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Effective Date: 12/08/2010 |
Title: Platelet Rich Plasma
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Revision Date: 03/01/2017
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Document: BI288:00
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CPT Code(s): P9020, 0232T
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Public Statement
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Effective Date:
a)
This policy
will apply to all services performed on or after the above revision date which
will become the new effective date.
b)
For all
services referred to in this policy that were performed before the revision
date, contact customer service for the rules that would apply.
1)
Platelet
rich plasma injections are not covered.
2)
Platelet
rich plasma is injected into areas around damaged tendons with the intent of
stimulating healing.
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Medical Statement
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Blood products including platelet rich plasma used in the treatment of joints
and tendinopathies’, or for any other reason, are considered
experimental/investigational and are not covered.
Codes
Used In This BI:
P9020 - Platelet rich plasma unit
0232T -
Injection platelet plasma
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Background
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The
available evidence regarding the effectiveness of autologous blood injection for
the treatment of tendinopathies’ is largely based on non-randomized studies.
Randomized studies have not consistently supported effectiveness. Furthermore,
available guidelines from the American College of Occupational and Environmental
Medicine, National Institute for Health and Clinical Excellence (NICE), and Work
Loss Data Institute do not support the use of autologous blood injection for
tendinopathies’.
The
American College of Occupational and Environmental Medicine (2007) did not
recommend autologous blood injection for managing patients with elbow
disorders. The NICE`s guideline on autologous blood injection for tendinopathy
(2009) states that current evidence on the safety and effectiveness of
autologous blood injection for tendinopathy is inadequate in quantity and
quality. In addition, the NICE Committee notes that some of the published
studies involved the use of dry needling prior to the injection of autologous blood,
but it was not possible to differentiate between effects of these two components
of the procedure. The Committee also states that future research should be in
the context of randomized controlled studies that define chronicity of
tendinopathy and describe any previous or adjunctive therapies (e.g.,
physiotherapy and dry needling) as well as the tendons treated. These
studies should address the role of ultrasound guidance and include functional
and quality of life outcomes with a minimum follow-up of 1 year. It is also
interesting to note that the Work Loss Data Institute`s guideline on the
management of acute and chronic shoulder disorders (2007) did not mention the
use of autologous blood injection as a means of therapy.
Besides autologous blood injection, other blood product injection therapies for
the treatment of patients with tendinopathies’ include platelet-rich plasma
(PRP) and bone marrow plasma.
PRP for Elbow Injuries:
In a pilot study, Mishra and Pavelko (2006) reported their findings on the
treatment of chronic elbow tendinosis with PRP. A total of 140 patients were
evaluated in this study. Subjects were initially given a standardized physical
therapy protocol and various non-operative treatments. Twenty of these patients
had significant persistent pain (mean of 82 of 100; range of 60 to 100 of 100 on
VAS) for a mean of 15 months despite these interventions. All patients were
considering surgery. This cohort of patients was then given either a single
percutaneous injection of PRP (n = 15) or bupivacaine (n = 5). Eight weeks
after the treatment, the PRP-injected patients noted a 60 % improvement in their
VAS versus 16 % improvement in bupivacaine-treated patients (p = 0.001). Three
of 5 of the control subjects (bupivacaine-treated) withdrew or sought other
treatments after the 8-week period, preventing further direct analysis. Thus,
only PRP-treated patients were available for continued evaluation. At 6 months,
PRP-treated subjects noted an 81 % improvement in their VAS (p = 0.0001). At
final follow-up (mean of 25.6 months; range of 12 to 38 months), the PRP-treated
patients reported a 93 % reduction in pain compared with before the treatment (p
< 0.0001). The authors concluded that treatment of patients with chronic elbow
tendinosis with PRP reduced pain significantly. Moreover, they stated that
further evaluation of this novel treatment is warranted. Controlled studies by
Creaney (2011) and Thanasas (2011) failed to show significant benefit of PRP
injections compared to autologous blood injections. A single RCT by Peerbooms
(2010) did show improvement in the Disabilities of the Arm, Shoulder, and Hand
score compared to corticosteroid injection. Studies comparing PRP to sham
treatment have not been reported.
PRP for ACL Injuries:
Randomized controlled trials have provided mixed results for the use of PRP in
ACL injuries. Cervellin (2012) reported that PRP improved knee function, but
not pain, at one year. Vogrin (2010) found that at 3 and 6 months after
treatment with PRP during ACL surgery patients had statistically significant
improvements in knee stability, but other outcome measures were not reported.
De Almeida (2012) reported improvement in patellar tendon gap area and pain
score in patients who had PRP added to the patellar tendon harvest site in
patients having ACL surgery; there were no significant improvements in
functional outcomes or strength testing. Orrego (2008) reported acceleration in
ACL graft maturation but no improvements in functional outcomes. Rupreht (2012)
reported improvement in MRI indicators of healing at 1 and 2.5, but not at 6
months; no functional outcomes were reported. Nin (2009) found that PRP
treatment as an adjunct to ACL surgery was not associated with any significant
improvements in pain or knee function. Figueroa (2010) and Silva and Sampaio
(2009) did not find any statistically significant benefits for PRP injection
during ACL surgery, based on MRI and histologic exams. Thus, there is minimal
evidence for benefits.
PRP for Rotator Cuff Injuries:
Controlled studies by Rodeo (2012) and Castricini (2011) did not show any
significant benefit to use of platelet-rich fibrin matrix during arthroscopic
rotator cuff tendon repair. In contract, Gumina (2012) reported better tendon
repair integrity after 13 months of follow-up. Randelli (2011) reported that
autologous PRP lowered pain scores up to 30 days after surgery and improved
clinical ratings scale scores at 3 months, but not thereafter. Rha (2012)
reported that two injections of PRP in patients with tendinosis or partial tears
of the rotator cuff significantly improved Shoulder Pain and Disability Index
scores at 6 weeks, 3 months, and 6 months compared to dry needling.
PRP for Achilles Tendon Injuries:
Two controlled trials failed to demonstrate improved outcome with use of PRP in
patients with Achilles tendinopathy or tendon rupture.
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Reference
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Suresh SP, Ali KE, Jones H, Connell DA.
Medial epicondylitis: Is ultrasound guided autologous blood injection an
effective treatment? Br J Sports Med. 2006; 40(11):935-939; discussion 939.
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Connell DA, Ali KE, Ahmad M, et al.
Ultrasound-guided autologous blood injection for tennis elbow. Skeletal
Radiol. 2006; 35(6):371-377.
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Mishra A, Pavelko T. Treatment of chronic
elbow tendinosis with buffered platelet-rich plasma. Am J Sports Med. 2006;
34(11):1774-1778.
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James SL, Ali K, Pocock C, Robertson C, et
al. Ultrasound guided dry needling and autologous blood injection for
patellar tendinosis. Br J Sports Med. 2007; 41(8):518-521; discussion 522.
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American College of Occupational and
Environmental Medicine (ACOEM). Elbow disorders. Elk Grove Village, IL:
American College of Occupational and Environmental Medicine (ACOEM); 2007.
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Work Loss Data Institute. Shoulder (acute &
chronic). Corpus Christi, TX: Work Loss Data Institute; July 5, 2007.
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Moon YL, Jo SH, Song CH, et al. Autologous
bone marrow plasma injection after arthroscopic debridement for elbow
tendinosis. Ann Acad Med Singapore. 2008; 37(7):559-563.
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National Institute for Health and Clinical
Excellence (NICE). Autologous blood injection for tendinopathy.
Interventional Procedure Guidance 279. London, UK: NICE; January 2009.
Available at:
http://www.nice.org.uk/nicemedia/pdf/IPG279Guidance.PDF
. Accessed November 8, 2010.
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Rompe JD, Furia JP, Maffulli N. Mid-portion
Achilles tendinopathy -- current options for treatment. Disabil Rehabil.
2008; 30(20-22):1666-1676.
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Rabago D, Best TM, Zgierska A, et al. A
systematic review of four injection therapies for lateral epicondylitis:
Prolotherapy, polidocanol, whole blood and platelet rich plasma. Br J Sports
Med. 2009 Jan 21. [Epub ahead of print].
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Hayes Medical Technology Assessment.
Platelet-Rich Plasma for Ligament and Tendon Injuries. Published Dec 24,
2012.
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Castricini R, et al. Platelet-rich plasma
augmentation for arthroscopic rotator cuff repair: a randomized controlled
trial. Am J Sports Med 2011; 39(2):258-265.
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Cervellin M, et al. Autologous platelet-rich
plasma gel to reduce donor-site morbidity after patellar tendon graft
harvesting for anterior cruciate ligament reconstruction: a randomized,
controlled clinical study. Knee Surg Sports Traumatol Arthrosc.
2012;20(1):114-120
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Creaney L, et al. Growth factor-based
therapies provide additional benefit beyond physical therapy in resistant
elbow tendinopathy: a prospective, dingle-blind, randomized trial of
autologous blood injections versus platelet-rich plasma injections. Br J
Sports Med 2011;45(12):966-971
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De Almeida AM, et al. Patellar tendon
healing with platelet-rich plasma: a prospective randomized controlled
trial. Am J Sports Med 2012;40(6): 1623-1629
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Peerbooms JC, et al. Positive effect of an
autologous platelet concentrate in lateral epicondylitis in a double-blind
randomized controlled trial: platelet-rich plasma versus corticosteroid
injection with a 1-year follow-up. Am J Sports Med 2010;38(2):255-262
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Thanasas C, et al. Platelet-rich plasma
versus authologous whole blood for the treatment of chronic lateral elbow
epicondylitis: a randomized controlled clinical trial. Am J Sports Med
2011;39(10):2130-2134
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Vogrin M, et al. The effect of
platelet-derived growth factors on knee stability after anterior cruciate
ligament reconstruction: a prospective randomized clinical study. Wein
Klin Wochenschr 2010; 122(Suppl 2):91-95
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Orrego M, et al. Effects of platelet
concentrate and a bone plug on the healing of hamstring tendons in a bone
tunnel. Arthroscopy 2008;24(12):1373-1380
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Nin JR, et al. Has platelet-rich plasma any
role in anterior cruciate ligament allograft healing? Arthroscopy
2009;25(11):1206-1213
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Figueroa D, et al. Magnetic resonance
imaging evaluation of the integration and maturation of
semitendinosus-gracilis graft in anterior cruciate ligament reconstruction
using autologous platelet concentrate. Arthroscopy 2010; 26(10):1318-1325.
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Silva A, Sampaio R. Anatomic ACL
reconstruction: does the platelet-rich plasma accelerate tendon healing?
Knee Surg Sports Traumatol Arthrosc 2009; 17(6):676-682.
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Rodeo SA, et al. The effect of platelet-rich
fibrin matrix on rotator cuff tendon healing: a prospective, randomized
clinical study. Am J Sports Med 2012;40(6):1234-1241
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Randelli P, et al. Platelet rich plasma in
arthroscopic rotator cuff repair: a prospective RCT study, 2-year follow-up.
J Shoulder Elbow Surg 2011;20(4):518-528
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Browning SR, Weiser AM, et. al.
Platelet-Rich Plasma Increases Matrix Metalloproteinases in Cultures of
Human Synovial Fibroblasts. J Bone Joint Surg Am, 2012 Dec 05; 94(23): e172.
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Cavallo C, Filardo G, et. al.
Comparison of Platelet-Rich Plasma Formulations for Cartilage Healing. J
Bone Joint Surg Am 2014 Mar 05; 96(5) 423-429.
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Feller J. Platelet-Rich Plasma
Injections Were Not Better Than Hyaluronic Acid Injections for Knee Joint
Degeneration. J Bone Joint Surg Am 2016 Feb 17; 98(4): 315.
Addendum:
1.
Effective
03/01/2017:
Updated
references.
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Application to Products
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This policy applies to all health plans administered by QualChoice, both those insured by QualChoice and those that are self-funded by the sponsoring employer, unless there is indication in this policy otherwise or a stated exclusion in your medical plan booklet. Consult the individual plan sponsor Summary Plan Description (SPD) for self-insured plans or the specific Evidence of Coverage (EOC) for those plans insured by QualChoice. In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC, the SPD or EOC, as applicable, will prevail. State and federal mandates will be followed as they apply.
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Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed.
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