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Clinical Trials/NCT03499470
NCT03499470
Unknown
Not Applicable

The Effectiveness of Structured Discharge and Follow-up Protocol on Readmission Rate in COPD Patients Receiving LTOT and NIV: A Multicenter Randomized Trial

Dokuz Eylul University10 sites in 1 country160 target enrollmentNovember 7, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD Exacerbation
Sponsor
Dokuz Eylul University
Enrollment
160
Locations
10
Primary Endpoint
Readmission rate
Last Updated
6 years ago

Overview

Brief Summary

Readmission to hospital is one of the most important problems in chronic obstructive pulmonary disease (COPD) patients who developed chronic respiratory failure. Patients receiving long-term oxygen therapy (LTOT) and noninvasive ventilation (NIV) constitute the most vulnerable group because of the need for comprehensive care. However, because of lack of health care support systems in Turkey, many advanced COPD patients are hospitalized due to preventable problems such as insufficient knowledge about the therapies, nonadherence to therapy and technical issues related to LTOT/NIV equipment. The aim of this multicenter randomized trial is to find out whether a structured discharge and follow-up protocol reduce the rate of unplanned, COPD-related hospital readmissions over 90 days in patients receiving LTOT or NIV.

Detailed Description

The study is planned with Turkish Thoracic Society and Global Alliance Against Respiratory Disease-Turkey partnership and being carried out 10 centers throughout Turkey. COPD patients who are prescribed long-term oxygen therapy for hypoxemic respiratory failure and/or noninvasive ventilation for hypercapnic respiratory failure will be included in the study and will be randomized to either intervention or control arm. The intervention mainly consists of not only education about the disease and medications but also the education of the equipment and how to use it to have the best benefit. Control arm patients will receive usual care, which consists of basic education of the patient about the therapies. The primary outcome of the study is readmission in 90 days.

Registry
clinicaltrials.gov
Start Date
November 7, 2016
End Date
August 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Begum Ergan

Instructor

Dokuz Eylul University

Eligibility Criteria

Inclusion Criteria

  • COPD patients who developed chronic respiratory failure and are eligible for long-term oxygen therapy (LTOT) or noninvasive ventilation (NIV) according to Turkish National Social Security regulations
  • Definitions:
  • COPD: The diagnosis of COPD is made according to GOLD criteria Chronic respiratory failure: PaO2\>60mmHg at room air and/or PaCO2\> 45
  • Eligibility for LTOT:
  • PaO2 ≤ 55 mmHg or SaO2 ≤ 88% under room air
  • PaO2 value of 55-59 mmHg or SaO2 ≤ 89% and cor pulmonale with hematocrit \>55 or p pulmonale in ECG or congestive heart failure.
  • Eligibility for NIV:
  • PaCO2≥55 mmHg or
  • PaCO2 50 to 54 mmHg and nocturnal desaturation ≤ %88 for 5 minutes under 2lt/min nasal O2 therapy
  • PaCO2 50 to 54 mmHg and \>2 exacerbations within the last year

Exclusion Criteria

  • Patients receiving LTOT or NIV for a different cause
  • Patients who do not give consent
  • Patients who are unable to be followed up regularly due to reasons such as living far from study center, lack of family support, unwillingness or inability to contact regularly.

Outcomes

Primary Outcomes

Readmission rate

Time Frame: 90days

The rate of unplanned, COPD-related hospital readmissions over 90 days after discharge

Secondary Outcomes

  • Rate of hospitalization(90 days)
  • Long term survival(One year)
  • Rate of exacerbation(90 days)
  • Compliance to treatment(90 days)
  • Time to first exacerbation(90 days)

Study Sites (10)

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