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* From Pulmonary Flight (Drs. Chaney and Olivier, and Mr. Jones) and Anesthesia Flight (Dr. Grathwohl), Wilford Hall Medical Center, Lackland AFB, TX.
Correspondence to: John C. Chaney, MD, 59 MDW/MCCP, Lackland AFB, TX 78236; e-mail: John.Chaney{at}lackland.af.mil
| Abstract |
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Design: Cross-sectional observational study.
Setting: Military-affiliated, tertiary care hospital.
Patients or participants: Current users of LTOT at our institution and patients with new oxygen prescriptions between June 2000 and May 2001.
Intervention: The OTC evaluation consisted of a focused medical interview and physical examination by a respiratory therapist. Demographic data, indications for supplemental oxygen, oxygen-related diagnoses, cardiopulmonary review of systems, pertinent physical examination findings, pulmonary function testing, and oximetry data were recorded. Patients prescribed oxygen during hospitalization were followed up for recertification within 90 days based on the recommendations of the Fifth Oxygen Consensus Conference. Also, patients with existing oxygen prescriptions and new oxygen prescriptions during the study period were evaluated in the OTC. Data are provided for the initial evaluation in this clinic.
Measurements and results: A total of 283 patients were evaluated in the OTC during the study period. Ninety-seven patients with a new oxygen prescription during hospitalization were evaluated, with a mean ± SE time from discharge to evaluation of 2.6 ± 0.4 months. At follow-up, 50.5% of these patients no longer met Medicare guidelines for LTOT. A significant change in oxygen prescription was required in 27.9% of these patients. A total of 95 outpatients with existing oxygen prescriptions were contacted for recertification in the OTC. Of these patients, 31.6% no longer met Medicare criteria for LTOT and 26% required a significant change to their oxygen prescription. Oxygen therapy was discontinued in 22% of the 91 patients who were referred from other outpatient clinics, and the oxygen prescription was changed in another 29.7%.
Conclusions: Results of this initial evaluation suggest that the institution of a respiratory therapist-managed OTC to manage home oxygen patients can significantly decrease inappropriate supplemental oxygen use, which can result in significant cost savings while providing improved health-care delivery. Further evaluation is necessary to identify the long-term benefits and cost savings in this population.
Key Words: COPD obstructive lung disease oxygen therapy reimbursement
| Introduction |
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| Materials and Methods |
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Exercise oximetry was performed on all patients who were physically capable. Patients were asked to walk at their own pace to cover as much distance as possible in 6 min (as measured by a pedometer). A portable pulse oximeter with printer (N-20 PA; Nellcor) was used to record SpO2 and heart rate at 30-s intervals via a reflectance oxygen transducer placed on the patients forehead (RS-10; Nellcor). The test was terminated if the patient experienced extreme dyspnea or fatigue to the extent that they could not continue, or if the patient experienced chest pain. Patients with significant oxyhemoglobin desaturations during the test were placed on supplemental oxygen or an increased flow of oxygen delivered via a nasal cannula. The respiratory therapist pulled a wheeled d-cylinder setup (cylinder plus regulator plus two-wheeled cart) and titrated oxygen flow to keep SpO2 > 90% during the test. After the test was completed, the patient was asked to quantitate his or her level of exertion to compare to the level that they exert themselves at home. This data were compiled and used to help determine supplemental oxygen need.
Arterial blood gas analysis was obtained when patients demonstrated borderline SpO2 (89 to 92%) on repeated measurements, or if the patient actively used tobacco. Patients who met Medicare guidelines for supplemental oxygen at rest were given prescriptions for oxygen to use continuously. Patients who had adequate oxygenation during rest but demonstrated a significant desaturation during exercise were given prescriptions for oxygen for use during exertion at a flow rate equal to the minimum flow required to keep SpO2 > 90% during exercise testing.
Overnight oximetry was performed based on the patients answers to the following screening factor for nocturnal desaturations and obstructive sleep apnea (OSA): excessive daytime sleepiness, nocturnal awakening/choking, witnessed apneas, or high score (> 9) on an Epworth sleepiness scale.9 A pulse oximeter capable of printing a sleep hypnogram (Biox 3740; Ohmeda; Madison, WI) was used. Patients with an oxygen requirement at rest continued their current oxygen flow rate during overnight oximetry. If a prolonged desaturation (averaging < 89% for at least 5 min) was observed, the patient was prescribed oxygen for use during sleep at a flow rate of 2 L/min. Patients were referred to the sleep disorders clinic if the history suggested significant OSA or the patient experienced nocturnal desaturations in a pattern suggestive of OSA.10 If overnight oximetry was not performed, the patient was prescribed oxygen during sleep at a flow rate equal to their requirement during exertion.
A pulmonary physician directly supervised the OTC respiratory therapist on a daily basis, and all prescriptions were reviewed and signed by a pulmonary physician. During the study period, patients who had been prescribed oxygen in the past and were receiving oxygen or who had oxygen equipment in their possession were required to come to the OTC to determine eligibility for recertification. As part of the standard evaluation in the OTC, patients were provided with education on safe home oxygen therapy. Appropriate follow-up was arranged at the time of the visit based on the recommendations of the Fifth Oxygen Consensus Conference.4 New referrals and patients discharged from the hospital with a new oxygen prescription were required to be evaluated in the OTC. Patients with conditions such as congestive heart failure or pneumonia where the oxygen requirement may not be stable were followed up within 1 month, and patients with chronic conditions such as COPD or interstitial lung disease were evaluated between 1 month and 3 months at the discretion of the pulmonary physician. Referrals to other clinics (ie, pulmonary medicine, cardiology, sleep disorders, cardiopulmonary rehabilitation, and smoking cessation) were made by the supervising pulmonary physician based on subjective and objective data obtained during the evaluation.
Data Analysis
Standardized clinical intake forms were developed to store key tracking variables. These data were collected and entered into a database created using Microsoft Access software (Microsoft; Seattle, WA) during the clinical evaluation. The database was programmed to generate all necessary forms for home oxygen therapy utilizing data entered during the visit. It also served as a tracking tool to prompt appropriately timed scheduling of follow-up appointments. Various end points were automatically calculated and updated in a real-time manner. These included the proportion of patients requiring a change in oxygen prescription, proportion of patients discontinued from oxygen therapy, average duration of oxygen therapy, and proportion of patients referred to other clinics.
| Results |
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Most of the new referrals were from either the internal medicine or pulmonary medicine clinics. Of these 91 patients, 27.0% had prescriptions for LTOT initiated as a result of this evaluation, 22.0% were discontinued from LTOT, 29.7% were continued on LTOT with changes to either the dose or delivery system, one patient died prior to the scheduled evaluation, and the prescriptions for 9.9% were continued without change (Fig 1 , bottom).
Table 2 lists patient characteristics sorted by action taken in the OTC. The values listed in Table 2 for exertional SpO2 may be falsely elevated because the respiratory technician often began oxygen titration immediately once the SpO2 dropped below 88% during ambulation rather than observing a true nadir. Also, the resting and exertional saturation values for new referrals who were begun on LTOT are higher than expected due to a high proportion of patients started on nocturnal oxygen therapy based on results of overnight oximetry (36%).
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| Discussion |
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The OTC provides a unique concept with multiple benefits. The clinic manages all patients placed on home oxygen to ensure the following: (1) appropriate up-to-date evaluation of oxygen needs, (2) identification of related medical conditions that may impact on oxygen need or delivery, (3) education on safe home oxygen therapy, (4) tailoring of the oxygen delivery system to the patient, and (5) appropriately timed follow-up and reevaluation. It improves communication and facilitates initial prescription and reevaluation, as well as serves as a centralized resource for patients, primary care providers, and vendors. By providing case management of patients and strictly adhering to Medicare guidelines for LTOT and the recommendations of the Fifth Oxygen Consensus Conference,4 a significant impact on oxygen expenditures and patient care was realized. More than one half of patients who were prescribed oxygen during hospitalization could have oxygen discontinued at the initial follow-up visit in the OTC. Not only does this translate into obvious cost savings, but it also directly relates to quality of life for patients by discontinuing an inconvenient and potentially hazardous treatment in those patients without continued need. Also, active case management allows tailoring of treatment to the clinical requirement, lifestyle, and home environment of those patients with a persistent home oxygen need.
ODonohue12 expressed concerns regarding the discontinuation of LTOT after 3 months of treatment in patients with previously established supplemental oxygen need who experience an improvement in PaO2 during oxygen therapy. This improvement may be related to the beneficial effects of oxygen therapy rather than a change in the patients clinical condition. This is a legitimate concern when such strict adherence to Medicare guidelines is enforced. Therefore, a case management approach to individualize the care of these patients is extremely important including regular follow-up in patients who are discontinued from LTOT. The rate of reinitiation of LTOT or long-term outcome in patients whose treatment has been discontinued is not known and is currently being explored by our group.
The institution of the OTC was an efficient utilization of resources that lead to significant cost savings. Typical LTOT costs per patient at our institution are approximately $3,855/yr (OxeNET; Lubbock, TX) for 2 L of continuous flow via an oxygen concentrator system. If one extrapolates the number of patients taken off oxygen during the first year of operation of the OTC (130 patients), the estimated cost savings in oxygen expenditures is > $500,000. This estimation assumes that the patients no longer meeting requirements for LTOT would not have had therapy discontinued by another provider, an assumption that is validated by the high percentage of patients who had established oxygen prescriptions that no longer met Medicare requirements or who had died (31.6% and 32.6%, respectively). In order to accurately analyze the cost benefit of establishing an OTC, one must also consider personnel cost, facility cost, and equipment cost. A typical respiratory therapist working in the United States earns a median base salary of $42,063.13 Required equipment includes a portable pulse oximeter, a sleep oximeter, a stationary and portable oxygen source, and oxygen tubing. Laboratory support for arterial blood gas analysis and CBC count determinations is also necessary.
The institution of a respiratory therapist-managed OTC to manage patients receiving home oxygen can result in a significant cost savings while providing improved health-care delivery by ensuring appropriately timed follow-up care, education on safe home oxygen therapy, and timely identification of related and potentially modifiable comorbid conditions such as tobacco abuse, deconditioning, or sleep-related breathing disorders. Further studies are needed to determine if the practice of discontinuing patients from LTOT after improvement in oxygenation occurs will have any detrimental effects on exercise capacity, quality of life, or mortality.14 Whether or not the use of an oxygen therapy clinic translates into significant alterations in emergency department treatments, hospital admissions, or long-term health-care expenditures is yet to be determined.
| Footnotes |
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The views expressed in this article are those of the authors and do not reflect the official policy of the Department of Defense or other Departments of the US Government.
Received for publication September 5, 2001. Accepted for publication June 4, 2002.
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