New Integrated Weaning Indexes (NIWIs)

January 28, 2013 updated by: Amir Vahedian-Azimi, Baqiyatallah Medical Sciences University

New Integrated Weaning Indexes From Mechanical Ventilation: A Prospective Clinical Trial

The purpose of this study is to determine whether introducing the new weaning indexes can predict better than traditional ones?

Study Overview

Status

Completed

Detailed Description

The study was divided into two parts: First, the threshold values of the indexes that discriminated best between successful weaning and weaning failure were determined in training set (n = 208). Second, the accuracy of each index was scrutinized prospectively in an additional group of patients (prospective-validation data set, n = 967). One thousand one hundred and seventy-five patients who were on mechanical ventilation for more than 24 hours were evaluated.Informed consent was obtained from each patient, whenever possible, or from the patient's next of kin. The samples were selected using a simple random sampling method in which the entry number of eligible patients was considered to be the sampling ID number. Using Random Allocation Software (RAS), random numbers were generated to select the study participant.

The ventilators used were Evita XL and Evita 4 edition (Draeger, Lubeck, Germany).

According to a protocol that have introduced in two studies, the protocol established. All of the mechanically ventilated patients undergoing assessment for extubation undergo a daily SBT if predetermined eligibility criteria for weaning are met . According to this protocol, sedation would be discontinued before evaluation of weaning. Patients who meet these criteria are initially placed on SBT (continuous positive airway pressure of 5 mmHg, FiO2≤0.4) for 3 minutes to obtain weaning parameters. If the Oxygen saturation is ≥ 92% on pulse oximetry with FiO2≤0.4 and RSBI <104 breaths/minute/L, patients are continued on the SBT for 30 to 120 minutes. All clinical and ventilator parameters are monitored closely for signs of respiratory distress (respiratory rate > 30 breaths/minute, SaO2< 90%, heart rate > 140 breaths/minute, or a sustained increase or decrease of heart rate of >20%, blood pressure>200 mm Hg or <80 mm Hg, and agitation, diaphoresis, or anxiety). At the end of the SBT, the RSBI is measured again, ABG is obtained, and the predetermined values are calculated and measured. The decision to return to mechanical ventilation made by the two subspecialists in pulmonary and lung diseases, who were chief supervisor of both ICU in two cities (who were completely blind to the study and the results of the indexes evaluated), based on airway competence (cough, sputum production, neurologic status, level of consciousness, and maximal inspiratory pressure). Patients who remain extubated at 48 hours are classified as having had a successful extubation. Baseline demographics, initial diagnosis, and pre-extubation clinical, ventilator, laboratory, and radiographic data are collected for each patient.

To assess the prognostic value of new indices, receiver operator characteristic (ROC) curves was drawn for each formula in addition for other conventional criteria used in this area. For each ROC curve analysis, sensitivity, Specificity, Positive Predictive Value, Negative Predictive Value, diagnostic accuracy, likelihood ratio of a positive test (LR+) and the likelihood ratio of a negative test (LR-), probability for weaning success when test is positive and probability for weaning success when test is negative of the indexes were used to predict the weaning outcome in the prospective-validation data set.

Hanley and McNeil method was used to calculate the area under curve (AUC) for each formula and then the methods developed by the same authors were used to compare these AUCs. Bayes' theorem was used to compute the weaning outcome the probability for weaning success when test is positive and negative (post-test probability) in the prospective-validation data set to assess the perform

Study Type

Observational

Enrollment (Actual)

1175

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

One thousand one hundred and seventy-five patients who were on mechanical ventilation for more than 24 hours were evaluated.

Description

Inclusion Criteria:

  • Patients (both males and females) more than 24 hours in mechanical ventilation in weaning process.

Exclusion Criteria:

  1. Hypercapnic respiratory failure attributable to COPD exacerbation or post-respiratory arrest;
  2. underlying moderate to severe obstructive airways disease, defined as forced expiratory volume in 1 second of < 50% of predicted value, or baseline PaCO2 > 50 mmHg,
  3. concurrent neurological and neuromuscular or drug intoxication contributing to respiratory failure; and finally younger than 18 years of age

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Better accuracy in predicting weaning outcome
Time Frame: Four years
Four years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Adequate prognosis
Time Frame: Four years

The following measurements were taken for weaning indexes:

  1. RSBI
  2. NIF
  3. P0.1
  4. CROP
  5. IWI
  6. PaO2: PALVO2 ration (PPR)
  7. PaO2:FiO2 ratio (PFR)
  8. RR
  9. VT
  10. MV
  11. C Dynamic
  12. C Static
  13. Pimax
  14. PaO2
  15. PaCO2
  16. FiO2
  17. SaO2
  18. Respiratory index
  19. Formula one [(PPR)/ (RSBI*FiO2)]
  20. Formula two [(PPR)/ (RSBI*FiO2*P0.1)]
  21. Formula three [(PPR)*(NIF)/ (RSBI*FiO2)]
  22. Formula four [(PPR)*(NIF)/ (RSBI*FiO2*P0.1)]
  23. Formula five [(NIF)/ (P0.1)]
  24. Formula six [(SaO2)/ ((P (A-a) O2)*RSBI*FiO2)]
  25. Formula seven [(SaO2)/ ((P (A-a) O2)*RSBI*FiO2*P0.1)]
  26. Formula eight [(SaO2*NIF)/ ((P (A-a) O2)*RSBI*FiO2)]
  27. Formula nine [(SaO2*NIF)/ ((P (A-a) O2)*RSBI*FiO2*P0.1)]
  28. Formula ten [(SaO2)/ ((P (A-a) O2)*P0.1)] These are newly proposed indexes, used in some hospitals in Iran.
Four years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2007

Primary Completion (Actual)

January 1, 2008

Study Completion (Actual)

December 1, 2012

Study Registration Dates

First Submitted

January 23, 2013

First Submitted That Met QC Criteria

January 28, 2013

First Posted (Estimate)

January 30, 2013

Study Record Updates

Last Update Posted (Estimate)

January 30, 2013

Last Update Submitted That Met QC Criteria

January 28, 2013

Last Verified

January 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • BMSU & TUMS

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Mechanical Ventilation Weaning

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