📄 Extracted Text (1,772 words)
BioRe ference
LABORATORI ES FINAL REPORT
Sr OFVCCIHealth Company
rPsTEIN, 7EFFREY Specimen IR: 104659439
D08: 81/28/1953 Age: 64 y Sex: m
Date Of Report: 89/21/2017 10:08
U/FL: Bed: S
Rm: A Date Collected: 09/15/2017 08:57
Date Received: 09/15/2017 23:06
Patient ED:
0
Address:9 EAST 715T STREET,
NEW YORK, MY 10021
11:
1. North America Eastern Ttnie
I Nores: NCN
FASTING
NOTE: SST tube submitted was inadequatel
y spun. Serum was found to
contain RBCs. Certain tests, e.g. Glucose,
may be decreased while
others e.g. Potassium or LOH may be elevated.
CLINICAL REPORT
Clinical Abnormalities Summary: rmay not contain all abnormal results; narrative results may not have abnormal
flags. Please review entire report.)
Cholesterol 224 HI Triglycerides 646 HI ROL CHOL., DIRECT 29 LO
HDL as % of 13 • Choi/HDL Ratio 7.7 • NON-HDL 195 HI
Cholesterol
CHOLESTEROL
HEP. A Ab., TOTAL Reactive * HEP. H SURF. AR. Reactive • 250H, VITAMIN D 31.5 LO
PTH(3), INTACT 196.9 HI PNEUMO Ab TYPE 1 0.3 LO PNEUMO Ab TYPE 4 8.8 LO
(58) (58)
PNEUMO Ab TYPE 8 0.6 LO PNEUMO Ab TYPE 9 (9N) 8.7 LO PNEUMO Ab TVPE 12 (12F)
(58) (58) (58)
PNEUMO Ab TYPE 19 (19F) 1.1 LO PNEUMO Ab TYPE 23 (23F) 0.3 LD PRELIM° Ab TYPE 26 (68) 8.9 LO
(58) (58) (58)
PNEUMO Ab TYPE 68 (9V) 9.5 LO B.Henselae IgG Ab 1:64 •
(58) (3)
Albumin 4.7 3.5.5.2 g/dL 4.5 08/30/1017
.Calcium 9.8 8.6-12.4 Ing/ill• • 9.7 30 -
-* CARDIOVASCULAR/LIPIDS *--
cholesterol 224HI <200 mg/dL 226 HI 8/30/2017
Triglycerides 646 MI <Ise :mg/dL IS29 Mt 8E/80/2017
BBL 0440L'eroEcr . 29 LO >40 mg/a TNP 08/39iidij .
HDL es t.0 Choles —11-1--- >14 yNp 08/30/2017
Evaluation: ABOVE AVG.(OWDERATE RISK)
Ratio 7.7 a <7.4 • avaiiiiii7
•-•
•.
Evaluation: ABM AVO.(MODERATE RISK)
to HDL Ratio 7.-- - com et:MR- Aa,
tote-
ot/30/2e0
i98 MI 4136 mg/dL
ELbranCeitiirer <lee esini2015
44041:. uoioto to coiculate.m. due to a Triglycerido level of greater tton 408 Ii/dL. , • • "
VLDL, CALCULATED Can't Calm 7-32 mg/di (._.Can't CaLc 108/39/2017
...._... . •--
BioReference Laboratories, Inc. James Weisberger M.D. Page 1 of
481 Edward H. Ross Dr I Elammod Park, NO B7407 I Laboratory Director 'rioted ,i 9/22/2917 89:57
EFTA00299765
Bio
LAB Ref
oRA ere
ToR nce
i Es
an OPKO Health Company
FINAL REPORT
ORSHER, STUART
EPSTEIN, JEFFREY
Specimen ID: 104659439
DOB: 01/20/1953 Age: 64 y Sex: m
U C3870 - STUART ORSHER, U/FL:
Date Of Report: 09/21/2017 10:88
N.D. Bed:
9 EAST 79TM 5T, Na: a Date Collected: 09/15/2017 88:57
Date Received: 09/15/2017 23:06
Patient ID:
NEW YORK, NY 10021 Address:9 EAST 71ST STREET, p
Acct #: (C3070) MO NEW YORK, HY 10021
P: E
North Americo Eastern Time
CLINICAL REPORT
Can't Calc: One or more components was
outside the measurable
range. We are unable to calculate.
--* MISCELLANEOUS
T5H
1.770 0.178-4.530 uIU/aIL TNP 08/30/2017
7.3 4.9-12.9
ill UPTAKE (13U) ug/dL TNP 08/30/2017
31.0 24.3-39.0
rffirmodat, FREE (aT4Y • 3.11
TNP 08/30/2017
— 6710--1.71r ng/d1 TNP
: FREE T4 INDEX . . 08/30/2017 •
2.3 1.5-3.8
1T3 (THYRONINE), TOTAL TNP 98/30/2017
127 -180
HEP: A Ab:,. -IgM r&dL --14NP B/30/1017 •
Non- Non-Reactive .•• .•
Reactive
NOTE: Hep A Ab,IgM is positive or reacti
ve during the acute phase.
Hep A Ab/Total is positive or reacti
ve during the recovery phase
or is indicative of a past infection.
; MEP. B CORE Ab. I66 • Non-
-Non-Reactive TNP 88/30/2017
Non-Reactive TAP . 08/30/2017
Reactive
Ramage • Na7kaaifive
B SURF. A4 TNP BB/30/2917
• tioh- Non-Reactive
Reactive eaftifidi7 •
NEP. IT-417' Negative legative 88/30/2017
BE AO.- Negative • Negative • 08/30/2017
WTOSTERDNE; TOT.,S: 194.3 193.44463---- 018/10/1017
NOTE: Patients receiving the drug Nandrolone cannot
be tested for
TESTOSTERONE, total using the EIA method (test code
0379-8)
due to a strong interference from the drug. Clinic
ians are
asked to request Testosterone, Total by LC/H5/
MS (test code
)4516) for these Patients.
gii Nakk.RiN15.0. .6e. 14 10-57 nmol/L
'tl.e4 30.00-150.00 pg/mL
LH 3.8 1.74.6 mIU/mi
Ci 280
i ll QUINTANA AB 6/N (30
39-308 Q/L 08/362017
s€t BELOW
' B. quintana Ab, IgM . < 2:16
--INTERPRETIVE INFORMAT/ON: Bartonella Quintana
Ab, lgm
-- Less than 1:16 Negative-No significant level of
.... . .
BioReference Laboratories, Inc.
481 Edward R. Ross Dr I Elmwood Park. NJ James Weisberger M.D. Page 2 of 5
07407 t Laboratory Director Printed 09/22/2017 09:57
EFTA00299766
13ioReference
LASORATOR/ES FINAL REPORT
an OPKO Health Company
ORSHER, STUART
EPSTEIN, JEFFREY Specimen ID: 104659439
DOB: 01/20/1953 Age: 64 y Sex:
C3070 - STUART ORSHER, M.O. H Date Of Report: 89/21/2017 10:08
U/FL: Bed: S
Date Collected:09/15/2817 88:57
Rm: A
9 EAST 79TH 57, ate Received: 09/15/2017 23:06
Patient ID:
NEW YORK, NY 10021 Address:9 EAST 71ST STREET, p
Acct a: (C3070) NEW YORK, NY 10821 L
P.
North Americo Eastern Time
Bartonel a quintana IgN antibody
detected.
1:16 or greater Positive-Presence of IgM antibody
to Bartonella quintana detected,
suggestive of current or recent
infection.
--The presence of 1.0( antibodies sugges
ts recent infection. Low
--levels of IgM antibodies may occasionally
persist for more than 12
. --months post-infection.
--Test developed and characteristics determ
ined by ARUP
--Laboratories. See Compliance Statement
A: aruplab.com/CS
--www.aruplab.com, Julio Delgado, MD - Lab.
Director
B. quintana Ab, Ig6 <1:64
--INTERPRETIVE INFORMATION: ilartonella quinta
na Antibody, IgG
-- Less than 1:64 Negative: No significant level of
Bartonella quintana Ig6 antibody
detected.
1:64 - 1:128 Equivocal: Questionable presence
of Bartonella quintana Ig6
antibody detected. Repeat testing
in 20-14 days may be helpful.
1:256 or greater Positive: Presence of IgG
antibody to Bartonella quintana
detected, suggestive of current
or past infection.
--A low positive suggests past exposure or infect
ion, while high
--positivB reSUltS may indicate recent or current infect
ion, but is
--inconclusive for diagnosis. Seroconversion betwee
n acute and
--convalescent sera is considered strong evidence of
recent
--infection. The best evidence for infection is
a significant change
--on two.appropriately timed specimens where
both tests are done in
--the same laboratory at the same time.
--Test developed and characteristics determined by AK,
i --Labo ratories. See Compliance Statement A: aruplab.con/CS
'HEP. C Ab. Non- Non-Reactive VIP
ML*(
NEPCA5CCORAne
(314
: performed .by: fIRU7
.
Reactive
0.03 0.80 MP .
I
• 08/30/2017
SOO Chipeta Way.
Salt Lake City, UT 841011
Hepatitis 8 Result Interpretation
(for reference. use only)
Master il/EAs Acute Oast Chronic IMV
•
atessamilmit eat
+ t - .t
SioReference Laboratories, Inc.
481 Edward H. Ross Dr I Elmwood Park, N3 07487 JainesWelabargeril.D. Page 3 of 5
Laborator/Director Printed 09/22/2917 09:57
EFTA00299767
BioReference
LABORATOR I ES FINAL REPORT
an OPKOHealth Company
mom, STUART
EPSTEIN, 7EFFREY Specimen ID: 18404430
D DOB: 01/20/1963 Age: 64 V Sex: e Date Of Report: 09/21/2017 10:08
a C3070 - STUART ORSHER, N.D. U/FL: Bed: ate Collected: 09/15/2017 08:57
R
Ie:
9 EAST 791N ST, Date Received: 40/13/2017 23:06
Patient ID:
EA YORK, NY 10021 Address:9 EAST 11ST STREET,
r. cct 8: (C3070) MO NEW NUFK, Pe 10821
P:
P: I
II Atrit, AmPrica fs5terr
mBeAg +-
HEP.B.CORE AB,IgM
HEP.B.CORE AB. +
N8eAb +/- +/.
MBSAb +/-
"Late Incubation/Early Acute
. NOTE: In remote past infection,
HBsAb level may be Negative or
Mon-Reactive in Some patients.
ACID 7.77 >5.38 ng/oL tep 040/241i
: Folic Acid Range
Units (ng/eL)
Weal >5.38
Borderline deficient 3.38-5.38
Deficient 0.35-3.37
EXCe8Sive >24.00
:
114114exitil 359 niaar Tip-
,2SON, VITAMIN 0 •- "." 'heir ' '"
VITAMIN 0,25-0H TEST INFORMATION
Range (ng/mL) Suggested Interpretation
<20.8 Deficient
20.0-31.9 Insufficient
32.0-100.0 Sufficient
>100.0 Possible Adverse Effects
Tgrolasobwo0dict . .....
52.8 ' ii7iciic5-----'-iiiii7 I....
n.77 1WW--
IPTH(3), INTACT
14/31755ii-
106.0 HI i3.1:44.8-. nenL " -- 71143 0/36/2817-,
:PERM Ablwq 1 (58) 0.3 LO 51.3 . ug/fiL (0.3 D 08/30/2017
ANEUMO Ab TYPE 3 (58). 1.8
1.---__,,-,__...... >1.3 ' ' Ug/iL 1.4 08/3e/2017
mum AD TYPE nal .. 0.8 LO cCI-- . Ug/IL .. 9.6 L BB/38/ 8i7
PRES Ab TYPE 8 (58) -.
0.6 tO >2.3 Ug/mi ' 4:4 LO ' 08/30/24317
— Th
iani i firi 9 (48) (se) 0.7 LO >4.1 ' • UgieL: /30/2817
POOSo-An DOELi-(11O)(41)"' - 4.1 L0 >1:3 ' -6024L. 08/30/2017
NEUMD Ab TYPE 14 010 7---' >it.3 >1.3 Wet 23.2 08 30/1017
TPNEUNO Ab TYPE 19 (19F) (58) ' 1.1 L0 ii:i -. ueini - 9.8 to 00/30/2017
WOW -a TYPE 10 (20)(037— Ira >1.3 . 4717
8 - i t'0.3 LO Os/ /2817
pwuko Ab TYPE 26 (GB) (58) 8.4 LO )1.3 wi/wL ti.s tO 08/3e/2017 -
iiPECIMO Ab TYPE 5 8.i---
. ... ...... >1.3 48/71C
pili(446 6 WOE if(10j .(34)- — I:4 •
...'≥LS' ug/iL 1.5 08/30/2017
-0140413743T*E - T6-titC71413- 1.8 >1.3 80/0 • I.3 0 --- beWeifrozl .
meupb At; TYPE 66 (9w) ( 51). • •
0.0 Lo . . i1:3 - ug/nL 4:4 io 08/30/2017 •
......_
*This test was developed and its performance characteris
tics determined by
bloaelerence Laboratories, Inc.
JanemONebelmwDereeD. Page 4 of 5
481 Edward H. Ross Dr I Elmwood Park, 83 07407
Laboratory okootor Printed 49/22/2027 09:57
EFTA00299768
Bio Reference
sORATORIEs
en Orlin" Health
FINAL REPORT
Company
WISNER, STUART
(EPSTEIN, 3EFFREY Specimen ID: 104659439
DOD: 01/20/1953 Age: 64 Y Ser: M
[3070 - STUART ORSHER, M.D. Date Of Report: 09/21/2017 10:08
Red: S
Date Collected: 09/15/2817 04:S7
A
9 EAST 79TH ST, Date Received: 09/15/2017 23:0S
Patient ID:
0 NEW YORK, NY 184321 Address:9 EAST 71ST STREET,
Acct #: (C3078) MD NEN YORK, NY 10821
P: E
P:
North America Eastern Tier
CLINICAL REPORT
I Viracor EurofinS. It as no, teen " • . 4.-4,: ••• • • • •• • ••••••It • i• "41.1 • '•• ••• ••'• .•'•• • "
clear? or aPPrOve
. Drug Administration.
Testing Performed At:
Viracor Eurofins
1001 NW Technology Drive
. Lee's Summit, MO 64886
IIIMM
CLIM ESI 643
e.11eitflfliekid Ab (3) 1:64 •
piiieriieile l`gM Ab (3) titer 1:64 g '08/30/aiii'l.
<1:20 • ie
•••• • -••• • titer <1:20 08/30/2017
•
This test was developed and its analyt
ical performance characteristics have
been determined by Quest Diagnostics
Nichols Institute Valencia. It has not
been cleared or approved by the US Food
and Drug Administration. This assay
has been validated pursuant to the CLIA
regulations and is used for clinical
purposes.
(3)
Performed by: Quest Diagnostics Nichols
Institute of Valencia
27027 Tourney Road
Valencia, CA 9135S-5386
(S8)
Performed by: viracor Eurofins Clinical
Diagnostic
1001 NW Technology brive
Lees Summit, MO 64086
NOTE: Specimen submitted is LIPEMIC. This
may cause inaccurate rnsults.
Please resubmit a fasting specimen at your
earliest convenience.
SioReference laboratories, Inc.
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LaboretopylDkeclor Printed 09/22/2017 09:57
EFTA00299769
ℹ️ Document Details
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35987932be870204c391c1e65c83d7b27da87739fcf39f1656b1ec0c14abe445
Bates Number
EFTA00299765
Dataset
DataSet-9
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document
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5
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