Oxygen is one of the countrys most billed and reimbursed items through the DME benefit of Medicare Part B, and even though the fee schedule for oxygen has been reduced by over 25% in recent years, it remains, in my opinion, an excellent source of revenue and profit.
The main reason oxygen is still a money maker is that, prior to the reimbursement cut, a good five-liter concentrator with a 5-year warranty cost around $1,100. Since the cut, that same concentrator now sells for $700 to $800 and still has an estimated useful life of at least 60 months. Medicares reimbursement averages $207 per patient per month. This amount times 60 months yields $12,420 with a cost of goods of $750. Granted, there are ancillary costs such as cannulas, tubing, humidifier bottles, and water traps, but overall the profit picture is favorable.
To develop or improve your current oxygen business, start by identifying what a Medicare oxygen patient looks like. To begin with, the patients physician must determine that the patient has a severe lung disease or hypoxia-related symptoms that will likely improve by the patients use of oxygen therapy. Second, the patients blood gas study must meet Medicares guidelines for oxygen coverage. Last, but not least, the physician must have tried or considered alternative treatment measures and deemed them clinically ineffective.
Not All Tests Are the Same
Key to the qualification of the patient is the blood gas study, and Medicare is therefore understandably concerned about who performs the study. According to its criteria, the study can be completed only by an entity qualified to bill Medicare for the test, such as a Part A provider, a laboratory, an Independent Diagnostic Testing Facility (IDTF), or a physician. This study must also be one that complies with Fiscal Intermediary or Local Carrier policy and is covered by Medicare Part A or Medicare Part B. A supplier is not qualified (per these requirements) and is therefore not allowed to supply test results for use on a Medicare Certificate of Medical Necessity (CMN). Suppliers also may not reimburse any provider of laboratory services for the performance of blood gas studies.
Now that we know who can, and who cannot, perform these tests, a provider must determine whether the patient will qualify for reimbursement under Medicare guidelines. The two acceptable tests, an oximetry or an arterial blood gas study (ABG), have a range of acceptable values that qualify the patient for Medicare coverage. Acceptable test results place the patient into one of two covered groups, Group I and Group II.
Group I
To be covered as a Group I patient, the Medicare beneficiarys laboratory test results must meet one of the following four criteria:
1. An ABG (aka arterial pulse oxygen or PO2) at or below 55 mg Hg or an arterial oxygen saturation (aka oxygen saturation or O2 sat) at or below 88% taken at rest, but not while asleep.
2. An ABG at or below 55 mg Hg or an arterial oxygen saturation at or below 88% for at least 5 minutes taken during sleep for patients with an arterial PO2 at or above 56 mm Hg or an arterial oxygen saturation at or above 89% while awake.
3. A decrease in arterial PO2 by more than 10 mm Hg or a decrease in arterial oxygen saturation of more than 5% for at least 5 minutes taken during sleep associated with symptoms or signs reasonable attributable to hypoxemia. (Note that the 5 minutes need not be continuous.)
4. An ABG at or below 55 mg Hg or an arterial oxygen saturation at or below 88% taken during exercise for patients with an arterial PO2 at or above 56 mm Hg or an arterial oxygen saturation at or above 89% at rest. In this case the oxygen is provided for during exercise if it is documented that the use of oxygen improves the hypoxemia associated with exercise when the patient was breathing room air.
Group II
To be covered as a Group II patient under Medicare, the patients laboratory test results must be derived under the same circumstances as a Group I patient and demonstrate an arterial PO2 of 56-59 mm Hg or an arterial blood gas saturation of 89%, and any of the following three symptoms:
1. Dependent edema suggesting congestive heart failure.
2. Pulmonary hypertension or cor pulmonale.
3. Erythrocythemia with a hematocrit greater than 56%.
Medicare does have a Group III for oxygen patients. These are patients with an arterial PO2 at or above 60 mm Hg or an arterial oxygen saturation at or above 90%. For these patients, Medicare concludes there is a rebuttable presumption of noncoverage.
Coverage Periods
Medicare CMN periods and patient retesting are directly related to these test results and must be completed and obtained on the following schedules:
Group I: The first (initial) CMN covers the shorter of 12 months or the physicians specified length of need. The laboratory results reported on the initial CMN must be the most recent obtained prior to the CMNs initial date and must be obtained within 30 days prior to that initial date.
The one exception to this rule is for patients coming off Medicare HMO coverage in which case the 30-day rule does not apply and the provider must obtain the patients most recent test results from when the patient was enrolled in the Medicare HMO. Recertifications for months 13 and beyond where the physician indicated 99 as the estimated length of need require only a recertification CMN. The original laboratory results on the initial CMN need only be transposed by the physician to the recertification CMN. If the physician indicated any length of need less than 99, the patient must be retested within 30 days of the recertification date.
Group II: The first (initial) CMN covers the shorter of 3 months or the physicians specified length of need. The laboratory results reported on the initial CMN must be the most recent obtained prior to the CMNs initial date and must be obtained within 30 days prior to that initial date. The same transition Medicare HMO rules apply. Recertifications for months 4 and beyond require the patient to be retested regardless of the physicians notation of estimated length of need.
As you can tell, furnishing oxygen is complex, and there is much more to know, including requirements for retesting and portable oxygen. But if I were to get back into the DME business and open a new DME company, oxygen would be at the top of my list of items to provide, despite the reimbursement cuts.
Bruce Brothis is president and CEO of Centralized Billing & Intake, a DME billing and consulting company located in Parker, Colo. A former DME company owner, Brothis has more than 24 years of industry experience. Contact him at (800) 396-9910 ext 13.
| Respiratory Insider Ralph Spang Products cannot be chosen based on price alone, says Ralph Spang, senior product manager of Medical Industries America, Adel, Iowa. Providers must consider effective disease management, especially when choosing a nebulizer, Spang says. Dealer/Provider spoke with Spang about his companys recent partnership with Aerogen to provide a micropump aerosol delivery device and how that product can improve patient outcome and supplier profitability. Why did Medical Industries decide to team up with Aerogen to market and distribute the Aeroneb Go nebulizer? Our mission has been to become the single leading provider of aerosol delivery devices both domestically and abroad. Aerogen was looking for a distributor and manufacturer that would use its OnQ aerosol generator technology to introduce the Aeroneb Go to the home care market. As we have an already established reputation as a premier provider of aerosol devices, Aerogen saw us an ideal partner. What is the main difference between a conventional nebulizer and an electronic micropump nebulizer? There is a significant difference between a traditional nebulizer and our micropump aerosol delivery device. Our unit uses an aperture plate with an oscillating washer that vibrates in excess of 100,000 times per second. This is not an ultrasonic device. The aperture is smaller than a dime with more than 1,000 uniform holes. The medication is gravity fed through these uniform holes, meaning that the medication has a consistent 2.4 micron particle size time after time. Being the only gravity-fed device in this market means the unit never reconstitutes the medication, treatment times are shorter (6 minutes for 3 mL), and residual amount of medication is less than .1 cc or 97% of the aerosol medication is available to the patient. We also have a unique 42-cc reservoir (spacer) built into the unit, providing the patient with readily available aerosol at the beginning of the inspiratory cycle. How can this product help dealers maximize profit? For dealers with an established medication program, our Aeroneb Go helps keep their patient base compliant and in most cases increases patient compliance. The goal is keeping patients healthier, which means a dealers physician base is happier, and positive feedback from the patient to the doctor leads to more referrals. Chronic obstructive pulmonary disease (COPD) patients will need medications for the rest of their lives as well as a myriad of other products dealers traditionally carry. Our Aeroneb Go is a device that can help move patients to the dealers, increase their medication business, increase their market share in a region, and increase their opportunity to both rent and sell more of their product line. |