REVIEW REQUEST FOR
Autologous, Allogeneic, Xenographic, Synthetic and
Composite Products for Wound Healing and
Soft Tissue Grafting
Provider Data Collection Tool Based on Medical Policies 2.01.16; SURG.00011
Policy Last
05/19/2011
Review
Date:
12/7/2011;
Policy Effective Date: 01/01/2012; 01/19/2012
Provider Tool Effective Date: 03/06/2012
Individual’s Name:
Date of Birth:
Insurance Identification Number:
Individual’s Phone Number:
Ordering Provider Name & Specialty:
Provider ID Number:
Office Address:
Office Phone Number:
Office Fax Number:
Rendering Provider Name & Specialty:
Provider ID Number:
Office Address:
Office Phone Number:
Office Fax Number:
Facility Name:
Facility ID Number:
Facility Address:
Date/Date Range of Service:
Place of Service:
Service Requested (CPT if known):
Outpatient
Home
Inpatient
Other:
Diagnosis (ICD-9) if known):
Please check all that apply to the individual:
SYNTHETIC PRODUCTS
Becaplermin gel (Regranex®) for Neuropathic Diabetic Ulcers:
Request is for becaplermin gel (Regranex®) recombinant human platelet-derived growth factor for neuropathic diabetic
ulcers extending into subcutaneous tissue or beyond
There is adequate tissue oxygenation, as measured by a transcutaneous partial pressure of oxygen of 30 mm Hg or
greater on the foot dorsum or at the margin of the ulcer
The individual has a full-thickness ulcer (i.e., Stage III or IV), extending through dermis into subcutaneous tissues
There is documentation of participation in a wound management program, which includes sharp debridement,
pressure relief (i.e., non-weight-bearing), and infection control
Other: (please list)
Becaplermin gel (Regranex®) for Pressure Ulcers:
Request is for becaplermin gel (Regranex®) recombinant human platelet-derived growth factor for pressure ulcers
The individual has a full-thickness ulcer (i.e., Stage III or IV), extending through dermis into subcutaneous tissues
The ulcer is in an anatomic location that can be offloaded for the duration of treatment
Page 1 of 4
REVIEW REQUEST FOR
Autologous, Allogeneic, Xenographic, Synthetic and
Composite Products for Wound Healing and
Soft Tissue Grafting
Provider Data Collection Tool Based on Medical Policies 2.01.16; SURG.00011
Policy Last
05/19/2011
Review
Date:
12/7/2011;
Policy Effective Date: 01/01/2012; 01/19/2012
Provider Tool Effective Date: 03/06/2012
There is recent documentation that the serum albumin concentration is greater than 2.5 dL
There is recent documentation that the serum total lymphocyte count is greater than 1,000
There are recent documented normal values of vitamins A and C.
Other: (please list)
Becaplermin gel (Regranex®) for Other Uses:
Request is for becaplermin gel (Regranex®) recombinant human platelet-derived growth factor for the treatment of
ischemic ulcers
Request is for becaplermin gel (Regranex®) recombinant human platelet-derived growth factor for the treatment of
venous stasis ulcers
Request is for becaplermin gel (Regranex®) recombinant human platelet-derived growth factor for the treatment of
ulcers which do not extend through the dermis into the subcutaneous tissue
Other: (please list)
Other synthetic products:
Request is for antimicrobial silver wound dressings, (e.g., Acticoat, Actisorb ™ , and Silversorb® ) therapy and dressings
Request is for synthetic Silicone/Nylon Membrane wound dressing (e.g., Biobrane®)
Request is for synthetic fistula plugs (e.g. GORE BIO-A Fistula Plug)
Request is for a synthetic product or use not described in the synthetic product section: (please specify):
AUTOLOGOUS PRODUCTS
Request is for (check all that apply):
Blood derived wound products, (e.g., Autologel™ , SafeBlood™ , Vitagel® )
Platelet rich plasma (PRP) for the treatment of cutaneous wounds, soft tissue injuries (including epicondylitis and sinus
surgery), or bone injuries (including surgically created wounds and non-unions)
Request is for an autologous product or use not described in the autologous product section: (please specify)
ALLOGENEIC PRODUCTS (Alloderm®, Apligraf®, Dermagraft®, OrCel™, TransCyte™, Cymetra® , GraftJacket™, and
Neoform Dermis™)
Request is for Alloderm® for breast reconstruction surgery
Request is for Alloderm® for surgical repair of complex abdominal wall wounds (e.g., due to infection, fascial defect,
etc.)
Request is for Alloderm® for other use (please list):
Request is for Apligraf® in conjunction with standard therapeutic compression for the treatment of chronic, non-infected,
partial or full-thickness skin ulcers due to venous insufficiency of greater than one month duration and which have not
adequately responded following a one month period of conventional ulcer therapy (such as standard dressing changes,
and standard therapeutic compression)
Request is for Apligraf® in conjunction with standard diabetic foot ulcer care for the treatment of full-thickness
neuropathic diabetic foot ulcers of greater than three weeks duration which have not adequately responded following at
least a three week period of conventional ulcer therapy (such as surgical debridement, complete off-loading and standard
dressing changes) and which extend through the dermis but without tendon, muscle, joint capsule, or bone exposure
Request is for Apligraf® use on clinically infected wounds
Page 2 of 4
REVIEW REQUEST FOR
Autologous, Allogeneic, Xenographic, Synthetic and
Composite Products for Wound Healing and
Soft Tissue Grafting
Provider Data Collection Tool Based on Medical Policies 2.01.16; SURG.00011
Policy Last
05/19/2011
Review
Date:
12/7/2011;
Policy Effective Date: 01/01/2012; 01/19/2012
Provider Tool Effective Date: 03/06/2012
Request is for Apligraf® in individuals with known allergies to bovine collagen
Request is for Apligraf®in individuals with a known hypersensitivity to the components of the Apligraf® agarose
shipping medium
Request is for Apligraf® for other use (please list):
Request is for Dermagraft® for the treatment of full-thickness diabetic foot ulcers of greater than six weeks duration that
extend through the dermis, but without tendon, muscle, joint capsule, or bone exposure
Request is for Dermagraft® for wounds with dystrophic epidermolysis bullosa
Request is for Dermagraft® for infected ulcers and ulcers with sinus tracts
Request is for Dermagraft® for other use (please list):
Request is for OrCel™ for children with recessive dystrophic epidermolysis bullosa who are undergoing reconstructive
hand surgery
Request is for OrCel™ for other use (please list):
Request is for TransCyte™ as a temporary wound covering to treat second and third degree burns
Request is for TransCyte™ for other use (please list):
Request is for Cymetra®
Request is for GraftJacket™
Request is for Neoform Dermis™
Request is for C-QUR™ biosynthetic mesh
Request is for a use or product not specificed above (please list):
XENOGRAPHIC PRODUCTS
Request is for: Integra™ Bilayer Matrix Wound Dressing, in the post-excisional treatment of full- thickness or deep
partial-thickness burns when autografting is not feasible due to the individual's weakened physiological condition or a
lack of suitable healthy tissue
Request is one of the following xenographic products (please check appropriate product)
Avaulta Plus™
CellerateRX®
Collamend
CorMatrix®
CRXa™
Cuffpatch™
ENDURAgen™
E-Z Derm™
Integra™ Matrix Wound Dressing
Matristem®
Mediskin®
Menaflex™ Collagen Meniscus Implant
Oasis™
Page 3 of 4
REVIEW REQUEST FOR
Autologous, Allogeneic, Xenographic, Synthetic and
Composite Products for Wound Healing and
Soft Tissue Grafting
Provider Data Collection Tool Based on Medical Policies 2.01.16; SURG.00011
Policy Last
05/19/2011
Review
Date:
12/7/2011;
Policy Effective Date: 01/01/2012; 01/19/2012
Provider Tool Effective Date: 03/06/2012
OrthADAPT™
Pelvicol®
Pelvisoft®
Permacol™
PriMatrix
Strattice™
SurgiMend®
Surgisis® (including Surgisis AFP™ Anal Fistula Plug
TenoGlide™
Unite™
Veritas® Collagen Matrix
Request is for a xenographic product not listed above other (please list):
COMPOSITE AUTOLOGOUS / ALLOGENEIC / XENOGRAPHIC PRODUCTS
Request is for a product made from a combination of human autologous and xenographic cellular materials (e.g.
Epicel®)
Request is for a product made from a combination of human allogeneic and xenographic cellular materials
Other: (please list)
This request is being submitted:
Pre-Claim
Post– Claim. If checked, please attach the claim or indicate the claim number
I attest the information provided is true and accurate to the best of my knowledge. I understand that Anthem may perform a
routine audit and request the medical documentation to verify the accuracy of the information reported on this form.
_____________________________________________________________
Name and Title of Provider or Provider Representative Completing Form and Attestation (Please Print)*
Date
*The attestation fields must be completed by a provider or provider representative in order for the tool to be accepted
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