Case File
efta-efta00520767DOJ Data Set 9OtherSCHAFFER, SCHONHOLZ & DROSSMAN. LLP — BREAST MRI
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Unknown
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DOJ Data Set 9
Reference
efta-efta00520767
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10
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0
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Text extracted via OCR from the original document. May contain errors from the scanning process.
SCHAFFER, SCHONHOLZ & DROSSMAN. LLP — BREAST MRI
315 West 57th Street (between 8TH Avenue and 9" Avenue)
Tel:
New York. New York 10019
Fax:
PATIENT'S NAME
APPOINTMENT DATE:
REF PHYSICIAN:
BREAST MRI APPPOINTMENT INFORMATION
2- \lc)
\Coi Kc
MRI PACKET PROVIDED TO PATIENT ON:
TIME: X. s
MRN:
SCHEDULER:
in office 0
USPS mail 0
At your physician's request. you have been scheduled for an MRI examination of the breast. The examination will be
performed at cur Breast MRI office located on the Concourse Level at 315 West 57' Street between 8th and 9th Avenue.
Below. you will find important information regarding the procedure. Please read these instructions carefully and call our
office at 212.755.7656 if you have any questions.
•
Please arrive to the MRI Office at your scheduled lime so you can review your identifying documentation and
prepare for the examination.
•
The day before your appointment. PLEASE DRINK six to eight 8oz GLASSES OF WATER.
•
If you are 60 years old or over or have a history of diabetes or renal disease, a recent (within two weeks of your
appointment) BUN and Creatlnine blood test is required to assess renal function in association with a
contrast agent which may be administered during your MRI examination. Should these results not be available
at the time of your examination, a "finger-stick" laboratory screening test will be performed just prior to your
MRI examination.
NOTE: If you are having the MRI exam for assessment of breast implant rupture, the previous two paragraphs
do not apply to you.)
•
Bring your completed MRI Screening sheet.
•
You may continue to take all medications you currently take as prescribed.
•
It is extremely important to bring any previous studies related to this procedure for comparison with your
current examination. If you have any films related to this procedure please bring them with you.
•
Also, if your Referring Physician has given you any notes that pertain to the study, please bring those with you
as well.
•
Allow one to one and a half hours for the MRI exam.
•
Our Physicians will contact you within 48 hours to discuss the MRI results. A detailed medical report will be
sent to your Referring Physician.
BILLING PROCEDURES
The fee for the procedure(s) that has been scheduled is: S
Please be advised that our office does not participate with any commercial insurance plans. The foe for this examination will
be billed to you to the address we have on file. Please note that most insurance companies require pre-certification for
this examination. We suggest that you contact your Insurance carrier for information regarding pre-certification
requirements so you may be reimbursed for this service according to your policy's allowances.
If you have any billing questions, please call our Billing Department at 212-755-7656 Ext 17
• PLEASE SEE OTHER ATTACHMENTS FOR ADDITIONAL INFORMATION •
EFTA00520767
DIRECTIONS TO THE MRI OFFICE
The Breast MRI office is located at 315 West 571h Street between 8th and 9 th Avenues -
Concourse Level, Suite LL4
Transportation:
o
By Subway:
A, B, C, D or 1 to Columbus Circle
o
By Bus:
M5, M6, M7, M30, M31, M57 and M104 stop nearby.
Parking:
o
The nearest parking facility is on 571° Street between
8th and 91° Avenue - directly across the street from our office.
• C. •
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EFTA00520768
Schaffer, Schonholz & Drossman, LLP — Breast MRI
315 West 57'" Street - Concourse Level
Tel
New York, New York 10019
Fax
BREAST MRI GUIDELINES
• Please bring anything in writing from your referring doctor.
• Take all medications as prescribed.
• Leave all valuables at home.
• Allow one hour for each MRI exam scheduled.
• Results will be sent to your referring doctor in 2-3 business days.
• Please call us prior to appointment if you are pregnant or have a cardiac
pacemaker, cardiac valves, implanted cardiac defibrillator, aneurysm clips,
cochlear ear implants, heart stents, and retinal implants.
• Your appointment time includes a 15 minute registration period.
IMPORTANT;
The MRI must be performed on days 7 - 12 of your menstrual cycle.
• The day before and the day after your MRI examination, PLEASE DRINK
SIX TO EIGHT 8oz glasses of water.
• If you are 60 years old or over, or have a history of diabetes, renal
disease or are on dialysis, please inform us when you schedule your
appointment. We will need results of a recent (within 2 weeks of your
appointment) BUN and Creatinine blood test to assess renal function in
association with the contrast agent which may be administered during
your MRI examination.
If you have any questions or concerns, please call our office at
EFTA00520769
Patient's Name:
SCHAFFER, SCHONHOLZ & DROSSMAN, LLP
488 Madison Avenue • New York, NY 10022
31! West 57" Street • New York, NY 10019
PRE-CERTIFICATION INFORMATION
DOB:
I am aware that the MRI procedure I have scheduled may need to be pre-certified by my
insurance carrier in order for me to receive full or partial reimbursement.
I am aware that the pre-certification process may take several days to be completed and
that it is my responsibility to initiate the process in a timely fashion.
I am aware that I am responsible for the full fee as stated below.
2(
Breast MRI
o MRI Guided Breast Biopsy
o MRI Guided Wire Localization
$ 2,200.00
$ 3,600.00
$ 2,700.00
Patient's Signature:1(
EFTA00520770
SCHAFFER, SCHONHOLZ & DROSSNIAN, LLP
315 West 57th Street - LL4
New York, NY 10019
Patient's Name:
Date of Exam:
.Bwkayfrilirgigytscmgittiqp.HEn (Plen,. print legibly)
Mc 0:
MRN:
Age:
•
DOB:
Sex: F
Tel: 11.
1
Fax:
Have you had a prior mammogram: 0 Yes
0 No
Where?:
Have you had arecent clinical breast exam by your physician/practitioner (within the past year)? ODYaetes:
0 No
Reason for Today's Exam:
0 Annual screening exam (no problems)
1St
Last CBE Date:
0 Diagnostic Exam (Check all that apply)
0 Left 0 Right 0 Both
0 NEW lumps in your breast?
0 NEW pain in your breast?
0 Abnormal discharge from nipple?
family History:
Do you have a family history of breast cancer?
If yes, who?
who?
Personal History:
Have you ever had breast cancer?
If yes, please check the following boxes:
Which breast?
What surgery?
Radiation therapy?
Type of cancer?
Are you BRCA positive? (Breast cancer gene)
Surgical History:
Have you ever had ANY previous breast surgery?
If yes, please check the following boxes:
Medical Information:
Are you pregnant? 0 Yes 0 No
Benign excision
Aspiration
Needle biopsy
Breast reduction/breast lift
Implants
0 6 month follow-up exam
0 Call back examination
0 Other changes?
Explain:
O Yes
0 No
Age when diagnosed?
Age when diagnosed?
O Yes
0 No
When?
O Left
0 Right
0 Both
O Mastectomy 0 Lumpectomy (for breast cancer)
0 Yes 0 No
0 Invasive 0 DCIS
0 Not sure
0 Yes
0 No 0 Have not been tested
O Yes
0 No
O Left 0 Right
0 Both
When?
O Left
0 Right
0 Both
When?
O Left
0 Right
0 Both
When?
0 Yes
0 No
When?
0 Yes 0 No
When?
implant Type
0 Silicone 0 Saline
Are you currently breast feeding? 0 Yes 0 No
Do you have monthly menstrual periods?
0 Yes
0 No (post menopausal)
0 No (post hysterectomy)
Date of last menstrual period:
Are you on hormone supplement? 0 Yes 0 No
Are you on birth control? 0 Yes 0 No
Personal history of any cancer other than breast cancer? 0 Yes 0 No Explain:
Personal history of any other medical condition? 0 Yes 0 No Explain:
Patient Signature:
Technologist initials:
EFTA00520771
SCHAFFER, SCHONHOLZ & DROSSMAN, LLP
315 West 57th Street - LL4
New York, NY 10019
Tel:
Fax:
PATIENT MEDICATION GUIDE FOR GADOLINIUM-BASED CONTRAST
Patient Name:
MRN:
Contrast Type Being Administered:
S00tarem
nEoviSt
DMullThance
D0ther:
A
The United States Food & Drug Administration requires imaging centers to share this information with
patients scheduled to receive gadolinium-based contrast agents for magnetic resonance imaging.
What is a GADOLINIUM-BASED CONTRAST AGENT (GBCA)?
• The injection you are scheduled to receive is a prescription medicine called a gadolinium-based contrast agent (GBCA).
GBCAs are injected into your vein and used with a magnetic resonance Imaging (MRI) scanner.
• An MRI exam with a GBCA helps your doctor to see problems better than an MRI exam without a GBCA.
• Your doctor has reviewed your medical records and determined that you would benefit from using GBCA with your MRI.
What Is the most important Information I should know about GADOLINIUM-BASED CONTRAST AGENTS?
• This injection contains a metal called gadolinium. Small amounts of gadolinium can stay in your body including the brain,
bones, skin and other parts of your body for a long time (several months to years).
• His not known how GBCAs may affect you, but solar, studies have not found harmful effects in patients with normal kidneys.
• Rarely patients have reported pains, tiredness, and skin, muscle or bone ailments for a long time, but these symptoms
have not been directly linked to gadolinium.
• There are different GBCAs that can be used for your MRI exam. The amount of gadolinium that stays In the body is
different for different gadolinium medicines. Gadolinium stays In the body more after Omniscan or Optimark than after
Eovist, Magnevist or MulliHance. Gadolinium stays in the body the least after Dotarem, Gadavist or ProHance.
• People who get many doses of gadolinium medicines, women who are pregnant and young children may be at increased
risk from gadolinium staying in the body.
• Some people with kidney problems who get gadolinium medicines can develop a condition with severe thickening of the
skin, muscles and other organs in the body (nephrogenic systemic fibrosis). Your healthcare provider should screen you to
see how well your kidneys are working before you receive GADOLINIUM-BASED CONTRAST.
Do not receive a GADOLINIUM-BASED CONTRAST if you have had a prior severe allergic reaction to it.
Before receiving GADOLINIUM-BASED CONTRAST, tell us about all your medical conditions, including If you:
• Have had any MRI procedures in the past where you received a GBCA. Your healthcare provider may ask you for more
information including the dates of these MRI procedures.
• Are pregnant or plan to become pregnant. It is not knoWn if GADOLINIUM CONTRAST can harm your unborn baby. Talk
to your healthcare provider about the possible risks to an unborn baby if a GBCA is received during pregnancy.
• Have kidney problems. diabetes, or high blood pressure.
• Have had an allergic reaction to dyes (contrast agents) including GBCAs.
What are possible side effects of GADOLINIUM-BASED CONTRAST?
• See above 'What is the most important information I should know aboutGADOLINIUM-BASED CONTRAST AGENTS?".
• Allergic reactions: GADOLINIUM-BASED CONTRAST can cause allergic reactions that can sometimes be serious. Your
healthcare provider will monitor you closely for symptoms of an allergic reaction.
Most common side effects of GBCAS: Nausea, headache, dizziness and cold feeling or burning at the injection site.
Other common side effects can include: Rash, pain, vasodllatlon, tingling in hands or feet, and taste perversion.
These are not all the possible side effects of GADOLINIUM-BASED CONTRASTAGENTS.
Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1.800-FDA-1088.
General Information about the safe and effective uses and Ingredients of GADOLINIUM-BASED CONTRAST.
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. You can ask your healthcare
provider for information about GADOLINIUM-BASED CONTRAST that is written for health professionals.
Dotarem
Active Ingredient: Gadoterate meglumine
Inactive Ingredients: DOTA water
erbet
Gui e approv
y the FDA 4/2018
Eovist
Active Ingredient: Gadoxelate disodium
Inactive Ingredients: Caloxetate trisodium,
trometamol, hydrochloric acid and/or sodium
hydroxide (for pH), water
Manufacturer: Bayer HealthCare
h rrnaceuticals
e approv
by the FDA 4/2018
MultlHance
Active Ingredient: Gadobenale
dimeglumine
Inactive Ingredient: water
Manufacturer. Bracco Dia
A 4/2018
I acknowledge that I was provided the above Information regardin Gadolinium-Based Contrast Agents.
Patient Signature:
Witness Signature:
Job Title:
EFTA00520772
MEDICATION GUIDE
DOTAREM® (doh TAH rem)
(gadoterate meglumine)
Injection for Intravenous use
What Is DOTAREM?
• DOTAREM is a prescription medicine called a gadolinium-based contrast agent (GBCA). DOTAREM, like other
GBCAs, Is injected into your vein and used with a magnetic resonance Imaging (MRI) scanner.
•
An MRI exam with a GBCA, Including DOTAREM, helps your doctor to see problems better than an MRI exam
without a GBCA.
•
Your doctor has reviewed your medical records and has determined that you would benefit from using a GBCA
with your MRI exam.
What is the most Important information I should know about DOTAREM?
•
DOTAREM contains a metal called gadolinium. Small amounts of gadolinium can stay in your body including the
brain, bones, skin and other parts of your body for a long time (several months to years).
•
It is not known how gadolinium may affect you, but so far, studies have not found harmful effects in patients with
normal kidneys.
•
Rarely patients have reported pains, tiredness, and skin, muscle or bone ailments for a long time, but these
symptoms have not been directly linked to gadolinium.
•
There are different GBCAs that can be used for your MRI exam. The amount of gadolinium that stays In the body Is
different for different gadolinium medicines. Gadolinium stays in the body more after Omniscan or Optimark than after
Eovist, Magnevist or MultiHance. Gadolinium stays in the body the least after Dotarem, Gadavist or ProHance.
•
People who get many doses of gadolinium medicines, women who are pregnant and young children may be al
increased risk from gadolinium staying in the body.
•
Some people with kidney problems who get gadolinium medicines can develop a condition with severe thickening of
the skin, muscles and other organs in the body (nephrogenic systemic fibrosis). Your healthcare provider should
screen you to see how well your kidneys are working before you receive DOTAREM.
Do not receive DOTAREM if you have had a severe allergic reaction to DOTAREM.
Before receiving DOTAREM, tell your healthcare provider about all your medical conditions, Including if you:
•
have had any MRI procedures in the past where you received a GBCA. Your healthcare provider may ask you for
more information including the dates of these MRI procedures.
• are pregnant or plan to become pregnant. It Is not known If DOTAREM can harm your unborn baby. Talk to your
healthcare provider about the possible risks to an unborn baby if a GBCA such as DOTAREM is received during
pregnancy.
• have kidney problems, diabetes, or high blood pressure.
•
have had an allergic reaction to dyes (contrast agents) including GBCAs.
What are possible side effects of DOTAREM?
•
See "What is the most important information I should know about DOTAREM?"
•
Allergic reactions. DOTAREM can cause allergic reactions that can sometimes be serious. Your healthcare
provider will monitor you closely for symptoms of an allergic reaction.
The most common side effects of DOTAREM Include: nausea, headache, pain, or cold feeling at the injection
site, and rash.
These are not all the possible side effects of DOTAREM.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
General information about the safe and effective uses of DOTAREM.
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. You can ask your
healthcare provider for information about DOTAREM that is written for health professionals.
What are the ingredients in DOTAREM?
Active Ingredient: gadoterate meglumine
Inactive ingredients: DOTA, water for injection
Manufactured by: Catelent
and Recipharm (vials) for Guerbet
For more Information, go to
-
or call allalialls
This Medication Guide has been approved by the U.S. Food and Drug Administration.
Rev. 412018
EFTA00520773
SCHAFFER, SCHONHOLZ & DROSSMAN, LLP
315 West 57th Street - LL4
New York, NY 10019
Tel:
Fax
hi PAIIENNgiagg.Bablic,rcz%:" ; ';;; , '
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Patient Name:
Medical Record #:
Date of Exam:
Referring Dr.:
Date of Birth:
Age:
Height:
Weight:
O Male O Female
WARMNG:TtlaMig,§XSTENI:M.40N.atr.14i40.1fi.YS.ON
• ,' I.
•
Certain implants, devices or objects may be hazardous and/or may interfere with your MRI procedure.
0
Do not enter the MRI exam room if you have questions or concern regarding an implant, device or object.
k
Consult the MRI Technologist BEFORE entering the MRI exam room.
DO YOU.HAVE.ANY OF THE'FOALOWINGt `. -
.
. IMPORTANT INSTRUOTIONS ' -
OYES ONO Injury to your eye involving metal
OYES ONO My metallic fragment or foreign body
OYES ONO Aneurysm clip(s)
OYES ONO Cardiac pacemaker
DYES ONO Implanted cardioverter defibrillator (ICD)
OYES ONO Electronic implant or device
OYES ONO Magnetically-activated implant or device
OYES D NO Neurostimulation system
OYES ONO Spinal cord stimulator
OYES ONO Internal electrodes or wires
OYES ONO Bone growth / bone fusion stimulator
DYES ONO Cochlear, otologic or other ear implant
DYES ONO Insulin or other infusion pump
DYES • NO Implanted drug Infusion device
OYES ONO Any type of prosthesis (eye, penile, etc.)
OYES ONO Heart valve prosthesis
OYES ONO Eyelid spring or wire
OYES ONO Artificial or prosthetic limb
DYES ONO Metallic stent, filter or coil
OYES ONO Shunt (spinal or intraventricular)
OYES ONO Vascular access port and/or catheter
OYES ONO Radiation seeds or implants
OYES ONO Swan-Ganz or thermodilution catheter
OYES ONO Medication patch (Nicotine, Nitroglycerine, etc.)
OYES ONO Wire mesh implant
DYES O NO Tissue expander (breast or other)
DYES ONO Surgical staples, clips or metallic sutures
OYES ONO Joint replacement (hip, knee, etc.)
OYES ONO Bone/joint pin, screw, nail, wire, plate, etc.
OYES ONO IUD, diaphragm or pessary
OYES ONO Other implant:
Mark
implant
on the
or
C
—
•
-
-
_
figure
metal
-
below the
inside of or
t ''
location
on
J
-\
your
l.
,r
of
body
If
any
RIGHT
Remove ALL
including:
- hearing
-
_ dentures
cell phone
- keys
- eyeglasses
- hair pins
- jewelry
- safety
- money
- credit cards,
- pens
- pocket
- nail clipper
- clothing
- steel-toed
- tools
- all loose
aids
and
and
and
pins
clip
knife
with
metallic
I
metallic
and
watch,
and
bank
boots/shoes
LEFT
LEFT
objects in the
partial plates
pagers
barrettes
Including body
coins
cards and
metal fasteners and
objects
1
dressing
piercing
magnetic
metallic
RIGHT
room,
jewelry
strip cards
threads
OYES ONO Dentures or partial plates
OYES O NO Tattoo or permanent makeup
OYES ONO Body piercing jewelry
O YES O NO Hearing aid (remove before entering exam room)
OYES ONO Breathing problem or motion disorder
OYES ONO Claustrophobia
* Consult the MRI Technologist if you have any questions or concerns BEFORE you enter the exam
Technologist Notes:
* Aft patients •having MRI studies MUST wear hearing protection (ear. pitigs or earmuffs)...No exceptions.
EFTA00520774
PREGNANCY and BREASTFEEDING STATUS
* If a mother desires, she may refrain from breastfeeding for 24 hours and discard milk after gadolinium injections.
Are you: Pregnant? K Yes K No
Possibly Pregnant? 0 Yes O NO
Breast Feeding? K Yes K No
Date of Last Menstrual Period:
SKINWARMIN(3,. .. .
* MRI Radiofrequency has the potential to cause tissue heating. Precautions will be taken to avoid this.
Alert the technologist Immediately if you notice any heating sensations during your MRI scan.
PIERCINGS; COSMETIC IMPLANTS, TATTOOS ANDPERMANENT MAKEUP
* A small number of patients have experienced transient skin irritation, swelling, bruising or heating sensations at the site of
piercings, cosmetic implants, tattoos and permanent makeup in association with MR procedures.
Individuals with these items should Inform the technologist so precautions can be taken.
_MEDICAL HISTORY
Why are you having this test done? What is the reason? List surgeries you have had and date of surgery:
Where/What area is the problem? Body part involved?
Do you have or ever had cancer? K Yes K No
If yes: What Type — Where (body part)
Which side (left/right/upper/lower)?
When did your symptoms start?
Describe the problem it is giving you.
What type of treatment did you receive and when?
Did you injure the area of interest? K Yes K No
If yes, describe:
Check all that are applicable to your symptoms:
K Acute
(present or a severe and intense degree)
K Chronic (persisting a long time / constantly recurring)
O Intermittent
K Transient (lasts only a short time)
O Primary issue K Secondary due to another issue
List any tests you had at other facilities for this problem:
Ex: Lab, X-Ray, Upper GI, BE, Ultrasound, MRI, CT
Test
—
Date
—
Where
List all medications you are taking and what they're for:
Have you been In the hospital within the last week?
O Yes K No
If yes, describe below:
Have you ever experienced any problem related to a
previous MRI procedure or MRI contrast? K Yes K No
DO YOU HAVE ANY OF THE FOLLOWING?
TECHNOLOGIST NOTES
K YES ONO Kidney disease or kidney Injury
K YES ONO Kidney surgery, transplant, single kidney
❑YES ONO Kidney tumor or cancer
❑YES ONO Diabetes
OYES K NO Are on dialysis
❑YES O NO Chemotherapy in the past 3 months
OYES K NO Take medication for hypertension (follow local protocol)
K YES ONO Past allergic reaction to gadolinium or Iodine contrast
OYES ONO Asthma or allergy
CONTRAST CONSENT
Due to your medical history, or as requested by your physician, an injection of MRI gadolinium contrast
may be necessary to aid the radiologist in evaluating your MRI scan.
The Food and Drug Administration has approved this agent. A very small percentage of patients receiving gadolinium may develop a
headache or experience mild nausea. Rarely, local Inflammation may occur at the Injection site.
O I CONSENT to having Gadolinium contrast as needed. (Check box if you agree to contrast)
O I DECLINE having a Gadolinium contrast injection at this time. (Check box if you disagree to contrast)
I attest that the information on this form Is correct to the best of my knowledge. I have read and understand the contents of this form
and had the opportunity to ask questions regarding the MR procedure I am about to undergo.
I understand that emergency or follow-up care, if needed, is the direct financial responsibility of the patient receiving
additional 3rd party services (ambulance transport to a hospital, 911 call, medical care, etc.).
PatienliGuardian Signature:
FOR STAFF USE: Screening Performed By: O MR Technologist
Staff Signature:
O Nurse O Radiologist O Other:
Print Name:
EFTA00520775
SCHAFFER, SCHONHOLZ & DROSSMAN, LLP
C Tax ID tt 13-198-5544
MRI PROCEDURES PRE-CERTIFICATION INFORMATION
Most insurance companies require pre-certification for MRI examinations. Below, you will find the procedure codes your insurance carrier will need to pre-
certify your MRI. Please note that it is the patient's responsibility to initiate the pre-certification process by calling the insurance carrier and notifying them
of the procedure to be performed. Your insurance company pre-cert specialist may also request to speak with your Referring Physician during the pre-
certification process. Should they have any additional questions, please have them contact our Billing Department at
Ext. 17. Thank you.
BREAST MRI - BILATERAL
CPT-4 CODE
DESCRIPTION
FEE
77049
$ Z200
MRI BREAST - BILATERAL w/wo CONTRAST and 3D RECONSTRUCTION and ANALYSIS ON INDEPENDENT WORKSTATION
BREAST MRI - UNILATERAL
CPT-4 CODE
DESCRIPTION
FEE
77048
MRI BREAST - UNILAT w/wo CONTRAST and 3D RECONSTRUCTION and ANALYSIS ON INDEPENDENT WORKSTATION
$ 2,100
•
MRI GUIDED BREAST BIOPSY
CPT-4 CODE
DESCRIPTION
FEE
19085
MRI GUIDED BIOPSY, BREAST, WITH OR WITHOUT PLACEMENT OF CUP AND IMAGING OF THE BIOPSY SPECIMEN,
PERCUTANEOUS, FIRST LESION
$ 3,275
G0206
DIGITAL MAMMOGRAPHY/UNILATERAL
325
TOTAL FEE:
$ 3,600
19086
MRI GUIDED BIOPSY, BREAST, + EACH ADDITIONAL SITE WITH OR WITHOUT alp PLACEMENT
$ 3,275
NOTE: Breast biopsies require that we send the tissue specimen obtained during the procedure to a pathologist for microscopic examination and reporting.
The specimen obtained will be sent to Mount Sinai Pathology Associates or to the University of Pennsylvania Surgical Pathology Department. New York
State Law (Section 394-E) requires that clinical laboratories bill patients directly. The lab processing your specimen(s) will bill you separately for their
services. If you have any questions regarding the laboratory billing, please contact:
Mt Sinai Pathology Associates: 1-800-542-5760
UCKlatei 05/33/19
University of Pennsylvania Pathology:
EFTA00520776
Technical Artifacts (7)
View in Artifacts BrowserEmail addresses, URLs, phone numbers, and other technical indicators extracted from this document.
Phone
1-800-542-5760Phone
212-755-7656Phone
212.755.7656Wire Ref
REF PHYSICIANWire Ref
ReferringWire Ref
Wire LocalizationWire Ref
referringForum Discussions
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