- Joined
- Aug 11, 2008
- Messages
- 1,483
Test Name Result Flag Reference Range Lab
FASTING:YES
LIPID PANEL
CHOLESTEROL, TOTAL 209 HIGH 125-200 mg/dL 01
HDL CHOLESTEROL 14 LOW > OR = 40 mg/dL 01
TRIGLYCERIDES 129 <150 mg/dL 01
LDL-CHOLESTEROL 169 HIGH <130 mg/dL (calc) 01
Desirable range <100 mg/dL for patients with CHD or
diabetes and <70 mg/dL for diabetic patients with
known heart disease.
CHOL/HDLC RATIO 14.9 HIGH < OR = 5.0 (calc) 01
NON HDL CHOLESTEROL 195 HIGH mg/dL (calc) 01
Target for non-HDL cholesterol is 30 mg/dL higher than
LDL cholesterol target.
GGT
GGT 23 3-70 U/L 01
IRON, TOTAL
IRON, TOTAL 54 50-195 mcg/dL 01
LD
LD 233 HIGH 100-220 U/L 01
PHOSPHATE (AS PHOSPHORUS)
PHOSPHATE (AS PHOSPHORUS) 3.4 2.5-4.5 mg/dL 01
URIC ACID
URIC ACID 3.6 LOW 4.0-8.0 mg/dL 01
Therapeutic target for gout patients: <6.0 mg/dL
COMPREHENSIVE METABOLIC PANEL
GLUCOSE 77 65-99 mg/dL 01
Fasting reference interval
UREA NITROGEN (BUN) 12 7-25 mg/dL 01
CREATININE 1.24 0.60-1.35 mg/dL 01
eGFR NON-AFR. AMERICAN 79 > OR = 60 mL/min/1.73m2 01
eGFR AFRICAN AMERICAN 92 > OR = 60 mL/min/1.73m2 01
BUN/CREATININE RATIO NOT APPLICABLE 6-22 (calc) 01
SODIUM 137 135-146 mmol/L 01
POTASSIUM 4.8 3.5-5.3 mmol/L 01
CHLORIDE 103 98-110 mmol/L 01
CARBON DIOXIDE 23 19-30 mmol/L 01
CALCIUM 10.0 8.6-10.3 mg/dL 01
PROTEIN, TOTAL 7.0 6.1-8.1 g/dL 01
ALBUMIN 4.2 3.6-5.1 g/dL 01
GLOBULIN 2.8 1.9-3.7 g/dL (calc) 01
ALBUMIN/GLOBULIN RATIO 1.5 1.0-2.5 (calc) 01
BILIRUBIN, TOTAL 0.6 0.2-1.2 mg/dL 01
ALKALINE PHOSPHATASE 33 LOW 40-115 U/L 01
AST 42 HIGH 10-40 U/L 01
ALT 30 9-46 U/L 01
IGF I, LC/MS
1 of 3
IGF I, LC/MS 97 63-373 ng/mL 02
Z SCORE (MALE) -1.2 -2.0 - +2.0 SD 02
This test was developed and its analytical performance
characteristics have been determined by Quest Diagnostics
Nichols Institute San Juan Capistrano. It has not been
cleared or approved by FDA. This assay has been validated
pursuant to the CLIA regulations and is used for clinical
purposes.
Z SCORE (FEMALE) DNR 02
CBC (INCLUDES DIFF/PLT)
WHITE BLOOD CELL COUNT 7.3 3.8-10.8 Thousand/uL 01
RED BLOOD CELL COUNT 5.88 HIGH 4.20-5.80 Million/uL 01
HEMOGLOBIN 16.6 13.2-17.1 g/dL 01
HEMATOCRIT 53.1 HIGH 38.5-50.0 % 01
MCV 90.3 80.0-100.0 fL 01
MCH 28.3 27.0-33.0 pg 01
MCHC 31.3 LOW 32.0-36.0 g/dL 01
RDW 16.5 HIGH 11.0-15.0 % 01
PLATELET COUNT 461 HIGH 140-400 Thousand/uL 01
MPV 7.5 7.5-11.5 fL 01
ABSOLUTE NEUTROPHILS 5074 1500-7800 cells/uL 01
ABSOLUTE BAND NEUTROPHILS DNR 0-750 cells/uL 01
ABSOLUTE METAMYELOCYTES DNR 0 cells/uL 01
ABSOLUTE MYELOCYTES DNR 0 cells/uL 01
ABSOLUTE PROMYELOCYTES DNR 0 cells/uL 01
ABSOLUTE LYMPHOCYTES 1818 850-3900 cells/uL 01
ABSOLUTE MONOCYTES 197 LOW 200-950 cells/uL 01
ABSOLUTE EOSINOPHILS 175 15-500 cells/uL 01
ABSOLUTE BASOPHILS 37 0-200 cells/uL 01
ABSOLUTE BLASTS DNR 0 cells/uL 01
ABSOLUTE NUCLEATED RBC DNR 0 cells/uL 01
NEUTROPHILS 69.5 % 01
BAND NEUTROPHILS DNR % 01
METAMYELOCYTES DNR % 01
MYELOCYTES DNR % 01
PROMYELOCYTES DNR % 01
LYMPHOCYTES 24.9 % 01
REACTIVE LYMPHOCYTES DNR 0-10 % 01
MONOCYTES 2.7 % 01
EOSINOPHILS 2.4 % 01
BASOPHILS 0.5 % 01
BLASTS DNR % 01
NUCLEATED RBC DNR 0 /100 WBC 01
COMMENT(S) DNR 01
DHEA SULFATE
DHEA SULFATE 457 85-690 mcg/dL 01
TSH
TSH 2.51 0.40-4.50 mIU/L 01
ESTRADIOL
ESTRADIOL 34 < OR = 39 pg/mL 01
Reference range established on post-pubertal patient
population. No pre-pubertal reference range
established using this assay. For any patients for
whom low Estradiol levels are anticipated (e.g. males,
pre-pubertal children and hypogonadal/post-menopausal
females), the Quest Diagnostics Nichols Institute
Estradiol, Ultrasensitive, LCMSMS assay is recommended
(order code 30289).
Please note: patients being treated with the drug
fulvestrant (Faslodex(R)) have demonstrated significant
interference in immunoassay methods for estradiol
measurement. The cross reactivity could lead to falsely
2 of 3
elevated estradiol test results leading to an
inappropriate clinical assessment of estrogen status.
Quest Diagnostics order code 30289-Estradiol,
Ultrasensitive LC/MS/MS demonstrates negligible cross
reactivity with fulvestrant.
PSA, TOTAL
PSA, TOTAL 0.4 < OR = 4.0 ng/mL 01
This test was performed using the Siemens
chemiluminescent method. Values obtained from
different assay methods cannot be used
interchangeably. PSA levels, regardless of
value, should not be interpreted as absolute
evidence of the presence or absence of disease.
TESTOSTERONE,FR(DIALYSIS) AND TOTAL(LC/MS/MS)
TESTOSTERONE, TOTAL, LC/MS/MS 4622 HIGH 250-1100 ng/dL 03
FREE TESTOSTERONE 1479.1 HIGH
Thoughts?
My plan is to add in Citrus Bergamot 2x a day for cholsterol..any other advice?
FASTING:YES
LIPID PANEL
CHOLESTEROL, TOTAL 209 HIGH 125-200 mg/dL 01
HDL CHOLESTEROL 14 LOW > OR = 40 mg/dL 01
TRIGLYCERIDES 129 <150 mg/dL 01
LDL-CHOLESTEROL 169 HIGH <130 mg/dL (calc) 01
Desirable range <100 mg/dL for patients with CHD or
diabetes and <70 mg/dL for diabetic patients with
known heart disease.
CHOL/HDLC RATIO 14.9 HIGH < OR = 5.0 (calc) 01
NON HDL CHOLESTEROL 195 HIGH mg/dL (calc) 01
Target for non-HDL cholesterol is 30 mg/dL higher than
LDL cholesterol target.
GGT
GGT 23 3-70 U/L 01
IRON, TOTAL
IRON, TOTAL 54 50-195 mcg/dL 01
LD
LD 233 HIGH 100-220 U/L 01
PHOSPHATE (AS PHOSPHORUS)
PHOSPHATE (AS PHOSPHORUS) 3.4 2.5-4.5 mg/dL 01
URIC ACID
URIC ACID 3.6 LOW 4.0-8.0 mg/dL 01
Therapeutic target for gout patients: <6.0 mg/dL
COMPREHENSIVE METABOLIC PANEL
GLUCOSE 77 65-99 mg/dL 01
Fasting reference interval
UREA NITROGEN (BUN) 12 7-25 mg/dL 01
CREATININE 1.24 0.60-1.35 mg/dL 01
eGFR NON-AFR. AMERICAN 79 > OR = 60 mL/min/1.73m2 01
eGFR AFRICAN AMERICAN 92 > OR = 60 mL/min/1.73m2 01
BUN/CREATININE RATIO NOT APPLICABLE 6-22 (calc) 01
SODIUM 137 135-146 mmol/L 01
POTASSIUM 4.8 3.5-5.3 mmol/L 01
CHLORIDE 103 98-110 mmol/L 01
CARBON DIOXIDE 23 19-30 mmol/L 01
CALCIUM 10.0 8.6-10.3 mg/dL 01
PROTEIN, TOTAL 7.0 6.1-8.1 g/dL 01
ALBUMIN 4.2 3.6-5.1 g/dL 01
GLOBULIN 2.8 1.9-3.7 g/dL (calc) 01
ALBUMIN/GLOBULIN RATIO 1.5 1.0-2.5 (calc) 01
BILIRUBIN, TOTAL 0.6 0.2-1.2 mg/dL 01
ALKALINE PHOSPHATASE 33 LOW 40-115 U/L 01
AST 42 HIGH 10-40 U/L 01
ALT 30 9-46 U/L 01
IGF I, LC/MS
1 of 3
IGF I, LC/MS 97 63-373 ng/mL 02
Z SCORE (MALE) -1.2 -2.0 - +2.0 SD 02
This test was developed and its analytical performance
characteristics have been determined by Quest Diagnostics
Nichols Institute San Juan Capistrano. It has not been
cleared or approved by FDA. This assay has been validated
pursuant to the CLIA regulations and is used for clinical
purposes.
Z SCORE (FEMALE) DNR 02
CBC (INCLUDES DIFF/PLT)
WHITE BLOOD CELL COUNT 7.3 3.8-10.8 Thousand/uL 01
RED BLOOD CELL COUNT 5.88 HIGH 4.20-5.80 Million/uL 01
HEMOGLOBIN 16.6 13.2-17.1 g/dL 01
HEMATOCRIT 53.1 HIGH 38.5-50.0 % 01
MCV 90.3 80.0-100.0 fL 01
MCH 28.3 27.0-33.0 pg 01
MCHC 31.3 LOW 32.0-36.0 g/dL 01
RDW 16.5 HIGH 11.0-15.0 % 01
PLATELET COUNT 461 HIGH 140-400 Thousand/uL 01
MPV 7.5 7.5-11.5 fL 01
ABSOLUTE NEUTROPHILS 5074 1500-7800 cells/uL 01
ABSOLUTE BAND NEUTROPHILS DNR 0-750 cells/uL 01
ABSOLUTE METAMYELOCYTES DNR 0 cells/uL 01
ABSOLUTE MYELOCYTES DNR 0 cells/uL 01
ABSOLUTE PROMYELOCYTES DNR 0 cells/uL 01
ABSOLUTE LYMPHOCYTES 1818 850-3900 cells/uL 01
ABSOLUTE MONOCYTES 197 LOW 200-950 cells/uL 01
ABSOLUTE EOSINOPHILS 175 15-500 cells/uL 01
ABSOLUTE BASOPHILS 37 0-200 cells/uL 01
ABSOLUTE BLASTS DNR 0 cells/uL 01
ABSOLUTE NUCLEATED RBC DNR 0 cells/uL 01
NEUTROPHILS 69.5 % 01
BAND NEUTROPHILS DNR % 01
METAMYELOCYTES DNR % 01
MYELOCYTES DNR % 01
PROMYELOCYTES DNR % 01
LYMPHOCYTES 24.9 % 01
REACTIVE LYMPHOCYTES DNR 0-10 % 01
MONOCYTES 2.7 % 01
EOSINOPHILS 2.4 % 01
BASOPHILS 0.5 % 01
BLASTS DNR % 01
NUCLEATED RBC DNR 0 /100 WBC 01
COMMENT(S) DNR 01
DHEA SULFATE
DHEA SULFATE 457 85-690 mcg/dL 01
TSH
TSH 2.51 0.40-4.50 mIU/L 01
ESTRADIOL
ESTRADIOL 34 < OR = 39 pg/mL 01
Reference range established on post-pubertal patient
population. No pre-pubertal reference range
established using this assay. For any patients for
whom low Estradiol levels are anticipated (e.g. males,
pre-pubertal children and hypogonadal/post-menopausal
females), the Quest Diagnostics Nichols Institute
Estradiol, Ultrasensitive, LCMSMS assay is recommended
(order code 30289).
Please note: patients being treated with the drug
fulvestrant (Faslodex(R)) have demonstrated significant
interference in immunoassay methods for estradiol
measurement. The cross reactivity could lead to falsely
2 of 3
elevated estradiol test results leading to an
inappropriate clinical assessment of estrogen status.
Quest Diagnostics order code 30289-Estradiol,
Ultrasensitive LC/MS/MS demonstrates negligible cross
reactivity with fulvestrant.
PSA, TOTAL
PSA, TOTAL 0.4 < OR = 4.0 ng/mL 01
This test was performed using the Siemens
chemiluminescent method. Values obtained from
different assay methods cannot be used
interchangeably. PSA levels, regardless of
value, should not be interpreted as absolute
evidence of the presence or absence of disease.
TESTOSTERONE,FR(DIALYSIS) AND TOTAL(LC/MS/MS)
TESTOSTERONE, TOTAL, LC/MS/MS 4622 HIGH 250-1100 ng/dL 03
FREE TESTOSTERONE 1479.1 HIGH
Thoughts?
My plan is to add in Citrus Bergamot 2x a day for cholsterol..any other advice?