EFTA00804474.pdf
dataset_9 pdf 346.1 KB • Feb 3, 2026 • 6 pages
Report Status: Final
(0) Quest
Diagnostics EPSTEIN, JEFFREY
Patient Information Specimen Information Client Information
Specimen: MR8391 ION Client #: 78300020 56W5265
EPSTEIN, JEFFREY
Requisition: 0006872 MOSKOWITZ, BRUCE W
DOB: 01/20/1953 AGE: 65 BRUCE MOSKOWITZ, MD
Gender: M Attn: NATIONWIDE ACCOUNT
Collected: 11/23/2018
Phone: 561.366.0084 1411 N FLAGLER DR STE 7100
Received: 11/27/2018 109:51 EST
Patient ID: 19530120MJE WEST PALM BEACH, FL 33401-3418
Reported: 11/28/2018 109:22 EST
Health ID: 8573003290851249
Test Hams In Range Out Of Range Reference Range Lab
PROTEIN, TOTAL AND PROTEIN ELECTROPHORESIS
PROTEIN, TOTAL, SERUM MI
PROTEIN, TOTAL 7.1 6.1-8.1 g/dL
PROTEIN ELECTROPHORESIS TP
ALBUMIN 4.2 3.8-4.8 g/dL
ALPHA 1 GLOBULIN 0.3 0.2-0.3 g/dL
ALPHA 2 GLOBULIN 0.7 0.5-0.9 g/dL
BETA 1 GLOBULIN 0.6 0.4-0.6 g/dL
BETA 2 GLOBULIN 0.4 0.2-0.5 g/dL
GAMMA GLOBULIN 1.0 0.8-1.7 g/dL
INTERPRETATION
Normal Electrophoretic Pattern
The above test was performed; however,
the specimen was lipemic.
LIPID PANEL, STANDARD
CHOLESTEROL, TOTAL 216 H <200 mg/dL MI
HDL CHOLESTEROL 23 L >40 mg/dL MI
TRIGLYCERIDES 935 H <150 mg/dL MI
LDL-CHOLESTEROL mg/dL (talc) MI
LDL cholesterol not calculated. Triglyceride levels
greater than 400 mg/dL invalidate calculated LDL results.
Reference range: <100
Desirable range <100 mg/dL for primary prevention;
<70 mg/dL for patients with CHD or diabetic patients
with > or = 2 CHD risk factors.
LDL-C is now calculated using the Martin-Hopkins
calculation, which is a validated novel method providing
better accuracy than the Friedewald equation in the
estimation of LDL-C.
Martin SS et al. JAMA. 2013;310(19): 2061-2068
(http://education.QuestDiagnostics.com/faq/FAQ164)
CHOL/HDLC RATIO 9.4 H <5.0 (talc) MI
NON HDL CHOLESTEROL 193 H <130 mg/dL (talc) MI
For patients with diabetes plus 1 major ASCVD risk
factor, treating to a non-HDL-C goal of <100 mg/dL
(LDL-C of <70 mg/dL) is considered a therapeutic
option.
HS CRP 1.1 mg/L TP
The above test was performed; however,
the specimen was lipemic.
Average relative cardiovascular risk according to
AHA/CDC guidelines.
CLIENT SERVICES:866.697.8378 SPECIMEN: MR8391 ION PAGEI0F6
Quest. Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics.
EFTA00804474
Report Status: Final
Quest
—• Diagnostics EPSTEIN, JEFFREY
Patient Information Specimen Information Client Information
Specimen: MR8391 ION Client #: 78300020
EPSTEIN, JEFFREY
Collected: 11/23/2018 MOSKOWITZ, BRUCE W
DOB: 01/20/1953 AGE: 65 Received: 11/27/2018 / 09:51 EST
Gender: M Reported: 11/28/2018 / 09:22 EST
Patient ID: 19530120MJE
Health ID: 8573003290851249
Test Name In Range Out Of Range Reference Range Lab
For ages >17 Years:
hs-CRP mg/L Risk According to AHA/CDC Guidelines
<1.0 Lower relative cardiovascular risk.
1.0-3.0 Average relative cardiovascular risk.
3.1-10.0 Higher relative cardiovascular risk.
Consider retesting in 1 to 2 weeks to
exclude a benign transient elevation
in the baseline CRP value secondary
to infection or inflammation.
>10.0 Persistent elevation, upon retesting,
may be associated with infection and
inflammation.
HONOCYSTEINE 12.7 H <11.4 umol/L MI
Homocysteine is increased by functional deficiency of
folate or vitamin B12. Testing for methylmalonic acid
differentiates between these deficiencies. Other causes
of increased homocysteine include renal failure, folate
antagonists such as methotrexate and phenytoin, and
exposure to nitrous oxide.
COMPREHENSIVE METABOLIC MI
PANEL
GLUCOSE 111 H 65-99 mg/dL
Fasting reference interval
For someone without known diabetes, a glucose value
between 100 and 125 mg/dL is consistent with
prediabetes and should be confirmed with a
follow-up test.
UREA NITROGEN (BUN) 20 7-25 mg/dL
CREATININE 0.95 0.70-1.25 mg/dL
For patients >49 years of age, the reference limit
for Creatinine is approximately 13% higher for people
identified as African-American.
eGFR NON-AFR. AMERICAN 84 > OR 60 mL/min/1.73m2
eGFR AFRICAN AMERICAN 97 > OR 60 mL/min/1.73m2
BUN/CREATININE RATIO NOT APPLICABLE 6-22 (calc)
SODIUM 138 135-146 mmol/L
POTASSIUM 4.4 3.5-5.3 mmol/L
CHLORIDE 105 98-110 mmol/L
CARBON DIOXIDE 24 20-32 mmol/L
CALCIUM 9.9 8.6-10.3 mg/dL
PROTEIN, TOTAL 7.1 6.1-8.1 g/dL
ALBUMIN 4.4 3.6-5.1 g/dL
GLOBULIN 2.7 1.9-3.7 g/dL (calc)
ALBUMIN/GLOBULIN RATIO 1.6 1.0-2.5 (calc)
BILIRUBIN, TOTAL 0.7 0.2-1.2 mg/dL
ALKALINE PHOSPHATASE 60 40-115 U/L
AST 23 10-35 U/L
ALT 36 9-46 U/L
HEMOGLOBIN Ale 5.7 H <5.7 % of total Hgb MI
CLIENTSERIIICES:866.6971378 SPECIMEN: MR839110N PAGE 2 OF 6
Quest. Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics.
EFTA00804475
Report Status: Final
raj Quest
Diagnostics EPSTEIN, JEFFREY
Patient Information Specimen Information Client Information
Specimen: MR8391 ION Client #: 78300020
EPSTEIN, JEFFREY
Collected: 11/23/2018 MOSKOWITZ, BRUCE W
DOB: 01/20/1953 AGE: 65 Received: 11/27/2018 109:51 EST
Gender: M Reported: 11/28/2018 / 09:22 EST
Patient ID: 19530120MJE
Health ID: 8573003290851249
Test Name In Range Out Of Range Reference Range Lab
For someone without known diabetes, a hemoglobin
Alc value between 5.7% and 6.4% is consistent with
prediabetes and should be confirmed with a
follow-up test.
For someone with known diabetes, a value <7%
indicates that their diabetes is well controlled. Alc
targets should be individualized based on duration of
diabetes, age, comorbid conditions, and other
considerations.
This assay result is consistent with an increased risk
of diabetes.
Currently, no consensus exists regarding use of
hemoglobin Alc for diagnosis of diabetes for children.
CALCIUM, IONIZED 5.2 4.8-5.6 mg/dL TP
URIC ACID 6.9 4.0-8.0 mg/dL MI
Therapeutic target for gout patients: <6.0 mg/dL
IMMUNOFIXATION, SERUM TP
INTERPRETATION NO MONOCLONAL PROTEIN
DETECTED
TSH 2.44 0.40-4.50 mIU/L MI
T4 (THYROXINE), TOTAL 7.6 4.9-10.5 mcg/dL MI
FREE T4 INDEX (T7) 2.3 1.4-3.8
T3 UPTAKE 30 22-35 % MI
SED RATE BY MODIFIED MI
WESTERGREN 11 < OR = 20 mm/h
CBC (INCLUDES DIFF/PLT) MI
WHITE BLOOD CELL COUNT 6.0 3.8-10.8 Thousand/uL
RED BLOOD CELL COUNT 5.28 4.20-5.80 Million/uL
HEMOGLOBIN 15.4 13.2-17.1 g/dL
HEMATOCRIT 44.3 38.5-50.0 %
MCV 83.9 80.0-100.0 fL
MCH 29.2 27.0-33.0 pg
MCHC 34.8 32.0-36.0 g/dL
RDW 13.0 11.0-15.0 %
PLATELET COUNT 273 140-400 Thousand/uL
MPV 10.6 7.5-12.5 fL
ABSOLUTE NEUTROPHILS 2892 1500-7800 cells/uL
ABSOLUTE LYMPHOCYTES 2298 850-3900 cells/uL
ABSOLUTE MONOCYTES 492 200-950 cells/uL
ABSOLUTE EOSINOPHILS 270 15-500 cells/uL
ABSOLUTE BASOPHILS 48 0-200 cells/uL
NEUTROPHILS 48.2
LYMPHOCYTES 38.3
MONOCYTES 8.2
EOSINOPHILS 4.5
BASOPHILS 0.8
URINALYSIS, COMPLETE MI
Sim Endhoto I
IRON AND TOTAL IRON MI
BINDING CAPACITY
CLIENT SERVICES: 866.697.8378 SPECIMEN: MR839110N PAGE30F6
Quest. Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics.
EFTA00804476
Report Status: Final
Quest
Diagnostics EPSTEIN, JEFFREY
Patient Information Specimen Information Client Information
Specimen: MR8391 ION Client #: 78300020
EPSTEIN, JEFFREY
Collected: 11/23/2018 MOSKOWITZ, BRUCE W
DOB: 01/20/1953 AGE: 65 Received: 11/27/2018 / 09:51 EST
Gender: M Reported: 11/28/2018 / 09:22 EST
Patient ID: 19530120MJE
Health ID: 8573003290851249
Test Name In Range Out Of Range Reference Range Lab
IRON, TOTAL 91 50-180 mcg/dL
IRON BINDING CAPACITY 336 250-425 mcg/dL (calc)
% SATURATION 27 15-60 % (calc)
FERRITIN 57 20-380 ng/mL MI
VITAMIN B12 325 200-1100 pg/mL MI
Please Note: Although the reference range for vitamin
B12 is 200-1100 pg/mL, it has been reported that between
5 and 10% of patients with values between 200 and 400
pg/mL may experience neuropsychiatric and hematologic
abnormalities due to occult B12 deficiency; less than 1₹
of patients with values above 400 pg/mL will have symptoms.
C-REACTIVE PROTEIN 1.3 <8.0 mg/L MI
MERCURY, BLOOD <5 <OR=10 mcg/L AT
This test was developed and its analytical performance
characteristics have been determined by Quest
Diagnostics. It has not been cleared or approved by the
FDA. This assay has been validated pursuant to the CLIA
regulations and is used for clinical purposes.
PSA, TOTAL 0.6 < OR = 4.0 ng/mL MI
The total PSA value from this assay system is
standardized against the WHO standard. The test
result will be approximately 20% lower when compared
to the equimolar-standardized total PSA (Beckman
Coulter). Comparison of serial PSA results should be
interpreted with this fact in mind.
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, FREE AMD
(DIALYSIS) AND TOTAL,MS
TESTOSTERONE, TOTAL, MS 153 L 250-1100 ng/dL
Men with clinically significant hypogonadal
symptoms and testosterone values repeatedly in
the range of the 200-300 ng/dL or less, may
benefit from testosterone treatment after
adequate risk and benefits counseling.
For additional information, please refer to
http://education.questdiagnostics.com/faq/
TotalTestosteroneLCMSMSFAQ165
(This link is being provided for informational/
educational purposes only.)
This test was developed and its analytical performance
characteristics have been determined by Quest
Diagnostics Nichols Institute Chantilly, VA. It has
not been cleared or approved by the U.S. Food and Drug
CLIENTSERIIICES:866.697.8378 SPECIMEN: MR839110N PAGE 4 OF6
Quest. Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics.
EFTA00804477
Report Status: Final
Quest
—00 Diagnostics EPSTEIN, JEFFREY
Patient Information Specimen Information Client Information
Specimen: MR839110N Client #: 78300020
EPSTEIN, JEFFREY
Collected: 11/23/2018 MOSKOWITZ, BRUCE W
DOB: 01/20/1953 AGE: 65 Received: 11/27/2018 I 09:51 EST
Gender: M Reported: 11/28/2018 / 09:22 EST
Patient ID: 19530120MJE
Health ID: 8573003290851249
Test Name In Range Out Of Range Reference Range Lab
Administration. This assay has been validated pursuant
to the CLIA regulations and is used for clinical
purposes.
TESTOSTERONE, FREE 42.5 35.0-155.0 pg/mL
This test was developed and its analytical performance
characteristics have been determined by Quest
Diagnostics Nichols Institute Chantilly, VA. It has
not been cleared or approved by the U.S. Food and Drug
Administration. This assay has been validated pursuant
to the CLIA regulations and is used for clinical
purposes.
Endnote I
* Test not performed. *
* No specimen received. *
CLIENT SERVICES: 866.697.8378 SPECIMEN: MR8391 ION PAGE5OF6
Quest. Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics.
EFTA00804478
Report Status: Final
raj Quest
Diagnostics EPSTEIN, JEFFREY
Patient Information Specimen Information Client Information
Specimen: MR8391 ION Client #: 78300020
EPSTEIN, JEFFREY
Collected: 11/23/2018 MOSKOWITZ, BRUCE W
DOB: 01/20/1953 AGE: 65 Received: 11/27/2018 / 09:51 EST
Gender: M Reported: 11/28/2018 / 09:22 EST
Patient ID: 19530120MJE
Health ID: 8573003290851249
Endocrinology
Test Name Result Reference Range Lab
VITAMIN D,25-OH,TOTAL,IA 24 L 30-100 ng/mL MI
Vitamin D Status 25-OH Vitamin D:
Deficiency: <20 ng/mL
Insufficiency: 20 - 29 ng/mL
Optimal: > or = 30 ng/mL
For 25-OH Vitamin D testing on patients on D2-supplementation and patients for whom quantitation of D2 and D3 fractions is required, the
QuestAssureD(TM) 25-OH VIT D, (D2,D3), LC/MS/MS is recommended: order code 92888 (patients >2yrs).
For more information on this test, go to: httpJ/education.questdiagnostics.com/faq/FAO163 (This link is being provided for informational/
educational purposes only.)
Physician Comments:
PERFORMING SITE:
AMD QUEST DIAGNOSTICS/NIOIOLS CHANTILLY. 1422.5 NEWBROOK DRJVE CHANTILL Y. VA 201SI -2225 Laboratory Ducar PATRICK W. MASONAID.PHD.CLIA: 1900221801
AT QUEST DIAGNOSTICS...JUNTA. 1777 MONTREAL CIRCLE. IIICICER GA 30014.6802 Laboratory Director. ANDREW N YOUNG.AID.PHD.CLIA: 1100255931
MI QUEST DIAGNOSTICS.NIIAMI HMO COMMERCE PARKWAY. MIRAMAR. FL 330254938 Laboratory DUCCIOI: JULIE I. FRIEDMAN.MD.CLIA: If/002773M
TP QUEST DIAGNOSTICSTAMPA.1223 E FOWLER AVE TAMPA. It 33617.2026 Laboratory Ihrector GLEN L IIORTIN.MD.PHD. CUA: 1000291120
CLIENT SERVICES: 866.697.8378 SPECIMEN: MR839110N PAGE 6 OF 6
Quest. Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics.
EFTA00804479
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