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Mechanical Ventilation Discontinuation Practices (IOS)

2021년 3월 30일 업데이트: Unity Health Toronto

Practice Pattern Variation in Discontinuing Mechanical Ventilation in Critically Ill Adults: An International Prospective Observational Study

Background: The requirement for ventilator support is a defining feature of critical illness. Weaning is the process during which the work of breathing is transferred from the ventilator back to the patient. Approximately 40% of the total time spent on ventilators is dedicated to weaning. The extent of practice variation in how this complex and expensive technology is discontinued from critically ill patients is unknown. Meanwhile, practice variation has been shown to adversely impact upon patient safety and clinical outcomes.

Purpose: To characterize practice pattern variation in weaning and the consequences of weaning variation by implementing an international, prospective observational study in Canada, the United States, the United Kingdom, Europe, India and Australia/New Zealand.

Primary Objectives: To describe

  1. weaning practice variation among regions in 5 domains (the use of daily screening, preferred methods of support used before initial discontinuation attempts, use of written protocols, preferred methods of evaluating spontaneous breathing, and sedation and mobilization practices).
  2. the assocation between selected discontinuation strategies and important clinical outcomes (length of stay, mortality, duration of ventilation).

Methods: The investigators propose to conduct a large scale, observational study involving critically ill adults requiring ventilator support for at least 24 hours to evaluate practices in discontinuing ventilators in 150 centres. The investigators will classify each new admission over the observation period according to the initial strategy that precipitated or facilitated ventilator discontinuation.

Relevance: This novel study will build collaborations with critical care investigators from around the world and industry

연구 개요

상세 설명

Background: The requirement for mechanical ventilation is a defining feature of critical illness. Weaning is the process during which the work of breathing is transferred from the ventilator back to the patient. Approximately 40% of the total time spent on mechanical ventilation is dedicated to weaning. The extent and predictors of practice variation in how this complicated and expensive technology is discontinued from critically ill patients remains unknown. Meanwhile, practice pattern variability has been shown to adversely impact upon patient safety and important clinical outcomes.

Primary Objectives:

  1. To describe weaning practice variation with regard to the (i) use of daily screening, (ii) preferred methods of support used before initial discontinuation attempts, (iii) use of written weaning and spontaneous breathing trial (SBT) protocols, (iv) preferred methods used to conduct SBTs and (v) sedation and mobilization practices among geographic regions.
  2. To describe the association between variation in weaning practices (direct extubation, tracheostomy, SBT conduct) and important clinical outcomes.

    Secondary Objectives:

  3. To identify baseline and time-dependent factors associated with use of selected strategies.
  4. Among critically ill adults who undergo an initial SBT, the investigators will: a) investigate associations between SBT outcome (success/failure) and clinical outcomes, b) explore differences between critically ill patients who undergo an SBT early versus later in their intensive care unit (ICU) stay, and c) investigate the impact of different SBT techniques and humidification strategies on outcomes.
  5. To identify important predictors (patient, clinician, SBT, institutional and regional) of SBT outcome.

Study Design and Population: The investigators propose to conduct an international prospective observational study of mechanical ventilation discontinuation practices in 150 ICUs involving all newly admitted critically ill adults requiring invasive ventilation for at least 24 hours.

Study Centres: Interested centres have been identified through completion of an information card enclosed in a previously administered International Weaning Survey. The investigators will use a multimodal approach to identify participating centers in each of the 6 geographic regions (Canada, the United States, the United Kingdom, Europe, India and Australia/New Zealand).

Study Outcomes: The investigators will classify each new admission over the study week according to the initial strategy that precipitated or facilitated mechanical ventilation discontinuation into one of five categories: direct extubation, tracheostomy, SBT success, SBT failure or death. The investigator will describe the association between the use of alternative discontinuation strategies and important clinical outcomes (e.g., mortality, ICU and hospital stay, ICU readmission and reintubation rates).

Relevance: Through collaborations with industry partners and international colleagues we will implement this large scale observational study to quantify the existence and extent of practice variation in weaning. Information obtained from this study will inform the design of future studies aimed at reducing weaning practice variation and improving outcomes in critically ill patients receiving invasive mechanical ventilation

연구 유형

관찰

등록 (실제)

1868

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Massachusetts
      • Boston, Massachusetts, 미국, 02111
        • Tufts Medical Center
    • Michigan
      • Ann Arbor, Michigan, 미국, 48109
        • University of Michigan Health System
    • Ontario
      • Hamilton, Ontario, 캐나다
        • St. Joseph's Hospital
      • Hamilton, Ontario, 캐나다, L8L2X2
        • Hamilton Health Sciences Hamilton General Hospital
      • Hamilton, Ontario, 캐나다
        • Juravinski Hospital Cancer Centre
      • London, Ontario, 캐나다, N6A 5A5
        • London Health Sciences Centre - University Hospital Campus
      • Ottawa, Ontario, 캐나다
        • Ottawa Civic Hospital
      • Ottawa, Ontario, 캐나다
        • Ottawa General Hospital
      • Toronto, Ontario, 캐나다, M5B 1W8
        • St. Michael's Hospital
      • Toronto, Ontario, 캐나다
        • Mount Sinai Hospital
    • Quebec
      • Montréal, Quebec, 캐나다, H2X 3J4
        • Hôpital Saint-Luc
      • Sherbrooke, Quebec, 캐나다
        • Université de Sherbrooke
      • Sherbrooke, Quebec, 캐나다
        • Universite Hopitalier de Sherbrooke
      • Trois-Rivières, Quebec, 캐나다, G9A5C5
        • Ciusss McQ

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

16년 이상 (어린이, 성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

비확률 샘플

연구 인구

We propose to conduct an International, Prospective Observational Study of Mechanical Ventilation Discontinuation Practices among critically ill adults who receive invasive mechanical ventilation for at least 24 (i.e., > or equal to 24) hours in approximately 150 international ICUs

설명

Inclusion Criteria:

  • All newly admitted critically ill adults after study initiation at participating ICUs.
  • Requiring invasive mechanical ventilation for at least 24 (i.e. > or equal to 24) hours

Exclusion Criteria:

  • Transferred to a participating ICU without a clear time of intubation
  • Tracheotomy/tracheostomy present at the time of ICU admission
  • Already on ventilator settings compatible with a SBT [e.g., T-piece or Continuous Positive Airway Pressure < or =5 cm H2O (water) or Pressure Support < or = 8 cm H2O (with or without PEEP) or Automatic Tube Compensation (ATC) or equivalent] at the time of ICU admission
  • Patient residing in ICU for > or = 24 hours at the time of the study activation (i.e., not a new admission from the time of study activation).
  • Patient readmitted to this ICU during the study period (i.e., would constitute a second inclusion) unless they were ineligible during their first admission
  • Patients participating in studies (e.g., randomized controlled trials) with explicit weaning protocols incorporated into the study design

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
INITIAL SBT
Patients who underwent an Spontaneous Breathing Trial prior to extubation. This cohort will be further subdivided into initial patients who initially pass an SBT successes and those who initially fail an SBT.
DIRECT EXTUBATION
Patients that were directly extubated without conduct of a prior SBT or tracheostomy
DIRECT TRACHEOSTOMY
Patients who underwent a direct tracheostomy without conduct of a prior SBT or extubation
No attempt at mechanical ventilation discontinuation
Patients who died without conduct of a prior SBT, extubation or tracheostomy

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Practice variation among geographic regions in the use of daily screening to identify candidates to undergo an SBT
기간: Through study completion (approximately 4 years)
Use of once daily screening in clinical practice
Through study completion (approximately 4 years)
Practice variation among geographic regions in the preferred methods of ventilator support used before initial discontinuation attempts
기간: Through study completion (approximately 4 years)
Differences in ventilator modes (Pressure Support, Assist Control, other) prior to discontinuation attempts
Through study completion (approximately 4 years)
Practice variation among geographic regions in the use of written weaning and SBT protocols
기간: Through study completion (approximately 4 years)
Use of written protocols to liberate patients from ventilators
Through study completion (approximately 4 years)
Practice variation among geographic regions in the methods used to conduct SBTs (and humidify oxygen)
기간: Through study completion (approximately 4 years)
Use of different techniques to conduct SBTs (Pressure Support, T-piece, etc.)
Through study completion (approximately 4 years)
Practice variation among geographic regions in the sedation and mobilization practices during weaning
기간: Through study completion (approximately 4 years)
Use of different levels of sedation (Sedation Agitation Scale) and levels of mobilization (active, passive, none)
Through study completion (approximately 4 years)
Association between variation in the weaning practices and total duration of ventilation.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and the total duration of ventilation.
Through study completion (approximately 4 years)
Association between variation in the weaning practices and ICU mortality
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and ICU mortality.
Through study completion (approximately 4 years)
Association between variation in the weaning practices and hospital mortality.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and hospital mortality.
Through study completion (approximately 4 years)
Association between variation in the weaning practices and the proportion of patients off the ventilator at day 28.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and the proportion of patients off the ventilator at day 28.
Through study completion (approximately 4 years)
Association between variation in the weaning practices and the proportion of patients out of the ICU at day 28.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and the proportion of patients out of the ICU at day 28.
Through study completion (approximately 4 years)
Association between variation in the weaning practices and ICU LOS.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and ICU LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Association between variation in the weaning practices and hospital LOS.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and hospital LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Association between variation in the weaning practices and ICU readmission.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and ICU readmission (during the current hospitalization).
Through study completion (approximately 4 years)
Association between variation in the weaning practices and reintubation.
기간: Through study completion (approximately 4 years)
We will describe the association between variation in the weaning practices and reintubation (or repeat ventilation following disconnection in tracheostomized patients) within 48 hours of extubation.
Through study completion (approximately 4 years)

2차 결과 측정

결과 측정
측정값 설명
기간
Identify baseline characteristics and time-dependent factors associated with use of selected strategy (direct extubation, direct tracheostomy, Initial SBT) to discontinue mechanical ventilation
기간: Through study completion (approximately 4 years)
We will use cox proportion hazards modelling to identify baseline characteristics and time-dependent factors (development of adult respiratory distress syndrome, heart failure, acute kidney injury requiring dialysis) associated with the use of selected discontinuation strategies (direct extubation, direct tracheostomy, Initial SBT)
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and total duration of ventilation.
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and the total duration of ventilation.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and ICU mortality.
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and ICU mortality.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and hospital mortality.
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and hospital mortality.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and the proportion of patients off of the ventilator at day 28
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and the proportion of patients off the ventilator at day 28.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and the proportion of patients out of the ICU at day 28.
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and the proportion of patients out of the ICU at day 28.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and ICU LOS.
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and ICU LOS (total and among survivors and non survivors.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and hospital LOS.
기간: Through study completion (approximately 4 years)
Describe the associations between SBT outcome (success/failure) and hospital LOS (total and among survivors and non survivors.
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and ICU readmission.
기간: Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and ICU readmission (during the current hospitalization).
Through study completion (approximately 4 years)
Association between initial SBT outcome (success/failure) and reintubation.
기간: Through study completion (approximately 4 years)

Describe the associations between SBT outcome (success/failure) and reintubation (or repeat ventilation following disconnection in tracheostomized patients) within 48 hours of extubation

c) Describe the association between different SBT techniques on clinical outcomes and d) Describe the association between use of selected humidification strategies and clinical outcomes.

Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on the total duration of ventilation.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on the total duration of ventilation.
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on ICU mortality.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on ICU mortality.
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on hospital mortality.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on hospital mortality.
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on the proportion of patients off the ventilator at day 28.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on the proportion of patients off the ventilator at day 28.
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on the proportion of patients out of the ICU at day 28.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on the proportion of patients out of the ICU at day 28.
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on ICU LOS.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on ICU LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on hospital LOS.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on hospital LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on ICU readmission.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on ICU readmission (during the current hospitalization).
Through study completion (approximately 4 years)
Differences in clinical outcomes between patients who undergo an SBT early versus later in their ICU stay on reintubation.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on reintubation (or repeat ventilation following disconnection in tracheostomized patients) within 48 hours of extubation.
Through study completion (approximately 4 years)
Association between different SBT techniques and total duration of ventilation.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on the total duration of ventilation.
Through study completion (approximately 4 years)
Association between different SBT techniques and ICU mortality.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on ICU mortality.
Through study completion (approximately 4 years)
Association between different SBT techniques and hospital mortality.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on hospital mortality.
Through study completion (approximately 4 years)
Association between different SBT techniques and the proportion of patients off the ventilator at day 28.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on the proportion of patients off the ventilator at day 28.
Through study completion (approximately 4 years)
Association between different SBT techniques and the proportion of patients out of the ICU at day 28.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on the proportion of patients out of the ICU at day 28.
Through study completion (approximately 4 years)
Association between different SBT techniques and ICU LOS.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on ICU LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Association between different SBT techniques and hospital LOS.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on hospital LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Association between different SBT techniques and ICU readmission.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on ICU readmission (during the current hospitalization).
Through study completion (approximately 4 years)
Association between different SBT techniques and reintubation.
기간: Through study completion (approximately 4 years)
Associations between use of different SBT technique (e.g., Pressure Support, T-piece) and the impact on reintubation (or repeat ventilation following disconnection in tracheostomized patients) within 48 hours of extubation
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and the total duration of ventilation.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on the total duration of ventilation.
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and ICU mortality.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on ICU mortality.
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and hospital mortality.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on hospital mortality.
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and the proportion of patients off the ventilator at day 28.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on the proportion of patients off the ventilator at day 28.
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and the proportion of patients out of the ICU at day 28.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on the proportion of patients out of the ICU at day 28.
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and ICU LOS.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on ICU LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and hospital LOS.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on hospital LOS (total and among survivors and non survivors).
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and ICU readmission.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on ICU readmission (during the current hospitalization).
Through study completion (approximately 4 years)
Association between use of selected humidification strategies and reintubation.
기간: Through study completion (approximately 4 years)
Associations between use of different humidification strategies (e.g., Heat and Moisture Exchanger, heated humidifier) and the impact on reintubation (or repeat ventilation following disconnection in tracheostomized patients) within 48 hours of extubation.
Through study completion (approximately 4 years)

기타 결과 측정

결과 측정
측정값 설명
기간
Predictors of initial SBT outcome.
기간: Through study completion (approximately 4 years)
Describe important predictors (patient, clinician, SBT, institutional and regional-related) of initial SBT outcome (SBT success and failure) using a single regression analysis. One analysis will be conducted to describe significant predictors.
Through study completion (approximately 4 years)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Karen E.A. Burns, MD, FRCPC, MSc, St. Michael's Hospital, Li Ka Shing Knowledge Institute, University of Toronto

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2013년 11월 4일

기본 완료 (실제)

2016년 12월 17일

연구 완료 (실제)

2016년 12월 17일

연구 등록 날짜

최초 제출

2019년 5월 3일

QC 기준을 충족하는 최초 제출

2019년 5월 16일

처음 게시됨 (실제)

2019년 5월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 4월 2일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 3월 30일

마지막으로 확인됨

2021년 3월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • 11-024

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

3
구독하다