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Transfusion Strategies in Weaning Patients

Liberal Versus Restrictive Transfusion Management in Patients Being Weaned From Prolonged Mechanical Ventilation

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01256645
Acronym
WTT
Enrollment
120
Registered
2010-12-08
Start date
2010-12-31
Completion date
2013-02-28
Last updated
2010-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weaning Patients

Keywords

weaning, mechanical ventilation, blood transfusion, spontaneous breathing trials

Brief summary

The aim of this study is to determine, whether a liberal transfusion strategy is helpful to liberate patients from prolonged invasive mechanical ventilation. Patients who are difficult to wean according to the criteria by Boles et al \[1\] are limited by the capacity of their respiratory muscles. Improved oxygen delivery achieved by blood transfusions however is known to decrease the work of breathing \[2\] and thus in theory can improve weaning success \[3\]. This study is designed as a prospective, randomized, open labeled blinded End-point evaluation to test the hypothesis that a liberal transfusion strategy decreases the time needed for weaning. 1. Boles, JM, J Bion, A Connors, M Herridge, B Marsh, C Melot, R Pearl, H Silverman, M Stanchina, A Vieillard-BaronandT Welte, Weaning from mechanical ventilation. Eur Respir J, 2007. 29(5): p. 1033. 2. Schonhofer, B, M Wenzel, M GeibelandD Kohler, Blood transfusion and lung function in chronically anemic patients with severe chronic obstructive pulmonary disease. Crit Care Med, 1998. 26(11): p. 1824. 3. Schonhofer, B, H BohrerandD Kohler, Blood transfusion facilitating difficult weaning from the ventilator. Anaesthesia, 1998. 53(2): p. 181.

Detailed description

Liberation from invasive mechanical ventilation has a huge impact on quality of life and healthcare expenses. Weaning is more difficult and complex in patients who have been ventilated for a longer time (i.e. more than seven days) or have undergone multiple failed weaning attempts and thus are classified weaning category three according to Boles at al. \[1\] Current national and international guidelines are in favour of a rather restrictive transfusion regime. This recommendation is mainly based on the work of Hebert et al. \[2\] where no benefit or a liberal transfusion approach could be found. Patients in the Hebert study however had become acutely ill and did not show any impairment or dysfunction of the respiratory muscles Weaning class 3 patients however suffer from an overload of their respiratory muscles either cause by an increased load or decreased capacity. In either instance unloading of the respiratory muscles is key to improve the capability of spontaneous breathing. One possible way to achieve this goal is to improve oxygen delivery. Oxygen delivery is determined by the cardiac output times the oxygen content of the blood. The latter is mainly determined by the haemoglobin concentration and the oxygen saturation (Hb x 1.34 x SaO2 + PO2 x 0.003). Previous studies have shown that in patients with a strained respiratory pump blood transfusions improve the work of breathing \[3\]. A more liberal transfusion strategy therefore might improve the weaning outcome ventilator dependant patients \[4\] This study is designed as a prospective, randomized, open labeled blinded End-point evaluation to test the hypothesis that a liberal transfusion strategy decreases the time needed for weaning. Patients who are anemic (Hb \< 9 mg/dl) and were admitted to our specialized weaning unit are either randomized to a conservative or liberal transfusion regime if they are agreed to participate. The goal in the liberal transfusion group is to keep the Hb at \> 12 mg/dl and transfusions are given in single units until this threshold is achieved. Patients then undergo routine weaning procedures consistent of daily or multiple daily weaning trials paired with intermittent ventilation targeted do rest the respiratory muscles. Daily physiologic data are recorded as well as adverse events. Primary outcome is the time needed to wean the patients off invasive mechanical ventilation, mortality is a secondary criterium. The study is planned to include 120 patients in blocks of 40 patients. Interim analysis will be performed after each block and the study will be terminated if a significant result is achieved. 1. Boles, JM, J Bion, A Connors, M Herridge, B Marsh, C Melot, R Pearl, H Silverman, M Stanchina, A Vieillard-BaronandT Welte, Weaning from mechanical ventilation. Eur Respir J, 2007. 29(5): p. 1033. 2. Hebert, PC, G Wells, MA Blajchman, J Marshall, C Martin, G Pagliarello, M Tweeddale, I SchweitzerandE Yetisir, A multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. Transfusion Requirements in Critical Care Investigators, Canadian Critical Care Trials Group. N Engl J Med, 1999. 340(6): p. 409. 3. Schonhofer, B, M Wenzel, M GeibelandD Kohler, Blood transfusion and lung function in chronically anemic patients with severe chronic obstructive pulmonary disease. Crit Care Med, 1998. 26(11): p. 1824. 4. Sato, T, EJ BedrickandC Tsai, Model Selection for Multivariate Regression in Small Samples. Biometrics, 1998. 54(1): p. 391.

Interventions

OTHERblood transfusion

application of single units of red blood cell transfusions

Sponsors

Krankenhaus Kloster Grafschaft
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hb \< 9g/dl * Prolonged mechanical ventilation for \> 14 days * Hemodynamically stable / no acute ongoing disease * weainingfailure * spontaneous breathing capacity less than four hours * Euvolemia * Consent

Exclusion criteria

* Age \< 18 years * Pregnancy * known blood incompatibility * acute indications to give blood products or previous transfusions within the last three days * previously known chronic anemia * coma * ongoing dialysis

Design outcomes

Primary

MeasureTime frameDescription
Time to sucessfull weaning14 daysTime between randomisation an sucessfull liberation from invasive mechanical ventilation

Secondary

MeasureTime frameDescription
mortalitywithin hospitalmortality during the hospital stay

Countries

Germany

Contacts

Primary ContactDieter Köhler, Prof
d.koehler@fkkg.de+49 2972
Backup ContactDominic Dellweg, M.D.
d.dellweg@fkkg.de+49 2972

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026