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Information

Protein, Blood, Total and Fractions and Protein, Urine

Synonym/Acronym

TP, SPEP (fractions include albumin, alpha1-globulin, alpha2-globulin, beta-globulin, and gamma-globulin).

Rationale

Blood: To assess nutritional status related to various disease and conditions such as burns, edema, dehydration, and malabsorption. Urine: To assess for the presence of protein in the urine toward diagnosing disorders affecting the kidneys and urinary tract, such as cancer, infection, and pre-eclampsia.

Patient Preparation

There are no food, fluid, activity, or medication restrictions unless by medical direction. For urine studies, usually a 24-hr urine collection is ordered. As appropriate, provide the required urine collection container and specimen collection instructions.

Normal Findings

Method: Blood and Urine: Spectrophotometry for total protein, electrophoresis for protein fractions.

Blood: Total Protein

AgeConventional UnitsSI Units (Conventional Units × 10)
Newborn–5 days3.8–6.2 g/dL38–62 g/L
1–3 yr5.9–7 g/dL59–70 g/L
4–6 yr5.9–7.8 g/dL59–78 g/L
7–9 yr6.2–8.1 g/dL62–81 g/L
10–19 yr6.3–8.6 g/dL63–86 g/L
Adult6–8 g/dL60–80 g/L

Values may be slightly decreased in older adults due to insufficient intake or the effects of medications and the presence of multiple chronic or acute diseases with or without muted symptoms.

Blood: Protein Fractions

Conventional UnitsSI Units (Conventional Units × 10)
Albumin3.4–4.8 g/dL34–48 g/L
alpha1-Globulin0.2–0.4 g/dL2–4 g/L
alpha2-Globulin0.4–0.8 g/dL4–8 g/L
beta-Globulin0.5–1 g/dL5–10 g/L
gamma-Globulin0.6–1.2 g/dL6–12 g/L

Values may be slightly decreased in older adults due to insufficient intake or the effects of medications and the presence of multiple chronic or acute diseases with or without muted symptoms.

Normal 24-Hour Urine Volume

The ranges are very general averages and were not calculated on the basis of normal average body weights. Literature shows that the expected urinary output can be estimated by formula where the expected output is as follows:

Infants: 1–2 mL/kg/hr

Children and adolescents: 0.5–1 mL/kg/hr

Adults: 1 mL/kg/hr

Newborns15–60 mL
Infants
3–10 days100–300 mL
11–59 days250–450 mL
2–12 mo400–500 mL
Children and adolescents
13 mo–4 yr500–700 mL
5–7 yr650–1,000 mL
8–14 yr800–1,400 mL
Adults and older adults800–2,500 mL (average 1,200 mL)
Normally, more urine is produced during the day than at night. With advancing age, the reverse will often occur. The total expected outcome for adults appears to remain the same regardless of age.
24-Hr Total Urine ProteinConventional UnitsSI Units (Conventional Units × 0.001)
Normal excretion30–150 mg/24 hr0.03–0.15 g/24 hr
ProteinuriaGreater than 300 mg/24 hrGreater than 0.3 g/24 hr

The 24-hr urine volume is recorded and provided with the results of the protein measurement. Electrophoresis for fractionation is qualitative: No monoclonal gammopathy detected. (Urine protein electrophoresis should be ordered along with serum protein electrophoresis.)

Spot or Random Urine Protein/Creatinine Ratio—useful in situations where 24-hr urine collection is not feasible (e.g., urgent such as with pre-eclampsia, patients unable to reliably cooperate such as pediatric patients, etc.)
AgeMaleFemale
7–9 yr61–220 mg/g70–548 mg/g
10–12 yr59–220 mg/g57–334 mg/g
13–15 yr41–371 mg/g33–307 mg/g
16–17 yr31–242 mg/g36–329 mg/g
Greater than 17 yr15–68 mg/g10–107 mg/g

Critical Findings and Potential Interventions

N/A

Overview

Study type: Blood collected in a gold-, red-, or red/gray-top tube; Urine from an unpreserved random or timed specimen collected in a clean plastic collection container; related body system: Digestive, Immune, and Urinary systems.

Protein is essential to all physiological functions. Proteins consist of amino acids, the building blocks of blood and body tissues. Protein is also required for the regulation of metabolic processes, immunity, and proper water balance. Total protein includes albumin and globulins. Albumin, the protein present in the highest concentrations, is the main transport protein in the body. Albumin also significantly affects plasma oncotic pressure, which regulates the distribution of body fluid between blood vessels, tissues, and cells.

Globulin is calculated from the following formula: Total protein - albumin = globulin

After an acute infection or trauma, levels of many of the liver-derived proteins increase, whereas albumin level decreases; these conditions may not reflect an abnormal total protein determination.

Most proteins, with the exception of the immunoglobulins, are synthesized and catabolized in the liver, where they are broken down into amino acids. The amino acids are converted to ammonia and ketoacids. Ammonia is converted to urea via the urea cycle. Urea is excreted in the urine. Normally, proteins do not pass from the blood through the kidneys’ filtration process into the urine. The presence of protein in the urine (proteinuria) is a significant indication of kidney disease. Proteinuria is defined as greater than 300 mg/day on a 24-hr urine or 30 mg/dL on a random or spot urine.

The predominant causes of proteinuria are (1) lack of filtration due to damaged glomeruli and (2) a breakdown in the kidneys’ tubular reabsorption process. Chronic conditions such as diabetes, hypertension, and sickle cell anemia cause incremental and potentially irreversible kidney damage. Proteinuria is present in many cases of pre-eclampsia, especially those with associated hypertension. Acute conditions such as urinary tract infections and kidney stones can also damage the kidneys. Collection of 24-hr urine samples in certain urgent conditions may not be feasible (e.g., pre-eclampsia); spot urine protein/creatinine ratios are considered reliable indicators of proteinuria. Proteinuria can also be the result of extremely elevated serum protein levels, as seen with immunoglobulin-secreting malignancies such as multiple myeloma. The kappa and lambda light chain portions of the immunoglobulins, also known as Bence Jones proteins, are detected using electrophoresis techniques and are classic findings in conditions such as myeloma, Waldenström macroglobulinemia, and lymphoma.

Indications

Blood

Urine

Interfering Factors

Factors That May Alter the Results of the Study

Blood

  • Drugs and other substances that may increase protein levels include amino acids (if given by IV), anabolic steroids, anticonvulsants, corticosteroids, furosemide, hormones (angiotensin, corticotropin, insulin, growth hormone, oral contraceptives, progesterone), and thyroid drugs.
  • Hemolysis can falsely elevate results.
  • Venous stasis can falsely elevate results; the tourniquet should not be left on the arm for longer than 60 sec.
  • Drugs and other substances that may decrease protein levels include acetylsalicylic acid, ammonium ions, arginine, benzene, carvedilol, floxuridine, laxatives, mercury compounds, oral contraceptives, pyrazinamide, and rifampin.
  • Values are significantly lower (5% to 10%) in recumbent patients.

Urine

  • Drugs and other substances that may increase urine protein levels include acetaminophen, aminosalicylic acid, amphotericin B, ampicillin, antimony compounds, antipyrine, arsenicals, ascorbic acid, bacitracin, bismuth subsalicylate, bromate, capreomycin, captopril, carbamazepine, carbarsone, cephaloglycin, cephaloridine, chlorpromazine, chlorpropamide, chlorthalidone, chrysarobin, colistimethate, colistin, contrast medium (iopanoic acid, ipodate sodium), corticosteroids, cyclosporine, demeclocycline, diatrizoic acid, dihydrotachysterol, doxycycline, enalapril, gentamicin, gold salts, hydrogen sulfide, iodopyracet, iophenoxic acid, kanamycin, corn oil (Lipomul), lithium, mefenamic acid, mercury compounds, methicillin, methylbromide, mezlocillin, mitomycin, nafcillin, naphthalene, neomycin, oxacillin, paraldehyde, penicillamine, penicillin, phenolphthalein, phensuximide, piperacillin, plicamycin, polymyxin, probenecid, pyrazolones, rifampin, sodium bicarbonate, streptokinase, sulfisoxazole, suramin, tetracyclines, thallium, thiosemicarbazones, tolbutamide, tolmetin, triethylenemelamine, and vitamin D.
  • Drugs and other substances that may decrease urine protein levels include benazepril, captopril, cyclosporine, diltiazem, enalapril, fosinopril, interferon, lisinopril, losartan, lovastatin, prednisolone, prednisone, and quinapril.
  • All urine voided for the timed collection period must be included in the collection, or else falsely decreased values may be obtained. Compare output records with volume collected to verify that all voids were included in the collection.

Potential Medical Diagnosis: Clinical Significance of Results

Increased In

Blood

  • alpha1-Globulin proteins in acute and chronic inflammatory diseases
  • alpha2-Globulin proteins occasionally in diabetes, pancreatitis, and hemolysis
  • beta-Globulin proteins in hyperlipoproteinemias and monoclonal gammopathies
  • gamma-Globulin proteins in chronic liver diseases, chronic infections, autoimmune disorders, hepatitis, cirrhosis, and lymphoproliferative disorders
  • Total protein:
    • Chronic infection or inflammation (related to increased production of inflammatory proteins)
    • Dehydration (related to hemoconcentration)
    • Monoclonal and polyclonal gammopathies (related to excessive gamma-globulin protein synthesis)
    • Myeloma (related to excessive gamma-globulin protein synthesis)
    • Sarcoidosis(related to excessive gamma-globulin protein synthesis)
    • Some types of chronic liver disease
    • Tropical diseases (e.g., leprosy) (related to inflammatory reaction)
    • Waldenström macroglobulinemia (related to excessive gamma-globulin protein synthesis)

Urine

  • Diabetic nephropathy(related to disease involving renal glomeruli, which increases permeability of protein)
  • Fanconi syndrome(related to abnormal protein deposits in the kidney, which can cause Fanconi syndrome)
  • Heavy metal poisoning (related to disease involving renal glomeruli, which increases permeability of protein)
  • Malignancies of the urinary tract (tumors secrete protein into the urine)
  • Monoclonal gammopathies (evidenced by large amounts of Bence Jones protein light chains excreted in the urine)
  • Multiple myeloma (evidenced by large amounts of Bence Jones protein light chains excreted in the urine)
  • Nephrotic syndrome(related to disease involving renal glomeruli, which increases permeability of protein)
  • Postexercise period (related to muscle exertion)
  • Pre-eclampsia (numerous factors contribute to increased permeability of the kidneys to protein)
  • Sickle cell disease (related to increased destruction of red blood cells and excretion of hemoglobin protein)
  • Urinary tract infections (related to disease involving renal glomeruli, which increases permeability of protein)

Decreased In

Blood

  • alpha1-Globulin proteins in hereditary deficiency
  • alpha2-Globulin proteins in nephrotic syndrome, malignancies, numerous subacute and chronic inflammatory disorders, and recovery stage of severe burns
  • beta-Globulin proteins in hypo-beta-lipoproteinemias and IgA deficiency
  • gamma-Globulin proteins in immune deficiency or suppression
  • Total protein:
    • Administration of IV fluids (related to hemodilution)
    • Burns (related to fluid retention, loss of albumin from chronic open burns)
    • Chronic ulcerative colitis (related to poor intestinal absorption)
    • Cirrhosis (related to damaged liver, which cannot synthesize adequate amount of protein)
    • Crohn disease(related to poor intestinal absorption)
    • Glomerulonephritis(related to alteration in permeability that results in excessive loss by kidneys)
    • Heart failure (related to fluid retention)
    • Hyperthyroidism (possibly related to increased metabolism and corresponding protein synthesis)
    • Malabsorption (related to insufficient intestinal absorption)
    • Malnutrition(related to insufficient intake)
    • Nephrotic syndrome (related to alteration in permeability that results in excessive loss by kidneys)
    • Pregnancy (related to fluid retention, dietary insufficiency, increased demands of growing fetus)
    • Prolonged immobilization (related to fluid retention)
    • Protein-losing enteropathies (related to excessive loss)
    • Severe skin disease
    • Starvation(related to insufficient intake)
    • Substance use disorder (alcohol) (related to insufficient dietary intake; diminished protein synthesis by damaged liver)
    • Tumors

Urine

N/A

Nursing Implications, Nursing Process, Clinical Judgement

Before the Study: Planning and Implementation

Teaching the Patient What to Expect

  • Discuss how the blood test can assist in assessing nutritional status related to disease process; discuss how the urine test can assist in assessing the cause of protein in the urine.
  • Explain that a blood or urine sample is needed for the test. Information regarding urine specimen collection is presented with other general guidelines in Appendix A: Patient Preparation and Specimen Collection.

Potential Nursing Actions

  • Include on the collection container’s label urine total volume, test start and stop times/dates, and any medications that may interfere with test results.

After the Study: Implementation & Evaluation Potential Nursing Actions

Treatment Considerations

  • Monitor and trend TP. Compare with other LFTs (Alb, ALP, ALT, AST, TBil, DBil) to track the course of liver disease and response to treatment. If liver function is significantly damaged, PT will be prolonged and INR increased.
  • Discuss how there are not always obvious symptoms of protein in the urine.
  • Observable symptoms of excessive protein loss include urine appearing foamy and edema of the hands, feet, face, and abdomen.

Nutritional Considerations

  • Discuss good dietary sources of complete protein (containing all eight essential amino acids) including meat, fish, eggs, and dairy products and that good sources of incomplete protein (lacking one or more of the eight essential amino acids) include grains, nuts, legumes, vegetables, and seeds.
  • Discuss general symptoms of insufficient nutrition; dry skin, thin brittle nails, hair loss and thinning, hypoactive bowel sounds, fatigue, muscle wasting, decreased ability to perform activities of daily living.

Clinical Judgement

  • Consider which cultural barriers impact the patient’s ability to embrace dietary changes that would improve health. Also consider ways to reinforce the necessity of following therapeutic recommendations to facilitate kidney health.

Follow-Up and Desired Outcomes

  • Understands that depending on the results of this procedure, additional testing may be performed to evaluate or monitor disease progress and determine the need for a change in therapy.
  • Acknowledges that information related to proteinuria can be found at Kidney and Urology Foundation of America at https://www.cdc.gov/kidneydisease/publications-resources/kidney-tests.html.