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HPV: Diagnostics, Coding and Insurance Coverage

HPV:  Diagnostics, Coding and Insurance Coverage
October 8, 2016
Lori-Lynne A. Webb
Human Papilloma Virus also known as HPV is the most common sexually transmitted infection in the United States. HPV is a virus, and is so common that nearly all sexually active men and women get it at some point in their lives. There are more than 150 different types and strains of HPV, and some of the types can cause health problems including genital warts and cancers. HPV is so common that nearly all sexually active men and women get it at some point in their lives.
HPV is named for the warts (papillomas) some HPV types can cause. There are some strains of HPV that can lead to cancer.  Most commonly these HPV strains have been linked to cervical cancer in women.  Unfortunately, there are more than 40 HPV types that can infect the genital areas of both men and women.  However, research has created vaccines that can prevent infection with some of the most common types of HPV.
Human Papillomavirus (HPV), low-risk types are associated with strain(s)  6, 11, 42, 43, 44.  High risk strains have been identified as strain(s) 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68. 
According to the Advisory Committee on Immunization Practices (ACIP) during its February 2015 meeting, it has been recommended that the  9-valent (9 different strains HPV vaccine; also known as 9vHPV) as one of three HPV targeted vaccines that can be used for routine vaccination.  The HPV vaccine is recommended for routine vaccination at age 11 or 12 years and they also recommend vaccination for females aged 13 through 26 years and males aged 13 through 21 years not vaccinated previously.  
Previously, the quadravalent (4-strain) HPV vaccine was only effective against HPV strain(s) 6, 11, 16 and 18.  The 9-valent vaccine is effective against HPV strains 6, 11, 16, 18, 31, 33, 45, 52, and 58.  
Prevention of cervical cancer due to HPV can be initiated with regular screening performed at the same time as the Papanicolaou screening test, also known as a Pap Smear, for cervical cancer.   The PAP looks for abnormal cells on the cervix that could turn into cancer over time. Screening does not eliminate the problem, it allows for these types of diagnoses to be found and treated before they turn into cancer.
ACOG has recommended that women should start getting regular Pap tests at age 21. For women ages 30 and older, the HPV test can be used along with the Pap test. Cervical cancer often does not cause symptoms until it is advanced. The Pap Smear and the HPV tests look for different things: The Pap test is a screening to check the cervix for abnormal cells that could turn into cervical cancer. The HPV test is performed to check the cervix for the virus (HPV) that can cause abnormal cells and cervical cancer.
CMS Policy:
In July of 2015, the Centers for Medicare & Medicaid Services (CMS) came out with the implementation of payment for screening for cervical cancer with HPV testing under National Coverage Determination policy 210.2.1.  Up until this change was implemented, Medicare was covering a screening pap and pelvic exam for its female beneficiaries every 12 or 24 month interval, based upon whether the patient was considered low or high risk.  Unfortunately, at that time HPV screening and testing was not paid for by CMS.   However, CMS has since determined that HPV screening/testing    
In conjunction with the Pap and Pelvic exam is of value, and will allow a screening test once per every 5 years, for beneficiaries aged 30 to 65 years
For Medicare beneficiaries (and some private payers too) HCPCS has implemented code G0476.  HCPCS 2017 Code : G0476; Infectious Agent Detection By Nucleic Acid (Dna Or Rna); Human Papillomavirus (Hpv), High-Risk Types (Eg, 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68) For Cervical Cancer Screening, Must Be Performed In Addition To Pap Test . 
The ICD-10cm codes used in conjunction with G0476 are:
1.     ICD-10 Z11.51 Encounter for screening for human papillomavirus (HPV) and Z01.411 Encounter for gynecological examination (general)(routine) with abnormal findings  
OR
2.     Z01.419 Encounter for gynecological examination (general)(routine) without abnormal findings
Once the claim is submitted to your CMS carrier (Such as Medicare,  True Blue, etc) 
a)     Medicare/Medicaid will not apply beneficiary coinsurance and deductibles to claims with the HCPCS code  G0476, HPV screening
 
b)    Part B claims can only be accepted with a Place of Service Code equal to ‘81’, Independent Lab or ‘11’, Office;

c)     This is only effective for claims with dates of service on or after July 9, 2015

d)    If your clams contain HCPCS G0476, HPV screening, more than once in a 5-year period [at least 4 years and 11 months (59 months total) must elapse from the date of the last screening] they will be denied.

e)     CMS will deny line-items on claims containing HCPCS G0476, HPV screening, If the beneficiary is less than 30 years of age or older than 65 years of age.

f)      If you know that the patient is not eligible for payment, then be sure to have the ABN signed, on file and submit the claim with the GA modifier. 
Some provider offices were having problems getting the code G0476 paid, with diagnosis code Z12.4 Encounter for screening for malignant neoplasm of cervix.  The issue with this ICD-10 code is that
a)     CMS policies are only for those FEDERAL programs such as Medicare/Medicaid/Tricare. and they don’t necessarily pertain to private insurance payers (such as Blue Cross/Blue Shield/Aetna/etc… )
b)    The HCPCS code G0476 is actually the HCPCS code for the “lab test itself”    therefore that is why only those particular ICD-10 codes would be applicable. 
c)     The ICD-10cm code Z12.4 Encounter for screening for malignant neoplasm of cervix is exactly that –  it is for the“Encounter”  the Office/Visit  aka E&M code.  It not appropriate to append a ICD-10 “encounter for” code to a “lab test” code such as the G00476.
In January of 2015, CPT has revised the HPV test codes by deleting laboratory codes  87620-87622 and adding three new codes 87623-87625 Human Papilloma Virus (HPV).  These new codes have been added to differentiate between high and low risk HPV types.  Low-risk types would be reported with code 87623 and high-risk types with code 87624. Again, these are laboratory codes, not the codes you would normally use in the providers office. 
HPV Vaccinations and Cervical Cancer
Cervical Cancer has been one of the most common causes of cancer death for American women prior to Pap test.
Since the Pap test, cervical cancer mortality has declined by almost 70%.  Most cervical cancers occur in unscreened or
inadequately screened women. According to the American Cancer society, most cases of cervical cancer are diagnosed in women younger than 50, and more than 20% are diagnosed in women over the age of 65.  In the U.S., Hispanic women have been shown to be the most likely demographic to get cervical cancer, followed by African-Americans, Asians, Pacific Islanders, and Whites.  In women over the age of 30 HPV infections are more likely to be persistent and/or  high-grade.  Most HPV-related lesions progress slowly into a cervical cancer.  This slow rate of growth is somewhere between 3 – 7 years on average for a severe dysplasia to progress to invasive cancer.
The HPV strain 16 accounts for nearly 55 – 60%, and the HPV 18 strain accounts for approximately 10 – 15% of those that develop cervical cancer.  The ACS notes that about 10 other HPV strains cause remaining 25 – 35% of cervical cancers.  HPV vaccines are used to prevent HPV infection and therefore cervical cancer.  ACOG and the World Health Organization (WHO) have recommended for women who are 9 to 25 years old, and who have not been exposed to HPV receive the vaccination for HPV virus.  Since the vaccine only covers the partial listing of HPV strains, routine PAP smears should still be a part of cervical cancer screening.  Normally, the vaccines require two or three doses depending on how old the patient is. Vaccinating girls around the ages of nine to thirteen is typically recommended. The vaccines provide protection for at least eight years.  It has also been recommended that young and adolescent men ages 9–26 receive the HPV vaccine for the prevention of genital warts and anal cancer. 
The first FDA approved HPV vaccination came out in 2006 and were targeted to the four most common strains of HPV.  However, improvements and more research has continued to develop better vaccines which now target up to nine of the most common strains of HPV that can potentially cause cervical cancer. 
Coding, Clinical Documentation and Reimbursement
When coding the vaccinations for the HPV vaccine (such as GARDASIL®9 Human Papillomavirus 9-valent Vaccine, Recombinant) Below represents what would normally be coded from the physician/provider office. Modifier -51 should not be reported for vaccines  when performed with the administration procedure code .
90649
CPT
Human Papillomavirus vaccine, types 6, 11, 16, 18, quadrivalent (4vHPV), 3 dose schedule, for intramuscular use
90650
CPT
Human Papillomavirus vaccine, types 16, 18, bivalent (2vHPV), 3 dose schedule, for intramuscular use
90651
CPT
Human Papillomavirus vaccine types 6, 11, 16, 18, 31, 33, 45, 52, 58, nonavalent (9vHPV), 3 dose schedule, for intramuscular use
90471
CPT
Immunization administration (includes percutaneous, intradermal, subcutaneous, or intramuscular injections); one vaccine (single or combination vaccine/toxoid)
Z23
ICD-10-CM
Encounter for Immunization
The clinical documentation for injections and infusions that are “vaccination” based need to clearly reflect this is a “vaccine” as a prophylactic measure and not a diagnostic or therapeutic service.  In addition be sure to inform the provider that these items should be clearly reflected in the record:
·         The site of the injection/infusion
·         The route of the administration (eg.  Intramuscular, subcutaneous, subdermal, intradermal)
·         The substance administered (eg Gardasil-9)
·         The number of units administered  
·         The medical necessity (eg diagnosis)
As, HPV vaccines are fairly new on the market not all insurance payers will reimburse for this service.   CMS/Medicaid eligible or those that have no insurance, may qualify for the Vaccines for Children (VFC) program or have these vaccines proved at a local Health Departments.   Private insurance payers such as Blue Cross, Blue Shield, Aetna, UHC, etc.. will varies based upon how the patient’s insurance plan is written and whether they have immunization coverage as a benefit
As a provider office, it is important that you check with the patients’ plan ahead of time to determine if they will pay for the cost of the vaccine.  If the private insurance payer does not cover the vaccine, the patient would be responsible for the cost.   In this instance it would be advisable to have the patient also sign an Advance Notice of potential non-payment and collect the cost of the service in advance. 
The “average” cost per single dose of an HPV vaccine can ranges between $ 175 – 250.00 per vial of vaccine serum,  plus an administration fee for the administration of the serum.   Three doses of the vaccine, spaced one month apart  are required to complete the series.  It is imperative that the patient understands the financial cost and the requirement of 3 visits to the provider to obtain the complete series for protection against HPV.

Lori-Lynne A. Webb, CPC, CCS-P, CCP, CHDA, COBGC and ICD10 cm/pcs Ambassador/trainer is an E&M, and Procedure based Coding, Compliance, Data Charge entry and HIPAA Privacy specialist, with over 25 years of experience.  Lori-Lynne’s coding specialty is OB/GYN office & Hospitalist Services, Maternal Fetal Medicine, OB/GYN Oncology, Urology, and general surgical coding.  She can be reached via e-mail at [email protected]or you can also find current coding information on her blog site: http://lori-lynnescodingcoachblog.blogspot.com/.   

Lori-Lynne’s Coding Coach Blog

diagnostics with embolizations

Hi,

I have an embolization case that seems to indicate that they did diagnostic workup before the decision to embolize. According to Dr. Z, "embolization codes (37241-37244) allow separate coding of catheter placements and associated diagnostic imaging." Since the report says that "transarterial embolization was elected" after all of the diagnostic imaging, wouldn’t I code that imaging?

For the angiography leading up to the decision to embolize, I thought 36245-59 for catheter position in the iliac limb, and 75625 for aortography along with 75710-59 for the iliac imaging, and 75774×2 for imaging of the celiac and SMA.
Then for the embolization, I thought 37242 with 36245-59 for placement in the SMA, and 36246 for catheter placement in the middle colic artery.

I hope I’m close.

Thanks for any input and thoughts on this!

PROCEDURES PERFORMED:
Abdominal aortography, mesenteric angiography, transmesenteric arterial
abdominal aortic aneurysm Endosac embolization and proximal inferior
mesenteric artery embolization.
IMAGING MODALITY UTILIZED:
Color Doppler ultrasonography and fluoroscopy.
FLUOROSCOPY TIME: 46.9 minutes, 4933 mGy.
MODERATE SEDATION: Moderate sedation was utilized.
ANESTHESIA: Local.
ACCESS SITE:
Right common femoral artery retrograde.
CATHETER POSITION:
Proximal abdominal aorta, abdominal aortic aneurysm endograft iliac limb
(left), celiac artery, superior mesenteric artery, inferior mesenteric
artery (via SMA/IMA collateral), abdominal aortic aneurysm sac via
transarterial mesenteric approach.
CONTRAST UTILIZED: Omnipaque.
TECHNIQUE: The right common femoral artery was interrogated with color Doppler
ultrasonography. The right common femoral artery demonstrates normal color
Doppler waveform analysis, and appears patent. Under ultrasound guidance,
after achieving local anesthesia with 1 percent lidocaine, right common
femoral artery was accessed in retrograde fashion. Over a guidewire a 6
French sheath was inserted. Over the guidewire, through the sheath a 5
French pigtail catheter was placed in the proximal abdominal aorta. AP
abdominal aortography was performed. Catheter was exchanged over a
guidewire for a 5 French Reuter catheter which is positioned in the left
iliac limb. Selective injection was performed. Catheter was repositioned
in the celiac artery. Injection performed. Catheter was repositioned in
the SMA, injection performed. Correlation is made with CTA from ****.
There is a prominent meandering SMA to IMA collateral with the IMA filling
the aneurysm sac. This is the suspected source is a type II endoleak.
Transarterial embolization attempt was elected. Patient received a total
of 2000 units of heparin during the course of the procedure.
Subsequently, a coaxial 3 French Renegade (150 cm) microcatheter was
advanced into the proximal superior mesenteric artery. Using a series of
0.018 inch and 0.014 inch guidewires, negotiation into the middle colic
artery supplying the meandering artery was unsuccessful. As such, a 4
French C2 glide catheter was positioned into the proximal SMA. Through
this a 3 French Direxion Renegade STC (150 cm) straight microcatheter was
inserted. Through this a 0.018 inch double-angled glide wire GT was placed
into the acutely-angled origin of the middle colic artery. Over this the
microcatheter was advanced into the proximal middle colic artery.
Superselective injection performed. Intra-arterial nitroglycerin was
utilized throughout this phase of the procedure. The meandering artery
has a long serpiginous course.
Subsequently, over the 0.018 inch double-angled and curved Glidewire, as
well as a 0.014 inch Fathom guidewire, the catheter was carefully advanced
through the left upper quadrant, into the origin of the IMA. Injection was
performed. The catheter was further advanced into the endosac. Injections
were performed into the endosac. With the catheter in this position, three
0.018 inch detachable interlock coils were deployed (one-2 mm x 4 cm, two-3
mm x 6 cm). The catheter was carefully retracted across the endo-channel
to the origin of the IMA. At this level, an additional 3 mm x 6 cm
interlock coil was deployed. Completion injection demonstrates complete
occlusion of the IMA at the level of its origin, preservation of the
superior rectal, sigmoid branches as well as left colic branch. The
catheter was removed. With removal, additional intra-arterial
nitroglycerin was administered. Via the 4 French C2 glide catheter
positioned in the proximal and middle colic artery, completion injection
performed demonstrates preservation of SMA, middle colic and IMA arterial
circulation to the gut. Catheter removed. Sheath removed. Groin closed
using StarClose without incident. Sterile dressing applied.
FINDINGS:
Patent AneuRx aortic endograft. No type I, type III, type IV endoleak.
Patent celiac artery. Patent SMA. There is an SMA to IMA meandering
artery that retrograde fills the endosac, constituting a type II IMA
endoleak. As described in detail above, the endosac channel, and IMA
origin were embolized using transarterial approach via the SMA-IMA
meandering artery.
COMPLICATIONS: None.
IMPRESSION:
ABDOMINAL AORTOGRAPHY, MESENTERIC ANGIOGRAPHY DEMONSTRATES PATENT ANEURX
ENDOGRAFT DEVICE. NO TYPE I, TYPE III, TYPE IV ENDOLEAK. THE PROXIMAL
STENT RING OF THE ANEURX DEVICE IS CAUDALLY DISPLACED WITH RESPECT TO THE
ORIGIN OF THE RENAL ARTERIES. IT IS UNCERTAIN AS TO WHETHER THIS REFLECTS
MIGRATION OR INITIAL PLACEMENT. INITIAL PLACEMENT IMAGES ARE NOT AVAILABLE
TO DETERMINE ACCORDINGLY.
TYPE II IMA ENDOLEAK AS DESCRIBED IN DETAIL ABOVE, TREATED WITH
TRANSCATHETER ARTERIAL EMBOLIZATION VIA SMA/IMA COLLATERAL.

Medical Billing and Coding | AAPC Forum