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The following is a table of reference values, meth- suggesting an endorsement of commercial products
ods, and conversion factors for tests commonly or- by the hospital or the Journal. Because reference val-
dered at the Massachusetts General Hospital (MGH) ues are affected by many variables, the ranges used
and recorded in the Case Records. The table revises at MGH may not be appropriate for other insti-
the most recently published data (Normal Reference tutions. Furthermore, the methods and units report-
Laboratory Values. N Engl J Med 1992;327:718- ed should not be interpreted as a judgment about
24). Laboratory values are expressed in the units the optimal way to perform or report a given labo-
used at MGH (MGH units) and the units of the ratory test.
Système International d’Unités (SI units), with a The table was compiled with the aid of Dr. Mi-
factor to convert MGH units to SI units by multi- chael Laposata, Dr. James Flood, Dr. Neal Smith,
plication. This table is not intended to provide a Dr. Kathryn Ruoff, Dr. Mary Jane Ferraro, Dr. Eliz-
comprehensive review of reference values, since this abeth Van Cott, William Young, Catherine Tuttle,
information is widely available in standard text- Patricia Puopolo, Linda Ardisson, Ela Dhanak, Ed-
books. Detailed information on specific methods ward Masley, Fu-Mei Huang, Stephen Johnson, Lin-
and instruments is not provided, in order to avoid da Jennings, Jeanne Casey, and Debera Grzybek.
CHEMISTRY
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
Vo l u m e 3 3 9 Nu m b e r 15 · 1063
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The Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
CHEMISTRY (Continued)
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
1064 · O c to b e r 8 , 19 98
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C AS E R EC O R D S O F T H E M AS SAC H U S ET T S G E N E R A L H O S P I TA L
CHEMISTRY (Continued)
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
Vo l u m e 3 3 9 Nu m b e r 15 · 1065
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The Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
CHEMISTRY (Continued)
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
1066 · O c to b e r 8 , 19 98
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C AS E R EC O R D S O F T H E M AS SAC H U S ET T S G E N E R A L H O S P I TA L
CHEMISTRY (Continued)
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
Vo l u m e 3 3 9 Nu m b e r 15 · 1067
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The Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
Acetaminophen, toxicity S >120 µg/ml at 2–4 hr >794 µmol/liter at 2–4 hr Liquid chromatography 6.62
Amikacin S Immunoassay 1.71
Trough 1–7 µg/ml 1.7–12 µmol/liter
Peak 15–25 µg/ml 26–43 µmol/liter
Amitriptyline S Liquid chromatography 3.61
Amitriptyline 120–250 µg/liter 433–903 nmol/liter
Nortriptyline 50–150 µg/liter 181–542 nmol/liter
Barbiturate screen S Negative Negative Liquid chromatography
Basic drug screen S Negative Negative Liquid chromatography
Benzodiazepine screen S Negative Negative Liquid chromatography
Carbamazepine (adult) S 4–12 µg/ml 17–51 µmol/liter Immunoassay 4.23
Chlordiazepoxide S 1.0–3.0 mg/liter 3.3–10 µmol/liter Liquid chromatography 3.336
Clomipramine S 150–450 µg/liter 476–1427 nmol/liter Liquid chromatography 3.17
Clonazepam S 10–70 µg/liter 32–222 nmol/liter Liquid chromatography 3.17
Clozapine S Liquid chromatography
Clozapine 150–500 µg/liter 459–1530 nmol/liter 3.06
Norclozapine 100–450 µg/liter 320–1440 nmol/liter 3.20
Desipramine S 150–300 µg/liter 563–1125 nmol/liter Liquid chromatography 3.75
Diazepam S 100–1000 µg/liter 0.35–3.50 µmol/liter Liquid chromatography 0.0035
Digoxin S 0.9–2.0 ng/ml 1.2–2.6 nmol/liter Immunoassay 1.28
Doxepin S 150–250 µg/liter 537–895 nmol/liter Liquid chromatography 3.58
Ethanol S Clinical intoxication: Clinical intoxication: Gas chromatography 0.001
>1000 mg/liter >1 g/liter
Fluoxetine S Liquid chromatography
Fluoxetine 50–450 µg/liter 162–1454 nmol/liter 3.23
Norfluoxetine 50–450 µg/liter 169–1521 nmol/liter 3.38
Fluvoxamine S 12–240 µg/liter 38–756 nmol/liter Liquid chromatography 3.15
Gentamicin S Immunoassay
Trough <2.1 µg/ml <4.4 µmol/liter 2.09
Peak 4–8 µg/ml 8.4–16.7 µmol/liter 2.09
Imipramine S Liquid chromatography
Imipramine 150–250 µg/liter 536–893 nmol/liter 3.57
Desipramine 150–300 µg/liter 563–1125 nmol/liter 3.75
Lithium S, P 0.5–1.5 mmol/liter 0.5–1.5 mmol/liter Ion-selective electrode 1
Methadone S 50–800 µg/liter 0.16–2.58 µmol/liter Liquid chromatography 0.00323
Methotrexate S Immunoassay 1
24 hr after high-dose infusion <10 µmol/liter <10 µmol/liter
48 hr after high-dose infusion <1 µmol/liter <1 µmol/liter
72 hr after high-dose infusion <0.4 µmol/liter <0.4 µmol/liter
Nordiazepam S 100–800 µg/liter 0.37–2.95 µmol/liter Liquid chromatography 0.00369
Paroxetine S 20–190 µg/liter 61–576 nmol/liter Liquid chromatography 3.03
Phenobarbital S 15–50 µg/ml 65–216 µmol/liter Immunoassay 4.31
Phenytoin S 5–20 µg/ml 20–79 µmol/liter Immunoassay 3.96
Quinidine S 1.2–4.0 µg/ml 3.7–12.3 µmol/liter Liquid chromatography 3.08
Salicylate intoxication >500 mg/liter >3.62 mmol/liter 0.00724
Sertraline S 40–160 µg/liter 130–522 nmol/liter Liquid chromatography 3.26
Sulfamethoxazole S 5–15 mg/dl 19.8–59.2 nmol/liter Liquid chromatography 3.95
Theophylline S 10–20 µg/ml 56–111 µmol/liter Immunoassay 5.55
For apnea control 5–15 µg/ml 28–83 µmol/liter
Thiocyanate, toxic range S >100 mg/liter >1720 µmol/liter Spectrophotometry 17.2
Tobramycin S Immunoassay 2.14
Trough <2.0 µg/ml <4.3 µmol/liter
Peak 4.0–8.0 µg/ml 8.6–17.1 µmol/liter
Trazodone S 800–1600 µg/liter 2152–4304 nmol/liter Liquid chromatography 2.69
Valproic acid S 50–100 µg/ml 347–693 µmol/liter Immunoassay 6.93
Vancomycin S Immunoassay 0.690
Trough <10.1 µg/ml <7.0 µmol/liter
Peak (2 hr after infusion) 18–26 µg/ml 12–18 µmol/liter
1068 · O c to b e r 8 , 19 98
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C AS E R EC O R D S O F T H E M AS SAC H U S ET T S G E N E R A L H O S P I TA L
IMMUNOLOGY
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT† TO SI UNIT
Vo l u m e 3 3 9 Nu m b e r 15 · 1069
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The Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT‡ SI UNIT METHOD OR INSTRUMENT† TO SI UNIT
Activated protein C resistance (factor V P Ratio >2.0 Not applicable Automated clotting assay
Leiden)
Alpha2-antiplasmin P 80–130% 0.80–1.30 Chromogenic assay 0.01
Antiphospholipid-antibody panel
Partial-thromboplastin time–lupus P Negative Negative Dilute phospholipid clotting
anticoagulant screen assay
Platelet-neutralization procedure P Negative Negative Clotting assay
Anticardiolipin antibody S
IgG 0–15 GPL units 0–15 arbitrary units ELISA 1
IgM 0–15 MPL units 0–15 arbitrary units ELISA 1
Antithrombin III P
Immunologic 22–39 mg/dl 220–390 mg/liter Immunoassay 10
Functional 80–130% 0.8–1.30 U/liter Chromogenic assay 0.01
Anti-Xa assay (heparin assay) P Chromogenic assay
Unfractionated heparin 0.3–0.7 IU/ml 0.3–0.7 kIU/liter 1
Low-molecular-weight heparin 0.5–1.0 IU/ml 0.5–1.0 kIU/liter 1
Danaparoid 0.5–0.8 IU/ml 0.5–0.8 kIU/liter 1
Bleeding time (adult) 2–9.5 min 2–9.5 min Surgicutt 1
Clot retraction WB 50–100%/2 hr 0.50–1.00/2 hr Manual method 0.01
D -Dimer P <0.5 µg/ml <0.5 mg/liter Latex agglutination 1
Differential blood count WB Automated cell counter or
manual method
Neutrophils 45–75% 0.45–0.75 0.01
Bands 0–5% 0.0–0.05 0.01
Lymphocytes 16–46% 0.16–0.46 0.01
Monocytes 4–11% 0.04–0.11 0.01
Eosinophils 0–8% 0.0–0.8 0.01
Basophils 0–3% 0.0–0.03 0.01
Erythrocyte count (adult) WB Automated cell counter
Male 4.50–5.30¬106/mm3 4.50–5.30¬1012/liter 1¬10 6
Female 4.10–5.10¬106/mm3 4.10–5.10¬1012/liter 1¬10 6
Erythrocyte sedimentation rate WB Automated erythrocyte-sedi- 1
mentation-rate instrument
Female 1–25 mm/hr 1–25 mm/hr
Male 0–17 mm/hr 0–17 mm/hr
Factor II, prothrombin P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor V P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor VII P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor VIII P 50–200% 0.50–2.00 Automated clotting assay 0.01
Factor IX P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor X P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor XI P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor XII P 60–140% 0.60–1.40 Automated clotting assay 0.01
Factor XIII screen P No deficiency detected Not applicable Urea clot dissolution
Factor-inhibitor assay P <0.5 Bethesda unit <0.5 Bethesda unit Automated clotting assay 1
Ferritin S Immunoassay 1
Male 30–300 ng/ml 30–300 µg/liter
Female 10–200 ng/ml 10–200 µg/liter
Fibrin(ogen)-degradation products P <2.5 µg/ml <2.5 mg/liter Latex agglutination 1
Fibrinogen P 175–400 mg/dl 1.75–4.00 µmol/liter Automated clotting assay 0.01
Folate (folic acid) S, P Immunoassay 2.266
Normal 3.1–17.5 ng/ml 7.0–39.7 nmol/liter
Borderline deficient 2.2–3.0 ng/ml 5.0–6.8 nmol/liter
Deficient <2.2 ng/ml <5.0 nmol/liter
Excessive >17.5 ng/ml >39.7 nmol/liter
Glucose-6-phosphate dehydrogenase WB No gross deficiency Not applicable Visual fluorescence screening
(erythrocyte)
Hematocrit (adult) WB Automated cell counter
Male 37.0–49.0 0.37–0.49 0.01
Female 36.0–46.0 0.36–0.46 0.01
Hemoglobin (adult) WB Automated cell counter 0.6206
Male 13.0–18.0 g/dl 8.1–11.2 mmol/liter
Female 12.0–16.0 g/dl 7.4–9.9 mmol/liter
Hemoglobin A2 WB <3.5% <0.04 Spectrophotometry 0.01
Hemoglobin F WB <0.02% <0.0002 Spectrophotometry 0.01
Heparin-induced thrombocytopenia P Negative Negative ELISA
antibody
Iron S 30–160 µg/dl 5.4–28.7 µmol/liter Colorimetry 0.1791
Iron-binding capacity S 228–428 µg/dl 40.8–76.7 µmol/liter Colorimetry 0.1791
Leukocyte count (WBC) WB 4.5–11.0¬103/mm3 4.5–11.0¬109/liter Automated cell counter 1¬106
Mean corpuscular hemoglobin (MCH) WB 25.0–35.0 pg/cell 25.0–35.0 pg/cell Automated cell counter 1
1070 · O c to b e r 8 , 19 98
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C AS E R EC O R D S O F T H E M AS SAC H U S ET T S G E N E R A L H O S P I TA L
FACTOR FOR
CONVERSION
ANALYTE SPECIMEN* MGH UNIT SI UNIT METHOD OR INSTRUMENT TO SI UNIT
Mean corpuscular hemoglobin concen- WB 31.0–37.0 g/dl 310–370 g/liter Automated cell counter 10
tration (MCHC)
Mean corpuscular volume (MCV) WB Automated cell counter 1
(adult)
Male 78–100 µm 3 78–100 fl
Female 78–102 µm3 78–102 fl
Osmotic fragility of erythrocytes WB Increased hemolysis as Not applicable Spectrophotometry
compared with normal
control
Partial-thromboplastin time, activated P 22.1–34.1 sec 22.1–34.1 sec Automated clotting assay 1
Plasminogen P
Antigen 8.4–14.0 mg/dl 84–140 mg/liter Immunoassay 10
Functional 80–130% 0.80–1.30 Chromogenic assay 0.01
Platelet aggregation PRP >65% aggregation in Not applicable Platelet aggregometry
response to adenosine
diphosphate, epineph-
rine, collagen, ristoce-
tin, and arachidonic
acid
Platelet count WB 150–350¬103/mm3 150–350¬109/liter Automated cell counter 1¬106
Platelet, mean volume WB 6.4–11.0 µm3 6.4–11.0 fl Automated cell counter 1
Prekallikrein assay P 60–140% 0.60–1.40 Chromogenic assay 0.01
Prekallikrein screen P No deficiency detected Automated clotting assay
Protein C P
Total antigen 70–140% 0.70–1.40 Immunoassay 0.01
Functional 70–140% 0.70–1.40 Chromogenic assay 0.01
Protein S P
Total antigen 70–140% 0.70–1.40 Immunoassay 0.01
Functional 70–140% 0.70–1.40 Automated clotting assay 0.01
Free antigen 70–140% 0.70–1.40 Immunoassay 0.01
Prothrombin time P 11.2–13.2 sec 11.2–13.2 sec Automated clotting assay 1
Red-cell distribution width WB 11.5–14.5% 0.115–0.145 Automated cell counter 0.01
Reptilase time P 16–24 sec 16–24 sec Automated clotting assay 1
Reticulocyte count WB 0.5–2.5% red cells 0.005–0.025 red cells Flow cytometry 0.01
Ristocetin cofactor (functional P Platelet aggregometry 0.01
von Willebrand factor)
Blood group O 75% mean of normal 0.75 mean of normal
Blood group A 105% mean of normal 1.05 mean of normal
Blood group B 115% mean of normal 1.15 mean of normal
Blood group AB 125% mean of normal 1.25 mean of normal
Sucrose hemolysis WB <10% <0.1 Spectrophotometry 0.01
Thrombin time P 16–24 sec 16–24 sec Automated clotting assay 1
Total eosinophils WB 70–440/mm3 70–440¬106/liter Automated cell counter 1¬103
Vitamin B12 S, P Immunoassay 0.7378
Normal >250 pg/ml >184 pmol/liter
Borderline 125–250 pg/ml 92–184 pmol/liter
Deficient <125 pg/ml <92 pmol/liter
von Willebrand factor (vWF) antigen P Immunoassay
(factor VIII:R antigen)
Blood group O 75% mean of normal 0.75 mean of normal 0.01
Blood group A 105% mean of normal 1.05 mean of normal 0.01
Blood group B 115% mean of normal 1.15 mean of normal 0.01
Blood group AB 125% mean of normal 1.25 mean of normal 0.01
von Willebrand factor multimers P Normal distribution Normal distribution Western blot assay
Vo l u m e 3 3 9 Nu m b e r 15 · 1071
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The Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
MICROBIOLOGY
Throat Group A beta-hemolytic streptococci, If a complete throat culture is request- Alpha-hemolytic streptococci, non-
pyogenic groups C and G beta- ed, it will be examined for Haemoph- hemolytic streptococci, diphtheroids,
hemolytic streptococci, Arcanobac- ilus influenzae, Staphylococcus aureus, coagulase-negative staphylococci,
terium haemolyticum Streptococcus pneumoniae, Neisseria saprophytic neisseria
meningitidis, and yeast
Sputum Pneumococci, H. influenzae, beta- Presence or absence of normal throat Carefully collected specimens should
hemolytic streptococci, Staph. aureus, flora contain few or no normal throat flora
Moraxella (Branhamella) catarrhalis,
pseudomonas, Enterobacteriaceae,
yeast
Urine Aerobic bacteria and yeast: abundant, Few, 103–104 colony-forming units/ml; Carefully collected specimens should not
>105 colony-forming units/ml; rare, 102 –103 colony-forming units/ contain mixed bacterial species (i.e., two
moderate, 10 4–105 colony-forming ml; no growth, <102 colony-forming or more of the following: lactobacilli,
units/ml units/ml; these amounts may indicate non–beta-hemolytic streptococci, diph-
clinically significant bacteriuria if ac- theroids, coagulase-negative staphylo-
companied by pyuria, clinical symp- cocci, Gardnerella vaginalis)
toms, or both
Blood Aerobic and anaerobic bacteria, yeasts Growth in both bottles is usually more None; aerobic and anaerobic diphtheroids
clinically significant than growth in a and coagulase-negative staphylococci are
single bottle common contaminants
Cerebrospinal and Aerobic and anaerobic bacteria; yeasts, Any organism isolated None
other fluids including cryptococcus
Feces Enteric pathogens: salmonella, shigella, Moderate or abundant yeast or Staph. Enterobacteriaceae, streptococci, pseudo-
campylobacter, plesiomonas, and aer- aureus; presence or absence of nor- monas, small numbers of staphylococci,
omonas when predominant mal gram-negative enteric flora; spe- and yeast (and anaerobes that are not
cial cultures can be specifically re- cultured routinely)
quested for yersinia, Vibrio cholerae,
V. parahaemolyticus, or hemorrhagic
(O157) strains of Escherichia coli
Wounds Aerobic and anaerobic bacteria, yeasts
Cervical or vaginal Gonococci, beta-hemolytic streptococ- Enteric gram-negative rods and candi-
ci, Staph. aureus, and G. vaginalis da, if present in large numbers
when predominant
*P denotes plasma, S serum, U urine, WB whole blood, CSF cerebrospinal fluid, JF joint fluid, and PRP platelet-rich plasma.
†ELISA denotes enzyme-linked immunosorbent assay.
‡GPL denotes IgG phospholipid, and MPL IgM phospholipid.
1072 · O c to b e r 8 , 19 98
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