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Evaluation of a "Fast Track" Respiratory Therapy Clinic for Patients With Suspected Severe Sleep-Disordered Breathing

Not Applicable
Conditions
Sleep Disordered Breathing
Interventions
Procedure: Fast Track
Registration Number
NCT02191085
Lead Sponsor
University of Calgary
Brief Summary

Access to medical care for patients with breathing disorders during sleep is a major problem for Canadians. Recently, there has been increasing interest in how health care providers who are not physicians can help to improve access to medical care for these patients, but it is unclear whether patients with severe sleep-disordered breathing who receive care from these non-physician providers have the same response to treatment as patients who receive care from physicians. Since these severe have a high risk of developing cardiac and respiratory complications and of being hospitalized, an initiative to improve access such as the use of non-physician providers could be of great benefit to individual patients and the health care system.

The objectives of this project are:

1. to determine whether patients with severe breathing disorders during sleep have the same response to treatment when cared for by non-physician health care providers (respiratory therapists) as they do when cared for by physicians;

2. to determine the effects of non-physician health care provider treatment to patient access;

3. to determine health care utilization and related costs associated with non-physician health care provider treatment.

Detailed Description

The difficulty in providing timely access to sleep specialists is widespread. These delays are particularly important for patients with severe SDB due to the increased risk of adverse clinical outcomes and potential associated healthcare costs. The lack of timely access has sparked an interest in the use of alternate care providers (ACPs) to manage patients with SDB. Our group and others have demonstrated that ACPs are an effective and efficient substitute for physicians for patients with uncomplicated SDB. However, the role of ACPs in the management of patients with severe SDB remains unclear.

Prompted by wait times that far exceed current Canadian guidelines, we have recently implemented an ACP-led "Fast Track" clinic for patients who are referred to the Foothills Medical Centre (FMC) Sleep Centre with suspected severe SDB. In this clinic, patients with suspected severe SDB are assessed by a sleep-trained registered respiratory therapist functioning as an ACP. Decisions regarding further sleep testing and treatment are made by the patient and ACP, under the guidance of a sleep physician. This model of care differs from a physician-led model that is used at the FMC Sleep Centre.

To evaluate this novel care delivery model, we have designed a randomized trial comparing outcomes for patients in the "Fast Track" clinic to those who undergo conventional, physician-led care. The specific goals of this study are:

1. to compare the clinical effectiveness of an ACP-led clinic for patients with suspected severe SDB to physician-led management;

2. to determine whether cycle times from referral to diagnosis and treatment for patients referred with suspected severe SDB can be reduced by an ACP-led clinic;

3. to determine the impact of an ACP-led clinic on the demand for sleep physicians, ACPs and diagnostic testing;

4. to compare the cost-effectiveness of these models of care using data on healthcare utilization, costs, and patient reported health-related quality of life (HRQOL).

Patients in the "Standard Management" arm will be assessed by a sleep respirologist and follow a management plan that is determined by the sleep physician and patient. This plan may involve polysomnography or the initiation of PAP therapy. If further testing is ordered, follow-up may occur with the physician or with an ACP, at the physician's discretion. For patients initiating PAP therapy, the decision to delegate follow-up to an ACP will be left up to the physician, as the intent of this study is to observe real-world practice and not to change the management of individual patients.

In the "Fast Track" arm, an ACP will perform the initial assessment and will determine the management plan with the patient. To ensure patient safety, the management plan will be discussed with a sleep respirologist, who will be designated as the patient's primary sleep physician. This sleep physician will be available at the FMC Sleep Centre during the "Fast Track" clinic to assist with the assessment of patients who appear unwell (e.g. severe hypoxemia, decompensated cardiorespiratory failure, etc.). As in the "Standard Management" arm, follow-up visits to review test results, discuss and initiate treatment, or to assess treatment response may occur with the ACP who performed the initial assessment or may be delegated to any other ACP.

As is usual procedure at the FMC Sleep Centre, ambulatory sleep test requisitions will be completed by ACPs or physicians, whereas all polysomnogram requisitions will be completed by the primary sleep physician to ensure adequate blinding of patient assignment. The research associate will ensure that all tests are interpreted in advance of clinic visits. Patients who are followed by ACPs in either arm can be referred to the primary sleep physician for assessment of non-respiratory sleep disorders, or for persistent symptoms such as daytime sleepiness.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
164
Inclusion Criteria
  • referred to the FMC Sleep Centre for assessment of SDB

  • meet one of the three criteria for suspected severe SDB:

    1. Respiratory disturbance index (RDI) >/= 30 events/hour on an ambulatory sleep test
    2. Mean nocturnal oxygen saturation </= 85% on an ambulatory sleep test
    3. Suspected hypoventilation, defined by an RDI >/= 15 events/hour on an ambulatory sleep test and partial pressure of carbon dioxide >/= 45 mmHg on arterial blood gas
    4. On supplemental oxygen therapy with high suspicion of SDB (as determined by physician review of referral)
Exclusion Criteria
  • Suspected concomitant sleep disorder other than SDB
  • A previous diagnosis of OSA treated with PAP or dental appliance
  • Primary health insurance provided by a province other than Alberta
  • Failure to provide consent to participate in the study
  • Under the age of 18

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Fast TrackFast TrackIn the "Fast Track" arm, an ACP will perform the initial assessment and will determine the management plan with the patient.
Primary Outcome Measures
NameTimeMethod
Adherence to positive airway pressure (PAP) therapy3 months after treatment initiation

Data includes number of days of PAP use and number of hours used per day.

Secondary Outcome Measures
NameTimeMethod
Change in daytime sleepiness1 year after treatment initiation

Epworth Sleepiness Scale

Health care utilization1 year after treatment initiation

Combination of physician visits, emergency department visits, hospitalizations

Incremental cost-effectiveness ratio1 year after treatment initiation

Comparing cost/QALY for intervention vs. control arm (QALY determined from Health Utilities Index

Time from date of referral to date of treatment initiationExpected within 1 year (unknown due to nature of outcome)

Comparing cycle times for intervention vs. control arm

Adherence to positive airway pressure (PAP) therapy1 year after treatment initiation

Data includes number of days of PAP use and number of hours used per day.

Change in disease specific health-related quality of life1 year after treatment initiation

Sleep Apnea Quality of Life Index

Patient experience1 year after treatment initiation

Visit-Specific Instrument (VSQ-9)

Number of sleep diagnostic tests and sleep ambulatory care visits1 year after treatment initiation

Will measure sleep physician and ACP visits as well as polysomnography and ambulatory testing

Change in severity of sleep-disordered breathing1 year after treatment initiation

Respiratory disturbance index from ambulatory testing

Change in general health-related quality of life1 year after treatment initiation

Health Utilities Index

Trial Locations

Locations (1)

Foothills Medical Centre Sleep Centre

🇨🇦

Calgary, Alberta, Canada

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