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January 1, 2026 By Rebecca Summers, OT, CLT-LANA, CSR

Lymphedema Maintenance (part 2 of 2)

Last month, we discussed phase I (decongestion therapy) in lymphedema treatment. This month, we’ll pick up with phase II & also discuss adjuncts. If you’ve got lymphedema & made a New Year’s resolution, this post may help.

Phase II: Lymphedema Maintenance

Assuming a patient is compliant with guidelines, they should progress to phase II fairly predictably (the maintenance phase). This begins immediately after phase I & involves being fit with a compression garment to maintain the volume loss & fibrosis reduction attained in phase I. Sometimes the garment doesn’t fit quite right in the first try. So, a revised garment must be ordered. In my experience, patients frequently try to short cut this phase, too, by:

  • wearing elastic garments (off the shelf, circular-knit garments) instead of resuming bandaging while waiting for the revised garment
  • wearing the garment to be returned (which is improperly fit)
  • not wearing a night garment or using an inappropriate night garment.

These decisions can cause refilling & regression.

As noted earlier, if a person begins phase I in stage II or III lymphedema, fibrosis is likely still going to be present to some extent at the end of treatment. But it should continue to gradually reduce in phase II with the appropriate compression & compliance.7

Phase II is generally “maintenance for life.”9 In my experience, when a person is compliant & sticks to the above protocol, phase II will maintain their lymphedema. And, lymphedema can continue to improve. However, people often, again, try shortcuts (i.e. no night garment, noncompliance with daily use of their daytime garment, etc.). On occasion, particularly if a person is in stage II or III lymphedema (or if they took shortcuts or have not been compliant), they may need to resume intensive phase I treatment in the future.

Phase II Adjuncts

There are several adjuncts to lymphedema maintenance. We just talked about one the past two blog posts. “Adjunct” means “supplement” or “auxiliary function,” not a standalone or essential role. In other words, these aren’t necessary components to maintenance. But some people may find some beneficial effects.

A chameleon appears to be one thing but is actually another. Like a chameleon, certain adjunct therapies may be seem to be a “cure” for lymphedema, but they may not be what they appear.

The following are examples of adjuncts for lymphedema.

  • Compression pumps10, 18
  • Medications: Flavonoids, benzopyrones11 & synbiotics18
  • Aquatics12, 18 – compression applied by water during exercise
  • Ultrasound13, 18 – uses sound waves to cause vibrations which may help with fibrosis but it can create friction & heat (which increases fluid creation).**
  • Hivamat13, 18 -uses an electrostatic field to create a deep, gentle oscillation in the tissue, which helps reduce fibrosis, inflammation & improve lymphatic flow
  • Rebounders16 – trampolines require you to use your muscles. As encouraged by any exercise, muscle contraction impacts lymphatic function by squeezing lymph vessels, which helps to propel lymph fluid through the body. While contraction increases interstitial fluid pressure and can compress vessels, the relaxation phase is crucial for allowing fluid to enter the lymphatics. Exercise causes an increase in blood flow (increasing fluid in the tissue spaces). Compression garments counteract this process by providing working pressure that promotes lymph fluid removal from the tissue space. So, it’s important to wear compression during any exercise to prevent refilling & to aid in the uptake of fluid in the lymphatic vessels.
  • Vibration14, 18 – stimulates the lymphatic system by causing rapid muscle contractions that help pump lymph fluid through the vessels. As with any exercise, it’s important to wear compression during use.
  • Diet17 – despite books & social media posts, there is no “lymphedema diet.” Nothing you eat is going to cure lymphedema. However, eating a poor diet & gaining weight can exacerbate lymphedema. Salt, sugar & alcohol consumption can negatively impact water retention & inflammation, thus exacerbating lymphedema.
  • Kinesio taping18 (elastic taping) may facilitate lymphatic drainage
  • Photobiomodulation (low-level laser)18 – red light therapy & near-infrared light can stimulate cellular function, reduce inflammation & enhance lymphangiogenesis & lymphatic motility
  • Extracorporeal shock wave therapy (ESWT)18 – a noninvasive treatment that uses acoustic shock waves to reduce fibrosis & enhance lymphangiogenesis (new lymphatic vessel growth).
  • Acupuncture and Moxibustion18** Acupuncture works by inserting fine needles into specific points on the body (up to two inches deep into skin) to stimulate biochemical reactions, while moxibustion uses heat from burning mugwort to warm acupuncture points.
  • Negative pressure (cupping)18** – creates suction, drawing the skin and tissue upward. This suction increases blood flow. It can also cause skin redness & discoloration that persists for some time after the procedure. According to Foldi, manual lymph drainage should be gentle & light in pressure (pressure sufficient to stretch the skin, not heavy enough to cause redness). This is because the lymph vessels are less than one millimeter in diameter on average with more superficial vessels being even smaller. (As a reference, 1 millimeter = 0.03937 inches.) If too much force is used in MLD (or otherwise), the delicate anchoring filaments can be injured or deeper lymphangions can go into spasm.”20 Note: MLD force and compression-garment pressure behave completely differently physiologically and mechanically, even though both affect lymph flow. MLD involves directional shear, not uniform compression. That’s why pressure must be extremely low. Compression garments apply broad, evenly distributed, static external pressure across the entire limb (not directional shear).

Personally, I would avoid the above adjuncts marked with an asterisks as they cause hyperemia (an increase in blood flow) which increases lymphatic load & could exacerbate lymphedema. The exception is activities in which you have or use compression (such as aquatics or exercise). In Foldi’s words, “[a]t a minimum, methods that result in hyperemia should be avoided wherever possible.19, 20

References
1 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 273. Germany: Urban and Fisher.
2 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 245, 322. Germany: Urban and Fisher.
3 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 246. Germany: Urban and Fisher.
4 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 272. Germany: Urban and Fisher.
5 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 281. Germany: Urban and Fisher.
6 Adjuncts – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 282. Germany: Urban and Fisher.
7 Fibrosis – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 273-274. Germany: Urban and Fisher.
8 Inpatient – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 273. Germany: Urban and Fisher.
9 For life – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 274. Germany: Urban and Fisher.
10 Pumps – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 283. Germany: Urban and Fisher.
11 Meds – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 283. Germany: Urban and Fisher.
12 Aquatics – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 559 Germany: Urban and Fisher.
13 Ultrasound & Hivamat – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 560. Germany: Urban and Fisher.
14 Vibration – Rauch F, Sievanen H, Boonen S, et al. Whole-body vibration and blood flow and muscle oxygenation: a meta-analysis. Clin Physiol Funct Imaging. 2015;35(2):97–104. (This meta-analysis shows that whole-body vibration (WBV) increases peripheral blood flow — a mechanism potentially relevant to lymphatic drainage.)// Casarotto RA, Tonezzer T, Munaretto Timm Baiocchi J, Harari D. Effects of the vibratory platform on the treatment of lymphedema post-breast cancer surgery: case studies. World Physiotherapy Congress Proceedings. 2022.
15 RLT – Carati CJ, Anderson SN, Gannon BJ, Piller NB. Treatment of postmastectomy lymphedema with low-level laser therapy: a double-blind, placebo-controlled trial. Cancer. 2003;98(6):1114–1122. // Ridner SH, Poage-Hooper E, Kanar C, Doersam JK, Bond SM, Dietrich MS. A pilot randomized trial evaluating low-level laser therapy as an alternative treatment to manual lymphatic drainage for breast cancer–related lymphedema. Oncol Nurs Forum. 2013;40(4):383–393. // Li K, Zhang Z, Liu NF, Feng SQ, Tong Y, Zhang JF, et al. Efficacy and safety of far infrared radiation in lymphedema treatment: clinical evaluation and laboratory analysis. Lasers Med Sci. 2017;32(3):485–494. // Ueno N, Fukuzawa H, Oshima T, et al. Far infrared radiation therapy for gynecological cancer–related lymphedema is an effective and oncologically safe treatment: a randomized-controlled trial. Lymphology. 2021;54(3):141–150.
16 Rebounders – https://www.thecancerspecialist.com/2019/08/01/the-benefits-of-rebounding-in-the-prevention-and-management-of-lymphedema/
17 Diet – Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 269, 305. Germany: Urban and Fisher.
18 https://lymphnet.org/page/position-papers (National Lymphedema Network Position Paper on maintenance)
19 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 559. Germany: Urban and Fisher.
20 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 526. Germany: Urban and Fisher.

Filed Under: Lymphedema Maintenance Tagged With: compression pumps for swelling, laser therapy for lymphedema, lymphedema adjuncts, lymphedema maintenance, lymphedema therapy, medications for lymphedema, modalities for lymphedema, phase II lymphedema maintenance, RLT for lymphedema

December 1, 2025 By Rebecca Summers, OT, CLT-LANA, CSR

Lymphedema Maintenance (part 1 of 2)

The past two months we reviewed compression pumps. Pumps can be an adjunct to therapy maintenance.6 But pump use shouldn’t be a standalone plan for lymphedema treatment or maintenance. What is the recommended maintenance program for lymphedema?

Phase I: Decongestive Lymphedema Treatment

First, a person should complete phase I (decongestion) which involves complete decongestive therapy (CDT). CDT is composed of:

  1. manual lymph drainage
  2. multi-layer short-stretch bandaging
  3. skin care
  4. decongestive exercise.

Duration

The duration of this phase depends on the severity of lymphedema. It also depends on the frequency of treatment (which should be daily & bandages should remain on until the next therapy session).4 And it depends on comorbidities (such as vein disease, heart failure, renal failure, etc.) being diagnosed & properly treated.5

If a person is in stage I lymphedema, CDT generally lasts about 2 weeks. If stage II lymphedema (depending on how advanced within stage II), CDT lasts approximately 4-6 weeks. If stage III lymphedema, CDT may last 6-8 weeks or more (& it’s recommended to be treated several times a day according to Foldi).1 Below is a reference for the stages.

If a person is in stage I lymphedema, CDT generally lasts about 2 weeks. If stage II lymphedema (depending on how advanced within stage II), CDT lasts approximately 4-6 weeks. If stage III lymphedema, CDT may last 6-8 weeks or more (& it’s recommended to be treated several times a day according to Foldi).1 Below is a reference for the stages.

Lymphedema Stages

  • Stage I (the reversible stage) – It’s caused by accumulation of interstitial (lymph) fluid.2 And it’s characterized by pitting edema & reduction in swelling with elevation. There isn’t usually pain in lymphedema,3 but there may be pain in this stage associated with early congestion.
  • Stage II (the spontaneously irreversible stage) – It’s caused by excess growth of connective (scar) tissue. It’s characterized by fibrosis & fat tissue growth. The swelling becomes more hard & doesn’t go down with elevation. There may be discoloration (brownish discoloration) to the involved tissue.
  • Stage III (elephantiasis) – It’s caused by the accumulation effect of stage II leading to extensive fibrosis & fat tissue growth. There are deep creases, fungal infections, recurrent cellulitis infections & some people may even become immobile.

In my experience, people get tired of bandaging after 2 weeks. They often seek shortcuts. For example:

– ending therapy before fibrosis is adequately reduced (note: some fibrosis will likely persist if a person initiates therapy during stages II or III of their lymphedema)7
– removing bandages before the next session
– using only (1) set of bandages, not washing bandages between sessions for better recoil & compression
– canceling a session here & there, missing consistent daily treatment.

These behaviors impact outcome. Of course, there can also be other “hiccups” during therapy. For example, a pressure wound develops & must be addressed, compression slips down between sessions or gets wet during toileting or bathing. These events are more likely when people aren’t treated as they are in Germany (i.e. inpatient hospitalization with focused, daily lymphedema therapy).8 Sometimes things just happen. But these events can prolong phase I & expectations should be clear in advance to avoid added disappointment.

Next month, we’ll pick up with phase II in part 2 of this blog on Lymphedema Maintenance. (References will be cited in that post.)

Filed Under: Lymphedema Maintenance Tagged With: CDT, complete decongestive therapy, lymphedema maintenance, lymphedema therapy, lymphedema treatment, phase I lymphedema care

November 1, 2025 By Rebecca Summers, OT, CLT-LANA, CSR

Compression Pumps (part 2)

Last month we noted there are several differences among pumps. And not all pumps are appropriate for all conditions. When it comes to lymphedema, the wrong pump has potential to do more harm than good. This month, we’re picking up with the types of compression pumps available.

Types of Compression Pumps (continued)

2. Non-Pneumatic Pumps – Non-pneumatic compression pumps use mechanical forces (rather than air) to apply compression. For example, Koya Medical (Dayspring device) uses shape-memory alloy springs that generate compression when activated by electrical current, causing the alloys to contract. This creates mechanical compression without air. These systems typically consist of a sleeve placed on a limb, and compression is delivered in a sequential or gradient pattern. Because they are lightweight, battery-powered, and allow mobility, users can often move or walk during treatment. (This is unique for lymphedema.) They are also generally quieter than pneumatic systems. (For those located in Dallas, Tx, Koya Medical relocated to the state in 2025.)

Common Uses:

  • Management of chronic lymphedema
  • Supporting lymphatic drainage in active patients
  • Enhancing treatment adherence through mobility

Examples of Devices:

  • Dayspring by Koya Medical

It’s important to note: Because they are lighter, less bulky and allow mobility, compliance may be improved. However, one downside from a therapist’s perspective is the sleeve doesn’t cover the hand (or the foot if on the leg). The concern is the potential to contribute to swelling in the hand and foot. Koya Medical believes that hand swelling is unlikely as they provide a mild compression glove and people are meant to be active, so a person is using their hand muscles to help reduce swelling. Another downside is the pump doesn’t first decongest the trunk as we do in manual lymph drainage lymphedema treatment. This is important in pure lymphedema as the swelling involves a quadrant of the trunk due to the drainage path of the lymph system. So, a patient may need to be taught how to first open the lymph drainage path and initiate drainage if using this pump, etc.1

Well Pump – Public Domain (Pixabay)

Are Pumps Necessary for Lymphedema?

Many people (especially pump manufacturers & distributors) won’t agree, but in my experience treating patients with lymphedema, pumps are generally not needed. In fact, Foldi’s Textbook of Lymphology doesn’t recommend them. However, compression pumps have advanced since their writing. The National Lymphedema Network (NLN) recognizes this, but the NLN still considers a pump to be an adjunct to therapy, not a standalone or a necessary component to treatment.1,2

I would agree & have a few reservations about pumps in general:

  1. Insurance may pay several thousand dollars for one (as much as $8,000 in some cases – or more) but patients grow tired of using them. Patient complaints include:
    • pump hoses are heavy & hard to put on or take off (elderly may not have the strength)
    • the daily pumping schedule recommended (sometimes twice a day) is too time-consuming
    • doesn’t always seem to help or the improvement doesn’t last without using compression garments
  2. Patients are frequently not informed about the contraindications or don’t know when they should stop using a pump
  3. Frequent pump use may worsen heart or kidney disease as it moves more fluid through the body & increases the load these organs must process. Too often, this isn’t well-monitored. At a minimum, people should monitor weight & blood pressure regularly in cases of “compensated” heart or kidney disease (as well as taking note of how they feel after pump use).

What are the best pumps for lymphedema?

Assuming you, your therapist & doctor have decided a pump would be beneficial for you, what are the best compression pumps for lymphedema? If dealing with pure lymphedema, first, ensure there is a trunk component like a vest or shorts. If there isn’t, ensure you’ve been taught how to decongest before pumping & how to clear after pumping. Second, ensure there are several chambers which pump proximally (at the root of the extremity) & works outward to decongest before pumping distal to proximal. For example, in right arm lymphedema due to breast cancer, be sure the pump begins pumping to decongest nearer the axilla & works outward toward your hand slowly, in segments, before pumping from the hand up to the axilla. Below are a list of potential manufacturers, but be sure the model chosen fits the recommendation: advanced, programmable, sequentially gradient compression (pneumatic or not). (Note this rules out most inexpensive, Amazon-purchased pumps.)

  1. Bio Compression Systems
  2. Lympha Press
  3. Airos Medical
  4. Tactile Medical
    Runner-up: Koya Medical

References
1 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 282. Germany: Urban and Fisher.
2 https://lymphnet.org/page/position-papers

Filed Under: Blog, Lymphedema Maintenance, Treatment Tagged With: arm pump, compression pump, intermittet pneumatic compression, leg pump, lymphedema pump, sequential pump

September 1, 2025 By Rebecca Summers, OT, CLT-LANA, CSR

Can You Cheat in Lymphedema? (part 2)

We’re continuing a patient story from last month. (Click here for part 1)

The patient we’ve been following received a daytime CCL 2 sleeve & glove (she also wanted to try a gauntlet). She also received her CCL 1 sleeve & glove which she wanted to try for night use (instead of the recommended protocol of bandaging or a foam sleeve).

What Happened?

Five weeks after getting her daytime sleeve/glove, she had issues with finger swelling & arm refilling. She wasn’t resting well at night either. She stopped using the CCL 1 garment & used the same CCL 2 sleeve at night. When she returned to see me, she seemed angry (with me) for her outcome. When there’s a deviation from the protocol, the outcome will be affected.

I noted the likelihood of using a CCL 2 daytime sleeve/glove at night, especially when sleeping with elbow bent, as contributing to her forearm swelling & worsening fibrosis. While resuming bandaging was the best idea, she was adamant she wasn’t going to do that again. I said the next best option would be to get a nighttime foam sleeve. It should help reduce the forearm fibrosis which would help reduce the swelling. She agreed.

(collaboration with a local garment rep on best night garment in this case)

Intervention

This patient chose to continue wearing her daytime CCL 2 sleeve/glove (23-32 mmHg) before being fit for the night garment. (She hadn’t been re-reduced with bandaging.) That meant, the nighttime garment would likely be bigger than it should be. The fitter tried to compensate for this by decreasing the circumferences. (I had the manufacturer’s local rep do the fitting.)

Outcome

It took several weeks for the nighttime garment to arrive. The patient continued wearing the CCL 2 sleeve & glove during this time. (She did come in for bandaging one session prior to the arrival of the night garment.) The night garment was a little short & a little big, but the patient agreed to try it at night. After a few nights, she felt she was doing well & seeing progress.

(photo sent by pt after removing the night garment in the morning; she had worn it several nights)

When she returned to see me, she was happy with her status. Because the night sleeve wasn’t quite as long as it could have been (or the patient hadn’t been able to keep it up near the shoulder because it was a too large around the upper arm), there was some refilling around the shoulder. But her other numbers were improved as her fibrosis softened with the chipped foam sleeve.

(final visit after wearing night foam sleeve: volume 26.3 cm)

Can You Cheat the System?

Short answer: No. The protocol for lymphedema treatment exists to maximize the best outcome by softening fibrosis & decongesting tissue. Once this process is complete, a patient is ready for their maintenance day & night garment fitting. They should remain bandaged until both garments are in place.

This patient’s course was prolonged & a bumpy ride to get to her conclusion. But in the end, she was happy with her status. That’s what matters most. Sometimes a patient’s goals aren’t solely to maximize reduction. Convenience or interference with daily routines may trump the “ideal outcome.” It’s important to ask a patient what their goal is & to monitor this goal during the course of therapy as it may change.

Filed Under: Blog, Breast Cancer, Lymphedema Maintenance, Treatment Tagged With: arm lymphedema, breast cancer, lymphedema therapy

August 1, 2025 By Rebecca Summers, OT, CLT-LANA, CSR

Can You Cheat in Lymphedema? (part 1)

Many people are tempted to shortcut the therapy process in lymphedema. Instead of bandaging, they only want manual lymph drainage (MLD). Or instead of MLD, they only want to bandage. Or they may stop treatment early (or skip therapy & go right to a compression garment). Is it possible to “cheat” in therapy? Yes, it is. But just like shortcutting or changing a recipe, the outcome will be affected.

Protocol

The recommended protocol for lymphedema treatment (according to Foldi) is to bandage daily during the decongestion phase.1 Once volume plateaus & a patient is not expected to make further progress, they are fit with a custom, flat-knit, daytime sleeve/glove & they are to bandage at night for the maintenance phase.2 (Or, alternatively, a special nighttime garment like a foam sleeve might be used.)

A patient with left arm lymphedema due to breast cancer was tiring of bandaging & driving to appointments after ~10 sessions of daily treatment. Her arm fibrosis hadn’t maximized in reduction nor had the swelling, but she had made decent progress.

(evaluation – visit 1: total left arm volume 27.9 cm)

(after 10 sessions: total left arm volume 26.9 cm)

She wanted to proceed with getting fit for her custom, flat-knit sleeve & glove in a class 2 (23-32 mmHg). She would continue working on her arm fibrosis herself. In addition, she didn’t want to bandage at night (or get an alternative night garment like a foam sleeve which looked hot & bulky). She wanted to try using a daytime sleeve and glove at night in less compression instead – a class 1 (18-21 mmHg). I wasn’t wholly supportive of this idea, but I agreed to try it.

Waiting for the custom sleeve & glove

Custom garments can take 2-3 weeks to receive. During the waiting period, a person should remain bandaged. However, therapy sessions can usually reduce in frequency. In this case, the pt remained bandaged 3x/week until the daytime garments arrived.

What was the outcome? Find out next month.

References
1 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 272. Germany: Urban and Fisher.
2 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 273, 574-581. Germany: Urban and Fisher.

Filed Under: Blog, Lymphedema Maintenance, Treatment Tagged With: arm lymphedema, breast cancer, lymphedema treatment

June 17, 2024 By Rebecca Summers, OT, CLT-LANA, CSR

Billing for Compression (part 3)

We’ve been talking about how a therapist can bill for compression in light of the passage of the Lymphedema Treatment Act. Last month, we noted there were (3) models. The third model involved:

  • a therapist billing Medicare for compression as a supplier & for service as a provider for their own patients, and
  • the same therapist also billing for compression for people who are not their patients.

This gets tricky because the model gives rise to unique ownership concerns related to Medicare & Medicaid payments. (Government complicates things.) These concerns revolve around federal statutes & criminal liability. That’s the focus of this month’s blog.

Disclaimer: Information is not guaranteed to be comprehensive or accurate. Consult a healthcare law attorney for guidance.

Model 3

You would think billing for other people’s patients could be done in your therapy business. But that’s not the case – unless the individual is your patient. And would another therapist want to refer their patients to you – a competitor? Of course, there are several people seeking compression that aren’t wanting treatment. They just need someone who can bill insurance. But does billing for a supply item constitute someone becoming a patient?  Besides that, the 42 CFR has special considerations for therapists billing for compression for their own patients that doesn’t apply to therapists billing for individuals who are not their patients. (See April’s blog update.) A seemingly easy solution is to have a second business.

If you have a second business for DME, why not simplify things? Keep your therapy services in the therapy business & the DME in a DME business. You could have both businesses in the same location & save on costs (like rent). Additional benefits could include having a different taxonomy code (for potential better reimbursement rates), less confusion among insurance payors, & legal protection from financial losses.  You could refer your therapy patients to the DME business. Right? Wrong. (Why not? Well, government complicates things.)

Medicare Supplier Standards2

Anyone who plans to bill federal healthcare programs for DME must be mindful of the 42 CFR Supplier Standards. One of those standards states a supplier is prohibited from sharing a practice location with another Medicare provider or supplier. But there are a few exceptions. Two of these include:

  • a therapist (i.e. provider) who is billing DME for their own patients only
  • a DME supplier can be co-located with & owned by a Medicare provider (e.g. therapist), but the businesses must operate separately (separate phone lines, separate computers, separate staff, etc.). You must also meet the definition of a Medicare provider.7,8

It would seem you actually could separate the therapy business & refer your patients to your DME company. But that’s not the case. (Did I mention government complicates things?)

The Anti-Kickback Statute

The Anti-Kickback Statute is one of the fraud & abuse laws mentioned last month. It was an amendment added to the Social Security Act & first passed by Congress in 1972 as an effort to prevent fraud & abuse of federal healthcare programs (i.e. Medicare & Medicaid).6 It can be found in Title 42 of the U.S. code which covers public health & welfare. (These laws are broken down into titles, chapters, subchapters, parts & sections.)3,4 Specifically, Section 1320a-7b talks about the Anti-Kickback Statute. This amendment prevents giving or receiving anything of value (e.g. money, free rent or other perks) for generating healthcare business paid for by federal programs.

In other words, if you had two businesses that billed Medicare or Medicaid, & you wanted to refer patients from one to the other, you can’t. (Unless, of course, you don’t mind jail time & hefty monetary penalties. Most therapists try to avoid these.) There are a few “safe harbor” exclusions that will allow such business transactions.5 But all elements of a safe harbor must be met. (And these have pros & cons.)

Two notes: First, this only applies to providers/suppliers billing federal healthcare programs (clarification is needed as to whether the non-direct plans like the exchange programs provided by commercial plans are included in this). Second, you can still have a therapy business providing therapy services & DME to your own patients. You can also have a separate DME business for other people’s patients in addition. But these must operate entirely separately & cannot refer business between them if you bill federal healthcare programs unless you fall within one of the safe harbor exclusions. You would also be wise to consider other mitigating factors to prevent implication of Anti-Kickback Statute violation.

There’s one more question that comes to mind regarding billing. What if a Medicare patient wants to pay cash for an item? We’ll look at that next month.

References
1 https://oig.hhs.gov/compliance/physician-education/fraud-abuse-laws/
2 (supplier standards) https://www.ecfr.gov/current/title-42/chapter-IV/subchapter-B/part-424/subpart-D/section-424.57
3 https://www.govinfo.gov/app/details/USCODE-2010-title42/USCODE-2010-title42-chap7-subchapXI-partA-sec1320a-7b
4 https://uscode.house.gov/
5 (safe harbors) https://www.ecfr.gov/current/title-42/chapter-V/subchapter-B/part-1001/subpart-C/section-1001.952
6 https://www.whistleblowerllc.com/anti-kickback-statute/#:~:text=Congress%20first%20enacted%20the%20AKS,physicians%20corrupt%20medical%20decision%2Dmaking.
7 (clinic definition) https://www.govinfo.gov/content/pkg/USCODE-2011-title42/html/USCODE-2011-title42-chap7-subchapXVIII-partE-sec1395x.htm, https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/downloads/R5BP.pdf & https://www.ssa.gov/OP_Home/ssact/title18/1861.htm
8 (OTPP definition) https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/downloads/R5BP.pdf

Attribution
Photo by Olia Danilevich Pexels

Filed Under: Blog, Lymphedema Maintenance, Treatment Tagged With: compression, hose, lymphedema compression, lymphedema garment, lymphedema treatment, lymphedema treatment act, sleeve

March 1, 2024 By Rebecca Summers, OT, CLT-LANA, CSR

Compression Garments & Insurance (part 5/5)

Because of the Lymphedema Treatment Act, Medicare will now cover lymphedema compression, supplies & aids with the appropriate diagnosis code & medical necessity. What items are covered & how do you get them?

Diagnosis Codes

A diagnosis code must be written on a physician order. Appropriate diagnosis codes1 to qualify for the new lymphedema benefit category are

  • I89.0 Lymphedema, not elsewhere classified
  • I97.2 Post-mastectomy lymphedema
  • I97.89 Other postprocedural complications & disorders of the circulatory system, not elsewhere classified
  • Q82.0 Hereditary lymphedema

Medical Necessity

A patient must have a medical necessity for the ordered item(s). Medical necessity is proven by physician order & supportive documentation. A physician order can be signed by a “treating practitioner,” meaning, a medical doctor, doctor of osteopathy, podiatrist, physician’s assistant (PA), nurse practitioner (NP), or clinical nurse specialist (CNS).2,3 The following must be on the “standard written order.”2

  • The name of the treating practitioner, their NPI (national provider identifier), their signature & the date
    • stamps can’t be used; signatures & dates can be electronic or handwritten1,4
  • The beneficiary’s name (the patient’s name) & Medicare number
  • Description of the item(s) (such as the HCPCS code1)
    • options or features constituting an upgrade above the basic item must be listed separately on the order (such as upgrading from an off-the-shelf hose to a custom hose or adding a lining, zipper or pocket to a custom garment, etc.)
    • supplies must be listed separately on the order (such as a donning frame, donning gloves, etc.)
  • The quantity to be dispensed.

Supportive documentation (if requested) would include medical or therapy notes. (Note: Some DME requires a face-to-face encounter with the treating practitioner within 6 months of an order.5 Lymphedema items are not currently on that list.)

Compression Supplies Covered

Phase 1 of lymphedema treatment (the reduction or decongestion phase) requires decongestion supplies. This typically includes a cotton liner, a padding layer & several short-stretch bandages. At times, a Velcro reduction garment or wound kit might be used instead.

For coverage, supportive documentation must include justification for the quantity & frequency of these items. In my experience, two sets of supplies are needed (one to use & one to wash). Each set can be laundered & reused each session. (Avoid bleach, fabric softener, Woolite, dryer use or placing items in the sun as these things can damage the elastic fibers.)

When it comes to billing, a supplier will need to line-item each compression bandaging supply, accessory, wrap or garment that doesn’t have a unique HCPCS code with one of the following best-matched HCPCS codes:

  • A6549 – Gradient compression garment, not otherwise specified
  • A6584 – Gradient compression wrap with adjustable straps, not otherwise specified
  • A6593 – Accessory for gradient compression garment or wrap with adjustable straps, not otherwise specified
  • A6609 – Gradient compression bandaging supply, not otherwise specified.

The supplier will also need to add:1

  • a description of the item (including the inch, foot or yard for supplies)
  • manufacturer name
  • product name & number
  • supplier price list
  • HCPCS of a related item.

Billing modifiers are needed as well (right, left, replacement – if an item is lost, stolen or damaged, etc.).

All therapists & patients should be good stewards & conservative in their utilization of this benefit. Abuse & waste will cause problems down the road (be it increased government debt, higher taxes or another outcome).

Compression Garments Covered

Phase 2 of lymphedema treatment is the maintenance phase. This is when compression garments are needed to maintain the volume loss attained in Phase 1. Medicare covers these garments which may include:

  • off-the-shelf or custom (for all body parts) (typically flat-knit, circular-knit or Velcro)
  • day &/or night garments (typically Velcro or foam garments).

Medicare allows for:

  • (3) daytime garments every 6 months
  • (2) nighttime garments every 24 months

    (Note: There are two situations in which additional compression may be covered. The first is if an item is lost, stolen or damaged. The second is if there is a change in the patient’s status or condition. Either situation will require a new order & the replacement clock will start over.1)

Garment Aids Covered

Many patients are not aware there are several donning & doffing aids available to help get compression on or to remove it. There are donning frames, slippery material, gloves & other tools your therapist may know about. Justification for the quantity of supplies & the frequency of dispensing must be supported by documentation.

YouTube
Check out the Lymphedema Savvy YouTube channel for an upcoming treatment vlog. Information about the Lymphedema Treatment Act & billing will be included in a future video.

*****UPDATE 07/22/24*****

The following educational handouts were provided by the Lymphedema Treatment Act:

Patients
Providers
Suppliers

*****UPDATE 02/19/25*****

The current list of HCPCS lymphedema compression billing codes can be found here. The US Medical Compression Alliance has noted Medicare approval of additional codes here (effective April 1, 2025). They are specifically listed in Medicare’s Final Rule here. Medicare Learning Network (MLN Matters publication) provides billing tips here.

References
1 (coverage) https://www.cgsmedicare.com/jc/pubs/news/2023/12/cope147943.html
2 (orders) https://www.cms.gov/medicare-coverage-database/view/article.aspx?articleid=55426
3 (physician) https://www.ssa.gov/OP_Home/ssact/title18/1861.htm
4 (signatures) https://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/downloads/pim83c03.pdf
5 (face to face) https://www.cms.gov/data-research/monitoring-programs/medicare-fee-service-compliance-programs/medical-review-and-education/dmepos-order-requirements or https://www.federalregister.gov/documents/2023/01/17/2023-00718/medicare-program-updates-to-face-to-face-encounter-and-written-order-prior-to-delivery-list#:~:text=For%20items%20on%20the%20F2F,of%20the%20written%20order%2Fprescription.

Filed Under: Lymphedema Maintenance Tagged With: hose, lymphedema garment, lymphedema garments, lymphedema treatment, lymphedema treatment act

February 1, 2024 By Rebecca Summers, OT, CLT-LANA, CSR

Compression Garments & Insurance (part 4)

Requirements for Medicare Coverage of Lymphedema Compression, Supplies & Accessories

The last post on the Lymphedema Treatment Act (LTA) passage was in December. (The LTA passed December, 2022, & became effective Jan 1, 2024, providing coverage to Medicare beneficiaries for lymphedema compression garments, supplies & accessories.) Since my last post on the topic, I’ve had questions about what’s needed for Medicare coverage. The following are required:

  • DMEPOS Enrolled Supplier – a supplier can be a DME supplier or a medical professional providing items to their own patients after enrolling with Medicare to do so. (To learn about becoming a supplier or how a medical professional can become a supplier for their own patients, click here.)

    Note: A therapist cannot be a provider & a DME supplier in the same space unless solely providing these items to their own patients. They must still become an enrolled supplier & meet certain requirements to bill for items provided to their own patients. (Such therapists cannot bill items for people who are not their own patients. They can fit patients, however. See below.) (CFR, Title 42)

    Note: A trained, experienced fitter is recommended to measure lymphedema compression (particularly custom) & to recommend appropriate accessories. If measurements have been obtained from a therapist who is not enrolled as a DMEPOS supplier, a 3rd party supplier can be used for ordering & billing Medicare. However, payment for the fitting itself is included in the garment payment amount. So, therapists fitting patients & submitting an order to a 3rd party must get payment for their service from that supplier (if payment is desired). Fitting Medicare patients is not a separate, billable service under this law.
  • Script – there are specific items that must be on the physician’s order (i.e. script).2

    Note: A physician, nurse practitioner, or clinical nurse specialist is considered a “treating practitioner.”

    Note: A supplier must have additional information such as supportive documentation. They will likely ask for medical records (such as progress notes, therapist notes, etc.) verifying medical necessity.

    Items Needed on Order:
    – Beneficiary’s name or Medicare beneficiary identifier (i.e. Medicare number)
    – Order date
    – A lymphedema diagnosis (acceptable ICD-10 diagnosis codes include: I89.0, Q82.0, I97.2, I97.89)
    – Item description (the HCPCS billing code). For a list of lymphedema compression HCPCS codes, click here.
    – Quantity of item to be dispensed (i.e. how many are being ordered)
    – Treating practitioner’s name or NPI
    – Treating practitioner’s signature (no signature stamp is allowed)

Next month, we’ll review what Medicare covers, the frequency & allowable amounts.

************UPDATE 02/19/24**********

The Lymphedema Treatment Act recently published an article summarizing the above. Here’s that pdf.

Coverage-for-Lymphedema-Compression-Supplies-copyDownload

References
1 https://med.noridianmedicare.com/web/jddme/dmepos/lymphedema-compression-treatment
2 https://www.cms.gov/medicare-coverage-database/view/article.aspx?articleid=55426
3 https://www.cgsmedicare.com/jc/pubs/news/2023/12/cope147943.html
4 https://lymphedematreatmentact.org/final-coverage-rules/

Filed Under: Blog, Lymphedema Maintenance Tagged With: lymphedema compression, lymphedema garment, lymphedema garments, lymphedema treatment act, medicare payment for lymphedema supplies

November 1, 2023 By Rebecca Summers, OT, CLT-LANA, CSR

Compression Garments & Insurance (part 2)

As you know from last month’s blog, the Lymphedema Treatment Act (LTA) was passed in December of 2022. Most of 2023 has been spent with Heather Ferguson & others communicating with legislators & Medicare on what should be included in the bill coverage.

Flat-knit hose & a toe cap

Bill Coverage

On page 45 of the “Medicare and You 2024” handbook,1 it states if you have a diagnosis of lymphedema, Medicare will cover your medically gradient compression garments (with a physician’s prescription) at 80%. Coverage is for standard, off-the-shelf garments or custom-fitted garments. You’ll pay your 20% (unless you have a supplemental plan). Your part B deductible applies.

The proposed final rule is a more specific.2 It states medically gradient compression garments (readymade or custom, Velcro or other) will be covered as well as bandaging supplies. Anyone providing these items must be enrolled with Medicare as a DME supplier & meet supplier standard requirements.

Where You Can Find a Supplier Who Can Bill For Compression Garments

You can use Medicare’s online search tool3 to search for a supplier capable of billing for the items. One concern I have is whether these will be competent fitters (vs standard DME suppliers whose knowledge is typically limited to basic sleeves & hose). Lymphedema Therapy Source plans to use a second business to bill for lymphedema supplies & compression (including pneumatic compression pumps). This will include a lengthy process of becoming an enrolled DMEPOS supplier, becoming accredited, meeting all DME supplier and quality standards, obtaining a surety bond & submitting claims to the appropriate Medicare contractor for DME. (No small task!)

circular-knit hose

Billing Codes4 (see updates at the end of page)

While therapy services are billed using CPT codes, products (or DME supplies) are billed with HCPCS Level II codes. Below is a list of expected codes & descriptions for lymphedema compression items covered by Medicare as a result of the Lymphedema Treatment Act.

HCPCS Codes for Compression Treatment Items:
Compression Hose
A6530 Gradient compression stocking, below knee, 18-30 mmHg each
A6531 Gradient compression stocking, below knee, 30-40 mmHg, each*
A6532 Gradient compression stocking, below knee, 40-50 mmHg, each*
A6533 Gradient compression stocking, thigh length, 18-30 mmHg, each
A6534 Gradient compression stocking, thigh length, 30-40 mmHg, each
A6535 Gradient compression stocking, thigh length, 40-50 mmHg, each
A6536 Gradient compression stocking, full length/chap style, 18-30 mmHg, each
A6537 Gradient compression stocking, full length/chap style, 30-40 mmHg, each
A6538 Gradient compression stocking, full length/chap style, 40-50 mmHg, each
A6539 Gradient compression stocking, waist length, 18-30 mmHg, each
A6540 Gradient compression stocking, waist length, 30-40 mmHg, each
A6541 Gradient compression stocking, waist length, 40-50 mmHg, each

Velcro (or other)
A6545 Gradient compression wrap, non-elastic, below knee, 30-50 mmHg, each*
A6549 Gradient compression stocking/sleeve, not otherwise specified

Compression Sleeves & Gloves
S8420 Gradient pressure aid (sleeve and glove combination), custom made
S8421 Gradient pressure aid (sleeve and glove combination), readymade
S8422 Gradient pressure aid (sleeve), custom made, medium -weight
S8423 Gradient pressure aid (sleeve), custom made, heavy -weight
S8424 Gradient pressure aid (sleeve), readymade
S8425 Gradient pressure aid (glove), custom made, medium -weight
S8426 Gradient pressure aid (glove), custom made, heavy -weight
S8427 Gradient pressure aid (glove), readymade
S8428 Gradient pressure aid (gauntlet), readymade

Other (including treatment supplies)
S8429 Gradient pressure exterior wrap
S8430 Padding for compression bandage, roll
S8431 Compression bandage, roll

There may be changes to some of these codes. For those with an asterisks (*), new HCPCS codes may be assigned when these items are used as surgical dressings (such as in the case of an open venous stasis ulcer).

Velcro leg & foot compression

***UPDATE 11/30/23***

Beginning in 2024, there will be 81 HCPSC codes specifically for lymphedema compression supplies (most will be new).

Where You Can Find More Information

Visit the Lymphedema Treatment Act for more information & an up-to-date status on the bill & its coverage: https://lymphedematreatmentact.org/faqs/.

A special thank-you to Heather Ferguson & her team for their ongoing fight to get the LTA passed.

***UPDATE 01/05/24***

Lymphedema HCPCS billing codes have been published & are listed here. A person must have one of the following diagnosis codes:

  • I89.0 (lymphedema, not elsehwere classified)
  • I97.2 (postmastectomy lymphedema)
  • I97.89 (Other postprocedural complications and disorders of the circulatory system, not elsewhere classified)
  • Q82.0 (hereditary/primary lymphedema)

References
1 https://www.medicare.gov/publications/10050-Medicare-and-You.pdf
2 https://lymphedematreatmentact.org/wp-content/uploads/2023/07/LTA-Section-Home-Health-Rule.pdf
3 https://www.medicare.gov/medical-equipment-suppliers/
4 LTA Home Health Rule, p. 13

Filed Under: Blog, Lymphedema Maintenance Tagged With: compression, gloves, gradient compression, hose, lymphedema garment, lymphedema hose, medically gradient, surgical dressing

October 1, 2023 By Rebecca Summers, OT, CLT-LANA, CSR

Compression Garments & Insurance Coverage

Even though the legislation was submitted over 10 years ago to government delegates, the Lymphedema Treatment Act is still not widely recognized by most people who have lymphedema. Yet passage of the bill (which was accomplished Dec. 23, 2022) is so important to lymphedema care. It will become effective Jan. 1, 2024. Why is it important to lymphedema?

Lymphedema Care

Lymphedema treatment has two phases. Phase I is decongestion. This is the therapy phase when CDT is administered. (CDT is complete decongestive therapy & involves manual lymph drainage, bandaging, skin care & exercise.) Once maximum reduction is attained in therapy, the next step is fitting with a compression garment (usually for day & night). This is a part of Phase II (the maintenance phase).

Maintenance Phase

Compression garments are mandatory for lymphedema maintenance. Without them, swelling will promptly recur, & the reduction obtained during therapy will be lost. There are a few different types of compression.

  • Flat-knit (usually custom-made, but readymade is available) – daytime garment
  • Circular-knit (usually readymade, but custom is available) – daytime
  • Velcro (commonly used in wound care or as a night option) – day or night
  • Foam sleeves (nighttime use) – night
    (Note: Self-bandaging at night is the textbook recommendation for lymphedema maintenance.)

Recommended Compression

While circular-knit & Velcro can be used in some edema-related cases (such as venous edema) or combination edema-lymphedema cases (such as phlebolymphedema), the recommended compression for lymphedema is custom, flat-knit. One reason is the fact the many lymphedematous extremities don’t fit into the readymade dimensions. Another reason is the way flat-knit garments are made. While other garments provide compression, flat-knit provides the best containment. Flat-knit also aids in softening hardened, fibrotic tissue caused by lympedema. Finally, flat-knit is a thicker fabric less prone to bunching & causing pain in joints (such as ankles & behind knees).

Cost & Insurance

The downside to compression is cost. Compression should be replaced every 6 months (to a year) because it loses its effectiveness as fibers wear out.1 Many insurance carriers follow Medicare’s guidelines, & until 2024, Medicare won’t cover the cost of lymphedema compression. Here’s where you come in! (For more on cost, see the below video clip.)

Lymphedema Treatment Act (LTA)

The Lymphedema Treatment Act was passed in December of 2022. But the legislation details are still being worked out. Heather Ferguson is the founder of this legislation. She sends out a newsletter with updates. And she needs your help. Please read the below letter, & contact your insurance company. Heather makes it easy for you by providing templates & links.

LETTER: https://ltstherapy.com/wp-content/uploads/2023/09/LTA-1.pdf
Action Item #1: click here
Action Item #2: click here

References
1 Foldi, M, Foldi, E. (2006). Foldi’s Textbook of Lymphology (2nd ed.), p. 595. Germany: Urban and Fisher. Foldi, M., & Foldi, E. (2012). Foldi’s Textbook of Lymphology (3rd ed.). Urban and Fisher.

Filed Under: Blog, Lymphedema Maintenance Tagged With: compression gloves, garment, hose, lymphedema garment, sleeves

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