through the glomerular capsule).
∏_{B}
This value is almost always taken to be equal to zero because, in a healthy nephron, there should be no proteins in the Bowman's Capsule.^{[5]}
Creatininebased approximations of GFR
In clinical practice, however, creatinine clearance or estimates of creatinine clearance based on the serum creatinine level are used to measure GFR. Creatinine is produced naturally by the body (creatinine is a breakdown product of creatine phosphate, which is found in muscle). It is freely filtered by the glomerulus, but also actively secreted by the peritubular capillaries in very small amounts such that creatinine clearance overestimates actual GFR by 1020%. This margin of error is acceptable, considering the ease with which creatinine clearance is measured. Unlike precise GFR measurements involving constant infusions of inulin, creatinine is already at a steadystate concentration in the blood, and so measuring creatinine clearance is much less cumbersome. However, creatinine estimates of GFR have their limitations. All of the estimating equations depend on a prediction of the 24hour creatinine excretion rate, which is a function of muscle mass which is quite variable. One of the equations, the Cockcroft and Gault equation (see below) does not correct for race. With a higher muscle mass, serum creatinine will be higher for any given rate of clearance.
A common mistake made when just looking at serum creatinine is the failure to account for muscle mass. Hence, an older woman with a serum creatinine of 1.4 mg/dL may actually have a moderately severe degree of renal insufficiency, whereas a young muscular male can have a normal level of renal function at this serum creatinine level. Creatininebased equations should be used with caution in cachectic patients and patients with cirrhosis. They often have very low muscle mass and a much lower creatinine excretion rate than predicted by the equations below, such that a cirrhotic patient with a serum creatinine of 0.9 mg/dL may have a moderately severe degree of renal insufficiency.
Creatinine Clearance C_{Cr}
One method of determining GFR from creatinine is to collect urine (usually for 24 hours) to determine the amount of creatinine that was removed from the blood over a given time interval. If one removes 1440 mg in 24 hours, this is equivalent to removing 1 mg/min. If the blood concentration is 0.01 mg/mL (1 mg/dL), then one can say that 100 mL/min of blood is being "cleared" of creatinine, since, to get 1 mg of creatinine, 100 mL of blood containing 0.01 mg/mL would need to have been cleared.
Creatinine clearance (C_{Cr}) is calculated from the creatinine concentration in the collected urine sample (U_{Cr}), urine flow rate (Vdt), and the plasma concentration (P_{Cr}). Since the product of urine concentration and urine flow rate yields creatinine excretion rate, which is the rate of removal from the blood, creatinine clearance is calculated as removal rate per min (U_{Cr}×Vdt) divided by the plasma creatinine concentration. This is commonly represented mathematically as
 C_{Cr} = \frac { U_{Cr} \times \dot{V} }{ P_{Cr} }
Example: A person has a plasma creatinine concentration of 0.01 mg/ml and in 1 hour produces 60ml of urine with a creatinine concentration of 1.25 mg/mL.
 C_{Cr} = \frac {1.25 mg/mL \times \frac{60mL}{60min}}{0.01 mg/mL} = \frac { {1.25 mg/mL} \times {1 mL/min}}{0.01 mg/mL} = \frac {1.25 mg/min}{0.01 mg/mL} = {125 mL/min}
The common procedure involves undertaking a 24hour urine collection, from emptybladder one morning to the contents of the bladder the following morning, with a comparative blood test then taken. The urinary flow rate is still calculated per minute, hence:
 C_{Cr} = \frac { U_{Cr} \ \times \ \mbox{24hour volume} }{P_{Cr} \ \times \ 24 \times 60 mins}
To allow comparison of results between people of different sizes, the C_{Cr} is often corrected for the body surface area (BSA) and expressed compared to the average sized man as mL/min/1.73 m^{2}. While most adults have a BSA that approaches 1.7 (1.61.9), extremely obese or slim patients should have their C_{Cr} corrected for their actual BSA.
 C_{Crcorrected} = \frac \ \times \ {1.73}} {BSA}
 BSA can be calculated on the basis of weight and height.
Twentyfour hour urine collection to assess creatinine clearance is no longer widely performed, due to difficulty in assuring complete specimen collection. To assess the adequacy of a complete collection, one always calculates the amount of creatinine excreted over a 24hour period. This amount varies with muscle mass, and is higher in young people vs. old, in blacks vs. whites, and in men vs. women. An unexpectedly low or high 24hour creatinine excretion rate voids the test. Nevertheless, in cases where estimates of creatinine clearance from serum creatinine are unreliable, creatinine clearance remains a useful test. These cases include "estimation of GFR in individuals with variation in dietary intake (vegetarian diet, creatine supplements) or muscle mass (amputation, malnutrition, muscle wasting), since these factors are not specifically taken into account in prediction equations."^{[7]}
Estimated values
A number of formulae have been devised to estimate GFR or C_{cr} values on the basis of serum creatinine levels.
Estimated creatinine clearance rate (eC_{Cr}) using CockcroftGault formula
A commonly used surrogate marker for estimate of creatinine clearance is the CockcroftGault (CG) formula, which in turn estimates GFR in ml/min:^{[8]} It is named after the scientists who first published the formula, and it employs serum creatinine measurements and a patient's weight to predict the creatinine clearance.^{[9]}^{[10]} The formula, as originally published, is:
 eC_{Cr} = \frac { \mbox{(140  Age)} \ \times \ \mbox{Mass (in kilograms)} \ \times \ } {\mbox{72} \ \times \ \mbox{Serum Creatinine (in mg/dL)}}
 This formula expects weight to be measured in kilograms and creatinine to be measured in mg/dL, as is standard in the USA. The resulting value is multiplied by a constant of 0.85 if the patient is female. This formula is useful because the calculations are simple and can often be performed without the aid of a calculator.
When serum creatinine is measured in µmol/L:
 eC_{Cr} = \frac { \mbox{(140  Age)} \ \times \ \mbox{Mass (in kilograms)} \ \times \ {Constant} } {\mbox{Serum Creatinine (in } \mu \mbox{mol/L)}}
 Where Constant is 1.23 for men and 1.04 for women.
One interesting feature of the Cockcroft and Gault equation is that it shows how dependent the estimation of CCr is based on age. The age term is (140  age). This means that a 20yearold person (14020 = 120) will have twice the creatinine clearance as an 80yearold (14080 = 60) for the same level of serum creatinine (120 is twice as great as 60). The CG equation assumes that a woman will have a 15% lower creatinine clearance than a man at the same level of serum creatinine.
Estimated GFR (eGFR) using Modification of Diet in Renal Disease (MDRD) formula
The most recently advocated formula for calculating the GFR is the one that was developed by the Modification of Diet in Renal Disease Study Group.^{[11]} Most laboratories in Australia,^{[12]} and The United Kingdom now calculate and report the MDRD estimated GFR along with creatinine measurements and this forms the basis of chronic kidney disease.^{[13]} The adoption of the automatic reporting of MDRDeGFR has been widely criticised.^{[14]}^{[15]}^{[16]}
The most commonly used formula is the "4variable MDRD," which estimates GFR using four variables: serum creatinine, age, ethnicity, and gender.^{[17]} The original MDRD used six variables with the additional variables being the blood urea nitrogen and albumin levels.^{[11]} The equations have been validated in patients with chronic kidney disease; however both versions underestimate the GFR in healthy patients with GFRs over 60 mL/min.^{[18]}^{[19]} The equations have not been validated in acute renal failure.
For creatinine in µmol/L:
 \mbox{eGFR} = \mbox{32788}\ \times \ \mbox{Serum Creatinine}^{1.154} \ \times \ \mbox{Age}^{0.203} \ \times \ \ \times \
For creatinine in mg/dl:
 \mbox{eGFR} = \mbox{186}\ \times \ \mbox{Serum Creatinine}^{1.154} \ \times \ \mbox{Age}^{0.203} \ \times \ \ \times \
 Creatinine levels in µmol/L can be converted to mg/dL by dividing them by 88.4. The 32788 number above is equal to 186×88.4^{1.154}.
A more elaborate version of the MDRD equation also includes serum albumin and blood urea nitrogen (BUN) levels:
 \mbox{eGFR} = \mbox{170}\ \times \ \mbox{Serum Creatinine}^{0.999} \ \times \ \mbox{Age}^{0.176} \ \times \ \ \times \ \ \times \ \mbox{BUN}^{0.170} \ \times \ \mbox{Albumin}^{+0.318}
 Where the creatinine and blood urea nitrogen concentrations are both in mg/dL. The albumin concentration is in g/dL.
These MDRD equations are to be used only if the laboratory has NOT calibrated its serum creatinine measurements to isotope dilution mass spectrometry (IDMS). When IDMScalibrated serum creatinine is used (which is about 6% lower), the above equations should be multiplied by 175/186 or by 0.94086.^{[20]}
Since these formulae do not adjust for body mass, they (relative to the CockcroftGault formula) underestimate eGFR for heavy people and overestimate it for underweight people. (see CockcroftGault formula above).
Estimated GFR (eGFR) using the CKDEPI formula
The CKDEPI (Chronic Kidney Disease Epidemiology Collaboration) formula was published in May 2009. It was developed in an effort to create a formula more accurate than the MDRD formula, especially when actual GFR is greater than 60 mL/min per 1.73 m2.
Researchers pooled data from multiple studies to develop and validate this new equation. They used 10 studies that included 8254 participants, randomly using 2/3 of the data sets for development and the other 1/3 for internal validation. Sixteen additional studies, which included 3896 participants, were used for external validation.
The CKDEPI equation performed better than the MDRD (Modification of Diet in Renal Disease Study) equation, especially at higher GFR, with less bias and greater accuracy. When looking at NHANES (National Health and Nutrition Examination Survey) data, the median estimated GFR was 94.5 mL/min per 1.73 m2 vs. 85.0 mL/min per 1.73 m2, and the prevalence of chronic kidney disease was 11.5% versus 13.1%. Despite its overall superiority to the MDRD equation, the CKDEPI equations performed poorly in certain populations, like black women, the elderly and the obese, so has yet to overtake the MDRD in popularity among clinicians.^{[21]}
The CKDEPI equation, expressed as a single equation, is:
 \mbox{eGFR} = \mbox{141}\ \times \ \mbox{min(SCr/k,1)}^{a} \ \times \ \mbox{max(SCr/k,1)}^{1.209} \ \times \ \mbox{0.993}^{Age} \ \times \ \ \times \ \
where SCr is serum creatinine (mg/dL), k is 0.7 for females and 0.9 for males, a is 0.329 for females and 0.411 for males, min indicates the minimum of SCr/k or 1, and max indicates the maximum of SCr/k or 1.
A clearer version may be as follows: For creatinine (IDMS calibrated) in mg/dL:
Black Female
If serum creatinine (Scr) <= 0.7
 \mbox{eGFR} = \mbox{166}\ \times \ \mbox{(SCr/0.7)}^{0.329} \ \times \ \mbox{0.993}^{Age} \
If serum creatinine (Scr) > 0.7
 \mbox{eGFR} = \mbox{166}\ \times \ \mbox{(SCr/0.7)}^{1.209} \ \times \ \mbox{0.993}^{Age} \
Black male
If serum creatinine (Scr) <= 0.9
 \mbox{eGFR} = \mbox{163}\ \times \ \mbox{(SCr/0.9)}^{0.411} \ \times \ \mbox{0.993}^{Age} \
If serum creatinine (Scr) > 0.9
 \mbox{eGFR} = \mbox{163}\ \times \ \mbox{(SCr/0.9)}^{1.209} \ \times \ \mbox{0.993}^{Age} \
White or other race female
If serum creatinine (Scr) <= 0.7
 \mbox{eGFR} = \mbox{144}\ \times \ \mbox{(SCr/0.7)}^{0.329} \ \times \ \mbox{0.993}^{Age} \
If serum creatinine (Scr) > 0.7
 \mbox{eGFR} = \mbox{144}\ \times \ \mbox{(SCr/0.7)}^{1.209} \ \times \ \mbox{0.993}^{Age} \
White or other race male
If serum creatinine (Scr) <= 0.9
 \mbox{eGFR} = \mbox{141}\ \times \ \mbox{(SCr/0.9)}^{0.411} \ \times \ \mbox{0.993}^{Age} \
If serum creatinine (Scr) > 0.9
 \mbox{eGFR} = \mbox{141}\ \times \ \mbox{(SCr/0.9)}^{1.209} \ \times \ \mbox{0.993}^{Age} \
This formula was developed by Levey et al.^{[22]}
The formula CKDEPI may provide improved cardiovascular risk prediction over the MDRD Study formula in a middleage population.^{[23]}
Estimated GFR (eGFR) using the Mayo Quadratic formula
Another estimation tool to calculate GFR is the Mayo Quadratic formula. This formula was developed by Rule et al,^{[18]} in an attempt to better estimate GFR in patients with preserved kidney function. It is well recognized that the MDRD formula tends to underestimate GFR in patients with preserved kidney function.
The equation is:
 \mbox{eGFR} = \mbox{exp}{(1.911+ 5.249/{Serum\ Creatinine}  2.114/{Serum\ Creatinine}^2  0.00686 \ \times \ \mbox{Age}  )}
If Serum Creatinine < 0.8 mg/dL, use 0.8 mg/dL for Serum Creatinine.
Estimated GFR for children using Schwartz formula
In children, the Schwartz formula is used.^{[24]}^{[25]} This employs the serum creatinine (mg/dL), the child's height(cm) and a constant to estimate the glomerular filtration rate:
 \mbox{eGFR} = \frac{ {k} \times {Height} }{Serum\ Creatinine}

Where k is a constant that depends on muscle mass, which itself varies with a child's age:
 In first year of life, for preterm babies K=0.33^{[26]} and for fullterm infants K=0.45^{[25]}
 For infants and children of age 1 to 12 years, K=0.55.^{[24]}
The method of selection of the Kconstant value has been questioned as being dependent upon the goldstandard of renal function used (i.e., creatinine clearance, inulin clearance, etc.) and also may be dependent upon the urinary flow rate at the time of measurement.^{[27]}
In 2009, the formula was updated to use standardized serum creatinine (recommend k=0.413) and additional formulas that allow improved precision were derived if serum cystatin measured in addition to serum creatinine.^{[28]}
Importance of calibration of the serum creatinine level and the IDMS standardization effort
One problem with any creatininebased equation for GFR is that the methods used to assay creatinine in the blood differ widely in their susceptibility to nonspecific chromogens, which cause the creatinine value to be overestimated. In particular, the MDRD equation was derived using serum creatinine measurements that had this problem. The NKDEP program in the United States has attempted to solve this problem by trying to get all laboratories to calibrate their measures of creatinine to a "gold standard", which in this case is isotope dilution mass spectrometry (IDMS). In late 2009 not all labs in the U.S. had changed over to the new system. There are two forms of the MDRD equation that are available, depending on whether or not creatinine was measured by an IDMScalibrated assay. The CKDEPI equation is designed to be used with IDMScalibrated serum creatinine values only.
Cystatin C
Problems with creatinine (varying muscle mass, recent meat ingestion, etc.) have led to evaluation of alternative agents for estimation of GFR. One of these is cystatin C, a ubiquitous protein secreted by most cells in the body (it is an inhibitor of cysteine protease).
Cystatin C is freely filtered at the glomerulus. After filtration, Cystatin C is reabsorbed and catabolized by the tubular epithelial cells, with only small amounts excreted in the urine. Cystatin C levels are therefore measured not in the urine, but in the bloodstream.
Equations have been developed linking estimated GFR to serum cystatin C levels. Most recently, some proposed equations have combined (sex, age and race) adjusted cystatin C and creatinine. The most accurate is (sex, age and race) adjusted cystatin C, followed by (sex, age and race) adjusted creatinine and then cystatine C alone in slightly different with adjusted creatinine.^{[29]}
Normal ranges
The normal range of GFR, adjusted for body surface area, is 100130 ml/min/1.73m^{2} in men and women. In children, GFR measured by inulin clearance is 110 ml/min/1.73m^{2} until 2 years of age in both sexes, and then it progressively decreases. After age 40, GFR decreases progressively with age, by about 0.4  1.2 mL/min per year.
Chronic kidney disease stages
Risk factors for kidney disease include diabetes, high blood pressure, family history, older age, ethnic group and smoking. For most patients, a GFR over 60 mL/min/1.73m^{2} is adequate. But significant decline of the GFR from a previous test result can be an early indicator of kidney disease requiring medical intervention. The sooner kidney dysfunction is diagnosed and treated the greater odds of preserving remaining nephrons, and preventing the need for dialysis.
CKD stage  GFR level (mL/min/1.73 m^{2}) 

Stage 1  ≥ 90 
Stage 2  60 – 89 
Stage 3  30 – 59 
Stage 4  15 – 29 
Stage 5  < 15 
The severity of chronic kidney disease (CKD) is described by six stages; the most severe three are defined by the MDRDeGFR value, and first three also depend on whether there is other evidence of kidney disease (e.g., proteinuria):
 0) Normal kidney function – GFR above 90mL/min/1.73m^{2} and no proteinuria
 1) CKD1 – GFR above 90mL/min/1.73m^{2} with evidence of kidney damage
 2) CKD2 (mild) – GFR of 60 to 89 mL/min/1.73m^{2} with evidence of kidney damage
 3) CKD3 (moderate) – GFR of 30 to 59 mL/min/1.73m^{2}
 4) CKD4 (severe) – GFR of 15 to 29 mL/min/1.73m^{2}
 5) CKD5 kidney failure  GFR less than 15 mL/min/1.73m^{2} Some people add CKD5D for those stage 5 patients requiring dialysis; many patients in CKD5 are not yet on dialysis.
Note: others add a "T" to patients who have had a transplant regardless of stage.
Not all clinicians agree with the above classification, suggesting that it may mislabel patients with mildly reduced kidney function, especially the elderly, as having a disease.^{[30]}^{[31]} A conference was held in 2009 regarding these controversies by Kidney Disease: Improving Global Outcomes (KDIGO) on CKD: Definition, Classification and Prognosis, gathering data on CKD prognosis to refine the definition and staging of CKD.^{[32]}
See also
 Clearance
 Dialysis
 Filtration fraction
 Kt/V
 Pharmacokinetics
 Renal clearance ratio
 Renal failure
 Standardized Kt/V
 Tubuloglomerular feedback
 Urea reduction ratio
References
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 ^ Stevens, Paul E.; Levin, Adeera (Jun 4, 2013). "Evaluation and management of chronic kidney disease: synopsis of the kidney disease: improving global outcomes 2012 clinical practice guideline". Annals of Internal Medicine 158 (11): 825–830.
 ^ Physiology: 7/7ch04/7ch04p11  Essentials of Human Physiology  "Glomerular Filtration Rate"
 ^ GFR (Cockcroft & MDRD) calculator at medicalcalculator.nl  Cockcroft and MDRD calculator and details about inulin clearance
 ^ ^{a} ^{b} ^{c} ^{d} Guyton, Arthur; Hall, John (2006). "Chapter 26: Urine Formation by the Kidneys: I. Glomerular Filtration, Renal Blood Flow, and Their Control". In Gruliow, Rebecca. Textbook of Medical Physiology (Book) (11th ed.). Philadelphia, Pennsylvania: Elsevier Inc. pp. 308–325.
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 ^ "KDOQI CKD Guidelines". Retrieved 20100825.
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 ^ Cockcroft DW, Gault MH (1976). "Prediction of creatinine clearance from serum creatinine". Nephron 16 (1): 31–41.
 ^ Gault MH, Longerich LL, Harnett JD, Wesolowski C (1992). "Predicting glomerular function from adjusted serum creatinine". Nephron 62 (3): 249–56.
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 ^ Mathew TH, Johnson DW, Jones GR (October 2007). "Chronic kidney disease and automatic reporting of estimated glomerular filtration rate: revised recommendations". The Medical Journal of Australia 187 (8): 459–63.
 ^ Joint Specialty Committee on Renal Disease (June 2005). "Chronic kidney disease in adults: UK guidelines for identification, management and referral" (PDF).
 ^ Davey RX (January 2006). "Chronic kidney disease and automatic reporting of estimated glomerular filtration rate". The Medical Journal of Australia 184 (1): 42–3; author reply 43.
 ^ Twomey PJ, Reynolds TM (November 2006). "The MDRD formula and validation". QJM 99 (11): 804–5.
 ^ Kallner A, Ayling PA, Khatami Z (2008). "Does eGFR improve the diagnostic capability of SCreatinine concentration results? A retrospective population based study". International Journal of Medical Sciences 5 (1): 9–17.
 ^ National Kidney Foundation (February 2002). "K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification". American Journal of Kidney Diseases 39 (2 Suppl 1): S1–266.
 ^ ^{a} ^{b} Rule AD, Larson TS, Bergstralh EJ, Slezak JM, Jacobsen SJ, Cosio FG (December 2004). "Using serum creatinine to estimate glomerular filtration rate: accuracy in good health and in chronic kidney disease". Annals of Internal Medicine 141 (12): 929–37.
 ^ Levey AS, Coresh J, Greene T, et al. (August 2006). "Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate". Annals of Internal Medicine 145 (4): 247–54.
 ^ "GFR MDRD Calculator for Adults". National Kidney Disease Education Program. United States:
 ^ Hougardy, JM; Delanaye, P; Le Moine, A; Nortier, J (2014). "Estimation of the glomerular filtration rate in 2014 by tests and equations: strengths and weaknesses.". Rev Med Brux. (in French) 35 (4): 250–7.
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 ^ Matsushita K, Selvin E, Bash LD, Astor BC, Coresh J (April 2010). "Risk implications of the new CKD Epidemiology Collaboration (CKDEPI) equation compared with the MDRD Study equation for estimated GFR: the Atherosclerosis Risk in Communities (ARIC) Study". American Journal of Kidney Diseases 55 (4): 648–59.
 ^ ^{a} ^{b} Schwartz GJ, Haycock GB, Edelmann CM, Spitzer A (August 1976). "A simple estimate of glomerular filtration rate in children derived from body length and plasma creatinine". Pediatrics 58 (2): 259–63.
 ^ ^{a} ^{b} Schwartz GJ, Feld LG, Langford DJ (June 1984). "A simple estimate of glomerular filtration rate in fullterm infants during the first year of life". The Journal of Pediatrics 104 (6): 849–54.
 ^ Brion LP, Fleischman AR, McCarton C, Schwartz GJ (October 1986). "A simple estimate of glomerular filtration rate in low birth weight infants during the first year of life: noninvasive assessment of body composition and growth". The Journal of Pediatrics 109 (4): 698–707.
 ^ Haenggi MH, Pelet J, Guignard JP (February 1999). "[Estimation of glomerular filtration rate by the formula GFR = K x T/Pc]". Archives De Pédiatrie (in French) 6 (2): 165–72.
 ^ Schwartz GJ, Muñoz A, Schneider MF, et al. (March 2009). "New equations to estimate GFR in children with CKD". Journal of the American Society of Nephrology 20 (3): 629–37.
 ^ Stevens LA, Coresh J, Schmid CH, et al. (March 2008). "Estimating GFR using serum cystatin C alone and in combination with serum creatinine: a pooled analysis of 3,418 individuals with CKD". American Journal of Kidney Diseases 51 (3): 395–406.
 ^ Bauer C, Melamed ML, Hostetter TH (2008). "Staging of Chronic Kidney Disease: Time for a Course Correction". American Society of Nephrology 19 (5): 844–46.
 ^ Eckardt KU, Berns JS, Rocco MV, Kasiske BL (June 2009). "Definition and Classification of CKD: The Debate Should Be About Patient Prognosis—A Position Statement From KDOQI and KDIGO" (PDF). American Journal of Kidney Diseases 53 (6): 915–920.
 ^ "KDIGO Controversies Conference: Definition, Classification and Prognosis in CKD, London, October 2009". Kidney Disease: Improving Global Outcomes (KDIGO). 2009.
External links
Online calculators
 Online GFR Calculator
 Schwartz formula for estimating pediatric renal function
 Creatinine clearance calculator (CockcroftGault Equation) by MDCalc
 MDRD GFR Equation
Reference links
 National Kidney Disease Education Program website. Includes professional references and GFR calculators
 eGFR at Lab Tests Online
